composition for cleaning and / or caring for keratinous material
A composition with alpha-hydroxy acid, selenium sulfide, and cellulose addresses stability issues in cosmetic products, effectively reducing dandruff and itching at high temperatures.
Patent Information
- Application Number
- FR2024004799
- Authority / Receiving Office
- FR · FR
- Patent Type
- Utility models
- Current Assignee / Owner
- Priority Date
- 2024-03-21
- Filing Date
- 2024-05-07
- Publication Date
- 2025-09-26
- Estimated Expiration
- 2034-05-07
AI Technical Summary
Cosmetic products containing anti-dandruff agents often lack stability at high temperatures, leading to social disability due to unsightly dandruff and itching.
A composition comprising alpha-hydroxy acid, selenium sulfide, and cellulose, which provides improved stability over time even at high temperatures.
The composition maintains stability at 50°C for 5 days, reducing dandruff and itching effectively.
Abstract
Description
Title of the invention: composition for cleaning and / or caring for keratinous material Technical field
[0001] The present invention relates to a composition for cleaning and / or caring for keratinous material, preferably hair and scalp. The present invention also relates to a process for cleaning and / or caring for the scalp and hair. STATE OF THE ART
[0002] The scalp is an epidermis that undergoes continuous renewal, like the rest of the skin tissue, and is rich in sebaceous glands. Normally, the scalp is renewed by an imperceptible and invisible elimination of superficial skin cells. However, excessive renewal of cells in the horny layer of the scalp, for various reasons, can lead to the formation of large, thick patches of cells visible to the naked eye, known as "dandruff".
[0003] Dandruff is a chronic, frequent and recurring condition that is socially disabling due to its manifestly unsightly nature. These dandruff-like conditions of the scalp result in an alteration of the barrier function of the epidermis. In addition, these conditions can give rise to sensations of itching or pruritus, leading to scratching behavior that amplifies the phenomenon of the appearance of dandruff.
[0004] Many cosmetic products for cleaning and / or caring for keratinous material have been developed so as to comprise at least one anti-dandruff agent in order to solve the aforementioned problems. However, it is often difficult for cosmetic products comprising an anti-dandruff agent to be stable over time, particularly at a high temperature.
[0005] Therefore, there is a need for a composition for cleaning and / or caring for keratinous material, which comprises at least one anti-dandruff agent, and can provide improved stability over time even at high temperature. Summary of the invention
[0006] The inventors have discovered that such a need can be satisfied by the composition according to the present invention.
[0007] According to a first aspect, the present invention provides a composition, preferably for cleaning and / or caring for keratinous material, comprising: a. from 0.6% by weight to 30% by weight of at least one alpha-hydroxy acid, relative to the total weight of the composition; and b. at least one selenium sulfide; and c. at least one cellulose.
[0008] According to a second aspect, the present invention provides the use of a cellulose for improving the stability of a composition comprising at least one anti-dandruff agent, wherein the anti-dandruff agent comprises an alpha-hydroxy acid and / or a selenium sulfide, and optionally a beta-hydroxy acid and / or its derivatives.
[0009] According to a third aspect, the present invention provides a process for cleaning and / or caring for keratinous material, preferably hair and scalp, comprising the following steps: a. applying the composition as described above to a wet keratinous material; b. massaging the keratinous material for 2 seconds to 120 seconds; and c. rinsing the keratinous material with water.
[0010] The inventors have discovered that the composition according to the present invention can provide improved stability over time even at a high temperature, for example at 50°C for 5 days.
[0011] Other subjects and characteristics, aspects and advantages of the present invention will become even more apparent from the detailed description and examples which follow. DETAILED DESCRIPTION OF THE INVENTION
[0012] In the following 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...".
[0013] The articles "a" and "an", as used herein, mean one or more when applied to any feature in embodiments of the present invention described in the specification and claims. The use of "a" and "an" does not limit the meaning to a single feature, unless such a limitation is specifically stated. Furthermore, the expression "at least one" as used in this specification is equivalent to the expression "one or more".
[0014] Throughout this application, the term "comprising" should be interpreted to encompass all of the specifically mentioned features as well as optional, additional, unspecified features. As used herein, the use of the term "comprising" also discloses the embodiment in which no material features or features other than the specifically cited features are present (such as "consisting essentially of" or "consisting of"). In the case of "consisting essentially of", any Any additional composition, material and / or component that materially affects the fundamental and novel characteristics are excluded from such an embodiment, but any composition, material and / or component that does not materially affect the fundamental and novel characteristics may be included in the embodiment.
[0015] Unless otherwise specified, all numerical values expressing an amount of ingredients and the like used in the description and claims are to be understood as being modified by the term "about". Accordingly, unless otherwise specified, the numerical values and parameters described herein are approximate values which may be modified depending on the desired performance obtained as required. The term "about" denoting a certain value is intended to denote a range within ± 5% of the value, for example: within ± 3%, ± 2%, ± 1% and ± 0.5% of the value.
[0016] As used herein, the expression "keratinous material(s)" means at least one material selected from hair, eyelashes, eyebrows, skin, nails, mucous membranes and scalp, and preferably hair and scalp.
[0017] For the purposes of the present invention, and unless otherwise indicated:
[0018] - an “alkyl” radical denotes a linear or branched saturated radical containing, for example example, from 1 to 30 carbon atoms.
[0019] - an “alkenyl” radical designates a hydrocarbon group formed when an atom hydrogen is removed from an alkene group.
[0020] - an “alkoxy” radical designates an alkyl attached to the parent molecule by an atom of oxygen (i.e., “-O-alkyl”), where “alkyl” is as defined above.
[0021] - a “heterocyclyl” radical designates a monovalent group derived from a chosen cycle among monocyclic, bicyclic or polycyclic rings of 3 to 8 members, preferably of 4 to 6 members, saturated, partially unsaturated or totally unsaturated comprising at least one carbon atom in addition to 1, 2, 3 or 4 heteroatoms chosen from oxygen, sulfur and nitrogen.
[0022] - an “aryl” radical denotes a monovalent hydrocarbon radical derived from a monocyclic, fused bicyclic, or polycyclic ring system (in which at least one ring contains a fully conjugated ir electron system) with known aromatic characteristics. Alpha-hydroxy acid
[0023] The composition according to the present invention comprises from 0.6% by weight to 30% by weight of at least one alpha-hydroxy acid, relative to the total weight of the composition.
[0024] The term "alpha-hydroxy acid" is intended to mean, according to the present invention, a carboxylic acid having at least one occupying hydroxyl functional group an alpha position on said acid (carbon adjacent to a carboxylic acid functional group).
