EP3897547A1 - Method for dyeing or making up eyebrows - Google Patents
Method for dyeing or making up eyebrowsInfo
- Publication number
- EP3897547A1 EP3897547A1 EP19829120.5A EP19829120A EP3897547A1 EP 3897547 A1 EP3897547 A1 EP 3897547A1 EP 19829120 A EP19829120 A EP 19829120A EP 3897547 A1 EP3897547 A1 EP 3897547A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- extract
- eyebrows
- coloring
- keratin fibers
- 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.)
- Pending
Links
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- 238000000034 method Methods 0.000 title claims abstract description 33
- 238000004043 dyeing Methods 0.000 title abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 303
- 102000011782 Keratins Human genes 0.000 claims abstract description 70
- 108010076876 Keratins Proteins 0.000 claims abstract description 70
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- 229930182559 Natural dye Natural products 0.000 claims abstract description 28
- 239000002537 cosmetic Substances 0.000 claims abstract description 28
- 239000000978 natural dye Substances 0.000 claims abstract description 28
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- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical class [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 claims abstract description 6
- 239000005569 Iron sulphate Substances 0.000 claims abstract description 6
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims abstract description 6
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- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229950009195 phenylpropanol Drugs 0.000 description 1
- GVKCHTBDSMQENH-UHFFFAOYSA-L phloxine B Chemical compound [Na+].[Na+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 GVKCHTBDSMQENH-UHFFFAOYSA-L 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 235000010204 pine bark Nutrition 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 239000001120 potassium sulphate Substances 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical compound CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- NGSRGPMIUOKCKY-UHFFFAOYSA-M sodium;2,2-bis(prop-2-enoxy)acetate Chemical compound [Na+].C=CCOC(C(=O)[O-])OCC=C NGSRGPMIUOKCKY-UHFFFAOYSA-M 0.000 description 1
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 description 1
- JJMIAJGBZGZNHA-UHFFFAOYSA-N sodium;styrene Chemical compound [Na].C=CC1=CC=CC=C1 JJMIAJGBZGZNHA-UHFFFAOYSA-N 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 229940074067 terminalia chebula fruit extract Drugs 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- DWKARHJHPSUOBW-UHFFFAOYSA-N trimethyl-[3-[(2e)-2-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)hydrazinyl]phenyl]azanium;chloride Chemical compound [Cl-].CC1=NN(C=2C=CC=CC=2)C(O)=C1N=NC1=CC=CC([N+](C)(C)C)=C1 DWKARHJHPSUOBW-UHFFFAOYSA-N 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
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- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
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- 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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/23—Sulfur; Selenium; Tellurium; Compounds thereof
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
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- A—HUMAN NECESSITIES
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- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
- A61K8/602—Glycosides, e.g. rutin
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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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
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- 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
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
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- 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
- A61K2800/432—Direct dyes
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- 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
- A61K2800/432—Direct dyes
- A61K2800/4322—Direct dyes in preparations for temporarily coloring the hair further containing an oxidizing agent
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- 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
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/88—Two- or multipart kits
- A61K2800/884—Sequential application
Definitions
- the present invention relates to the field of coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows.
- compositions for coloring or making up keratin materials comprising natural dyes, in particular plant extracts comprising polyphenols.
- Dyeing processes using natural products which are more respectful of the nature of the fibers and the environment, are in fact increasingly appreciated by users.
- the coloring or makeup result in particular when it comes to keratin fibers, is not always satisfactory in terms of intensity and / or homogeneity and / or resistance over time.
- compositions and methods for coloring or making up keratin fibers in particular the eyelashes and / or the eyebrows and preferably the eyebrows, comprising natural dyes based on polyphenols, with improved chromatic properties ( intensity and homogeneity of the color) and which are resistant to washing, perspiration and / or sebum.
- compositions for coloring or making up keratin fibers in particular the eyebrows by using specific plant extracts and iron salts and / or aluminum salts , especially iron gluconate.
- specific penetration boosters improves the intensity and color fastness over time.
- compositions in the form of gels comprising iron gluconate have also demonstrated, for coloring or make-up compositions in the form of gels comprising iron gluconate, that the use of a particular acrylate copolymer was advantageous for the stability and the texture of the compositions.
- a first subject of the invention is therefore a cosmetic process for coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, comprising the application to said keratin fibers, of at least: a) A cosmetic composition A dye comprising, in a physiologically acceptable medium, one or more natural dye (s) chosen from the group consisting of neoflavonoids, gallic tannins and catechic tannins, proanthocyanidins and their derivatives , and mixtures thereof, or preferably one or more plant extracts containing them, and advantageously an antioxidant agent, b) A revealing cosmetic composition B comprising, in a physiologically acceptable medium, at least one iron salt and / or one salt aluminum, in particular an iron gluconate or an iron sulphate, composition A being applied before or after composition B, preferably before composition B.
- a cosmetic composition A dye comprising, in a physiologically acceptable medium, one or more natural dye (s) chosen from the group consisting of neof
- composition A further comprises an agent promoting and / or increasing the penetration of the natural dye into keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, chosen from bicyclic ethers , fatty acid esters comprising polyethoxylated C6 to C18 hydrocarbon chains, and their mixtures, preferably bicyclic ethers, each cycle of the bicycle comprising a number n of links between 3 and 10, the fatty acid esters comprising a C6 to C18 hydrocarbon chain, saturated or unsaturated, linear or branched using other C6 to C18 hydrocarbon chains, each of the hydrocarbon chains being polyethoxylated, with a degree of ethoxylation of at least 2, in particular of 2 to 12, and mixtures thereof, more preferably dimethyl isosorbide.
- PEG-7 glyceryl cocoate, and their mixture.
- the invention also relates to a kit or device for coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, with several separate compartments and comprising:
- the coloring composition A as defined in the invention in another separate compartment the revealing composition B as defined in the invention and characterized in that it does not include the iron salt and / or aluminum, and
- the iron and / or aluminum salt intended to be mixed extemporaneously with the revealing composition B before application to the keratin fibers,
- the kit or device for coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, with several separate compartments comprises:
- the revealing composition B as defined in the invention and characterized in that it comprises the iron and / or aluminum salt,
- kits according to the invention may also optionally comprise, in another separate compartment, a composition C comprising an oxidizing agent for pretreatment of the keratin fibers before treatment with compositions A and B.
- an agent oxidant such as hydrogen peroxide produces a slight alteration of the cuticles or scales, outer part of the keratin fibers, allowing them to open and therefore better penetration of the active ingredients.
- the use of a pre-treatment with an oxidizing agent makes it possible to promote better penetration of the coloring agents.
