cleansing and / or makeup-removing composition for keratinous materials

A soap-free composition with hydrophobic silica aerogel, cellulose, and amino acid surfactants addresses the need for effective and non-drying skin cleansing by providing a strong squeaking sensation and thorough makeup removal.

FR3132021B1Active Publication Date: 2025-11-21LOREAL SA
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Patent Information

Application Number
FR2022001662
Authority / Receiving Office
FR · FR
Patent Type
Patents
Current Assignee / Owner
Priority Date
2022-01-26
Filing Date
2022-02-25
Publication Date
2025-11-21
Estimated Expiration
2042-02-25

AI Technical Summary

Technical Problem

Existing skin cleansers either cause skin dryness and irritation due to high pH and removal of surface lipids or lack the desired squeaking sensation associated with soap, making them ineffective for thorough cleansing.

Method used

A soap-free composition comprising hydrophobic silica aerogel particles, cellulose particles, and surfactants, particularly amino acid surfactants, to provide a squeaking sensation and effective cleansing without drying the skin.

Benefits of technology

The composition achieves a strong squeaking sensation and effective cleansing, maintaining skin hydration and removing makeup without causing dryness or irritation.

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Abstract

Cleansing and / or Makeup-Removing Composition for Keratinous Materials. The present invention relates to a soap-free composition for cleansing and / or removing makeup from keratinous materials, comprising: a) at least one hydrophobic silica aerogel particle; b) at least one cellulose particle; and c) at least one surfactant. The present invention also relates to a process for cleansing and / or removing makeup from keratinous materials, particularly the skin, comprising applying the composition according to the present invention to the keratinous materials, particularly the skin, and rinsing off said composition after a period of massage. Figure for the abstract: NONE
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Description

Title of the invention: cleansing and / or makeup-removing composition for keratinous materials technical field

[0001] The present invention relates to a cosmetic composition, in particular, a composition for cleansing and / or removing makeup from keratinous materials. The present invention also relates to a process for cleansing and / or removing makeup from keratinous materials using said composition. CONTEXT

[0002] Cleansing the skin or removing makeup is very important for skin care. It must be as effective as possible because oily residues, such as excess sebum, remnants of cosmetics used daily, and makeup products, especially waterproof products, accumulate in skin folds and can clog pores and lead to the appearance of pimples.

[0003] Several types of skin cleansing or makeup removal products are known, for example rinse-off anhydrous oils and gels, foaming creams and lotions.

[0004] The soap is well-received by the consumer because of its good lather, the feeling of freshness it provides, and the squeaking sensation it produces when all the oily sebum is removed. The squeaking sensation of the soap comes from the metallic soap (soap lather).

[0005] Metallic soap is insoluble in water and can settle on the skin, causing a grinding sensation because the water-insoluble compound can prevent fingers from moving easily on the face during washing. It removes all sebum and viscous cleansing surfactants from the skin.

[0006] However, the soap is somewhat hard due to the dryness resulting from the rapid evaporation of water. Reasons for the deterioration of the skin barrier include a high pH and the removal of excessive amounts of surface lipids from the skin, which have an occlusive effect on the skin to prevent water loss.

[0007] On the other hand, amino acid surfactants are increasingly popular due to their gentleness. They can produce foams at a lower pH than soap. They are less damaging to the skin barrier. However, cleansers based on amino acid surfactants do not produce as much metallic soap; therefore, consumers do not experience a squeaking sensation on their skin and consider amino acid surfactants ineffective for cleansing.

[0008] Moreover, compared to soap, it is difficult to stabilize the cleaner obtained with An amine surfactant alone. Thus, polymers and / or fillers, nonionic surfactants, and amphoteric surfactants are usually added to stabilize the cleaner. However, the presence of polymers and / or fillers, nonionic surfactants, and amphoteric surfactants also causes a non-squeaking sensation.

[0009] Thus, there remains a need for a soap-free cleanser that can cause a squeaking sensation and does not dry out the skin. Summary of the invention

[0010] The inventors have found that such a need can be satisfied by the present invention.

[0011] Thus, according to one aspect, the present invention provides a soap-free composition for cleansing and / or removing makeup from keratinous materials comprising:

[0012] a) at least one hydrophobic silica aerogel particle;

[0013] b) at least one cellulose particle; and

[0014] c) at least one surfactant.

[0015] When the composition according to the present invention is used to wash the skin, a very strong squeaking sensation can be quickly obtained.

[0016] In addition, the composition according to the present invention also makes it possible to obtain a good finish on the skin (i.e. a feeling of non-dry skin) after application.

[0017] The composition according to the present invention can be used to cleanse and / or remove makeup from keratinous materials, in particular, the skin, especially the face, lips and / or eyes.

