JPS61172807A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPS61172807A
JPS61172807A JP1231185A JP1231185A JPS61172807A JP S61172807 A JPS61172807 A JP S61172807A JP 1231185 A JP1231185 A JP 1231185A JP 1231185 A JP1231185 A JP 1231185A JP S61172807 A JPS61172807 A JP S61172807A
Authority
JP
Japan
Prior art keywords
protein
cosmetic
high polymer
skin
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP1231185A
Other languages
Japanese (ja)
Other versions
JPH0514682B2 (en
Inventor
Masao Motoki
本木 正雄
Noriki Nio
式希 丹尾
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP1231185A priority Critical patent/JPS61172807A/en
Publication of JPS61172807A publication Critical patent/JPS61172807A/en
Publication of JPH0514682B2 publication Critical patent/JPH0514682B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • 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
    • 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
    • A61K8/645Proteins of vegetable origin; Derivatives or degradation products 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
    • A61K8/64Proteins; 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
    • A61Q19/00Preparations for care of the skin

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)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:A cosmetic, containing a crosslinked proteinaceous high polymer obtained by reacting transglutaminase with protein in a liquid, and having good humectant property and remarkably improved extensibility. CONSTITUTION:A cosmetic obtained by incorporating a crosslinked high polymer prepared by reacting transglutaminase with protein, e.g. vegetable protein such as defatted oil seed, or animal protein such as milk protein or gelatin collagen, in the form of a mixture with water, oil-in-water type or water-in-oil type emulsion to give a highly viscous material or gelatinous material when the liquid contains >=2wt%, preferably >=5wt% protein or solutional material when the liquid contains <=2wt% protein with a cosmetic, etc. The amount of the crosslinked high polymer is 5-10% expressed in terms of dry material. The crosslinked high polymer incorporated with the cosmetic imparts moderate moisture to the skin or hair, and the skin or hair surface can be protected. EFFECT:Stable with prolonged action.

Description

【発明の詳細な説明】 本発明は液体中でトランスグルタミナーゼを蛋白質に作
用させることにより、得られた蛋白質の架橋高分子化物
を含有してなる保湿効果の優れた化粧料に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cosmetic with excellent moisturizing effects, which contains a crosslinked polymer of protein obtained by allowing transglutaminase to act on protein in a liquid.

従来の技術 化粧品においては皮膚又は頭髪表面の水分を一定に保ち
、皮膚又は毛髪表面を保護する目的で保湿効果を有する
湿潤剤を配合するのが常である。
Conventional cosmetics usually contain humectants that have a moisturizing effect in order to maintain a constant level of moisture on the skin or hair surface and protect the skin or hair surface.

このような化粧品としては化粧水、クリーム、ノ4ツク
剤などの基礎化粧品、7アンデーシ冒ン、口紅類、メイ
クアップ製品などの仕上げ化粧品、ヘアーコンディジ1
ナー、ヘアークリームなどの頭髪用化粧品等があり、b
ずれも湿潤剤を配合し、皮膚表面に潤いを与えることK
より皮膚の健康及び衛生を保持し生理機能を扶助すると
共に美容上の効果をもたせている。一方頭髪用化粧品に
あっては毛髪表面に潤いを与えることによりて、毛髪の
表面を滑らかにし、切れ毛、枝毛を防止し、静電気の帯
電を防止し、毛髪のパサツキ、はこりの付着を防いでい
る。このような目的のために用いられる湿潤剤は一般に
は蛋白加水分解物、DL−2−ピロリドン−5−カルボ
ン酸、ヒヤルロン酸、有機酸塩、およびレシチンなどが
あり、これらのうち単独で又はいくつかを適宜組合わせ
て使用している。化粧品に用いられる湿潤剤の効果は、
皮膚又は毛髪に常時皮膚又は毛髪に適度の潤いをもたせ
皮膚又は毛髪を健康的に、衛生的に保持することKある
。従って湿潤剤は大気中の湿度の影響を受けずに常に一
定の水分を保持することが望ましく、大気中の湿度の高
い環境下では必要以上に吸湿せず、又大気中の湿度の低
い環境下では吸湿性を有していることが望ましいが現在
このように理想的な湿潤剤はまだ確認されていない。
Such cosmetics include basic cosmetics such as lotions, creams, and creams, finishing cosmetics such as 7-and-a-shine creams, lipsticks, and makeup products, and hair conditioners.
There are hair cosmetics such as nail polish, hair cream, etc.
Both products contain humectants to moisturize the skin surface.
It maintains skin health and hygiene, supports physiological functions, and has cosmetic effects. On the other hand, hair cosmetics moisturize the surface of the hair, making it smooth, preventing hair breakage and split ends, preventing static electricity, and preventing dryness and frizz from forming on the hair. Preventing. Wetting agents used for this purpose generally include protein hydrolysates, DL-2-pyrrolidone-5-carboxylic acid, hyaluronic acid, organic acid salts, and lecithin, which may be used alone or in combination. They are used in appropriate combinations. The effects of humectants used in cosmetics are
To keep the skin or hair healthy and hygienic by always keeping the skin or hair properly moisturized. Therefore, it is desirable for a wetting agent to always maintain a constant level of moisture without being affected by atmospheric humidity, and should not absorb more moisture than necessary in an environment with high atmospheric humidity, and should not absorb moisture in an environment with low atmospheric humidity. Although it is desirable that the wetting agent has hygroscopic properties, such an ideal wetting agent has not yet been identified.

