JP7261591B2 - Hair composition and hair treatment method - Google Patents
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Description
本発明は、毛髪用組成物、及びこの組成物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 composition for hair and a method of treating hair using this composition.
タンパク質を加水分解して得られるペプチドは、毛髪の修復効果やコンディショニング効果を期待して、毛髪用途とされる組成物に配合される。そのようなペプチドの効果の向上や機能の付加を目指した研究開発が行われており、カチオン化、アシル化又はシリル化したペプチド誘導体が知られている。 Peptides obtained by hydrolyzing proteins are incorporated into compositions intended for use in hair, in anticipation of hair repairing and conditioning effects. Research and development aimed at improving the effects of such peptides and adding functions are being carried out, and cationized, acylated or silylated peptide derivatives are known.
また、特許文献1には、毛髪内における修復効果が期待されるペプチド誘導体として、チオグリコール酸塩を用いてカルボキシメチルジスルフィド基をペプチドに導入した変性ペプチドが開示されている。更に、特許文献2には、特許文献1の変性ペプチド、又は当該変性ペプチド以外の所定の変性ペプチドが配合されたpH3.5以上5.5以下の毛髪処理剤において、アニオン界面活性剤をも配合すれば、その変性ペプチドの毛髪内部への浸透性が向上することが開示されている。 Further, Patent Document 1 discloses a modified peptide obtained by introducing a carboxymethyl disulfide group into a peptide using thioglycolate as a peptide derivative expected to have a repairing effect in hair. Furthermore, in Patent Document 2, a hair treatment agent with a pH of 3.5 or more and 5.5 or less, which contains the modified peptide of Patent Document 1 or a predetermined modified peptide other than the modified peptide, also contains an anionic surfactant. It is disclosed that the penetration of the modified peptide into the hair is improved by doing so.
ところで、上記特許文献2は、pH3.5以上5.5以下の組成物における変性ペプチドに関する技術を開示するに留まり、当該変性ペプチドについて、他の有効な毛髪補修を開示するものではない。 By the way, the above-mentioned Patent Document 2 merely discloses a technique relating to a modified peptide in a composition having a pH of 3.5 or more and 5.5 or less, and does not disclose other effective hair repairing methods using the modified peptide.
本発明は、上記事情に鑑み、所定の変性ペプチドによる有効な毛髪補修を可能とする毛髪用組成物、及び当該組成物を使用する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 hair composition that enables effective hair repair with a given modified peptide, and a hair treatment method using the composition.
本発明者が鋭意検討を行った結果、所定の変性ペプチドを配合する組成物のpHを3.5未満に設定すれば、密度向上に優れた毛髪補修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, it was found that if the pH of a composition containing a predetermined modified peptide is set to less than 3.5, hair repair with excellent hair density improvement is possible, and the present invention has been developed. Completed.
すなわち、本発明に係る毛髪用組成物は、pHが3.5未満、かつ、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変性ペプチドが配合されたものである。
-S-S-(CH2)n-COOH (I)
(式(I)中、nは1又は2である。)
-S-S-CH(CH3)-COOH (II)
-S-S-CH(COOH)-CH2-COOH (III)
That is, the composition for hair according to the present invention has a pH of less than 3.5 and a side chain having a unit selected from structures represented by the following formulas (I) to (III) and salts of these structures Modified peptides having one or more groups are blended.
—S—S—(CH 2 )n—COOH (I)
(In formula (I), n is 1 or 2.)
—S—S—CH(CH 3 )—COOH (II)
—S—S—CH(COOH)—CH 2 —COOH (III)
本発明に係る毛髪用組成物のpHは、3.0未満が良い。pH3.0未満であれば、変性ペプチドの水中分散性に優れるから、毛髪内への浸透性の向上が期待される。 The pH of the hair composition according to the present invention is preferably less than 3.0. If the pH is less than 3.0, the denatured peptide is excellent in dispersibility in water, and an improvement in penetration into the hair is expected.
