CA2539982A1 - Pantoprazole multiparticulate formulations - Google Patents
Pantoprazole multiparticulate formulations Download PDFInfo
- Publication number
- CA2539982A1 CA2539982A1 CA002539982A CA2539982A CA2539982A1 CA 2539982 A1 CA2539982 A1 CA 2539982A1 CA 002539982 A CA002539982 A CA 002539982A CA 2539982 A CA2539982 A CA 2539982A CA 2539982 A1 CA2539982 A1 CA 2539982A1
- Authority
- CA
- Canada
- Prior art keywords
- pantoprazole
- multiparticulates
- core
- multiparticulate
- coat
- 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.)
- Granted
Links
- IQPSEEYGBUAQFF-UHFFFAOYSA-N Pantoprazole Chemical compound COC1=CC=NC(CS(=O)C=2NC3=CC=C(OC(F)F)C=C3N=2)=C1OC IQPSEEYGBUAQFF-UHFFFAOYSA-N 0.000 title claims abstract description 92
- 229960005019 pantoprazole Drugs 0.000 title claims abstract description 89
- 239000000203 mixture Substances 0.000 title claims description 59
- 238000009472 formulation Methods 0.000 title claims description 45
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims abstract description 42
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims abstract description 36
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims abstract description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000004094 surface-active agent Substances 0.000 claims abstract description 15
- 229960003943 hypromellose Drugs 0.000 claims abstract description 13
- 150000003839 salts Chemical class 0.000 claims abstract description 9
- 239000003814 drug Substances 0.000 claims description 26
- 239000002775 capsule Substances 0.000 claims description 21
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 20
- 229960000913 crospovidone Drugs 0.000 claims description 19
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 claims description 19
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 239000011248 coating agent Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 17
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 16
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 claims description 14
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims description 14
- 229940068968 polysorbate 80 Drugs 0.000 claims description 14
- 229920000053 polysorbate 80 Polymers 0.000 claims description 14
- 239000000454 talc Substances 0.000 claims description 12
- 229910052623 talc Inorganic materials 0.000 claims description 12
- 229920003138 Eudragit® L 30 D-55 Polymers 0.000 claims description 11
- GDCRSXZBSIRSFR-UHFFFAOYSA-N ethyl prop-2-enoate;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.CCOC(=O)C=C GDCRSXZBSIRSFR-UHFFFAOYSA-N 0.000 claims description 11
- -1 pantoprazole compound Chemical class 0.000 claims description 11
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims description 10
- 229940016286 microcrystalline cellulose Drugs 0.000 claims description 10
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims description 10
- 239000008108 microcrystalline cellulose Substances 0.000 claims description 10
- 229920003130 hypromellose 2208 Polymers 0.000 claims description 9
- 229940031707 hypromellose 2208 Drugs 0.000 claims description 9
- 239000007884 disintegrant Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 8
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 claims description 6
- 239000002702 enteric coating Substances 0.000 claims description 6
- 238000009505 enteric coating Methods 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 239000003002 pH adjusting agent Substances 0.000 claims description 6
- 239000001069 triethyl citrate Substances 0.000 claims description 6
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 claims description 6
- 235000013769 triethyl citrate Nutrition 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 5
- 239000000725 suspension Substances 0.000 claims description 5
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 4
- 229920003145 methacrylic acid copolymer Polymers 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 230000007935 neutral effect Effects 0.000 claims description 4
- 239000011888 foil Substances 0.000 claims description 3
- 230000002496 gastric effect Effects 0.000 claims description 3
- 229920000136 polysorbate Polymers 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 claims description 2
- 238000005563 spheronization Methods 0.000 claims description 2
- 229950008882 polysorbate Drugs 0.000 claims 2
- 229920001688 coating polymer Polymers 0.000 claims 1
- 229960004048 pantoprazole sodium Drugs 0.000 abstract description 15
- YNWDKZIIWCEDEE-UHFFFAOYSA-N pantoprazole sodium Chemical compound [Na+].COC1=CC=NC(CS(=O)C=2[N-]C3=CC=C(OC(F)F)C=C3N=2)=C1OC YNWDKZIIWCEDEE-UHFFFAOYSA-N 0.000 abstract description 14
- 229940079593 drug Drugs 0.000 description 25
- 239000003826 tablet Substances 0.000 description 25
- 239000000546 pharmaceutical excipient Substances 0.000 description 15
- 238000004090 dissolution Methods 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000011734 sodium Substances 0.000 description 10
- 229910052708 sodium Inorganic materials 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
- 239000008213 purified water Substances 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 8
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 7
- 230000009471 action Effects 0.000 description 7
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 229940061276 protonix Drugs 0.000 description 6
- 241000282472 Canis lupus familiaris Species 0.000 description 5
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- 238000010521 absorption reaction Methods 0.000 description 5
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- 239000012530 fluid Substances 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 210000001035 gastrointestinal tract Anatomy 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
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- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 235000013311 vegetables Nutrition 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000013341 scale-up Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000003981 vehicle Substances 0.000 description 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
- 229920003134 Eudragit® polymer Polymers 0.000 description 2
- 206010017999 Gastrointestinal pain Diseases 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920003091 Methocel™ Polymers 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 208000021302 gastroesophageal reflux disease Diseases 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000333 poly(propyleneimine) Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000009747 swallowing Effects 0.000 description 2
- 206010000087 Abdominal pain upper Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229920000623 Cellulose acetate phthalate Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 102000007530 Neurofibromin 1 Human genes 0.000 description 1
- 108010085793 Neurofibromin 1 Proteins 0.000 description 1
- 102100021904 Potassium-transporting ATPase alpha chain 1 Human genes 0.000 description 1
- 108010083204 Proton Pumps Proteins 0.000 description 1
- PQUGCKBLVKJMNT-UHFFFAOYSA-N SC560 Chemical compound C1=CC(OC)=CC=C1N1C(C=2C=CC(Cl)=CC=2)=CC(C(F)(F)F)=N1 PQUGCKBLVKJMNT-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 201000008629 Zollinger-Ellison syndrome Diseases 0.000 description 1
- 229940121353 acid pump inhibitor Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229940069428 antacid Drugs 0.000 description 1
- 239000003159 antacid agent Substances 0.000 description 1
- 230000001458 anti-acid effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
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- 230000036765 blood level Effects 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000007894 caplet Substances 0.000 description 1
- 229940081734 cellulose acetate phthalate Drugs 0.000 description 1
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
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- 229940126534 drug product Drugs 0.000 description 1
- 210000001198 duodenum Anatomy 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000013265 extended release Methods 0.000 description 1
- 230000009246 food effect Effects 0.000 description 1
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- 238000012395 formulation development Methods 0.000 description 1
- 230000030136 gastric emptying Effects 0.000 description 1
- 210000001914 gastric parietal cell Anatomy 0.000 description 1
- 201000000052 gastrinoma Diseases 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 229940031704 hydroxypropyl methylcellulose phthalate Drugs 0.000 description 1
- 229920003132 hydroxypropyl methylcellulose phthalate Polymers 0.000 description 1
- 239000012729 immediate-release (IR) formulation Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 210000003750 lower gastrointestinal tract Anatomy 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 230000003232 mucoadhesive effect Effects 0.000 description 1
- 210000001711 oxyntic cell Anatomy 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229940104721 pantoprazole 20 mg Drugs 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940068965 polysorbates Drugs 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229940069328 povidone Drugs 0.000 description 1
- 229940126409 proton pump inhibitor Drugs 0.000 description 1
- 239000000612 proton pump inhibitor Substances 0.000 description 1
- 238000012419 revalidation Methods 0.000 description 1
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- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical class [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
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Classifications
-
- 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
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- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
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- 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
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- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
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- A61K9/5005—Wall or coating material
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- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
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- 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
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- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1611—Inorganic compounds
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- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
Abstract
Pantoprazole sodium multiparticulates are described which avoid sticking to nasogastric and gastronomy tubes. The pantoprazole multiparticulates have a spheroid core of pantoprazole or an enantiomer thereof, or a salt thereof, a surfactant, and a distintegrant; a sub coat which is comprised of hydroxypropyl methylcellulose (hypromellose) and water, an enteric coat on the sub-coat, and a final seal coat over the enteric coat, which is composed of hydroxypropyl methylcellulose (hypromellose) and water.
Description
PANTOPRAZOLE MULTIPARTICULATE FORMULATIONS
BACKGROUND OF THE INVENTION
Pantoprazole, 5-(difluoromethoxy)-2-[(3,4-dimethoxy-2-pyridyl)methylsulphinyl]-1H-benzimidazole, is a H+/I~+-adenosine triphosphate (ATP) inhibitor (also known as acid pump or proton pump inhibitor (PPI), is an enzyme present in the gastric parietal cells. It is believed that these drugs are metabolized in the parietal cells to active sulfenamide metabolites that inactivate the sulfhydryl group of the proton pump, thus reducing the hydrogen ion secretion.
PPIs are generally lipophilic wealc bases with poor aqueous solubility at low pH.
Many PPIs are unstable in low pH solutions and undergo rapid acid-catalyzed degradation, and they are relatively stable at neutral or high pH.
The current commercial oral formulations of sodimn pantoprazole are single unit coated tablets. See, e.g., US Patent 5997903, which describes oral forms of pantoprazole that consist of a core, an intermediate layer and an outer layer.
The current coating has a tendency to cause undesirable sticking of the tablet to the gastrointestinal tract.
Multipat-ticulate formulations, because of their nature of dispersing in the gastrointestinal tract, show a reduced food effect and variability in gastric emptying times, thereby providing for reduced inter and intra subject variability, as compared to single unit tablets (Intl. Journal of Pharmaceutics 140 [1996] 229-235).
Several unsuccessful attempts have been made in the past to develop a multiparticulate formulation of pantoprazole. However, these attempts yielded multiparticulates that were not bioequivalent to tablets, only 70% relative bioavailability was found. Another attempt using different technologies- non-pareil seed coating and extrusionspheronization, resulted in a product that did not provide the appropriate release in acid conditions. In addition, these attempts yielded product that was unstable, as observed by discoloration, when stored at room temperature.
SUMMARY OF THE INVENTION
The invention provides a stable multiparticulate pantoprazole formulation that provides reduced inter and intra subject variability.
In one embodiment, the pantoprazole multiparticulates of the invention is composed of a spheroid core comprising pantoprazole or an enantiomer thereof, or a salt or hydrate thereof, at least one surfactant, at least one distintegrant, and about 1 to about 2% w/w water; an enteric coat on the core, said enteric coat comprising a copolymer of methacrylic acid and methacrylates in the range of about 15 to about 45 w/w of the spheroid core; wherein said multiparticulates have an average size of about 1 mm in diameter.
Advantageously, the multipanticulate formulations of the invention are stable under room temperatw-e storage conditions for at least twelve months. Based on the trend analysis using the twelve month room temperature data and 6 month 40 °C/75%
relative humidity (RH) data available to date, the multiparticulates of the invention should have a shelf life of over 2 years. Typically, a multiparticulate formulation of the invention is considered stable if it retains 90% to 110% of its potency during shelf life storage.
This pantoprazole multiparticulate formulation of the invention is less prone to adherence to the intestinal walls, nasogastric and gastromy tubes, and pouch material thereby giving predictable delivery of the drug product to the site of drug release. It also provides for an early onset of action for relief of gastro-intestinal pain and has a prolonged duration of action. This formulation allows dosing to pediatric patients and patients who have difficulty swallowing solid foods. This formulation also allows for drug delivery via nasogastric and gastrostomy tubes.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides a multiparticulate formulation of pantoprazole having a unique combination of excipients and a surfactant (e.g., polysorbate 80) that are compatible with pantoprazole sodium in the presence of an alkaline pH
environment. Further, the invention provides a process that utilizes low shear during granulation and low temperature during drying for preparation of the multiparticulate.
