 ANHYDROUS SOLID COMPOSITION COMPRISING AN ISETHIONIC ACID DERIVATIVE, A GLUTAMIC ACID DERIVATIVE, AN
专利摘要:
The subject of the present invention is a composition, preferably a cosmetic composition, in the form of an anhydrous solid comprising at least one anionic surfactant chosen from isethionic acid derivatives and their salts, at least one anionic surfactant chosen from glutamic acid derivatives and their salts, at least one amphoteric surfactant, and at least 20% by weight relative to the total weight of fillers. The composition of the invention is advantageously in the form of granules whose particle size is homogeneous. It disintegrates or disintegrates easily, is easy to apply on keratinous materials, and allows a rapid foam start, when the composition is applied to said keratin materials, as well as a good quality of foam. 公开号:FR3068243A1 申请号:FR1756220 申请日:2017-06-30 公开日:2019-01-04 发明作者:Audrey SEGALEN-GUIRAUD；Nadine LAVABLE 申请人:LOreal SA； IPC主号:
专利说明:
Anhydrous solid composition comprising an isethionic acid derivative, a glutamic acid derivative, an amphoteric surfactant and fillers The present invention relates to a composition in the form of an anhydrous solid comprising suitably selected anionic surfactants, at least one amphoteric surfactant, and at least 20% by weight, preferably at least 25% by weight relative to the total weight of the composition , fillers, and its use for cleaning and / or removing make-up from keratin materials such as the skin and the hair. Many cosmetic washing products are known in the field of body and / or hair hygiene. They are generally intended for cleaning keratin materials while providing them with good cosmetic properties. Conventional products for cleaning keratin materials, such as shower gels and shampoos, most often come in the form of more or less thickened liquids. But these products can prove to be difficult to dose: the more liquid they are, the more they tend to escape between the fingers, making their dosing difficult and generating waste, and / or tend to leak out of their packaging, which can be very annoying when they come into contact with clothing, for example when traveling. To modify the texture, and in particular to make it more compact, the conventional means consist in using gelling or thickening agents, but this is often done to the detriment of the cosmetic effects of the composition. In addition, these gelling or thickening agents can have the disadvantage of inhibiting the development of foam. In addition, it has been found that the thicker compositions often require a lot of rinse water in order to remove the excess product on the hair. In many countries where access to water is restricted, the rinsing time and therefore the quantity necessary to rinse the product well are key indicators of the qualities of use of a composition. For these reasons, it may be advantageous to provide foaming products in solid form which do not contain water or very little water, and also have the advantage of avoiding microbiological problems, and therefore of not requiring the use of preservatives. For example, from document FR 2 779 648, solid compositions are known in the form of a deformable paste based on anionic surfactants and on specific powdery fillers. These compositions can only be obtained using an extruder, which can be restrictive in terms of process. In order to overcome some of these problems, other solid cosmetic formulations have been proposed, in particular shower products or shampoos in the form of granules or solid powder. Mention may in particular be made to US 4,330,438 which describes shampoo concentrates in powder form comprising anionic surfactants and nonionic derivatives of galactomannan, which form shampoos after dilution with water. Mention may also be made of EP 0 796 318 which describes solid compositions obtained by drying and granulating aqueous surfactant pastes in the presence of solid fillers, such as wood flour. Mention may also be made of WO 2009/153311 which describes granulated shampoos comprising at least one surfactant deposited on solid particles. In this document, an aqueous phase comprising the surfactant is brought into contact with a solid phase consisting of fillers, so that the surfactant agglomerates on the fillers. This step can be carried out in a granulator mixer, in a mixer or in a fluidized bed granulator. Patent application FR 2 969 925 describes cosmetic compositions for cleaning anhydrous keratin materials, comprising the combination of a nonionic surfactant with an anionic surfactant and at least 25% by weight of fillers and / or fiber. These compositions can be in the form of a deformable solid, as well as in powder form. Finally, patent application FR 3 030 269 describes cosmetic compositions for cleaning keratin materials such as the hair or the skin, anhydrous, solid in the form of particles, comprising at least 30% by weight of anionic surfactants, at least 5 % by weight of amphoteric surfactants, and at least 10% by weight of fillers. However, the solid compositions thus prepared can disintegrate or disintegrate with difficulty in the presence of water, and do not always make it possible to obtain a rapid start of foam and / or an abundance of sufficient foam. They can also be difficult to remove on rinsing, and can leave residues on the skin or hair, which can then impact the cosmetic or aesthetic performance of the product. There is therefore a need to have compositions for washing keratin materials, which do not flow, which are more compact, moldable and economical. The desired compositions must disintegrate or disintegrate easily, be easy to apply to keratin materials, and allow rapid foaming, that is to say rapid obtaining of an adequate and sufficiently abundant foam, when the composition is applied, generally by rubbing, onto said keratin materials which may have been previously moistened. In addition, in recent years, the cosmetic market has been marked by a very strong demand for formulations containing ingredients of natural origin. Consumers want formulations free from chemical substances to which they prefer ingredients of natural origin, known for their better tolerance and affinity with the skin, and which are more respectful of the environment. We therefore seek to obtain foaming cleaning products containing compounds of natural origin having good harmlessness with respect to keratin materials, having good microbiological preservation, easy and pleasant to use while nevertheless having the properties required for foaming products, i.e. good mixing with water, rapid foaming and good rinsing. By “natural compound” is meant a compound which is obtained directly from the ground or soil, or from plants or animals, via, where appropriate, one or more physical processes, such as for example grinding. , refining, distillation, purification or filtration. By compounds "of natural origin" is understood a natural compound having undergone one or more chemical or industrial treatments, generating modifications which do not affect the essential qualities of this compound and / or a compound mainly comprising natural constituents having or not undergone transformations, as indicated above. By way of nonlimiting example of chemical or industrial annex treatment generating modifications which do not affect the essential qualities of a natural compound, mention may be made of those authorized by control bodies such as Ecocert (Standard for organic cosmetic products and ecological, January 2003) or defined in recognized manuals in the field, such as "Cosmetics and Toiletries Magazine", 2005, vol. 120, 9:10. The Applicant has discovered that a composition in the form of an anhydrous solid comprising a particular combination of anionic surfactants, at least one amphoteric surfactant, and a high level of charges makes it possible to achieve these objectives. More specifically, the subject of the invention is a composition, preferably a cosmetic composition, in the form of an anhydrous solid comprising at least one anionic surfactant chosen from isethionic acid derivatives and their salts, at least one anionic surfactant chosen from derivatives of glutamic acid and their salts, at least one amphoteric surfactant, and at least 20% by weight relative to the total weight of the composition of fillers. According to a particular embodiment of the invention, the composition comprises, as amphoteric surfactant, at least one betaine derivative. The compositions according to the invention are advantageously in the form of granules with a uniform particle size. The compositions according to the invention are easier to dose, which allows less loss of the product. They disintegrate or disintegrate easily, dissolution in water is rapid. They are easy to apply to keratin materials, and allow rapid foaming, that is to say rapid obtaining of an adequate and sufficiently abundant foam, when the composition is applied, generally by rubbing, on said keratin materials possibly moistened beforehand, as well as a good quality of foam, in particular a creamy, creamy and abundant foam. After application, good persistence of the perfume is obtained and, when the composition is applied to the skin, good softness of the skin. Another subject of the invention is a process for cleaning or removing make-up from keratin materials such as the skin, including the scalp, keratin fibers such as the eyelashes, the hair, and / or the lips, characterized by the fact which is applied to said keratin materials, a cosmetic composition as defined above. The composition according to the invention is intended for topical application and therefore contains a physiologically acceptable medium. The term “physiologically acceptable medium” is understood here to mean a medium compatible with keratin materials. In the context of the present invention, the term “keratin material” is understood in particular to mean the skin, the scalp, keratin fibers such as the eyelashes, the eyebrows, the hair, and the hair, the nails, the mucous membranes such as the lips , and more particularly the skin (body, face, eye area, eyelids). In what follows, the expression "at least one" is equivalent to "one or more" and, unless otherwise indicated, the limits of a range of values are included in this field. Anhydrous solid composition The composition according to the invention is in the form of a solid, that is to say that it does not flow under their own weight. According to a particular embodiment, they are in powder form, in particular in the form of particles such as granules or granules, or else in the form of powder. According to a particular embodiment of the invention, the composition is in the form of granules. Preferably, the particles according to the invention are presented as small fractionated objects formed of solid particles aggregated together, of varying shapes and sizes. They can be regular or irregular in shape. They can in particular be spherical, square, rectangular, elongated like sticks. In particular, the composition according to the invention is in the form of small fractionated objects, which can be of various shapes, generally of regular shape and preferably of spherical shape, even better of well calibrated spherical shape (homogeneous). Particularly preferred are spherical particles. The size of the particles can be, in its largest