WO2001097773A1 - Emulsion solide a phase grasse liquide structuree par un polymere - Google Patents
Emulsion solide a phase grasse liquide structuree par un polymere Download PDFInfo
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- WO2001097773A1 WO2001097773A1 PCT/FR2001/001958 FR0101958W WO0197773A1 WO 2001097773 A1 WO2001097773 A1 WO 2001097773A1 FR 0101958 W FR0101958 W FR 0101958W WO 0197773 A1 WO0197773 A1 WO 0197773A1
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- composition
- phase
- liquid fatty
- emulsion
- fatty phase
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Classifications
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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
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
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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
- A61K8/0216—Solid or semisolid forms
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/88—Polyamides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
Definitions
- the present invention relates to a composition for caring for and / or treating and / or making up the skin, including the scalp, and / or the lips of human beings of the emulsion type, containing a liquid fatty phase structured by a special polymer.
- This composition is in particular in the form of a makeup product, in particular poured in a stick or in a cup and more especially a concealer stick, a makeup for the body, a foundation or a lip product, the application of which leads to a natural deposit, light and of good behavior over time. More specifically, this composition is in the form of a solid water-in-oil emulsion (W / O).
- liquid fatty phase within the meaning of the invention, is meant a fatty phase liquid at room temperature (25 ° C) and atmospheric pressure (760mm Hg), composed of one or more non-aqueous compounds liquid at room temperature , also called oils, generally compatible with each other and insoluble at least in part in an aqueous phase.
- the non-aqueous compounds or oils can be volatile or non-volatile.
- the liquid fatty phase may contain one or more volatile compounds, one or more non-volatile compounds or a mixture of these volatile and non-volatile compounds.
- volatile compound is meant within the meaning of the invention any non-aqueous medium capable of evaporating on contact with the skin or the lips in less than one hour, at room temperature and atmospheric pressure.
- volatile solvent (s) of the invention are organic solvents and in particular volatile cosmetic oils, liquid at room temperature, having a non-zero vapor pressure, at room temperature and atmospheric pressure, ranging in particular from 10 "3 to 300mm Hg and preferably greater than 0.3mm Hg.
- the structuring of the liquid fatty phase makes it possible in particular to limit its exudation from solid compositions in particular in hot and humid regions and, in addition, to limit, after deposition on the skin or the lips, the migration or propagation of this phase in the fine lines and wrinkles, which is particularly sought after for a lipstick, a concealer or an eyeshadow.
- migration is meant an overflow of the liquid fatty phase outside the initial makeup line. This migration of the liquid fatty phase, in particular when it is significant and when this phase is loaded with coloring matters, leads to an unsightly effect around the lips and eyes, particularly accentuating wrinkles and fine lines. This migration is often cited by women as a major defect in colored makeup products such as lipsticks, concealer and classic eyeshadow.
- makeup or care compositions cast are most often in anhydrous form resulting, in particular on the face and the body but also on the eyelashes, phenomena of discomfort, heaviness, greasiness and sometimes impressions. mask or suffocation, which can become prohibitive.
- compositions due to the presence of a high level of wax, still have the disadvantage of being heavy, of being difficult to spread and of generally giving the composition an unpleasant feel.
- the presence of these waxes generally causes a matification of the makeup which is not always desirable for a lipstick or an eyeshadow.
- compositions which does not have the above drawbacks, and which in particular has properties of freshness, lightness, good resistance over time, not drying out the skin or the lips to which it is applied, both during application and over time.
- this composition is stable over time and easy to manufacture.
- the makeup obtained is natural, without a mask or suffocation sensation, and homogeneous.
- the subject of the invention is precisely a solid emulsion for caring for and / or making up and / or treating the skin and / or the lips of the face and / or the integuments making it possible to remedy the drawbacks mentioned above.
- emulsion is meant a composition containing an aqueous phase and a liquid fatty phase in which one of the two phases is dispersed in the other phase with or without emulsifier, the whole being homogeneous with the naked eye.
- solid emulsion is meant an emulsion which does not flow under its own weight at room temperature and atmospheric pressure.
- stable is meant a composition which does not exude at room temperature for at least 2 months, or even up to 9 months.
- the invention applies not only to products for making up the lips, such as lipsticks, lip glosses and lip pencils and for making up the skin, both of the face and of the human body, such as dyes possibly poured in sticks, jars or cups, concealer products, eyeshadows or blushes and temporary tattoo products but also skin care and / or treatment products, including leather scalp, and lips such as products, in particular sun protection sticks for the skin of the face or lips, body hygiene products such as deodorants, in particular sticks, thickened shampoos and conditioners, and eye makeup products such as eyeliners, pencils and mascaras more especially poured in the form of bread, as well as products for making up or caring for keratin fibers such as the hair and the eyebrows.
