US20100330150A1 - Orally Disintegrating Tablet Compositions Comprising Combinations of High and Low-Dose Drugs - Google Patents

Orally Disintegrating Tablet Compositions Comprising Combinations of High and Low-Dose Drugs Download PDF

Info

Publication number
US20100330150A1
US20100330150A1 US12/772,770 US77277010A US2010330150A1 US 20100330150 A1 US20100330150 A1 US 20100330150A1 US 77277010 A US77277010 A US 77277010A US 2010330150 A1 US2010330150 A1 US 2010330150A1
Authority
US
United States
Prior art keywords
coating
dose drug
drug
dose
low
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/772,770
Inventor
Gopi Venkatesh
Michael Gosselin
James Clevenger
Jin-Wang Lai
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Adare Pharma Solutions Inc
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US12/772,770 priority Critical patent/US20100330150A1/en
Application filed by Individual filed Critical Individual
Assigned to EURAND, INC. reassignment EURAND, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CLEVENGER, JAMES, GOSSELIN, MICHAEL, LAI, JIN-WANG, VENKATESH, GOPI
Publication of US20100330150A1 publication Critical patent/US20100330150A1/en
Assigned to BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT reassignment BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT SECURITY AGREEMENT Assignors: EURAND, INCORPORATED
Assigned to APTALIS PHARMATECH, INC. reassignment APTALIS PHARMATECH, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: EURAND, INCORPORATED
Assigned to APTALIS PHARMATECH, INC. reassignment APTALIS PHARMATECH, INC. RELEASE OF LIEN ON PATENTS Assignors: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Assigned to BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT reassignment BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT PATENT SECURITY AGREEMENT Assignors: APTALIS PHARMA CANADA INC., APTALIS PHARMA US, INC., APTALIS PHARMATECH, INC.
Assigned to APTALIS PHARMA US, INC., APTALIS PHARMATECH, INC., APTALIS PHARMA CANADA INC. reassignment APTALIS PHARMA US, INC. TERMINATION AND RELEASE Assignors: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Assigned to ADARE PHARMACEUTICALS, INC. reassignment ADARE PHARMACEUTICALS, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: APTALIS PHARMATECH, INC.
Assigned to BANK OF MONTREAL reassignment BANK OF MONTREAL U.S. PATENT SECURITY AGREEMENT Assignors: ADARE PHARMACEUTICALS, INC.
Assigned to ADARE PHARMACEUTICALS USA, INC., ADARE PHARMACEUTICALS, INC., ADARE DEVELOPMENT I, L.P. reassignment ADARE PHARMACEUTICALS USA, INC. RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAMES 037246/0313, 047807/0967, 053474/0276 Assignors: BANK OF MONTREAL, AS COLLATERAL AGENT
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4415—Pyridoxine, i.e. Vitamin B6
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/485—Morphinan derivatives, e.g. morphine, codeine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/5415—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with carbocyclic ring systems, e.g. phenothiazine, chlorpromazine, piroxicam
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/60—Salicylic acid; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
    • A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
    • A61K9/2081—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets with microcapsules or coated microparticles according to A61K9/50
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5005—Wall or coating material
    • A61K9/5021—Organic macromolecular compounds
    • A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
    • A61K9/5042—Cellulose; Cellulose derivatives, e.g. phthalate or acetate succinate esters of hydroxypropyl methylcellulose
    • A61K9/5047—Cellulose ethers containing no ester groups, e.g. hydroxypropyl methylcellulose
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
    • A61K9/5078—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings with drug-free core
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5084—Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • opioid analgesics such as hydrocodone.
  • opioid analgesics such as hydrocodone.
  • opioid analgesics such as hydrocodone.
  • a non-opioid analgesic such as acetaminophen, aspirin, ibuprofen, etc.
  • Other medical conditions such as diabetes (hyperglycemia), cardiovascular disease, and schizophrenia are also effectively treated with drug combinations.
  • the need to administer multiple dosage forms can result in problems such as patient compliance issues or dosage administration errors.
  • Vicodin® is an immediate-release (IR) tablet containing 5 mg of hydrocodone bitartrate and 500 mg of acetaminophen, intended for the management of severe pain.
  • IR immediate-release
  • it is very difficult to reproducibly prepare homogeneous blends of hydrocodone and acetaminophen at the required 1:100 weight ratio e.g., with a content uniformity having an RSD of 6% or less, as required by regulatory agencies worldwide).
  • Orally disintegrating tablet (ODT) dosage forms have been introduced to address such problems, because ODTs rapidly dissolve or disintegrate in the buccal cavity and the resulting slurry or suspension of the drug is more readily swallowed by the patient. Such dosage forms are also more convenient because they need not be administered with water.
  • the ODT dosage form disintegrates in the oral cavity of the patient, the disintegrated ODT must be palatable.
  • the drug-containing particles comprising the ODT must be taste-masked, e.g., by coating the drug-containing particles with a polymeric membrane to prevent release of the drug in the oral cavity.
  • taste-masking is slower dissolution of the drug(s) from effectively taste-masked microparticles. The more bitter the drug, the thicker the taste-masking coating required and hence, the slower the drug release from the taste-masked drug-containing particles.
  • the very process of effectively taste-masking the drug-containing particles results in a substantially slower drug release, with concomitant slower systemic absorption of the drug in the gastrointestinal tract.
  • slower drug release is a particular problem for ODT dosage forms which are intended to be bioequivalent to a reference listed immediate-release (IR) dosage form of the drug, for example bioequivalent to conventional tablet or effervescent tablet based IR dosage forms having a T max of less than an hour, and rapid-onset of action.
  • IR immediate-release
  • ODT compositions containing combinations of two or more drugs e.g., a high-dose/low-dose drug formulation
  • this problem is particularly acute, because the different drug components of the combination ODT may require different levels of taste-masking depending on the degree of bitterness of the drugs (i.e., drugs with low bitterness levels may require little or no taste-masking, while highly bitter drugs may require substantial taste-masking layers).
  • taste-masking layers reduce the release rate of poorly soluble drugs more than for more soluble drugs.
  • an ODT composition comprising taste-masked low-dose drug particles combined with sustained release coated high-dose drug particles may be more desirable.
  • ODTs must rapidly disintegrate on contact with the saliva in the oral cavity while also providing sufficient tablet hardness and strength sufficient to withstand attrition during packaging, storage, transportation, distribution, and end use, and also provide acceptable organoleptic properties (e.g., be palatable as described above, and exhibit a smooth (non-gritty) mouthfeel), and acceptable pharmacokinetic properties (i.e., rapid onset, C max , AUC properties similar to the reference listed drugs). Achieving all of these properties is often quite difficult because thicker taste-masking layers may be required for adequate taste-masking of more soluble and/or more bitter drugs, which may make it difficult to obtain the required rapid drug release.
  • acceptable organoleptic properties e.g., be palatable as described above, and exhibit a smooth (non-gritty) mouthfeel
  • acceptable pharmacokinetic properties i.e., rapid onset, C max , AUC properties similar to the reference listed drugs.
  • compositions comprising at least a high-dose and a low-dose drug, particularly in the form of an ODT, is quite difficult and requires the balancing of many different and often competing requirements.
  • the present invention is directed to a pharmaceutical composition
  • a pharmaceutical composition comprising a plurality of modified-release coated high-dose/low-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
  • the present invention is directed to a pharmaceutical composition
  • a pharmaceutical composition comprising a plurality of taste-masked non-opioid analgesic drug/opioid analgesic drug-containing microparticles, wherein the drug-containing microparticles comprise:
  • the present invention is directed to a pharmaceutical composition
  • a pharmaceutical composition comprising a plurality of high-dose/low-dose drug-containing microparticles in combination with high-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
  • sustained-release coating layer comprises a water-insoluble polymer optionally in combination with one or more of a water soluble or enteric polymer; thereby imparting taste-masking and/or sustained release properties to the high-dose drug-containing microparticles; and the taste-masking layer disposed over the low-dose drug-containing microparticles comprises a water-insoluble polymer optionally in combination with a gastrosoluble polymer or a gastrosoluble pore-former.
  • the present invention is directed to a pharmaceutical composition
  • a pharmaceutical composition comprising a plurality of modified-release coated high-dose/low-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
  • the present invention is directed to an ODT dosage form comprising the combination of one of the pharmaceutical compositions of the present invention, rapidly dispersing microgranules, and optionally a second population of high-dose drug containing particles comprising a high-dose drug-containing core coated with a modified-release coating layer.
  • the present invention is directed to a method for preparing the pharmaceutical compositions disclosed herein, comprising:
  • the present invention is directed to a method for preparing an ODT pharmaceutical composition as disclosed herein, further comprising:
  • the present invention is directed to a method of treating a patient subject to a disease or condition, comprising administering a therapeutically effective amount of the high-dose drug and low-dose drug-containing compositions of the present invention to the patient in need thereof.
  • FIG. 1 illustrates a schematic of one embodiment of a modified release coated microparticle comprising a high-dose drug-containing core, as well as a taste-masked low-dose/high-dose drug-containing microparticle.
  • FIG. 2 illustrates the plasma concentration-time profiles for acetaminophen of hydrocodone bitartrate/acetaminophen tablets observed in the pilot PK (pharmacokinetics) study.
  • FIG. 3 illustrates the plasma concentration-time profiles for hydrocodone bitartrate of hydrocodone bitartrate/acetaminophen tablets observed in the pilot PK (pharmacokinetics) study.
  • FIG. 4 illustrates the plasma concentration-time profiles for acetaminophen of Acetaminophen ODTs versus Panadol® observed in the pilot PK (pharmacokinetics) study.
  • the present invention is directed to pharmaceutical compositions comprising a plurality of modified-release coated high-dose/low-dose drug-containing microparticles as described herein.
  • the compositions of the present invention provide combination high-dose drug/low-dose drug-containing oral dosage forms meeting one or more of the following specifications:
  • drug includes a pharmaceutically acceptable and therapeutically effective compound, pharmaceutically acceptable salts, stereoisomers and mixtures of stereoisomers, solvates (including hydrates), polymorphs, and/or esters thereof.
  • pharmaceutically acceptable salts pharmaceutically acceptable salts, stereoisomers and mixtures of stereoisomers, solvates (including hydrates), polymorphs, and/or esters thereof.
  • the reference encompasses the base drug, pharmaceutically acceptable salts, stereoisomers and mixtures of stereoisomers, solvates (including hydrates), polymorphs, and/or esters thereof, unless otherwise indicated.
  • sealant layer or “coating” as used herein are synonymous.
  • sealant layer or “coating” as used herein are synonymous with sealant coating, drug coating, etc.
  • orally disintegrating tablet refers to a tablet which disintegrates rapidly in the oral cavity of a patient after administration, without the need for chewing.
  • the rate of disintegration can vary, but is faster than the rate of disintegration of conventional solid dosage forms (e.g., tablets or capsules) which are intended to be swallowed immediately after administration, or chewable solid dosage forms.
  • Orally disintegrating compositions of the present invention can contain pharmaceutically acceptable ingredients which swell, dissolve or otherwise facilitate the disintegration or dissolution of the ODT composition.
  • Such ingredients can include pharmaceutical disintegrant such as crospovidone, water-soluble sugar alcohol such as mannitol, a saccharide such as lactose, or a mixture thereof, a water-soluble binder such as povidone, a meltable solid (e.g., a hydrophobic wax such as polyethylene glycol, glyceryl behenate, stearic acid, hydrogenated castor oil, etc.) which can release the drugs upon entering the stomach.
  • Orally disintegrating compositions of the present invention may be in the form of a tablet, a minitablet, a capsule or a monodose sachet, or a dry powder for reconstitution.
  • the amount of the various coatings or layers described herein is expressed as the percentage weight gain of the particles or beads provided by the dried coating, relative to the initial weight of the particles or beads prior to coating.
  • a 10% coating weight refers to a dried coating which increases the weight of a particle by 10%.
  • immediate-release refers to release of greater than or equal to about 50%, or greater than about 75%, or greater than about 90%, or greater than about 95% of the drug within about 2 hours, more particularly within about one hour following administration of the dosage form.
  • substantially disintegrates means a level of disintegration amounting to disintegration of at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or about 100% disintegration of the ODT composition.
  • modified-release coating encompasses coatings that delay release, sustain release, extend release, prevent release, and/or otherwise prolong the release of a drug relative to formulations lacking such coatings which release a drug relatively quickly (i.e., “immediate release” compositions).
  • controlled-release encompasses “sustained release,” “extended release,” “delayed release,” and “timed, pulsatile release.”
  • lag-time refers to a particular type of “controlled release” coating in which the lag time coating delays release of a drug after administration.
  • controlled release is also used interchangeably with “modified release.”
  • controlled-release particle refers to a particle showing one or more controlled-release properties, as described herein.
  • controlled-release particle also refers to a drug-containing particle coated with one or more controlled-release coatings, as described herein.
  • the term “substantially masks the taste” in reference to the taste-masking layer of the IR particles (when present) refers to the ability of the taste-masking layer to substantially prevent release of a bitter tasting drug in the oral cavity of a patient.
  • a taste-masking layer which “substantially masks” the taste of the drug typically releases less than about 10% of the drug in the oral cavity of the patient, in other embodiments, less than about 5%, less than about 1%, less than about 0.5%, less than about 0.1%, less than about 0.05%, less than about 0.03%, less than about 0.01% of the drug.
  • the taste-masking properties of the taste-masking layer of the compositions of the present invention can be measured in vivo (e.g., using conventional organoleptic testing methods known in the art) or in vitro (e.g., using dissolution tests as described herein).
  • the skilled artisan will recognize that the amount of drug release associated with a taste-masking layer than “substantially masks” the taste of a drug is not limited to the ranges expressly disclosed herein, and can vary depending on other factors, such as the perceived the bitterness of the drug and the presence of other flavoring agents in the composition.
  • substantially modifies release in reference to a layer refers to the ability of the layer to provide modified release properties, i.e., delay release, sustain release, extend release, prevent release, and/or otherwise prolong the release of a drug relative to formulations lacking such coatings which release a drug relatively quickly (i.e., “immediate release” compositions), as described herein.
  • sustained-release refers to the property of slow release of a drug from a drug-containing core particle, without an appreciable lag time.
  • sustained-release coating or “SR coating” refers to a coating showing sustained-release properties.
  • sustained-release particle refers to a drug-containing particle showing sustained-release properties.
  • a sustained-release coating comprises a water-insoluble polymer and optionally a water-soluble polymer.
  • An SR coating can optionally contain a plasticizer or other ingredients that do not interfere with the “sustained-release” properties of the coating.
  • timed, pulsatile release refers to the property of modified release of a drug after a pre-determined lag time.
  • timed, pulsatile-release coating or “TPR coating” refers to a coating showing timed, pulsatile-release properties.
  • timed, pulsatile-release particle refers to a drug-containing particle showing timed, pulsatile-release properties.
  • a lag time of from at least about 2 to about 10 hours is achieved by coating the particle with, e.g.
  • a TPR coating can optionally contain a plasticizer or other ingredients which do not interfere with the “timed, pulsatile release” properties of the coating.
  • modified-release coated drug-containing microparticles refers generally to drug-containing microparticles (e.g., crystals, granules, pellets produced by controlled spheronization, or drug layered particles/beads) coated with one or more functional polymers to achieve effective taste-masking and/or extended/sustained release properties.
  • drug-containing microparticles e.g., crystals, granules, pellets produced by controlled spheronization, or drug layered particles/beads
  • functional polymers e.g., a functional polymers to achieve effective taste-masking and/or extended/sustained release properties.
  • high-dose/low-dose drug-containing microparticles this term refers to modified-release coated high-dose/low-dose drug containing microparticles as described herein.
  • disposed over means that a second material is deposited over a first material, wherein the second material may or may not be in direct physical contact with the first material. Thus it is possible, but not necessary, that an intervening material lies between the first and second materials.
  • Combination drug therapies are increasingly useful in treating diseases or conditions which are advantageously treated by the administration of two or more drugs.
  • pain treatments benefit from the administration of low doses of opioid analgesics combined with relatively high-doses of non-opioid analgesics (e.g., an NSAID), which effectively treat moderate to severe pain, yet reduce the amount of potentially habit forming opioid drug administered.
  • non-opioid analgesics e.g., an NSAID
  • the combination of drugs can interact synergistically to provide greater clinical benefits compared to either drug administered individually.
  • the need to administer multiple dosage forms, each containing a single drug can result in problems such as reduced patient compliance, errors in administering the proper doses of each drug, etc.
  • the present invention is directed to pharmaceutical compositions comprising a plurality of taste-masked high-dose/low-dose drug-containing microparticles, each containing both the high-dose drug (or drugs) and the low-dose drug (or drugs).
  • the core of the taste-masked high-dose/low-dose drug-containing microparticles comprises the high-dose drug, and the low-dose drug is provided in a low-dose drug layer disposed over the high-dose drug-containing core.
  • Suitable core compositions include particles of the high-dose drug itself (e.g., formed by recrystallization or precipitation of the high-dose drug from solution, or by milling and sieving the high-dose drug, etc., such that high-dose drug-containing particles of a desired particle size and particle size distribution are obtained).
  • the core can comprise a granulate comprising particles of the high-dose drug in combination one or more pharmaceutically acceptable excipients (e.g., lactose, mannitol, microcrystalline cellulose, etc.) and an optional binder, prepared by wet or dry granulation.
  • the core can comprise extruded and spheronized particles comprising the high-dose drug (e.g., in combination with suitable pharmaceutically acceptable excipients as described herein) or high-dose drug pellets are produced by controlled spheronization in a Granurex VEC-35 or VEC-40 from Vector Corporation, and these pellets are coated with polymers or polymer blends providing target drug release profiles suitable for once- or twice-daily dosing regimen.
  • the core comprises drug layered beads—i.e., an inert core (e.g., sugar spheres, microcrystalline cellulose, mannitol-microcrystalline cellulose, silicon dioxide, etc.) layered with the high-dose drug and an optional binder.
  • the core can comprise the high-dose drug in combination with pharmaceutically acceptable excipients, compressed into “minitabs” having a particle diameter in the range of about 2-5 mm.
  • the core comprises particles of the high-dose drug.
  • the core has an average particle size of less than about 500 ⁇ m, or less than about 400 ⁇ m, or less than about 300 ⁇ m, or less than about 200 ⁇ m.
  • Any pharmaceutically acceptable high-dose/low-dose drug combination that is efficacious in the treatment of disease states or conditions including, for example, cardiovascular diseases, diabetes, moderate to severe pain, gastrointestinal disorders, etc. can be selected in accordance with certain embodiments of the present invention to create pharmaceutical compositions comprising one or more populations of modified release coated high-dose/low-dose drug-containing microparticles exhibiting desired in vitro/in vivo drug release profiles.
  • any pharmaceutically acceptable polymeric binder which is compatible with the high-dose drug and/or other components of the composition may be used in preparing the high-dose drug-containing cores (e.g., a binder used in forming a granulate, in forming drug-layered beads, etc.).
  • Suitable polymeric binders include for example, polymers selected from the group consisting of hydroxypropylcellulose, povidone, methylcellulose, hydroxypropyl methylcellulose, carboxyalkylcelluloses, polyethylene oxides, polysaccharides, acacia, alginic acid, agar, calcium carrageenan, sodium carboxymethylcellulose, microcrystalline cellulose, dextrin, ethylcellulose, gelatin, liquid glucose, guar gum, hydroxypropyl methylcellulose, methylcellulose, pectin, PEG, povidone, pregelatinized starch, etc.
  • the high-dose drug-containing core can be coated directly with the low-dose drug layer, or can be first coated with a sealant layer.
  • Suitable sealant layers comprise a hydrophilic water-soluble polymer.
  • suitable hydrophilic polymers include hydrophilic hydroxypropyl cellulose (e.g., Klucel® LF), hydroxypropyl methylcellulose or hypromellose (e.g., Opadry® Clear or PharmacoatTM 603), vinylpyrrolidone-vinylacetate copolymer (e.g., Kollidon® VA 64 from BASF), and ethylcellulose, e.g. low-viscosity ethylcellulose.
  • the compositions of the present invention do not require a sealant layer coated directly over the core.
  • the sealant layer can be applied at a coating weight of about 1% to about 10%, for example about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10%, inclusive of all ranges and subranges therebetween.
  • compositions of the present invention are intended to disintegrate in the oral cavity of the patient upon administration (e.g., the ODT dosage form as described herein).
  • the high-dose drug and/or the low-dose drug has unpleasant sensory properties (e.g., is bitter tasting)
  • the high-dose drug-containing core and/or the low-dose drug-containing layer is taste-masked to prevent the patient from tasting the high-dose and/or low dose drug, e.g. by coating the high-dose drug-containing core and/or the low-dose drug-containing layer with a taste-masking layer.
  • compositions of the present invention can include a single taste-masking layer as described herein disposed between the high-dose drug-containing core and the low-dose drug-containing layer, a single taste-masking layer as described herein disposed over the low-dose drug-containing layer, or two taste-masking layers disposed respectively between the high-dose drug-containing core and the low-dose drug-containing layer and over the low-dose drug-containing layer.
  • the taste-masking layer can be coated directly onto the high-dose drug-containing core and/or the low-dose drug-containing layer, or the high-dose drug-containing core and/or low-dose drug-containing layer can be first coated with a sealant layer (e.g., as described herein) for example to minimize or prevent static charging and/or particle attrition, followed by the taste-masking polymer coating.
  • a sealant layer e.g., as described herein
  • the taste-masking layers can be independently selected from any of the taste-masking layer compositions described herein.
  • Suitable taste-masking layers can comprise a water-insoluble polymer or the combination of a water-insoluble polymer and a gastrosoluble pore-former (e.g., gastrosoluble and pharmaceutically acceptable organic, inorganic, or polymeric materials.
  • a gastrosoluble pore-former e.g., gastrosoluble and pharmaceutically acceptable organic, inorganic, or polymeric materials.
  • the taste-masking layer can be coated onto the high-dose drug-containing core and/or low-dose drug-containing layer by any suitable method, e.g., fluid bed coating or coacervation.
  • the taste-masking polymer coating can be deposited in the core to provide a weight gain (after coating and drying) of from about 3% to about 50%, including about 3%, about 5%, about 7%, about 10%, about 12%, about 15%, about 17%, about 20%, about 22%, about 25%, about 27%, about 30%, about 35%, about 40%, about 45%, or about 50%, inclusive of all ranges and subranges therebetween.
  • Non-limiting examples of suitable water-insoluble polymers include ethylcellulose, cellulose acetate, cellulose triacetate, cellulose acetate butyrate, polyvinyl acetate, neutral methacrylic acid-methylmethacrylate copolymers (e.g., Eudragit RL, RS, and NE30D, etc.), and mixtures thereof.
  • the water-insoluble polymer comprises ethylcellulose.
  • the water-insoluble polymer comprises ethylcellulose with a mean viscosity of 10 cps (e.g., Ethocel Standard 10 Premium) or about 100 cps (Ethocel Standard 100 Premium) in a 5% solution in 80/20 toluene/ethanol, measured at 25° C. with an Ubbelohde viscometer.
  • 10 cps e.g., Ethocel Standard 10 Premium
  • 100 cps Ethocel Standard 100 Premium
  • the taste-masking layer(s) independently comprises the combination of a water-insoluble polymer (as described herein) and a gastrosoluble pore-former.
  • Pore-formers include polymeric and non-polymeric pharmaceutically acceptable gastrosoluble materials.
  • Non-limiting examples of non-polymeric gastrosoluble pore-formers include pharmaceutically acceptable inorganic materials such as calcium carbonate, magnesium carbonate, calcium phosphate, ferric hydroxide, ferric phosphate, magnesium hydroxide, magnesium phosphate, etc.; pharmaceutically acceptable non-polymeric organic materials such as calcium saccharide, calcium succinate, calcium tartrate, magnesium citrate, ferric acetate, etc.; pharmaceutically acceptable gastrosoluble polymers including maltrin, aminoalkyl methacrylate copolymers available under the trade name of Eudragit® (type E100 or EPO), polyvinylacetal diethylaminoacetate e.g., AEA® available from Sankyo Company Limited, Tokyo (Japan), and the like; and mixtures thereof.
  • pharmaceutically acceptable inorganic materials such as calcium carbonate, magnesium carbonate, calcium phosphate, ferric hydroxide, ferric phosphate, magnesium hydroxide, magnesium phosphate, etc.
  • pharmaceutically acceptable non-polymeric organic materials such as calcium
  • the gastrosoluble polymer is a terpolymer based on dimethylaminoethyl methacrylate, butyl methacrylate, and methyl methacrylate.
  • the terpolymer has an average molecular weight of 150,000 and the ratio of the monomers is 1:2:1 of methyl methacrylate, N,N-dimethylaminoethyl methacrylate, and butyl methacrylate, and mixtures thereof.
  • the ratio of water-insoluble polymer to gastrosoluble pore-former ranges from about 95/5 to about 50/50 including about 90/10, about 85/15, about 80/20, about 75/25, about 70/30, about 65/35, about 60/40, or about 55/45.
  • the coating weight of the taste-masking layer comprising a water-insoluble polymer and a gastrosoluble pore-former ranges from about 5% to about 30%, or about 5%-25%, about 5%-20%, about 5%-15%, about 5%-10%, about 10%-30%, about 10%-25%, about 10%-20%, about 10%-15%, about 15%-30%, about 50%-25%, about 15%-20%, about 20%-30%, about 20%-25%, or about 25%-30%.
  • the ratio of the water-insoluble polymer to the gastrosoluble polymer ranges from about 9/1 to about 1/1, including the range of about 6/3 to about 2/1. In other embodiments, the ratio of water-insoluble polymer to gastrosoluble polymer is about 95/5, about 90/10, about 85/15, about 80/20, about 75/25, about 70/30, about 65/35, about 60/40, about 55/45, or about 50/50, inclusive of all values, ranges, and subranges therebetween.
  • the taste-masking layer comprising the combination of a water-insoluble polymer and gastrosoluble polymer has a coating weight of about 10% to about 40% by weight, including the ranges from about 12% to about 30%, about 15% to about 25%, and from about 20% to about 30%.
  • the coating weight of the taste-masking layer comprising a combination of water-insoluble and gastrosoluble polymers is about 10%, about 12.5%, about 13%, about 15%, about 17%, about 18%, about 20%, about 22%, about 24%, about 25%, about 27%, about 30%, about 35%, or about 40%, inclusive of all ranges and subranges therebetween.
  • an extended-release coating layer over the high-dose drug-containing cores in order to modify the release of the high-dose drug.
  • the extended-release coating disposed over the high-dose drug-containing cores can comprise a water-insoluble polymer, thereby providing a sustained release (SR) coating; a water-insoluble polymer in combination with an enteric or water-soluble polymer, thereby providing a timed pulsatile release (TPR) coating.
  • the extended-release coating comprises an enteric polymer disposed on the high-dose drug-containing particle, thereby providing a delayed release (DR) coating.
  • the extended-release coating provides suitable properties (e.g., extended release characteristics, mechanical properties, and coating properties) without the need for a plasticizer.
  • ethylcellulose without a plasticizer is used for coating drug-containing cores by solvent coacervation via phase separation for taste-masking, and or can be applied e.g. from a suitable solvent to provide sustained-release properties.
  • coatings comprising polyvinyl acetate (PVA), neutral and cationic copolymers of acrylate/methacrylate esters (e.g., NE30D and EPO), waxes, etc. can be applied without plasticizers.
  • Non-limiting examples of suitable enteric polymers include cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, hydroxypropyl methylcellulose acetate succinate, polyvinyl acetate phthalate, pH-sensitive methacrylic acid/methylmethacrylate copolymers (e.g., Eudragit® L, S and FS polymers), shellac, and mixtures thereof.
