MXPA99005507A - Cosmetic composition containing an anionic polymer and an acrylic terpolime and use of this composition for the treatment of queratini matters - Google Patents

Cosmetic composition containing an anionic polymer and an acrylic terpolime and use of this composition for the treatment of queratini matters

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Publication number
MXPA99005507A
MXPA99005507A MXPA/A/1999/005507A MX9905507A MXPA99005507A MX PA99005507 A MXPA99005507 A MX PA99005507A MX 9905507 A MX9905507 A MX 9905507A MX PA99005507 A MXPA99005507 A MX PA99005507A
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Mexico
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acid
composition according
copolymers
acrylic
weight
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MXPA/A/1999/005507A
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Spanish (es)
Inventor
Dupuis Christine
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L´Oreal
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Publication of MXPA99005507A publication Critical patent/MXPA99005507A/en

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Abstract

The present invention relates to cosmetic compositions comprising, in a cosmetically acceptable aqueous medium, at least one anionic polymer and an acrylic terpolymer as well as the use of these compositions for treating keratin materials. The acrylic terpolymer comprises: a) about 20 to 70% by weight of a carboxylic acid having alpha, beta-monoethylenic unsaturation, b) about 20 to 80% by weight of a monomer having monoethylenic, non-surfactant unsaturation, different from a ) and c) about 0.5 to 60% by weight of a nonionic urethane monomer which is the reaction product of a monohydric nonionic surfactant with a monoisocyanate having monoethylenic unsaturation. The invention is concerned in particular with unclarified hair products such as gels, foams, lacquers as well as solar compositions.

Description

COSMETIC COMPOSITION CONTAINING AN ANIONIC POLYMER AND A ACRILICO TERPOLIMERO AND USE OF THIS COMPOSITION FOR THE TREATMENT OF KERATINIC MATTERS Description of the invention The present invention relates to cosmetic compositions containing in association at least one anionic polymer and an acrylic terpolymer, as well as the use of these compositions for the treatment of keratin materials, in particular the skin and hair. ~~ The anionic polymers are generally used for their binding properties, in particular for the formulation of combing hair gels or head and fixation gels. It is interesting to formulate hair care compositions that contain anionic polymers having a high viscosity and are in the form of well-extending gels for care and combing. For this, thickener and / or gelling polymers have generally been used. However, the introduction of anionic polymers in the thickeners frequently leads to problems of fluidization and loss of limpidity and the cosmetic performances obtained are insufficient for the care and combing products. Thickening and / or gelling polymers are known which comprise in their chain a part REF .: 30468 hydrophilic and a hydrophobic part consisting of a fatty chain such as the product * PEMULEN TR1"marketed by the company GOODRICH or the polymers" CRYSOL "marketed by the company ROHM & HAAS. The polymer ^ PEMULEN TR1"used in association with anionic polymers does not lead to a gel of sufficient texture and does not give satisfactory results in the cosmetic plane, in particular as regards fixation power, softness and touch. * CRYSOL polymer 44"used in association with an anionic polymer leads to a cloudy and liquid product. It has surprisingly been discovered that by using a new families of thickening and / or gelling polymers and by associating them with cationic polymers, cosmetic formulations can be obtained which have a satisfactory viscosity at a relatively low pH, not doughy, non-greasy, which They extend well on the skin and the hair and give the latter good properties of softness, touch and carmenadura or desenredoredo while they have good properties of fixation. Thus, the subject of the present invention is cosmetic compositions for the treatment of keratin materials containing, in a cosmetically acceptable aqueous support, at least one anionic polymer. and an acrylic terpolymer which will be defined more in detail in the continuation of the description. This polymer makes it possible in particular to prepare aqueous or hydro-organic compositions containing cosmetically acceptable, clarified or unclarified solvents ranging from gelled products to solid sticks or pastes. The advantages of this polymer are to be stable in an electrolytic medium and to have a very good thickening power at pH equal to or greater than 5.5, which makes it possible to reach a good level of viscosity and be able to use high concentrations