[0018] According to another aspect, the present invention proposes a process for cleaning and / or removing makeup from keratinous materials, in particular from the skin, comprising applying the composition according to the present invention to the keratinous materials, in particular the skin, and rinsing off said composition after a period of massage.

[0019] Other subjects, features, aspects, and advantages of the invention will become even clearer upon reading the description and examples that follow. DETAILED DESCRIPTION OF THE INVENTION

[0020] Unless otherwise defined, all technical and scientific terms used in this document have the same meaning as that commonly understood by those skilled in the art to which the present invention relates. Where the definition of a term in this description is inconsistent with the meaning commonly understood by those skilled in the art to which the present invention relates, the definition described in this document shall apply.

[0021] In what follows and unless otherwise indicated, the limits of a range of values ​​are included in this range, in particular in the expressions "between ... and ..." and "ranging from ... to ...".

[0022] Furthermore, the expression "at least one" used in this description is equivalent to the expression "one or more".

[0023] Throughout this application, the term "comprising" shall be interpreted as encompassing all the specifically mentioned features as well as any optional, additional, and unspecified features. As used herein, the use of the term "comprising" also discloses the embodiment in which no features other than the specifically mentioned features are present (i.e., "consisting of").

[0024] Unless otherwise stated, all numerical values ​​expressing the quantity of ingredients and the like used in the description and claims shall be understood as modified by the term "approximately". Consequently, unless otherwise stated, the numerical values ​​and parameters described in this document are approximate values ​​that may be modified as needed for the intended purpose.

[0025] For the purposes of the present invention, the term "keratinous material" is intended to cover human skin. The face, lips, and eyes are considered more particularly according to the present invention.

[0026] All percentages in the present invention refer to a percentage by weight, unless otherwise indicated.

[0027] According to one aspect, the present invention relates to a soap-free composition for cleansing and / or removing makeup from keratinous materials comprising:

[0028] a) at least one hydrophobic silica aerogel particle;

[0029] b) at least one cellulose particle; and

[0030] c) at least one surfactant. Hydrophobic silica aerogel particles

[0031] The composition according to the present invention comprises at least one hydrophobic silica aerogel particle.

[0032] As used in this document, silica aerogels are porous materials obtained by replacing (by drying) the liquid component of a silica gel with air.

[0033] They are generally synthesized by a sol-gel process in a liquid medium, then dried, most often by extraction from a supercritical fluid, the most commonly used being supercritical CO2. This type of drying prevents shrinkage of the pores and the material. The sol-gel process and the various drying processes are described in detail in Brinker C J., and Scherer GW, Sol-Gel Science: New York: Academie Press, 1990.

[0034] Preferably, the hydrophobic silica aerogel particles that can be used in the present invention have a specific surface area per unit mass (SM) of 500 to 1500 m2 / g, preferably 600 to 1200 m2 / g and even better 600 to 800 m2 / g.

[0035] The specific surface area per unit mass can be determined by the BET (Brunauer-Emmett-Teller) nitrogen absorption process described in the Journal of the American Chemical Society, vol. 60, page 309, February 1938, and corresponding to the international standard ISO 5794 / 1 (Annex D). The BET specific surface area corresponds to the total specific surface area of ​​the particles considered.

[0036] Preferably, the hydrophobic silica aerogel particles usable in the present invention have a size expressed in average volume diameter (D[0.5]), ranging from 0.1 to 150 µm, preferably from 1 to 50 µm, in particular from 3 to 30 µm, more preferably from 5 to 20 µm, and even better from 5 to 15 µm.

[0037] The particle size of hydrophobic silica aerogel can be measured by static light scattering using a commercial particle size analyzer such as the Malvern MasterSizer 2000. The data are processed based on Mie scattering theory. This theory, which is accurate for isotropic particles, allows the determination of an "effective" particle diameter in the case of non-spherical particles. This theory is described in particular in the publication by Van de Hulst, H.C., "Light Scattering by Small Particles," Chapters 9 and 10, Wiley, New York, 1957.

[0038] According to an advantageous embodiment, the hydrophobic silica aerogel particles used in the present invention have a specific surface area per unit mass (SM) ranging from 600 to 800 m2 / g and a size expressed by the average volumetric diameter (D[0,5]) ranging from 5 to 20 qm and even better from 5 to 15 qm.

[0039] The hydrophobic silica aerogel particles used in the present invention may advantageously have a packed density p ranging from 0.04 g / cm3 to 0.10 g / cm3 and preferably from 0.05 g / cm3 to 0.08 g / cm3.

[0040] In the context of the present invention, this density, referred to as packed density, can be evaluated according to the following protocol:

[0041] 40 g of powder are poured into a measuring cylinder; the measuring cylinder is The measuring cylinder is then placed on a Stampf Volumeter Stay 2003 machine; it is then subjected to a series of 2500 compaction movements (this operation is repeated until the volume difference between two consecutive tests is less than 2%); the final volume Vf of compacted powder is then measured directly on the measuring cylinder. The compacted density is determined by the ratio m / Vf, in this case 40 / Vf (Vf being expressed in cm³ and m in g).

