WO2002047606A2 - Compositions cosmetiques transparentes ou translucides colorees par des pigments - Google Patents
Compositions cosmetiques transparentes ou translucides colorees par des pigments Download PDFInfo
- Publication number
- WO2002047606A2 WO2002047606A2 PCT/FR2001/003941 FR0103941W WO0247606A2 WO 2002047606 A2 WO2002047606 A2 WO 2002047606A2 FR 0103941 W FR0103941 W FR 0103941W WO 0247606 A2 WO0247606 A2 WO 0247606A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- transparent
- translucent
- colored
- cosmetic composition
- composition according
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/26—Optical properties
- A61K2800/262—Transparent; Translucent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
Definitions
- the present invention relates to transparent or translucent cosmetic compositions colored with pigments.
- the coloring of transparent or translucent cosmetic compositions is usually obtained by dyes soluble in the cosmetic support which have the advantage of not diffusing light and thus preserving the transparency properties of the compositions containing them.
- US Patent 3,148,125 describes transparent lipsticks colored with dyes.
- the Applicant has surprisingly discovered that it is possible to obtain translucent or transparent colored cosmetic compositions by incorporating into transparent or translucent cosmetic supports a very small fraction of pigments having dimensions greater than those of the nanopigments used in the art.
- the present invention therefore relates to transparent or translucent colored cosmetic compositions having a turbidity of less than 800 NTU and containing, in a transparent or translucent cosmetic base, an amount of less than 0.03% by weight, based on the final cosmetic composition , at least one colored pigment, insoluble in the cosmetic base, having an average particle size greater than 100 nm.
- the colored pigments which can be used according to the present invention for coloring transparent or translucent compositions are chosen from the very wide variety of inorganic, organic or composite colored pigments usually used in the cosmetic field.
- mineral pigments examples include iron oxides, chromium oxide, chromium hydrate, ultramarines (aluminosilicate polysulphides), cobalt blue, Prussian blue (ferric ferrocyanide) , manganese violet, manganese pyrophosphate and certain metallic powders such as silver or aluminum powders.
- the organic pigments are chosen, for example, from carbon black, thioindigo or flaming red.
- the composite pigments which can be used according to the present invention include in particular lacquers, that is to say salts of certain metals (calcium, barium, aluminum, strontium, zirconium and their mixtures) of acid organic dyes, immobilized on an organic support such as rosin, or on a mineral support such as alumina, barium sulphate, calcium carbonate, talc, clay, zinc oxide, dioxide of titanium and combinations thereof.
- lacquers that is to say salts of certain metals (calcium, barium, aluminum, strontium, zirconium and their mixtures) of acid organic dyes, immobilized on an organic support such as rosin, or on a mineral support such as alumina, barium sulphate, calcium carbonate, talc, clay, zinc oxide, dioxide of titanium and combinations thereof.
- lakes examples include the calcium salt of lithol red B on rosin and barium sulfate (D&C Red n ° 7 calcium lake), the aluminum salt of tartrazine on alumina (FD&C Yellow n ° 5 aluminum lake), the aluminum salt of eosin on alumina and titanium dioxide (D&C Red n ° 21 aluminum lake), the aluminum salt of phloxine B on alumina (D&C Red n ° 27 aluminum lake), the bright yellow aluminum salt FCF on alumina (FD&C Yellow n ° 6 aluminum lake) and the bright blue aluminum salt on alumina (FD&C Blue n ° 1 aluminum lake).
- D&C Red n ° 7 calcium lake examples include the calcium salt of lithol red B on rosin and barium sulfate (D&C Red n ° 7 calcium lake), the aluminum salt of tartrazine on alumina (FD&C Yellow n ° 5 aluminum lake), the aluminum salt of eosin on alumina and titanium dioxide (D&
- the colored pigments described above can be coated with different materials chosen, for example, from silicones, amino acids or fluorinated compounds. Such a coating may be useful, or even necessary, to improve the compatibility of the pigments with certain cosmetic bases and to stabilize the dispersions obtained over time.