of alcohol. The acrylic terpolymer used according to the invention is soluble or dilatable in alkalis. It is characterized in that it comprises a) about 20 to 70% by weight, preferably 25 to 55% by weight, of a carboxylic acid having α, β-monoethylenic unsaturation; b) about 20 to 80% by weight, preferably 30 to 65% by weight, of a monomer having monoethylenic, non-surfactant unsaturation, different from a) c) about 0.5 to 60% by weight, preferably 10 to 50% by weight, of a non-ionic urethane monomer which is the reaction product of a non-ionic surfactant. monohydric ion with a monoisocyanate having monoethylenic unsaturation. The carboxylic acid with α, β-monoethylenic unsaturation: a) can be chosen from numerous acids and in particular from acrylic acid, methacrylic acid, itaconic acid and maleic acid. Methacrylic acid is preferred. A large proportion of acid is essential to give a polymeric structure which is solubilized and gives a thickener by reaction with an alkaline compound, such as sodium hydroxide, alkanolamines, amino methyl propanol or amino methyl propanediol. The terpolymer must also contain an important proportion indicated hereinabove of a monomer b) having monoethylenic unsaturation which has no surfactant property. Preferred monomers are those which give water-insoluble polymers when they are homopolymerized and are illustrated by alkyl acrylates and methacrylates of 1 to 4 carbon atoms, such as methyl acrylate, ethyl acrylate, butyl acrylate or the corresponding methacrylates. The most particularly preferred monomers are methyl and ethyl acrylates. Other monomers that can be used are styrene, vinyltoluene, vinyl acetate, acrylonitrile and vinylidene chloride. Non-reactive monomers are preferred, these monomers are those in which the Unique ethylene group is the only reactive group under the conditions of polymerization. However, monomers containing reactive groups under the action of heat can be used in certain situations, such as hydroxyethyl acrylate. The monohydric nonionic surfactants used to obtain the nonionic urethane monomer c) are well known and are in general alkoxylated hydrophobic compounds containing an alkylene oxide which forms the hydrophilic part of the molecule. The hydrophobes are generally constituted by an aliphatic alcohol or an alkylphenol in which a carbon chain containing at least six carbon atoms constitutes the hydrophobic part of the surfactant. Preferred monohydric nonionic surfactants have the formula: wherein R is an alkyl group of 6 to 30 carbon atoms or aralkyl of 8 to 30 carbon atoms, R 'is an alkyl group of 1 to 4 carbon atoms, n is an average number of about 5 to 150 and m it is an average number of approximately 0 to 50, with the proviso that n is at least as large as -m and that n + m = 5 - 150.
Preferred alkyl groups of 6 to 30 carbon atoms include dodecyl and alkyl radicals of 18 to 26 carbon atoms. As aralkyl groups, mention may be made in particular of alkyl groups (from 8 to 13 carbon atoms) phenyl. The preferred R 'group is the methyl group. Monoisocyanate with monoethylenic unsaturation used to form the nonionic urethane monomer c) can be chosen from a variety of compounds. A compound containing any copolymerizable unsaturation such as an acrylic or methacrylic unsaturation can be used. An allylic unsaturation conferred by allyl alcohol can also be used. The preferred monoethylenic monoisocyanate is 1'-a, a-dimethyl-m-isopropenyl-benzylisocyanate. The acrylic terpolymer defined hereinabove is obtained by means of aqueous emulsion copolymerization of components a), b) and c) which is quite usual and is described in the patent application EP-A-0 173 109. As terpolymers that can be to be used according to the invention, mention may be made of the reaction products of methacrylic acid as component a), ethyl acrylate as component b) and a non-ionic urethane macromonomer such as compound c) having the following structure: wherein p 'is from 6 to 150 and preferably is equal to 130 and R2 is an alkyl radical of 8 to 13 carbon atoms, as described in Example 3 of the patent application EP-A-0 173 109. The preferred acrylic terpolymer used according to the invention is obtained from methacrylic acid as component a), methyl acrylate as component b) and a non-ionic urethane macromonomer as component c), which has the structure following: wherein p is from 6 to 150 and R1 is an alkyl radical of 18 to 26 carbon atoms, preferably 20 to 24 carbon atoms, linear, of plant origin, such as the docosyl radical. The acrylic terpolymer is present in the cosmetic compositions of the invention in concentrations from 0.01 to 20% by weight in relation to the total weight of the composition and preferably from 0.1 to 10% by weight. According to the invention, any anionic polymer known per se can be used. Of course, one or more anionic polymers can be used.