- products for making up the lips such as lipsticks, lip glosses and lip pencils and for making up the skin
- both of the face and of the human body such as dyes possibly poured in sticks, jars or cups, concealer products, eyeshadows or blushes and temporary tattoo products but also skin care and
- the subject of the invention is a solid emulsion containing an aqueous phase and a liquid fatty substance dispersed one inside the other, the liquid fatty phase being structured by at least one polymer of average molecular mass by weight less than 100,000, and in particular ranging from 1,000 to 30,000, comprising a) a polymer backbone having hydrocarbon repeating units provided with at least one heteroatom, and b) pendant and / or optionally functionalized fatty chains having 12 to 120 carbon atoms and being linked to these hydrocarbon units, the aqueous phase, the liquid fatty phase and the polymer forming a physiologically acceptable medium.
- the liquid fatty phase being structured by at least one polymer of average molecular mass by weight less than 100,000, and in particular ranging from 1,000 to 30,000, comprising a) a polymer backbone having hydrocarbon repeating units provided with at least one heteroatom, and b) pendant and / or optionally functionalized fatty chains having 12 to 120 carbon atoms and being linked to these hydrocarbon units, the a
- the weight average molecular weight is less than 100,000 and better still less than 50,000.
- composition of the invention may be in the form of a paste or solid, more or less hard, deformable or not. It can be an oil-in-water (O / W) or water-in-oil (W / O) emulsion, or even in the form of a triple emulsion. In particular, it is in the form of stick or cup casting and more especially in the form of a rigid water-in-oil emulsion, in particular casting.
- the structuring of the liquid fatty phase is modular according to the nature of the heteroatom polymer used and can be such that a more or less hard structure is obtained, in particular in the form of a stick or a stick.
- These rigid compositions when they are colored make it possible, after application, to obtain a deposit, homogeneous in color more or less shiny, fresh, not heavy, flexible, not migrating and of good behavior, in particular of the color over time.
- the polymer structuring the composition of the invention is a solid which is not deformable at room temperature (25 ° C) and atmospheric pressure (760mm of Hg, ie approximately 1.013. 10 5 Pa). He is able to structure the composition without clouding it.
- “functionalized chains” within the meaning of the invention is meant an alkyl chain comprising one or more functional or reactive groups chosen in particular from hydroxyl, ether, oxyalkylene or polyoxyalkylene, halogen groups, including fluorinated or perfluorinated groups, ester, siloxane , polysiloxane.
- the hydrogen atoms of one or more fatty chains can be substituted at least partially by fluorine atoms.
- polymer is meant within the meaning of the invention a compound having at least 2 repeating units.
- hydrocarbon repeating units is meant within the meaning of the invention a unit comprising from 2 to 80 carbon atoms, and preferably from 2 to 60 carbon atoms, carrying hydrogen atoms and optionally atoms of oxygen, which can be linear, branched or cyclic, saturated or unsaturated.
- These patterns further include each of one to more non-pendant heteroatoms located in the polymer backbone. These heteroatoms are chosen from nitrogen, sulfur and phosphorus atoms and their associations, possibly associated with one or more oxygen atoms.
- These units can, in addition, comprise a polar group of the carbonyl type.
- heteroatom units are in particular amide units forming a skeleton of the polyamide type, carbamate and / or urea units forming a polyurethane, polyurea and / or polyurea-urethane skeleton.
- these units are amide units.
- the pendant chains are linked directly to at least one of the heteroatoms of the polymer backbone.
- the polymer can comprise silicone units or oxyalkylenated units.
- the polymer of the composition of the invention advantageously comprises from 40 to 98% of fatty chains relative to the total number of units with a heteroatom and of fatty chains and better still from 50 to 95%.
- the nature and proportion of the heteroatom units depends on the nature of the liquid fatty phase and is in particular similar to the nature of the fatty phase.
- the more polar the heteroatom units and in high proportion in the polymer, which corresponds to the presence of several hetero atoms the more polymer has affinity with polar oils.
- the heteroatom units are not very polar or even non-polar or in low proportion, the more the polymer has affinity with non-polar oils.
- the subject of the invention is also a solid emulsion containing an aqueous phase and a liquid fatty phase dispersed one inside the other, the liquid fatty phase being structured by at least one polyamide of average molecular mass by weight less than 100,000, and in particular ranging from 1000 to 30,000, comprising a) a polymer backbone, having repeating amide units, and b) optionally pendant and / or terminal fatty chains optionally functionalized, having from 8 to 120 carbon atoms and being linked to these amide units, the aqueous phase, the liquid fatty phase and the polymer forming a physiologically acceptable medium.
- the liquid fatty phase being structured by at least one polyamide of average molecular mass by weight less than 100,000, and in particular ranging from 1000 to 30,000, comprising a) a polymer backbone, having repeating amide units, and b) optionally pendant and / or terminal fatty chains optionally functionalized, having from 8 to 120 carbon atoms and being linked to these amide units, the aque
- This emulsion can be used as it is or introduced into a more complex composition with a physiologically acceptable medium.
- the pendant fatty chains are linked to at least one of the nitrogen atoms of the amide units.
- the fatty chains of this polyamide represent from 40 to 98% of the total number of amide units and fatty chains, and better still from 50 to 95%.
