EP3980132A1 - Neuartige haarfärbezusammensetzung - Google Patents
Neuartige haarfärbezusammensetzungInfo
- Publication number
- EP3980132A1 EP3980132A1 EP20742316.1A EP20742316A EP3980132A1 EP 3980132 A1 EP3980132 A1 EP 3980132A1 EP 20742316 A EP20742316 A EP 20742316A EP 3980132 A1 EP3980132 A1 EP 3980132A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- oil
- protein
- optionally hydrolyzed
- composition according
- chosen
- 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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- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- RTMBGDBBDQKNNZ-UHFFFAOYSA-L C.I. Acid Blue 3 Chemical compound [Ca+2].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=C(O)C=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1.C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=C(O)C=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 RTMBGDBBDQKNNZ-UHFFFAOYSA-L 0.000 description 1
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- 239000004215 Carbon black (E152) Substances 0.000 description 1
- GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical compound CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 241000581002 Murex Species 0.000 description 1
- 241000123069 Ocyurus chrysurus Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 241000238370 Sepia Species 0.000 description 1
- 230000002009 allergenic effect Effects 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- WHBMBENUJOTNGS-UHFFFAOYSA-J aluminum potassium sulfonato sulfate Chemical compound [Al+3].[K+].[O-]S(=O)(=O)OS([O-])(=O)=O.[O-]S(=O)(=O)OS([O-])(=O)=O WHBMBENUJOTNGS-UHFFFAOYSA-J 0.000 description 1
- 239000004410 anthocyanin Substances 0.000 description 1
- 235000010208 anthocyanin Nutrition 0.000 description 1
- 229930002877 anthocyanin Natural products 0.000 description 1
- 150000004636 anthocyanins Chemical class 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 description 1
- YBHILYKTIRIUTE-UHFFFAOYSA-N berberine Chemical compound C1=C2CC[N+]3=CC4=C(OC)C(OC)=CC=C4C=C3C2=CC2=C1OCO2 YBHILYKTIRIUTE-UHFFFAOYSA-N 0.000 description 1
- 229940093265 berberine Drugs 0.000 description 1
- QISXPYZVZJBNDM-UHFFFAOYSA-N berberine Natural products COc1ccc2C=C3N(Cc2c1OC)C=Cc4cc5OCOc5cc34 QISXPYZVZJBNDM-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- -1 carbohydrate compound Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 235000012730 carminic acid Nutrition 0.000 description 1
- 239000004106 carminic acid Substances 0.000 description 1
- PMRJYBALQVLLSJ-UHFFFAOYSA-N chamazulene Natural products CCC1=CC2=C(C)CCC2=CC=C1 PMRJYBALQVLLSJ-UHFFFAOYSA-N 0.000 description 1
- OJYGBLRPYBAHRT-IPQSZEQASA-N chloralose Chemical compound O1[C@H](C(Cl)(Cl)Cl)O[C@@H]2[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]21 OJYGBLRPYBAHRT-IPQSZEQASA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229940080423 cochineal Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000004148 curcumin Substances 0.000 description 1
- 235000012754 curcumin Nutrition 0.000 description 1
- 229940109262 curcumin Drugs 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- VFLDPWHFBUODDF-UHFFFAOYSA-N diferuloylmethane Natural products C1=C(O)C(OC)=CC(C=CC(=O)CC(=O)C=CC=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-UHFFFAOYSA-N 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 210000004709 eyebrow Anatomy 0.000 description 1
- 210000000720 eyelash Anatomy 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000003806 hair structure Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- KQSBZNJFKWOQQK-UHFFFAOYSA-N hystazarin Natural products O=C1C2=CC=CC=C2C(=O)C2=C1C=C(O)C(O)=C2 KQSBZNJFKWOQQK-UHFFFAOYSA-N 0.000 description 1
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
- KHLVKKOJDHCJMG-QDBORUFSSA-L indigo carmine Chemical compound [Na+].[Na+].N/1C2=CC=C(S([O-])(=O)=O)C=C2C(=O)C\1=C1/NC2=CC=C(S(=O)(=O)[O-])C=C2C1=O KHLVKKOJDHCJMG-QDBORUFSSA-L 0.000 description 1
- 229960003988 indigo carmine Drugs 0.000 description 1
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- 235000012738 indigotine Nutrition 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011021 lapis lazuli Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 238000007431 microscopic evaluation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000004177 patent blue V Substances 0.000 description 1
- 235000012736 patent blue V Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 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
- 239000002243 precursor Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- BBNQQADTFFCFGB-UHFFFAOYSA-N purpurin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC(O)=C3C(=O)C2=C1 BBNQQADTFFCFGB-UHFFFAOYSA-N 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
Classifications
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- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
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- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
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- A61K2800/4324—Direct dyes in preparations for permanently dyeing the hair
Definitions
- the present invention relates to a new composition for coloring the hair comprising an amino acid, a protein, an alcohol, a mineral powder, a vegetable oil and a dye or a pigment, as well as a process for coloring the hair using implement said composition.
