JPS60204708A - Humectant - Google Patents

Humectant

Info

Publication number
JPS60204708A
JPS60204708A JP6121684A JP6121684A JPS60204708A JP S60204708 A JPS60204708 A JP S60204708A JP 6121684 A JP6121684 A JP 6121684A JP 6121684 A JP6121684 A JP 6121684A JP S60204708 A JPS60204708 A JP S60204708A
Authority
JP
Japan
Prior art keywords
water
skin
soluble
aqueous solution
humectant
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
JP6121684A
Other languages
Japanese (ja)
Other versions
JPH0557968B2 (en
Inventor
Seiji Noda
野田 誠二
Tomoko Yasumasu
安増 知子
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.)
Lion Corp
Original Assignee
Lion Corp
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 Lion Corp filed Critical Lion Corp
Priority to JP6121684A priority Critical patent/JPS60204708A/en
Priority to GB08506618A priority patent/GB2159408B/en
Priority to DE19853511135 priority patent/DE3511135C2/en
Priority to FR8504702A priority patent/FR2561915A1/en
Publication of JPS60204708A publication Critical patent/JPS60204708A/en
Publication of JPH0557968B2 publication Critical patent/JPH0557968B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • 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
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • 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
    • A61K8/65Collagen; Gelatin; Keratin; 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/735Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair

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)
  • Cosmetics (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は新規な保湿剤、さらに詳しくいえば、特定の水
溶性ケイ素化合物と水溶性高分子物質との組合せから成
る、優れた保湿効果を有する保湿剤に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel moisturizing agent, and more specifically, to a moisturizing agent that has an excellent moisturizing effect and is composed of a combination of a specific water-soluble silicon compound and a water-soluble polymeric substance. .

皮膚は外界と生体との界面にsb、湿度、光線、微生物
、化学物質、機械的刺激などから生体を守シ、水分の蒸
発などを適度に調節して生体の恒常性を保つ働きをして
いる。このうち角質層は皮膚の最外殻にあシ、通常適度
の水分を保持しているが、種々の外的、内的要因によシ
水分を保持できなくなった場合、皮膚は乾燥粗粋を示し
、柔軟性や伸展性が低下して前記の機能を全うしなくな
る。
The skin acts as the interface between the outside world and the living body, protecting the living body from SB, humidity, light, microorganisms, chemicals, mechanical stimuli, etc., and maintaining the homeostasis of the living body by appropriately regulating moisture evaporation. There is. The stratum corneum is the outermost layer of the skin and normally retains a moderate amount of moisture, but when it is no longer able to retain moisture due to various external and internal factors, the skin becomes dry and coarse. This results in a decrease in flexibility and extensibility, and the above-mentioned functions are no longer fulfilled.

このためには、何らかの方法で角質層に水分を補給、保
持させたシ、角質層の水分が過度に蒸発しないようにす
ることが必要で、通常皮膚用剤や化粧料などにはこの目
的で保湿剤が配合されている。
To achieve this, it is necessary to supply and retain moisture in the stratum corneum in some way, and to prevent the moisture in the stratum corneum from evaporating excessively. Contains moisturizer.

このような保湿剤として、従来、プロピレングリコール
、グリセリン、ピロリドンカルボン酸ナトリウム、乳酸
ナトリウム、ソルビットなどが、皮膚に対する親和性や
使用感の点から化粧料中に比較的多量に用いられている
。しかしながら、これらの保湿剤は皮膚に対するペタツ
キ感が生じやすく、その上低湿度での使用においては、
皮膚中から保湿剤配合の化粧料へと逆に水分がとシ込ま
れて、皮膚を乾燥させる場合もあるなどの欠点を有して
いる。
As such humectants, propylene glycol, glycerin, sodium pyrrolidone carboxylate, sodium lactate, sorbitol, and the like have conventionally been used in relatively large amounts in cosmetics from the viewpoint of their affinity for the skin and their feel when used. However, these moisturizers tend to cause a sticky feeling on the skin, and when used at low humidity,
They have the disadvantage that moisture may be drawn into the skin from the skin into cosmetics containing moisturizers, causing the skin to become dry.

