Cosmetic composition comprising a combination of fillers

Abstract

Cosmetic composition comprising a combination of fillers The present invention relates to a cosmetic composition in invert (water-in-oil) emulsion form comprising: (a) starch, (b) cellulose particles, (c) perlite, (d) lauroyl lysine or one of its salts, and (e) boron nitride. The invention also relates to the use of such a composition for skin care, and a skin care method comprising the application of the composition according to the invention on the skin.

Description

Cosmetic composition comprising a combination of fillersThe present invention relates to a cosmetic composition in invert (water-in-oil) emulsion form comprising:(a) starch,(b) cellulose particles,(c) perlite,(d) lauroyl lysine or one of its salts, and(e) boron nitride.To enhance the sensory properties of cosmetic products, and in particular care products, it is common to use fillers of different kinds.This type of product, and in particular for eye contour care, often exhibit a so-called "pilling" defect. "Pilling" consists of the appearance of particles disintegrating on the skin during or after spreading.In the context of cosmetic care compositions, in particular for the eye contour, it is desirable to have compositions with a soft and light texture, with no pilling effect, and inducing the formation of a smooth and occlusive homogeneous film (with no tightening effect). Moreover, it is preferable for this type of composition to have a visual blemish blurring and mattifying effect.The formulator therefore seeks raw materials making it possible to obtain compositions that have such texture and application properties, while avoiding a pilling effect.A composition is therefore sought which has a light and soft texture, a sensation of thickness under the finger when spreading, a thin and occlusive film, and mattifying and blemish blurring properties.The aim of the present invention is therefore that of providing compositions in the form of emulsion having a light and soft texture, a sensation of thickness under the finger when spreading, a thin and occlusive film, and mattifying and blemish blurring properties.It was discovered that combining specific fillers with particular surface effects and physicochemical properties makes it possible to obtain such an effect.Furthermore, the formulation of environmentally friendly cosmetic products, i.e. the design and development of which account for environmental concerns, is becoming a major concern to help meet global challenges.It has therefore become essential to propose more sustainable compositions and / or preparation processes and / or ingredients to meet these environmental challenges.In this context, it is important to develop novel cosmetic compositions with a better carbon footprint, in particular by promoting the use of renewable raw materials and / or those with a good wilderness quality index and / or of natural origin, and more particularly those of plant origin, while reducing the use of compounds of petrochemical origin.The combination of fillers according to the present invention contributes in this respect.The present invention relates to a cosmetic composition in invert (water-in-oil) emulsion form comprising:(a) starch,(b) cellulose particles,(c) perlite,(d) lauroyl lysine or one of its salts, and(e) boron nitride.In particular, the composition according to the invention is a skin care composition, in particular for eye contour skin care.The invention also relates to a cosmetic composition in invert (water-in-oil) emulsion form comprising, with respect to the total weight of the composition:- from 0.1 to 5% by weight of starch,- from 0.05% to 1% by weight of cellulose particles,- from 0.05% to 1% by weight of perlite,- from 0.05% to 1% by weight of lauroyl lysine or one of its salts, and- from 0.01% to 1% by weight of boron nitride.The invention also relates to the use of a composition according to the invention for skin care, in particular for eye contour skin care.The invention also relates to a skin care method, wherein the composition according to the invention is applied on the skin. In particular, the skin is that of the eye contour.StarchStarch(es) that can be used in this invention are particularly macromolecules in the form of polymers composed of elementary structural units that are anhydroglucose units. The number of these structural units and their assembly provide a means of distinguishing amylose (linear polymer) and amylopectin (ramified polymer).The starch molecules used in this invention may originate from a plant source such as cereals, tubercles, roots, vegetables and fruits. Thus, the starch(es) may originate from a plant source chosen from among corn, peas, potatoes, sweet potatoes, banana, barley, wheat, rice, oat, sago, tapioca and sorghum. The starch is preferably obtained from corn.Hydrolysates from starches mentioned above may also be used.Starches are usually in the form of a white powder, insoluble in cold water, with an elementary particle size ranging from 3 to 100 microns.The starches used in the composition according to the invention may be native, or modified, in particular chemically modified, preferably by one or several of the following reactions: pregelatinization, oxidation, crosslinking, esterification, heat treatments.Preferably, the starch present in the composition is chosen from among native starches. Mention may be made for example of BEAUTE-BY-ROQUETTE ST005 from ROQUETTE.Alternatively, if the starch is a modified starch, the chemical modification reactions may be carried out as follows:- pregelatinization by splitting starch granules (for example drying and baking in a dryer drum);- oxidation by strong oxidants leading to the introduction of carboxyl groups in the starch molecule and depolymerization of the starch molecule (for example by treating an aqueous solution of starch by sodium hypochlorite);- crosslinking by functional agents capable of reacting with hydroxyl groups of starch molecules that will thus be bonded to each other (for example with glyceryl and / or phosphate groups);- esterification in an alkaline medium for grafting of functional groups, particularly acyl C1 -C6 (acetyl), hydroxyalkylated C1 -C6 (hydroxyethyl, hydroxypropyl), carboxyalkyl (in particular carboxymethyl), octenylsuccinic. Mention may be made in particular of starches modified by sodium carboxymethyl.In particular, monostarch phosphates (of the Am-O-PO-(OX)2type), distarch phosphates (of the Am-O-PO-(OX)-O-Am type) or even tristarch phosphates (of the Am-O- PO-(O-Am)2type) or mixtures thereof may be obtained by crosslinking with phosphorated compounds.In particular, X denotes alkaline metals (for example sodium or potassium), alkaline earth metals (for example calcium, magnesium), ammonia salts, amine salts like monoethanolamine, diethanolamine, triethanolamine, amino-3 propanediol-1 ,2 salts, ammonium salts derived from basic amino acids such as