- the present invention therefore relates to a cosmetic process for coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, comprising the application to said keratin fibers, of at least:
- a cosmetic composition A dye comprising, in a physiologically acceptable medium, one or more natural dye (s) chosen from the group consisting of neoflavonoids, gallic tannins and catechic tannins, proanthocyanidins and their derivatives , and mixtures thereof, or preferably one or more plant extracts containing them, and advantageously an antioxidant agent
- a revealing cosmetic composition B comprising, in a physiologically acceptable medium, at least one iron salt and / or one salt aluminum, in particular an iron gluconate or an iron sulphate, composition A being applied before or after composition B, preferably before composition B.
- the compositions A and B do not contain an oxidizing agent and the keratin fibers are not treated, before or after treatment with the compositions A and B, with an oxidizing agent.
- the keratin fibers in particular the eyelashes and / or the eyebrows and preferably the eyebrows, are pretreated with an oxidizing agent, before the application of said compositions A and B.
- this oxidizing pretreatment makes it possible to open the scales of the keratin fibers and thus make it possible to promote the penetration of the coloring agents.
- the oxidizing agent can be chosen from the group formed by hydrogen peroxide, urea peroxide, bromates or ferricyanides of alkali metals, peroxygenated salts such as for example persulfates, perborates, peracids and their precursors and alkali or alkaline earth metal percarbonates.
- hydrogen peroxide is used.
- a pretreatment composition C comprising hydrogen peroxide as an oxidizing agent is applied to the keratin fibers, in particular the eyelashes and / or the eyebrows, before the application of the coloring compositions A and revealing B.
- a pre-treatment with an oxidizing agent makes it possible to improve the intensity and the color fastness over time.
- the oxidizing agent may be present in the pretreatment composition C in a content ranging from 1 to 15% by weight, preferably from 1 to 12% by weight relative to the total weight of said composition.
- the composition comprises from 1 to 12% by weight of hydrogen peroxide or, by volume, from 3 volumes to 40 volumes of the total composition.
- the cosmetic composition A dye according to the invention comprises one or more natural dye (s) chosen from the group consisting of neoflavonoids, gallic tannins and catechic tannins, proanthocyanidins and their derivatives, and mixtures thereof, or preferably one or more plant extracts containing it.
- the natural dye or dyes suitable for the invention can be chosen from hematoxylin, hematinin, brazilein, brazilin, gallic acid, catechin, castalagin, vescalagin, procyanidins, and their mixtures.
- Plant extracts comprising polyphenols
- the plant extracts which can be used according to the invention are plant extracts comprising at least polyphenols chosen from the group consisting of neoflavonoids, gallic tannins and catechic tannins, proanthocyanidins and their derivatives, and their mixtures. These polyphenols are predominant in the composition of said plant extracts.
- the plant extracts which are suitable for the invention are chosen from plant extracts containing at least one colorant chosen from the group consisting of hematoxylin, hematein, brazilein, brazilin, gallic acid, catechin, castalagine, vescalagine, procyanidins.
- plant extracts (genus and species) can in particular be used:
- - chestnut extract (Castanea sativa) containing in particular hydrolysable tannins of the ellagitannin type such as vescalagine and castalagine and gallic tannins such as the monomers of gallic acid and derivatives;
- extracts of hibiscus and strawberry including anthocyanins, and mixtures thereof.
- the coloring composition A comprises a natural dye chosen from the group consisting of hematoxylin, hematein, brazilein, brazilin, gallic acid, catechin, castalagin, vescalagin, and / or procyanidins and their mixtures, or a plant extract containing them, in particular a plant extract chosen from the group consisting of a log extract, a red wood extract, chestnut extract, gall nut extract (Rhus semialata gall extract), Anogeissus bark extract pine extract, tea extract, vine extract, Sorghum extract , a cocoa extract, a myrobalan extract, a hibiscus extract, a strawberry extract and their mixtures, preferably a log extract, a red wood extract, a chestnut extract, and their mixtures.
- a natural dye chosen from the group consisting of hematoxylin, hematein, brazilein, brazilin, gallic acid, catechin, castalagin, vescalagin, and
- the coloring composition A comprises at least one plant extract chosen from an extract of logwood, an extract of chestnut, an extract of red wood, and their mixtures.
- the extracts are obtained by extracting various parts of plants, such as for example the root, the wood, the bark or the leaf.
- an extract from logwood, wood or chestnut bark, sorghum leaf or stem, pine bark, tea leaf, gall nut, cocoa bean, wood is used. or red wood bark and mixtures thereof.
- the coloring composition A comprises at least one extract of logwood.
- Campeche extract Hematoxylon Campechianum
- SCRD company SCRD
- Logwood extract also known under the name Hematin N0200.
- Hematin N0200 a dark brown burgundy powder comprising 20-40% hematoxylin (polyphenol neoflavonoid type) by weight of dry extract.
- It is a pure vegetable dye of non-oxidized extraction obtained from Campeche wood. The degree of oxidation comes from the natural oxidation of the Hematoxylin contained in the product without any chemical oxidation.
- Campeche extract consists mainly of the Hematoxylin dye, more or less condensed glucosides and tannins.
- the chemical structure of the two coloring principles, Hematoxylin and Hematein, allows them to be classified in the group of neoflavonoids.
- the range of colors that can be obtained with Campeche extract is one of the most extensive in vegetable dye.
- the coloring composition A comprises at least one extract of wood or chestnut bark of INCI name Castanea sativa (chestnut) bark extract.
- the bark and the chestnut wood contain in particular eight polyphenolic compounds, including ellagitannins, castaline, vescalagine, castalagine, acutissimine A, kurigaline, chestanine.
- the coloring composition A comprises at least one extract of wood or bark of Brasiletto (or red wood).
- the Redwood Haematoxylum Brasiletto or Brasilensis
- the extract of Brasiletto wood or red wood is rich in Bréziline (its oxidized form is Braziléine).
- SCRD an extract of Brasiletto sold by the company SCRD.
- the coloring composition A can also comprise a mixture of plant extracts according to the invention, depending on the desired shade. According to a particular mode, the coloring composition A comprises a mixture of logwood extract and chestnut extract.
- the natural dye (s) or the plant extract (s) containing it are present in the dye composition A of the invention in a total content ranging from 0.1 to 10%, preferably from 2 to 5% by weight relative to the weight total of the composition.
- a person skilled in the art will know how to adapt the total content of plant extracts to be used in the composition according to the desired effect and to the nature and content of natural dye (s) of said extracts.
- Antioxidant agent oxidation reducing agent
- the coloring composition A also advantageously comprises at least one antioxidant agent (otherwise called oxidation reducing agent).
- This antioxidant agent both protects the plant extract from oxidation and acts on the keratin fiber and in particular on the eyebrow to break the disulphide bridges and thus improve coloring.
- the antioxidant agent can be chosen in particular from sulfites, bisulfites, thiols and phosphines, preferably sulfites and bisulfites of alkali or alkaline earth metals. Mention may in particular be made of sodium sulfite or bisulfite.
- the coloring composition A comprises a sodium bisulfite (sodium metabisulfite) as an antioxidant agent.
