SKINCARE AND / OR MAKE-UP COMPOSITION OF KERATINOUS MATERIALS

FR3163562B3Active Publication Date: 2026-07-31LOREAL SA
View PDF 0 Cites 0 Cited by

Patent Information

Authority / Receiving Office
FR · FR
Patent Type
Utility models
Current Assignee / Owner
LOREAL SA
Filing Date
2024-07-22
Publication Date
2026-07-31

AI Technical Summary

Technical Problem

Conventional cosmetic compositions struggle to simultaneously achieve a matte appearance and provide a cushioning sensation during application.

Method used

A composition comprising at least 0.1% by weight of starch grafted with an acrylic polymer, at least one hydroxyalkyl-modified starch, and at least one alkyl polyglucoside, which delivers a matte appearance and cushioning feel.

Benefits of technology

The composition achieves a desirable matte appearance and cushioning sensation, enhancing the application experience.

✦ Generated by Eureka AI based on patent content.
Patent Text Reader

Abstract

CARE AND / OR MAKE-UP COMPOSITION FOR KERATINOUS MATERIALS The present invention relates to a care and / or make-up composition for keratinous materials, comprising the following components: (i) at least 0.1% by weight of at least one starch grafted with an acrylic polymer, relative to the total weight of the composition; (ii) at least one starch modified with a hydroxyalkyl; and (iii) at least one alkyl polyglucoside. The present invention also relates to a non-therapeutic method for the care and / or make-up of keratinous materials. Figure for the abstract: none
Need to check novelty before this filing date? Find Prior Art

Description

Title of the invention: SKINCARE AND / OR MAKE-UP COMPOSITION OF KERATINOUS MATERIALS Technical field

[0001] The present invention relates to a cosmetic composition. In particular, the present invention relates to a composition for the care and / or makeup of keratinous materials. The present invention further relates to a non-therapeutic method for the care and / or makeup of keratinous materials. STATE OF THE ART

[0002] The development of formulations dedicated to the care and / or makeup of the skin and / or lips is ongoing.

[0003] A matte appearance like cashmere in a cosmetic composition is preferable because its use could provide a more pleasant sensation.

[0004] It is desirable that a cosmetic composition have a good texture, such as a "cushioning" sensation during application. The "cushioning sensation" here means that the fingers feel the presence of the cosmetic composition, which could be felt as if there were a cushion between the fingers.

[0005] However, it is difficult for a conventional cosmetic composition to simultaneously satisfy the above requirements.

[0006] Consequently, there is always a need to formulate a composition, preferably for the care and / or makeup of keratinous materials, particularly skin, that has a matte appearance and / or can provide a cushioning sensation. Summary of the invention

[0007] The inventors have now discovered that it is possible to formulate such compositions having the desired properties as described above.

[0008] More specifically, the inventors discovered that it is possible to formulate skincare and / or makeup compositions of keratinous materials, in particular of the skin, which have a matte appearance and / or can deliver a cushioning sensation.

[0009] Consequently, according to a first aspect, the present invention relates to a composition, preferably for the care and / or makeup of keratinous materials, comprising the following components: i. at least 0.1% by weight of at least one starch grafted with an acrylic polymer, relative to the total weight of the composition; ii. at least one hydroxyalkyl-modified starch; and iii. at least one alkyl polyglucoside.

[0010] The inventors have discovered that the composition according to the present invention has a matte appearance and / or delivers a cushioning feel.

[0011] According to a second aspect, the present invention relates to a non-therapeutic method for the care and / or makeup of keratinous materials, comprising the application of the composition according to the present invention on the keratinous materials.

[0012] Other subjects and features, aspects and advantages of the present invention will be presented in the following description and, in part, will emerge from the description, or can be learned through practice of the present invention. DETAILED DESCRIPTION OF THE INVENTION

[0013] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as that commonly understood by a person skilled in the art of the present invention. Where the definition of a term in this description conflicts with the meaning commonly understood by a person skilled in the art of the present invention, the definition described herein shall apply.

[0014] In what follows and unless otherwise indicated, the limits of a range of values ​​are included in that range, in particular in the expressions "between...and..." and "from...to...".

[0015] Furthermore, the expression "at least one" used in this description is equivalent to the expression "one or more".

[0016] Throughout this application, the term "including" shall be interpreted as encompassing all the specifically mentioned features as well as optional, additional, unspecified features. As used herein, the use of the term "including" also discloses the embodiment in which no features other than the specifically mentioned features are present (i.e., "consisting of").

[0017] Unless otherwise stated, all numerical values ​​expressing a quantity of ingredients and the like used in the description and claims are to be understood as modified by the term "approximately". Consequently, unless otherwise stated, the numerical values ​​and parameters described herein are approximate values ​​which, if necessary, can be changed according to the desired purpose.