BACKGROUND OF THE INVENTION
Pantoprazole, 5-(difluoromethoxy)-2-[(3,4-dimethoxy-2-pyridyl)methylsulphinyl]-1H-benzimidazole, is a H+/I~+-adenosine triphosphate (ATP) inhibitor (also known as acid pump or proton pump inhibitor (PPI), is an enzyme present in the gastric parietal cells. It is believed that these drugs are metabolized in the parietal cells to active sulfenamide metabolites that inactivate the sulfhydryl group of the proton pump, thus reducing the hydrogen ion secretion.
PPIs are generally lipophilic wealc bases with poor aqueous solubility at low pH.
Many PPIs are unstable in low pH solutions and undergo rapid acid-catalyzed degradation, and they are relatively stable at neutral or high pH.
The current commercial oral formulations of sodimn pantoprazole are single unit coated tablets. See, e.g., US Patent 5997903, which describes oral forms of pantoprazole that consist of a core, an intermediate layer and an outer layer.
The current coating has a tendency to cause undesirable sticking of the tablet to the gastrointestinal tract.
Multipat-ticulate formulations, because of their nature of dispersing in the gastrointestinal tract, show a reduced food effect and variability in gastric emptying times, thereby providing for reduced inter and intra subject variability, as compared to single unit tablets (Intl. Journal of Pharmaceutics 140 [1996] 229-235).
Several unsuccessful attempts have been made in the past to develop a multiparticulate formulation of pantoprazole. However, these attempts yielded multiparticulates that were not bioequivalent to tablets, only 70% relative bioavailability was found. Another attempt using different technologies- non-pareil seed coating and extrusionspheronization, resulted in a product that did not provide the appropriate release in acid conditions. In addition, these attempts yielded product that was unstable, as observed by discoloration, when stored at room temperature.
SUMMARY OF THE INVENTION
The invention provides a stable multiparticulate pantoprazole formulation that provides reduced inter and intra subject variability.
In one embodiment, the pantoprazole multiparticulates of the invention is composed of a spheroid core comprising pantoprazole or an enantiomer thereof, or a salt or hydrate thereof, at least one surfactant, at least one distintegrant, and about 1 to about 2% w/w water; an enteric coat on the core, said enteric coat comprising a copolymer of methacrylic acid and methacrylates in the range of about 15 to about 45 w/w of the spheroid core; wherein said multiparticulates have an average size of about 1 mm in diameter.
Advantageously, the multipanticulate formulations of the invention are stable under room temperatw-e storage conditions for at least twelve months. Based on the trend analysis using the twelve month room temperature data and 6 month 40 °C/75%
relative humidity (RH) data available to date, the multiparticulates of the invention should have a shelf life of over 2 years. Typically, a multiparticulate formulation of the invention is considered stable if it retains 90% to 110% of its potency during shelf life storage.
This pantoprazole multiparticulate formulation of the invention is less prone to adherence to the intestinal walls, nasogastric and gastromy tubes, and pouch material thereby giving predictable delivery of the drug product to the site of drug release. It also provides for an early onset of action for relief of gastro-intestinal pain and has a prolonged duration of action. This formulation allows dosing to pediatric patients and patients who have difficulty swallowing solid foods. This formulation also allows for drug delivery via nasogastric and gastrostomy tubes.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides a multiparticulate formulation of pantoprazole having a unique combination of excipients and a surfactant (e.g., polysorbate 80) that are compatible with pantoprazole sodium in the presence of an alkaline pH
environment. Further, the invention provides a process that utilizes low shear during granulation and low temperature during drying for preparation of the multiparticulate.
This process contributes to the stability of the core of the multiparticulates of the invention.
In one aspect, the invention provides multiparticulate formulations of pantoprazole having reduced release under gastric conditions and fast release at neutral pH, i.e., in the lower gastrointestinal tract.
The multi particulate formulation of sodium pantoprazole of the invention provides an enhanced system for the delivery of pantoprazole to patients. The current marlceted formulation is a single monolithic tablet. The present formulation of multiparticulate spheroids, which is adaptable for use in a capsule or a foil packet, can be prepared by extrusion/spheronization plus coating technology.
The composition of the multiparticle of the invention, and the enteric coat, e. g. , Eudragit, allows for reduced release at low pH (~ 1 ) and fast release at a neutral pH (~7). This provides faster blood levels of the drug, in patients, and thereby a faster onset of action. The smaller T,ag value of multiparticulate formulation as compared to that of a single monolithic tablet based on the results from dog data indicates faster onset of action of multiparticulate formulation.
The use of a mufti particulate formulation facilitates dosing to pediatric patients and patients who have trouble swallowing, by dispersing the spheroids in a suspending liquid or sprinlcling/dispersing in a low pH liquid like applesauce, prior to administration. The suspending liquid could be made prior to administration by mixing a blend of powder material with water. The smaller size of the mufti pat-ticulates, in a capsule or pouch or any other container, also allows dosing through nasogastric or gastrostomy tube.
This formulation allows for a faster relief of GI pain, and prolonged duration of action (extended release), as compared to the current marketed tablet.
Multiparticulates of the Invention Suitably, the multiparticles are in the range of about 0.1 to 2 mm, or 0.5 mm to 1.5 mm, or 0.7 mm to 1.25 mm, or 0.8 mm to 1 mm. In one embodiment, the multiparticulates in a composition of the invention average about 1 iron in diameter.
Typically, the multiparticles of the invention are no greater than about 1mm in size in order to facilitate passage through nasogastric tubes The multiparticulates of the invention are composed, at a minimum, of a spheroid core with an enteric coat over the core. In between the core and enteric coat an initial seal coat may be applied, e.g., comprising a coating of hydroxylpropyl methylcellulose (hypromellose). Also, over the enteric coat a final seal coat may be applied, e.g., a coating of hydroxylpropyl methyl cellulose (hypromellose).
The spheroid core is composed of, at a minimum, a pantoprazole or a salt thereof, and a surfactant.
As used herein unless the context requires otherwise, the term 'pantoprazole' refers to 5-(difluoromethoxy)-2-[(3,4-dimethoxy-2-pyridyl)methylsulphinyl]-1H-benzimidazole and enantiomers thereof and the term 'pantoprazole compound' includes pantoprazole and enantiomers and salts and hydrates thereof . The active compound, pantoprazole is described in European Patent 166 287, which describes the preparation thereof, and is available commercially under the brand name PROTONIX ~. Examples of pharmaceutically acceptable salts of pantoprazole include, e.g., sodium, magnesium, and calcium, among others; still others are described in the European Patent 166 286, which is incorporated by reference herein.
The selection of a suitable salt is not a limitation of the invention. In one embodiment, the salt is sodium. Typically, the pantoprazole compound is present in the range of from about 5 to 50 % w/w, more preferably about 20 to 45 % w/w, of the total multiparticulate.
Suitable surfactants are known to those of slcill in the an. However, particularly desirable are sodium lauryl sulfate, polysorbates, including, e.g., polysorbate 80, and mixtures of these components. Typically, the surfactant is present in the core in an amount of about 2 to about 7 % w/w, and desirably, about 5%
w/w of the core. In another embodiment, the surfactant is present in a ratio of about 5:3 drug: surfactant (e.g., pantoprazole sodium sesquihydrate to sodium lauryl sulfate) to about 10:1 drug: surfactant (e.g., pantoprazole sodium sesquihydrate to polysorbate 80). Advantageously, the surfactants in the multiparticulate formulation have been found to enhance the wettability and, thus, the speed and extent of release and absorption of the sodium pantoprazole, from the mufti particulate formulation of the invention.
The spheroid core can further contain a disintegrant, a pH adjuster and, optionally a binder or another excipient such as hydroxypropyl methylcellulose (e.g., hypromellose 2208). Suitably, the total amount of disintegrant(s) present in the core is an amount of about 15 % w/w to about 80 % w/w, or about 20% w/w to about 70 w/w, or about 25% w/w to about 45% w/w, or about 30% w/w to about 42 % w/w.
In one emboeiiment, the total amount of drug to binder is represented by a ratio of from about S 0:1 to about 40:1 by weight drug:binder. The total amount of a pH
adjuster in the formulation can range from about 0.1 % w/w to about 10% w/w of the multiparticulate, or about 1% w/w to about 8% w/w, or about 3% w/w to about 7%
w/w. However, these percentages can be adjusted as needed or desired by one of skill in the art.
The disintegrant may be selected from among other l~nomn disintegrants, including, e.g., cellulose, and crospovidone, among others. In one embodiment, the disintegrant is selected from among microcrystalline cellulose and crospovidone, and mixtures thereof. The binder may be selected from among known binders, including e.g., cellulose, and povidone, among others. In one embodiment, the binder is hydroxylpropyl methyl cellulose (hypromellose). Suitable pH adjusters include, e.g., sodium carbonate, sodium bicarbonate, potassium carbonate, lithium carbonate, among others. Still other suitable components will be readily apparent to one of skill in the art.
In one embodiment, the spheroid core contains, w/w based on the dry uncoated cor e, about 45% pantoprazole sodium sesquihydrate (about 40% free pantoprazole~ , about 25 to 30%, and preferably about 27% microcrystalline cellulose, about 4 to 6%, and preferably about 5% polysorbate 80, about 14 to 16%, and preferably about 15% crospovidone, about 0.5 to 2 %, and preferably about 1%
hypromellose 2208, about 5 to 8%, and preferably about 6.5% sodium carbonate.
In one embodiment, the spheroid core contains:
In one aspect, the invention provides multiparticulate formulations of pantoprazole having reduced release under gastric conditions and fast release at neutral pH, i.e., in the lower gastrointestinal tract.
The multi particulate formulation of sodium pantoprazole of the invention provides an enhanced system for the delivery of pantoprazole to patients. The current marlceted formulation is a single monolithic tablet. The present formulation of multiparticulate spheroids, which is adaptable for use in a capsule or a foil packet, can be prepared by extrusion/spheronization plus coating technology.
The composition of the multiparticle of the invention, and the enteric coat, e. g. , Eudragit, allows for reduced release at low pH (~ 1 ) and fast release at a neutral pH (~7). This provides faster blood levels of the drug, in patients, and thereby a faster onset of action. The smaller T,ag value of multiparticulate formulation as compared to that of a single monolithic tablet based on the results from dog data indicates faster onset of action of multiparticulate formulation.
The use of a mufti particulate formulation facilitates dosing to pediatric patients and patients who have trouble swallowing, by dispersing the spheroids in a suspending liquid or sprinlcling/dispersing in a low pH liquid like applesauce, prior to administration. The suspending liquid could be made prior to administration by mixing a blend of powder material with water. The smaller size of the mufti pat-ticulates, in a capsule or pouch or any other container, also allows dosing through nasogastric or gastrostomy tube.
This formulation allows for a faster relief of GI pain, and prolonged duration of action (extended release), as compared to the current marketed tablet.
Multiparticulates of the Invention Suitably, the multiparticles are in the range of about 0.1 to 2 mm, or 0.5 mm to 1.5 mm, or 0.7 mm to 1.25 mm, or 0.8 mm to 1 mm. In one embodiment, the multiparticulates in a composition of the invention average about 1 iron in diameter.
Typically, the multiparticles of the invention are no greater than about 1mm in size in order to facilitate passage through nasogastric tubes The multiparticulates of the invention are composed, at a minimum, of a spheroid core with an enteric coat over the core. In between the core and enteric coat an initial seal coat may be applied, e.g., comprising a coating of hydroxylpropyl methylcellulose (hypromellose). Also, over the enteric coat a final seal coat may be applied, e.g., a coating of hydroxylpropyl methyl cellulose (hypromellose).
