WO1992016182A2 - Method for inactivating enveloped viruses and sperm - Google Patents

Method for inactivating enveloped viruses and sperm Download PDF

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Publication number
WO1992016182A2
WO1992016182A2 PCT/US1992/002427 US9202427W WO9216182A2 WO 1992016182 A2 WO1992016182 A2 WO 1992016182A2 US 9202427 W US9202427 W US 9202427W WO 9216182 A2 WO9216182 A2 WO 9216182A2
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WO
WIPO (PCT)
Prior art keywords
gelatin
solution
composition according
cellulose
betaine
Prior art date
Application number
PCT/US1992/002427
Other languages
French (fr)
Other versions
WO1992016182A3 (en
Inventor
Edwin B. Michaels
Original Assignee
E.B. Michaels Research Associates, Inc.
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 E.B. Michaels Research Associates, Inc. filed Critical E.B. Michaels Research Associates, Inc.
Priority to DE69206976T priority Critical patent/DE69206976T2/en
Priority to EP92909110A priority patent/EP0576585B1/en
Priority to KR1019930702779A priority patent/KR100202057B1/en
Priority to JP50884992A priority patent/JP3347727B2/en
Priority to CA002106682A priority patent/CA2106682C/en
Priority to AU19835/92A priority patent/AU663506B2/en
Publication of WO1992016182A2 publication Critical patent/WO1992016182A2/en
Publication of WO1992016182A3 publication Critical patent/WO1992016182A3/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/65Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • 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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2065Polyhydric alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/221Mono, di- or trisaccharides or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/225Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/384Animal products
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2041Dihydric alcohols
    • C11D3/2044Dihydric alcohols linear

Definitions

  • the present invention relates to novel viscous surfactant compositions that liquify or become less viscous under elevated conditions of shear or
  • compositions comprising amphoteric surface active agents having a high viscosity and which produce good lather or foam.
  • This invention also relates to a process for preparing these compositions. More particularly, the invention is concerned with compositions comprising betaines and amine oxides.
  • compositions of this invention can be used to prepare hair and body shampoos; hand cleansers; antiviral, antimicrobial or spermicidal compositions; and
  • gelatin can be used in creams and hair wave set lotions to raise the viscosity of the formulation.
  • gelatin forms rigid gels below 35'C, thereby making its use in personal hair care products, such as hand cleansers, hair and body shampoos difficult.
  • concentrations high enough to increase viscosity gelatin forms solid gels which become nonadherent and lumpy when subjected to mechanical stress.
  • Useful viscosities of personal care products for efficient delivery to the hair, hands, body and teeth for cleansing purposes are generally in the range of 500 to 30 , 000 cps .
  • Usual viscosity enhancing excipients such as natural and synthetic gums when used with amphoteric surfactants can increase the viscosity of such
  • U.S. Patent 4,451,385 discloses a liquid detergent composition comprising an anionic surfactant and a partially hydrolyzed protein fraction, rich in positively charged amino acids, having an isoionic point of 7 to 11 and a Bloom gel value of zero. This composition counters the irritation to the skin and eyes caused by the anionic surfactant, without
  • a specified surface active system which includes an anionic surfactant; a Type B gel-forming gelatin, having a Bloom strength of 50 - 300 and an isoelectric point between pH 4.6 and 5.0, and an amine oxide.
  • This composition forms a hydrophilic film on the surface of dishes when used as intended.
  • Type A gelatin is used in the compositions of the present invention.
  • the compositions of the present invention form a hydrophobic film on the treated
  • U.S. Patent 4,554,097 discloses an elastic detergent bar type product comprising a mixture of anionic and amphoteric synthetic organic detergents, gelatin and water, that is of use as a novelty to encourage children to bathe.
  • An amphoteric synthetic organic detergent can be triethanolammonium-1- carboxymethyl-1-carb ⁇ xyethoxyethyl-2-cocoimidazoliniumbetaine.
  • the product comprises 5 - 30% of gelatin, preferably Type A gelatin having a Bloom strength of 300.
  • the product can also contain 3 - 20% of lower dihydric or polyhydric alcohols.
  • U.S. Patents 4,207,198 and 4,439,355 disclose similar elastic detergent bars of improved foaming power after use. These bars comprise a mixture of anionic detergent with amphoteric synthetic organic detergents. Amphoteric detergents that can be used are imidazolinium betaines. The composition also comprises about 8 - 35% of gelatin having a Bloom strength of 100 - 300g and about 20 - 65% of a lower polyhydric alcohol.
  • Crotein Q a product of Croda Inc. of New York, is a cationic quaternary derivative of hydrolyzed collagen protein and has been used as an ingredient in hair cream rinses and other compositions containing anionic and other surface active agents.
  • compositions can be prepared from amphoteric surfactants, a Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 - 300,000 and polyhydric alcohols and minor amounts of nonionic cellulose gums.
  • composition comprising an amphoteric surfactant comprising a mixture of betaines and amine oxides; Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 - 300,000, polyhydric alcohols and nonionic cellulose gums and optionally lower aliphatic alcohols have increased viscosity and exhibit good lathering and foaming.
  • a primary object of the present invention is to provide personal care compositions, such as hand cleansers, hair and body shampoos having
  • Another object of the invention is to provide antiviral, antimicrobial or spermicidal compositions that are less toxic to mammalian tissues or cells.
  • Still another object of the invention is to provide a composition that can be used in dentrifices.
  • Another object of this invention is to provide a process for producing these compositions.
  • compositions comprising a mixture of an amine oxide and betaines as amphoteric surfactants; Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 - 300,000; polyhydric alcohols and nonionic cellulose gums and optionally lower aliphatic alcohols have increased viscosity with good lathering and foaming properties.
