WO2018153763A1 - Composition cosmétique multi-phase et procédé de traitement cosmétique - Google Patents
Composition cosmétique multi-phase et procédé de traitement cosmétique Download PDFInfo
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- WO2018153763A1 WO2018153763A1 PCT/EP2018/053736 EP2018053736W WO2018153763A1 WO 2018153763 A1 WO2018153763 A1 WO 2018153763A1 EP 2018053736 W EP2018053736 W EP 2018053736W WO 2018153763 A1 WO2018153763 A1 WO 2018153763A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/03—Liquid compositions with two or more distinct layers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/002—Preparations for repairing the hair, e.g. hair cure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
Definitions
- the invention relates to a multi-phase composition
- a multi-phase composition comprising visually distinct phases, a first phase comprising thickening polymers, and a second phase comprising plant oils of particular triglyceride type.
- the invention also relates to a cosmetic treatment process, in particular for the hair, using said composition.
- Hair is generally damaged and embrittled by the action of external atmospheric agents such as light and bad weather, and by mechanical or chemical treatments, such as brushing, combing, dyeing, bleaching, permanent-waving and/or relaxing.
- external atmospheric agents such as light and bad weather
- mechanical or chemical treatments such as brushing, combing, dyeing, bleaching, permanent-waving and/or relaxing.
- Mention may thus in particular be made of leave-on haircare products, which can be applied to dry or wet hair and which are not rinsed off, and which can advantageously be in the form of a multi-phase composition, in particular comprising two or three visually distinct phases.
- These care products generally comprise at least one aqueous phase and at least one fatty phase, the latter comprising mineral oils such as alkanes (isododecane in particular) and/or volatile or non-volatile silicone oils.
- compositions can also be improved, in particular with regard to their performances relating to fibre strengthening and protection, and provision of sheen and of frizziness control, this being by using mainly starting materials of natural origin.
- the objective of the present invention is to meet this demand and it therefore pro- vides a multi-phase composition which makes it possible to nourish the hair, to strengthen it and to give it protection, while at the same time conferring on it softness, suppleness, straightness, lightness, and a natural non-greasy and non-charged feel, and also good individualization of the hairs.
- This composition also gives the hair an improved ability to disentangle, and good volume control, and makes it manageable, in particular in terms of reducing frizziness.
- composition according to the invention has an attractive visual appearance, since it is in the form of several visually distinct phases, in particular in two-phase form.
- a subject of the present invention is therefore a multi-phase composition
- a multi-phase composition comprising at least two visually distinct phases, a first phase comprising one or more thickening polymers, and a second phase comprising: - one or more plant oils of triglyceride type, the C12 fatty acid content of which is greater than or equal to 40% by weight, relative to the total weight of fatty acids of said triglycerides of said oil and
- one or more additional plant oils of triglyceride type different from the plant oils of triglyceride type, the C12 fatty acid content of which is greater than or equal to 40% by weight, relative to the total weight of fatty acids of said triglycerides of said oil.
- the expression “at least one” is equivalent to the expression “one or more” and can be substituted for said expression;
- the expression “be- tween” is equivalent to the expression “ranging from” and can be substituted for said expression, and implies that the limits are included.
- composition according to the present invention has two phases that are visually distinct or more than two visually distinct phases, and preferably two visually distinct phases.
- phase can be distinguished from each other by a person's naked eye, unlike phases forming homogeneous particle dispersions or emulsions. Thus, one of the two phases is not finely dispersed in the other, as is the case for example for emulsions.
- the phases of the composition according to the invention are liquid, and, at rest, occupy zones one above the other; when the container is inverted, the phases can mix together.
- the composition according to the invention is advantageously a two-phase liquid.
- composition according to the invention comprises a first phase which comprises one or more thickening polymers.
- This phase is advantageously aqueous, that is to say it comprises water, in particu- lar at a content greater than or equal to 40% by weight, in particular ranging from 40% to 99.5% by weight, in particular ranging from 50% to 99% by weight and better still ranging from 70% to 98% by weight, relative to the total weight of said phase.
- This first phase also comprises one or more thickening polymers.
