WO1997009029A1 - Composition pour traitement capillaire - Google Patents

Composition pour traitement capillaire Download PDF

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Publication number
WO1997009029A1
WO1997009029A1 PCT/JP1996/002559 JP9602559W WO9709029A1 WO 1997009029 A1 WO1997009029 A1 WO 1997009029A1 JP 9602559 W JP9602559 W JP 9602559W WO 9709029 A1 WO9709029 A1 WO 9709029A1
Authority
WO
WIPO (PCT)
Prior art keywords
acid
weight
hair
composition
hair treatment
Prior art date
Application number
PCT/JP1996/002559
Other languages
English (en)
Japanese (ja)
Inventor
Bettina Fath
Original Assignee
Kao Corporation
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7771605&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO1997009029(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kao Corporation filed Critical Kao Corporation
Priority to GB9803642A priority Critical patent/GB2321595B/en
Publication of WO1997009029A1 publication Critical patent/WO1997009029A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—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
    • A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4913—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
    • 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
    • A61K8/30—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
    • 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

Definitions

  • the present invention relates to an aqueous hair treatment composition, and more particularly, to imparting gloss and volume to hair, improving combability, and particularly, when applied to hair that has become dry due to damage, has improved gloss and flexibility. And a hair conditioning composition.
  • Some hair conditioning compositions left the ingredients in the hair, and some were rinsed after application.
  • compositions had insufficient conditioning effects, especially when used on hair that had become dry due to damage.
  • an object of the present invention is to provide a hair treatment composition which imparts gloss and volume to hair, improves combability, and imparts flexibility.
  • an aqueous hair treatment composition containing a fixed amount of lactic acid, citric acid, and pyrrolidone carboxylic acid has a sufficient hair conditioning effect. That is, the present invention has been completed.
  • the present invention provides the following components (a), (b) and (c)
  • the present invention provides a water or water-based hair treatment composition containing the following.
  • the hair treatment composition of the present invention is used for the final treatment of hair after shampooing, perming, hair dyeing and the like.
  • the above-mentioned weight% refers to the weight% in the whole composition.
  • the lactic acid as the component (a) is contained in an amount of not less than 0.01% by weight in the whole composition. It is preferable to include them.
  • citric acid of the component (b) should be contained in an amount of not less than 0.01% by weight in the total composition. Is preferred.
  • the component (c), pyrrolidone carboxylic acid is 5-oxo-pyrrolidine-12-carboxylic acid known as pyroglutamic acid, which is contained in an amount of not less than 0.01% by weight in the total composition. However, it is particularly preferable to add 0.05 to 2% by weight, more preferably 0.1 to 1% by weight.
  • the hair treatment composition of the present invention may further contain an organic acid in order to further increase the hair conditioning effect.
  • organic acids include one or more selected from glycolic acid, malic acid, glyoxylic acid, tartaric acid, mandelic acid, and pyruvic acid. It is preferable that the organic acid is contained in the entire composition in an amount of at least 0.01% by weight, particularly at least 0.05% by weight.
  • the upper limit of the content of the organic acid is not particularly limited, but in the composition of the present invention, it is determined mainly by the desired pH of the composition. Preferred pH values are between 2 and 7, especially between 4 and 5.5. In general, the upper limit of the content of the organic acid is preferably about 5% by weight, particularly about 2.5% by weight in the total composition. On the other hand, the lower limit of the content of the organic acid is preferably about 0.05% by weight, particularly preferably about 0.25% by weight in the whole composition. These organic acids may be obtained from plants, juices or extracts thereof.
  • Another preferable optional component is glycerin, which is added in an amount of 0.5% by weight or more, particularly preferably 1 to 10% by weight, in the composition of the present invention.
  • hair treatment is used here for shampoo, permanent treatment or after hair dyeing This definition is described in K. Schrader, "Grundlagen und printeduren der Kosmetika", 2nd Ed. (1989), Huthing Buchverlag Heidelberg, pp. 722-724.
  • composition of the present invention may be water-based or water-alcohol-based, may be emulsified or dispersed, or may be an aerosol, particularly an aerosol sol form.
  • the amount of the cationic surfactant to be added is preferably 0.1 to 7.5% by weight, particularly preferably 0.25 to 5% by weight in the whole composition.
  • Preferred examples of the cationic surfactant include one or a mixture of two or more long-chain quaternary ammonium salts, and in particular, cetyltrimethylammonium chloride, dimethyldicetylammonium chloride, Trimethylcetylammonium amide, stearyltrimethylammonium chloride, dimethylstearylbenzylbenzylammonium chloride, benzyltetradecyldimethylammonium chloride, dimethyldihydrogenated tallow ammonium chloride, laurylpyri Preferred are divinyl chloride, lauryldimethylbenzylammonium chloride, laurinoretrimethylammonium chloride, tris (oligoxitytyl) alkyl ammonium phosphate, cetylpyridinium chloride and the like.
  • composition of the present invention can be blended with known components used in ordinary hair conditioning compositions. These include those described in K. Schrader, "Grundlagen und printeduren der Kosmetika", 2nd Ed. (1989), Huthing Buchverlag Heidelberg. PP. 722-771.
  • nonionic surfactant can be used in the composition of the present invention, it is preferable to use a nonionic surfactant together with a cationic surfactant.
  • the nonionic surfactant, aminoxide be used in an amount of 0.25 to 5% by weight, preferably 0.5 to 3.5% by weight in the total composition.
  • Aminoxides include those already known.
  • C 12 -C 18 alkyl dimethyl aminoxides such as lauryl dimethyl aminoxide, C 12 -C 18 alkyl aminaminopropyl or ethyl aminoxide, C ] 2 -C 18 alkyl di (hydroxicetyl) or (hydroxydipropyl)
  • Examples include aminoxide, ethylenoxide in the alkyl chain, or aminoquinide having Z and propylene oxide.
  • These aminoxides can be obtained commercially. This includes, for example, those with the registered trademarks "Ammonyx", "Aromox” or "Genaminox".
  • C 8 -C 18 alkyl glucosides having a degree of condensation of 1.2 to 2.5 are also preferable nonionic surfactants.
  • the composition of the present invention may further contain an amphoteric or zwitterionic surfactant, but is preferably used together with a cationic surfactant.
  • the content of the amphoteric or zwitterionic surfactant is preferably from 0.1 to 5% by weight, preferably from 0.5 to 3% by weight in the whole composition.
  • Examples of the amphoteric or zwitterionic surfactant include known betaines such as fatty acid amide alkyl betaines and sulfobetaine, and specific examples include lauryl hydroxysulfobetaine.
  • composition of the present invention includes complexing agents, dyes, preservatives, ⁇ regulators, thickeners such as inorganic salts, fragrances, pearling agents, sizing agents, wetting agents, plant and animal oils such as jojoba oil, etc. Can be added.
  • Particularly preferred additives are hair conditioning agents, especially cationic polymers, which are added in an amount of 0.05 to 2.5% by weight, especially 0.2 to 1.5% by weight in the total composition. % Is preferable.
  • EP 337,354 discloses the use of alkylpolyglycoside surfactants in conjunction with cationic polymers, but the cationic polymers described on pages 3 to 7 also apply to the invention. And can be suitably used as a conditioning agent. Also, the ones listed under the name “Polyquaternium” in the “CTFA Cosmetic Ingredient Dictionary, 4th. Ed. Can be.
  • composition J of the present invention may further contain a protein hydrolyzate as a conditioning agent, in an amount of 0.25 to 5% by weight, preferably 0.5 to 2.5% by weight of the total composition. Preferably it is 5% by weight.
  • a protein hydrolyzate as a conditioning agent
  • Conductors can also be used.
  • various polysiloxanes may be used as a conditioning agent, and the added amount is 0.25 to 5% by weight, particularly 0.5 to 2% by weight of the whole composition. 5% by weight is preferred.
  • the polysiloxane may be volatile or non-volatile, cyclic or linear. Examples of polysiloxanes include those known under the names “dimethicone”, “phenyldimethicone” and “cyclomethicone”.
  • silicone derivatives described in EP 398,177 with alkylpolyglycosides can also be used in the present invention.
  • composition of the present invention various components may be mixed in water or water-alcohol by a conventional method, and it may be used as a premix.
  • Hair treatment compositions were prepared with the compositions shown in Examples 1 to 5 below.
  • Isopropyl alcohol 150 Isopropyl myristate 1 2 0 Panthenol 0 5 0 Flavor 0 4 0 Lactic acid 0 5 5 Cunic acid 0 0 5 Pyrrolidone carboxylic acid 0 0 2 Tartaric acid 0 0 2 Lingic acid 0 0 1 Preservative
  • the hair after shampooing was treated with the compositions of Examples 1 to 3 and subjected to a half-side test.As a result, the product of the present invention had better combability than the composition not containing the mixture of hydroxycarboxylic acids. Improves both wet and dry, making your hair soft and shiny I was able to.
  • Example 4 In addition to the conditioning effect of the compositions of Examples 1-3, the composition of Example 4 further restored the shine of the hair.
  • the hair treatment composition of the present invention imparts gloss to hair, and further imparts combability and flexibility.

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

La présente invention concerne une composition pour traitement capillaire à base d'eau ou de mélange eau/alcool comprenant en proportion massique: (a) au moins 0,01 % d'acide lactique, (b) au moins 0,01 % d'acide citrique et (c) au moins 0,01 % d'acide pyrrolidonecarboxylique. Cette composition confère aux cheveux brillant, aptitude au peignage, et douceur.
PCT/JP1996/002559 1995-09-08 1996-09-09 Composition pour traitement capillaire WO1997009029A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB9803642A GB2321595B (en) 1995-09-08 1996-09-09 Hair conditioning composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19533211.3 1995-09-08
DE1995133211 DE19533211B4 (de) 1995-09-08 1995-09-08 Haarnachbehandlungsmittel

Publications (1)

Publication Number Publication Date
WO1997009029A1 true WO1997009029A1 (fr) 1997-03-13

Family

ID=7771605

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP1996/002559 WO1997009029A1 (fr) 1995-09-08 1996-09-09 Composition pour traitement capillaire

Country Status (6)

Country Link
JP (1) JPH09110650A (fr)
CN (1) CN1199332A (fr)
DE (1) DE19533211B4 (fr)
GB (1) GB2321595B (fr)
TW (1) TW427910B (fr)
WO (1) WO1997009029A1 (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9704050D0 (en) * 1997-02-27 1997-04-16 Unilever Plc Hair treatment composition
DE19720366A1 (de) * 1997-05-15 1998-11-19 Wella Ag Haarreinigungsmittel mit glanzverbessernden Eigenschaften
EP0978272A1 (fr) * 1998-08-07 2000-02-09 Kao Corporation Préparation pour les soins de la medulla
JP3208381B2 (ja) 1998-12-28 2001-09-10 花王株式会社 毛髪化粧料
DE10009439A1 (de) * 2000-02-29 2001-08-30 Schwarzkopf Gmbh Hans Neue Verwendung von kationischen Proteinhydrolysaten
DE10009438A1 (de) * 2000-02-29 2001-08-30 Schwarzkopf Gmbh Hans Neue Verwendung von Pyrrolidinoncarbonsäuren und Polymeren
BRPI0311568B1 (pt) * 2002-07-05 2017-06-20 Unilever N.V Use of a topical composition and uses of an α-hydroxy acid
JP4926371B2 (ja) * 2002-11-26 2012-05-09 花王株式会社 毛髪化粧料
US7981405B2 (en) 2002-11-26 2011-07-19 Kao Corporation Cosmetic hair preparation
EP1649847B1 (fr) 2003-08-01 2013-09-18 Kao Corporation Methode de soin des cheveux
CN100444821C (zh) * 2003-08-01 2008-12-24 花王株式会社 毛发化妆品
JP2006193461A (ja) * 2005-01-13 2006-07-27 Pola Chem Ind Inc 毛髪用の洗浄料
JP5168996B2 (ja) 2007-04-13 2013-03-27 味の素株式会社 アミノ酸類高配合防腐水溶液
JP5496456B2 (ja) * 2007-12-28 2014-05-21 花王株式会社 毛髪化粧料
ATE524160T1 (de) * 2008-02-14 2011-09-15 Kpss Kao Gmbh Haarpflegemittel enthaltend pca und pca-ester
JP2010065022A (ja) * 2008-08-12 2010-03-25 Kao Corp 毛髪処理用組成物
WO2011124560A2 (fr) * 2010-04-09 2011-10-13 Dsm Ip Assets B.V. Compositions de soin capillaire
BR112018074006B1 (pt) * 2016-05-23 2021-06-15 Symrise Ag Mistura para cuidado capilar, seu uso, composição e método para cuidado capilar ou pessoal
CN108403554B (zh) * 2018-04-27 2021-03-05 北京杼宸医学研究院 一种育发洗发露及其制备方法
US20210275418A1 (en) * 2020-03-09 2021-09-09 Colgate-Palmolive Company Personal Care Compositions
CN114712267A (zh) * 2022-04-06 2022-07-08 王洪伟 烫发缓冲剂

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07112921A (ja) * 1993-10-13 1995-05-02 Sunstar Inc 毛髪化粧料
JPH08239312A (ja) * 1995-02-15 1996-09-17 Kao Corp ヘアシャンプー組成物

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07112921A (ja) * 1993-10-13 1995-05-02 Sunstar Inc 毛髪化粧料
JPH08239312A (ja) * 1995-02-15 1996-09-17 Kao Corp ヘアシャンプー組成物

Also Published As

Publication number Publication date
JPH09110650A (ja) 1997-04-28
GB2321595A (en) 1998-08-05
DE19533211B4 (de) 2005-12-01
GB9803642D0 (en) 1998-04-15
CN1199332A (zh) 1998-11-18
DE19533211A1 (de) 1996-02-08
GB2321595B (en) 2000-01-26
TW427910B (en) 2001-04-01

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