The spheroid core is composed of, at a minimum, a pantoprazole or a salt thereof, and a surfactant.
As used herein unless the context requires otherwise, the term 'pantoprazole' refers to 5-(difluoromethoxy)-2-[(3,4-dimethoxy-2-pyridyl)methylsulphinyl]-1H-benzimidazole and enantiomers thereof and the term 'pantoprazole compound' includes pantoprazole and enantiomers and salts and hydrates thereof . The active compound, pantoprazole is described in European Patent 166 287, which describes the preparation thereof, and is available commercially under the brand name PROTONIX ~. Examples of pharmaceutically acceptable salts of pantoprazole include, e.g., sodium, magnesium, and calcium, among others; still others are described in the European Patent 166 286, which is incorporated by reference herein.
The selection of a suitable salt is not a limitation of the invention. In one embodiment, the salt is sodium. Typically, the pantoprazole compound is present in the range of from about 5 to 50 % w/w, more preferably about 20 to 45 % w/w, of the total multiparticulate.
Suitable surfactants are known to those of slcill in the an. However, particularly desirable are sodium lauryl sulfate, polysorbates, including, e.g., polysorbate 80, and mixtures of these components. Typically, the surfactant is present in the core in an amount of about 2 to about 7 % w/w, and desirably, about 5%
w/w of the core. In another embodiment, the surfactant is present in a ratio of about 5:3 drug: surfactant (e.g., pantoprazole sodium sesquihydrate to sodium lauryl sulfate) to about 10:1 drug: surfactant (e.g., pantoprazole sodium sesquihydrate to polysorbate 80). Advantageously, the surfactants in the multiparticulate formulation have been found to enhance the wettability and, thus, the speed and extent of release and absorption of the sodium pantoprazole, from the mufti particulate formulation of the invention.
The spheroid core can further contain a disintegrant, a pH adjuster and, optionally a binder or another excipient such as hydroxypropyl methylcellulose (e.g., hypromellose 2208). Suitably, the total amount of disintegrant(s) present in the core is an amount of about 15 % w/w to about 80 % w/w, or about 20% w/w to about 70 w/w, or about 25% w/w to about 45% w/w, or about 30% w/w to about 42 % w/w.
In one emboeiiment, the total amount of drug to binder is represented by a ratio of from about S 0:1 to about 40:1 by weight drug:binder. The total amount of a pH
adjuster in the formulation can range from about 0.1 % w/w to about 10% w/w of the multiparticulate, or about 1% w/w to about 8% w/w, or about 3% w/w to about 7%
w/w. However, these percentages can be adjusted as needed or desired by one of skill in the art.
The disintegrant may be selected from among other l~nomn disintegrants, including, e.g., cellulose, and crospovidone, among others. In one embodiment, the disintegrant is selected from among microcrystalline cellulose and crospovidone, and mixtures thereof. The binder may be selected from among known binders, including e.g., cellulose, and povidone, among others. In one embodiment, the binder is hydroxylpropyl methyl cellulose (hypromellose). Suitable pH adjusters include, e.g., sodium carbonate, sodium bicarbonate, potassium carbonate, lithium carbonate, among others. Still other suitable components will be readily apparent to one of skill in the art.
In one embodiment, the spheroid core contains, w/w based on the dry uncoated cor e, about 45% pantoprazole sodium sesquihydrate (about 40% free pantoprazole~ , about 25 to 30%, and preferably about 27% microcrystalline cellulose, about 4 to 6%, and preferably about 5% polysorbate 80, about 14 to 16%, and preferably about 15% crospovidone, about 0.5 to 2 %, and preferably about 1%
hypromellose 2208, about 5 to 8%, and preferably about 6.5% sodium carbonate.
In one embodiment, the spheroid core contains:
pantoprazole sodium sesquihydrate 45.24% w/w microcrystalline cellulose 27.25% w/w polysorbate 80 5 % w/w crospovidone 15 % w/w hypromellose 2208 1 % w/w sodium carbonate 6.5% w/w In another embodiment, the spheroid core contains:
Ingredients Amount/ % w/w, based on total Capsule weight multiparticulate Pantoprazole Sodium Sesquihydrate 45.11 21.911 Microcrystalline Cellulose,27.39 13.304 NF/EP
(Avicel PH 101) Polysorbate 80, NF 5.00 2.429 Vegetable source Crospovidone, NF 15.00 7.286 (Polyplasdone XL) HPMG USP/EP (Methocel) 1.00 0.486 I~3 Sodium Carbonate, NF 6.50 3.157 Purified Water, USP/BP/EP q.s. to malce wet mass Total 100.00 mg 48.573 Although moisture is removed from the core during the drying process which is described below, the core preferably retains about 1% to about 2% w/w water.
Without wishing to be bound by theory, the inventors believe that this water content contributes the stability of this multiparticulate as compared to the failed prior art attempts at forming a multiparticulate pantoprazole.
Optionally, an initial seal coat (or subcoat) can be applied directly to the core prior to coating with the enteric coat. Although the components of this seal coat can be modified by one of slcill in the art, a particularly suitable initial seal coat is composed of hydroxypropyl methylcellulose (hypromellose) and water. For example, a suitable initial seal coat can be applied as a 7.5% w/w hypromellose solution.
Ingredients Amount/ % w/w, based on total Capsule weight multiparticulate Pantoprazole Sodium Sesquihydrate 45.11 21.911 Microcrystalline Cellulose,27.39 13.304 NF/EP
(Avicel PH 101) Polysorbate 80, NF 5.00 2.429 Vegetable source Crospovidone, NF 15.00 7.286 (Polyplasdone XL) HPMG USP/EP (Methocel) 1.00 0.486 I~3 Sodium Carbonate, NF 6.50 3.157 Purified Water, USP/BP/EP q.s. to malce wet mass Total 100.00 mg 48.573 Although moisture is removed from the core during the drying process which is described below, the core preferably retains about 1% to about 2% w/w water.
Without wishing to be bound by theory, the inventors believe that this water content contributes the stability of this multiparticulate as compared to the failed prior art attempts at forming a multiparticulate pantoprazole.
Optionally, an initial seal coat (or subcoat) can be applied directly to the core prior to coating with the enteric coat. Although the components of this seal coat can be modified by one of slcill in the art, a particularly suitable initial seal coat is composed of hydroxypropyl methylcellulose (hypromellose) and water. For example, a suitable initial seal coat can be applied as a 7.5% w/w hypromellose solution.
Typically, such a seal coat is in the range of about 2% w/w to about 4% w/w of the uncoated core or about 1 % w/w to about 2% w/w of the coated multiparticulate.
In one embodiment, a multiparticulate with a subcoat contains:
Ingredients Amount/ %w/w, based Capsule on total weight multiparticul ate A. Sub Coat: 4.00 mg 1.943 Pantoprazole Sodium Pellets 100.00 mg 48.573 (40 mg pantoprazole per 100 mg pellets) Hydroxypropylmethyl cellulose4.00 mg 1.943 2910, USP, 6cps Purified water, USP/BP/EP 9.33 mg~
removed during processing Total 104.00 mg 50.516 The enteric coat is applied over the initial seal coat, if present, or directly to the uncoated spheroid core. Suitably, the enteric coat is applied such that it coats the core in an amount of about 15 to 45 % w/w, or about 20 % wlw to about 30% w/w, or about 25% w/w to 30% w/w of the multipauticulate. In one embodiment, the enteric coat is about 27.5 to 32.5 % w/w of the multiparticulate. Suitably, the enteric coat contains a product which is a copolymer of methacrylic acid and methacrylates, such as the commercially available Eudragit L 30D-55. In one embodiment, the enteric coat is composed of a Eudragit L30D-55 copolymer, talc, triethyl citrate, sodium hydroxide and water. More particularly, the enteric coating may contain about 30%
w/w of multiparticulate ( applied as a 30 wt% dispersion) of Eudragit L 30D-55 coating; about 15% w/w talc, about 3% triethyl citrate; a pH adjuster such as sodium hydroxide and water. Other suitable materials may be selected for use in the enteric coat including, e.g., hydroxypropyl methylcellulose phthalate, cellulose acetate phthalate and the like.
In one embodiment, a multiparticulate of the invention is provided with a subcoat over the core and an enteric coat as follows:
In one embodiment, a multiparticulate with a subcoat contains:
Ingredients Amount/ %w/w, based Capsule on total weight multiparticul ate A. Sub Coat: 4.00 mg 1.943 Pantoprazole Sodium Pellets 100.00 mg 48.573 (40 mg pantoprazole per 100 mg pellets) Hydroxypropylmethyl cellulose4.00 mg 1.943 2910, USP, 6cps Purified water, USP/BP/EP 9.33 mg~
removed during processing Total 104.00 mg 50.516 The enteric coat is applied over the initial seal coat, if present, or directly to the uncoated spheroid core. Suitably, the enteric coat is applied such that it coats the core in an amount of about 15 to 45 % w/w, or about 20 % wlw to about 30% w/w, or about 25% w/w to 30% w/w of the multipauticulate. In one embodiment, the enteric coat is about 27.5 to 32.5 % w/w of the multiparticulate. Suitably, the enteric coat contains a product which is a copolymer of methacrylic acid and methacrylates, such as the commercially available Eudragit L 30D-55. In one embodiment, the enteric coat is composed of a Eudragit L30D-55 copolymer, talc, triethyl citrate, sodium hydroxide and water. More particularly, the enteric coating may contain about 30%
w/w of multiparticulate ( applied as a 30 wt% dispersion) of Eudragit L 30D-55 coating; about 15% w/w talc, about 3% triethyl citrate; a pH adjuster such as sodium hydroxide and water. Other suitable materials may be selected for use in the enteric coat including, e.g., hydroxypropyl methylcellulose phthalate, cellulose acetate phthalate and the like.
In one embodiment, a multiparticulate of the invention is provided with a subcoat over the core and an enteric coat as follows:
Ingredients Azzzouzztlcapsule%w/w, based on total weight zzzultipazticulate Core + Subcoat 100.20 mg 48.67 Eudragit L30D-55 208.00 mg 30.309 62.40 (solids) Talc, USP, Altalc SOOV 31.20 mg 15.155 Sodium Hydroxide, NF 9.30 mg 0.175 solution 0.36 (solids) Triethyl Citrate, PG/NF6.24 mg 3.031 Purified Water, USPBP/EP183.38 mg*
'~ removed during processing Total 204.20 mg 99.186 In one embodiment, the enteric-coated multiparticulate is further coated with a final seal coat. Suitably, this final seal coat is comprises hydroxypropyl methylcellulose, and about 0.1% w/w to 10 % w/w of the coated multipa~.-ticle, 0.1%
w/w to about 5% w/w, or about 0.2% w/w to about 4% w/w.
In one embodiment, a final seal coat of hydroxypropyl methylcellulose in an amount of O.5 to 1 % w/w of the multiparticulate in water (which is removed during processing) is applied over the enteric coat. Following this, a coating of talc can optionally be applied over the final seal coat, in an amount of about 0.05 w/w to about 1 % w/w, and pr efer ably 0.1 % w/w to 0.5 % w/w.
