[go: up one dir, main page]

WO2002056845B1 - Composition structured in rigid form by a polymeric compound - Google Patents

Composition structured in rigid form by a polymeric compound

Info

Publication number
WO2002056845B1
WO2002056845B1 PCT/FR2002/000185 FR0200185W WO02056845B1 WO 2002056845 B1 WO2002056845 B1 WO 2002056845B1 FR 0200185 W FR0200185 W FR 0200185W WO 02056845 B1 WO02056845 B1 WO 02056845B1
Authority
WO
WIPO (PCT)
Prior art keywords
composition according
lipophilic
composition
carbon atoms
hydrocarbon
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/FR2002/000185
Other languages
French (fr)
Other versions
WO2002056845A1 (en
Inventor
Richard Kolodziej
Veronique Ferrari
Jean Mondet
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LOreal SA
Original Assignee
LOreal SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by LOreal SA filed Critical LOreal SA
Publication of WO2002056845A1 publication Critical patent/WO2002056845A1/en
Publication of WO2002056845B1 publication Critical patent/WO2002056845B1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/89—Polysiloxanes
    • A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
    • A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
    • 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
    • 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
    • A61K8/87—Polyurethanes
    • 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
    • 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
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/892—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a hydroxy group, e.g. dimethiconol
    • 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
    • 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
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • 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
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06—Lipsticks
    • 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
    • A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

The invention concerns a composition containing a liquid lipophilic body and an organic polymeric compound comprising: a) a polar part having at least two repeat units including at least a group capable of forming hydrogen interactions with the lipophilic body, said group including at least a heteroatom; and b) a lipophilic part comprising a carbonaceous chain with at least four carbon atoms or a silicon chain including at least two silicon atoms, the organic polymeric compound having a mean mole weight less than 1000, the lipophilic body and the organic compound forming a physiologically acceptable medium. Said composition constitutes in particular a non-greasy make-up base or a lipstick having non-transfer properties. The polymer is in particular a polyamide comprising a hydroxylated fatty acid ester chain.