- the antioxidant agent may be present in the coloring composition A in a content ranging from 0.01 to 0.5%, preferably from 0.05 to 0.1% by weight relative to the total weight of said composition Agent promoting and / or increasing the penetration of the dye (otherwise called 'penetration booster')
- composition A further comprises an agent promoting and / or increasing the penetration of the natural dye into keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows.
- This agent promoting and / or increasing the penetration of the natural dye into the keratin fiber and in particular the eyebrow, is distinct from benzyl alcohol.
- This agent promoting and / or increasing the penetration of the natural dye into the keratin fiber and in particular the eyebrow is in particular chosen from bicyclic ethers, fatty acid esters comprising C6 to C18 polyethoxylated hydrocarbon chains, and mixtures thereof.
- the agent promoting and / or increasing the penetration of the natural dye into the keratin fiber is chosen from bicyclic ethers, each cycle of the bicycle comprising a number n of links between 3 and 10, the esters d fatty acids comprising a C6 to C18 hydrocarbon chain, saturated or unsaturated, linear or branched using other C6 to C18 hydrocarbon chains, each of the hydrocarbon chains being polyethoxylated, with a degree of ethoxylation of at least 2, in particular from 2 to 12, and their mixtures.
- the bicyclic ether is dimethyl isosorbide.
- the polyethoxylated fatty acid ester is PEG-7 glyceryl cocoate.
- the coloring composition A comprises at least dimethyl isosorbide, such as that marketed under the names ARLASOLVE TM DMI or GRANSOLVE TM DMI by the company CRODA, Dottisol TM by the company Dottikon ES AG, NEX-DMI TM by the Nexgen Biotechnologies, Inc; or OriStar DMI TM by Orient Stars LLC.
- dimethyl isosorbide such as that marketed under the names ARLASOLVE TM DMI or GRANSOLVE TM DMI by the company CRODA, Dottisol TM by the company Dottikon ES AG, NEX-DMI TM by the Nexgen Biotechnologies, Inc; or OriStar DMI TM by Orient Stars LLC.
- the coloring composition A comprises at least PEG-7 glyceryl cocoate, such as that sold under the names CETIOL® HE by the company BASF, or Chemonic LI-7 Surfactant by the company Lubrizol Advanced Materials, Inc, or Tegosoft GC by Evonik Nutrition & Care GmbH or Nikkol SG-CG700 by Nikko Chemicals Co., Ltd or Glycerox HE by Croda.
- the coloring composition A can also comprise aromatic alcohols chosen in particular from benzyl alcohol, phenyl ethanol and phenyl propanol, as preservatives.
- the coloring composition A also comprises phenoxyethanol and benzyl alcohol as preservatives.
- the content of preservatives may range from 0.1 to 5%, in particular from 0.3 to 3% and preferably from 0.5 to 2% by weight relative to the total weight of said composition.
- the coloring composition A also advantageously comprises a nonionic surfactant, in particular an alkyl glucoside, preferably decyl glucoside.
- nonionic surfactant which can be used in the dye composition A of the invention, mention may in particular be made of alkylpolyglucosides.
- an alkyl glucoside will be used as a nonionic surfactant according to the invention.
- These surfactants known from the prior art can be more represented by the following general formula: R 1 0- (R 2 0) t (G) v in which:
- R1 represents a linear or branched alkyl and / or alkenyl radical containing approximately from 8 to 24 carbon atoms, an alkylphenyl radical in which the linear or branched alkyl radical contains from 8 to 24 carbon atoms,
- R2 represents an alkylene radical comprising approximately 2 to 4 carbon atoms
- G represents a sugar unit comprising from 5 to 6 carbon atoms
- t denotes a value ranging from 0 to 10, preferably 0 to 4, preferably 0 to 4 and v denotes a value ranging from 1 to 15.
- the alkylpolyglucoside surfactants are compounds of formula described above in which R1 more particularly denotes a saturated or unsaturated, linear or branched alkyl radical containing from 8 to 18 carbon atoms, t denotes a value ranging from 0 to 3 and more particularly still equal to 0, G can denote glucose, fructose or galactose, preferably glucose.
- the degree of polymerization ie the value of v in the above formula, can range from 1 to 15, preferably from 1 to 4.
- the average degree of polymerization is more particularly between 1 and 2.
- the glucosidic bonds between the sugar units are of the 1-6 or 1-4 type and preferably 1-4.
- the coloring composition A comprises a decyl glucoside such as that sold under the name PLANTACARE 2000® UP or PLANTACARE 2000® UP / MB by the company BASF, or Triton CG-50 Surfactant by the company Dow Chemical Company , or Blanova Tens APG 2000 by Azelis Deutschland Kosmetik GmbH or Oramix NS 10 by Seppic.
- a decyl glucoside such as that sold under the name PLANTACARE 2000® UP or PLANTACARE 2000® UP / MB by the company BASF, or Triton CG-50 Surfactant by the company Dow Chemical Company , or Blanova Tens APG 2000 by Azelis Deutschland Kosmetik GmbH or Oramix NS 10 by Seppic.
- the content of nonionic surfactant, preferably alkylpolyglucoside and more preferably decyl glucoside in the dye composition A of the invention will range from 0.5 to 10% by weight, preferably from 3% to 5% by weight relative to the total weight of composition A.
- the coloring composition A will also comprise a polymeric gelling agent, preferably an acrylic polymeric gelling agent.
- a polymeric gelling agent preferably an acrylic polymeric gelling agent.
- This polymeric gelling agent makes it possible to structure the composition by increasing its viscosity.
- hydrophilic polymeric gelling agent capable of gelling the aqueous phase of the compositions according to the invention.
- the gelling agent can be water-soluble or water-dispersible.
- the polymeric gelling agent according to the invention is a polymeric gelling agent, preferably synthetic, in other words it is neither naturally existing nor derived from a polymer of natural origin (ex: polysaccharides, celluloses, etc.).
- the synthetic polymeric gelling agent considered according to the invention may or may not be particulate; in particular it is in the form of particles, preferably spherical.
- the polymeric gelling agent according to the invention is an acrylic polymeric gelling agent chosen from carboxyvinyl polymers, modified or not.
- carboxyvinyl polymers may be copolymers resulting from the polymerization of at least one monomer (a) chosen from a, b-ethylenically unsaturated carboxylic acids or their esters, with at least one ethylenically unsaturated monomer (b) comprising a group hydrophobic.
- the term “copolymers” means both the copolymers obtained from two kinds of monomers as well as those obtained from more than two kinds of monomers such as the terpolymers obtained from three kinds of monomers.
- hydrophobic group or unit is meant a radical with a hydrocarbon chain, saturated or unsaturated, linear or branched, comprising at least 8 carbon atoms, preferably from 10 to 30 carbon atoms, in particular from 12 to 30 carbon atoms and more preferably from 18 to 30 carbon atoms.
- polymeric gelling agents are, for example, polymers or copolymers of acrylic and methacrylic acids such as acrylic acid / ethyl acrylate copolymers and carboxyvinyl polymers.
