US20060188528A1 - Spreadable warming lubricant - Google Patents

Spreadable warming lubricant Download PDF

Info

Publication number
US20060188528A1
US20060188528A1 US11/063,711 US6371105A US2006188528A1 US 20060188528 A1 US20060188528 A1 US 20060188528A1 US 6371105 A US6371105 A US 6371105A US 2006188528 A1 US2006188528 A1 US 2006188528A1
Authority
US
United States
Prior art keywords
condom
lubricant
spreadable
warming lubricant
latex
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/063,711
Inventor
Beng Sim Chuah
David Lucas
Tsui Shih Yeun
Dave Narasimhan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ansell Healthcare Products LLC
Original Assignee
Ansell Healthcare Products LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ansell Healthcare Products LLC filed Critical Ansell Healthcare Products LLC
Priority to US11/063,711 priority Critical patent/US20060188528A1/en
Assigned to ANSELL HEALTHCARE PRODUCTS LLC reassignment ANSELL HEALTHCARE PRODUCTS LLC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHUAH, BENG SIM, LUCAS, DAVID M., YEUN, TSUI SHIH, NARASIMHAN, DAVE
Priority to JP2007556394A priority patent/JP2008531085A/en
Priority to KR1020077021849A priority patent/KR20070121695A/en
Priority to AU2006216807A priority patent/AU2006216807B2/en
Priority to CA002598653A priority patent/CA2598653A1/en
Priority to MX2007010230A priority patent/MX2007010230A/en
Priority to NZ556299A priority patent/NZ556299A/en
Priority to PCT/US2006/006063 priority patent/WO2006091576A2/en
Priority to EP06735632A priority patent/EP1850828A4/en
Priority to BRPI0608428-1A priority patent/BRPI0608428A2/en
Priority to RU2007135226/15A priority patent/RU2376036C2/en
Priority to CN2006800056528A priority patent/CN101128184B/en
Publication of US20060188528A1 publication Critical patent/US20060188528A1/en
Priority to IL184323A priority patent/IL184323A0/en
Priority to US12/756,510 priority patent/US8303969B2/en
Abandoned legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0034Urogenital system, e.g. vagina, uterus, cervix, penis, scrotum, urethra, bladder; Personal lubricants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F6/00Contraceptive devices; Pessaries; Applicators therefor
    • A61F6/02Contraceptive devices; Pessaries; Applicators therefor for use by males
    • A61F6/04Condoms, sheaths or the like, e.g. combined with devices protecting against contagion
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry

Definitions

  • the present invention relates to personal lubricants, which are highly spreadable on latex rubber and human skin and which provide a lubricious warming effect upon contact with moisture.
  • Lubricants have been employed for a number of applications, including lubrication of latex condoms and lubrication of skin. More recently, lubricants have been designed to take advantage of the heat that is generated when glycerin or propylene glycol is dissolved in water. Unfortunately, glycerin and propylene glycol do not spread readily on skin and other surfaces and irritate skin after prolonged use, since glycerin extracts water from the skin surface. The spreadability of such lubricants is further compromised by the addition of one or more insulating agents, such as honey, isopropyl myristate and/or isopropyl palmitate, which reportedly help to retain the heat of the lubricant (see, e.g., U.S. Pat.
  • U.S. Pat. No. 4,851,434 (the '434 patent) to Deckner discloses a non-greasy, non-irritating moisturizer, and compositions containing as the major moisturizing component the di-, tri- or polyglycol amide or glucamine reaction product with an a-hydroxy-substituted fatty acid, with the formula containing hydrogen or a lower alkyl, preservatives, thickeners, skin-soothing agents, such as allantoin and/or dl-panthenol, and water.
  • the non-irritating moisturizer disclosed in the '434 patent does not produce a warming effect when it contacts body-generated moisture and does not spread spontaneously on latex and human skin.
  • U.S. Pat. No. 4,952,560 to Kigasawa et al. discloses an ointment base containing a water-soluble protein consisting of gelatin, casein and soybean protein and a monohydric alcohol with a carbon number of 2 to 4 and/or an oleginous substance and additionally containing a wetting agent selected from the group consisting of an alkylene glycol containing 2 to 6 carbon atoms, polyethylene glycol having an average molecular weight of about 200 to 800, glycerin, trimethylolpropane and sorbitol, in a range of 1 to 35 weight % based on the weight of the whole ointment. While the ointment base improves percutaneous absorption of drugs, it is too thick to function as a lubricant.
  • U.S. Pat. No. 5,441,723 to Simmons discloses a non-toxic hypocompatible biodegradable germicide.
  • the non-toxic hypocompatible biodegradable germicide is effective against a wide range of pathogenic organisms and comprises 65-75 wt % of a monohydric alcohol selected from the group consisting of isopropyl, methyl, ethyl, n-propyl, n-butyl, tert-butyl, allyl, or mixtures thereof, and from about 4% to about 16% by weight of at least one polyhydric alcohol selected from the group consisting of propylene glycol, 1,3 propanediol, 1,2 butanediol, PEG 400, glycerol or 1,4 butanediol, or mixtures thereof in proportion by weight.
  • the monohydric alcohol in the germicide provides the primary disinfecting or killing effect on the pathogenic organisms, while the polyhydric alcohol reduces the surface glaze formed by the monohydric alcohol and the surface tension formed by water or water-based body fluids, thereby enabling the disinfectant/antiseptic to kill pathogenic organisms and act equally effectively on a patient or inanimate surface without deleterious effects.
  • the monohydric alcohol also lowers the flash point of the composition, soothes the skin, and slows the rate of evaporation.
  • the germicide is not a lubricant and does not include a warming constituent.
  • the polyhydric alcohol by reducing the rate of evaporation of the monohydric alcohol, essentially cools the surface by evaporative cooling.
  • U.S. Pat. No. 5,512,289 to Tseng et al. discloses a spermicidal anti-viral lubricant composition containing a water-soluble polymeric gel matrix comprising a hydroxyalkyl cellulose with 2 to 6 carbon atoms; an alkylphenoxypolyethoxyethanol spermicide; and a solubilizing moiety comprising a polyethoxylated non-ionic compound, such as polyethoxylated castor oil.
  • the use of an alkylphenoxypolyethoxyethanol spermicide prevents collapse of the hydroxyalkyl cellulose gel.
  • the addition of a solubilizer substantially prevents the collapse of the gel matrix and permits the gel matrix to maintain its properties in the composition.
  • the spermicidal composition can be dispersed by use of a pharmaceutically acceptable vehicle, such as water, alcohols, e.g., ethanol, glycerin, propylene glycol, and mixtures thereof.
  • a pharmaceutically acceptable vehicle such as water, alcohols, e.g., ethanol, glycerin, propylene glycol, and mixtures thereof.
  • a typical formulation of the spermicidal lubricant can include water 75.50 wt %, glycerin 17.00 wt %, hydroxyethyl cellulose 1.00 wt %, polyvinyl pyrrolidone 0.90 wt %, carboxymethyl cellulose 1.00 wt %, Nonoxynol-9 spermicide 2.00 wt %, polyethoxylated castor oil 2.00 wt %, methylparaben 0.20 wt %, sorbic acid 0.05 wt %, and citric acid 0.35 w
  • U.S. Pat. No. 5,514,698 to Ahmad et al. discloses an antifungal vaginal cream composition.
  • the composition has stable viscosity at human body temperature and comprises about 0.4 to 10.0% of an imidazole antifungal agent (of miconazole, econazole, terconazole, saperconazole, itraconazole, ketoconazole, and clotrimazole), about 1.0% to 5.0% of a fatty acid ester (isopropyl stearate, isopropyl myristate, isopropyl palmitate, and isopropyl laurate), about 1.0% to 25.0% of aliphatic alcohols (cetyl alcohol, stearyl alcohol and propylene glycol), about 2.0% to 5.0% of a surfactant (polysorbate 60 or polysorbate 80), about 0.02% to 0.20% of an antioxidant (butylated hydroxyanisole), a sufficient amount of inorganic base (NaOH or KOH
  • vaginal cream is not a lubricant and is expected to maintain its viscosity for prolonged time periods at body temperature. Even though propylene glycol is used in the composition, it is already mixed with water and, therefore, no warming effect takes place when the cream contacts body-generated moisture.
  • U.S. Pat. No. 5,649,825 to Ratkus discloses a dental root canal bacterialcidal lubricant, which allows the cleaning wires or files to move more freely when removing a nerve from a tooth.
  • the composition reduces packing of tissue and dentin debris within the nerve cavity.
  • This formulation is also resistive to decomposition during cold weather shipping, and includes cetyl alcohol, stearyl alcohol, sodium lauryl sulfate, stearic acid, propylene glycol, methyl paraben, propyl paraben, and butyl paraben in a purified water solution.
  • the lubricant does not provide a warming effect.
  • U.S. Pat. No. 5,885,591 to Ahmad et al. discloses highly lubricious personal lubricant compositions containing one or more polyhydric alcohols, one or more water-soluble polymers derived from cellulose, water, and, optionally, preservatives and alkali metal or alkaline earth metal bases. These compositions can provide a vehicle for delivering medicaments for contraception and for the treatment and prevention of disease.
  • the personal lubricant composition contains about 30% glycerin, about 5% propylene glycol, about 10% sorbitol, about 0.4% preservative, about 0.4% hydroxyethylcellulose, about 0.01% sodium hydroxide, and about 50% water.
  • the composition has a lubricity of 33 to about 466.
  • the personal lubricant composition attaches to mucous membranes and is not readily washed off. Since the composition already contains water, no heating or warming reaction occurs when the lubricant is applied to the body and the glycerin comes in contact with body-generated moisture.
  • U.S. Pat. No. 6,139,848 to Ahmad et al. discloses stable personal lubricant compositions containing at least one water-soluble polyhydric alcohol, a water-soluble polymer derived from cellulose, tocopherol or a tocopherol derivative, a nonionic water-soluble or dispersible emulsifier, and water.
  • the lubricious, oily tocopherol or tocopherol derivative is present as an emulsion in the personal lubricant.
  • the emulsifier preferably is a polyalkylene emulsifier chosen from the group consisting of polyoxyethylene (20) sorbitan monostearate, commonly known as Tween 60 or Polysorbate 60, and polyethylene glycol ether of isocetyl alcohol (commonly known as Isoceteth 20 or Arlasolve 200, which is available from ICI Americas, Inc., New Castle, Del.).
  • the water-soluble polyhydric alcohol serves to increase the lubriciousness of the compositions.
  • the water-soluble cellulose-derived polymer serves to impart the desired slipperiness and viscosity to the composition. Water is desired in sufficient quantity to be delivered as moisture to the mucous membranes and to provide consistency and viscosity to the composition.
  • the nonionic surfactants emulsify tocopherol, tocopherol acetate or other tocopherol derivatives into a microemulsion in which the internal or oil phase is reduced to very small globules measuring 2 or less than 2 microns in size. Due to their enormous small size, the emulsion globules do not coalesce and serve to assist in maintaining the homogeneity of the emulsions and to preserve physical stability of the compositions. Since the polyhydric alcohol (glycerin) is already combined with water, no heating or warming reaction occurs when the lubricant is applied to the body.
  • U.S. Patent Application Publication No. 2001/0039380 to Larson et al. discloses in vivo biocompatible acoustic coupling media comprising polyethylene oxide (PEO), at least one of polyalkylene glycols and polyhydric alcohols, and the balance water. Since water is already added to polypropylene alcohol, the exothermic reaction of mixing has already occurred, and no additional warming occurs when the lubricant is used.
  • PEO polyethylene oxide
  • U.S. Patent Application Publication No. 2003/0207772 and International Patent Application Publication No. WO 03/092651 to Ahmad et al. disclose warming and nonirritating lubricating compositions containing polyhydric alcohols and an insulating agent.
  • the polyhydric alcohol comprises glycerin, alkylene glycol, or a mixture thereof.
  • the alkylene glycol is selected from the group consisting of propylene glycol, butylene glycol and hexalene glycol
  • the polyethylene glycol is selected from the group consisting of polyethylene glycol 300 and polyethylene glycol 400.
  • the insulating agent is selected from the group consisting of honey, isopropyl myristate and isopropyl palmitate.
  • a warming action is created by the heat released during dissolution of the polyhydric alcohol in water, and the insulating agent retains the heat.
  • the insulating agent is an essential part of the composition of the lubricant, and reduces the spreading capability of the warming lubricant.
  • U.S. Patent Application Publication No. 2003/0232090 and International Patent Application Publication No. WO 03/092650 to Ahmad et al. disclose warming and nonirritating lubricating compositions. Also disclosed are substantially anhydrous, warming, non-toxic and nonirritating lubricating compositions containing polyhydric alcohols, a gelling agent and, alternatively, a pH-adjusting agent for treating fungal and bacterial infections.
  • the polyhydric alcohol comprises glycerin, alkylene glycol, polyethylene glycol, or a mixture thereof.
  • the alkylene glycol is selected from the group consisting of propylene glycol, butylene glycol and hexalene glycol
  • the polyethylene glycol is selected from the group consisting of polyethylene glycol 300 and polyethylene glycol 400.
  • the insulating agent is selected from the group consisting of honey, isopropyl myristate and isopropyl palmitate. The use of insulating agents reduces the spreading capability of the warming lubricant.
  • U.S. Patent Application Publication No. 2004/0037911 to Letoumeau et al. discloses a genital lubricating composition.
  • the composition comprises (i) fatty acids and/or homeopathic dilutions of plant extracts and (ii) a physiologically acceptable carrier.
  • the genital lubricant composition comprises about 0.05% to about 0.5% hemp seed oil and a physiologically acceptable carrier so that it forms a lotion, a cream or a gel.
  • the composition is particularly useful for use as a vaginal moisturizer, or as a personal lubricant for use prior or during sexual intercourse.
  • the fatty acids can be hemp oil, linoleic (CI8:2) acid or linolenic (C18:3) acid.
  • the plant extracts include extracts from Caladium seguinum, Sepia officianalis, Lycopodium clavatum, and Onosmodium virginanium. The exact composition of the carrier is not disclosed. This lubricant does not have any polyhydric alcohol and does not produce a warming sensation.
  • the anti-viral compositions contain at least one zinc compound, at least one phenolic antioxidant (and optionally other ingredients), and a pharmaceutical carrier.
  • the zinc compound is selected from the group consisting of zinc, zinc chloride, zinc acetate, zinc citrate, zinc sudoxicam, zinc sulfate, zinc nitrate, zinc carbonate, zinc tartrate, zinc maliate, zinc lactate, zinc aminoacetate, zinc aspartate, zinc glutamate, zinc propionate, zinc oleate, zinc benzoate, zinc gluconate, zinc butyrate, zinc formate, zinc glycerate, zinc glycolate, zinc oxide, zinc ethylenediamine tetraacetate, zinc pentosan polysulfate, zinc oxyacetate, and hydrates.
  • the phenolic antioxidant comprises at least one compound represented by the formula:
  • each R is independently an aliphatic hydrocarbon residue, with or without oxygen, comprising 1 to about 12 carbon atoms, x is from 1 to 3, y is from 0 to 3, z is from 1 to 3, and x+y+z is 6 or less.
  • the pharmaceutical carrier comprises at least one of water, alcohol, fatty acids, fatty acid esters, and waxes. The composition does not function as a lubricant.
  • U.S. Patent Application Publication No. 2004/0138074 to Ahmad et al. discloses substantially anhydrous, warming, non-toxic and nonirritating lubricating compositions containing polyols and preferably an insulating agent.
  • the substantially anhydrous lubricant composition comprises a polyol, which increases in temperature by at least about 5° C. upon exposure to moisture and which has a maximum Energy Release Index of at least about 11 mJ/mg.
  • the polyhydric alcohol is selected from glycerin, alkylene glycol, polyethylene glycol, polypropylene glycol, PEGylated compounds, block copolymers comprising polyalkylene glycol, and their mixtures.
  • insulating agents such as honey, isopropyl myristate and isopropyl palmitate, reduces the spreading capability of the warming lubricant.
  • European patent document EP 0636374 to Tseng discloses a spermicidal anti-viral lubricating composition containing an antiviral alkylphenoxypolyethoxyethanol spermicide, a water-soluble polymeric gel matrix, and a solubilizer, which permits the spermicide to be compatible with the gel matrix.
  • a polyethoxylated compound such as polyethoxylated castor oil, is used.
  • There is no warming agent present in the lubricant since the water-soluble polymer functions as the lubricating agent.
  • Japanese patent document JP 2292212 to Hans Eke Rennaruto Bidesutoreemu discloses a sterilizable gel.
  • This sterilizing gel comprises a carboxypolymethylene polymer (carboma) and 1-90% polyhydric alcohol for stabilization (e.g., ethylene glycol).