- the first polymer, and in particular the polyamide, of the composition according to the invention has a weight-average molecular mass of less than 100,000 (in particular ranging from 1,000 to 100,000), in particular less than 50,000 (in particular ranging from 1000 to 50,000), and more particularly ranging from 1000 to 30,000, preferably from 2000 to 20,000, and better still from 2000 to 10,000.
- polyamides branched by pendant fatty chains and / or chains terminal fatty groups having from 12 to 120 carbon atoms and in particular from 12 to 68 carbon atoms, the terminal fatty chains being linked to the polyamide skeleton by ester groups.
- These first polymers are preferably polymers resulting from a polycondensation between a dicarboxylic acid having at least 32 carbon atoms (notably having from 32 to 44 carbon atoms) with a diamine having at least 2 carbon atoms (especially from 2 36 carbon atoms).
- the diacid is preferably a dimer derived from ethylenically unsaturated fatty acid having at least 16 carbon atoms, preferably from 16 to 24 carbon atoms, such as oleic, linoleic or linolenic acid.
- the diamine is preferably ethylene diamine, hexylene diamine, hexamethylene diamine.
- polymers comprising one or 2 terminal carboxylic acid groups
- esterify them with a monoalcohol having at least 4 carbon atoms, preferably from 10 to 36 carbon atoms and better still from 12 to 24 and even better from 16 to 24, for example 18 carbon atoms.
- n denotes an integer number of amide units such that the number of ester groups represents from 10% to 50% of the total number of ester groups and amide
- R 1 is independently at each occurrence an alkyl or alkenyl group having at least 4 carbon atoms and in particular from 4 to 24 carbon atoms
- R 2 independently represents at each occurrence a C 4 to C 42 saturated or unsaturated hydrocarbon group, provided that 50% of the R 2 groups represent a C 30 to C 42 saturated or unsaturated hydrocarbon group
- R 3 independently represents, on each occurrence, an organic group provided with at least 2 carbon atoms, hydrogen atoms and optionally one or more oxygen or nitrogen atoms
- R 4 independently represents, at each occurrence, a hydrogen atom, a saturated or unsaturated C 1 to C 10 alkyl group or a direct bond to R 3 or to another R 4 so that the nitrogen atom to which are bound to both R 3 and R 4 is part of a heterocyclic structure defined by R 4 -NR 3 , with at least 50% of
- terminal fatty chains optionally functionalized within the meaning of the invention are terminal chains linked to the last heteroatom, here nitrogen, of the polyamide skeleton.
- ester groups of formula (I), which are part of the terminal and / or pendant fatty chains within the meaning of the invention, represent from 15 to 40% of the total number of ester and amide groups and better still from 20 to 35%.
- n advantageously represents an integer ranging from 1 to 5.
- R 1 is a saturated or unsaturated C 12 -C 22 and preferably C 16 -C 22 alkyl group.
- R 2 can be a C 10 to C 42 hydrocarbon (alkylene) group.
- at least 50% and better still 75% of the R 2 are groups having from 30 to 42 carbon atoms.
- the other R 2 are hydrogenated groups from C 4 to C 19 and even from C 4 to C 12 .
- R 3 represents a C 2 to C 36 hydrocarbon group or a polyoxyalkylene group and R 4 represents a hydrogen atom.
- R 3 represents a C 2 to C 12 hydrocarbon group, saturated or not.
- the hydrocarbon groups can be linear, cyclic or branched, saturated or unsaturated groups.
- the alkyl and alkylene groups can be linear or branched groups.
- the polymer of the composition of the invention comprises a weight-average molecular mass ranging from 2,000 to 20,000 and better still from 2,000 to 10,000.
- the structuring of the liquid fatty phase is obtained using one or more polymers of formula (I).
- the polymers of formula (I) are in the form of polymer blends, these blends can also contain a synthetic product of formula (I) corresponding to a compound with n being 0, that is to say a diester.
- polyamide resins resulting from the condensation of an aliphatic di-carboxylic acid and a diamine (including the compounds having respectively more than 2 carboxyl groups and more than 2 amino groups ), the carboxyl and amine groups of adjacent unit units being condensed in the form of an amide bond.
- These polyamide resins are especially those sold under the Versamid® brand by the companies General Mills, Inc. and Henkel Corp. (Versamid 930, 744 or 1655) or by the company Olin Mathieson Chemical Corp., under the brand Onamid®, in particular Onamid S or C. These resins have a molecular mass weight average ranging from 6000 to 9000.
- Versamid® 930 or 744 are used.
- the structuring polymers of the composition of the invention advantageously have a softening temperature greater than 65 ° C and up to 190 ° C. Preferably, they have a softening temperature ranging from 70 to 130 ° C and better still from 80 to 105 ° C. This softening temperature is lower than that of known structuring polymers, which facilitates the use of the polymers which are the subject of the invention and limits the deterioration of the liquid fatty phase. These polymers are in particular non-waxy polymers.