  • This invention overcomes a problem in the art, namely to increase the viscosity of personal care
  • This invention overcomes inherent problems when gums or other thickening agents are added to amphoteric surfactants.
  • compositions relate to skin integrity, antimicrobial activity (i.e. antibacterial, antiviral, antifungal) and oral health.
  • antimicrobial activity i.e. antibacterial, antiviral, antifungal
  • oral health i.e. antibacterial, antiviral, antifungal
  • formulations are of special value for cosmetic and pharmaceutical preparations.
  • Amphoteric surfactants agents of use in the present invention include those of the type disclosed in U.S. Patent 4,839,158, which describes mixtures of betaines and amine oxides.
  • the betaines used in this invention are selected from the group consisting of (a) alkyl-N-betaines, alkyl-N-sulfobetaines, acyl-N- betaines, and mixtures of two or more thereof.
  • the amine oxides used in this invention are selected from the group consisting of b) alkyl-N,N-dimethylamine oxides, alkyl-N,N-dihydroxyethylamine oxides or
  • betaine when used herein means N-dimethyl glycine and its lower alkyl homologs. Unless otherwise specified an N-dimethyl compound is intended.
  • sulfobetaine or sultaine means the sulfuric acid analog of such betaines.
  • the acid necessary to supply the required pH to the amphoteric surfactants can be any organic or
  • inorganic acid such as hydrochloric acid, phosphoric acid, sulfuric acid, citric acid, acetic acid or
  • the operating pH for the surfactant composition is 4.5 to 7.0 preferably, from about 4.5 to 6.5.
  • the pH of an aqueous solution comprising the above enumerated components is determined by employing an aqueous solution of 0.5%, by weight, total of active components typically at a glass electrode, to precisely define the acidity.
  • alkyl-N-betaine, the alkyl-N-sulfobetaine and the acyl-N-betaine employed as the components (a) of the composition of the invention have structures, respectively, as follows:
  • R is a higher alkyl group having from 10 to 18 carbon atoms, preferably from 12 - 16 carbon atoms and where n is from 1 to 3.
  • coco-N-betaine cetyl-N-betaine, stearyl-N-betaine, isostearyl-N-betaine, oleyl-N- betaine
  • coco-N-sulphobetaine cetyl-N- sulphobetaine, stearyl-N-sulfobetaine, isostearyl-N- sulfobetaine, oleyl-N-sulfobetaine
  • cocoamido-N- betaine cetylamido-N-betaine, stearylamido-N-betaine, isostearylamido-N-betaine, oleyl-amino-N-betaine.
  • coco is that used in the CTFA (designations of Cosmetic and Toiletry and Fragrance Association, Wash., D.C.) and is used to indicate alkyl groups present in coconut oil, i.e. a mixture of alkyl groups of from 10 to 18 carbon atoms.
  • CTFA Cosmetic and Toiletry and Fragrance Association, Wash., D.C.
  • alkyl groups present in coconut oil i.e. a mixture of alkyl groups of from 10 to 18 carbon atoms.
  • the designations of the compounds listed herein are those of the CTFA.
  • R is a higher alkyl group of from 10 to 18 carbon atoms for instance a radical such as decyl, undecyl, lauryl, tridecyl, myristyl, cetyl, stearyl, isostearyl or oleyl.
  • amine oxides are: decylN,N-dimethylamine oxide, lauryl-N,N-dimethylamine oxide, stearyl-N-N-dimethylamine oxide, oleyl-N,N-dimethylamine oxide, coco-N,N dihydroxyethylamine oxide, cetyl-N,N-dihydroxyethylamine oxide, oleyl-N,N-dihydroxyethylamine oxide, N,N-dihydroxyethylamine oxide, oleyl-N,-N-dihydroxyethyl-amine oxide and mixtures of the same.
  • the betaine can be a alkyl-N-di (lower alkyl) betaine preferably an alkyl N-dimethyl betaine and the amine oxide can be an alkyl-N-di (lower alkyl) amine oxide preferably an alkyl N-dimethyl amine oxide.
  • the lower alkyl is C 1-3 .
  • hydrolyzed collagen has inherently low viscosity under conditions where it is not forming rigid gels, is used in these compositions to form high
  • Gelatins such as those used in this invention are characterized by their Bloom Strength (Standard Methods for Sampling and Testing of Gelatins, Gelatin Manufacturers Institute of America, Inc., New York).
  • Type A gelatins as used in this invention are produce by acid processing of collagenous raw materials and have an isoelectric point between pH 7 and 9.
  • Type B gelatins are produced by alkaline or lime processing and have an isoelectric point between pH 4.6 and 5.2.
  • Use of Type B gelatin in compositions analogous to those of this invention inhibits the properties which are useful in this invention as the properties of the surfactants used in this invention are not compatible with Type B gelatin.
  • Type A gelatins useful in this invention will have Bloom strengths of 100 to 300. Such gelatins will have average molecular weights from about 75,000 to 300,000.
  • Illustrative of the polyhydric alcohols useful in this invention are glycerine, propylene gly ⁇ ol, xylitol, sorbitol, and mannitol.
  • Cellulose gums useful in this invention are the nonionic gums such as
  • cellulose gums are those of high
  • cellulose gums are, synthetic materials having some properties analogous to said gums such as polyvinyl alcohol, polyvinyl pyrrolidone and some polyacrylic acid polymer.