- examples of such polymers or copolymers are in particular the "carbomers” (CTFA) sold under the name Carbopol® by the company GOODRICH or by the company LUBRIZOL. Mention may also be made of the polyglyceryl methacrylate sold by the company
- GUARDIAN under the name Lubragel or even the polyglycerylacrylate marketed under the name Hispagel by the company HISPANO CHIMICA or finally the polyacrylamide / C1 3-C14 lsoparaffin / Laureth7 mixture marketed by the company SEPPIC under the name Sepigel.
- the coloring composition A comprises a homopolymer of polyacrylic acid with the name INCI Carbomer.
- the content of polymeric gelling agent in the coloring composition A of the invention will generally range from 0.1% to 5% by weight, preferably from 1% to 2% by weight relative to the total weight of the composition.
- the coloring composition A of the invention may also advantageously comprise at least one additional coloring matter chosen from pigments, dyes and their mixtures.
- the coloring material (s) can be chosen from water-soluble or non-soluble, liposoluble or not, organic or inorganic coloring materials, materials with an optical effect, and mixtures thereof.
- the term “coloring matter” is intended to mean a compound capable of producing a colored optical effect when it is formulated in a sufficient amount in an appropriate cosmetic medium.
- the dye (s) are chosen in particular from mineral and / or organic pigments, composite pigments (based on mineral and / or organic materials), dyes, and mixtures thereof.
- pigments should be understood to mean colored particles, inorganic (mineral) or organic, insoluble in the liquid organic phase.
- mineral pigments there may be mentioned, by way of example, black, yellow, red and brown iron oxides; manganese violet; ultramarine blue, chromium oxide, hydrated chromium oxide and ferric blue.
- water-soluble dyes mention may be made of Yellow 5, Yellow 6, Blue 1, Green 5, Green 3, Green 6, Orange 4, Red 4, Red 21, Red 22, Red 27, Red 28, Red 33, Red 40, cochineal carmine (Cl 15850, Cl 75470).
- the coloring composition A comprises at least one coloring matter chosen from direct dyes, preferably direct cationic dyes.
- direct dyes are, for example, chosen from all the aromatic and / or non-aromatic dyes in common use such as neutral benzene, acid or cationic direct dyes, neutral azo, acid or cationic direct dyes, quinone direct dyes and particularly neutral, acidic or cationic anthraquinones, direct azine, triarylmethane, indoamine dyes, methines, styriles, porphyrins, metalloporphyrins, phthalocyanines, methine cyanines, and fluorescent dyes.
- aromatic and / or non-aromatic dyes such as neutral benzene, acid or cationic direct dyes, neutral azo, acid or cationic direct dyes, quinone direct dyes and particularly neutral, acidic or cationic anthraquinones, direct azine, triarylmethane, indoamine dyes, methines, styriles, porphyrins, metalloporphyrins
- the coloring composition A will comprise one or more cationic direct dyes. Mention may in particular be made of the following cationic direct dyes of INCI name: BASIC RED 76, BASIC YELLOW 57, HC BLUE NO. 15, and their mixtures.
- the content of additional dyes, in particular direct dyes, in particular direct cationic dyes, in the dye composition A of the invention will go generally from 0.005 to 5% by weight, preferably from 0.005% to 0.5% by weight relative to the total weight of the composition
- the color-revealing composition B comprises at least one iron salt and / or aluminum salt.
- Iron salts in particular make it possible to obtain sought-after dark shades ranging from brown to black. These salts allow metal complexation on the keratin fiber, and in particular the eyebrow.
- iron salts and / or aluminum salts is meant according to the invention the oxides of these metals and the actual salts derived in particular from the action of an acid on a metal.
- the salts are not oxides.
- halides such as chlorides, fluorides and iodides; sulfates, phosphates; nitrates; perchlorates and salts of carboxylic acids and polymer complexes which can support said salts, as well as their mixtures.
- the carboxylic acid salts which can be used in the invention also include salts of hydroxylated carboxylic acids such as gluconate.
- iron or aluminum salts there may be mentioned sulfates, gluconates, chlorides, lactates, acetates, glycinates, aspartates, and citrates.
- alum that is to say one or more mixed sulphates of aluminum and of monovalent cation, chosen in particular from aluminum and potassium sulphate (potassium alum), aluminum and sodium sulfate (sodium alum), and aluminum and ammonium sulfate (ammonium alum).
- iron gluconate potassium, sodium or ammonium alums and mixtures of these salts will be used.
- the revealing composition B comprises at least one iron gluconate.
- Mention may in particular be made of iron gluconate sold by the company Givaudan-Lavirotte under the name GIVOBIO Fe 601 or Gluconal FE from the company Glucona America, Inc.
- the iron salt (s) and / or aluminum salt (s) used in the revealing composition B advantageously represent from 0.1% to 10 %%, preferably from 3% to 5% by weight of the total weight of the composition.
- the iron salt and / or the aluminum salt preferably iron gluconate or an iron sulphate, more preferably iron gluconate, can be incorporated into the revealing composition B, but preferably it is added extemporaneously to revealing composition B, before application thereof on said keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows
- the revealing composition B comprises at least one film-forming polymer.
- This film-forming polymer makes it possible to improve the behavior of the coloring or make-up on keratin materials, in particular the eyelashes and / or the eyebrows and preferably the eyebrows.
- This film-forming polymer can in particular be chosen from cationic, anionic, amphoteric or nonionic polymers conventionally used in the hair field, or from film-forming polymers used in the field of mascaras.
- the film-forming polymer is chosen from acrylic copolymers.
- an aqueous dispersion of C1-C6 alkyl non-ionic film-forming polymer (meth) acrylate and in particular of polymer consisting essentially of one or more C1-C6 alkyl (meth) acrylates.
- These polymers can be chosen from polymers of C1 -C4 alkyl (meth) acrylate, and in particular copolymers of C1 -C4 alkyl acrylate and C1 -C4 alkyl methacrylate, and mixtures thereof. .
- C1-C4 alkyl (meth) acrylate mention may be made of methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate.
- a copolymer of ethyl acrylate and methyl methacrylate such as that sold under the name "DAITOSOL 5000 AD" by the company DAITO KASEY KOGYO.
- the film-forming polymer advantageously used in the revealing composition B can be present in a content ranging from 1% to 10%, preferably from 1% to 5% by weight (of dry polymer extract) of the total weight of the composition.
- compositions of the invention described above can be found independently of one another in various dosage forms, such as a powder, a lotion, a foam, a cream, an emulsion, a gel or under any other suitable form for dyeing keratin fibers, in particular the eyebrows.
- the keratin fibers in particular the eyelashes and / or the eyebrows, and preferably the eyebrows, using a brush or a brush.
- compositions used in the process according to the invention comprise a medium suitable for dyeing or making up keratin fibers, which may contain water, a mixture of water and one or more organic solvents.