[0018] As used herein, the expression "keratinous materials" refers to the skin and lips. "Skin" means all the skin of the body, including the scalp. Preferably, the keratinous material is the skin of the face.

[0019] In the present invention, all percentages refer, unless otherwise indicated, to a percentage by weight.

[0020] The composition according to the present invention comprises the following components: i. at least 0.1% by weight of at least one starch grafted with an acrylic polymer, relative to the total weight of the composition; ii. at least one hydroxyalkyl-modified starch; and iii. at least one alkyl polyglucoside.

[0021] As used herein, the term "starch" refers to a basic starch. Basic starch, as used herein, is intended to include all starches derived from any native source, any of which may be suitable for use herein. A native starch, as used herein, is a starch found in nature. Starches derived from a plant obtained by standard breeding techniques, including crossing, translocation, inversion, transformation, or any other genetic or chromosomal engineering process, to include their variations, are also suitable. In addition, starches derived from a plant obtained by artificial mutations and variations of the above generic starches, which may be produced by known standard processes of mutation breeding, are also suitable herein.

[0022] Typical sources of starch are cereals, tubers, roots, legumes, and fruits. The native source may be waxy varieties of maize, peas, potato, sweet potato, banana, barley, wheat, rice, oats, sago, amaranth, tapioca (cassava), arrowroot, canna, and sorghum, as well as their low- and high-amylose varieties.

[0023] As used herein, the expression "low amylose" starch is intended to include starch containing not more than about 10%, in particular not more than 5%, and more particularly not more than 2% by weight of amylose.

[0024] As used herein, the expression "high amylose" starch is intended to include starch containing at least about 50%, in particular at least about 70%, and more particularly at least about 80% by weight of amylose. Starch grafted with an acrylic polymer

[0025] According to the first aspect, the composition of the present invention comprises at least 0.1% by weight of at least one starch grafted with an acrylic polymer, relative to the total weight of the composition.

[0026] The acrylic polymer can be a homopolymer or a copolymer, preferably a homopolymer.

[0027] Preferably, the acrylic polymer is a sodium polyacrylate.

[0028] More preferably, the starch grafted with an acrylic polymer used comprises from 1% by weight to 30% by weight of starch and from 70% by weight to 99% by weight of an acrylic polymer, preferably from 5% by weight to 20% by weight of starch and from 80% by weight to 95% by weight of an acrylic polymer, more preferably from 8% by weight to 15% by weight of starch and from 85% by weight to 92% by weight of an acrylic polymer.

[0029] In some preferred embodiments, the starch grafted with an acrylic polymer used consists of 90% by weight of sodium polyacrylate and 10% by weight of starch.

[0030] The starch grafted with an acrylic polymer used in the present invention can be cross-linked or non-cross-linked.

[0031] The number average molecular weight of the starch grafted with an acrylic polymer used is preferably greater than 1000 daltons.

[0032] Examples include starches grafted with an acrylic polymer and in particular with a sodium polyacrylate, such as those sold under the name Sanfresh ST-100MC by Sanyo Chemical Industries or Makimousse 25, Makimousse 12 or Makimousse 7 by Daito Kasei (INCI name: Sodium polyacrylate starch).

[0033] Advantageously, the starch grafted with an acrylic polymer is present in the composition according to the present invention in an amount ranging from 0.1% by weight to 10% by weight, preferably from 0.1% by weight to 5% by weight, more preferably from 0.15% by weight to 3% by weight, even more preferably from 0.2% by weight to 1.5% by weight, most preferably from 0.2% by weight to 1% by weight, relative to the total weight of the composition. Hydroxyalkyl modified starch

[0034] According to the first aspect, the composition of the present invention comprises at least one hydroxyalkyl modified starch.

[0035] Hydroxyalkyl modified starch is a modified starch in which the hydroxyl group is linked via an alkyl group, such that there are 2 to 10 carbon atoms in the alkyl group. The position of the hydroxyl group is not critical and can be in the alpha to omega positions. Hydroxyalkyl modified starch can also contain more than one hydroxyl group per alkyl group. In some suitable embodiments, the degree of substitution of the hydroxyalkylation is approximately 0.08 to 0.3. The degree of substitution is the average number of substituted OH groups in the starch molecule per anhydroglucose unit. The hydroxyalkylation of a starch can be induced by reacting a native starch with alkylene oxides having the appropriate number of carbon atoms, including, but not limited to, hydroxypropylation by reacting the starch with propylene oxide.

[0036] Preferably, the hydroxyalkyl in the hydroxyalkyl-modified starch is a C2-C6 hydroxyalkyl.