大気中の湿度の影響を受けずに常に一定の水分を保持す
るような湿潤剤は理想的であるが現実には確認されてい
ない。現在、使われている湿潤剤は吸湿性ではあるが、
環境の変化に影響を受は吸湿した水分をさらに増加し友
り、又減少したりし、常時水分を一定に保つ保湿性が充
分でない。
A wetting agent that maintains a constant level of moisture without being affected by atmospheric humidity would be ideal, but it has not been confirmed in reality. Although currently used wetting agents are hygroscopic,
Affected by changes in the environment, the absorbed moisture may further increase or decrease, and the moisture retaining ability to keep the moisture constant at all times is not sufficient.

前記のような化粧品に配合された湿潤剤として具有しな
ければならない性状を更に前進させる目的で検討を重ね
た結果、液体中でトランスグルタミナーゼを蛋白質に作
用させることにより得られた蛋白質の架橋高分子化物を
含有させることにより、保湿効果が良く著しく伸展性に
優れ九化粧品を得ることを見い出し、本発明を完成する
に至った。
As a result of repeated studies with the aim of further advancing the properties that should be possessed by a humectant added to cosmetics as described above, we have developed a cross-linked polymer of protein obtained by allowing transglutaminase to act on protein in a liquid. The present inventors have discovered that a cosmetic product with a good moisturizing effect and extremely excellent spreadability can be obtained by containing a compound, and the present invention has been completed.

トランスグルタミナーゼ(EC2、3、2、13)は蛋
白質中のりジン残基のε−NH2とグルタミン残基のγ
−カルデキシアミド基間のアシル転移反応を触媒し、ε
−(γ−グルタミル)リジル架橋を形成させるCa  
依存性の酵素であることが知られている( J、E、F
olk and J、S、Finla!son ”Ad
vancesin Protein Chemistr
y″vol 31. ed、 by C,B。
Transglutaminase (EC2, 3, 2, 13) consists of ε-NH2 of lysine residues and γ of glutamine residues in proteins.
-catalyzes the acyl transfer reaction between caldexamide groups, and
-Ca that forms a (γ-glutamyl)lysyl bridge
It is known to be a dependent enzyme (J, E, F
olk and J, S, Finla! son” Ad
vancein Protein Chemistry
y″vol 31. ed, by C,B.

AnflnI!en  at  ml、Academi
c  Press  Inc、New York197
7)。この酵素は血液中(血液凝固因子庫 @Factor )(lla″)、毛のう、脳、水晶体
、肝酔といった各種臓器に存在し1モルモット肝臓より
Connellanらの方法(J、Blol、 Che
m、 2461093(1971) )に従って調製さ
れたものが好適である。
AnflnI! en at ml, Academy
c Press Inc, New York 197
7). This enzyme exists in various organs such as the blood (blood coagulation factor storehouse @Factor) (lla''), hair follicle, brain, crystalline lens, and hepatotoxicity.
Preferably, those prepared according to J. M., 2461093 (1971)) are suitable.