  • non-polymeric enteric materials such as non-polymeric waxes and fatty acid compositions may be used instead of enteric polymers, provided they have the pH sensitive solubility associate with enteric polymers.
  • These enteric polymers may be used as a solution in a solvent mixture or an aqueous dispersion.
  • methacrylic acid copolymers sold under the trademark Eudragit (L100, S100, L30D) manufactured by Rohm Pharma, Cellacefate (cellulose acetate phthalate) from Eastman Chemical Co., Aquateric (cellulose acetate phthalate aqueous dispersion) from FMC Corp., and Aqoat (hydroxypropyl methylcellulose acetate succinate aqueous dispersion) from Shin Etsu K.K.
  • the coating weight of the extended-release coating comprising the combination of a water-insoluble polymer and an enteric polymer ranges from about 10 to 60%, more particularly from about 30% to 60%, including about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, or about 55%, inclusive of all ranges and sub ranges therebetween.
  • the ratio of water insoluble polymer to enteric polymer may vary from about 10:1 to 1:2, more particularly from about 2:1 to 1:1, including about 9:1, about 8:1, about 7:1 about 6:1, about 5:1 about 4:1, about 3:1, about 2:1, or about 1:1.
  • the extended-release layer comprises the combination of a water-insoluble polymer (as described herein) in combination with a water-soluble polymer.
  • suitable water-soluble polymers include polyvinylpyrrolidone (e.g., Povidone K-25), polyethylene glycol (e.g., PEG 400), hydroxypropyl methylcellulose, and hydroxypropylcellulose.
  • the ratio of the water-insoluble polymer to the water-soluble polymer ranges from about 95/5 to about 50/50, including ratios of about 95/5, about 90/10, about 85/15, about 80/20, about 75/25, about 70/30, about 65/35, about 60/40, about 55/45, or about 50/50, inclusive of all ranges and subranges therebetween.
  • the taste-masking layer comprising the combination of a water-insoluble polymer and a water-soluble polymer is deposited over the high-dose drug-containing core at a coating weight of about 3%, about 5%, about 7%, about 10%, about 12%, about 15%, about 17%, about 20%, about 22%, about 25%, about 27%, about 30%, about 35%, about 40%, about 45%, and about 50% by weight, inclusive of all values, ranges, and subranges therebetween.
  • the present invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising modified-release coated high-dose drug cores comprising at least one therapeutic agent or a pharmaceutically acceptable salt, solvate, and/or ester thereof; a water-insoluble polymer (e.g., ethylcellulose), a second optional coating disposed over the first coating, comprising an enteric polymer and optionally a water-insoluble polymer (e.g., ethylcellulose and hypromellose phthalate at a ratio of from about 9:1 to about 5:5).
  • a water-insoluble polymer e.g., ethylcellulose
  • a second optional coating disposed over the first coating, comprising an enteric polymer and optionally a water-insoluble polymer (e.g., ethylcellulose and hypromellose phthalate at a ratio of from about 9:1 to about 5:5).
  • the modified-release or taste-masking layer can be unplasticized or plasticized.
  • drug-containing particles can be taste-masked with ethylcellulose by solvent coacervation via phase separation without requiring a plasticizer, or from suitable pharmaceutically acceptable solvent using a fluid bed coater.
  • Modified-release coatings comprising various polymers such as Eudragit NE30D or various hydrophobic waxes in a fluid bed coater typically do not require a plasticizer.
  • suitable plasticizers include glycerol and esters thereof (e.g., acetylated mono- or diglycerides including commercially available Myvacet® 9-45), glyceryl monostearate, glyceryl triacetate, glyceryl tributyrate, phthalates (e.g., dibutyl phthalate, diethyl phthalate, dimethyl phthalate, dioctyl phthalate, etc.), acetylcitric acid tributyl ester, acetylcitric acid triethyl ester, tributyl citrate, acetyltributyl citrate, triethyl citrate, glyceroltributyrate; diethyl sebacate, dibutyl sebacate, dibutyl adipates, dibutyl azelates, dibutyl benzoates, chlorobutan
  • the amount of plasticizer in the taste-masking layer, relative to the amount of water-insoluble polymer ranges from about 3% to about 30% by weight. In another embodiment, the amount of plasticizer ranges from 10% to about 25% by weight of the water-insoluble polymer. In still other embodiments, the amount of plasticizer relative to the weight of the water-insoluble polymer is about 3%, about 5%, about 7%, about 10%, about 12%, about 15%, about 17%, about 20%, about 22%, about 25%, about 27%, and about 30%, inclusive of all ranges and subranges therebetween.
  • plasticizer based on the polymer or polymers and nature of the coating system (e.g., aqueous or solvent-based, solution or dispersion-based and the total solids).
  • the plasticizer is castor oil.
  • the taste-masking layer can further comprise an anti-tacky agent to reduce aggregation of the taste-masked particles.
  • Suitable anti-tacky agents include talc and/or magnesium stearate.
  • the taste-masking polymer coating comprises a plasticized water-insoluble polymer, such as ethylcellulose (EC-10), at a coating weight of about 5-50% by weight.
  • EC-10 ethylcellulose
  • the modified-release (sustained-release and/or taste-masked) high-dose drug-containing core is coated with a sealant layer, for example to minimize attrition or agglomeration of the taste-masked cores, or alternatively to prevent contact between the high-dose drug in the core and e.g., the low-dose drug in the low-dose drug layer.
  • a sealant layer for example to minimize attrition or agglomeration of the taste-masked cores, or alternatively to prevent contact between the high-dose drug in the core and e.g., the low-dose drug in the low-dose drug layer.
  • the composition and coating weight of the sealant layer is as described herein.
  • the low-dose drug layer is disposed directly over the high-dose drug-containing core, or over a sealant coated core, and/or a taste-masked core.
  • the low-dose drug can be coated onto the high-dose drug-containing core by any suitable method, e.g., pan coating or fluid bed coating using a solution of the low-dose drug (in a pharmaceutically acceptable solvent), optionally in combination with a polymeric binder as described herein.
  • the low-dose drug coating solution can comprise a suitable solvent (e.g.
  • a pharmaceutically acceptable organic solvent such as acetone or alcohol, or aqueous organic solvents
  • a binder e.g., hydroxypropylcellulose, polyvinylpyrrolidone, etc.
  • the resulting high-dose drug/low-dose drug-containing microparticle can then be coated, if needed, with an additional sealant layer (as described herein), and/or a taste-masking layer (also as described herein).
  • the ultimate high-dose drug/low-dose drug-containing microparticles comprise a high-dose drug-containing core (as described herein), coated with an optional sealant coating, a taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer), a low-dose drug layer, a second optional sealant layer, and a second taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer).
  • a taste-masking layer e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer
  • the high-dose drug/low-dose drug-containing microparticles can optionally comprise one or more sealant layers, wherein the sealant layers can have the same composition or different compositions, and can be coated at the same coating weight or different coating weights.
  • the high-dose drug/low-dose drug-containing microparticles comprise two taste-masking layers
  • the two taste-masking layers can have the same composition or a different composition and/or the same coating weight or different coating weights.
  • the inner taste-masking layer can comprise a water-insoluble polymer
  • the outer taste-masking layer can comprise the combination of a water-insoluble polymer and a water-soluble polymer and/or gastrosoluble polymer, etc.
  • a flavorant coating layer (which can include a sweetener and/or a flavoring agent as described herein) can be disposed over the low-dose drug-containing layer (e.g., instead of a taste-masking layer), such that the high-dose drug/low-dose drug-containing microparticles comprise, for example a high-dose drug-containing core (as described herein), coated with an optional sealant coating, a taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer), a low-dose drug layer, a second optional sealant layer, and the flavorant coating layer.
  • a high-dose drug/low-dose drug-containing microparticles comprise, for example a high-dose drug-containing core (as described herein), coated with an optional sealant coating, a taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a
  • the flavorant coating layer comprises a combination of a flavorant and a binder.
  • Suitable binders include those described herein.
  • the flavorant includes water soluble sweeteners such as sucralose, saccharine, aspartame, neotame, acesulfame K, sodium saccharinate, neohesperidine, lactitol, maltitol, sorbitol, and mixtures thereof, or alternatively flavoring agents such as strawberry cherry, peppermint, strawberry and mixtures thereof.
  • the binder is hydroxypropyl cellulose and the flavorant is sucralose.
  • the coating weight of the flavorant coating layer can range from about 1% to about 10% by weight, including the ranges from about 3.0% to about 8%, about 5% to about 7.5%, and from about 5% to about 10%, of the weight of the coated core, or about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10%, inclusive of all ranges and subranges therebetween.
  • the taste-masked high-dose/low-dose drug-containing microparticles can include various layers in addition to the taste-masking layer (e.g. optional sealant layers, etc.).
  • the taste-masking layer can be disposed directly over the high-dose drug-containing core, or a sealant layer can be interposed between the high-dose drug-containing core and a taste-masking layer.
  • the low-dose drug-containing layer is coated with a taste-masking layer comprising a water-insoluble polymer combined with a gastrosoluble polymer such as a cationic dimethylaminoethyl methacrylate copolymer.
  • the taste-masking layer disposed over the low-dose drug layer comprises a water-insoluble polymer and no water-soluble or gastrosoluble polymer.
  • a flavorant coating layer e.g., at coating weight of about 1% to about 10%
  • a sealant layer e.g., hydroxypropyl cellulose at a coating weight of about 1% to about 10%
  • the high-dose drug/low-dose drug-containing microparticles of the present invention provide rapid dissolution of the high-dose and low-dose drugs when dissolution tested using USP Apparatus 1 (baskets@ 100 RPM) or USP Apparatus 2 (paddles@ 50 RPM) in 900 mL media (pH 1.2, pH 5.8, pH 6.8, or pH 7 (water)) at 37° C.
  • the pharmaceutical compositions comprising the modified-release coated high-dose drug/low-dose drug-containing microparticles of the present invention provide blend homogeneity as well as uniformity of dosage units as per the USP requirements which are difficult to achieve by other methods (e.g., by blending particles comprising the high-dose drug with a second population of particles comprising the low-dose drug), particularly when the ratio of the high-dose drug to the low-dose drug is about 20/1 or higher (e.g., about 20/1, about 25/1, about 30/1, about 35/1, about 40/1, about 45/1, about 50/1, about 60/1, about 70/1, about 80/1, about 90/1, about 100/1, etc.).
  • the high-dose drug and the low-dose drug can comprise any drugs which are intended to be used in combination to treat a condition or disease in a patient.
  • pharmaceutical compositions of the present invention can include combinations of high-dose and low-dose drugs such as non-opioid analgesics (e.g., acetaminophen and non-steroidal anti-inflammatory drugs such as aspirin, ibuprofen, ketoprofen, meloxicam, diclofenac potassium, etodolac, sulindac, indomethacin, celecoxib, etc.) in combination with one or more opioid analgesics (hydrocodone bitartrate, oxymorphone, buprenorphine, fentanyl, hydromorphone) for the treatment of moderate-to-severe pain.
  • opioid analgesics hydrocodone bitartrate, oxymorphone, buprenorphine, fentanyl, hydromorphone
  • an anti-diabetic combination of high-dose and low-dose drugs suitable for the treatment of diabetes mellitus include at least one biguanide (e.g., metformin) in combination with at least one sulfonylurea (e.g., glipizide, gliclazide, glyburide, gliquidone, glyclopyamide, glimepiride), meglitinide (e.g. repaglinide, nateglinide) or thiazolidinedione (e.g., roseglitazone, pioglitazone, troglitazone).
  • biguanide e.g., metformin
  • sulfonylurea e.g., glipizide, gliclazide, glyburide, gliquidone, glyclopyamide, glimepiride
  • meglitinide e.g. repaglinide, nateglinide
  • a high-dose drug e.g., nicotinic acid
  • a low-dose drug e.g., lovastatin, fluvastatin, atorvastatin, cerivastatin, simvastatin, mevastatin, rosuvastatin, pravastatin
  • cholesterol very low density lipoproteins
  • Combinations of a high-dose drug such as pseudoephedrine hydrochloride, pseudoephedrine sulfate, or fexofenadine and a low-dose drug such as cetirizine, loratidine, and phenylephrine are useful for treating indoor and outdoor allergies.
  • the low-dose drug is a therapeutically effective amount of hydrocodone bitartrate and the high-dose drug is a therapeutically effective amount of acetaminophen for treating pain.
  • the high-dose drug is a therapeutically effective amount of metformin and the low-dose drug is a therapeutically effective amount of roseglitazone for treating hyperglycemia.
  • the pharmaceutical compositions of the present invention can comprise niacin (nicotinic acid) as the high-dose drug, formulated as taste-masked high-dose drug particles with an immediate-release (IR) profile, layered with a statin and taste-masking coating.
  • the niacin can be formulated as sustained-release (SR) coated high-dose drug particles to produce modified-release pharmaceutical compositions.
  • the pharmaceutical compositions of the present invention comprise high-dose/low-dose drug-containing microparticles.
  • the pharmaceutical compositions of the present invention can further comprise a second population of high-dose drug containing microparticles.
  • the high-dose drug-containing microparticles comprise, for example, a high-dose drug-containing core (as described herein) coated with a water-insoluble polymer, e.g., at a coating weight of about 15% to about 35%, thereby providing sustained-release (SR) high-dose drug-containing particles.
  • SR sustained-release
  • the combination of high-dose/low-dose drug-containing microparticles and SR high-dose drug-containing particles exhibit rapid low-dose drug release profiles and prolonged high-dose drug release (modified release) profiles.
  • compositions of the present invention can be used to prepare oral dosage forms such as tablets, capsules, and ODTs.
  • Tablets can be prepared by combining the pharmaceutical compositions of the present invention with suitable pharmaceutically acceptable excipients, and then compressing the resulting mixture to form tablets.
  • capsules can be filled with the pharmaceutical compositions of the present invention (and optional excipients).
  • the pharmaceutical compositions of the present invention can be combined with rapidly dispersing microgranules to form an orally disintegrating tablet (ODT).
  • ODT is a tablet designed to substantially disintegrate in the oral cavity after administration (without chewing) within about 60 seconds after contact with saliva (i.e., in the oral cavity) or with simulated saliva fluid (e.g., tested according to the USP ⁇ 701> Disintegration Test). In particular embodiments, the ODT substantially disintegrates within about 30 seconds.
  • the disintegration of the ODT in the oral cavity of the patient provides a smooth, easy-to-swallow suspension having no gritty mouthfeel or aftertaste, while still providing pharmacokinetic profiles for the drugs contained in the ODT (e.g., plasma concentration vs. time profiles) which are bioequivalent to the respective reference listed drugs (RLDs).
  • pharmacokinetic profiles for the drugs contained in the ODT e.g., plasma concentration vs. time profiles
  • the ODTs of the present invention comprise the pharmaceutical compositions of the present invention combined with rapidly dispersing microgranules.
  • Rapidly dispersing microgranules can be prepared as described in US Publication Nos. 2006/0078614, 2006/0105038, 2005/0232988 or 2003/0215500 (each of which is herein incorporated by reference in its entirety for all purposes) by granulating a disintegrant with a sugar alcohol and/or saccharide having an average particle size of not more than about 30 ⁇ m.
  • the granulation can be carried out, for example, in a high shear granulator with approximately 20-25% water as the granulating fluid, and if needed wet milled and dried to produce rapidly dispersing microgranules, for example having an average particle size of not more than about 300 ⁇ m (e.g., about 175-300 ⁇ m).
  • the ratio of the disintegrant to the sugar alcohol, saccharide, or mixture thereof in the rapidly dispersing microgranules ranges from about 90/10 to about 99/01, for example about 90/10, about 91/9, about 92/8, about 93/7, about 94/6, about 95/5, about 96/4, about 97/3, about 98/2, about 99/1, inclusive of all values, ranges, and subranges therebetween.
  • the ratio of the rapidly dispersing microgranules to taste-masked drug-containing particles ranges from about 5/1 to about 1/1, including about 5/1, 4/1, 3/1, 2/1, 1/1, inclusive of all values, ranges, and subranges therebetween.
  • the taste-masked high-dose/low-dose drug-containing microparticles incorporated into the ODT dosage form should also have a small enough particle size such that after disintegration of the ODT in the oral cavity of the patient, a smooth, easy-to-swallow suspension results.
  • the average particle size of the taste-masked high-dose/low-dose drug-containing microparticles is not more than about 400 ⁇ m, or in some embodiments not more than about 300 ⁇ m.
  • the ODT dosage form may also include pharmaceutically acceptable excipients typically used in disintegrating tablet formulations such as microcrystalline cellulose and spray dried mannitol (compressible diluents), croscarmellose sodium or crospovidone (super disintegrant), coloring agents, and optionally magnesium stearate or sodium stearyl fumarate (lubricant intragranularly mixed or used externally to lubricate die and punch surfaces).
  • pharmaceutically acceptable excipients typically used in disintegrating tablet formulations such as microcrystalline cellulose and spray dried mannitol (compressible diluents), croscarmellose sodium or crospovidone (super disintegrant), coloring agents, and optionally magnesium stearate or sodium stearyl fumarate (lubricant intragranularly mixed or used externally to lubricate die and punch surfaces).
  • Tablet dosage forms comprising the pharmaceutical composition of the present invention have a low friability, e.g., less than about 1%, (e.g., less than about 0.9%, less than about 0.8%, less than about 0.7%, less than about 0.6%, less than about 0.5%, less than about 0.4%, less than about 0.3%, etc., inclusive of all ranges and subranges therebetween) in order to have sufficient durability to withstand handling, shipping, and/or packaging in push-through blister packaging.
  • a low friability e.g., less than about 1%, (e.g., less than about 0.9%, less than about 0.8%, less than about 0.7%, less than about 0.6%, less than about 0.5%, less than about 0.4%, less than about 0.3%, etc., inclusive of all ranges and subranges therebetween) in order to have sufficient durability to withstand handling, shipping, and/or packaging in push-through blister packaging.
  • a non-limiting list of suitable disintegrants for the rapidly dispersing microgranules includes crospovidone (cross-linked PVP), sodium starch glycolate, cross-linked sodium carboxymethylcellulose, calcium silicate, and low substituted hydroxypropyl cellulose.
  • the amount of disintegrant in the ODT is typically in the range of about 1% to about 10% by weight, including about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10%, inclusive of all ranges and subranges therebetween.
  • the disintegrant for the rapidly dispersing microgranules is selected from the group consisting of crospovidone, cross-linked sodium carboxymethylcellulose, and low substituted hydroxypropyl cellulose. In a more particular embodiment, the disintegrant for the rapidly dispersing microgranules is crospovidone.
  • a non-limiting list of suitable sugar alcohols includes mannitol, sorbitol, xylitol, maltitol, arabitol, ribitol, dulcitol, iditol, isomalt, lactitol, erythritol and combinations thereof.
  • the sugar alcohol is mannitol.
  • a non-limiting list of suitable saccharides includes lactose, sucrose, maltose, and combinations thereof.
  • the saccharide is lactose.
  • the amount of sugar alcohol and/or saccharide in the ODT ranges from about 30% to about 70% by weight, including, for example, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, or about 70%, inclusive of all ranges and subranges therebetween.
  • compositions include fillers, diluents, glidants, disintegrants, binders, lubricants etc.
  • Other pharmaceutically acceptable excipients include acidifying agents, alkalizing agents, preservatives, antioxidants, buffering agents, chelating agents, coloring agents, complexing agents, emulsifying and/or solubilizing agents, flavors and perfumes, humectants, sweetening agents, wetting agents etc.
  • suitable fillers, diluents and/or binders include lactose (e.g.
  • lactose various grades of Pharmatose®, Microtose® or Fast-Flo®
  • microcrystalline cellulose various grades of Avicel®, Ceolus®, Elcema®, Vivacel®, Ming Tai® or Solka-Floc®
  • hydroxypropylcellulose L-hydroxypropylcellulose (low substituted), low molecular weight hydroxypropyl methylcellulose (HPMC) (e.g.
  • Methocel E, F and K from Dow Chemical, Metolose SH from Shin-Etsu, Ltd), hydroxyethylcellulose, sodium carboxymethylcellulose, carboxymethylhydroxyethylcellulose and other cellulose derivatives, sucrose, agarose, sorbitol, mannitol, dextrins, maltodextrins, starches or modified starches (including potato starch, maize starch and rice starch), calcium phosphate (e.g. basic calcium phosphate, calcium hydrogen phosphate, dicalcium phosphate hydrate), calcium sulfate, calcium carbonate, sodium alginate, collagen etc.
  • phosphate e.g. basic calcium phosphate, calcium hydrogen phosphate, dicalcium phosphate hydrate
  • calcium sulfate calcium carbonate, sodium alginate, collagen etc.
  • Suitable diluents include e.g. calcium carbonate, dibasic calcium phosphate, tribasic calcium phosphate, calcium sulfate, microcrystalline cellulose, powdered cellulose, dextrans, dextrin, dextrose, fructose, kaolin, lactose, mannitol, sorbitol, starch, pregelatinized starch, sucrose, sugar etc.
  • Suitable disintegrants include e.g. alginic acid or alginates, microcrystalline cellulose, hydroxypropyl cellulose and other cellulose derivatives, croscarmellose sodium, crospovidone, polacrillin potassium, sodium starch glycolate, starch, pregelatinized starch, carboxymethyl starch (e.g. Primogel® and Explotab®) etc.
  • glidants and lubricants include stearic acid, magnesium stearate, calcium stearate or other metallic stearates, talc, waxes and glycerides, light mineral oil, PEG, glyceryl behenate, colloidal silica, hydrogenated vegetable oils, corn starch, sodium stearyl fumarate, polyethylene glycols, alkyl sulfates, sodium benzoate, sodium acetate etc.
  • excipients include e.g. flavoring agents, coloring agents, taste-masking agents, pH-adjusting agents, buffering agents, preservatives, stabilizing agents, anti-oxidants, wetting agents, humidity-adjusting agents, surface-active agents, suspending agents, absorption enhancing agents, agents for modified release etc.
  • the present invention is also directed to methods of preparing the pharmaceutical compositions and dosage forms described herein.
  • the high-dose/low-dose drug-containing microparticles are prepared by a method comprising:
  • the step (a) of preparing the core may be accomplished by any of the methods known in the art; for example, layering an inert bead (e.g., sugar, microcrystalline cellulose, mannitol-microcrystalline cellulose, silicon dioxide, etc.) with a solution comprising the drug and optionally a polymeric binder (e.g., by fluid-bed or pan coating).
  • the core may comprise drug crystals of the desired particle size (e.g., about 50-500 ⁇ m, including 100-250 ⁇ m), prepared by crystallization of the drug from a suitable solvent, or by milling drug crystals to a desired particle size.
  • the core can comprise a pellet prepared by controlled-spheronization.
  • the microgranules comprising a high-dose drug may be prepared by a conventional high-shear or planetary granulation process or high-dose drug-containing pellets may be prepared by a conventional granulation-extrusion-spheronization process comprising e.g. acetaminophen, a polymer binder and one or more fillers/diluents.
  • Step (b) comprises coating the taste-masked high-dose drug-containing core with the low-dose drug using a drug-layering solution as described herein (e.g., comprising a solution of the low-dose drug and optionally a binder).
  • a drug-layering solution as described herein (e.g., comprising a solution of the low-dose drug and optionally a binder).
  • the low-dose drug layer can be applied using any suitable method, for example fluid bed, pan coating, coacervation, etc.
  • Step (c) comprises coating the high-dose drug-containing core and/or the low-dose drug containing layer with a taste-masking layer.
  • a taste-masking layer is coated directly over the high-dose-drug containing core, or a sealant layer is coated onto the high-dose drug-containing core before coating with the low-dose drug-containing layer and/or a taste-masking layer.
  • a sealant layer may be coated onto the low-dose drug-containing layer before coating with a taste-masking layer or a flavorant layer as described herein (e.g., comprising a sweetener and/or flavoring agent and an optional polymeric binder such as hydroxypropylcellulose, applied as a solution or suspension).
  • the taste-masking layer comprises a water-insoluble polymer or a water-insoluble polymer combined with a water-soluble or gastrosoluble polymer (and optionally a binder), for example any of the compositions described herein such as ethylcellulose (Ethocel Standard 100 Premium, at a coating weight of about 10%), or a combination of ethylcellulose with a gastrosoluble polymer (e.g., Eudragit E100) at coating weight of about 25%.
  • ethylcellulose Ethocel Standard 100 Premium, at a coating weight of about 10%
  • gastrosoluble polymer e.g., Eudragit E100
  • the resulting particles can optionally be coated with a sealant coat (as described herein) and then coated with a taste-masking layer or flavorant layer (as described herein).
  • the taste-masking layer applied over the low-dose drug layer can comprise a water-insoluble polymer (e.g. ethylcellulose) or the combination of a water-insoluble polymer and a water soluble or gastrosoluble polymer (e.g., ethylcellulose in combination with Eudragit E100).
  • a flavorant coating can be applied over the low-dose drug layer, or over a protective sealant layer applied over the low-dose drug layer.
  • the method comprises coating by solvent coacervation a taste-masking layer directly over the high-dose drug-containing core or over a sealant layer disposed on the high-dose drug-containing core, wherein the taste-masking layer comprises water-insoluble ethylcellulose (Ethocel Standard 100 Premium) at coating weight of about 6%.
  • the method comprises coating water-insoluble ethylcellulose (Ethocel Standard 10 Premium) in combination with water-soluble hydroxypropylcellulose at a ratio of 7:3 or gastrosoluble Eudragit E100 at a ratio of 8:7 at a coating weight of about 20% by fluid bed coating.
  • the method comprises coating by solvent coacervation a taste-masking layer directly over the low-dose drug-containing layer or over a sealant layer disposed on the low-dose drug-containing layer, e.g. with water-insoluble ethylcellulose (Ethocel Standard 100 Premium) at a coating weight of about 6%.
  • the method comprises coating water-insoluble ethylcellulose (Ethocel Standard 10 Premium) in combination with water-soluble hydroxypropylcellulose at a ratio of 7:3 or gastrosoluble Eudragit E100 at a ratio of 8:7 at a level of about 20% by weight based on the total weight of the coated particles by fluid bed coating.
  • Taste-masking coatings can be prepared and applied as described, for example in U.S. Patent Publ. Nos. 2006/0078614 and 2006/0105038.
  • the method comprises coating the low-dose drug-containing layer with a sealant layer comprising hydrophilic hydroxypropylcellulose at a coating weight of about 5%, then coating with a taste-masking layer comprising a sweetener such as sucralose at a coating weight of about 5% by weight.
  • the ultimate dosage form comprising the taste-masked high-dose/low-dose drug-containing microparticles of the present invention can then be prepared by various methods known in the pharmaceutical arts, such as filling an appropriate amount of the taste-masked high-dose/low-dose drug-containing microparticles into e.g. a gelatin capsule or a container suitable for storing a suspension, sachet, etc.
  • the taste-masked high-dose/low-dose drug-containing microparticles of the present invention are combined with suitable pharmaceutically acceptable excipients and compressed to form a tablet.
  • Tablets comprising the pharmaceutical compositions of the present invention can contain an internal lubricant (e.g., magnesium stearate), or can be compressed into tablets using an external lubrication process, in which the lubricant is sprayed onto the surface of the die and punch surfaces, rather than incorporated into the compression blend.
  • an internal lubricant e.g., magnesium stearate
  • external lubrication process in which the lubricant is sprayed onto the surface of the die and punch surfaces, rather than incorporated into the compression blend.
  • External lubrication and compression methods than can be used to prepare oral dosage forms (e.g., tablets, ODTs) comprising the pharmaceutical compositions of the present invention are described for example in U.S. Pat. No. 5,996,902 and U.S. Pat. No. 6,776,361.
  • the method further comprises preparing rapidly dispersing microgranules comprising a disintegrant and a sugar alcohol, a saccharide or a mixture thereof, wherein each of the disintegrant, sugar alcohol and/or saccharide have an average particle diameter of not more than 30 ⁇ m; then combining the rapidly dispersing microgranules with taste-masked high-dose/low-dose drug-containing microgranules and optionally other pharmaceutically acceptable excipients, e.g., in a mixer or V-blender; and finally compressing the blend of rapidly dispersing microgranules and taste-masked high-dose/low-dose drug-containing microgranules into an ODT, e.g., using an externally lubricated tablet press to provide ODTs with desired tableting characteristics (e.g., adequate hardness, friability of ⁇ 0.6%, low disintegration time, and rapid dissolution). Rapidly dispersing microgranules can be prepared following the procedures disclosed
  • the rapidly dispersing microgranules and taste-masked drug-containing microparticles may be present in the ratio of about 4/1 to 2/1 to achieve a smooth mouthfeel.
  • Rapidly dispersing microgranules may be produced as described herein by granulating a disintegrant such as Crospovidone XL-10 with a sugar alcohol or a saccharide, or a combination thereof, each having an average particle diameter of not more than about 30 ⁇ m, with water or an alcohol-water mixture in a conventional or high shear granulator and drying in a fluid bed equipment or a tray drying oven to produce granules with an average particle size not more than about 400 ⁇ m (preferably not more than about 300 ⁇ m).
  • a disintegrant such as Crospovidone XL-10
  • a sugar alcohol or a saccharide or a combination thereof