- the transparent or translucent cosmetic compositions of the present invention is linked to the particle size of the colored pigment (s) used.
- the average particle size of the pigments used according to the present invention is greater than 100 nm and preferably greater than 200 nm.
- the colored pigments used therefore do not present the problems of instability of the dispersed state of the cosmetic compositions of the prior art containing nanopigments having a size less than 100 nm.
- the pigments thus dispersed do not require as thorough grinding, therefore as long and costly, as pigments of size less than 100 nm.
- the transparent or translucent dispersions colored by the pigments indicated above having an average size greater than 100 nm have satisfactory long-term stability and require only small amounts of dispersing agent, or even no dispersing agent at all.
- the quantity of pigments used in the transparent or translucent colored cosmetic compositions of the present invention depends on certain parameters such as the nature, the average size and the coloring power of the pigment particles, the shade, the transparency and the intensity of color desired. or the chemical nature of the cosmetic base used. It is most often a question of finding the best compromise between minimum turbidity and maximum color intensity.
- the concentration of the colored pigment (s) in the transparent or translucent cosmetic compositions of the present invention is less than 0.03% by weight and preferably less than 0.01% by weight, relative to the cosmetic composition final.
- the transparent or translucent cosmetic compositions contain at most 0.001% by weight of colored pigment.
- compositions according to the present invention means compositions having a turbidity, measured according to the method described below, of less than 800 NTU (Nephelometric Turbidity
- the turbidity is measured using a model 2100 P turbidimeter from the company HACH at room temperature (20 to 25 ° C).
- the tubes used for the measurement are referenced AR 397 A cat 24347-06.
- the device is calibrated by suspensions of formazine of different concentrations.
- any known cosmetic base can be used as transparent or translucent base for the preparation of the transparent or colored translucent cosmetic compositions of the present invention, provided that it satisfies the transparency requirements indicated above. It goes without saying that the cosmetic base used, free of colored pigments, must have sufficient transparency or translucency so that the value of the turbidity of the final composition colored by pigments does not exceed the limit values indicated above.
- the transparent or translucent cosmetic base can be a hydrophilic or lipophilic phase, of liquid, thickened, gelled, pasty or solid consistency. It may for example be a water-in-oil emulsion, an oil-in-water emulsion, a solid, hydrophilic or lipophilic gel, a flexible gel, an oily lotion.
- the base of the composition is in the form of a more or less rigid, aqueous or oily gel. More specifically, this gel is a rigid gel, presented in a dish or in a stick, preferably in a stick and in anhydrous form.
- the lipophilic base can be an oily phase liquid at room temperature such as those conventionally used in cosmetics.
- This fatty phase can contain polar oils and / or non-polar oils.
- the polar oils of the invention are: - hydrocarbon vegetable oils with a high triglyceride content consisting of fatty acid and glycerol esters, the fatty acids of which can have varying chain lengths from C 4 to C 24 , the latter may be 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, seed grape or blackcurrant, evening primrose, millet, barley, quinoa, olive, rye, safflower,nadooulier, passionflower, or 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 Dynamit Nobel;
- R a COOR b synthetic oils or synthetic esters of formula R a COOR b in which R a represents the remainder of a linear or branched fatty acid containing from 1 to 40 carbon atoms and R represents a hydrocarbon chain, in particular branched, containing 1 to 40 carbon atoms provided that R a + R is ⁇ 10, such as Purcellin oil
- 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 or alkoxy groups, lateral and / or at the chain end, groups each having from 2 to 24 carbon atoms; phenylated silicones such as phenyltrimethicones, phenyldimethicones, phenyltrimethylsiloxydiphenylsiloxanes, diphenyldimethicones, diphenylmethyldiphenyltrisiloxanes, 2-phenylethyltrimethylsiloxy silicates; linear or branched hydrocarbons of synthetic or mineral origin, volatile or not, such as volatile paraffin oils (isoparaffins like isododecane) or non-volatile, and their derivatives, petrolatum, liquid lanolin, polydecenes, polyisobistene hydrogenated such as Parleam oil
- the 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 alkanes such as Parleam oil, isoparaffins such as isododecane, 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 99.95%, preferably from 10 to 80%, and better still from 20 to 75% of the total weight of the composition.