また、最近では、皮膚に存在し、保湿効果を有する化合
物として、コンドロイチン硫酸、ヒアルロン酸、ムコタ
ンパク、カロニン硫酸などのムコ多糖類や、コラーゲン
、ポリペブタイドなどが見出され、化粧料などに用いら
れている。しかしながら、これらは皮膚の老化現象をあ
る程度防止しうる効果を有しているものの、保湿効果に
ついては必ずしも十分とはいえない。
Recently, mucopolysaccharides such as chondroitin sulfate, hyaluronic acid, mucoprotein, and caronine sulfate, collagen, and polypeptides have been discovered as compounds that exist in the skin and have a moisturizing effect, and are used in cosmetics. There is. However, although these have the effect of preventing the aging phenomenon of the skin to some extent, their moisturizing effect is not necessarily sufficient.

本発明者らは、このような事情に鑑み、ペタツキ感がな
く、かつ保湿効果の優れた保湿剤を提供すべく鋭意研究
を重ねた結果、シラノール基を含む水溶性ケイ素化合物
と水溶性高分子物質との組合せから成るものが、その目
的に適合しうろことを見出し、この知見に基づいて本発
明を完成するに至った。
In view of these circumstances, the present inventors conducted intensive research to provide a moisturizing agent that does not have a sticky feeling and has an excellent moisturizing effect. It was discovered that a combination of substances is suitable for the purpose, and based on this knowledge, the present invention was completed.

すなわち、本発明は、(勾分子中に少なくとも1個のシ
ラノール基を有するケイ素化合物と■)水溶性高分子物
質との組合せから成る保湿剤を提供するものである。
That is, the present invention provides a humectant comprising a combination of (a) a silicon compound having at least one silanol group in the gradient molecule and (i) a water-soluble polymeric substance.

本発明の保湿剤において(Al成分として用いるケイ素
化合物は、分子中に少なくとも1個のシラノール基を有
するものであシ、このようなものとしては、分子中にケ
イ素原子1個を有するモノシラノール化合物及びケイ素
原子2個以上を有するポリシラノール化合物があるが、
好ましくは分子中にケイ素原子1〜3個を有するシラノ
ール化合物であシ、さらに好ましくは、一般式 %式%() (式中のRは炭素数1〜6のアルキル基、アラルキル基
、アルケニル基、シクロアルキル基又はアルコキシ基で
、2以上のRはたがいに同一でも異なっていてもよ<s
”は0又は1〜3の整数である) で示されるシラノール化合物又はその水酸基の水素原子
の一部が塩基性物質例えばアルカリ金属、アルカリ土類
金属又はアミン類で置換されたシラノエートである。
In the humectant of the present invention, the silicon compound used as the Al component must have at least one silanol group in the molecule, and examples of such compounds include monosilanol compounds having one silicon atom in the molecule. and polysilanol compounds having two or more silicon atoms,
Preferably, it is a silanol compound having 1 to 3 silicon atoms in the molecule, and more preferably a silanol compound having the general formula % (%) (in which R is an alkyl group having 1 to 6 carbon atoms, an aralkyl group, or an alkenyl group). , cycloalkyl group or alkoxy group, two or more R's may be the same or different <s
is 0 or an integer from 1 to 3) or a silanoate in which some of the hydrogen atoms of its hydroxyl group are substituted with a basic substance, such as an alkali metal, an alkaline earth metal, or an amine.