  • the ultimate dosage forms can comprise a single population of taste-masked high-dose/low-dose drug-containing microparticles of the present invention in combination with excipients, rapidly dispersing microgranules, etc, or can include a combination of the taste-masked high-dose/low-dose drug-containing microparticles in combination with high-dose drug-containing particles, or alternatively two or more populations of different taste-masked high-dose/low-dose drug-containing microparticles.
  • the ratio of the different populations of high-dose/low-dose drug-containing microparticles or high-dose/low-dose drug-containing microparticles and high-dose drug containing particles can be varied to provide suitable dosages of the high-dose and low-dose drugs.
  • the ultimate dosage forms can comprise a single population of taste-masked high-dose/low-dose drug-containing microparticles of the present invention in combination with excipients, rapidly dispersing microgranules, etc, or can include a combination of the taste-masked high-dose/low-dose drug-containing microparticles in combination with modified release (e.g., taste-masked or sustained release) coated high-dose drug-containing microparticles, or alternatively two or more populations of different taste-masked high-dose/low-dose drug-containing microparticles, wherein the sustained release coated high-dose drug-containing microparticles comprise a water insoluble polymer optionally in combination with a water soluble or enteric polymer applied prior to low-dose drug layering.
  • modified release e.g., taste-masked or sustained release
  • the ratio of the different populations of high-dose/low-dose drug-containing microparticles or high-dose/low-dose drug-containing microparticles and taste-masked or sustained release coated high-dose drug-containing microparticles can be varied to provide suitable dosages of the high-dose and low-dose drug components.
  • the oral dosage forms of the present invention provide in vivo plasma concentrations and release profiles which mimic RLD's.
  • the pharmaceutical compositions of the present invention comprise microgranules or extruded/spheronized pellets comprising acetaminophen, a polymeric binder, which imparts resilient characteristics to the dried microgranules/pellets, a hydrophilic filler/diluent, and optionally a flavor, a sweetener and/or a disintegrant.
  • the present invention is directed to compositions of the present invention comprising at least one population of non-opioid analgesic/opioid analgesic drug-containing microparticles combined with non-opioid analgesic drug-containing microparticles with drug release properties suitable for a twice- or once-daily dosing regimen, wherein the one or more of the non-opioid analgesic drug-containing microparticle populations comprise non-opioid analgesic drug-containing microparticles with one or more coating layers comprising a water-insoluble polymer, an enteric polymer, or an enteric polymer in combination with a water-insoluble polymer.
  • the taste-masked pharmaceutical compositions of the present invention exhibit the following properties:
  • the pharmaceutical composition of the present invention comprises acetaminophen as the high-dose drug and hydrocodone bitartrate as the low-dose drug.
  • acetaminophen is rapidly and almost completely absorbed from the GI tract. Peak plasma concentrations are attained within 30-60 minutes (binding to serum protein is about 25% after normal therapeutic dosages) and plasma half-life is between 1-2.5 hours in normal, healthy patients. After about 8 hours, only traces of the drug are detectable.
  • compositions of the present invention comprising therapeutically effective amounts of taste-masked high-dose/low-dose drug-containing microparticles are effective in treating various diseases or conditions.
  • pharmaceutical compositions of the present invention comprising therapeutically effective amounts of a non-steroidal anti-inflammatory drug such as aspirin, ibuprofen, ketoprofen, meloxicam, diclofenac potassium, etodolac, sulindac, indomethacin, celecoxib, or mixtures thereof, in combination with an opioid analgesic such as hydrocodone bitartrate, oxymorphone, buprenorphine, fentanyl, hydromorphone, or mixtures thereof (e.g. a combination of acetaminophen and hydrocodone) are effective for relief of mild to moderate pain of acute, chronic, or post-operative pain, or disabling pain of terminal conditions such as cancer.
  • a non-steroidal anti-inflammatory drug such as aspirin, ibuprofen, ketoprofen,
  • the pharmaceutical compositions of the present invention comprise therapeutically effective amounts of acetaminophen in combination with therapeutically effective amount of hydrocodone or salts thereof, e.g. hydrocodone bitartrate.
  • the pharmaceutical compositions of the present invention comprise 500 mg of acetaminophen and 5 mg of hydrocodone bitartrate, or 300 mg of acetaminophen and 100 mg of hydrocodone bitartrate.
  • the acetaminophen/hydrocodone-containing compositions of the present invention are bioequivalent to known acetaminophen/hydrocodone compositions such as Vicodin®, Panadol®, and Xodol®.
  • compositions of the present invention comprising 500 mg of acetaminophen/5 mg of hydrocodone bitartrate have an acetaminophen C max of 80-125% of 6115 ng/mL, a hydrocodone bitartrate C max of 80-125% of 20.14 ng/mL, an acetaminophen AUC of 80-125% of 19920 ng ⁇ hr/mL, and a hydrocodone bitartrate AUC of 80-125% of 141 ng ⁇ hr/mL.
  • compositions of the present invention comprising 300 mg acetaminophen/10 mg hydrocodone bitartrate have an acetaminophen C max of 80-125% of 3915 ng/mL, a hydrocodone bitartrate C max of 80-125% of 40.53 ng/mL, an acetaminophen AUC of 80-125% of 12794 ng ⁇ hr/mL, and a hydrocodone bitartrate AUC of 80-125% of 280 ng ⁇ hr/mL.
  • compositions of the present invention comprising therapeutically effective amounts of niacin in combination with a statin such as atorvastatin, lovastatin, fluvastatin, cerivastatin, simvastatin, mevastatin, rosuvastatin, pravastatin or mixtures thereof are effective to lower cholesterol (very low density lipoproteins) and triglycerides levels in patients with or at risk of cardiovascular disease.
  • a statin such as atorvastatin, lovastatin, fluvastatin, cerivastatin, simvastatin, mevastatin, rosuvastatin, pravastatin or mixtures thereof are effective to lower cholesterol (very low density lipoproteins) and triglycerides levels in patients with or at risk of cardiovascular disease.
  • compositions of the present invention comprising therapeutically effective amounts of metformin in combination with a drug such as glipizide, glyburide, glimepiride, repaglinide, nateglinide, rosiglitazone, pioglitazone, troglitazone (e.g., a combination of metformin and rosiglitazone) are effective to treat hyperglycemia, e.g., in diabetic patients.
  • a drug such as glipizide, glyburide, glimepiride, repaglinide, nateglinide, rosiglitazone, pioglitazone, troglitazone (e.g., a combination of metformin and rosiglitazone) are effective to treat hyperglycemia, e.g., in diabetic patients.
  • compositions of the present invention comprising therapeutically effective amounts of pseudoephedrine hydrochloride, pseudoephedrine sulfate, or fexofenadine, in combination with a drug such as cetirizine or loratidine are effective to treat indoor or outdoor allergies.
  • Hydrocodone bitartrate (81.1 g) was slowly added to an acetone/water (1453/782) solution of hydroxypropyl cellulose (8.1 g of Nisso HPC-L-FP) and mixed well to dissolve.
  • 60-80 mesh sugar spheres (1500 g) were coated with the drug-layering formulation in a Glatt fluid-bed coater (Glatt GPCG 3, equipped with a 7′′ bottom-spray Wurster insert, 7 13/16′′ column, 25 mm column height, ‘C’ air distribution plate, and 200 mesh product retention screen) under the following conditions—inlet air temperature: 70 ⁇ 5° C.; product temperature: 45 ⁇ 5° C.; atomization air pressure 2.43 bar; port size: 1.0 mm; flow rate: 2 g/min increased in steps to 15 g/min, air flow: 25% flap.
  • a sealant coating solution of hydroxypropylcellulose (32.4 g in 457/51 acetone/water) was sprayed onto the drug layered beads for a coating weight of 2%.
  • the dried immediate release (IR) beads were sieved through 50 and 80 mesh screens for a usable total yield of 88.4%.
  • IR beads 140 g from Example 1.A, above were coated with ethylcellulose (Ethocel Standard Premium 100 from Dow Chemicals) by solvent coacervation at a coating weight of 30%.
  • the tank was heated to 80° C. to dissolve the ethylcellulose, and thereafter, the tank was cooled to below 30° C. to achieve taste-masked hydrocodone bitartrate microcapsules.
  • the microcapsules were separated by decanting, then filtered and washed with fresh cyclohexane and air dried in a fume hood.
  • IR Beads (1001.3 g) prepared as described in Example 1.A, above were coated with a solution of ethylcellulose (Ethocel Standard Premium 10 cps, hereafter referred as EC-10)/Eudragit E100 (188.6 g each) plasticized with diacetylated monoglycerides (Myvacet 9-45; 30.0 g) and kosher magnesium stearate (30.0 g) dissolved in 80/20 acetone (3086 g)/water (771 g) for a coating weight of 30%. Samples were pulled during the coating process at coating weights of about 10%, 15%, 20%, and 25% and dissolution tested to evaluate the effect of coating level on dissolution and organoleptic properties. The coated beads were dried/cured at 60° C. for 10 minutes in the Glatt GPCG 3 and sieved to discard agglomerates.
  • EC-10 ethocel Standard Premium 10 cps
  • the microcapsule bed Upon controlled cooling to ⁇ 30° C., the microcapsule bed is subjected to vacuum filtration and rinsing with cyclohexane to wash off residual polyethylene.
  • the microcapsules were transferred to a fluid bed dryer, subjected to a drying procedure, and dried for a period of 4-6 hrs to reduce the cyclohexane level to not more than 1000 ppm.
  • Rapidly dispersing microgranules comprise a sugar alcohol such as mannitol and/or a saccharide such as lactose and a disintegrant such as Crospovidone.
  • the sugar alcohol and/or saccharide and disintegrant will typically be present in the rapidly dispersing microgranules at a ratio of from about 99:1 to about 90:10 (sugar alcohol and/or saccharide:disintegrant).
  • the rapidly dispersing microgranules used in the ODT formulations disclosed in the various examples in accordance with the present invention were produced by granulating 95 parts of D-mannitol with an average particle size of about 15 ⁇ m, and 5 parts of crospovidone (Crospovidone XL-10) in a high shear mixer (e.g., GMX 600 from Vector Corporation) with water as the granulating fluid, drying the wet mass in a fluid bed dryer (e.g., Glatt GPCG 200 or Fluid Air FA0300), and sieving/milling to obtain granules with an average particle size of less than 400 ⁇ m.
  • a fluid bed dryer e.g., Glatt GPCG 200 or Fluid Air FA0300
  • the wet milled granules are dried in a tray drying oven for a loss on drying value of less than 1% by weight.
  • Example 1E Beads (172.4 g) prepared as described in Example 1.B (30% coating weight), above; standard acetaminophen microcapsules (PE004, 531.9 g) produced in Example 1D, above, and rapidly dispersing microgranules (803.4 g) from Example 1E above, were blended with a pre-blend comprising crospovidone (XL-10, 80.0 g), sucralose (5.6 g), and strawberry flavor (6.7 g) before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (19 mm in diameter) weighing approximately 1600 mg using a Carver tablet press at a compression force of 1 metric ton.
  • crospovidone crospovidone
  • sucralose 5.6 g
  • strawberry flavor 6.7 g
  • Hydrocodone bitartrate (47.5 g) was slowly added to a 50/50 acetone/water (each 452 g) solution of hydroxypropylcellulose (5.3 g of Nisso HPC-L-FP) and mixed well to dissolve.
  • Acetaminophen microcapsules (PE004) from Example 1.D with a 6% EC-100 coating (1500.0 g) were coated with the drug-layering formulation in a Glatt fluid-bed coater Glatt GPCG 3.
  • a sealant coating solution of hydroxypropylcellulose (31.7 g in 447/50 acetone/water) was sprayed onto the drug layered beads at a coating weight 2%.
  • the dried IR beads were sieved through 35 and 80 mesh screens for a usable total yield of 99.0%.
  • IR particles 1100.0 g prepared as described in Example 2.A, above were coated with a solution of ethylcellulose (EC-10; 43%)/Eudragit E100 (43%) plasticized with diacetylated monoglycerides (Myvacet 9-45 at 7%) and kosher magnesium stearate (7%) dissolved in 80/20 acetone (3294 g)/water (848 g) for a 30% weight gain. Samples were pulled during the coating process at coating weights of about 5%, 10%, 15%, 20%, and 25% and dissolution tested to evaluate the effect of coating level on dissolution as well as organoleptic properties. The coated beads were dried at the same temperature settings in the Glatt GPCG 3 and sieved to discard agglomerates for a total useable yield of 98.9%.
  • Example 2.B 20% EC-10/E100 coated (10.01% of hydrocodone bitartrate/Acetaminophen beads at 15% hydrocodone bitartrate load) from Example 2.B, above; standard acetaminophen microcapsules (PE004, 35.46%) from Example 1.D, above, and rapidly dispersing microgranules (48.76%) from Example 1.E above, were blended with a pre-blend comprising crospovidone (XL-10 at 5.0%), sucralose (0.35%), and strawberry flavor (0.42%) before compressing into 10 mg/300 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (15 mm in diameter) weighing approximately 900 mg using a Carver tablet press at a compression force of 1 metric ton.
  • crospovidone crospovidone
  • sucralose 0.35%
  • strawberry flavor 0.42%
  • Example 1.E 30% coated beads (10.78%) from Example 2.B, above, standard acetaminophen microcapsules (PE004, 33.24%) from Example 1.D, above, and rapidly dispersing microgranules (37.71%) from Example 1.E above, were blended with a pre-blend comprising microcrystalline cellulose (Avicel PH101 at 12.5%), crospovidone (XL-10 at 5.0%), sucralose (0.35%), and strawberry flavor (0.42%) before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (17 mm in diameter) weighing approximately 1600 mg using a rotary Hata tablet press equipped with an external lubrication system (Matsui Ex-Lub System) to lubricate the die/punch surfaces by spraying magnesium stearate prior to each compression.
  • a pre-blend comprising microcrystalline cellulose (Avicel PH101 at 12.5%), crospovidone (XL-10 at 5.0%), sucralose (
  • Acetaminophen (Granular grade from Covidien (A100); 2000.0 g) was coated in a Glatt GPCG 3 (7′′ bottom spray Wurster insert and nozzle with 1.00 mm port size) with a solution of ethylcellulose (10 cps; 114.3 g)/Eudragit E100 (100.0 g) plasticized with polyethylene glycol (PEG 400; 42.9 g) and kosher magnesium stearate (28.6 g) homogeneously suspended in acetone (1359.5 g)/isopropyl alcohol (672.7 g)/water (770.8 g) for a 12.5% weight gain. The dried particles were sieved with 35 and 80 mesh screens to discard agglomerates/fines (useable yield: 93.6%).
  • Hydrocodone bitartrate was layered onto acetaminophen (Granular A100) by spraying the drug-layering formulation (see Table 1—Low Potency for compositions) in a Glatt GPCG 3 fluid-bed coater. Following the drug layering, the sealant coating solution was sprayed onto the drug layered particles at a coating weight of 2%, followed by a taste-masking coating with EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 at a coating weight of 22% using the method disclosed in Example 3.A above.
  • Hydrocodone bitartrate was layered onto acetaminophen (Granular A100) by spraying the drug-layering formulation (see Table 1—High Potency for compositions) in a Glatt GPCG 3 fluid-bed coater. Following the drug layering, the sealant coating solution was sprayed onto the drug layered particles at a coating weight of 2%, followed by a taste-masking coating with EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 at a coating weight of 27%.
  • Example 3A 12.5% coated acetaminophen from Example 3A, above, 22% coated hydrocodone/acetaminophen from Example 3B, above, rapidly dispersing microgranules from Example 1.E above, were blended with a pre-blend comprising microcrystalline cellulose (Avicel PH101), (Parteck M200), crospovidone, sucralose, and strawberry flavor before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (17 mm in diameter) weighing approximately 1600 mg using a using a rotary Hata tablet press equipped with an external lubrication system (Matsui Ex-Lub System) to lubricate the die/punch surfaces prior to each compression at a compression force of 18 to 24 kN.
  • a pre-blend comprising microcrystalline cellulose (Avicel PH101), (Parteck M200), crospovidone, sucralose, and strawberry flavor before compressing into 5 mg/500 mg hydrocodone bitartrate
  • Example 3.A 12.5% coated acetaminophen from Example 3.A, above, 27% coated hydrocodone/acetaminophen from Example 3.C, above, and rapidly dispersing microgranules from Example 1.E above, were blended with a pre-blend comprising microcrystalline cellulose (Avicel PH101), mannitol (Parteck M200), crospovidone, sucralose, and strawberry flavor before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (17 mm in diameter) weighing approximately 1000 mg using a using a rotary Hata tablet press equipped with an external lubrication system (Matsui Ex-Lub System) to lubricate the die/punch surfaces prior to each compression at a compression force of 10 to 15 kN (see Table 2 for details).
  • a pre-blend comprising microcrystalline cellulose (Avicel PH101), mannitol (Parteck M200), crospovidone, sucralose, and strawberry
  • A100 standard particle size, i.e., 177-350 ⁇ m
  • the taste-masking coating was compositionally the same for all particles, but the amount of coating on a w/w basis varies from 12.5% on acetaminophen (PE380), 22% on 1.75% hydrocodone bitartrate/acetaminophen (PE382) used in 5 mg/500 mg ODTs (PF401) to 27% on 7% hydrocodone bitartrate/acetaminophen (PE384) used in 10 mg/300 mg ODTs (PF402).
  • the compression blend is compressed into hydrocodone bitartrate/acetaminophen ODTs using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant.
  • Each of the dosages has a unique blend and was prepared using different tableting parameters (see Table 3 below for details). These ODT batches were prepared as described in Examples 3.A to 3.E (see Tables 1 and 2 for compositions. The intermediate and finished products were tested using qualified analytical test methods and used in the pilot PK study in healthy volunteers.
  • Hydrocodone bitartrate/acetaminophen ODTs 5 mg/500 mg and 10 mg/300 mg dosages were tested in a 4-arm pilot PK (pharmacokinetics) study involving 16 healthy subjects per arm in comparison to the corresponding RLDs, Abbott's VICODIN® 5 mg/500 mg, Mikart's Xodol®, 10 mg/300 mg.
  • Acetaminophen and hydrocodone bitartrate plasma concentration vs. time profiles for these ODTs are shown in FIGS. 2 and 3 .
  • FIG. 4 shows the plasma concentration-time profiles for acetaminophen observed in another 3-arm pilot PK study involving 24 healthy subjects per arm wherein Acetaminophen ODT, 500 mg with or without water was administered to fasted healthy volunteers in comparison to the corresponding RLD, GSK's Panadol® 500 mg.
  • Acetaminophen of semi-fine grade (A137) with a smaller particle size distribution of 53-177 ⁇ m were taste-masked by solvent coacervation with Ethocel Standard Premium 100 cps for a coating weight of 10-12%.
  • microcapsules were blended with rapidly dispersing microgranules (PE378 prepared from mannitol 25/crospovidone at 95/5 as disclosed in Example 1.E, above), crospovidone, microcrystalline cellulose, aspartame (sweetener) and strawberry flavor in a V-blender and then compressed on a rotary tablet press equipped with an external lubrication system.
  • P378 prepared from mannitol 25/crospovidone at 95/5 as disclosed in Example 1.E, above
  • crospovidone microcrystalline cellulose
  • aspartame sweetener
  • strawberry flavor in a V-blender
  • Acetaminophen ODTs Quantity % per ODT (mg/tablet) (kg)/Batch Ingredients tablet 250 mg 500 mg 250 mg/500 mg Taste-masked (10-12%) 39.68 277.8 555.5 63.5 Acetaminophen (A137) Rapidly Dispersing 42.12 294.8 589.7 67.4 Granules (PE375) Microcrystalline 10.00 70.0 140.0 8.0 Cellulose (Avicel PH101) Crospovidone NF (XL-10) 5.00 35.0 70.0 16.0 Sucralose NF 1.60 11.2 22.4 2.56 Strawberry Flavor 1.60 11.2 22.4 2.56 Total 100.0 700.0 1400.0 160.0
  • test product Acetaminophen ODT
  • 500 mg when administered with and without water is bioequivalent to the reference product, Panadol®, 500 mg swallowed with water.
  • Multi-speed (50, 75 and 100 rpm) and multi-pH in vitro dissolution (water, pH 1.2, 4.5, 5.8, 6.8) data were generated on batches of 5 mg/500 mg and 10 mg/300 mg ODT tablets of Example 3 and 4 and 250 mg and 500 mg ODT tablets of Example 4, and a comparative data set is presented in Table 6.
  • Acetaminophen/Hydrocodone ODT tablets (5 mg/500 mg or 10 mg/300 mg ODTs) contain two of three types of microencapsulated acetaminophen drug particles—granular grade acetaminophen and granular grade acetaminophen drug particles layered with hydrocodone at a low or high drug load, all taste-masked with a coating of ethylcellulose/Eudragit EPO.
  • Acetaminophen (Semi-fine grade from Covidien with a particle size of 80-270 mesh or 53-177 ⁇ m (A137); 1800.0 g) was taste-masked by solvent coacervation in a 5-gallon system.
  • the 5-gallon system filled with 10,000 g of cyclohexane was charged with ethylcellulose (Ethocel Standard Premium 100 from Dow Chemicals; 114.9 g), polyethylene (Epolene C-10; 50 g), and the drug.
  • the system was subjected to a controlled heating cycle to achieve a temperature of 80° C. to dissolve ethylcellulose while agitating the contents at a speed of 300 RPM.
  • the system was subjected to a computer controlled cooling cycle to ⁇ 28° C. in not less than 45 min to encapsulate the drug crystals with a smooth coating at a coating weight of 6%, and avoiding formation of agglomerates.
  • the microcapsules were separated by decanting, washed with fresh cyclohexane, and dried in a fume hood. The microcapsules with a size less than 35 mesh were collected for taste-masking (useable yield: 98.0%).
  • Hydrocodone bitartrate (57.4 g), acetaminophen (semi-finer grade A137; 1742.6 g), ethylcellulose (156.5 g), polyethylene (50.0 g) were suspended in cyclohexane in the 5 gallon system, and HCB/Acetaminophen microencapsulated particles at an EC-100 coating of 8% by weight were produced following the procedure of Example 5.A.
  • Hydrocodone bitartrate/Acetaminophen microencapsulated particles (1518.8 g) were sealant coating with Klucel LF (288.6 g)/magnesium stearate (15.2 g) and further provided with a second taste-masking membrane comprising ethylcellulose (EC-10)/Eudragit E100/Myvacet/magnesium stearate at a ratio of 286.6/253.5/31.8/35.7 in a Glatt GPCG 3 for a coating weight of 25% as described in Example 3.
  • EC-10 ethylcellulose
  • E100/Myvacet/magnesium stearate at a ratio of 286.6/253.5/31.8/35.7 in a Glatt GPCG 3 for a coating weight of 25% as described in Example 3.
  • Hydrocodone bitartrate (60.0 g and 6.7 g of Klucel LF) was layered onto acetaminophen microcapsules (Semi-fine A137 with an EC-100 coating weight of 6% from Example 5.A; 1205.3 g) in the Glatt GPCG 3 for a coating weight of 8% as described in Example 3.
  • a sealant coating with Klucel LF (28.0 g) was sprayed onto the hydrocodone-layered particles, followed by a taste-masking coating with EC-10/E100/PEG 400/Myvacet 9-45 at a ratio of 40/35/15/10 for a coating weight of 35%.
  • the compression blend comprising taste-masked Hydrocodone/Acetaminophen microparticles from Example 5.B, above or taste-masked Hydrocodone/Acetaminophen microparticles from Example 5.C, above was combined with the rapidly dispersing microgranules from 1.E, above, and a pre-blend comprising microcrystalline cellulose, crospovidone, sucralose, and strawberry flavor, and compressed into hydrocodone bitartrate/acetaminophen ODTs, 5 mg/500 mg and 10 mg/300 mg (see Table 8 for compositions) using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant.
  • Table 9 presents the dissolution profiles of hydrocodone bitartrate and acetaminophen from ODTs.
  • a 200-gallon solvent coacervation system (146 kg) was charged with acetaminophen (Semifine grade A137; 75.5 kg), Ethylcellulose (EC-100; 4.8 kg), Epolene; 2.1 kg) and the acetaminophen was taste-masked by solvent coacervation in a 200-gallon system while agitating at 80 ⁇ 5 RPM.
  • a computer controlled “heat to 80° C.- and hold” cycle was used to achieve a temperature of 80° C. to dissolve the ethylcellulose in the coacervation system.
  • microcapsules were vacuum-filtered, washed with cyclohexane, and dried in a fluid bed dryer using a 3-step temperature (e.g., 25° C., 35° C., 99° C.) for 4 to 6 hrs to achieve a residual cyclohexane level of less than 1000 ppm.
  • the microcapsules were sieved through a US 35 mesh sieve. Following the same procedure, several batches of microcapsules (batch size: 80 kg) were prepared at a coating weight of 6% in the 200 gallon system.
  • Hydrocodone bitartrate (see Table 10 for compositions and batch quantities) was layered onto acetaminophen microcapsules (6% EC-100 coating; 3375.0 g) from Example 6.A, above by spraying the drug-layering formulation comprising hydroxypropylcellulose (10% solids) in a Glatt GPCG 5 (9′′ Wurster, 25 mm partition gap, 200 mesh product retention screen, 1.0 mm nozzle tip diameter, ‘C’ bottom air distribution plate; product temperature: 37 ⁇ 3° C.; inlet air volume: 40-45 CFM; spray rate: 8-24 ml/min) for a hydrocodone bitartrate load of 9.0%.
  • a sealant coating solution of hydroxypropyl (5.0% or 73.68 g dissolved in 50/50 acetone/water at 10% solids) was sprayed onto the drug-layered particles (1400 g) in a Glatt GPCG 3, for a coating weight of 5%, followed by a taste-masking coating with sucralose (5.0%) dissolved in an aqueous solution of hydroxypropylcellulose (1.24%; at a ratio of 80/20 sucralose/HPC) using the following process conditions: Inlet temperature: 57 ⁇ 2° C.; product temperature: 37 ⁇ 2° C.; spray rate: 8 mL/min; inlet air volume: 6 CFM.
  • Hydrocodone bitartrate (see Table 10 for compositions and batch quantities) was layered onto acetaminophen microcapsules (6% EC-100 coating; 3733.3 g) from Example 6.A, above by spraying a drug-layering formulation comprising hydroxypropylcellulose (10% solids) in a Glatt GPCG 5 as described in Example 6.B, above. Following the coating, the microparticles were sealant coated with hydroxypropylcellulose at 5% in the same unit, dried for 5 minutes to reduce residual moisture and sieved through 30 and 80 mesh sieves to discard over sized particles and fines.
  • a compression blend comprising taste-masked hydrocodone/acetaminophen microparticles from Example 6.B, above or taste-masked Hydrocodone/Acetaminophen microparticles from Example 6.C, above was combined with the rapidly dispersing microgranules from 1.E, above, and a pre-blend comprising microcrystalline cellulose, crospovidone, sucralose, and strawberry flavor, and compressed into Hydrocodone bitartrate/Acetaminophen ODTs, 10 mg/300 mg and 5 mg/500 mg (see Table 11 for compositions) using an Elizabeth Hata tablet press.
  • ODT lot # 1334-JMC-142 was compressed using magnesium stearate as an external lubricant
  • ODT lot # 1198-JMC-046 and 1198-JMC-062 were compressed using Sodium stearyl fumarate (PRUV) as an internal lubricant.
  • PRUV Sodium stearyl fumarate
  • Metformin hydrochloride (1000.0 g) is coated in a Glatt GPCG 3 with a solution of ethylcellulose (Ethocel Standard 10 Premium; 78.5 g)/Eudragit E100 (75.0 g) plasticized with polyethylene glycol (PEG 400; 25.9 g) and kosher magnesium stearate (15.6 g) dissolved in 80/20 acetone (1359.5 g)/isopropyl alcohol (672.7 g)/water (770.8 g) for a coating weight of 17.5%. The dried particles are sieved using 35 and 80 mesh sieves to discard agglomerates/fines. A batch of taste-masked metformin microcapsules are also prepared at a coating weight of 25%.
  • a 5% sealant coating with Klucel LF is also applied to avoid potential interaction between the cationic polymer of the taste-masking membrane and low-dose drug (e.g., rosiglitazone).
  • Another batch of taste-masked metformin microparticles is also prepared with the coating formulation at the same ratio and same % solids for a coating weight of 25%, for directly incorporating in the ODT formulation.
  • Rosiglitazone maleate is layered onto sealant-coated metformin microcapsules from Example 7.A, above in the Glatt GPCG 3 for a coating weight gain of 2.5%, using a method similar to that described in Example 5.B, above.
  • a sealant coating of a 2% by weight Klucel LF solution at is sprayed onto the rosiglitazone-layered particles, followed by coating with a taste-masking coating of EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 at a coating weight of 20%.
  • Rosiglitazone maleate/Metformin hydrochloride microparticles from Example 7.B, above, taste-masked Metformin hydrochloride microparticles from Example 7.A, above, rapidly dispersing microgranules from Example 1.E, above and a pre-blend comprising microcrystallinecellulose, sucralose, strawberry flavor, and crospovidone are blended together in a V-blender and compressed into Rosiglitazone/Metformin ODTs, 1 mg/500 mg, 2 mg/500 mg, 4 mg/500 mg, and 4 mg/1 g using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant to lubricate punch and die surfaces prior to compression.
  • ODT formulations comprising microparticles comprising high-dose metformin HCl/low-dose rosiglitazone maleate (e.g., 500 mg/l mg, 500 mg/2 mg, or 500 mg/4 mg) exhibit acceptable tableting properties (e.g., hardness, friability, uniformity of dosage forms, low in vitro/in vivo disintegration time, rapid dissolution, acceptable organoleptic properties which significantly improve patient-compliance.
  • the pharmaceutical compositions (and oral dosage forms prepared therefrom) of the present invention exhibit acceptable taste-masking and provides rapid, substantially-complete release of the dose on entry into the stomach, thereby providing bioequivalence to the appropriate reference immediate release (IR) product.
  • IR immediate release
  • Povidone (PVP K-30; 50 g) is slowly added to purified water (500 g) while constantly stirring to prepare a polymer binder solution at 10% w/w solids.
  • Niacin or nicotinic acid from Lonza Corporation; 2000 g
  • colloidal silica a flow aid, Cab-O-Sil M-5P from Cabot Corporation
  • povidone 50 g
  • the 10% PVP binder solution is sprayed into the rotating material bed at a controlled rate.
  • Optimized process parameters during pellet formation process air temperature: ⁇ 19-20° C.; product temperature: 16 ⁇ 2° C.; Rotor speed: 425 RPM; External air supply: 150 L/min; Spray rate: 15 RPM ( ⁇ 8 mL/min); pressure drop across slit: 1.3-11 mm in water.
  • Optimized process parameters during drying of pellets Process air temperature: ⁇ 19-20° C.; product temperature: 16 ⁇ 2° C.; Rotor speed: 425 RPM; External air supply: 150 L/min; Spray rate: 15 RPM ( ⁇ 8 mL/min); pressure drop across slit: 1.3-11 mm in water.
  • Optimized process parameters during drying of pellets Process air temperature: ⁇ 60° C.; Product temperature: 35° C. (to stop drying); Rotor speed: 180 RPM; Slit air volume: 10 CFM; Processing time: 40 min. About 65% of the pellets thus prepared have a size in the range of 40-80 mesh.
  • Niacin microparticles (1600 g) from step 8.A, above are provided with an SR coating with ethylcellulose (Ethocel Standard 10 Premium; 180 g)/TEC (triethyl citrate, a plasticizer; 20 g) dissolved in 90/10 acetone/water for a 15% weight gain. Samples are pulled at a coating of 7.5, 10, 12.5% by weight for drug release testing. The dried particles are sieved using 30 and 80 mesh sieves to discard agglomerates/fines. A 2% seal coat with Klucel LF is also applied to avoid potential interaction between the polymer/plasticizer and low-dose drug (e.g., atorvastatin).
  • ethocel Standard 10 Premium 180 g
  • TEC triethyl citrate, a plasticizer
  • Another batch of taste-masked niacin microparticles is also be prepared with the coating formulation at the same ratio and same % solids for a weight gain of 15% based on the total weight of the coated microparticles for directly incorporating in the ODT formulation.
  • Atorvastatin calcium is layered onto seal-coated niacin microcapsules from step 8.B, above in the Glatt GPCG 3 for a weight gain of 4% as described in Example 1.C, above.
  • a seal coating of Klucel LF at 2% by weight is sprayed onto the atorvastatin-layered particles, followed by a taste-masking coating with EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 for a weight gain of 20%.