[0025] The alpha-hydroxy acid present in the composition, according to the present invention, includes, but is not limited to, glycolic acid, citric acid, lactic acid, methyllactic acid, glucuronic acid, 2-hydroxybutanoic acid, 2-hydroxypentanoic acid, 2-hydroxyhexanoic acid, 2-hydroxyheptanoic acid, 2-hydroxyoctanoic acid, 2-hydroxynonanoic acid, 2-hydroxydecanoic acid, 2-hydroxyundecanoic acid, 2-hydroxydodecanoic acid, 2-hydroxytetradecanoic acid, 2-hydroxyhexadecanoic acid, 2-hydroxyoctadecanoic acid, 2-hydroxytetracosanoic acid, 2-hydroxyeicosanoic acid, mandelic acid, phenyllactic acid, gluconic acid, galacturonic acid, ribonic acid, tartronic acid, tartaric acid, malic acid, fumaric acid, and mixtures thereof.
[0026] Preferably, the alpha-hydroxy acid is a lower acid having 2 to 12 carbon atoms, more preferably 2 to 8 carbon atoms, even more preferably 2 to 6 carbon atoms.
[0027] Suitable alpha-hydroxy acids include glycolic acid, lactic acid, tartaric acid, citric acid, gluconic acid, and combinations thereof.
[0028] Preferably, the alpha-hydroxy acid is a monocarboxylic acid.
[0029] More preferably, the alpha-hydroxy acid is a lower monocarboxylic acid having 2 to 8 carbon atoms, even more preferably 2 to 6 carbon atoms such as lactic acid.
[0030] The most preferable alpha-hydroxy acid is lactic acid, for example, that sold under the trade name L-LACTIC ACID (90%) (CRG) by the company MUSASHINO CHEMICAL LABORATORY, and that sold under the trade name L(4)-LACTIC ACID 90% HEAT STABLE PERSONAL CARE by the company JUNGBUNZLAUER.
[0031] Advantageously, the alpha-hydroxy acid is in an amount ranging from 0.6% by weight to 20% by weight, preferably from 0.6% by weight to 10% by weight, more preferably from 0.8% by weight to 8% by weight, and even more preferably from 1% by weight to 6% by weight, relative to the total weight of the composition. Selenium sulfide
[0032] The composition according to the present invention comprises at least one selenium sulfide (or selenium disulfide).
[0033] Selenium sulfide is a basic commercial item. Selenium sulfide is generally considered to be a compound containing one mole of selenium and two moles of sulfur. However, it can take the form of a ring structure, SexSy , in which x + y = 8. Since sulfur and selenium readily form rings and chains, selenium sulfide is not a pure chemical compound, but a mixture, for example, a mixture of eight-membered ring compounds where the overall Se:S ratio is 1:2 (often abbreviated as SeS2).
[0034] Selenium sulfide is used to treat dandruff and certain scalp infections (seborrheic dermatitis). It reduces itching, irritation, and redness of the scalp.
[0035] According to the present invention, selenium sulfide is added as a raw material in the form of a powder whose particles generally have a particle size (D90) of less than 200 qm, preferably less than 100 qm, preferably less than 150 qm, preferably less than 100 qm, preferably less than 50 qm, and more preferably less than 25 qm. For example, selenium sulfide, as a raw material, may have a particle size (D90) ranging from 1 qm to 24 qm, preferably from 3 qm to 15 qm, and more preferably from 5 qm to 10 qm, for example, 24 qm, 20 qm, 18 qm, 15 qm, 10 qm, 8 qm, 7 qm, 5 qm, 3 qm, 2 qm or 1 qm. For the purposes of the present invention, the particle size (D90) corresponds to the particle size defined such that 90% by volume of the particles have a size smaller than the particle size (D90).Particle size can be measured by a forward laser light scattering device (e.g., a Malvem 3600 instrument).
[0036] A particularly preferable example of selenium sulfide is that sold under the trade name SELENIUM SULPHIDE EP / USP MICRONIZED by the company ESKAY FINE CHEMICALS.
[0037] Advantageously, the selenium sulfide is present in an amount ranging from 0.001% by weight to 10% by weight, preferably from 0.005% by weight to 5% by weight, and more preferably from 0.01% by weight to 3% by weight, and even more preferably from 0.1% by weight to 2% by weight, relative to the total weight of the composition. Cellulose
[0038] The composition according to the present invention comprises at least one cellulose.
[0039] As used herein, the term "cellulose" is intended to refer to any polysaccharide compound having within its structure sequences of glucose residues linked together via beta-1,4 linkages. Cellulose may be unsubstituted or substituted. Further, cellulose may be anionic, cationic, amphoteric, or nonionic.
[0040] Preferably, the cellulose used according to the invention is chosen from unsubstituted celluloses, including those in microcrystalline form; cellulose esters; cellulose ethers; cellulose ester ethers; and mixtures thereof.
[0041] Among the cellulose esters are inorganic cellulose esters (cellulose nitrates, sulfates, phosphates, etc.), organic cellulose esters (cellulose monoacetates, triacetates, amidopropionates, acetate butyrates, acetate propionates and acetate trimellitates, etc.) and mixed organic / inorganic cellulose esters, such as cellulose acetate butyrate sulfates and cellulose acetate propionate sulfates.
[0042] Cellulose ethers include nonionic cellulose ethers, anionic cellulose ethers, and cationic cellulose ethers.
[0043] Examples of non-ionic cellulose ethers include (Ci-C4)alkylcelluloses, such as methylcelluloses and ethylcelluloses (e.g., Ethocel Standard 100 Premium from Dow Chemical); (poly)hydroxy(Ci-C4)alkylcelluloses, such as hydroxymethylcelluloses, hydroxyethylcelluloses (e.g., Natrosol 250 HHR supplied by Ashland) and hydroxypropylcelluloses (e.g., Klucel EF from Aqualon); mixed (poly)hydroxy(Ci-C4)alkyl(Ci-C4)alkylcelluloses, such as hydroxypropylmethylcelluloses (e.g., Methocel E4M from Dow Chemical), hydroxyethylmethylcelluloses, hydroxyethylethylcelluloses (e.g., Bermocoll 20 E 481 FQ from Akzo Nobel) and hydroxybutylmethylcelluloses.
[0044] Among the anionic cellulose ethers, mention may be made of (poly)carboxy(C i-C4)alkylcelluloses and their salts. By way of example, mention may be made of carboxymethylcelluloses (for example Blanose 7M from the company Aqualon) and carboxymethylhydroxyethylcelluloses, and their sodium salts.
[0045] Among the cationic cellulose ethers, mention may be made of cationic cellulose derivatives such as cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, and described in particular in US patent 4,131,576, such as (poly)hydroxy(Ci-C4)alkyl celluloses, for example hydroxymethyl, hydroxyethyl or hydroxypropylcelluloses grafted in particular with a methacryloylethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyldiallylammonium salt.
[0046] Among the cellulose ester ethers, mention may be made of hydroxypropylmethylcellulose phthalates and ethylcellulose sulfates.
[0047] According to the present invention, the cellulose is preferably chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, more preferably chosen from unsubstituted celluloses.
[0048] Advantageously, the cellulose is present in an amount ranging from 0.01% by weight to 10% by weight, preferably from 0.05% by weight to 5% by weight, and more preferably from 0.1% by weight to 1% by weight, relative to the total weight of the composition. Beta-hydroxy acid and / or its derivatives
[0049] According to the present invention, the composition may further comprise at least one beta-hydroxy acid and / or its derivatives.