  • the carboma can be sterilized by assistance of the polyhydric alcohol and avoids deterioration of the gel when the gel is sterilized by ⁇ -radiation derived from cobalt 60. This is not a warming gel and polyhydric alcohol is only used to prevent discoloration during ⁇ -radiation.
  • Japanese patent document JP 2003183115 to Saijo discloses a poikilothermal lubricant.
  • the lubricant may contain ingredients that cause cooling or warming.
  • the warming or cooling ingredient is a dispersant that is not water-soluble and is protected by a polymeric coating. It is unclear what is the nature of the warming agent and what is the mechanism of the warming action.
  • the water-based, non-foaming, shaving gel comprises from 0.05 to 4.0% of a carboxypolymethylene, from 2.00 to 52.0% of a polyhydric alcohol, and, optionally, a silicone derivative, an antipruritic agent, preservative agents, a chelating agent, a neutralizing agent, a solubilizing agent, a UV light-absorbing agent, or a perfume.
  • the preferred polyhydric alcohol is glycerin.
  • the gel is applied directly to dry skin and hair prior to shaving with a razor blade and provides a close, comfortable and well-lubricated shave. The shaving gel does not provide a warming effect.
  • the present invention provides a spreadable warming lubricant that exhibits excellent spreadability and low surface tension and contact angle, thereby providing a well-wetted, uniform, thin layer during skin to skin contact and condom latex film to skin contact.
  • the warming lubricant composition has sufficient viscosity to establish easily a thin film on either skin or condom latex film with a film thickness ranging from 0.01 to 0.1 mm.
  • the spreadable warming lubricant composition is substantially anhydrous and comprises a mixture of glycerin with another polyhydric alcohol in the range of 40%-60% each and a non-ionic surfactant in the range of 0.1 to 3%.
  • the polyhydric alcohol is preferably propylene glycol
  • the non-ionic surfactant is preferably polysorbate 20, polysorbate 40, polysorbate 60 or polysorbate 80.
  • the preferred spreadable warming composition comprises 49.75% glycerin, 49.75% propylene glycol, and 0.5% polyoxyethylene sorbitan monolaurate (polysorbate 20).
  • the spreadable warming lubricant releases heat when mixed with moisture, which can be skin-generated.
  • the temperature rise is optimal when nearly equal volumes of the spreadable warming lubricant and moisture are mixed.
  • An excess of either moisture or the warming lubricant reduces the temperature rise because the heat released has to heat a larger mass. Therefore, the quantity of the warming lubricant desirably is limited to the quantity of moisture available during use.
  • the spreadable warming lubricant desirably coats the surface of the condom as a thin layer. When the interior and exterior of a latex condom is not coated with a lubricant, there is rubbing between skin and latex, which produces friction and irritation.
  • the presence of a thin, well-spread layer of spreadable warming lubricant minimizes, if not eliminates, friction and irritation and assures uniform heat release, which, in turn, provides a comfortable warming sensation.
  • the thin, well-wetted, warming lubricant layer that is in contact with (i) a condom latex surface and skin or (ii) skin and skin results in elastohydrodynamic lubrication that effectively reduces friction even when the contacting surfaces deform.
  • the present inventive spreadable warming lubricant wets latex with a small contact angle. Therefore, the addition of a small quantity of about 0.2-5 ml of spreadable warming lubricant to a condom package results in the migration of the warming lubricant over the internal and external surfaces of the condom. This migration process coats essentially the complete internal and external surfaces of the latex condom with a thin layer of warming lubricant within a period of approximately a week.
  • the present inventive spreadable warming lubricant is advantageous in that it enables uniform coating of a lubricant on a condom. Accordingly, the present invention also provides a latex condom, onto which a spreadable warming lubricant has been applied in accordance with such a method.
  • the warming lubricant When the spreadable warming lubricant is used as skin lubricant, the warming lubricant is applied to the skin in an amount that approximates the available skin moisture.
  • moisture can be added to the skin prior to the application of the spreadable warming lubricant.
  • the reaction between moisture and the spreadable warming lubricant results in the release of heat, thereby creating a warming sensation.
  • the spreadability of the warming lubricant is essential for this warming effect, since the quantity of moisture available on skin is generally small and the quantity of spreadable warming lubricant applied desirably is matched with this quantity of moisture so as to optimize the warming effect. In the absence of spreadability, the warming lubricant would be concentrated in the area of initial application to the skin and the desired effects of lubrication and warmth would not be optimized.
  • the present invention provides an improved warming lubricant that provides and maintains a thin elastohydrodynamic lubricating film between skin and either skin or latex.
  • the lubricant exhibits excellent spreadability due to sufficient viscosity, a low surface tension, and a low contact angle.
  • the lubricant is substantially anhydrous, preferably containing less than about 5% water, more preferably containing less than about 3% water, and most preferably containing less than about 2% water, such as less than about 1% water. Having sufficient viscosity, a film thickness ranging from about 0.01 to 0.10 mm, such as about 0.05 to 0.10 mm, can be achieved on skin or latex rubber.
  • the present invention provides a spreadable warming lubricant comprising glycerin with another polyhydric alcohol and a non-ionic surfactant.
  • glycerin is present in an amount from about 40% to 60%
  • the polyhydric alcohol is present in an amount from about 40% to 60%
  • the non-ionic surfactant is present in an amount from about 0.1% to 3%.
  • polyhydric alcohol Any suitable polyhydric alcohol can be used.
  • the polyhydric alcohol is propylene glycol.
  • Other polyhydric alcohols, such as butylene glycol, hexalene glycol, and polyethylene glycol, are known in the art.
  • the warming lubricant has constituents that release heat by exothermic heat of dissolution when mixed with moisture, such as skin-generated moisture. Since skin-generated moisture is generally small in quantity, the quantity of warming lubricant desirably is small in quantity to take advantage of the exothermic heat release to provide a warming effect. An excessive amount of the warming lubricant in the presence of a small amount of skin-generated moisture results in only a small temperature rise resulting in a minimal warming effect. The small quantity of spreadable warming lubricant can only be effective if it creates a stable elastohydrodynamic film over the skin or between skin and a latex article.
  • the spreadable warming lubricant has glycerin and a polyhydric alcohol, preferably propylene glycol, mixed in an appropriate ratio to ensure that the viscosity of the mixture provides sufficient lubricating properties.
  • the higher the viscosity the higher is the drag when the contacting surfaces are moved with respect to one another.
  • higher viscosity compositions tend to form thick lubricating films, since gravitational forces are inadequate to form a thin film, whereas lower viscosity compositions run off easily, forming very thin lubricating films.
  • the viscosity of a glycerin—propylene glycol mixture as a function of composition is shown in Table 1 below. Propylene glycol viscosity is too low to be useful as a lubricant, while glycerin has too high a viscosity to produce evenly a thin lubricating film. Table 1 also documents the warming effect of the lubricant composition in three trials. Propylene glycol provides the largest warming effect, while glycerin produces the smallest warming effect. TABLE 1 % Propylene Glycol 0 50 100 % Glycerin 99.7% 100 50 0 Test No.
  • the lubricant must wet the surfaces in question and must have a low contact angle. This requirement is even more important when the surfaces in contact are deformable and the adhesion of the film to the surface needs to be better, thus demanding even a smaller contact angle. If the contact angle is large, the lubricating fluid film disrupts creating islands, which are physically separated, and rubbing now occurs between skin and skin or between skin and latex, both of which are high friction coefficient couples providing skin irritation. Improved wetting of a glycerin-propylene glycol mixture is accomplished by addition of 0.1 to 3 percent of non-ionic surfactants.
  • Non-ionic surfactants do not contain ionic constituents. They are “ionically” inert. A vast majority of all non-ionic detergents are condensation products or ethylene oxide with a hydrophobe. This group of detergents is enormous, and the permutations endless. They are the single largest group of all surfactants.
  • Nonionic Surfactants Organic Chemistry, Nico M. van Os, ed., Marcel Dekker (1998), specifically incorporated by reference herein, discusses a number of non-ionic surfactants, including polyoxyethylene alkylphenols, alcohols, esters of fatty acids, mercaptans, and alkylamines, nonionic surfactants containing an amide group, and polyol ester surfactants.
  • Dow Chemical Co. markets a number of non-ionic surfactants under the trade name ‘DOWFAX’. These polyethylene glycol formulations provide superior softening, conditioning, and skin-smoothing characteristics, since polyglycols dissolve or are compatible and miscible in various organic liquids.
  • Polysorbate compositions are also non-ionic surfactants and are available as polysorbate-20, 40, 60; 65 and 80. They are polyoxyethylene sorbitan monoesters (PS) of the general formula:
  • R is laureate, palmitate, stearate or oleate and each of w, x, y and z is independently 1 or 2; or each of w, x, y and z is independently less than or equal to 17 and the sum of w, x, y and z is 20.
  • Polysorbate-20 is polyoxyethylenesorbitan monolaurate, CAS #9005-64-5, with a chemical composition of sorbitan mono-9-octadecenoate poly(oxy-1,1-ethanediyl).
  • Polysorbate 40 is polyethylene glycol sorbitan monopalmitate, polyoxyethylene sorbitanmonopalmitate, CAS# 9005-66-7
  • Polysorbate 60 is polyethylene glycol sorbitan monostearate, polyoxyethylene sorbitanmonostearate, CAS #9005-67-8
  • Polysorbate 80 is polyoxyethylenesorbitan monooleate, CAS# 9005-65-6.
  • Tables 2 A, B and C show the effect of the addition of polysorbate 20 to warming lubricant compositions containing propylene glycol and glycerin on drop diameter, when a fixed volume of liquid is applied to a substrate, including glass, latex condom film and skin, and the corresponding contact angle.
  • This contact angle is determined by dropping a fixed volume of 25 ⁇ l of lubricant mixture using a microsyringe on a flat substrate of glass, condom latex film or skin, respectively, and measuring the diameter of the spread of the warming lubricant as a function of time.
  • Substrate GLASS Average Base Diameter of Drop (mm) & Contact Angle (degrees) 50% 49.50% Propylene Propylene Propylene Glycol, 49.5% Glycol, Lapse Drop Glycol, glycerin, Glycerin, Propylene 0.5% time Vol.
  • the propylene glycol can be in the range of 40% to 60%, glycerin can be in the range of 40 to 60%, and polysorbate 20 or other non-ionic surfactant can be in the range of 0.1 to 3%.
  • the viscosity of glycerin propylene glycol is relatively stable in this compositional range, and polysorbate 20 and other non-ionic surfactants are effective in improving the contact angle.
  • the warming lubricant can be used as a skin lubricant wherein a small drop [VOLUME] of the warming lubricant is applied over skin and rubbed. Any skin-generated moisture quickly produces a warming effect as the warming lubricant combines with moisture.
  • the warming lubricant is highly spreadable and produces a soothing effect.
  • the spreadable warming lubricant can be applied to a condom latex surface. Due to its enhanced spreading character, the warming lubricant spreads over the internal and external surface of the condom latex.
  • the utility of a lubricated condom is related to distribution of the lubricating agent on the condom surface, since this lubrication is what prevents irritation. Any lubricant that does not spread well has bare spots, where latex condom surface rubs directly on skin and creates increased friction, stickiness and irritation. In order to quantify this effect, a small amount of spreadable warming lubricant was applied on the external surface of a condom, and the spreading of the warming lubricant was measured. The results are shown below in Table 2F.
  • the 50%-50% mixture of glycerin and propylene glycol had a higher migration distance up the condom shaft as compared to pure glycerin.
  • polysorbate 20 was added to the lubricant, both glycerin and the 50%-50% mixture of glycerin and propylene glycol showed improvement in the migration distance of the lubricant up the condom shaft, particularly within one week.
  • the mode of application of the spreadable warming lubricant in condoms includes dropping a measured quantity of warming lubricant consistent with the skin-generated moisture. Since the skin-generated moisture is generally in the range of 0.2 to 5 ml, the quantity of the warming lubricant desirably is less than 5 ml. This small quantity of the warming lubricant has to be spread all over the internal and external surface of the condom latex to provide effective lubrication and warming effect. During packaging of a condom, the measured quantity of lubricant is added, and the spreading effect is relied on to disperse the lubricant across the internal and external surfaces of the condom.
  • the lubricant When the spreadable warming lubricant is used as skin lubricant, the lubricant is applied to the skin in an amount that approximates the available skin moisture.
  • moisture can be added to the skin prior to the application of the spreadable warming lubricant.
  • the reaction between moisture and spreadable warming lubricant results in the release of heat, thereby creating a warming sensation.
  • the spreadability of the warming lubricant is essential for this warming effect, since the quantity of moisture available on skin is generally small and the quantity of spreadable warming lubricant applied desirably is matched with this quantity of available moisture so as to optimize the warming effect.
  • the warming lubricant In the absence of spreadability, the warming lubricant would be concentrated in the area of initial application to the skin and the desired effects of lubrication and warmth would not be optimized.
  • the combination of suitable viscosity, low surface tension and contact angle with respect to human skin results in spreading of the warming lubricant on the skin so as to provide an optimal, soothing warming effect.