[0042] According to one embodiment, the hydrophobic silica aerogel particles that can be used in the present invention have a specific surface area per SV volume unit ranging from 5 to 60 m2 / cm3, preferably from 10 to 50 m2 / cm3 and even better from 15 to 40 m2 / cm3.

[0043] The specific surface area per unit volume is given by the relation: SV=SM. p ; where p is the packed density expressed in g / cm3 and SM is the specific surface area per unit mass expressed in m2 / g, as defined above.

[0044] Preferably, the hydrophobic silica aerogel particles according to the invention have an oil absorption capacity, measured at the wet point, ranging from 5 to 18 mL / g, preferably from 6 to 15 mL / g and even better from 8 to 12 mL / g.

[0045] The oil absorption capacity measured at the wet point, denoted Wp, corresponds to the amount of water that must be added to 100 g of particles to obtain a homogeneous paste.

[0046] It is measured according to the wet point method or the method for determining the oil absorption of a powder described in standard NF T 30-022. It corresponds to the quantity of oil adsorbed on the available surface of the powder and / or absorbed by the powder by the wet point measurement, described below:

[0047] A quantity m = 2 g of powder is placed on a glass plate, and then the oil (isononyl isononanoate) is added drop by drop. After adding 4 to 5 drops of oil to the powder, the mixture is stirred with a spatula, and the addition of oil is continued until a conglomerate of oil and powder has formed. At this stage, the oil is added one drop at a time, and the mixture is then triturated with the spatula. The addition of oil is stopped when a firm, smooth paste is obtained. This paste must be able to be spread on the glass plate without cracking or forming lumps. The volume Vs (expressed in mL) of oil used is then recorded.

[0048] Oil absorption corresponds to the ratio Vs / m.

[0049] By "hydrophobic silica" is meant any silica whose surface is treated with silylation agents, for example halogenated silanes such as alkylchlorosilanes, alkylsiloxanes, in particular dimethylsiloxanes or hexamethyldisiloxane, or silazanes, so as to functionalize the OH groups with Si-Rn silyl groups, for example trimethylsilyl groups.

[0050] With regard to the preparation of hydrophobic particles of silica aerogels which have been surface modified by silylation, reference may be made to US patent document no. 7,470,725.

[0051] In particular, hydrophobic silica aerogel particles whose surface has been modified by trimethylsilyl groups and whose INCI name is Silica silylate will be used.

[0052] In a preferred embodiment, the hydrophobic silica aerogel particle used is the aerogel sold under the name VM-2270 (INCI name: Silica silylate, 98% active), by Dow Corning, the particles of which have an average size ranging from 5 to 15 microns and a specific surface area per unit mass ranging from 600 to 800 m² / g (oil absorption equal to 1080 mL / 100 g).

[0053] Thanks to the pores of the hydrophobic silica aerogel particles, oil and water can be absorbed so that an oil / water balance can be achieved.

[0054] Advantageously, the hydrophobic silica aerogel particle is present in the composition according to the present invention in an amount ranging from 0.05% by weight to 1% by weight, preferably from 0.1% by weight to 0.5% by weight, more preferably from 0.15% by weight to 0.3% by weight, relative to the total weight of the composition. Cellulose particles

[0055] The composition according to the present invention comprises at least one cellulose particle.

[0056] As used in this document, the term "cellulose" refers to any polysaccharide compound having in its structure sequences of glucose residues linked together by β-1,4 bonds, and in addition to unsubstituted celluloses, a derivative thereof may be used. For example, cellulose ethers, cellulose esters, and cellulose ester ethers (such as carboxymethylcellulose, hydroxyethylcellulose, and hydroxypropylmethylcellulose) may be used.

[0057] Preferably, the cellulose is microcrystalline cellulose.

[0058] Microcrystalline cellulose is a purified and partially depolymerized cellulose obtained from fibrous plant material in the form of a paste.

[0059] Cellulose preferably has an average particle size of 10 µm to 150 µm, preferably 30 µm to 100 µm, and more preferably 50 µm to 80 µm. The average particle size means the average particle size by volume.

[0060] It may be more preferable that the microcrystalline cellulose be "Avicel® PH Microcrystalline Cellulose" and Avicel® PC 611 sold by FMC Corporation, "MICROCRYSTALLINE CELLULOSE" sold by ACCENT, "VIVAPUR CS 70 FM" by JRS.

[0061] It may be preferable for microcrystalline cellulose to be the isolated and crystalline portion of the cellulose fibers from the wood pulp which can be used in colloidal form (i.e. co-treated with a soluble hydrocolloid) or non-colloidal form.