dimension, between 1 and 5000 μm, preferably between 50 and 5000 μm, even more preferably between 100 and 3500 μm, and better still between 200 and 3000 μm. The particle size can be determined by manual sieving or via a mechanical calibrator, as well as by laser granulometry, using for example the Masterizer 3000 model sold by the company Malvern. This solid presentation has many advantages such as better preservation of the homogeneity of the mixture, better flow and a reduction in dust generation. Thus, it allows easier handling of the compositions, as well as easier storage and transport. The composition according to the invention is anhydrous, that is to say that it does not comprise water (0%) or, if it does, the water content is less than or equal to 5% by weight, in particular less than or equal to 2% by weight, or even less than or equal to 1% by weight, even better less than or equal to 0.5% by weight, relative to the total weight of the composition. surfactants The anionic surfactant (s) chosen from isethionic acid derivatives, the anionic surfactant (s) chosen from glutamic acid derivatives, the amphoteric surfactant (s) present in the composition of the invention are generally foaming. Foaming surfactants are detergents and differ from emulsifying surfactants by the value of their HLB (Hydrophilic Lipophilie balance), HLB being the ratio between the hydrophilic part and the lipophilic part in the molecule. The term HLB is well known to those skilled in the art and is described for example in "The HLB System. A timesaving guide to Emulsifier Sélection ”(published by ICI Americas Inc; 1984). The term HLB (from the English "Hydrophilic Lipophilie Balance") is well known to those skilled in the art, and designates the hydrophilic-lipophilic balance of a surfactant. The HLB or hydrophilic-lipophilic balance of the surfactant (s) used according to the invention can be determined by the GRIFFIN method or the DAVIES method. The higher the value, the higher the solubility in water and conversely, the lower the value, the more the surfactant will have an affinity for oil. The HLB according to GRIFFIN is defined in the publication J. Soc. Cosm. Chem. 1954 (Volume 5), pages 249-256 or the HLB determined experimentally and as described in the work by authors F. PUISIEUX and M. SEILLER, entitled GALENICA 5: Dispersed systems - Tome I - Surface active agents and emulsions - Chapter IV - Notions of HLB and HLB review, pages 153-194 - paragraph 1.1.2. HLB determination experimentally, pages 164-180. Preferably, it is the value of the calculated HLB which must be taken into account. The calculated HLB is defined as the following coefficient: HLB calculated = 20 x molar mass hydrophilic part / total molar mass. The HLB according to DAVIES consists in summing up the hydrophilic and lipophilic contributions made by each of the structural groups of the surfactant: HLB = £ HLB hydrophilic groups Σ H LB hydrophobic groups + 7 Thus, the HLB of the surfactant is equal to the sum of the HLBs of the hydrophilic groups minus the sum of the HLBs of the hydrophobic groups plus 7. There are HLB tables for the different classic groups that can be found in particular in the following collection: Surfactants in cosmetics, second edition, surfactant science seriés volume 68, edited by Martin M.Rieger & Linda D.Rhein, p. 134, table 4. Reference may be made to the document "Encyclopedia of Chemical Technology, KIRKOTHMER", volume 22, p. 333-432, 3 rd edition, 1979, WILEY, for the definition of the properties and emulsifying functions of surfactants, in particular p. 347377 of this reference, for anionic and nonionic surfactants. According to a particular embodiment of the invention, the HLB values of the surfactant (s) are determined according to the DAVIES method which defines a scale varying from 0 to several tens (generally up to 50). For emulsifying surfactants, the HLB generally ranges from 3 to 8 for the preparation of water-in-oil (W / O) emulsions and from 8 to 18 for the preparation of oil-in-water (O / W) emulsions, while the Foaming surfactants generally have an HLB greater than 18, and better still greater than 20. Isethionic acid derivatives The composition according to the invention comprises at least one anionic surfactant chosen from isethionic acid derivatives and their salts, in particular their cosmetically acceptable salts. This or these anionic surfactants can for example be chosen from acyl isethionic acids, their salts (isethionates) and mixtures thereof, preferably from the salts of acyl isethionic acid in which the hydrocarbon chain R1 of the acyl group R1C = O, is linear or branched, saturated or unsaturated, and comprises from 8 to 30 carbon atoms, preferably from 10 to 22 carbon atoms, and better still from 12 to 18 carbon atoms. The acyl group can in particular be chosen from the lauroyl, myristoyl, palmitoyl, stearoyl, olivoyl, cocoyl, oleoyl groups and their mixtures. By “cosmetically acceptable salts” is meant that the hydrogen atom of the acid function of isethionic acid is replaced by an M + cation, for example chosen from the ions of alkali metals such as Na, Li, K, preferably Na or K, among the ions of alkaline earth metals such as Mg, ammonium groups and their mixtures. Mention may be made in particular of the compounds of the following formula: in which : R1 represents a linear or branched, saturated or unsaturated hydrocarbon chain, comprising from 8 to 30 carbon atoms, preferably from 10 to 22 carbon atoms and better still from 12 to 18 carbon atoms, M + represents H + or a cation, preferably chosen from ions of alkali metals such as Na, Li, K, from ions of alkaline earth metals, ammonium groups and mixtures thereof, and R2, R3, R4 and R5 represent, independently of each other, a hydrogen atom or an alkyl group, linear or branched, comprising from 1 to 4 carbon atoms. Preferably, R1 represents an alkyl group, linear or branched, comprising from 10 to 20 carbon atoms, better still from 12 to 18 carbon atoms. Preferably, R2 represents a hydrogen atom or a linear alkyl group comprising from 1 to 4 carbon atoms such as methyl, ethyl, propyl or butyl, in particular a methyl group. Even more preferably, R2 represents a hydrogen atom. Preferably, R3 represents a hydrogen atom. Preferably, R4 and R5 represent, independently of one another, a hydrogen atom or an alkyl group comprising from 1 to 4 carbon atoms. Even more preferably, R4 and R5 represent a hydrogen atom. As isethionic acid derivatives which can be used in the context of the invention, mention may be made, for example, of the compound bearing the name INCI sodium lauroyl methyl isethionate such as the references Iselux LQ-CLR, Iselux LQ-CLR-SB, or the mixture sodium lauroyl methyl isethionate / sodium methyl isethionate such as ISELUX (Pellets) offered by the company INNOSPEC. One can also cite the compound bearing the name INCI sodium cocoyl isethonate as the references HOSTAPON SCI marketed by the company CLARIANT or PUREACT I-85EC marketed by the company INNOSPEC ACTIVE CHEMICALS. Mention may also be made of sodium cocoyl isethionate sold under the name JORDAPON Cl P® by the company BASF. The isethionic acid derivative (s) and their salts may be present in the composition in an active material content ranging from 1 to 60% by weight, preferably from 2 to 40% by weight, and better still from 5 to 30% by weight. weight relative to the total weight of the composition. Glutamic acid derivatives The composition according to the invention comprises at least one anionic surfactant chosen from glutamic acid derivatives and their salts, in particular their cosmetically acceptable salts. This or these anionic surfactants can for example be chosen from acyl glutamic acids (acyl glutamic acid) and their salts (acyl glutamates). According to a particular embodiment, they are chosen from acyl glutamic acids, the acyl group of which comprises from 10 to 30 carbon atoms, preferably from 12 to 22 carbon atoms, such as, for example, lauroyl glutamic acids, myristoyl glutamic acids, palmitoyl glutamic, stearoyl glutamic, behenoyl glutamic, olivoyl glutamic, cocoyl glutamic and the salts of these acids, in particular the alkali metal salts such as Na, Li, K, preferably Na or K, the alkaline earth metal salts such as Mg , or the ammonium salts of said acids. Mention may be made, for example, of the compounds bearing the name INCI lauroyl glutamic acid, cocoyl glutamic acid, sodium stearoyl glutamate, potassium lauroyl glutamate, potassium cocoyl glutamate, sodium olivoyl glutamate, and their mixtures. Such compounds are marketed under the name AMISOFT by the company AJINOMOTO and in particular under the references Amisoft CA, Amisoft LA, Amisoft HS 11 PF, Amisoft MK-11, Amisoft LK-11, Amisoft CK-11, or even under the name EUMULGIN SG by COGNIS. Mention may also be made of triethanolamine cocoyl glutamate sold under the name AMISOFT CT 12 by the company AJINOMOTO, disodium cocoyl glutamate sold by the company Ajinomoto under the name Amisoft ECS-22SB, and sodium lauroyl glutamate sold under the name AMISOFT LS -11 by the company AJINOMOTO. Mention may also be made of sodium cocoyl glutamate sold under the name Amisoft CS-11 by the company AJINOMOTO. As acyl glutamic acid salt, mention may also be made of sodium hydrogenated tallowoyl glutamate such as that sold under the reference ACYLGLUTAMATE GS 11 by the company AJINOMOTO and disodium hydrogenated tallow glutamate such as that sold under the reference ACYLGLUTAMATE HS-21 AJINOMOTO company. Mention may also be made of commercial mixtures of surfactants comprising at least one glutamic acid derivative or a salt of said derivative such as for example the mixture of acyl glutamate salts such as Amisoft CS 22 marketed by AJINOMOTO. According to a particular embodiment of the invention, the mono-sodium salt of N-lauroyl L-glutamic acid is used, such as that sold by the company AJINOMOTO under the reference Amisoft HS 11 PF. The acyl glutamic acid (s) and their salts may be present in the composition according to the invention in an active material content (AM) ranging from 1 to 60% by weight, preferably from 2 to 40% by weight and better still from 5 to 30% by weight relative to the total weight of the composition. Amphoteric surfactants The composition according to the invention also comprises one or more amphoteric surfactants. The amphoteric surfactant (s) are chosen from amphoteric surfactants well known to those skilled in the art (this term including amphoteric and zwitterionic surfactants). According to a particular embodiment of the invention, the amphoteric surfactant (s) are chosen from the compounds of secondary or tertiary aliphatic amines, optionally quaternized, comprising a hydrocarbon chain, linear or branched, containing from 8 to 22 carbon atoms, or a mixture of such hydrocarbon chains, and comprising at least one anionic group, such as for example a carboxylate, sulfonate, sulfate group. The amphoteric surfactant (s) can be chosen from N-alkyl (C8-C22) betaines, N-alkyl (C8-C22) sulfobetaines, N-alkyl (C8-C22) amidoalkyl (Ci-C6) betaines, Nalkyl (C8-C22) sultaines, N-alkyl (Cs-C22) hydroxysultaines, N-alkyl (CsC22) amidoalkyl (Ci-C6) hydroxysultaines, N-alkyl (Cs-C22) amphoacetates, N-alkyl (CsC22 ) amphodiacetates, N-alkyl (Cs-C22) amphopropionates, N-alkyl (Cs-C22) amphodipropionates, N-alkyl (C8-C22) amphohydroxypropylsulfonates, diethylaminopropyl cocoaspartamide, and mixtures thereof. These surfactants are referenced in particular in the catalog of The Personnal Care Product Council. The Cs-C 2 2 alkyl group may be chosen from octyl (or caprylyl), decyl (or capryl), lauryl, myristyle, palmityl, stearyl, arachidyl, behenyl, and mixtures thereof. As N-alkyl (C8-C 2 2) betaines, mention may in particular be made of coco-betaine, such as the product sold under the name DEHYTON AB-30® by the company BASF, decyl betaine (or decyl dimethyl glycine), lauryl betaine (or lauryl dimethyl glycine) such as the product sold under the name GENAGEN KB® by the company Clariant, myristyle betaine (or myristyl dimethyl glycine), cetylbetaine (or cetyl dimethyl glycine), stearyl betaine (or stearyl dimethyl glycine). In known manner, the coconut group denotes the alkyl group deriving from coconut oil. It mainly comprises a mixture of lauryl and myristyle group. Advantageously, the N-alkyl (C8-C 2 2) betaines are coco-betaine. Among the N-alkyl (C8-C 2 2) amidoalkyl (Ci-C6) betaines, mention may, for example, be made of cocamidopropyl betaine (or coamidopropyl dimethyl glycine), for example marketed under the name DEHYTON® PK45 by the company BASF or under the name TEGO BETAIN CK D by the company EVONIK GOLDSCHMIDT, lauramidopropyl betaine marketed under the name REWOTERIC AMB12P® by the company EVONIK GOLDSCHMIDT, myristamidopropyl betaine, stearamidopropyl betaine, caprylitaine betaine / caprylitin Advantageously, the N-alkyl (C8-C 2 2) amidoalkyl (Ci-C6) betaines are chosen from N-alkyl (C8-C 2 2) amidopropyl betaines, such as those mentioned above, and preferably are cocamidopropyl betaine. Like the N-alkyl (C8-C 2 2) sulfobetaines, mention may be made of lauryl sulfobetaine. As N-alkyl (C8-C 2 2) sultaines, mention may be made of capryl sultaine, lauryl sultaine, myristyl sultaine, coco-sultaine. As N-alkyl (C8-C 2 2) hydroxysultaines, mention may be made of capryl hydroxysultaine, lauryl hydroxysultaine (for example BETADET® S-20 from Kao), myristyl hydroxysultaine, coco hydroxysultaine, cetyl hydroxysultaine. As N-alkyl (C8-C 2 2) amidoalkyl (Ci-C6) hydroxysultaines, mention may be made of cocamidopropyl hydroxysultaine (such as that sold under the name AMONYL675SB by the company Seppic or BETADET® SHR from Kao, lauramidopropyl hydroxysultaine, myristamidopropyl hydroxysultaine. As N-alkyl (C8-C 2 2) amphoacetates, there may be mentioned for example: N’-cocoyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium cocamphoacetate); N’-caproyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium caproamphoacetate); N’-capryloyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium capryloamphoacetate); N’-isostearoyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium isostearoamphoacetate); N-lauroyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium lauroamphoacetate); N’-myristoyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium myristoamphoacetate); N’-palmitoyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium palmamphoacetate); N’-stearoyl-N-hydroxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: sodium stearoamphoacetate). As N-alkyl (C8-C22) amphodiacetates, there may be mentioned for example: - N’-cocoyl-N-carboxymethoxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: disodium cocamphodiacetate) as the product marketed under the name MIRANOL C2M CONCENTRE NP® by the company Rhodia Chimie; - N’-caproyl-N-carboxymethoxyethyl-N-carboxymethyl-ethylenediamine di-sodium (CTFA name: disodium coproamphodiacetate); - N’-capryloyl-N-carboxymethoxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: disodium copryloamphodiacetate); - N’-isostearoyl-N-carboxymethoxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: disodium isostearoamphodiacetate); - N’-lauroyl-N-carboxymethoxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: disodium lauroamphodiacetate); - N’-stearoyl-N-carboxymethoxyethyl-N-carboxymethyl-ethylenediamine sodium (CTFA name: disodium stearoamphodiacetate) Advantageously, the N-alkyl (C8-C22) amphodiacetates are disodium cocamphodiacetate. As N-alkyl (Cs-C22) amphopropionates, there may be mentioned for example: N’-cocoyl-N-hydroxyethyl-N-carboxyethyl-ethylenediamine sodium (CTFA name: sodium cocamphopropionate) such as that sold under the name REWOTERIC AM KSF 40 by the company Evonik Goldschmidt (code 52683); N’-caproyl-N-hydroxyethyl-N-carboxyethyl-ethylenediamine sodium (CTFA name: sodium caproamphopropionate); N’-capryloyl-N-hydroxyethyl-N-carboxyethyl-ethylenediamine sodium (CTFA name: sodium capryloamphopropionate); N’-isostearoyl-N-hydroxyethyl-N-carboxyethyl-ethylenediamine sodium (CTFA name: sodium isostearoamphopropionate); N’-lauroyl-N-hydroxyethyl-N-carboxyethyl-ethylenediamine sodium (CTFA name: sodium lauroamphopropionate); N’-stearoyl-N-hydroxyethyl-N-carboxyethyl-ethylenediamine sodium (CTFA name: sodium stearoamphopropionate). As N-alkyl (Cs-C22) amphodipropionates, there may be mentioned: cocoamphodipropionic acid lauroamphodipropionic acid diethanolamine cocoamphodipropionate N'-cocoyl-N-carboxyethoxyethyl-N-carboxyethyl-ethylenediamine disodium (CTFA name: disodium cocoamphodipropionate) such as that sold under the name MACKAM 2CSF 40 ; disodium N-caproyl-N-carboxyethoxyethyl-N-carboxyethyl-ethylenediamine (CTFA name: disodium caproamphodipropionate); disodium capryloyl-N-carboxyethoxyethyl-N-carboxyethyl-ethylenediamine (CTFA name: disodium capryloamphodipropionate); disodium isostearoyl-N-carboxyethoxyethyl-N-carboxyethyl-ethylenediamine (CTFA name: disodium isostearoamphodipropionate); disodium N-lauroyl-N-carboxyethoxyethyl-N-carboxyethyl-ethylenediamine (CTFA name: disodium lauroamphodipropionate). As N- (C8-C22 alkyl) amphohydroxypropylsulfonates, mention may be made of sodium caproamphohydroxypropylsulfonate, sodium capryloamphohydroxypropylsulfonate, sodium cocoamphohydroxypropylsulfonate, such as that sold under the name MIRANOL CS CONCENTROHYRUS Sodium hydroxypropylsulfonyl, CONCONYPROSYLON, N-alkyl (Cs-C22) amphoacetates, N-alkyl (C8-C22) amphodiacetates, N-alkyl (Cs-C22) amphopropionates, N-alkyl (Cs-C22) amphodipropionates, N- (alkyl CsC22) amphohydroxypropylsulfonates may be in free acid form or in the form of salts, in particular alkaline (such as sodium, potassium) or alkaline earth (calcium, magnesium) salts, and preferably in the form of sodium salt. Monodiethylaminopropyl cocoaspartamide sodium can also be used, such as that sold under the name Chimexane HB by the company Chimex. According to a particular embodiment of the invention, the amphoteric surfactant (s) may be chosen from N-alkyl (C8-C22) betaines, N-alkyl (C8-C22) amidoalkyl (C6Cslbétaines, N-alkyl (C8 -C22) amphoacetates, N-alkyl (C8-C20) amphodiacetates, and mixtures thereof. According to a preferred embodiment, the composition according to the invention comprises at least one N-alkyl (C8-C22) amidoalkyl (Ci-C6) betaine, and preferably cocamidopropyl betaine. The amphoteric surfactant (s) are generally present in the anhydrous composition according to the invention in an amount of active material of between 0.5% and 40% by weight, relative to the total weight of the composition, in particular ranging from 1% to 30 % by weight, better from 1% to 20% by weight. Additional surfactants The composition according to the invention may comprise additional surfactants different from anionic surfactants and amphoteric surfactants such as those described above, but only insofar as the presence of these surfactants does not affect the comfort (safety) of the composition. . These additional surfactants can also be foaming within the meaning of the present invention. The additional surfactant (s), when they are present in the composition in accordance with the invention, can be chosen from anionic surfactants other than isethionic acid derivatives, glutamic acid derivatives, and their salts, non-surfactants ionic, and cationic surfactants. Preferably, they are chosen from anionic surfactants other than isethionic acid derivatives, glutamic acid derivatives, and their salts, and nonionic surfactants. The nonionic surfactants can be chosen for example from phospholipids, alkyl polyglucosides (APG), maltose esters, sucrose esters, hydrophobic gums, polyglycerolated fatty alcohols, glyceryl and fatty acid esters, oxyalkylenated glycerol esters, oxyalkylenated sugar esters, fatty acid and polyethylene glycol esters, fatty acid and sorbitan esters, glucamine derivatives such as 2-ethylhexyl oxy-carbonyl n-methyl glucamine , and mixtures thereof. The phospholipids used in the composition according to the invention may be of plant or animal origin and be in pure form or in the form of a mixture. The phospholipids used in the composition can in particular be lecithins which are a complex mixture of phosphatides chosen mainly from phosphatidic acid, phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, lysophosphatidylcholine and / or phosphatidylinositol, associated with variable amounts of other substances such as triglycerides, glycolipids, sphingolipids, fatty acids and carbohydrates. We can therefore choose either the phospholipids mentioned above, or the lecithins containing these phospholipids. According to a particular embodiment of the invention, the phospholipid (s) are chosen from non-hydrogenated lecithins and hydrogenated lecithins. Non-hydrogenated lecithins are generally obtained by lipid extraction using non-polar solvents, from vegetable or animal fats. This lipid fraction usually comprises, for the most part, glycerophospholipids, including phosphatidylcholine. Animal or plant sources that can be used to extract non-hydrogenated lecithins are, for example, soy, sunflower, or eggs. The glycerophospholipids included, in high proportion, in these lecithins are mainly phosphatidylcholine and phosphatidylethanolamine. The non-hydrogenated lecithins suitable for the implementation of the present invention may be lecithins derived from soybeans, sunflowers, eggs and / or their mixtures. Lecithins are usually supplied in dissolved form in fatty acids, triglycerides or other solvents, or in the form of powders or breads. These are usually mixtures of lecithins, the glycerophospholipid content of which, in the products as marketed, generally varies from approximately at least 15% to approximately at least 95%. Among the non-hydrogenated lecithins which may be suitable for the use of cosmetic compositions in accordance with the present invention, mention may be made of the lecithins sold under the references PHOSPHOLIPON 80® and Alcolec F100, PHOSALE 75® by the company AMERICAN LECITHIN COMPANY, EPIKURON 145V from CARGILL, EMULMETIK 320 or 100J from Cargill, OVOTHIN 200 and ORGANIC LECITHIN sold by the company LUCAS MEYER. Hydrogenated lecithins are obtained by controlled hydrogenation of non-hydrogenated lecithins as described above. As hydrogenated lecithin which can be used in the composition according to the invention, there may be mentioned, for example, that which is marketed under the reference NIKKOL LECINOL S 10 by NIKKO. As alkylpolyglucosides, use is preferably made of those containing an alkyl group comprising from 6 to 30 carbon atoms and preferably from 8 to 16 carbon atoms, and containing a hydrophilic group (glucoside) preferably comprising 1.2 to 3 saccharide units . Mention may be made, for example, of decylglucoside (Alkyl-C9 / C11 -polyglucoside (1.4)) as the product sold under the name MYDOL 10® by the company KAO, the product sold under the name PLANTAREN 2000 UP® by the company BASF, and the product marketed under the name ORAMIX NS 10 ® by the company SEPPIC; caprylyl / capryl glucoside such as the product sold under the name ORAMIX CG 110® by the company SEPPIC; laurylglucoside such as the products marketed under the names PLANTAREN 1200 N ® and PLANTACARE 1200 ® by the company BASF; and coco-glucoside such as the product marketed under the name PLANTACARE 818 / UP ® by the company BASF, ketostearyl glucoside optionally in mixture with cetostearyl alcohol, marketed for example under the name MONTANOV 68 by the company SEPPIC, under the name TEGO CARE CG90 by the company EVONIK GOLDSCHMIDT and under the name EMULGADE KE3302 by the company BASF; arachidyl glucoside, for example in the form of the mixture of arachidic and behenic alcohols and of arachidyl glucoside marketed under the name MONTANOV 202 by the company SEPPIC; cocoylethylglucoside, for example in the form of the mixture (35/65) with cetyl and stearyl alcohols, sold under the name MONTANOV 82 by the company SEPPIC and their mixtures. The oxyalkylenated glycerol esters are in particular the polyoxyethylenated derivatives of the glyceryl and fatty acid esters and of their hydrogenated derivatives. These oxyalkylenated glycerol esters can be chosen, for example, from glyceryl esters and from hydrogenated and oxyethylenated fatty acids such as PEG-200 hydrogenated glyceryl palmate sold under the name Rewoderm Ll-S 80 by the company Evonik Goldschmidt; oxyethylenated glyceryl cocoates such as PEG-7 glyceryl cocoate sold under the name Tegosoft GC by the company Evonik Goldschmidt, and PEG-30 glyceryl cocoate sold under the name Rewoderm LI-63 by the company Evonik Goldschmidt; and their mixtures. The oxyalkylenated sugar esters are in particular the polyethylene glycol ethers of the fatty acid and sugar esters. These oxyalkylenated sugar esters can be chosen, for example, from oxyethylenated glucose esters such as PEG-120 methyl glucose dioleate sold under the name Glucamate DOE 120 by the company LUBRIZOL. The fatty acid and polyethylene glycol esters are preferably esters of C16-C22 fatty acids comprising from 8 to 100 units of ethylene oxide. The fatty chain of the esters can be chosen in particular from stearyl, behenyl, arachidyl, palmityl, cetyl units and their mixtures such as cetearyl, and preferably a stearyl chain. The number of ethylene oxide units can range from 8 to 100, preferably from 10 to 80, and better still from 10 to 50. According to a particular embodiment of the invention, this number can range from 20 to 40. As an example of a fatty acid ester of polyethylene glycol, mention may be made of esters of stearic acid comprising respectively 20, 30.40, 50.100 ethylene oxide units, such as the products sold respectively under the name Myrj 49 P (polyethylene glycol stearate 20 OE; CTFA name: PEG-20 stearate), Myrj 51, Myrj 52 P (polyethylene glycol 40 stearate; CTFA name: PEG-40 stearate), Myrj 53, Myrj 59 P by CRODA. The esters of C16-C22 fatty acids and of sorbitan are in particular esters of C16-C22 acids and of sorbitan and are formed by esterification of at least one fatty acid comprising at least one saturated or unsaturated linear alkyl chain , having respectively from 16 to 22 carbon atoms, with sorbitol. These esters can in particular be chosen from stearates, behenates, arachidates, palmitates, sorbitan oleates, and their mixtures. Preferably sorbitan stearates and palmitates are used, and preferably sorbitan stearates. As an example of a sorbitan ester which can be used in the composition according to the invention, sorbitan monostearate (CTFA name: Sorbitan stearate) sold by the company Croda under the name Span 60 may be cited, sorbitan tristearate sold by the company Croda company under the name Span 65 V, sorbitan monopalmitate (CTFA name: Sorbitan palmitate) sold by the company Croda under the name Span 40, sorbitan monoleate sold by Croda under the name Span 80 V, the trioleate sorbitan sold by the company Uniqema under the name Span 85 V. preferably, the sorbitan ester used is sorbitan tristearate. The glyceryl and fatty acid esters can be obtained in particular from an acid comprising a linear saturated alkyl chain having from 16 to 22 carbon atoms. As glyceryl ester and fatty acid, there may be mentioned in particular glyceryl stearate (mono-, di- and / or glyceryl tri-stearate) (CTFA name: Glyceryl stearate), glyceryl ricinoleate, and mixtures thereof. Preferably, the glyceryl ester and fatty acid used is chosen from glyceryl stearates. Mention may also be made of the mixture of glyceryl stearate and of polyethylene glycol 100 OE monostearate, and in particular that comprising a 50/50 mixture, sold under the name Arlacel 165 by the company Croda. The sucrose and fatty acid esters are preferably chosen from the esters resulting from the reaction of sucrose (saccharose) and fatty acid (s) comprising from 10 to 24 carbon atoms, preferably from 12 to 20 carbon atoms, better from 12 to 18 carbon atoms and even better from 12 to 16 carbon atoms. Fatty acids comprising from 10 to 24 carbon atoms can be linear or branched, saturated or unsaturated. The fatty acids can be chosen from oleic acid, lauric acid, palmitic acid, myristic acid, stearic acid, linoleic acid, capric acid, or mixtures thereof According to one embodiment, the sucrose and fatty acid ester is chosen from the esters resulting from the sucrose and fatty acid reaction comprising from 12 to 18 carbon atoms, preferably from 12 to 16 carbon atoms such as lauric acid and / or palmitic acid such as, for example, sucrose laurate, sucrose palmitate or a mixture. The sucrose and fatty acid esters can be chosen from mono-, di-, tri- and tetra-esters, polyesters and their mixtures. Esters with a low degree of esterification, such as, for example, monoesters, diesters, triesters of sucrose and fatty acid or a mixture, are preferably used. The sucrose and fatty acid ester can be in the form of a mixture of esters with a low degree of esterification, for example a mixture of monoester and diester or a mixture of monoester, diester and triester. In the case where a mixture of sucrose and fatty acid esters is used, a mixture is preferred in which the esters with a low degree of esterification, in particular monoesters, are predominant and represent for example at least 50 %, preferably at least 60% by weight of the mixture of sucrose esters and fatty acid. Use may in particular be made of a mixture of sucrose esters and of fatty acids comprising from 12 to 16 carbon atoms, in particular a mixture of mono, di and triesters of lauric acid or palmitic acid, said mixture possibly comprising in a minority (in a content less than or equal to 40% by weight relative to the weight of the mixture of sucrose esters and fatty acid) of sucrose esters of fatty acids in which the fatty acid comprises more than 16 carbon atoms. Preferably, the sucrose and fatty acid ester which can be used in the present invention has an HLB greater than or equal to 10, preferably greater than or equal to 12. As is well known, the term HLB (Hydrophilic-Lipophilic Balance) means the balance between the size and strength of the hydrophilic group and the size and strength of the lipophilic group of the surfactant. The HLB value according to GRIFFIN is defined in J. Soc. Cosm. Chem. 1954 (volume 5), pages 249-256. Examples of esters or mixtures of sucrose and fatty acid esters that may be mentioned include the products marketed by the company MITSUBISHI KAGAKU FOODS below: the Surfhope SE COSME C-1416, having an HLB of 16, which is a myristate sucrose comprising approximately 80% of monoester, the rest of the mixture being composed of di and triesters, the Surfhope SE COSME C-1216 whose INCI name is sucrose laurate, of HLB equal to 16 and comprises from 75 to 90% of monoester, the rest of the mixture being composed of di and triesters, the Surfhope SE COSME C-1215L whose INCI name is sucrose laurate, of HLB HLB equal to 15, comprising approximately 70% of monoesters, the remainder of the mixture being composed of diesters and other polyetsers, the Surfhope SE COSME C-1616, having an HLB of 16, which is a mixture of sucrose esters and palmitic acids and / or stearic (INCI name sucrose palmitate), comprising from 75 to 90% of monoester, the rest of the mixture being composed of di and triesters, and may include sucrose stearate and sucrose palmitate stearate. One can also cite the ester bear the name INCI sucrose laurate marketed by the company Daiichi Kogyo Seiyaku under the reference DK ester S-L18A, of HLB equal to 17, comprising 70% of monoesters and 30% of di- and tri-esters . Examples of esters or mixtures of fatty acid sucrose esters that may also be mentioned: - the products sold under the names F160, F140, F110, F90, F70, SL40 by the company CRODESTA, designating respectively the palmito-stearates of sucrose formed from 73% of monoester and 27% of di- and tri-ester, from 61 % of monoester and 39% of di-, tri-, and tetra-ester, of 52% of monoester and 48% of di-, tri-, and tetra-ester, of 45% of monoester and 55% of di-, tri-, and tetra-ester, 39% monoester and 61% di-, tri-, and tetra-ester, and sucrose mono-laurate; - the products sold under the name RYOTO SUGAR ESTERS, for example referenced B370 and corresponding to the sucrose behenate formed from 20% monoester and 80% di-triester-polyester; - the sucrose mono-di-palmito-stearate sold by the company EVONIK GOLDSCHMIDT under the name TEGOSOFT PSE. According to one embodiment, sucrose laurate is used. According to one embodiment, the composition comprises at least one nonionic surfactant chosen from sucrose esters, in particular sucrose laurate. The amount of nonionic surfactants can range, for example, from 0.1 to 20% by weight, preferably from 0.5 to 15% by weight, better from 1 to 10% by weight, even better from 2 to 8% by weight relative to the total weight of the composition. The anionic surfactants other than the derivatives of isethionic acid, derivatives of glutamic acid, and their salts can be chosen in particular from anionic derivatives of proteins of vegetable origin, amino acids and amino acid derivatives, alkyl sulfates, alkyl ether sulfates, sulfonates, taurates, sulfosuccinates, alkyl sulfoacetates, phosphates and alkylphosphates, polypeptides, anionic derivatives of alkyl polyglucoside, soaps (fatty acid salts), derivatives of oil soy, lactic acid derivatives, their salts and mixtures. The anionic derivatives of proteins of vegetable origin are protein hydrolysates with a hydrophobic group, said hydrophobic group being able to be naturally present in the protein or to be added by reaction of the protein and / or the protein hydrolyzate with a hydrophobic compound. The proteins are of plant origin, and the hydrophobic group can in particular be a fatty chain, for example an alkyl chain containing from 10 to 22 carbon atoms. As anionic derivatives of proteins of vegetable origin, usable in the composition according to the invention, one can more particularly quote hydrolysates of proteins of wheat, soya, oats or silk, comprising an alkyl chain having from 10 to 22 carbon atoms and their salts. The