本発明に係る毛髪用組成物において、アニオン界面活性剤は1質量%以下配合又は無配合が良い。1質量%以下又は無配合であると、毛髪内への変性ペプチドの定着性の向上が期待される。 In the composition for hair according to the present invention, it is preferable that the anionic surfactant is blended in an amount of 1% by mass or less or not blended. If it is 1% by mass or less or if it is not blended, it is expected that the fixation of the denatured peptide into the hair will be improved.
本発明に係る毛髪用組成物は、酸性染料が配合されたものが良い。本発明の毛髪用組成物のpHは3.5未満であるから、酸性染料の染毛性は優れる。 The composition for hair according to the present invention preferably contains an acid dye. Since the pH of the hair composition of the present invention is less than 3.5, the acid dye has excellent hair dyeing properties.
本発明に係る毛髪処理方法は、本発明に係る毛髪用組成物を毛髪に塗布した後、水又はpHが3.5以上の組成物を前記毛髪に接触させるものである。本発明に係る毛髪用組成物における変性ペプチドは、pH3.5未満で水中分散性に優れるから毛髪内部に高浸透し、水又はpH3.5以上の組成物との接触により、変性ペプチドが毛髪において凝集することで、変性ペプチドの定着性が向上し、毛髪密度が高まると考えられる。 In the hair treatment method according to the present invention, after applying the hair composition according to the present invention to the hair, water or a composition having a pH of 3.5 or higher is brought into contact with the hair. The modified peptide in the composition for hair according to the present invention has excellent dispersibility in water at a pH of less than 3.5, so that it penetrates into the hair at a high level. Aggregation is thought to improve fixation of the denatured peptide and increase hair density.
本発明に係る毛髪用組成物によれば、pHが3.5未満に設定されるから、所定の変性ペプチドによる毛髪密度の向上が優れる。 According to the composition for hair according to the present invention, since the pH is set to less than 3.5, the hair density is excellently improved by the predetermined modified peptide.
また、本発明に係る毛髪処理方法によれば、毛髪に塗布される所定の変性ペプチドが配合された毛髪用組成物のpHが3.5未満に設定されるから、毛髪密度の向上が優れる。 Moreover, according to the hair treatment method of the present invention, the pH of the hair composition containing the predetermined modified peptide is set to be less than 3.5, so that the hair density is excellently improved.
本発明の実施形態に基づき、本発明を以下に説明する。
(毛髪用組成物)
本実施形態に係る毛髪用組成物は、所定pHであり、水及び所定の変性ペプチドが配合されたものである(水の配合量は、例えば70質量%以上)。また、本実施形態の毛髪用組成物には、使用目的に応じて、公知の毛髪用組成物原料が任意に配合される。
The present invention will be described below based on the embodiments of the present invention.
(Composition for hair)
The composition for hair according to the present embodiment has a predetermined pH and contains water and a predetermined modified peptide (the amount of water is, for example, 70% by mass or more). In addition, the composition for hair according to the present embodiment is optionally blended with known ingredients for the composition for hair according to the purpose of use.
pH
本実施形態の毛髪用組成物のpHは、25℃において、3.5未満であり、3.0未満が良く、2.8未満が好ましく、2.6未満がより好ましく、2.5未満が更に好ましい。3.5未満であれば、配合される所定の変性ペプチドによる毛髪密度向上に優れる。この密度向上は、pH3.5未満であれば所定の変性ペプチドの水中分散性が高まるから、当該変性ペプチドが毛髪内に浸透し易くなるためと考えられる。なお、本実施形態の毛髪用組成物のpHの下限は、特に限定されるものではないが、例えば2.0である。
pH
The pH of the hair composition of the present embodiment is less than 3.5, preferably less than 3.0, preferably less than 2.8, more preferably less than 2.6, and less than 2.5 at 25°C. More preferred. If it is less than 3.5, it is excellent in hair density improvement by the predetermined modified peptide to be blended. This increase in density is considered to be due to the fact that when the pH is less than 3.5, the dispersibility of a given modified peptide in water increases, and the modified peptide easily penetrates into the hair. The lower limit of the pH of the hair composition of the present embodiment is not particularly limited, but is, for example, 2.0.