- gelling polyamides in particular of molecular mass less than 100,000 and preferably less than 50,000, for example of molecular mass ranging from 2000 to 20,000, optionally comprising alkyl groups at the side or at the end of the chain, having from 8 with 120 carbon atoms and preferably from 12 to 60 carbon atoms,
- hydrophobic galactomannans comprising in particular from 1 to 6, and preferably from 2 to 4 OH groups, by dare unit, substituted by a C ⁇ alkyl group. 6 , preferably in C ⁇ . ,
- the gelling polyamides are, for example, the polyamide resins resulting from the condensation of an aliphatic dicarboxylic acid and a diamine, including compounds having more than 2 carboxyl groups and more than 2 amine groups, the carboxyl and amine groups of adjacent unit units being condensed by an amide bond.
- These polyamide resins include those marketed under the Versamid ® trademark by 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 weight average molecular weight ranging from 6000 to 9000. For more information on these polyamides, reference can be made to documents US-A-3645705 and US-A-3148125. More specifically, Versamid ® 930 or 744 are used.
- the polyamides can also be those resulting from a polycondensation between a dicarboxylic acid comprising at least 32 carbon atoms (in particular from 32 to 44 carbon atoms) and a diamine having at least 2 carbon atoms (in particular from 2 to 36 atoms of carbon).
- the diacid is preferably a fatty acid dimer having at least 16 carbon atoms such as oleic, linoleic or linolenic acid.
- the diamine is preferably ethylenediamine, hexylenediamine or hexamethylenediamine.
- the polymers contain one or two terminal carboxylic acid groups, it is advantageous to esterify them with a monoalcohol having at least 4 carbon atoms, preferably from 10 to 36 carbon atoms, better still from 12 to 24 and even better still 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 and amide groups; each of the symbols independently denotes an alkyl or alkenyl group having at least 4 carbon atoms and in particular from 4 to 24 carbon atoms; each of the symbols R 2 independently represents a C 4 to C 42 hydrocarbon group, provided that 50% of the R 2 groups represent a C 30 to C 42 hydrocarbon group; each of the symbols R 3 independently represents an organic group provided with at least 2 carbon atoms, hydrogen atoms and optionally one or more oxygen or nitrogen atoms; and each R represents mdépendamment a hydrogen atom, an alkyl group Ci-C ⁇ 0 or a direct bond to R 3 or to another so that the nitrogen atom to which are linked to both R 3 and R 4 is part of a heterocyclic structure defined by R 4 - NR 3 , with at least 50% of R 4 representing a hydrogen atom.
- 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 side 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 and preferably greater than 2.
- Ri is a C 2 to C 22 alkyl group and more preferably C 16 to C 22 -
- R 2 may be a C ⁇ 0 to C 42 hydrocarbon (alkylene) group.
- at least 50% and more preferably at least 75% of the symbols R 2 are groups having 30 to 42 carbon atoms.
- the other symbols R 2 are hydrogenated groups in C to C ⁇ 9 and even in C 4 to C ⁇ 2 .
- R 3 represents a C 2 to C 36 hydrocarbon group or a polyoxyalkylenated group and R 4 represents a hydrogen atom. More preferably, R 3 represents a hydrocarbon group, C 2 C ⁇ 2.
- the hydrocarbon groups can be linear, cyclic or branched, saturated or unsaturated groups.
- the alkyl and alkylene groups may be linear or branched groups, saturated or not.
- the structuring of the liquid fatty phase is preferably 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 corresponding to a compound of formula (I) where n is 0, that is to say a diester.