Abstract

The present invention is directed to pharmaceutical compositions comprising a plurality of taste-masked high-dose/low-dose drug-containing microparticles, dosage forms comprising such pharmaceutical compositions (such as an orally disintegrating tablet), and methods of making the pharmaceutical compositions and dosage forms of the present invention. Dosage forms comprising the pharmaceutical compositions of the present invention are improved homogeneous blends of high-dose and low-dose drugs which provide for more convenient and palatable administration of drug combinations, for example for treating pain, hyperglycemia, cardiovascular disease, and allergies.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • The present application claims priority to U.S. Provisional Application Nos. 61/174,780 and 61/174,788, both filed May 1, 2009.
    • BACKGROUND OF THE INVENTION
  • Moderate to severe pain can be effectively treated with opioid analgesics such as hydrocodone. However since many opioids are habit forming, the risk of abuse can be moderated by combining the opioid with a non-opioid analgesic such as acetaminophen, aspirin, ibuprofen, etc., thereby allowing effective pain management at lower doses of the opioid analgesic. Other medical conditions such as diabetes (hyperglycemia), cardiovascular disease, and schizophrenia are also effectively treated with drug combinations. However, the need to administer multiple dosage forms can result in problems such as patient compliance issues or dosage administration errors.
  • One approach to preventing such problems is to combine multiple drugs into a single dosage form in order to minimize the number of different dosage forms to be administered, and to ensure that the combination of drugs are administered in the correct relative dosages. For example, Vicodin® is an immediate-release (IR) tablet containing 5 mg of hydrocodone bitartrate and 500 mg of acetaminophen, intended for the management of severe pain. However, it is very difficult to reproducibly prepare homogeneous blends of hydrocodone and acetaminophen at the required 1:100 weight ratio (e.g., with a content uniformity having an RSD of 6% or less, as required by regulatory agencies worldwide). Thus, there is a need for methods for uniformly and reproducibly combining a high-dose drug and a low-dose drug in a single dosage form.
  • The two most widely used types of oral dosage forms are tablets and capsules. However, such dosage forms have several disadvantages. For example, it is estimated that 50% of the population have problems swallowing tablets (see Seager, Journal of Pharmacol. and Pharm. 50, pages 375-382, 1998). It is especially hard for the elderly or for children to swallow tablets or capsules, or to medicate patients who are unable or unwilling to swallow tablets or capsules. Furthermore, conventional tablets or capsules usually must be administered with water, which is not always possible or convenient. This leads to poor or even non-compliance with the treatment which consequently has a negative impact on the efficacy of the treatment. Orally disintegrating tablet (ODT) dosage forms have been introduced to address such problems, because ODTs rapidly dissolve or disintegrate in the buccal cavity and the resulting slurry or suspension of the drug is more readily swallowed by the patient. Such dosage forms are also more convenient because they need not be administered with water.
  • Because the ODT dosage form disintegrates in the oral cavity of the patient, the disintegrated ODT must be palatable. For example, if one or more of the drugs in the ODT are bitter tasting, the drug-containing particles comprising the ODT must be taste-masked, e.g., by coating the drug-containing particles with a polymeric membrane to prevent release of the drug in the oral cavity. However, the main drawback of taste-masking is slower dissolution of the drug(s) from effectively taste-masked microparticles. The more bitter the drug, the thicker the taste-masking coating required and hence, the slower the drug release from the taste-masked drug-containing particles. Thus the very process of effectively taste-masking the drug-containing particles results in a substantially slower drug release, with concomitant slower systemic absorption of the drug in the gastrointestinal tract.
  • In some cases, slower drug release is a particular problem for ODT dosage forms which are intended to be bioequivalent to a reference listed immediate-release (IR) dosage form of the drug, for example bioequivalent to conventional tablet or effervescent tablet based IR dosage forms having a Tmax of less than an hour, and rapid-onset of action. For such bioequivalent immediate release ODT products, it is essential that the taste-masking layer should not substantially lower the release rate of the drug. For ODT compositions containing combinations of two or more drugs (e.g., a high-dose/low-dose drug formulation) this problem is particularly acute, because the different drug components of the combination ODT may require different levels of taste-masking depending on the degree of bitterness of the drugs (i.e., drugs with low bitterness levels may require little or no taste-masking, while highly bitter drugs may require substantial taste-masking layers). Adding further complication, taste-masking layers reduce the release rate of poorly soluble drugs more than for more soluble drugs. In certain cases, an ODT composition comprising taste-masked low-dose drug particles combined with sustained release coated high-dose drug particles may be more desirable.
  • In addition, ODTs must rapidly disintegrate on contact with the saliva in the oral cavity while also providing sufficient tablet hardness and strength sufficient to withstand attrition during packaging, storage, transportation, distribution, and end use, and also provide acceptable organoleptic properties (e.g., be palatable as described above, and exhibit a smooth (non-gritty) mouthfeel), and acceptable pharmacokinetic properties (i.e., rapid onset, Cmax, AUC properties similar to the reference listed drugs). Achieving all of these properties is often quite difficult because thicker taste-masking layers may be required for adequate taste-masking of more soluble and/or more bitter drugs, which may make it difficult to obtain the required rapid drug release.
  • Thus, the preparation of clinically effective pharmaceutical compositions comprising at least a high-dose and a low-dose drug, particularly in the form of an ODT, is quite difficult and requires the balancing of many different and often competing requirements.
    • SUMMARY OF THE INVENTION
  • In one embodiment, the present invention is directed to a pharmaceutical composition comprising a plurality of modified-release coated high-dose/low-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
      • (a) a core comprising a high-dose drug;
      • (b) a first coating comprising a low-dose drug disposed over the core; and
      • (c) a second coating disposed over the core, modified-release coating (e.g., a taste-masking or sustained release coating to achieve taste-masking and/or extended/sustained release properties), comprising a comprising a water-insoluble polymer.
  • In another embodiment, the present invention is directed to a pharmaceutical composition comprising a plurality of taste-masked non-opioid analgesic drug/opioid analgesic drug-containing microparticles, wherein the drug-containing microparticles comprise:
      • (a) a core comprising a high dose drug such as a non-opioid analgesic drug;
      • (b) a layer comprising a low dose drug such as an opioid analgesic drug disposed over the high-dose drug-containing core; and
      • (c) at least one modified-release coating layer (e.g., a taste-masking or sustained release coating layer) disposed over the high-dose drug core as well as the high-dose/low-dose drug-containing core, wherein the at least one taste-masking or sustained release coating layer comprises a water-insoluble polymer, or the combination of a water-insoluble polymer with one or more of a water-soluble polymer, an enteric polymer, or a gastrosoluble pore-former.
  • In still another embodiment, the present invention is directed to a pharmaceutical composition comprising a plurality of high-dose/low-dose drug-containing microparticles in combination with high-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
      • (a) a core comprising a high-dose drug;
      • (b) an optional sealant coat disposed over the high-dose drug-containing core;
      • (c) a sustained-release coating layer disposed over the high-dose drug-containing core;
      • (d) a low-dose drug layer disposed over the sustained-release coating layer;
      • (e) a sealant coat disposed over the low-dose drug layer; and
      • (f) a taste-masking layer disposed over the sealant coat;
  • wherein the sustained-release coating layer comprises a water-insoluble polymer optionally in combination with one or more of a water soluble or enteric polymer; thereby imparting taste-masking and/or sustained release properties to the high-dose drug-containing microparticles; and the taste-masking layer disposed over the low-dose drug-containing microparticles comprises a water-insoluble polymer optionally in combination with a gastrosoluble polymer or a gastrosoluble pore-former.
  • In yet another embodiment, the present invention is directed to a pharmaceutical composition comprising a plurality of modified-release coated high-dose/low-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
      • (a) a core comprising a high-dose drug;
      • (b) an optional sealant coat disposed over the high-dose drug-containing core;
      • (c) a taste-masking coating layer disposed over the sealant coating layer;
      • (d) a low-dose drug layer disposed over the taste-masking coating layer;
      • (e) a sealant coat disposed over the low-dose drug layer; and
      • (f) a flavorant layer disposed over the sealant coat.
  • In still yet another embodiment, the present invention is directed to an ODT dosage form comprising the combination of one of the pharmaceutical compositions of the present invention, rapidly dispersing microgranules, and optionally a second population of high-dose drug containing particles comprising a high-dose drug-containing core coated with a modified-release coating layer.
  • In a further embodiment, the present invention is directed to a method for preparing the pharmaceutical compositions disclosed herein, comprising:
      • (1) preparing cores comprising a high-dose drug;
      • (2) coating the high-dose drug-containing cores of step (1) with a low-dose drug layer, thereby forming high-dose/low-dose drug-containing microparticles; and
      • (3) coating the high-dose drug-containing cores of step (1) and/or the high-dose/low-dose drug-containing microparticles of step (2) with a coating layer comprising a water-insoluble polymer, thereby forming taste-masked and sustained-release high-dose/low-dose drug-containing microparticles.
  • In a further embodiment, the present invention is directed to a method for preparing an ODT pharmaceutical composition as disclosed herein, further comprising:
      • (1) preparing rapidly dispersing microgranules comprising a sugar alcohol, a saccharide, or a mixture thereof with an average particle size of not more than 30 μm and a super disintegrant;
      • (2) preparing a blend comprising high-dose/low-dose drug-containing microparticles with high-dose drug-containing microparticles and rapidly dispersing microgranules
      • (3) compressing the blend into orally disintegrating tablets.
  • In a further embodiment, the present invention is directed to a method of treating a patient subject to a disease or condition, comprising administering a therapeutically effective amount of the high-dose drug and low-dose drug-containing compositions of the present invention to the patient in need thereof.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 illustrates a schematic of one embodiment of a modified release coated microparticle comprising a high-dose drug-containing core, as well as a taste-masked low-dose/high-dose drug-containing microparticle.
  • FIG. 2 illustrates the plasma concentration-time profiles for acetaminophen of hydrocodone bitartrate/acetaminophen tablets observed in the pilot PK (pharmacokinetics) study.
  • FIG. 3 illustrates the plasma concentration-time profiles for hydrocodone bitartrate of hydrocodone bitartrate/acetaminophen tablets observed in the pilot PK (pharmacokinetics) study.
  • FIG. 4 illustrates the plasma concentration-time profiles for acetaminophen of Acetaminophen ODTs versus Panadol® observed in the pilot PK (pharmacokinetics) study.
    •  DETAILED DESCRIPTION OF THE INVENTION
  • All documents cited herein are incorporated by reference in their entirety for all purposes. The citation of any document is not to be construed as an admission that it is prior art with respect to the present invention.
  • The present invention is directed to pharmaceutical compositions comprising a plurality of modified-release coated high-dose/low-dose drug-containing microparticles as described herein. The compositions of the present invention provide combination high-dose drug/low-dose drug-containing oral dosage forms meeting one or more of the following specifications:
      • Taste-masked and/or sustained release coated microparticles wherein the low-dose drug is layered onto high-dose drug-containing microparticles having a blend homogeneity meeting United States Pharmacopoeia requirements;
      • effectively taste-masked microparticles, irrespective of the differences in solubility and bitterness of the high-dose and low-dose drugs;
      • in some embodiments further comprising rapidly dispersing granules so as to provide an ODT dosage form which rapidly disintegrates on contact with saliva in the oral cavity, and form a smooth, easy-to-swallow suspension containing taste-masked drug particles;
      • drug particles with an average particle diameter of not more than about 400 μm to provide a smooth mouthfeel leaving no aftertaste (i.e., little or minimal drug release with a non-gritty or non-chalky taste) until swallowed;
      • providing rapid, substantially-complete release of the dose from the taste-masked immediate-release drug particles upon arrival in the stomach, thereby enhancing the probability of being bioequivalent to the corresponding immediate-release reference-listed-drug product(s) or providing a target release profile of the high-dose drug to be suitable for a once- or twice-daily dosing regimen; and
      • providing robust tablet formulations exhibiting acceptable tablet hardness and friability suitable for packaging in HDPE bottles, and/or transportation in bulk or as packaged tablets for commercial distribution and end use.
  • The term “drug”, “active” or “active pharmaceutical ingredient” as used herein includes a pharmaceutically acceptable and therapeutically effective compound, pharmaceutically acceptable salts, stereoisomers and mixtures of stereoisomers, solvates (including hydrates), polymorphs, and/or esters thereof. When referring to a drug in the descriptions of the various embodiments of the invention, the reference encompasses the base drug, pharmaceutically acceptable salts, stereoisomers and mixtures of stereoisomers, solvates (including hydrates), polymorphs, and/or esters thereof, unless otherwise indicated.
  • The terms “layer” or “coating” as used herein are synonymous. For example, the terms sealant layer, drug layer, etc., are synonymous with sealant coating, drug coating, etc.
  • The terms “orally disintegrating tablet” or “ODT” refers to a tablet which disintegrates rapidly in the oral cavity of a patient after administration, without the need for chewing. The rate of disintegration can vary, but is faster than the rate of disintegration of conventional solid dosage forms (e.g., tablets or capsules) which are intended to be swallowed immediately after administration, or chewable solid dosage forms. Orally disintegrating compositions of the present invention can contain pharmaceutically acceptable ingredients which swell, dissolve or otherwise facilitate the disintegration or dissolution of the ODT composition. Such ingredients can include pharmaceutical disintegrant such as crospovidone, water-soluble sugar alcohol such as mannitol, a saccharide such as lactose, or a mixture thereof, a water-soluble binder such as povidone, a meltable solid (e.g., a hydrophobic wax such as polyethylene glycol, glyceryl behenate, stearic acid, hydrogenated castor oil, etc.) which can release the drugs upon entering the stomach. Orally disintegrating compositions of the present invention may be in the form of a tablet, a minitablet, a capsule or a monodose sachet, or a dry powder for reconstitution.
  • The term “about”, as used herein to refer to a numerical quantity, includes “exactly”. For example, “about 60 second” includes 60 seconds, exactly, as well as values close to 60 seconds (e.g., 50 seconds, 55 seconds, 59 seconds, 61 seconds, 65 seconds, 70 seconds, etc.).
  • Unless stated otherwise, the amount of the various coatings or layers described herein (the “coating weight”) is expressed as the percentage weight gain of the particles or beads provided by the dried coating, relative to the initial weight of the particles or beads prior to coating. Thus, a 10% coating weight refers to a dried coating which increases the weight of a particle by 10%.
  • As used herein, the term “immediate-release” or IR refers to release of greater than or equal to about 50%, or greater than about 75%, or greater than about 90%, or greater than about 95% of the drug within about 2 hours, more particularly within about one hour following administration of the dosage form.
  • The term “substantially disintegrates” means a level of disintegration amounting to disintegration of at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, or about 100% disintegration of the ODT composition.
  • As used herein, the term “modified-release” coating encompasses coatings that delay release, sustain release, extend release, prevent release, and/or otherwise prolong the release of a drug relative to formulations lacking such coatings which release a drug relatively quickly (i.e., “immediate release” compositions). The term “controlled-release” encompasses “sustained release,” “extended release,” “delayed release,” and “timed, pulsatile release.”The term “lag-time” coating refers to a particular type of “controlled release” coating in which the lag time coating delays release of a drug after administration. The term “controlled release” is also used interchangeably with “modified release.” The term “controlled-release particle” refers to a particle showing one or more controlled-release properties, as described herein. The term “controlled-release particle” also refers to a drug-containing particle coated with one or more controlled-release coatings, as described herein.
  • The term “substantially masks the taste” in reference to the taste-masking layer of the IR particles (when present) refers to the ability of the taste-masking layer to substantially prevent release of a bitter tasting drug in the oral cavity of a patient. A taste-masking layer which “substantially masks” the taste of the drug typically releases less than about 10% of the drug in the oral cavity of the patient, in other embodiments, less than about 5%, less than about 1%, less than about 0.5%, less than about 0.1%, less than about 0.05%, less than about 0.03%, less than about 0.01% of the drug. The taste-masking properties of the taste-masking layer of the compositions of the present invention can be measured in vivo (e.g., using conventional organoleptic testing methods known in the art) or in vitro (e.g., using dissolution tests as described herein). The skilled artisan will recognize that the amount of drug release associated with a taste-masking layer than “substantially masks” the taste of a drug is not limited to the ranges expressly disclosed herein, and can vary depending on other factors, such as the perceived the bitterness of the drug and the presence of other flavoring agents in the composition.
  • The term “substantially modifies release” in reference to a layer refers to the ability of the layer to provide modified release properties, i.e., delay release, sustain release, extend release, prevent release, and/or otherwise prolong the release of a drug relative to formulations lacking such coatings which release a drug relatively quickly (i.e., “immediate release” compositions), as described herein.
  • As used herein, the term “sustained-release” (SR) refers to the property of slow release of a drug from a drug-containing core particle, without an appreciable lag time. The term “sustained-release coating” or “SR coating” refers to a coating showing sustained-release properties. The term “sustained-release particle” refers to a drug-containing particle showing sustained-release properties. In one embodiment, a sustained-release coating comprises a water-insoluble polymer and optionally a water-soluble polymer. An SR coating can optionally contain a plasticizer or other ingredients that do not interfere with the “sustained-release” properties of the coating.
  • As used herein, the term “timed, pulsatile release” (TPR) refers to the property of modified release of a drug after a pre-determined lag time. The term “timed, pulsatile-release coating” or “TPR coating” refers to a coating showing timed, pulsatile-release properties. The term “timed, pulsatile-release particle” refers to a drug-containing particle showing timed, pulsatile-release properties. In some embodiments, a lag time of from at least about 2 to about 10 hours is achieved by coating the particle with, e.g. a combination of at least one water-insoluble polymer and at least one enteric polymer (e.g., a combination of ethylcellulose and hypromellose phthalate). A TPR coating can optionally contain a plasticizer or other ingredients which do not interfere with the “timed, pulsatile release” properties of the coating.
  • The term “modified-release coated drug-containing microparticles” refers generally to drug-containing microparticles (e.g., crystals, granules, pellets produced by controlled spheronization, or drug layered particles/beads) coated with one or more functional polymers to achieve effective taste-masking and/or extended/sustained release properties. With respect to high-dose/low-dose drug-containing microparticles, this term refers to modified-release coated high-dose/low-dose drug containing microparticles as described herein.
  • The terms “plasma concentration-time profile”, “Cmax”, “AUC”, “Tmax”, and “elimination half life” have their generally accepted meanings as defined in the FDA Guidance to Industry: Bioequivalence.
  • Unless otherwise indicated, all percentages and ratios are calculated by weight based on the total composition.
  • The term “disposed over” means that a second material is deposited over a first material, wherein the second material may or may not be in direct physical contact with the first material. Thus it is possible, but not necessary, that an intervening material lies between the first and second materials.
  • Combination drug therapies are increasingly useful in treating diseases or conditions which are advantageously treated by the administration of two or more drugs. For example, pain treatments benefit from the administration of low doses of opioid analgesics combined with relatively high-doses of non-opioid analgesics (e.g., an NSAID), which effectively treat moderate to severe pain, yet reduce the amount of potentially habit forming opioid drug administered. For other indications (e.g., diabetes), the combination of drugs can interact synergistically to provide greater clinical benefits compared to either drug administered individually. However, the need to administer multiple dosage forms, each containing a single drug, can result in problems such as reduced patient compliance, errors in administering the proper doses of each drug, etc. It is therefore beneficial in such situations to prepare a single dosage form combining the two (or more) drugs, thereby permitting the administration of a single dosage form rather than two (or more) dosage forms. However, it can be difficult to prepare such combination pharmaceutical formulations, when one of the drugs is present in a relatively high concentration compared to one or more of the other drugs; as a practical matter it is difficult to obtain a uniform mixture of a high-dose drug and a low-dose drug, such that the high-dose drug and the low-dose drug are both reproducibly provided at their respective correct dosages.
  • The present invention is directed to pharmaceutical compositions comprising a plurality of taste-masked high-dose/low-dose drug-containing microparticles, each containing both the high-dose drug (or drugs) and the low-dose drug (or drugs). The core of the taste-masked high-dose/low-dose drug-containing microparticles comprises the high-dose drug, and the low-dose drug is provided in a low-dose drug layer disposed over the high-dose drug-containing core.
  • Suitable core compositions include particles of the high-dose drug itself (e.g., formed by recrystallization or precipitation of the high-dose drug from solution, or by milling and sieving the high-dose drug, etc., such that high-dose drug-containing particles of a desired particle size and particle size distribution are obtained). Alternatively, the core can comprise a granulate comprising particles of the high-dose drug in combination one or more pharmaceutically acceptable excipients (e.g., lactose, mannitol, microcrystalline cellulose, etc.) and an optional binder, prepared by wet or dry granulation. In still other embodiments, the core can comprise extruded and spheronized particles comprising the high-dose drug (e.g., in combination with suitable pharmaceutically acceptable excipients as described herein) or high-dose drug pellets are produced by controlled spheronization in a Granurex VEC-35 or VEC-40 from Vector Corporation, and these pellets are coated with polymers or polymer blends providing target drug release profiles suitable for once- or twice-daily dosing regimen. In yet other embodiments, the core comprises drug layered beads—i.e., an inert core (e.g., sugar spheres, microcrystalline cellulose, mannitol-microcrystalline cellulose, silicon dioxide, etc.) layered with the high-dose drug and an optional binder. In further embodiments, the core can comprise the high-dose drug in combination with pharmaceutically acceptable excipients, compressed into “minitabs” having a particle diameter in the range of about 2-5 mm. In a particular embodiment, the core comprises particles of the high-dose drug. In many embodiments, the core has an average particle size of less than about 500 μm, or less than about 400 μm, or less than about 300 μm, or less than about 200 μm.
  • Any pharmaceutically acceptable high-dose/low-dose drug combination that is efficacious in the treatment of disease states or conditions including, for example, cardiovascular diseases, diabetes, moderate to severe pain, gastrointestinal disorders, etc. can be selected in accordance with certain embodiments of the present invention to create pharmaceutical compositions comprising one or more populations of modified release coated high-dose/low-dose drug-containing microparticles exhibiting desired in vitro/in vivo drug release profiles.
  • Any pharmaceutically acceptable polymeric binder which is compatible with the high-dose drug and/or other components of the composition may be used in preparing the high-dose drug-containing cores (e.g., a binder used in forming a granulate, in forming drug-layered beads, etc.). Suitable polymeric binders include for example, polymers selected from the group consisting of hydroxypropylcellulose, povidone, methylcellulose, hydroxypropyl methylcellulose, carboxyalkylcelluloses, polyethylene oxides, polysaccharides, acacia, alginic acid, agar, calcium carrageenan, sodium carboxymethylcellulose, microcrystalline cellulose, dextrin, ethylcellulose, gelatin, liquid glucose, guar gum, hydroxypropyl methylcellulose, methylcellulose, pectin, PEG, povidone, pregelatinized starch, etc.
  • The high-dose drug-containing core can be coated directly with the low-dose drug layer, or can be first coated with a sealant layer. Suitable sealant layers comprise a hydrophilic water-soluble polymer. Non-limiting examples of suitable hydrophilic polymers include hydrophilic hydroxypropyl cellulose (e.g., Klucel® LF), hydroxypropyl methylcellulose or hypromellose (e.g., Opadry® Clear or Pharmacoat™ 603), vinylpyrrolidone-vinylacetate copolymer (e.g., Kollidon® VA 64 from BASF), and ethylcellulose, e.g. low-viscosity ethylcellulose. In many embodiments, particularly when the high-dose drug-containing core is particles of the high-dose drug, the compositions of the present invention do not require a sealant layer coated directly over the core.
  • The sealant layer can be applied at a coating weight of about 1% to about 10%, for example about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10%, inclusive of all ranges and subranges therebetween.
  • In some embodiments, the compositions of the present invention are intended to disintegrate in the oral cavity of the patient upon administration (e.g., the ODT dosage form as described herein). In such embodiments, when the high-dose drug and/or the low-dose drug has unpleasant sensory properties (e.g., is bitter tasting), the high-dose drug-containing core and/or the low-dose drug-containing layer is taste-masked to prevent the patient from tasting the high-dose and/or low dose drug, e.g. by coating the high-dose drug-containing core and/or the low-dose drug-containing layer with a taste-masking layer. For example, the compositions of the present invention can include a single taste-masking layer as described herein disposed between the high-dose drug-containing core and the low-dose drug-containing layer, a single taste-masking layer as described herein disposed over the low-dose drug-containing layer, or two taste-masking layers disposed respectively between the high-dose drug-containing core and the low-dose drug-containing layer and over the low-dose drug-containing layer. The taste-masking layer can be coated directly onto the high-dose drug-containing core and/or the low-dose drug-containing layer, or the high-dose drug-containing core and/or low-dose drug-containing layer can be first coated with a sealant layer (e.g., as described herein) for example to minimize or prevent static charging and/or particle attrition, followed by the taste-masking polymer coating. When the compositions of the present invention comprise two or more taste-masking layers, the taste-masking layers can be independently selected from any of the taste-masking layer compositions described herein.
  • Suitable taste-masking layers can comprise a water-insoluble polymer or the combination of a water-insoluble polymer and a gastrosoluble pore-former (e.g., gastrosoluble and pharmaceutically acceptable organic, inorganic, or polymeric materials.
  • The taste-masking layer can be coated onto the high-dose drug-containing core and/or low-dose drug-containing layer by any suitable method, e.g., fluid bed coating or coacervation. For example the taste-masking polymer coating can be deposited in the core to provide a weight gain (after coating and drying) of from about 3% to about 50%, including about 3%, about 5%, about 7%, about 10%, about 12%, about 15%, about 17%, about 20%, about 22%, about 25%, about 27%, about 30%, about 35%, about 40%, about 45%, or about 50%, inclusive of all ranges and subranges therebetween.
  • Non-limiting examples of suitable water-insoluble polymers include ethylcellulose, cellulose acetate, cellulose triacetate, cellulose acetate butyrate, polyvinyl acetate, neutral methacrylic acid-methylmethacrylate copolymers (e.g., Eudragit RL, RS, and NE30D, etc.), and mixtures thereof. In one embodiment, the water-insoluble polymer comprises ethylcellulose. In another embodiment, the water-insoluble polymer comprises ethylcellulose with a mean viscosity of 10 cps (e.g., Ethocel Standard 10 Premium) or about 100 cps (Ethocel Standard 100 Premium) in a 5% solution in 80/20 toluene/ethanol, measured at 25° C. with an Ubbelohde viscometer.
  • As described herein, in some embodiments the taste-masking layer(s) independently comprises the combination of a water-insoluble polymer (as described herein) and a gastrosoluble pore-former. Pore-formers include polymeric and non-polymeric pharmaceutically acceptable gastrosoluble materials. Non-limiting examples of non-polymeric gastrosoluble pore-formers, include pharmaceutically acceptable inorganic materials such as calcium carbonate, magnesium carbonate, calcium phosphate, ferric hydroxide, ferric phosphate, magnesium hydroxide, magnesium phosphate, etc.; pharmaceutically acceptable non-polymeric organic materials such as calcium saccharide, calcium succinate, calcium tartrate, magnesium citrate, ferric acetate, etc.; pharmaceutically acceptable gastrosoluble polymers including maltrin, aminoalkyl methacrylate copolymers available under the trade name of Eudragit® (type E100 or EPO), polyvinylacetal diethylaminoacetate e.g., AEA® available from Sankyo Company Limited, Tokyo (Japan), and the like; and mixtures thereof. In one embodiment, the gastrosoluble polymer is a terpolymer based on dimethylaminoethyl methacrylate, butyl methacrylate, and methyl methacrylate. In another embodiment, the terpolymer has an average molecular weight of 150,000 and the ratio of the monomers is 1:2:1 of methyl methacrylate, N,N-dimethylaminoethyl methacrylate, and butyl methacrylate, and mixtures thereof.
  • The ratio of water-insoluble polymer to gastrosoluble pore-former ranges from about 95/5 to about 50/50 including about 90/10, about 85/15, about 80/20, about 75/25, about 70/30, about 65/35, about 60/40, or about 55/45.
  • The coating weight of the taste-masking layer comprising a water-insoluble polymer and a gastrosoluble pore-former ranges from about 5% to about 30%, or about 5%-25%, about 5%-20%, about 5%-15%, about 5%-10%, about 10%-30%, about 10%-25%, about 10%-20%, about 10%-15%, about 15%-30%, about 50%-25%, about 15%-20%, about 20%-30%, about 20%-25%, or about 25%-30%.
  • The ratio of the water-insoluble polymer to the gastrosoluble polymer ranges from about 9/1 to about 1/1, including the range of about 6/3 to about 2/1. In other embodiments, the ratio of water-insoluble polymer to gastrosoluble polymer is about 95/5, about 90/10, about 85/15, about 80/20, about 75/25, about 70/30, about 65/35, about 60/40, about 55/45, or about 50/50, inclusive of all values, ranges, and subranges therebetween.
  • In some embodiments, the taste-masking layer comprising the combination of a water-insoluble polymer and gastrosoluble polymer has a coating weight of about 10% to about 40% by weight, including the ranges from about 12% to about 30%, about 15% to about 25%, and from about 20% to about 30%. In other embodiments, the coating weight of the taste-masking layer comprising a combination of water-insoluble and gastrosoluble polymers is about 10%, about 12.5%, about 13%, about 15%, about 17%, about 18%, about 20%, about 22%, about 24%, about 25%, about 27%, about 30%, about 35%, or about 40%, inclusive of all ranges and subranges therebetween.
  • In various embodiments, it is desirable to provide an extended-release coating layer over the high-dose drug-containing cores in order to modify the release of the high-dose drug. The extended-release coating disposed over the high-dose drug-containing cores can comprise a water-insoluble polymer, thereby providing a sustained release (SR) coating; a water-insoluble polymer in combination with an enteric or water-soluble polymer, thereby providing a timed pulsatile release (TPR) coating. In still other embodiments, the extended-release coating comprises an enteric polymer disposed on the high-dose drug-containing particle, thereby providing a delayed release (DR) coating.
  • In some embodiments, the extended-release coating provides suitable properties (e.g., extended release characteristics, mechanical properties, and coating properties) without the need for a plasticizer. For example, ethylcellulose without a plasticizer is used for coating drug-containing cores by solvent coacervation via phase separation for taste-masking, and or can be applied e.g. from a suitable solvent to provide sustained-release properties. Also, coatings comprising polyvinyl acetate (PVA), neutral and cationic copolymers of acrylate/methacrylate esters (e.g., NE30D and EPO), waxes, etc. can be applied without plasticizers.
  • Non-limiting examples of suitable enteric polymers include cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, hydroxypropyl methylcellulose acetate succinate, polyvinyl acetate phthalate, pH-sensitive methacrylic acid/methylmethacrylate copolymers (e.g., Eudragit® L, S and FS polymers), shellac, and mixtures thereof. In certain embodiments, non-polymeric enteric materials such as non-polymeric waxes and fatty acid compositions may be used instead of enteric polymers, provided they have the pH sensitive solubility associate with enteric polymers. These enteric polymers may be used as a solution in a solvent mixture or an aqueous dispersion. Some commercially available materials that may be used are methacrylic acid copolymers sold under the trademark Eudragit (L100, S100, L30D) manufactured by Rohm Pharma, Cellacefate (cellulose acetate phthalate) from Eastman Chemical Co., Aquateric (cellulose acetate phthalate aqueous dispersion) from FMC Corp., and Aqoat (hydroxypropyl methylcellulose acetate succinate aqueous dispersion) from Shin Etsu K.K.
  • The coating weight of the extended-release coating comprising the combination of a water-insoluble polymer and an enteric polymer ranges from about 10 to 60%, more particularly from about 30% to 60%, including about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, or about 55%, inclusive of all ranges and sub ranges therebetween. The ratio of water insoluble polymer to enteric polymer may vary from about 10:1 to 1:2, more particularly from about 2:1 to 1:1, including about 9:1, about 8:1, about 7:1 about 6:1, about 5:1 about 4:1, about 3:1, about 2:1, or about 1:1.
  • In other embodiments, the extended-release layer comprises the combination of a water-insoluble polymer (as described herein) in combination with a water-soluble polymer. Non-limiting examples of suitable water-soluble polymers include polyvinylpyrrolidone (e.g., Povidone K-25), polyethylene glycol (e.g., PEG 400), hydroxypropyl methylcellulose, and hydroxypropylcellulose.