変性ペプチド
本実施形態の毛髪用組成物には、所定の変性ペプチドが配合される。この変性ペプチドは、2以上のアミノ酸のペプチド結合によって形成された主鎖と、この主鎖に結合する側鎖基を備える。
Modified Peptide The hair composition of the present embodiment contains a predetermined modified peptide. The modified peptide comprises a backbone formed by peptide bonds of two or more amino acids and side groups attached to the backbone.
本実施形態の変性ペプチドの上記主鎖は、特に限定されない。この主鎖の例としては、システインを構成アミノ酸の一種としているペプチドの主鎖と同じものが挙げられる。また、システインを構成アミノ酸の一種としているペプチドの例としては、ケラチン、カゼインが挙げられる。ケラチンは、天然物由来のペプチドの中でもシステイン比率が高いものとして知られており、当該変性ペプチドが効率よく得られる原料となる。かかる観点から、変性ペプチドの主鎖はケラチンの主鎖と同じものが好適である。 The main chain of the modified peptide of this embodiment is not particularly limited. An example of this main chain is the same as the main chain of peptides in which cysteine is one of the constituent amino acids. Examples of peptides containing cysteine as one of the constituent amino acids include keratin and casein. Keratin is known to have a high cysteine ratio among peptides derived from natural products, and is a raw material from which the modified peptide can be efficiently obtained. From this point of view, the main chain of the modified peptide is preferably the same as that of keratin.
上記変性ペプチドは、下記式(I)で表される構造を有する側鎖基、下記式(I)で表される構造の塩を有する側鎖基、下記式(II)で表される構造を有する側鎖基、下記式(II)で表される構造の塩を有する側鎖基、下記式(III)で表される構造を有する側鎖基、下記式(III)で表される構造の塩を有する側鎖基から選ばれる側鎖基を一種又は二種以上備える。
-S-S-(CH2)n-COOH (I)
(式(I)中、nは1又は2である。)
-S-S-CH(CH3)-COOH (II)
-S-S-CH(COOH)-CH2-COOH (III)
The modified peptide has a side chain group having a structure represented by the following formula (I), a side chain group having a salt having a structure represented by the following formula (I), and a structure represented by the following formula (II). a side chain group having a salt of the structure represented by the following formula (II), a side chain group having a structure represented by the following formula (III), a structure represented by the following formula (III) One or two or more side chain groups selected from salt-containing side chain groups are provided.
—S—S—(CH 2 )n—COOH (I)
(In formula (I), n is 1 or 2.)
—S—S—CH(CH 3 )—COOH (II)
—S—S—CH(COOH)—CH 2 —COOH (III)
上記式(I)で表される構造の塩、式(II)で表される構造の塩、式(III)で表される構造の塩は、それぞれ、カルボキシラートアニオンとカチオンとのイオン結合体である。そのカチオンとなる単位としては、例えば、NH4などのアンモニウム;Na、Kなどの金属原子;が挙げられる。 The salt having the structure represented by formula (I), the salt having the structure represented by formula (II), and the salt having the structure represented by formula (III) are each an ionic combination of a carboxylate anion and a cation. is. Examples of units that become cations include ammonium such as NH4 ; metal atoms such as Na and K;
上記変性ペプチドの毛髪内部への浸透性は、分子量が小さいほど高く、分子量が大きいほど低い。この観点から、上記変性ペプチドの分子量は、70000以下が良く、50000以下が好ましく、30000以下がより好ましい。同分子量の下限は、特に限定されないが、例えば10000である。ここで、変性ペプチド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)による変性ペプチド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、変性ペプチドの分子量とみなして採用する。 The penetrability of the modified peptide into the inside of the hair is higher when the molecular weight is smaller, and lower when the molecular weight is higher. From this point of view, the molecular weight of the modified peptide is preferably 70,000 or less, preferably 50,000 or less, and more preferably 30,000 or less. Although the lower limit of the molecular weight is not particularly limited, it is 10,000, for example. Here, the molecular weight of the denatured peptide is calculated from the relative distance between the denatured peptide band and the molecular weight marker band by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE method). considered and adopted.