- polymers exhibit, due to their fatty chain (s), good solubility in oils and therefore lead to macroscopically homogeneous compositions even with a high level (at least 25%) of polymer, unlike polymers free from fatty chains.
- polyamides modified by side fatty chains and / or terminal fatty chains having from 8 to 120 carbon atoms and in particular from 12 to 68 carbon atoms , the fatty, terminal chains being linked to the polyamide skeleton by ester groups.
- these polymers comprise a fatty chain at each end of the polymer backbone and in particular of the polyamide backbone.
- structuring polyamides of formula (I) used in the composition according to the invention include the commercial products sold by the company Arizona Chemical under the names Uniclear® ® 80 and Uniclear® ® 100. They are sold respectively under 80% gel form (active ingredient) in mineral oil and 100% gel (active ingredient) active). They have a softening point of 88 to 94 ° C. These commercial products are a mixture of copolymers of a C 36 diacid condensed on ethylenediamine, of average molecular weight by weight of approximately 600 or 4000 respectively. The terminal ester groups result from the esterification of the remaining acid terminations by cetyl or stearyl alcohol or their mixtures (also called cetylstearyl alcohol).
- the galactomannans are in particular ethyl guar derivatives having in particular a degree of substitution of 2 to 3, such as those marketed by the company AQUALON under the names N-Hance-
- the fumed silica preferably has a particle size which can be nanometric to micrometric, for example ranging from approximately 5 to 200 nm.
- Pyrogenic silicas can be obtained by high-temperature hydrolysis of a volatile silicon compound in an oxyhydrogen flame, producing a finely divided silica. This process makes it possible in particular to obtain hydrophilic silicas which have a large number of silanol groups on their surface.
- Such hydrophilic silicas are, for example, marketed under the names AEROSIL 130 ® , "AEROSIL 200 ® , AEROSIL 255 ® , AEROSIL 300 ® , AEROSIL 380 ® by the company Degussa, or under the names CAB-O-SIL HS-5 ® , "CAB-O-SIL EH-5 ® , CAB-O-SIL LM-130 ® , CAB-O-SIL MS-55 ® , and CAB-O-SIL M-5 ® by Cabot.
- hydrophobic groups can be:
- Trimethylsiloxy groups which are obtained in particular by treatment of fumed silica in the presence of hexamethyldisilazane. of the silicas thus treated are called "Silica silylate” according to the CTFA (6 th edition, 1995). They are for example marketed under the name AEROSIL R812 ® by the company Degussa, and under the name CAB-O-SIL TS-530 ® by the company Cabot. - Dimethylsilyloxy or polydimethylsiloxane groups, which are obtained in particular by treatment of fumed silica in the presence of polydimethylsiloxane or dimethyldichlorosilane.
- Silicas thus treated are called "Silica dimethyl Silylate” according to the CTFA (6th edition, 1995). They are for example marketed under the names AEROSIL R972 ® and AEROSIL R974 ® by the company Degussa, and under the names
- any gelling agent of the aqueous phase of the cellulose derivative type such as hydroxyethylcellulose and carboxymethylcellulose or acrylic derivative, such as copolymers of acrylic acid and of C 1 0 alkyl acrylates, can be used.
- the aqueous gel can be a gel based on water or based on a hydroalcoholic mixture.
- the gelling agent represents from 0.05 to 90% by weight, preferably from 2 to 60% by weight and in particular from 5 to 40% by weight, of the total weight of the colored cosmetic composition.
- the cosmetic base is therefore an anhydrous lipophilic base.
- the transparent or translucent colored cosmetic compositions according to the present invention may contain, in addition to the colored pigments described above, one or more white pigments such as titanium dioxide, zirconium dioxide, cerium dioxide or oxide of zinc.
- the transparent or translucent colored cosmetic compositions according to the present invention may also contain additives commonly used in the cosmetic field, such as, for example, dispersing agents, perfumes, sunscreens, preservatives, antioxidants or principles. cosmetic active agents, provided of course that the addition of these optional constituents does not alter the transparency or translucency properties inherent in the cosmetic compositions of the present invention.