[0037] Preferably, the hydroxyalkyl modified starch is chosen from hydroxyethyl starch, hydroxypropyl starch, hydroxyethyl starch phosphate, hydroxypropyl starch phosphate and one of their mixtures.

[0038] More preferably, the hydroxyalkyl modified starch is chosen from hydroxyethyl starch phosphate, hydroxypropyl starch phosphate, and one of their mixtures.

[0039] Hydroxyalkyl modified starch can be pregelatinized. Pregelatinization and techniques for achieving pregelatinization are known in the art and disclosed, for example, in US patents Nos. 4,465,702, 5,037,929, 5,131,953 and 5,149,799. See also Chapter XXIL, "Production and Use of Pregelatinized Starch," in Starch: Chemistry and Technology, Vol. III - Industrial Aspects, R.L. Whistler and E.F. Paschall, Editors, Academy Press, New York, 1967.

[0040] As used herein, the term "pregelatinized" is intended to refer to swollen starch particles that have lost their birefringence and / or Maltese crosses under polarized light. These pregelatinized starch derivatives are substantially soluble in cold water without cooking.

[0041] In this context, the term "soluble" does not necessarily mean the formation of a true molecular solution, but can also mean a colloidal dispersion.

[0042] In a preferred embodiment, the hydroxyalkyl modified starch is completely pregelatinized.

[0043] In a preferred embodiment, the starch molecules used in the present invention may be unmodified or chemically or physically modified. Examples of unmodified starches include unmodified corn starches (INCI name: Zea mays starch), for example, products sold under the trade name Farmal CS®, in particular the Farmal CS 3650® product from Corn Products International. Examples also include unmodified rice starches (INCI name: Oryza sativa (rice) starch), for example, the Remy DR I® product sold by Beneo-Remy.

[0044] In a preferred embodiment, the hydroxyalkyl modified starch of the present invention uses starches modified by crosslinking with functional agents capable of reacting with the hydroxyl groups of starch molecules, which thus bind together (for example with glyceryl and / or phosphate groups).

[0045] Mono-starch phosphates (of the type St-O-PO-(OX)2), distarch phosphates (of the type St-O-PO-(OX)-O-St), or even tri-starch phosphates (of the type St-O-PO-(O-St)2), or mixtures thereof, can be obtained, in particular, by crosslinking with phosphorus compounds. X designates, in particular, alkali metals (for example, sodium or potassium), alkaline earth metals (for example, calcium or magnesium), ammonium salts, amine salts, for example, those of monoethanolamine, diethanolamine, triethanolamine, 3-amino-1,2- Propanediol, or ammonium salts derived from basic amino acids, such as lysine, arginine, sarcosine, ornithine, or citrulline. Phosphorus compounds may include, for example, sodium tripolyphosphate, sodium orthophosphate, phosphorus oxychloride, or sodium trimetaphosphate.

[0046] Preferably, the hydroxyalkyl modified starch consists of distarch phosphates or distarch phosphate-rich compounds, in particular distarch phosphate hydroxypropyl ethers bearing the INCI name: Hydroxypropyl Starch Phosphate, for example the products sold under the trade names Farinex VA70 C or Farmal MS 689® from Avebe Stadex; the products sold under the trade names Structure BTC®, Structure HVS®, Structure XL® or Structure Zea® from National Starch (corn distarch phosphate).

[0047] More preferably, the hydroxyalkyl modified starch made from starch will be chosen from unmodified maize starches, unmodified rice starches and maize distarch phosphates, or mixtures thereof; even more preferably, the starch will be chosen from maize distarch phosphates.

[0048] Examples of hydroxyalkyl modified starch used in the present invention may include the following:

[0049] hydroxypropyl starch phosphate (pregelatinized maize starch) marketed by Akzo Nobel under the names Structure ZEA and XL; and

[0050] modified maize starch (hydroxypropyl, pregelatinized, high amylose) marketed by Akzo Nobel under the name AMAZE.

[0051] Preferably, the composition of the present invention comprises hydroxypropyl starch phosphate.

[0052] Advantageously, the hydroxyalkyl modified starch is present in the composition according to the present invention in an amount ranging from 0.01% by weight to 10% by weight, preferably from 0.05% by weight to 5% by weight, more preferably from 0.1% by weight to 3% by weight, even more preferably from 0.2% by weight to 1.5% by weight, relative to the total weight of the composition.

[0053] Preferably, the composition comprises starch grafted with an acrylic polymer and starch modified by hydroxyalkyl with the weight ratio between starch grafted with an acrylic polymer and starch modified by hydroxyalkyl not less than 0.05, preferably from 0.08 to 10, more preferably from 0.1 to 5, even more preferably from 0.2 to 3. Alkyl polyglucosides

[0054] According to the first aspect, the composition of the present invention comprises at least one alkyl polyglucoside.