本実施形態の毛髪用組成物における上記変性ペプチドの配合量の下限は、特に限定されないが、変性ペプチドによる毛髪密度向上の観点から、例えば0.001質量%が良く、0.005質量%が好ましく、0.01質量%がより好ましく、0.1質量%が更に好ましい。一方、変性ペプチド配合量の上限は、多量配合によるコスト上昇抑制の観点から、5質量%が良く、3質量%が好ましく、2質量%がより好ましく、0.5質量%が更に好ましい。 The lower limit of the content of the modified peptide in the composition for hair of the present embodiment is not particularly limited, but from the viewpoint of improving hair density by the modified peptide, it is preferably 0.001% by mass, preferably 0.005% by mass. , more preferably 0.01% by mass, and even more preferably 0.1% by mass. On the other hand, the upper limit of the modified peptide content is preferably 5% by mass, preferably 3% by mass, more preferably 2% by mass, and still more preferably 0.5% by mass, from the viewpoint of suppressing cost increases due to blending in a large amount.
本実施形態の上記変性ペプチドは、例えば、特許第5798741号に開示されるような公知の製造方法により製造することができる。 The modified peptide of the present embodiment can be produced by a known production method such as that disclosed in Japanese Patent No. 5798741, for example.
任意原料
本実施形態の毛髪用組成物には、上記の通り、使用目的に応じて、公知の毛髪用組成物原料が任意に配合される。この任意原料は、アニオン界面活性剤、カチオン界面活性剤、両性界面活性剤、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、染料、香料、防腐剤、金属イオン封鎖剤、紫外線吸収剤などである。
Optional Ingredients As described above, the hair composition of the present embodiment is arbitrarily blended with known hair composition ingredients depending on the purpose of use. The optional raw materials include anionic surfactants, cationic surfactants, amphoteric surfactants, alcohols, polyhydric alcohols, sugars, ester oils, fats and oils, fatty acids, hydrocarbons, waxes, silicones, polymer compounds, amino acids, animal and plant extracts. substances, substances derived from microorganisms, inorganic compounds, dyes, fragrances, preservatives, sequestering agents, ultraviolet absorbers, and the like.
本実施形態の毛髪用組成物にアニオン界面活性剤を配合する場合、カルボン酸系アニオン界面活性剤、スルホン酸系アニオン界面活性剤、硫酸系アニオン界面活性剤、リン酸系アニオン界面活性剤などの公知のアニオン界面活性剤から選ばれた一種又は二種以上が配合される。本実施形態の毛髪用組成物におけるアニオン界面活性剤の配合量は、1質量%以下が良く、0.5質量%以下が好ましく、0.1質量%以下がより好ましく、0.05質量%以下が更に好ましい。本実施形態の変性ペプチドはpH3.5以上で凝集し易くなるので、本実施形態の毛髪用組成物を塗布した後の毛髪に対して、水又はpH3.5以上の組成物を接触させれば、毛髪における変性ペプチドの凝集定着を期待できるが、アニオン界面活性剤はその凝集を阻害する場合があるから、本実施形態の毛髪用組成物におけるアニオン界面活性剤の配合量は1質量%以下が良い(アニオン界面活性剤が無配合であれば、同界面活性剤による変性ペプチドの凝集定着を妨げる虞はない。)。 When blending an anionic surfactant in the composition for hair of the present embodiment, carboxylic acid-based anionic surfactants, sulfonic acid-based anionic surfactants, sulfate-based anionic surfactants, phosphoric acid-based anionic surfactants, etc. One or two or more selected from known anionic surfactants are blended. The content of the anionic surfactant in the hair composition of the present embodiment is preferably 1% by mass or less, preferably 0.5% by mass or less, more preferably 0.1% by mass or less, and 0.05% by mass or less. is more preferred. Since the modified peptide of the present embodiment easily aggregates at pH 3.5 or higher, if water or a composition having a pH of 3.5 or higher is brought into contact with the hair after application of the hair composition of the present embodiment, However, since the anionic surfactant may inhibit the aggregation, the content of the anionic surfactant in the hair composition of the present embodiment should be 1% by mass or less. Good.