alkyl chain can in particular be a lauryl chain and the salt can be a sodium, potassium and / or ammonium salt. Mention may be made, for example, of the sodium, potassium and / or ammonium salts of silk protein hydrolysates modified with lauric acid, such as the product sold under the name KAWA SILK by the company Kawaken; sodium, potassium and / or ammonium salts of wheat protein hydrolysates modified by lauric acid, such as the potassium salt marketed under the name AMINOFOAM W OR by the company Croda (CTFA name: Potassium lauroyl wheat aminoacids) and the sodium salt sold under the name PROTEOL LW 30 by the company Seppic (CTFA name: sodium lauroyl wheat aminoacids); the sodium, potassium and / or ammonium salts of oat protein hydrolysates comprising an alkyl chain having from 10 to 22 carbon atoms, and more especially the sodium, potassium and / or ammonium salts of oat protein hydrolysates modified by lauric acid, such as the sodium salt marketed under the name PROTEOL OAT (CTFA name: Sodium lauroyl oat aminoacids), PROTEOL SAV 50S (INCI name: Sodium cocoyl aminoacid), PROTEOL APL (INCI name: sodium cocoyl apple amino acids) by the company Seppic, AMARANTH S (INCI name: sodium cocoyl hydrolyzed amaranth proteins) by the company LONZA; and their mixtures. As alkyl ether sulphates, mention may, for example, be made of sodium lauryl ether sulphate (C12-14 70/30) (2.2 EO) sold under the names SIPON AOS 225® or TEXAPON N702 PATE® by the company Cognis, lauryl ammonium ether sulfate (C1214 70/30) (3 EO) sold under the name SIPON LEA 370® by the company Cognis, the alkyl (C12-C14) ether (9 EO) ammonium sulphate sold under the name RHODAPEX AB / 20® by the company Rhodia Chimie. As sulfonates, there may be mentioned, for example, the sulfonate alpha-olefins such as sodium alpha-olefin sulfonate (C14-16) sold under the name BIO-TERGE AS-40® by the company Stepan, sold under the names WITCONATE AOS PROTEGE® and SULFRAMINE AOS PH 12® by the company Witco or marketed under the name BIO-TERGE AS-40 CG® by the company Stepan, the secondary sodium olefin sulfonate marketed under the name HOSTAPUR SAS 30® by the company Clariant; linear alkyl aryl sulfonates such as sodium xylene sulfonate sold under the names MANROSOL SXS30®, MANROSOL SXS40®, MANROSOL SXS93® by the company Manro. As alkyl sulfoacetates, mention may be made of laurylsulfoacetate, for example that which is sold as a mixture with sodium methyl-2-sulfolaurate and disodium 2-sulfolaurate under the reference STEPAN MILD PCL by the company Stepan. As taurates, mention may be made of the sodium salt of palm kernel oil methyltaurate sold under the name HOSTAPON CT PATE® by the company Clariant; N-acyl N-methyltaurates such as sodium N-cocoyl N-methyltaurate sold under the name HOSTAPON LT-SF® by the company Clariant or marketed under the name NIKKOL CMT-30-T® by the company Nikko, palmitoyl methyltaurate sodium sold under the name NIKKOL PMT® by the company Nikko. As sulfosuccinates, mention may be made, for example, of lauryl alcohol mono-sulfosuccinate (C12 / C14 70/30) oxyethylenated (3 EO) sold under the names SETACIN 103 SPECIAL® by the company Z SCHIMMER & SCHWARZ or REWOPOL SB-FA 30 K 4 ® by the company EVONIK GOLDSCHMIDT, the sodium salt of a hemisulfosuccinate of C12-C14 alcohols, marketed under the name SETACIN F SPECIAL PASTE® by the company Z SCHIMMER & SCHWARZ, the oleamidosulfosuccinate disodium oxyethylenated (2 EO) marketed under the name STANDAPOL SH 135® by the company Cognis, the oxyethylenated lauric amide mono-sulfosuccinate (5 EO) marketed under the name LEBON A-5000® by the company Sanyo, the disodium salt of oxyethylenated lauryl citrate mono-sulfosuccinate (10 EO) ) marketed under the name REWOPOL SB CS 50® by the company EVONIK GOLDSCHMIDT, the disodium salt of lauric alcohol mono-sulfosuccinate marketed under the name REWOPOL SB F12P® mination by the company EVONIK GOLDSCHMIDT, ricinoleic mono-ethanolamide mono-sulfosuccinate marketed under the name REWODERM S 1333® by the company Witco. As phosphates and alkylphosphates, mention may, for example, be made of monoalkylphosphates and dialkyl phosphates, such as lauryl mono-phosphate sold under the name MAP 20® by the company Kao, the potassium salt of dodecyl phosphoric acid, mixture of mono- and di-ester (majority diester) marketed under the name CRAFOL AP-31® by the company PULCRA, the mixture of monoester and di-ester of octylphosphoric acid, marketed under the name CRAFOL AP-20® by PULCRA, the mixture of monoester and diophoric acid diester of ethoxylated 2-butyloctanol (7 moles of EO), marketed under the name ISOFOL 12 7 EO-PHOSPHATE ESTER® by the company SASOL, the potassium or mono-alkyl (C12-C13) phosphate triethanolamine marketed under the references ARLATONE MAP230K-40® and ARLATONE MAP230T60® by the company Uniqema, potassium lauryl phosphate marketed under the name DERMALCARE MAP XC-99 / 09® nation by Rhodia. The anionic derivatives of alkyl polyglucosides can in particular be citrates, tartrates, sulfosuccinates, carbonates and glycerol ethers obtained from alkyl polyglucosides. Mention may be made, for example, of the sodium salt of cocoylpolyglucoside (1,4) tartaric ester, sold under the name EUCAROL AGE-ET® by the company LAMBERTI, the sodium salt of cocoylpolyglucoside sulfosuccinic ester (1,4 ), sold under the name ESSAI 512 MP® by the company Seppic, the sodium salt of cocoyl polyglucoside (1,4) citric ester sold under the name EUCAROL AGE-EC® by the company LAMBERTI. Soaps are obtained from a fatty acid which is partially or totally saponified (neutralized) by a basic agent. These are soaps of alkali or alkaline earth metal or organic bases. As fatty acids, saturated linear or branched fatty acids may be used, having from 8 to 30 carbon atoms, and preferably having from 8 to 22 carbon atoms. This fatty acid can in particular be chosen from palmitic acid, stearic acid, myristic acid, lauric acid and their mixtures. As basic agents, it is possible, for example, to use alkali metal hydroxides (sodium hydroxide and potassium hydroxide or potassium hydroxide), alkaline earth metal hydroxides (for example magnesium), ammonium hydroxide, or alternatively organic bases such as triethanolamine, N-methylglucamine, lysine and arginine. The soaps may in particular be alkaline fatty acid salts, the basic agent being an alkali metal hydroxide, and preferably potassium or potassium hydroxide (KOH). The amount of basic agent must be sufficient for the fatty acid to be at least partially neutralized. Mention may in particular be made of sodium or potassium laurate, potassium myristate, potassium palmitate, potassium stearate, potassium cocoate or else the stearic acid salts of KOH formed in situ. Soybean oil derivatives and their salts are in particular fatty acids and fatty acid salts derived from soybean oil (whose INCI name is “glycine soybean oil” or “soybean oil”) and in particular the alkali metal salts such as Na, Li, K, preferably Na or K, and fatty acids derived from soya, such as potassium soyate, for example that which is sold by the company Noveon, As acylamino acids other than glutamic acid derivatives, mention may, for example, be made of sodium cocoylglycinate sold by the company Ajinomoto under the name Amilite GCS-12, analinates and their derivatives such as that which is marketed under the name AMILITE ACS-12 by the company AMILON, the sodium cocoylglycinate marketed by the company Ajinomoto under the name Amilite GCK-12, the sodium lauroyl sarcosinate marketed by the company Seppic under the name ORAMIX L 30, the sodium and disodium stearoyl glutamate marketed by the company Ajinomoto under the name Amisoft HS21 P and HS11 PF and sodium cocoyl sarcosinate marketed by the company ZSCHIMMER & SCHWARZ under the name Protelan LS 9011 / C. Mention may also be made of the sodium salt of lauroyl amino acids from oats such as the Proteol OAT sold by the company Seppic or the compound bearing the name INCI sodium cocoyl amino acids such as the Proteol SAV 50 S from Seppic. The amino acid derivatives can be chosen, for example, from sarcosinates and in particular acylsarcosinates such as sodium lauroyl sarcosinate sold under the name ORAMIX L 30® by the company Seppic, sodium myristoyl sarcosinate, sold under the name NIKKOL SARCOSINATE MN® the company Nikko, sodium palmitoyl sarcosinate, sold under the name NIKKOL SARCOSINATE PN ® by the company Nikko; alaninates such as sodium N-lauroyl-Nmethylamidopropionate, sold under the name SODIUM NIKKOL ALANINATE LN 30® by the company Nikko, and N-lauroyl N-methylalanine triethanolamine, sold under the name ALANONE ALTA ® by the company KAWAKEN FINE ; aspartates such as the mixture of triethanolamine N-lauroylaspartate and triethanolamine N-myristoylaspartate, sold under the name ASPARACK® by the company Mitsubishi; citrates. The lactic acid derivatives or their salts can be chosen from the acyl lactylic acid derivatives, their salts (lactylates) such as sodium stearoyl lactylate, offered for example by the company AARHUSKARL SHAMN under the name Akoline SL, or also by Dr Straetmans under the name Dermofeel SL; isostearoyl lactylate sodium such as that sold by RITA under the name PATIONIC ISL; sodium behenoyl lactylate, for example sold by the company AMERICAN INGREDIENTS under the name PATIONIC SBL; sodium cocoyl lactylate such as that sold by the company RITA under the name PATIONIC SCL, sodium oleoyl lactylate, sodium lauroyl lactylate (PATIONIC 138C from CARAVAN INGREDIENTS), sodium caproyl lactylate (CAPMUL S8L-G from ABITEC). Mention may also be made of the mixture of sodium cocoamphoacetate, glycerin, lauryl glucoside, sodium cocoylglutamate, sodium lauryl glucose carboxylate sold by the company Cognis under the reference Plantapon SF. The additional anionic surfactants can be present in a content ranging from 0.1 to 20% by weight, preferably from 0.5 to 15% by weight, better from 1 to 10% by weight, even better from 2 to 8% by weight. weight relative to the total weight of the composition. According to a particular embodiment of the invention, the total amount of active ingredient in foaming surfactants is between 5% and 80% by weight, preferably between 10% and 60% by weight, and even more preferably between 3 and 50 % by weight of the total weight of the composition. According to a particular embodiment of the invention, the composition comprises less than 5% by weight of anionic surfactant comprising at least one sulphate group, in particular less than 2% by weight, even less than 1% by weight, even better less than 0.5% by weight, relative to the total weight of the composition. Preferably, the composition is free from an anionic surfactant comprising at least one sulphate group, such as, for example, alkyl sulphates and alkyl ether sulphates. loads The fillers are present in the composition according to the invention in a content greater than or equal to 20% by weight relative to the total weight of the composition, preferably greater than or equal to 25% by weight, better still greater than or equal to 45% by weight. weight. The amount of fillers in the composition according to the invention can range from 20% to 80% by weight, better still from 30% to 75% by weight relative to the total weight of the composition. By fillers, it is necessary to understand solid particles insoluble in the medium of the composition regardless