Thus, the anionic polymers used in general are polymers comprising groups derived from carboxylic, sulphonic or phosphoric acid and have a molecular weight between about 500 and 5,000,000. The carboxylic groups are provided by unsaturated mono- or dicarboxylic carboxylic monomers such as those which correspond to the formula: wherein n is an integer from 0 to 10, A designates a methylene group, optionally attached to the carbon atom of the unsaturated group or to a neighboring methylene group when n is greater than 1 by means of a heteroatom such as oxygen or sulfurRi denotes a hydrogen atom, a phenyl or benzyl group, R2 denotes a hydrogen atom, a lower alkyl or carboxyl group, R3 denotes a hydrogen atom, a lower alkyl group, a -CH2COOH group, phenyl or benzyl. In the aforementioned formula, a lower alkyl radical preferably designates a group having 1 to 4 carbon atoms and in particular methyl and ethyl. The anionic polymers having preferred carboxylic groups according to the invention are: A) homo- or copolymers of acrylic or methacrylic acid or their salts and in particular the products sold under the names' VERSICOL E 'or' VERSICOL K 'by the company ALLIED COLLOID and' ULTRAHOLD 'by the company BASF, the copolymers of acrylic acid and acrylamide sold in the form of its sodium salt, under the names' RETEN 421"," RETEN 423"or" RETEN 425"by the company HERCULES; the sodium salts of polyhydroxycarboxylic acids. B) Copolymers of acrylic or methacrylic acids with at least one onoethylene monomer such as ethylene, styrene, vinyl esters, esters of acrylic or methacrylic acid, acrylamide or its derivatives and vinylpyrrolidone, optionally grafted to a polyalkylene glycol such as polyethylene glycol and optionally crosslinked . Such polymers are described in particular in French patent 1,222,944 and German application 2,330,956. Copolymers of this type comprising in their chain an optionally N-alkylated and / or hydroxyalkylated acrylamide portion are described in particular in the patents FR 2 360 615 and FR 2 432 528 or proposed under the name 'QUADRAMER' by the company AMERICAN CYANAMID Mention may also be made of the copolymers of acrylic acid and alkyl methacrylate of 1 to 4 carbon atoms and the terpolymers of vinyl pyrrolidone, (meth) acrylic acid and alkyl (meth) acrylate of 1 to 20 carbon atoms, for example , of lauril such as the one sold by the ISP company under the name 'ACRYLIDONE LM', of tert.-butyl, for example, 'LUVIFLEX VBM 70' marketed by BASF or methyl, such as 'STEPANHOLD EXTRA' marketed by STEPAN. "Copolymers of methacrylic acid or ethyl acrylate may also be mentioned such as the one sold under the name 'LUVIMER MAEX' by the company BASF and the terpolymers of methacrylic acid / ethyl acrylate / tertiobutyl acrylate such as the product 'LUVIMER 100P' marketed by BASF C) Copolymers derived from crotonic acid such as those which comprise in their chain portions of vinyl acetate or propionate and optionally other monomers such as allyl or metalyl esters, vinyl ether or vinyl ester of a linear or branched saturated carboxylic acid of long hydrocarbon chain such as those which comprise minus 5 carbon atoms, these polymers can eventually be grafted to a polyalkylene glycol and cross-linked or also a vinyl, allyl or metalyl ester of an α-, or β-cyclic carboxylic acid. Such polymers are further described in French patents 1,222,944, 1,580,545, 2,265,782, 2,265,781, 1,564,110 and 2,439,798. Commercial products that fall into this class are resins 28-29-30, 26-13-14 and 28-13-10 sold by the company NATIONAL STARCH. Mention may also be made of the acetate terpolymer of vinyl / p-tert-butylbenzoate vinyl / crotonic acid (65/25/10). D) Copolymers derived from monounsaturated carboxylic acids or anhydrides of 4 to 8 carbon atoms selected from: - the copolymers comprising (i) one or more maleic, fumaric, itaconic anhydrides or anhydrides and (ii) at least one monomer selected from the vinyl esters, vinyl esters, vinyl halides, phenyl vinyl derivatives, acrylic acid and their esters, the anhydride functions of these copolymers which are optionally onesterified or monoamidified. Such polymers are described in particular in U.S. Patent Nos. 2,047,398, 2,723,248, 2,102,113, British Patent 839,805 and are sold in particular under the names 'G7? NTREZ AN' or 'GANTREZ ES' or 'AVANTAGE CP' by the company ISP. copolymers comprising (i) one or more maleic, citraconic or itraconic anhydrides and (ii) at least one monomer chosen from allyl or metalyl esters optionally comprising one or more acrylamide, methacrylamide, α-olefin groups in its chain , acrylic or methacrylic