酸性染料による染毛性はpH3.5未満で良好であるから、本実施形態の毛髪用組成物に酸性染料を配合し、染毛料として使用すると良い。その酸性染料としては、例えば、赤色2号(Amaranth)、赤色3号(Erythrosine)、赤色102号(New Coccine)、赤色104号の(1)(Phloxine B)、赤色105号の(1)(Rose Bengal)、赤色106号(Acid Red)、赤色201号(Lithol Rubine B)、赤色227号(Fast Acid Magenta)、赤色230号の(1)(Eosine YS)、赤色230号の(2)(Eosine YSK)、赤色231号(Phloxine BK)、赤色232号(Rose Bengal K)、赤色401号(Violamine R)、赤色502号(Ponceau 3R)、赤色503号(Ponceau R)、赤色504号(Ponceau SX)、赤色506号(Fast Red S)、黄色4号(Tartrazine)、黄色5号(Sunset Yellow FCF)、黄色202号の(1)(Uranine)、黄色202号の(2)(Uranine K)、黄色203号(Quinoline Yellow WS)、黄色402号(Polar Yellow 5G)、黄色403号の(1)(Naphthol Yellow S)、黄色406号(Metanil Yellow)、黄色407号(Fast Light Yellow 3G)、橙色205号(Orange II)、橙色207号(Erythrosine Yellowish NA)、橙色402号(Orange I)、緑色3号(Fast Green FCF)、緑色204号(Pyranine Conc)、緑色205号(Light Green SF Yellowish)、緑色401号(Naphthol Green B)、緑色402号(Guinea Green B)、紫色401号(Alizurol Purple)、青色1号(Brilliant Blue FCF)、青色2号(Indigo Carmine)、青色202号(Patent Blue NA)、青色203号(Patent Blue CA)、青色205号(Alphazurine FG)、褐色201号(Rezorich Brown)、黒色401号(Naphthol Blue Black)が挙げられる。本実施形態の毛髪用組成物における酸性染料の配合量は、特に限定されないが、例えば0.01~5質量%である。 Since the hair dyeing property with an acid dye is good at a pH of less than 3.5, it is preferable to mix an acid dye with the hair composition of the present embodiment and use it as a hair dye. The acid dyes include, for example, Red No. 2 (Amaranth), Red No. 3 (Erythrosine), Red No. 102 (New Coccine), Red No. 104 (1) (Phloxine B), Red No. 105 (1) ( Rose Bengal), Red No. 106 (Acid Red), Red No. 201 (Lithol Rubine B), Red No. 227 (Fast Acid Magenta), Red No. 230 (1) (Eosine YS), Red No. 230 (2) ( Eosine YSK), Red No. 231 (Phloxine BK), Red No. 232 (Rose Bengal K), Red No. 401 (Violamine R), Red No. 502 (Ponceau 3R), Red No. 503 (Ponceau R), Red No. 504 (Ponceau) SX), Red No. 506 (Fast Red S), Yellow No. 4 (Tartrazine), Yellow No. 5 (Sunset Yellow FCF), Yellow No. 202 (1) (Uranine), Yellow No. 202 (2) (Uranine K) , Yellow No. 203 (Quinoline Yellow WS), Yellow No. 402 (Polar Yellow 5G), Yellow No. 403 (1) (Naphthol Yellow S), Yellow No. 406 (Metanil Yellow), Yellow No. 407 (Fast Light Yellow 3G), Orange No. 205 (Orange II), Orange No. 207 (Erythrosine Yellowish NA), Orange No. 402 (Orange I), Green No. 3 (Fast Green FCF), Green No. 204 (Pyranine Conc), Green No. 205 (Light Green SF Yellowish) ), Green No. 401 (Naphthol Green B), Green No. 402 (Guinea Green B), Purple No. 401 (Alizurol Purple), Blue No. 1 (Brilliant Blue FCF), Blue No. 2 (Indigo Carmine), Blue No. 202 (Patent Blue NA), Blue No. 203 (Patent Blue CA), Blue No. 205 (Alphazurine FG), Brown No. 201 (Rezorich Brown), and Black No. 401 (Naphthol Blue Black). The content of the acid dye in the hair composition of the present embodiment is not particularly limited, but is, for example, 0.01 to 5% by mass.