lysine, arginine, sarcosine, ornithine, citrulline.The phosphorated compounds may for example be sodium tripolyphosphate, sodium orthophosphate, phosphorus oxychloride or sodium trimetaphosphate.Among starch phosphates, mention may be made in particular of hydroxypropylated starch phosphates, or compounds rich in starch phosphate, particularly hydroxypropylated, such as the products marketed under references PREJEL VA-70-T AGGL (gelatinized hydroxypropylated manioc distarch phosphate) or PREJEL TK1 (gelatinized manioc distarch phosphate) or PREJEL 200 (gelatinized acetylated manioc distarch phosphate) by AVEBE or STRUCTURE ZEA from NATIONAL STARCH (gelatinized hydroxypropylated corn distarch phosphate).When starches are chemically modified by an esterification reaction, carboxyalkyl starches may be obtained as mentioned above.The carboxyalkyl starches are preferably carboxyalkyl (C1-C4) starch and more particularly carboxymethyl starches.The salts are particularly alkali or alkali earth metal salts such as Na, K, Li, NH4, a quaternary ammonium or an organic amine such as mono, di or triethanolamine.Carboxyalkyl starches are obtained by grafting carboxyalkyl groups on one or several alcohol functions of starch, particularly by reacting starch and sodium monochloroacetate in alkaline medium.Carboxyalkyl groups are usually fixed by means of an ether function, more particularly on carbon 1 .The degree of substitution preferably varies from 0.1 to 1 and more particularly from 0.15 to 0.5. The degree of substitution is defined according to this invention as being the average number of hydroxyl groups substituted by an ester or ether group (in this case ether for carboxymethyl starches) per monosaccharide unit of polysaccharide.Carboxyalkyl starches preferably comprise structural units with the following formula: [Chem 1]X denotes a hydrogen atom, an alkali or alkali earth metal such as Na, K 1 / 2, Li, NH4, a quaternary ammonium or an organic amine. Preferably X denotes an Na+ ion.The carboxyalkyl starches that may be used in this invention are preferably nonpregelatinized carboxyalkyl starches.The carboxyalkyl starches that may be used in this invention are preferably partially or totally crosslinked carboxyalkyl starches.The carboxyalkyl starches that can be used in this invention are preferably sodium salts of carboxyalkyl starch, particularly a sodium salt of carboxymethyl starch from potatoes, sold particularly under the trade name PRIMOJEL by DMV International. The diameter of more than 95% of particles of this starch is less than 100 microns and more particularly less than 65 microns.Alternatively, amphoteric starches may also be used, these amphoteric starches contain one or several anionic groups and one or several cationic groups. The anionic and cationic groups may be related to the same reactive site of the starch molecule or to different reactive sites, but they are preferably related to the same reactive site. The anionic groups may be of the carboxylic, phosphate or sulfate type, and preferably carboxylic. Cationic groups may be of the primary, secondary, tertiary of quaternary amine type.Amphoteric starches are chosen particularly from among compounds with the following formulas:[Chem 2]R' RCH— CH-COOMSt-O-(CH2)-N[Chem 3]R" (ID[Chem 4][Chem 5]formulas wherein:St-0 represents a starch molecule,R, identical or different, represents a hydrogen atom or a methyl radical,R', identical or different, represents a hydrogen atom, a methyl radical or a COOH group, n is an integer equal to 2 or 3,M, identical or different, denotes a hydrogen atom, an alkali metal or alkali earth metal such as Na, K, Li, NH4, a quaternary ammonium or an organic amine,R" represents a hydrogen atom or an alkyl radical having from 1 to 18 carbon atoms.These compounds are described particularly in patents US 5,455,340 and US 4,017,460.Starches with formulas (I) or (II) may be used in particular as amphoteric starches. More particularly, starches modified by 2-chloroethyl aminodipropionic acid are used, in other words starches with formula (I) or (II) wherein R, R', R" and M represent a hydrogen atom and n is equal to 2. In particular, potato starch modified by 2-chloroethyl aminodipropionic acid neutralized with soda may be used, marketed under the reference STRUCTURE SOLANACE by NATIONAL STARCH.Starches and derivatives suitable for the invention include particularly:- modified starch (amylopectin / amylose crosslinked by epichlorhydrin) sold under the trade name "Amidon de riz insoluble non mucilagineux' (non-mucilaginous insoluble rice starch) by REMY,- native waxy corn starch (essentially amylopectin) sold under the trade name "WAXY MAIS" by BLATTMANN,- pre-baked modified wheat starch sold under the trade name "MIDSOL KRISP" by MIDWEST GRAIN PRODUCTS,- refined modified wheat starch sold under the trade name "MIDSOL ADHERE" by MIDWEST GRAIN PRODUCTS,- modified wheat starch powder sold under the trade name "MIDSOL 35" by MIDWEST GRAIN PRODUCTS,- modified potato starch sold under the trade name "PERFECTAGEL MPT" by AVEBE,- the "corn starch B" product sold by ROQUETTE FRERES, the "corn starch" product sold by NATIONAL STARCH.According to one variant, a monostarch phosphate; a glycerol starch; a distarch phosphate esterified with sodium trimetaphosphate; a phosphated distarch phosphate, an acetylated distarch phosphate; a starch acetate esterified with acetic anhydride; a starch acetate esterified with vinyl acetate; an acetylated distarch adipate; an acetylated distarch glycerol; a hydroxypropylic starch; a hydroxypropylic distarch phosphate; a hydroxypropylic distarch glycerol; a sodium starch succinate octenyl, and any mixture thereof may be used.The composition according to the invention preferably comprises at least 0.01 % by weight of starch with respect to the total weight of the composition.Preferably, the quantity of starch in the composition is between 0.01 % and 10% by weight, preferably between 0.05% and 8% by weight, preferably between 0.1% and 6% by weight, preferably between 0.5 and 5% by weight, preferably between 1 % and 4% by weight, even more preferably between 2 and 3% by weight with respect to the total weight of the composition.Cellulose particlesThe cellulose particles that may be used according to the invention are preferably spherical (cellulose beads).For the purposes of this invention, spherical particles means solid or porous particles with a circularity parameter of at least 0.95. The circularity parameter is defined as the ratio of the circumference of a disk having the same area as the particle to the perimeter of the particle. A value of 1 characterizes particles that are perfectly spherical.They preferably have an average size of less than 40 pm, preferably ranging from 1 to 20 pm, even more preferably from 2 to 10 pm.Among the cellulose particles that may be used according to the invention, particular mention may be made of those marketed by Daito under the trademark CELLULOBEADS®, such as CELLULOBEADS USF® (D