Claims

REVENDICATIONS MODIFIEES[reçues par le Bureau International le 23 juillet 2002 (23.07.02); revendications originales 1-48 remplacées par les revendications modifiées 1-44 (5 pages)] AMENDED CLAIMS [received by the International Bureau on 23 July 2002 (23.07.02); original claims 1-48 replaced by the amended claims 1-44 (5 pages)] 1. Composition contenant un corps lipophile liquide hydrocarboné, un composé polymérique organique comprenant a) une partie polaire ayant au moins deux motifs de répétition comportant au moins un groupement apte à former des interactions hydrogène avec le corps lipophile hydrocarboné, ce groupement comprenant au moins un hétéroatome, b) au moins une partie lipophile comportant une chaîne carbonée à au moins quatre atomes de carbone ou une chaîne siliconée comportant au moins deux atomes de silicium, le composé polymérique organique ayant une masse moléculaire moyenne en poids inférieure à 1 000, le corps lipophile hydrocarboné et le composé organique formant un milieu physiologiquement acceptable, et au moins une matière colorante. 1. A composition containing a liquid hydrocarbon lipophilic body, an organic polymeric compound comprising a) a polar part having at least two repeating units comprising at least one group capable of forming hydrogen interactions with the hydrocarbon lipophilic body, this group comprising at least one heteroatom, b) at least one lipophilic part comprising a carbon chain containing at least four carbon atoms or a silicone chain comprising at least two silicon atoms, the organic polymeric compound having a weight average molecular mass of less than 1000, the body lipophilic hydrocarbon and the organic compound forming a physiologically acceptable medium, and at least one dyestuff. 2. Composition selon la revendication 1 , caractérisée en ce que le groupement apte à former des interactions hydrogène est un groupement amide, carbamate, urée, thiocarbamate, thiourée, hydroxyle ou association.2. Composition according to claim 1, characterized in that the group capable of forming hydrogen interactions is an amide group, carbamate, urea, thiocarbamate, thiourea, hydroxyl or combination. 3. Composition selon la revendication 1 ou 2, caractérisée en ce que ledit hétéroatome est l'atome d'azote.3. Composition according to claim 1 or 2, characterized in that said heteroatom is the nitrogen atom. 4. Composition selon l'une des revendications précédentes, caractérisée en ce que le composé organique comprend au moins deux groupements aptes à former des interactions hydrogène.4. Composition according to one of the preceding claims, characterized in that the organic compound comprises at least two groups capable of forming hydrogen interactions. 5. Composition selon l'une des revendications précédentes, caractérisée en ce que la partie lipophile comporte au moins un groupement fonctionnel ou réactif.5. Composition according to one of the preceding claims, characterized in that the lipophilic portion comprises at least one functional or reactive group. 6. Composition selon l'une des revendications précédentes, caractérisée en ce que la partie polaire comprend au moins deux azotes qui sont sous forme de liaisons :6. Composition according to one of the preceding claims, characterized in that the polar part comprises at least two nitrogens which are in the form of bonds: OO . amide, soit - C - N (R) - avec R = H ou alkyle en C^ à C50 et mieux de C-i à C40. O O. amide, that is - C - N (R) - with R = H or C 1 to C 50 alkyl and better still from C 1 to C 40 . OO I l nI l n . uréthane, soit - O- C- NH- ou thiocarbamate, soit - S-C-NH- O O O I I" I l I I. urethane, either - O-C-NH- or thiocarbamate, or - SC-NH-OOOII " II . urée, soit - NH- C- NH, ou biuret - NH - C - N(R) - C - NH - ou thiourée, avec R un radical alkyle linéaire ou ramifiée ayant de 1 à 50 atome de carbone et mieux de 2 à 40. . urea, that is - NH - C - NH, or biuret - NH - C - N (R) - C - NH - or thiourea, with R a linear or branched alkyl radical having from 1 to 50 carbon atoms and better still from 2 to 40. 7. Composition selon l'une des revendications précédentes, caractérisée en ce que la partie lipophile comporte une chaîne alkyle ou alcoxy, linéaire ou ramifiée pouvant présenter des insaturations et/ou des cycles, ayant de 8 à 60 atomes de carbone et mieux de 12 à 40 atomes de carbone. 7. Composition according to one of the preceding claims, characterized in that the lipophilic portion comprises a linear or branched alkyl or alkoxy chain which may have unsaturations and / or rings, having from 8 to 60 carbon atoms and better still 12 at 40 carbon atoms. 8. Composition selon l'une des revendications précédentes, caractérisée en ce que la partie lipophile comporte une chaîne siliconée du type polyorganosiloxane, comportant éventuellement des radicaux alkyle ou alkoxy en Ci à C30 et mieux en C6 à C24 ou des radicaux phényle.8. Composition according to one of the preceding claims, characterized in that the lipophilic portion comprises a silicone chain of the polyorganosiloxane type, optionally comprising alkyl or alkoxy radicals C 1 to C 30 and better still C 6 to C 24 or phenyl radicals . 44 44 9. Composition selon l'une des revendications précédentes, caractérisée en ce que le composé organique comprend au moins deux parties lipophiles situées de part et d'autre de la partie polaire. 9. Composition according to one of the preceding claims, characterized in that the organic compound comprises at least two lipophilic parts located on either side of the polar part. 10. Composition selon l'une des revendications précédentes, caractérisée en ce que les motifs sont des motifs amide.10. Composition according to one of the preceding claims, characterized in that the patterns are amide units. 