  • Lower aliphatic alcohols useful in this invention are ethyl, n-propyl and
  • compositions of this invention contain generally the following components in aqueous solution:
  • Type A gelatin having a Bloom strength of 100-300 and a molecular weight from 75,000 to 300,000;
  • compositions of the present invention are preferably, compositions of the present invention.
  • compositions of the present invention may include a polishing agent. Any such agent used however should not be one that absorbs the surfactant. Thus most silica based polishing agents should be avoided.
  • One polishing agent that is of use is dicalcium
  • This improvement is related to a moisturizing effect obtained by conserving skin hydration, which is enhanced by formulation with the above excipients.
  • compositions can be used as topical antiinfective compositions.
  • compositions along the lines disclosed above have been used to prepare gel dentifrices which rapidly become low viscosity fluids at the mechanical stress levels and body temperatures experienced in tooth
  • compositions of this invention have been used to prepare antiviral compositions for prophylactic use in preventing sexually transmitted diseases. This is the subject of a copending U.S. application filed on March 22, 1991, Attorney Docket no. U8185. Compositions of this type are non-irritating to mammalian cells and decrease the toxicity of antimicrobial agents. These compositions can also be used to aid wound healing.
  • Amphoteric surfactants that can be used in this invention are described in Examples 1 - 5.
  • composition described below is a concentrate of C31G, an equimolar preparation of
  • cocobetaine and cocodimethylamine oxides (designations of CTFA Cosmetic and Toiletry and Fragrance Association, Wash., D.C.) [CFTA] which can be used in a number of different configurations.
  • This composition is disclosed in US Patent # 4,839,158 issued to E.B. Michaels.
  • Cocobetaine 31.5% active ingredient (Al) :
  • Citric acid monohydrate USP: 26 lb.
  • Concentrate ⁇ CCon ⁇ comprises:
  • Lauryl Betaine (30% ai) 1000 pts Lauramine Oxide (30% ai) 870 pts
  • the composition should have a pH of 4.85 at the glass electrode.
  • Citric acid monohydrate 6.8 lbs
  • Purified water 100 lbs.
  • Citric acid monohydrate USP 60 lbs
  • Purified water USP: 100 lbs
  • the excipients are dyes and fragrances.
  • Viscosity was measured by using a Brookfield viscometer at low stress level equivalent to pouring. 3. Method of Hand Lathering
  • Method of shower lathering Foam level 0 - 5 based upon a volume of shampoo used. The amount of lathering produced on hair and body using a standard washing polyurethane sponge. Rating of 5 would be equivalent to use with a natural soap (Ivory liquid soap) . Amount of soap used per shower would vary between 10 and 30 gms.
  • gelatin should be added by sprinkling into vortex of water heated to 60oC. and stirred for short period of time to complete solution, maintaining the temperature between 40 - 50oC.
  • the gelatin solution is then transferred to the mixture of surfactants with residual water containing excipients and finally stirred with the hydrated cellulose gum to uniform solution. Note - high speed agitation should not be used as cellulose gum will be degraded.
  • Agitation should be strong enough as to avoid the partially hydrated cellulose gum from escaping agitation as the partially hydrated gum will have specific gravity greater than water.
  • the flavors are stirred into the glycerine mixed with the alcohol.
  • the gelatin and cellulose gums are triturated together and added to surfactant which is warmed to 30 - 35oC. and stirred to hydrate the gum and gelatin.
  • the saccharin and fluoride are dissolved in a small portion of water at 50oC. and are added to the hydrated solution of gums and surfactants.
  • glycerine and alcohol solution of the flavors are then added and the mixtures maintained at a temperature of 30 - 35oC.
  • the dentrifice can be packaged before the mixture has cooled below 30oC.
  • Clear fluid contraceptive jellies are prepared by substitution of 1.5 pts or high viscosity grade of hydroxypropyl or hydroxypropylmethyl cellulose for the gelatin and hydroxyethyl cellulose of the above
  • Creme formulations by incorporation of 0.5 pts of cetyl alcohol in Gel 1 or 2 formulations by dissolving the alcohol in the glycerine at 40oC. before trituration of the gelatin and cellulose gum.

Abstract

High viscosity fluids comprising amphoteric surfactants and Type A gelatin. These compositions can be used in shampoos, dentrifices and cosmetic and pharmaceutical preparations.

Description

METHOD FOR INACTIVATING ENVELOPED VIRUSES AND SPERM BACKGROUND OF THE INVENTION FIELD OF THE INVENTION
The present invention relates to novel viscous surfactant compositions that liquify or become less viscous under elevated conditions of shear or
temperature. In particular it relates to compositions comprising amphoteric surface active agents having a high viscosity and which produce good lather or foam. This invention also relates to a process for preparing these compositions. More particularly, the invention is concerned with compositions comprising betaines and amine oxides. Type A gelatin, non-ionic cellulose and polyhydric alcohols. These compositions can also optionally include lower aliphatic alcohols.
Compositions of this invention can be used to prepare hair and body shampoos; hand cleansers; antiviral, antimicrobial or spermicidal compositions; and
dentrifices.
DESCRIPTION OF THE PRIOR ART
It is known to add viscosity enhancing agents such as gums or other thickening compounds to amphoteric surfactants.
It is known that gelatin can be used in creams and hair wave set lotions to raise the viscosity of the formulation. However, gelatin forms rigid gels below 35'C, thereby making its use in personal hair care products, such as hand cleansers, hair and body shampoos difficult. At concentrations high enough to increase viscosity, gelatin forms solid gels which become nonadherent and lumpy when subjected to mechanical stress.
Useful viscosities of personal care products for efficient delivery to the hair, hands, body and teeth for cleansing purposes are generally in the range of 500 to 30 , 000 cps .