剤型
毛髪用組成物の使用時の剤型は、特に限定されず、例えば、液状、乳液状、ローション状、クリーム状、ワックス状、ゲル状、固形状、フォーム状(泡状)、霧状が挙げられる。
Dosage form The dosage form of the composition for hair is not particularly limited, and examples thereof include liquid, milky lotion, lotion, cream, wax, gel, solid, foam (foam), and mist. is mentioned.
(毛髪処理方法)
本実施形態の毛髪処理方法は、本実施形態の毛髪用組成物を毛髪に塗布した後に、この塗布後の毛髪に水又はpHが3.5以上の組成物(当該組成物における水の配合量は、例えば60質量%以上)を接触させるものである。この接触によるpHの上昇は、変性ペプチドの凝集を促進し、その結果、毛髪における変性ペプチドの定着性が高まると考えられる。
(Hair treatment method)
In the hair treatment method of the present embodiment, after the hair composition of the present embodiment is applied to the hair, water or a composition having a pH of 3.5 or more (the amount of water in the composition) is applied to the hair after application. is, for example, 60% by mass or more). It is believed that the increase in pH due to this contact promotes aggregation of the denatured peptide and, as a result, enhances fixation of the denatured peptide on the hair.
水又はpH3.5以上の組成物を接触させる態様は、例えば、噴霧などによる水又はpH3.5以上の組成物の連続塗布、水洗による本実施形態の毛髪用組成物の除去、が挙げられる。 Examples of contact with water or a composition with a pH of 3.5 or higher include continuous application of water or a composition with a pH of 3.5 or higher by spraying, and removal of the hair composition of the present embodiment by washing with water.
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 The present invention will be described in detail below based on examples, but the present invention is not limitedly interpreted based on the description of these examples.
実施例及び比較例の毛髪用組成物を製造し、これら毛髪用組成物による毛髪処理を行ってから、毛髪密度の測定を行った。詳細は、次の通りである。 After the hair compositions of Examples and Comparative Examples were produced and hair was treated with these hair compositions, the hair density was measured. Details are as follows.
(毛髪用組成物)
成分、成分配合量が下記表1に記載の通りである実施例1、比較例1a~1dの液状毛髪用組成物を製造した(表1における「残部」とは、全量を100質量%とする量である。)。
(Composition for hair)
Liquid hair compositions of Example 1 and Comparative Examples 1a to 1d having the components and their blending amounts as shown in Table 1 below were produced (the "remainder" in Table 1 means the total amount of 100% by mass). quantity.).
表1における変性ペプチド(I)は、上記式(I)で表される側鎖基(n=1)を備える変性ペプチドなどが分散する透明の変性ペプチド(I)液として得たものであり、以下の還元工程、酸化剤混合工程、固液分離工程、回収工程、及び加水分解工程に従い、変性ペプチド(I)液を製造した。 Modified peptide (I) in Table 1 was obtained as a transparent modified peptide (I) solution in which modified peptides having a side chain group (n=1) represented by the above formula (I) were dispersed. A modified peptide (I) solution was produced according to the following reduction step, oxidant mixing step, solid-liquid separation step, recovery step, and hydrolysis step.