前記一般式(1)で表わされる化合物としては、例えば
シラノール、トリメチルシラノール、ジメチルシランジ
オール、メチルエチルシランジオール、メチルシラント
リオール、トリエチルシラノール、ジエチルシランジオ
ール、エチルシラントリオール、ジ−n−1日ピルシラ
ンジオール、ジイソプロピルシランジオール、ジ−n−
ブチルシランジオール、ジイソブチルシランジオール、
ジーtert−プチルシ2ンジオール、ジアリルシラン
ジオール、トリフェニルシラノール、ジフェニルシラン
ジオール、フェニルシラントリオール、メチルシクロヘ
キシルシランジオール、ジシクロへキシルシランジオー
ルなどが挙げられる。また、ポリシラノール化合物とし
ては、例えばナト2メチルジシロキサン−1,3−ジオ
ール、テトラメチルジシルメチレン−1,3−ジオール
、テトラメチルジシルエチレン−1,4−ジオール、ビ
ス(メチルビニル)ジシロキサンジオールなどが挙げら
れる。
Examples of the compound represented by the general formula (1) include silanol, trimethylsilanol, dimethylsilanediol, methylethylsilanediol, methylsilanetriol, triethylsilanol, diethylsilanediol, ethylsilanetriol, and di-n-1 day pill. Silanediol, diisopropylsilanediol, di-n-
Butylsilanediol, diisobutylsilanediol,
Examples include di-tert-butylsilanediol, diallylsilanediol, triphenylsilanol, diphenylsilanediol, phenylsilanetriol, methylcyclohexylsilanediol, dicyclohexylsilanediol, and the like. Examples of polysilanol compounds include nato-2methyldisiloxane-1,3-diol, tetramethyldisylmethylene-1,3-diol, tetramethyldisylethylene-1,4-diol, and bis(methylvinyl). Examples include disiloxane diol.

これらのシラノール化合物は、一般に不安定で重合しや
すいが、(Bl成分の水溶性高分子物質と組み合わせる
ことによ多安定化される。この安定化の機構については
必ずしも明確ではないが、水溶性高分子物質中の一〇H
基や−NH2基とシラノール化合物中の810Hとの間
に水素結合が形成されて安定化されるものと思われる。
These silanol compounds are generally unstable and easily polymerized, but they become multi-stabilized when combined with a water-soluble polymer substance (Bl component). Although the mechanism of this stabilization is not necessarily clear, water-soluble 10H in polymeric substances
It is thought that a hydrogen bond is formed between the group or -NH2 group and 810H in the silanol compound to stabilize it.

本発明の保湿剤において(B)成分として用いる水溶性
高分子物質としては、分子中に少なくとも1個のヒドロ
キシル基又はアミン基若しくはその両方を有するものが
好ましく、このようなものとしては、例えばムコ多糖類
や水溶性タンパク質などの水溶性生体高分子物質、セル
ロース誘導体、デンプン誘導体、ポリビニルアルコール
などが挙げられ、これらはそれぞれ単独で用いてもよい
し、2種以上組み合わせて用いてもよい。
The water-soluble polymer used as component (B) in the moisturizing agent of the present invention preferably has at least one hydroxyl group or amine group or both in the molecule. Examples include water-soluble biopolymer substances such as polysaccharides and water-soluble proteins, cellulose derivatives, starch derivatives, and polyvinyl alcohol, and each of these may be used alone or in combination of two or more.

前記ムコ多糖類は広義のムコ多糖類を指し、例えば中性
ムコ多糖、ヒアルロン酸、コンドロイチン、コンドロイ
チン硫酸、ヘパリン、ヘパラン硫酸などの酸性ムコ多糖
、ムコタンパク、糖タンパり、糖脂質などが用いられる
。また水溶性タンノくり質としては、例えばタンパク加
水分解物のアミノ基と脂肪酸のカルボキシル基を縮合し
て得られる、リボ−ペプチド、あるいは可溶性コラーゲ
ン、可溶性エラスチン、可溶性ケラチンなどを用いるこ
とができる。セルロース誘導体としては、例えばカルボ
キシメチルセルロース(OMO) 、メチルセルロース
(MC)sヒドロキシエチルセルロース(110)、ヒ
ドロキシグロビルセルロースなどが挙げられ、デンプン
誘導体としては、通常のデンプンより水溶性のものがよ
く、例えば若干加水分解されたデキストリン、デンプン
の酢酸誘導体、リン酸誘導体、ヒドロキシアルキル誘導
体などが挙げられる。
The mucopolysaccharides refer to mucopolysaccharides in a broad sense, and examples include acidic mucopolysaccharides such as neutral mucopolysaccharides, hyaluronic acid, chondroitin, chondroitin sulfate, heparin, and heparan sulfate, mucoproteins, glycoproteins, and glycolipids. As the water-soluble tannin, for example, ribo-peptide obtained by condensing the amino group of a protein hydrolyzate with the carboxyl group of a fatty acid, soluble collagen, soluble elastin, soluble keratin, etc. can be used. Examples of cellulose derivatives include carboxymethylcellulose (OMO), methylcellulose (MC), hydroxyethylcellulose (110), and hydroxyglobilcellulose.As for starch derivatives, those that are more water-soluble than normal starch are preferred, for example, slightly Examples include hydrolyzed dextrin, acetic acid derivatives of starch, phosphoric acid derivatives, and hydroxyalkyl derivatives.