- compositions A and B used in the process according to the invention each comprise water or a mixture of water and one or more organic solvents or a mixture of organic solvents.
- organic solvent mention may, for example, be made of CC 4 mono-alcohols, such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, monoethyl ether and diethylene glycol monomethyl ether, hexylene glycol, as well as aromatic alcohols such as benzyl alcohol or phenoxyethanol.
- the organic solvents are generally present in the compositions of the invention in contents ranging from 0.1 to 5%, preferably from 1% to 2% by weight relative to the total weight of the composition.
- compositions of the invention may also contain various adjuvants such as antioxidants, sequestering agents, perfumes, pH adjusters otherwise called acidifying or basifying agents, dispersing agents, conditioning agents and their mixtures.
- adjuvants such as antioxidants, sequestering agents, perfumes, pH adjusters otherwise called acidifying or basifying agents, dispersing agents, conditioning agents and their mixtures.
- the coloring composition A and / or the revealing composition B advantageously comprise a pH adjuster.
- the pH of said compositions will range from 6 to 8.5, preferably from 7 to 8. According to a particular mode, the pH of the compositions ranges from 7 to 7.5.
- the pH of the compositions used in the process according to the invention can thus be adjusted to the desired value by means of acidifying or basifying agents usually used in cosmetics or even using conventional buffer systems.
- acidifying agents of the compositions used in the invention mention may be made, for example, of citric acid.
- an advantageous variant is to add an basifying agent to the composition or compositions of the process according to the invention, containing the (bi) carbonate (s). More particularly, this alkaline agent is chosen from ammonia, alkali carbonates or bicarbonates such as sodium or potassium carbonates or bicarbonates, alkanolamines such as mono-, di- and triethanolamines as well as their derivatives, hydroxides of sodium or potassium, and mixtures thereof.
- this alkaline agent is chosen from ammonia, alkali carbonates or bicarbonates such as sodium or potassium carbonates or bicarbonates, alkanolamines such as mono-, di- and triethanolamines as well as their derivatives, hydroxides of sodium or potassium, and mixtures thereof.
- composition or compositions of the invention comprise alkaline bicarbonates, in particular sodium bicarbonate.
- the coloring composition A and the revealing composition B are in the form of gels, preferably in the form of aqueous gels.
- aqueous gels are characterized by an aqueous phase generally comprising water and water-soluble organic solvents as described above, and one or more gelling agents, preferably acrylic polymeric gelling agents.
- compositions A and B by increasing their viscosity.
- the viscosity of compositions A and B will range from 2000 cps to 10 OOOcps, preferably from 4000 cps to 7000 cps, measured with Rheolab with a mobile fin.
- the coloring composition A comprises a polymeric gelling agent, as described above.
- the polymeric gelling agent used according to the invention is not a natural polymeric gelling agent (ex: polysaccharides, celluloses, etc.).
- the polymeric gelling agent according to the invention is an acrylic polymeric gelling agent.
- These polymeric gelling agents are, for example, polymers or copolymers of acrylic and methacrylic acids such as acrylic acid / ethyl acrylate copolymers and carboxyvinyl polymers.
- Examples of such polymers or copolymers are in particular the "carbomers" (CTFA) sold under the name Carbopol® by the company GOODRICH or by the company LUBRIZOL.
- CTFA carboxyvinyl polymers
- GUARDIAN under the name Lubragel or even the polyglycerylacrylate marketed under the name Hispagel by the company HISPANO CHIMICA or finally the polyacrylamide / C1 3-C14 lsoparaffin / Laureth7 mixture marketed by the company SEPPIC under the name Sepigel.
- the coloring composition A comprises a homopolymer of polyacrylic acid with the name INCI Carbomer.
- the content of polymeric gelling agent in the coloring composition A of the invention will generally range from 0.1% to 3 %% by weight, preferably from 1% to 2 %% by weight relative to the total weight of the composition
- the revealing composition B comprises a hydrophilic polymeric gelling agent chosen from associative polymers.
- This polymeric gelling agent in a revealing composition B in gel form makes it possible to improve the stability of the composition, in particular in contact with iron gluconate, capable of impacting the stability and / or the structure of said composition.
- the revealing composition B in the form of an aqueous gel comprises at least one associative polymer.
- associative polymer is meant any amphiphilic polymer comprising in its structure at least one fatty chain and at least one hydrophilic portion.
- the associative polymers in accordance with the present invention can be anionic, cationic, nonionic or amphoteric. Preferably, it will be an associative anionic polymer.
- B denotes the ethyleneoxy radical
- n is zero or denotes an integer ranging from 1 to 100
- R denotes a hydrocarbon radical chosen from alkyl, arylalkyl, aryl, alkylaryl, cycloalkyl radicals, comprising 8 with 30 carbon atoms, preferably 10 to 24, and more particularly still from 12 to 18 carbon atoms.
- associative anionic polymers mention may also be made of terpolymers of maleic anhydride / C 3 oC 38 olefin / alkyl maleate such as the maleic anhydride / cc-olefin C 30 -C 38 / maleate copolymer product. isopropyl sold under the name PERFORMA V 1608 by the company NEWPHASE TECHNOLOGIES.
- the associative anionic polymers comprising, among their monomers, an a, (3-monoethylenically unsaturated) carboxylic acid and an a, b- monoethylenically unsaturated carboxylic acid ester and Oxyalkylenated fatty alcohol
- these compounds also comprise, as monomer, an ester of a, b- monoethylenically unsaturated carboxylic acid and of C1-C4 alcohol.
- this type of compound examples include Aculyn 22 ® sold by the company Rohm & Haas, which is a terpolymer of methacrylic acid / ethyl acrylate / stearyl methacrylate oxyalkylenated (comprising 20 EO units) or 'ACULYN 28 (terpolymer of methacrylic acid / ethyl acrylate / behenyl methacrylate oxyethylene (25 EO).
- Aculyn 22 ® sold by the company Rohm & Haas, which is a terpolymer of methacrylic acid / ethyl acrylate / stearyl methacrylate oxyalkylenated (comprising 20 EO units) or 'ACULYN 28 (terpolymer of methacrylic acid / ethyl acrylate / behenyl methacrylate oxyethylene (25 EO).
- anionic polymers comprising at least one hydrophilic unit of olefinic unsaturated carboxylic acid type, and at least one hydrophobic unit exclusively of unsaturated carboxylic acid (C10-C30) alkyl ester type.
- anionic associative polymers mention may also be made of anionic terpolymers.
- the anionic terpolymer can be a linear or branched and / or crosslinked terpolymer of at least one monomer (1) carrying an acid function in free form, partially or totally salified with a nonionic monomer (2) chosen from NN. dimethylacrylamide and 2-hydroxyethyl acrylate and at least one polyoxyethylenated alkyl acrylate monomer (3) of formula (II) below:
- R1 represents a hydrogen atom
- R represents a linear or branched C 2 -C 8 alkyl radical
- n represents a number ranging from 1 to 10.