In one embodiment, the resulting multiparticttlate formulation of the invention achieves a geometric mean AUC ratio of test/reference of 89 to 94 with a 90%
confidence interval of 84 to 100 for the ratio or achieving a geometric mean Cmax ratio of test/reference of 62 to 66 with a 90% confidence interval of 56 to 74 for the ratio or an ah-vitro dissolution profile as shown below:
'~ removed during processing Total 204.20 mg 99.186 In one embodiment, the enteric-coated multiparticulate is further coated with a final seal coat. Suitably, this final seal coat is comprises hydroxypropyl methylcellulose, and about 0.1% w/w to 10 % w/w of the coated multipa~.-ticle, 0.1%
w/w to about 5% w/w, or about 0.2% w/w to about 4% w/w.
In one embodiment, a final seal coat of hydroxypropyl methylcellulose in an amount of O.5 to 1 % w/w of the multiparticulate in water (which is removed during processing) is applied over the enteric coat. Following this, a coating of talc can optionally be applied over the final seal coat, in an amount of about 0.05 w/w to about 1 % w/w, and pr efer ably 0.1 % w/w to 0.5 % w/w.
In one embodiment, the resulting multiparticttlate formulation of the invention achieves a geometric mean AUC ratio of test/reference of 89 to 94 with a 90%
confidence interval of 84 to 100 for the ratio or achieving a geometric mean Cmax ratio of test/reference of 62 to 66 with a 90% confidence interval of 56 to 74 for the ratio or an ah-vitro dissolution profile as shown below:
Dru Release Media Time Initial 6 Months 6 Months @ Target @ 40C/75%RH
25C/60%RH
Acid 2 hrs 0.33 0.45 0.6 NMT 10%
( H 1.0) 3 min - 0.91 0.85 -Foll wed b o y 6 min - 3.61 1.83 -Alkaline 9 min - 52.25 16.45 -Buffer (pH 6.8) 12 min - 89.65 75.15 -15 min 101.58 97.15 91.92 -30 min 105.29 100.67 98.96 -45 min 105.29 100.57 99.14 NLT 75%
60 min 105.06 100.52 99.07 -In another embodiment, the resulting multiparticulate formulation of the invention achieves a mean AUC of 5451 to 5629 ng.h/ml and mean Cmax of 1865 to 1929 ng/ml or an ifz-vitro dissolution profile as shown below:
Batch % Drug Release Acid Buffer (mirc) 2hrs I S 30 45 Initial 0.08 101.77 107.44107.38 6 Months @40C/75%RH 0.73 95.44 101.12101.21 12 Months @25C/60%RH 0.30 96.11 101.92102.20 *Specifications: Acid at 21 s-NMT 10.0%; Buffer at 45 min-NLT 75%
However, the invention is not limited to these exemplary profiles.
Without wishing to be bound by theory, it is believed that final seal coat layer of hydroxypropyl methylcellulose provides a physical barrier for reduced contact between the mucoadhesive Eudragit layer and the upper GI tract, and thereby allows the reliable transit of the multiparticulates to the proper pH environment in the GI
tract for effective release and absorption of the drug. In addition, the final seal coat layer of hydroxypropyl methylcellulose imparts anti-sticking properties to the multiparticulates and thus the multipaniculates are not sticking to the pouch material andlor nasogastric tube. The multiparticulates of the invention are useful for administration via the nasogastric tube and via food vehicles, particularly acidic food vehicles.
II. Meth od of Producing Multiparticulate Formulations of Invention In another aspect, the invention provides a method of producing the multiparticulate formulations of the invention.
Typically, the uncoated pantoprazole compounds are prepared are follows.
The dry components, including, at least the pantoprazole compound and the binder are dry blended in a suitable mixer under low shear conditions. Suitable low shear conditions can be readily achieved using, e.g., a Hobart mixer, at a range of about 25 rpm to 35 rprn, and most desirably, 32 rpm. However, one of skill in the art will be able to achieve comparable low shear conditions using different equipment, with the rpm adjusted to the appropriate low shear settings for the selected equipment.
Optionally, hydroxypropyl methylcellulose or crospovidone may be substituted or additionally included in this step. Additionally, a pH adjuster may be included in this step.
Subsequently, the liquid components, e.g., the surfactant and water, are mixed in to afford a granulated product by mixing under low shear conditions.
Suitable low shear conditions can be readily achieved using, e.g., a Hobart mixer, at a range of about 25 rpm to 35 rpm, and most desirably, 32 rpm. However, one of skill in the art will be able to achieve comparable low shear conditions using different equipment, with the rpm adjusted to the appropriate low shear settings for the selected equipment.
The granulation is then extruded and spheronized through a suitable device (e.g., a NICA extruder/spheronizer) axed the resulting spheroids are dried, sifted, and optionally blended prior to storage.
The inventors have found that a significant advantage is provided to the stability of the compound when the multiparticulates of the invention are dried at low temperature. Desirably, the spheroid cores of the pantoprazole multiparticulates of the invention are dried to a percent (%) loss-on-drying (LOD) of 3.4% to 4.3%.
As used herein, low temperature drying refers to a temperature not exceeding about 40°C
for a period of 10 to 12 hours. When the drying conditions exceed this temperature and time period, impurities are observed that contribute to instability. In one embodiment, drying of the core is performed in the range of 35°C to 40°C, or about 37 °C to 39 °C for about 8 to 72 hours. In another embodiment, the core is dryed at about 40°C for 10 to 12 hours. Suitably, when coating layers are applied as described, the drying temperature for the various coating layers is also in this range.
Optionally, an initial seal coat of a hydrophilic polymer can be applied to the uncoated multiparticulates. For example, an initial seal coat composed of hydroxypropyl methylcellulose and purified water can be applied on a fluid bed coater, e. g. , by spraying.
The enteric coat can be applied directly to the uncoated spheroid core, i.e., the uncoated multipaxticulate, or may be applied over an initial seal coat. The enteric coat as described above, is typically applied on a fluid bed wurster coater.
In one embodiment, a final seal coat is applied over the enteric coat and, optionally, talc is utilized in the final step prior to filling the multiparticulates into a suitable packaging unit.
The multipauticulate of the invention may be in any suitable form including, e.g., granules, pellets, beads, minitabs, spherules, beadlets, microcapsules, millispheres, nonocapsules, microspheres, platelets, tablets, and capsules, depending upon the desired route of delivery.
III. Formulations, Kits and Methods of delivery In another embodiment, the present invention provides products containing the pantoprazole multiparticulates of the invention.
Suitably, the multiparticulate compositions of the invention are formulated such that a patient receives a suitable amount of the pantoprazole, e.g., 5 mg to 200 mg, about 10 mg to about 100 mg, or about 40 mg (measured based upon free pantoprazole). Preferably, the formulations are such that a suitable dose is delivered in a single dosage unit. These doses may be administered daily for a suitable period of time, e.g., 4 weeks to 8 weelcs, but can be delivered for a shorter period oftime, e.g., 3 days to 3 weelcs, one week to 3 months, or over a longer period, e.g., over 6 months, or longer. These compositions can be delivered alone or in combination with an antacid or other suitable composition.
In one embodiment, the invention provides a method of treating humans by admiW stering an effective dose of the pantoprazole multiparticulates such that an area under curve (AUC) at least bioequivalent to Protonix" 40mg tablet and Cmax as listed in Table VI are achieved.
In one embodiment, the pantoprazole multiparticulates are packaged for use by the patient or his caregiver. For example, the multiparticulates can be packaged in a foil or other suitable package and is suitable for mixing into a food product (e.g., applesauce and other acidic food vehicles) or into a drinlc for consumption by the patient.
The pantoprazole multiparticulate formulations of the invention are useful for treatment of gastroesophageal reflux disease (GERD), ulcers of the stomach and duodenum, and Zollinger-Ellison Syndrome.
In another embodiment, the pantoprazole multiparticulates are suspended in a physiologically compatible suspending liquid.
In yet another embodiment, the pantoprazole multiparticulates are filled in capsules, caplets or the like for oral delivery.
In still a further embodiment, the invention provides method of treating a subject in need thereof by administering an effective dose of the pantoprazole multiparticles of the invention.
The following examples illustrate specific embodiments of the invention and are not a limitation on the present invention.
Example 1 -PANTOPRAZOLE SODIUM MULTIPARTICULATE
FORMULATIONS
Using a NICA extruder/spheronizer, during initial formulation development, several prototypes of uncoated multiparticulates were manufactured to obtain a target immediate release profile similar to or faster than the pantoprazole sodium uncoated tablet, currently available as Protonix (20 mg and 40 mg) tablets. Levels of the disintegrant crospovidone fiom 5 to 28.5% and the binder hydroxypropyl methyl cellulose from 0.5 to 1% were evaluated during preparation of uncoated multiparticulates over four batches.
A. Poepa~atioh of Uncoated Pantop~~azole Sodium Multipaf ticulates More particularly, pantoprazole sodium sesquihydrate, microcrystalline cellulose, hydroxypropyl methylcellulose (hypromellose 2208), crospovidone and sodium carbonate are dry blended in a Hobart mixer.
Thereafter, polysorbate 80, NF (vegetable source) and purified water, USP, are added to the Hobart mixer. The resulting granulated produce is extruded and spheronized in a NICA 't extruder/spheronizer and the spheroids are tray dried at a temperature not beyond 40°C and sifted, followed by transfer to a PK blender. The final spheroids are stored in drums.
One of the batches (an approximately 200 gm batch) with 15%
disintegrant crospovidone and with 1 % hydroxypropyl methylcellulose (Hypromellose 2208)-was selected as a prototype with similar release profile.
The sieve cut of the uncoated spheroids from this batch was between 500 -1000 microns.
B. P~~ototype Lab Batch (Batch A) Approximately 100 grams of these uncoated spheroids were coated in a 3" Wurster Fluid Bed coater with Eudragit L30D-55 and hypromellose to result in Enteric coated multiparticulates.
During coating for this batch, the level of hydroxypropyl methyl cellulose (HPMC) initial seal coat was 4% of the weight of the uncoated multipaxticulates. The % w/w of the dry polymer Eudragit L30D-55 used was 22.16°fo. In the coating batch, talc was introduced as dry powder in the coating chamber instead of being a part of the suspension. This was due to the small nozzle size (0.5 mm) used for coating the 100 g batch, which could potentially be clogged.
The percent of talc and triethyl citrate used for the lab batch was less as compared to the clinical batches which were subsequently prepared. The multiparticulates were hand filled into size #2 HPMC capsules at a fill weight of 206 mg. The capsules were tested i~c vitro in 0.1 N HCl and pH 6.8 phosphate buffer. Less than 1% was released in acid media in 2 hours and greater than 80% was released in basic media in minutes as desired.
These capsules were tested in dogs. The C",aX and AUC were compared against the current marketed Protonix 20 mg tablet (and values were extrapolated to the 40 mg strength). It was seen that these multiparticulates released drug at a much faster rate than the current Protonix tablet in pH 6.8 phosphate buffer as desired. The final seal coat comprises hydroxypropyl methylcellulose (hypromellose) and water. This batch was paclcaged as spheroids in clear glass vials and placed on stability at accelerated conditions (30 °C/65% relative humidity (RH) and 40 °C/75% RH). The stability was monitored for 3 months. The potency and dissolution results are presented in Table I. The multiparticulates were stable over the three month period and a 40 mg equivalent dose of multiparticulates filled into capsules at each stability time point met all dissolution and stability criteria Dissolution was tested by filling the stored spheroids into capsule shells, and dissolving in 0.1 N HCl (target release at 2 hours: not more than (NMT) 10%), followed by dissolution in pH 6.8 phosphate buffer (target release at 45 min:
not less than (NLT) 75%. The acceptance criteria further required a strength of 90 to 110% of the label claim.
Table I: Stability of multiparticulates in clear glass vials.