Usual viscosity enhancing excipients such as natural and synthetic gums when used with amphoteric surfactants can increase the viscosity of such
solutions. However, when they are used to raise the viscosity much above 500 centipoises (cps) there is a marked decrease in the lathering properties of the surfactants.
U.S. Patent 4,451,385 (Tavss et al.) discloses a liquid detergent composition comprising an anionic surfactant and a partially hydrolyzed protein fraction, rich in positively charged amino acids, having an isoionic point of 7 to 11 and a Bloom gel value of zero. This composition counters the irritation to the skin and eyes caused by the anionic surfactant, without
decreasing the foaming and detergency properties
imparted to the composition by said anionic surfactant.
U.S. Patent 3,898,186 (Mermelstein et al.) discloses a mild liquid dishwashing composition
containing a specified surface active system which includes an anionic surfactant; a Type B gel-forming gelatin, having a Bloom strength of 50 - 300 and an isoelectric point between pH 4.6 and 5.0, and an amine oxide. This composition forms a hydrophilic film on the surface of dishes when used as intended.
Type A gelatin is used in the compositions of the present invention. The compositions of the present invention form a hydrophobic film on the treated
surfaces.
U.S. Patent 4,554,097 (Schebece) discloses an elastic detergent bar type product comprising a mixture of anionic and amphoteric synthetic organic detergents, gelatin and water, that is of use as a novelty to encourage children to bathe. An amphoteric synthetic organic detergent can be triethanolammonium-1- carboxymethyl-1-carbσxyethoxyethyl-2-cocoimidazoliniumbetaine. The product comprises 5 - 30% of gelatin, preferably Type A gelatin having a Bloom strength of 300. The product can also contain 3 - 20% of lower dihydric or polyhydric alcohols.
U.S. Patents 4,207,198 and 4,439,355 (Kenkare) disclose similar elastic detergent bars of improved foaming power after use. These bars comprise a mixture of anionic detergent with amphoteric synthetic organic detergents. Amphoteric detergents that can be used are imidazolinium betaines. The composition also comprises about 8 - 35% of gelatin having a Bloom strength of 100 - 300g and about 20 - 65% of a lower polyhydric alcohol.
Crotein Q, a product of Croda Inc. of New York, is a cationic quaternary derivative of hydrolyzed collagen protein and has been used as an ingredient in hair cream rinses and other compositions containing anionic and other surface active agents.
None of the above cited art discloses a gel type or high viscosity liquid composition having
increased viscosity with good lathering or forming potential. I have found that such compositions can be prepared from amphoteric surfactants, a Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 - 300,000 and polyhydric alcohols and minor amounts of nonionic cellulose gums.
The characteristics of gels formed by gelatin alone even when diluted or prepared with gelatin of low Bloom strength, show poor adherence and lack of
uniformity. In contrast to the present invention, such products are not useful for a high viscosity fluid cosmetic or pharmaceutical products.
SUMMARY OF THE INVENTION
It has been found that a composition comprising an amphoteric surfactant comprising a mixture of betaines and amine oxides; Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 - 300,000, polyhydric alcohols and nonionic cellulose gums and optionally lower aliphatic alcohols have increased viscosity and exhibit good lathering and foaming.
Accordingly, a primary object of the present invention is to provide personal care compositions, such as hand cleansers, hair and body shampoos having
enhanced viscosity and good lathering or foaming
properties.
Another object of the invention is to provide antiviral, antimicrobial or spermicidal compositions that are less toxic to mammalian tissues or cells.
Still another object of the invention is to provide a composition that can be used in dentrifices.
Another object of this invention is to provide a process for producing these compositions.
DETAILED DESCRIPTION OF THE INVENTION
Compositions comprising a mixture of an amine oxide and betaines as amphoteric surfactants; Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 - 300,000; polyhydric alcohols and nonionic cellulose gums and optionally lower aliphatic alcohols have increased viscosity with good lathering and foaming properties.
This invention overcomes a problem in the art, namely to increase the viscosity of personal care
products without decreasing the lathering or foaming potential of the products. This invention overcomes inherent problems when gums or other thickening agents are added to amphoteric surfactants.
Other unexpected advantages of these compositions relate to skin integrity, antimicrobial activity (i.e. antibacterial, antiviral, antifungal) and oral health. These formulations are of special value for cosmetic and pharmaceutical preparations.
Amphoteric surfactants agents of use in the present invention include those of the type disclosed in U.S. Patent 4,839,158, which describes mixtures of betaines and amine oxides. The betaines used in this invention are selected from the group consisting of (a) alkyl-N-betaines, alkyl-N-sulfobetaines, acyl-N- betaines, and mixtures of two or more thereof. The amine oxides used in this invention are selected from the group consisting of b) alkyl-N,N-dimethylamine oxides, alkyl-N,N-dihydroxyethylamine oxides or
acylamide t-amine oxides and mixtures of two or more thereof. The term betaine when used herein means N-dimethyl glycine and its lower alkyl homologs. Unless otherwise specified an N-dimethyl compound is intended. The term sulfobetaine or sultaine means the sulfuric acid analog of such betaines.
Typically, the betaine and amine oxide
components are present in a molar ratio of from 1:5 to 5:1, preferably in a molar ratio of about 1:1. In general, the acid necessary to supply the required pH to the amphoteric surfactants can be any organic or
inorganic acid, such as hydrochloric acid, phosphoric acid, sulfuric acid, citric acid, acetic acid or
nicotinic acid. The operating pH for the surfactant composition is 4.5 to 7.0 preferably, from about 4.5 to 6.5. The pH of an aqueous solution comprising the above enumerated components is determined by employing an aqueous solution of 0.5%, by weight, total of active components typically at a glass electrode, to precisely define the acidity.