- a colored transparent lip balm is prepared from the following ingredients:
- a dispersion of the pigments in Parléam oil is prepared in the presence of the dispersing agent. This dispersion is incorporated into the other ingredients (Uniclear ® 100 and octyldodecanol) heated to 100 ° C keeping the mixture under gentle stirring for 30 minutes. After pouring into molds and cooling to room temperature, a solid pinkish beige composition is obtained having a turbidity of 87.3 NTU.
- a transparent anhydrous scent gel colored for the body is prepared by mixing the following ingredients:
- the gel obtained is blue in color and has a turbidity of
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01270299A EP1359896A2 (fr) | 2000-12-12 | 2001-12-11 | Compositions cosmetiques transparentes ou translucides colorees par des pigments |
US10/203,382 US6761881B2 (en) | 2000-12-12 | 2001-12-11 | Transparent or translucent cosmetic compositions colored by pigments |
JP2002549182A JP2004515509A (ja) | 2000-12-12 | 2001-12-11 | 顔料で着色した透明又は半透明な化粧組成物 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0016176A FR2817742B1 (fr) | 2000-12-12 | 2000-12-12 | Compositions cosmetiques transparentes ou translucides colorees par des pigments |
FR00/16176 | 2000-12-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2002047606A2 true WO2002047606A2 (fr) | 2002-06-20 |
WO2002047606A3 WO2002047606A3 (fr) | 2002-08-01 |
Family
ID=8857562
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2001/003941 WO2002047606A2 (fr) | 2000-12-12 | 2001-12-11 | Compositions cosmetiques transparentes ou translucides colorees par des pigments |
Country Status (5)
Country | Link |
---|---|
US (1) | US6761881B2 (fr) |
EP (1) | EP1359896A2 (fr) |
JP (1) | JP2004515509A (fr) |
FR (1) | FR2817742B1 (fr) |
WO (1) | WO2002047606A2 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7749524B2 (en) | 2003-07-11 | 2010-07-06 | L'oreal S.A. | Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent |
EP2706108A1 (fr) * | 2011-05-04 | 2014-03-12 | Shiseido Company, Ltd. | Composition de fragrance semi-transparente |
US9238786B2 (en) | 2011-05-04 | 2016-01-19 | Shiseido Company, Ltd. | Translucent fragrance composition |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2810562B1 (fr) * | 2000-06-23 | 2003-04-18 | Oreal | Emulsion solide a phase grasse liquide structuree par un polymere |
US20030082126A9 (en) * | 2000-12-12 | 2003-05-01 | Pinzon Carlos O. | Cosmetic compositions containing heteropolymers and oil-soluble cationic surfactants and methods of using same |
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 |
US20020168335A1 (en) * | 2000-12-12 | 2002-11-14 | Nathalie Collin | Cosmetic composition comprising a wax and a polymer |
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 |
FR2817739B1 (fr) * | 2000-12-12 | 2005-01-07 | Oreal | Composition cosmetique coloree transparente ou translucide |
US20060018854A1 (en) * | 2002-10-02 | 2006-01-26 | Christophe Dumousseaux | Cosmetic compositions |
US8007772B2 (en) * | 2002-10-02 | 2011-08-30 | L'oreal S.A. | Compositions to be applied to the skin and the integuments |
US20050074473A1 (en) * | 2003-10-07 | 2005-04-07 | Cabot Corporation | Soft-focus cosmetic composition comprising fumed alumina |
US7981404B2 (en) * | 2004-04-08 | 2011-07-19 | L'oreal S.A. | Composition for application to the skin, to the lips, to the nails, and/or to hair |