11. Composition structurée contenant au moins un corps lipophile liquide hydrocarboné structuré par au moins un polyamide de masse moléculaire moyenne en poids inférieure à 1 000, comportant a) un squelette polymérique ayant au moins deux motifs de répétition amide, et b) au moins une chaîne carbonée pendante et/ou au moins une chaîne carbonée terminale éventuellement fonctionnalisées, ayant au moins quatre atomes de carbone, ces chaînes étant liées à ces motifs amide, ce corps lipophile et ce polyamide formant un milieu physiologiquement acceptable.A structured composition containing at least one hydrocarbon liquid lipophilic body structured with at least one polyamide of weight average molecular weight of less than 1000, comprising a) a polymeric backbone having at least two amide repeating units, and b) at least one pendant carbon chain and / or at least one optionally functionalized terminal carbon chain having at least four carbon atoms, these chains being linked to these amide units, this lipophilic body and this polyamide forming a physiologically acceptable medium. 12. Composition selon la revendication précédente, caractérisée en ce que le polyamide comporte deux chaînes carbonées situées de part et d'autres des motifs amide.12. Composition according to the preceding claim, characterized in that the polyamide comprises two carbon chains located on either side of the amide units. 13. Composition selon la revendication 11 ou 12, caractérisée en ce que les chaînes carbonées comportent de 8 à 60 atomes de carbone et mieux de 12 à 40 atomes de carbone.13. Composition according to claim 11 or 12, characterized in that the carbon chains contain from 8 to 60 carbon atoms and better still from 12 to 40 carbon atoms. 14. Composition selon l'une des revendications 8 à 11, caractérisée en ce que les motifs amide sont au nombre de deux.14. Composition according to one of claims 8 to 11, characterized in that the amide units are two in number. 15. Composition selon l'une des revendications précédentes, caractérisée en ce que le composé polymérique organique ou le polyamide résulte de la polymérisation d'une diamine comportant un radical alkyle linéaire ou ramifiée ayant de 1 à 50 atomes de carbone et mieux de 2 à 40 atomes de carbone avec au moins un monacide carboxylique comportant un groupe alkyle de 8 à 60 atomes de carbone.15. Composition according to one of the preceding claims, characterized in that the organic polymeric compound or the polyamide results from the polymerization of a diamine having a linear or branched alkyl radical having from 1 to 50 carbon atoms and better still from 2 to 40 carbon atoms with at least one monocarboxylic acid having an alkyl group of 8 to 60 carbon atoms. 16. Composition selon la revendication précédente, caractérisée en ce que la diamine est choisie parmi l'éthylène diamine, la propylène diamine, le 1 ,6-diamino hexane, le cyclohexane diamine, l'isophorone diamine, la 2 méthyl-1 ,5 pentane diamine, le 1,12- diamino dodécane, la phénylène diamine.16. Composition according to the preceding claim, characterized in that the diamine is chosen from ethylene diamine, propylene diamine, 1, 6-diamino hexane, cyclohexane diamine, isophorone diamine, 2-methyl-1,5 pentane diamine, 1,12-diamino dodecane, phenylene diamine. 17. Composition selon la revendication précédente, caractérisée en ce que la diamine est l'éthylène diamine. 17. Composition according to the preceding claim, characterized in that the diamine is ethylene diamine. 18. Composition selon l'une des revendications 15 à 17, caractérisée en ce que le monoacide carboxylique comporte au moins un groupement hydroxyle.18. Composition according to one of claims 15 to 17, characterized in that the carboxylic monoacid comprises at least one hydroxyl group. 19. Composition selon l'une des revendications 15 à 18, caractérisée en ce que le monoacide carboxylique comporte au moins un groupe ester d'acide carboxylique ayant un groupe alkyle en C8 à C6o, notamment en C12 à C40.19. Composition according to one of claims 15 to 18, characterized in that the monocarboxylic acid comprises at least one carboxylic acid ester group having a C 8 -C 6 alkyl group, especially C 12 to C 40 . 20. Composition selon l'une des revendications 15 à 19, caractérisée en ce que le monoacide carboxylique est choisi parmi les esters de monoacides aliphatiques mono hydroxylés insaturés tels que les esters de l'acide ricinoléique ; les esters de monoacides aliphatiques mono hydroxylés linéaires saturés tels que les esters de l'acide lactique, le palmitate d'éthyl 2 hexyle, les esters de l'acide 12-hydroxy octadécanoïque ; leurs mélanges.20. Composition according to one of claims 15 to 19, characterized in that the carboxylic monoacid is chosen from unsaturated monohydroxylated aliphatic monoacid esters such as esters of ricinoleic acid; saturated linear monohydroxylated aliphatic monoacid esters such as esters of lactic acid, ethyl 2 hexyl palmitate, esters of 12-hydroxy octadecanoic acid; their mixtures. 45 45 21. Composition selon l'une des revendications précédentes, caractérisée en ce que le composé polymérique organique ou le polyamide résulte de l'amidification d'un triglycéride par une diamine éventuellement en présence d'un monoacide carboxylique en G|2 à C40.21. Composition according to one of the preceding claims, characterized in that the organic polymeric compound or the polyamide results from the amidation of a triglyceride with a diamine optionally in the presence of a monocarboxylic acid in G | 2 to C 40 . 