[0055] Preferably, the alkyl polyglucoside is chosen from those of formula (I):

[0056] RO-Gx (I)

[0057] in which

[0058] - R is an alkyl group in C6-C22,

[0059] - G is a glucose motif, and

[0060] - x' represents the average degree of polymerization of the alkyl polyglucoside from 1 to 10.

[0061] For a specific alkyl polyglucoside molecule, x' can only take integer values. In any physical sample of alkyl polyglucosides, there will generally be molecules with different values ​​of x'. The physical sample can be characterized by the average value of x', which can take non-integer values. In this disclosure, the values ​​of x' should be understood as average values.

[0062] The hydrophilic part of the alkyl polyglucoside is the polyglucoside which contains from about 1 to about 10, preferably from 1 to 3 glucoside motifs on average.

[0063] The hydrophobic group on the alkyl polyglucoside is an alkyl group, linear or branched, containing from about 6 to about 22 carbon atoms on average. Preferably, the alkyl group contains from 8 to 22 carbon atoms, more preferably the alkyl group contains from 12 to 20 carbon atoms.

[0064] More preferably, in formula (I):

[0065] - R is a C12-C20 alkyl group,

[0066] - G is a glucose motif,

[0067] - x' is worth from 1 to 3.

[0068] Preferably, the alkyl polyglucoside is selected from lauryl glucoside, myristyl glucoside, cetyl glucoside, cetearyl glucoside, a (C12-20 alkyl) glucoside, octyldodecyl glucoside, stearyl glucoside, isostearyl glucoside, and one of their combinations.

[0069] Advantageously, the alkyl polyglucoside is present in the composition according to the present invention in an amount ranging from 0.01% by weight to 10% by weight, preferably from 0.05% by weight to 5% by weight, more preferably from 0.1% by weight to 3% by weight, even more preferably from 0.15% by weight to 1.5% by weight, most preferably from 0.2% by weight to 0.8% by weight, relative to the total weight of the composition. Fatty alcohols

[0070] Preferably, the composition of the present invention comprises at least one fatty alcohol.

[0071] The expression "fatty alcohol" means an alcohol comprising at least one hydroxyl group (OH), and comprising at least 8 carbon atoms, and which is neither oxyalkylated (in particular neither oxyethylated, nor oxypropylated), nor glycerolated.

[0072] Fatty alcohols can be represented by R-OH, in which R designates a linear or branched alkyl or alkenyl comprising 8 to 40 carbon atoms, preferably 10 to 30 carbon atoms, more preferably 12 to 24 carbon atoms, and even more preferably 14 to 22 carbon atoms.

[0073] Non-limiting examples of useful fatty alcohols include lauryl alcohol; myristyl alcohol (1-tetradecanol); cetyl alcohol (1-hexadecanol); stearyl alcohol (1-octadecanol); arachidyl alcohol (1-eicosanol); behenyl alcohol (1-docosanol); lignoceryl alcohol (1-tetracosanol); ceryl alcohol (1-hexacosanol); montanyyl alcohol (1-octacosanol); myricyl alcohol (1-triacontanol), and mixtures thereof.

[0074] Preferably, the composition according to the present invention comprises one or more fatty alcohols having 12 to 24 carbon atoms. Specific non-limiting examples of fatty alcohols having 12 to 24 carbon atoms include C14-22 alcohols, cetyl alcohol, stearyl alcohol, cetearyl alcohol, behenyl alcohol, lauryl alcohol, myristyl alcohol, arachidyl alcohol and mixtures thereof.

[0075] More preferably, the composition according to the present invention comprises one or more fatty alcohols selected from the alcohols in Cl4-22, dodecyl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, cetearyl alcohol, isostearyl alcohol, isocetyl alcohol, behenyl alcohol, oleyl alcohol and one of their mixtures.

[0076] Advantageously, the fatty alcohol is present in the composition according to the present invention in an amount ranging from 0.2% by weight to 10% by weight, preferably from 0.6% by weight to 5% by weight, more preferably from 0.8% by weight to 2% by weight, relative to the total weight of the composition. Aqueous phase

[0077] Preferably, the composition of the present invention comprises an aqueous phase.

[0078] The aqueous phase is preferably present in an amount of 10% by weight at 96% by weight, more preferably from 30% by weight to 90% by weight, even more preferably from 50% by weight to 85% by weight, relative to the total weight of the composition.

