CA2106682C - Viscous surface active composition - Google Patents

Viscous surface active composition Download PDF

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CA2106682C
CA2106682C CA002106682A CA2106682A CA2106682C CA 2106682 C CA2106682 C CA 2106682C CA 002106682 A CA002106682 A CA 002106682A CA 2106682 A CA2106682 A CA 2106682A CA 2106682 C CA2106682 C CA 2106682C
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composition
alkyl
solution
betaine
constitute
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CA2106682A1 (en
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Edwin B. Michaels
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Biosyn Inc
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Biosyn Inc
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    • 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

Abstract

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

Description

Viscous Surface Active Composition The present invention relates to novel viscous surfactant compositions that liquefy 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;
1o hand cleansers; antiviral, antimicrobial or spermicidal compositions; and dentrifices.
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 non-adherent 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 S00 to 30,000 2o 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 ? to 11 and a Bloom gel value of zero. This composition counters the irntation 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 to 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-carboxyethoxyethyl-2-coco-imidazoliniumbetaine. 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 2o dihydric or polyhydric alcohols.
U.S. Patents 4,207,198 and 4,439,355 (Kenkare) disclose similar elastic detergent bars of improved foaming power a$er 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 foaming 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.
An 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.
2o Still another object of the invention is to provide a composition that can be used in dentifrices.
Another object of this invention is to provide a process for producing these compositions.
Accordingly, one aspect of the present invention relates to a viscous fluid composition comprising:

(a) 0.2 to 40% of an aqueous amphoteric surfactant which comprises a mixture of at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide;
(b) 0.3 to 10% of Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000;
(c) 0.5 to 30% polyhydric alcohol;
(d) 0.1 to 1.5% nonionic cellulose gum or synthetic analog thereof; and (e) 0.0 to 5% lower aliphatic alcohol.
Another aspect of the present invention relates to a method of preparing a shampoo comprising:
(a) adding cellulose gum to water;
(b) stirring the solution to hydrate the cellulose gum;
(c) separately preparing a solution of gelatin in water;
(d) transfernng the gelatin solution to a mixture of amphoteric surfactants comprising at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine, and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide;
(e) adding the solution containing gelatin and surfactants from step (d) to the solution of hydrated cellulose gum from step (b); and stirring to form a uniform product solution.
Another aspect relates to a method of preparing a dentifrice composition comprising:

(a) mixing glycerine and an additional polyhydric alcohol in an amount to constitute 0.5 to 30% of the dentifrice;
(b) triturating Type A gelatin having a Bloom strength of 100 to 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 at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine, and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide, the gelatin being present in an amount to constitute 0.3 to 10% of the dentifrice, the cellulose gum being 1o present in an amount to constitute 0.1 to 1.5% of the dentifrice, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the dentifrice:
(c) warming the solution of step (b) to 30° to 35° C. and stirring to hydrate the gum and gelatin;
(d) adding the solution of step (a) to the solution of step (c) while maintaining the combined solution at 30° to 35° C.; and cooling the combined solution of step (d).
Another aspect relates to a method of preparing a shampoo comprising:
(a) adding a nonionic cellulose gum to water in an amount to constitute 0.1 to 1.5% of the shampoo;
(b) stirnng the solution of step (a) to hydrate the cellulose gum;
2o (c) preparing a separate solution of gelatin by adding Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000 to water in an amount to constitute 0.3 to 10% of the shampoo;
(d) transfernng the gelatin solution to a mixture of amphoteric surfactants, the mixture comprising at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine, and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide, so that the amphoteric surfactant comprises 0.2 to 40% of the shampoo;
(e) adding the solution of step (c) containing gelatin and surfactants to the solution of step (d) containing hydrated cellulose gums; and (f) stirnng to form a uniform product solution.
Still another aspect of the invention is a method of preparing a gel composition comprising:
(a) triturating Type A gelatin having a Bloom strength of 100 to 300 and a molecular 1o weight from 75,000 to 300,000 and hydroxyethyl cellulose in glycerine;
(b) adding the mixture of step (a) to water at 45° C and stirring to form a solution;
(c) adding to the solution of step (b) an aqueous amphoteric surfactant solution comprising:
at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N
dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide and an acylamide t-amine oxide;
the gelatin being in an amount to constitute 0.3 to 10% of the composition, the 2o hydroxyethyl cellulose gum being in an amount to constitute 0.1 to 1.5% of the composition, the glycerine being in an amount to constitute 0.5 to 30% of the composition, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the composition; and (d) cooling the solution of step (c) to form the gel composition.