さらにポリビニルアルコールについては、重合度やけん
化度によって水に対する溶解度が異なるが、一般にけん
化度がそれほど高くないもの(約97モルチ以下)を使
用することが望ましい。
Furthermore, the solubility of polyvinyl alcohol in water varies depending on the degree of polymerization and degree of saponification, but it is generally desirable to use one whose degree of saponification is not so high (approximately 97 mole or less).

これらの水溶性高分子物質の中で、ムコ多糖類や水溶性
タンパク質などの水溶性生体高分子物質は、それ自体皮
膚に対して有効な薬理作用を有し、かつ保湿効果も有す
るので好適である。
Among these water-soluble polymer substances, water-soluble biopolymer substances such as mucopolysaccharides and water-soluble proteins are suitable because they themselves have an effective pharmacological effect on the skin and also have a moisturizing effect. be.

本発明の保湿剤においては、(勾成分のシラノール化合
物と(B)成分の水溶性高分子物質との好ましい配合割
合は、重量基準で1:10ないし10:1の範囲で選ば
れる。
In the humectant of the present invention, the preferred blending ratio of the silanol compound as the gradient component and the water-soluble polymer substance as the component (B) is selected in the range of 1:10 to 10:1 on a weight basis.

本発明の保湿剤は、 (A)成分のシラノール化合物を
(B)成分の水溶性高分子物質で安定化することによっ
て得られる。この安定化の方法については、水溶性高分
子物質の水性溶液中にシラノール化合物を配合してもよ
いが、該シラノール化合物は一般に不安定で重合しやす
いので、次に示すような方法を用いることが好ましい。
The humectant of the present invention is obtained by stabilizing the silanol compound (A) with the water-soluble polymer substance (B). As for this stabilization method, a silanol compound may be added to the aqueous solution of the water-soluble polymer substance, but since the silanol compound is generally unstable and easily polymerized, the following method should be used. is preferred.

すなわち、まず比較的安定なシラノエート化合物の水性
溶液を調製し、これに水溶性高分子物質の水性溶液を加
えたのち、H型カチオン交換樹脂などを用いて該シラノ
エート化合物をシラノール化合物に変換することによシ
ラノエ−ト化合物は安定化されて本発明の保湿剤が得ら
れる。
That is, first, a relatively stable aqueous solution of a silanoate compound is prepared, an aqueous solution of a water-soluble polymer substance is added thereto, and then the silanoate compound is converted into a silanol compound using an H-type cation exchange resin or the like. The silanoate compound is stabilized to obtain the humectant of the present invention.