[0079] Preferably, the aqueous phase comprises at least one water-miscible organic solvent at an ambient temperature of 25 °C, such as monoalcohols having 2 to 6 carbon atoms such as ethanol, isopropanol; polyols having 2 to 6 carbon atoms, such as glycerin, propylene glycol, butylene glycol, pentylene glycol; glycol ethers (having in particular 3 to 16 carbon atoms) such as mono-, di- or tri-propylene glycol (C1-C4 alkyl) ethers, mono-, di- or tri-ethylene glycol (C1-C4 alkyl) ethers; and mixtures thereof.

[0080] More preferably, the organic solvent is present in an amount ranging from 0.5% by weight to 20% by weight, preferably from 1% by weight to 15% by weight, more preferably from 2% by weight to 10% by weight, relative to the total weight of the composition.

[0081] Preferably, the aqueous phase comprises water, preferably in an amount ranging from 10% by weight to 90% by weight, preferably from 30% by weight to 80% by weight, even more preferably from 50% by weight to 75% by weight, relative to the total weight of the composition.

[0082] In some preferred embodiments, the aqueous phase comprises water and a polyol having 2 to 6 carbon atoms, preferably selected from glycerin, pentylene glycol and mixtures thereof.

[0083] In some preferred embodiments, the composition of the present invention comprises 50% by weight to 75% by weight of water and 2% by weight to 10% by weight of a combination of glycerin and pentylene glycol, relative to the total weight of the composition. Oils

[0084] The composition of the present invention may include an oil.

[0085] The oily phase contains at least one oil, in particular a cosmetic oil. It may also contain other fatty substances.

[0086] The term "oil" refers to a non-aqueous compound that is immiscible with water and is liquid at room temperature (20 °C) and atmospheric pressure (760 mmHg).

[0087] Oils can be volatile or non-volatile.

[0088] The expression "non-volatile" refers to an oil whose vapor pressure at ambient temperature and atmospheric pressure is non-zero and is less than 103 mmHg (0.13 Pa).

[0089] The term “volatile oil” means any oil which is capable of evaporating on contact with the skin in less than one hour, at room temperature and atmospheric pressure.

[0090] Preferably, the composition according to the present invention comprises at least one oil selected from ethers of formula ROR', carbonates of formula ROC(O)OR', and one of their mixtures, in which the groups R and R', which may be identical or different, represent a saturated or unsaturated hydrocarbon group, branched or unbranched.

[0091] Preferably, in the formula ROR', the groups R and R', which may be identical or different, represent a saturated or unsaturated hydrocarbon group, branched or unbranched, comprising 1 to 16 carbon atoms, preferably 3 to 16 carbon atoms, more preferably 8 to 16 carbon atoms.

[0092] More preferably, in the formula ROR', the groups R and R', which may be identical or different, represent a C3-C16 alkyl, even more preferably a C8-C16 alkyl.

[0093] Preferably, in the formula ROC(O)OR', the groups R and R', which may be identical or different, represent a saturated or unsaturated hydrocarbon group, branched or unbranched, comprising 3 to 16 carbon atoms, more preferably 8 to 16 carbon atoms.

[0094] More preferably, in the formula ROC(O)OR', the groups R and R', which may be identical or different, represent a C3-C16 alkyl, even more preferably a C8-C16 alkyl.

[0095] Preferably, the composition according to the present invention comprises at least one oil selected from dicaprylyl ether, dipropyl carbonate, diethylhexyl carbonate, dicaprylyl carbonate, a C14-15 dialkyl carbonate, and mixtures thereof.

[0096] More preferably, the composition according to the present invention comprises at least one oil selected from dicaprylyl ether, dicaprylyl carbonate, and mixtures thereof.

[0097] Advantageously, the oil is present in the composition of the present invention in an amount ranging from 0.1% by weight to 20% by weight, preferably from 0.5% by weight to 10% by weight, more preferably from 0.5% by weight to 5% by weight, even more preferably from 1% by weight to 4% by weight, relative to the total weight of the composition. Waxes

[0098] The composition of the present invention may include a wax.

[0099] As used herein, the term "wax" is intended to refer to a lipophilic compound with reversible solid / liquid phase change, which is solid at room temperature (25 °C) and atmospheric pressure (760 mmHg).

[0100] Preferably, the composition of the present invention comprises at least one wax whose melting point is less than 50 °C.

[0101] For the purposes of the present invention, the melting point corresponds to the temperature of the most endothermic peak observed by thermal analysis (DSC) as described in ISO 11357-3: 1999.

[0102] Preferably, the wax is selected from hydrogenated coco-glyceride, stearyl heptanoate, stearyl stearate, myristyle myristate, cetyl myristate, stearyl myristate, myristyle palmitate, cetyl palmitate, stearyl palmitate, myristyle stearate, cetyl stearate, stearyl stearate and mixtures thereof.

[0103] More preferably, the composition of the present invention comprises at least one wax selected from hydrogenated coco-glyceride, stearyl heptanoate and mixtures thereof.