of the temperature at which the composition is produced. The fillers can be colorless or white, mineral or organic, of any physical form (platelet, spherical or oblong), and of any crystallographic form (for example in sheets, cubic, hexagonal, orthorhombic, etc.). The fillers can be porous or non-porous. As fillers, mention may be made of mineral fillers such as silica, clays, ceramic beads, calcium carbonate, titanium oxides, talc or magnesium silicate (particle size: 5 microns) sold under the name LUZENAC 15 M00 ® by the company IMERYS, talcs marketed under the names LYZENAC 00 and LUZENAC PHARMA M by the company IMERYS, kaolin or aluminum silicate, for example that marketed under the name KAOLIN SUPREME® by the company, grain size between 1 and 1000 microns, or organic fillers such as starches, in particular corn starch such as for example the product sold under the name AMIDON DE MAIS B ® by the company ROQUETTE, rice starch, Arrow root starch, as well as their derivatives, the NATPURE HOLLOW BEAD spheres marketed by the company SENSIENT, celluloses such as celluloid beads dares CELLULOBEAD D-10 from the company DAITOKA SEIKOGYO, colloidal silicas, sodium carbonate, nylon microspheres such as those marketed under the name ORGASOL2002 UD NAT COS® by the company ATOCHEM, micronized or non-micronized plant powders such as powders fruit from the company LESSONIA or bamboo powders, or powdered rice hulls, and mixtures thereof. The starch derivatives used in the present invention can come from a vegetable source such as cereals, tubers, roots, vegetables and fruits. Thus, the starch (s) can come from a vegetable source chosen from corn, peas, potato, sweet potato, banana, barley, wheat, rice, oats, sago, tapioca and sorghum. Starches are generally in the form of a white powder, insoluble in cold water, the size of the elementary particles of which ranges from 15 to 100 microns. It is possible in particular to use, within the framework of the invention, starches used in a crosslinked form and in a chemically modified form by functionalization with carboxyalkyl units. The purpose of crosslinking is to form a network that is much more stable to heat and better resistant to heat and acidity. The starch chains are linked together by linking molecules: phosphate derivatives, chloroepoxide derivatives, acid dianhydrides and aldehyde derivatives. The (C1-C4) carboxyalkyls of starch also referred to below as "carboxyalkyl starch" are obtained by grafting carboxyalkyl groups onto one or more alcohol functions of the starch, in particular by reaction of starch and sodium monochloroacetate in the medium alkaline. The carboxyalkyl groups are generally fixed via an ether function, more particularly on carbon 1. The degree of substitution in carboxyalkyl unit of the C1-C4 carboxyalkyl of starch preferably ranges from 0.1 to 1 and more particularly from 0.15 to 0.5. The degree of substitution is defined according to the present invention as being the average number of hydroxyl groups substituted by an ester or ether group per monosaccharide unit of the polysaccharide. The carboxyalkyl starches are advantageously used in the form of salts and in particular of alkali or alkaline earth metal salts such as Na, K, Li, NH 4 , of a quaternary ammonium or of an organic amine such as mono, di or triethanolamine. Carboxyalkyl Ci-C 4 starch are advantageously in the context of the present invention carboxymethyl. The carboxymethyl starches preferably comprise units of the following formula: ch 2 och 2 coox ch 2 och 2 coox OH OH in which X, linked or not covalently to the carboxylic unit, denotes a hydrogen atom, an alkali or alkaline earth metal such as Na, K, Li, NH 4 , a quaternary ammonium or an organic amine such as for example mono, di or triethanolamine. Preferably, X denotes a Na + cation. The carboxyalkyl starches which can be used according to the present invention are partially or totally crosslinked carboxyalkyl starches. In general, a cross-linked carboxyalkyl starch has, in contrast to a non-cross-linked carboxyalkyl starch, an increased, controllable viscosity and increased stability. Cross-linking thus makes it possible to reduce the phenomena of syneresis and to increase the resistance of the gel to the effects of shearing. It also makes it possible to increase the hydrophilicity of the material as well as its speed of disintegration. The carboxyalkyl starches considered according to the invention are more particularly carboxyalkyl starches of potatoes. Thus, the carboxyalkyl starches which can be used according to the present invention are preferably sodium salts of carboxyalkyl starch, in particular a sodium salt of carboxymethyl starch of potato sold in particular under the name PRIMOJEL by the company DMV International or GLYCOLYS® and GLYCOLYS LV® by the Company Roquette. According to a particular mode, the potato carboxymethyl starch sold in particular under the name GLYCOLYS® by the company Roquette will be used. Mention may also be made, as fillers, of exfoliating particles which will allow the exfoliation of the skin. As exfoliating particles, one can use exfoliating or exfoliating particles of mineral, vegetable or organic origin. Thus, it is possible, for example, to use beads or polyethylene powder, such as those sold under the name Microthene MN 727 or Microthene MN 710-20 by the company Equistar or as the powder sold under the name Gotalene 120 Incolore 2 by the company Dupont ; nylon particles such as those sold by the company ATOCHEM under the name Orgasol 2002 EXD NAT COS; polyvinyl chloride powder; pumice stone (INCI name: pumice) such as pumice 3 / B from Eyraud; crushed fruit kernel hulls such as apricot kernel or nut shell hulls; sawdust, wood flour, cork flour; glass beads; alumina (aluminum oxide) (INCI name: Alumina) as the product sold under the name Dermagrain 900 by the company Marketech International; sugar crystals; beads which melt during application to the skin, such as, for example, the spheres based on mannitol and cellulose sold under the names Unisphères by the company Induchem, the capsules based on agar sold under the names Primasponge by the Cognis, and the spheres based on jojoba esters sold under the names Florasphères by the company Floratech; and their mixtures. According to one embodiment, the composition according to the invention comprises at least one filler chosen from talcs, starches, in particular rice starch and corn starch, and their mixtures. Binding agents According to a particular embodiment of the invention, the composition comprises at least one binding agent. According to a preferred embodiment, the binding agent or agents are liquid, hydrophilic or lipophilic, preferably hydrophilic (aqueous binders). For the purpose of the present invention, the term “binding agent, hydrophilic or lipophilic liquid” means a liquid which interacts with at least one solid raw material. In the context of the invention, the binding agent (s) can be chosen from: polyols such as glycerol, 1,3 propanediol, propylene glycol, butylene glycol, hexylene glycol, polyethylene glycols such as PEG-8, dipropylene glycol, sugars such as mannitol, maltodextrin, sorbitol, xylitol, sucrose, glucose, and mixtures thereof. According to a particular embodiment of the invention, the composition comprises at least one binding agent chosen from polyols. Preferably, it is propylene glycol. The binding agent (s) may represent from 1% to 30% by weight relative to the total weight of the composition, preferably from 2% to 20% by weight relative to the total weight of the composition, and at best 5% to 18 %. cyclodextrins According to a particular embodiment of the invention, the composition comprises at least one cyclodextrin. By cyclodextrin is meant within the meaning of the present invention, a non-chemically modified cyclodextrin. The cyclodextrins which can be used according to the present application are in particular oligosaccharides of formula: in which x can be a number equal to 4 (which corresponds to Ι'α-cyclodextrin), to 5 (β-cyclodextrin) or to 6 (γ-cyclodextrin). Preferably, the cyclodextrin according to the invention is chosen from β-cyclodextrin and γ-cyclodextrin. Preferably it is β-cyclodextrin. One can in particular use a β-cyclodextrin sold by the company WACKER under the name CAVAMAX W7 PHARMA® and a γ-cyclodextrin sold by the company WACKER under the name CAVAMAX W8®. The cyclodextrin (s) may represent from 1% to 70% by weight relative to the total weight of the composition, preferably from 2% to 30% by weight relative to the total weight of the composition, and at best 2% to 20% . Fatty acid salts According to a particular embodiment of the invention, the composition comprises at least one fatty acid salt. The fatty acid salt is advantageously a monocarboxylic acid salt comprising from 8 to 20 carbon atoms, preferably from 10 to 18 carbon atoms. It is more particularly a fatty acid salt chosen from caprylic, capric, lauric, myristic, palmitic, stearic, oleic acids, or their mixtures such as coconut salts. The fatty acid salt can be chosen from alkali metal, alkaline earth metal, or amine salts. The salt can be chosen from sodium, potassium, calcium, magnesium, ammonium, diethanolamine, triethanolamine, triisopropanolamine salts. As examples of fatty acid salts, there may be mentioned: sodium or potassium caprate; sodium or potassium caprylate; sodium or potassium or magnesium or calcium or ammonium or triethanolamine laurate; sodium or potassium or magnesium or calcium myristate or diethanolamine or triethanolamine or triisopropanolamine; sodium or potassium or magnesium palmitate or triethanolamine; sodium or potassium or magnesium or triethanolamine cocoate; sodium or potassium or magnesium or ammonium stearate or diethanolamine or triethanolamine; sodium or potassium or ammonium oleate; sodium peanutate; behenate sodium or potassium or calcium. Advantageously, a salt of monocarboxylic acid having 12 to 18 carbon atoms or of their mixture, such as those described above, is used. In particular, a salt of stearic acid can be used. According to one embodiment, the composition of the invention comprises magnesium stearate. The fatty acid salt or salts may be present in the composition according to the invention in a content ranging from 0% to 5% by weight, preferably ranging from 0.1% to 2% by weight relative to the total weight of the composition. admixtures The compositions of the invention may contain adjuvants usually used in the cosmetic field, and in particular those used in cleaning products. The compositions of the invention can in particular comprise at least one disintegrating agent. In the context of the present invention, the term "disintegrating agent" means a component capable of accelerating the speed of separation of the particles forming the granules, for example in contact with water when the composition is used. By way of example, mention may be made, for example, of effervescent agents such as sodium bicarbonate and citric acid. As adjuvants, mention may also be made of perfumes, preservatives, sequestrants (EDTA, sodium phytate), pigments, pearlescent agents, soluble dyes, sun filters, cosmetic or dermatological active agents such as water-soluble or liposoluble vitamins, antiseptics, antiseborrheics, antimicrobials such as benzoyl peroxide, salicylic acid, triclosan, azelaic