- thickening polymer is intended to mean a polymer which, when introduced at 1 % by weight in an aqueous solution or an aqueous- alcoholic solution containing 30% ethanol, and at pH 7, or in an oil chosen from liquid petroleum jelly, isopropyl myristate or cyclopentadimethylsiloxane, makes it possible to achieve a viscosity of at least 100 cps (centipoises), in particular of at least 200 cps, preferably of at least 500 cps, at 25°C and at a shear rate of 1 s ⁇ 1 . This viscosity may be measured using a cone/plate viscometer (Haake R600 rhe- ometer or the like).
- the thickening polymers according to the invention may be of natural or synthetic origin, but are advantageously of natural origin.
- the thickening polymers according to the invention can be chosen from, alone or as a mixture, thickening polymers comprising a sugar unit, in particular thickening pol- ysaccharides, even better still bio-heteropolysaccharides.
- the thickening polymers according to the invention may be non-ionic, anionic, amphoteric or cationic.
- the base units of the polymers of the invention can be mono- or disaccharides.
- sugar unit is intended to mean a unit derived from a carbohydrate of formula Cn(H2O) n -i or (ChbOJn, which may be optionally modified by substitution and/or by oxidation and/or by dehydration.
- the sugar units capable of participating in the composition of the polymers of the invention preferably result from the following sugars: glucose, galactose, arabinose, rhamnose, mannose, xylose, fucose, fructose, anhydrogalactose, galacturonic acid, glucuronic acid, mannuronic acid, galactose sulfate or anhydrogalactose sulfate.
- a) tree or shrub exudates including:
- gums resulting from algae including:
- gums resulting from seeds or tubers including:
- locust bean gum polymer of mannose and galactose
- microbial gums including: - xanthan gum (polymer of glucose, mannose acetate, mannose/pyruvic acid and glucuronic acid),
- e) plant extracts including:
- polymers can be physically or chemically modified. Mention may in particular be made, as physical treatment, of the temperature. Chemical treatments that may be mentioned include esterification, etherification, amidation and oxidation reactions. These treatments make it possible to result in polymers which can be non-ionic, anionic, cationic or amphoteric.
- non-ionic guar gums may be modified with C1 -C6 hydroxyalkyl groups. Mention may be made, among the hydroxyalkyl groups, of the hydroxymethyl, hy- droxyethyl, hydroxypropyl and hydroxybutyl groups.
- guar gums are well known in the prior art and may be prepared, for example, by reacting the corresponding alkene oxides, for instance, propylene oxides, with the guar gum so as to obtain a guar gum modified with hydroxypropyl groups.
- the degree of hydroxyalkylation preferably varies from 0.4 to 1 .2 and corresponds to the number of alkylene oxide molecules consumed by the number of free hydroxyl functions present on the guar gum.
- Such non-ionic guar gums optionally modified with hydroxyl groups are for example sold under the trade names Jaguar HP8, Jaguar HP60 and Jaguar HP120 by the company Rhodia Chimie.
- the guar gums can be modified with cationic groups; mention may particularly be made of guar gums comprising trialkylammonium cationic groups. Preferably, from 2% to 30% of the number of the hydroxyl functional groups of these guar gums carry trialkylammonium cationic groups. More preferably still, from 5% to 20% of the num- ber of the hydroxyl functional groups of these guar gums are branched with trialkylammonium cationic groups. Mention may very particularly be made, among these trialkylammonium groups, of the trimethylammonium and triethylammonium groups. More preferably still, these groups represent from 5% to 20% by weight, relative to the total weight of the modified guar gum.
- guar gums modified with 2,3-epoxypropyltrimethylammonium chloride are products already known per se and are, for example, described in Patents US 3 589 578 and US 4 0131 307. Such products are moreover sold especially under the trade names Jaguar C13 S, Jaguar C 15 and Jaguar C 17 by the company Rhodia Chimie.
- modified locust bean gum of the cationic locust bean gum containing hydroxypropyltrimonium groups, such as Catinal CLB 200 provided by Toho.
- the starch molecules used in the present invention can originate from any plant starch source, in particular cereals and tubers; more particularly, they can be starches from maize, rice, cassava, barley, potato, wheat, sorghum, pea, oat or tap- ioca. It is also possible to use the hydrolysates of the starches mentioned above.
- the starch is preferably derived from potato.