- the polymer is associated with at least one amphiphilic liquid and non-volatile compound at room temperature, with a hydrophilic / lipophilic balance value (HLB) of less than 12 and in particular ranging from 1 to 8 and preferably from 1 to 5.
- HLB hydrophilic / lipophilic balance value
- the polymer can use one or more amphiphilic compounds.
- the purpose of these amphiphilic compounds is to reinforce the structuring properties of the heteroatom polymer, to facilitate the processing of the polymer and to improve the capacity to deposit solid emulsion.
- the composition of emulsion type can have a hardness ranging from 10g to 200g and better still from 30g to 100g.
- This hardness can be measured according to a method of penetration of a probe into said composition and in particular using a texture analyzer (for example TA-XT2 from Rhéo) equipped with an ebonite cylinder of 5 mm high and 8 mm in diameter.
- the hardness measurement is carried out at 20 ° C. in the center of 5 samples of the said composition.
- the cylinder is introduced into each composition sample at a pre-speed of 2mm / s then at a speed of 0.5 mm / s and finally at a post-speed of 2mm / s, the total displacement being 1mm.
- the value recorded for hardness is that of the maximum peak.
- the sample is approximately 1cm thick.
- the hardness of the composition (or of the emulsion) according to the invention is such that the composition is self-supporting and can disintegrate easily to form a satisfactory deposit on the skin and / or the lips and / or the integuments.
- the composition of the invention resists impact well.
- the solid emulsion in particular cast in a cup or possibly in the form of a stick, has the behavior of a deformable and flexible elastic solid, giving the application remarkable elastic softness.
- the cast compositions of the prior art do not have this property of elasticity and flexibility.
- amphiphilic compound or compounds which can be used in the composition of the invention comprise a lipophilic part linked to a polar part, the lipophilic part comprising a carbon chain having at least 8 carbon atoms in particular, from 18 to 32 carbon atoms and better still from 18 to 28 carbon atoms.
- the polar part of this or these amphiphilic compounds is the remainder of a compound chosen from alcohols and polyols having from 1 to 12 hydroxyl groups, polyoxyalkylenes comprising at least 2 oxyalkylenated units and having from 0 to 20 units oxypropylenated and / or from 0 to 20 oxyethylenated units.
- the amphiphilic compound is an ester chosen from hydro-xystearates, oleates, iso-stearates of glycerol, sorbitan or methylglucose or else branched fatty alcohols in C 12 to C 26 such as octyldodecanol and their mixtures .
- esters monoesters and mixtures of mono- and di-esters are preferred.
- the level of amphiphilic compound and that of the heteroatom polymer are chosen according to the desired gel hardness and according to the particular application. considered.
- the respective amounts of polymer and of amphiphilic compound must be such that they allow obtaining a disintegrating stick.
- the amount of polymer (in active material) represents from 0.5 to 80% of the total weight of the composition and better still from 5 to 40%, or even from 7 to 20%.
- the amount of amphiphilic compound represents in practice from 0.1% to 35% of the total weight of the composition and better still from 1% to 15%, if it is present.
- the liquid fatty phase of the composition contains at least 40% liquid oil (s) having a group similar to that of the heteroatom units and better from 50 to 100%.
- the liquid fatty phase structured by a polyamide-type skeleton contains a majority amount, namely at least equal to 40% of the total weight of the liquid fatty phase and better still from 50 to 100%, of oil or mixture of non-polar liquid oils, and more particularly hydrocarbon oil (s).
- this fatty phase preferably contains at least
- this fatty phase advantageously contains at least 40% by weight and better still from 50 to 100%, of oil or mixture of liquid non-polar oils, in particular hydrocarbon, relative to the total weight of the liquid fatty phase.
- hydrocarbon oil any oil containing carbon and hydrogen atoms and optionally an ether, ester, acid or hydroxyl function.