Test Time Strength Dissolution (HPLC) - Percentage Label Released (av Unit 0.1 N HCl Secondary dissolution in hos hate buffer Initial 100.0% 0.9% 91.6%
Ambient Room Temp1 month 97.2% 0.8% 88.5%
7 month 108.5% 0.8% 94.1%
30 C/60% RH 1 month 99.3% 0.5% 83.4%
2 month 98.3% NA NA
3 month 104.4% 0.7% 82.2%
40 C/75% RH 1 month 95.4% 0.7% 86.1 2 month 97. 3 % NA NA
3 month 102.7% 0.7% 89.4%
One capsule - 78% released.
Example 2 - COATED PANTOPRAZOLE SODIUM MULTIPARTICULATE
FORMULATIONS (BATCH B) Based upon the lab batch A, a further scale-up batch of 1400 g was manufactured using a 7" wurster fluid bed coater. During coating for this batch, the level of hydroxypropyl methyl cellulose initial seal coat was 2% of the weight of the uncoated multiparticulates as compared to 4% for the coated Batch A. The % w/w of the dry polymer, Eudragit L30D-55 used was 22.16% w/w. Also, the talc was added directly to the coating suspension as a larger nozzle size (1 mm) was used.
Initial release of coated multiparticulates in 0.1 N acid was high (9.0%) and very close to the limit of 10%. This Batch (B) did not meet the stability and dissolution criteria when tested at accelerated conditions (30 °C/60%
relative humidity (RH) and 40 °C/75% RH). Trial from this batch indicated that an initial seal coat of greater than 2% of uncoated multiparticulates enhances stability of the multiparticulates. Additionally, more enteric polymer loading may be beneficial to control the release in acid media as the process is scaled up.
Example 3 - PREPARATION OF PANTOPRAZOLE MULTIPARTICULATES
SCALE-UP BATCH
A. Tech~zical Batch Using a NICA extruder/spheronizer, a 36 lcg technical batch of 6 uncoated multiparticulates was prepared and 20 kg of this batch were enteric coated in a Glatt GPCG-15 machine to result in a 32 kg batch of coated multiparticulates. The w/w of the dry polymer, Eudragit L30D-55 used was 22.16% w/w. This batch was filled into size #3 HPMC capsules at a fill weight of 156 mg. The release in 0.1 N
HCl at 2 hours was greater than the desired 10%. Based on this, taking into account scale-up effects, minor adjustments were made to the formula and process for clinical batch.
B. Clinical Batch Two 12 kg sub batches of a wet granulated mass were extruded and spheronized on a NICA extruder/spheronizer resulting in wet multiparticulates.
The multipaxticulates were tray dried at 40 °C for 10 to 12 hours to the desired % LOD of 3.4% to 4.3%. The batch was screened and only 16 lcg of uncoated multiparticulates were used for coating to ensure uniformity and completeness of coating in the GPCG-15 machine. The sieved uncoated multiparticulates were coated with an initial hydroxypropyl methycellulose seal coat, followed by an Eudragit L30D-55 enteric coat, followed by a hydroxypropyl methycellulose final coat to result in 33 lcg of coated multiparticulates. This batch was filled into size #2 HPMC capsules at a fill weight of 206 mg.
The release in 0.1 N HCl at 2 hours was less than the 10% limit and in pH 6.8 phosphate buffer, it was greater than the 80% limit at 45 minutes. The batch met ifz vit~~o release characteristics. The one month stability date showed that the multiparticulates were stable at 40 °C/75% RH for one month. Currently, this batch is stable up to one year at room temperature and upto 6 months at 40 deg.C/ 75%
RH.
Stability study at room temperature condition beyond one year is ongoing. The one year room temperature stability results of this batch are shown in the following Table II.
The spheroid filled capsule had a faster ih oitr~o release (dissolution) as compared to the Protonix 40 mg tablet in pH 6.8 phosphate buffer.
Table II: Stability of Pantoprazole Sodium Spheroid-filled Capsules, 40 mg AppearaStrengthWater (KF) Test nce (HPLC) Purity Dissolution and Descripti on Specifi#2 90.0- For InformationLargestTotal DissolutionDissolution Opaque in in ca white 110.0% SingleKnown O.1N HCI Phosphate tion capsulesLabel Known and NMT 10% Buffer Claim Unknownin NLT 75%
in (cap (LC) or Impurities2 hrs. 45 min.
and Conforms Conforms body) Unknown_<2.0 to USP to USP
<724> <724>
containing Impurity white <0.5 to off white colored (RRT) s heroids Unit InitialConforms100.3 5.1 BRL B1RL, 0 105 Initial 0 107 (Spher oids Only) 0%RH
1 No 99.5 5.2 0.17 0.17 1 103 MonthChange (1.39) 2 No 101.4 4.6 0.15 0.23 0 101 MonthChange (1.38)b 3 No 101.2 4.5 0.17 0.17 0 100 MonthChange (1.39) 6 No 101.3 4.5 0.18 0.24 0 100 MonthChange (1.38)v Month (Spher olds onl )'' Stability of Pantoprazole Sodium Spheroid-filled Capsules, 40 mg (Cont'd) AppearaStrength Test nce (HPLC) Water Purity Dissolution and (KF) Descripti on Specific#2 90.0-110.0%For LargestTotal DissolutionDissolution Opaque Known in in Ation white Label InformationSingleand UnknownO.1N HCl Phosphate Claim NMT
capsules(LC) Known Impurities10% in Buffer or 2 hrs.
(cap Unknown_<2.0 Conforms NLT
and to 75%
in body) Impurity USP <724> 45 min.
containing <-0.5 Conforms to white USP
to <724>
off (RRT) white colored spheroids Unit 9 MonthsNo 99.2 5.1 0.21 0.33 0 101 Change ( 1.40)v 9 Months 0 108 (Spheroids onl )"
12 MonthsNo 99.1 5.1 0.08 0.23 0 102 Change (0.14) 12 Months 0 104 (Spheroids onl )~
BRL = Below Reporting Limit (0.05%). NMT = Not more than. NLT = Not less than. RRT = Relative retention tune.
a: Initial and revalidation dissolution results are provided for Pantoprazole Sodium Spheroids, 40 mg/206 mg, which is the ingoing batch of spheroids used for manufacture of Pantoprazole Sodimn Spheroid-filled Capsules, 40 mg.
b. Corresponds to the impurity at RRT=1.39.
Example 4 - Evaluation of Batch A Formulation in Beagle Dogs The in-vity~o release data of the sodium pantoprazole mufti particulate formulation shows a faster release than the current marketed tablet. This provides earlier absorption and thereby a faster onset of action. The dog data clearly shows earlier drug levels of sodium pantoprazole from multiparticulates as compared to the single monolithic tablets. Earlier onset of action provides faster relief from gastric pain and other gastrointestinal (GIj disorders.
Pantoprazole sodium formulations have been evaluated in Beagle Dogs (n=5).
The mean (SD) pharmacokinetic parameters and relative bioavailability of pantoprazole is illustrated in the Table III below.
As illustrated, the non-optimized lab batch of sodium pantoprazole multiparticulate formulation dosed in dogs shows smaller lag time than the current marlceted tablet. In the following table, AUC refers to the area under a curve plotting mean concentration against protocol time. C",aX refers to the maximum observed concentration value in the blood sample after administration. T",~ refers to the time point when C max occurs. Tlag refers to the time following administration before effective amounts of the drug are observed in the circulation; t~z (hr) provides the half life for drug elimination. Relative bioavailability compares the absorption of a product from the gut in comparison with a dose given intravenously (assumed 100%).
Table III
The mean (SD) pharmacolcinetic parameters and relative bioavailability of pantopr azole 20mg Market Tablet 40mg Multiparticulate Batch A Capsule Parameter Pantoprazole Naa Batch A with enteric coat -Panto razole Na AUC (~,g*hr/mL) 16.3 (2.46) 17.3 (2.33) Cmax (yg/mL) 11.7 (3.55) 7.10 (1.76) Tmax (hr) 1.70 (0.84) 1.20 (0.27) tlag (hr) 1.10 (0.91) 0.25 (0.18) t'/~ (br) 0.62 (0.17) 0.77 (0.21) Relative Bioavailability-- AUC: 106/v Cmax: 61 / v a: AUC and Cmax are normalized to a 40mg dose b: Relative to Marke t Product Tablet The dog data of the sodium pantoprazole multi particulate formulation gives a similar AUC as the current marketed tablet. Without wishing to be bound by theory, it is believed that the faster release and similar AUC of the multi particulates is achieved by lowering the level of the disintegrating agent crospovidone (as compared to the level in the tablet) and incorporating the functional excipient polysorbate 80 in the core of the spheroids.
EXAMPLE 5 - PANTOPRAZOLE SODIUM SESQUIHYDRATE :EXCIPIENT
FORMULATIONS
This study was performed to determine the compatibility of pantoprazole sodium sesquihydrate with hypromellose 2208, sodium lauryl sulfate (SLS), crospovidone, and polysorbate-80.
A. Study Design The study consists of two sets of samples. The first set contained drug and excipient. The second set contained drug, excipient and approximately 2 p,1 water.
The reason for the water along with the drug and the excipient is to see whether additional water present causes any incompatibility.
The excipients were mixed with the drug in the ratio indicated in the following table. The excipients and the drug were weighed into a glass vial.
Then the vials were vortexed for 15 seconds. Similarly, a second set of samples was prepared.
Approximately 2 ~.l (the smallest amount of water that can be added with the pipette in the lab) was added to these vials. Then the vials were vortexed for 5 seconds.
Finally, the first and second set of vials were capped and placed in stability chambers.
The conditions tested were 40°/75%RH and 51 °C for 3 weelcs.
B. Results The results of this drug-excipient compatibility study are presented as recovery in the Table IV below. The selection criteria for the compatibility or in-compatibility are based on the % recovery between 90-110%.
Table IV: Drug: Excipient Compatibility Results Excipient Ratio of Drug:
Excipient% Recovery Drug + Excipient Drug + Excipient + Water 40C/75%RH 51C 40C/75% 51C
RH
3 weeks 3 weeks 3 weeks 3 weeks Control (Drug _ 94.67 100.53 94.60 96.64 alone) Hypromellose 10:1 99.209 93.248 93.811 97.421 2208, USP, 3cps Sodium Lauryl 5:3 99.947 98.763 95.466 95.088 Sulfate (SLS) Crospovidone, 10:1 100.080 98.908 97.201 105.716 NF
Polysorbate-80,10:1 98.301 90.961 99.908 81.405 NF
BP/EP (vegetable source) From the results shown in the table, the following conclusions can be drawn.
Hypermellose 2208, SLS, crospovidone and polysorbate-80 are compatible with pantoprazole sodium sequihydrate at 40°C/75%RH for 3 weeks.
Hypromellose 2208, SLS and crospovidone are compatible with pantoprazole sodium sequihydrate at 40°C/75%RH and 51°C with and without additional water for 3 weeks.
In this study degradation compounds were not studied. However, the pediatric clinical formulation, [pantoprazole sodium sesquihydrate 45.24% w/w;
microcrystalline cellulose 27.25% w/w; polysorbate 80 5 % w/w; crospovidone 15 w/w; hypromellose 2208 1% w/w; sodium carbonate 6.5% w/w; purified water q.s.], was studied under accelerated conditions of 40°C/75%RH and is stable up to 6 months, providing a 2 year room temperature shelf life.
The components of the pediatric formulation are provided in the following Table V.