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5.0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 process:
Merino wool washed with a neutral detergent and dried was cut into pieces of about 5 mm. 5.0 parts by mass of this wool, 15.4 parts by mass of a 30% by mass sodium thioglycolate aqueous solution and 8.5 parts by mass of a 6 mol/L sodium hydroxide aqueous solution were mixed, and further mixed with water to give a total amount of 150 parts by mass and a pH of 11. was prepared. This liquid to be treated was stirred at 45° C. for 1 hour. Next, water was further mixed to make the total amount 200 parts by mass, left at 45° C. for 2 hours, and then naturally cooled until the liquid temperature reached normal 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、その上昇は約20質量%酢酸水溶液を混合することでpH10以上11以下の範囲に調整した。)。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。
Oxidant mixing process:
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 solution was mixed with the liquid over about 30 minutes with stirring (peroxidation The pH of the liquid to be treated rises with the mixing of hydrogen water, and the rise was adjusted to a range of pH 10 or more and 11 or less by mixing about 20 mass % acetic acid aqueous solution.). After that, about 20% by mass of acetic acid aqueous solution was gradually mixed, and the pH of the liquid to be treated was gradually adjusted from 11 to 7.
固液分離工程及び回収工程:
酸化剤混合工程で得られた液をろ過することによりその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質量部を添加して液のpHを7から3.8にすることにより、変性ペプチド(I)の沈殿を生じさせた。この沈殿を回収、水洗し、固形状の変性ペプチド(I)を得た。
Solid-liquid separation step and recovery step:
The liquid obtained in the oxidizing agent mixing step was filtered to remove insoluble matter from the liquid. After that, 160 parts by mass of an aqueous solution containing 97.2 parts by mass of a 36% by mass hydrochloric acid aqueous solution was added to the collected liquid portion (filtrate) to adjust the pH of the liquid from 7 to 3.8, thereby obtaining a modified peptide (I ) resulted in precipitation. This precipitate was collected and washed with water to obtain a solid denatured peptide (I).
加水分解工程:
回収工程で得た固形状の変性ペプチド(I)を配合し、2-アミノ-2-メチル-1-プロパノールでpH10.5とした水溶液を、80℃で2時間加熱した。この加熱後の水溶液をろ過し、ろ液を変性ペプチド(I)液として得た。当該変性ペプチド(I)液における変性ペプチド(I)は、SDS-PAGE法では、変性ペプチド(I)のバンドが44000の分子量で認められた。
Hydrolysis step:
An aqueous solution containing the solid modified peptide (I) obtained in the recovery step and adjusted to pH 10.5 with 2-amino-2-methyl-1-propanol was heated at 80° C. for 2 hours. The heated aqueous solution was filtered to obtain a filtrate as a modified peptide (I) solution. Denatured peptide (I) in the denatured peptide (I) solution was found to have a denatured peptide (I) band with a molecular weight of 44,000 in the SDS-PAGE method.
(毛髪処理)
50代の日本人女性3名(女性A、女性B、女性C)から毛髪を採取した毛髪を、ミルボン社製シャンプー「ディーセス ノイ ウィローリュクス シャンプー」を使用して洗浄した後、乾燥させた。実施例及び比較例の毛髪用組成物のそれぞれに、乾燥後の各女性の毛髪9本(女性Aの毛髪3本、女性Bの毛髪3本、女性Cの毛髪3本)を30分間浸漬し、浸漬後の毛髪を、精製水で水洗した後、25℃、湿度50%の条件で自然乾燥させた。これら毛髪を0.5mm程度に細断してから、下記毛髪密度の測定を行った。
(hair treatment)
Hair was collected from three Japanese women in their 50s (Female A, Female B, and Female C), washed with Milbon's shampoo "Deese's Neu Willow Luxe Shampoo", and then dried. Nine hairs of each woman after drying (three hairs of woman A, three hairs of woman B, and three hairs of woman C) were soaked in each of the hair compositions of Examples and Comparative Examples for 30 minutes. After the soaked hair was rinsed with purified water, it was naturally dried under the conditions of 25° C. and 50% humidity. After cutting these hairs into pieces of about 0.5 mm, the hair density was measured as described below.
(毛髪密度の測定)
各毛髪処理後の毛髪の30細断片(女性Aの毛髪:10細断片、女性Bの毛髪:10細断片、女性Cの毛髪:10細断片)について、毛髪密度の測定を行った。その測定方法は、特開2016-61664号公報の実施例と同様、密度勾配液体を使用する方法を使用した。
(Measurement of hair density)
The hair density was measured on 30 pieces of hair after each hair treatment (hair of female A: 10 pieces, hair of female B: 10 pieces, hair of female C: 10 pieces). As the measurement method, a method using a density gradient liquid was used as in the example of JP-A-2016-61664.