- the polar oils of the invention are: - hydrocarbon-based vegetable oils with a high triglyceride content consisting of fatty acid and glycerol esters, the fatty acids of which may have varying chain lengths from C 4 to C 24 , the latter possibly being linear or branched, saturated or unsaturated ; these oils are in particular the oils of wheat germ, corn, sunflower, shea, castor, sweet almonds, macadamia, apricot, soy, cotton, alfalfa, poppy, pumpkin, sesame, squash, rapeseed, avocado, hazelnut, grape or blackcurrant seed, evening primrose, millet, barley, quinoa, olive, rye, safflower,nadooulier , passion flower, muscat rose; or the triglycerides of caprylic / capric acids such as those sold by the company Stearineries Dubois or those sold under the names Miglyol 810, 812 and 818 by the company
- R. represents the remainder of a linear or branched fatty acid containing from 1 to 40 carbon atoms and R 2 represents a hydrocarbon chain in particular branched containing 1 to 40 carbon atoms provided that R 1 + R 2 is> 10, such as Purcellin oil (ketostearyl octanoate), isononyl isononanoate, C 12 to C 15 alcohol benzoate , isopropyl myristate, ethyl 2-hexyl palmitate, isostearate isostearate, octanoates, decanoates or ricinoleates of alcohols or polyalcohols; hydroxylated esters such as isostearyl lactate, di-isostearyl malate; and pentaerythritol esters;
- apolar oils according to the invention are in particular silicone oils such as polydimethylsiloxanes (PDMS) volatile or not, linear or cyclic, liquid at room temperature; polydimethylsiloxanes comprising alkyl, alkoxy or phenyl groups, pendant and / or at the end of the silicone chain, groups each having from 2 to 24 carbon atoms; phenylated silicones such as phenyl trimethicones, phenyl dimethicones, phenyl trimethylsiloxy diphenylsiloxanes, diphenyl dimethicones, diphenyl methyldiphenyl trisiloxanes, 2-phenylethyl trimethylsiloxysilicates; linear or branched hydrocarbons of synthetic or mineral origin, volatile or not, such as paraffin oils, volatile or non-volatile, and its derivatives, petrolatum, liquid lanolin, polydecenes, hydrogenated polyisobutene such as parlam, squalane
- the structured oils are nonpolar oils and more especially an oil or a mixture of oils of the hydrocarbon type of mineral or synthetic origin, chosen in particular from hydrocarbons, in particular alkanes such as parlameam oil, isoparaffins such as isododecane and squalane and their mixtures.
- these oils are combined with one or more phenylated silicone oils.
- the liquid fatty phase contains at least one non-volatile oil chosen in particular from hydrocarbon oils of mineral, vegetable or synthetic origin, synthetic esters or ethers, silicone oils and their mixtures.
- the total liquid fatty phase represents, in practice, from 5 to 98% of the total weight of the composition, preferably from 20 to 75%.
- the liquid fatty phase of the composition according to the invention may also contain at least one non-aqueous volatile compound, namely one or more volatile compounds.
- Volatile compounds are generally solvents of non-volatile compounds.
- these volatile compounds facilitate, in particular, the application of the composition to the skin, the lips or the integuments.
- These volatile compounds can be hydrocarbon compounds, silicone compounds optionally comprising pendant or end-to-end alkyl or alkoxy groups. silicone or a mixture of these volatile compounds.
- silicone oils having a viscosity at room temperature of less than 10 cSt and having in particular from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups having from 1 to 10 carbon atoms.
- silicone oil As silicone oil.
- volatile which can be used in the invention, there may be mentioned in particular octamethyl cyclotetrasiloxane, decamethyl cyclopentasiloxane, dodecamethyl cyclohexasiloxane, heptamethyl hexyltrisiloxane, heptamethyloctyl trisiloxane, hexamethyl disiloxane, octamethyl trisethylamisane tetamethylane tisiloxane, pentasiloxane and their mixtures.
- volatile hydrocarbon oils having from 8 to 16 carbon atoms and their mixtures and in particular branched C 8 -C 16 alkanes such as iso-alkanes (also called isoparaffins).
- C 8 -C 16 isododecane, isodecane, isohexadecane and for example the oils sold under the trade names of Isopars 1 or Permyls, the branched esters of C 8 -C 16 such as iso neopentanoate -hexyl and their mixtures.
- the volatile compound (or solvent) is chosen from volatile hydrocarbon oils having from 8 to 16 carbon atoms and their mixtures.
- volatile compounds represent in particular a mass rate of 0 to 97.5% relative to the total weight of the composition, preferably from 1 to 75% and better still from 3 to 45% (if present).
- the amount of volatile compound is used in an amount sufficient to obtain sliding and spreading properties. This amount will be adapted by a person skilled in the art depending on the intensity of the spreading properties sought.
- the composition of the invention additionally contains an aqueous phase immiscible with the liquid fatty phase containing water optionally thickened or gelled with one or more thickeners or gelling agents of aqueous phase and optionally containing compounds miscible with water , like C 2 to C 7 lower alcohols, polyols having at least two hydroxyl groups and from 2 to 10 carbon atoms such as glycerol, propylene glycol, D-panthenol, polyethylene glycols.
- the aqueous phase represents in particular from 1 to 80% of the total weight of the composition and better still from 5 to 70%.
- the emulsions according to the invention can be obtained using a surfactant or a mixture of surfactants whose HLB (hydrophilic / lipophilic balance) is adapted to the direction of the emulsion.
- HLB hydrophilic / lipophilic balance
- surfactant which can be used in the invention, suitable for obtaining a W / O emulsion, mention may be made of those having a lower HLB 7 and in particular the fatty acid esters of polyols such as mono-, di-, tri- or sesqui-oleates or stearates of sorbitol or glycerol, glycerol or polyethylene glycol laurates; alkyl or alkoxy dimethicone copolyols with an alkyl or alkoxy chain hanging or at the end of a silicone skeleton having, for example, from 6 to 22 carbon atoms.