Formulation: ~ Multiparticulates Core:
Ingredients Amount/C% w/w apsule Pantoprazole Sodium Sesquihydrate45.11 21.911 Microcrystalline Cellulose,27.39 13.304 NF/EP
(Avicel PH 101) Polysorbate 80, NF 5.00 2.429 Vegetable source Crospovidone, NF 15.00 7.286 (Polyplasdone XL) HPMC USP/EP (Methocel) 1.00 0.486 Sodium Carbonate, NF 6.50 3.157 Purified Water, USP/BP/EP q.s. to make wet massT
Total 100.00 48.573 mg Enteric Coat: 100.20 48.67 mg Eudragit L30D-55 208.00 30.309 mg 62.40 (solids) Talc, USP, Altalc SOOV 31.20 15.155 mg Sodium Hydroxide, NF 1 9.30 mg 0.175 N solution 0.36 (solids) Triethyl Citrate, PG/NF 6.24 mg 3.031 Purified Water, USP/BP/EP 183.38 * removed during mg processing Total 204.20 99.186 mg Final Seal Coat: 1.54 mg 0.748 Hydroxypropyl Methylcellulose,1.54 mg 0.748 USP 2910, 6cps Purified water, USP/BP/EP 18.99 * removed during mg* processing Total 205.74 99.934 mg Talc, USP, Altalc SOOV 0.14 mg 0.068 Total 205.88 100.002 mg EXAMPLE 6 - Evaluation of Pantoprazole Sodium Formulation in Human Adult Subjects In this study, 40 mg pantoprazole sodium, formulated as described, clinical pediatric formulation, was administered to healthy human adults (n=24) by sprinl~ling in applesauce, in tablet fomn, or as an aqueous suspension prepared using an inactive powder blend and water (8 in each group).
In the following Table VI, column 1 provides the pharmacolcinetic (PK) parameters, AUC (area under the concentration curve), AUCT is the area under the concentration time curve, and C",~, maximum concentration. The second column provides the test/reference geometric mean (GM) ratio. The third column provides the confidence interval for the GM ratio. [The FDA considers a test product to be bioequivalent to a reference product if the 90% confidence interval (CI) of the geometric mean ratio of AUC and CmaX between the test and reference fall within 80-125%]. -The confidence interval is calculated using WinNonlin software.
Table VI: Human PK study Results A. Spheroids sprinkled irz applesauce:
PK parameter Test/Reference 90% CI for ratio*
GM ratio Cmax 62 56-70 B. Spheroids ifz sus~ensiofz:
PK parameter Test/Reference 90% CI for ratio GM r atio Cmax 66 60-74 The lag time in the absorption of the tablet was higher compared to the sprinkle and suspension formulations. The entire drug in the tablet is released over a small time interval and therefore a higher C",~ is obtained. With the spheroid formulations, drug from each spheroid is released over a longer time interval and therefore the C",~ is lower than the tablet. However, the period of time following administration that pantoprazole remained in the circulation is similar for the 3 formulations.
All documents identified herein are incorporated by reference. One of shill in the art will recognize that minor modifications to the conditions and techniques described in the specific embodiments described herein can be varied without departing from the present invention. Such minor modification and variants are within the scope of the invention as defined by the following claims.
25C/60%RH
Acid 2 hrs 0.33 0.45 0.6 NMT 10%
( H 1.0) 3 min - 0.91 0.85 -Foll wed b o y 6 min - 3.61 1.83 -Alkaline 9 min - 52.25 16.45 -Buffer (pH 6.8) 12 min - 89.65 75.15 -15 min 101.58 97.15 91.92 -30 min 105.29 100.67 98.96 -45 min 105.29 100.57 99.14 NLT 75%
60 min 105.06 100.52 99.07 -In another embodiment, the resulting multiparticulate formulation of the invention achieves a mean AUC of 5451 to 5629 ng.h/ml and mean Cmax of 1865 to 1929 ng/ml or an ifz-vitro dissolution profile as shown below:
Batch % Drug Release Acid Buffer (mirc) 2hrs I S 30 45 Initial 0.08 101.77 107.44107.38 6 Months @40C/75%RH 0.73 95.44 101.12101.21 12 Months @25C/60%RH 0.30 96.11 101.92102.20 *Specifications: Acid at 21 s-NMT 10.0%; Buffer at 45 min-NLT 75%
However, the invention is not limited to these exemplary profiles.
Without wishing to be bound by theory, it is believed that final seal coat layer of hydroxypropyl methylcellulose provides a physical barrier for reduced contact between the mucoadhesive Eudragit layer and the upper GI tract, and thereby allows the reliable transit of the multiparticulates to the proper pH environment in the GI
tract for effective release and absorption of the drug. In addition, the final seal coat layer of hydroxypropyl methylcellulose imparts anti-sticking properties to the multiparticulates and thus the multipaniculates are not sticking to the pouch material andlor nasogastric tube. The multiparticulates of the invention are useful for administration via the nasogastric tube and via food vehicles, particularly acidic food vehicles.
II. Meth od of Producing Multiparticulate Formulations of Invention In another aspect, the invention provides a method of producing the multiparticulate formulations of the invention.
Typically, the uncoated pantoprazole compounds are prepared are follows.
The dry components, including, at least the pantoprazole compound and the binder are dry blended in a suitable mixer under low shear conditions. Suitable low shear conditions can be readily achieved using, e.g., a Hobart mixer, at a range of about 25 rpm to 35 rprn, and most desirably, 32 rpm. However, one of skill in the art will be able to achieve comparable low shear conditions using different equipment, with the rpm adjusted to the appropriate low shear settings for the selected equipment.
Optionally, hydroxypropyl methylcellulose or crospovidone may be substituted or additionally included in this step. Additionally, a pH adjuster may be included in this step.
Subsequently, the liquid components, e.g., the surfactant and water, are mixed in to afford a granulated product by mixing under low shear conditions.
Suitable low shear conditions can be readily achieved using, e.g., a Hobart mixer, at a range of about 25 rpm to 35 rpm, and most desirably, 32 rpm. However, one of skill in the art will be able to achieve comparable low shear conditions using different equipment, with the rpm adjusted to the appropriate low shear settings for the selected equipment.
The granulation is then extruded and spheronized through a suitable device (e.g., a NICA extruder/spheronizer) axed the resulting spheroids are dried, sifted, and optionally blended prior to storage.
The inventors have found that a significant advantage is provided to the stability of the compound when the multiparticulates of the invention are dried at low temperature. Desirably, the spheroid cores of the pantoprazole multiparticulates of the invention are dried to a percent (%) loss-on-drying (LOD) of 3.4% to 4.3%.
As used herein, low temperature drying refers to a temperature not exceeding about 40°C
for a period of 10 to 12 hours. When the drying conditions exceed this temperature and time period, impurities are observed that contribute to instability. In one embodiment, drying of the core is performed in the range of 35°C to 40°C, or about 37 °C to 39 °C for about 8 to 72 hours. In another embodiment, the core is dryed at about 40°C for 10 to 12 hours. Suitably, when coating layers are applied as described, the drying temperature for the various coating layers is also in this range.
Optionally, an initial seal coat of a hydrophilic polymer can be applied to the uncoated multiparticulates. For example, an initial seal coat composed of hydroxypropyl methylcellulose and purified water can be applied on a fluid bed coater, e. g. , by spraying.
The enteric coat can be applied directly to the uncoated spheroid core, i.e., the uncoated multipaxticulate, or may be applied over an initial seal coat. The enteric coat as described above, is typically applied on a fluid bed wurster coater.
In one embodiment, a final seal coat is applied over the enteric coat and, optionally, talc is utilized in the final step prior to filling the multiparticulates into a suitable packaging unit.
The multipauticulate of the invention may be in any suitable form including, e.g., granules, pellets, beads, minitabs, spherules, beadlets, microcapsules, millispheres, nonocapsules, microspheres, platelets, tablets, and capsules, depending upon the desired route of delivery.
III. Formulations, Kits and Methods of delivery In another embodiment, the present invention provides products containing the pantoprazole multiparticulates of the invention.
Suitably, the multiparticulate compositions of the invention are formulated such that a patient receives a suitable amount of the pantoprazole, e.g., 5 mg to 200 mg, about 10 mg to about 100 mg, or about 40 mg (measured based upon free pantoprazole). Preferably, the formulations are such that a suitable dose is delivered in a single dosage unit. These doses may be administered daily for a suitable period of time, e.g., 4 weeks to 8 weelcs, but can be delivered for a shorter period oftime, e.g., 3 days to 3 weelcs, one week to 3 months, or over a longer period, e.g., over 6 months, or longer. These compositions can be delivered alone or in combination with an antacid or other suitable composition.
In one embodiment, the invention provides a method of treating humans by admiW stering an effective dose of the pantoprazole multiparticulates such that an area under curve (AUC) at least bioequivalent to Protonix" 40mg tablet and Cmax as listed in Table VI are achieved.
In one embodiment, the pantoprazole multiparticulates are packaged for use by the patient or his caregiver. For example, the multiparticulates can be packaged in a foil or other suitable package and is suitable for mixing into a food product (e.g., applesauce and other acidic food vehicles) or into a drinlc for consumption by the patient.
The pantoprazole multiparticulate formulations of the invention are useful for treatment of gastroesophageal reflux disease (GERD), ulcers of the stomach and duodenum, and Zollinger-Ellison Syndrome.
In another embodiment, the pantoprazole multiparticulates are suspended in a physiologically compatible suspending liquid.
In yet another embodiment, the pantoprazole multiparticulates are filled in capsules, caplets or the like for oral delivery.
In still a further embodiment, the invention provides method of treating a subject in need thereof by administering an effective dose of the pantoprazole multiparticles of the invention.
The following examples illustrate specific embodiments of the invention and are not a limitation on the present invention.
Example 1 -PANTOPRAZOLE SODIUM MULTIPARTICULATE
FORMULATIONS
Using a NICA extruder/spheronizer, during initial formulation development, several prototypes of uncoated multiparticulates were manufactured to obtain a target immediate release profile similar to or faster than the pantoprazole sodium uncoated tablet, currently available as Protonix (20 mg and 40 mg) tablets. Levels of the disintegrant crospovidone fiom 5 to 28.5% and the binder hydroxypropyl methyl cellulose from 0.5 to 1% were evaluated during preparation of uncoated multiparticulates over four batches.
A. Poepa~atioh of Uncoated Pantop~~azole Sodium Multipaf ticulates More particularly, pantoprazole sodium sesquihydrate, microcrystalline cellulose, hydroxypropyl methylcellulose (hypromellose 2208), crospovidone and sodium carbonate are dry blended in a Hobart mixer.
Thereafter, polysorbate 80, NF (vegetable source) and purified water, USP, are added to the Hobart mixer. The resulting granulated produce is extruded and spheronized in a NICA 't extruder/spheronizer and the spheroids are tray dried at a temperature not beyond 40°C and sifted, followed by transfer to a PK blender. The final spheroids are stored in drums.
One of the batches (an approximately 200 gm batch) with 15%
disintegrant crospovidone and with 1 % hydroxypropyl methylcellulose (Hypromellose 2208)-was selected as a prototype with similar release profile.
The sieve cut of the uncoated spheroids from this batch was between 500 -1000 microns.
B. P~~ototype Lab Batch (Batch A) Approximately 100 grams of these uncoated spheroids were coated in a 3" Wurster Fluid Bed coater with Eudragit L30D-55 and hypromellose to result in Enteric coated multiparticulates.
During coating for this batch, the level of hydroxypropyl methyl cellulose (HPMC) initial seal coat was 4% of the weight of the uncoated multipaxticulates. The % w/w of the dry polymer Eudragit L30D-55 used was 22.16°fo. In the coating batch, talc was introduced as dry powder in the coating chamber instead of being a part of the suspension. This was due to the small nozzle size (0.5 mm) used for coating the 100 g batch, which could potentially be clogged.