[0104] Advantageously, the wax is present in the composition of the present invention in an amount ranging from 0.1% by weight to 15% by weight, preferably from 0.5% by weight to 10% by weight, more preferably from 1% by weight to 8% by weight, even more preferably from 2% by weight to 5% by weight, relative to the total weight of the composition. cosmetic active ingredients

[0105] The composition according to the present invention may comprise one or more cosmetic active ingredients.

[0106] It is easy for a person skilled in the art to adjust the quantity of the cosmetic active ingredients according to the end use of the composition according to the present invention. Additional adjuvants or additives

[0107] The composition of the present invention may also contain conventional cosmetic adjuvants or additives, for example preservatives and bactericides, surfactants, pH correctors, and mixtures thereof.

[0108] A person skilled in the art can adjust the quantity of additional adjuvants or additives so as not to have a negative impact on the final use of the composition according to the present invention.

[0109] According to a preferred embodiment, the present invention proposes a composition, preferably for the care and / or makeup of keratinous materials, comprising, relative to the total weight of the composition: (i) from 0.2% by weight to 1.5% by weight of a sodium polyacrylate starch;

[0110] (ii) from 0.2% by weight to 1.5% by weight of at least one hydroxyalkyl modified starch selected from hydroxyethyl starch phosphate, hydroxypropyl starch phosphate and a mixture thereof; and

[0111] (iii) from 0.2% by weight to 0.8% by weight of at least one alkyl glucoside selected from lauryl glucoside, myristyl glucoside, cetyl glucoside, cetearyl glucoside, a (C12-20 alkyl) glucoside, octyldodecyl glucoside, stearyl glucoside, isostearyl glucoside, and one of their combinations.

[0112] According to a more preferred embodiment, the present invention proposes a composition, preferably for the care and / or makeup of keratinous materials, comprising, relative to the total weight of the composition:

[0113] (i) from 0.2% by weight to 1.5% by weight of a sodium polyacrylate starch;

[0114] (ii) from 0.2% by weight to 1.5% by weight of at least one hydroxyalkyl modified starch selected from hydroxyethyl starch phosphate, hydroxypropyl starch phosphate and a mixture thereof;

[0115] (iii) from 0.2% by weight to 0.8% by weight of at least one alkyl glucoside selected from lauryl glucoside, myristyl glucoside, cetyl glucoside, cetearyl glucoside, a (C12-20 alkyl) glucoside, octyldodecyl glucoside, stearyl glucoside, isostearyl glucoside, and one of their combinations; and

[0116] (iv) from 0.8% by weight to 2% by weight of at least one fatty alcohol represented by: R-OH, in which R designates a linear or branched alkyl or alkenyl comprising 12 to 24 carbon atoms. Method and use

[0117] Preferably, the composition of the present invention is used for the care and / or makeup of keratinous materials.

[0118] According to the second aspect, the present invention relates to a non-therapeutic method for the care and / or makeup of keratinous materials, comprising the application of the composition according to the present invention on the keratinous materials.

[0119] Preferably, the keratinous material is the skin, for example facial skin. EXAMPLES

[0120] The following examples are given by way of non-limiting illustrations of the present invention.

[0121] The main raw materials used, their trade names and their suppliers are listed in Table 1.

[0122] [Tables 1] INCI Name Trade Name Supplier Sodium polyacrylate starch (Sodium polyacrylate starch) MAKIMOUSSE 12 DAITO KASEI KOG YO (C12-20 alkyl glucoside) MONTANOV L SEPPIC Hydroxypropyl starch phosphate (Hydroxypropyl starch phosphate) STRUCTURE XL AKZO NOBEL (NOU RYON) Ammonium acryloyldimethyltaurate / VP copolymer (Ammonium acryloyldimethyltaurate / VP copolymer) AVC CLARIANT Polyacrylate crosspolymer-6 (Polyacrylate crosspolymer-6) ZEN SEPPIC Polyglyceryl-6 distearate (and) jojoba esters (and) cetyl alcohol (and) polyglyceryl-3 beeswax EMULIUM MELLI FERA MB GATTEFOSSE Polyglyceryl-2 stearate (Polyglyceryl-10 stearate) EMULGADE VER DE 10MS BASF Dimethicone (and) polysilicone-11 (Dimethicone (and) polysilicone-11) GRANSIL DMG-6 LC GRANT INDUSTRIE S

[0123] Examples of the invention 1 and 2 and Comparative examples 1 to 6

[0124] The compositions of the examples of the invention (Ev.) 1 and 2 and of the comparative examples (Ev.) 1 to 6 were prepared on the basis of the quantities given in Table 2. The quantities are given as % by weight of each ingredient relative to the total weight of the composition.