[0050] = 4 pm), CELLULOBEADS D-5® (D

[0050] < 10 pm), CELLULOBEADS D-10® (D

[0050] < 15 pm), CELLULOBEADS D-30® (D

[0050] < 30 pm).The composition according to the invention preferably comprises at least 0.01 % by weight of cellulose particles with respect to the total weight of the composition.Preferably, the cellulose particles are present in the composition in a quantity ranging from 0.01% to 10% by weight, preferably from 0.02% to 5% by weight, preferably from 0.03% to 3% by weight, preferably from 0.04% to 2% by weight, preferably from 0.05% to 1% by weight, even more preferably from 0.06% to 0.5% by weight, advantageously from 0.08% to 0.2% by weight with respect to the total weight of the composition.PerlitePerlite is a natural glass of volcanic origin, glossy light gray or black in color, resulting from the rapid cooling of lava and presented in the form of small particles resembling pearl.The perlites suitable for use according to the invention are generally aluminosilicates of volcanic origin and have by way of composition:70.0-75.0% by weight of silica SiO212.0-15.0% by weight of aluminum oxide AI2O33.0-5.0% of sodium oxide Na2O3.0-5.0% of potassium oxide K2O0.5-2% of iron oxide Fe2O30.2-0.7% of magnesium oxide MgO0.5-1 .5% of calcium oxide CaO, and0.05-0.15% of titanium oxide TiO2.Preferentially, the perlite particles used according to the invention will be in porous expanded form.The perlite is milled, dried then calibrated in a first step. The product obtained known as Perlite Ore is gray in color and of the order of 100 pm in size. The Perlite Ore is then expanded (1000°C / 2 seconds) to produce more or less white particles. When the temperature attains 850-900°C, the water trapped in the structure of the material evaporates and induces the expansion of the material relative to the original volume thereof. Theexpanded perlite particles according to the invention may be obtained by means of the expansion process described in patent US 5,002,698.Preferably, the particles of perlite used will be milled; they are in this case referred to as Expanded Milled Perlite (EMP).They preferably have a particle size defined by a median diameter D50 ranging from 0.5 to 50 pm and preferably from 0.5 to 40 pm.Preferably, the perlite particles according to the invention have a particle size distribution such that at least 50% of the particles have a size less than 20 pm. Furthermore, they preferentially have a particle size distribution such that 90% by weight of the particles have a size less than 55 pm and preferably a size less than 40 pm. It is preferred moreover that 90% by weight of the particles have a size greater than 5 pm.Preferably, the particles of perlite used have a loose bulk apparent density at 25°C ranging from 10 and 400 kg / m3 (Standard DIN 53468), and preferably from 10 and 300 kg / m3.Expanded perlite particles sold under the trade names OPTIMAT 1430 OR® or OPTIMAT 2550® by WORLD MINERALS or the commercial products GK-110 THIN® and GK-110 EXTRA THIN® by LANGFANG XINDAZHONG FILTER and HENAN ZHONGNAN FILTER AID will be used in particular.The composition according to the invention preferably comprises at least 0.01 % by weight of perlite with respect to the total weight of the composition.Preferably, perlite is present in the composition in a quantity ranging from 0.01% to 10% by weight, preferably from 0.02% to 5% by weight, preferably from 0.03% to 3% by weight, preferably from 0.04 to 2% by weight, preferably from 0.05% to 1 % by weight, even more preferably from 0.06 to 0.5% by weight, advantageously from 0.08% to 0.2% by weight with respect to the total weight of the composition.Lauroyl lysineThe composition according to the invention comprises lauroyl lysine or one of its salts. Lauroyl lysine denotes the compound of the following formula:[Chem 6]When it is present in salt form, lauroyl lysine has for example the following formula: [Chem 7]Lauroyl lysine is obtained by reacting lauric acid and lysine. It is an ingredient of interest for formulating cosmetic products such as makeup or care products.This compound is typically presented in powder form. Lauroyl lysine or one of its salts is generally used as a filler and / or non-coloring base.Lauroyl lysine is for example marketed under the name AMIHOPE LL by Ajinomoto.The composition according to the invention preferably comprises at least 0.01 % by weight of lauroyl lysine or one of its salts with respect to the total weight of the composition.Preferably, lauroyl lysine or one of its salts is present in the composition in a quantity ranging from 0.01 % to 10% by weight, preferably from 0.02% to 5% by weight, preferably from 0.03% to 3% by weight, preferably from 0.04 to 2% by weight, preferably from 0.05% to 1 % by weight, even more preferably from 0.06 to 0.5% by weight, advantageously from 0.08% to 0.2% by weight with respect to the total weight of the composition.Boron nitrideBoron nitride is a chemical compound of formula BN which exists in several polymorphic forms.In particular, the boron nitride according to the invention has a hexagonal shape and is present in the form of a white powder.This compound has good mattifying properties.Boron nitride is for example marketed by:- MOMENTIVE PERFORMANCE MATERIALS under the name SOFTOUCH BORON NITRIDE POWDER CC6058- MERCK under the name RONAFLAIR BORONEIGE SQ-6- SAINT GOBAIN CERAMICS under the name SP8 or- MIZUSHIMA FERROALLOY under the name BORON NITRIDE SHP 3The composition according to the invention preferably comprises at least 0.01 % by weight of boron nitride with respect to the total weight of the composition.Preferably, the composition according to the invention comprises between 0.01% and 10% by weight, preferably between 0.05 and 8% by weight, preferably between 0.1 % and 5% by weight, preferably between 0.2% and 3% by weight of boron nitride, with respect to the total weight of the composition. Preferably, the composition according to the invention preferably comprises between 0.1 and 1 % by weight, advantageously between 0.3% and 0.8% by weight of boron nitride with respect to the total weight of the composition.Aqueous phaseThe composition according to the invention comprises an aqueous phase, which forms the dispersed phase of the composition.According to an embodiment, the composition according to the invention comprises from 10% to 60% by weight, preferably 15% to 50% by weight, preferably from 25 to 45% by weight of water, with respect to the total weight of the composition.Preferably, the composition of the invention comprises more than 20% by weight, even more than 25% by weight of water with respect to the total weight of the composition.The water used may be sterile demineralized water and / or floral water such as rose water, cornflower water, chamomile water or linden water, and / or a spring or natural mineral water, such as for example: Vittel water, water from the basin of Vichy, Uriage water, la Roche Posay water, la Bourboule water, Enghien-les-Bains water, Saint Gervais-les-Bains water, Neris-les-Bains water, Allevar-les-Bains water, Digne water, Maizieres water, Neyrac-les-Bains water, Lons-le-Saunier water, les Eaux Bonnes, Rochefort water, Saint Christau water, Fumades water and Tercis-les-bains water, Avene water.In addition to water, the aqueous phase can also comprise at least one water-soluble solvent.The term "water-soluble solvent" in the present invention