- dyeing is a hairstyling technique that allows hair to be colored permanently or temporarily.
- oxidation dyes To modify the color of the hair in a lasting way, one generally uses chemical treatments called oxidation dyes. These treatments allow a pigmentary modification of the hair in its cortex by denaturing its melanin. Such treatments make it possible to achieve a colored visual appearance, for a resistance of several months.
- a first treatment allowing hair coloring is thus based on the principle of the oxidative combination of two precursor components called base and coupler.
- the oxidation phase is carried out in the presence of hydrogen peroxide in a basic medium (pH between 9.5 and 10.5) with the use of ammoniacal solutions with a high swelling capacity of the fiber.
- This technology is particularly robust and compatible with all types of hair, but nevertheless requires strict compliance with the application conditions recommended by the suppliers, in particular in terms of precautions for use and pause time. They are also recognized as sensitizing and with high allergenic potential.
- the base used consists of an aromatic diamine such as paraphenylenediamine (PPD), 1,4-piaminobenzene, p-phenylenediamine or p-aminoaniline.
- PPD paraphenylenediamine
- 1,4-piaminobenzene 1,4-piaminobenzene
- p-phenylenediamine p-aminoaniline.
- the coupler itself consists of a diphenol such as resorcinol, resorcinol, 1,3-benzenediol, 1,3-dihydroxybenzene or m-dihydrobenzene. These components are also classified as toxic and dangerous.
- a second treatment is based on the use of powders of dye plants or of henna. Although we speak of 'vegetable coloring' and these treatments are considered more natural, they are not without consequences. Indeed, henna powders naturally contain traces of mercury and arsenic.
- the use of henna must in general be accompanied by the use of couplers such as sodium picramates and / or aromatic diamines (PPD) in order to obtain a visible result, more or less covering and lasting. in time. This treatment therefore also presents a risk of toxicity by skin contact.
- these treatments are incompatible with any other chemical or organic treatment since they leave an impenetrable envelope around the fiber preventing the passage of any other product.
- the use of other treatments such as straighteners, perms or lightening can also be at the origin of the destruction of the hair due to the interaction of traces of mercury with the ammonia present in them. .
- New complementary treatments have been developed to provide hair coloring without chemical damage. These treatments are based on the use of cationic dyes called direct dyes or basic dyes. These have a great affinity with keratin but do not have the capacity to cling in a lasting way to the hair. In fact, the cationic dye is deposited only at the periphery of the fiber so as not to damage the latter. Not very robust, this treatment quickly fades after a few shampoos.
- a subject of the present invention is therefore a composition for dyeing the hair comprising:
- a proteinogenic amino acid chosen from aspartic acid, glutamic acid, asparagine, carnitine, cysteine, glutamine, histidine, leucine, isoleucine, methionine, N-phenylalanine, proline, hydroxyproline, threonine, tryptophan, tyrosine, valine, glycine, alanine, serine, beta alanine, taurine, lysine and arginine or a salt thereof, d acid or base, organic or inorganic;
- composition according to the present invention allows effective and long-lasting coloring of the hair, according to an easier application process (without oxidizing mixing to be carried out and without prolonged pause time, the color setting being instantaneous) and preserving the quality of the hair. , in particular due to the absence of an oxidation phase in a basic medium, of aromatic diamine, of diphenol and of ammonia.
- dyes in particular cationic dyes, direct dyes and plant dyes.