[0062] Advantageously, the cellulose particle is present in the composition according to the present invention in an amount ranging from 0.05% by weight to 5% by weight, preferably from 0.1% by weight to 4% by weight, more preferably from 0.5% by weight to 3% by weight, relative to the total weight of the composition.

[0063] With the hydrophobic silica aerogel particle and the cellulose particle, particularly with a small size and irregular shape, the composition according to the present invention can provide a squeaking sensation and good ability to cleaning even as a soap-free composition.

[0064] As used in this document, irregular shape means a shape not having a smooth spherical surface, for example a potato or plate shape, or having a porous structure or a rough surface.

[0065] Preferably, the particle size is smaller than the size of the skin pores, the composition according to the present invention can physically eliminate sebum and remove dirt from inside the skin pores.

[0066] Preferably, in the context of the present invention, the hydrophobic silica aerogel particle has an average volume diameter D[0.5] ranging from 5 to 15 pm and the cellulose particle has an average particle size ranging from 50 pm to 80 pm. Soap-free surfactants

[0067] The composition according to the present invention comprises at least one surfactant.

[0068] Since the composition according to the present invention is a soap-free composition, the ten The active ingredient contained in the composition is a soap-free surfactant.

[0069] Preferably, the surfactant is chosen from anionic surfactants, amphoteric surfactants and combinations thereof.

[0070] Examples of anionic surfactants include amino acid surfactants, isethionate surfactants and sulfosuccinate surfactants.

[0071] Preferably, the surfactant is chosen from amino acid surfactants, betaines and combinations thereof.

[0072] Preferably, said amino acid surfactant is derived from an amino acid carboxylate salt in which the amino group located on carbon a or carbon [3] of an amino acid salt is acylated with a C8-C22- fatty acid derivative

[0073] The carboxylate salts of these amino acids can be formed by conventional means such as the neutralization of the respective amino acid with a base. The amino group located on the α-carbon or the [3]-carbon of the neutralized amino acid is acylated with a fatty acid halide (acyl halide) in the presence of a base by the well-known Schotten-Baumann reaction, yielding the amide, thus forming the desired surfactant reaction product, i.e., the amino acid surfactant. Suitable acyl halides for the acylation of the amino acid carboxylate salt include acyl chlorides, bromides, fluorides, and iodides. Acyl halides can be prepared by reacting a saturated or unsaturated, linear or branched C8-C22 fatty acid with a thionyl halide (bromide, chloride, fluoride, and iodide).Representative acyl halides include, but are not limited to, acyl chlorides selected from decanoyl chloride, dodecanoyl chloride (lauroyl chloride), cocoyl chloride (coconut oil-derived fatty acid chlorides), tetradecanoyl chloride (myristoyl chloride), hexadecanoyl chloride (coconut oil chloride). palmitoyl), octadecanoyl chloride (stearoyl chloride), 9-octadecanoyl chloride (oleoyl chloride), eicosanoyl chloride (arachidoyl chloride), docosanoyl chloride (behenoyl chloride), and any mixture thereof. Other acyl halides include the bromides, fluorides, and iodides of the preceding fatty acids. A process for preparing acyl halides and an alternative process for acylating amino acids are described in Publication of US Patent Application No. 2008 / 0200704, published on August 21, 2008.

[0074] Preferably, said amino acid surfactant is represented by the formula (I): O (I) ^(CH2)n ^.COOM XY

[0075] in which

[0076] Z represents a linear or branched alkyl or alkenyl group having 8 to 22 carbon atoms,

[0077] X represents a hydrogen or a methyl group,

[0078] n is equal to 0 or 1,

[0079] Y is chosen from among hydrogen, -CH3, -CH(CH3)2, -CH2CH(CH3)2, -CH(CH3)CH2CH3, -CH2C6H5, -CH2C2H4OH, -CH2OH, -CH(OH)CH3, -(CH2)4NH2, -(CH2)3NHC(NH)NH2, -CH2C(O)O M+, -(CH2)2C(O)OH, -(CH2)2C(O)O M+, and

[0080] M is a salt-forming cation in which COO is the counter-anion, such as sodium, potassium, ammonium or triethanolamine.

[0081] According to a preferred embodiment of the invention, in formula (I):

[0082] Z represents a linear or branched C8-C22 alkyl or alkenyl group,

[0083] X represents a hydrogen or a methyl group,

[0084] n is equal to 0,

[0085] Y is chosen from hydrogen, -(CH2)2C(O)OH, -(CH2)2C(O)O M+, and

[0086] M is a salt-forming cation in which COO is the counter-anion, such as sodium, potassium, ammonium or triethanolamine.