- the starches may be chemically or physically modified, in particular by one or more of the following reactions: pregelatinization, oxidation, crosslinking, esterification, etherification, amidation, heat treatments.
- the phosphorus compounds can, for example, be sodium tripolyphosphate, sodium orthophosphate, phosphorus oxychloride or sodium trimetaphosphate.
- Distarch phosphates or compounds rich in distarch phosphate will preferentially be used, for instance the product sold under the references Prejel VA-70-T AGGL (ge- latinized hydroxypropyl cassava distarch phosphate), Prejel TK1 (gelatinized cassava distarch phosphate) or Prejel 200 (gelatinized acetyl cassava distarch phosphate) by the company Avebe, or Structure Zea from National Starch (gelatinized corn distarch phosphate).
- a preferred starch is a starch which has undergone at least one chemical modification, such as at least one esterification.
- amphoteric starches comprising one or more anionic groups and one or more cationic groups.
- the anionic and cationic groups can be bonded to the same reactive site of the starch molecule or to different reactive sites; they are preferably bonded to the same reactive site.
- the anionic groups can be of carboxylic, phosphate or sulfate type, preferably of carbox- ylic type.
- the cationic groups may be of primary, secondary, tertiary or quaternary amine type.
- amphoteric starches are in particular chosen from the compounds having the following formulae:
- St-O represents a starch molecule
- R which may be identical or different, represents a hydrogen atom or a methyl radical
- R' which may be identical or different, represents a hydrogen atom, a methyl radical or a -COOH group
- n is an integer equal to 2 or 3
- M which are identical or different, denote a hydrogen atom, an alkali metal or alkaline earth metal, such as Na, K, Li or NH 4 , a quaternary ammonium or an organic amine,
- R" represents a hydrogen atom or a C1 -C18 alkyl radical.
- the preferred amphoteric starch is a starch chloroethylamidodi- propionate.
- the celluloses and cellulose derivatives can be anionic, cationic, amphoteric or non- ionic. Among these derivatives, cellulose ethers, cellulose esters and cellulose ester ethers are distinguished.
- cellulose esters examples include inorganic cellulose esters (cellulose nitrates, sulfates and phosphates), organic cellulose esters (cellulose monoacetates, triacetates, amidopropionates, acetate butyrates, acetate propio- nates and acetate trimellitates), and mixed organic/inorganic cellulose esters, such as cellulose acetate butyrate sulfates and cellulose acetate propionate sulfates. Mention may be made, among the cellulose ester ethers, of hydroxypropyl methyl- cellulose phthalates and ethylcellulose sulfates.
- non-ionic cellulose ethers that may be mentioned are alkylcelluloses such as methylcelluloses and ethylcelluloses (for example Ethocel Standard 100 Premium from Dow Chemical); hydroxyalkylcelluloses such as hydroxymethylcellu- loses and hydroxyethylcelluloses (for example Natrosol 250 HHR sold by Aqualon) and hydroxypropylcelluloses (for example Klucel EF from Aqualon); mixed hydrox- yalkyl-alkylcelluloses such as hydroxypropylmethylcelluloses (for example Methocel E4M from Dow Chemical), hydroxyethylmethylcelluloses, hydroxyethylethylcellu- loses (for example Bermocoll E 481 FQ from Akzo Nobel) and hydroxybutylmethyl- celluloses.
- alkylcelluloses such as methylcelluloses and ethylcelluloses (for example Ethocel Standard 100 Premium from Dow Chemical); hydroxyalkylcelluloses such as hydroxymethylcellu- lose
- anionic cellulose ethers mention may be made of carboxyalkyl celluloses and salts thereof. Examples that may be mentioned include carboxymethyl celluloses, carboxymethyl methyl celluloses (for example Blanose 7M from the company Aqualon) and carboxymethyl hydroxyethyl celluloses, and also the sodium salts thereof.
- cationic cellulose ethers mention may be made of crosslinked or non- crosslinked quaternized hydroxyethylcelluloses.
- the quaternizing agent can in par- ticular be diallyldimethylammonium chloride (for example Celquat L200 from National Starch). Mention may be made, as other cationic cellulose ether, of hydroxy- ethylcellulose hydroxypropyltrimethylammonium (for example Ucare polymer JR 400 from Amerchol).
- the thickening polymers can be chosen from, alone or as a mixture, bio-heteropolysaccharides also called microbial gums.