実際の調選例は特開昭58−149645号に例示され
る。
An example of actual tuning is exemplified in Japanese Patent Laid-Open No. 149645/1983.

基質となるタンパク質は、リジン残基及びグルタミン残
基を有し、上述の酵素の触媒をうけるものであれば、そ
の起源、性状に制約されるものではなく植物性蛋伯質、
動物性蛋白質などいかなるものでも使用できる。植物性
蛋白質としては油糧種子の脱脂物及びそれらより分離し
た蛋白質を挙げることが出来る。また動物性蛋白質とし
ては乳蛋白質、ゼラチンコラ−ダン等を例示することが
できる。これらの蛋白質の2重量%以上好ましくは5重
量係以上の液体であれば、トランスグルタミナーゼの添
加により高粘性物、あるいはrル状物が形成され、2重
量%以下であれば、溶液状の架橋高分子化物が得られる
。トランスグルタミナーゼは蛋白IIに対して0.5二
二、ト以上添加、反応溶液の声は6ないしは9に調整し
、又5mM程度のC& を添加させてインキュベート(
20〜40℃)すると架橋高分子化物ないしはrル状物
を得ることができる。この蛋白含有溶液は単に蛋白質と
水との混合物に限らず、蛋白質、水及び油脂を混合した
水中油型又は油中水型エマルジ璽ンであってもよく、各
種塩類、澱粉、多糖類、香料、保湿剤、着色料などもト
ランスグルタミナーゼによる架橋高分子及びrル化を阻
害しない範囲で適宜選択して添加することができる。
The protein that serves as the substrate is not limited by its origin or properties, as long as it has lysine residues and glutamine residues and can be catalyzed by the enzymes mentioned above, and may include vegetable proteins,
Any animal protein can be used. Examples of vegetable proteins include defatted oilseed products and proteins separated from them. Examples of animal proteins include milk protein, gelatin colladan, and the like. If the liquid contains more than 2% by weight of these proteins, preferably more than 5% by weight, the addition of transglutaminase will form a highly viscous or ripple-like substance, and if it is less than 2% by weight, solution-like crosslinking will occur. A polymerized product is obtained. Transglutaminase was added at least 0.5 to protein II, the volume of the reaction solution was adjusted to 6 or 9, and approximately 5 mM C& was added and incubated (
(20 to 40°C), a crosslinked polymeric product or a rolled product can be obtained. This protein-containing solution is not limited to a simple mixture of protein and water, but may also be an oil-in-water type or water-in-oil type emulsion containing a mixture of protein, water, and oil, as well as various salts, starches, polysaccharides, and fragrances. , a moisturizing agent, a coloring agent, and the like can be appropriately selected and added within a range that does not inhibit the crosslinked polymer and phosphorization by transglutaminase.

又蛋白質の種類と量を調整することによって架橋高分子
化物の架橋度を変えることができこれによ〕、生成する
ダルの物性及び含水量をそれぞれの目的と用途に応じて
変えることができる。
Furthermore, by adjusting the type and amount of protein, the degree of crosslinking of the crosslinked polymer can be changed, and thereby the physical properties and water content of the resulting dal can be changed depending on the purpose and use.

このようにして得られた蛋白架橋高分子化物は食品用と
しても供せられるものであるので、化粧品用として用い
た場合にも皮膚及び粘膜への刺激性もなく、アレルギー
性の心配がなく、極めて安釜性の高い湿潤剤が得られる
The protein cross-linked polymer obtained in this way can also be used for food, so when used for cosmetics, there is no irritation to the skin or mucous membranes, and there is no risk of allergies. A wetting agent with extremely high potability can be obtained.

この架橋高分子化物及びゲル化物をそのまま又はこれを
乾燥させた形態で目的とする用途、形態に合わせて油脂
、他薬剤、柔軟剤、染料、香料、界面活性剤、保湿剤等
を配合して乳化混練して化粧料用配合基材とすることが
可能である。蛋白架橋高分子化物の添加量は乾物換算し
て5〜lO%が適当である。
These crosslinked polymers and gelled products may be used as they are or in dried form, and may be blended with oils and fats, other chemicals, softeners, dyes, fragrances, surfactants, humectants, etc., depending on the intended use and form. It can be emulsified and kneaded to form a formulation base for cosmetics. The appropriate amount of the protein crosslinked polymer added is 5 to 10% in terms of dry matter.

