WO2013138973A1 - Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne - Google Patents

Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne Download PDF

Info

Publication number
WO2013138973A1
WO2013138973A1 PCT/CN2012/072507 CN2012072507W WO2013138973A1 WO 2013138973 A1 WO2013138973 A1 WO 2013138973A1 CN 2012072507 W CN2012072507 W CN 2012072507W WO 2013138973 A1 WO2013138973 A1 WO 2013138973A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
methyl
trimethylpentyl
weight
hydroxy
Prior art date
Application number
PCT/CN2012/072507
Other languages
English (en)
Chinese (zh)
Inventor
吴桂谦
赵文忠
洪盛杰
李桂珠
余利
Original Assignee
Wu Guiqian
Zhao Wenzhong
Hong Shengjie
Li Guizhu
Yu Li
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wu Guiqian, Zhao Wenzhong, Hong Shengjie, Li Guizhu, Yu Li filed Critical Wu Guiqian
Priority to CN201280000167.7A priority Critical patent/CN103442681B/zh
Priority to PCT/CN2012/072507 priority patent/WO2013138973A1/fr
Publication of WO2013138973A1 publication Critical patent/WO2013138973A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4926Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4946Imidazoles or their condensed derivatives, e.g. benzimidazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/006Antidandruff preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair

Definitions

  • the invention belongs to the field of daily chemistry, in particular to a hair swarf group containing pyridone salt and allantoin.
  • the anti-dandruff agents commonly used in anti-dandruff shampoo are: zinc pyrithione, ganbaosu, undecylenic acid derivatives, ketoconazole, salicylic acid, etc., wherein zinc pyrithione is an efficient anti-dandruff Itching agents and broad-spectrum fungicides are also one of the most widely used anti-dandruff agents, but they are often used in shampoo formulations, and sedimentation often occurs. Occasionally, discoloration may occur when handling accidentally. Zinc pyrithione is not compatible with disodium edetate, and is unstable to light, and will cover the pearl of shampoo.
  • the biggest disadvantage is that it has strong degreasing ability, and long-term use will cause hair dryness and other problems.
  • the anti-dandruff effect of several other anti-dandruff agents does not meet the requirements of the regulations.
  • the popular dipyridinone has an effect on killing various fungi such as oocysts, oocysts, and Candida albicans, and its sensitivity to metal ions is small, and the color in the shampoo system is stable.
  • the property is improved, the water solubility is good, the compounding effect can be improved, and the degreasing ability is weak, but the anti-dandruff effect is not satisfactory.
  • a hair care composition comprising 1- a salt of hydroxy-4-methyl-6-(2,4,4-trimethylpentyl: )-2(1 ⁇ )-pyridone (pyrosterone) as an antibacterial active ingredient and containing allantoin .
  • the balance is water;
  • the antidandruff agent is an organic salt of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1H)-pyridone a combination with an inorganic salt;
  • the organic salt of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridone is selected from the group consisting of monoethanolamine, diethanolamine Or at least one of triethanolamine salts;
  • the inorganic salt of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1H)-pyridone is selected from the group consisting of sodium At least one of potassium, magnesium, calcium or zinc salts.
  • the technical solution of the present invention includes wherein the anionic surfactant is selected from ammonium lauryl sulfate or ammonium laureth sulfate, the amphoteric surfactant is cocamidopropyl betaine, and the conditioning agent is selected. At least one of a cationic cellulose polymer, a cationic guar gum, and an emulsified silicone oil.
  • the technical solution of the present invention includes wherein the antidandruff agent is 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridone monoethanolamine and 1- A composition of zinc hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridinone.
  • the technical solution of the invention includes wherein the 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-
  • the technical solution of the present invention includes wherein the molar ratio of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridone to monoethanolamine is 1:1; The molar ratio of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridone to zinc chloride is from 5:1 to 1:5.
  • the technical scheme of the present invention comprises that the molar ratio of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1H)-pyridone to zinc chloride is optimized to 1 :2.5.
  • the technical scheme of the present invention comprises 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridone monoethanolamine salt and 1-hydroxy-4 in the composition.
  • the weight percentage of the methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridinone zinc salt is 4:1 to 1:4.
  • the technical solution of the present invention includes, in the composition, 1 -hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridone monoethanolamine salt and 1-hydroxy-4-methyl-6-(2,4 , 4-trimethylpentyl)-2(1 ⁇ )-pyridone zinc salt weight percentage is further optimized to 1:2.8
  • the technical solution of the present invention comprises the composition further comprising from 0.25% to 8.0% by weight of the composition of behenyltrimethylammonium chloride.
  • the technical solution of the present invention comprises that the dodecyltrimethylammonium chloride in the composition accounts for 0.5% to 5.0% by weight of the composition.
  • the anti-dandruff composition has the following advantages over the prior art:
  • 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl:)-2(1 ⁇ )-pyridinone salt in combination with allantoin can effectively remove dandruff and solve Usually, the anti-dandruff shampoo uses ZPT degreasing, has problems such as cytotoxicity and hair dryness, and is more mild;
  • 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl) used in the present invention -2(1 ⁇ )-pyridone salt is a zinc salt compared to 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1 ⁇ )-pyridinone ethanolamine salt It can increase the adsorption of scalp and hair to a greater extent, and exert a longer lasting sterilization and anti-oxidation effect, thereby greatly reducing the amount of use and achieving mild anti-dandruff effect.
  • composition of the present invention contains an antimicrobially active substance such as a pyridone salt in an amount of 0.05% by weight to 5% by weight, further optimized to 0.05% by weight to 1% by weight, again optimized to 0.05% by weight. Percentage to 0.8% by weight.
  • R 2 is selected from -C 4 fluorenyl, C 2 -C 4 alkenyl or alkynyl, phenolic, phenyl; M+ is selected from H + ; inorganic salt is selected from chlorine Sodium, calcium chloride, potassium chloride, zinc chloride, and organic salts are selected from the group consisting of monoethanolamine, diethanolamine, and triethanolamine.
  • the preparation of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl:)-2(1 ⁇ )-pyridinone salt in the present invention can be carried out according to a conventional method such as pyridone and a single
  • the reaction of ethanolamine produces pyridone ethanolamine salt, wherein the molar ratio of pyridone to monoethanolamine is 1: 1, such as DF206, pyridone ethanolamine salt produced by Yantai Oriental Chemical Co., Ltd., the active content is 98%, and the average molecular weight is 298.4 g/mol. Loss on drying ⁇ 0.3%, PH (0.5% aqueous solution) 8.5-10;
  • Pyridone and sodium chloride, calcium chloride, potassium chloride, zinc chloride, etc. form pyridone inorganic salts.
  • the method for preparing a zinc pyridinium salt as preferred in the present invention may also be added to the formulation by a process in which an inorganic zinc salt such as zinc chloride is added, wherein the molar ratio of the pyridone to the zinc chloride is 5:1 to 1 : 5; The optimization is 1:2.5.
  • the weight percentage of the zinc salt of 6-(2,4,4-trimethylpentyl)-2(1H)-pyridone is from 4:1 to 1:4; further optimized to a ratio of 1:2.8 pyridone salt
  • the reaction with monoethanolamine and zinc chloride is not complete, meaning that the organic 2-aminoethanol and the inorganic salt zinc chloride are excessively present in the composition.
  • the invention uses a substance with synergistic anti-dandruff effect - allantoin, which is an odorless white or off-white crystalline powder having a melting point of 226-240 ° C, slightly soluble in propylene glycol, insoluble In glycerol, chloroform or ether, the solubility in room temperature water is about 0.4%, the solubility in hot water and alcohol increases, and the solubility in water increases with temperature (25 ° C, 5.7 g / L ; 40 ° C, l lg / L ; 75 °C, 40g/L).
  • a saturated aqueous solution of allantoin (about 0.5%:) is weakly acidic, and the pH is 4.5 - 6.0.
  • the allantoin used in the present invention is produced in Kunshan Shuangyou, molecular formula: C 4 H 6 N 4 0 3 Molecular mass: 158.12 Melting point: 230 ° C, Chinese name: 2,5-dioxo-4-imidazolium urea; allantoin; 1-ureido-diazepinedione-[2,4], the structural formula is as follows:
  • Luoxian Allantoin is an imidazole heterocyclic compound, a derivative of uric acid, present in sacs, fetal urine and some plants, but the cost of extracting vesicles from these substances is too high.
  • the methods for synthesizing allantoin are: high potassium oxysulfate method: dichloroacetic acid and urea are heated to synthesize allantoin, and glyoxylic acid and urea are directly condensed.
  • Glyoxylic acid is directly condensed with urea (glyoxylic acid is obtained by oxidation of glyoxal).
  • the white precipitate was collected by a Buchner funnel and precipitated in cold water several times to obtain crude allantoin. It was recrystallized from 1000 ml of distilled water. The white fine crystalline allantoin is 60-63%, and the melting point is 236 ° C (decomposition). Based on glyoxal, the allantoin yield is 38-40% of the theoretical (weight yield is 103-108%).
  • the function of allantoin in the present invention is to help soften the scalp stratum corneum and heal scalp wound healing, reduce the irritation of the surfactant, enhance the water retention capacity of the hair, and thereby synergize the antidandruff effect of the pyridone salt. ⁇ 0. 3 ⁇ 0. 3 ⁇ 0. 3 ⁇ 0. 3 ⁇ 0. Weight percentage.
  • Pyridone salt can be widely used in the preparation of cosmetic compositions such as anti-dandruff shampoo, hair conditioner, deodorant shower gel, etc.
  • the application of the present invention in hair and the like also includes: hair conditioner, hair nutrient solution, hair spray, Styling glue, hair oil, hair wax, shower gel, soap, hand soap, deodorant stick, deodorant spray, lotion, etc. Therefore, these products can be used for hair, scalp or skin depending on their respective uses, either as a rinse-off product or as a resident product.
  • composition of the present invention may be a transparent or non-transparent liquid if used in shampoos, shower gels or nourishing liquids, and the like. Or have a pearlescent look.
  • the surfactants used in the shampoos of the present invention are anionic, cationic, nonionic and zwitterionic.
  • the total amount of the surfactant in the present invention is from 5% by weight to 70% by weight, optimized from 10% by weight to 40% by weight, and further optimized to 12% by weight. Percentage to 35 percent by weight.
  • anionic surfactants include: C 1Q -C 2Q mercapto and alkene carboxylates, mercapto ether carboxylates, fatty alcohol sulfates, fatty alcohol ether sulfates, sterol amine sulfates and sulfonates, Fatty acid sterolamine polyglycol ether sulfate, decyl sulfonate, hydroxy sulfonium sulfonate, paraffin sulfonate, acyl ester of isethionate, a-sulfofatty acid ester, benzene Propylene sulfonate, nonylphenol polyglycol ether sulfonate, sulfosuccinate, sulfosuccinate monoester and diester, fatty alcohol ether phosphate, fatty acid monoglyceride sulfate and sulfonate, Mercaptoglyceride ether sulful
  • the anionic surfactant is used in an amount of 30% by weight of 7% by weight, preferably 10% by weight to 25% by weight, and further optimized to 12% by weight. Percentage to 22 percent by weight.
  • Cationic surfactants include: quaternary ammonium salts, such as bis(C 1Q -C 24 ) decyl dimethyl ammonium chloride or ammonium bromide, optimized for bis(C 12 -C 18 ) decyl dimethyl ammonium chloride Or ammonium bromide; C 1 (r C 2 4 mercapto dimethylethyl ammonium chloride or ammonium bromide; C 1 (r C 24 mercapto trimethyl ammonium chloride or ammonium bromide, optimized to sixteen Mercaptotrimethylammonium chloride or ammonium bromide and C 2Q -C 22 mercaptotrimethylammonium chloride or ammonium bromide; C 1Q -C 2 4 mercaptodimethylphenyl ammonium chloride or bromination Ammonium, optimized to 0 12 -0 18 mercaptotrimethylammonium chloride or ammonium bromide; the cationic polymer used in the present invention, also
  • the selection of the cationic polymer in the present invention is preferably selected from the group consisting of polyquaternium-7, polyquaternium-10 and cation cassia gum derivatives. Further optimized for polyquaternium-10 and cationic Cassia gum derivatives, the cationic Cassia gum derivatives are more in line with the "green" appeal.
  • the cationic polymer is used in the composition of the invention in an amount of from 1% by weight to 10% by weight, optimized from 2% by weight to 5% by weight, and further optimized to 3% by weight Weight percentage to 5 percent by weight.
  • an amphoteric surfactant such as: N-(C 12 -C 18 mercapto)-aminopropionate and N-(C 12 -C 18 mercapto:)-aminopropionate (alkali Metal salt, mono-, bis-decyl ammonium salt); sodium cocoamphoacetate; N-acylamine sulfhydryl-N, N-bismethylacetate betaine, cocamidopropyl betaine.
  • the amount of the amphoteric surfactant used in the present invention is from 0.5% by weight to 20% by weight, further optimized to from 1% by weight to 10% by weight.
  • Preferred surfactants for use in the present invention are, for example, lauryl sulfate, lauryl ether sulfate, cocamidopropyl betaine, sodium cocoyl glutamate, sodium lauryl sulfosuccinate, coconut fatty acid Diethanolamide, coconut fatty acid monoethanolamide.
  • the present invention also includes other additional ingredients such as: emulsifiers, co-emulsifiers, fatliquors, oils, waxes, stabilizers, bioactive agents, glycerin, preservatives, pearlizing agents, dyes, perfumes, solvents, sunscreens, Thickener, dispersant, hydrolyzed protein, natural and synthetic peptides, egg yolk, lecithin, lanolin And derivatives thereof, fatty alcohols, silicone oils and derivatives, such as quaternized polysiloxane polymers, and, in addition, some antimicrobial compositions of different structures not mentioned in the present invention can also be used in the present invention.
  • additional ingredients such as: emulsifiers, co-emulsifiers, fatliquors, oils, waxes, stabilizers, bioactive agents, glycerin, preservatives, pearlizing agents, dyes, perfumes, solvents, sunscreens, Thickener, dispersant, hydrolyzed protein, natural and synthetic
  • Some emulsifiers that may be used include: sorbitol esters, phosphate esters, monoglycerides, polysorbates, polyethylene glycol mono/di fatty acid esters, highly ethoxylated fatty acid esters, high molecular weight
  • a silicone oil compound such as dimethylpolysiloxane (molecular weight between 10,000 and 50,000) and the like.
  • nonionic 0/W co-emulsifiers are: Adding 2-30 moles of epoxy oxime and/or 0-5 moles of epoxy propylene to linear fatty alcohols with 8-22 carbons, or 12 a nonionic emulsifier formed from -22 carbon fatty acids or a nonyl phenol of 8-15 carbon atoms; containing 1-30 moles of ethoxy, glyceryl, glycerol mono/diester, sorbitol mono/diester a C 6 -C 22 saturated or unsaturated fatty acid and a fatty alcohol;
  • the fat-reducing agent is, for example, a polyethoxylated lanolin derivative, a lecithin derivative, a polyhydric alcohol fatty acid ester, a monoglyceride and a fatty acid sterol amide, a microcrystalline wax, a hexadecanol/octadecyl alcohol or the like.
  • Solubilizers such as metal salts of fatty acids such as manganese stearate, zinc stearate.
  • Biologically active ingredients such as plant extracts, vitamins, and the like.
  • Suitable preservatives such as: phenoxyethanol, nipa gold ester, pentanediol, formaldehyde emission, etc.; pearlescent agents such as: ethylene glycol stearate including ethylene glycol distearate, ethylene glycol single Stearate and the like.
  • Suitable thickeners such as: sodium chloride, potassium chloride, ammonium chloride, fatty acid sterol amides, cellulose derivatives such as hydroxyethyl methylcellulose, carboxyvinyl polymers such as Kappa 934, 940, 941 , 980, 981, 1342, etc.
  • Thickening and dispersing agents such as long carbon chain C 16 -22 amine oxides, long carbon chain fatty acid esters, long carbon chain ethylene glycol esters, sterol amide esters and the like.
  • Suitable carriers include: vegetable oils, natural and hydrogenated oils, waxes, deionized water, ethanol, polyols, glycerides, liquid paraffins, alcohols, and the like.
  • Antifungal active ingredients include: pyridone, zinc pyrithione (ZPT), ganbaosu, ketoconazole, oxyconazole, terbinaphthol, bifonazole, butoconazole, tribendazole, econazole , Enconazole, Fluconazole, Itraconazole, Miconazole, Thiconazole, Thiconazole, Fenticonazole, Teconazole, Naftifine.
  • ZPT zinc pyrithione
  • cationic guar gum In order to improve the adsorption of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl: )-2 (13 ⁇ 4-pyridone) salt on the skin/scalp, it is recommended to use cationic guar gum.
  • the polymer is used in an amount of from 0.01% by weight to 1.0% by weight, and further optimized to 0.02% by weight to 0.25% by weight.
  • the antimicrobial effect of 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl:)-2(1 ⁇ )-pyridinone salt is achieved by adding the following ingredients and having a coordinated effect : polyethylene glycol, polyethylene glycol with 6-22 moles of EO, polyethylene glycol-12, polypropylene glycol, polyethylene glycol/polypropylene glycol copolymer, silicone oil, polysulfonyl silicone oil, polydecyl aromatic Silicon siloxane, polyether-silicon oxime copolymer.
  • the anti-dandruff active ingredient is added in the formulation in an amount of 0.05% by weight to 5% by weight, optimized to 0.05% by weight to 1% by weight, and further optimized to 100% From 0.05% by weight to 0.6% by weight.
  • the anti-dandruff composition of the present invention can be prepared by any known or otherwise effective technique suitable for providing a shampoo composition, and the method of preparing the anti-dandruff composition of the present invention includes conventional formulation and mixing techniques.
  • the following is an example of the anti-dandruff composition of the present invention, which is a shampoo, which is a non-limiting example.
  • the examples are given for the purpose of illustration only, and are not to be construed as limiting the scope of the invention. In these examples, all concentrations are by weight unless otherwise stated.
  • the term "minor matter" refers to those materials which are optional, such as preservatives, viscosity modifiers, pH adjusters, perfumes, pigments, etc., which are selected with the particular ingredients selected for the preparation of the present invention.
  • EXAMPLE I - XV Suitable methods for preparing the anti-dandruff composition of Examples I - XV are as follows: A suitable amount of water is added to the reaction tank, and guar gum and polyquaternium-10 are added for dispersion under slow stirring.
  • pH adjusters such as citric acid
  • ammonium lauryl sulfate ammonium laureth sulfate
  • cocamidopropyl betaine fatty acid single Ethanolamide
  • sodium glycol distearate acrylic acid copolymers
  • phthalic acid amide disodium edetate (if these materials are used)
  • these materials are completely dispersed and then cooled.
  • the antidandruff agent 1-hydroxy-4-methyl-6-(2,4,4-trimethylpentyl)-2(1H)-pyridone and 1-hydroxy- are added.
  • the anti-dandruff composition of the present invention is used in a conventional manner for cleansing and conditioning hair, and mainly includes the following steps:
  • the efficacy evaluation method for the embodiment is divided into two parts: a sensory evaluation method and a combability test.
  • the sensory evaluation method was as follows: Preparation Examples I - X V were separately sent to 60 testers for comparison. The tester washes the hair in the same way when using the shampoo sample, and each shampoo is used for two weeks. The tester scores according to his or her own feelings, and the antipruritic effect is scored according to the time when the itching starts and the degree of itching. The anti-dandruff effect is scored according to the amount and size of the dandruff. The scoring standard is 7 points, 1 is the worst, 7 is the best, and the higher the score, the better.
  • Table 1 Evaluation of the use of shampoo compositions are shown in Table 1. Table 1 Evaluation of the use of shampoo compositions

Landscapes

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

Abstract

L'invention concerne une composition de shampooing ayant une fonction d'élimination des pellicules, qui contient : (A) des tensio-actifs anioniques représentant 5,0 % à 40 % du poids de la composition, des tensio-actifs ampholytiques représentant 1,0 % à 10,0 % du poids de la composition, des conditionneurs représentant 2,0 % à 10 % du poids de la composition ; (B) des agents antipelliculaires représentant 0,05 % à 0,8 % du poids de la composition, les agents antipelliculaires étant une composition de sel organique et de sel inorganique de la 1-hydroxyl-4-méthyl-6-(2,4,4-triméthylamyl)-2(1H)-pyridone ; (C) de l'uréidohydantoïne représentant 0,05 % à 0,3 % du poids de la composition ; et (D) de l'eau en tant que partie restante. La composition de shampooing a d'excellents effets d'élimination des pellicules et de soulagement du prurit.
PCT/CN2012/072507 2012-03-19 2012-03-19 Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne WO2013138973A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201280000167.7A CN103442681B (zh) 2012-03-19 2012-03-19 一种含有吡啶酮盐和尿囊素的头发去屑组合物
PCT/CN2012/072507 WO2013138973A1 (fr) 2012-03-19 2012-03-19 Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2012/072507 WO2013138973A1 (fr) 2012-03-19 2012-03-19 Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne

Publications (1)

Publication Number Publication Date
WO2013138973A1 true WO2013138973A1 (fr) 2013-09-26

Family

ID=49221776

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2012/072507 WO2013138973A1 (fr) 2012-03-19 2012-03-19 Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne

Country Status (2)

Country Link
CN (1) CN103442681B (fr)
WO (1) WO2013138973A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104546524A (zh) * 2015-01-19 2015-04-29 广州市科能化妆品科研有限公司 一种保湿抗菌头皮护理组合物
WO2021224118A1 (fr) * 2020-05-08 2021-11-11 Unilever Ip Holdings B.V. Compositions de soins personnels comprenant un complexe de piroctone métallique

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022533085A (ja) * 2019-05-14 2022-07-21 ユニリーバー・アイピー・ホールディングス・ベスローテン・ヴェンノーツハップ 2(1h)-ピリジノン及びピロクトンオラミンを含むヘアケア組成物
CN114259446A (zh) * 2022-01-26 2022-04-01 拉芳家化股份有限公司 一种含滋养复合剂的头皮精华液

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1293031A (zh) * 1999-09-29 2001-05-02 欧莱雅 含去头屑剂和丙烯酸类三元共聚物的头发和头皮处理用组合物
WO2009100999A1 (fr) * 2008-02-12 2009-08-20 Henkel Ag & Co. Kgaa Nettoyants capillaires et corporels à fragrance à effet prolongé

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1293031A (zh) * 1999-09-29 2001-05-02 欧莱雅 含去头屑剂和丙烯酸类三元共聚物的头发和头皮处理用组合物
WO2009100999A1 (fr) * 2008-02-12 2009-08-20 Henkel Ag & Co. Kgaa Nettoyants capillaires et corporels à fragrance à effet prolongé

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104546524A (zh) * 2015-01-19 2015-04-29 广州市科能化妆品科研有限公司 一种保湿抗菌头皮护理组合物
WO2021224118A1 (fr) * 2020-05-08 2021-11-11 Unilever Ip Holdings B.V. Compositions de soins personnels comprenant un complexe de piroctone métallique

Also Published As

Publication number Publication date
CN103442681B (zh) 2016-09-14
CN103442681A (zh) 2013-12-11

Similar Documents

Publication Publication Date Title
TWI442939B (zh) 水性毛髮洗淨劑
TWI547555B (zh) 水性毛髮洗淨劑
AU2012315728B2 (en) Regimen for reducing the appearance of thinning hair
JP7250396B2 (ja) ヘアケア組成物
JP2001172121A (ja) 化粧料調合物
US20140086893A1 (en) Regimen For Reducing The Appearance Of Thinning Hair
JP2011505398A (ja) 身体手入れ組成物
JP2018532812A (ja) ペットケア組成物
WO2013138973A1 (fr) Composition d'élimination des pellicules contenant du chlorhydrate de pyridine et de l'uréidohydantoïne
US20060128579A1 (en) Cleansing foaming lotion
EP1602355A1 (fr) Formulation nettoyante moussante
DE1950643A1 (de) Quaternaere Ammoniumverbindungen zur Herstellung von Koerperpflegemitteln
JPH0248516A (ja) 養毛料
JP2696523B2 (ja) ふけ防止剤及び頭髪化粧料
CN114366680A (zh) 用于养护头皮健康防脱固发的洗发组合物及其制备方法
JP3202135B2 (ja) 頭髪化粧料
JPH10203954A (ja) 抗菌性低刺激化粧料
JPH11302147A (ja) 化粧料
BR112020000120A2 (pt) uso novo
JP4327989B2 (ja) 頭髪化粧料
JPH10109923A (ja) 抗菌性低刺激化粧料
JPH07206647A (ja) 養毛料
JP2860124B2 (ja) 頭髪化粧料
JPH0227965B2 (ja) Yomoryo
JPH10182335A (ja) 抗菌性低刺激化粧料

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12872017

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 12872017

Country of ref document: EP

Kind code of ref document: A1