esters, acrylic or methacrylic acids or vinylpyrrolidone, the anhydride functions of these copolymers are optionally monoesterified or monoamified. These polymers are for example described in French patents 2,350,384 and 2,357,241 of the applicant. E) Polyacrylamides comprising carboxylate groups. Polymers comprising sulfonic groups are polymers comprising vinlsulfonic, styrenesulfonic, naphthalenesulfonic or acrylamido alkylsulfonic moieties. These polymers can be chosen in particular from: the polyvinyl sulphonic acid salts having a weight average molecular weight of between 1,000 and 100,000 as well as their copolymers with an unsaturated comonomer such as acrylic or methacrylic acids and their esters, acrylamide or their derivatives, vinyl ethers and vinylpyrrolidone, - the salts of polystyrenesulfonic acid, the sodium salts having a weight average molecular weight of approximately 500,000 and approximately 100,000 are respectively sold under the names 'FLEXAN 500' and 'FLEXAN 130' by NATIONAL STARCH These compounds are described by the French patent 2,198,719, the salts of polyacrylamide 'alkylsulfonic acids, such as those mentioned in US Patent 4,128,631 and more in particular polyacrylamidoethylpropane sulfonic acid sold under the name 'COSMEDIA POLYMER HSP 1180' by HENKEL and crosslinked and partially neutralized polyacrylamide ethylpropane sulfonic acid 50% by ammonia sold under the name 'HOSTACERIN AMPS' by the company HOECHST. According to the invention, the anionic polymers are preferably chosen from copolymers of acrylic or methacrylic acid with at least one monoethylene monomer, optionally grafted with a polyalkylene glycol and optionally crosslinked such as the terpolymer of acrylic acid / ethyl acrylate / N -tertyobutylacrylamide sold under the name 'ULTRAHOLD STRONG' by the company BASF, the copolymers of methacrylic acid and methyl methacrylate sold under the name 'EUDRAGIT L' by the company ROHM PHARMA, the copolymer of methacrylic acid and ethyl acrylate sold under the name 'LUVIMER MAEX' by the company BASF, the terpolymer of vinylpyrrolidone / acrylic acid / lauryl methacrylate sold under the name 'ACRYLIDONE LM' by the company ISP, copolymers derived from crotonic acid such as terpolymer acetate vinyl / tertiary-butyl benzoate vinyl / crotonic acid, terpolymer crotonic acid / vinyl acetate / inyl neododecanoate sold under the name 'Resine 28-29-30' by the company NATIONAL STARCH, the vinyl acetate / crotonic acid copolymer sold under the name 'LUVISET CA 66' by the company BASF and the terpolymer of vinyl acetate / crotonic acid / polyethylene glycol under the name 'ARISTOFLEX A' by the company BASF, copolymers derived from maleic, fumaric, itaconic acids or anhydrides such as the methylvinyl ether / maleic ester monohydride copolymer sold under the name 'GANTREZ ES 425' by the company ISP. ~ The most particularly preferred anionic polymers are chosen from the vinyl acetate / tertiary butyl benzoate / crotonic acid terpolymer, the methylvinyl ether / maleic ester anhydride copolymer sold under the name 'GANTREZ ES 425' by the ISP company , the copolymer of methacrylic acid and methyl methacrylate, sold under the name 'EUDRAGIT L' by the company ROHM PHARMA, the copolymer of methacrylic acid and ethyl acrylate sold under the name 'LUVIMER MAEX' by the company BASF, vinylpyrrolidone terpolymer / acrylic acid / lauryl ethacrylate sold under the name 'ACRYLIDONE LM' by the company ISP. According to the invention, anionic polymers in the form of latex or pseudolatex, that is to say in the form of an aqueous dispersion of insoluble polymer particles. For example, an aqueous dispersion comprising a copolymer formed of one or more alkyl acrylates can be used., one or more alkyl methacrylates and one and more ethylenic carboxylic acids having from 3 to 5 carbon atoms, alkyl radicals having from 1 to 5 carbon atoms and can be hydroxylated. The alkyl acrylate is preferably chosen from methyl acrylate, ethyl acrylate, propyl acrylate and butyl acrylate. Ethyl acrylate is particularly preferred. The concentration of alkyl acrylate is preferably between 40 and 70% by weight and more particularly between 50 and 60% by weight in proportion to the total weight of the copolymer. The alkyl methacrylate is preferably chosen from methyl methacrylate, ethyl methacrylate, propyl methacrylate and butyl methacrylate. Methyl methacrylate is particularly preferred. The concentration of the ethyl methacrylate is preferably between 30 and 50% by weight and more particularly between 30 and 40% by weight in proportion to the total weight of the copolymer.
Preferred ethylenic carboxylic acids are acrylic acid, methacrylic acid, crotonic acid, itaconic acid and mixtures thereof. Acrylic acid and methacrylic acid are particularly preferred. According to the invention, it is possible to apply the salts of these carboxylic acids. The concentration of ethylenic carboxylic acids or their salts is preferably between 5 and 15% by weight and more particularly between 8 and 12% by weight in proportion to the total weight of the copolymer. In a particularly preferred embodiment of the invention, the acrylic acid is used with the methacrylic acid, each in a concentration comprised between 2 and 10% by weight, the total of these two acids is not more than 15% by weight of the total weight of the copolymer. The copolymer may also contain minor amounts, that is, less than 10%, preferably less than 5% and more particularly less than 2% of a polymerizable monomer other than those mentioned hereinabove. According to a particularly preferred embodiment of the invention, a copolymer comprising 50 to 60% by weight of ethyl acrylate, 30 to 40% by weight of methyl methacrylate, 2 to 10% by weight of acid is used. acrylic, 2 to 10% by weight methacrylic acid, the The total concentration of acrylic and methacrylic acid is not more than 15% by weight in proportion to the total weight of the acrylic copolymer. A copolymer as such is for example described in the patent application EP-A-590604 which is included herein by way of reference. An aqueous dispersion of the acrylic copolymer described hereinabove comprises 25% by weight of a copolymer of ethyl acrylate / methyl methacrylate / ethacrylic acid / acrylic acid sold in particular under the trade name 'AMERHOLD DR-25"by the company According to the invention, it is also possible to use an aqueous dispersion of copolymer of hydroxyethyl methacrylate / butyl methacrylate / methacrylic acid / butyl acrylate, such as, for example, the product sold by the company SEPPIC under the name 'ACUDYNE 255". According to the invention, it is also possible to use an aqueous dispersion of the ethyl acrylate / methacrylic acid / tert-butyl acrylate copolymer such as, for example, the product sold by the company BASF under the name 'LUVIMER LOW VOC'. are used in the compositions of the invention in proportions comprised between 0.01 and 20% by weight and preferably between 0.1 and 8% by weight in proportion to the total weight of the composition. The compositions according to the invention contain a cosmetically acceptable aqueous medium. They have a pH of 3.5 to 11, preferably between 5.5 and 11 and even more preferably between 5.5 and 8.5. The cosmetically acceptable medium of the compositions according to the invention is more particularly constituted by water and optionally of cosmetically acceptable organic solvents.Organic solvents can represent 0. 5 to 90% of the total weight of the composition. They can be chosen from the group consisting of hydrophilic organic solvents, lipophilic organic solvents, amphiphilic solvents or their mixtures. Among the hydrophilic organic solvents, mention may be made, for example, of linear or branched lower monohydric alcohols having from 1 to 8 carbon atoms, polyethylene glycols having from 6 to 80 ethylene oxide units and polyols. As amphiphilic organic solvents, mention may be made of polypropylene glycol (PPG) derivatives such as polypropylene glycol and fatty acid esters, PPG and fatty alcohol such as PPG-23 oleyl ether and PPG-36 oleate.
Examples of lipophilic organic solvents include fatty esters such as diisopropyl adipate, dioctyl adipate, alkyl benzoates, dioctyl maleate. In order that the cosmetic compositions of the invention are more pleasant to use (softer in the application, more nutritious, more emollient) it is possible to add a fat phase in the middle of these compositions. The fat phase can represent 50% of the total weight of the composition. This fat phase can comprise an oil or a wax or its mixtures and can also comprise fatty acids, fatty alcohols and esters of fatty acids. The oils may be chosen from animal, vegetable, mineral or synthetic oils and in particular from petrolatum oil, paraffin oil, isoparaffins, poly-α-olefins, fluorinated and perfluorinated oils. Also, the waxes can be chosen from the animal, fossil, vegetable, mineral or synthetic waxes known per se. The compositions of the invention may contain the usual adjuvants in the cosmetic domain as other conventional gelling agents and / or thickeners; emulsifiers; surfactants; moisturizing agents; emollients; hydrophilic or lipophilic active agents such as ceramides; anti-aging agents free radicals; sequestrants; antioxidants; conservatives; alkalizing or acidifying agents; perfumes; charges; coloring matters; volatile silicones or not, modified or not, reducing. The amounts of these different adjuvants are those used classically in the domains considered. Of course, those skilled in the art will choose the optional compound or compounds to be added to the composition according to the invention, in such a way that the advantageous properties obtained intrinsically with the composition according to the invention are not substantially altered by the contemplated addition. The compositions according to the invention can be presented in any form suitable for a topical application, in particular in the form of a thick lotion, in the form of aqueous or hydroalcoholic gels, in the form of vesicular dispersions, in the form of simple or complex emulsions (( O / W, W / O, 0 / W / O or W / O / W, where W = water, 0 = oil) and can be of liquid, semi-liquid or solid consistency, such as creams, milks, gels, gels -creams, pastes, sticks and possibly can be packaged in aerosol and presented in the form of foams or sprays.These compositions are prepared according to the usual methods.
The compositions according to the invention are preferably used as clarified or unclarified hair products, in particular for washing, coloring, care, conditioning, straightening, maintaining the hairstyle or headdress or the permanent or non-permanent formation of the hair. hair. They may be styling or headdressing products, such as application lotions, lotions for brushing, fixing and combing compositions or headdressing. The lotions can be conditioned in various forms, in particular in vaporizers, pump bottles or aerosol containers in order to ensure an application of the composition in vaporized form or in the form of foam. Such forms of conditioning are indicated for example when it is desired to obtain a spray or a foam for fixing or treating the hair. The compositions of the invention can also be shampoos, clarifying compositions or not, for applying before or after shampooing, coloring, decolouring, perming or straightening or straightening. The compositions of the invention can also be used as toilet or hygiene products, such as protective creams, for treatment or for face care, for hands or for the body, in milk bodily protection or toilet, lotions, gels or foams for the care or cleaning of the skin. The compositions of the invention can also be used as antisun compositions. The compositions may also consist of solid preparations constituting cleaning soaps or bars. The compositions of the invention can also be used as oral care products such as toothpastes, mouthwashes. The compositions can be make-up products such as face creams, bases, mascaras, eyeliners, lipsticks, nail varnish. Another object of the invention is a method of non-therapeutic cosmetic treatment of the skin, scalp, hair, eyelashes, eyebrows, nails or mucous membranes, characterized in that a composition is applied to the keratin support. as defined hereinabove, according to the technique of habitual use of this composition, for example application of creams, gels, serums, lotions, milks on the skin, scalp or mucous membranes. The following examples illustrate the invention without presenting a limiting character.