[0050] The term "beta-hydroxy acid" is understood, according to the present invention, to mean a carboxylic acid having a hydroxyl functional group and a carboxylic functional group separated by two carbon atoms.
[0051] Preferably, the "derivative" in the expression "beta-hydroxy acid and / or its derivatives" means that the hydroxyl functional group of the beta-hydroxy acid, rather than the carboxylic functional group, is derivatized and preferably acylated.
[0052] Preferably, the beta-hydroxy acid and / or its derivatives are chosen from salicylic acid, its acylated derivatives on the hydroxyl group, and its derivative of the following formula (I):
[0053] wherein, R represents a linear, branched or cyclic saturated aliphatic group or an unsaturated aliphatic group containing one or a number of double bonds, which may or may not be conjugated, these groups containing from 2 to 22, preferably from 3 to 11 carbon atoms and being optionally substituted by at least one substituent selected from (a) halogen atoms, (b) the trifluoromethyl group, (c) hydroxyl groups in free form or esterified by an acid having from 1 to 6 carbon atoms or (d) a carboxyl functional group which is free or esterified by a lower alcohol having from 1 to 6 carbon atoms;
[0054] R' represents a hydroxyl group or an ester functional group of the following formula (II): ---O--G— Rj (II) II O
[0055] in which Ri is a saturated or unsaturated, linear or branched aliphatic group having from 1 to 18 carbon atoms, preferably from 4 to 15 carbon atoms.
[0056] More preferably, the beta-hydroxy acid and / or its derivatives is (are) that having a salicylic moiety, including salicylic acid, acetylsalicylic acid, capryloylsalicylic acid, 5-n-decanoylsalicylic acid, 5-n-dodecanoylsalicylic acid, 5-propanoylsalicylic acid, 5-n-hexadecanoylsalicylic acid, 5-n-oleoylsalicylic acid and mixtures thereof.
[0057] Non-limiting examples of other useful beta-hydroxy acids and / or derivatives thereof include 5-n-octylsalicylic acid, 5-n-heptyloxysalicylic acid, 4-n-heptyloxysalicylic acid, 5-tert-octylsalicylic acid, 3-tert-butyl-5-methyl salicylic acid, 3-tert-butyl-6-methylsalicylic acid, 3,5-diisopropylsalicyl acid, 5-butoxysalicylic acid, 5-octyloxysalicylic acid, 5-benzoylsalicylic acid, beta-hydroxypropionic acid, beta-hydroxybutyric acid, beta-hydroxybeta-methylbutyric acid, carnitine, lipohydroxy acid, 3-hydroxyvaleric acid, and their mixtures.
[0058] According to the present invention, the beta-hydroxy acid and / or its derivatives are preferably particularly chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof, and are more preferably salicylic acid.
[0059] A particularly preferable beta-hydroxy acid and / or its derivatives are salicylic acid, for example, that sold under the trade name AMIPRESERVE by the company ALBAN MULLER (CRODA), and that sold under the trade name SALICYLIC ACID USP by the company CELLMARK.
[0060] Advantageously, the beta-hydroxy acid and / or its derivatives is (are) present in an amount ranging from 0.05% by weight to 10% by weight, preferably from 0.1% by weight to 8% by weight, more preferably from 0.2% by weight to 6% by weight, and even more preferably from 0.2% by weight to 3% by weight, relative to the total weight of the composition. Anionic surfactant
[0061] According to the present invention, the composition may comprise at least one anionic surfactant.
[0062] In the present description, a species is said to be “anionic” when it carries at least one permanent negative charge or when it can be ionized in the form of a negatively charged species, under the conditions of use of the composition of the invention (for example, the medium or the pH).
[0063] Preferably, the anionic surfactant is chosen from alkyl ether sulfates.
[0064] In some cases, the alkyl ether sulfates include those having the following formula (III): (III)
[0065] in which R represents a hydrogen or an alkyl chain having 6 to 24 carbon atoms, preferably an alkyl chain having 8 to 18 carbon atoms, and more preferably an alkyl chain having 12 to 18 carbon atoms, said alkyl chain being saturated or unsaturated, linear or branched, substituted or unsubstituted;
[0066] M represents a solubilizing cation such as alkali metal ions, for example sodium or potassium, ammonium or substituted ammonium ions, or alkanolammonium ions, for example monoethanolammonium or triethanolammonium ions; and
[0067] n is an integer from 0 to 3, preferably between 1 and 3, more preferably between 2 and 3.
[0068] Preferably, the anionic surfactant is sodium laureth sulfate, for example, that sold under the trade name EMAL 170S by the company KAO, or under the trade name KOPACOL N701 S RENU ULTRA / MB MASPHATE ES70 IM LD RSPO MB by the company KENSING PT MUSIM MAS.
[0069] Advantageously, the anionic surfactant is present in an amount ranging from 1% by weight to 30% by weight, preferably from 5% by weight to 25% by weight, and more preferably from 10% by weight to 20% by weight, relative to the total weight of the composition. Fatty amine
[0070] According to the present invention, the composition may comprise at least one fatty amine as a conditioning agent. Two or more fatty amines may be used in combination. Thus, a single type of fatty amine or a combination of different types of fatty amines may be used.
[0071] The term "fatty amines" means primary, secondary or tertiary fatty amines, which are optionally (poly)oxyalkylenated, or their salts. The fatty amines generally comprise at least one C6-C30 hydrocarbon-based chain. Preferably, the fatty amines according to the present invention are not quaternized. Preferably, the fatty amines according to the present invention are not (poly)oxyalkylenated.
[0072] Preferably, the composition according to the present invention comprises at least one fatty amine comprising at least one C6-C30 hydrocarbon-based chain.
[0073] Preferably, the composition according to the present invention comprises at least one fatty amine chosen from tertiary fatty amines.
[0074] More preferably, the composition according to the present invention comprises one or more tertiary fatty amines chosen from amidoamines.
[0075] Amidoamines are a class of chemical compounds formed from fatty acids and diamines. Non-limiting examples of amidoamines include those of the following formula (IV):
[0076] RCONHR'N(R")2(IV)
[0077] in which R represents a hydrocarbon radical containing at least 6 carbon atoms, preferably from 6 to 30 carbon atoms, preferably from 8 to 24 carbon atoms, and in particular a C6-C30, preferably C8-C24, linear or branched, saturated or unsaturated and substituted or unsubstituted hydrocarbon radical, preferably a C6-C30, preferably C8-C24, linear or branched alkyl radical, or a C6-C30, preferably C8-C24, linear or branched alkenyl radical; and R' represents a divalent hydrocarbon radical containing less than 6 carbon atoms, preferably from 1 to 4 carbon atoms, which may be linear or branched, saturated or unsaturated, and substituted or unsubstituted; and R" which may be the same or different, represents a hydrogen or a hydrocarbon radical containing less than 6 carbon atoms, preferably from 1 to 4 carbon atoms.Additionally, R" may be linear or branched, acyclic or cyclic, saturated or unsaturated, substituted or unsubstituted. Preferably, R" is a linear or branched acyclic alkyl or alkenyl group. More preferably, R" is hydrogen or a methyl group.