The percent of talc and triethyl citrate used for the lab batch was less as compared to the clinical batches which were subsequently prepared. The multiparticulates were hand filled into size #2 HPMC capsules at a fill weight of 206 mg. The capsules were tested i~c vitro in 0.1 N HCl and pH 6.8 phosphate buffer. Less than 1% was released in acid media in 2 hours and greater than 80% was released in basic media in minutes as desired.
These capsules were tested in dogs. The C",aX and AUC were compared against the current marketed Protonix 20 mg tablet (and values were extrapolated to the 40 mg strength). It was seen that these multiparticulates released drug at a much faster rate than the current Protonix tablet in pH 6.8 phosphate buffer as desired. The final seal coat comprises hydroxypropyl methylcellulose (hypromellose) and water. This batch was paclcaged as spheroids in clear glass vials and placed on stability at accelerated conditions (30 °C/65% relative humidity (RH) and 40 °C/75% RH). The stability was monitored for 3 months. The potency and dissolution results are presented in Table I. The multiparticulates were stable over the three month period and a 40 mg equivalent dose of multiparticulates filled into capsules at each stability time point met all dissolution and stability criteria Dissolution was tested by filling the stored spheroids into capsule shells, and dissolving in 0.1 N HCl (target release at 2 hours: not more than (NMT) 10%), followed by dissolution in pH 6.8 phosphate buffer (target release at 45 min:
not less than (NLT) 75%. The acceptance criteria further required a strength of 90 to 110% of the label claim.
Table I: Stability of multiparticulates in clear glass vials.
Test Time Strength Dissolution (HPLC) - Percentage Label Released (av Unit 0.1 N HCl Secondary dissolution in hos hate buffer Initial 100.0% 0.9% 91.6%
Ambient Room Temp1 month 97.2% 0.8% 88.5%
7 month 108.5% 0.8% 94.1%
30 C/60% RH 1 month 99.3% 0.5% 83.4%
2 month 98.3% NA NA
3 month 104.4% 0.7% 82.2%
40 C/75% RH 1 month 95.4% 0.7% 86.1 2 month 97. 3 % NA NA
3 month 102.7% 0.7% 89.4%
One capsule - 78% released.
Example 2 - COATED PANTOPRAZOLE SODIUM MULTIPARTICULATE
FORMULATIONS (BATCH B) Based upon the lab batch A, a further scale-up batch of 1400 g was manufactured using a 7" wurster fluid bed coater. During coating for this batch, the level of hydroxypropyl methyl cellulose initial seal coat was 2% of the weight of the uncoated multiparticulates as compared to 4% for the coated Batch A. The % w/w of the dry polymer, Eudragit L30D-55 used was 22.16% w/w. Also, the talc was added directly to the coating suspension as a larger nozzle size (1 mm) was used.
Initial release of coated multiparticulates in 0.1 N acid was high (9.0%) and very close to the limit of 10%. This Batch (B) did not meet the stability and dissolution criteria when tested at accelerated conditions (30 °C/60%
relative humidity (RH) and 40 °C/75% RH). Trial from this batch indicated that an initial seal coat of greater than 2% of uncoated multiparticulates enhances stability of the multiparticulates. Additionally, more enteric polymer loading may be beneficial to control the release in acid media as the process is scaled up.
Example 3 - PREPARATION OF PANTOPRAZOLE MULTIPARTICULATES
SCALE-UP BATCH
A. Tech~zical Batch Using a NICA extruder/spheronizer, a 36 lcg technical batch of 6 uncoated multiparticulates was prepared and 20 kg of this batch were enteric coated in a Glatt GPCG-15 machine to result in a 32 kg batch of coated multiparticulates. The w/w of the dry polymer, Eudragit L30D-55 used was 22.16% w/w. This batch was filled into size #3 HPMC capsules at a fill weight of 156 mg. The release in 0.1 N
HCl at 2 hours was greater than the desired 10%. Based on this, taking into account scale-up effects, minor adjustments were made to the formula and process for clinical batch.
B. Clinical Batch Two 12 kg sub batches of a wet granulated mass were extruded and spheronized on a NICA extruder/spheronizer resulting in wet multiparticulates.
The multipaxticulates were tray dried at 40 °C for 10 to 12 hours to the desired % LOD of 3.4% to 4.3%. The batch was screened and only 16 lcg of uncoated multiparticulates were used for coating to ensure uniformity and completeness of coating in the GPCG-15 machine. The sieved uncoated multiparticulates were coated with an initial hydroxypropyl methycellulose seal coat, followed by an Eudragit L30D-55 enteric coat, followed by a hydroxypropyl methycellulose final coat to result in 33 lcg of coated multiparticulates. This batch was filled into size #2 HPMC capsules at a fill weight of 206 mg.
The release in 0.1 N HCl at 2 hours was less than the 10% limit and in pH 6.8 phosphate buffer, it was greater than the 80% limit at 45 minutes. The batch met ifz vit~~o release characteristics. The one month stability date showed that the multiparticulates were stable at 40 °C/75% RH for one month. Currently, this batch is stable up to one year at room temperature and upto 6 months at 40 deg.C/ 75%
RH.
Stability study at room temperature condition beyond one year is ongoing. The one year room temperature stability results of this batch are shown in the following Table II.
The spheroid filled capsule had a faster ih oitr~o release (dissolution) as compared to the Protonix 40 mg tablet in pH 6.8 phosphate buffer.
Table II: Stability of Pantoprazole Sodium Spheroid-filled Capsules, 40 mg AppearaStrengthWater (KF) Test nce (HPLC) Purity Dissolution and Descripti on Specifi#2 90.0- For InformationLargestTotal DissolutionDissolution Opaque in in ca white 110.0% SingleKnown O.1N HCI Phosphate tion capsulesLabel Known and NMT 10% Buffer Claim Unknownin NLT 75%
in (cap (LC) or Impurities2 hrs. 45 min.
and Conforms Conforms body) Unknown_<2.0 to USP to USP
<724> <724>
containing Impurity white <0.5 to off white colored (RRT) s heroids Unit InitialConforms100.3 5.1 BRL B1RL, 0 105 Initial 0 107 (Spher oids Only) 0%RH
1 No 99.5 5.2 0.17 0.17 1 103 MonthChange (1.39) 2 No 101.4 4.6 0.15 0.23 0 101 MonthChange (1.38)b 3 No 101.2 4.5 0.17 0.17 0 100 MonthChange (1.39) 6 No 101.3 4.5 0.18 0.24 0 100 MonthChange (1.38)v Month (Spher olds onl )'' Stability of Pantoprazole Sodium Spheroid-filled Capsules, 40 mg (Cont'd) AppearaStrength Test nce (HPLC) Water Purity Dissolution and (KF) Descripti on Specific#2 90.0-110.0%For LargestTotal DissolutionDissolution Opaque Known in in Ation white Label InformationSingleand UnknownO.1N HCl Phosphate Claim NMT
capsules(LC) Known Impurities10% in Buffer or 2 hrs.
(cap Unknown_<2.0 Conforms NLT
and to 75%
in body) Impurity USP <724> 45 min.
containing <-0.5 Conforms to white USP
to <724>
off (RRT) white colored spheroids Unit 9 MonthsNo 99.2 5.1 0.21 0.33 0 101 Change ( 1.40)v 9 Months 0 108 (Spheroids onl )"
12 MonthsNo 99.1 5.1 0.08 0.23 0 102 Change (0.14) 12 Months 0 104 (Spheroids onl )~
BRL = Below Reporting Limit (0.05%). NMT = Not more than. NLT = Not less than. RRT = Relative retention tune.
a: Initial and revalidation dissolution results are provided for Pantoprazole Sodium Spheroids, 40 mg/206 mg, which is the ingoing batch of spheroids used for manufacture of Pantoprazole Sodimn Spheroid-filled Capsules, 40 mg.
b. Corresponds to the impurity at RRT=1.39.
Example 4 - Evaluation of Batch A Formulation in Beagle Dogs The in-vity~o release data of the sodium pantoprazole mufti particulate formulation shows a faster release than the current marketed tablet. This provides earlier absorption and thereby a faster onset of action. The dog data clearly shows earlier drug levels of sodium pantoprazole from multiparticulates as compared to the single monolithic tablets. Earlier onset of action provides faster relief from gastric pain and other gastrointestinal (GIj disorders.
Pantoprazole sodium formulations have been evaluated in Beagle Dogs (n=5).
The mean (SD) pharmacokinetic parameters and relative bioavailability of pantoprazole is illustrated in the Table III below.
As illustrated, the non-optimized lab batch of sodium pantoprazole multiparticulate formulation dosed in dogs shows smaller lag time than the current marlceted tablet. In the following table, AUC refers to the area under a curve plotting mean concentration against protocol time. C",aX refers to the maximum observed concentration value in the blood sample after administration. T",~ refers to the time point when C max occurs. Tlag refers to the time following administration before effective amounts of the drug are observed in the circulation; t~z (hr) provides the half life for drug elimination. Relative bioavailability compares the absorption of a product from the gut in comparison with a dose given intravenously (assumed 100%).
Table III
The mean (SD) pharmacolcinetic parameters and relative bioavailability of pantopr azole 20mg Market Tablet 40mg Multiparticulate Batch A Capsule Parameter Pantoprazole Naa Batch A with enteric coat -Panto razole Na AUC (~,g*hr/mL) 16.3 (2.46) 17.3 (2.33) Cmax (yg/mL) 11.7 (3.55) 7.10 (1.76) Tmax (hr) 1.70 (0.84) 1.20 (0.27) tlag (hr) 1.10 (0.91) 0.25 (0.18) t'/~ (br) 0.62 (0.17) 0.77 (0.21) Relative Bioavailability-- AUC: 106/v Cmax: 61 / v a: AUC and Cmax are normalized to a 40mg dose b: Relative to Marke t Product Tablet The dog data of the sodium pantoprazole multi particulate formulation gives a similar AUC as the current marketed tablet. Without wishing to be bound by theory, it is believed that the faster release and similar AUC of the multi particulates is achieved by lowering the level of the disintegrating agent crospovidone (as compared to the level in the tablet) and incorporating the functional excipient polysorbate 80 in the core of the spheroids.
EXAMPLE 5 - PANTOPRAZOLE SODIUM SESQUIHYDRATE :EXCIPIENT
FORMULATIONS
This study was performed to determine the compatibility of pantoprazole sodium sesquihydrate with hypromellose 2208, sodium lauryl sulfate (SLS), crospovidone, and polysorbate-80.
A. Study Design The study consists of two sets of samples. The first set contained drug and excipient. The second set contained drug, excipient and approximately 2 p,1 water.
The reason for the water along with the drug and the excipient is to see whether additional water present causes any incompatibility.
The excipients were mixed with the drug in the ratio indicated in the following table. The excipients and the drug were weighed into a glass vial.
Then the vials were vortexed for 15 seconds. Similarly, a second set of samples was prepared.
Approximately 2 ~.l (the smallest amount of water that can be added with the pipette in the lab) was added to these vials. Then the vials were vortexed for 5 seconds.
Finally, the first and second set of vials were capped and placed in stability chambers.
The conditions tested were 40°/75%RH and 51 °C for 3 weelcs.
B. Results The results of this drug-excipient compatibility study are presented as recovery in the Table IV below. The selection criteria for the compatibility or in-compatibility are based on the % recovery between 90-110%.