Example 1: Non-clarified ungelled capillary product - Methacrylic acid / methyl acrylate / dimethyl metaisopropenylbenzyl isocyanate ethoxylated behenyl ester (40 OE) in 25% aqueous dispersion 0.5 g MA - Vinyl acetate / p-tert-butyl benzoate vinyl / crotonic acid terpolymer (65/25/10) 0.5 g MA -2-amino-2-methylpropanol-l "(AMP) pH adjusted to 7.5, how much is enough -Perfume, conservative, coloring, how much is enough - Demineralized water as long as it is enough for 100 g A thick, non-pasty, non-greasy gel is obtained and it spreads well in the hair. This gel gives the hair a soft touch and a good unraveling ability and has a good fixing power. If the aforementioned terpolymer is replaced by the same amount of the polyurethane 'ACRYSOL 44"of ROHM and HAAS, a liquid and turbid product is obtained If the terpolymer is replaced by the copolymer of acrylic acid / alkyl acrylate of 10/30 atoms carbon, crosslinked, 'PEMULEN TR1"sold by GOODRICH, you get a slightly pasty gel that has a power very poor fixative and rather less good cosmetic and contact properties.
Example 2: High protection solar gel -4-terbutyl 4 '-methoxy dibenzoylmethane (' PARSOL 1789 'sold by the company ROCHE) 2 g-Benzene-1,4-di (3-methylidene-10-camphorsulphonic acid) ) in 33% aqueous solution 3 g -2-cyano-3, 3-diphenylacrylate 2-ethylhexyl ('UVINUL N 539"sold by BASF) 10 g - Methacrylic acid / methyl acrylate / dimethyl metaisopropenylbenzyl isocyanate terpolymer of ethoxylated behenyl alcohol (40 OE) in 25% aqueous dispersion 0.45 g MA - Crosslinked polyacrylamidomethyl-propanesulfonic acid 50% partially neutralized by ammonia, sold under the name 'HOSTACERIN AMPS' by the company HOECHST 0.8 g -2.2, 4, 4, 6, 6, 8-heptamethylnonano 9 g - Glycerol 6 g - Propylene glycol 6 g - Ethylenediaminetetra (methylene phosphonic acid) salt pentasodium in 33% aqueous solution 0.3 g - Triethanolamine 0.85 g - Denatured 96 ° ethyl alcohol 4.5 g - De-mineralized water sterilized as much as 100 g. An unctuous gel is obtained that spreads well on the skin. It is noted that, with regard to this date, the best method known to the applicant to carry out the aforementioned invention is that which is clear from the present description of the invention.

Claims (26)

  1. Claims Having described the invention as above, the content of the following claims is claimed as property: 1. A cosmetic composition intended for the treatment of keratin materials, characterized in that it comprises, in a cosmetically acceptable aqueous support, at least one anionic polymer and a acrylic terpolymer comprising: a) about 20 to 70% in. weight and preferably 25 to 55% by weight of a carboxylic acid having α, β-monoethylenic unsaturation; b) about 20 to 80% by weight and preferably 30 to 65% by weight of a monomer having monoethylenic, non-surfactant unsaturation, different from a) and c) about 0.5 to 60% by weight and preferably 10 to 50% by weight weight, of a non-ionic urethane monomer, which is the reaction product of a monohydric nonionic surfactant with a monoisocyanate having monoethylenic unsaturation.
  2. 2. The composition according to claim 1, characterized in that the carboxylic acid having α, β-monoethylenic unsaturation a) is chosen from between acrylic acid, methacrylic acid, itaconic acid and maleic acid.
  3. The composition according to claim 2, characterized in that the carboxylic acid having α, β-monoethylenic unsaturation a) is methacrylic acid.
  4. 4. The composition according to any of claims 1 to 3, characterized in that the monomer having non-surfactant monoethylenic unsaturation b) is selected from alkyl acrylates and methacrylates of 1 to 4 carbon atoms, styrene, vinyltoluene, acetate of vinyl, acrylonitrile and vinylidene chloride.
  5. The composition according to claim 4, characterized in that the monomer having non-surfactant monoethylenic unsaturation is methyl or ethyl acrylate.