- bio-heteropolysaccharides is intended to mean substances synthesized by sugar fermentation by microorgan- isms.
- the bio-heteropolysaccharides often in particular have units chosen from mannose units, glucose units and glucuronic or galacturonic acids in their chain, these units being optionally acylated.
- xanthan gums Preferably, use is made of xanthan gums.
- the thickening polymers according to the invention may optionally be associative. Mention may be made, among the associative thickening polymers having a sugar unit or sugar units, of celluloses or their derivatives, modified with groups comprising at least one fatty chain, such as alkyl, arylalkyl or alkylaryl groups or their mixtures where the alkyl groups are C8-C22 groups; non-ionic alkyl hydroxyethylcelluloses, such as the products Natrosol Plus Grade 330 CS and Polysurf 67 (C16 alkyl) sold by the company Aqualon; quaternized alkyl hydroxyethylcelluloses, such as the products Quatrisoft LM 200, Quatrisoft LM-X 529-18-A, Quatrisoft LM-X 529-18-B (C12 alkyl) and Quatrisoft LM-X 529-8 (C18 alkyl) sold by the company Amerchol, the products Crodacel QM, Crodacel Q
- hydroxypropyl guars modified with a fatty chain such as the product Esaflor HM 22 (modified with a C22 alkyl chain) sold by the company Lamberti; the product Miracare XC 95-3 (modified with a C14 alkyl chain) and the product RE 205-146 (modified with a C20 alkyl chain) sold by Rhodia Chimie.
- the thickening polymers according to the invention are chosen from bio- heteropolysaccharides or microbial gums, and in particular from, alone or as a mixture, xanthan gums, scleroglucan guns, gellan gums, pullulan gums, Curdlar gums, grifolan gums, lentinan gums, Schizophyllan gums, spirulinan gums and krestin gums, and also derivatives thereof; preferentially xanthan gums, gellan gums and scleroglucan gums, and derivatives thereof; and most particularly xanthan gums.
- composition according to the invention can comprise said thickening polymer(s) in a total amount ranging from 0.001 % to 10% by weight, in particular from 0.01 % to 5% by weight and preferentially from 0.02% to 1 % by weight, relative to the total weight of the phase which comprises them.
- composition according to the invention can comprise said thickening polymer(s) in a total amount ranging from 0.001 % to 10% by weight, in particular from 0.01 % to 5% by weight and preferentially from 0.02% to 1 % by weight, relative to the total weight of the composition.
- Said first phase can also comprise one or more polyols, in particular one or more C2-C6, preferably C2-C4, diols or triols, such as glycerol, propylene glycol, 1 ,3-pro- panediol or butylene glycol.
- This or these polyol(s) may be present in a total content ranging from 0.01 % to 15% by weight, especially from 0.1 % to 10% by weight and better still from 0.5% to 5% by weight, relative to the total weight of the phase which comprises them.
- composition according to the invention may comprise this or these polyol(s) in a total content ranging from 0.01 % to 15% by weight, in particular from 0.1 % to 10% by weight and better still from 0.5% to 5% by weight relative to the total weight of the composition.
- Said first phase preferably aqueous phase
- This or these salt(s) may be present in a total content ranging from 0.01 % to 5% by weight, in particular from 0.1 % to 2% by weight, relative to the total weight of the phase which comprises them.
- composition according to the invention comprises at least one second phase which comprises several particular plant oils.
- This second phase which can be referred to without distinction, and interchangeably and equivalently, as fatty phase or oily phase, is advantageously anhydrous, that is to say it preferably comprises less than 5% by weight of water, in particular less than 2% by weight of water, relative to the total weight of said phase, and advantageously does not comprise water (0%).
- Said fatty phase comprises one or more plant oils of triglyceride type, of wh ich the content of fatty acid having a carbon-chain length equal to 12 (C12 fatty acid) is greater than or equal to 40% by weight, relative to the total weight of fatty acids of said triglycerides of said oil.
- plant oils comprise mainly triglycerides, which are esters of glycerol in which, generally, the three hydroxyl groups of the glycerol are esterified with fatty acids, in particular C8-C22 acids.