acid, and also optical brighteners, nonionic polymers such as polyvinylpyrrolidone, anionic polymers, fatty substances such as oils or waxes. The amounts of these various adjuvants are those conventionally used in the field under consideration, and for example from 0.01 to 20% of the total weight of the composition. These adjuvants and their concentrations must be such that they do not modify the property sought for the composition of the invention. As active agents, mention may be made of any care or cleaning active agent usually used in the cosmetic field, and in particular antibacterials such as octopirox and triclosan, keratolytic agents such as salicylic acid and its derivatives, lactic acid or glycolic acid, essential oils, vitamins such as vitamin C (ascorbic acid, vitamin A (retinol), vitamin PP (niacinamide), vitamin B3 (panthenol) and their derivatives. Preparation process According to a particular embodiment of the invention, the composition is in the form of granules. Generally, the process used to obtain these granules calls for an agglomeration operation without compression called wet granulation. This granulation technique aims to transform generally powdery materials into small grains, by introducing a liquid making it possible to create bridges between the particles. The agglomeration is done by introducing into a shearing granulator (example: coulters or vertical), rotary (example: drum mixer or granulating plate, or on a fluidized bed), on the one hand the pulverulent powder, on the other hand a small amount of a liquid which is usually water. This has the effect of causing the particles to agglomerate together, thus leading to the formation of agglomerates which take a spherical shape when rolling and rubbing between them. Among the many factors that characterize the granules and the efficiency of the granulation operation, the main ones are the size of the particles and their distribution, as well as the hardness of the granules obtained. The use of one or more binding agents such as those defined above makes it possible to reduce the amount of water used and therefore the cost of the drying operation. According to a particular embodiment, all or part of the mixture is prepared beforehand dry, that is to say that all of the powders are dry mixed before granulation. The binder (s), alone or diluted in water or another solvent, or water, are then added to the pulverulent phase, then the granules obtained are dried, for example in a ventilated oven and / or in a fume cupboard or in a fluidized air bed. The particle size distribution is generally done by using sieves of different sizes or via a calibrator. Wet granulation consists of the agglomeration of powders using a wetting liquid. The different stages of wet granulation are as follows, some of which can take place simultaneously: - mixing of the pulverulent raw materials in a homogeneous manner in the granulator such as for example a baker perkins or Loedige granulator; - Preparation of the wetting solution, this solution possibly containing at least one binding agent, and transfer to the granulator; - wetting the powders and mixing; - granulation: the purpose of this step is to mix powder and liquid to reach the granular structure, by mechanical shearing or by spraying; - drying, in order to reduce the moisture content of the granules. When the drying is carried out in an oven, a preliminary step consists in distributing the wet granule on a tray. - calibration, which allows a good particle size distribution to be obtained by passing through a calibrated grid (sieve). - Optionally, addition of lubricating and / or disintegrating agents, the purpose of lubrication being to facilitate the flow and avoid sticking of the dried granule in the feed hoppers of the packaging equipment and / or the placing machines. shaped like tablet presses. The compositions according to the invention may in particular constitute cleaning or make-up removing products for the skin (body, face, eyes), scalp and / or hair. Another subject of the invention is a process for cleaning or removing make-up from keratin materials such as the skin, including the scalp, keratin fibers such as the eyelashes, the hair, and / or the lips, characterized by the fact which is applied to said keratin materials, a cosmetic composition as defined above. According to a particular embodiment of the invention, the cosmetic process for cleaning keratin materials consists in applying the composition of the invention to keratin materials in the presence of water, and in removing the foam formed and the dirt residues by rinsing at the water. Another object of the invention consists in the cosmetic use of the composition as defined above, as cleaning and / or make-up removing products for keratin materials. The following examples are given by way of illustration of the invention and are not intended to be limiting. All the amounts are given as a percentage by weight relative to the total weight of the composition. The names of the compounds are indicated as appropriate in chemical names or in INCI names. EXAMPLES The compositions described in the examples are prepared by wet granulation according to the procedure below. Procedure The powders are mixed in a 1 L baker perkins granulator. The perfume, then the binding agent, are added using a pipette, with stirring. Agitation is maintained to obtain granulation of the mixture by mechanical shearing. The granules thus obtained are distributed over a 160 micron sieve. They are then placed in a ventilated oven at 50 ° C and then in a fume cupboard for drying. The composition is then calibrated on a sieve in order to obtain a particle size between 400 microns and 2500 microns. The compositions thus obtained are then evaluated either qualitatively or quantitatively according to the tests below. In vitro dispersion test 0.5 g of granules are mixed with 1 g of Hepar hard water at room temperature in a 15 mL graduated tube. The mixture is stirred for 10 seconds, in a Vortex genie 2 apparatus from Scientific Industries, at the speed of vortex 1. In vitro foam test 0.5 g of granules are mixed with 1 g of Hepar hard water at room temperature in a 15 mL graduated tube. The mixture is stirred for 40 seconds, in a Vortex genie 2 apparatus from Scientific Industries, at the speed of vortex 1. The amount of foam generated is measured in mL on the pipette. Example 1 according to the invention: shower granules The composition below is prepared. Pulverulent phase SODIUM COCOYL ISETHIONATE(PUREACT I-85 from INNOSPEC ACTIVECHEMICALS orHOSTAPON SCI 85 by CLARIANT) 16.65 SODIUM N-LAUROYL L-GLUTAMATE(AMISOFT LS 11 from AJINOMOTO) 8.33 COCAMIDOPROPYLBETAINE POWDER (TEGO BETAIN CK D by EVONIK GOLDSCHMIDT) 5.56 Beta-cyclodextrin(CAVAMAX W7 PHARMA by WACKER) 10.17 Rice starch(REMY DR I (IRRADIATED) from BENEO-REMY) 18,01 Talc(IMERCARE PHARMA of IMERYS) 21.43 Dye (s) qs Liquid phase Propylene glycol 18.91 Perfume (s) 0.93 The above composition is evaluated qualitatively. It is in the form of granules with a uniform particle size. It mixes well with water and breaks up easily. Its application on the skin and the hair is easy. It has good foaming properties: the foam starts up quickly, that is to say that an adequate and sufficiently abundant foam is quickly obtained, and the quality of the foam is good, in particular the foam is smooth and abundant. Comparative Example 2 The composition below is prepared. Composition AT B VS Pulverulent phase SODIUM LAURYL SULPHATE POWDER(TEXAPON Z 95 P from BASF) 8.33 14.65 22.98 SODIUM COCOYL ISETHIONATE (PUREACT I-85 from INNOSPEC ACTIVE CHEMICALS orHOSTAPON SCI 85 by CLARIANT) 16.65 SODIUM N-LAUROYL L-GLUTAMATE(AMISOFT LS 11 from AJINOMOTO)8.33COCAMIDOPROPYLBETAINE INPOWDER(TEGO BETAIN CK D by EVONIK GOLDSCHMIDT) 5.56 5.56 5.56 Beta-cyclodextrin(CAVAMAX W7 PHARMA by WACKER) 10.17 12,17 12,17 Rice starch 18,01 18,01 18,01 Talc(IMERCARE PHARMA of IMERYS) 21.43 21.43 21.43 Dye (s) qs qs qs Liquid phase Propylene glycol 18.91 18.91 18.91 Perfume (s) 0.93 0.93 0.93 Dispersion results obtained Composition Example 1(invention) AT(comparative) B(comparative) VS(comparative) Dispersion instant Partial, slow Partial, slow Partial, slow Foam results obtained Composition Example 1(invention) AT(comparative) B(comparative) VS(comparative) Foam 6 ml 3 mL 4 mL 4 mL The composition of Example 1 according to the invention disperses better and faster and makes it possible to obtain more foam under hard water conditions at room temperature than the comparative compositions A, B and C. Example 3 according to the invention: shower granules The composition below is prepared. Pulverulent phase SODIUM COCOYL ISETHIONATE(PUREACT I-85 from INNOSPEC ACTIVECHEMICALS orHOSTAPON SCI 85 by CLARIANT) 17.43 SODIUM N-LAUROYL L-GLUTAMATE(AMISOFT LS 11 from AJINOMOTO) 8.71 COCAMIDOPROPYLBETAINE POWDER (TEGO BETAIN CK D by EVONIK GOLDSCHMIDT) 5.82 Beta-cyclodextrin(CAVAMAX W7 PHARMA by WACKER) 10.65 Corn starch 41.27 Dye (s) qs Liquid phase Propylene glycol 15.14 Perfume (s) 0.98 The above composition is evaluated gualitatively. It is in the form of granules with a uniform particle size. It mixes well with water and breaks up easily. Its application on the skin and the hair is easy. It has good foaming properties: the foam starts up quickly, that is to say that an adequate and sufficiently abundant foam is quickly obtained, and the quality of the foam is good, in particular the foam is smooth and abundant . Example 4 according to the invention: shower granules The composition below is prepared. Pulverulent phase SODIUM COCOYL ISETHIONATE(PUREACT 1-85 from INNOSPEC ACTIVECHEMICALS orHOSTAPON SCI 85 by CLARIANT) 16.65 SODIUM N-LAUROYL L-GLUTAMATE(AMISOFT LS 11 from AJINOMOTO) 8.33 COCAMIDOPROPYLBETAINE POWDER (TEGO BETAIN CK D by EVONIK GOLDSCHMIDT) 5.56 CARBOXYMETHYLAMIDON SODIUM (APPLEDETERRE) CROSSLINKED(GLYCOLYS de ROQUETTE) 9.31 Rice starch 18,01 Talc(IMERCARE PHARMA of IMERYS) 22,30 Dye (s) qs Liquid phase Propylene glycol 18.91 Perfume (s) 0.93 The above composition is evaluated qualitatively. It is in the form of granules with a uniform particle size. It mixes well with water and breaks up easily. Its application on the skin and the hair is easy. It has good foaming properties: the foam starts up quickly, that is to say that an adequate and sufficiently abundant foam is quickly obtained, and the quality of the foam is good, in particular the foam is smooth and abundant. Example 5 according to the invention: shower granules The composition below is prepared. Pulverulent phase SODIUM COCOYL ISETHIONATE(PUREACT 1-85 from INNOSPEC ACTIVECHEMICALS orHOSTAPON SCI 85 by CLARIANT) 16.65 SODIUM N-LAUROYL L-GLUTAMATE(AMISOFT LS 11 from AJINOMOTO) 8.33 COCAMIDOPROPYLBETAINE POWDER (TEGO BETAIN CK D by EVONIK GOLDSCHMIDT) 5.56 Rice starch 18,01 Talc(IMERCARE PHARMA of IMERYS) 31.60 Dye (s) qs Liquid phase Propylene glycol 18.91 Perfume (s) 0.93 The above composition is evaluated qualitatively. It is in the form of granules with a uniform particle size. It mixes well with water and breaks up easily. Its application on the skin and the hair is easy. It has good foaming properties: the foam starts up quickly, that is to say that an adequate and sufficiently abundant foam is quickly obtained, and the quality of the foam is good, in particular the foam is smooth and abundant.