denotes a compound that is liquid at ambient temperature and water-miscible (miscibility in water greater than 50% by weight at 25°C and atmospheric pressure).The water-soluble solvents suitable for use in the compositions according to the invention may further be volatile.Among the water-soluble solvents that may be used in the compositions in accordance with the invention, mention may be made in particular of monoalcohols having from 1 to 5 carbon atoms such as ethanol and isopropanol, C3 and C4 ketones and C2-C4 aldehydes, and preferably monoalcohols having from 1 to 5 carbon atoms such as ethanol and isopropanol.Preferably, the composition according to the invention preferably comprises a total monoalcohol concentration comprising between 2 and 8 carbon atoms between 0 and 15% by weight (limits included) with respect to the total weight of the composition.Preferably, the composition according to the invention comprises a total concentration of monoalcohols comprising between 2 and 8 carbon atoms between 0 and 10% by weight (limits included), advantageously between 0 and 5% by weight (limits included), in relation to the total weight of the composition.C2-C8 polyolThe composition may also comprise at least one C2-C8, preferably C3-C6, polyol, saturated or not, linear or branched, comprising from 2 to 6 hydroxyl groups.Preferably, the polyol is chosen from glycerin, propylene glycol, 1 ,3-butylene glycol and dipropylene glycol, tripropylene glycol, diglycerin, 1 ,2-octanediol (caprylyl glycol), and mixtures thereof,Preferably, the polyol concentration represents from 0.05% to 10% by weight, particularly from 0.1% to 10% by weight, and more particularly from 1 % to 6% by weight, with respect to the weight of the composition.Oily phaseThe composition according to the invention comprises an oil phase, which forms the continuous phase of the composition.It may comprise an oil, and / or another fatty substance such as a fatty acid, a wax, a solid fatty alcohol, a pasty compound.OilOil denotes any fatty substance in liquid form at ambient temperature (20 - 25°C) and at atmospheric pressure (760 mm Hg). An oil according to the invention may be volatile or non-volatile. The oil may be hydrocarbon or silicone.A hydrocarbon oil suitable for the invention may be an animal hydrocarbon oil, a plant hydrocarbon oil or a synthetic hydrocarbon oil."Hydrocarbon oif' denotes an oil essentially formed, or consisting, of carbon and hydrogen atoms, and optionally oxygen, nitrogen atoms, and containing no silicon or fluorine. The hydrocarbon oil is therefore distinct from a silicone oil and from a fluorine oil.It may contain alcohol, ester, ether, carboxylic acid, amine and / or amide groups. Preferably, the hydrocarbon oil is free of heteroatoms such as nitrogen, sulfur and phosphorus.The oil may be volatile or non-volatile.The term "volatile oil" according to the invention denotes any oil capable of evaporating in contact with skin or keratin fiber, in less than one hour, at ambient temperature and atmospheric pressure. The volatile oil(s) according to the invention is (are) volatile cosmetic oils that are liquid at ambient temperature, having a vapor pressure different from zero at ambient temperature and atmospheric pressure, particularly ranging from 0.13 Pa to 40,000 Pa (10-3to 300 mm Hg), particularly ranging from 1.3 Pa to 13,000 Pa (0.01 to 100 mm Hg), and more specifically ranging from 1.3 Pa to 1300 Pa (0.01 to 10 mm Hg).The term "non-volatile oil" denotes an oil remaining on skin or keratin fiber at ambient temperature and atmospheric pressure for at least several hours and particularly having a vapor pressure less than 10-3mm Hg (0.13 Pa).Among the non-volatile hydrocarbon oils that may be used, mention may be made in particular of:(i) hydrocarbon oils of plant origin such as triglyceride esters that are generally triesters of fatty acids and glycerols, the fatty acids of which may have chain lengths ranging from C4 to C24, with the latter able to be linear or branched, saturated or unsaturated; these oils are in particular wheat germ, sunflower, grape seed, sesame, corn, apricot, castor, shea, avocado, olive, soybean oils, almond and particularly sweet almond, palm, rapeseed, cotton, hazelnut, macadamia, jojoba, alfalfa, poppy seed, pumpkin, sesame, squash, rapeseed, blackcurrant, evening primrose, millet, barley, quinoa, rye, safflower, candlenut, passiflora, musk rose, coconut oils; or caprylic / capric acid triglycerides such as those sold by Stearineries Dubois or those sold under the trade names Miglyol 810®, 812® and 818® by Dynamit Nobel,(ii) synthetic ethers, for example linear or branched dialkyl ethers, symmetrical or non- symmetrical, containing 6 to 22 carbon atoms per alkyl group, such as dicaprylyl ether (Cetiol® OE);(iii) linear or branched hydrocarbons of mineral or synthetic origin, such as petrolatum oil, polydecenes, hydrogenated polyisobutene such as Parleam, squalane, and mixtures thereof (inorganic oils);(iv) synthetic esters such as oils having the formula RCOOR' in which R represents the residue of a linear or branched fatty acid comprising 1 to 40 carbon atoms and R’ represents a hydrocarbon chain, particularly branched containing 1 to 40 carbon atoms on the condition that R + R’ is > 10, such as for example Purcellin oil (cetostearyl octanoate), isononyl isononanoate, isopropyl myristate, ethyl-2-hexyl palmitate, octyl-2-dodecyl stearate, octyl-2-dodecyl erucate, isostearyl isostearate, isopropyl palmitate, C12 to C15 alcohol benzoates like the product sold under the trade name "Finsolv TN®" or "Witconol TN®" by WITCO or "TEGOSOFT TN®" by EVONIK GOLDSCHMIDT, 2-ethylphenyl benzoate such as the commercial product sold under the name "X-TEND 226®" by ISP, isopropyl lanolate, hexyl laurate, diisopropyl adipate, isononyl isononanoate, oleyl erucate, 2-ethylhexyl palmitate, isostearyl isostearate, diisopropyl sebacate like the product sold under the trade name "Dub Dis®" by Stearinerie Dubois, octanoates, decanoates or ricinoleates of alcohols or polyalcohols such as propylene glycol dioctanoate; hydroxylated esters, such as isostearyl lactate, diisostearyl malate; pentaerythritol esters; citrates or tartrates such as C12-C13 linear di-alkyl tartrates like those sold under the name COSMACOL ETI® by ENICHEM AUGUSTA INDUSTRIALS and C14-C15 linear di-alkyl tartrates like those sold under the name COSMACOL ETL® by the same company; acetates;(y) fatty alcohols that are liquid at ambient temperature, with a branched and / or unsaturated carbon chain having 12 to 26 carbon atoms, such as octyldodecanol, isostearyl alcohol, oleic alcohol, 2-hexyldecanol, 2-butyloctanol, 2-undecylpentadecanol;(vi) higher fatty acids, such as oleic acid, linoleic acid, linolenic acid;(vii) carbonates such as dicaprylyl carbonate like the product sold under the trade name "Cetiol CC®" by Cognis, or propylene carbonate;(viii) fatty amides such as isopropyl N-lauroyl sarcosinate like the product sold under the trade name Eldew SL 205® by Ajinomoto and mixtures thereof.Volatile hydrocarbon oils that may be used may be chosen particularly from among hydrocarbon oils having 8 to 16 carbon atoms, and particularly branched C8-C16 alkanes such as petroleum-based C8-C16 isoalkanes (also referred to as isoparaffins) such as isododecane (also referred to as 2,2,4,4,6-pentamethylheptane), isodecane, isohexadecane, oils sold under the trade