  6. The composition according to any of claims 1 to 5, characterized in that the non-ionic monohydric surfactant used to obtain the nonionic urethane monomer c) has the formula: wherein R is an alkyl group of 6 to 30 carbon atoms or aralkyl of 8 to 30 carbon atoms, R 'is an alkyl group of 1 to 4 carbon atoms, n is a number average of about 5 to 150 and is an average number of about 0 to 50, with the proviso that, 'n is at least as large as and that n + = 5 - 150.
  7. 7. The composition in accordance with the claim 6, characterized in that R is chosen from among the radicals dodecyl, alkyl of 18 to 26 carbon atoms and alkyl '(of 8 to 13 carbon atoms) phenyl, m = 0 and n is an average number of about 5 to 150.
  8. 8 The composition according to any one of claims 1 to 7, characterized in that the monoisocyanate having monoethylenic unsaturation used to form the non-ionic urethane monomer c) is 1'-a, a-dimethyl-m-isopropenyl benzyl isocyanate.
  9. The composition according to any of claims 1 to 8, characterized in that the acrylic terpolymer is obtained in aqueous dispersion from methacrylic acid as component a), methyl acrylate as component b) and a non-urethane macromonomer Ionic of following structure: wherein p is from 6 to 150 and R1 is an alkyl radical of from 18 to 26 carbon atoms, preferably from 20 to 24 linear carbon atoms, of plant origin, such as the docosyl radical.
  10. 10. The composition according to any of claims 1 to 9, characterized in that the acrylic terpolymer is present in concentrations of 0.01 to 20% by weight and preferably 0.1 to 10% by weight in relation to the total weight of the composition.
  11. The composition according to any of claims 1 to 10, characterized in that the anionic terpolymer (s) are chosen from among the polymers containing carboxylic, sulfonic or phosphoric acid derivative groups.
  12. 12. The composition according to claim 11, characterized in that the anionic polymer (s) are selected from among the polymers comprising carboxylic groups derived from unsaturated mono- or dicarboxylic carboxylic monomers of the formula: wherein n is an integer from 0 to 10, A designates a methylene group, optionally bonded to the carbon atom of the unsaturated group or to a neighboring methylene group when n is greater than 1 by means of a heteroatom such as oxygen or sulfur, Ra designates a hydrogen atom, a phenyl or benzyl group, R 2 denotes a hydrogen atom, a lower alkyl or carboxyl group, R 3 denotes a hydrogen atom, hydrogen, a lower alkyl group, a group -CH2C00H, phenyl or benzyl, - polymers comprising two vinylsulfonic, styrene sulfonic, naphthalene sulphonic or acrylamido alkylsulfonic portions.
  13. 13. The composition according to any of claims 1 to 12, characterized in that the or the anionic polymers are chosen from: A) homo- or copolymers of acrylic or methacrylic acid or their salts, the copolymers of acrylic acid and acrylamide sodium salts of polyhydroxycarboxylic acids, B) copolymers of acrylic or methacrylic acids with at least one monoethylene monomer such as ethylene, styrene, violyl esters, esters of acrylic or methacrylic acid, acrylamide or its derivatives and vinylpyrrolidone, optionally grafted in a polyalkylene glycol such as polyethylene glycol and optionally crosslinked, C) copolymers derived from crotonic acid comprising in their chain portions of vinyl acetate or propionate and optionally other monomers such as allyl or metalyl esters, vinyl ether or vinyl ester of a carboxylic acid saturated linear or branched long chain hydrocarbon nothing they understand at least 5 carbon atoms or a vinyl, allyl or metalyl ester of an α- or β-cyclic carboxylic acid, these polymers may optionally be grafted onto a polyalkylene glycol and crosslinked, D) copolymers derived from monounsaturated carboxylic acid or anhydrides from 4 to 8 carbon atoms chosen from among the copolymers comprising (i) one or more maleic, fumaric, itaconic anhydrides or anhydrides and (ii) at least one monomer chosen from vinyl esters, vinyl ethers, vinyl halides , the phenyl vinyl derivatives, acrylic acid and its esters, the anhydride functions of these copolymers which are optionally onesterified or monoamidified and the copolymers comprising (i) one or more maleic, citraconic or itaconic anhydrides and (ii) one or more monomers selected from between the allylic or metalyl esters that eventually comprise in their chain one or more groups s acrylamide, methacrylamide, α-olefin, acrylic or methacrylic esters, acrylic or methacrylic acids or vinylpyrrolidone, the anhydride functions of these copolymers are optionally monoesterified or monoamidated, E) as polyacrylamides comprising carboxylate groups.