[0078] Non-limiting examples of amidoamines include, but are not limited to, oleamidopropyl dimethylamine, stearamidopropyl dimethylamine, isostearamidopropyl dimethylamine, stearamidoethyl dimethylamine, lauramidopropyl dimethylamine, myristamidopropyl dimethylamine, behenamidopropyl dimethylamine, dilinoleamidopropyl dimethylamine, palmitamidopropyl dimethylamine, ricinoleamidopropyl dimethylamine, sojamidopropyl dimethylamine, wheat germamidopropyl dimethylamine, toumesolamidopropyl dimethylamine, amandamidopropyl dimethylamine, avocatamidopropyl dimethylamine, babassuamidopropyl dimethylamine, cocamidopropyl dimethylamine, visonamidopropyl dimethylamine, avoinamidopropyl dimethylamine, sesamidopropyl dimethylamine, tallamidopropyl dimethylamine, brassicamidopropyl dimethylamine, olivamidopropyl dimethylamine, stearamidoethyl diethylamine, stearamidopropyl diethylamine, palmitamidopropyl diethylamine, palmitamidoethyl diethylamine, palmitamidoethyl dimethylamine, behenamidopropyl diethylamine, behenamidoethyl diethylamine, behenamidoethyl dimethylamine, arachidamidopropyl dimethylamine, arachidamidopropyl diethylamine, arachidamidoethyl diethylamine, arachidamidoethyl dimethylamine, diethylaminoethylstearamide, and mixtures thereof. Preferably, the fatty amine is brassicamidopropyl dimethylamine.
[0079] Other suitable fatty amines include, but are not limited to, octylamine, decylamine, dodecylamine, stearylamine, stearyldimethylamine, and mixtures thereof.
[0080] A particularly preferable example of Brassicamidopropyl Dimethylamine is that sold under the trade name PROCONDITION 2 by INOLEX CHEMICAL COMPANY.
[0081] Advantageously, the fatty acid is present in an amount ranging from 0.01% by weight to 10% by weight, preferably from 0.01% by weight to 3% by weight, more preferably from 0.05% by weight to 2% by weight, and even more preferably from 0.1% by weight to 1% by weight, relative to the total weight of the composition. Nitrogen-containing compound
[0082] The composition according to the present invention may comprise at least one nitrogen-containing compound corresponding to the following formula (V):
[0083] in which Rb R2, R3, R4 and R5, independently of each other, denote a radical chosen from:
[0084] - a hydrogen atom,
[0085] - a carboxyl group, and
[0086] - a linear or branched C1-C6 saturated or unsaturated alkyl group, which is optionally interrupted by one or more heteroatoms selected from O, S and N, and / or optionally substituted with one or more groups selected from amino, imino, amidino, guanidino, hydroxyl, sulfhydryl, carboxyl, amido, C1-C6 perfluoroalkyl, C1-C6 alkoxy, sulfate, phosphate, aryl and heterocyclyl, and
[0087] wherein R1 and R4 optionally form a ring which contains 5 or 6 atoms selected from carbon and nitrogen.
[0088] Preferably, RB R2, R3, R4 and R5, independently of one another, denote a radical chosen from:
[0089] - a hydrogen atom,
[0090] - a carboxyl group, and
[0091] - a linear or branched C1-C6 alkyl group, saturated or unsaturated, which is optionally interrupted by one or more heteroatoms selected from O, S and N, and / or optionally substituted with one or more groups selected from amino, imino, amidino, guanidino, hydroxyl, sulhydryl, carboxyl, amido, C1-C6 alkoxy, phenyl and heterocyclyl selected from pyrimidyl, piperidyl, morpholinyl, pyranyl, furyl, piperazinyl, pyridyl, imidazolyl and indolyl, and
[0092] wherein R1 and R4 optionally form a ring which contains 5 or 6 atoms selected from carbon or nitrogen.
[0093] According to the present invention, the nitrogen-containing compound may have a molecular weight of less than 500, preferably less than 400, and more preferably less than 250.
[0094] Non-limiting examples of the nitrogen-containing compound include, but are not limited to, arginine, including L-arginine, trolamine, diethanolamine, L-alanine, L-asparagine, L-aspartate, L-cysteine, L-glutamate, L-glutamine, L-glycine, L-histidine, L-isoleucine, L-leucine, L-lysine, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, L-valine, tris(hydroxymethyl)aminomethane, ethanolamine, diethanolamine, monoisopropanolamine, diisopropanolamine, N-dimethylaminoethanolamine, triisopropanolamine, 3-isopropoxypropylamine, 3-methoxypropylamine (3-MPA), 3-ethoxypropylamine, 3-(2-ethylhexyloxy)-propylamine, 2-(2-aminoethoxy)ethanol (2-2AEE), 3-butoxypropylamine (3-BPA) and monoethanolamine (MEA), and mixtures thereof.
[0095] Preferably, the nitrogen-containing compound is selected from the group consisting of L-arginine, trolamine, tris(hydroxymethyl)aminomethane, ethanolamine, diethanolamine, and mixtures thereof, more preferably L-arginine.
[0096] Preferably, the composition comprises at least 1% by weight to 10% by weight of the nitrogen-containing compound selected from the group consisting of L-arginine, trolamine, tris(hydroxymethyl)aminomethane, ethanolamine, diethanolamine and mixtures thereof, more preferably L-arginine.
[0097] One of the particularly preferable nitrogen-containing compounds is L-arginine sold under the trade name L ARGININE by the company KYOWA HAKKO.
[0098] Advantageously, the nitrogen-containing compound is present in an amount ranging from 1% by weight to 10% by weight, preferably from 1.2% by weight to 8% by weight, more preferably from 1.5% by weight to 5% by weight, and even more preferably from 1.8% by weight to 5% by weight, relative to the total weight of the composition. Amphoteric surfactant
[0099] The composition according to the present invention may comprise at least one amphoteric surfactant.
[0100] The term "amphoteric surfactant" refers to a surfactant that simultaneously carries the anionic and cationic hydrophilic group with its structure simultaneously containing hermaphroditic ions that are capable of forming cations or anions depending on ambient conditions (such as pH changes).
[0101] Useful amphoteric surfactants include betaines, sultaines (also known as sulfobetaines), alkyl amphoacetates and alkyl amphodiacetates, alkyl amphoproprionates, and mixtures thereof.
[0102] Preferably, the amphoteric surfactant is chosen from sultaines.
[0103] More preferably, the amphoteric surfactant is chosen from hydroxysultaine type surfactants.
[0104] In certain cases, the hydroxysultaine surfactant is chosen from (C8-C20 alkyl)amido(C1-C6 alkyl)hydroxylsulfobetaines.
[0105] Preferably, non-limiting examples of the hydroxysultaine surfactant include hydroxysultaines of formula (VI): O Œ3 (VI> RC—NH( CH2h—N+—CH2CHCH2SO f CIL OH
[0106] in which R represents an alkyl group having 7 to 18 carbon atoms.