- branched polymer is meant a non-linear polymer which has pendant chains so as to obtain, when this polymer is dissolved in water, a strong state of entanglement leading to viscosities, at low speed gradient very important.
- crosslinked polymer is meant a non-linear polymer in the state of a three-dimensional network insoluble in water but swellable with water and leading to the production of a chemical gel.
- the acid function of the monomer (1) is in particular the sulfonic acid, phosphonic acid function, said functions being in free form, partially or totally salified.
- the monomer (1) can be chosen from styrenesulfonic acid, ethylsulfonic acid or 2-methyl1-2 [(1-oxo-2-propenyl] amino] 1-propanesulfonic acid (also called Acryloyldimethyltaurate) , partially or totally salified. It is present in the anionic terpolymer preferably in molar proportions of between 5% and 95 mol% and more particularly between 10% and 90 molar.
- the monomer (1) will be more particularly acid 2 -methyl-2 - [(1-oxo-2-propenyl] amino] 1 - propanesulfonic in free form, partially or totally salified.
- the acid function in partially or fully salified form will preferably be an alkali metal salt such as a sodium or potassium salt, an ammonium salt, an amino alcohol salt such as a monoethanolamine salt or else a salt of amino acid such as a lysine salt.
- an alkali metal salt such as a sodium or potassium salt, an ammonium salt, an amino alcohol salt such as a monoethanolamine salt or else a salt of amino acid such as a lysine salt.
- the monomer (2) is preferably present in the anionic terpolymer in molar proportions of between 4.9% and 90 mol% and more particularly between 9.5% and 85% molar and even more particularly between 19.5% and 75 % molar.
- formula (II) as an example of a linear C 8 -C 16 alkyl radical, there may be mentioned octyl, decyl, undecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl.
- formula (II) as an example of a C 8 -C 16 branched alkyl radical, mention may be made of 2-ethylhexyl, 2-propylheptyl, 2-butyloctyl, 2-pentylnonyl, 2hexyldecyl, 4-methylpentyl, 5-methylhexyl, 6 -methylheptyl, 15-methylpentadecyl, 16-methylheptadecyl, 2-hexyloctyl.
- R denotes a C12-C16 alkyl radical.
- n varies from 3 to 5.
- monomer of formula (II) of tetraethoxylated lauryl acrylate.
- the monomer (3) of formula (II) is preferably present in the anionic terpolymer in molar proportions of between 0.1% and 10 mol% and more particularly between 0.5% and 5 mol%.
- the anionic terpolymer is crosslinked and / or branched with a diethylene or polyethylene compound in the proportion expressed relative to the total amount of monomers used, from 0.005% to 1 mol% and preferably from 0.01% to 0.5 mol% and more particularly from 0.01% to 0.25% molar.
- the crosslinking agent and / or the branching agent is preferably chosen from ethylene glycol dimethacrylate, diallyloxoacetic acid or one of its salts, such as sodium diallyloxyacetate, tetraallyloxyethane, ethylene glycol diacrylate, diallyl urea, triallyl amine, trimethylol propanetriacrylate, methylenebis- (acrylamide) or their mixtures.
- the anionic terpolymer can contain additives such as complexing agents, transfer agents, chain-limiting agents.
- composition B Use will be made more particularly in composition B revealing the invention of an anionic terpolymer of 2-methyl-2 - [(1-oxo-2-propenyl] amino] 1-propanesulfonic acid partially or totally salified in the form of a salt.
- the hydrophilic gelling polymer in particular the anionic associative polymer present in the revealing composition B, will be present in a content ranging from 0.1% to 5% by weight, preferably from 1% to 3% by weight relative to the total weight of said composition.
- compositions A and B can be applied to the keratin fibers, in particular the eyelashes and / or the eyebrows, preferably the eyebrows, separately and in particular sequentially, whatever their order of application (application of composition A then of composition B or application of composition B then of composition A).
- the coloring composition A is applied before the revealing composition B.
- the keratin fibers, preferably the eyebrows, may or may not be previously moistened.
- the coloring composition A will be applied to keratin fibers not previously moistened.
- the keratin fibers may or may not be previously treated with an oxidizing agent.
- the coloring composition A will be applied to keratin fibers which are not previously treated with an oxidizing agent.
- the coloring composition A will be applied to keratin fibers previously treated with an oxidizing agent, in particular hydrogen peroxide.
- compositions A and B can be preceded or followed by a step of rinsing and / or drying the keratin fibers.
- the method does not comprise a rinsing and / or drying step before the application of compositions A and B.
- the method nevertheless comprises a final rinsing step after application of composition B .
- the exposure time after application of the coloring composition A generally varies from 30 seconds to 30 minutes, preferably from 45 seconds to 10 minutes, and more preferably from 1 minute to 6 minutes.
- the exposure time after application of the revealing composition B generally varies from 30 seconds to 10 minutes, preferably from 45 seconds to 5 minutes.
- Compositions A and B are generally applied at room temperature.
- the invention also relates to a cosmetic process for coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, in which:
- the coloring composition A is applied to the keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, with an exposure time ranging from 30 seconds to 30 minutes, preferably from 45 seconds to 10 minutes, preferably from 1 minutes to 6 minutes
- the revealing composition B is applied to the keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, with an exposure time ranging from 30 seconds to 10 minutes, preferably from 45 seconds to 5 minutes
- composition A being applied before or after composition B, preferably before composition B, said keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, then being, in a final step and optionally, rinsed.
- the coloring composition A is applied before the revealing composition B.
- the coloring composition A is applied to keratin fibers which are not previously treated with an oxidizing agent.
- the coloring composition A is applied to keratin fibers previously treated with an oxidizing agent, preferably hydrogen peroxide.
- the pre-treatment time with the oxidizing agent will generally range from 30 seconds to 10 minutes, preferably from 30 seconds to 5 minutes.
- an intermediate rinsing step and optionally drying is carried out between the pre-treatment step with the oxidizing agent and the treatment step with the coloring composition.
- the invention also relates to a kit or device for coloring or making up keratin fibers, in particular the eyelashes and / or the eyebrows and preferably the eyebrows, with several separate compartments and comprising:
- the revealing composition B as defined in the invention, and characterized in that it does not include the iron and / or aluminum salt, and
- the iron and / or aluminum salt intended to be mixed extemporaneously with the revealing composition B before application to the keratin fibers,
- composition C comprising an oxidizing agent for a pretreatment of the keratin fibers before treatment with the compositions A and B,
- the kit or device according to the invention comprises:
- the coloring composition A as defined in the invention; in another separate compartment, the revealing composition B as defined in the invention and characterized in that it comprises the iron and / or aluminum salt,
- composition C comprising an oxidizing agent for a pretreatment of the keratin fibers before treatment with the compositions A and B,
- the kit or device according to the invention comprises:
- a natural dye chosen from the group consisting of log extract, chestnut extract, Sorghum extract, pine extract, tea extract, gall nut extract, cocoa extract, Brasiletto extract , and mixtures thereof;
- composition B comprising
- compositions A and B are as described above.