[0087] Examples of amino acid surfactants include the salts of alanine, arginine, aspartic acid, glutamic acid, glycine, isoleucine, leucine, lysine, phenylalanine, serine, tyrosine, valine, sarcosine, and any mixture thereof. More specifically, examples of amino acid surfactants include dipotassium capryloyl glutamate, dipotassium undecylenoyl glutamate, disodium capryloyl glutamate, disodium cocoyl glutamate, disodium lauroyl glutamate, disodium stearoyl glutamate, disodium undecylenoyl glutamate, and capryloyl glutamate of potassium, cocoyl glutamate de potassium, lauroyl glutamate de potassium, myristoyl glutamate de potassium, stéaroyl glutamate de potassium, undécylénoyl glutamate de potassium, capryloyl glutamate de sodium, cocoyl glutamate de sodium, lauroyl glutamate de sodium, myristoyl glutamate de sodium, olivoyl glutamate sodium, palmitoyl glutamate de sodium, stéaroyl glutamate de sodium, undécylénoyl glutamate de sodium, [3-alaninate de cocoyl méthyle, [3-alaninate de lauroyle, [3-alaninate de lauroyl méthyle, [3-alaninate de myristoyle, lauroyl méthyl [3-alaninate de potassium, cocoyl alaninate de sodium, cocoyl méthyl [3-alaninate de sodium et myristoyl méthyl [3-alaninate de sodium palmitoyl glycinate, lauroyl glycinate de sodium, cocoyl glycinate de sodium, myristoyl glycinate de sodium, lauroyl glycinate de potassium, cocoyl glycinate de potassium, lauroyl sarcosinate de potassium, cocoyl sarcosinate de potassium, cocoyl sarcosinate de sodium, lauroyl sarcosinate de sodium,myristoyl sarcosinate de sodium, oléoyl sarcosinate de sodium, palmitoyl sarcosinate de sodium, lauroyl sarcosinate d’ammonium, lauroyl aspartate de sodium, myristoyl aspartate de sodium, cocoyl aspartate de sodium, caproyl aspartate de sodium, lauroyl aspartate disodique, myristoyl aspartate disodique, cocoyl aspartate disodique, caproyl aspartate disodique, lauroyl aspartate de potassium, myristoyl aspartate de potassium, cocoyl aspartate de potassium, caproyl aspartate de potassium, lauroyl aspartate dipotassique, myristoyl aspartate dipotassique, cocoyl aspartate dipotassique, caproyl aspartate dipotassique, et des mélanges de ceux-ci. ,

[0088] Reference can be made to commercially available amino acid surfactants, for example acylsarcosinates, for example sodium lauroyl sarcosinate sold under the name Sarkosyl NL 97® by Ciba or sold under the name Oramix L 30® by SEPPIC, sodium myristoyl sarcosinate sold under the name Nikkol Sarcosinate MN® by Nikkol or sodium palmitoyl sarcosinate sold under the name Nikkol Sarcosinate PN® by Nikkol; alaninates, for example sodium N-lauroyl-N-methylamidopropionate sold as Sodium Nikkol Alaninate LN 30® by Nikkol or sold as Alanone ALE® by Kawaken, and N-lauroyl-N-methylalanine triethanolamine sold as Alanone Alta® by Kawaken;N-acylglutamates, for example triethanolamine monococoylglutamate sold under the name Acylglutamate CT-12® by Ajinomoto and triethanolamine lauroylglutamate sold under the name Acylglutamate LT-12® by Ajinomoto; glycinates, for example sodium N-cocoylglycinate sold under the name Amilite GCS-12® by Ajinomoto; aspartates, for example the mixture of triethanolamine N-lauroyl aspartate and triethanolamine N-myristoyl aspartate, sold under the name Asparack® by Mitsubishi; citrates, and any mixture thereof.

[0089] According to the present invention, the preferred amino acid surfactant is selected from sodium lauroyl sarcosinate, sodium cocoyl glycinate, sodium cocoyl glutamate, sodium stearoyl glutamate, disodium cocoyl glutamate, sodium lauroyl glutamate, potassium cocoyl glycinate, TEA-cocoyl glutamate, or a mixture thereof.

[0090] Among the preferred amino acid surfactants in the composition that are commercially available, we can mention sodium lauroyl sarcosinate (ORAMIX L 30 sold by Seppic), sodium cocoyl glycinate (and) water (AMILITE® GCS-12K sold by Ajinomoto), sodium cocoyl glutamate (and) disodium cocoyl glutamate (AMISOFT® CS-22 sold by Ajinomoto), and sodium lauroyl glutamate (AMISOFT® LS-11 sold by Ajinomoto).

[0091] According to a preferred embodiment, the amino acid surfactant is selected from sodium lauroyl sarcosinate, sodium cocoyl glycinate, sodium cocoyl glutamate, sodium stearoyl glutamate, disodium cocoyl glutamate, sodium lauroyl glutamate, potassium cocoyl glycinate, TEA-cocoyl glutamate, and a mixture thereof.