[0107] One of the particularly preferable hydroxysultaine surfactants is cocamidopropyl hydroxysultaine, for example, that sold under the trade name TC-SHD 50 RSPO MB by the company GUANGZHOU TINCI MATERIALS, or those available from SEPPIC or KAO CHEMICAL.
[0108] Advantageously, the amphoteric surfactant is present in an amount ranging from 0.1% by weight to 20% by weight, preferably from 0.5% by weight to 15% by weight, and more preferably from 1% by weight to 10% by weight, relative to the total weight of the composition. Cationic Polymer
[0109] The composition according to the present invention may comprise at least one cationic polymer, other than celluloses.
[0110] Preferably, said cationic polymer is chosen from polyquaterniums, cationic guar gum derivatives, and mixtures thereof.
[0111] In some cases, the cationic polymer may comprise monomer units derived from amine and / or quaternary ammonium substituted monomer and / or compatible spacer monomers.
[0112] A suitable cationic polymer includes, for example: copolymers of 1-vinyl-2-pyrrolidine and l-vinyl-3-methylimidazolium salt (e.g., the chloride salt) (referred to as Polyquaternium-16) such as those commercially available from BASF under the trade name LUVIQUAT (e.g., LUVIQUAT FC 370); copolymers of l-vinyl-2-pyrrolidine and dimethylaminoethyl methacrylate (referred to as Polyquaternium-11) such as those commercially available from Gar Corporation (Wayne, NJ, USA) under the trade name GAFQUAT (e.g., GAFQUAT 755N); and a cationic polymer containing diallyl quaternary ammonium including, for example, a homopolymer of dimethyldiallyammonium chloride and copolymers of acrylamide and dimethyldiallyammonium chloride (referred to as Polyquaternium-6 and Poly quaternium-7).
[0113] Un polymère cationique approprié peut inclure d’autres polyquaterniums, tels que polyquaternium-1, polyquaternium-2, polyquatemium-3, polyquatemium-4, polyquaternium-5, polyquaternium-8, polyquaternium-9, polyquaternium-10, polyquaternium-12, polyquaternium-13, polyquaternium-14, polyquaternium-15, polyquaternium-17, polyquaternium-18, polyquaternium-19, polyquaternium-20, polyquaternium-21, polyquaternium-22, polyquaternium-23, polyquaternium-24, polyquaternium-25, polyquaternium-26, polyquaternium-27, polyquaternium-28, polyquaternium-29, polyquaternium-30, polyquaternium-40, polyquaternium-41, polyquaternium-42, polyquaternium-43, polyquaternium-44, polyquaternium-45, polyquaternium-46, polyquaternium-47, polyquaternium-48, polyquaternium-49, polyquaternium-50, polyquaternium-51, polyquaternium-52, polyquaternium-53, polyquaternium-54, polyquatemium-55, polyquatemium-56, polyquatemium-57, polyquaternium-58, polyquaternium-59, polyquaternium-60, polyquaternium-61,polyquaternium-62, polyquaternium-63, polyquaternium-64, polyquaternium-65, polyquaternium-66, polyquaternium-67, and combinations thereof. ,
[0114] The preferable cationic guar gum derivative may be guar hydroxypropyltrimonium chloride, and preferably hydroxypropyl guar hydroxypropyltrimonium chloride.
[0115] According to the present invention, the cationic polymer, other than celluloses, is preferably chosen from polyquaterniums, cationic guar gum derivatives and their mixtures, more preferably chosen from derivatives of cationic guar gum, is even more preferably guar hydroxypropyltrimonium chloride, and most preferably hydroxypropyl guar hydroxypropyltrimonium chloride.
[0116] Advantageously, the cationic polymer is present in an amount ranging from 0.01% by weight to 10% by weight, preferably from 0.01% by weight to 3% by weight, more preferably from 0.05% by weight to 2% by weight, and even more preferably from 0.1% by weight to 1% by weight, relative to the total weight of the composition. Aqueous solvent
[0117] The composition of the present invention may comprise at least one aqueous solvent.
[0118] Preferably, the aqueous solvent of the composition according to the present invention includes water and one or more water-miscible or at least partially water-miscible compounds, for example C2-C8 polyols and monoalcohols.
[0119] The term “polyol” should be understood as designating any organic molecule comprising at least two free hydroxyl groups.
[0120] More preferably, the composition according to the present invention comprises water.
[0121] Advantageously, the water is present in an amount ranging from 30% by weight to 95% by weight, preferably from 40% by weight to 90% by weight, and more preferably from 50% by weight to 85% by weight, relative to the total weight of the composition. Additional ingredients
[0122] The composition according to the present invention may comprise one or more additional ingredients, chosen from those conventionally used in cleaning and / or care products for keratinous material, for example hair and scalp.
[0123] The composition according to the present invention may comprise any of the following additives: pH correcting agents, biological extracts, perfumes, preservatives and chelating agents.
[0124] According to the present invention, non-limiting examples of pH correcting agents include potassium acetate, potassium hydroxide, sodium carbonate, sodium hydroxide, sodium hydrogen carbonate, ethanol amines, and mixtures thereof. A particularly preferable pH correcting agent is sodium hydroxide.
[0125] A person skilled in the art can correct the type and amount 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 adversely affected by the additional ingredients. Composition
[0126] According to the present invention, the composition comprising the above components is a composition for cleaning and / or caring for keratinous material, preferably hair and scalp.
[0127] According to the present invention, the composition comprising the above components is preferably in the form of a fluid, for example a lotion, an emulsion, a paste, a cream or a gel. In the context of the present disclosure, the term "fluid" means that the composition can flow by means of an external force.
[0128] According to the present invention, the composition preferably has a pH value of 2 to 6.5, preferably 2 to 6, more preferably 3.5 to 5.2.
[0129] By means of the above specific components, the composition according to the present invention can provide improved stability over time even at a high temperature, for example, 50°C for 5 days, even at a lower pH value, for example, a pH value of 2 to 6.5.
[0130] According to the present invention, microorganisms include all microorganisms that can affect the skin, nails, hair, scalp, and mucous membranes. Examples of microorganisms include, but are not limited to, non-dermatophytes (Candida species such as C. albicans, etc., Scopulariopsis species such as S. brevicaulis, and Malassezia spp.). These are yeasts represented by the genus candida and by Malassezia furfur (formerly called pityrosporon). Candida affects the skin, nails, hair, and scalp, as well as mucous membranes. Malassezia furfur, which is a common saprophyte of the skin, especially seborrheic skin, is the agent of pityriasis versicolor.
[0131] Furthermore, by means of the specific fatty amine as defined above, the composition comprising it can further improve the smooth texture feeling of the keratinous material, even at a lower pH value, for example, a pH value of 2 to 6.5.
[0132] By means of the specific arginine and / or cationic polymer as defined above, the composition comprising them can further improve the smooth texture sensation and / or the softness sensation of the keratinous material, even at a lower pH value, for example a pH value of 2 to 6.5.