names Isopars® or Permetyls®, branched C8- C16 esters, iso-hexyl neopentanoate, and mixtures thereof.Mention may also be made of the alkanes described in patent applications W02007 / 068371 , or W02008 / 155059 made by Cognis (separate alkane mixtures and different by at least one carbon). These alkanes are obtained from fatty alcohols, themselves obtained from coconut or palm oil. Mention may be made of mixtures of n- undecane (C1 1 ) and n-tridecane (C13) obtained in examples 1 and 2 in application W02008 / 155059 made by Cognis.Mention may also be made of n-dodecane (C12) and n-tetradecane (C14) sold by Sasol under the references PARAFOL 12-97® and PARAFOL 14-97® respectively, and mixtures thereof.Further volatile hydrocarbon oils such as petroleum distillates, particularly those sold under the trade name Shell Soit® by SHELL, may also be used.The non-volatile silicone oils may be chosen particularly from among non-volatile polydimethylsiloxanes (PDMS), polydimethylsiloxanes comprising alkyl or alkoxy groups that are pendant and / or at the end of the silicone chain, groups each having 2 to 24 carbon atoms; phenylated silicones, such as phenyl trimethicones, phenyl dimethicones, phenyltrimethylsiloxydiphenylsiloxanes, diphenyl dimethicones, diphenylmethyldiphenyltrisiloxanes or (2-phenylethyl)trimethylsiloxysilicates.Volatile silicone oils that may be used include for example volatile linear or cyclic silicone oils, particularly those having a viscosity of 8 centistokes (8.106m2 / s), and in particular having 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups having 1 to 10 carbon atoms. Mention may be made, as a volatile silicone oil suitable for use in the invention, in particular, of octamethyl cyclotetrasiloxane, decamethyl cyclopentasiloxane, dodecamethyl cyclohexasiloxane, heptamethyl hexyltrisiloxane, heptamethyloctyl trisiloxane, hexamethyl disiloxane, octamethyl trisiloxane, decamethyl tetrasiloxane, dodecamethyl pentasiloxane, and mixtures thereof.Mention may also be made of volatile alkyl trisiloxane linear oils with general formula (X):[Chem 8]R(X) where R represents an alkyl group comprising 2 to 4 carbon atoms and in which one or several hydrogen atoms can be substituted by a fluorine or chlorine atom.Among the oils of general formula (X), mention may be made of: 3-butyl 1 ,1 ,1 , 3, 5,5,5- heptamethyl trisiloxane, 3-propyl 1 ,1 ,1 ,3,5,5, 5-heptamethyl trisiloxane, and 3-ethyl 1 ,1 ,1 ,3,5,5, 5-heptamethyl trisiloxane, corresponding to oils with formula (X) for which R is a butyl group, a propyl group or an ethyl group respectively.Preferably, the silicone oil is a non-volatile PDMS.Other fatty substanceAnother fatty substance (or lipophilic compound) may be chosen from:- fatty acids comprising 8 to 30 carbon atoms such as stearic acid, lauric acid, palmitic acid and oleic acid;- waxes such as lanolin, beeswax, Carnauba or Candelilla wax, paraffin or lignite waxes or microcrystalline waxes, ceresin or ozokerite, synthetic waxes such as polyethylene waxes, polymethylene waxes, microwaxes in particular of polyethylene, and Fischer-Tropsch waxes;- pasty compounds, such as butters of plant origin;- fatty alcohols solid at ambient temperature with a linear carbon chain having 12 to 26 carbon atoms, such as cetyl alcohol or cetylstearyl alcohol;- and mixtures thereofGenerally, a wax considered in the framework of this invention is a lipophilic compound, which is solid at ambient temperature (25°C), having a reversible solid / liquid change of state and a melting point greater than or equal to 30°C of up to 200°C and particularly up to 120°C.The melting point of a solid fat can be measured using a differential scanning calorimeter (DSC), for example the calorimeter sold under the trade name "DSC Q100" by TA Instruments with "TA Universal Analysis" software.The measurement protocol is as follows:A sample of solid fat of about 5 mg is placed in a "sealed aluminum capsule" crucible When the solid fat is soft (pasty fat), the sample is subjected to a first temperature rise from 20°C to 80°C, at a heating rate of 2°C / minute to 80°C, then left at the isotherm of 80°C for 20 minutes, then is cooled from 80°C to -80°C at a cooling rate of 2°C / minute, and finally subjected to a second temperature rise ranging from- 80°C to 20°C at a heating rate of 2°C / minute.The value of the melting temperature of the solid fat is the value of the top of the most endothermic peak of the fusion curve observed, representing the variation in the difference in power absorbed as a function of the temperature.Non-ionic silicone or hydrocarbon surfactantsThe compositions of the invention may furthermore comprise at least one hydrocarbon or silicone non-ionic surfactant.Said surfactant(s) are chosen such that the composition according to the invention is in the form of a water-in-oil emulsion.Preferably, the surfactant has an HLB (hydrophilic / lipophilic balance) less than or equal to 8, more particularly less than or equal to 7, preferably between 1 and 6. The HLB value as per GRIFFIN is defined in J. Soc. Cosm. Chem. 1954 (volume 5), pages 249-256.With regards to silicone surfactants, mention may be made of alkyl or alkoxy dimethicone copolyols with pendant alkyl or alkoxy chain or silicone backbone-end having for example from 6 to 22 carbon atoms; dimethicone copolyols, which are more particularly oxypropylene and / or oxyethylene polydimethyl methyl siloxanes, as well as crosslinked solid elastomeric organopolysiloxanes that comprise at least one oxyalkylene group, and mixtures thereof.Among the particularly preferred silicone surfactants, mention may be made of: dimethicone copolyols such as for example those sold under the trade names KF-6015 (PEG-3 dimethicone), KF-6016 (PEG-9 methyl ether dimethicone), KF-6017 (PEG-10 dimethicone), KF-6028 (PEG-9 polydimethylsiloxyethyl dimethicone), KF-6050 L (PEG / PPG 18 / 18 dimethicone in cyclopentasiloxane), X-22-671 1 D (dimethicone PEG / PPG-18 / 18 Dimethicone) by Shin-Etsu; alkyl dimethicone copolyols such as for example those sold under the trade names KF-6038 (Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone), the dimethicone copolyols marketed under the trade names Dow Corning 3225C® (PEG / PPG-18 / 18 DIMETHICONE in a mixture of cyclotetrasiloxane and cyclopentasiloxane), DC 5225 C Formulation Aid (PEG / PPG-18 / 18 dimethicone in cyclopentasiloxane); or the product marketed under the trade name SF 1528 GE (mixture of PEG / PPG-20 / 15 Dimethicone and cyclopentasiloxane) by Momentive Performance Materials.Alkyl-dimethicone copolyols may also be used such as Lauryl PEG / PPG-18 / 18 Methicone (which is more particularly an alkoxyl derivative of Lauryl Methicone containing on average 18 moles of ethylene oxide and 18 moles of propylene oxide, sold under the trade name "Dow Corning 5200 Formulation Aid" by Dow Corning; cetyl PEG / PPG-10 / 1 Dimethicone (which is more particularly a copolymer of Cetyl Dimethicone and an alkoxyl derivative of dimethicone containing on average 10 moles of ethylene oxide and 1 mole of propylene oxide) such as the product sold under the trade name Abil EM 90 by EvonikGoldschmidt as well as the mixture of cetyl PEG / PPG-10 / 1 Dimethicone, of polyglycerol isostearate (4 moles) and hexyl laurate sold under the trade name ABIL WE 09 by Evonik Goldschmidt.It is also possible to mention, as emulsion surfactants, in particular for water-in-oil