The alkyl-N-betaine, the alkyl-N-sulfobetaine and the acyl-N-betaine employed as the components (a) of the composition of the invention have structures, respectively, as follows:
Figure imgf000008_0001
Figure imgf000008_0002
or
Figure imgf000008_0003
Figure imgf000008_0004
where R is a higher alkyl group having from 10 to 18 carbon atoms, preferably from 12 - 16 carbon atoms and where n is from 1 to 3.
Illustrative of these aforementioned substances are: (1) coco-N-betaine, cetyl-N-betaine, stearyl-N-betaine, isostearyl-N-betaine, oleyl-N- betaine; (2) coco-N-sulphobetaine, cetyl-N- sulphobetaine, stearyl-N-sulfobetaine, isostearyl-N- sulfobetaine, oleyl-N-sulfobetaine; and (3) cocoamido-N- betaine, cetylamido-N-betaine, stearylamido-N-betaine, isostearylamido-N-betaine, oleyl-amino-N-betaine.
When used here the term "coco" is that used in the CTFA (designations of Cosmetic and Toiletry and Fragrance Association, Wash., D.C.) and is used to indicate alkyl groups present in coconut oil, i.e. a mixture of alkyl groups of from 10 to 18 carbon atoms. The designations of the compounds listed herein are those of the CTFA.
The (1) alkyl-N,N-diethylamine oxide, (2) alkyl-N,N-dihydroxylethylamine oxide, or (3)
acylamide t-amine oxide employed as component (b) of the aforementioned mixture, respectively, have the
structure:
Figure imgf000009_0001
Figure imgf000009_0002
Figure imgf000009_0003
where R is a higher alkyl group of from 10 to 18 carbon atoms for instance a radical such as decyl, undecyl, lauryl, tridecyl, myristyl, cetyl, stearyl, isostearyl or oleyl. Exemplary of the amine oxides are: decylN,N-dimethylamine oxide, lauryl-N,N-dimethylamine oxide, stearyl-N-N-dimethylamine oxide, oleyl-N,N-dimethylamine oxide, coco-N,N dihydroxyethylamine oxide, cetyl-N,N-dihydroxyethylamine oxide, oleyl-N,N-dihydroxyethylamine oxide, N,N-dihydroxyethylamine oxide, oleyl-N,-N-dihydroxyethyl-amine oxide and mixtures of the same.
The betaine can be a alkyl-N-di (lower alkyl) betaine preferably an alkyl N-dimethyl betaine and the amine oxide can be an alkyl-N-di (lower alkyl) amine oxide preferably an alkyl N-dimethyl amine oxide. The lower alkyl is C1-3. Gelatin, a high molecular weight
preparation of hydrolyzed collagen has inherently low viscosity under conditions where it is not forming rigid gels, is used in these compositions to form high
viscosity or non-rigid gel compositions.
Gelatins such as those used in this invention are characterized by their Bloom Strength (Standard Methods for Sampling and Testing of Gelatins, Gelatin Manufacturers Institute of America, Inc., New York).
Type A gelatins as used in this invention, are produce by acid processing of collagenous raw materials and have an isoelectric point between pH 7 and 9. Type B gelatins are produced by alkaline or lime processing and have an isoelectric point between pH 4.6 and 5.2. Use of Type B gelatin in compositions analogous to those of this invention inhibits the properties which are useful in this invention as the properties of the surfactants used in this invention are not compatible with Type B gelatin. In order to produce the high viscosity fluids. Type A gelatins useful in this invention will have Bloom strengths of 100 to 300. Such gelatins will have average molecular weights from about 75,000 to 300,000.
Without wishing to be bound by any particular theories, it is generally believed that solid gel formation of gelatin is the result of hydrogen bond formation between the peptide chains of hydrolyzed collagen. These bonds are readily broken by increasing the temperature to above the melting point of the aqueous gel (usually about 35º - 40ºC). The bonds reform upon cooling. It should be noted that the viscosity of gelatins are usually independent of Bloom strength, however, in the range of Bloom strength noted above (100 - 300), the viscosity in the compositions of this disclosure, increase with the molecular weight of the gelatin.
Illustrative of the polyhydric alcohols useful in this invention are glycerine, propylene glyσol, xylitol, sorbitol, and mannitol. Cellulose gums useful in this invention are the nonionic gums such as
hydroxyethyl, hydroxypropyl and hydroxypropylmethyl celluloses. The cellulose gums are those of high
molecular weight. Other possible polymers are that may be used in place of the cellulose gums are, synthetic materials having some properties analogous to said gums such as polyvinyl alcohol, polyvinyl pyrrolidone and some polyacrylic acid polymer. Lower aliphatic alcohols useful in this invention are ethyl, n-propyl and
isopropyl alcohols.
The compositions of this invention contain generally the following components in aqueous solution:
0.2 - 40% Active Ingredient Amphoteric surfactant;
0.3 - 10% Type A gelatin having a Bloom strength of 100-300 and a molecular weight from 75,000 to 300,000;
0.5 - 30% polyhydric alcohols;
0.1% - 1.5% cellulose gums; and
0.0 - 5% lower aliphatic alcohols.
Lower chain length surfactants (e.g. coco derivatives) of the amphoteric surfactants have
inherently low viscosities at useful concentrations and have the most useful foaming and lathering properties as compared to longer chain lengths.
Higher chain length derivatives (e.g. myristyl or cetyl derivatives) are useful at low
concentration in oral hygiene products such as
dentifrices which can benefit from having a high
viscosity for dose delivery.