[0133] By means of the specific hydroxysultaine surfactant as defined above, the foaming property of the composition comprising it can be improved, even at a lower pH value, for example, a pH value of 2 to 6.5.
[0134] By means of the relatively smaller particle size of the selenium sulfide raw material as defined above, the selenium sulfide can better disperse in the composition, and further provide smooth texture sensations and / or improved softness for the composition comprising it, even at a lower pH value, for example, a pH value of 2 to 6.5.
[0135] According to a preferred embodiment, the present invention relates to a composition for cleaning and / or caring for keratinous material, relative to the total weight of the composition, comprising: a. 0.8% by weight to 8% by weight of at least one alpha-hydroxy acid being a lower acid having 2 to 12 carbon atoms, more preferably 2 to 8 carbon atoms, even more preferably 2 to 6 carbon atoms; b. 0.005% by weight to 5% by weight of at least one selenium sulfide; and c. 0.05% by weight to 5% by weight of at least one cellulose;
[0136] wherein the composition optionally has a pH value of 2 to 6.5.
[0137] In a more preferred embodiment, the present invention relates to a composition for cleaning and / or caring for keratinous material, relative to the total weight of the composition, comprising: a. 0.8% by weight to 8% by weight of at least one alpha-hydroxy acid being a lower acid having 2 to 12 carbon atoms, more preferably 2 to 8 carbon atoms, even more preferably 2 to 6 carbon atoms; b. 0.005% by weight to 5% by weight of at least one selenium sulfide; c. 0.05% by weight to 5% by weight of at least one unsubstituted cellulose; and optionally at least one of the following components: d. 0.1% by weight to 8% by weight of at least one beta-hydroxy acid and / or its derivatives chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof; e. 0.05% by weight to 2% by weight of at least one amidoamine; f. 0.5% by weight to 15% by weight of at least one hydroxysultaine surfactant; g. 1.2% by weight to 8% by weight of at least one nitrogen-containing compound selected from L-arginine, trolamine, tris(hydroxymethyl)aminomethane, ethanolamine, diethanolamine, and mixtures thereof; and h. 0.05% by weight to 2% by weight of at least one cationic guar gum derivative,
[0138] wherein the composition optionally has a pH value of 2 to 6.5.
[0139] In a more preferred embodiment, the present invention relates to a hair and scalp cleansing and / or care composition, relative to the total weight of the composition, comprising: a. 1% by weight to 6% by weight of at least one alpha-hydroxy acid being a lower monocarboxylic acid having 2 to 8 carbon atoms, even more preferably 2 to 6 carbon atoms, more preferably lactic acid; b. 0.2% by weight to 6% by weight of at least one beta-hydroxy acid and / or its derivatives chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof; c. 0.01% by weight to 3% by weight of selenium sulfide; d. 0.1% by weight to 1% by weight of at least one cellulose selected from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably unsubstituted celluloses; and optionally at least one of the following components: e. 0.1% by weight to 1% by weight of brassicamidopropyl dimethylamine; f. 1% by weight to 10% by weight of cocamidopropyl hydroxysultaine; g. 1.5% by weight to 5% by weight of L-arginine; and h. 0.1% by weight to 1% by weight of hydroxypropyl guar chloride hydroxypropyltrimonium;
[0140] wherein the composition optionally has a pH value of 3.5 to 5.2.
[0141] In a more preferred embodiment, the present invention relates to a hair and scalp cleansing and / or care composition, relative to the total weight of the composition, comprising: a. 1% by weight to 6% by weight of lactic acid; b. 0.2% by weight to 6% by weight of salicylic acid; c. 0.01% by weight to 3% by weight of selenium sulfide; and d. 0.1% by weight to 1% by weight of an unsubstituted cellulose;
[0142] wherein the composition optionally has a pH value of 3.5 to 5.2.
[0143] In an even more preferred embodiment, the present invention relates to a composition for cleaning and / or caring for the hair and scalp, relative to the total weight of the composition, comprising: a. 1% by weight to 6% by weight of lactic acid; b. 0.2% by weight to 6% by weight of salicylic acid; c. 0.01% by weight to 3% by weight of selenium sulfide; d. 0.1% by weight to 1% by weight of an unsubstituted cellulose; and optionally at least one of the following components: e. 0.1% by weight to 1% by weight of brassicamidopropyl dimethylamine; f. 1% by weight to 10% by weight of cocamidopropyl hydroxysultaine; g. 1.5% by weight to 5% by weight of L-arginine; and h. 0.1% by weight to 1% by weight of hydroxypropyl guar chloride hydroxypropyltrimonium;
[0144] wherein the composition optionally has a pH value of 3.5 to 5.2. Process and use
[0145] The composition according to the present invention can be used in a process of cleaning and / or caring for keratinous material, preferably hair and scalp, by being applied to the keratinous material.
[0146] It has been found that the composition according to the present invention can provide improved stability over time even at high temperature.
[0147] According to a second aspect, the present invention provides the use of a cellulose for improving the stability of a composition comprising at least one anti-dandruff agent, wherein the anti-dandruff agent comprises an alpha-hydroxy acid and / or a selenium sulfide, and optionally a beta-hydroxy acid and / or its derivatives, wherein the alpha-hydroxy acid, the beta-hydroxy acid and / or its derivatives, the selenium sulfide and the cellulose are preferably defined above.
[0148] Preferably, the composition comprises a mixture of an alpha-hydroxy acid, a beta-hydroxy acid and / or their derivatives, and a selenium sulfide.
[0149] Preferably, the cellulose is chosen from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably chosen from unsubstituted celluloses.
[0150] In some cases, the composition has a pH value of 2 to 6.5, preferably 2 to 6, more preferably 3.5 to 5.2.
[0151] According to a third aspect, the present invention provides a process for cleaning and / or caring for keratinous material, preferably hair and scalp, comprising the following steps: a. applying the above composition to a wet keratinous material; b. massaging the keratinous material for 2 seconds to 120 seconds; and c. rinsing the keratinous material with water.
[0152] Optionally, the process according to the present invention further comprises step d) of drying the keratinous material.
[0153] The present invention is illustrated in more detail by the examples described below, which are given by way of non-limiting illustrations. EXAMPLES
[0154] The main raw materials used, their trade names and suppliers are listed in Table 1, and materials not specified here were all commercially available.
[0155] [Table 1] Table 1 INCI Name Trade Name Supplier Lactic Acid (Lactic Acid) L-LACTIC ACID (90%) (CRG) MUSASHINO CHEMI CAL LABORATORY SALICYLIC ACID (ACIDE SALI CYLIQUE) AMIPRESERVE ALBAN MULLER (C RODA) Selenium sulfide (Séléni um sulfide) SELENIUM SULPHIDE EP / USP MICR ONIZED ESKAY FINE CHEMI CALS SODIUM LAURETH SULFATE (LAURETH SULFATE DE SODIUM) EMAL 170S KAO COCAMIDOPROPYL HYDROXY SULTAINE (COCAMIDOPROPY L HYDROXYSULTAINE) TC-SHD 50 RSPO MB GUANGZHOU TINCI MATERIALS ARGININE L ARGININE KYOWA HAKKO CELLULOSE AQUALON CMC 7 H3SXF ASHLAND
[0156] Comparative Examples 1 to 4 and Inventive Examples 1 to 4
[0157] The compositions according to Comparative Examples (CE.) 1 to 4 and Inventive Examples (Ex.) 1 to 4 comprising the active ingredients indicated in Table 2 were prepared, all quantities being expressed as percentages by weight of active material relative to the total weight of each composition.