- polyols such as mono-, di-, tri- or sesqui-oleates or stearates of sorbitol or glycerol, glycerol or polyethylene glycol laurates
- surfactant which can be used in the invention for obtaining an O / W emulsion, mention may be made of those having an HLB greater than 7 such as the fatty acid esters of polyethylene glycol (monostearate or polyethylene glycol monolaurate); polyoxyethylenated sorbitol fatty acid esters (stearate, oleate); polyoxyethylenated alkyl (lauryl, cetyl, stearyl, octyl) ethers and dimethicone copolyols.
- any ionic (cationic or anionic) amphoteric surfactant and any nonionic surfactant can be used.
- composition of the invention may also comprise any additive usually used in the field concerned, chosen in particular from coloring matters, antioxidants, essential oils, preservatives, perfumes, electrolytes (cation or polycations), fillers, waxes, pasty products at room temperature, neutralizers, water-soluble or dispersible polymers in the medium, cosmetic or dermatological active ingredients such as emollients, moisturizers, vitamins, essential fatty acids, sunscreens, dispersants such as acid poly (12-hydroxystearic) and mixtures thereof.
- additives can be present in the composition at a rate of 0 to 20% (in particular from 0.01 to 20%) of the total weight of the composition and better still from 0.01 to 10%.
- the composition contains at least one cosmetic or dermatological active ingredient.
- the composition according to the invention can be in the form of a dermatological tinting composition or for caring for keratin materials such as the skin, the lips and / or the integuments such as keratin fibers, in the form of a sun protection composition or personal hygiene in particular in the form of a deodorant or make-up remover product in cast form. It can in particular be used as a care base for the skin, the integuments or the lips (lip balms protecting the lips from the cold and / or from the sun and / or wind, care product for the skin, the nails or the hair ).
- composition of the invention may also be in the form of a colored product for making up the skin, in particular a foundation, optionally having care or treatment properties, a blush, a blush or eyelids, concealer, eyeliner, body makeup; make-up of the lips such as a lipstick, a lip gloss or a pencil possibly having care or treatment properties; make-up of the integuments such as the eyelashes and the hair, in particular in the form of a bread mascara, the eyebrows in particular in the form of a pencil, the nails.
- the composition of the invention must be cosmetically or dermatologically acceptable, ie contain a physiologically acceptable medium which is non-toxic and capable of being applied to the skin, the integuments or the lips of human beings.
- cosmetically acceptable is meant within the meaning of the invention a composition of pleasant appearance, odor and feel.
- the composition contains at least one cosmetic active and / or one dermatological active and / or at least one coloring matter. Thanks to the use of at least one polymer of weight average molecular weight ranging from 1000 to 30,000, as defined above in an emulsion, a trapping of the active agents and the coloring matters present in the composition is obtained, making it possible to maintain where they were applied, namely the lips, the skin or the integuments.
- the coloring matter according to the invention can be chosen from lipophilic dyes, hydrophilic dyes, pigments and nacres usually used in cosmetic or dermatological compositions, and mixtures thereof.
- This coloring material is generally present in an amount of 0.01 to 50% of the total weight of the composition, preferably from 5 to 30%, if it is present.
- Iosoluble dyes are for example Sudan red, DC Red 17, DC Green 6, ⁇ -carotene, soybean oil, Sudan brown, DC Yellow 11, DC Violet 2, DC orange 5, quinoline yellow. They can represent from 0.1 to 20% of the weight of the composition and better still from 0.1 to 6% (if present).
- the pigments can be white or colored, mineral and / or organic, coated or not.
- mineral pigments mention may be made of titanium dioxide, optionally surface-treated, zirconium or cerium oxides, as well as iron or chromium oxides, manganese violet, ultramarine blue, hydrate of chrome and ferric blue.
- organic pigments mention may be made of carbon black, pigments of the D & C type, and lakes based on cochineal carmine, barium, strontium, calcium, aluminum.
- the pigments can represent from 0.1 to 50% and better still from 2 to 30% of the total weight of the composition, if they are present.
- the pearlescent pigments can be chosen from white pearlescent pigments such as mica coated with titanium or bismuth oxychloride, colored pearlescent pigments such as mica titanium with iron oxides, mica titanium with especially ferric blue or chromium oxide, titanium mica with an organic pigment of the aforementioned type as well as pearlescent pigments based on bismuth oxychloride. They can represent from 0.1 to 20% of the total weight of the composition and better still from 0.1 to 15%, if they are present.
- the composition may optionally contain one or more waxes to improve the structuring in the form of a stick, although this rigid form can be obtained in the absence of wax.
- a wax within the meaning of the present invention, is a lipophilic fatty compound, solid at room temperature (25 ° C), with reversible solid / liquid state change, having a melting temperature above 40 ° C which can range up to at 200 ° C, and having an anisotropic crystalline organization in the solid state.
- the size of the crystals is such that the crystals diffract and / or scatter light, giving the composition a cloudy, more or less opaque appearance.