- the plant oils that can be used in the context of the present invention are triglycerides, the C12 fatty acid content of which is greater than or equal to 40% by weight, relative to the total weight of fatty acids of said triglycerides.
- Said fatty phase also comprises one or more additional plant oils of triglyceride type, different from the plant oils of triglyceride type, the C12 fatty acid content of which is greater than or equal to 40% by weight, relative to the total weight of fatty acids of said triglycerides of said oil.
- said fatty phase comprises at least three different plant oils of triglyceride type, including at least one plant oil of triglyceride type, the C12 fatty acid content of which is greater than or equal to 40% by weight, relative to the total weight of fatty acids of said triglycerides of said oil.
- said fatty phase comprises:
- said fatty phase comprises: - one or more plant oils of triglyceride type, the C12 fatty acid content of which is greater than or equal to 40% by weight, and
- said fatty phase comprises:
- the fatty acid percentage is indicated by weight, relative to the total weight of fatty acids of said triglycerides of said oil.
- the fatty (or oily) phase preferably comprises a total content of plant oils of triglyc- eride type of greater than or equal to 90% by weight of said oily phase.
- It comprises in particular from 90% to 100% by weight, in particular from 95% to 99% by weight, relative to the total weight of said phase, of one or more plant oils of triglyceride type.
- the fatty (or oily) phase comprises from 0.1 % to 20% by weight, in par- ticular from 0.5% to 15% by weight, or even from 1 % to 10% by weight, relative to the total weight of said phase, of one or more plant oils of triglyceride type, the C12 fatty acid content of which is greater than or equal to 40% by weight.
- the fatty (or oily) phase preferably comprises from 20% to 80% by weight, in particular from 30% to 70% by weight, or even from 40% to 65% by weight, even better still from 50% to 60% by weight, relative to the total weight of said phase, of one or more plant oils of triglyceride type, the Cie fatty acid content of which is greater than or equal to 40% by weight.
- the fatty (or oily) phase preferably comprises from 5% to 60% by weight, in particular from 10% to 50% by weight, or even from 20% to 40% by weight, even better still from 30% to 40% by weight, relative to the total weight of said phase, of one or more plant oils of triglyceride type, the C20 fatty acid content of which is greater than or equal to 40% by weight.
- composition according to the invention may comprise a total content of plant oils of triglyceride type ranging from 1 % to 50% by weight, preferably from 5% to 30% by weight and better still from 10% to 30% by weight relative to the total weight of the composition.
- coconut oil also called copra oil (INCI: COCOS NUCIFERA (COCONUT) OIL).
- the C12 fatty acid content of which is greater than or equal to 40% by weight that can be used in the context of the invention, mention may be made of:
- avocado oil and/or argan oil are used.
- jojoba oil (INCI name: SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL).
- the oily phase advantageously comprises coconut oil, alone or as a mixture with at least one oil chosen from argan oil, avocado oil and jojoba oil; better still coconut oil as a mixture with at least one oil chosen from argan oil and/or avocado oil; and even better still coconut oil, jojoba oil and at least one oil chosen from avocado oil and/or argan oil.
- coconut oil alone or as a mixture with at least one oil chosen from argan oil, avocado oil and jojoba oil
- better still coconut oil as a mixture with at least one oil chosen from argan oil and/or avocado oil
- even better still coconut oil, jojoba oil and at least one oil chosen from avocado oil and/or argan oil 3/ Composition
- composition according to the invention comprises at least two visually distinct phases as defined above, which are preferably located one above the other.
- composition according to the invention can comprise more than two visually distinct phases, but it preferentially comprises only two visually distinct phases, one aqueous phase and one fatty (or oily) phase as defined above.
- the first phase preferably aqueous phase
- the first phase may represent from 20% to 99% by weight, preferably from 30% to 95% by weight, better still from 50% to 90% by weight and even better still from 70% to 85% by weight of the total weight of the composition.
- the fatty (or oily) phase may represent from 1 % to 80% by weight, preferably from 5% to 70% by weight, better still from 10% to 50% by weight and even better still from 15% to 30% by weight of the total weight of the composition.
- the composition according to the invention does not comprise any sili- cone-comprising fatty substance (less than 1 % by weight, preferably 0%) and does not comprise any mineral oil (less than 1 % by weight, preferably 0%).