[0158] [Table 2] Table 2 Components Ex. 1 Ex. 2 Ex. 3 Ex. 4 EC. 1 EC. 2 CE. 3 EC. 4 Phase A WATER QSP 100 QSP 100 QSP 100 QSP 100 QSP 100 QSP 100 QSP 100 QSP 100 CELLULOSE 0.2 0.2 0.2 0.2 / / 0.2 0.2 CARBOMER / / / / 0.2 / / / XANTH ANE GUM / / / / 0.2 / / HYD ROXYPROPYL GUA R HYDROXYPROPY L-TRIMONIUM CHLORIDE / / 0.3 / / / / / BRASSICAMIDOPROPYL DIMETHYLA MINE / / 0.4 / / / / / Phase eB COCAMIDOPROPYL HYDROXYSULTAIN / / 2.5 / / / / / SODIUM LAURETH SULFATE 14 14 14 14 14 14 14 14 Phase eC SALICYLIC ACID 0.5 / 0.5 / 0.5 0.5 0.5 0.5 ARGININE / / 2 / / / / / LACTIC ACID 3 3 3 1 3 3 / 0.2 Phase eD SELENIUM SULFIDE 0.6 0.6 0.6 0.6 0.6 0.6 0.6 0.6 pH (SODIUM HYDROXIDE) 3.8 3.8 3.8 3.8 3.8 3.8 3.8 3.8 Preparation process
[0159] The composition was prepared from a process comprising the following steps: 1. mixing each component of phase A until Premix 1 is formed; 2. adding each component of Phase B into Premix 1 and mixing them until transparent to form Premix 2; 3. addition of each component of phase C into Premix 2 to form Premix 3; 4. adding phase D selenium sulfide to Premix 3 and mixing them until homogenized to form Mix 1; and 5. Correction of the pH value of Mixture 1 to 3.8 by adding sodium hydroxide to form the final composition. Evaluation of compositions
[0160] The compositions as prepared were evaluated for stability. Stability test
[0161] For each of the compositions of Inventive Examples 1 to 4 and Comparative Examples 1 to 4, stability was tested using the EPPENDORF 5702 / 5702 R / 5702 RH low-speed centrifuge, comprising the following steps: 1. adding each composition to a 15 ml centrifuge tube; 2. centrifugation of each sample for 1 hour at a speed of 900 rpm, and 3. observation of the samples to determine whether precipitation has occurred.
[0162] Further, stability was tested by storing each composition at a temperature of 50°C for 5 days.
[0163] The stability results of the compositions of Inventive Examples 1 to 4 and Comparative Examples 1 to 4 were presented respectively in the following Table 3.
[0164] [Table 3] Table 3 Properties Ex. 1 Ex. 2 Ex. 3 Ex. 4 EC. 1 EC. 2 EC. 3 EC. 4 Stability after No No No No No One pr One pr One pr One pr centrifugation precip precip precip precip precip ecipita ecipita ecipita ecipita for 1 hour at a speed of 900 rpm itation itation itation itation tion is t appear tion is t appear tion is t appear Stability after No No No No One pr One pr One pr One pr storage at 50 precip precip precip precip ecipita ecipita ecipita °C for 5 days itation itation itation itation tion is t appear tion is t appear tion is t appear
[0165] From Table 3, it can be seen that only the composition of Inventive Examples 1 to 4, comprising an amount of 0.6 wt% or more of an alpha-hydroxy acid, based on the total weight of each composition, a selenium sulfide and a cellulose, can provide desired stability after centrifugation for 1 h at 900 rpm and after storage at an elevated temperature of 50°C for 5 days.
[0166] In contrast, each of the compositions of Comparative Examples 1 to 4, which does not comprise the cellulose of the present invention, but rather comprises carbomer or xanthan gum, or comprises an amount outside the scope of the present invention of alpha-hydroxy acid, or does not comprise alpha-hydroxy acid, cannot provide desired stability after centrifugation or after storage at 50°C for 5 days.
[0167] In summary, the composition according to the present invention can provide improved stability over time at elevated temperature.
Claims
Claims
1. Composition, preferably for cleaning and / or caring for keratinous material, comprising: a) from 0.6% by weight to 30% by weight of at least one alpha-hydroxy acid, relative to the total weight of the composition; b) at least one selenium sulfide; and c) at least one cellulose.
2. A composition according to claim 1, wherein the alpha-hydroxy acid is a lower acid having 2 to 12 carbon atoms, preferably a lower monocarboxylic acid having 2 to 8 carbon atoms, preferably 2 to 6 carbon atoms, and is more preferably lactic acid.
3. A composition according to any preceding claim, wherein the cellulose is selected from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers and mixtures thereof, preferably selected from unsubstituted celluloses.