emulsions, crosslinked solid elastomeric organopolysiloxanes comprising at least one oxyalkylene group, such as those obtained according to the operating procedure in examples 3, 4 and 8 of document US-A-5, 412,004 and the examples of document US-A- 5,811 ,487, particularly the product of example 3 (example of synthesis) of the patent US-A- 5,412,004 and such as the products marketed under the references KSG 21 , KSG-210, by Shin Etsu.Non-ionic surfactants may be chosen in particular from alkyl(C8-Cso) ethers of polyethylene oxide), alkyl(C8-Cso)- and polyalkyl(C8-C3o)- esters of ethylene oxide, of propylene, of polyethylene oxide) or of poly(propylene oxide); fatty acid polyesters, preferably polyhydroxylated, C12-C20, polyoxyalkylenated, having from 4 to 50 moles of ethylene oxide; alkyl- and polyalkyl- esters of sorbitan; alkyl- and polyalkyl- esters of (poly)glycerol and mixtures thereof.As other surfactants that may be used, mention may be made of C12-C20 fatty acid polyesters, preferably polyhydroxylated, polyoxyalkylenated, having from 4 to 50 moles of ethylene oxide, that have water-in-oil emulsifying properties.According to a particularly preferred embodiment, the composition comprises at least one silicone non-ionic surfactant.Advantageously, the silicone surfactant or surfactants are chosen from dimethicone copolyols, alkyl dimethicone copolyols, in particular alkyl C8-C22 dimethicone copolyols, alone or in mixtures.The concentration of silicone or hydrocarbon non-ionic surfactant(s) represents more particularly a concentration ranging from 10 to 40% by weight, and preferably ranging from 15 to 35% by weight, and preferably ranging from 15 to 25% by weight with respect to the total weight of the composition.C-glvcoside derivativeThe composition according to the invention may also comprise a C-glycoside derivative.The C-glycoside (or C-glycoside derivative) according to the invention is preferably according to the following general formula (A):[Chem 9]X— g__ / / A X vV whereinR represents a C1 to C10, in particular C1 to C4, saturated alkyl radical, optionally substituted by at least one radical chosen from OH, COOH or COOR"2, where R"2 is a saturated C1 -C4 alkyl radical,S represents a monosaccharide or a polysaccharide including up to 20 sugar units, in particular up to 6 sugar units, in pyranose and / or furanose form and of L and / or D series, said mono- or polysaccharide optionally being substituted by an obligatorily free hydroxyl group, and optionally one or more optionally protected amine function(s), andX represents a radical chosen from the groups -CO-, -CH(OH)-, -CH(NH2)-, - CH(NHCH2CH2CH2OH)-, -CH(NHPh)- and -CH(CH3)- and in particular a radical -CO-, - CH(OH)- or -CH(NH2)- and more particularly a radical -CH(OH)-, and the bond S-CH2-X represents a C-anomeric type bond, which can be a or p, as well as the cosmetically acceptable salts thereof, the solvates thereof such as hydrates and the optical and geometric isomers thereof.The C-glycosides of formula (V) usable for the implementation of the invention are in particular those for which R denotes a C1 to C6, in particular C1 to C4, preferably C1 to C2, saturated linear alkyl radical and more preferably a methyl radical.Among the alkyl groups suitable for the implementation of the invention, mention may in particular be made of the methyl, ethyl, isopropyl, n-propyl, n-butyl, t-butyl, isobutyl, sec-butyl, pentyl, n-hexyl, cyclopropyl, cyclopentyl, cyclohexyl groups.According to an embodiment of the invention, a C-glycoside derivative complying with the formula (V) can be used for which S may represent a monosaccharide or a polysaccharide containing up to 6 sugar units, in pyranose and / or furanose form and of L and / or D series, said mono- or polysaccharide having at least one obligatorily free hydroxyl function and / or optionally one or more obligatorily protected amine functions, X and R retaining moreover all of the definitions previously given. Advantageously, a monosaccharide according to the invention may be chosen from D-glucose, D-galactose, D-mannose, D-xylose, D-lyxose, L-fucose, L-arabinose, L-rhamnose, D-glucuronic acid, D- galacturonic acid, D-iduronic acid, N-acetyl-D-glucosamine, N-acetyl-D-galactosamine andadvantageously denotes D-glucose, D-xylose, N-acetyl-D-glucosamine or L-fucose, and in particular D-xylose. More particularly, a polysaccharide according to the invention containing up to 6 sugar units may be chosen from D-maltose, D-lactose, D-cellobiose, D- maltotriose, a disaccharide associating a uronic acid chosen from D-iduronic acid or D- glucuronic acid with a hexosamine chosen from D-galactosamine, D-glucosamine, N- acetyl-D-galactosamine, N-acetyl-D-glucosamine, an oligosaccharide containing at least one xylose which can advantageously be chosen from xylobiose, methyl1 -6-xylobioside, xylotriose, xylotetraose, xylopentaose and xylohexaose and in particular xylobiose which is composed of two xylose molecules bonded by a 1 -4 bond. More particularly, S may represent a monosaccharide chosen from D-glucose, D-xylose, L-fucose, D-galactose, D- maltose and in particular D-xylose. Preferably, a C-glycoside derivative is used having formula (V) for which: R represents a C1 -C4, in particular C1 -C2, in particular methyl, nonsubstituted linear alkyl radical; S represents a monosaccharide as described above and in particular chosen from D-glucose, D-xylose, N-acetyl-D-glucosamine or L-fucose, and in particular D-xylose; X represents a group chosen from -CO-, -CH(OH)-, -CH(NH2)-, and preferably a group -CH(OH)-.The acceptable salts of the compounds described in the present invention comprise conventional non-toxic salts of these compounds, such as those formed from organic or inorganic acids. By way of example, mention may be made of the salts of mineral acids, such as sulfuric acid, hydrochloric acid, hydrobromic acids, hydroiodic acid, phosphoric acid, boric acid. Mention may also be made of organic salts, which may include one or more carboxylic, sulfonic, or phosphonic acid groups. They may consist of linear, branched or cyclic aliphatic acids or indeed aromatic acids. These acids may further include one or more heteroatoms selected from O and N, for example in the form of hydroxyl groups. Mention may particularly be made of propionic acid, acetic acid, terephthalic acid, citric acid, and tartaric acid. When the compound of formula (V) includes an acid group, the neutralization of the acid group(s) may be performed by a mineral base, such as LiOH, NaOH, KOH, Ca(OH)2, NH4OH, Mg(OH)2or Zn(OH)2; or by an organic base such as a primary, secondary or tertiary alkylamine, for example triethylamine or butylamine. This primary, secondary or tertiary alkylamine may include one or nitrogen and / or oxygen atoms and may therefore include for example one or more alcohol functions; mention may in particular be made of amino-2-methyl-2-propanol, triethanolamine, dimethylamino-2-propanol, 2-amino-2- (hydroxymethyl)-l ,3- propanediol. Mention may furthermore be made of lysine or 3- (dimethylamino)propylamine. The acceptable solvates for the compounds described in the present invention comprise conventional solvates such as those formed during the final preparation step of said compounds due to the presence of solvents. By way of example,mention may be made of solvates due to the presence of water or linear or branched alcohols