US20050257715A1 (en) * | 2004-04-08 | 2005-11-24 | Christophe Dumousseaux | Compositions for application to the skin, to the lips, to the nails, and/or to hair |
US20050238979A1 (en) * | 2004-04-08 | 2005-10-27 | Christophe Dumousseaux | Compositions for application to the skin, to the lips, to the nails, and/or to hair |
WO2006028931A2 (fr) * | 2004-09-03 | 2006-03-16 | Interpolymer Corporation | Systeme polymere olefinique greffe a base d'eau pour applications cosmetiques polyvalentes |
FR2876011B1 (fr) * | 2004-10-05 | 2006-12-29 | Oreal | Procede de maquillage d'un support et kit pour la mise en oeuvre de ce procede |
WO2006037901A1 (fr) * | 2004-10-05 | 2006-04-13 | L'oreal | Kit et procede de maquillage |
US9649261B2 (en) | 2004-10-05 | 2017-05-16 | L'oreal | Method of applying makeup to a surface and a kit for implementing such a method |
FR2888115B1 (fr) * | 2005-07-08 | 2013-02-15 | Oreal | Fond de teint liquide, procede de maquillage et kit pour la mise en oeuvre d'un tel procede. |
FR2889921B1 (fr) | 2005-08-30 | 2007-12-28 | Oreal | Ensemble de conditionnement et d'application comportant un dispositif magnetique. |
JP6390756B2 (ja) * | 2017-02-24 | 2018-09-19 | 堺化学工業株式会社 | 硫酸バリウム球状複合粉末及びその製造方法 |
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DE19707309A1 (de) * | 1997-02-11 | 1998-08-13 | Lancaster Group Gmbh | Feste kosmetische Zusammensetzung auf Basis verfestigter Öle |
EP0879592A2 (fr) * | 1997-04-17 | 1998-11-25 | Henkel Kommanditgesellschaft auf Aktien | Compositions de protection solaire |
FR2804014A1 (fr) * | 2000-01-21 | 2001-07-27 | Oreal | Nanoemulsion a base de lipides amphiphiles et de polymeres cationiques et utilisations |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3148125A (en) * | 1961-03-22 | 1964-09-08 | Yardley Of London Inc | Clear lipstick |
-
2000
- 2000-12-12 FR FR0016176A patent/FR2817742B1/fr not_active Expired - Fee Related
-
2001
- 2001-12-11 US US10/203,382 patent/US6761881B2/en not_active Expired - Fee Related
- 2001-12-11 JP JP2002549182A patent/JP2004515509A/ja active Pending
- 2001-12-11 EP EP01270299A patent/EP1359896A2/fr not_active Withdrawn
- 2001-12-11 WO PCT/FR2001/003941 patent/WO2002047606A2/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19707309A1 (de) * | 1997-02-11 | 1998-08-13 | Lancaster Group Gmbh | Feste kosmetische Zusammensetzung auf Basis verfestigter Öle |
EP0879592A2 (fr) * | 1997-04-17 | 1998-11-25 | Henkel Kommanditgesellschaft auf Aktien | Compositions de protection solaire |
FR2804014A1 (fr) * | 2000-01-21 | 2001-07-27 | Oreal | Nanoemulsion a base de lipides amphiphiles et de polymeres cationiques et utilisations |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7749524B2 (en) | 2003-07-11 | 2010-07-06 | L'oreal S.A. | Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent |
EP2706108A1 (fr) * | 2011-05-04 | 2014-03-12 | Shiseido Company, Ltd. | Composition de fragrance semi-transparente |
EP2706108A4 (fr) * | 2011-05-04 | 2015-03-25 | Shiseido Co Ltd | Composition de fragrance semi-transparente |
US9238786B2 (en) | 2011-05-04 | 2016-01-19 | Shiseido Company, Ltd. | Translucent fragrance composition |
Also Published As
Publication number | Publication date |
---|---|
WO2002047606A3 (fr) | 2002-08-01 |
FR2817742A1 (fr) | 2002-06-14 |
JP2004515509A (ja) | 2004-05-27 |
FR2817742B1 (fr) | 2004-12-24 |
US20030012752A1 (en) | 2003-01-16 |
US6761881B2 (en) | 2004-07-13 |
EP1359896A2 (fr) | 2003-11-12 |
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