4. A composition according to any one of the preceding claims, further comprising at least one beta-hydroxy acid and / or its derivatives, which is preferably selected from salicylic acid, its derivatives acylated on the hydroxyl group and its derivatives of formula (I): / OH (I) K rr O in which, R represents a linear, branched or cyclic saturated aliphatic group or an unsaturated aliphatic group containing one or a number of double bonds, which may or may not be conjugated, these groups containing from 2 to 22, preferably from 3 to 11 carbon atoms and being optionally substituted by at least one substituent selected from (a) halogen atoms, (b) the trifluoromethyl group, (c) hydroxyl groups in free form or esterified by an acid having from 1 to 6 carbon atoms or (d) a carboxyl functional group which is free or esterified by a lower alcohol having 1 to 6 carbon atoms;
5. R' represents a hydroxyl group or an ester functional group of the following formula (II): ---O--C — Ri (II) O in which Ri is a saturated or unsaturated, linear or branched aliphatic group having from 1 to 18 carbon atoms, preferably from 4 to 15 carbon atoms; and is more preferably chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid and mixtures thereof, and more preferably salicylic acid, and in which the beta-hydroxy acid and / or its derivatives is (are) preferably present in an amount ranging from 0.05% to 10% by weight, preferably from 0.1% to 8% by weight, more preferably from 0.2% to 6% by weight, and even more preferably from 0.2% to 3% by weight, relative to the total weight of the composition. Composition according to any one of the preceding claims, further comprising at least one fatty amine, which is preferably chosen from amidoamines corresponding to the following formula (IV): RCONHR'N(R")2(IV) in which R represents a hydrocarbon radical containing at least 6 carbon atoms, R' represents a divalent hydrocarbon radical containing less than 6 carbon atoms, and R" which may be the same or different, represents hydrogen or a hydrocarbon radical containing less than 6 carbon atoms, and more preferably, is chosen from the group consisting of oleamidopropyl dimethylamine, stearamidopropyl dimethylamine, isostearamidopropyl dimethylamine, stearamidoethyl dimethylamine, lauramidopropyl dimethylamine, myristamidopropyl dimethylamine, behenamidopropyl dimethylamine, dilinoleamidopropyl dimethylamine, palmitamidopropyl dimethylamine, ricinoleamidopropyl dimethylamine, sojamidopropyl dimethylamine, wheat germamidopropyl dimethylamine, toumesolamidopropyl dimethylamine, amandamidopropyl dimethylamine, avocatamidopropyl dimethylamine, babassuamidopropyl dimethylamine, cocamidopropyl dimethylamine, visonamidopropyl dimethylamine,avoinamidopropyl dimethylamine, sesamidopropyl,
6. dimethylamine, tallamidopropyl dimethylamine, brassicamidopropyl dimethylamine, olivamidopropyl dimethylamine, stearamidoethyl diethylamine, stearamidopropyl diethylamine, palmitamidopropyl diethylamine, palmitamidoethyl diethylamine, palmitamidoethyl dimethylamine, behenamidopropyl diethylamine, behenamidoethyl diethylamine, behenamidoethyl dimethylamine, arachidamidopropyl dimethylamine, arachidamidopropyl diethylamine, arachidamidoethyl diethylamine, arachidamidoethyl dimethylamine, diethylaminoethylstearamide, and mixtures thereof; and most preferably, is brassicamidopropyl dimethylamine, and wherein the fatty amine is preferably present in an amount ranging from 0.01% to 10% by weight, preferably from 0.01% to 3% by weight, more preferably from 0.05% to 2% by weight, and even more preferably from 0.1% by weight to 1% by weight, relative to the total weight of the composition. Composition according to any one of the preceding claims, further comprising at least one amphoteric surfactant, which is preferably chosen from betaines, sultaines, alkyl amphoacetates and alkyl amphodiacetates, alkyl amphopropionates, and mixtures thereof, more preferably chosen from sultaines, even more preferably chosen from hydroxysultaine surfactants, even more preferably chosen from alkyl(C8-C2o)amidoalkyl(C1-C6)hydroxyl sulfobetaines, and is even more preferably a hydroxysultaine surfactant corresponding to the following formula (VI): O CH3 (VI> RC—W(CH3h—N+—CH2CHCH2SO3- CH3 OH in which R represents an alkyl group having 7 to 18 carbon atoms; and is most preferably cocamidopropyl hydroxysultaine, and wherein the hydroxysultaine surfactant is preferably present in an amount ranging from 0.1% by weight to 20% by weight, preferably from 0.5% by weight to 15% by weight, and more preferably from 1% by weight to 10% by weight, relative to the total weight of the composition.
7. A composition according to any preceding claim, further comprising at least one nitrogen-containing compound of the following formula (V): in which Rb R2, R3, R4 and R5, independently of each other, denote a radical chosen from: - a hydrogen atom, - a carboxyl group, and - a saturated or unsaturated linear or branched C3-C6 alkyl group, which is optionally interrupted by one or more heteroatoms selected from O, S and N, and / or optionally substituted by one or more groups selected from amino, imino, amidino, guanidino, hydroxyl, sulhydryl, carboxyl, amido, perfluoroC1-C6 alkyl, C1-C6 alkoxy, sulfate, phosphate, aryl (preferably phenyl), and heterocyclyl which is preferably selected from pyrimidyl, piperidyl, morpholinyl, pyranyl, furyl, piperazinyl, pyridyl, imidazolyl and indolyl, and wherein R 1 and R 4 optionally form a ring which contains 5 or 6 atoms selected from carbon and nitrogen, preferably the nitrogen-containing compound is selected from arginine, including L-arginine, trolamine, diethanolamine, L-alanine, L-asparagine, L-aspartate, L-cysteine, L-glutamate, L-glutamine, L-glycine, L-histidine, L-isoleucine, L-leucine, L-lysine, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, L-valine, tris(hydroxymethyl)aminomethane, ethanolamine, diethanolamine, monoisopropanolamine, diisopropanolamin e, N-dimethylaminoethanolamine, triisopropanolamine, 3-isopropoxypropylamine, 3-methoxypropylamine (3-MPA), 3-ethoxypropylamine, 3-(2-ethylhexyloxy)-propylamine, 2-(2-aminoethoxy)ethanol (2-2AEE), 3-butoxypropylamine (3-BPA) and monoethanolamine (MEA), and mixtures thereof,
8.
9. more preferably, is chosen from L-arginine, trolamine, tris(hydroxymethyl)amino-methane, ethanolamine, diethanolamine and mixtures thereof, and even more preferentially, is L-arginine; and wherein the nitrogen-containing compound is preferably present in an amount ranging from 1% by weight to 10% by weight, preferably from 1.2% by weight to 8% by weight, and more preferably from 1.5% by weight to 5% by weight, and even more preferably from 1.8% by weight to 5% by weight, relative to the total weight of the composition. A hair and scalp cleansing and / or care composition, relative to the total weight of the composition, comprising a) 1% by weight to 6% by weight of at least one alpha-hydroxy acid being a lower monocarboxylic acid having 2 to 8 carbon atoms, even more preferably 2 to 6 carbon atoms, more preferably lactic acid; b) 0.2% by weight to 6% by weight of at least one beta-hydroxy acid and / or its derivatives chosen from salicylic acid, acetylsalicylic acid, capryloyl salicylic acid, and mixtures thereof; c) 0.01% by weight to 3% by weight of selenium sulfide; (d) 0.1% by weight to 1% by weight of at least one cellulose selected from unsubstituted celluloses, cellulose esters, cellulose ethers, cellulose ester ethers, and mixtures thereof, preferably unsubstituted celluloses; and optionally at least one of the following components: e) 0.1% by weight to 1% by weight of brassicamidopropyl dimethylamine; f) 1% by weight to 10% by weight of cocamidopropyl hydroxysultaine; (g) 1.5% by weight to 5% by weight of L-arginine; and (h) 0.1% by weight to 1% by weight of hydroxypropyl guar hydroxypropyltrimonium chloride; wherein the composition optionally has a pH value of 3.5 to 5.
2. Use of a cellulose for improving the stability of a composition comprising at least one anti-dandruff agent, wherein the anti-dandruff agent comprises an alpha-hydroxy acid and / or a selenium sulfide, and optionally a beta-hydroxy acid and / or its derivatives, and preferably comprises a mixture of an alpha-hydroxy acid, a beta-hydroxy acid and / or its derivatives, and a selenium sulfide; and wherein the composition is preferably defined according to any one of claims 1 to 8.
10. A process for cleaning and / or caring for keratinous material, more preferably hair and scalp, comprising the following steps: a) applying the composition according to any one of claims 1 to 8 to a wet keratinous material; b) massaging the keratinous material for 2 seconds to 120 seconds; and c) rinsing the keratinous material with water.
Citation Information
Patent Citations
Process for the preparation of graft copolymers of a water soluble monomer and polysaccharide employing a two-phase reaction system
US4131576A