Yet another aspect is a method of preparing a jelly composition comprising:
(a) triturating in glycerine a cellulose gum selected from the group consisting of hydroxypropyl cellulose and hydroxypropylmethyl cellulose;
(b) adding the mixture of step (a) to water at 45° C and stirnng to form a solution;
(c) adding to the solution of step (b) an aqueous amphoteric surfactant solution comprising:
at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N
1o dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide and an acylamide t-amine oxide;
the cellulose gum being in an amount to constitute 1.5% of the composition, the glycerine being in an amount to constitute 0.5 to 30% of the composition, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the composition; and (d) cooling the solution of step (c) to form the jelly composition.
A further aspect of the invention is a method of preparing a creme composition comprising:
(a) dissolving cetyl alcohol in glycerine at 40° C to make an alcohol-glycerine solution;
20 (b) triturating Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000 and hydroxyethyl cellulose in the alcohol-glycerine solution of step (a);
(c) adding the mixture of step (b) to water at 45° C and stirring to form a solution;
(d) adding to the solution of step (c) an aqueous amphoteric surfactant solution comprising:

at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N
dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide and an acylamide t-amine oxide;
the gelatin being in an amount to constitute 0.3 to 10% of the composition, the hydroxyethyl cellulose gum being in an amount to constitute 0.1 to 1.5% of the composition, the glycerine being in an amount to constitute 0.5 to 30% of the composition, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of 1 o the composition; and (e) cooling the solution of step (d) to form a creme.
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 2o 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 for 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 1o from 1:5 to S:l, 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 component (a) of the composition of the invention have structures, respectively, as follows:

R N+ tCH2)nC00-'CH

R N+ (CH2)NSO3_ 'CH3 O p R C N+ CHZCOO- or RC - NH(CHz)3 -- N+ ~ CH2C00-\ CH3 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-sulfobetaine, cetyl-N-sulfobetaine, stearyl-N-sulfobetaine; isostearyl-N-sulfobetaine, oleyl-N-sulfobetaine; and (3) cocoamido-N-betaine, cetylamido-N-betaine, stearylamido-N-betaine, isostearylamido-N-betaine, oleylamido-N-betaine.
When used here the term "coco" is that used in the CTFA (designations of l0 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-dimethylamine 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:

R N+ = O

(CHz)zOH
R N+ ---~ O_ ~CH ) OH
2z O ~H3 R C NH (CHz)3 N+ --~ O

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: decyl-N,N-dimethylamine oxide, lauryl-N,N-dimethylamine oxide, stearyl-N,N-dimethylamine, oleyl-N,N-dimethylamine oxide; coco-N,N-dihydroxyethylamine oxide, cetyl-N,N-dihydroxyethylamine oxide, oleyl-N,N-dihydroxyethyl-amine oxide, and mixtures of the same. The betaine can be preferably an alkyl-N-betaine and the amine oxide can be an alkyl-N,N-di(lower alkyl)amine oxide, preferably an alkyl-N,N-dimethylamine oxide. The lower alkyl is C1_3. Gelatin, a high molecular weight preparation of hydrolyzed collagen that 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 produced 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 to 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 35° - 40° C.).
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 glycol, xylitol, sorbitol, and mannitol. Cellulose gums useful in this invention are the nonionic gums such as hydroxyethyl, hydroxypropyl and hydroxypropylmethyl 2o celluloses. The cellulose gums are those of high molecular weight. Other possible polymers 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 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 composition, 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 dehydrate.
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.
1o In accordance with this invention, it is possible to provide high viscosity fluids which liquefy 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 2o 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.
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.
Amphoteric surfactants that can be used in this invention are described in Examples 1 - 5.
1o Example 1 The composition described below is a concentrate of C31GTM, 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 # 4,839,1 S 8 issued to E.B. Michaels.
Cocobetaine; 31.5% active ingredient (AI): 405.5 lb, Cocamine oxide, 31.5% (AI): 325 Ib, Citric acid monohydrate, USP: 26 lb Purified water, USP: 26 Ib 2o To make about 782.5 lb C31 G at 29.6% AI at a dilution 1 % AI; pH = 4.9.
Formulations for Contraceptive/Antilnfective Preparations Example 2 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 to Purified water: 100 lbs To make about 402 lbs at 17% AI, at dilution 1 % AI; pH 4.9.
Example 4 Cocoamido propylbetaine 30% AI: 530 Ibs Cocoamido propylamine oxide 30% AI: 470 lbs Citric acid monohydrate, USP 60 Ibs 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 Ibs 2o Citric acid monohydrate 24 lbs Water 100 lbs To make about 711 lb at 24.8% AI at a dilution 1% AI, pH = 5Ø

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W o\ , ~ , W O , , ~
a ~
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x .~ XI X O N O M V1 , ~ U1 v'1 v~ ~ W W o, a .-. p O M v v a x z a ~ .-'"' i~~X O O ~ O
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.

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x V ~ ~ J

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 l0 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 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.
2o Pert Plus"' 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 (lOX weight of cellulose gum to be used) is heated to 80° C. Cellulose gum is sprinkled into the vortex of water creating a slurry that is quickly transferred to at least SX vol. of cold water and stirred for complete hydration by rapidly cooling to below 35° C.
Separately, gelatin should be added by sprinkling into vortex of water heated to 60° C and stirred for short period of time to complete solution, maintaining the temperature between 40 - SO° C. The gelatin solution is then transferred to the mixture of surfactants with residual water containing excipients and finally stirred with the hydrated to 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. l4 Ex.lS Ex. l6 Ex. l7 Ex. l8 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 0.2 0.4 0.4 0.4 1.5 Cellulose %

Glycerine % 11.0 6.0 6.0 6.0 2.0 Alcohol SDA38B - - 5.0 - 5.0 %

Excipient' Viscosity' 3700 3500 3900 28000 52000 CUSP 200 proof alcohol, denatured with 1.5% mint flavor ZExcipients 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 70° F. over viscosity at brush stress at 95° F.
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 1o 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 therapeutic agent.
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 -35° C and stirred to hydrate the gum and gelatin. The saccharin and fluoride are dissolved in a small portion of water at SO° C 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 - 35° C. The dentrifice can be packaged 2o before the mixture has cooled below 30° C.
Spermicidal Gels, Cremes or Jellies for use with Cervical Caps, Condoms, Diaphragms or alone prior to coitus.

Example 19 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 45° C 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 of high viscosity grade of hydroxypropyl or hydroxypropylmethyl cellulose for the gelatin and hydroxyethyl cellulose of the above examples.
Example 21 20 Creme 1 The Gel formulation above is converted to a Creme formulation by incorporation of 0.5 pts of cetyl alcohol in Gel-1 formulations by dissolving the alcohol in the glycerine at 40° C, 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 1 S lbs of water. Warm to 40° C. Mix until gums and gelatin are completely hydrated. Solution is poured on polyethylene sheet to be used as contraceptive films after cooling.
Example 23 Ointment for Xeroderma l0 2.5 lbs of petroleum jelly is warmed to 40° C, then mixed with 1 lb of shampoo of Example 6. Stir while cooling.
It is used for moisturizing and eliminating scaly skin caused by xeroderma.