作用 かかる蛋白架橋高分子化物を化粧品に配合すると皮膚又
は毛髪に適度な湿り気を与え皮膚及び毛髪表面を保護す
ることができる。さらに蛋白質の種類及び量を変えるこ
とにより異った保湿性があり、かつ、これらを配合する
ことにより、それぞれの目的と用途に合り危化粧料を得
ることができ発明の効果 かくして得られた化粧品の特徴を列記すると次の通りで
ある。
Effect: When such protein crosslinked polymers are blended into cosmetics, they can provide appropriate moisture to the skin or hair and protect the skin and hair surfaces. Furthermore, by changing the type and amount of protein, different moisturizing properties can be obtained, and by blending these together, it is possible to obtain hazardous cosmetics suitable for each purpose and use, thus achieving the effect of the invention. The characteristics of cosmetics are listed below.

l)クリーム類においては、安定性、光沢性が非常に良
好で皮膚にしっとりとした滑らかな感触を与え、しかも
伸展性に優れる 2)乳液においても安定性が良く、浸透性に優れ皮膚に
湿潤性を与え、かつ持続性があるので保湿効果がある 3)口紅、ファンデージ讐ン類においては顔料の分散力
にすぐれかつのびがよく、とれにくく持続性がある 4)クリームあるいは乳液状で手に塗布し、やや乾燥さ
せると薄くコーティングされ皮膚にfltされる次めに
、水洗作業等による手あれを軽減させることができる。
l) In creams, it has very good stability and gloss, giving a moist and smooth feel to the skin, and has excellent spreadability.2) In emulsions, it has good stability and has excellent permeability and moisturizes the skin. 3) Lipsticks and foundations have excellent pigment dispersibility and spread well, and are difficult to remove and have a long-lasting effect. 4) Cream or emulsion-like cream or emulsion that can be used on the hands. When applied to the skin and allowed to dry slightly, a thin coating is applied to the skin, which can reduce hand roughness caused by washing with water, etc.

以下、実施例により具体的に説明する。Hereinafter, this will be explained in detail using examples.

実施例1 特開昭58−149645号の実施例2に記載された方
法により調製された牛乳蛋白αs1−カゼインを5 m
M CaCl2.20 mMジチオスレイトール(DT
T)含有のO,l M )リスー塩酸バッファー(pH
7、6) K O,5%になるように溶解し、これに特
開昭58−149645号の実施例1に記載された方法
により調製されたトランスグルタミナーゼを蛋白質11
1#9に対して0.05unit加え、37℃で30分
間インキュベートし反応させた。反応終了後、透析ある
いはミリポアフィルタ−で脱塩し、凍結乾燥し粉末状の
白色架橋高分子化物を得た(蛋白収率98チ)。この白
色粉末5チ、デロデュウ100(味の素@)製配合湿潤
剤)3チ、トリエタノールアミン0.5%、水70.5
 %を水相とし、流動パラフィン3チ、スダアリン酸8
チ、イソデロビルノルミテート3%、水添ラノリン2チ
、グリセリンモノステアレート(自己乳化W)3%’t
−油相とし混練しバニシングクリームを調製した。上記
の処方でトランスグルタミナーゼによる架橋高分子化物
の粉末囚の代りに未反応のα81−カゼインを同量配合
したもの(B)を各々調製して、男子20人、女子20
人計略0名の18〜25才までの成人に対してブライン
ドで官能検査を行なった。その結果を次表に示す。
Example 1 5 m of milk protein αs1-casein prepared by the method described in Example 2 of JP-A-58-149645
M CaCl2.20 mM dithiothreitol (DT
T) Containing O, l M) Li-HCl buffer (pH
7,6) Protein 11 was dissolved in KO to a concentration of 5%, and transglutaminase prepared by the method described in Example 1 of JP-A-58-149645 was added to the solution.
0.05 unit was added to 1#9 and incubated at 37°C for 30 minutes to react. After the reaction was completed, the product was desalted by dialysis or using a Millipore filter, and lyophilized to obtain a powdery white crosslinked polymer (protein yield: 98 cm). 5 grams of this white powder, 3 grams of Derodew 100 (wetting agent made by Ajinomoto), 0.5% triethanolamine, 70.5 grams of water
% aqueous phase, 3 tbsp liquid paraffin, 8 tbsp sudaric acid.
3% isoderovir normitate, 2% hydrogenated lanolin, 3% glycerin monostearate (self-emulsifying W)
- A vanishing cream was prepared by kneading the oil phase. 20 boys and 20 girls were prepared with the same amount of unreacted α81-casein (B) in place of the powdered cross-linked polymer by transglutaminase using the above formulation.
A blind sensory test was conducted on 0 adults between the ages of 18 and 25. The results are shown in the table below.