22. Composition selon la revendication 21, caractérisée en ce que le monoacide carboxylique est l'acide 12-hydroxystéarique et le triglycéride un triglycéride d'acide gras hydroxylé ayant de 12 à 30 atomes de carbone. 22. Composition according to Claim 21, characterized in that the mono-carboxylic acid is 12-hydroxystearic acid and the triglyceride is a hydroxylated fatty acid triglyceride having from 12 to 30 carbon atoms. 23. Composition selon l'une des revendications précédentes, caractérisée en ce que le corps lipophile liquide est choisi parmi :23. Composition according to one of the preceding claims, characterized in that the liquid lipophilic body is chosen from: - les huiles végétales hydrocarbonées à forte teneur en triglycérides constitués d'esters d'acides gras et de glycérol dont les acides gras peuvent.avoir des longueurs de chaînes variées de C à C24, ces dernières pouvant être linéaires ou ramifiées, saturées ou insaturées ; ces huiles sont notamment les huiles de germe de blé, de maïs, de tournesol, de karité, de ricin, d'amandes douces, de macadamia, d'abricot, de soja, de coton, de luzerne, de pavot, de potimarron, de sésame, de courge, de colza, d'avocat, de noisette, de pépins de raisin ou de cassis, d'onagre, de millet, d'orge, de quinoa, d'olive, de seigle, de carthame, de bancoulier, de passiflore, de rosier muscat ; ou encore les triglycérides des acides caprylique/caprique ; ;hydrocarbon vegetable oils with a high triglyceride content consisting of esters of fatty acids and of glycerol, the fatty acids of which may have chain lengths varying from C to C 24 , the latter possibly being linear or branched, saturated or unsaturated ; these oils include wheat germ, corn, sunflower, shea, castor oil, sweet almond, macadamia, apricot, soya, cotton, alfalfa, poppy, pumpkin, sesame, pumpkin, rapeseed, avocado, hazelnut, grape seed or black currant, evening primrose, millet, barley, quinoa, olive, rye, safflower, bancoulier passionflower, muscat rose; or the triglycerides of caprylic / capric acids; ; - les huiles de synthèse ou esters de synthèse de formule R5COOR6 dans laquelle R5 représente le reste d'un acide gras linéaire ou ramifié comportant de 1 à 40 atomes de carbone et R6 représente une chaîne hydrocarbonée notamment ramifiée contenant de 1 à 40 atomes de carbone à condition que R5 + R6 soit > 10, comme par exemple l'huile de Purcellin (octanoate de cétostéaryle), l'isononanoate d'isononyle, le benzoate d'alcool en C12 à C 5, le myristate d'isopropyle, le palmitate d'éthyl 2-hexyle, l'isostéarate d'isostéarate, des octanoates, décanoates ou ricinoléates d'alcools ou de polyalcools ; les esters hydroxylés comme le lactate d'isostéaryle, le malate de di-isostéaryle ; et les esters du pentaérythritol ; - les éthers de synthèse ayant de 10 à 40 atomes de carbone ;the synthetic oils or synthetic esters of formula R 5 COOR 6 in which R 5 represents the residue of a linear or branched fatty acid comprising from 1 to 40 carbon atoms and R 6 represents a hydrocarbon chain, in particular branched, containing from 1 at 40 carbon atoms provided that R 5 + R 6 is> 10, such as, for example, purcellin oil (cetostearyl octanoate), isononyl isononanoate, C 12 -C 5 alcohol benzoate, isopropyl myristate, 2-hexyl ethyl palmitate, isostearate isostearate, octanoates, decanoates or ricinoleates of alcohols or polyalcohols; hydroxylated esters such as isostearyl lactate, diisostearyl malate; and pentaerythritol esters; synthetic ethers having from 10 to 40 carbon atoms; - les alcools gras en C8 à C26 comme l'alcool oléique ;- C 8 to C 26 fatty alcohols such as oleic alcohol; - leurs mélanges.- their mixtures. 24. Composition selon l'une des revendications précédentes, caractérisée en ce que la composition contient au moins une huile non volatile choisie en particulier parmi les huiles hydrocarbonées d'origine minérale, végétale ou synthétique, les esters ou éthers de synthèse, les huiles de silicone et leurs mélanges.24. Composition according to one of the preceding claims, characterized in that the composition contains at least one non-volatile oil chosen in particular from hydrocarbon oils of mineral, vegetable or synthetic origin, synthetic esters or ethers, silicone and mixtures thereof. 25. Composition selon l'une des revendications précédentes, caractérisée en ce que la composition contient une phase grasse liquide qui représente de 5 à 99 % du poids total de la composition, de préférence de 20 à 75 %.25. Composition according to one of the preceding claims, characterized in that the composition contains a liquid fatty phase which represents from 5 to 99% of the total weight of the composition, preferably from 20 to 75%. 26. Composition selon la revendication précédente, caractérisée en ce que le composé lipophile liquide représente tout ou partie de la phase grasse liquide.26. Composition according to the preceding claim, characterized in that the liquid lipophilic compound represents all or part of the liquid fatty phase. 27. Composition selon l'une des revendications précédentes, caractérisée en ce que la composition contient, en outre, au moins un solvant volatil.27. Composition according to one of the preceding claims, characterized in that the composition contains, in addition, at least one volatile solvent. 28.. Composition selon la revendication précédente, caractérisée en ce que solvant volatil est choisi parmi les solvants hydrocarbonés, les solvants siliconés comportant éventuellement des groupements alkyle ou alkoxy pendants ou en bout de chaîne siliconée et les mélanges de ces solvants.28. Composition according to the preceding claim, characterized in that volatile solvent is selected from hydrocarbon solvents, silicone solvents optionally comprising pendant alkyl or alkoxy groups or at the end of the silicone chain and mixtures of these solvents. 