  14. 14. The composition according to claim 13, characterized in that the anionic polymer or polymers are selected from the copolymers of methacrylic acid and methyl methacrylate, copolymers of methacrylic acid and ethyl acrylate, terpolymers of vinylpyrrolidone / acrylic acid / methacrylate of lauryl, methacrylic acid terpolymer / ethyl acrylate / tertiary butyl acrylate, terpolymers of acrylic acid / ethyl acrylate / N-tert-butyl-butylacrylamide, vinyl acetate / crotonic acid copolymers, terpolymers of. vinyl acetate / vinyl tertiary butylbenzoate / crotonic acid, crotonic acid terpolymers / vinyl acetate / vinyl neododecanoate, vinyl acetate / crotonic acid / polyethylene glycol terpolymers and monoesterified methyl vinyl ether / maleic anhydride copolymers.
  15. 15. The composition according to claim 14, characterized in that the anionic polymer (s) is selected from vinyl acetate / tert-butylbenzoate / crotonic acid polymers, monovinterified methyl vinyl ether / maleic anhydride copolymers, methacrylic acid copolymers and methyl methacrylate, copolymers of methacrylic acid and ethyl acrylate and terpolymers of vinylpyrrolidone / acrylic acid / lauryl methacrylate.
  16. 16. The composition according to claim 12, characterized in that the one or more anionic polymers are chosen from: the polyvinyl sulfonic acid salts having a weight average molecular weight of between about 1,000 and 100,000 and their copolymers with acrylic or methacrylic acids or their esters, acrylamide and its derivatives, vinyl ethers and vinylpyrrolidone; - salts of polystyrenesulfonic acid; - salts of polyacrylamide alkylsulfonic acid
  17. 17. The composition according to claim 16, characterized in that the anionic polymer (s) comprise sulphonic groups selected from polyacryl amidoethylpropane sulfonic acid and crosslinked and partially neutralized polyacryl amidomethylpropane sulfonic acid. 50% by ammonia
  18. 18. The composition according to any of claims 1 to 10, characterized in that the anionic polymer or polymers are in the form of an aqueous dispersion of insoluble particles of anionic polymers selected from the copolymers formed of one or several of alkyl acrylate, of one or more alkyl methacrylates and of one or more ethylenic carboxylic acids having from 3 to 5 carbon atoms, alkyl radicals having from 1 to 5 carbon atoms and can be hydroxylated.
  19. 19. The composition according to claim 18, characterized in that the aqueous dispersion of insoluble particles of anionic polymers comprises a copolymer of ethyl acrylate / methyl methacrylate / methacrylic acid / acrylic acid, a copolymer of hydroxyethyl methacrylate / methyl methacrylate / acid methacrylic / butyl-acrylate or a copolymer of ethyl acrylate / methacrylic acid / tert-butyl acrylate.
  20. The composition according to any of claims T to 19, characterized in that the anionic polymer or polymers are present in concentrations of 0.01 to 20% by weight and preferably of 0.1 to 8% by weight in proportion to the total weight of the composition.
  21. 21. The composition according to any of claims 1 to 20, characterized in that it has a pH of 3.5 to 11, preferably of 5.5 to 11 and still more preferably of 5.5 to 8.5.
  22. 22. The composition according to any of claims 1 to 21, characterized in that the cosmetically acceptable aqueous medium is constituted by water or water and at least one organic solvent selected from the group consisting of hydrophilic, lipophilic, amphiphilic organic solvents or their mixtures
  23. 23. The composition according to any of claims 1 to 22, characterized in that further comprises at least one usual cosmetic adjuvant selected from among conventional fatty, gelling and / or thickening substances, surfactants, moisturizing agents, emollients, sunscreens, hydrophilic or lipophilic active agents such as ceramides, anti-free radicals, sequestering agents, antioxidants, preservatives, alkalizing or acidifying agents, perfumes, fillers, coloring matters, silicones and reducers.
  24. 24. The composition according to any of claims 1 to 23, characterized in that it is in the form of an emulsion, thick lotion, gel, vesicular dispersion, paste, solid stick or is packaged in an aerosol and is presented as a foam or spray.
  25. 25. The composition according to any of claims 1 to 24, characterized in that it is used as a clarified or unclarified hair product for washing, dyeing, caring, conditioning, caring or unraveling, maintaining the hairstyle or headdress or permanent application or not to the hair or as an antisun composition.
  26. 26. A process of non-therapeutic, cosmetic treatment for the treatment of skin, scalp, hair, eyelashes, eyebrows, nails and mucous membranes, characterized in that it is applied in the latter an effective amount of a composition as defined in any of claims 1 to 25.
MXPA/A/1999/005507A 1998-06-15 1999-06-14 Cosmetic composition containing an anionic polymer and an acrylic terpolime and use of this composition for the treatment of queratini matters MXPA99005507A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9807514 1998-06-15

Publications (1)

Publication Number Publication Date
MXPA99005507A true MXPA99005507A (en) 2000-07-01

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