前記シラノエート化合物の水性溶液は、例えば、出発原
料としてノ・ロゲンを含む炭化水素置換シラン誘導体を
用い、このシ2ン誘導体を加水分解して生成した加水分
解物を回収し、この加水分解物を、ケイ素原子1個当シ
、少なくとも1轟量の塩基が存在するような割合でアル
カリ金属水酸化物の水性溶液中に添加する方法〔ジャー
ナル・オプ・ザ・ケミカル’71サイ文ティ(Jour
nal of thechemi、ca180Qiet
7 ) 、第105巻、679ページ〕、ハロゲンを含
む炭化水素置換シラン誘導体を、該誘導体のハロゲンか
ら由来する中和当量に加えて、ケイ素原子1個当シ、少
なくとも1当量の塩基が存在するように調製されたアル
カリ金属水酸化物の水性溶液中に添加する方法、などに
よって調製される。
The aqueous solution of the silanoate compound can be prepared by, for example, using a hydrocarbon-substituted silane derivative containing a silane as a starting material, hydrolyzing this silane derivative, collecting the generated hydrolyzate, and recovering the resulting hydrolyzate. , into an aqueous solution of an alkali metal hydroxide in such a proportion that at least one amount of base is present per silicon atom [Journal of the Chemical '71 Sci.
nal of thechemi, ca180Qiet
7), Vol. 105, p. 679], a halogen-containing hydrocarbon-substituted silane derivative is prepared by adding at least 1 equivalent of a base per silicon atom in addition to the neutralization equivalent derived from the halogen of the derivative. It is prepared by adding it to an aqueous solution of an alkali metal hydroxide prepared as described above.

このようなシラノエート化合物の水性溶液の調製に用い
る出発原料のノーロゲンを含む炭化水素置換シラン誘導
体としては、例えばモノシラノエート化合物の水性溶液
を調製する場合は、四塩化ケイ素、メチルトリクロロシ
ラン、フェニルトリクロロシラン、ジフェニルジクロロ
シラン、ジメチルジクロロシラン、クロロメチルトリク
ロロシラン、トリメチルクロロシラン、クロロフェニル
トリクロロシラン、メチルシ20ヘキシルジクロpシラ
ン、ベンジルトリクロロシランなどが挙げられる。
For example, when preparing an aqueous solution of a monosilanoate compound, silicon tetrachloride, methyltrichlorosilane, and phenyl trichlorosilane are used as starting materials for preparing an aqueous solution of a monosilanoate compound. Examples include chlorosilane, diphenyldichlorosilane, dimethyldichlorosilane, chloromethyltrichlorosilane, trimethylchlorosilane, chlorophenyltrichlorosilane, methylcyclosilane, benzyltrichlorosilane, and the like.

本発明の保湿剤は、例えば通常の整肌、栄養化粧水の他
に、アストリンゼンローション、シェーブローション、
ボディローション、液状パックなどの水系化粧用ローシ
ョン類、栄養クリーム、アイクリーム、ボディクリーム
、ノ・ンドクリーム、マツサージクリーム、コールドク
リーム、エモリエントクリームなどのクリーム類、栄養
乳液、ボディ乳液、ネック乳液、ノ・ンド乳液などの乳
液類、パック類などの皮膚用化粧料に用いられ、さらに
シャンプーやリンスなどの毛髪用化粧料にも用いること
ができる。
The moisturizer of the present invention can be used, for example, in addition to regular skin conditioning and nutritional lotions, astringent lotion, shave lotion,
Water-based cosmetic lotions such as body lotions and liquid packs, creams such as nutritional creams, eye creams, body creams, neck creams, pine surge creams, cold creams, and emollient creams, nutritional emulsions, body emulsions, neck emulsions,・It is used in skin cosmetics such as emulsions such as skin milk lotions and packs, and can also be used in hair cosmetics such as shampoos and conditioners.

このような用途に本発明の保湿剤を用いる場合、該保湿
剤に必要な成分を加えて用いてもよいし、該保湿剤を必
要な成分を含有する水性溶液や水性分散液、あるいは固
形基剤に適尚量添加してもよく、その配合量は通常、化
粧料に対して0.1〜10重量%の範囲で好ましく用い
られる。
When using the humectant of the present invention for such purposes, the humectant may be used with the necessary ingredients added, or the humectant may be used as an aqueous solution or dispersion containing the necessary ingredients, or as a solid base. It may be added in an appropriate amount to the cosmetic composition, and the amount thereof is usually preferably used in the range of 0.1 to 10% by weight based on the cosmetic composition.