46 46 29. Composition selon la revendication précédente, caractérisée en ce que solvant volatil est choisi parmi les huiles de silicones linéaires ou cycliques ayant une viscosité à température ambiante inférieure à 8 cSt et ayant notamment de 2 à 7 atomes de silicium, ces silicones comportant éventuellement des groupes alkyle ou alkoxy ayant de 1 à 10 atomes de carbone, les huiles volatiles hydrocarbonées ayant de 8 à 16 atomes de carbone et leurs mélanges.29. Composition according to the preceding claim, characterized in that the volatile solvent is chosen from linear or cyclic silicone oils having a viscosity at room temperature of less than 8 cSt and having in particular from 2 to 7 silicon atoms, these silicones possibly comprising alkyl or alkoxy groups having 1 to 10 carbon atoms, volatile hydrocarbon oils having 8 to 16 carbon atoms and mixtures thereof. 30. Composition selon l'une des revendications 27 à 29, caractérisée en ce que solvant volatil est choisi parmi l'isododécane, les isoparaffines en Cδ-Cι6, leurs mélanges, éventuellement associés au décaméthyl tétrasiloxane ou au cyclopentasiloxane.30. Composition according to one of claims 27 to 29, characterized in that volatile solvent is selected from isododecane, isoparaffins Cδ-Cι 6 , mixtures thereof, optionally combined with decamethyl tetrasiloxane or cyclopentasiloxane. 31. Composition selon l'une des revendications 27 à 30, caractérisée en ce que solvant volatil est utilisé en une quantité suffisante pour obtenir des propriétés de sans transfert. 31. Composition according to one of claims 27 to 30, characterized in that volatile solvent is used in an amount sufficient to obtain non-transfer properties. 32. Composition selon la revendication précédente, caractérisée en ce que la matière colorante est choisie parmi les colorants lipophiles, les colorants hydrophiles, . les pigments, les nacres et leurs mélanges.32. Composition according to the preceding claim, characterized in that the dyestuff is chosen from lipophilic dyes, hydrophilic dyes. pigments, nacres and their mixtures. 33. Composition selon la revendication 31 ou 32, caractérisée en ce que la matière colorante est présente à raison de 0,01 à 50 % du poids total de la composition, de préférence de 5 à 30 %.33. A composition according to claim 31 or 32, characterized in that the dyestuff is present in a proportion of 0.01 to 50% of the total weight of the composition, preferably 5 to 30%. 34. Composition selon l'une des revendications précédentes, caractérisée en ce qu'elle contient au moins un additif choisi parmi l'eau, les antioxydants, les huiles essentielles, les conservateurs, les parfums, les charges, les cires, les composés gras pâteux à température ambiante, les neutralisants, les polymères liposolubles ou dispersibles dans le milieu, les actifs cosmétiques ou dermatologiques, les dispersants, et leurs mélanges.34. Composition according to one of the preceding claims, characterized in that it contains at least one additive selected from water, antioxidants, essential oils, preservatives, perfumes, fillers, waxes, fatty compounds. pastes at room temperature, neutralizers, liposoluble or dispersible polymers in the medium, cosmetic or dermatological active agents, dispersants, and mixtures thereof. 35. Composition selon l'une des revendications précédentes, caractérisée en ce qu'elle contient au moins une charge inerte.35. Composition according to one of the preceding claims, characterized in that it contains at least one inert filler. 36. Composition selon l'une des revendications précédentes, caractérisée en ce qu'elle se présente sous forme d'un gel rigide, et notamment de stick anhydre. 36. Composition according to one of the preceding claims, characterized in that it is in the form of a rigid gel, including anhydrous stick. 37. Composition selon l'une des revendications précédentes, caractérisée en ce qu'elle se présente sous forme de mascara, d'eye-liner, de fond de teint, de rouge à lèvres, de blush, de produit déodorant ou démaquillant, de produit de maquillage du corps, de fard à paupières ou à joues, de produit anti-cerne, de shampoing, d'après shampoing, de protection solaire, de produit de soin du visage ou du corps.37. Composition according to one of the preceding claims, characterized in that it is in the form of mascara, eyeliner, foundation, lipstick, blush, deodorant or makeup remover, body make-up, eye shadow or cheek product, anti-skin product, shampoo, conditioner, sunscreen, facial or body care product. 38. Composition selon l'une des revendications précédentes, caractérisée en ce qu'elle se présente sous forme d'un fond de teint.38. Composition according to one of the preceding claims, characterized in that it is in the form of a foundation. 39. Procédé cosmétique de soin, de maquillage ou de traitement des matières kératiniques des êtres humains, comprenant l'application sur les matières kératiniques d'une composition cosmétique conforme à l'une des revendications précédentes.39. A cosmetic process for the care, make-up or treatment of keratinous substances of human beings, comprising the application to the keratin materials of a cosmetic composition according to one of the preceding claims. 