Abstract

A substantially anhydrous, spreadable warming lubricant composition comprising a mixture of glycerin, a polyhydric alcohol, and a non-ionic surfactant, the viscosity of the composition being less than that of glycerin but greater than that of the polyhydric alcohol, thereby promoting formation of a useful thin layer on a surface with which the composition is brought into contact, the surfactant improving wetting and spreadability of the composition on skin and latex, such that the composition can be applied to skin or a condom and provide an optimal warming effect upon contact with ambient moisture during use and such that the composition can be added to a condom package and, over the course of about a week, spread and coat nearly the entire internal and external surfaces of the condom.

Description

    FIELD OF THE INVENTION
  • The present invention relates to personal lubricants, which are highly spreadable on latex rubber and human skin and which provide a lubricious warming effect upon contact with moisture.
  • BACKGROUND OF THE INVENTION
  • Lubricants have been employed for a number of applications, including lubrication of latex condoms and lubrication of skin. More recently, lubricants have been designed to take advantage of the heat that is generated when glycerin or propylene glycol is dissolved in water. Unfortunately, glycerin and propylene glycol do not spread readily on skin and other surfaces and irritate skin after prolonged use, since glycerin extracts water from the skin surface. The spreadability of such lubricants is further compromised by the addition of one or more insulating agents, such as honey, isopropyl myristate and/or isopropyl palmitate, which reportedly help to retain the heat of the lubricant (see, e.g., U.S. Pat. App. Pub. Nos. 2004/0138074, 2003/0232090, 2003/0211161 and 2003/0207772, and Int'l App. Pub. Nos. WO 03/092652, WO 03/092651 and WO 09/092650, discussed below).
  • U.S. Pat. No. 4,851,434 (the '434 patent) to Deckner discloses a non-greasy, non-irritating moisturizer, and compositions containing as the major moisturizing component the di-, tri- or polyglycol amide or glucamine reaction product with an a-hydroxy-substituted fatty acid, with the formula containing hydrogen or a lower alkyl, preservatives, thickeners, skin-soothing agents, such as allantoin and/or dl-panthenol, and water. The non-irritating moisturizer disclosed in the '434 patent does not produce a warming effect when it contacts body-generated moisture and does not spread spontaneously on latex and human skin.
  • U.S. Pat. No. 4,952,560 to Kigasawa et al. discloses an ointment base containing a water-soluble protein consisting of gelatin, casein and soybean protein and a monohydric alcohol with a carbon number of 2 to 4 and/or an oleginous substance and additionally containing a wetting agent selected from the group consisting of an alkylene glycol containing 2 to 6 carbon atoms, polyethylene glycol having an average molecular weight of about 200 to 800, glycerin, trimethylolpropane and sorbitol, in a range of 1 to 35 weight % based on the weight of the whole ointment. While the ointment base improves percutaneous absorption of drugs, it is too thick to function as a lubricant.
  • U.S. Pat. No. 5,441,723 to Simmons discloses a non-toxic hypocompatible biodegradable germicide. The non-toxic hypocompatible biodegradable germicide is effective against a wide range of pathogenic organisms and comprises 65-75 wt % of a monohydric alcohol selected from the group consisting of isopropyl, methyl, ethyl, n-propyl, n-butyl, tert-butyl, allyl, or mixtures thereof, and from about 4% to about 16% by weight of at least one polyhydric alcohol selected from the group consisting of propylene glycol, 1,3 propanediol, 1,2 butanediol, PEG 400, glycerol or 1,4 butanediol, or mixtures thereof in proportion by weight. The monohydric alcohol in the germicide provides the primary disinfecting or killing effect on the pathogenic organisms, while the polyhydric alcohol reduces the surface glaze formed by the monohydric alcohol and the surface tension formed by water or water-based body fluids, thereby enabling the disinfectant/antiseptic to kill pathogenic organisms and act equally effectively on a patient or inanimate surface without deleterious effects. The monohydric alcohol also lowers the flash point of the composition, soothes the skin, and slows the rate of evaporation. In this regard, the germicide is not a lubricant and does not include a warming constituent. The polyhydric alcohol, by reducing the rate of evaporation of the monohydric alcohol, essentially cools the surface by evaporative cooling.
  • U.S. Pat. No. 5,512,289 to Tseng et al. discloses a spermicidal anti-viral lubricant composition containing a water-soluble polymeric gel matrix comprising a hydroxyalkyl cellulose with 2 to 6 carbon atoms; an alkylphenoxypolyethoxyethanol spermicide; and a solubilizing moiety comprising a polyethoxylated non-ionic compound, such as polyethoxylated castor oil. The use of an alkylphenoxypolyethoxyethanol spermicide prevents collapse of the hydroxyalkyl cellulose gel. The addition of a solubilizer substantially prevents the collapse of the gel matrix and permits the gel matrix to maintain its properties in the composition. The spermicidal composition can be dispersed by use of a pharmaceutically acceptable vehicle, such as water, alcohols, e.g., ethanol, glycerin, propylene glycol, and mixtures thereof. A typical formulation of the spermicidal lubricant can include water 75.50 wt %, glycerin 17.00 wt %, hydroxyethyl cellulose 1.00 wt %, polyvinyl pyrrolidone 0.90 wt %, carboxymethyl cellulose 1.00 wt %, Nonoxynol-9 spermicide 2.00 wt %, polyethoxylated castor oil 2.00 wt %, methylparaben 0.20 wt %, sorbic acid 0.05 wt %, and citric acid 0.35 wt %. Since glycerin and glycol are already dissolved in water, the lubricant does not provide a warming effect.
  • U.S. Pat. No. 5,514,698 to Ahmad et al. discloses an antifungal vaginal cream composition. The composition has stable viscosity at human body temperature and comprises about 0.4 to 10.0% of an imidazole antifungal agent (of miconazole, econazole, terconazole, saperconazole, itraconazole, ketoconazole, and clotrimazole), about 1.0% to 5.0% of a fatty acid ester (isopropyl stearate, isopropyl myristate, isopropyl palmitate, and isopropyl laurate), about 1.0% to 25.0% of aliphatic alcohols (cetyl alcohol, stearyl alcohol and propylene glycol), about 2.0% to 5.0% of a surfactant (polysorbate 60 or polysorbate 80), about 0.02% to 0.20% of an antioxidant (butylated hydroxyanisole), a sufficient amount of inorganic base (NaOH or KOH) to adjust the pH range to a value of about 3.0 to 7.0, and water. This vaginal cream is not a lubricant and is expected to maintain its viscosity for prolonged time periods at body temperature. Even though propylene glycol is used in the composition, it is already mixed with water and, therefore, no warming effect takes place when the cream contacts body-generated moisture.
  • U.S. Pat. No. 5,649,825 to Ratkus discloses a dental root canal bacterialcidal lubricant, which allows the cleaning wires or files to move more freely when removing a nerve from a tooth. The composition reduces packing of tissue and dentin debris within the nerve cavity. This formulation is also resistive to decomposition during cold weather shipping, and includes cetyl alcohol, stearyl alcohol, sodium lauryl sulfate, stearic acid, propylene glycol, methyl paraben, propyl paraben, and butyl paraben in a purified water solution. The lubricant does not provide a warming effect.
  • U.S. Pat. No. 5,885,591 to Ahmad et al. discloses highly lubricious personal lubricant compositions containing one or more polyhydric alcohols, one or more water-soluble polymers derived from cellulose, water, and, optionally, preservatives and alkali metal or alkaline earth metal bases. These compositions can provide a vehicle for delivering medicaments for contraception and for the treatment and prevention of disease. The personal lubricant composition contains about 30% glycerin, about 5% propylene glycol, about 10% sorbitol, about 0.4% preservative, about 0.4% hydroxyethylcellulose, about 0.01% sodium hydroxide, and about 50% water. The composition has a lubricity of 33 to about 466. The personal lubricant composition attaches to mucous membranes and is not readily washed off. Since the composition already contains water, no heating or warming reaction occurs when the lubricant is applied to the body and the glycerin comes in contact with body-generated moisture.
  • U.S. Pat. No. 6,139,848 to Ahmad et al. discloses stable personal lubricant compositions containing at least one water-soluble polyhydric alcohol, a water-soluble polymer derived from cellulose, tocopherol or a tocopherol derivative, a nonionic water-soluble or dispersible emulsifier, and water. The lubricious, oily tocopherol or tocopherol derivative is present as an emulsion in the personal lubricant. The emulsifier preferably is a polyalkylene emulsifier chosen from the group consisting of polyoxyethylene (20) sorbitan monostearate, commonly known as Tween 60 or Polysorbate 60, and polyethylene glycol ether of isocetyl alcohol (commonly known as Isoceteth 20 or Arlasolve 200, which is available from ICI Americas, Inc., New Castle, Del.). The water-soluble polyhydric alcohol serves to increase the lubriciousness of the compositions. The water-soluble cellulose-derived polymer serves to impart the desired slipperiness and viscosity to the composition. Water is desired in sufficient quantity to be delivered as moisture to the mucous membranes and to provide consistency and viscosity to the composition. The nonionic surfactants emulsify tocopherol, tocopherol acetate or other tocopherol derivatives into a microemulsion in which the internal or oil phase is reduced to very small globules measuring 2 or less than 2 microns in size. Due to their immensely small size, the emulsion globules do not coalesce and serve to assist in maintaining the homogeneity of the emulsions and to preserve physical stability of the compositions. Since the polyhydric alcohol (glycerin) is already combined with water, no heating or warming reaction occurs when the lubricant is applied to the body.
  • U.S. Patent Application Publication No. 2001/0039380 to Larson et al. discloses in vivo biocompatible acoustic coupling media comprising polyethylene oxide (PEO), at least one of polyalkylene glycols and polyhydric alcohols, and the balance water. Since water is already added to polypropylene alcohol, the exothermic reaction of mixing has already occurred, and no additional warming occurs when the lubricant is used.
  • U.S. Patent Application Publication No. 2003/0207772 and International Patent Application Publication No. WO 03/092651 to Ahmad et al. (see also U.S. Pat. App. Pub. No. 2003/0211161 and Int'l Pat. App. Pub. No. WO 03/092652) disclose warming and nonirritating lubricating compositions containing polyhydric alcohols and an insulating agent. The polyhydric alcohol comprises glycerin, alkylene glycol, or a mixture thereof. The alkylene glycol is selected from the group consisting of propylene glycol, butylene glycol and hexalene glycol, whereas the polyethylene glycol is selected from the group consisting of polyethylene glycol 300 and polyethylene glycol 400. The insulating agent is selected from the group consisting of honey, isopropyl myristate and isopropyl palmitate. A warming action is created by the heat released during dissolution of the polyhydric alcohol in water, and the insulating agent retains the heat. The insulating agent is an essential part of the composition of the lubricant, and reduces the spreading capability of the warming lubricant.
  • U.S. Patent Application Publication No. 2003/0232090 and International Patent Application Publication No. WO 03/092650 to Ahmad et al. disclose warming and nonirritating lubricating compositions. Also disclosed are substantially anhydrous, warming, non-toxic and nonirritating lubricating compositions containing polyhydric alcohols, a gelling agent and, alternatively, a pH-adjusting agent for treating fungal and bacterial infections. The polyhydric alcohol comprises glycerin, alkylene glycol, polyethylene glycol, or a mixture thereof. The alkylene glycol is selected from the group consisting of propylene glycol, butylene glycol and hexalene glycol, whereas the polyethylene glycol is selected from the group consisting of polyethylene glycol 300 and polyethylene glycol 400. The insulating agent is selected from the group consisting of honey, isopropyl myristate and isopropyl palmitate. The use of insulating agents reduces the spreading capability of the warming lubricant.