[0092] Thanks to the use of amino acid surfactant, the composition according to the present invention does not cause any irritation to keratinous materials.

[0093] Examples of isethionates include acylisethionates, such as sodium cocoylisethionate.

[0094] Examples of sulfosuccinates include disodium lauryl sulfosuccinate, disodium laureth sulfosuccinate, diammonium lauryl sulfosuccinate, and sodium diethylhexyl sulfosuccinate.

[0095] Examples of betaines include coco betaine, cocamidopropyl betaine, lauryl betaine, laurylhydroxy sulfobetaine, lauryldimethyl betaine, cocamidopropyl hydroxysultaine, behenyl betaine, capryl / capramidopropyl betaine, lauryl hydroxysultaine, stearyl betaine and mixtures thereof.

[0096] Preferably, the surfactant is selected from sodium lauroyl sarcosinate, sodium cocoyl glycinate, sodium cocoyl glutamate, sodium stearoyl glutamate, disodium cocoyl glutamate, sodium lauroyl glutamate, potassium cocoyl glycinate, TEA-cocoyl glutamate, sodium cocoyl isethionate, disodium lauryl sulfosuccinate, disodium laureth sulfosuccinate, diammonium lauryl sulfosuccinate, and sodium diethylhexyl sulfosuccinate, coco betaine, cocamidopropyl betaine, lauryl betaine, lauryl hydroxy sulfobetaine, lauryl dimethyl betaine, cocamidopropyl hydroxy-sultaine, behenyl betaine, capryl / capramidopropyl betaine, lauryl hydroxysultaine, stearyl betaine, and a combination thereof of these.

[0097] Advantageously, the surfactant is present in the composition according to the present invention in an amount ranging from 0.1% by weight to 50% by weight, preferably of 5% by weight to 30% by weight, more preferably 10% by weight to 25% by weight, relative to the total weight of the composition.

[0098] Even more advantageously, the composition according to the present invention comprises from 10% by weight to 25% by weight of at least one amino acid surfactant, relative to the total weight of the composition. Aqueous phase

[0099] The composition of the present invention comprises an aqueous phase.

[0100] The aqueous phase of the composition according to the present invention comprises water and optionally one or more water-miscible or at least partially water-miscible compounds, for example C2-C8 polyols or monoalcohols, such as ethanol, isopropanol, hexylene glycol, dipropylene glycol.

[0101] The term "polyol" should be understood as meaning any organic molecule comprising at least two free hydroxyl groups. Examples of polyols that may be cited include glycols, for example butylene glycol, propylene glycol, dipropylene glycol, isoprene glycol, hexylene glycol, caprylyl glycol, glycerol, and polyethylene glycols.

[0102] Preferably, the composition according to the present invention comprises water, glycerin and caprylyl glycol. Additional ingredients

[0103] The composition according to the present invention may include one or more additional ingredients, chosen from those conventionally used in skin cleansers.

[0104] The composition according to the present invention may include an additional ingredient selected from pH adjusting agents (e.g. citric acid, potassium hydroxide), preservatives (e.g. hydroxyacetophenone, chlorphenesin) and bactericides (e.g. hydroxyacetophenone), thickeners (e.g. hydroxypropylmethylcellulose, C10-30 acrylate / alkyl acrylate crosslinked polymer), colorants, scrubbing agents (e.g. lactic acid), and perfumes (e.g. perfumes, essential oils), etc.

[0105] A person skilled in the art can adjust the type and quantity of additional ingredients present in the compositions according to the present invention by means of routine operations, so that the desired properties of these compositions are not negatively affected by the additional ingredients.

[0106] According to a preferred embodiment, the present invention provides a soap-free composition for cleansing and / or removing makeup from keratinous materials comprising, relative to the total weight of the composition

[0107] a) from 0.15% by weight to 0.3% by weight of silica silylate;

[0108] b) from 0.5% by weight to 3% by weight of microcrystalline cellulose; and

[0109] c) from 10% by weight to 25% by weight of at least one amino acid surfactant. Use

[0110] The composition according to the present invention can be used to cleanse and / or remove makeup from keratinous materials, in particular the skin, especially the face, lips and / or eyes.

[0111] It can be used as a daily facial cleanser and / or makeup remover. The composition of the present invention is a rinse-off product. Thus, such a composition can be applied to the skin (for example, the face, lips, eyes) and then rinsed off with clean water after a period of massage.

[0112] Thus, according to another aspect, the present invention proposes a process for cleaning and / or removing makeup from keratinous materials, in particular from the skin, comprising applying the composition according to the present invention to the keratinous materials, in particular the skin, and rinsing off said composition after a period of massage.