- compositions A and B are in the form of an aqueous gel, the composition A comprising an aqueous phase gelled by a carboxyvinyl polymer and the composition B comprising an aqueous phase gelled by an associative polymer, in particular an associative anionic polymer.
- the compositions of the kit are packaged in separate compartments, possibly accompanied by appropriate means of application, identical or different, such as brushes, brushes or sponges.
- the kit comprises a brush or a brush for applying the compositions of the invention.
- the coloring composition A is prepared according to the following procedure:
- dimethyl isosorbide, glycerol, sodium metabisulfite and preservatives are mixed with water with stirring;
- the carbomer (gelling agent) is then added to the previous phase and mixed until complete dissolution;
- the logwood extract is then added and mixed until complete dissolution; finally the alkyl glucoside surfactant and water are added and the gel thus obtained is homogenized;
- Disclosure composition B comprising iron gluconate
- the revealing composition B is prepared according to the following procedure:
- the gelling agent is then added until perfect dissolution and formation of the gel
- iron gluconate is added immediately to composition B, before application of the product to the eyebrows
- the revealing composition B is then applied to the eyebrows using a brush or a brush, with an exposure time of 2 minutes;
- a brown color is obtained on the eyebrows with good resistance over time.
- Example 2 Selection of penetration booster agents, alone or in combination
- the Applicant has shown that the use of one or more penetration booster agent (s) makes it possible to improve the color result on the eyebrows and its hold over time. It tested various agents including phospholipids, ceramides, saponins, fatty acids and selected from among the best performing agents, in particular dimethyl isosorbide (Arlasolve DMI from Univar) and PEG-7 Glyceryl Cocoate (Cetiol ® HE from BASF ). The results presented below illustrate the effect of phospholipids and dimethyl isosorbide respectively.
- Composition A1 log extract + DMI 2%
- Composition A2 extract of logwood + cationic dyes (low quantity) without DMI
- Composition A3 extract of logwood + lecithin (phospholipid) 1%
- Composition B comprising iron gluconate
- compositions A1 to A3 are prepared according to example 1 and composition B corresponds to the example described in example 1.
- compositions A1 to A4 are applied for 4 minutes.
- Composition B is applied for 2 minutes.
- the effect of the presence or absence of the color penetration booster agent in the coloring composition A is evaluated by carrying out observations under a microscope on sections of keratin fibers treated or not treated with said compositions (FIG. 1).
- An untreated fiber is characterized by a white halo (white rim) while a treated (colored) fiber is characterized by a black halo. The thicker this halo, the deeper the color diffusion in the keratin fiber.
- Figure 1a corresponds to the untreated condition; a thicker colored halo is observed in FIG. 1 b (treated with a composition A1 comprising DMI), compared to the treatments with cationic dyes without DMI (FIG. 1 c) or phospholipids (FIG. 1 d).
- dimethyl isosorbide promotes and / or increases the penetration of the natural dye (logwood) into keratin fibers in an improved manner compared to phospholipids.
- compositions similar to those described in Example 1 are reproduced; two natural dyes are used in a total content of 5%, namely a logwood extract (Logwood extract from SCRD) and a chestnut extract (for example, that of the company Couelles de plantes) in a 60/40 proportion (60 % log extract and 40% chestnut extract).
- a logwood extract Logwood extract from SCRD
- a chestnut extract for example, that of the company Couelles de plantes
- the DMI is replaced by water.
- the two compositions are evaluated at T0, T3, T7, T9 and T21 (expressed in days) according to the color parameters L (intensity) and delta E1 (color fastness over time) using and the apparatus.
- photo capture Visia
- image analysis software Visilog.
- Delta E0 (DE0) V ((L0-Li) 2 + (a0-ai) 2 + (b0-bi) 2 ) and
- Delta E1 (DE1) V ((L1 -Li) 2 + (a1-ai) 2 + (b1-bi) 2 )
- the hold of the product is validated when there is a difference between the time before application and the other measurement times for the parameters L * and DeltaEI.
- Example 2.1 is repeated, replacing the DMI with 1% of PEG-7 Glyceryl Cocoate (Cetiol HE).
- the coloring composition A is applied with an exposure time of 6 minutes. According to an alternative, it is applied with an exposure time of 3 minutes.
- Example 3 Effect of an oxidizing pretreatment on the coloring or makeup result
- Composition A1 log extract + DMI 1%
- Composition A2 log extract + Cetiol HE 1%
- Composition A3 extract of logwood alone
- Composition A4 log extract + DMI 1% + Cetiol HE 1%
- Composition B comprising iron gluconate
- compositions A1 to A4 are prepared according to example 1 and composition B corresponds to the example described in example 1.
- compositions A1 to A4 are applied for 4 or 6 minutes.
- Composition B is applied for 2 minutes.
- compositions are tested with or without pre-treatment of keratin fibers (hair and eyebrows) with an oxidizing agent, in particular 12% hydrogen peroxide.
- an oxidizing agent in particular 12% hydrogen peroxide.
- the pre-treatment with the oxidizing agent is carried out for 2 minutes or for 10 minutes. This oxidizing pre-treatment will allow, by opening the cuticles or scales of the keratin fibers, to promote better penetration of the coloring agents.
- the effect of the oxidizing pre-treatment and the presence or absence of the color penetration booster agent in the coloring composition A are evaluated by carrying out observations under a microscope on sections of treated / untreated keratin fibers.
- a fiber not treated with the oxidizing agent is characterized by a white halo (white rim) while a treated (colored) fiber is characterized by a black halo. The thicker this halo, the deeper the color diffusion in the keratin fiber.
- na not determined (not measured)
- the coloring composition A is prepared according to the following procedure: - dimethyl isosorbide, glycerol, sodium metabisulfite and preservatives are mixed with water with stirring;
- Composition A is prepared according to the protocol described above.
- Composition A coloring with an extract of red wood, an extract of chestnut and an extract of logwood
- DMI Dimethyl isosorbide
- Carbomer Carbopol Ultrez 30
- composition B comprising iron qluconate
- the revealing composition B is prepared according to the following procedure:
- composition B the iron gluconate is added extemporaneously to composition B, before application of the product to the eyebrows
- composition A The protocol for coloring or making up the eyebrows successively using composition A and composition B described above is as follows:
- composition A in a thick layer, carefully following the eyebrow line so to cover all the hairs well (Exposure time: 4 min. Do not wipe the product)
- composition B add the iron gluconate to the white jar containing composition B and mix until there is no more grain
- composition B thus prepared extemporaneously in a thick layer over composition A, carefully following the eyebrow line so as to cover all the hairs (Exposure time: 2 min. During this time, correct if necessary eyebrow contour using a cotton swab).