下表1に、実施例及び比較例の毛髪用組成物の成分及び配合量、毛髪密度の測定結果、毛髪密度比(比較例1aの毛髪を100とした場合の比率)を示す。また、図1に、その毛髪密度比の算出値を表すグラフを示す。
表1において以下の(1)~(3)を確認できる。
(1)実施例1と比較例1bとの対比により、pHが3未満であった実施例1は、pHが3以上である比較例1bよりも、毛髪密度比に優れていたこと(なお、実施例1及び比較例1bの毛髪用組成物は、共に、変性ペプチド(I)が分散し、かつ、変性ペプチド(I)の凝集のないものであった。)。
(2)実施例1とこれよりも毛髪密度比が低い比較例1cとの対比により、pHを3.0未満にするための乳酸が毛髪密度比の差を生じさせたものではないこと。
(3)変性ペプチド(I)を配合した実施例1と羊毛由来加水分解ケラチンを配合した比較例1dとの対比により、実施例1の方が毛髪密度比が高いから、変性ペプチド(I)特有の毛髪密度向上が認められたこと(なお、比較例1dの毛髪用組成物は、羊毛由来加水分解ケラチンの凝集が認められた。)。
In Table 1, the following (1) to (3) can be confirmed.
(1) By comparing Example 1 and Comparative Example 1b, it was found that Example 1, in which the pH was less than 3, was superior to Comparative Example 1b, in which the pH was 3 or more, in terms of hair density ratio. In both the hair compositions of Example 1 and Comparative Example 1b, modified peptide (I) was dispersed and there was no aggregation of modified peptide (I).).
(2) By comparing Example 1 with Comparative Example 1c, which has a lower hair density ratio, the lactic acid used to make the pH less than 3.0 did not cause a difference in the hair density ratio.
(3) By comparing Example 1 containing modified peptide (I) and Comparative Example 1d containing wool-derived hydrolyzed keratin, Example 1 has a higher hair density ratio, and therefore, it is unique to modified peptide (I). (In addition, aggregation of wool-derived hydrolyzed keratin was observed in the hair composition of Comparative Example 1d.).
Claims (5)
-S-S-(CH2)n-COOH (I)
(式(I)中、nは1又は2である。)
-S-S-CH(CH3)-COOH (II)
-S-S-CH(COOH)-CH2-COOH (III) A modified peptide having a pH of less than 3.0 and 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 is blended. A hair composition that is applied to the treated hair .
—S—S—(CH 2 )n—COOH (I)
(In formula (I), n is 1 or 2.)
—S—S—CH(CH 3 )—COOH (II)
—S—S—CH(COOH)—CH 2 —COOH (III)
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010132595A (en) | 2008-12-04 | 2010-06-17 | Nicca Chemical Co Ltd | Hair-treating agent having effect of protecting hair, and damage prevention and hair restoration |
JP2010229106A (en) | 2009-03-27 | 2010-10-14 | Milbon Co Ltd | Hair coloring agent and hair bleach |
JP2012121831A (en) | 2010-12-08 | 2012-06-28 | Milbon Co Ltd | Multi-agent type hair treating agent |
JP2015137242A (en) | 2014-01-21 | 2015-07-30 | 株式会社ミルボン | liquid composition |
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JP2010132595A (en) | 2008-12-04 | 2010-06-17 | Nicca Chemical Co Ltd | Hair-treating agent having effect of protecting hair, and damage prevention and hair restoration |
JP2010229106A (en) | 2009-03-27 | 2010-10-14 | Milbon Co Ltd | Hair coloring agent and hair bleach |
JP2012121831A (en) | 2010-12-08 | 2012-06-28 | Milbon Co Ltd | Multi-agent type hair treating agent |
JP2015137242A (en) | 2014-01-21 | 2015-07-30 | 株式会社ミルボン | liquid composition |
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