[0113] The composition according to the present invention can have a good rinsing effect and provide a feeling of non-dry skin.

[0114] The present invention is illustrated in more detail by the examples described below, which are given by way of non-limiting illustrations. EXAMPLES

[0115] The main raw materials used, their trade names and their suppliers are listed in Table 1. JM Ct Nom commercial Fountisseüir DÎsoÆshe Glutamate (and) Sodium Glutamate AMISQFT* CS 22 AJMOMOTO Soctois ÀMIUTE^GCS-^K AJiMOMOTO Sodium GSSSXI PÜREÀCT I-85E FLAKES INNOSPEQ ACTIVE CHE^CALS FS431P GUANGZHOU FLOWER4S SWGFSNECHEMÏC DEHYTOH PS 45 BASF DOW CORNING* W-2270 AEROGEL FINE P ARTICLES DOW CORNING Cefcfese WÂPLSR* OS 70 FM tRS EDEHOR 012-90. MY RSPO MB EM ER Y OLEOCHEMICALS ÉDENOR Ct 4-98 MY RSPO MB EMERY QLEDQHEMICALS WfcAeKl EDENORC1S-90.MY RSPO MB EMERY OLEOCHEMiCALS Àaè PALMES 50-IS^B IOI GROUP OLEOCHEMICALS CREME RGLYC RE FIN ED GLYCERINE 797¾ RSPO MB CREME R OLEO ¢101} GwîMGiyMi QLEANBIO-OG KOLON LIFE SCIENCE GLUCOtiAL MG-P PURAC Potassium CLORETC DE POTASSiO U.S.P / F.C.C LABSVNTH UefeAcid L-LACTiC ACID ®G% j fCRGL MüSASHiN O CHEMICAL LABORATORY METHOCEL E4 M PREMIUM DOW Aerytates / C 18-30 Alttÿl Acr / iate towtet ____ GARBOPOL^ ULTREZ 20 POLYMER LUSRIZOL SYMSAVE HO SYMRISE SodwK' Stear&ÿi Giisiamate AMI SOFT HS 11 PF A^OMOTO GF-A390 FOSHAR GAOFENG STARCHTECHNOLOGY HSOLVE EPH TGH O CHEMICALS LAN El If" 22 BASF LANETTE*16 BASF à&o^^mfetSE TEGM PELLETS EVOm GOLDSCHMIDT PEG-45S DAPRACARE P6SGÛ DS NV ITALMATGH CHEMICALS PEG-32 ■CARBOWAX SEMTRY PEG1450NF FLAKE(INH) BASF P^yQuàtepi|.um-7 MERQUAT^ 7SPR PQLYMER. MALCO EQTA-4^A SHUSAZHUA^G. 4ACKCHEM.

[0117] Comparative Examples 1 to 4 and Invention Example 1

[0118] The compositions of comparative examples (CE.) 1 to 4 and of the invention example (IE.) 1 were prepared according to the quantities indicated in Table 2. The quantity of Each component is given as a percentage by weight of the total weight of the composition containing it. IE.1 CE.1 CE.2 CE.3 CE.4 % by weight % by weight % by weight % by weight % by weight Disodium cocoyl glutamate (and) Sodium cocoyl glutamate (25%)*. 20 20 20 20 2 Sodium cocoyl glycinate (30%)**.25 25 25 25 - Sodium stearoyl glutamate 0.5 0.5 0.5 0.5 - Sodium cocoyl isethionate 2 2 2 2 - Disodium lauryl sulfosuccinate 2 2 2 2 - Cocamidopropyl betaine 7 7 7 7 - Silica silylate 0.3 - 0.3 - - Microcrystalline cellulose 3 3 - - - Lauric acid - - - - 4.0 Myristic acid - - - - 15.8 Palmitic acid - - - - 1.0 Stearic acid - - - - 13.24 Potassium hydroxide 3.4 3.4 3.4 3.4 13.37 Glycerin 13 13 13 13 21 Caprylyl glycol 0.3 0.3 0.3 0.3 - Magnesium gluconate 0.5 0.5 0.5 0.5 - Potassium chloride 5 5 5 5 - Lactic acid 6.4 6.4 6.4 6.4 - Hydroxypropyl methylcellulose 0.15 0.15 0.15 0.15 - Crosslinked acrylates / C alkyl acrylate polymer 10-30 0.4 0.4 0.4 0.4 - Hydroxyacetophenone 0.5 0.5 0.5 0.5 0.5 Oxidized starch acetate 1.5 1.5 1.5 1.5 - Phenoxyethanol 0.5 0.5 0.5 0.5 0.6 . Water Up to 100 Up to 100 Up to 100 Up to 100 Up to 100 Glyceryl Stearate SE - - - - 1.0 PEG-150 Distearate - - - - 0.8 PEG-32 - - - - 1.5 Polyquatemium-7 - - - - 9.0 Tetrasodium EDTA - - - - 0.36

[0120] * : added as a dispersion at 25% by weight in water, the quantity indicates that of dispersion.