本 表中の数値は最良と判定した人数を示す以上の結果
からトランスグルタミナーゼによる架橋高分子化物を配
合することにより伸展性、湿潤性、使用感のいずれも優
れていることが示された。
The numbers in this table indicate the number of people who judged it to be the best.The above results showed that blending the cross-linked polymer with transglutaminase resulted in excellent spreadability, wettability, and feel when used.

実施例2 市販の牛乳蛋白Na−カゼネー) (5olac :8
成共益(株))を5 mM CaCl2  含む水に1
0%になるように溶解し、これに実施例1で用いたもの
と同じトランスグルタミナーゼを蛋白質1■当v0.1
unit加え、37℃で1時間インキュベートすると系
全体がrル化したものが得られた。このグル状物50チ
に流動ノ4ラフイン13%、セチルアルコール5係、ミ
ツロウ2%、イソプロピルミリステー)51 ソルビタ
ンモノステアレー)1.71?リオキシエチレン(20
)セチルエーテル0.8%、ピログルタミン酸ソーダ3
壬、水19.5%を乳化混練してハンドクリームを得た
。上記配合組成物により皮膚に対して柔軟性、滑らかな
感触を有し、更に持続感のあるクリームを得た。
Example 2 Commercially available milk protein Na-cazene) (5olac:8
Seikyoei Co., Ltd.) in water containing 5 mM CaCl2.
The same transglutaminase used in Example 1 was added to this solution at a volume of 0.1% per protein.
unit was added and incubated at 37° C. for 1 hour to obtain a system in which the entire system was hydrated. 50 parts of this glue-like material, 13% of the liquid, 5 parts of cetyl alcohol, 2% of beeswax, 51 parts of isopropyl myrite, 1.71 parts of sorbitan monosteare) Lioxyethylene (20
) Cetyl ether 0.8%, sodium pyroglutamate 3
A hand cream was obtained by emulsifying and kneading 19.5% water. By using the above-mentioned compounded composition, a cream was obtained which had a soft and smooth feel on the skin and also had a long-lasting feeling.

実施例3 市販のゼラチン(メルク社製)5%溶液100m/に対
し大豆油30*(27,6,9)を混合し超音波処理(
60W、20kHz、3分間)で0/W型に乳化せしめ
これに実施例1で使用のものと同じトランスグルタミナ
ーゼを250ユニツト添加し37℃にインキュベートす
ることによって乳化グル状物を得た。この乳化グル状物
全量に対しスクワレンー固形ノやラフイン−セチルアル
コール−ピログルタミン酸モノオレイン−グリセリンモ
ノステアレート(17:3:2:3:2η〜)の混合物
2711加え更に酸化チタン−カオリン−タルク(B:
s:2w/w)の混合物33I、弁柄−黄酸化鉄−酸化
クロムの混合物2.4 、P 、水14.2.9を加え
、混練乳化しファンデージ1ンクリームを調製した。上
記配合組成物により光沢、キメの良い、又持続性の良い
7アンデーシ曹ンクリームヲ得急。
Example 3 Soybean oil 30* (27,6,9) was mixed with 100ml of a 5% solution of commercially available gelatin (manufactured by Merck & Co., Ltd.) and subjected to ultrasonic treatment (
60 W, 20 kHz, 3 minutes) to obtain a 0/W emulsification, 250 units of the same transglutaminase used in Example 1 was added thereto, and the mixture was incubated at 37°C to obtain an emulsified glutinous product. To the total amount of this emulsified glue, 2711 parts of a mixture of squalene-solid or roughin-cetyl alcohol-monoolein pyroglutamate-glycerol monostearate (17:3:2:3:2η~) was added, and furthermore, titanium oxide-kaolin-talc ( B:
Mixture 33I of Bengara-yellow iron oxide-chromium oxide 2.4, P and 14.2.9 of water were added and kneaded and emulsified to prepare foundation 1 cream. By using the above-mentioned compounded composition, you can quickly obtain a 7-andesin soda cream that has good gloss, texture, and long-lasting properties.