  • U.S. Patent Application Publication No. 2004/0037911 to Letoumeau et al. discloses a genital lubricating composition. The composition comprises (i) fatty acids and/or homeopathic dilutions of plant extracts and (ii) a physiologically acceptable carrier. According to a preferred embodiment, the genital lubricant composition comprises about 0.05% to about 0.5% hemp seed oil and a physiologically acceptable carrier so that it forms a lotion, a cream or a gel. The composition is particularly useful for use as a vaginal moisturizer, or as a personal lubricant for use prior or during sexual intercourse. The fatty acids can be hemp oil, linoleic (CI8:2) acid or linolenic (C18:3) acid. The plant extracts include extracts from Caladium seguinum, Sepia officianalis, Lycopodium clavatum, and Onosmodium virginanium. The exact composition of the carrier is not disclosed. This lubricant does not have any polyhydric alcohol and does not produce a warming sensation.
  • U.S. Patent Application Publication No. 2004/0086575 to Smith discloses anti-viral compositions. The anti-viral compositions contain at least one zinc compound, at least one phenolic antioxidant (and optionally other ingredients), and a pharmaceutical carrier. The zinc compound is selected from the group consisting of zinc, zinc chloride, zinc acetate, zinc citrate, zinc sudoxicam, zinc sulfate, zinc nitrate, zinc carbonate, zinc tartrate, zinc maliate, zinc lactate, zinc aminoacetate, zinc aspartate, zinc glutamate, zinc propionate, zinc oleate, zinc benzoate, zinc gluconate, zinc butyrate, zinc formate, zinc glycerate, zinc glycolate, zinc oxide, zinc ethylenediamine tetraacetate, zinc pentosan polysulfate, zinc oxyacetate, and hydrates. The phenolic antioxidant comprises at least one compound represented by the formula:
    Figure US20060188528A1-20060824-C00001
  • wherein each R is independently an aliphatic hydrocarbon residue, with or without oxygen, comprising 1 to about 12 carbon atoms, x is from 1 to 3, y is from 0 to 3, z is from 1 to 3, and x+y+z is 6 or less. The pharmaceutical carrier comprises at least one of water, alcohol, fatty acids, fatty acid esters, and waxes. The composition does not function as a lubricant.
  • U.S. Patent Application Publication No. 2004/0138074 to Ahmad et al. discloses substantially anhydrous, warming, non-toxic and nonirritating lubricating compositions containing polyols and preferably an insulating agent. The substantially anhydrous lubricant composition comprises a polyol, which increases in temperature by at least about 5° C. upon exposure to moisture and which has a maximum Energy Release Index of at least about 11 mJ/mg. The polyhydric alcohol is selected from glycerin, alkylene glycol, polyethylene glycol, polypropylene glycol, PEGylated compounds, block copolymers comprising polyalkylene glycol, and their mixtures. The use of insulating agents, such as honey, isopropyl myristate and isopropyl palmitate, reduces the spreading capability of the warming lubricant.
  • European patent document EP 0636374 to Tseng discloses a spermicidal anti-viral lubricating composition containing an antiviral alkylphenoxypolyethoxyethanol spermicide, a water-soluble polymeric gel matrix, and a solubilizer, which permits the spermicide to be compatible with the gel matrix. Preferably, a polyethoxylated compound, such as polyethoxylated castor oil, is used. There is no warming agent present in the lubricant, since the water-soluble polymer functions as the lubricating agent.
  • Japanese patent document JP 2292212 to Hans Eke Rennaruto Bidesutoreemu discloses a sterilizable gel. This sterilizing gel comprises a carboxypolymethylene polymer (carboma) and 1-90% polyhydric alcohol for stabilization (e.g., ethylene glycol). The carboma can be sterilized by assistance of the polyhydric alcohol and avoids deterioration of the gel when the gel is sterilized by γ-radiation derived from cobalt 60. This is not a warming gel and polyhydric alcohol is only used to prevent discoloration during γ-radiation.
  • Japanese patent document JP 2003183115 to Saijo discloses a poikilothermal lubricant. The lubricant may contain ingredients that cause cooling or warming. The warming or cooling ingredient is a dispersant that is not water-soluble and is protected by a polymeric coating. It is unclear what is the nature of the warming agent and what is the mechanism of the warming action.
  • International Patent Application Publication No. WO 93/18740 to Dunbar discloses a shaving gel. The water-based, non-foaming, shaving gel comprises from 0.05 to 4.0% of a carboxypolymethylene, from 2.00 to 52.0% of a polyhydric alcohol, and, optionally, a silicone derivative, an antipruritic agent, preservative agents, a chelating agent, a neutralizing agent, a solubilizing agent, a UV light-absorbing agent, or a perfume. The preferred polyhydric alcohol is glycerin. The gel is applied directly to dry skin and hair prior to shaving with a razor blade and provides a close, comfortable and well-lubricated shave. The shaving gel does not provide a warming effect.
  • Notwithstanding the advances in the field of lubricants and more particularly in the field of warming lubricants and related articles, there remains a need in the art for a warming lubricant that provides effective elastohydrodynamic lubrication as evidenced by improved spreadability on skin, condoms and other surfaces with which it is brought in contact.
  • SUMMARY OF THE INVENTION
  • The present invention provides a spreadable warming lubricant that exhibits excellent spreadability and low surface tension and contact angle, thereby providing a well-wetted, uniform, thin layer during skin to skin contact and condom latex film to skin contact. The warming lubricant composition has sufficient viscosity to establish easily a thin film on either skin or condom latex film with a film thickness ranging from 0.01 to 0.1 mm. The spreadable warming lubricant composition is substantially anhydrous and comprises a mixture of glycerin with another polyhydric alcohol in the range of 40%-60% each and a non-ionic surfactant in the range of 0.1 to 3%. The polyhydric alcohol is preferably propylene glycol, and the non-ionic surfactant is preferably polysorbate 20, polysorbate 40, polysorbate 60 or polysorbate 80. The preferred spreadable warming composition comprises 49.75% glycerin, 49.75% propylene glycol, and 0.5% polyoxyethylene sorbitan monolaurate (polysorbate 20).
  • The spreadable warming lubricant releases heat when mixed with moisture, which can be skin-generated. The temperature rise is optimal when nearly equal volumes of the spreadable warming lubricant and moisture are mixed. An excess of either moisture or the warming lubricant reduces the temperature rise because the heat released has to heat a larger mass. Therefore, the quantity of the warming lubricant desirably is limited to the quantity of moisture available during use. Thus, when used with a latex condom, for example, the spreadable warming lubricant desirably coats the surface of the condom as a thin layer. When the interior and exterior of a latex condom is not coated with a lubricant, there is rubbing between skin and latex, which produces friction and irritation. The presence of a thin, well-spread layer of spreadable warming lubricant minimizes, if not eliminates, friction and irritation and assures uniform heat release, which, in turn, provides a comfortable warming sensation. The thin, well-wetted, warming lubricant layer that is in contact with (i) a condom latex surface and skin or (ii) skin and skin results in elastohydrodynamic lubrication that effectively reduces friction even when the contacting surfaces deform.
  • Incorporation of lubricant on a condom latex surface as a uniform coating in general is difficult to achieve. However, the present inventive spreadable warming lubricant wets latex with a small contact angle. Therefore, the addition of a small quantity of about 0.2-5 ml of spreadable warming lubricant to a condom package results in the migration of the warming lubricant over the internal and external surfaces of the condom. This migration process coats essentially the complete internal and external surfaces of the latex condom with a thin layer of warming lubricant within a period of approximately a week. Thus, the present inventive spreadable warming lubricant is advantageous in that it enables uniform coating of a lubricant on a condom. Accordingly, the present invention also provides a latex condom, onto which a spreadable warming lubricant has been applied in accordance with such a method.
  • When the spreadable warming lubricant is used as skin lubricant, the warming lubricant is applied to the skin in an amount that approximates the available skin moisture. Optionally, moisture can be added to the skin prior to the application of the spreadable warming lubricant. The reaction between moisture and the spreadable warming lubricant results in the release of heat, thereby creating a warming sensation. The spreadability of the warming lubricant is essential for this warming effect, since the quantity of moisture available on skin is generally small and the quantity of spreadable warming lubricant applied desirably is matched with this quantity of moisture so as to optimize the warming effect. In the absence of spreadability, the warming lubricant would be concentrated in the area of initial application to the skin and the desired effects of lubrication and warmth would not be optimized.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The present invention provides an improved warming lubricant that provides and maintains a thin elastohydrodynamic lubricating film between skin and either skin or latex. The lubricant exhibits excellent spreadability due to sufficient viscosity, a low surface tension, and a low contact angle. The lubricant is substantially anhydrous, preferably containing less than about 5% water, more preferably containing less than about 3% water, and most preferably containing less than about 2% water, such as less than about 1% water. Having sufficient viscosity, a film thickness ranging from about 0.01 to 0.10 mm, such as about 0.05 to 0.10 mm, can be achieved on skin or latex rubber.
  • Accordingly, the present invention provides a spreadable warming lubricant comprising glycerin with another polyhydric alcohol and a non-ionic surfactant. Preferably, glycerin is present in an amount from about 40% to 60%, the polyhydric alcohol is present in an amount from about 40% to 60%, and the non-ionic surfactant is present in an amount from about 0.1% to 3%.
  • Any suitable polyhydric alcohol can be used. Preferably, the polyhydric alcohol is propylene glycol. Other polyhydric alcohols, such as butylene glycol, hexalene glycol, and polyethylene glycol, are known in the art.
  • The warming lubricant has constituents that release heat by exothermic heat of dissolution when mixed with moisture, such as skin-generated moisture. Since skin-generated moisture is generally small in quantity, the quantity of warming lubricant desirably is small in quantity to take advantage of the exothermic heat release to provide a warming effect. An excessive amount of the warming lubricant in the presence of a small amount of skin-generated moisture results in only a small temperature rise resulting in a minimal warming effect. The small quantity of spreadable warming lubricant can only be effective if it creates a stable elastohydrodynamic film over the skin or between skin and a latex article.
  • Polyhydric alcohols react with water to release heat by an exothermic dissolution reaction. This effect is well-known and documented in several chemistry textbooks including supplier literature of Dow Chemical Company (Midland, Mich.). Any of the polyhydric alcohols, including glycerin, propylene glycol, butylene glycol, hexalene glycol, and polyethylene glycol, exhibit this exothermic reaction. The spreadable warming lubricant has glycerin and a polyhydric alcohol, preferably propylene glycol, mixed in an appropriate ratio to ensure that the viscosity of the mixture provides sufficient lubricating properties. The higher the viscosity, the higher is the drag when the contacting surfaces are moved with respect to one another. In addition, higher viscosity compositions tend to form thick lubricating films, since gravitational forces are inadequate to form a thin film, whereas lower viscosity compositions run off easily, forming very thin lubricating films.
  • The viscosity of a glycerin—propylene glycol mixture as a function of composition is shown in Table 1 below. Propylene glycol viscosity is too low to be useful as a lubricant, while glycerin has too high a viscosity to produce evenly a thin lubricating film. Table 1 also documents the warming effect of the lubricant composition in three trials. Propylene glycol provides the largest warming effect, while glycerin produces the smallest warming effect.
    TABLE 1
    % Propylene Glycol
     0 50 100
    % Glycerin 99.7%
    100 50  0
    Test No. 1 2 3 1 2 3 1 2 3
    Tmax (° C.) 35.7 35.8 35.8 37.2 37.5 37.6 38.5 38.1 38.5
    Tb (° C.) 23.8 23.8 24.1 24.1 24.0 24.0 23.8 24.0 24.1
    ΔTsample = Tmax − Tb (° C.) − Tsf 5.7 5.8 5.5 6.9 7.3 7.4 8.5 7.9 8.2
    Avg warming, ΔT (° C.) 5.7 7.2 8.2
    Viscosity (at 25° C.) ˜565.5 cps ˜140 cps ˜32 cps