[0121] ** : added as a dispersion at 30% by weight in water, the quantity indicates that of dispersion. Preparation process

[0122] The compositions were prepared by combining all the components and heating to 80 °C to be mixed by stirring, then cooling to approximately 25 °C. Evaluation

[0123] The compositions prepared above have been evaluated.

[0124] 0.5 g of the sample was taken to wet the hands. Then, 1 g of tap water was used. The foam was applied and rubbed in 20 times (3 sets). The foam in the palm was then collected. The foam was removed by washing the hand with tap water. The intensity and duration of hand contact before the squeaking sensation was recorded. The finish on the skin was assessed 2 minutes after towel drying. The intensity of the squeaking sensation was evaluated according to the following standard:

[0125] Very strong: strong sensation of finger stopping

[0126] Strong: sensation of finger stopping

[0127] Acceptable: no viscous sensation or sensation of stopping.

[0128] Bad: viscous sensation • The speed of the squeaking was evaluated according to the following standard:

[0129] Very fast: < 2 touch washes

[0130] Fast: >=2, <4 touch washes

[0131] Acceptable: >=4, <6 touch washes

[0132] Slow: >=6, <8 touch washes

[0133] Very slow: > 8 touch washes

[0134] The finish on the skin was evaluated 2 minutes after towel drying according to the following standards.

[0135] [Tables3] Skin Finish Rating: Very good. Feels hydrated, skin smooth. Good. No feeling of dryness. Dry. Feels dry, rough surface.

[0136] The results of the evaluations have been summarized in Table 4.

[0137] [Tables4] Ex. 1 CE. 1 CE. 2 CE. 3 CE. 4 Rinse Squeaking intensity Very loud Loud Loud Bad Very loud Squeaking speed Very fast Fast Slow Very slow Very fast Finish on skin No dry skin Good Good Good Good Dry

[0138] It has been found that the composition of example of invention 1 provides a very strong squeaking intensity and a very fast squeaking speed.

[0139] In addition, the composition of example of invention 1 also provides a good finish on skin after application.

Claims

Demands

1. Soap-free composition for the cleansing and / or removal of keratinous materials comprising: a) at least one hydrophobic silica aerogel particle; b) at least one cellulose particle; and c) at least one surfactant selected from amino acid surfactants, isethionate surfactants, sulfosuccinate surfactants, betaines and combinations thereof.

2. Composition according to claim 1, wherein the hydrophobic silica aerogel particle is selected from a silica whose surface is treated with silylation agents such as halogenated silanes, alkylsiloxanes or silazanes.

3. Composition according to any one of claims 1 to 2, wherein the hydrophobic silica aerogel particle is a silica silylate.

4. Composition according to any one of claims 1 to 3, wherein the cellulose particle is selected from celluloses, cellulose ethers, cellulose esters, cellulose ester ethers and a combination thereof.

5. Composition according to any one of claims 1 to 4, wherein the cellulose particle is selected from microcrystalline cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl methylcellulose, and a combination thereof.

6. Composition according to any one of claims 1 to 5, wherein the surfactant is a soap-free surfactant.

7. Composition according to any one of claims 1 to 6, wherein the surfactant is selected from sodium lauroyl sarcosinate, sodium cocoyl glycinate, sodium cocoyl glutamate, sodium stearoyl glutamate, disodium cocoyl glutamate, sodium lauroyl glutamate, potassium cocoyl glycinate, TEA-cocoyl glutamate, sodium cocoyl sethionate, disodium lauryl sulfosuccinate, disodium laureth sulfosuccinate, diammonium lauryl sulfosuccinate and sodium diethylhexyl sulfosuccinate, coco betaine, cocamidopropyl betaine, lauryl betaine, laurylhydroxysulfobetaine, lauryldimethyl betaine, cocamidopropyl hydroxysultaine, behenyl betaine, capryl / capramidopropyl betaine, lauryl hydroxysultaine, stearyl betaine, and a combination thereof.

8. Composition according to claim 1, comprising, in relation to the total weight of the composition: a) 0.15% to 0.3% by weight of silica silylate; b) 0.5% to 3% by weight of microcrystalline cellulose; and c) 10% to 25% by weight of at least one amino acid surfactant.

9. Composition according to any one of claims 1 to 8, wherein both silica silylate and microcrystalline cellulose have an irregular shape.

10. Method for cleaning and / or removing makeup from keratinous materials, comprising applying the composition according to any one of claims 1 to 9 to the keratinous materials, and rinsing off said composition after a period of massage.