40. Utilisation de l'association d'au moins un solvant vplatil, d'au moins un corps lipophile hydrocarboné et d'au moins un composé polymérique de masse moléculaire moyenne en poids inférieure à 1000, comprenant a) une partie polaire ayant au moins deux motifs de répétition carbonés comportant au moins un groupement apte à former des interactions hydrogène avec le corps lipophile hydrocarboné, ce groupement comprenant au moins un hétéroatome, et b) au moins une partie lipophile comportant une chaîne carbonée à au moins quatre atomes de carbone ou une chaîne siliconée comportant au moins deux atomes de silicium, dans une composition cosmétique ou pour la fabrication d'une composition physiologiquement acceptable, pour diminuer le transfert et/ou le dépôt de traces d'un film de ladite composition, appliqué sur les matières kératiniques, sur un support mis au contact dudit film et/ou augmenter la tenue dudit film.40. Use of the combination of at least one vplatil solvent, at least one hydrocarbon lipophilic body and at least one polymer compound having a weight average molecular weight of less than 1000, comprising a) a polar part having at least two carbon repeating units comprising at least one group capable of forming hydrogen interactions with the lipophilic hydrocarbon body, this group comprising at least one heteroatom, and b) at least one lipophilic part comprising a carbon chain containing at least four carbon atoms or a silicone chain comprising at least two silicon atoms, in a cosmetic composition or for the manufacture of a physiologically acceptable composition, for reducing the transfer and / or the deposition of traces of a film of said composition, applied to the keratin materials, on a support put in contact with said film and / or increase the holding of said film. 41. Utilisation, dans une composition cosmétique ou pour la fabrication d'une composition physiologiquement acceptable, solide, contenant un corps lipophile liquide hydrocarboné, d'au moins un composé polymérique de masse moléculaire moyenne en poids inférieure à 1000, comprenant a) une partie polaire ayant au moins deux motifs de répétition carbonés comportant au moins un groupement apte à former des interactions hydrogène avec l corps lipophile hydrocarboné, ce groupement comprenant au moins un hétéroatome, et b) au moins une partie lipophile comportant une chaîne carbonée à au moins quatre atomes de carbone ou une chaîne siliconée comportant au moins deux atomes de silicium, pour diminuer le toucher gras ou huileux de ladite composition.41. Use, in a cosmetic composition or for the manufacture of a physiologically acceptable, solid composition, containing a liquid hydrocarbon lipophilic body, of at least one polymeric compound having a weight-average molecular mass of less than 1000, comprising a) a part polar element having at least two carbon repeating units comprising at least one group capable of forming hydrogen interactions with the lipophilic hydrocarbon body, this group comprising at least one heteroatom, and b) at least one lipophilic part comprising a carbon chain containing at least four carbon atoms or a silicone chain comprising at least two silicon atoms, to reduce the greasy or oily feel of said composition. 42. Utilisation selon l'une des revendications 40 ou 41 , caractérisée en ce que la composition est anhydre.42. Use according to one of claims 40 or 41, characterized in that the composition is anhydrous. 43. Utilisation selon l'une des revendications 40 à 42, caractérisée en ce que le composé polymérique est un polyamide comportant deux parties lipophiles situées de part et d'autre du squelette polyamide.43. Use according to one of claims 40 to 42, characterized in that the polymeric compound is a polyamide having two lipophilic parts located on either side of the polyamide backbone. 44. Procédé cosmétique pour diminuer le transfert et/ou le dépôt de traces d'un film d'une composition physiologiquement acceptable, appliqué sur des matières kératiniques vers un support mis au contact dudit film et/ou pour augmenter la tenue dudit film, consistant à introduire dans la composition l'association d'au moins un solvant volatil, d'au moins un corps lipophile hydrocarboné et d'au moins un composé polymérique de masse moléculaire moyenne en poids inférieure à 1000, comprenant a) une partie polaire ayant au moins deux motifs de répétition carbonés comportant au moins un groupement apte à former des interactions hydrogène avec le corps lipophile hydrocarboné, ce groupement comprenant au moins un hétéroatome, et b) au moins une partie lipophile comportant une chaîne carbonée à au moins quatre atomes de carbone ou une chaîne siliconée comportant au moins deux atomes de silicium.44. Cosmetic process for reducing the transfer and / or the deposition of traces of a film of a physiologically acceptable composition, applied to keratin materials to a support placed in contact with said film and / or to increase the holding of said film, to introduce into the composition the combination of at least one volatile solvent, at least one hydrocarbon lipophilic body and at least one polymer compound having a weight average molecular weight of less than 1000, comprising a) a polar part having at least at least two carbon repeating units comprising at least one group capable of forming hydrogen interactions with the lipophilic hydrocarbon body, this group comprising at least one heteroatom, and b) at least one lipophilic part comprising a carbon chain containing at least four carbon atoms or a silicone chain comprising at least two silicon atoms. 48 48
PCT/FR2002/000185 2001-01-17 2002-01-17 Composition structured in rigid form by a polymeric compound Ceased WO2002056845A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0100620A FR2819398A1 (en) 2001-01-17 2001-01-17 STRUCTURED COMPOSITION IN A RIGID FORM BY A POLYMERIC COMPOUND
FR01/00620 2001-01-17