Typically, compositions of the present
invention have a viscosity in the range 500 to 100,000 cps, preferably 1,000 to 30,000 cps. Dentrifices of this invention typically have a viscosity of 20,000 - 50,000 cps, preferably about 30,000 cps. When used as a dentrifice compositions of the present invention may include a polishing agent. Any such agent used however should not be one that absorbs the surfactant. Thus most silica based polishing agents should be avoided. One polishing agent that is of use is dicalcium
phosphate dihydrate.
Compositions of this invention have shown particular advantages such as:
1. Gelation of the product is avoided at the ambient temperature that personal care products are normally stored and used. The viscosity remains high enough to use in the higher ambient temperatures without dripping from areas of use. 2. Synergistic effects are experienced in the combination of the mild low toxicity surfactants with the compositions above, in sharply reducing dry skin (xeroderma). This problem is serious with older people using surfactants, particularly in winter climates.
This improvement is related to a moisturizing effect obtained by conserving skin hydration, which is enhanced by formulation with the above excipients.
3. These compositions can be used as topical antiinfective compositions.
In accordance with this invention, it is possible to provide high viscosity fluids which liquify under mechanical stress and at body temperature. Such products have special application in dentifrices and, in antiinfective topical agents where the high viscosity aids in dose delivery and the decrease in viscosity results in dose efficacy.
It has been demonstrated that liquid products applied in oral hygiene are more effective than the gels or pastes which are commonly used as dentifrices. Gels and pastes inhibit delivery to interproxal and sulces areas of dentition.
Compositions along the lines disclosed above have been used to prepare gel dentifrices which rapidly become low viscosity fluids at the mechanical stress levels and body temperatures experienced in tooth
brushing. This results in enhanced therapeutic
properties of dentifrices having germicidal properties, in that the stress of brushing and the temperature in the oral cavity results in the penetration and
adsorption of the therapeutic and cleansing ingredients to the subgingival sulcus and intraproximal areas of dentition.
Compositions of this invention have been used to prepare antiviral compositions for prophylactic use in preventing sexually transmitted diseases. This is the subject of a copending U.S. application filed on March 22, 1991, Attorney Docket no. U8185. Compositions of this type are non-irritating to mammalian cells and decrease the toxicity of antimicrobial agents. These compositions can also be used to aid wound healing.
A fuller understanding of the present invention will be gained from the following illustrative examples.
Example 1
Amphoteric surfactants that can be used in this invention are described in Examples 1 - 5.
The composition described below is a concentrate of C31G, an equimolar preparation of
cocobetaine and cocodimethylamine oxides (designations of CTFA Cosmetic and Toiletry and Fragrance Association, Wash., D.C.) [CFTA] which can be used in a number of different configurations. This composition is disclosed in US Patent # 4,839,158 issued to E.B. Michaels.
Cocobetaine; 31.5% active ingredient (Al) :
405.5 lb,
Cocamine oxide, 31.5% (Al) : 325 lb.
Citric acid monohydrate, USP: 26 lb.
Purified water, USP: 26 lb.
To make about 782.5 lb C31G at 29.6% Al at a dilution 1% Al; pH - 4.9.
Example 2
Formulations for Contraceptive/Antilnfective
Preparations
Concentrate {CCon} comprises:
Lauryl Betaine (30% ai) 1000 pts Lauramine Oxide (30% ai) 870 pts
Citric Acid monohydrate 69 pts
The above are stirred to a uniform solution. At a dilution of one part to 30, the composition should have a pH of 4.85 at the glass electrode. Putative
concentration equal to 28.5% active ingredients (ai). Example 3
Cetyl betaine 20% AI: 200 lbs
Myristamine oxide 30% AI: 95 lbs
Citric acid monohydrate: 6.8 lbs
Purified water: 100 lbs.
To make about 402 lbs at 17% AI, at dilution 1% AI; pH 4.9.
Example 4
Coco amido propylbetaine 30% AI: 530 lbs Cocoamido propylamine oxide 30% AI: 470 lbs
Citric acid monohydrate, USP 60 lbs Purified water, USP: 100 lbs
To make about 1160 lbs at 25.9% AI at a dilution 1% AI, pH = 4.9.
Example 5
Cocosultaine, 30% AI 347 lbs
Cocoamine oxide 30% AI 240 lbs
Citric acid monohydrate 24 lbs
Water 100 lbs
To make about 711 lb at 24.8% AI at a dilution % AI, pH = 5.0.
BODY AND HAIR SHAMPOO EXAMPLES
(Examples 6 - 13)
Ex 12 Ex . 15
Ex Ex Ex Ex Ex 10 Ex 117 Prell7 Pert plus6
Surfactant Ex. 1 Ex. 1 Ex. 1 Ex. 1 Ex. 1 Ex . 2 anionic anionic % 7.5 9.0 9.0 9.0 9.0 9.0 N/A N/A
Gelatin Type A200 - - A200 A200 B250 - - % 1.0 - - 1.0 1.0 1.25 - -
Hydroxy Propyl 0.4 0.6 - 0.3 - - - - Cellulose %
Glycerine % 1.0 1.0 - 0.5 - - - -
Excipient + + - - - + + +
Viscosity (cps) 4 .00 800 80 3000 300-3000 1500 5000 4000
Lathering hand3 4.0 3.0 3.5 4.5 4.05 2.5 4.0 4.5 Lathering shower4 4.0 3.0 3.0 4.5 - 2.5 4.0 4.5
Notes
1. The excipients are dyes and fragrances.
2. Viscosity was measured by using a Brookfield viscometer at low stress level equivalent to pouring. 3. Method of Hand Lathering
a) clean hands
b) dilute concentrate 1:5
c) rubbing hand against other hand for 60 sec.
d) observe foam level at rating 0 - 5
4. Method of shower lathering Foam level 0 - 5 based upon a volume of shampoo used. The amount of lathering produced on hair and body using a standard washing polyurethane sponge. Rating of 5 would be equivalent to use with a natural soap (Ivory liquid soap) . Amount of soap used per shower would vary between 10 and 30 gms.