Table IV: Drug: Excipient Compatibility Results Excipient Ratio of Drug:
Excipient% Recovery Drug + Excipient Drug + Excipient + Water 40C/75%RH 51C 40C/75% 51C
RH
3 weeks 3 weeks 3 weeks 3 weeks Control (Drug _ 94.67 100.53 94.60 96.64 alone) Hypromellose 10:1 99.209 93.248 93.811 97.421 2208, USP, 3cps Sodium Lauryl 5:3 99.947 98.763 95.466 95.088 Sulfate (SLS) Crospovidone, 10:1 100.080 98.908 97.201 105.716 NF
Polysorbate-80,10:1 98.301 90.961 99.908 81.405 NF
BP/EP (vegetable source) From the results shown in the table, the following conclusions can be drawn.
Hypermellose 2208, SLS, crospovidone and polysorbate-80 are compatible with pantoprazole sodium sequihydrate at 40°C/75%RH for 3 weeks.
Hypromellose 2208, SLS and crospovidone are compatible with pantoprazole sodium sequihydrate at 40°C/75%RH and 51°C with and without additional water for 3 weeks.
In this study degradation compounds were not studied. However, the pediatric clinical formulation, [pantoprazole sodium sesquihydrate 45.24% w/w;
microcrystalline cellulose 27.25% w/w; polysorbate 80 5 % w/w; crospovidone 15 w/w; hypromellose 2208 1% w/w; sodium carbonate 6.5% w/w; purified water q.s.], was studied under accelerated conditions of 40°C/75%RH and is stable up to 6 months, providing a 2 year room temperature shelf life.
The components of the pediatric formulation are provided in the following Table V.
Formulation: ~ Multiparticulates Core:
Ingredients Amount/C% w/w apsule Pantoprazole Sodium Sesquihydrate45.11 21.911 Microcrystalline Cellulose,27.39 13.304 NF/EP
(Avicel PH 101) Polysorbate 80, NF 5.00 2.429 Vegetable source Crospovidone, NF 15.00 7.286 (Polyplasdone XL) HPMC USP/EP (Methocel) 1.00 0.486 Sodium Carbonate, NF 6.50 3.157 Purified Water, USP/BP/EP q.s. to make wet massT
Total 100.00 48.573 mg Enteric Coat: 100.20 48.67 mg Eudragit L30D-55 208.00 30.309 mg 62.40 (solids) Talc, USP, Altalc SOOV 31.20 15.155 mg Sodium Hydroxide, NF 1 9.30 mg 0.175 N solution 0.36 (solids) Triethyl Citrate, PG/NF 6.24 mg 3.031 Purified Water, USP/BP/EP 183.38 * removed during mg processing Total 204.20 99.186 mg Final Seal Coat: 1.54 mg 0.748 Hydroxypropyl Methylcellulose,1.54 mg 0.748 USP 2910, 6cps Purified water, USP/BP/EP 18.99 * removed during mg* processing Total 205.74 99.934 mg Talc, USP, Altalc SOOV 0.14 mg 0.068 Total 205.88 100.002 mg EXAMPLE 6 - Evaluation of Pantoprazole Sodium Formulation in Human Adult Subjects In this study, 40 mg pantoprazole sodium, formulated as described, clinical pediatric formulation, was administered to healthy human adults (n=24) by sprinl~ling in applesauce, in tablet fomn, or as an aqueous suspension prepared using an inactive powder blend and water (8 in each group).
In the following Table VI, column 1 provides the pharmacolcinetic (PK) parameters, AUC (area under the concentration curve), AUCT is the area under the concentration time curve, and C",~, maximum concentration. The second column provides the test/reference geometric mean (GM) ratio. The third column provides the confidence interval for the GM ratio. [The FDA considers a test product to be bioequivalent to a reference product if the 90% confidence interval (CI) of the geometric mean ratio of AUC and CmaX between the test and reference fall within 80-125%]. -The confidence interval is calculated using WinNonlin software.
Table VI: Human PK study Results A. Spheroids sprinkled irz applesauce:
PK parameter Test/Reference 90% CI for ratio*
GM ratio Cmax 62 56-70 B. Spheroids ifz sus~ensiofz:
PK parameter Test/Reference 90% CI for ratio GM r atio Cmax 66 60-74 The lag time in the absorption of the tablet was higher compared to the sprinkle and suspension formulations. The entire drug in the tablet is released over a small time interval and therefore a higher C",~ is obtained. With the spheroid formulations, drug from each spheroid is released over a longer time interval and therefore the C",~ is lower than the tablet. However, the period of time following administration that pantoprazole remained in the circulation is similar for the 3 formulations.
All documents identified herein are incorporated by reference. One of shill in the art will recognize that minor modifications to the conditions and techniques described in the specific embodiments described herein can be varied without departing from the present invention. Such minor modification and variants are within the scope of the invention as defined by the following claims.
Claims (30)
1. Pantoprazole multiparticulates having reduced release under gastric conditions and fast release at neutral pH, wherein each of said multiparticulates comprises:~
a spheroid core comprising pantoprazole or an enantiomer thereof, or a salt or hydrate thereof, at least one surfactant, at least one distintegrant, and about 1%
to about 2% w/w water;
an enteric coat on the core, said enteric coat comprising a copolymer of methacrylic acid and methacrylates in the range of about 15 to about 45 % w/w of the spheroid core; and wherein said multiparticulates have an average size of about 1mm in diameter.
a spheroid core comprising pantoprazole or an enantiomer thereof, or a salt or hydrate thereof, at least one surfactant, at least one distintegrant, and about 1%
to about 2% w/w water;
an enteric coat on the core, said enteric coat comprising a copolymer of methacrylic acid and methacrylates in the range of about 15 to about 45 % w/w of the spheroid core; and wherein said multiparticulates have an average size of about 1mm in diameter.
2. The pantoprazole multiparticulates according to claim 1, further comprising a final seal coat on the enteric coat.
3. The pantoprazole multiparticulates according to claim 2, wherein the final seal coat comprises about 0.1 to 10 wt% of the multiparticle.
4. The pantoprazole multiparticulates according to claim 2 or claim 3, wherein the final seal coat comprises hydroxypropyl methylcellulose (hypromellose).
5. The pantoprazole multiparticulates according to any one of claims 1 to, wherein said multiparticulate further comprises an initial seal coat on the core.
6. The pantoprazole multiparticulates according to claim 4, wherein said said initial seal coat is in the range of about 2 to 4 % w/w of the weight of the uncoated core multiparticle.
7. The pantoprazole multiparticulates according to claim 4 or claim 5, wherein the initial seal coat comprises hypromellose.
8. The pantoprazole multiparticulates according to any one of claims 1 to 7, wherein the surfactant comprises from about 2 to about 7% by weight of the uncoated core.
9. The pantoprazole multiparticulates according to any one of claims 1 to 8, wherein the surfactant is a polysorbate.
10. The pantoprazole multiparticulates according to claim 9, wherein the polysorbate is polysorbate 80.
11. The pantoprazole multiparticulates according to any one of claims 1 to 10, wherein the enteric coat comprises 27.5 to 32.5 % w/w of the multiparticulate.
12. The pantoprazole multiparticulates according to claim 1, wherein the enteric coating comprises about 30% w/w of Eudragit L 30 D-55 coating, about 15%
w/w talc, about 3% triethyl citrate and a pH adjuster; said amounts being by weight of the microparticulate..
w/w talc, about 3% triethyl citrate and a pH adjuster; said amounts being by weight of the microparticulate..
13. The pantoprazole multiparticulates according to any one of claims 1 to 12, wherein the pantoprazole compound is present in the range of from about 5 to 50 w/w, of the spheroid core.
14. The pantoprazole multiparticulates according to any one of claims 1 to 12 , in which the core comprises pantoprazole compound in an amount equivalent to about 40 mg pantoprazole per 100 mg uncoated multiparticulate.
15. The pantoprazole multiparticulates according to any one of claims 1 to 15, wherein said spheroid core further comprises a pH adjuster and hypromellose.
16. The pantoprazole multiparticulates according to any of claims 1 to 15, wherein the disintegrant is selected from the group consisting of microcrystalline cellulose and crospovidone, and mixtures thereof.
17. The pantoprazole multiparticulates according to claim 16, wherein the microcrystalline cellulose comprises about 25 to about 30% by weight of the core.
18. The pantoprazole multiparticulates according to claim 16 or claim 17, wherein the crospovidone comprises about 14 to about 16% by weight of the core.
19. The pantoprazole multiparticulates according to claim 1, wherein the spheroid core consists essentially of:
pantoprazole sodium sesquihydrate ~45 % w/w microcrystalline cellulose~~27 % w/w polysorbate 80 ~~~5 % w/w crospovidone ~~~15 % w/w hypromellose 2208 ~~~1 % w/w and sodium carbonate ~~~7 % w/w.
pantoprazole sodium sesquihydrate ~45 % w/w microcrystalline cellulose~~27 % w/w polysorbate 80 ~~~5 % w/w crospovidone ~~~15 % w/w hypromellose 2208 ~~~1 % w/w and sodium carbonate ~~~7 % w/w.
20. A pantoprazole formulation for use in dosing to pediatric patients, said formulation comprising a suspension comprising the pantoprazole multiparticulates of any one of Claims 1 to 19 and a physiologically compatible suspending liquid.
21. A capsule comprising the pantoprazole multiparticulates of any one of Claims 1 to 19.
22. A foil packet comprising the pantoprazole multiparticulates of any one of Claims 1 to 19.
23. A method of treating humans in need of pantoprazole, said method comprising the step of administering an effective dose of the pantoprazole multiparticulates of any one of Claims 1 to 19.
24. A method of producing a multiparticle formulation of pantoprazole, said method comprising the steps of:
producing a spheroid core comprising pantoprazole or an entantiomer thereof, or a salt thereof, a surfactant, a distintegrant, via extrusion and spheronization, said core containing about 1 to about 2% w/w water;
applying an initial seal coat to the spheroid core, said seal coat being about 1 % w/w to about 20 % w/w of the multiparticulate;
applying an enteric coating over the initial seal coat, said enteric coating comprising a copolymer of methacrylic acid and methacrylates in an amount that provides the multiparticulate with 15 to 45 % w/w dry enteric coating polymer;
and optionally applying a final seal coat to the enteric-coated spheroid core, said final seal coat being about 1 wt% of the multiparticulate;
wherein said multiparticulates have an average size of no greater than about 1mm in diameter.
producing a spheroid core comprising pantoprazole or an entantiomer thereof, or a salt thereof, a surfactant, a distintegrant, via extrusion and spheronization, said core containing about 1 to about 2% w/w water;
applying an initial seal coat to the spheroid core, said seal coat being about 1 % w/w to about 20 % w/w of the multiparticulate;
applying an enteric coating over the initial seal coat, said enteric coating comprising a copolymer of methacrylic acid and methacrylates in an amount that provides the multiparticulate with 15 to 45 % w/w dry enteric coating polymer;
and optionally applying a final seal coat to the enteric-coated spheroid core, said final seal coat being about 1 wt% of the multiparticulate;
wherein said multiparticulates have an average size of no greater than about 1mm in diameter.
25. The method according to claim 24, wherein the spheroid core is prepared by mixing the ingredients in a low shear mixer at low shear conditions at a range of about 25 rpm to 35 rpm.
26. The method according to claim 25, wherein the low shear conditions are 32 rpm.
27. The method according to claim 25 or claim 26 , wherein the spheroid cores are dried at a low temperature not exceeding about 40°C for a period of 8 to 72 hours to a percent (%) loss-on-drying (LOD) of 3.4% to 4.3 %.
28 28. The method according to claim 24, further comprising the step of applying an layer of talc in an amount of 0.05% w/w to 0.1% w/w of the multiparticulate.
29. The method according to claim 24, wherein the enteric coating is sprayed as a suspension onto the spheroid core.
30. Use of pantoprazole multiparticulates according to any of claims 1 to 19 in preparing a medicament.
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