    Tb = room temperature of sample

    Tmax = highest temperature of sample upon mixing with equal amount of water at 37° C.

    Tsf = 6.2° C., inherent effect of mixing water at 37° C. with water at room temperature

    ΔTsample = increase in temperature of sample after mixing with equal amount of water at 37° C.

    cps = centipoises
  • The lubricant must wet the surfaces in question and must have a low contact angle. This requirement is even more important when the surfaces in contact are deformable and the adhesion of the film to the surface needs to be better, thus demanding even a smaller contact angle. If the contact angle is large, the lubricating fluid film disrupts creating islands, which are physically separated, and rubbing now occurs between skin and skin or between skin and latex, both of which are high friction coefficient couples providing skin irritation. Improved wetting of a glycerin-propylene glycol mixture is accomplished by addition of 0.1 to 3 percent of non-ionic surfactants.
  • Non-ionic surfactants, as the name implies, do not contain ionic constituents. They are “ionically” inert. A vast majority of all non-ionic detergents are condensation products or ethylene oxide with a hydrophobe. This group of detergents is enormous, and the permutations endless. They are the single largest group of all surfactants. Nonionic Surfactants: Organic Chemistry, Nico M. van Os, ed., Marcel Dekker (1998), specifically incorporated by reference herein, discusses a number of non-ionic surfactants, including polyoxyethylene alkylphenols, alcohols, esters of fatty acids, mercaptans, and alkylamines, nonionic surfactants containing an amide group, and polyol ester surfactants. Dow Chemical Co. markets a number of non-ionic surfactants under the trade name ‘DOWFAX’. These polyethylene glycol formulations provide superior softening, conditioning, and skin-smoothing characteristics, since polyglycols dissolve or are compatible and miscible in various organic liquids.
  • Polysorbate compositions are also non-ionic surfactants and are available as polysorbate-20, 40, 60; 65 and 80. They are polyoxyethylene sorbitan monoesters (PS) of the general formula:
    Figure US20060188528A1-20060824-C00002
  • wherein R is laureate, palmitate, stearate or oleate and each of w, x, y and z is independently 1 or 2; or each of w, x, y and z is independently less than or equal to 17 and the sum of w, x, y and z is 20. Polysorbate-20 is polyoxyethylenesorbitan monolaurate, CAS #9005-64-5, with a chemical composition of sorbitan mono-9-octadecenoate poly(oxy-1,1-ethanediyl). Polysorbate 40 is polyethylene glycol sorbitan monopalmitate, polyoxyethylene sorbitanmonopalmitate, CAS# 9005-66-7, Polysorbate 60 is polyethylene glycol sorbitan monostearate, polyoxyethylene sorbitanmonostearate, CAS #9005-67-8, and Polysorbate 80 is polyoxyethylenesorbitan monooleate, CAS# 9005-65-6.
  • Tables 2 A, B and C show the effect of the addition of polysorbate 20 to warming lubricant compositions containing propylene glycol and glycerin on drop diameter, when a fixed volume of liquid is applied to a substrate, including glass, latex condom film and skin, and the corresponding contact angle. This contact angle is determined by dropping a fixed volume of 25 μl of lubricant mixture using a microsyringe on a flat substrate of glass, condom latex film or skin, respectively, and measuring the diameter of the spread of the warming lubricant as a function of time. The contact angle is calculated using a well-known formula (Roberts et al., Surface Treatments to Reduce Friction—Rubber Chemistry and Technology, 63:722 (1990)) as shown below, wherein D is the diameter of the lubricant and V is the volume of the warming liquid:
    TABLE 2 A
    D 3 V = 24 Sin 3 θ π ( 2 - 3 Cos θ + Cos 3 θ ) .
    Substrate: GLASS
    Average Base Diameter of Drop (mm) & Contact Angle (degrees)
    50% 49.50% Propylene Propylene
    Propylene Glycol, 49.5% Glycol,
    Lapse Drop Glycol, glycerin, Glycerin, Propylene 0.5%
    time Vol. 50% glycerin 0.5% PS20 Glycerin 0.5% PS20 Glycol PS20
    (mins) (μL) mm deg mm deg mm, deg mm, deg mm deg mm deg
    1 25 7.0 39 8.0 27.4 6.0 56.4  6.5 41.5 7.0 39 8.0 27.4
    10 25 7.0 39 9.5 16.8 6.0 56.4  8.0 27.4 8.0 27.4 10.0 14.4
    60 25 7.5 32.7 10.5 12.5 7.0 39 10.0 14.4 8.0 27.4 11.5 9.5
    135 25 7.5 32.7 12.0 8.4 7.5 32.7 8.0 27.4 12.5 7.4
    300 25 8.0 27.4 12.5 7.4 8.0 27.4 12.0  8.4 8.5 23.1 13.5 5.9
  • TABLE 2B
    Substrate: CONDOM LATEX FILM Average Base Diameter
    of Drop (mm) & Contact Angle (degrees)
    49.50%
    50% Propylene
    Propylene Glycol, Propylene
    Lapse Drop Glycol, 49.5% glycerin, Glycerin, Propylene Glycol,
    time Vol. 50% glycerin 0.5% PS20 Glycerin 0.5% PS20 Glycol 0.5% PS20
    (mins) (μL) mm deg mm deg mm deg mm deg mm deg mm deg
    1 25 5.0 78.9 6.0 56.4 5.0 78.9 6.0 56.4 6.0 56.4 7.0 39
    10 25 5.0 78.9 7.0 39 5.0 78.9 6.0 56.4 6.0 56.4 7.0 39
    60 25 5.0 78.9 9.0 19.6 5.5 67.5 8.5 23.1 6.0 56.4 8.0 27.4
    135 25 6.0 56.4 9.0 19.6 6.5 41.5 9.0 19.6 7.0 39 9.0 19.6
    300 25 6.0 56.4 9.0 19.6 7.0 39 10.0 14.4 7.5 32.7 9.5 16.8
  • TABLE 2C
    Substrate: SKIN ON ARM Average Base Diameter of Drop (mm) & Contact Angle (degrees)
    49.75%
    50% Propylene
    Propylene Glycol, Propylene
    Lapse Drop Glycol, 49.75% glycerin, Glycerin, Propylene Glycol,
    time Vol. 50% glycerin 0.5% PS20 Glycerin 0.5% PS20 Glycol 0.5% PS20
    (mins) (μL) mm deg mm deg mm deg mm deg mm deg mm deg
    1 25 6.0 56.4 6.5 41.5 5.0 78.9 6.0 56.4 7.0 39 7.0 39
    5 25 7.5 32.7 10.5 12.5 5.5 41.5 8.0 27.4 8.0 27.4 8.0 27.4
  • The contact angle measured by this spreading drop measurement compares well with the Kruss Contact Angle measurement as shown in Table 2D below. Skin tests could not be successfully conducted using the Kruss contact angle meter since the applied drop spreads too rapidly.
    TABLE 2D
    Substrate CONDOM LATEX FILM Contact Angle (degrees)
    49.75%
    Propylene Glycol,
    50% Propylene Glycol, 49.75% glycerin,
    Lapsed time 50% glycerin 0.5% PS20 Glycerin
    (mins) (deg) (deg) (deg)
    1 85.06 57.45 84.86
    5 88.14 50.75 82.9
    10 86.26 48.48 79.25
  • The surface tensions of the warming lubricants were measured and are shown below in Table 2E.
    TABLE 2E
    Surface Tension (N/m)
    49.75% Propylene Glycol Propylene
    50% Propylene Glycol, 49.75% glycerin, Glycerin, Propylene Glycol,
    50% glycerin 0.5% PS20 Glycerin 0.5% PS20 Glycol 0.5% PS20
    (N/m) (N/m) (N/m) (N/m) (N/m) (N/m)
    0.046 0.037 0.067 0.036 0.0385 0.03825
  • It is, therefore, very clear that adding 0.5% of polysorbate 20 increases the spread diameter of the lubricant, and decreases contact angle and surface tension in all cases. The combination of appropriate lubricant viscosity and lubricant spreading capability generates an effective warming lubricant as demonstrated by the warming lubricant composition having 49.75% propylene glycol, 49.75% glycerin, and 0.5% polysorbate 20.
  • Even though this specific composition is shown in Tables 2A-C, the propylene glycol can be in the range of 40% to 60%, glycerin can be in the range of 40 to 60%, and polysorbate 20 or other non-ionic surfactant can be in the range of 0.1 to 3%. The viscosity of glycerin propylene glycol is relatively stable in this compositional range, and polysorbate 20 and other non-ionic surfactants are effective in improving the contact angle.
  • The warming lubricant can be used as a skin lubricant wherein a small drop [VOLUME] of the warming lubricant is applied over skin and rubbed. Any skin-generated moisture quickly produces a warming effect as the warming lubricant combines with moisture. The warming lubricant is highly spreadable and produces a soothing effect.
  • The spreadable warming lubricant can be applied to a condom latex surface. Due to its enhanced spreading character, the warming lubricant spreads over the internal and external surface of the condom latex. The utility of a lubricated condom is related to distribution of the lubricating agent on the condom surface, since this lubrication is what prevents irritation. Any lubricant that does not spread well has bare spots, where latex condom surface rubs directly on skin and creates increased friction, stickiness and irritation. In order to quantify this effect, a small amount of spreadable warming lubricant was applied on the external surface of a condom, and the spreading of the warming lubricant was measured. The results are shown below in Table 2F.
    TABLE 2F
    Migration Up Condom Shaft (weeks)
    Time
    1 2 3 1 2 3
    week weeks weeks week weeks weeks
    Propylene 0 0 0 50 50 50
    glycol %
    Glycerin % 100 100 100 50 50 50
    Migration up 5 4.5 5.7 13.3 18.5 18.5
    condom shaft
    after 1, 2,
    3 wks (cm)*
    Migration up 15 15.5 16.8 16.8 17.5 17
    condom shaft
    with 0.5%
    Polysorbate 20
    after 1, 2,
    3 wks (cm)
  • The 50%-50% mixture of glycerin and propylene glycol had a higher migration distance up the condom shaft as compared to pure glycerin. When polysorbate 20 was added to the lubricant, both glycerin and the 50%-50% mixture of glycerin and propylene glycol showed improvement in the migration distance of the lubricant up the condom shaft, particularly within one week.
  • The mode of application of the spreadable warming lubricant in condoms includes dropping a measured quantity of warming lubricant consistent with the skin-generated moisture. Since the skin-generated moisture is generally in the range of 0.2 to 5 ml, the quantity of the warming lubricant desirably is less than 5 ml. This small quantity of the warming lubricant has to be spread all over the internal and external surface of the condom latex to provide effective lubrication and warming effect. During packaging of a condom, the measured quantity of lubricant is added, and the spreading effect is relied on to disperse the lubricant across the internal and external surfaces of the condom.
  • When the spreadable warming lubricant is used as skin lubricant, the lubricant is applied to the skin in an amount that approximates the available skin moisture. Optionally, moisture can be added to the skin prior to the application of the spreadable warming lubricant. The reaction between moisture and spreadable warming lubricant results in the release of heat, thereby creating a warming sensation. The spreadability of the warming lubricant is essential for this warming effect, since the quantity of moisture available on skin is generally small and the quantity of spreadable warming lubricant applied desirably is matched with this quantity of available moisture so as to optimize the warming effect. In the absence of spreadability, the warming lubricant would be concentrated in the area of initial application to the skin and the desired effects of lubrication and warmth would not be optimized. The combination of suitable viscosity, low surface tension and contact angle with respect to human skin results in spreading of the warming lubricant on the skin so as to provide an optimal, soothing warming effect.
  • All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.
  • The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.
  • Preferred embodiments of this invention are described herein, including the best mode known to the inventors for carrying out the invention. It should be understood that the illustrated embodiments are exemplary only, and should not be taken as limiting the scope of the invention.

Claims (26)

1. A spreadable warming lubricant comprising:
a. a mixture of glycerin and polyhydric alcohol; and
b. a non-ionic surfactant incorporated in said mixture;
wherein the spreadable warming lubricant is substantially anhydrous, produces a thin lubricious layer on skin or a condom, and produces a warming effect upon contact with moisture.
2. The spreadable warming lubricant of claim 1, wherein glycerin is present in an amount from about 40% to 60%, the polyhydric alcohol is present in an amount from about 40% to 60%, and the non-ionic surfactant is present in an amount from about 0.1% to 3%.
3. The spreadable warming lubricant of claim 1, wherein the polyhydric alcohol is propylene glycol.
4. The spreadable warming lubricant of claim 2, wherein the polyhydric alcohol is propylene glycol.
5. The spreadable warming lubricant of claim 1, wherein the non-ionic surfactant is a polyoxyethylene sorbitan monoester.
6. The spreadable warming lubricant of claim 2, wherein the non-ionic surfactant is a polyoxyethylene sorbitan monoester.
7. The spreadable warming lubricant of claim 5, wherein the polyoxyethylene sorbitan monoester is polyoxyethylene sorbitan monolaurate.
8. The spreadable warming lubricant of claim 6, wherein the polyoxyethylene sorbitan monoester is polyoxyethylene sorbitan monolaurate.
9. The spreadable warming lubricant of claim 1, wherein the warming lubricant has a thickness of 0.05 to 0.1 mm when applied to skin.
10. The spreadable warming lubricant of claim 1, wherein the warming lubricant has a thickness of 0.01 to 0.1 mm when applied to skin.
11. A spreadable warming lubricant consisting of 49.75% glycerin, 49.75% propylene glycol and 0.5% polyoxyethylene sorbitan monolaurate.
12. The spreadable warming lubricant of claim 11, wherein the warming lubricant has a thickness of 0.05 to 0.1 mm when applied to the surface of a latex condom.
13. The spreadable warming lubricant of claim 11, wherein the warming lubricant has a thickness of 0.01 to 0.1 mm when applied to skin.
14. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 1;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
15. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 2;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
16. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 3;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
17. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 4;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
18. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 5;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
19. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 6;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
20. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 7;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
21. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 8;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
22. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 9;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
23. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 10;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
24. A method of applying a spreadable warming lubricant onto the internal and external surfaces of a latex condom, which method comprises:
a. contacting the latex condom with about 0.2 to 5 ml of the spreadable warming lubricant of claim 11;
b. packaging the condom, and
c. maintaining the packaged condom under conditions, which promote migration of the spreadable lubricant on the condom, for at least about 1 week,
whereupon the spreadable warming lubricant is applied onto the internal and external surfaces of the latex condom.
25. A method of applying spreadable warming lubricant of claim 1 to skin, which method comprises:
a. applying one to five drops of the warming lubricant consistent with the degree of skin-generated or applied moisture present;
b. rubbing the lubricant to produce lubrication and a warming effect;
whereby the warming effect is generated by the contact between the warming lubricant and the moisture.
26. A method of applying spreadable warming lubricant of claim 2 to skin, which method comprises:
a. applying one to five drops of the warming lubricant consistent with the degree of skin-generated or applied moisture present;
b. rubbing the lubricant to produce lubrication and a warming effect;
whereby the warming effect is generated by the contact between the warming lubricant and the moisture.
US11/063,711 2005-02-23 2005-02-23 Spreadable warming lubricant Abandoned US20060188528A1 (en)

Priority Applications (14)

Application Number Priority Date Filing Date Title
US11/063,711 US20060188528A1 (en) 2005-02-23 2005-02-23 Spreadable warming lubricant
CN2006800056528A CN101128184B (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
NZ556299A NZ556299A (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
EP06735632A EP1850828A4 (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
AU2006216807A AU2006216807B2 (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
CA002598653A CA2598653A1 (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
MX2007010230A MX2007010230A (en) 2005-02-23 2006-02-21 Spreadable warming lubricant.
JP2007556394A JP2008531085A (en) 2005-02-23 2006-02-21 Spreading temperature rising lubricant
PCT/US2006/006063 WO2006091576A2 (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
KR1020077021849A KR20070121695A (en) 2005-02-23 2006-02-21 Spreadable warming lubricant
BRPI0608428-1A BRPI0608428A2 (en) 2005-02-23 2006-02-21 dispersible heating lubricant, method for applying said lubricant and article
RU2007135226/15A RU2376036C2 (en) 2005-02-23 2006-02-21 Flowing heating lubricant
IL184323A IL184323A0 (en) 2005-02-23 2007-07-01 Spreadable warming lubricant
US12/756,510 US8303969B2 (en) 2005-02-23 2010-04-08 Spreadable warming lubricant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11/063,711 US20060188528A1 (en) 2005-02-23 2005-02-23 Spreadable warming lubricant

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/756,510 Division US8303969B2 (en) 2005-02-23 2010-04-08 Spreadable warming lubricant

Publications (1)