5. Preparation was uneven and lumpy and was difficult to pour uniform amounts of preparation.
Viscosity varied according to amount of premixing of preparation.
6. These shampoos were used as controls. They are available commercial shampoos that have been rated by expert panels. Prell is an average foaming shampoo. Pert PlusR is the highest foaming shampoo available on the commercial market Consumer Reports, Feb. 1989
7. Viscosity is uneven, solution is very cloudy.
Method for Preparing Shampoos
An adequate portion of water (10X weight of cellulose gum to be used) is heated to 80ºC. Cellulose gum is sprinkled into the vortex of water creating a slurry that is quickly transferred to at least 5X vol. of cold water and stirred for complete hydration by rapidly cooling to below 35ºC.
Separately, gelatin should be added by sprinkling into vortex of water heated to 60ºC. and stirred for short period of time to complete solution, maintaining the temperature between 40 - 50ºC. The gelatin solution is then transferred to the mixture of surfactants with residual water containing excipients and finally stirred with the hydrated cellulose gum to uniform solution. Note - high speed agitation should not be used as cellulose gum will be degraded.
Agitation should be strong enough as to avoid the partially hydrated cellulose gum from escaping agitation as the partially hydrated gum will have specific gravity greater than water.
DENTIFRICE EXAMPLES
(Examples 14 - 18)
Ex. 14 Ex. 15 Ex. 16 Ex. 17 Ex. 18
Surfactant Ex. 3 Ex. 3 Ex. 3 Ex. 3 Ex. 3
0.9 0.9 0.9 0.9 0.9
% AI
Gelatin Type A200 A300 A300 A200 -
% 2.0 1.0 1.0 1.5 -
Hydroxy Ethyl
Cellulose % 0.2 0.4 0.4 0.4 1.5
Glycerine % 11.0 6.0 6.0 6.0 2.0
Alcohol SDA38B1% - - 5.0 - 5.0
Excipient2
Viscosity3 3700 3500 3900 28000 52000
300 1000 1000 100 170001USP 200 proof alcohol, denatured with 1.5% mint flavor 2Excipients are 0.375% mint flavor N.F.
0.02% soluble saccharin U.S.P.
0.04% sodium fluoride U.S.P.
3Brookfield viscosity at pour stress at 70ºF. over viscosity at brush stress at 95ºF.
All of the gelatin gels are firm enough gels to stand up on the toothbrush. Upon delivery of the dentrifice to the dentition on brushing, the viscosity drops by about 99%, whereas with high viscosity
cellulose gum (without gelatin), the dentrifice
viscosity will drop less than 70% under same conditions and will be less effective. This dentrifice (without the gelatin) retains a high viscosity which inhibits the energy of tooth brushing, gum massage and diffusion of the therapeuticagent.
Preparation of Dentrifices
The flavors are stirred into the glycerine mixed with the alcohol. The gelatin and cellulose gums are triturated together and added to surfactant which is warmed to 30 - 35ºC. and stirred to hydrate the gum and gelatin. The saccharin and fluoride are dissolved in a small portion of water at 50ºC. and are added to the hydrated solution of gums and surfactants. The
glycerine and alcohol solution of the flavors are then added and the mixtures maintained at a temperature of 30 - 35ºC. The dentrifice can be packaged before the mixture has cooled below 30ºC.
Example 19
Spermicidal Gels, Cremes or Jellies for use with Cervical Caps, Condoms, Diaphragms or alone prior to coitus.
Gel-1
CCon of Example 2 7.0 pts
Gelatin A200 1.5 pts
Glycerine 10.0 pts
Hydroxyethyl Cellulose
(high viscosity Grade) 0.4 pts
Water 81.1 pts
Procedure - The gelatin and cellulose gum are triturated in the glycerine and added to the water at 45ºC. and stirred to solution. The surfactants are added to the vessel and the warm solution removed for packaging. A uniform fluid high viscosity gel forms on cooling. Example 20
Jelly 1 and 2
Clear fluid contraceptive jellies are prepared by substitution of 1.5 pts or high viscosity grade of hydroxypropyl or hydroxypropylmethyl cellulose for the gelatin and hydroxyethyl cellulose of the above
examples.
Example 21
Cremes 1 and 2
The Gel formulations above are converted to
Creme formulations by incorporation of 0.5 pts of cetyl alcohol in Gel 1 or 2 formulations by dissolving the alcohol in the glycerine at 40ºC. before trituration of the gelatin and cellulose gum.
Example 22
Contraceptive Film
6.2 lbs of gelatin A100 is triturated with 0.5 lbs of hydroxyethylcellulose. 31 lbs of glycerine are added. Solution is mixed thoroughly to form a slurry. Add 33 lbs of CCon of Example 2 and 15 lbs of water.
Warm to 40ºC. Mix until gums and gelatin are completely hydrated. Solution is poured on polyethylene sheet to cast a film of about 3 mm thick to be cut for films to be used as contraceptive films after cooling.
Example 23
Ointment for Xeroderma
2.5 lbs of petroleum jelly is warmed to 40ºC. Then mixed with 1 lb of shampoo of Example 6. Stir while cooling.