such as ethanol or isopropanol.By way of illustration and not limitation of the C-glycosides derivatives more specifically suitable for the invention, mention may in particular be made of the following compounds:- C-p-D-xylopyranoside-n-propane-2-one,- C-a-D-xylopyranoside-n-propane-2-one,- C-p-D-xylopyranoside-2-hydroxy-propane,- C-a-D-xylopyranoside-2-hydroxy-propane,- 1 -(C-p-D-fucopyranoside)-propane-2-one,- 1 -(C-a-D-fucopyranoside)-propane-2-one,- 1 -(C-p-L-fucopyranoside)-propane-2-one,- 1 -(C-a-L-fucopyranoside)-propane-2-one,- 1 -(C-p-D-fucopyranoside)-2-hydroxy-propane,- 1 -(C-a-D-fucopyranoside)-2-hydroxy-propane,- 1 -(C-p-L-fucopyranoside)-2-hydroxy-propane,- 1 -(C-a-L-fucopyranoside)-2-hydroxy-propane,- 1 -(C-p-D-glucopyranosyl)-2-hydroxyl-propane,- 1 -(C-a-D-glucopyranosyl)-2-hydroxyl-propane,- 1 -(C-p-D-galactopyranosyl)-2-hydroxyl-propane,- 1 -(C-a-D-galactopyranosyl)-2-hydroxyl-propane,- 1 -(C-p-D-fucofuranosyl)-propane-2-one,- 1 -(C-a-D-fucofuranosyl)-propane-2-one,- 1 -(C-p-L-fucofuranosyl)-propane-2-one,- 1 -(C-a-L-fucofuranosyl)-propane-2-one,- C-p-D-maltopyranoside-n-propane-2-one,- C-a-D-maltopyranoside-n-propane-2-one,- C-p-D-maltopyranoside-2-hydroxy-propane,- C-a-D-maltopyranoside-2-hydroxy-propane, isomers thereof and mixtures thereof.According to an embodiment, C-p-D-xylopyranoside-2-hydroxy-propane or C-a-D- xylopyranoside-2-hydroxy-propane, and still better C-p-D-xylopyranoside-2-hydroxy- propane, may advantageously be used for the preparation of a composition according to the invention.A C-glycoside derivative that is suitable for the invention may be obtained in particular through the synthesis method described in the document WO 02 / 051828.In particular, the composition according to the invention comprises C-beta-D- xylopyranoside-2-hydroxy-propane, the INCI name of which is HYDROXYPROPYL TETRAHYDROPYRANTRIOL particularly marketed under the trade name MEXORYL SBB® or MEXORYL SCN® by NOVEAL. MEXORYL SBB® for example contains 35% by weight of hydroxypropyl tetrahydropyrantriol in 40% by weight of water and 25% propylene glycol.The composition according to the invention may comprise from 3 to 25% by weight of C-glycoside compound, preferably from 5 to 20% by weight, preferably from 8 to 15% with respect to the total weight of the composition.Other ingredientsThe composition may contain one or more of the usual active agents or excipients in the cosmetic and dermatological fields, such as hydrating agents; emollients; gelling agents, for example natural gelling agents; active agents; antioxidants; perfumes; filmforming agents; dyestuffs; sequestering agents; electrolytes; pH adjusters; fillers; preservatives; antioxidants; plant extracts and mixtures thereof. The quantities of these different excipients are those conventionally used in the fields in question. In particular, these quantities vary according to the sought purpose and can for example range from 0.01% to 20%, and preferably from 0.1% to 10% by weight of the total weight of the composition.Obviously, a person skilled in the art will take care to choose the optional active agent(s) or excipient(s) added to the composition according to the invention in such a way that the advantageous properties intrinsically associated with the composition according to the invention are not altered, or are not substantially altered, by the envisaged addition.The composition according to the invention may be obtained conventionally by those skilled in the art.The expressions "between ... and ..." and "ranging from ... to ..." are to be understood to be inclusive of the limits, unless specified otherwise.The following examples make it possible to understand the invention better, without being in any way limitative. The raw materials are referred to with the chemical or INCI namethereof. The amounts indicated are as a % by weight of raw materials with respect to the total weight of the composition (% w / w), unless specified otherwise.ExamplesExample 1 : Preparation of the comparative compositions and a composition according to the inventionComposition 11 according to the invention comprises starch, cellulose, perlite, lauroyl lysine and boron nitride.Comparative compositions C1 to C6 are respectively free from cellulose, boron nitride, lauroyl lysine, perlite, starch and lauroyl lysine.Composition according to the invention 11 and comparative compositions C1 to C6 are prepared as follows:The oily phase and the aqueous phase containing xanthan gum are heated to 75°C. The aqueous phase is incorporated slowly to perform the emulsification. The cooling is launched and Mexoryl SCN (HYDROXYPROPYL TETRAHYDROPYRANTRIOL) is added. The mixture of starch and fillers is added at ambient temperature and dispersed until a homogeneous mixture is obtained.[Table 1]Example 2: Evaluation of the comparative compositions and the composition according to the inventionSensory evaluation:A sensory evaluation of compositions 11 and C1 to C6 was carried out, on a panel of 20 trained people. The evaluation consists of applying 50pL of composition on the back of thehand. The following sensory criteria are then rated: softness, lightness, film thickness, freshness, penetration rate, matt effect, blurring of blemishes.A score of 1 to 5 is assigned for each criterion:1 : None / 2: slight / 3: moderate / 4: substantial / 5: very substantialThe results are detailed in the table hereinbelow.[Table 2]Following the sensory evaluation, the following results are observed:- composition 11 is considered soft and light, with a thickness effect under the finger when spreading, a mattifying effect, and a blemish blurring effect. Furthermore, a pilling test was performed on 6 volunteers by an expert beauty therapist, and no pilling was observed;- composition C1 is considered rough to the touch and more difficult to spread on the skin than composition 11 ;- composition C2 is considered shinier and as leaving a less smooth and homogeneous skin texture than composition 11 ;- composition C3 is considered thicker and more difficult to spread on the skin than composition 11 ;- composition C4 is considered too slippery, and shinier than composition 11 ;- composition C5 is considered too slippery, too soft, too light, and shinier than composition 11 ;- composition C6 is considered too dry and not soft enough, compared to composition 11 .Spectrophotometer evaluation:Haze measurements to evaluate the blurring of compositions 11 and C1 to C6 were performed.The measurements are made on a dry deposit of 25 pm of composition after 1 hour of drying.The Haze parameter is defined as a percentage of scattered light with respect to the total light passing through a sample.The Haze parameter is given by the following relation:[Math 1 ] 100where- HT = Hemispheric or Total transmission;- DT = Direct transmission.The results are detailed in the table hereinbelow.[Table 3]The results show that the highest Haze value is obtained in the composition according to the invention 11 , and therefore that the combination of starch, cellulose, perlite, lauroyl lysine and boron nitride fillers, allows superior blurring.In conclusion, it is demonstrated that the combination of starch, cellulose, perlite, lauroyl lysine and boron nitride filler is necessary to obtain a light and soft texture, a sensation of thickness under the finger when spreading, a thin and occlusive film, and mattifying and blemish blurring properties.