  • The ratio of the water-insoluble polymer to the water-soluble polymer ranges from about 95/5 to about 50/50, including ratios of about 95/5, about 90/10, about 85/15, about 80/20, about 75/25, about 70/30, about 65/35, about 60/40, about 55/45, or about 50/50, inclusive of all ranges and subranges therebetween. In other embodiments, the taste-masking layer comprising the combination of a water-insoluble polymer and a water-soluble polymer is deposited over the high-dose drug-containing core at a coating weight of about 3%, about 5%, about 7%, about 10%, about 12%, about 15%, about 17%, about 20%, about 22%, about 25%, about 27%, about 30%, about 35%, about 40%, about 45%, and about 50% by weight, inclusive of all values, ranges, and subranges therebetween.
  • In some other embodiments, the present invention relates to a pharmaceutical composition comprising modified-release coated high-dose drug cores comprising at least one therapeutic agent or a pharmaceutically acceptable salt, solvate, and/or ester thereof; a water-insoluble polymer (e.g., ethylcellulose), a second optional coating disposed over the first coating, comprising an enteric polymer and optionally a water-insoluble polymer (e.g., ethylcellulose and hypromellose phthalate at a ratio of from about 9:1 to about 5:5).
  • The modified-release or taste-masking layer can be unplasticized or plasticized. For example, drug-containing particles can be taste-masked with ethylcellulose by solvent coacervation via phase separation without requiring a plasticizer, or from suitable pharmaceutically acceptable solvent using a fluid bed coater. Modified-release coatings comprising various polymers such as Eudragit NE30D or various hydrophobic waxes in a fluid bed coater typically do not require a plasticizer.
  • When it is desirable or convenient to use a plasticizer, non-limiting examples of suitable plasticizers include glycerol and esters thereof (e.g., acetylated mono- or diglycerides including commercially available Myvacet® 9-45), glyceryl monostearate, glyceryl triacetate, glyceryl tributyrate, phthalates (e.g., dibutyl phthalate, diethyl phthalate, dimethyl phthalate, dioctyl phthalate, etc.), acetylcitric acid tributyl ester, acetylcitric acid triethyl ester, tributyl citrate, acetyltributyl citrate, triethyl citrate, glyceroltributyrate; diethyl sebacate, dibutyl sebacate, dibutyl adipates, dibutyl azelates, dibutyl benzoates, chlorobutanol, polyethylene glycols, vegetable oils, diethyl fumarate, diethyl malates, diethyl oxalate, dibutyl succinate, dibutyl butyrate, cetyl alcohol esters, malonates (e.g., diethyl malonate etc.), castor oils, polysorbates, N-butylbenzenesulfonamide, N-methylpyrrolidone, and mixtures thereof. In some embodiments, it is desirable to use a non-phthalate plasticizer. In various embodiments of the present invention, the amount of plasticizer in the taste-masking layer, relative to the amount of water-insoluble polymer, ranges from about 3% to about 30% by weight. In another embodiment, the amount of plasticizer ranges from 10% to about 25% by weight of the water-insoluble polymer. In still other embodiments, the amount of plasticizer relative to the weight of the water-insoluble polymer is about 3%, about 5%, about 7%, about 10%, about 12%, about 15%, about 17%, about 20%, about 22%, about 25%, about 27%, and about 30%, inclusive of all ranges and subranges therebetween. One of ordinary skill in the art would know to select the type of plasticizer based on the polymer or polymers and nature of the coating system (e.g., aqueous or solvent-based, solution or dispersion-based and the total solids). In a particular embodiment, the plasticizer is castor oil.
  • In some embodiments, the taste-masking layer can further comprise an anti-tacky agent to reduce aggregation of the taste-masked particles. Suitable anti-tacky agents include talc and/or magnesium stearate.
  • In one embodiment, the taste-masking polymer coating comprises a plasticized water-insoluble polymer, such as ethylcellulose (EC-10), at a coating weight of about 5-50% by weight.
  • In some embodiments, the modified-release (sustained-release and/or taste-masked) high-dose drug-containing core is coated with a sealant layer, for example to minimize attrition or agglomeration of the taste-masked cores, or alternatively to prevent contact between the high-dose drug in the core and e.g., the low-dose drug in the low-dose drug layer. The composition and coating weight of the sealant layer is as described herein.
  • The low-dose drug layer is disposed directly over the high-dose drug-containing core, or over a sealant coated core, and/or a taste-masked core. The low-dose drug can be coated onto the high-dose drug-containing core by any suitable method, e.g., pan coating or fluid bed coating using a solution of the low-dose drug (in a pharmaceutically acceptable solvent), optionally in combination with a polymeric binder as described herein. For example, the low-dose drug coating solution can comprise a suitable solvent (e.g. water, a pharmaceutically acceptable organic solvent such as acetone or alcohol, or aqueous organic solvents) in which the low-dose drug and an optionally a binder (e.g., hydroxypropylcellulose, polyvinylpyrrolidone, etc.) are dissolved.
  • The resulting high-dose drug/low-dose drug-containing microparticle can then be coated, if needed, with an additional sealant layer (as described herein), and/or a taste-masking layer (also as described herein). Thus, in some embodiments, the ultimate high-dose drug/low-dose drug-containing microparticles comprise a high-dose drug-containing core (as described herein), coated with an optional sealant coating, a taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer), a low-dose drug layer, a second optional sealant layer, and a second taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer).
  • The high-dose drug/low-dose drug-containing microparticles can optionally comprise one or more sealant layers, wherein the sealant layers can have the same composition or different compositions, and can be coated at the same coating weight or different coating weights. Similarly, if the high-dose drug/low-dose drug-containing microparticles comprise two taste-masking layers, the two taste-masking layers can have the same composition or a different composition and/or the same coating weight or different coating weights. For example, the inner taste-masking layer can comprise a water-insoluble polymer, and the outer taste-masking layer can comprise the combination of a water-insoluble polymer and a water-soluble polymer and/or gastrosoluble polymer, etc.
  • In other embodiments, a flavorant coating layer (which can include a sweetener and/or a flavoring agent as described herein) can be disposed over the low-dose drug-containing layer (e.g., instead of a taste-masking layer), such that the high-dose drug/low-dose drug-containing microparticles comprise, for example a high-dose drug-containing core (as described herein), coated with an optional sealant coating, a taste-masking layer (e.g., comprising a water-insoluble polymer or a water insoluble polymer in combination with a water-soluble or gastrosoluble polymer), a low-dose drug layer, a second optional sealant layer, and the flavorant coating layer.
  • The flavorant coating layer comprises a combination of a flavorant and a binder. Suitable binders include those described herein. The flavorant includes water soluble sweeteners such as sucralose, saccharine, aspartame, neotame, acesulfame K, sodium saccharinate, neohesperidine, lactitol, maltitol, sorbitol, and mixtures thereof, or alternatively flavoring agents such as strawberry cherry, peppermint, strawberry and mixtures thereof. In one embodiment, the binder is hydroxypropyl cellulose and the flavorant is sucralose.
  • The coating weight of the flavorant coating layer can range from about 1% to about 10% by weight, including the ranges from about 3.0% to about 8%, about 5% to about 7.5%, and from about 5% to about 10%, of the weight of the coated core, or about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10%, inclusive of all ranges and subranges therebetween.
  • As described herein, the taste-masked high-dose/low-dose drug-containing microparticles can include various layers in addition to the taste-masking layer (e.g. optional sealant layers, etc.). Thus, the taste-masking layer can be disposed directly over the high-dose drug-containing core, or a sealant layer can be interposed between the high-dose drug-containing core and a taste-masking layer. In other embodiments, the low-dose drug-containing layer is coated with a taste-masking layer comprising a water-insoluble polymer combined with a gastrosoluble polymer such as a cationic dimethylaminoethyl methacrylate copolymer. In another embodiment, the taste-masking layer disposed over the low-dose drug layer comprises a water-insoluble polymer and no water-soluble or gastrosoluble polymer. In an alternative embodiment, a flavorant coating layer (e.g., at coating weight of about 1% to about 10%) comprising a water-soluble sweetener is disposed directly over the low-dose drug layer, or over a sealant layer (e.g., hydroxypropyl cellulose at a coating weight of about 1% to about 10%) disposed over the low-dose drug layer. The high-dose drug/low-dose drug-containing microparticles of the present invention provide rapid dissolution of the high-dose and low-dose drugs when dissolution tested using USP Apparatus 1 (baskets@ 100 RPM) or USP Apparatus 2 (paddles@ 50 RPM) in 900 mL media (pH 1.2, pH 5.8, pH 6.8, or pH 7 (water)) at 37° C.
  • As described herein, the pharmaceutical compositions comprising the modified-release coated high-dose drug/low-dose drug-containing microparticles of the present invention provide blend homogeneity as well as uniformity of dosage units as per the USP requirements which are difficult to achieve by other methods (e.g., by blending particles comprising the high-dose drug with a second population of particles comprising the low-dose drug), particularly when the ratio of the high-dose drug to the low-dose drug is about 20/1 or higher (e.g., about 20/1, about 25/1, about 30/1, about 35/1, about 40/1, about 45/1, about 50/1, about 60/1, about 70/1, about 80/1, about 90/1, about 100/1, etc.).
  • The high-dose drug and the low-dose drug can comprise any drugs which are intended to be used in combination to treat a condition or disease in a patient. For example, pharmaceutical compositions of the present invention can include combinations of high-dose and low-dose drugs such as non-opioid analgesics (e.g., acetaminophen and non-steroidal anti-inflammatory drugs such as aspirin, ibuprofen, ketoprofen, meloxicam, diclofenac potassium, etodolac, sulindac, indomethacin, celecoxib, etc.) in combination with one or more opioid analgesics (hydrocodone bitartrate, oxymorphone, buprenorphine, fentanyl, hydromorphone) for the treatment of moderate-to-severe pain. Similarly, an anti-diabetic combination of high-dose and low-dose drugs suitable for the treatment of diabetes mellitus (by lowering glucose levels in the blood) include at least one biguanide (e.g., metformin) in combination with at least one sulfonylurea (e.g., glipizide, gliclazide, glyburide, gliquidone, glyclopyamide, glimepiride), meglitinide (e.g. repaglinide, nateglinide) or thiazolidinedione (e.g., roseglitazone, pioglitazone, troglitazone). Alternatively, a high-dose drug (e.g., nicotinic acid) in combination with a low-dose drug (e.g., lovastatin, fluvastatin, atorvastatin, cerivastatin, simvastatin, mevastatin, rosuvastatin, pravastatin) is useful for lowering cholesterol (very low density lipoproteins) and triglycerides levels in people with, or at risk of cardiovascular disease. Combinations of a high-dose drug such as pseudoephedrine hydrochloride, pseudoephedrine sulfate, or fexofenadine and a low-dose drug such as cetirizine, loratidine, and phenylephrine are useful for treating indoor and outdoor allergies.
  • In a particular embodiment, the low-dose drug is a therapeutically effective amount of hydrocodone bitartrate and the high-dose drug is a therapeutically effective amount of acetaminophen for treating pain. In another particular embodiment, the high-dose drug is a therapeutically effective amount of metformin and the low-dose drug is a therapeutically effective amount of roseglitazone for treating hyperglycemia.
  • In one embodiment, the pharmaceutical compositions of the present invention can comprise niacin (nicotinic acid) as the high-dose drug, formulated as taste-masked high-dose drug particles with an immediate-release (IR) profile, layered with a statin and taste-masking coating. Alternatively, the niacin can be formulated as sustained-release (SR) coated high-dose drug particles to produce modified-release pharmaceutical compositions.
  • The pharmaceutical compositions of the present invention comprise high-dose/low-dose drug-containing microparticles. In an alternative embodiment, the pharmaceutical compositions of the present invention can further comprise a second population of high-dose drug containing microparticles. The high-dose drug-containing microparticles comprise, for example, a high-dose drug-containing core (as described herein) coated with a water-insoluble polymer, e.g., at a coating weight of about 15% to about 35%, thereby providing sustained-release (SR) high-dose drug-containing particles. The combination of high-dose/low-dose drug-containing microparticles and SR high-dose drug-containing particles exhibit rapid low-dose drug release profiles and prolonged high-dose drug release (modified release) profiles.
  • The pharmaceutical compositions of the present invention can be used to prepare oral dosage forms such as tablets, capsules, and ODTs. Tablets can be prepared by combining the pharmaceutical compositions of the present invention with suitable pharmaceutically acceptable excipients, and then compressing the resulting mixture to form tablets. Alternatively, capsules can be filled with the pharmaceutical compositions of the present invention (and optional excipients).
  • In a particular embodiment, the pharmaceutical compositions of the present invention can be combined with rapidly dispersing microgranules to form an orally disintegrating tablet (ODT). An ODT is a tablet designed to substantially disintegrate in the oral cavity after administration (without chewing) within about 60 seconds after contact with saliva (i.e., in the oral cavity) or with simulated saliva fluid (e.g., tested according to the USP <701> Disintegration Test). In particular embodiments, the ODT substantially disintegrates within about 30 seconds. The disintegration of the ODT in the oral cavity of the patient provides a smooth, easy-to-swallow suspension having no gritty mouthfeel or aftertaste, while still providing pharmacokinetic profiles for the drugs contained in the ODT (e.g., plasma concentration vs. time profiles) which are bioequivalent to the respective reference listed drugs (RLDs).
  • The ODTs of the present invention comprise the pharmaceutical compositions of the present invention combined with rapidly dispersing microgranules. Rapidly dispersing microgranules can be prepared as described in US Publication Nos. 2006/0078614, 2006/0105038, 2005/0232988 or 2003/0215500 (each of which is herein incorporated by reference in its entirety for all purposes) by granulating a disintegrant with a sugar alcohol and/or saccharide having an average particle size of not more than about 30 μm. The granulation can be carried out, for example, in a high shear granulator with approximately 20-25% water as the granulating fluid, and if needed wet milled and dried to produce rapidly dispersing microgranules, for example having an average particle size of not more than about 300 μm (e.g., about 175-300 μm).
  • The ratio of the disintegrant to the sugar alcohol, saccharide, or mixture thereof in the rapidly dispersing microgranules ranges from about 90/10 to about 99/01, for example about 90/10, about 91/9, about 92/8, about 93/7, about 94/6, about 95/5, about 96/4, about 97/3, about 98/2, about 99/1, inclusive of all values, ranges, and subranges therebetween.
  • The ratio of the rapidly dispersing microgranules to taste-masked drug-containing particles ranges from about 5/1 to about 1/1, including about 5/1, 4/1, 3/1, 2/1, 1/1, inclusive of all values, ranges, and subranges therebetween.
  • The taste-masked high-dose/low-dose drug-containing microparticles incorporated into the ODT dosage form should also have a small enough particle size such that after disintegration of the ODT in the oral cavity of the patient, a smooth, easy-to-swallow suspension results. In most embodiments in which the pharmaceutical compositions of the present invention as provided as an ODT dosage form, the average particle size of the taste-masked high-dose/low-dose drug-containing microparticles is not more than about 400 μm, or in some embodiments not more than about 300 μm.
  • The ODT dosage form, as described herein, may also include pharmaceutically acceptable excipients typically used in disintegrating tablet formulations such as microcrystalline cellulose and spray dried mannitol (compressible diluents), croscarmellose sodium or crospovidone (super disintegrant), coloring agents, and optionally magnesium stearate or sodium stearyl fumarate (lubricant intragranularly mixed or used externally to lubricate die and punch surfaces).
  • Tablet dosage forms, including ODT dosage forms, comprising the pharmaceutical composition of the present invention have a low friability, e.g., less than about 1%, (e.g., less than about 0.9%, less than about 0.8%, less than about 0.7%, less than about 0.6%, less than about 0.5%, less than about 0.4%, less than about 0.3%, etc., inclusive of all ranges and subranges therebetween) in order to have sufficient durability to withstand handling, shipping, and/or packaging in push-through blister packaging.
  • A non-limiting list of suitable disintegrants for the rapidly dispersing microgranules includes crospovidone (cross-linked PVP), sodium starch glycolate, cross-linked sodium carboxymethylcellulose, calcium silicate, and low substituted hydroxypropyl cellulose. The amount of disintegrant in the ODT is typically in the range of about 1% to about 10% by weight, including about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, or about 10%, inclusive of all ranges and subranges therebetween. In a particular embodiment, the disintegrant for the rapidly dispersing microgranules is selected from the group consisting of crospovidone, cross-linked sodium carboxymethylcellulose, and low substituted hydroxypropyl cellulose. In a more particular embodiment, the disintegrant for the rapidly dispersing microgranules is crospovidone.
  • A non-limiting list of suitable sugar alcohols includes mannitol, sorbitol, xylitol, maltitol, arabitol, ribitol, dulcitol, iditol, isomalt, lactitol, erythritol and combinations thereof. In a particular embodiment, the sugar alcohol is mannitol. A non-limiting list of suitable saccharides includes lactose, sucrose, maltose, and combinations thereof. In a particular embodiment, the saccharide is lactose. The amount of sugar alcohol and/or saccharide in the ODT ranges from about 30% to about 70% by weight, including, for example, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, or about 70%, inclusive of all ranges and subranges therebetween.
  • Pharmaceutically acceptable excipients include fillers, diluents, glidants, disintegrants, binders, lubricants etc. Other pharmaceutically acceptable excipients include acidifying agents, alkalizing agents, preservatives, antioxidants, buffering agents, chelating agents, coloring agents, complexing agents, emulsifying and/or solubilizing agents, flavors and perfumes, humectants, sweetening agents, wetting agents etc. Examples of suitable fillers, diluents and/or binders include lactose (e.g. spray-dried lactose, α-lactose, β-lactose, Tabletose®, various grades of Pharmatose®, Microtose® or Fast-Flo®), microcrystalline cellulose (various grades of Avicel®, Ceolus®, Elcema®, Vivacel®, Ming Tai® or Solka-Floc®), hydroxypropylcellulose, L-hydroxypropylcellulose (low substituted), low molecular weight hydroxypropyl methylcellulose (HPMC) (e.g. Methocel E, F and K from Dow Chemical, Metolose SH from Shin-Etsu, Ltd), hydroxyethylcellulose, sodium carboxymethylcellulose, carboxymethylhydroxyethylcellulose and other cellulose derivatives, sucrose, agarose, sorbitol, mannitol, dextrins, maltodextrins, starches or modified starches (including potato starch, maize starch and rice starch), calcium phosphate (e.g. basic calcium phosphate, calcium hydrogen phosphate, dicalcium phosphate hydrate), calcium sulfate, calcium carbonate, sodium alginate, collagen etc.
  • Examples of suitable diluents include e.g. calcium carbonate, dibasic calcium phosphate, tribasic calcium phosphate, calcium sulfate, microcrystalline cellulose, powdered cellulose, dextrans, dextrin, dextrose, fructose, kaolin, lactose, mannitol, sorbitol, starch, pregelatinized starch, sucrose, sugar etc.
  • Examples of suitable disintegrants include e.g. alginic acid or alginates, microcrystalline cellulose, hydroxypropyl cellulose and other cellulose derivatives, croscarmellose sodium, crospovidone, polacrillin potassium, sodium starch glycolate, starch, pregelatinized starch, carboxymethyl starch (e.g. Primogel® and Explotab®) etc.
  • Specific examples of glidants and lubricants include stearic acid, magnesium stearate, calcium stearate or other metallic stearates, talc, waxes and glycerides, light mineral oil, PEG, glyceryl behenate, colloidal silica, hydrogenated vegetable oils, corn starch, sodium stearyl fumarate, polyethylene glycols, alkyl sulfates, sodium benzoate, sodium acetate etc.
  • Other excipients include e.g. flavoring agents, coloring agents, taste-masking agents, pH-adjusting agents, buffering agents, preservatives, stabilizing agents, anti-oxidants, wetting agents, humidity-adjusting agents, surface-active agents, suspending agents, absorption enhancing agents, agents for modified release etc.
  • The present invention is also directed to methods of preparing the pharmaceutical compositions and dosage forms described herein. In one embodiment, the high-dose/low-dose drug-containing microparticles are prepared by a method comprising:
      • (a) preparing a core comprising a high-dose drug as described herein (e.g., a non-opioid analgesic such as acetaminophen, diclofenac potassium, etc.;
      • (b) coating a low-dose drug layer (e.g., comprising a low-dose drug as described herein, such as hydrocodone bitartrate) over the high-dose drug-containing core;
      • (c) coating the high-dose drug-containing core of step (a) with at least one taste-masking and/or modified-release coating layer and the high-dose/low-dose drug-containing particles of step (b) with at least one taste-masking layer or flavorant layer.
  • The step (a) of preparing the core may be accomplished by any of the methods known in the art; for example, layering an inert bead (e.g., sugar, microcrystalline cellulose, mannitol-microcrystalline cellulose, silicon dioxide, etc.) with a solution comprising the drug and optionally a polymeric binder (e.g., by fluid-bed or pan coating). Alternatively, the core may comprise drug crystals of the desired particle size (e.g., about 50-500 μm, including 100-250 μm), prepared by crystallization of the drug from a suitable solvent, or by milling drug crystals to a desired particle size. In still other embodiments, the core can comprise a pellet prepared by controlled-spheronization.
  • In a particular embodiment, the microgranules comprising a high-dose drug (e.g., a non-opioid analgesic or anti-diabetic drug) may be prepared by a conventional high-shear or planetary granulation process or high-dose drug-containing pellets may be prepared by a conventional granulation-extrusion-spheronization process comprising e.g. acetaminophen, a polymer binder and one or more fillers/diluents.
  • Step (b) comprises coating the taste-masked high-dose drug-containing core with the low-dose drug using a drug-layering solution as described herein (e.g., comprising a solution of the low-dose drug and optionally a binder). The low-dose drug layer can be applied using any suitable method, for example fluid bed, pan coating, coacervation, etc.
  • Step (c) comprises coating the high-dose drug-containing core and/or the low-dose drug containing layer with a taste-masking layer. In some embodiments, a taste-masking layer is coated directly over the high-dose-drug containing core, or a sealant layer is coated onto the high-dose drug-containing core before coating with the low-dose drug-containing layer and/or a taste-masking layer. Likewise, a sealant layer may be coated onto the low-dose drug-containing layer before coating with a taste-masking layer or a flavorant layer as described herein (e.g., comprising a sweetener and/or flavoring agent and an optional polymeric binder such as hydroxypropylcellulose, applied as a solution or suspension). The taste-masking layer comprises a water-insoluble polymer or a water-insoluble polymer combined with a water-soluble or gastrosoluble polymer (and optionally a binder), for example any of the compositions described herein such as ethylcellulose (Ethocel Standard 100 Premium, at a coating weight of about 10%), or a combination of ethylcellulose with a gastrosoluble polymer (e.g., Eudragit E100) at coating weight of about 25%.
  • After depositing the low-dose drug layer, the resulting particles can optionally be coated with a sealant coat (as described herein) and then coated with a taste-masking layer or flavorant layer (as described herein). For example, the taste-masking layer applied over the low-dose drug layer (or over a sealant coat deposited on the low-dose drug layer) can comprise a water-insoluble polymer (e.g. ethylcellulose) or the combination of a water-insoluble polymer and a water soluble or gastrosoluble polymer (e.g., ethylcellulose in combination with Eudragit E100). Alternatively, instead of a taste-masking layer, a flavorant coating can be applied over the low-dose drug layer, or over a protective sealant layer applied over the low-dose drug layer.
  • In particular embodiments, the method comprises coating by solvent coacervation a taste-masking layer directly over the high-dose drug-containing core or over a sealant layer disposed on the high-dose drug-containing core, wherein the taste-masking layer comprises water-insoluble ethylcellulose (Ethocel Standard 100 Premium) at coating weight of about 6%. In other embodiments, the method comprises coating water-insoluble ethylcellulose (Ethocel Standard 10 Premium) in combination with water-soluble hydroxypropylcellulose at a ratio of 7:3 or gastrosoluble Eudragit E100 at a ratio of 8:7 at a coating weight of about 20% by fluid bed coating.
  • In another particular embodiment, the method comprises coating by solvent coacervation a taste-masking layer directly over the low-dose drug-containing layer or over a sealant layer disposed on the low-dose drug-containing layer, e.g. with water-insoluble ethylcellulose (Ethocel Standard 100 Premium) at a coating weight of about 6%. In other embodiments, the method comprises coating water-insoluble ethylcellulose (Ethocel Standard 10 Premium) in combination with water-soluble hydroxypropylcellulose at a ratio of 7:3 or gastrosoluble Eudragit E100 at a ratio of 8:7 at a level of about 20% by weight based on the total weight of the coated particles by fluid bed coating. Taste-masking coatings can be prepared and applied as described, for example in U.S. Patent Publ. Nos. 2006/0078614 and 2006/0105038.
  • In yet another particular embodiment, the method comprises coating the low-dose drug-containing layer with a sealant layer comprising hydrophilic hydroxypropylcellulose at a coating weight of about 5%, then coating with a taste-masking layer comprising a sweetener such as sucralose at a coating weight of about 5% by weight.
  • The ultimate dosage form comprising the taste-masked high-dose/low-dose drug-containing microparticles of the present invention can then be prepared by various methods known in the pharmaceutical arts, such as filling an appropriate amount of the taste-masked high-dose/low-dose drug-containing microparticles into e.g. a gelatin capsule or a container suitable for storing a suspension, sachet, etc. In other embodiments, the taste-masked high-dose/low-dose drug-containing microparticles of the present invention are combined with suitable pharmaceutically acceptable excipients and compressed to form a tablet. Tablets comprising the pharmaceutical compositions of the present invention can contain an internal lubricant (e.g., magnesium stearate), or can be compressed into tablets using an external lubrication process, in which the lubricant is sprayed onto the surface of the die and punch surfaces, rather than incorporated into the compression blend. External lubrication and compression methods than can be used to prepare oral dosage forms (e.g., tablets, ODTs) comprising the pharmaceutical compositions of the present invention are described for example in U.S. Pat. No. 5,996,902 and U.S. Pat. No. 6,776,361.
  • When the ultimate dosage form is an ODT, the method further comprises preparing rapidly dispersing microgranules comprising a disintegrant and a sugar alcohol, a saccharide or a mixture thereof, wherein each of the disintegrant, sugar alcohol and/or saccharide have an average particle diameter of not more than 30 μm; then combining the rapidly dispersing microgranules with taste-masked high-dose/low-dose drug-containing microgranules and optionally other pharmaceutically acceptable excipients, e.g., in a mixer or V-blender; and finally compressing the blend of rapidly dispersing microgranules and taste-masked high-dose/low-dose drug-containing microgranules into an ODT, e.g., using an externally lubricated tablet press to provide ODTs with desired tableting characteristics (e.g., adequate hardness, friability of <0.6%, low disintegration time, and rapid dissolution). Rapidly dispersing microgranules can be prepared following the procedures disclosed in US Patent Publ. Nos. 2006/0078614, 2006/0105038, 2006/0105039 and 2005/0232988.
  • In particular embodiments, the rapidly dispersing microgranules and taste-masked drug-containing microparticles may be present in the ratio of about 4/1 to 2/1 to achieve a smooth mouthfeel. Rapidly dispersing microgranules may be produced as described herein by granulating a disintegrant such as Crospovidone XL-10 with a sugar alcohol or a saccharide, or a combination thereof, each having an average particle diameter of not more than about 30 μm, with water or an alcohol-water mixture in a conventional or high shear granulator and drying in a fluid bed equipment or a tray drying oven to produce granules with an average particle size not more than about 400 μm (preferably not more than about 300 μm).
  • The ultimate dosage forms can comprise a single population of taste-masked high-dose/low-dose drug-containing microparticles of the present invention in combination with excipients, rapidly dispersing microgranules, etc, or can include a combination of the taste-masked high-dose/low-dose drug-containing microparticles in combination with high-dose drug-containing particles, or alternatively two or more populations of different taste-masked high-dose/low-dose drug-containing microparticles. The ratio of the different populations of high-dose/low-dose drug-containing microparticles or high-dose/low-dose drug-containing microparticles and high-dose drug containing particles can be varied to provide suitable dosages of the high-dose and low-dose drugs.
  • Alternately, the ultimate dosage forms can comprise a single population of taste-masked high-dose/low-dose drug-containing microparticles of the present invention in combination with excipients, rapidly dispersing microgranules, etc, or can include a combination of the taste-masked high-dose/low-dose drug-containing microparticles in combination with modified release (e.g., taste-masked or sustained release) coated high-dose drug-containing microparticles, or alternatively two or more populations of different taste-masked high-dose/low-dose drug-containing microparticles, wherein the sustained release coated high-dose drug-containing microparticles comprise a water insoluble polymer optionally in combination with a water soluble or enteric polymer applied prior to low-dose drug layering. The ratio of the different populations of high-dose/low-dose drug-containing microparticles or high-dose/low-dose drug-containing microparticles and taste-masked or sustained release coated high-dose drug-containing microparticles can be varied to provide suitable dosages of the high-dose and low-dose drug components.
  • The oral dosage forms of the present invention, prepared by the methods described herein, provide in vivo plasma concentrations and release profiles which mimic RLD's. In accordance with certain embodiments, the pharmaceutical compositions of the present invention comprise microgranules or extruded/spheronized pellets comprising acetaminophen, a polymeric binder, which imparts resilient characteristics to the dried microgranules/pellets, a hydrophilic filler/diluent, and optionally a flavor, a sweetener and/or a disintegrant.
  • In certain embodiments, the present invention is directed to compositions of the present invention comprising at least one population of non-opioid analgesic/opioid analgesic drug-containing microparticles combined with non-opioid analgesic drug-containing microparticles with drug release properties suitable for a twice- or once-daily dosing regimen, wherein the one or more of the non-opioid analgesic drug-containing microparticle populations comprise non-opioid analgesic drug-containing microparticles with one or more coating layers comprising a water-insoluble polymer, an enteric polymer, or an enteric polymer in combination with a water-insoluble polymer.
  • In most embodiments, the taste-masked pharmaceutical compositions of the present invention exhibit the following properties:
      • 1) acceptable taste-masking leaving no aftertaste when the composition is placed in the oral cavity for 3 minutes, more particularly for 2 minutes and in certain embodiments for 60 seconds, and in still other embodiments, until it is swallowed;
      • 2) acceptable homogeneity of blends as per United States Pharmacopoeia requirements; and
      • 3) rapid substantially complete release of the dose upon entry into the stomach, i.e., release of not less than 75% of the total dose in 30 min when tested for dissolution using United States Pharmacopoeia Apparatus 1 (Baskets @ 100 rpm) or Apparatus 2 (paddles @ 50 rpm in 900 mL of dissolution media at 37±0.5° C.).
  • An ODT prepared in accordance with certain embodiments of the present invention may exhibit the following properties:
      • 1) exhibits acceptable uniformity of dosage forms as defined in United States Pharmacopoeia;
      • 2) disintegrates on contact with the saliva in the oral cavity forming a smooth, easy-to-swallow suspension comprising taste-masked microparticles;
      • 3) leaves no aftertaste after swallowing (no gritty or chalky mouthfeel);
      • 4) provides rapid, substantially-complete release of the total dose upon entry into the stomach; or
      • 5) the ODT when tested for dissolution using United States Pharmacopoeia Apparatus 1 (baskets @ 100 rpm) or Apparatus 2 (paddles @ 50 rpm) in 900 mL buffer releases not less than 75% of the total dose in about 30 minutes.
  • In another particular embodiment, the pharmaceutical composition of the present invention comprises acetaminophen as the high-dose drug and hydrocodone bitartrate as the low-dose drug. Following oral administration, acetaminophen is rapidly and almost completely absorbed from the GI tract. Peak plasma concentrations are attained within 30-60 minutes (binding to serum protein is about 25% after normal therapeutic dosages) and plasma half-life is between 1-2.5 hours in normal, healthy patients. After about 8 hours, only traces of the drug are detectable.
  • Pharmaceutical compositions of the present invention comprising therapeutically effective amounts of taste-masked high-dose/low-dose drug-containing microparticles are effective in treating various diseases or conditions. For example, pharmaceutical compositions of the present invention comprising therapeutically effective amounts of a non-steroidal anti-inflammatory drug such as aspirin, ibuprofen, ketoprofen, meloxicam, diclofenac potassium, etodolac, sulindac, indomethacin, celecoxib, or mixtures thereof, in combination with an opioid analgesic such as hydrocodone bitartrate, oxymorphone, buprenorphine, fentanyl, hydromorphone, or mixtures thereof (e.g. a combination of acetaminophen and hydrocodone) are effective for relief of mild to moderate pain of acute, chronic, or post-operative pain, or disabling pain of terminal conditions such as cancer.
  • In a particular embodiment, the pharmaceutical compositions of the present invention comprise therapeutically effective amounts of acetaminophen in combination with therapeutically effective amount of hydrocodone or salts thereof, e.g. hydrocodone bitartrate. In a specific embodiment, the pharmaceutical compositions of the present invention comprise 500 mg of acetaminophen and 5 mg of hydrocodone bitartrate, or 300 mg of acetaminophen and 100 mg of hydrocodone bitartrate. The acetaminophen/hydrocodone-containing compositions of the present invention are bioequivalent to known acetaminophen/hydrocodone compositions such as Vicodin®, Panadol®, and Xodol®. Compositions of the present invention comprising 500 mg of acetaminophen/5 mg of hydrocodone bitartrate have an acetaminophen Cmax of 80-125% of 6115 ng/mL, a hydrocodone bitartrate Cmax of 80-125% of 20.14 ng/mL, an acetaminophen AUC of 80-125% of 19920 ng·hr/mL, and a hydrocodone bitartrate AUC of 80-125% of 141 ng·hr/mL. compositions of the present invention comprising 300 mg acetaminophen/10 mg hydrocodone bitartrate have an acetaminophen Cmax of 80-125% of 3915 ng/mL, a hydrocodone bitartrate Cmax of 80-125% of 40.53 ng/mL, an acetaminophen AUC of 80-125% of 12794 ng·hr/mL, and a hydrocodone bitartrate AUC of 80-125% of 280 ng·hr/mL.
  • Likewise, pharmaceutical compositions of the present invention comprising therapeutically effective amounts of niacin in combination with a statin such as atorvastatin, lovastatin, fluvastatin, cerivastatin, simvastatin, mevastatin, rosuvastatin, pravastatin or mixtures thereof are effective to lower cholesterol (very low density lipoproteins) and triglycerides levels in patients with or at risk of cardiovascular disease.
  • Similarly, pharmaceutical compositions of the present invention comprising therapeutically effective amounts of metformin in combination with a drug such as glipizide, glyburide, glimepiride, repaglinide, nateglinide, rosiglitazone, pioglitazone, troglitazone (e.g., a combination of metformin and rosiglitazone) are effective to treat hyperglycemia, e.g., in diabetic patients.
  • Finally, pharmaceutical compositions of the present invention comprising therapeutically effective amounts of pseudoephedrine hydrochloride, pseudoephedrine sulfate, or fexofenadine, in combination with a drug such as cetirizine or loratidine are effective to treat indoor or outdoor allergies.