Publications (2)

Publication Number Publication Date
WO2002056845A1 WO2002056845A1 (en) 2002-07-25
WO2002056845B1 true WO2002056845B1 (en) 2003-02-13

Family

ID=8858934

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/FR2002/000185 Ceased WO2002056845A1 (en) 2001-01-17 2002-01-17 Composition structured in rigid form by a polymeric compound

Country Status (2)

Country Link
FR (1) FR2819398A1 (en)
WO (1) WO2002056845A1 (en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2796271B1 (en) 1999-07-15 2002-01-11 Oreal COMPOSITION WITHOUT WAX STRUCTURED IN A RIGID FORM BY A POLYMER
FR2796272B1 (en) 1999-07-15 2003-09-19 Oreal COMPOSITION WITHOUT WAX STRUCTURED IN A RIGID FORM BY A POLYMER
FR2817739B1 (en) 2000-12-12 2005-01-07 Oreal TRANSPARENT OR TRANSLUCENT COLORED COSMETIC COMPOSITION
AU2001225389A1 (en) 2000-12-12 2002-06-24 L'oreal S.A. Composition comprising at least one heteropolymer and at least one inert filler and methods for use
AU2002256544A1 (en) 2000-12-12 2002-06-24 L'oreal Sa Cosmetic compositions containing at least one heteropolymer and at least one gelling agent and methods of using the same
AU2002217252A1 (en) 2000-12-12 2002-06-24 L Oreal Cosmetic composition comprising a mixture of polymers
WO2002047626A1 (en) 2000-12-12 2002-06-20 L'oreal Sa Cosmetic composition comprising heteropolymers and a solid substance and method of using same
US6835399B2 (en) 2000-12-12 2004-12-28 L'ORéAL S.A. Cosmetic composition comprising a polymer blend
US7276547B2 (en) 2000-12-12 2007-10-02 L'oreal S.A. Compositions comprising heteropolymers and at least one oil-soluble polymers chosen from alkyl celluloses and alkylated guar gums
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
WO2002047628A1 (en) * 2000-12-13 2002-06-20 L'oréal Composition structured with a polymer containing a heteroatom and an organogelator
US7025953B2 (en) 2001-01-17 2006-04-11 L'oreal S.A. Nail polish composition comprising a polymer
FR2819399B1 (en) 2001-01-17 2003-02-21 Oreal COSMETIC COMPOSITION CONTAINING POLYMER AND FLUORINATED OIL
US6716420B2 (en) 2001-10-05 2004-04-06 L′Oreal Methods of use and of making a mascara comprising at least one coloring agent and at least one heteropolymer
US20050008598A1 (en) 2003-07-11 2005-01-13 Shaoxiang Lu Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent
US7008629B2 (en) 2002-07-22 2006-03-07 L'ORéAL S.A. Compositions comprising at least one heteropolymer and fibers, and methods of using the same
FR2858214B1 (en) * 2003-08-01 2006-01-27 Oreal COSMETIC BILOUCHE PRODUCT, USES THEREOF, AND MAKE-UP KIT CONTAINING THE SAME
FR2860433B1 (en) * 2003-10-03 2005-12-30 Oreal NON-AEROSOL ANTI-TRANSFERING COMPOSITION CONTAINING A NON-MISCIBLE LIQUID ORGANIC PHASE IN WATER SOLIDIFIED OR THICKENED BY NON-CYCLIC DIAMIDE