- the wax By bringing the wax to its melting point, it is possible to make it miscible with oils and to form a homogeneous mixture microscopically, but by bringing the temperature of the mixture to room temperature, the wax is recrystallized from the oils of the mixed. It is this recrystallization from the mixture which is responsible for the reduction in the gloss of said mixture. Also, advantageously the composition contains little or no wax.
- Waxes in the sense of demand, are those generally used in the cosmetic and dermatological fields; they are in particular of natural origin such as beeswax, Camauba, Candellila, Ouricoury, Japanese wax, cork or sugar cane fibers, paraffin waxes, lignite, microcrystalline waxes, lanolin wax, Montan wax, ozokerites, hydrogenated oils such as hydrogenated jojoba oil, but also of synthetic origin such as polyethylene waxes resulting from the polymerization of ethylene, waxes obtained by Fischer-Tropsch synthesis, fatty acid esters and concrete glycerides at 40 ° C, silicone waxes such as alkyl, alkoxy and / or poly (di) methylsiloxane esters at 40 ° C.
- natural origin such as beeswax, Camauba, Candellila, Ouricoury, Japanese wax, cork or sugar cane fibers, paraffin waxes, lignite, microcrystalline waxes, lanolin wax
- the composition according to the invention can be produced by known methods, generally used in the cosmetic or dermatological field. It can be manufactured by the process which consists in heating the polymer at least to its softening temperature, in adding thereto the amphiphilic compound or compounds, the emulsifiers, the coloring matters and the possibly melted additives then mixing the whole until the '' obtaining a clear, transparent solution. Then added to the mixture obtained, after lowering the temperature, the volatile compound or compounds, then the aqueous phase. The whole is then homogenized. The homogeneous mixture obtained can then be poured into a suitable mold such as a cup or a jar of lip gloss or directly into the packaging articles (case or cup in particular).
- the subject of the invention is also a cosmetic process for caring for, making up or treating keratin materials of human beings and in particular of the skin, lips and integuments, comprising the application to the keratin materials of the composition in particular cosmetic such as defined above.
- Titanium dioxide 4.1%
- Phase (B) is heated to 120 ° C, with stirring, then homogenized using a Rainery homogenizer rotating at 300 rpm. Phase A is then added, followed by phase C pre-ground using a three-cylinder mill. Phase D and phase E are then added slowly and regularly to the previous mixture brought to 100 ° C. with a Heidolph homogenizer. The whole is left in contact for 10 min and then poured into cups.
- the product obtained is solid, easy to finger grip; it is fresh and spreads well and forms a uniform, light deposit on the skin.
- the makeup obtained is natural and satin. Its hardness in g (on the texturometer) is 35.
- Example 2 W / O solid foundation
- Sorbitan isostearate (Ariacel 987 from Uniquema) 4.5%
- Titanium dioxide 4.1%
- Example 3 W / O foundation Phase A
- Sorbitan isostearate (Ariacel 987 from Uniquema) 6%. Preservative 0.2%
- Titanium dioxide 4.1%
- the product obtained still has a beautiful solid texture and has the same cosmetic properties as that of Example 1.
- This foundation differs from that of Example 1 by the use of 17% of Uniclear 80 instead of 15%.
- the product obtained is solid and has a hardness in g of 49.2.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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JP2002503250A JP2003535883A (ja) | 2000-06-23 | 2001-06-21 | ポリマーで構造が与えられた液体脂肪相を含む固形エマルション |
EP01947570A EP1296641A1 (fr) | 2000-06-23 | 2001-06-21 | Emulsion solide a phase grasse liquide structuree par un polymere |
US12/543,346 US20090324534A1 (en) | 2000-06-23 | 2009-08-18 | Solid emulsion containing a liquid fatty phase structured with a polymer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR00/08084 | 2000-06-23 | ||
FR0008084A FR2810562B1 (fr) | 2000-06-23 | 2000-06-23 | Emulsion solide a phase grasse liquide structuree par un polymere |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US10/312,083 A-371-Of-International US20040151686A2 (en) | 2000-06-23 | 2003-03-26 | Cosmetic composition comprising an emulsion containing a liquid fatty phase structured with a polymer, and an alkylene-oxide-containing emulsion stabilizer |
US12/543,346 Continuation US20090324534A1 (en) | 2000-06-23 | 2009-08-18 | Solid emulsion containing a liquid fatty phase structured with a polymer |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001097773A1 true WO2001097773A1 (fr) | 2001-12-27 |