    • Example 1 1.A IR Beads Drug Load: Approximately 5% Hydrocodone Bitartrate
  • Hydrocodone bitartrate (81.1 g) was slowly added to an acetone/water (1453/782) solution of hydroxypropyl cellulose (8.1 g of Nisso HPC-L-FP) and mixed well to dissolve. 60-80 mesh sugar spheres (1500 g) were coated with the drug-layering formulation in a Glatt fluid-bed coater (Glatt GPCG 3, equipped with a 7″ bottom-spray Wurster insert, 7 13/16″ column, 25 mm column height, ‘C’ air distribution plate, and 200 mesh product retention screen) under the following conditions—inlet air temperature: 70±5° C.; product temperature: 45±5° C.; atomization air pressure 2.43 bar; port size: 1.0 mm; flow rate: 2 g/min increased in steps to 15 g/min, air flow: 25% flap. Following the drug layering, a sealant coating solution of hydroxypropylcellulose (32.4 g in 457/51 acetone/water) was sprayed onto the drug layered beads for a coating weight of 2%. The dried immediate release (IR) beads were sieved through 50 and 80 mesh screens for a usable total yield of 88.4%.
    • 1.B Taste-Masked Beads Drug Load: Approximately 3.5% Hydrocodone Bitartrate
  • IR beads (140 g) from Example 1.A, above were coated with ethylcellulose (Ethocel Standard Premium 100 from Dow Chemicals) by solvent coacervation at a coating weight of 30%. The ethylcellulose (60 g) and polyethylene (40 g Epolene C-10 from Eastman Chemicals) were dissolved/suspended in 2000 g cyclohexane at an agitation speed of 300 RPM. The tank was heated to 80° C. to dissolve the ethylcellulose, and thereafter, the tank was cooled to below 30° C. to achieve taste-masked hydrocodone bitartrate microcapsules. The microcapsules were separated by decanting, then filtered and washed with fresh cyclohexane and air dried in a fume hood.
    • 1.C Taste-Masked Microparticles by Fluid-Bed Coating
  • IR Beads (1001.3 g) prepared as described in Example 1.A, above were coated with a solution of ethylcellulose (Ethocel Standard Premium 10 cps, hereafter referred as EC-10)/Eudragit E100 (188.6 g each) plasticized with diacetylated monoglycerides (Myvacet 9-45; 30.0 g) and kosher magnesium stearate (30.0 g) dissolved in 80/20 acetone (3086 g)/water (771 g) for a coating weight of 30%. Samples were pulled during the coating process at coating weights of about 10%, 15%, 20%, and 25% and dissolution tested to evaluate the effect of coating level on dissolution and organoleptic properties. The coated beads were dried/cured at 60° C. for 10 minutes in the Glatt GPCG 3 and sieved to discard agglomerates.
    • 1.D Standard Acetaminophen Microcapsules (PE004)
  • Production of industrial scale acetaminophen microcapsules using Acetaminophen Granular (Particle size: 45-80 mesh or 177-350 μm) from Covidien were coated using a method similar to that described above in Example 1.B using a 200-gallon, 500-gallon or 1000-gallon system, and using a computerized recipe for the process (e.g., quantities for the 200-gallon system at 10% coating—Acetaminophen: 94.1 kg; Ethocel 100: 10.5 kg, Epolene: 2.1 kg and Cyclohexane: 146.0 gallons or 547.5 L). Upon controlled cooling to <30° C., the microcapsule bed is subjected to vacuum filtration and rinsing with cyclohexane to wash off residual polyethylene. The microcapsules were transferred to a fluid bed dryer, subjected to a drying procedure, and dried for a period of 4-6 hrs to reduce the cyclohexane level to not more than 1000 ppm.
    • 1.E Rapidly Dispersing Microgranules
  • Rapidly dispersing microgranules comprise a sugar alcohol such as mannitol and/or a saccharide such as lactose and a disintegrant such as Crospovidone. The sugar alcohol and/or saccharide and disintegrant will typically be present in the rapidly dispersing microgranules at a ratio of from about 99:1 to about 90:10 (sugar alcohol and/or saccharide:disintegrant). For example, the rapidly dispersing microgranules used in the ODT formulations disclosed in the various examples in accordance with the present invention were produced by granulating 95 parts of D-mannitol with an average particle size of about 15 μm, and 5 parts of crospovidone (Crospovidone XL-10) in a high shear mixer (e.g., GMX 600 from Vector Corporation) with water as the granulating fluid, drying the wet mass in a fluid bed dryer (e.g., Glatt GPCG 200 or Fluid Air FA0300), and sieving/milling to obtain granules with an average particle size of less than 400 μm. Alternately, the wet milled granules are dried in a tray drying oven for a loss on drying value of less than 1% by weight.
    • 1.F Hydrocodone Bitartrate/Acetaminophen ODTs, 5 mg/500 mg
  • Beads (172.4 g) prepared as described in Example 1.B (30% coating weight), above; standard acetaminophen microcapsules (PE004, 531.9 g) produced in Example 1D, above, and rapidly dispersing microgranules (803.4 g) from Example 1E above, were blended with a pre-blend comprising crospovidone (XL-10, 80.0 g), sucralose (5.6 g), and strawberry flavor (6.7 g) before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (19 mm in diameter) weighing approximately 1600 mg using a Carver tablet press at a compression force of 1 metric ton.
    • Example 2 2.A Hydrocodone Bitartrate/Acetaminophen Microparticles Drug Load: 3%
  • Hydrocodone bitartrate (47.5 g) was slowly added to a 50/50 acetone/water (each 452 g) solution of hydroxypropylcellulose (5.3 g of Nisso HPC-L-FP) and mixed well to dissolve. Acetaminophen microcapsules (PE004) from Example 1.D with a 6% EC-100 coating (1500.0 g) were coated with the drug-layering formulation in a Glatt fluid-bed coater Glatt GPCG 3. Following drug layering, a sealant coating solution of hydroxypropylcellulose (31.7 g in 447/50 acetone/water) was sprayed onto the drug layered beads at a coating weight 2%. The dried IR beads were sieved through 35 and 80 mesh screens for a usable total yield of 99.0%.
    • 2.B Taste-Masked Hydrocodone Bitartrate/Acetaminophen Microparticles
  • IR particles (1100.0 g) prepared as described in Example 2.A, above were coated with a solution of ethylcellulose (EC-10; 43%)/Eudragit E100 (43%) plasticized with diacetylated monoglycerides (Myvacet 9-45 at 7%) and kosher magnesium stearate (7%) dissolved in 80/20 acetone (3294 g)/water (848 g) for a 30% weight gain. Samples were pulled during the coating process at coating weights of about 5%, 10%, 15%, 20%, and 25% and dissolution tested to evaluate the effect of coating level on dissolution as well as organoleptic properties. The coated beads were dried at the same temperature settings in the Glatt GPCG 3 and sieved to discard agglomerates for a total useable yield of 98.9%.
    • 2.C Hydrocodone Bitartrate/Acetaminophen ODTs, 10 mg/300 mg
  • 20% EC-10/E100 coated (10.01% of hydrocodone bitartrate/Acetaminophen beads at 15% hydrocodone bitartrate load) from Example 2.B, above; standard acetaminophen microcapsules (PE004, 35.46%) from Example 1.D, above, and rapidly dispersing microgranules (48.76%) from Example 1.E above, were blended with a pre-blend comprising crospovidone (XL-10 at 5.0%), sucralose (0.35%), and strawberry flavor (0.42%) before compressing into 10 mg/300 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (15 mm in diameter) weighing approximately 900 mg using a Carver tablet press at a compression force of 1 metric ton.
    • 2.D Hydrocodone Bitartrate/Acetaminophen ODTs, 5 mg/500 mg
  • 30% coated beads (10.78%) from Example 2.B, above, standard acetaminophen microcapsules (PE004, 33.24%) from Example 1.D, above, and rapidly dispersing microgranules (37.71%) from Example 1.E above, were blended with a pre-blend comprising microcrystalline cellulose (Avicel PH101 at 12.5%), crospovidone (XL-10 at 5.0%), sucralose (0.35%), and strawberry flavor (0.42%) before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (17 mm in diameter) weighing approximately 1600 mg using a rotary Hata tablet press equipped with an external lubrication system (Matsui Ex-Lub System) to lubricate the die/punch surfaces by spraying magnesium stearate prior to each compression.
    • Example 3 3.A Taste-Masked Acetaminophen Microparticles
  • Acetaminophen (Granular grade from Covidien (A100); 2000.0 g) was coated in a Glatt GPCG 3 (7″ bottom spray Wurster insert and nozzle with 1.00 mm port size) with a solution of ethylcellulose (10 cps; 114.3 g)/Eudragit E100 (100.0 g) plasticized with polyethylene glycol (PEG 400; 42.9 g) and kosher magnesium stearate (28.6 g) homogeneously suspended in acetone (1359.5 g)/isopropyl alcohol (672.7 g)/water (770.8 g) for a 12.5% weight gain. The dried particles were sieved with 35 and 80 mesh screens to discard agglomerates/fines (useable yield: 93.6%).
    • 3.B Low Potency Hydrocodone Bitartrate/Acetaminophen
  • Hydrocodone bitartrate was layered onto acetaminophen (Granular A100) by spraying the drug-layering formulation (see Table 1—Low Potency for compositions) in a Glatt GPCG 3 fluid-bed coater. Following the drug layering, the sealant coating solution was sprayed onto the drug layered particles at a coating weight of 2%, followed by a taste-masking coating with EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 at a coating weight of 22% using the method disclosed in Example 3.A above.
    • 3.C High Potency Hydrocodone Bitartrate/Acetaminophen
  • Hydrocodone bitartrate was layered onto acetaminophen (Granular A100) by spraying the drug-layering formulation (see Table 1—High Potency for compositions) in a Glatt GPCG 3 fluid-bed coater. Following the drug layering, the sealant coating solution was sprayed onto the drug layered particles at a coating weight of 2%, followed by a taste-masking coating with EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 at a coating weight of 27%.
  • TABLE 1
    Taste-Masked Low Potency (PE382)/High Potency ((PE384)
    Hydrocodone Bitartrate/Acetaminophen (A100)
    Percent Quantity Required. (g)
    Taste-masked Hydrocodone/Acetaminophen - PE382
    (LP)/PE384 (HP) or Acetaminophen PE380
    Low High Low High
    Ingredients Potency Potency PE380 Potency Potency
    LP/HP HCB on Acetaminophen (A100)
    Acetaminophen Granular (A100) 96.06 90.22 2500.0 2000.0
    Hydrocodone Bitartrate, NF 1.75 7.00 45.5 155.2
    Hydroxypropylcellulose, NF 0.196 0.78 5.1 17.2
    (Klucel LF)
    Acetone, NF 432.7 1474.1
    Purified Water, USP 432.7 1474.1
    Hydroxypropylcellulose 1.70 1.70 44.2 37.7
    (Klucel ® LF)
    Magnesium Stearate NF 0.30 0.30 7.8 6.7
    Acetone NF* 611.6 520.9
    Purified Water USP * 203.9 173.6
    Total 100.0 100.0 2602.6 2216.8
    Taste-masking Coating - (5% Solids)
    LP/HP Hydrocodone-layered 78.00 73.00 2000.0 1500.0
    Acetaminophen
    Acetaminophen Granular (A100) 2000.0
    Ethylcellulose NF 8.80 10.80 114.3 225.6 221.9
    (Ethocel ® Standard 10 Premium)
    Aminoalkyl Methacrylate 7.70 9.48 100.0 197.4 194.2
    Copolymer E (Eudragit ® E 100)
    Polyethylene Glycol 3.30 4.05 42.9 84.6 83.2
    (Carbowax ® 400)
    Magnesium Stearate NF 2.20 2.70 28.6 56.4 55.5
    Acetone NF* Traces Traces 1359.5 2684.1 2639.8
    Isopropyl Alcohol USP* Traces Traces 672.7 1328.2 1306.3
    Purified Water USP* Traces Traces 770.8 1521.9 1496.8
    Total 100.0 100.0 2285.8 2564.0 2054.8
    • 3.D Hydrocodone Bitartrate/Acetaminophen ODTs, 5 mg/500 mg
  • 12.5% coated acetaminophen from Example 3A, above, 22% coated hydrocodone/acetaminophen from Example 3B, above, rapidly dispersing microgranules from Example 1.E above, were blended with a pre-blend comprising microcrystalline cellulose (Avicel PH101), (Parteck M200), crospovidone, sucralose, and strawberry flavor before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (17 mm in diameter) weighing approximately 1600 mg using a using a rotary Hata tablet press equipped with an external lubrication system (Matsui Ex-Lub System) to lubricate the die/punch surfaces prior to each compression at a compression force of 18 to 24 kN.
    • 3.E Hydrocodone Bitartrate/Acetaminophen ODTs, 10 mg/300 mg
  • 12.5% coated acetaminophen from Example 3.A, above, 27% coated hydrocodone/acetaminophen from Example 3.C, above, and rapidly dispersing microgranules from Example 1.E above, were blended with a pre-blend comprising microcrystalline cellulose (Avicel PH101), mannitol (Parteck M200), crospovidone, sucralose, and strawberry flavor before compressing into 5 mg/500 mg hydrocodone bitartrate/acetaminophen orally disintegrating tablets (17 mm in diameter) weighing approximately 1000 mg using a using a rotary Hata tablet press equipped with an external lubrication system (Matsui Ex-Lub System) to lubricate the die/punch surfaces prior to each compression at a compression force of 10 to 15 kN (see Table 2 for details).
  • TABLE 2
    Hydrocodone Bitartrate/Acetaminophen ODTs, 5 mg/500 mg & 10 mg/300 mg
    Hydrocodone/Acetaminophen ODTs
    PF401 (5 mg/500 mg) PF402 (10 mg/300 mg)
    Item Ingredient %/tablet g/Batch %/tablet g/Batch
    1 Low-potency Taste-masked Hydrocodone 22.89 572.25
    Bitartrate/Acetaminophen (PE382)
    2 High-potency Taste-masked 15.66 391.5
    Hydrocodone/Acetaminophen (PE384)
    3 Acetaminophen Microcapsules (PE380) 16.11 402.75 15.60 390.0
    4 Rapidly Dispersing Granules 40.15 1003.75 49.70 1242.5
    5 Mannitol, USP (Parteck ® M200) 4.25 106.25 5.00 125.0
    6 Microcrystalline Cellulose, NF 10.00 250.0 10.00 250.0
    7 Crospovidone, NF (XL-10) 5.25 131.25 5.26 131.3
    8 Sucralose, NF 0.35 8.75 0.35 8.8
    9 Artificial Strawberry Flavor 1.00 25.00 1.00 25.0
    10 Magnesium Stearate Traces Traces Traces Traces
    Total 100.0 2500.0 100.0 2500.0
    Tablet Weight (mg) 1600.0 1250.0
    • Example 4 4.A Pilot PK Trial Supplies
  • Two tablet strengths of hydrocodone bitartrate/acetaminophen ODTs—5 mg/500 mg and 10 mg/300 mg, and three different taste-masked particle compositions were used between these two strengths: 1) acetaminophen crystals (A100—standard particle size, i.e., 177-350 μm) with a taste-masking coating composition used in both ODT formulations; 2) acetaminophen crystals (standard particle size) with a 1.75% w/w drug layer of hydrocodone bitartrate and a subsequent taste-masking coating, used in the 5 mg/500 mg strength; and 3) acetaminophen crystals (standard particle size) with a 7% w/w drug layer of hydrocodone bitartrate and a subsequent taste-masking coating, used in the 10 mg/300 mg strength. The taste-masking coating was compositionally the same for all particles, but the amount of coating on a w/w basis varies from 12.5% on acetaminophen (PE380), 22% on 1.75% hydrocodone bitartrate/acetaminophen (PE382) used in 5 mg/500 mg ODTs (PF401) to 27% on 7% hydrocodone bitartrate/acetaminophen (PE384) used in 10 mg/300 mg ODTs (PF402). The compression blend is compressed into hydrocodone bitartrate/acetaminophen ODTs using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant. Each of the dosages has a unique blend and was prepared using different tableting parameters (see Table 3 below for details). These ODT batches were prepared as described in Examples 3.A to 3.E (see Tables 1 and 2 for compositions. The intermediate and finished products were tested using qualified analytical test methods and used in the pilot PK study in healthy volunteers.
  • TABLE 3
    Tableting Parameters for Hydrocodone
    Bitartrate/Acetaminophen ODTs:
    5 mg/500 10 mg/300
    Parameter mg ODT mg ODT
    Tooling - round, flat face, radius edge 17 mm 15 mm
    Target tablet weight (mg) 1600 1250
    Lower target tablet weight × 0.985 (mg) 1576 1231
    Target tablet weight × 1.015 (mg) 1624 1269
    Turn table speed with range (rpm) 15 (10-20) 15 (10-20)
    Fill depth (mm) 10.94-10.98 5.11
    Main position (mm) 10.6-11.1 4.44
    Pre. Position (mm) 6.2-6.4 4.61
    Scale on the feed shoe 2 (0-4)  2 (0-4) 
    Tablet Weight (mg) 1597 1248.6
    Hardness with range (n) 6.80 6.92-6.95
    Thickness with range (mm) 47-49 40-42
    Friability with range (%) 0.25-0.31 0.24-0.31
    • 4.B Pilot PK (Pharmacokinetics) Study
  • Hydrocodone bitartrate/acetaminophen ODTs, 5 mg/500 mg and 10 mg/300 mg dosages were tested in a 4-arm pilot PK (pharmacokinetics) study involving 16 healthy subjects per arm in comparison to the corresponding RLDs, Abbott's VICODIN® 5 mg/500 mg, Mikart's Xodol®, 10 mg/300 mg. Acetaminophen and hydrocodone bitartrate plasma concentration vs. time profiles for these ODTs are shown in FIGS. 2 and 3.
  • TABLE 4
    PK Parameters for Hydrocodone/Acetaminophen ODTs
    Ratio
    Test# ODT RLD IR Active Test ODT RLD Test/RLD Min-Max
    Cmax (ng/mL)
     5/500 mg Vicodin Acetaminophen  5013.86  6115.49 81.99 67.79-99.15
    AUC0→inf (ng · hr/mL)
    19205.98 19917.76 96.43 79.17-117.4
    Cmax (ng/mL)
    10/300 mg Xodol Acetaminophen  3159.55  3914.16 80.72 67.80-96.10
    AUC0→inf (ng · hr/mL)
    12196.49 12794.85 95.32 79.55-114.2
    Cmax (ng/mL)
     5/500 mg Vicodin Hydrocodone   19.708   20.139 97.86 90.44-105.9
    AUC0→inf (ng · hr/mL)
     141.36  141.40 99.97 93.56-106.8
    Cmax (ng/mL)
    10/300 mg Xodol Hydrocodone   38.719   40.530 95.53 88.87-102.7
    AUC0→inf (ng · hr/mL)
     286.33  279.06 102.6  96.25-109.4
  • FIG. 4 shows the plasma concentration-time profiles for acetaminophen observed in another 3-arm pilot PK study involving 24 healthy subjects per arm wherein Acetaminophen ODT, 500 mg with or without water was administered to fasted healthy volunteers in comparison to the corresponding RLD, GSK's Panadol® 500 mg. Acetaminophen of semi-fine grade (A137) with a smaller particle size distribution of 53-177 μm were taste-masked by solvent coacervation with Ethocel Standard Premium 100 cps for a coating weight of 10-12%. To produce orally disintegrating tablets, these microcapsules were blended with rapidly dispersing microgranules (PE378 prepared from mannitol 25/crospovidone at 95/5 as disclosed in Example 1.E, above), crospovidone, microcrystalline cellulose, aspartame (sweetener) and strawberry flavor in a V-blender and then compressed on a rotary tablet press equipped with an external lubrication system. These tablets (see Table 5 for compositions) released not less than 85% in 15 min when tested using the USP apparatus 2 (paddles@ 75 rpm in pH 5.8 buffer (see Table 6 for dissolution data).
  • TABLE 5
    Compositions of Acetaminophen ODTs
    Quantity
    % per ODT (mg/tablet) (kg)/Batch
    Ingredients tablet 250 mg 500 mg 250 mg/500 mg
    Taste-masked (10-12%) 39.68 277.8 555.5 63.5
    Acetaminophen (A137)
    Rapidly Dispersing 42.12 294.8 589.7 67.4
    Granules (PE375)
    Microcrystalline 10.00 70.0 140.0 8.0
    Cellulose (Avicel PH101)
    Crospovidone NF (XL-10) 5.00 35.0 70.0 16.0
    Sucralose NF 1.60 11.2 22.4 2.56
    Strawberry Flavor 1.60 11.2 22.4 2.56
    Total 100.0 700.0 1400.0 160.0
  • The PK parameters for Acetaminophen ODTs in comparison to Panadol® are given below:
      • Regimen T1: Acetaminophen (P-300) ODT with water
      • Regimen T2: Acetaminophen (P-300) ODT without water
      • Regimen 3: Reference tablet (Panadol®) swallowed with water
  • 90% Confidence 90% Confidence
    Test 1 (ODT) Test 2 (ODT) Interval Interval
    PK Parameter With water W/O water Test T1 vs. RLD Test T2 vs. RLD
    Cmax (ng/mL) 7.240 7.635 90.94-110.25 94.04-114.01
    AUC0-t (ng · hr/mL) 21.44 21.00 99.61-106.19 98.06-104.53
    AUC0-INF (ng · hr/mL) 22.43 21.69 99.41-106.33 96.82-103.57
  • The above results confirm that the test product, Acetaminophen ODT, 500 mg when administered with and without water is bioequivalent to the reference product, Panadol®, 500 mg swallowed with water. Multi-speed (50, 75 and 100 rpm) and multi-pH in vitro dissolution (water, pH 1.2, 4.5, 5.8, 6.8) data were generated on batches of 5 mg/500 mg and 10 mg/300 mg ODT tablets of Example 3 and 4 and 250 mg and 500 mg ODT tablets of Example 4, and a comparative data set is presented in Table 6. Since different grades of the drug substance such as Acetaminophen Granular and Acetaminophen Semi-fine were used to manufacture batches of 5 mg/500 mg-10 mg/300 mg ODT tablets and 250 mg-500 mg ODT tablets, respectively, the particle size distributions of several lots of the drug substance and the corresponding batches of microcapsules were determined. Table 7 shows the mean particle size distribution data.
  • TABLE 6
    Dissolution Data for Hydrocodone/Acetaminophen
    IR Tablets and ODTs and Acetaminophen ODT
    Time PF401EA0001 PF402EA0001 Vicodin* Xodol PF407EA0001A PF408EA0002A
    (min) 5 mg/500 mg 10 mg/300 mg 5/500 mg 10/300 mg 250 mg 500 mg
    0 0 0 0 0 0 0
    5 23 28 49 40
    10 53 60 65 87 75
    15 75 87 71 84 95 88
    30 101 103 76 93
    *→ Vicodin is released by USP test 2 which is 0.1N HCl media
  • TABLE 7
    Particle Size Distributions of Acetaminophen Drug Substance and Microcapsules
    Acetaminophen Drug Substance Microcapsules
    % Particles % Particles % Assay
    Grade Retained on Coating Retained (STD)
    Granular
    (Mean of   >80% <425-180 μm>     6% (500/1000 gallon) 95% <425-180 μm> 93 ± 1.37
    multiple batches)
    Semi-fine
    Mean of   90% <150-53 μm> 12% (5-gallon)  87% <250-74 μm> 87.9
    multiple batches
    A13709532 89.5% <150-53 μm> 12% (500-gallon) 90% <250-74 μm> 86.8
    A13709533 86.2% <150-53 μm> 10% (500-gallon) 89.5% <250-74 mesh 89.7
  • Acetaminophen/Hydrocodone ODT tablets (5 mg/500 mg or 10 mg/300 mg ODTs) contain two of three types of microencapsulated acetaminophen drug particles—granular grade acetaminophen and granular grade acetaminophen drug particles layered with hydrocodone at a low or high drug load, all taste-masked with a coating of ethylcellulose/Eudragit EPO. To improve dissolution and bioequivalence to the RLDs and to improve the stability of hydrocodone when directly layered onto acetaminophen particles, it was decided to use the drug substance with a smaller particle size distribution (e.g., Acetaminophen Semi-fine) in the tablet formulation to manufacture “smaller acetaminophen microcapsules”.
  • During the evaluation of different taste-masking coatings applied on microparticles comprising hydrocodone bitartrate for their ability to impart acceptable organoleptic properties, it was discovered that a coating comprising a sweetener in combination with a seal coating layer comprising hydroxypropylcellulose (Klucel LF) was effective in masking the bitter taste of hydrocodone bitartrate.
    • Example 5 5.A Taste-Masked Acetaminophen Microparticles (6%)
  • Acetaminophen (Semi-fine grade from Covidien with a particle size of 80-270 mesh or 53-177 μm (A137); 1800.0 g) was taste-masked by solvent coacervation in a 5-gallon system. The 5-gallon system filled with 10,000 g of cyclohexane was charged with ethylcellulose (Ethocel Standard Premium 100 from Dow Chemicals; 114.9 g), polyethylene (Epolene C-10; 50 g), and the drug. The system was subjected to a controlled heating cycle to achieve a temperature of 80° C. to dissolve ethylcellulose while agitating the contents at a speed of 300 RPM. Thereafter the system was subjected to a computer controlled cooling cycle to <28° C. in not less than 45 min to encapsulate the drug crystals with a smooth coating at a coating weight of 6%, and avoiding formation of agglomerates. The microcapsules were separated by decanting, washed with fresh cyclohexane, and dried in a fume hood. The microcapsules with a size less than 35 mesh were collected for taste-masking (useable yield: 98.0%).
    • 5.B Taste-Masked Hydrocodone Bitartrate/Acetaminophen Microcapsules
  • Hydrocodone bitartrate (57.4 g), acetaminophen (semi-finer grade A137; 1742.6 g), ethylcellulose (156.5 g), polyethylene (50.0 g) were suspended in cyclohexane in the 5 gallon system, and HCB/Acetaminophen microencapsulated particles at an EC-100 coating of 8% by weight were produced following the procedure of Example 5.A. Hydrocodone bitartrate/Acetaminophen microencapsulated particles (1518.8 g) were sealant coating with Klucel LF (288.6 g)/magnesium stearate (15.2 g) and further provided with a second taste-masking membrane comprising ethylcellulose (EC-10)/Eudragit E100/Myvacet/magnesium stearate at a ratio of 286.6/253.5/31.8/35.7 in a Glatt GPCG 3 for a coating weight of 25% as described in Example 3.
    • 5.C Taste-Masked Hydrocodone Bitartrate/Acetaminophen Microcapsules
  • Hydrocodone bitartrate (60.0 g and 6.7 g of Klucel LF) was layered onto acetaminophen microcapsules (Semi-fine A137 with an EC-100 coating weight of 6% from Example 5.A; 1205.3 g) in the Glatt GPCG 3 for a coating weight of 8% as described in Example 3. Following the drug layering, a sealant coating with Klucel LF (28.0 g) was sprayed onto the hydrocodone-layered particles, followed by a taste-masking coating with EC-10/E100/PEG 400/Myvacet 9-45 at a ratio of 40/35/15/10 for a coating weight of 35%.
    • 5.D Hydrocodone Bitartrate/Acetaminophen ODTs
  • The compression blend comprising taste-masked Hydrocodone/Acetaminophen microparticles from Example 5.B, above or taste-masked Hydrocodone/Acetaminophen microparticles from Example 5.C, above was combined with the rapidly dispersing microgranules from 1.E, above, and a pre-blend comprising microcrystalline cellulose, crospovidone, sucralose, and strawberry flavor, and compressed into hydrocodone bitartrate/acetaminophen ODTs, 5 mg/500 mg and 10 mg/300 mg (see Table 8 for compositions) using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant.
  • TABLE 8
    Compositions of Acetaminophen ODTs
    ODTs, 5 mg/500 mg ODTs 10 mg/300 mg
    Ingredients (mg/tablet) 1300-086 1300-088 1300-085 1300-087
    Taste-masked Hydrocodone/ 287.4 344.8
    Acetaminophen (Example 5.B)
    Taste-masked Hydrocodone/ 172.4 344.8
    Acetaminophen (Example 5.C)
    Acetaminophen Microcapsules (PE378) 378.4 445.4 123.3 123.3
    Rapidly Dispersing Granules 496.9 544.9 445.5 445.5
    Microcrystalline Cellulose (Avicel 140.0 140.0 110.0 110.0
    PH101)
    Crospovidone NF (XL-10) 70.0 70.0 55.0 55.0
    Sucralose NF 4.9 4.9 3.85 3.85
    Strawberry Flavor 22.4 22.4 17.6 17.6
    Total 1400.0 1400.0 1100.0 1100.0
  • Table 9 presents the dissolution profiles of hydrocodone bitartrate and acetaminophen from ODTs. A slightly thicker coating on acetaminophen drug particles by coacervation (EC-100) or a thicker fluid-bed coating (EC-10/E100) appeared to have little impact on drug dissolution rates.
  • TABLE 9
    Dissolution Data for Hydrocodone Bitartrate/Acetaminophen ODTS
    Hydrocodone Bitartrate Released (%) Acetaminophen Released (%)
    Time ODT (10 mg/300 mg) ODT (5 mg/500 mg) ODT (10 mg/300 mg) ODT (5 mg/500 mg)
    (min) 1300-085 1300-087 1300-086 1300-088 1300-085 1300-087 1300-086 1300-088
    0 0 0 0 0 0 0 0 0
    5 90 101 87 98 54 49 47 51
    10 94 104 91 101 91 80 81 81
    15 94 104 92 101 102 95 93 92
    30 95 104 93 102 105 103 98 98
    • Example 6 6.A Microencapsulation of Acetaminophen
  • A 200-gallon solvent coacervation system (146 kg) was charged with acetaminophen (Semifine grade A137; 75.5 kg), Ethylcellulose (EC-100; 4.8 kg), Epolene; 2.1 kg) and the acetaminophen was taste-masked by solvent coacervation in a 200-gallon system while agitating at 80±5 RPM. A computer controlled “heat to 80° C.- and hold” cycle was used to achieve a temperature of 80° C. to dissolve the ethylcellulose in the coacervation system. Thereafter the system was subjected to a cooling cycle to <28° in not less than 45 min to encapsulate the acetaminophen crystals with a smooth coating at 6% by weight, and avoiding the formation of agglomerate's. The microcapsules were vacuum-filtered, washed with cyclohexane, and dried in a fluid bed dryer using a 3-step temperature (e.g., 25° C., 35° C., 99° C.) for 4 to 6 hrs to achieve a residual cyclohexane level of less than 1000 ppm. The microcapsules were sieved through a US 35 mesh sieve. Following the same procedure, several batches of microcapsules (batch size: 80 kg) were prepared at a coating weight of 6% in the 200 gallon system.
    • 6.B Taste-Masked Hydrocodone/Acetaminophen Microparticles
  • Hydrocodone bitartrate (see Table 10 for compositions and batch quantities) was layered onto acetaminophen microcapsules (6% EC-100 coating; 3375.0 g) from Example 6.A, above by spraying the drug-layering formulation comprising hydroxypropylcellulose (10% solids) in a Glatt GPCG 5 (9″ Wurster, 25 mm partition gap, 200 mesh product retention screen, 1.0 mm nozzle tip diameter, ‘C’ bottom air distribution plate; product temperature: 37±3° C.; inlet air volume: 40-45 CFM; spray rate: 8-24 ml/min) for a hydrocodone bitartrate load of 9.0%. A sealant coating solution of hydroxypropyl (5.0% or 73.68 g dissolved in 50/50 acetone/water at 10% solids) was sprayed onto the drug-layered particles (1400 g) in a Glatt GPCG 3, for a coating weight of 5%, followed by a taste-masking coating with sucralose (5.0%) dissolved in an aqueous solution of hydroxypropylcellulose (1.24%; at a ratio of 80/20 sucralose/HPC) using the following process conditions: Inlet temperature: 57±2° C.; product temperature: 37±2° C.; spray rate: 8 mL/min; inlet air volume: 6 CFM.
    • 6.C Taste-Masked Hydrocodone/Acetaminophen Microparticles
  • Hydrocodone bitartrate (see Table 10 for compositions and batch quantities) was layered onto acetaminophen microcapsules (6% EC-100 coating; 3733.3 g) from Example 6.A, above by spraying a drug-layering formulation comprising hydroxypropylcellulose (10% solids) in a Glatt GPCG 5 as described in Example 6.B, above. Following the coating, the microparticles were sealant coated with hydroxypropylcellulose at 5% in the same unit, dried for 5 minutes to reduce residual moisture and sieved through 30 and 80 mesh sieves to discard over sized particles and fines.
  • TABLE 10
    5.0% Sucralose/5.0% HPC/Hydrocodone Bitartrate/Acetaminophen Microparticles
    Ingredients
    5.0% Sucralose/5.0% HPC Coated Percent Quantity Required (g)
    Hydrocodone/Acetaminophen Microcapsules Formula A Formula B Formula A Formula B
    Drug Layering - (10% solids)
    Microcaps APAP (A137) (6% Coating) 80.16 84.24 3375.0 3733.3
    Hydrocodone Bitartrate, NF 8.02 5.41 337.5 240.0
    Hydroxypropyl Cellulose, NF (Klucel LF) 0.89 0.60 37.5 26.7
    Acetone, NF Traces Traces 2400.0
    Purified Water, USP Traces Traces 3375.0 2400.0
    HPC Sealant Coat - (6% solids)
    Hydrocodone/Acetaminophen Microcapsules 89.07 90.25 1400.0 4000.0
    Hydroxypropyl Cellulose, NF (Klucel LF) 4.69 4.75 73.68 210.5
    Acetone, NF Traces Traces 614.0 1649.1
    Purified Water, USP Traces Traces 614.0 1649.1
    Sucralose Coat (15% solids)
    HPC Coated Hydrocodone/Acetaminophen 93.76 95.00 1300.0 3400.0
    Sucralose, NF 5.00 5.00 69.33 179.0
    Hydroxypropyl Cellulose, NF (Klucel LF) 1.24 17.19
    Purified Water, USP Traces Traces 490.27 1014.0
    Total 100.0 100.0 1386.52 3578.9
    • 6.D Hydrocodone/Acetaminophen ODTs
  • A compression blend comprising taste-masked hydrocodone/acetaminophen microparticles from Example 6.B, above or taste-masked Hydrocodone/Acetaminophen microparticles from Example 6.C, above was combined with the rapidly dispersing microgranules from 1.E, above, and a pre-blend comprising microcrystalline cellulose, crospovidone, sucralose, and strawberry flavor, and compressed into Hydrocodone bitartrate/Acetaminophen ODTs, 10 mg/300 mg and 5 mg/500 mg (see Table 11 for compositions) using an Elizabeth Hata tablet press. While ODT lot # 1334-JMC-142 was compressed using magnesium stearate as an external lubricant, ODT lot # 1198-JMC-046 and 1198-JMC-062 were compressed using Sodium stearyl fumarate (PRUV) as an internal lubricant. The tableting properties are listed in Table 12.
  • TABLE 11
    Hydrocodone Bitartrate/Acetaminophen ODTs, 5 mg/500 mg & 10 mg/300 mg
    Hydrocodone/Acetaminophen ODTs
    10 mg/300 mg 10 mg/300 mg 5 mg/500 mg
    1334-JMC-142 1198-JMC-062 1198-046
    Item Ingredient (mg/tablet) mg/tablet mg/tablet mg/tablet
    1 Sucralose/HPC/9% Hydrocodone/ 123.11
    Acetaminophen (from Example 6.B)
    Sucralose/HPC/5.7% Hydrocodone/ 184.50 92.25
    Acetaminophen (from Example 6.C)
    2 Acetaminophen Microcapsules (10%) 225.88 172.33 476.35
    3 Rapidly Dispersing Granules 542.01 443.97 454.10
    4 Microcrystalline Cellulose, NF 110.00 110.00 140.00
    5 Mannitol, USP (Parteck ® M200) 110.00 140.00
    6 Crospovidone 55.00
    Croscarmellose Sodium (Ac-Di-Sol) 33.00 42.00
    7 Sucralose, NF 13.75 18.70 23.80
    8 Artificial Cherry Flavor 19.25 16.50 17.50
    9 Citric Acid 11.00
    Magnesium stearate (External) Traces
    Sodium Stearyl Fumarate (PRUV) 11.00 14.00
    Total 1100.0 1100.0 1400.0
  • TABLE 12
    Tableting Properties of Hydrocodone
    Bitartrate/Acetaminophen ODTs
    Compression
    Lot# Force Weight Thickness Hardness Friability
    ODTs 10-mg/300-mg
    1334-142 13 kN 1102 mg 6.12 mm 41.3 N 0.51%
    14 kN 1101 mg 6.03 mm 46.4 N 0.37%
    1198-062 12.5 kN   1099 mg 6.09 mm 46.0 N 0.20%
    ODTs 5-mg/500-mg
    1198-046 18 kN 1402 mg 6.11 mm   53 N 0.18%
    20 kN 1394 mg 6.03 mm   61 N 0.05%
    22 kN 1390 mg 5.97 mm   67 N 0.17%
    • Example 7 7.A Taste-Masked Metformin Microparticles
  • Metformin hydrochloride (1000.0 g) is coated in a Glatt GPCG 3 with a solution of ethylcellulose (Ethocel Standard 10 Premium; 78.5 g)/Eudragit E100 (75.0 g) plasticized with polyethylene glycol (PEG 400; 25.9 g) and kosher magnesium stearate (15.6 g) dissolved in 80/20 acetone (1359.5 g)/isopropyl alcohol (672.7 g)/water (770.8 g) for a coating weight of 17.5%. The dried particles are sieved using 35 and 80 mesh sieves to discard agglomerates/fines. A batch of taste-masked metformin microcapsules are also prepared at a coating weight of 25%. A 5% sealant coating with Klucel LF is also applied to avoid potential interaction between the cationic polymer of the taste-masking membrane and low-dose drug (e.g., rosiglitazone). Another batch of taste-masked metformin microparticles is also prepared with the coating formulation at the same ratio and same % solids for a coating weight of 25%, for directly incorporating in the ODT formulation.
    • 7.B Taste-Masked Rosiglitazone/Metformin
  • Rosiglitazone maleate is layered onto sealant-coated metformin microcapsules from Example 7.A, above in the Glatt GPCG 3 for a coating weight gain of 2.5%, using a method similar to that described in Example 5.B, above. Following the drug layering, a sealant coating of a 2% by weight Klucel LF solution at is sprayed onto the rosiglitazone-layered particles, followed by coating with a taste-masking coating of EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 at a coating weight of 20%.
    • 7.C Rosiglitazone/Metformin ODT
  • Rosiglitazone maleate/Metformin hydrochloride microparticles from Example 7.B, above, taste-masked Metformin hydrochloride microparticles from Example 7.A, above, rapidly dispersing microgranules from Example 1.E, above and a pre-blend comprising microcrystallinecellulose, sucralose, strawberry flavor, and crospovidone are blended together in a V-blender and compressed into Rosiglitazone/Metformin ODTs, 1 mg/500 mg, 2 mg/500 mg, 4 mg/500 mg, and 4 mg/1 g using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant to lubricate punch and die surfaces prior to compression.
  • These examples demonstrate that the ODT formulations comprising microparticles comprising high-dose metformin HCl/low-dose rosiglitazone maleate (e.g., 500 mg/l mg, 500 mg/2 mg, or 500 mg/4 mg) exhibit acceptable tableting properties (e.g., hardness, friability, uniformity of dosage forms, low in vitro/in vivo disintegration time, rapid dissolution, acceptable organoleptic properties which significantly improve patient-compliance. In addition, the pharmaceutical compositions (and oral dosage forms prepared therefrom) of the present invention exhibit acceptable taste-masking and provides rapid, substantially-complete release of the dose on entry into the stomach, thereby providing bioequivalence to the appropriate reference immediate release (IR) product.
    • Example 8 8.A Niacin Microparticles by Controlled Spheronization
  • Povidone (PVP K-30; 50 g) is slowly added to purified water (500 g) while constantly stirring to prepare a polymer binder solution at 10% w/w solids. Niacin (or nicotinic acid from Lonza Corporation; 2000 g) is blended with 10 g of colloidal silica (a flow aid, Cab-O-Sil M-5P from Cabot Corporation) and povidone (50 g) in a V-blender and charged into the product bowl of Granurex GX-35 from Vector Corporation (Iowa, USA). The 10% PVP binder solution is sprayed into the rotating material bed at a controlled rate. Optimized process parameters during pellet formation—process air temperature: ˜19-20° C.; product temperature: 16±2° C.; Rotor speed: 425 RPM; External air supply: 150 L/min; Spray rate: 15 RPM (˜8 mL/min); pressure drop across slit: 1.3-11 mm in water. Optimized process parameters during drying of pellets—Process air volume: 30 CFM; Process air temperature: ˜60° C.; Product temperature: 35° C. (to stop drying); Rotor speed: 180 RPM; Slit air volume: 10 CFM; Processing time: 40 min. About 65% of the pellets thus prepared have a size in the range of 40-80 mesh.
    • 8.B SR Coated Niacin Microparticles
  • Niacin microparticles (1600 g) from step 8.A, above are provided with an SR coating with ethylcellulose (Ethocel Standard 10 Premium; 180 g)/TEC (triethyl citrate, a plasticizer; 20 g) dissolved in 90/10 acetone/water for a 15% weight gain. Samples are pulled at a coating of 7.5, 10, 12.5% by weight for drug release testing. The dried particles are sieved using 30 and 80 mesh sieves to discard agglomerates/fines. A 2% seal coat with Klucel LF is also applied to avoid potential interaction between the polymer/plasticizer and low-dose drug (e.g., atorvastatin).
  • Another batch of taste-masked niacin microparticles is also be prepared with the coating formulation at the same ratio and same % solids for a weight gain of 15% based on the total weight of the coated microparticles for directly incorporating in the ODT formulation.
    • 8.C Atorvastatin Coated Niacin Microparticles
  • Atorvastatin calcium is layered onto seal-coated niacin microcapsules from step 8.B, above in the Glatt GPCG 3 for a weight gain of 4% as described in Example 1.C, above. Following the drug layering, a seal coating of Klucel LF at 2% by weight is sprayed onto the atorvastatin-layered particles, followed by a taste-masking coating with EC-10/E100/PEG 400/Mg stearate at a ratio of 40/35/15/10 for a weight gain of 20%.
    • 8.D Atorvastatin/Niacin SR ODT
  • Taste-masked Atorvastatin calcium/Niacin microparticles from step 8.C, above, taste-masked Niacin microparticles from step 8.B, above, rapidly dispersing microgranules from step 1.E, above and a pre-blend comprising microcrystalline cellulose, sucralose, strawberry flavor, and crospovidone are blended together in a V-blender and compressed into Atorvastatin/Niacin ODTs, 2.5-mg/500-mg, 5-mg/500-mg, and 10-mg/500-mg using an Elizabeth Hata tablet press equipped with a Matsui Ex-Lub lubricating system that uses magnesium stearate as an external lubricant to lubricate punch and die surfaces prior to compression.
  • Changes may be made by persons skilled in the art in the construction and the various components and assembly described herein or in the steps or the sequence of steps of the method of manufacture described therein without departing from the spirit and scope of the invention as described herein.