Claims (21)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A viscous fluid composition comprising:
(a) 0.2 to 40% of an aqueous amphoteric surfactant which comprises a mixture of:
at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide;
(b) 0.3 to 10% of Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000;
(c) 0.5 to 30% polyhydric alcohol;
(d) 0.1 to 1.5% nonionic cellulose gum or synthetic analog thereof; and (e) 0.0 to 5% lower aliphatic alcohol.
2. The composition according to claim 1, wherein the amphoteric surfactant comprises an alkyl-N-betaine and an alkyl-N,N-dimethylamine oxide.
3. The composition according to claim 1 or 2, wherein the betaine is selected from the group consisting of cocobetaine, lauryl betaine, cetyl betaine, cocamido propyl betaine, and coco sultaine; and wherein the amine oxide is selected from the group consisting of cocoamine oxide, lauramine oxide, myristamine oxide, and cocoamido propyl amine oxide.
4. The composition according to claim 1, 2 or 3; wherein the polyhydric alcohol is selected from the group consisting of glycerine, propylene glycol, xylitol, sorbitol, and mannitol.
5. The composition according to any one of claims 1 to 4, wherein the cellulose gum is selected from the group consisting of hydroxyethyl cellulose, hydroxypropyl cellulose, and hydroxypropylmethyl cellulose.
6. The composition according to any one of claims 1 to 5, wherein the aliphatic alcohol is selected from the group consisting of ethyl, n-propyl, and isopropyl alcohol.
7. The composition according to any one of claims 1 to 6, wherein the cellulose gum analog is selected from the group consisting of polyvinyl alcohol, polyvinyl pyrolidone, and polyacrylic acid polymers.
8. The composition according to any one of claims 1 to 7, wherein the betaine and the amine oxide are present in a ratio of from 1 : 5 to 5 : 1.
9. The composition of any one of claims 1 to 8, wherein the composition is formulated for use as an ointment or jelly, and further comprises petroleum jelly.
10. The composition according to any one of claims 1 to 8, wherein the composition is formulated for use as a spermicide.
11. The composition of any one of claims 1 to 8, wherein the composition is formulated for use as a dentifrice, and further comprises a flavouring agent.
12. The composition according to any one of claims 1 to 8, wherein the composition is formulated for use as a shampoo, and further comprises a dye and a fragrance.
13. A method of preparing a shampoo comprising:
(a) adding cellulose gum to water;
(b) stirring the solution to hydrate the cellulose gum;
(c) separately preparing a solution of gelatin in water;
(d) transferring the gelatin solution to a mixture of amphoteric surfactants comprising at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine, and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide;
(e) adding the solution containing gelatin and surfactants from step (d) to the solution of hydrated cellulose gum from step (b); and (f) stirring to form a uniform product solution.
14. A method of preparing a dentifrice composition comprising:
(a) mixing glycerine and an additional polyhydric alcohol in an amount to constitute 0.5 to 30% of the dentifrice;
(b) triturating Type A gelatin having a Bloom strength of 100 to 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 at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine, and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide, the gelatin being present in an amount to constitute 0.3 to 10% of the dentifrice, the cellulose gum being present in an amount to constitute 0.1 to 1.5% of the dentifrice, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the dentifrice;
(c) warming the solution of step (b) to 30° to 35° C and stirring to hydrate the gum and gelatin;

(d) adding the solution of step (a) to the solution of step (c) while maintaining the combined solution at 30° to 35° C; and (e) cooling the combined solution of step (d).
15. A method of preparing a shampoo comprising:
(a) adding a nonionic cellulose gum to water in an amount to constitute 0.1 to 1.5% of the shampoo;
(b) stirring the solution of step (a) to hydrate the cellulose gum;
(c) preparing a separate solution of gelatin by adding Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000 to water in an amount to constitute 0.3 to 10% of the shampoo;
(d) transferring the gelatin solution to a mixture of amphoteric surfactants, the mixture comprising at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine, and at least one amine oxide selected from the group consisting of an alkyl-N,N-dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide, and an acylamide t-amine oxide, so that the amphoteric surfactant comprises 0.2 to 40% of the shampoo;
(e) adding the solution of step (d) containing gelatin and surfactants to the solution of step (b) containing hydrated cellulose gum; and (f) stirring to form a uniform product solution.
16. A method of preparing a gel composition comprising:
(a) triturating Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000 and hydroxyethyl cellulose in glycerine;
(b) adding the mixture of step (a) to water at 45° C and stirring to form a solution;
(c) adding to the solution of step (b) an aqueous amphoteric surfactant solution comprising:

at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N
dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide and an acylamide t-amine oxide;
the gelatin being in an amount to constitute 0.3 to 10% of the composition, the hydroxyethyl cellulose gum being in an amount to constitute 0.1 to 1.5% of the composition, the glycerine being in an amount to constitute 0.5 to 30% of the composition, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the composition; and (d) cooling the solution of step (c) to form the gel composition.
17. The method according to claim 16, the gelatin being in an amount to constitute 1.5% of the composition, the hydroxyethyl cellulose gum being in an amount to constitute 0.4% of the composition, the glycerine being in an amount to constitute 10% of the composition, and the amphoteric surfactant being in an amount to constitute 7%
of the composition.
18. A method of preparing a jelly composition comprising:
(a) triturating in glycerine a cellulose gum selected from the group consisting of hydroxypropyl cellulose and hydroxypropylmethyl cellulose;
(b) adding the mixture of step (a) to water at 45° C and stirring to form a solution;
(c) adding to the solution of step (b) an aqueous amphoteric surfactant solution comprising:
at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N
dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide and an acylamide t-amine oxide;
the cellulose gum being in an amount to constitute 1.5% of the composition, the glycerine being in an amount to constitute 0.5 to 30% of the composition, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the composition; and (d) cooling the solution of step (c) to form the jelly composition.
19. The method according to claim 19, the glycerine being in an amount to constitute 10% of the composition, and the amphoteric surfactant being in an amount to constitute 7% of the composition.
20. A method of preparing a creme composition comprising:
(a) dissolving cetyl alcohol in glycerine at 40° C to make an alcohol-glycerine solution;
(b) triturating Type A gelatin having a Bloom strength of 100 to 300 and a molecular weight from 75,000 to 300,000 and hydroxyethyl cellulose in the alcohol-glycerine solution of step (a);
(c) adding the mixture of step (b) to water at 45° C and stirring to form a solution;
(d) adding to the solution of step (c) an aqueous amphoteric surfactant solution comprising:
at least one betaine selected from the group consisting of an alkyl-N-betaine, an alkyl-N-sulfobetaine, and an acyl-N-betaine; and at least one amine oxide selected from the group consisting of an alkyl-N,N
dimethylamine oxide, an alkyl-N,N-dihydroxyethylamine oxide and an acylamide t-amine oxide;
the gelatin being in an amount to constitute 0.3 to 10% of the composition, the hydroxyethyl cellulose gum being in an amount to constitute 0.1 to 1.5% of the composition, the glycerine being in an amount to constitute 0.5 to 30% of the composition, and the amphoteric surfactant being in an amount to constitute 0.2 to 40% of the composition; and (e) cooling the solution of step (d) to form a creme.
21. The method according to claim 20, the cetyl alcohol being in an amount to constitute 0.5 parts of the composition, the gelatin being in an amount to constitute 1.5%
of the composition, the hydroxyethyl cellulose gum being in an amount to constitute 0.4%
of the composition, the glycerine being in an amount to constitute 10% of the composition, and the amphoteric surfactant being in an amount to constitute 7%
of the composition.
CA002106682A 1991-03-22 1992-03-20 Viscous surface active composition Expired - Fee Related CA2106682C (en)

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KR19980076072A (en) * 1997-04-04 1998-11-16 이명환 Mouthwash
DE19930335A1 (en) * 1999-07-02 2001-01-18 Henkel Kgaa Composite materials made from calcium compounds and protein components
BRPI0109078B8 (en) * 2000-03-07 2021-05-25 Rush Presbyterian St Lukes Medical Center antimicrobial and contraceptive composition that reduces the risk of transmission or infection by a sexually transmitted disease through sexual activity
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