- silicone-comprising fatty substance is intended to mean an organic compound that is water-insoluble at ordinary atmospheric temperature and pressure (25°C, 1 atm.) (solubility less than 5%, preferably less than 1 %, and more preferentially less than 0.1 %), comprising at least one sequence of at least two siloxane groups.
- mineral oil is intended to mean hydrocarbons and in particular alkanes.
- the pH of the aqueous phase of the composition according to the invention generally ranges from 1 to 7, preferably from 2 to 6, preferentially from 2.5 to 5 and even better still from 3 to 4.5.
- the cosmetic composition according to the invention in particular finds a particularly advantageous application in the hair feel, in particular for caring for, strengthening and/or conditioning keratin materials, in particular the hair.
- the cosmetic composition according to the invention is advantageously in the form of a haircare product, in particular a leave-on care product, such as a two-phase lotion.
- the cosmetic composition may be thus rinsed off or left on after having been applied to the keratin materials, for example rinsed off with water, after an optional leave-on time.
- the composition is preferably a leave-on composition.
- the competition according to the invention can advantageously be packaged in a pump dispenser bottle.
- a subject of the invention is also a cosmetic treatment method, in particular for caring for and/or conditioning keratin materials, in particular the hair, which consists in applying a composition as described above to said keratin materials, and in optionally rinsing, for example with water, after an optional leave-on time. There is prefer- ably no rinsing off.
- composition according to the invention was prepared from the ingredients indicated in the table below.
- composition in the two-phase form according to the invention is obtained.
- This composition can be packaged in a pump dispenser bottle and can then be sprayed onto the head of hair.
- the treated hair is less frizzy, in particular when there is high hygrometry (80%); this effect can still be seen 72 hours after application.
- pH agent qs pH 3.6 ⁇ 0.5 qs pH 3.6 ⁇ 0.5
- phase A 20% by weight of phase A are mixed with 80% by weight of phase B.
- phase B 20% by weight of phase A are mixed with 80% by weight of phase B.
- Each of the compositions thus obtained is packaged in a pump dispenser bottle and sprayed onto a lock of moderately sensitized hair, then the locks are left to dry in the open air.
- a lock of hair treated with the composition of the invention is compared with a lock of hair treated with the comparative composition.
- the hair is judged to be suppler when treated with the composition according to the invention.
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Abstract
La présente invention concerne une composition cosmétique multi-phase comprenant au moins deux phases visuellement distinctes, et en particulier une première phase comprenant un ou plusieurs polymères épaississants, et une seconde phase comprenant une ou plusieurs huiles végétales du type triglycéride, dont la teneur en acide gras en C12 est supérieure ou égale à 40 % en poids, par rapport au poids total des acides gras desdits triglycérides de ladite huile, et une ou plusieurs huiles végétales additionnelles. L'invention concerne également un procédé de traitement cosmétique, en particulier pour le soin et/ou le conditionnement de matériaux kératiniques, en particulier du cheveu, en utilisant une telle composition.
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FR1751496A FR3063222B1 (fr) | 2017-02-24 | 2017-02-24 | Composition cosmetique multiphasique et procede de traitement cosmetique |
FR1751496 | 2017-02-24 |
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WO2018153763A1 true WO2018153763A1 (fr) | 2018-08-30 |
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US4031307A (en) | 1976-05-03 | 1977-06-21 | Celanese Corporation | Cationic polygalactomannan compositions |
US20120220510A1 (en) * | 2005-12-15 | 2012-08-30 | Mannie Lee Clapp | Non-Migrating Colorants In Multi-Phase Personal Cleansing Compositions |
FR3005859A1 (fr) * | 2013-05-24 | 2014-11-28 | Oreal | Composition cosmetique comprenant une phase aqueuse et une phase grasse visuellement distinctes |
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DATABASE GNPD [online] MINTEL; 1 December 2016 (2016-12-01), XP002779897, Database accession no. 4518205 * |
DATABASE GNPD [online] MINTEL; 1 November 2016 (2016-11-01), XP002779896, Database accession no. 4391611 * |
DATABASE GNPD MINTEL; 1 July 2016 (2016-07-01), XP002779898, Database accession no. 4171883 * |
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FR3063222A1 (fr) | 2018-08-31 |
FR3063222B1 (fr) | 2021-06-11 |
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