- a brown color is obtained on the eyebrows with good resistance over time.
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Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1873629A FR3090377B1 (en) | 2018-12-20 | 2018-12-20 | Eyebrow coloring or makeup process |
PCT/EP2019/085862 WO2020127431A1 (en) | 2018-12-20 | 2019-12-18 | Method for dyeing or making up eyebrows |
Publications (1)
Publication Number | Publication Date |
---|---|
EP3897547A1 true EP3897547A1 (en) | 2021-10-27 |
Family
ID=67660153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19829120.5A Pending EP3897547A1 (en) | 2018-12-20 | 2019-12-18 | Method for dyeing or making up eyebrows |
Country Status (7)
Country | Link |
---|---|
US (1) | US11547658B2 (en) |
EP (1) | EP3897547A1 (en) |
JP (1) | JP2022514357A (en) |
KR (1) | KR20210105937A (en) |
CN (1) | CN113453658B (en) |
FR (1) | FR3090377B1 (en) |
WO (1) | WO2020127431A1 (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102020215695A1 (en) * | 2020-12-11 | 2022-06-15 | Henkel Ag & Co. Kgaa | One-step hair coloring with vegetable dyes |
FR3117360B1 (en) * | 2020-12-15 | 2023-05-26 | Oreal | Process for coating two-component keratinous materials consisting in applying to said materials a composition with a polyphenol and a composition with a compound capable of forming hydrogen bonds with said polyphenol |
FR3117849A1 (en) * | 2020-12-17 | 2022-06-24 | L'oreal | Process for dyeing keratinous fibers using two distinct compounds capable of forming covalent bonds together as well as a particular metal salt |
WO2022128901A1 (en) * | 2020-12-17 | 2022-06-23 | L'oreal | Process for dyeing keratin fibres using two different compounds that are capable of forming covalent bonds together and also a particular metal salt or a salt of a metal belonging to the rare-earth metal group or a particular organometallic compound |
FR3130574A1 (en) * | 2021-12-17 | 2023-06-23 | L'oreal | Process for dyeing keratin fibers using a copolymer based on acetoacetate functions, a crosslinking agent, a coloring agent and a metal compound |
FR3130559A1 (en) * | 2021-12-17 | 2023-06-23 | L'oreal | Process for dyeing keratin fibers using a (co)polymer based on acetoacetate functions, a crosslinking agent, a coloring agent and a metal compound |
FR3134988A1 (en) * | 2022-04-28 | 2023-11-03 | L'oreal | Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylenated and/or polyglycerol compound, and a coloring material then application of an anhydrous composition |
FR3134987A1 (en) * | 2022-04-28 | 2023-11-03 | L'oreal | Makeup process using a polyphenol and at least one polyoxyethylene silicone, compositions for implementing the process |
WO2023208806A1 (en) * | 2022-04-28 | 2023-11-02 | L'oreal | Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylenated compound, and a dyestuff, followed by the application of an anhydrous or emulsified composition |
FR3134980A1 (en) * | 2022-04-28 | 2023-11-03 | L'oreal | Care and/or makeup composition comprising a polyphenol, a compound capable of reacting by hydrogen bonds with the polyphenol, a monoalcohol and an antioxidant agent |
FR3134978A1 (en) * | 2022-04-28 | 2023-11-03 | L'oreal | Makeup composition comprising a polyphenol, a polyoxyalkylenated and/or polyglycerol silicone compound, a monoalcohol, and process using it |
FR3134989A1 (en) * | 2022-04-28 | 2023-11-03 | L'oreal | Makeup process with the application of a composition comprising a polyphenol and a polyoxyalkylene compound, and a coloring material then application of an anhydrous composition |
KR20240059685A (en) * | 2022-10-25 | 2024-05-08 | 코스맥스 주식회사 | Hair dye composition comprising potassium alum and polyurethane-10 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101278051B (en) * | 2005-05-05 | 2011-10-05 | 金克克国际有限公司 | Personal care compositions and methods for their use |
US7749286B2 (en) * | 2006-05-01 | 2010-07-06 | Advanced Cosmetic Technologies, Llc | Composition for dyeing keratin fibers and a method of dyeing hair using same |
US7772181B2 (en) * | 2008-10-15 | 2010-08-10 | Danisco Us Inc. | Personal care compositions comprising modified variant Bowman Birk Protease Inhibitors |
CN101445508B (en) * | 2008-11-21 | 2011-08-31 | 南京威尔化工有限公司 | Method for synthesizing isosorbide dimethyl ether |
JP5770107B2 (en) * | 2009-02-20 | 2015-08-26 | 浙江養生堂天然薬物研究所有限公司 | Mordants and hair dye products containing mordants |
WO2012139948A2 (en) * | 2011-04-13 | 2012-10-18 | Unilever Plc | Hair care composition |
FR2994694B1 (en) * | 2012-08-23 | 2014-12-05 | Oreal | BLUE COLORING COMPOSITION AND ITS USE IN COSMETICS |
FR3000385B1 (en) * | 2012-12-27 | 2015-04-17 | Oreal | A CAPILLARY COLORING PROCESS USING A CHROMENIC OR CHROMANIC COLOR, A PARTICULAR ORGANIC COMPOUND, AN OXIDIZING AGENT, AN ALKALI AGENT AND A METAL SALT |
FR3000387B1 (en) * | 2012-12-27 | 2015-10-09 | Oreal | A CAPILLARY COLORING PROCESS USING CHROMENIC OR CHROMANIC COLOR AND ALUN |
EP2941240A1 (en) * | 2013-01-03 | 2015-11-11 | Unilever PLC | Hair care composition |
DE102015223855A1 (en) * | 2015-12-01 | 2017-06-01 | Henkel Ag & Co. Kgaa | Powerful hair treatment with anti-washout effect |
-
2018
- 2018-12-20 FR FR1873629A patent/FR3090377B1/en active Active
-
2019
- 2019-12-18 EP EP19829120.5A patent/EP3897547A1/en active Pending
- 2019-12-18 CN CN201980092524.9A patent/CN113453658B/en active Active
- 2019-12-18 JP JP2021535574A patent/JP2022514357A/en active Pending
- 2019-12-18 WO PCT/EP2019/085862 patent/WO2020127431A1/en unknown
- 2019-12-18 US US17/415,996 patent/US11547658B2/en active Active
- 2019-12-18 KR KR1020217022402A patent/KR20210105937A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CN113453658A (en) | 2021-09-28 |
US11547658B2 (en) | 2023-01-10 |
FR3090377A1 (en) | 2020-06-26 |
WO2020127431A1 (en) | 2020-06-25 |
KR20210105937A (en) | 2021-08-27 |
FR3090377B1 (en) | 2021-09-10 |
US20210378946A1 (en) | 2021-12-09 |
CN113453658B (en) | 2024-05-03 |
JP2022514357A (en) | 2022-02-10 |
WO2020127431A9 (en) | 2020-08-13 |
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