Claims

CLAIMS1. Cosmetic composition in the form of an invert emulsion comprising:(a) starch,(b) cellulose particles,(c) perlite,(d) lauroyl lysine or one of its salts, and(e) boron nitride.

2. Composition according to claim 1 , wherein the quantity of starch is between 0.01 % and 10% by weight, preferably between 0.05% and 8% by weight, preferably between 0.1% and 6% by weight, preferably between 0.5 and 5% by weight, preferably between 1% and 4% by weight, even more preferably between 2 and 3% by weight with respect to the total weight of the composition.

3. Composition according to claim 1 or 2, wherein the quantity of cellulose particles is between 0.01% and 10% by weight, preferably between 0.02% and 5% by weight, preferably between 0.03% and 3% by weight, preferably between 0.04 and 2% by weight, preferably between 0.05% and 1% by weight, even more preferably between 0.06 and 0.5% by weight, advantageously between 0.08% and 0.2% by weight with respect to the total weight of the composition.

4. Composition according one of the preceding claims, wherein the quantity of perlite is between 0.01% and 10% by weight, preferably between 0.02% and 5% by weight, preferably between 0.03% and 3% by weight, preferably between 0.04 and 2% by weight, preferably between 0.05% and 1% by weight, even more preferably between 0.06 and 0.5% by weight, advantageously between 0.08% and 0.2% by weight with respect to the total weight of the composition.

5. Composition according to one of the preceding claims, wherein the quantity of lauroyl lysine or one of its salts is between 0.01 % and 10% by weight, preferably between 0.02% and 5% by weight, preferably between 0.03% and 3% by weight, preferably between 0.04 and 2% by weight, preferably between 0.05% and 1% by weight, even more preferably between 0.06 and 0.5% by weight, advantageously between 0.08% and 0.2% by weight with respect to the total weight of the composition.

6. Composition according to one of the preceding claims, wherein the quantity of boron nitride is between 0.01 % and 10% by weight, preferably between 0.05 and 8% by weight, preferably between 0.1 % and 5% by weight, preferably between 0.2% and 3% by weight of boron nitride, even more preferably between 0.1 and 1% by weight, advantageously between 0.3% and 0.8% by weight with respect to the total weight of the composition.

7. Composition according to one of the preceding claims, which comprises from 3 to 25% by weight, preferably from 5 to 20% by weight, preferably from 8 to 15% by weight, with respect to the total weight of the composition, of a C-glycoside derivative of formula (A)X— RC3— — / , « , (A) wherein- R represents a C1 to C10, in particular C1 to C4, saturated alkyl radical, optionally substituted by at least one radical chosen from OH, COOH or COOR"2, where R"2 is a saturated C1 -C4 alkyl radical,- S represents a monosaccharide or a polysaccharide including up to 20 sugar units, in particular up to 6 sugar units, in pyranose and / or furanose form and of L and / or D series, said mono- or polysaccharide optionally being substituted by an obligatorily free hydroxyl group, and optionally one or more optionally protected amine function(s), and- X represents a radical chosen from the groups -CO-, -CH(OH)-, -CH(NH2)-, - CH(NHCH2CH2CH2OH)-, -CH(NHPh)- and -CH(CH3)- and in particular a radical -CO-, - CH(OH)- or -CH(NH2)- and more particularly a radical -CH(OH)-, and- the bond S-CH2-X represents a C-anomeric type bond, which can be a or p, as well as the cosmetically acceptable salts thereof, the solvates thereof such as hydrates and the optical and geometric isomers thereof.

8. Composition according to one of the preceding claims, which is a skin care composition, in particular for eye contour skin.

9. Use of a composition according to claims 1 to 8, for the skin care, in particular for eye contour care.

10. Skin care method, wherein a composition according to one of claims 1 to 8 is applied on the skin, in particular on eye contour skin.

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