权利要求:
Claims (22) [1" id="c-fr-0001] 1. Composition in the form of an anhydrous solid, preferably in the form of particles, comprising at least one anionic surfactant chosen from isethionic acid derivatives and their salts, at least one anionic surfactant chosen from glutamic acid derivatives and their salts , at least one amphoteric surfactant, and at least 20% by weight relative to the total weight of the composition of fillers. [2" id="c-fr-0002] 2. Composition according to claim 1, in which the isethionic acid derivative or derivatives and their salts are chosen from acyl isethionic acids, their salts and their mixtures, the hydrocarbon chain of the acyl group being linear or branched, saturated or unsaturated, and comprising from 8 to 30 carbon atoms, preferably from 10 to 22 carbon atoms and better still from 12 to 18 carbon atoms. [3" id="c-fr-0003] 3. Composition according to either of Claims 1 and 2, in which the isethionic acid derivative or derivatives and their salts are chosen from the compounds of formula: OR 2 R 4 . He II R 1 —C — O — G — C — SO3 ~ M>3'5 R 3 R 5 in which: R1 represents a linear or branched, saturated or unsaturated hydrocarbon chain, comprising from 8 to 30 carbon atoms, preferably from 10 to 22 carbon atoms and better still from 12 to 18 carbon atoms, M + represents H + or a cation, preferably chosen from ions of alkali metals such as Na, Li, K, from ions of alkaline earth metals, ammonium groups and their mixtures, and R2, R3, R4 and R5 independently represent a hydrogen atom or an alkyl group, linear or branched, preferably linear, comprising from 1 to 4 carbon atoms. [4" id="c-fr-0004] 4. Composition according to one of claims 1 to 3 wherein the isethionic acid derivative (s) are chosen from sodium lauroyl methyl isethionate, sodium methyl isethionate, sodium cocoyl-isethionate, and mixtures thereof. [5" id="c-fr-0005] 5. Composition according to any one of claims 1 to 4 in which the isethionic acid derivative (s) and their salts are present in an active material content ranging from 1 to 60% by weight, preferably from 2 to 40% by weight and better still from 5 to 30% by weight relative to the total weight of the composition. [6" id="c-fr-0006] 6. Composition according to any one of claims 1 to 5 in which the compound or derivatives of glutamic acid and their salts are chosen from acyl glutamic acids in which the acyl group comprises from 10 to 30 carbon atoms, preferably from 12 with 22 carbon atoms, such as for example lauroyl glutamic acids, myristoyl glutamic, palmitoyl glutamic, stearoyl glutamic, behenoyl glutamic, olivoyl glutamic, cocoyl glutamic and the salts of these acids, in particular the alkali metal salts such as Na, Li , K, preferably Na or K, the alkaline earth metal salts such as Mg, or the ammonium salts of said acids. [7" id="c-fr-0007] 7. Composition according to any one of claims 1 to 6 in which the glutamic acid derivative (s) and their salts are present in an active material content ranging from 1 to 60% by weight, preferably from 2 to 40% by weight and better from 5 to 30% by weight relative to the total weight of the composition. [8" id="c-fr-0008] 8. Composition according to one of claims 1 to 7 in which the amphoteric surfactant (s) are chosen from N-alkylfCe-CzObétaines, N-alkyl (CsCæjsulfobétaines, N-alkyl (C 8 -C 22 ) arnidoaikyl (Ci -C6) betaines, N-alkyl (C8C Z 2) sultaines, N-alkyl (C8-C 22 ) hydroxysultaines, N-alkyl (Ca-C22) amidoalkyl (C r C6) hydroxysultaines, Na! Kyl ( C8-C 22 ) amphoacetates, N-alkyl (C s -C 22 ) amphodiacetates, N-alkyl (Ce-C 2 2) amphopropionates, N-alkyliCs-Cæ) amphodipropionates, N-alkyl (C8-C22 ) amphohydroxypropylsulfonates, diethÿlaminopropyl cocoaspartamide, and their mixtures, preferably among N-alkyi (C8-C20) betaines, Na! kyl (C8C20) amidoalkyl (C1-C6) betaines, N-alkyl (C8-C20) amphoacetates and N-alkyl (C8C20) -modiacetates, and mixtures thereof. [9" id="c-fr-0009] 9. Composition according to any one of claims 1 to 8 comprising at least one N-alkyl (Ce-C22) to midoalkyl (Ci-C6) betaine. [10" id="c-fr-0010] 10. Composition according to one of claims 1 to 9 in which the amphoteric surfactant (s) are present in an amount of active material of between 0.5% and 40% by weight, relative to the total weight of the composition, in particular ranging from 1% to 30% by weight, better from 1% to 20% by weight. [11" id="c-fr-0011] 11. Composition according to any one of claims 1 to 10 in which the fillers are present in a content greater than or equal to 20% by weight relative to the total weight of the composition, preferably greater than or equal to 25% by weight, better greater than or equal to 45% by weight. [12" id="c-fr-0012] 12. Composition according to any one of claims 1 to 11 in which the amount of fillers ranges from 20% to 80% by weight, better still from 30% to 75% by weight relative to the total weight of the composition. [13" id="c-fr-0013] 13. Composition according to any one of claims 1 to 12 comprising at least one filler chosen from talcs, starches, in particular rice starch and corn starch, and mixtures thereof. [14" id="c-fr-0014] 14. Composition according to any one of claims 1 to 13 comprising at least one binding agent, preferably chosen from: polyols such as glycerol, 1,3 propanediol, propylene glycol, butylene glycol, hexylene glycol, polyethylene glycols such as PEG8, dipropylene glycol, - sugars such as mannitol, maltodextrin, sorbitol, xylitol, sucrose, glucose, and their mixtures. [15" id="c-fr-0015] 15. Composition according to any one of claims 1 to 14 comprising at least one binding agent chosen from polyols, preferably it is propylene glycol. [16" id="c-fr-0016] 16. Composition according to any one of claims 14 and 15 in which the binding agent (s) represent from 1% to 30% by weight relative to the total weight of the composition, preferably from 2% to 20% by weight relative to the total weight of the composition, and at best 5% to 18%. [17" id="c-fr-0017] 17. Composition according to any one of claims 1 to 16 comprising at least one cyclodextrin. [18" id="c-fr-0018] 18. Composition according to claim 17 in which the cyclodextrin or cyclodextrins are oligosaccharides of formula: in which x can be a number equal to 4 (which corresponds to Γα-cyclodextrin), to 5 (β-cyçlodextrin) or to 6 (γ-cyclodextrin). [19" id="c-fr-0019] 19. Composition according to either of Claims 17 and 18, in which the cyclodextrin or cyclodextrins are chosen from β-cyclodextrin and y-cyclodextrin, preferably it is β-cyclodextrin. [20" id="c-fr-0020] 20. Composition according to any one of claims 17 to 19 in which the cyclodextrin or cyclodextrins represent from 1% to 70% by weight relative to the total weight of the composition, preferably from 2% to 30.% by weight relative to the total weight of the composition, and at best 2% to 20%. [21" id="c-fr-0021] 21. A process for cleaning or removing make-up from keratin materials, in which a composition as defined in any one of claims 1 to 20 is applied to the keratin materials. [22" id="c-fr-0022] 22. Process for preparing a composition as defined in any one of claims 1 to 20 by wet granulation comprising in particular the following steps, some of which may take place simultaneously: - mixing of the pulverulent raw materials in a homogeneous manner in the granulator; - Preparation of the wetting solution, this solution possibly containing at least one binding agent, and transfer to the granulator; - wetting the powders and mixing; - granulation: the purpose of this step is to mix powder and liquid to reach the granular structure, by mechanical shearing or by spraying; - drying, in order to reduce the moisture content of the granules; - calibration, which makes it possible to obtain a good particle size distribution by passing through a calibrated grid or sieve; - possibly, addition of lubricants and / or disintegrants.
类似技术:
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同族专利:
公开号 | 公开日 CN110831568A|2020-02-21| WO2019001940A1|2019-01-03| FR3068243B1|2020-02-14| JP2020525514A|2020-08-27| EP3644948A1|2020-05-06| KR20200021096A|2020-02-27| US20210137800A1|2021-05-13|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 FR3030269A1|2014-12-19|2016-06-24|Oreal|SOLID ANHYDROUS COSMETIC COMPOSITION, PROCESS FOR PREPARING AND COSMETIC TREATMENT METHODSHUMID ANHYDROUS COSMETIC COMPOSITION, PROCESS FOR PREPARATION AND COSMETIC PROCESSING METHOD| US4330438A|1980-12-29|1982-05-18|Hoffmann-La Roche Inc.|Powdered shampoo concentrate| DE4443644A1|1994-12-08|1996-06-13|Henkel Kgaa|Solid, free-flowing preparations| FR2779648B1|1998-06-15|2001-07-20|Oreal|COSMETIC OR PHARMACEUTICAL COMPOSITION IN THE FORM OF A SOLID AND MAY BE DEFORMABLE| JP2002265990A|2001-03-13|2002-09-18|Kose Corp|Detergent composition| JP3957527B2|2002-03-04|2007-08-15|株式会社資生堂|Granular cleaning composition| JP5087245B2|2006-08-09|2012-12-05|花王株式会社|Granular skin cleanser| GB0811302D0|2008-06-20|2008-07-30|Dow Corning|Shampoo compositions| FR2952815B1|2009-11-25|2012-01-06|Oreal|COSMETIC PRODUCT| FR2969925B1|2011-01-04|2012-12-28|Oreal|FOAMING ANHYDROUS COMPOSITION| JP6666062B2|2014-05-30|2020-03-13|ロレアル|Foaming cleansing| WO2016096792A1|2014-12-19|2016-06-23|L'oreal|Solid anhydrous cosmetic composition, preparation process, cosmetic treatment processes and associated kit|DE102019210155A1|2019-07-10|2021-01-14|Henkel Ag & Co. Kgaa|Solid hair cosmetic composition| DE102019210159A1|2019-07-10|2021-01-14|Henkel Ag & Co. Kgaa|Solid hair cosmetic composition| DE102019210160A1|2019-07-10|2021-01-14|Henkel Ag & Co. Kgaa|Solid hair cosmetic composition| DE102019210154A1|2019-07-10|2021-01-14|Henkel Ag & Co. Kgaa|Solid hair cosmetic composition| USD939359S1|2019-10-01|2021-12-28|The Procter And Gamble Plaza|Packaging for a single dose personal care product| WO2021097691A1|2019-11-20|2021-05-27|The Procter & Gamble Company|Porous dissolvable solid structure| WO2021181099A1|2020-03-12|2021-09-16|Innospec Active Chemicals Llc|Solid cleansing composition comprising an acyl alkyl isethionate| USD941051S1|2020-03-20|2022-01-18|The Procter And Gamble Company|Shower hanger|
法律状态:
2019-01-04| PLSC| Search report ready|Effective date: 20190104 | 2019-05-10| PLFP| Fee payment|Year of fee payment: 3 | 2020-05-12| PLFP| Fee payment|Year of fee payment: 4 | 2021-05-14| PLFP| Fee payment|Year of fee payment: 5 |
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申请号 | 申请日 | 专利标题 FR1756220|2017-06-30| FR1756220A|FR3068243B1|2017-06-30|2017-06-30|SOLID ANHYDROUS COMPOSITION COMPRISING AN ISETHIONIC ACID DERIVATIVE, A GLUTAMIC ACID DERIVATIVE, AN AMPHOTERIC SURFACTANT AND FILLERS|FR1756220A| FR3068243B1|2017-06-30|2017-06-30|SOLID ANHYDROUS COMPOSITION COMPRISING AN ISETHIONIC ACID DERIVATIVE, A GLUTAMIC ACID DERIVATIVE, AN AMPHOTERIC SURFACTANT AND FILLERS| KR1020207002555A| KR20200021096A|2017-06-30|2018-06-11|Anhydrous solid composition comprising isethionic acid derivative, glutamic acid derivative, amphoteric surfactant and filler| PCT/EP2018/065376| WO2019001940A1|2017-06-30|2018-06-11|Anhydrous solid composition comprising an isethionic acid derivative, a glutamic acid derivative, an amphoteric surfactant and fillersanhydrous solid composition comprising an isethionic acid derivative, a glutamic acid derivative, an amphoteric surfactant and fillers| CN201880043690.5A| CN110831568A|2017-06-30|2018-06-11|Anhydrous solid composition comprising isethionic acid derivative, glutamic acid derivative, amphoteric surfactant and filler| US16/623,600| US20210137800A1|2017-06-30|2018-06-11|Anhydrous solid composition comprising an isethionic acid derivative, a glutamic acid derivative, an amphoteric surfactant and fillers| JP2019572600A| JP2020525514A|2017-06-30|2018-06-11|Anhydrous solid composition containing isethionic acid derivative, glutamic acid derivative, amphoteric surfactant and filler| EP18731785.4A| EP3644948A1|2017-06-30|2018-06-11|Anhydrous solid composition comprising an isethionic acid derivative, a glutamic acid derivative, an amphoteric surfactant and fillersanhydrous solid composition comprising an isethionic acid derivative, a glutamic acid derivative, an amphoteric surfactant and fillers| 相关专利
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