- hair coloring means any treatment making it possible to transform the natural color of hair in order to revive its shades or to transform it completely;
- vegetable oil is understood to mean any fatty substance extracted from an oleaginous plant, that is to say a plant whose seeds, nuts or fruits contain lipids;
- protein means any protein, heteroprotein or protein derivative such as a protein grafted onto a heteromolecule which may be silicone, a carbohydrate compound, a fatty acid or derivative, a surfactant of anionic, cationic or non- ionic or amphoteric, of variable size and shape, formed of one or more chain (s) charged with amino acids and linked by peptide bonds.
- the protein is of tertiary or quaternary structure;
- C x -C y -alkyl is understood to mean a saturated, linear or branched hydrocarbon-based chain, and comprising from x to y carbon atoms;
- alcohol means any linear or branched carbon chain containing from 1 to 10 carbon atoms substituted by a hydroxyl group, an aminoalcohol, an aldol or a ketol.
- alcohol denotes any linear or branched compound of formula C n H 2n + i OH in which n is an integer between 1 and 10;
- polyol is understood to mean any Ci-Cio-alkyl group substituted by at least two hydroxyl groups.
- polyol is understood to mean any compound chosen from glycerin, propylene glycol, propane-1,3-diol or sorbitol;
- mineral powder is understood to mean any powder prepared from a homogeneous natural solid in the form of a salt, comprising one or more elements chosen from magnesium (Mg 2+ ), calcium (Ca 26 ), sodium (Na + ) and potassium alum (KAI (S04) I 2 H 2 0);
- dye means any soluble substance consisting of a chromophore group and an auxochrome group.
- dyes mention may in particular be made of azo dyes (or naphthol) such as benzimidazolone yellows or oranges; anthraquinone dyes such as aliza rine, purpurine or indanthrene blue; indigo dyes such as indigo or indigo carmine; chlorine dyes such as chlorphylline; polymethine dyes such as rose or anthocyanin purple; acidic (or anionic) dyes such as patent blue V or fluorescine yellow; basic (or cationic) dyes such as malachite green, berberine yellow or fushin; direct dyes (or nouns) such as curcumin or cochineal; oxidation dyes requiring bases and couplers, such as para-phenylenediamine for the bases and 4-chloro-l 3-dinitrobenzene for the couplers
- pigment means any coloring substance of mineral or organic origin, natural or synthetic insoluble in the medium which it colors.
- inorganic pigments such as yellow ocher, red ocher or lapis lazuli; or organic pigments such as murex or sepia.
- composition according to the present invention therefore contains an amino acid, a protein, an alcohol, a mineral powder, a vegetable oil and a colorant or a pigment.
- the present invention relates to a composition as described. previously having the following characteristics, taken alone or in combination:
- the amino acid is chosen from aspartic acid, glutamic acid, asparagine, carnitine, cysteine, glutamine, histidine, methionine, proline, hydroxyproline, tyrosine, glycine , alanine, serine, beta alanine, taurine and arginine. Most preferably, the amino acid is chosen from glutamic acid, cysteine and arginine;
- composition contains from 0.1% to 20% amino acid as defined above, preferably from 0.1% to 5% amino acid as defined above, more preferably from 0.1% to 3 % amino acid as defined above;
- the protein is chosen from optionally hydrolyzed creatine, optionally hydrolyzed keratin, optionally hydrolyzed wheat protein, optionally hydrolyzed silk protein, optionally hydrolyzed vegetable keratin, optionally hydrolyzed soy protein, optionally hydrolyzed collagen, l ' optionally hydrolyzed elastin, optionally hydrolyzed pea protein, optionally hydrolyzed rice protein, optionally hydrolyzed conchioline protein and optionally hydrolyzed whey protein.
- the protein is chosen from optionally hydrolyzed creatine, optionally hydrolyzed keratin, optionally hydrolyzed silk protein, optionally hydrolyzed vegetable keratin, optionally hydrolyzed soy protein, optionally hydrolyzed collagen, optionally hydrolyzed elastin, optionally hydrolyzed pea protein, optionally hydrolyzed rice protein, optionally hydrolyzed conchiolin protein and optionally hydrolyzed whey protein.
- the protein is chosen from creatine, keratin, optionally hydrolyzed silk protein and optionally hydrolyzed soy protein;
- composition contains from 0.1% to 20% of protein as defined above, more preferably from 0.1% to 10% of protein as defined above, quite preferably from 0.1% to 5 % of protein as defined above;
- the alcohol is chosen from butanol, isopropanol, ethanol and benzyl alcohol. More preferably, the alcohol is chosen as being ethanol or benzyl alcohol;
- composition contains from 0.5% to 20% of alcohol as defined above, more preferably from 0.5% to 10% of alcohol as defined above, quite preferably from 0.5% 4% alcohol as defined above;
- the vegetable oil contains at least 1% chamazulene or carboxylic acids. More preferably, the vegetable oil is chosen from sweet almond oil, olive oil, argan oil, matricaria chamomile oil, Roman chamomile oil, Haarlem oil, babassu oil, broccoli oil, avocado oil, linseed oil, apricot oil, cucumber oil, black seed oil, brazil nut oil, grape seed oil, shea olein, sesame oil and tomato oil. Most preferably, the vegetable oil is chosen as being matricaria chamomile oil or Roman chamomile oil;
- composition contains from 1% to 15% of vegetable oil as defined above, more preferably from 1% to 10% of vegetable oil as defined above, most preferably from 1% to 8% d vegetable oil as defined above;
- the mineral powder contains at least 1% potassium or potassium aluminum disulphate.
- the mineral powder is chosen from kaolin powder, tartaric acid powder, alum powder, calcium carbonate powder, potassium carbonate powder, tara powder, titanium oxalate , magnesium powder.
- the mineral powder is chosen as being alum powder or tartaric acid powder;
- the composition contains from 0.1 to 20% of mineral powder as defined above, more preferably from 0.1 to 10% of mineral powder as defined above, quite preferably from 0.1 to 5% of mineral powder as defined above;
- the dyes are chosen from oxidation dyes, cationic dyes, plant dyes. More preferably, the dyes are chosen from cationic dyes and plant dyes. Most preferably, the dyes are chosen as being cationic dyes;
- the pigments are chosen as being inorganic pigments
- the composition contains from 0.1 to 10% of dye or pigment as defined above, more preferably from 0.1 to 8% of dye or pigment as defined above, most preferably 0, 1 to 5% of dye or pigment as defined above; and or
- composition also contains a polyol.
- composition according to the invention is in the form of a single composition ready for use.
- This can be in the form of a cream, a gel, an oil-in-water or water-in-oil emulsion, a hair lotion or a shampoo.
- the composition according to the invention is in the form of a cream.
- composition according to the present invention whether it is in the form of a cream, emulsion, lotion or shampoo, can be applied according to any known process. of the skilled person.
- the composition according to the present invention is applied according to the process comprising the following steps:
- composition according to the invention directly to dry hair
- the method according to the present invention can also be completed by:
- the method according to the present invention can be easily implemented and allows effective and lasting coloring of the hair without the use of ammonia, hydrogen peroxide, base or coupler, all in a medium with an acidic pH of 5.5, preserving thus the quality of the hair.
- composition according to the present invention can also be used to color the eyelashes or eyebrows.
- Example 1 Composition according to the invention
- a ready-to-use coloring cream comprising an amino acid, a protein, an alcohol, a mineral powder and a colorant, the composition of which is reported in the following Table 1, is prepared.
- Example 1 The cream described in Example 1 above is used with a view to coloring dehydrated hair sensitized by repetitive oxidation locks and dyes, which can no longer retain the dyes due to its porosity (FIG. 1).
- Step 1 Applying the coloring cream directly to dry hair
- the ready-to-use composition according to the invention is applied directly to dry hair, as a treatment for the entire hair from root to tip.
- composition is then left to act for 15 minutes.
- the entire hair is rinsed and a conventional shampoo free of sodium lauryl ether sulfate (i.e. Sodium Laureth Sulfate) is applied.
- sodium lauryl ether sulfate i.e. Sodium Laureth Sulfate
- the shampoo is then rinsed off and a classic detangling balm is applied.
- the hair is then styled in a conventional manner.
- the hair is colored in a deep shade and extremely shiny. We notice during styling that the hair is very soft and silky because it does not show any trace of sensitization. A colored hair is thus obtained simply without having to resort to any oxidation ( Figure 2).
- the microscopic analysis of a hair after treatment also reveals an intact cuticle, without any trace of corrosion in the fatty cells of the cortex.
- the fiber is completely healthy and intensely colored (Figure 3).
- Example 1 The cream described in Example 1 above is used with a view to carrying out the instantaneous transfer of coloring to hair in order to carry out wicking work.
- a photo taken before treatment shows the hair in its natural state ( Figure 4).
- composition according to the invention is carried out according to the following protocol.
- Step 1 Applying the coloring cream directly to dry hair
- the ready-to-use composition according to the invention is applied directly to the selected lock of dry hair.
- the entire hair is rinsed and a conventional shampoo free of sodium lauryl ether sulfate (i.e. Sodium Laureth Sulfate) is applied.
- sodium lauryl ether sulfate i.e. Sodium Laureth Sulfate
- the shampoo is then rinsed off and a classic detangling balm is applied.
- the hair is then styled in a conventional manner.
- the cream described in example 1 above and the Cream ref. are used in order to color dehydrated hair sensitized by repeated oxidation locks and dyes, which can no longer retain the dyes because of its porosity.
- the application of the compositions is carried out according to the protocol described in example 2 above (see 2.1).
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1906053A FR3096896A1 (fr) | 2019-06-07 | 2019-06-07 | Nouvelle composition pour la coloration des cheveux |
PCT/FR2020/050958 WO2020245546A1 (fr) | 2019-06-07 | 2020-06-05 | Nouvelle composition pour la coloration des cheveux |
Publications (1)
Publication Number | Publication Date |
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EP3980132A1 true EP3980132A1 (de) | 2022-04-13 |
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Family Applications (1)
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EP20742316.1A Pending EP3980132A1 (de) | 2019-06-07 | 2020-06-05 | Neuartige haarfärbezusammensetzung |
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US (1) | US11850296B2 (de) |
EP (1) | EP3980132A1 (de) |
JP (1) | JP2022535841A (de) |
KR (1) | KR20220018985A (de) |
CN (1) | CN114080218A (de) |
BR (1) | BR112021024484A2 (de) |
CA (1) | CA3139605A1 (de) |
FR (1) | FR3096896A1 (de) |
WO (1) | WO2020245546A1 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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FR3117821B1 (fr) * | 2020-12-23 | 2024-01-05 | Di Visco | Nouvelle composition pour boucler les cheveux |
FR3124732B1 (fr) * | 2021-06-30 | 2024-05-10 | Oreal | Composition comprenant du karité, un alkyl(poly)glycoside, un polysaccharide et un agent alcalin et/ou un colorant |
FR3127124A1 (fr) * | 2021-09-22 | 2023-03-24 | L'oreal | Composition comprenant de la cystéine et un triglycéride d’acide gras particulier |
WO2023006702A1 (en) * | 2021-07-27 | 2023-02-02 | L'oreal | Composition comprising cysteine, a particular fatty acid triglyceride and an additional reducing agent |
Family Cites Families (26)
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EP0634923B1 (de) * | 1992-04-06 | 1995-12-20 | Henkel Kommanditgesellschaft auf Aktien | Mittel zum färben von keratinhaltigen fasern |
JPH07330559A (ja) * | 1994-05-31 | 1995-12-19 | Shiseido Co Ltd | 染毛剤組成物 |
JPH0820518A (ja) * | 1994-07-06 | 1996-01-23 | Shiseido Co Ltd | 染毛剤組成物 |
US5843193A (en) * | 1997-03-18 | 1998-12-01 | Revlon Consumer Products Corporation | Hair dye compositions and process |
US20010042276A1 (en) * | 2000-03-30 | 2001-11-22 | Shiseido Co., Ltd. | Hair dye fixatives, hair dyes and hair dyeing methods |
JP4076492B2 (ja) * | 2003-12-10 | 2008-04-16 | ホーユー株式会社 | 酸化染毛処理用前処理剤組成物 |
JP4133785B2 (ja) * | 2003-12-16 | 2008-08-13 | ホーユー株式会社 | 半永久染毛剤組成物 |
JP4205602B2 (ja) * | 2004-02-02 | 2009-01-07 | ポーラ化成工業株式会社 | 2剤形態の染毛剤 |
JP2005255569A (ja) * | 2004-03-10 | 2005-09-22 | Kanebo Cosmetics Inc | 染毛剤組成物 |
US20070000070A1 (en) * | 2005-06-30 | 2007-01-04 | Vena Lou Ann C | Method and kit for applying lowlights to hair |
JP4931010B2 (ja) * | 2007-04-13 | 2012-05-16 | 東洋羽毛工業株式会社 | 毛髪処理方法 |
KR20090012647A (ko) * | 2007-07-31 | 2009-02-04 | 이선영 | 동백 오일과 올리브 오일이 함유된 염모제 및 그 제조방법 |
US7699897B2 (en) * | 2007-09-14 | 2010-04-20 | L'oreal | Method of coloring hair |
EP2272489A1 (de) * | 2009-07-09 | 2011-01-12 | KPSS-Kao Professional Salon Services GmbH | Verfahren zum Ausgleichen der Haarfarbe |
JP5759894B2 (ja) * | 2009-07-17 | 2015-08-05 | Rapas株式会社 | ゼオライトとセリサイトを配合してなる医療用又は医療補助組成物 |
CA2792018A1 (en) * | 2010-05-10 | 2011-11-17 | Segetis, Inc. | Fragrant formulations, methods of manufacture thereof and articles comprising the same |
JP4891449B1 (ja) * | 2011-05-25 | 2012-03-07 | 株式会社ピカソ美化学研究所 | 白髪染め用染毛剤組成物 |
FR2977489B1 (fr) * | 2011-07-07 | 2014-03-21 | Oreal | Procedes de traitement cosmetique et kit |
DE102012222768A1 (de) * | 2012-12-11 | 2014-06-12 | Henkel Ag & Co. Kgaa | Haarpflegemittel mit ausgewählten und/oder ausgewählten Oligopeptiden und/oder ausgewählten kationischen Proteinhydrolysaten und Silikonen enthaltend Zuckerstrukturen |
CN104177911A (zh) * | 2014-07-28 | 2014-12-03 | 蚌埠德美过滤技术有限公司 | 一种含醇溶蛋白的柔韧易附着印刷油墨 |
JP2018035103A (ja) * | 2016-09-01 | 2018-03-08 | 大同化成工業株式会社 | ヘアカラー組成物 |
KR101916539B1 (ko) * | 2016-11-21 | 2018-11-07 | 김숙희 | 천연재료를 포함하는 염모제 조성물 |
ES2947658T3 (es) * | 2017-07-11 | 2023-08-16 | Di Visco | Nueva composición para el alisado del cabello |
CN107890451A (zh) * | 2017-11-02 | 2018-04-10 | 杨寿 | 一种中老年人染发喷雾 |
RU2677275C1 (ru) * | 2018-01-17 | 2019-01-16 | Талагаева Елена Владимировна | Маски и бальзам для волос (варианты) |
RU2680841C1 (ru) * | 2018-02-28 | 2019-02-28 | Индивидуальный предприниматель Талагаева Елена Владимировна | Скраб-пилинг омолаживающий для тела |
-
2019
- 2019-06-07 FR FR1906053A patent/FR3096896A1/fr active Pending
-
2020
- 2020-06-05 KR KR1020217042224A patent/KR20220018985A/ko unknown
- 2020-06-05 BR BR112021024484A patent/BR112021024484A2/pt unknown
- 2020-06-05 WO PCT/FR2020/050958 patent/WO2020245546A1/fr unknown
- 2020-06-05 CN CN202080042126.9A patent/CN114080218A/zh active Pending
- 2020-06-05 EP EP20742316.1A patent/EP3980132A1/de active Pending
- 2020-06-05 JP JP2021571840A patent/JP2022535841A/ja active Pending
- 2020-06-05 US US17/616,743 patent/US11850296B2/en active Active
- 2020-06-05 CA CA3139605A patent/CA3139605A1/fr active Pending
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WO2020245546A1 (fr) | 2020-12-10 |
US11850296B2 (en) | 2023-12-26 |
BR112021024484A2 (pt) | 2022-01-18 |
JP2022535841A (ja) | 2022-08-10 |
KR20220018985A (ko) | 2022-02-15 |
US20220331215A1 (en) | 2022-10-20 |
FR3096896A1 (fr) | 2020-12-11 |
CN114080218A (zh) | 2022-02-22 |
CA3139605A1 (fr) | 2020-12-10 |
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