Claims (65)

1. A pharmaceutical composition comprising a plurality of high-dose/low-dose drug-containing microparticles, wherein the drug-containing microparticles comprise:
(a) a core comprising a high-dose drug;
(b) a first coating disposed over the core, comprising a low-dose drug; and
(c) a second coating disposed over the core, comprising a water-insoluble polymer.
2. The pharmaceutical composition of claim 1, wherein the weight ratio of high-dose drug to low-dose drug in the pharmaceutical composition is at least about 20:1.
3. The pharmaceutical composition of claim 1, wherein the high-dose drug-containing core comprises particles of the high-dose drug, wherein the second coating is a modified release coating comprising a water insoluble polymer.
4. (canceled)
5. (canceled)
6. (canceled)
7. The pharmaceutical composition of claim 1, wherein the second coating further comprises a plasticizer.
8. The pharmaceutical composition of claim 7, wherein the plasticizer is free of phthalates.
9. The pharmaceutical composition of claim 7, wherein the plasticizer is selected from the group consisting of glycerol, glycerol esters, acetylated mono- or diglycerides, glyceryl monostearate, glyceryl triacetate, glyceryl tributyrate, phthalates, dibutyl phthalate, diethyl phthalate, dimethyl phthalate, dioctyl phthalate, citrates, acetylcitric acid tributyl ester, acetylcitric acid triethyl ester, tributyl citrate, acetyltributyl citrate, triethyl citrate, glyceroltributyrate, sebacates, diethyl sebacate, dibutyl sebacate, adipates, azelates, benzoates, chlorobutanol, polyethylene glycols, vegetable oils, fumarates, diethyl fumarate, malates, diethyl malate, oxalates, diethyl oxalate, succinates, dibutyl succinate, butyrates, cetyl alcohol esters, malonates, diethyl malonate, castor oil, and combinations thereof.
10. The pharmaceutical composition of claim 1, wherein the second coating substantially masks the taste of the high-dose drug and/or the low-dose drug and is disposed below the first coating.
11. (canceled)
12. The pharmaceutical composition of claim 10, wherein the second coating further comprises a gastrosoluble polymer or a gastrosoluble pore-former.
13. (canceled)
14. The pharmaceutical composition of claim 12, wherein the water-insoluble polymer is selected from the group consisting of water-insoluble cellulose ethers, ethylcellulose, water-insoluble cellulose esters, cellulose acetate, cellulose triacetate, cellulose acetate butyrate, polyvinyl acetate, neutral methacrylic acid-methylmethacrylate copolymers, and mixtures thereof; and the gastrosoluble pore-former is selected from the group consisting of maltrin, aminoalkyl methacrylate copolymers, Eudragit® E100 Eudragit® EPO, polyvinylacetal diethylaminoacetate, AEA®, terpolymers based on dimethylaminoethyl methacrylate, butyl methacrylate, and methyl methacrylate, calcium carbonate, calcium phosphate, calcium saccharide, calcium succinate, calcium tartrate, ferric acetate, ferric hydroxide, ferric phosphate, magnesium carbonate, magnesium citrate, magnesium hydroxide, magnesium phosphate, and mixtures thereof.
15. (canceled)
16. The pharmaceutical composition of claim 1, wherein the second coating further comprises a water-soluble polymer or an enteric polymer.
17. The pharmaceutical composition of claim 16, wherein the water-insoluble polymer is selected from the group consisting of water-insoluble cellulose ethers, ethylcellulose, water-insoluble cellulose esters, cellulose acetate, cellulose triacetate, cellulose acetate butyrate, polyvinyl acetate, neutral methacrylic acid-methylmethacrylate copolymers, and mixtures thereof; the water-soluble polymer is selected from the group consisting of polyvinylpyrrolidone, polyethylene glycol, hydroxypropyl methylcellulose, and hydroxypropyl cellulose; and the enteric polymer is selected from the group consisting of cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, hydroxypropyl methylcellulose acetate succinate, polyvinyl acetate phthalate, pH-sensitive methacrylic acid/methylmethacrylate copolymers, shellac, and mixtures thereof.
18. The pharmaceutical composition of claim 1, wherein the second coating is disposed between the core and the first coating.
19. The pharmaceutical composition of claim 18, further comprising a third coating disposed over the first coating, wherein the third coating comprises a water-insoluble polymer which is the same as or different from the water-insoluble polymer of the second coating.
20. The pharmaceutical composition of claim 19, wherein the third coating substantially masks the taste of the low-dose drug.
21. The pharmaceutical composition of claim 1, further comprising a third coating disposed between the core and the first coating, wherein the third coating comprises a water-insoluble polymer which is the same as or different from the water-insoluble polymer and a second coating.
22. The pharmaceutical composition of claim 21, wherein the third coating substantially masks the taste of the high-dose drug.
23. The pharmaceutical composition of claim 22, wherein the third coating further comprises a gastrosoluble polymer or a gastrosoluble pore-former.
24. The pharmaceutical composition of claim 1, further comprising a flavorant coating disposed over the first coating, wherein the flavorant coating comprises a sweetener.
25. The pharmaceutical composition of claim 24, wherein the sweetener is selected from the group consisting of sucralose, lactitol, maltitol, sorbitol, and combinations thereof.
26. The pharmaceutical composition of claim 24, wherein the second coating is disposed between the core and the first coating.
27. The pharmaceutical composition of claim 26, wherein the second coating substantially modifies the release of the high-dose drug, and comprises a water insoluble or hydrophobic wax selected from the group consisting of glyceryl behenate, stearic acid, and hydrogenated castor oil.
28. The pharmaceutical composition of claim 1, wherein the high-dose drug comprises a non-opioid analgesic drug and the low-dose drug is comprises an opioid analgesic drug; or the high-dose drug comprises a bisguanidine and the low-dose drug comprises a sulfonylurea; or the high-dose drug comprises nicotinic acid and the low-dose drug comprises a statin; or the high-dose drug comprises a decongestant or a histamine antagonist and the low-dose drug comprises a histamine antagonist or a decongestant.
29. The pharmaceutical composition of claim 28, wherein the second coating is disposed between the core and the first coating, and the second coating substantially modifies the release of the high-dose drug.
30. The pharmaceutical composition of claim 29, further comprising a third coating disposed over the first coating, wherein the third coating comprises a water-insoluble polymer which is the same as or different from the water-insoluble polymer of the second coating, or the third coating comprises a flavorant coating; and the third coating substantially masks the taste of the low-dose drug.
31. The pharmaceutical composition of claim 28, wherein the high-dose drug is a non-steroidal anti-inflammatory drug and the low-dose drug is an opioid analgesic drug.
32. The pharmaceutical composition of claim 31, wherein the high-dose drug is selected from the group consisting of acetaminophen, aspirin, ibuprofen, ketoprofen, meloxicam, diclofenac potassium, etodolac, sulindac, indomethacin, and celecoxib; and the low-dose drug is selected from the group consisting of hydrocodone, oxymorphone, buprenorphine, fentanyl, and hydromorphone.
33. The pharmaceutical composition of claim 32, wherein the high-dose drug comprises acetaminophen, and the low-dose drug comprises hydrocodone.
34. The pharmaceutical composition of claim 33, further comprising a flavorant coating comprising a sweetener disposed over the first coating, wherein the second coating is disposed between the core and the first coating.
35. The pharmaceutical composition of claim 34, wherein the second coating comprises ethylcellulose, and the third coating comprises sucralose and an optional binder.
36. The pharmaceutical composition of claim 28, wherein the high-dose drug is metformin, and the low-dose drug is selected from the group consisting of glipizide, glyburide, glimepiride, repaglinide, nateglinide, rosiglitazone, pioglitazone, and troglitazone.
37. The pharmaceutical composition of claim 28, wherein the high-dose drug is nicotinic acid, and the low-dose drug is selected from the group consisting of lovastatin, fluvastatin, atorvastatin, cerivastatin, simvastatin, mevastatin, rosuvastatin, and pravastatin.
38. The pharmaceutical composition of claim 28, wherein the high-dose drug is selected from the group consisting of pseudoephedrine hydrochloride or sulfate, fexofenadine, and the low-dose drug is selected from the group consisting of cetirizine, loratidine, and phenylephrine.
39. The pharmaceutical composition of claim 1, further comprising a second population of high-dose drug-containing particles, wherein the second population of drug-containing particles comprises:
(i) a second core comprising the high-dose drug; and
(ii) a fourth coating comprising a water-insoluble polymer disposed over the second core, wherein the water-insoluble polymer of the fourth coating is the same as or different from the water-insoluble polymer of the second coating.
40. The pharmaceutical composition of claim 39, wherein the fourth coating further comprises a water-soluble polymer or an enteric polymer, and an optional gastrosoluble pore former.
41. (canceled)
42. (canceled)
43. (canceled)
44. A dosage form comprising the composition of claim 1 and one or more pharmaceutically acceptable excipients.
45. (canceled)
46. (canceled)
47. The dosage form of claim 44, wherein the dosage form further comprises rapidly dispersing granules comprising a disintegrant and a sugar alcohol and/or saccharide; wherein the dosage form is an ODT.
48. (canceled)
49. The dosage form of claim 47, wherein the ODT substantially disintegrates within about 30 seconds when tested according to the USP <701> Disintegration Test.
50. The dosage form of claim 47, wherein the ODT releases at least about 75% of the total amount of the high-dose drug and at least about 75% of the low-dose drug in 30 minutes, when dissolution tested using USP Apparatus 1 (Baskets @ 100 rpm) or Apparatus 2 (Paddles @ 50 rpm), in 900 mL of a pH 1.2 buffer.
51. The dosage form of claim 47 in the form of an ODT, comprising 500 mg of acetaminophen and 5 mg of hydrocodone bitartrate, wherein the ODT has an acetaminophen Cmaxof 80-125% of 6115 ng/mL, a hydrocodone bitartrate Cmax of 80-125% of 20.14 ng/mL, an acetaminophen AUC of 80-125% of 19920 ng·hr/mL, and a hydrocodone bitartrate AUC of 80-125% of 141 ng·hr/mL.
52. The dosage form of claim 47 in the form of an ODT, comprising 300 mg of acetaminophen and 10 mg of hydrocodone bitartrate, wherein the ODT has an acetaminophen Cmax of 80-125% of 3915 ng/mL, a hydrocodone bitartrate Cmax of 80-125% of 40.53 ng/mL, an acetaminophen AUC of 80-125% of 12794 ng·hr/mL, and a hydrocodone bitartrate AUC of 80-125% of 280 ng·hr/mL.
53. The dosage form of claim 47, wherein said the disintegrant is selected from the group consisting of crospovidone, sodium starch glycolate, crosslinked carboxymethyl cellulose of sodium, low-substituted hydroxypropylcellulose and mixtures thereof and the sugar alcohol or saccharide is selected from the group consisting of mannitol, xylitol, maltol, maltitol, sorbitol, lactose, sucralose, maltose, and combinations thereof.
54. The dosage form of claim 47, wherein the high-dose/low-dose drug-containing microparticles have an average particle size of less than about 400 μm, the rapidly dispersing granules have an average particle size of less than about 300 μm, and the disintegrant and sugar alcohol and/or saccharide have an average particle size of less than about 30 μm.
55. A method for preparing the pharmaceutical composition of claim 1, comprising:
(1) preparing cores comprising a high-dose drug;
(2) coating the high-dose drug-containing cores of step (1) with a low-dose drug layer, thereby forming high-dose/low-dose drug-containing microparticles; and
(3) coating the high-dose drug-containing cores of step (1) and/or the high-dose/low-dose drug-containing microparticles of step (2) with a second coating comprising a water-insoluble polymer.
56-65. (canceled)
66. A method of preparing the dosage form of claim 44, comprising:
(1) preparing cores comprising the high-dose drug;
(2) coating the high-dose drug-containing cores of step (1) with a sustained-release coating comprising a water-insoluble polymer, a pharmaceutically acceptable solvent, and an optional plasticizer;
(3) coating the sustained-release coated high-dose drug-containing cores of step (2) with the low-dose drug, a pharmaceutically acceptable solvent, and an optional binder, thereby forming high-dose/low-dose drug containing microparticles;
(4) coating the high-dose/low-dose drug-containing microparticles of step (3) with a taste-masking coating comprising a water-insoluble polymer and a pharmaceutically acceptable solvent; or a flavorant coating comprising a sweetener, a pharmaceutically acceptable solvent, and an optional binder;
(5) mixing the taste-masked or flavorant-coated high-dose/low-dose drug-containing microparticles of step (4) with at least one pharmaceutically acceptable excipient; and
(6) forming a tablet or a capsule.
67. The method of claim 66, further comprising:
(i) preparing a second population of cores comprising the high-dose drug, wherein the high-dose drug-containing cores of steps (1) and (i) are the same or different;
(ii) coating the second population of high-dose drug-containing cores of step (i) with a taste-masking layer, thereby forming taste-masked high-dose drug-containing cores;
wherein:
step (5) further comprises mixing the taste-masked or flavorant-coated high-dose/low-dose drug-containing microparticles of step (4) and the taste-masked high-dose drug-containing cores of step (ii).
68. The method of claim 66, further comprising:
(i) granulating a disintegrant and a sugar alcohol and/or saccharide each having an average particle size of less than about 30 μm, thereby forming rapidly-dispersing microgranules having an average particle size of less than about 300 μm;
wherein:
step (5) further comprises mixing the taste-masked high-dose/low-dose drug-containing microparticles of step (4) and the rapidly-dispersing microgranules of step (i); and
step (6) comprises compressing the mixture of step (5), thereby forming an ODT.
69. (canceled)
70. A method of treating pain comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 32 to a patient in need thereof.
71. A method of treating hyperglycemia comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 36 to a patient in need thereof.
72. A method of treating cardiovascular disease comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 37 to a patient in need thereof.
73. A method of treating hypercholesterolemia comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 37 to a patient in need thereof.
74. A method of treating indoor or outdoor allergies comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 38 to a patient in need thereof.
US12/772,770 2009-05-01 2010-05-03 Orally Disintegrating Tablet Compositions Comprising Combinations of High and Low-Dose Drugs Abandoned US20100330150A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/772,770 US20100330150A1 (en) 2009-05-01 2010-05-03 Orally Disintegrating Tablet Compositions Comprising Combinations of High and Low-Dose Drugs