Family
ID=8851614
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2001/001958 WO2001097773A1 (fr) | 2000-06-23 | 2001-06-21 | Emulsion solide a phase grasse liquide structuree par un polymere |
Country Status (5)
Country | Link |
---|---|
US (2) | US20040151686A2 (fr) |
EP (3) | EP1870076A3 (fr) |
JP (2) | JP2003535883A (fr) |
FR (1) | FR2810562B1 (fr) |
WO (1) | WO2001097773A1 (fr) |
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2000
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2001
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- 2001-06-21 WO PCT/FR2001/001958 patent/WO2001097773A1/fr not_active Application Discontinuation
- 2001-06-21 EP EP04011738A patent/EP1447078A1/fr not_active Ceased
- 2001-06-21 JP JP2002503250A patent/JP2003535883A/ja active Pending
- 2001-06-21 EP EP01947570A patent/EP1296641A1/fr not_active Ceased
-
2003
- 2003-03-26 US US10/312,083 patent/US20040151686A2/en not_active Abandoned
-
2004
- 2004-05-20 JP JP2004150989A patent/JP4227075B2/ja not_active Expired - Fee Related
-
2009
- 2009-08-18 US US12/543,346 patent/US20090324534A1/en not_active Abandoned
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EP0374332A1 (fr) * | 1987-06-23 | 1990-06-27 | Shiseido Company Limited | Cosmétiques solides du type à émulsion eau-dans-l'huile |
WO1995024887A1 (fr) * | 1994-03-17 | 1995-09-21 | The Mennen Company | Compositions desodorisantes et antisudorales |
WO1998017705A1 (fr) * | 1996-10-18 | 1998-04-30 | Union Camp Corporation | Polyamides a terminaisons ester d'acides gras polymerises servant a formuler des gels transparents dans des liquides a faible polarite |
WO1998047470A1 (fr) * | 1997-04-22 | 1998-10-29 | The Procter & Gamble Company | Compositions cosmetiques |
DE19750246A1 (de) * | 1997-11-13 | 1999-05-20 | Huels Chemische Werke Ag | Verwendung von Carbonamidgruppen-haltigen Geminitensiden |
EP0958811A1 (fr) * | 1998-05-20 | 1999-11-24 | Th. Goldschmidt AG | Dérivés d'acide polyaspartique modifié hydrophobes en émulsions H/E |
EP0959091A1 (fr) * | 1998-05-20 | 1999-11-24 | Th. Goldschmidt AG | Copolymère de polyesteramide-succinimide modifié et son utilisation |
EP1068855A1 (fr) * | 1999-07-15 | 2001-01-17 | L'oreal | Composition à phase grasse liquide gélifiée par un polyamide à groupements ester terminaux |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8080257B2 (en) | 2000-12-12 | 2011-12-20 | L'oreal S.A. | Cosmetic compositions containing at least one hetero polymer and at least one film-forming silicone resin and methods of using |
US7749524B2 (en) | 2003-07-11 | 2010-07-06 | L'oreal S.A. | Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent |
FR2873582A1 (fr) * | 2004-07-28 | 2006-02-03 | Oreal | Composition cosmetique comportant au moins une cire apolaire et au moins une huile alkyltrisiloxane volatile |
FR2873580A1 (fr) * | 2004-07-28 | 2006-02-03 | Oreal | Composition cosmetique comprenant un melange d'au moins une huile siliconee cyclique et d'au moins une huile alkyltrisiloxane volatile |
FR2873581A1 (fr) * | 2004-07-28 | 2006-02-03 | Oreal | Composition cosmetique comprenant au moins une huile lineaire alkyltrisiloxane volatile |
FR2873571A1 (fr) * | 2004-07-28 | 2006-02-03 | Oreal | Composition cosmetique pour le maquillage des fibres keratiniques comprenant une huile alkyltrisiloxane volatile |
FR2873583A1 (fr) * | 2004-07-28 | 2006-02-03 | Oreal | Composition cosmetique comprenant une emulsion a phase continue huileuse comprenant au moins une huile alkyltrisiloxane volatile |
WO2006013415A1 (fr) * | 2004-07-28 | 2006-02-09 | L'oreal | Composition cosmétique comportant une silicone cyclique et un trisiloxane alkyle |
WO2006013414A1 (fr) * | 2004-07-28 | 2006-02-09 | L'oreal | Composition cosmétique comportant une émulsion comportant un trisiloxane alkyle |
WO2006013412A1 (fr) * | 2004-07-28 | 2006-02-09 | L'oreal | Composition cosmétique comportant une cire polaire et un trisiloxane alkyle |
WO2006013413A1 (fr) * | 2004-07-28 | 2006-02-09 | L'oreal | Composition cosmétique comportant un trisiloxane alkyle linéaire volatile |
WO2006013411A1 (fr) * | 2004-07-28 | 2006-02-09 | L'oreal | Composition cosmétique pour fibres de kératine comportant un trisiloxane alkyle |
Also Published As
Publication number | Publication date |
---|---|
JP2003535883A (ja) | 2003-12-02 |
EP1296641A1 (fr) | 2003-04-02 |
EP1447078A1 (fr) | 2004-08-18 |
US20090324534A1 (en) | 2009-12-31 |
EP1870076A2 (fr) | 2007-12-26 |
JP4227075B2 (ja) | 2009-02-18 |
US20040151686A2 (en) | 2004-08-05 |
FR2810562A1 (fr) | 2001-12-28 |
FR2810562B1 (fr) | 2003-04-18 |
EP1870076A3 (fr) | 2009-07-22 |
JP2004231669A (ja) | 2004-08-19 |
US20030161807A1 (en) | 2003-08-28 |
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