[0125] [Tables2] Components El. 1 EL2 EC. 1 EC. 2 EC. 3 EC. 4 CE. 5 CE. 6 Glycerin 4 4 4 4 4 4 4 4 Pentylene glycol 2.5 2.5 2.5 2.5 2.5 2.5 2.5 2.5 Sodium polyacrylate starch 0.45 0.25 0.25 0 0.45 0.45 0 0.05 Hydroxypropyl starch phosphate 0.3 0.5 0 0.3 0.3 0.3 0 0.3 Dicaprylyl ether 1 1 1 1 1 1 1 1 Dicaprylyl carbonate 1 1 1 1 1 1 1 1 Stearyl heptanoate 3 3 3 3 3 3 3 3 Acryloyldimethyltaurate copolymer Ammonium / VP 0 0 0.44 0.45 0 0 0 0 Polyacrylate-6 cross-linked polymer (Polyacrylate cross-linked polymer-6) 0 0 0 0 0 0 0 0.71 0 (C12-20 alkyl glucoside) 0.3 (MA) 0.3 (MA) 0.3 (MA) 0.3 (MA) 0.3 (MA) 0 0 0.3 (MA) 0.3 (MA) Polyglyceryl-6 distearate (and) jojoba esters (and) cetyl alcohol (and) polyglyceryl-3 beeswax 0 0 0 0 0.3 0 0 0 Polyglyceryl-2 stearate (Polyglyceryl-10 stearate) 0 0 0 0 0 0.3 0 0 Water QS10 0 QS10 0 QS10 0 QS10 0 QS10 0 QS10 0 QS10 0 QS10 0

[0126] The compositions of examples 1 and 2 of the invention represent compositions according to the present invention.

[0127] The composition of comparative example 1 does not include hydroxyalkyl modified starch.

[0128] The composition of comparative example 2 does not include starch grafted with an acrylic polymer.

[0129] The composition of comparative example 3 does not include alkyl polyglucoside.

[0130] The composition of comparative example 4 does not include alkyl polyglucoside.

[0131] The composition of comparative example 5 does not include starch grafted with a hydroxyalkyl modified acrylic and starch polymer.

[0132] The composition of comparative example 6 comprises only 0.05% by weight of a starch grafted with an acrylic polymer.

[0133] Preparation process:

[0134] The compositions listed above were prepared as follows: 1. Phase A: Introduce glycerin and pentylene glycol into water at 85 °C while stirring at 200 rpm to obtain a clear liquid, then introduce hydroxypropyl starch phosphate (if applicable) while stirring at 400 rpm until a homogeneous phase A is obtained; 2. Phase B: Mix the C14-22 alcohols (and) the (C12-20 alkyl) glucoside (if present), the 6-polyglyceryl distearate (and) the jojoba esters (and) the cetyl alcohol (and) the 3-polyglyceryl beeswax (if applicable), and polyglyceryl-10 stearate (if applicable), dicaprylyl ether, dicaprylyl carbonate and stearyl heptanoate under stirring at 80 °C to obtain a clear oily phase B; 3. Introduce phase B into phase A at 70 °C under stirring at 900 rpm for 15 minutes to obtain a mixture; 4. Introduce sodium polyacrylate starch (if applicable) or ammonium acryloyldimethyltaurate / VP copolymer (if applicable) or polyacrylate-6 crosslinked polymer (if applicable) into a mixture obtained in step 3 under stirring until uniform, then cool to room temperature. Composition evaluation

[0135] The matte appearance and cushion-like feel delivered by the compositions of examples 1 and 2 of the invention and comparative examples 1 to 6 were evaluated. Matte finish

[0136] The matte appearance was evaluated as follows. Each composition of Examples 1 and 2 of the invention and of comparative examples 1 to 6 was coated onto a substrate to form a film with a thickness of 25 µm. The substrate bearing the film was placed in an oven at 37 °C for 10 minutes, and then the film was measured with a BYK haze-gard i_4775 hazemeter.

[0137] The higher the haze percentage, the higher the matte finish of the composition under test. For the purposes of the present invention, a haze percentage greater than 10% is acceptable. Cushioned feel

[0138] The cushioning sensation delivered by each of the compositions of Examples 1 and 2 of the invention and comparative examples 1 to 6 was evaluated by 10 skin experts during a blind test.

[0139] In order to evaluate the cushioning sensation (also called airy feel), the experts applied 0.3 g of each composition under test to the skin. The degree of cushioning sensation delivered by the composition under test was then rated on a scale of 1 to 5 according to the following standard, and the ratings were then averaged for each composition.