Claims (1)

【特許請求の範囲】[Claims] 液体中でトランスグルタミナーゼを蛋白質に作用させる
ことにより得られた蛋白質の架橋高分子化物を含有して
なる化粧料。
A cosmetic containing a cross-linked polymeric product of protein obtained by allowing transglutaminase to act on protein in a liquid.
JP1231185A 1985-01-25 1985-01-25 Cosmetic Granted JPS61172807A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1231185A JPS61172807A (en) 1985-01-25 1985-01-25 Cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1231185A JPS61172807A (en) 1985-01-25 1985-01-25 Cosmetic

Publications (2)

Publication Number Publication Date
JPS61172807A true JPS61172807A (en) 1986-08-04
JPH0514682B2 JPH0514682B2 (en) 1993-02-25

Family

ID=11801770

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1231185A Granted JPS61172807A (en) 1985-01-25 1985-01-25 Cosmetic

Country Status (1)

Country Link
JP (1) JPS61172807A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5525336A (en) * 1993-02-19 1996-06-11 Green; Howard Cosmetic containing comeocyte proteins and transglutaminase, and method of application
US6267957B1 (en) 1998-01-20 2001-07-31 Howard Green Attaching agents to tissue with transglutaminase and a transglutaminase substrate
WO2009090962A1 (en) * 2008-01-15 2009-07-23 Shiseido Company, Ltd. Microparticle film composition
US7727629B2 (en) 2002-04-11 2010-06-01 Ocean Nutrition Canada Limited Encapsulated agglomeration of microcapsules and method for the preparation thereof
KR101017461B1 (en) 2008-09-08 2011-02-25 주식회사 엘지생활건강 Damaged hair recovering composition containing transglutaminase, amino acid-glue and peptide
US8900630B2 (en) 2002-11-04 2014-12-02 Dsm Nutritional Products Microcapsules having multiple shells and method for the preparation thereof
US9056058B2 (en) 2006-06-05 2015-06-16 Dsm Nutritional Products Microcapsules with improved shells
US10166196B2 (en) 2007-01-10 2019-01-01 Dsm Nutritional Products Ag Vegetarian microcapsules

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5525336A (en) * 1993-02-19 1996-06-11 Green; Howard Cosmetic containing comeocyte proteins and transglutaminase, and method of application
US6267957B1 (en) 1998-01-20 2001-07-31 Howard Green Attaching agents to tissue with transglutaminase and a transglutaminase substrate
US7727629B2 (en) 2002-04-11 2010-06-01 Ocean Nutrition Canada Limited Encapsulated agglomeration of microcapsules and method for the preparation thereof
US8900630B2 (en) 2002-11-04 2014-12-02 Dsm Nutritional Products Microcapsules having multiple shells and method for the preparation thereof
US9056058B2 (en) 2006-06-05 2015-06-16 Dsm Nutritional Products Microcapsules with improved shells
US10166196B2 (en) 2007-01-10 2019-01-01 Dsm Nutritional Products Ag Vegetarian microcapsules
WO2009090962A1 (en) * 2008-01-15 2009-07-23 Shiseido Company, Ltd. Microparticle film composition
EP2229934A1 (en) * 2008-01-15 2010-09-22 Shiseido Company, Ltd. Microparticle film composition
EP2229934A4 (en) * 2008-01-15 2013-07-10 Shiseido Co Ltd Microparticle film composition
US8697136B2 (en) 2008-01-15 2014-04-15 Shiseido Company, Ltd. Transglutaminase crosslinked protein microparticle film composition
JP5562042B2 (en) * 2008-01-15 2014-07-30 株式会社 資生堂 Microparticle film composition
KR101017461B1 (en) 2008-09-08 2011-02-25 주식회사 엘지생활건강 Damaged hair recovering composition containing transglutaminase, amino acid-glue and peptide

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