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US17478009P 2009-05-01 2009-05-01
US17478809P 2009-05-01 2009-05-01
US12/772,770 US20100330150A1 (en) 2009-05-01 2010-05-03 Orally Disintegrating Tablet Compositions Comprising Combinations of High and Low-Dose Drugs

Publications (1)

Publication Number Publication Date
US20100330150A1 true US20100330150A1 (en) 2010-12-30

Family

ID=43032597

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/772,770 Abandoned US20100330150A1 (en) 2009-05-01 2010-05-03 Orally Disintegrating Tablet Compositions Comprising Combinations of High and Low-Dose Drugs
US12/772,776 Expired - Fee Related US9572781B2 (en) 2009-05-01 2010-05-03 Orally disintegrating tablet compositions comprising combinations of non-opioid and opioid analgesics

Family Applications After (1)

Application Number Title Priority Date Filing Date
US12/772,776 Expired - Fee Related US9572781B2 (en) 2009-05-01 2010-05-03 Orally disintegrating tablet compositions comprising combinations of non-opioid and opioid analgesics

Country Status (14)

Country Link
US (2) US20100330150A1 (en)
EP (2) EP2424504A4 (en)
JP (2) JP5845173B2 (en)
KR (2) KR101752014B1 (en)
CN (3) CN102458117B (en)
AR (2) AR076835A1 (en)
AU (2) AU2010242749B2 (en)
BR (1) BRPI1007636A2 (en)
CA (2) CA2760615A1 (en)
MX (2) MX2011011480A (en)
RU (2) RU2567032C2 (en)
TW (2) TW201041608A (en)
WO (2) WO2010127345A2 (en)
ZA (2) ZA201108780B (en)

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110003006A1 (en) * 2009-05-01 2011-01-06 Gopi Venkatesh Orally Disintegrating Tablet Compositions Comprising Combinations of Non-Opioid and Opioid Analgesics
WO2011066287A1 (en) 2009-11-30 2011-06-03 Eurand, Inc. Compressible-coated pharmaceutical compositions and tablets and methods of manufacture
US20130012524A1 (en) * 2010-03-15 2013-01-10 Inventia Healthcare Private Limited Stabilized prolonged release pharmaceutical composition comprising atypical antipsychotic
US20130143819A1 (en) * 2010-07-15 2013-06-06 Tedec Meiji Farma S.A. Ferrimannitol-ovalbumin tablet composition
WO2013089986A1 (en) * 2011-12-12 2013-06-20 Product And Technology Partners Llc Improved denaturants for sympathomimetic amines
US8637540B2 (en) 2003-11-26 2014-01-28 Acura Pharmaceuticals Compositions for deterring abuse of opioid containing dosage forms
WO2014017833A1 (en) * 2012-07-24 2014-01-30 Hanmi Pharm. Co., Ltd. Composite formulation for oral administration comprising metformin and rosuvastatin
US20140275149A1 (en) * 2013-03-15 2014-09-18 Inspirion Delivery Technologies, Llc Abuse deterrent compositions and methods of use
WO2014182003A1 (en) * 2013-05-06 2014-11-13 Hanmi Pharm. Co., Ltd. Composite formulation comprising a film coating layer containing rosuvastatin or a pharmaceutically acceptable salt thereof
KR20140131859A (en) * 2013-05-06 2014-11-14 한미약품 주식회사 Composite formulation comprising a film coating layer containing rosuvastatin or a pharmaceutically acceptable salt thereof
US8901113B2 (en) 2009-09-30 2014-12-02 Acura Pharmaceuticals, Inc. Methods and compositions for deterring abuse
US20150005334A1 (en) * 2013-03-15 2015-01-01 Inspirion Delivery Technologies, Llc Abuse deterrent compositions and methods of use
US9101636B2 (en) 2012-11-30 2015-08-11 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient
US20160346199A1 (en) * 2014-02-12 2016-12-01 Sawai Pharmaceutical Co., Ltd. Orally disintegrating tablet coated with film
US9616029B2 (en) 2014-03-26 2017-04-11 Sun Pharma Advanced Research Company Ltd. Abuse deterrent immediate release coated reservoir solid dosage form
US20180064663A1 (en) * 2014-05-01 2018-03-08 Sun Pharmaceutical Industries Limited Extended release liquid compositions of metformin
US9962336B2 (en) 2014-05-01 2018-05-08 Sun Pharmaceutical Industries Limited Extended release suspension compositions
US9962345B2 (en) 2014-05-01 2018-05-08 Sun Pharmaceutical Industries Limited Oral liquid compositions of guanfacine
US10010612B2 (en) 2007-05-25 2018-07-03 Indivior Uk Limited Sustained delivery formulations of risperidone compounds
US10022367B2 (en) 2014-03-10 2018-07-17 Indivior Uk Limited Sustained-release buprenorphine solutions
US10058554B2 (en) 2005-09-30 2018-08-28 Indivior Uk Limited Sustained release small molecule drug formulation
US10172849B2 (en) 2010-06-08 2019-01-08 Indivior Uk Limited Compositions comprising buprenorphine
US10198218B2 (en) 2010-06-08 2019-02-05 Indivior Uk Limited Injectable flowable composition comprising buprenorphine
US10238803B2 (en) 2016-05-02 2019-03-26 Sun Pharmaceutical Industries Limited Drug delivery device for pharmaceutical compositions
US10258583B2 (en) 2014-05-01 2019-04-16 Sun Pharmaceutical Industries Limited Extended release liquid compositions of guanfacine
US10285908B2 (en) 2014-07-30 2019-05-14 Sun Pharmaceutical Industries Ltd Dual-chamber pack
US10369078B2 (en) 2016-05-02 2019-08-06 Sun Pharmaceutical Industries Limited Dual-chamber pack for pharmaceutical compositions
US20200368117A1 (en) * 2018-02-06 2020-11-26 3M Innovative Properties Company Microcapsule with a porous or hollow core and ph-sensitive shell and use thereof
US11103581B2 (en) 2015-08-31 2021-08-31 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2648353C2 (en) * 2011-06-01 2018-03-23 Нитто Денко Корпорейшн Particulate composition and process for obtaining it
US10105330B2 (en) * 2012-01-04 2018-10-23 Wellesley Pharmaceuticals, Llc Extended, delayed and immediate release formulation method of manufacturing and use thereof
WO2013151754A1 (en) * 2012-04-02 2013-10-10 Teikoku Pharma Usa, Inc. Ibuprofen solid oral dosage composition comprising a methacrylic acid copolymer
US9301016B2 (en) * 2012-04-05 2016-03-29 Facebook, Inc. Sharing television and video programming through social networking
KR101397343B1 (en) * 2012-06-12 2014-05-19 씨제이제일제당 (주) Pharmaceutical preparation comprising metformin and HMG-CoA reductase inhibitor
US8993041B2 (en) * 2012-10-15 2015-03-31 New Jersey Institute Of Technology Taste masked active pharmaceutical powder compositions and processes for making them
AR096439A1 (en) * 2013-05-29 2015-12-30 Gruenenthal Gmbh DOSAGE METHOD RESISTING TO INDEED USE CONTAINING ONE OR MORE PARTICLES
US10195153B2 (en) 2013-08-12 2019-02-05 Pharmaceutical Manufacturing Research Services, Inc. Extruded immediate release abuse deterrent pill
KR101639692B1 (en) 2013-12-13 2016-07-14 제일약품주식회사 Orally dispersible, multiple-unit pharmaceutical composition comprising two or more active ingredients
US9649279B2 (en) * 2013-12-16 2017-05-16 Massachusetts Institute Of Technology Fortified micronutrient salt formulations
US10172797B2 (en) 2013-12-17 2019-01-08 Pharmaceutical Manufacturing Research Services, Inc. Extruded extended release abuse deterrent pill
US9492444B2 (en) 2013-12-17 2016-11-15 Pharmaceutical Manufacturing Research Services, Inc. Extruded extended release abuse deterrent pill
EP3169315B1 (en) 2014-07-17 2020-06-24 Pharmaceutical Manufacturing Research Services, Inc. Immediate release abuse deterrent liquid fill dosage form
US9132096B1 (en) * 2014-09-12 2015-09-15 Alkermes Pharma Ireland Limited Abuse resistant pharmaceutical compositions
EP3201823B1 (en) * 2014-10-02 2021-06-09 Trunomi Ltd. Systems and methods for context-based permissioning of personally identifiable information
US20160106737A1 (en) 2014-10-20 2016-04-21 Pharmaceutical Manufacturing Research Services, Inc. Extended Release Abuse Deterrent Liquid Fill Dosage Form
WO2017047586A1 (en) * 2015-09-14 2017-03-23 日本新薬株式会社 Tablet
JP6002870B1 (en) * 2015-10-16 2016-10-05 持田製薬株式会社 Orally disintegrating tablets containing low dose drugs
PL3398587T3 (en) * 2015-12-28 2024-01-22 Ssp Co., Ltd., Japan Compacted pharmaceutical preparation
JP6812104B2 (en) * 2015-12-28 2021-01-13 エスエス製薬株式会社 Oral solid composition
CN106619696A (en) * 2016-11-17 2017-05-10 郑州郑先医药科技有限公司 Compound blood glucose lowering preparation
US20180256515A1 (en) 2017-03-10 2018-09-13 Adare Pharmaceuticals, Inc. Oral amphetamine composition
CN107224439A (en) * 2017-06-13 2017-10-03 江苏黄河药业股份有限公司 It is a kind of to be used to treat oral loratadine disintegrating tablet of anaphylactia and preparation method thereof
WO2019131891A1 (en) * 2017-12-28 2019-07-04 大日本住友製薬株式会社 Bitterness-masked drug-containing particles and formulation containing said drug-containing particles
CN110840850B (en) * 2018-07-24 2023-03-17 烟台药物研究所 Celecoxib freeze-dried orally disintegrating tablet with high bioavailability and preparation method thereof
CN109701461B (en) * 2018-10-25 2021-06-08 西南交通大学 Preparation and application of PEG/Dex double aqueous phase-based calcium carbonate/calcium alginate composite microcapsule
CN109776873B (en) * 2018-12-12 2020-10-27 华南理工大学 Emulsion solvent volatilization method for preparing macroporous polymer microspheres
FR3093419B1 (en) * 2019-03-08 2021-06-18 Univ Grenoble Alpes Composition and associated method for measuring therapeutic compliance
WO2023095183A1 (en) * 2021-11-24 2023-06-01 Jordan University Of Science And Technology A pharmaceutical composition and a solid dosage form thereof

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4891223A (en) * 1987-09-03 1990-01-02 Air Products And Chemicals, Inc. Controlled release delivery coating formulation for bioactive substances
US5508044A (en) * 1991-08-12 1996-04-16 Euro-Celtique, S.A. Diltiazem pharmaceutical spheroid formulation
US6210714B1 (en) * 1993-11-23 2001-04-03 Euro-Celtique S.A. Immediate release tablet cores of acetaminophen having sustained-release coating
US6485747B1 (en) * 1998-10-30 2002-11-26 Monsanto Company Coated active tablet(s)
US20040091458A1 (en) * 2002-05-09 2004-05-13 Oncolytics Biotech Inc. Method for reducing pain using oncolytic viruses
US20050084536A1 (en) * 2001-10-26 2005-04-21 Van Buitenen Adrianus F.G. Method for the preparation of purified microparticles
US20060205674A2 (en) * 2004-08-26 2006-09-14 Nicholas Piramal India Ltd. Prodrugs containing novel bio-cleavable linkers
US20070036861A1 (en) * 2003-06-06 2007-02-15 Ethypharm Orally-dispersible multilayer tablet
WO2008015221A2 (en) * 2006-08-04 2008-02-07 Ethypharm Multilayer orally disintegrating tablet
US20080124398A1 (en) * 2003-11-14 2008-05-29 Gopi Venkatesh Modified release dosage forms of skeletal muscle relaxants
US20110003006A1 (en) * 2009-05-01 2011-01-06 Gopi Venkatesh Orally Disintegrating Tablet Compositions Comprising Combinations of Non-Opioid and Opioid Analgesics

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3826846A1 (en) 1988-08-06 1990-02-08 Goedecke Ag ALKOXY-4 (1H) -PYRIDONE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS DRUGS
US5500227A (en) * 1993-11-23 1996-03-19 Euro-Celtique, S.A. Immediate release tablet cores of insoluble drugs having sustained-release coating
AU752673B2 (en) * 1997-07-31 2002-09-26 Abbott Laboratories Combinations of HMG-CoA reductase inhibitors and nicotinic acid compounds and methods for treating hyperlipidemia once a day at night
RS49982B (en) * 1997-09-17 2008-09-29 Euro-Celtique S.A., Synergistic analgesic combination of opioid analgesic and cyclooxygenase-2 inhibitor
JP2004516234A (en) * 2000-05-01 2004-06-03 エアロファーム テクノロジー インコーポレイテッド Core preparation
EP1350512A1 (en) * 2002-04-03 2003-10-08 BOEHRINGER INGELHEIM INTERNATIONAL GmbH Combinations of epinastine, belladonna and pseudoephedrine as new pharmaceutical formulations
FR2850576B1 (en) * 2003-02-05 2007-03-23 Ethypharm Sa COMPOSITION COMPRISING A MIXTURE OF ACTIVE INGREDIENTS AND PROCESS FOR PREPARING THE SAME
FR2855756B1 (en) * 2003-06-06 2005-08-26 Ethypharm Sa MULTILAYER ORODISPERSIBLE TABLET
US8541026B2 (en) * 2004-09-24 2013-09-24 Abbvie Inc. Sustained release formulations of opioid and nonopioid analgesics
CN100404025C (en) * 2005-01-14 2008-07-23 信谊药厂 Oral disintegrating tablet containing tramadol hydrochloride and acetaminopher, and its preparation method
ZA200900640B (en) * 2006-08-04 2010-06-30 Ethypharm Sa Granule and orally disintegrating tablet comprising oxycodone
CN101352425B (en) * 2007-07-27 2010-11-10 鲁南制药集团股份有限公司 Compound osmotic pump controlled release preparation and preparation method thereof

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4891223A (en) * 1987-09-03 1990-01-02 Air Products And Chemicals, Inc. Controlled release delivery coating formulation for bioactive substances
US5508044A (en) * 1991-08-12 1996-04-16 Euro-Celtique, S.A. Diltiazem pharmaceutical spheroid formulation
US6210714B1 (en) * 1993-11-23 2001-04-03 Euro-Celtique S.A. Immediate release tablet cores of acetaminophen having sustained-release coating
US6485747B1 (en) * 1998-10-30 2002-11-26 Monsanto Company Coated active tablet(s)
US20050084536A1 (en) * 2001-10-26 2005-04-21 Van Buitenen Adrianus F.G. Method for the preparation of purified microparticles
US20040091458A1 (en) * 2002-05-09 2004-05-13 Oncolytics Biotech Inc. Method for reducing pain using oncolytic viruses
US20070036861A1 (en) * 2003-06-06 2007-02-15 Ethypharm Orally-dispersible multilayer tablet
US20080124398A1 (en) * 2003-11-14 2008-05-29 Gopi Venkatesh Modified release dosage forms of skeletal muscle relaxants
US20060205674A2 (en) * 2004-08-26 2006-09-14 Nicholas Piramal India Ltd. Prodrugs containing novel bio-cleavable linkers
WO2008015221A2 (en) * 2006-08-04 2008-02-07 Ethypharm Multilayer orally disintegrating tablet
US20110003006A1 (en) * 2009-05-01 2011-01-06 Gopi Venkatesh Orally Disintegrating Tablet Compositions Comprising Combinations of Non-Opioid and Opioid Analgesics

Cited By (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8637540B2 (en) 2003-11-26 2014-01-28 Acura Pharmaceuticals Compositions for deterring abuse of opioid containing dosage forms
US8822489B2 (en) 2003-11-26 2014-09-02 Acura Pharmaceuticals Abuse deterrent compositions and methods of making same
US9492443B2 (en) 2003-11-26 2016-11-15 Acura Pharmaceuticals, Inc. Abuse deterrent compositions and methods of making same
US11110093B2 (en) 2005-09-30 2021-09-07 Indivior Uk Limited Sustained release small molecule drug formulation
US10058554B2 (en) 2005-09-30 2018-08-28 Indivior Uk Limited Sustained release small molecule drug formulation
US11712475B2 (en) 2007-05-25 2023-08-01 Indivior Uk Limited Sustained delivery formulations of risperidone compound
US11013809B2 (en) 2007-05-25 2021-05-25 Indivior Uk Limited Sustained delivery formulations of risperidone compound
US10010612B2 (en) 2007-05-25 2018-07-03 Indivior Uk Limited Sustained delivery formulations of risperidone compounds
US10376590B2 (en) 2007-05-25 2019-08-13 Indivior Uk Limited Sustained delivery formulations of risperidone compound
US9572781B2 (en) 2009-05-01 2017-02-21 Adare Pharmaceuticals, Inc. Orally disintegrating tablet compositions comprising combinations of non-opioid and opioid analgesics
US20110003006A1 (en) * 2009-05-01 2011-01-06 Gopi Venkatesh Orally Disintegrating Tablet Compositions Comprising Combinations of Non-Opioid and Opioid Analgesics
US10155044B2 (en) 2009-09-30 2018-12-18 Acura Pharmaceuticals, Inc. Methods and compositions for deterring abuse
US8901113B2 (en) 2009-09-30 2014-12-02 Acura Pharmaceuticals, Inc. Methods and compositions for deterring abuse
WO2011066287A1 (en) 2009-11-30 2011-06-03 Eurand, Inc. Compressible-coated pharmaceutical compositions and tablets and methods of manufacture
US20160166510A1 (en) * 2010-03-15 2016-06-16 Inventia Healthcare Private Limited Stabilized prolonged release pharmaceutical composition comprising atypical antipsychotic
US9271939B2 (en) * 2010-03-15 2016-03-01 Inventia Healthcare Private Limited Stabilized prolonged release pharmaceutical composition comprising atypical antipsychotic
US20130012524A1 (en) * 2010-03-15 2013-01-10 Inventia Healthcare Private Limited Stabilized prolonged release pharmaceutical composition comprising atypical antipsychotic
US10558394B2 (en) 2010-06-08 2020-02-11 Indivior Uk Limited Injectable flowable composition comprising buprenorphine
US10592168B1 (en) 2010-06-08 2020-03-17 Indivior Uk Limited Injectable flowable composition comprising buprenorphine
US10198218B2 (en) 2010-06-08 2019-02-05 Indivior Uk Limited Injectable flowable composition comprising buprenorphine
US10172849B2 (en) 2010-06-08 2019-01-08 Indivior Uk Limited Compositions comprising buprenorphine
US9173925B2 (en) * 2010-07-15 2015-11-03 Tedee Meiji Farma, S.A. Ferrimannitol-ovalbumin tablet composition
US20130143819A1 (en) * 2010-07-15 2013-06-06 Tedec Meiji Farma S.A. Ferrimannitol-ovalbumin tablet composition
WO2013089986A1 (en) * 2011-12-12 2013-06-20 Product And Technology Partners Llc Improved denaturants for sympathomimetic amines
WO2014017833A1 (en) * 2012-07-24 2014-01-30 Hanmi Pharm. Co., Ltd. Composite formulation for oral administration comprising metformin and rosuvastatin
US10441657B2 (en) 2012-11-30 2019-10-15 Abuse Deterrent Pharmaceuticals, Llc Methods and compositions for self-regulated release of active pharmaceutical ingredient
US9320796B2 (en) 2012-11-30 2016-04-26 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient
US11857629B2 (en) 2012-11-30 2024-01-02 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient
US10688184B2 (en) 2012-11-30 2020-06-23 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient
US9101636B2 (en) 2012-11-30 2015-08-11 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient
US20140275149A1 (en) * 2013-03-15 2014-09-18 Inspirion Delivery Technologies, Llc Abuse deterrent compositions and methods of use
US20140275150A1 (en) * 2013-03-15 2014-09-18 Inspirion Delivery Technologies, Llc Abuse deterrent compositions and methods of use
US20150005334A1 (en) * 2013-03-15 2015-01-01 Inspirion Delivery Technologies, Llc Abuse deterrent compositions and methods of use
WO2014182003A1 (en) * 2013-05-06 2014-11-13 Hanmi Pharm. Co., Ltd. Composite formulation comprising a film coating layer containing rosuvastatin or a pharmaceutically acceptable salt thereof
KR102240429B1 (en) 2013-05-06 2021-04-15 한미약품 주식회사 Composite formulation comprising a film coating layer containing rosuvastatin or a pharmaceutically acceptable salt thereof
KR20140131859A (en) * 2013-05-06 2014-11-14 한미약품 주식회사 Composite formulation comprising a film coating layer containing rosuvastatin or a pharmaceutically acceptable salt thereof
US20160346199A1 (en) * 2014-02-12 2016-12-01 Sawai Pharmaceutical Co., Ltd. Orally disintegrating tablet coated with film
US10588856B2 (en) * 2014-02-12 2020-03-17 Sawai Pharmaceutical Co., Ltd. Orally disintegrating tablet coated with film
US10022367B2 (en) 2014-03-10 2018-07-17 Indivior Uk Limited Sustained-release buprenorphine solutions
US10517864B2 (en) 2014-03-10 2019-12-31 Indivior Uk Limited Sustained-release buprenorphine solutions
US9616029B2 (en) 2014-03-26 2017-04-11 Sun Pharma Advanced Research Company Ltd. Abuse deterrent immediate release coated reservoir solid dosage form
US9980917B2 (en) 2014-03-26 2018-05-29 Sun Pharma Advanced Research Company Ltd. Abuse deterrent immediate release coated reservoir solid dosage form
US10258583B2 (en) 2014-05-01 2019-04-16 Sun Pharmaceutical Industries Limited Extended release liquid compositions of guanfacine
US20180064663A1 (en) * 2014-05-01 2018-03-08 Sun Pharmaceutical Industries Limited Extended release liquid compositions of metformin
US9962336B2 (en) 2014-05-01 2018-05-08 Sun Pharmaceutical Industries Limited Extended release suspension compositions
US11504345B2 (en) * 2014-05-01 2022-11-22 Sun Pharmaceutical Industries Limited Extended release liquid compositions of metformin
US11523996B2 (en) * 2014-05-01 2022-12-13 Sun Pharmaceutical Industries Limited Extended release liquid compositions of metformin
US9962345B2 (en) 2014-05-01 2018-05-08 Sun Pharmaceutical Industries Limited Oral liquid compositions of guanfacine
US10285908B2 (en) 2014-07-30 2019-05-14 Sun Pharmaceutical Industries Ltd Dual-chamber pack
US11103581B2 (en) 2015-08-31 2021-08-31 Acura Pharmaceuticals, Inc. Methods and compositions for self-regulated release of active pharmaceutical ingredient
US10238803B2 (en) 2016-05-02 2019-03-26 Sun Pharmaceutical Industries Limited Drug delivery device for pharmaceutical compositions
US10369078B2 (en) 2016-05-02 2019-08-06 Sun Pharmaceutical Industries Limited Dual-chamber pack for pharmaceutical compositions
US20200368117A1 (en) * 2018-02-06 2020-11-26 3M Innovative Properties Company Microcapsule with a porous or hollow core and ph-sensitive shell and use thereof

Also Published As

Publication number Publication date
AR076540A1 (en) 2011-06-22
WO2010127345A2 (en) 2010-11-04
JP2012525444A (en) 2012-10-22
WO2010127346A1 (en) 2010-11-04
KR20120031002A (en) 2012-03-29
RU2011145432A (en) 2013-06-10
KR20120034630A (en) 2012-04-12
AR076835A1 (en) 2011-07-13
MX345942B (en) 2017-02-27
EP2424504A2 (en) 2012-03-07
AU2010242749B2 (en) 2015-05-07
WO2010127345A3 (en) 2011-01-06
JP5845172B2 (en) 2016-01-20
CA2760614A1 (en) 2010-11-04
AU2010242749A1 (en) 2011-11-24
RU2011145433A (en) 2013-06-10
CN102458117A (en) 2012-05-16
AU2010242748B2 (en) 2015-07-23
MX2011011478A (en) 2013-09-18
KR101752014B1 (en) 2017-06-28
EP2424365A1 (en) 2012-03-07
EP2424365A4 (en) 2012-11-28
RU2567032C2 (en) 2015-10-27
TW201041608A (en) 2010-12-01
TW201041607A (en) 2010-12-01
CN102458360A (en) 2012-05-16
ZA201108780B (en) 2012-09-26
JP5845173B2 (en) 2016-01-20
JP2012526047A (en) 2012-10-25
EP2424504A4 (en) 2012-11-28
ZA201108781B (en) 2012-08-29
CN102458117B (en) 2015-11-25
AU2010242748A1 (en) 2011-11-17
US9572781B2 (en) 2017-02-21
US20110003006A1 (en) 2011-01-06
BRPI1007636A2 (en) 2015-09-01
CN106390129A (en) 2017-02-15
CA2760615A1 (en) 2010-11-04
MX2011011480A (en) 2012-02-28
RU2554740C2 (en) 2015-06-27

Similar Documents

Publication Publication Date Title
AU2010242748B2 (en) Orally disintegrating tablet compositions comprising combinations of high and low-dose drugs
US10952971B2 (en) Taste-masked pharmaceutical compositions with gastrosoluble pore-formers
CA2782177C (en) Compressible-coated pharmaceutical compositions and tablets and methods of manufacture
US20120128764A1 (en) Controlled-release compositions comprising a proton pump inhibitor
US20090263480A1 (en) Taste-masked pharmaceutical compositions prepared by coacervation
US20120093938A1 (en) Orally disintegrating tablets comprising diphenhydramine
JP2013249305A (en) Drug delivery system containing weakly basic selective serotonin 5-ht3 blocking agent and organic acid
JP2014501224A (en) Orally disintegrating tablets
US20110256218A1 (en) Controlled release compositions comprising meclizine or related piperazine derivatives
WO2017017679A1 (en) Compositions comprising atorvastatin or a pharmaceutically acceptable salt thereof
US10335376B2 (en) Raloxifene sprinkle composition

Legal Events

Date Code Title Description
AS Assignment

Owner name: EURAND, INC., OHIO

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:VENKATESH, GOPI;GOSSELIN, MICHAEL;CLEVENGER, JAMES;AND OTHERS;REEL/FRAME:024977/0347

Effective date: 20100729

AS Assignment

Owner name: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT, NO

Free format text: SECURITY AGREEMENT;ASSIGNOR:EURAND, INCORPORATED;REEL/FRAME:025783/0548

Effective date: 20110211

AS Assignment

Owner name: APTALIS PHARMATECH, INC., OHIO

Free format text: CHANGE OF NAME;ASSIGNOR:EURAND, INCORPORATED;REEL/FRAME:027028/0048

Effective date: 20110712

AS Assignment

Owner name: APTALIS PHARMATECH, INC., NEW JERSEY

Free format text: RELEASE OF LIEN ON PATENTS;ASSIGNOR:BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT;REEL/FRAME:031494/0925

Effective date: 20131004

AS Assignment

Owner name: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT, NORTH CAROLINA

Free format text: PATENT SECURITY AGREEMENT;ASSIGNORS:APTALIS PHARMA CANADA INC.;APTALIS PHARMA US, INC.;APTALIS PHARMATECH, INC.;REEL/FRAME:031531/0488

Effective date: 20131004

Owner name: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT, NO

Free format text: PATENT SECURITY AGREEMENT;ASSIGNORS:APTALIS PHARMA CANADA INC.;APTALIS PHARMA US, INC.;APTALIS PHARMATECH, INC.;REEL/FRAME:031531/0488

Effective date: 20131004

AS Assignment

Owner name: APTALIS PHARMA CANADA INC., CANADA

Free format text: TERMINATION AND RELEASE;ASSIGNOR:BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT;REEL/FRAME:032149/0111

Effective date: 20140131

Owner name: APTALIS PHARMA US, INC., NEW JERSEY

Free format text: TERMINATION AND RELEASE;ASSIGNOR:BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT;REEL/FRAME:032149/0111

Effective date: 20140131

Owner name: APTALIS PHARMATECH, INC., NEW JERSEY

Free format text: TERMINATION AND RELEASE;ASSIGNOR:BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT;REEL/FRAME:032149/0111

Effective date: 20140131

AS Assignment

Owner name: ADARE PHARMACEUTICALS, INC., OHIO

Free format text: CHANGE OF NAME;ASSIGNOR:APTALIS PHARMATECH, INC.;REEL/FRAME:036090/0801

Effective date: 20150429

AS Assignment

Owner name: BANK OF MONTREAL, ILLINOIS

Free format text: U.S. PATENT SECURITY AGREEMENT;ASSIGNOR:ADARE PHARMACEUTICALS, INC.;REEL/FRAME:037246/0313

Effective date: 20151202

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: ADARE PHARMACEUTICALS, INC., NEW JERSEY

Free format text: RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAMES 037246/0313, 047807/0967, 053474/0276;ASSIGNOR:BANK OF MONTREAL, AS COLLATERAL AGENT;REEL/FRAME:053852/0697

Effective date: 20200922

Owner name: ADARE DEVELOPMENT I, L.P., NEW JERSEY

Free format text: RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAMES 037246/0313, 047807/0967, 053474/0276;ASSIGNOR:BANK OF MONTREAL, AS COLLATERAL AGENT;REEL/FRAME:053852/0697

Effective date: 20200922

Owner name: ADARE PHARMACEUTICALS USA, INC., NEW JERSEY

Free format text: RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAMES 037246/0313, 047807/0967, 053474/0276;ASSIGNOR:BANK OF MONTREAL, AS COLLATERAL AGENT;REEL/FRAME:053852/0697

Effective date: 20200922