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5010282B1 (en) * 1968-06-25 1975-04-19
US3857960A (en) * 1972-12-29 1974-12-31 Bristol Myers Co Toilet oil bar
JPH0615452B2 (en) * 1984-09-06 1994-03-02 株式会社資生堂 Makeup cosmetics
JPS6261911A (en) * 1985-09-12 1987-03-18 Noebia:Kk Makeup cosmetic
FR2674126B1 (en) * 1991-03-19 1995-03-10 Secma USE OF RED LIME ALGAE FOR THE PREPARATION OF COSMETIC COMPOSITIONS.
CA2197498C (en) * 1995-06-21 2002-12-17 Nathalie Mougin Cosmetic composition including a polymeric particle dispersion
FR2740330B1 (en) * 1995-10-27 1997-12-05 Oreal COMPOSITION CONSISTING OF A POLYMERIC SYSTEM AND USE OF THE SAID SYSTEM
US5837223A (en) * 1996-08-12 1998-11-17 Revlon Consumer Products Corporation Transfer resistant high lustre cosmetic stick compositions
GB2340838B (en) * 1998-08-21 2002-02-13 Cray Valley Ltd Resins and composites containing them
FR2785528B1 (en) * 1998-11-10 2002-08-30 Oreal COSMETIC COMPOSITION WITH CONTINUOUS LIPOPHILIC PHASE CONTAINING A NEW PIGMENT
FR2796273B1 (en) * 1999-07-15 2003-09-12 Oreal COMPOSITION WITH A LIQUID FATTY PHASE GELIFIED BY A POLYAMIDE WITH TERMINAL ESTER GROUPS

Also Published As

Publication number Publication date
WO2002056845A1 (en) 2002-07-25
FR2819398A1 (en) 2002-07-19

Similar Documents

Publication Publication Date Title
WO2002056845B1 (en) Composition structured in rigid form by a polymeric compound
EP0908175B1 (en) Stable topical composition containing a solid elastomeric organopolysiloxane and spherical particles
KR100883947B1 (en) Bis-urea type compounds, compositions comprising the same, uses and methods of cosmetic treatment
FR2944289A1 (en) VOLATILE OIL COMPOSITION
FR2968951A1 (en) COSMETIC COMPOSITION COMPRISING A CUCURBIC ACID COMPOUND AND A HYDROPHOBIC INULIN
EP1023890A1 (en) Anhydrous composition, use in cosmetics, in pharmacy or for hygiene
CA2223730A1 (en) Care composition containing an organopolysiloxane gel
EP1925292A1 (en) Cosmetic composition comprising at least one volatile carbonic acid ester
JP2005500249A (en) Nail polish with polymer
FR3035324A1 (en) EMULSION COMPRISING A GEMINE SURFACTANT HAVING TWO AMIDE FATTY GROUPS AND A TETRAHYDROJASMONIC ACID DERIVATIVE
FR2796270A1 (en) COMPOSITION WITH A LIQUID FATTY PHASE GELIFIED BY A POLYAMIDE WITH TERMINAL ESTER GROUPS
EP1938787A1 (en) Cosmetic composition including a bis-urea derivative
FR2973694A1 (en) COSMETIC COMPOSITION COMPRISING A CUCURBIC ACID COMPOUND AND A MIXTURE OF POLYMERS
EP1473017B1 (en) Solid oil-in-water emulsion suitable for use in cosmetics
FR2892303A1 (en) COSMETIC COMPOSITION TEXTURED BY A LIQUID-FILLED BIS-UREA DERIVATIVE TEXTURED BY A BIS-UREE COMPOUND
EP1938788A1 (en) Cosmetic composition including a bis-urea derivative
CA2374154C (en) Uses of derivatives of polyaminoacid as moisturizing agent, and cosmeticand pharmaceutical compositions containing them
FR2894476A1 (en) COSMETIC COMPOSITION TEXTURED BY A SPECIFIC SYMMETRIC BIS-UREA DERIVATIVE
FR2911496A1 (en) Solid water-in-oil emulsion useful as a cosmetic care or make-up product comprises salicylic acid or a 5-acylsalicylic acid
WO1998038979A1 (en) Homogeneous oil composition with silicon rubber base
EP1699873B1 (en) Cosmetic application of rod-coil polymers
FR2871054A1 (en) COSMETIC COMPOSITION COMPRISING A SEMI-CRYSTALLINE POLYMER AND A DIMERE DIOL ESTER
WO2011030036A1 (en) Composition comprising a polymer based on specific polyols, and cosmetic treatment method
FR2779440A1 (en) ANHYDROUS FLUID GEL BASED ON CROSS-LINKED ORGANOPOLYSILOXANE
FR2835529A1 (en) HYDROCARBON SKELETON COPOLYMERS AND COSMETIC OR DERMATOLOGICAL COMPOSITIONS COMPRISING THE SAME

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
AK Designated states

Kind code of ref document: B1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: B1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

B Later publication of amended claims
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase in:

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP