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JP6594114B2 - Multi-agent hair treatment agent and hair treatment method - Google Patents
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JP6594114B2 - Multi-agent hair treatment agent and hair treatment method - Google Patents

Multi-agent hair treatment agent and hair treatment method Download PDF

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JP6594114B2
JP6594114B2 JP2015170201A JP2015170201A JP6594114B2 JP 6594114 B2 JP6594114 B2 JP 6594114B2 JP 2015170201 A JP2015170201 A JP 2015170201A JP 2015170201 A JP2015170201 A JP 2015170201A JP 6594114 B2 JP6594114 B2 JP 6594114B2
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agent
hair
hydrolyzed keratin
treatment
hair treatment
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JP2017014182A (en
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紘介 渡邉
良介 山中
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Milbon Co Ltd
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    • 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
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • 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
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • 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
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • 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
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/65Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88Two- or multipart kits

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

Description

本発明は、多剤式毛髪処理剤、及びこの多剤式毛髪処理剤を使用する毛髪処理方法に関するものである。   The present invention relates to a multi-component hair treatment agent and a hair treatment method using the multi-component hair treatment agent.

加水分解タンパクなどのタンパク質誘導体は、毛髪の保護、補修成分として知られており、その誘導体を使用した様々な処理が提案されている。特許文献1には、アニオン界面活性剤を添加した可溶性ケラチンを含む毛髪化粧料を第1剤とし、ノニオン界面活性剤を含む毛髪化粧料を第2剤とする毛髪改質剤を使用し、その可溶性ケラチンを毛髪表面及び内部に固定することが開示されている。特許文献2には、加水分解ケラチンと共に特定のジエステルを含有させることで、加水分解ケラチンの毛髪への浸透を促進させることが開示されている。また、特許文献3には、ロイシンを配合することで、特定のタンパク質誘導体による毛髪補修を向上させることが開示されている。   Protein derivatives such as hydrolyzed proteins are known as hair protection and repair components, and various treatments using the derivatives have been proposed. Patent Document 1 uses a hair modifying agent having a hair cosmetic containing soluble keratin added with an anionic surfactant as a first agent and a hair cosmetic containing a nonionic surfactant as a second agent. It is disclosed to fix soluble keratin on and inside the hair. Patent Document 2 discloses that penetration of hydrolyzed keratin into hair is promoted by containing a specific diester together with hydrolyzed keratin. Patent Document 3 discloses that hair repair by a specific protein derivative is improved by blending leucine.

特開平8−109114号公報JP-A-8-109114 特開2013−53171号公報JP 2013-53171 A 特開2015−81245号公報Japanese Patent Laying-Open No. 2015-81245

上記の通り、タンパク質誘導体を利用した毛髪処理提案がある。そして、タンパク質誘導体であるケラチン誘導体として加水分解ケラチンや加水分解ケラチン誘導体が知られており、これらの毛髪への浸透性を制御できれば、毛髪の感触を調整可能になると期待される。   As described above, there are hair treatment proposals using protein derivatives. Further, hydrolyzed keratin and hydrolyzed keratin derivatives are known as keratin derivatives that are protein derivatives, and it is expected that the feel of hair can be adjusted if the permeability to these hairs can be controlled.

本発明は、上記事情に鑑み、加水分解ケラチンやその誘導体の毛髪への浸透性を制御できる多剤式毛髪処理剤、及び毛髪処理方法の提供を目的とする。   In view of the above circumstances, an object of the present invention is to provide a multi-component hair treatment agent and a hair treatment method capable of controlling the permeability of hydrolyzed keratin and its derivatives to hair.

本発明者等が鋭意検討を行った結果、加水分解ケラチン又はその誘導体を配合した処理剤を毛髪に適用する前に、タンニン酸を配合した処理剤を毛髪に適用すれば、加水分解ケラチン及びその誘導体の毛髪への浸透性を抑える制御が可能となることを見出し、本発明を完成するに至った。   As a result of intensive studies by the present inventors, if a treatment containing tannic acid is applied to the hair before applying the treatment containing hydrolyzed keratin or a derivative thereof to the hair, hydrolyzed keratin and its It has been found that it is possible to control the penetration of the derivative into hair, and the present invention has been completed.

すなわち、本発明に係る多剤式毛髪処理剤は、タンニン酸が配合された前処理剤と、加水分解ケラチン又は加水分解ケラチン誘導体が配合された後処理剤と、を備えることを特徴とする。   That is, the multi-component hair treatment agent according to the present invention is characterized by including a pretreatment agent containing tannic acid and a posttreatment agent containing hydrolyzed keratin or a hydrolyzed keratin derivative.

前記前処理剤におけるタンニン酸として、加水分解性タンニンが配合されていると良い。   It is preferable that hydrolyzable tannin is blended as tannic acid in the pretreatment agent.

前記後処理剤における加水分解ケラチン誘導体として、下記式(I)〜(III)で表される構造及びこれらの構造の塩から選ばれた単位を有する側鎖基を一種又は二種以上備えるものが配合されていると良い。
−S−S−(CH)n−COOH (I)
(式(I)中、nは1又は2である。)
−S−S−CH(CH)−COOH (II)
−S−S−CH(COOH)−CH−COOH (III)
As the hydrolyzed keratin derivative in the post-treatment agent, one having one or more side chain groups having units selected from the structures represented by the following formulas (I) to (III) and salts of these structures: It should be blended.
-S-S- (CH 2) n -COOH (I)
(In the formula (I), n is 1 or 2.)
-S-S-CH (CH 3 ) -COOH (II)
-S-S-CH (COOH) -CH 2 -COOH (III)

本発明に係る毛髪処理方法は、タンニン酸が配合された前処理剤を毛髪に塗布する前処理工程と、前記前処理工程後に、加水分解ケラチン又は加水分解ケラチン誘導体が配合された後処理剤を毛髪に塗布する後処理工程と、を備えることを特徴とする。   The hair treatment method according to the present invention comprises a pretreatment step of applying a pretreatment agent containing tannic acid to hair, and a posttreatment agent containing hydrolyzed keratin or a hydrolyzed keratin derivative after the pretreatment step. And a post-treatment step applied to the hair.

本発明によれば、タンニン酸が配合された前処理剤を毛髪に塗布後、加水分解ケラチン又はその誘導体が配合された後処理剤を毛髪に塗布するから、加水分解ケラチン及びその誘導体の毛髪への浸透性が抑えられる。   According to the present invention, after applying the pretreatment agent containing tannic acid to the hair, and then applying the posttreatment agent containing hydrolyzed keratin or a derivative thereof to the hair, the hydrolyzed keratin and the derivative thereof are applied to the hair. The permeability of is suppressed.

実施例の毛髪処理を行った毛髪の切断面を蛍光顕微鏡観察した撮影画像である。It is the picked-up image which observed the cut surface of the hair which performed the hair treatment of the Example by the fluorescence microscope. 比較例の毛髪処理を行った毛髪の切断面を蛍光顕微鏡観察した撮影画像である。It is the picked-up image which observed the cut surface of the hair which performed the hair treatment of the comparative example by the fluorescence microscope.

本発明の実施形態に基づき、本発明を以下に説明する。
本実施形態の多剤式毛髪処理剤は、前処理剤と、この前処理剤の後に使用される後処理剤を備えるものである。
Based on an embodiment of the present invention, the present invention will be described below.
The multi-component hair treatment agent of this embodiment comprises a pretreatment agent and a posttreatment agent used after the pretreatment agent.

(前処理剤)
本実施形態に係る前処理剤は、タンニン酸が水に配合されたものである(水の配合量は、例えば25質量%以上)。また、本実施形態の前処理剤には、用途に応じた任意原料として、公知の毛髪処理剤用の原料が配合されていても良い。
(Pretreatment agent)
The pretreatment agent according to this embodiment is obtained by blending tannic acid with water (the blending amount of water is, for example, 25% by mass or more). Moreover, the raw material for well-known hair treatment agents may be mix | blended with the pretreatment agent of this embodiment as an arbitrary raw material according to a use.

タンニン酸
本実施形態の前処理剤には、市販のタンニン酸又はタンニン酸を含む植物抽出物を配合すると良い。
Tannic acid Commercially available tannic acid or a plant extract containing tannic acid may be added to the pretreatment agent of the present embodiment.

上記タンニン酸として、加水分解性タンニンが配合されていると良い。ここで、加水分解性タンニンは、ブドウ糖と没食子酸とのエステル結合物、及び、そのエステル結合物と没食子酸とのデプシド結合物である。この加水分解性タンニンは、例えば下記一般式(A)で表される。   It is preferable that hydrolyzable tannin is blended as the tannic acid. Here, hydrolyzable tannin is an ester bond between glucose and gallic acid, and a depside bond between the ester bond and gallic acid. This hydrolyzable tannin is represented by the following general formula (A), for example.

[上記一般式(A)において、Gはエステル結合又はデプシド結合後の没食子酸残基を表し、k、l、m、及びnは、夫々、0又は正の整数を表す。] [In the general formula (A), G represents a gallic acid residue after an ester bond or a depside bond, and k, l, m, and n each represent 0 or a positive integer. ]

本実施形態の前処理剤におけるタンニン酸の配合量は、この前処理剤を安価にするために、0.1質量%以下が良く、0.05質量%以下が好ましく、0.02質量%以下がより好ましい。また、タンニン酸の配合量が微量であっても良く、その配合量は、例えば0.005質量%であり、0.008質量%以上が良く、0.01質量%以上が好ましい。   The blending amount of tannic acid in the pretreatment agent of this embodiment is preferably 0.1% by mass or less, preferably 0.05% by mass or less, and preferably 0.02% by mass or less in order to make the pretreatment agent inexpensive. Is more preferable. Moreover, the compounding quantity of a tannic acid may be trace amount, and the compounding quantity is 0.005 mass%, for example, 0.008 mass% or more is good, and 0.01 mass% or more is preferable.

任意原料
本実施形態の前処理剤に配合される任意原料は、公知の毛髪処理剤用の原料から適宜に選定される。この任意原料は、界面活性剤、高級アルコール、多価アルコール、糖類、エステル油、油脂、脂肪酸、炭化水素、ロウ、シリコーン、高分子化合物、アミノ酸、動植物抽出物、微生物由来物、無機化合物、香料、防腐剤、金属イオン封鎖剤、紫外線吸収剤などである。なお、前処理剤には、加水分解ケラチン及び/又は加水分解ケラチン誘導体が配合されていても良い。
Optional raw materials The optional raw materials blended in the pretreatment agent of the present embodiment are appropriately selected from known raw materials for hair treatment agents. These optional raw materials are surfactants, higher alcohols, polyhydric alcohols, saccharides, ester oils, fats and oils, fatty acids, hydrocarbons, waxes, silicones, polymer compounds, amino acids, animal and plant extracts, microorganism-derived substances, inorganic compounds, and fragrances. , Antiseptics, sequestering agents, UV absorbers and the like. The pretreatment agent may contain hydrolyzed keratin and / or hydrolyzed keratin derivative.

剤型
本実施形態の前処理剤は、毛髪に馴染み易くするため、外相が水相である水性のものが好ましい。そして、当該前処理剤の使用時の剤型は、特に限定されず、例えば、液状、クリーム状、ゲル状、フォーム状(泡状)、霧状が挙げられる。
Dosage Form The pretreatment agent of the present embodiment is preferably an aqueous one whose outer phase is an aqueous phase in order to make it easier to adjust to hair. And the dosage form at the time of use of the said pretreatment agent is not specifically limited, For example, liquid form, cream form, gel form, foam form (foam form), and mist form are mentioned.

pH
本実施形態の前処理剤のpHは、例えば4以上7以下であり、5以上が良い。
pH
The pH of the pretreatment agent of the present embodiment is, for example, 4 or more and 7 or less, and preferably 5 or more.

(後処理剤)
本実施形態に係る後処理剤は、加水分解ケラチン、加水分解ケラチン誘導体、又は、加水分解ケラチン及び加水分解ケラチン誘導体が水に配合されたものである(水の配合量は、例えば25質量%以上)。また、本実施形態の後処理剤には、用途に応じた任意原料として、公知の毛髪処理剤用の原料が配合されていても良い。
(Post-treatment agent)
The post-treatment agent according to this embodiment is hydrolyzed keratin, hydrolyzed keratin derivative, or hydrolyzed keratin and hydrolyzed keratin derivative blended in water (the blending amount of water is, for example, 25% by mass or more) ). Moreover, the raw material for well-known hair treatment agents may be mix | blended with the post-treatment agent of this embodiment as an arbitrary raw material according to a use.

加水分解ケラチン、加水分解ケラチン誘導体
本実施形態における「加水分解ケラチン」とは、化粧品原料の国際命名法(International Nomenclature Cosmetic Ingredient)に従って作成された国際的表示名称に基づき、日本化粧品工業連合会が「加水分解ケラチン」との表示名称を付与した成分が該当する。また、「加水分解ケラチン誘導体」とは、加水分解ケラチンに該当しないものであり、ケラチンの主鎖の切断を伴って製造されるケラチン誘導体である。これら加水分解ケラチン及び加水分解ケラチン誘導体は、安定入手し易い羊毛に由来するものであると良い。
Hydrolyzed keratin, hydrolyzed keratin derivative The “hydrolyzed keratin” in the present embodiment is based on the international labeling name created in accordance with the International Nomenclature Cosmetic Ingredient. The component which gave the display name "hydrolysis keratin" corresponds. Further, the “hydrolyzed keratin derivative” is a keratin derivative that does not correspond to the hydrolyzed keratin and is produced with cleavage of the main chain of keratin. These hydrolyzed keratin and hydrolyzed keratin derivative are preferably derived from wool that is easily available in a stable manner.

加水分解ケラチン誘導体としては、例えば、特開2012−224573号公報に開示されている下記式(I)〜(III)で表される構造及びこれらの構造の塩から選ばれた単位を有する側鎖基を一種又は二種以上備えるものが挙げられる。
−S−S−(CH)n−COOH (I)
(式(I)中、nは1又は2である。)
−S−S−CH(CH)−COOH (II)
−S−S−CH(COOH)−CH−COOH (III)
Examples of the hydrolyzed keratin derivative include a side chain having a unit selected from the structures represented by the following formulas (I) to (III) and salts of these structures disclosed in JP2012-224573A The thing provided with 1 type or 2 types or more of group is mentioned.
-S-S- (CH 2) n -COOH (I)
(In the formula (I), n is 1 or 2.)
-S-S-CH (CH 3 ) -COOH (II)
-S-S-CH (COOH) -CH 2 -COOH (III)

加水分解ケラチン及び加水分解ケラチン誘導体は、その分子量が小さなほど毛髪に浸透しやすい上に、後処理剤のpHを低く設定した際の溶解性への影響が小さい。そのため、加水分解ケラチン及び加水分解ケラチン誘導体は、分子量20000以下のものが含まれていると良く、分子量10000以下のものが含まれていると好ましく、分子量5000以下のものが含まれていると好ましい。一方で、毛髪への浸透性を抑えるには、加水分解ケラチン及び加水分解ケラチン誘導体は、分子量500以上のものが含まれていると良く、分子量1000以上のものが含まれていると好ましく、分子量2000以上のものが含まれているとより好ましい。ここで、前記の分子量については、Sodium Dodecyl Sulfate−ポリアクリルアミドゲル電気泳動法(SDS−PAGE法)による加水分解ケラチン等のバンドと分子量マーカーのバンドとの相対距離から算出した分子量を、加水分解ケラチン等の分子量とみなして採用する。   The smaller the molecular weight of the hydrolyzed keratin and hydrolyzed keratin derivative, the more easily it penetrates into the hair and the effect on the solubility when the pH of the post-treatment agent is set low. Therefore, the hydrolyzed keratin and the hydrolyzed keratin derivative may contain those having a molecular weight of 20000 or less, preferably those having a molecular weight of 10,000 or less, and preferably those having a molecular weight of 5000 or less. . On the other hand, in order to suppress the permeability to hair, the hydrolyzed keratin and hydrolyzed keratin derivative preferably contain those having a molecular weight of 500 or more, preferably those having a molecular weight of 1000 or more. More preferably 2000 or more are included. Here, with respect to the molecular weight, the molecular weight calculated from the relative distance between the band of hydrolyzed keratin and the like and the molecular weight marker band by Sodium Dodecyl Sulfate-polyacrylamide gel electrophoresis (SDS-PAGE method) The molecular weight is considered to be adopted.

本実施形態の後処理剤には、加水分解ケラチン及びその誘導体から選ばれた一種又は二種以上が配合される。この後処理剤における加水分解ケラチン及びその誘導体の配合量は、例えば0.0005質量%以上であり、0.001質量%以上が良く、0.01質量%以上が好ましい。一方、配合量の上限は、後処理剤を安価にする観点から、1質量%が良く、0.1質量%が好ましい。   In the post-treatment agent of this embodiment, one or more selected from hydrolyzed keratin and derivatives thereof are blended. The blending amount of hydrolyzed keratin and its derivative in this post-treatment agent is, for example, 0.0005 mass% or more, preferably 0.001 mass% or more, and preferably 0.01 mass% or more. On the other hand, the upper limit of the blending amount is preferably 1% by mass and preferably 0.1% by mass from the viewpoint of making the post-treatment agent inexpensive.

任意原料
本実施形態の後処理剤に配合される任意原料は、公知の毛髪処理剤用の原料から適宜に選定される。この任意原料は、界面活性剤、高級アルコール、多価アルコール、糖類、エステル油、油脂、脂肪酸、炭化水素、ロウ、シリコーン、高分子化合物、アミノ酸、動植物抽出物、微生物由来物、無機化合物、香料、防腐剤、金属イオン封鎖剤、紫外線吸収剤などである。なお、本実施形態の後処理剤にタンニン酸を配合しても良いが、その配合量は、前処理剤の配合量よりも少なくすると良い(例えば、前処理剤の配合量の1/100以下)。
Arbitrary raw material The arbitrary raw material mix | blended with the post-processing agent of this embodiment is suitably selected from the raw material for well-known hair processing agents. These optional raw materials are surfactants, higher alcohols, polyhydric alcohols, saccharides, ester oils, fats and oils, fatty acids, hydrocarbons, waxes, silicones, polymer compounds, amino acids, animal and plant extracts, microorganism-derived substances, inorganic compounds, and fragrances. , Antiseptics, sequestering agents, UV absorbers and the like. In addition, although tannic acid may be mix | blended with the post-processing agent of this embodiment, the compounding quantity is good to make it smaller than the compounding quantity of a pre-processing agent (for example, 1/100 or less of the compounding quantity of a pre-processing agent) ).

剤型
本実施形態の後処理剤は、毛髪に馴染み易くするため、外相が水相である水性のものが好ましい。そして、当該後処理剤の使用時の剤型は、特に限定されず、例えば、液状、クリーム状、ゲル状、フォーム状(泡状)、霧状が挙げられる。
Dosage Form The post-treatment agent of this embodiment is preferably an aqueous one in which the outer phase is an aqueous phase in order to make it easier to adjust to the hair. And the dosage form at the time of use of the said post-processing agent is not specifically limited, For example, liquid form, cream form, gel form, foam form (foam form), and mist form are mentioned.

pH
本実施形態の後処理剤のpHは、例えば4以上7以下である。pHを低く設定した場合に加水分解ケラチン及び/又は加水分解ケラチン誘導体の分散性が低い場合には、pH5以上が良く、6以上が好ましい。
pH
The pH of the post-treatment agent of this embodiment is, for example, 4 or more and 7 or less. When the pH is set low, when the dispersibility of the hydrolyzed keratin and / or hydrolyzed keratin derivative is low, the pH is preferably 5 or more, and preferably 6 or more.

(使用方法)
本実施形態の多剤式毛髪処理剤は、前処理剤を毛髪に塗布する前処理工程の後に、この前処理剤を洗い流し又は前処理剤を洗い流さずに、後処理剤を塗布する後処理工程で使用される。後処理剤は、塗布後に洗い流しても良いし、洗い流さなくても良い。
(how to use)
The multi-component hair treatment agent of the present embodiment is a post-treatment step of applying a post-treatment agent after washing the pre-treatment agent or without washing off the pre-treatment agent after the pre-treatment step of applying the pre-treatment agent to the hair. Used in. The post-treatment agent may be washed off after application or not.

本実施形態の多剤式毛髪処理剤は、前処理剤及び後処理剤に加えて、1以上の他の処理剤を備えるものであっても良い。例えば3剤式の毛髪処理後の場合の他の処理剤の使用順序は、前処理剤のタンニン酸が毛髪内に存在する状態で後処理剤を使用するのであれば限定されず、前処理剤の前に使用しても良く、前処理剤及び後処理剤の間に使用しても良く、後処理剤の後に使用しても良い。   The multi-component hair treatment agent of this embodiment may include one or more other treatment agents in addition to the pre-treatment agent and the post-treatment agent. For example, the order of use of other treatment agents after three-component hair treatment is not limited as long as the post-treatment agent is used in a state where the tannic acid of the pre-treatment agent is present in the hair. It may be used before, may be used between the pretreatment agent and the posttreatment agent, or may be used after the posttreatment agent.

本実施形態の多剤式毛髪処理剤は、ヘアケア剤などとして使用可能なものである。「ヘアケア剤」とは、毛髪の手入れ、手当て等を行うために用いられる毛髪処理剤である。ヘアケア剤としては、例えばシャンプー後に使用するトリートメント、パーマの前処理のためのトリートメント、パーマの後処理のためのトリートメント、カラーリングの前処理のためのトリートメント、カラーリングの後処理のためのトリートメント、ブリーチの前処理のためのトリートメント、ブリーチの後処理のためのトリートメントが挙げられる。   The multi-component hair treatment agent of this embodiment can be used as a hair care agent or the like. A “hair care agent” is a hair treatment agent used for the care and care of hair. Examples of hair care agents include treatments used after shampooing, treatments for pre-treatment of perms, treatments for post-treatment of perms, treatments for pre-treatment of coloring, treatments for post-treatment of coloring, Treatment for pre-treatment of bleach and treatment for post-treatment of bleach.

以下、実施例に基づき本発明を詳述するが、この実施例の記載に基づいて本発明が限定的に解釈されるものではない。   EXAMPLES Hereinafter, although this invention is explained in full detail based on an Example, this invention is not interpreted limitedly based on description of this Example.

前処理剤と後処理剤を製造し、実施例及び比較例の毛髪処理を行った。その詳細は、以下の通りである。   A pretreatment agent and a posttreatment agent were produced, and the hair treatment of Examples and Comparative Examples was performed. The details are as follows.

(前処理剤)
加水分解性タンニン(DSP五協フード&ケミカル社製「Gタンニン酸)の1質量%水溶液を前処理剤として製造した。
(Pretreatment agent)
A 1% by mass aqueous solution of hydrolyzable tannin (“G Tannic Acid” manufactured by DSP Gokyo Food & Chemical Co., Ltd.) was produced as a pretreatment agent.

(後処理剤)
ケラチン誘導体
以下の通り、還元工程及び酸化剤混合工程に従って−S−S−CH−COOH又はその塩を側鎖基に備えるケラチン誘導体を製造し、固液分離工程及び回収工程に従ってそのケラチン誘導体を回収し、加熱工程におけるケラチン誘導体の処理により、前記側鎖基を備える加水分解ケラチン誘導体の溶液を製造した。
(Post-treatment agent)
Follows keratin derivative, a -S-S-CH 2 -COOH or a salt thereof according to the reduction step and the oxidizing agent mixing process to produce a keratin derivative comprising a side group, the keratin derivative according to the solid-liquid separation step and the recovery step It collect | recovered and the solution of the hydrolysis keratin derivative provided with the said side chain group was manufactured by the process of the keratin derivative in a heating process.

還元工程
中性洗剤で洗浄、乾燥させたメリノ種羊毛を、約5mmに切断した。この羊毛5質量部、30質量%チオグリコール酸ナトリウム水溶液15.4質量部及び6mol/L水酸化ナトリウム水溶液8.5質量部を混合し、さらに水を混合して全量150質量部、pH11の被処理液を調製した。この被処理液を、45℃、1時間の条件で攪拌した。次いで、さらに水を混合して全量を200質量部とし、45℃、2時間の条件で放置し、その後、液温が常温になるまで自然冷却した。
Reduction step Merino wool, washed with a neutral detergent and dried, was cut to about 5 mm. 5 parts by weight of this wool, 15.4 parts by weight of a 30% by weight aqueous sodium thioglycolate solution and 8.5 parts by weight of a 6 mol / L aqueous sodium hydroxide solution are mixed, and water is further mixed to give a total amount of 150 parts by weight and a pH 11 coating. A treatment solution was prepared. This liquid to be treated was stirred at 45 ° C. for 1 hour. Subsequently, water was further mixed to make the total amount 200 parts by mass, left under conditions of 45 ° C. for 2 hours, and then naturally cooled until the liquid temperature reached room temperature.

酸化剤混合工程
還元工程後の被処理液を攪拌しながら、当該液に、35質量%過酸化水素水を15.26質量部配合した水溶液178質量部を、約30分かけて攪拌しながら混合した(過酸化水素水の混合に伴って被処理液のpHは上昇することになるが、約20質量%酢酸水溶液を混合することで、pH範囲を10以上11以下に調整した。)。その後、約20質量%酢酸水溶液を徐々に混合し、被処理液のpHが漸次11から7になるように調整した。以上によりケラチン誘導体溶液を得た。
Oxidant mixing step While stirring the liquid to be treated after the reduction step, 178 parts by mass of an aqueous solution containing 15.26 parts by mass of 35% by mass hydrogen peroxide was mixed with the liquid while stirring over about 30 minutes. (The pH of the liquid to be treated increased with the mixing of the hydrogen peroxide solution, but the pH range was adjusted to 10 or more and 11 or less by mixing an aqueous solution of about 20% by mass acetic acid.) Then, about 20 mass% acetic acid aqueous solution was mixed gradually, and it adjusted so that the pH of a to-be-processed liquid might become 11-7 gradually. Thus, a keratin derivative solution was obtained.

固液分離工程及び回収工程
ケラチン誘導体溶液をろ過することにより、その溶液の不溶物を除去した。その後、回収した液体部(ろ液)に36質量%塩酸水溶液97.2質量部を配合した水溶液160質量部を添加した。この添加で、ケラチン誘導体溶液のpHを7から4にすることにより、ケラチン誘導体の沈殿を生じさせた。この沈殿を回収、水洗し、固形状のケラチン誘導体を得た。
Solid-liquid separation step and recovery step By filtering the keratin derivative solution, insoluble matters in the solution were removed. Then, 160 mass parts of aqueous solution which mix | blended 97.2 mass parts of 36 mass% hydrochloric acid aqueous solution was added to the collect | recovered liquid part (filtrate). By this addition, the pH of the keratin derivative solution was changed from 7 to 4, thereby causing precipitation of the keratin derivative. This precipitate was recovered and washed with water to obtain a solid keratin derivative.

加熱工程
回収工程で得た固形状ケラチン誘導体が1質量%、かつ、2−アミノ−2−メチル−1−プロパノールでpH8とした水溶液を、85℃で5時間加熱した。その液を室温に冷却した後に、ろ過し、加水分解ケラチン誘導体の水溶液を得た。
Heating Step An aqueous solution in which the solid keratin derivative obtained in the recovery step was 1% by mass and the pH was 8 with 2-amino-2-methyl-1-propanol was heated at 85 ° C. for 5 hours. The liquid was cooled to room temperature and then filtered to obtain an aqueous solution of a hydrolyzed keratin derivative.

後処理剤の調製は、上記加熱工程で得られた加水分解ケラチン誘導体1質量%、1,3−ブチレングリコール3質量%、フェノキシエタノール1質量%、ラウリルジメチルアミノ酢酸ベタイン3質量%及び水(残部)を配合することにより行った。そして、後述の加水分解ケラチン誘導体の毛髪への浸透性の確認のために、後処理剤にFTSC−MESを添加し、ゲルろ過カラムにより未反応のFTSCを除去した。そのFTSC−MESは、1.065質量部の2−(N−Morpholino)ethanesulfonic Acid(MES)を40質量部の水に溶解させた液に、0.2M−NaOH水溶液を滴下することにより、pH5.5のMES水溶液を調製し、MES水溶液中に、0.00042質量部の蛍光色素Fluorescein−5−thiosemicarbazide(FTSC)を溶解させ、水を加えて全量約50質量部とすることで調製したものである。 The preparation of the post-treatment agent was 1% by mass of the hydrolyzed keratin derivative obtained in the heating step, 3% by mass of 1,3-butylene glycol, 1% by mass of phenoxyethanol, 3% by mass of lauryldimethylaminoacetic acid betaine and water (remainder). It was performed by blending. And in order to confirm the permeability of the hydrolyzed keratin derivative described later to the hair, FTSC-MES was added to the post-treatment agent, and unreacted FTSC was removed by a gel filtration column . The FTSC-MES has a pH of 5 by adding a 0.2M NaOH aqueous solution dropwise to a solution obtained by dissolving 1.065 parts by mass of 2- (N-Morpholino) ethansulfuric Acid (MES) in 40 parts by mass of water. Prepared by dissolving 0.00042 parts by mass of the fluorescent dye Fluorescein-5-thiosemicarbazide (FTSC) in MES aqueous solution and adding water to a total amount of about 50 parts by mass It is.

(実施例)
酸化染毛剤による染毛履歴がある毛先を含む毛髪を日本人女性から採取し、これに対して、市販のシャンプーによる洗浄処理、エタノール洗浄、水洗、乾燥を順次行い、この毛髪を実施例の毛髪処理対象として準備した。実施例の毛髪処理では、その毛髪を上記の製造した前処理剤に5分間浸漬し、次に、上記FTSC−MESを添加した後処理剤に30分間浸漬した。その後、毛髪を水洗し、乾燥させた。
(Example)
A hair sample containing hair with a history of hair dyeing with an oxidative hair dye is collected from a Japanese woman, and this is subjected to washing with a commercially available shampoo, ethanol washing, washing with water and drying in order. It was prepared as a hair treatment target. In the hair treatment of Examples, the hair was immersed in the prepared pretreatment agent for 5 minutes, and then the FTSC-MES was added and then immersed in the treatment agent for 30 minutes. Thereafter, the hair was washed with water and dried.

(比較例)
前処理剤を水に変更した以外は、実施例と同様にして毛髪処理を行った。
(Comparative example)
The hair treatment was performed in the same manner as in Example except that the pretreatment agent was changed to water.

(浸透性の評価)
実施例及び比較例の毛髪の毛先辺りをミクロトームで切断し、この切断面の蛍光顕微鏡観察(励起光波長:340nm)を行った。図1は、実施例の切断面の蛍光顕微鏡観察結果を示す撮影画像であり、図2は、比較例の切断面の蛍光顕微鏡観察結果を示す撮影画像である。図1及び図2に示す通り、比較例の撮影画像では切断面全体に均一性ある蛍光を確認できる一方で(図2参照)、実施例では中心部に向けて蛍光が弱まっている(図1参照)。つまり、前処理剤を使用した実施例の毛髪処理では、加水分解ケラチン誘導体の毛髪内部への浸透が抑えられていた。
(Evaluation of permeability)
The hair tips of Examples and Comparative Examples were cut with a microtome, and the cut surface was observed with a fluorescence microscope (excitation light wavelength: 340 nm). FIG. 1 is a photographed image showing the result of observation of the cut surface of the example with a fluorescence microscope, and FIG. 2 is a photographed image showing the result of observation of the cut surface of the comparative example with a fluorescence microscope. As shown in FIG. 1 and FIG. 2, while in the captured image of the comparative example, uniform fluorescence can be confirmed over the entire cut surface (see FIG. 2), in the example, the fluorescence is weakened toward the center (FIG. 1). reference). That is, in the hair treatment of the example using the pretreatment agent, the penetration of the hydrolyzed keratin derivative into the hair was suppressed.

Claims (4)

タンニン酸が配合された前処理剤と、
加水分解ケラチン又は加水分解ケラチン誘導体が配合された後処理剤と、を備えることを特徴とする多剤式毛髪処理剤。
A pretreatment agent containing tannic acid,
And a post-treatment agent containing hydrolyzed keratin or hydrolyzed keratin derivative.
前記前処理剤におけるタンニン酸として、加水分解性タンニンが配合された請求項1に記載の多剤式毛髪処理剤。   The multi-component hair treatment agent according to claim 1, wherein hydrolyzable tannin is blended as tannic acid in the pretreatment agent. 前記後処理剤における加水分解ケラチン誘導体として、下記式(I)〜(III)で表される構造及びこれらの構造の塩から選ばれた単位を有する側鎖基を一種又は二種以上備えるものが配合された請求項1又は2に記載の多剤式毛髪処理剤。
−S−S−(CH)n−COOH (I)
(式(I)中、nは1又は2である。)
−S−S−CH(CH)−COOH (II)
−S−S−CH(COOH)−CH−COOH (III)
As the hydrolyzed keratin derivative in the post-treatment agent, one having one or more side chain groups having units selected from the structures represented by the following formulas (I) to (III) and salts of these structures: The multi-component hair treatment agent according to claim 1 or 2, which is blended.
-S-S- (CH 2) n -COOH (I)
(In the formula (I), n is 1 or 2.)
-S-S-CH (CH 3 ) -COOH (II)
-S-S-CH (COOH) -CH 2 -COOH (III)
タンニン酸が配合された前処理剤を毛髪に塗布する前処理工程と、
前記前処理工程後に、加水分解ケラチン又は加水分解ケラチン誘導体が配合された後処理剤を毛髪に塗布する後処理工程と、
を備えることを特徴とする毛髪処理方法。
A pretreatment step of applying a pretreatment agent containing tannic acid to the hair;
After the pretreatment step, a posttreatment step of applying to the hair a posttreatment agent containing hydrolyzed keratin or hydrolyzed keratin derivative; and
A hair treatment method comprising:
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