Used for moisturizing and eliminating scaly skin caused by xeroderma.

Claims

C LA I MS
1. A high viscosity fluid composition comprising:
a) 0.2 - 40% of an amphoteric surfactant which comprises a mixture of betaines and amine oxides wherein the betaine is selected from the group consisting of alkyl-Nbetaines, alkyl-N-sulfobetaines and aσyl-N-betaines, and the amine oxide is selected from the group consisting of alkylN,N-dimethylamine oxide, alkyl-N,N-dihydroxyethylamine oxide and acylamide t-amine oxide;
b) 0.3 - 10% of Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 to 300,000;
c) 0.5 - 30% polyhydric alcohol;
d) 0.1 - 1.5% nonionic cellulose gum or synthetic analog thereof; and
e) 0.0 - 5% lower aliphatic alcohols.
2. A composition according to claim 1, wherein the amphoteric surfactant comprises an alkyl-N-di (methyl) betaine and an alkyl-N-di (methyl) amine oxide.
3. A composition according to any one of the previous claims, wherein the betaine is selected from the group consisting of cocobetaine, lauryl betaine, cetyl betaine, cocoamidopropyl betaine and coco sultaine, and the amine oxide is selected from the group consisting of cocamine oxide, lauramine oxide, myristamine oxide and cocoamido propyl amine oxide.
4. A composition according to any of the previous claims, wherein the polyhydric alcohol is selected from the group consisting of glycerine, propylene glycol, xylitol, sorbitol and mannitol.
5. A composition according to any of the previous claims, wherein the cellulose gum is selected from the group consisting of hydroxyethyl cellulose, hydroxypropyl
cellulose and hydroxypropylmethyl cellulose.
6. A composition according to any of the previous claims, wherein the aliphatic alcohol is selected from the group consisting of ethyl, n-propyl and isopropyl alcohol.
7. A composition according to any of the previous claims, wherein a cellulose gum analog is selected from the group consisting of polyvinyl alcohol, polyvinyl pyrrolidone and polyacrylic acid polymers.
8. A composition according to any of the previous claims, wherein said betaine and said amine oxide are present in a ratio of from 1:5 to 5:1.
9. A composition according to any one of the previous claims, suitable for use as a dentrifice further comprising flavoring agents.
10. A composition according to any one of claims 1-8, suitable for use as a shampoo further comprising dyes and fragrances.
11. A composition according to any one of claims 1-8, suitable for use as an ointment further comprising petroleum jelly.
12. A composition according to any one of claims 1-8, suitable for use with cervical caps, condoms, diaphragms or alone.
13. A method of preparing a high viscosity fluid according to any of the previous claims, comprising:
adding cellulose gum to water,
stirring the solution to hydrate the cellulose gum;
separately preparing a solution of gelatin in water.
transferring the gelatin solution to a mixture of amphoteric surfactants, comprising betaines and amine oxides;
adding the solution containing gelatin and surfactants to the solution of hydrated cellulose gums, and stirring to uniform solution.
14. A method according to any of the previous claims of preparing a composition which is a dentrifice comprising:
a) mixing glycerine and an additional polyhydric alcohol in an amount to constitute 0.5 - 30% of the
dentrifice;
b) triturating Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 to 300,000 and cellulose gums together and adding to an
amphoteric surfactant comprising a mixture of betaines and amine oxides; said gelatin being in an amount to constitute 0.3 - 10% of the dentrifice, said cellulose gums being in an amount to constitute 0.1 - 1.5% of the dentrifice, and said amphoteric surfactant being in an amount to constitute 0.2 - 40% of the dentrifice;
c) warming the solution of step (b) to 30 - 35ºC. and stirring to hydrate the gum and gelatin; and
d) adding the solution of step (a) to the
solution of step (σ) and maintaining the combined solution at 30 - 35ºC.
15. A method according to any of the previous claims for preparing a high viscosity fluid comprising:
adding a nonionic cellulose gum to water in an amount to constitute 0.1 - 1.5% of the fluid,
stirring the solution to hydrate the cellulose gum,
preparing a separate solution of gelatin by adding Type A gelatin having a Bloom strength of 100 - 300 and a molecular weight from 75,000 to 300,000 to water in an amount to constitute 0.3 - 10% of the fluid;
transferring the gelatin solution to a mixture of amphoteric surfactants, said mixture comprising a betaine or betaines, and an amine oxide or amine oxides, so that the amphoteric surfactant comprises 0.2 - 40% of the fluid,
adding the solution containing gelatin and surfactants to the solution of hydrated cellulose gums, and stirring to uniform solution.
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EP0719137A1 (en) * 1993-09-13 1996-07-03 E.B. Michaels Research Associates, Inc. Viscous surfactant emulsion compositions
EP0719137A4 (en) * 1993-09-13 1997-06-04 Michaels E B Res Ass Viscous surfactant emulsion compositions
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US6616922B2 (en) 2001-03-27 2003-09-09 The Dial Corporation Antibacterial compositions
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EP0576585A1 (en) 1994-01-05
EP0576585B1 (en) 1995-12-20
CA2106682C (en) 2005-10-18
AU1983592A (en) 1992-10-21
KR100202057B1 (en) 1999-06-15
WO1992016182A3 (en) 1992-12-23
JPH06506216A (en) 1994-07-14
AU663506B2 (en) 1995-10-12
DE69206976D1 (en) 1996-02-01
US5244652A (en) 1993-09-14
ATE131722T1 (en) 1996-01-15
JP3347727B2 (en) 2002-11-20
DE69206976T2 (en) 1996-08-14
CA2106682A1 (en) 1992-09-23

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