Publication Number Publication Date
US20060188528A1 true US20060188528A1 (en) 2006-08-24

Family

ID=36912974

Family Applications (2)

Application Number Title Priority Date Filing Date
US11/063,711 Abandoned US20060188528A1 (en) 2005-02-23 2005-02-23 Spreadable warming lubricant
US12/756,510 Active 2026-02-06 US8303969B2 (en) 2005-02-23 2010-04-08 Spreadable warming lubricant

Family Applications After (1)

Application Number Title Priority Date Filing Date
US12/756,510 Active 2026-02-06 US8303969B2 (en) 2005-02-23 2010-04-08 Spreadable warming lubricant

Country Status (13)

Country Link
US (2) US20060188528A1 (en)
EP (1) EP1850828A4 (en)
JP (1) JP2008531085A (en)
KR (1) KR20070121695A (en)
CN (1) CN101128184B (en)
AU (1) AU2006216807B2 (en)
BR (1) BRPI0608428A2 (en)
CA (1) CA2598653A1 (en)
IL (1) IL184323A0 (en)
MX (1) MX2007010230A (en)
NZ (1) NZ556299A (en)
RU (1) RU2376036C2 (en)
WO (1) WO2006091576A2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080118417A1 (en) * 2006-10-19 2008-05-22 Blaise Harrison, Llc Exothermic Personal Lubricant
US20080193492A1 (en) * 2007-02-09 2008-08-14 Nawaz Ahmad Complementary personal lubricant compositions
US20080193489A1 (en) * 2007-02-13 2008-08-14 Robert De Armond Personal Lubricant Compositions That Are Free Of Glycerin and Parabens
US20080210579A1 (en) * 2007-03-01 2008-09-04 Blaise Harrison, Llc Exothermic Condom Packaging
US20090107513A1 (en) * 2007-10-26 2009-04-30 Ansell Healthcare Products Llc Condom With Multifunctional Coating

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7709428B2 (en) * 2005-02-23 2010-05-04 Ansell Healthcare Products Llc Thickened spreadable warming lubricant
WO2011072097A1 (en) * 2009-12-09 2011-06-16 Glaxosmithkline Llc Coating for latex articles
CN103501887A (en) 2011-04-05 2014-01-08 Rj罗伯茨咨询有限公司 Wetting composition
CN103446630B (en) * 2013-08-23 2015-05-20 蔡智浙 Safe and easy-to-clean lubricating oil composition for condoms and preparation method thereof
US20190159986A1 (en) * 2016-06-30 2019-05-30 Sxwell Australia Pty. Ltd. Aesthetically Elegant Sexual Lubricants And Massage Gels
CN110121320B (en) * 2016-10-14 2022-06-03 海德鲁格莱德涂料有限责任公司 Hydrophilic polymer coating with long-lasting lubricity
US10912806B2 (en) 2018-09-26 2021-02-09 Michael MCGOWAN Composition comprising an essential oil and its packaging thereof

Citations (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4851434A (en) * 1983-05-27 1989-07-25 Deckner George E Novel non-irritating moisturizer, compositions containing same and method
US4930522A (en) * 1987-08-20 1990-06-05 Hutchinson Prophylactic device made of rupturable microencapsulated elastomeric material and process for its manufacture
US4952560A (en) * 1984-04-05 1990-08-28 Takeda Chemical Industries, Ltd. Ointment base
US4983404A (en) * 1989-06-05 1991-01-08 Warner-Lambert Company Controlled release flavor system and method of preparation
US5097697A (en) * 1990-06-06 1992-03-24 Ansell Incorporated Method and apparatus for airburst testing condoms and the like
US5323544A (en) * 1993-01-22 1994-06-28 Ansell Incorporated Method and apparatus for drying coatings or films
US5441723A (en) * 1989-01-31 1995-08-15 Rost, Incorporated Non-toxic hypocompatible biodegradable germicide
US5512289A (en) * 1993-07-28 1996-04-30 Johnson & Johnson Consumer Products, Inc. Spermicidal anti-viral lubricant composition and method of using same
US5514698A (en) * 1994-03-21 1996-05-07 Ortho Pharmaceutical Corporation Antifungal vaginal cream composition
US5549924A (en) * 1987-07-17 1996-08-27 Robin Renee Thill Shlenker Method of forming a membrane, especially a latex or polymer membrane, including a deactivating barrier and indicating layer
US5595980A (en) * 1993-09-29 1997-01-21 Medical College Of Hampton Roads Contraceptive compositions
US5649825A (en) * 1996-03-01 1997-07-22 Ratkus; Victor L. Dental root canal bacterialcidal lubricant
US5885591A (en) * 1996-07-02 1999-03-23 Johnson & Johnson Consumer Products, Inc. Personal lubricant compositions
US5888441A (en) * 1988-08-24 1999-03-30 Ansell Healthcare Products Inc. Preparation of antimicrobial articles
US5922336A (en) * 1996-01-03 1999-07-13 Deotexix Inc. Microcapsule-coated material
US5977223A (en) * 1997-12-12 1999-11-02 Ansell Healthcare Products, Inc. Elastomeric articles
US5985860A (en) * 1992-06-03 1999-11-16 Toppo; Frank System for transdermal delivery of pain relieving substances
US6007836A (en) * 1993-05-28 1999-12-28 Vericade, Inc. Transdermal vasodilator
US6075081A (en) * 1997-04-23 2000-06-13 Ansell Healthcare Products Inc. Manufacture of rubber articles
US6139848A (en) * 1999-02-12 2000-10-31 Mcneil-Ppc, Inc. Personal lubricant compositions
US6290981B1 (en) * 1992-08-24 2001-09-18 The United States Of America As Represented By The Department Of Health And Human Services Use of nitric oxide-releasing agents to treat impotency
US6306514B1 (en) * 1996-12-31 2001-10-23 Ansell Healthcare Products Inc. Slip-coated elastomeric flexible articles and their method of manufacture
US20010039380A1 (en) * 1999-07-01 2001-11-08 Larson Margaret J. In vivo biocompatible acoustic coupling media
US6378137B1 (en) * 1997-10-01 2002-04-30 Ansell Shah Alam Sdn Bhd Powder-free medical gloves
US20020103414A1 (en) * 2000-12-05 2002-08-01 Harrison Michael J. Condom with male genital desensitizer lubricant
US6428791B1 (en) * 1999-04-13 2002-08-06 Alphamed Pharmace Vticals, Corp Lubrication composition
US20020176892A1 (en) * 1995-09-29 2002-11-28 L.A.M. Pharmaceutical Corp. Topical drug preparations
US6541030B2 (en) * 2000-09-27 2003-04-01 Verion Inc. Instant water dissolvable encapsulate and process
US6551608B2 (en) * 2000-03-06 2003-04-22 Porex Technologies Corporation Porous plastic media with antiviral or antimicrobial properties and processes for making the same
US6620942B2 (en) * 1998-12-23 2003-09-16 Maxim Pharmaceuticals Synthesis of histamine dihydrochloride
US20030207772A1 (en) * 2002-05-01 2003-11-06 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US6664296B1 (en) * 1994-12-22 2003-12-16 Laboratoire Innothera Societe Anonyme Unit galenical formulation for vaginal use as a local contraceptive and/or to combat sexually-transmitted diseases and/or HIV
US20040037911A1 (en) * 2001-09-24 2004-02-26 Letourneau Lucie Elise Genital lubricating compositions and uses thereof
US6709725B1 (en) * 2000-02-29 2004-03-23 Ansell Medical Sdn, Bhd. Elasomeric article
US20040055094A1 (en) * 2002-09-16 2004-03-25 Jack Massoni Temporary hair dye composition
US20040086575A1 (en) * 2002-11-04 2004-05-06 Smith Jeffrey B. Anti-viral compositions and methods of making and using the anti-viral compositions
US20040115250A1 (en) * 2002-12-17 2004-06-17 Ansell Healthcare Products Inc. Camomile/aloe vera treated glove
US20040138074A1 (en) * 2002-05-01 2004-07-15 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20040167039A1 (en) * 2002-05-01 2004-08-26 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20040185065A1 (en) * 2002-05-01 2004-09-23 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US6840244B2 (en) * 2001-03-30 2005-01-11 Futura Medical Developments Limited Condom with an erectogenic composition
US20050042248A1 (en) * 2002-05-01 2005-02-24 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20050042249A1 (en) * 2002-05-01 2005-02-24 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20050066414A1 (en) * 2001-09-13 2005-03-31 Yu E. Anthony Microencapsulation coating for gloves
US20050130522A1 (en) * 2003-12-11 2005-06-16 Kaiyuan Yang Fiber reinforced elastomeric article
US20060070167A1 (en) * 2005-12-01 2006-04-06 Ansell Healthcare Products Llc Glove with hand-friendly coating and method of making
US7037579B2 (en) * 2003-12-19 2006-05-02 Ansell Healthcare Products Llc Polymer composite fibrous coating on dipped rubber articles and method
US7064114B2 (en) * 1999-03-19 2006-06-20 Parker Hughes Institute Gel-microemulsion formulations
US7084884B1 (en) * 1998-11-03 2006-08-01 Immersion Corporation Graphical object interactions
US7157393B2 (en) * 2001-12-18 2007-01-02 Arsell Healthcare Products Llc Carbide and nitride ternary ceramic glove and condom formers
US7176238B1 (en) * 1999-03-01 2007-02-13 Nitromed Inc. Nitrostated and nitrosylated prostaglandins, compositions and methods of use
US7214390B2 (en) * 2003-02-07 2007-05-08 Barmensen Labs, Llc Topical compositions for enhancing sexual responsiveness
US20070104766A1 (en) * 2005-11-10 2007-05-10 Shiping Wang Elastomeric article with antimicrobial coating
US20070287714A1 (en) * 2002-05-01 2007-12-13 Nawaz Ahmad Warming and Nonirritating Lubricant Compositions and Method of Comparing Irritation
US7405186B2 (en) * 2005-03-25 2008-07-29 Chemsil Silicones, Inc. Lubricant compositions, condom products and methods of making same

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02292212A (en) 1989-04-20 1990-12-03 Tremedic Ab Bactericide gel
GB9205988D0 (en) 1992-03-19 1992-04-29 Dunbar Peter Shaving gels
EP0860172B1 (en) * 1996-12-20 2003-06-18 Okamoto Industries, Inc. A water soluble lubricant for a condom and a condom spread with said water soluble lubricant
JP2003183115A (en) 2001-12-17 2003-07-03 Shoko Kagaku Kenkyusho:Kk Poikilothermal lubricant
CN1647376A (en) * 2002-04-11 2005-07-27 皇家飞利浦电子股份有限公司 Polyphase filter with integrators
CN1665484A (en) * 2002-05-01 2005-09-07 麦克内尔-Ppc股份有限公司 Warming and nonirritating lubricant compositions and method of comparing irritation
WO2005081952A2 (en) 2004-02-26 2005-09-09 Church & Dwight Co., Inc. Condom with warmth imparting lubricant