[0140] 1: means a very slight cushioning sensation,

[0141] 2: means a slight cushioning sensation,

[0142] 3: means a moderate cushioning sensation,

[0143] 4: means a moderate to strong cushioning sensation,

[0144] 5: means a very strong cushioning sensation.

[0145] During the test, dimethicone (and) polysilicone-11 were used as the standard sample and the cushioning sensation delivered was thus given a score of 5.

[0146] In the context of the present invention, the higher the value of the note, the better the sensation of transformation.

[0147] The results of the veil of each composition of examples 1 and 2 of the invention and of comparative examples 1 to 6 and of the cushion sensation thus delivered are summarized in Table 3.

[0148] [Tables3] Properties EI.l EI.2 EC.l EC.2 EC.3 EC.4 EC.5 EC.6 Voile (%) 12.8 10.5 6.5 6.9 17.8 8.8 9.5 7.5 Cushion feel s in 4.3 4.1 2.1 1.4 1.6 1.5 1.2 2.5

[0149] The compositions of examples 1 and 2 of the invention have a matte appearance and can deliver a desired cushioning feel.

Claims

Demands

1. Composition, preferably for the care and / or makeup of keratinous materials, comprising the following components: (i) at least 0.1% by weight of at least one starch grafted with an acrylic polymer, relative to the total weight of the composition; (ii) at least one starch modified by hydroxyalkyl; and (iii) at least one alkyl polyglucoside.

2. Composition according to claim 1, wherein the starch grafted with an acrylic polymer is present in an amount from 0.1% by weight to 10% by weight, preferably from 0.1% by weight to 5% by weight, more preferably from 0.15% by weight to 3% by weight, even more preferably from 0.2% by weight to 1.5% by weight, most preferably from 0.2% by weight to 1% by weight, relative to the total weight of the composition.

3. Composition according to any one of claims 1 or n2, wherein the hydroxyalkyl in the hydroxyalkyl modified starch is a C2-C6 hydroxyalkyl.

4. Composition according to any one of claims 1 to 3, wherein the hydroxyalkyl modified starch is present in an amount from 0.01% by weight to 10% by weight, preferably from 0.05% by weight to 5% by weight, preferably from 0.1% by weight to 3% by weight, and more preferably from 0.2% by weight to 1.5% by weight, relative to the total weight of the composition.

5. Composition according to any one of claims 1 to 4, wherein the alkyl polyglucoside is selected from those of formula (I): RO-Gx (I) in which - R is a C6-22 alkyl group, preferably a C8-22 alkyl group, and more preferably a C12-20 alkyl group, - G is a glucose motif, and - x' represents the average degree of polymerization of the alkyl polyglucoside from 1 to 10, preferably from 1 to 3.

6. Composition according to any one of claims 1 to 5, wherein the alkyl polyglucoside is selected from lauryl glucoside, myristyl glucoside, cetyl glucoside, cetearyl glucoside, (C12-20 alkyl)glucosides, octyldodecyl glucoside, stearyl glucoside, isostearyl glucoside, and any combination thereof.

7. Composition according to any one of claims 1 to 6, wherein the alkyl polyglucoside is present in an amount from 0.01% by weight to 10% by weight, preferably from 0.05% by weight to 5% by weight, preferably from 0.1% by weight to 3% by weight, more preferably from 0.15% by weight to 1.5% by weight, even more preferably from 0.2% by weight to 0.8% by weight, relative to the total weight of the composition.

8. Composition according to claim 1, comprising, relative to the total weight of the composition: (i) 0.2% by weight to 1.5% by weight of a sodium polyacrylate starch; (ii) 0.2% by weight to 1.5% by weight of at least one hydroxyalkyl modified starch selected from hydroxyethyl starch phosphate, hydroxypropyl starch phosphate and mixtures thereof; and (iii) 0.2% by weight to 0.8% by weight of at least one alkyl glucoside selected from lauryl glucoside, myristyl glucoside, cetyl glucoside, cetearyl glucoside, a (C12-20 alkyl) glucoside, octyldodecyl glucoside, stearyl glucoside, isostearyl glucoside, and combinations thereof.

9. Composition according to any one of claims 1 to 8, further comprising at least one fatty alcohol represented by R-OH, in which R denotes a linear or branched alkyl or alkenyl comprising from 8 to 40 carbon atoms, preferably from 10 to 30 carbon atoms, more preferably from 12 to 24 carbon atoms, and even more preferably from 14 to 22 carbon atoms, preferably the fatty alcohol is present in an amount from 0.2% by weight to 10% by weight, preferably from 0.6% by weight to 5% by weight, more preferably from 0.8% by weight to 2% by weight, relative to the total weight of the composition.

10. Non-therapeutic method of care and / or makeup of keratinous materials, comprising the application of the composition according to any one of claims 1 to 9 on keratinous materials.