Patent Citations (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4851434A (en) * 1983-05-27 1989-07-25 Deckner George E Novel non-irritating moisturizer, compositions containing same and method
US4952560A (en) * 1984-04-05 1990-08-28 Takeda Chemical Industries, Ltd. Ointment base
US5549924A (en) * 1987-07-17 1996-08-27 Robin Renee Thill Shlenker Method of forming a membrane, especially a latex or polymer membrane, including a deactivating barrier and indicating layer
US4930522A (en) * 1987-08-20 1990-06-05 Hutchinson Prophylactic device made of rupturable microencapsulated elastomeric material and process for its manufacture
US5024852A (en) * 1987-08-20 1991-06-18 Hutchinson Process for preparing a prophylactic device made of rupturable microcapsules and layers of elastomeric material
US5888441A (en) * 1988-08-24 1999-03-30 Ansell Healthcare Products Inc. Preparation of antimicrobial articles
US5441723A (en) * 1989-01-31 1995-08-15 Rost, Incorporated Non-toxic hypocompatible biodegradable germicide
US4983404A (en) * 1989-06-05 1991-01-08 Warner-Lambert Company Controlled release flavor system and method of preparation
US5097697A (en) * 1990-06-06 1992-03-24 Ansell Incorporated Method and apparatus for airburst testing condoms and the like
US5985860A (en) * 1992-06-03 1999-11-16 Toppo; Frank System for transdermal delivery of pain relieving substances
US6290981B1 (en) * 1992-08-24 2001-09-18 The United States Of America As Represented By The Department Of Health And Human Services Use of nitric oxide-releasing agents to treat impotency
US5323544A (en) * 1993-01-22 1994-06-28 Ansell Incorporated Method and apparatus for drying coatings or films
US6007836A (en) * 1993-05-28 1999-12-28 Vericade, Inc. Transdermal vasodilator
US5512289A (en) * 1993-07-28 1996-04-30 Johnson & Johnson Consumer Products, Inc. Spermicidal anti-viral lubricant composition and method of using same
US6347409B1 (en) * 1993-08-05 2002-02-19 Ansell Healthcare Products Inc. Manufacture of rubber articles
US6352666B1 (en) * 1993-08-05 2002-03-05 Ansell Healthcare Products Inc. Manufacture of rubber articles
US5595980A (en) * 1993-09-29 1997-01-21 Medical College Of Hampton Roads Contraceptive compositions
US5514698A (en) * 1994-03-21 1996-05-07 Ortho Pharmaceutical Corporation Antifungal vaginal cream composition
US6664296B1 (en) * 1994-12-22 2003-12-16 Laboratoire Innothera Societe Anonyme Unit galenical formulation for vaginal use as a local contraceptive and/or to combat sexually-transmitted diseases and/or HIV
US20020176892A1 (en) * 1995-09-29 2002-11-28 L.A.M. Pharmaceutical Corp. Topical drug preparations
US5922336A (en) * 1996-01-03 1999-07-13 Deotexix Inc. Microcapsule-coated material
US5649825A (en) * 1996-03-01 1997-07-22 Ratkus; Victor L. Dental root canal bacterialcidal lubricant
US5885591A (en) * 1996-07-02 1999-03-23 Johnson & Johnson Consumer Products, Inc. Personal lubricant compositions
US6306514B1 (en) * 1996-12-31 2001-10-23 Ansell Healthcare Products Inc. Slip-coated elastomeric flexible articles and their method of manufacture
US6075081A (en) * 1997-04-23 2000-06-13 Ansell Healthcare Products Inc. Manufacture of rubber articles
US6378137B1 (en) * 1997-10-01 2002-04-30 Ansell Shah Alam Sdn Bhd Powder-free medical gloves
US5977223A (en) * 1997-12-12 1999-11-02 Ansell Healthcare Products, Inc. Elastomeric articles
US7084884B1 (en) * 1998-11-03 2006-08-01 Immersion Corporation Graphical object interactions
US6620942B2 (en) * 1998-12-23 2003-09-16 Maxim Pharmaceuticals Synthesis of histamine dihydrochloride
US6139848A (en) * 1999-02-12 2000-10-31 Mcneil-Ppc, Inc. Personal lubricant compositions
US7176238B1 (en) * 1999-03-01 2007-02-13 Nitromed Inc. Nitrostated and nitrosylated prostaglandins, compositions and methods of use
US7064114B2 (en) * 1999-03-19 2006-06-20 Parker Hughes Institute Gel-microemulsion formulations
US6428791B1 (en) * 1999-04-13 2002-08-06 Alphamed Pharmace Vticals, Corp Lubrication composition
US20010039380A1 (en) * 1999-07-01 2001-11-08 Larson Margaret J. In vivo biocompatible acoustic coupling media
US6709725B1 (en) * 2000-02-29 2004-03-23 Ansell Medical Sdn, Bhd. Elasomeric article
US6551608B2 (en) * 2000-03-06 2003-04-22 Porex Technologies Corporation Porous plastic media with antiviral or antimicrobial properties and processes for making the same
US20040009227A1 (en) * 2000-03-06 2004-01-15 Porex Corporation Thermoplastic particles which comprise an antiviral or antimicrobial agent
US6541030B2 (en) * 2000-09-27 2003-04-01 Verion Inc. Instant water dissolvable encapsulate and process
US20020103414A1 (en) * 2000-12-05 2002-08-01 Harrison Michael J. Condom with male genital desensitizer lubricant
US6840244B2 (en) * 2001-03-30 2005-01-11 Futura Medical Developments Limited Condom with an erectogenic composition
US20050066414A1 (en) * 2001-09-13 2005-03-31 Yu E. Anthony Microencapsulation coating for gloves
US20040037911A1 (en) * 2001-09-24 2004-02-26 Letourneau Lucie Elise Genital lubricating compositions and uses thereof
US7157393B2 (en) * 2001-12-18 2007-01-02 Arsell Healthcare Products Llc Carbide and nitride ternary ceramic glove and condom formers
US20040138074A1 (en) * 2002-05-01 2004-07-15 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20030211161A1 (en) * 2002-05-01 2003-11-13 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20040185065A1 (en) * 2002-05-01 2004-09-23 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20030232090A1 (en) * 2002-05-01 2003-12-18 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20050042248A1 (en) * 2002-05-01 2005-02-24 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20050042249A1 (en) * 2002-05-01 2005-02-24 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US7417013B2 (en) * 2002-05-01 2008-08-26 Mcneil-Ppc, Inc. Warming and nonirritating lubricant compositions and method of comparing irritation
US20070287714A1 (en) * 2002-05-01 2007-12-13 Nawaz Ahmad Warming and Nonirritating Lubricant Compositions and Method of Comparing Irritation
US7005408B2 (en) * 2002-05-01 2006-02-28 Mcneil-Ppc, Inc. Warming and nonirritating lubricant compositions and method of comparing irritation
US7285517B2 (en) * 2002-05-01 2007-10-23 Mcneil-Ppc, Inc. Warming and nonirritating lubricant compositions and method of comparing irritation
US20040167039A1 (en) * 2002-05-01 2004-08-26 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20060094608A1 (en) * 2002-05-01 2006-05-04 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20030207772A1 (en) * 2002-05-01 2003-11-06 Nawaz Ahmad Warming and nonirritating lubricant compositions and method of comparing irritation
US20040055094A1 (en) * 2002-09-16 2004-03-25 Jack Massoni Temporary hair dye composition
US20040086575A1 (en) * 2002-11-04 2004-05-06 Smith Jeffrey B. Anti-viral compositions and methods of making and using the anti-viral compositions
US20040115250A1 (en) * 2002-12-17 2004-06-17 Ansell Healthcare Products Inc. Camomile/aloe vera treated glove
US7214390B2 (en) * 2003-02-07 2007-05-08 Barmensen Labs, Llc Topical compositions for enhancing sexual responsiveness
US20050130522A1 (en) * 2003-12-11 2005-06-16 Kaiyuan Yang Fiber reinforced elastomeric article
US20060141165A1 (en) * 2003-12-19 2006-06-29 Ansell Healthcare Products Llc Polymer composite fibrous coating on dipped rubber articles and method
US7037579B2 (en) * 2003-12-19 2006-05-02 Ansell Healthcare Products Llc Polymer composite fibrous coating on dipped rubber articles and method
US7405186B2 (en) * 2005-03-25 2008-07-29 Chemsil Silicones, Inc. Lubricant compositions, condom products and methods of making same
US20080210580A1 (en) * 2005-03-25 2008-09-04 Chemsil Silicones, Inc. Lubricant compositions, condom products and methods of making same
US20070104766A1 (en) * 2005-11-10 2007-05-10 Shiping Wang Elastomeric article with antimicrobial coating
US20060070167A1 (en) * 2005-12-01 2006-04-06 Ansell Healthcare Products Llc Glove with hand-friendly coating and method of making

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080118417A1 (en) * 2006-10-19 2008-05-22 Blaise Harrison, Llc Exothermic Personal Lubricant
US20080193492A1 (en) * 2007-02-09 2008-08-14 Nawaz Ahmad Complementary personal lubricant compositions
US8668913B2 (en) * 2007-02-09 2014-03-11 Personal Products Company Complementary personal lubricant compositions
US20080193489A1 (en) * 2007-02-13 2008-08-14 Robert De Armond Personal Lubricant Compositions That Are Free Of Glycerin and Parabens
US20080210579A1 (en) * 2007-03-01 2008-09-04 Blaise Harrison, Llc Exothermic Condom Packaging
US7882838B2 (en) * 2007-03-01 2011-02-08 Blaise Harrison, Llc Exothermic condom packaging
GB2459236B (en) * 2007-03-01 2011-08-10 Blaise Harrison Llc Exothermic condom packaging
US20090107513A1 (en) * 2007-10-26 2009-04-30 Ansell Healthcare Products Llc Condom With Multifunctional Coating
WO2009055652A1 (en) * 2007-10-26 2009-04-30 Ansell Healthcare Products Llc Condom with multifunctional coating
US8770201B2 (en) 2007-10-26 2014-07-08 Glycobiosciences Inc. Condom with multifunctional coating
AU2008316740B2 (en) * 2007-10-26 2015-07-16 Glycobiosciences Inc. Condom with multifunctional coating

Also Published As

Publication number Publication date
CN101128184A (en) 2008-02-20
EP1850828A2 (en) 2007-11-07
BRPI0608428A2 (en) 2009-12-29
CA2598653A1 (en) 2006-08-31
US20100186751A1 (en) 2010-07-29
WO2006091576A3 (en) 2006-11-02
IL184323A0 (en) 2007-10-31
AU2006216807A1 (en) 2006-08-31
RU2007135226A (en) 2009-03-27
AU2006216807B2 (en) 2010-09-16
JP2008531085A (en) 2008-08-14
MX2007010230A (en) 2007-11-07
RU2376036C2 (en) 2009-12-20
US8303969B2 (en) 2012-11-06
CN101128184B (en) 2011-08-03
KR20070121695A (en) 2007-12-27
WO2006091576A2 (en) 2006-08-31
EP1850828A4 (en) 2011-03-30
NZ556299A (en) 2009-06-26

Similar Documents

Publication Publication Date Title
US8303969B2 (en) Spreadable warming lubricant
US7709428B2 (en) Thickened spreadable warming lubricant
EP2108359B1 (en) Warming and nonirritating lubricant compositions
US20040138074A1 (en) Warming and nonirritating lubricant compositions and method of comparing irritation
JPH07145063A (en) Spermatocidal antiviral lubricant composition and its use
CA2484318C (en) Warming and nonirritating lubricant antifungal gel compositions
US7658941B2 (en) Warming and nonirritating lubricant compositions and method of comparing irritation
US20040167039A1 (en) Warming and nonirritating lubricant compositions and method of comparing irritation
US20050042249A1 (en) Warming and nonirritating lubricant compositions and method of comparing irritation
US20040185065A1 (en) Warming and nonirritating lubricant compositions and method of comparing irritation
US20130184233A1 (en) Personal Lubricant Compositions
WO2003092652A1 (en) Warming and nonirritating anhydrous lubricant compositions

Legal Events

Date Code Title Description
AS Assignment

Owner name: ANSELL HEALTHCARE PRODUCTS LLC, NEW JERSEY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:CHUAH, BENG SIM;LUCAS, DAVID M.;YEUN, TSUI SHIH;AND OTHERS;REEL/FRAME:016041/0331;SIGNING DATES FROM 20050412 TO 20050422

STCB Information on status: application discontinuation

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