次に参考例及び実施例によって本発明をさらに詳細に説
明する。
Next, the present invention will be explained in more detail with reference to Reference Examples and Examples.

参考例1 メチルトリクロロシランを加水分解して生じた沈殿を回
収し、これに等モルの水酸化ナトリウム水溶液を加え、
かきまぜて溶解させ10チ濃度(シラノール換算)のシ
ラノニー) (0H3Si(OH)2・QNa )水溶
液を得た。
Reference Example 1 Collect the precipitate generated by hydrolyzing methyltrichlorosilane, add an equimolar aqueous sodium hydroxide solution to it,
The mixture was stirred and dissolved to obtain a silanony (0H3Si(OH)2.QNa) aqueous solution with a concentration of 10% (in terms of silanol).

一方、別のビーカーで、ムコ多糖の1種である精製ヒア
ルロン酸(キューピー社製)の1%水溶液1ooccを
調製し、これに前記のシラノエート10チ水溶液10C
Cを加えたのち、H型カチオン交換樹脂でpH6,5に
中和し、次いで該イオン交換樹脂を除去後、水を加えて
約200 ccとし、保湿剤を得た。このものを減圧乾
燥したところ、固形分濃度は約1%であった。
On the other hand, in another beaker, prepare 100cc of a 1% aqueous solution of purified hyaluronic acid (manufactured by Kewpie), which is a type of mucopolysaccharide, and add to this 10C of the 10% aqueous solution of silanoate.
After adding C, the mixture was neutralized to pH 6.5 with an H-type cation exchange resin, and after removing the ion exchange resin, water was added to make a total volume of about 200 cc to obtain a moisturizer. When this product was dried under reduced pressure, the solid content concentration was about 1%.

参考例2 仔牛皮不溶性コラーゲンをペプシンで溶解、精製した水
可溶、性のアテロコラーゲンの4%水溶液を調製した。
Reference Example 2 A 4% aqueous solution of water-soluble atelocollagen was prepared by dissolving calf skin insoluble collagen with pepsin and purifying it.

この水溶液80 ccに、参考例1と同様にして調製し
たシラノエートの10%(シラノール換算)水溶液1Q
Ocを加えたのち、H型カチオン交換樹脂でPH(S、
5に中和し、次いで水を加えて全体を100 QCとし
、保湿剤を得た。このものを減圧乾燥したところ、固形
分濃度は5%であった。
To 80 cc of this aqueous solution, 1Q of a 10% (silanol equivalent) aqueous solution of silanoate prepared in the same manner as in Reference Example 1 was added.
After adding Oc, PH(S,
5, and then water was added to make the whole to 100 QC to obtain a moisturizer. When this product was dried under reduced pressure, the solid content concentration was 5%.

実施例1 市販のブタの皮を縦、横2a角に切ったものを用意した
Example 1 Commercially available pig skin cut vertically and horizontally into 2A squares was prepared.

別に、第1表に示すような各種の保湿剤水溶液を用意し
、これらの保湿剤一定量をそれぞれブタの皮2枚に塗p
付け、相対湿度65%及び30チに保たれたデシケータ
−中にそれぞれ24時間放置したのち、ブタの皮表面の
水分量をインピーダンス測定によ請求めた。その結果を
第2表に示す。
Separately, prepare various moisturizing aqueous solutions as shown in Table 1, and apply a certain amount of each of these moisturizing agents to two pieces of pig skin.
The samples were left in a desiccator maintained at a relative humidity of 65% and 30°C for 24 hours, and the amount of moisture on the surface of the pig's skin was determined by impedance measurement. The results are shown in Table 2.

なお、インピーダンス測定機はIBe社製のものを用い
、得られたインピーダンス値から検量線を用いて水分量
をめ、2枚の平均値を採用した。
An impedance measuring device manufactured by IBe was used, and the moisture content was determined from the obtained impedance value using a calibration curve, and the average value of the two sheets was used.

第 1 表 第 2 表 第2表から明らかに、本発明のヒアルロン酸で安定化さ
れた保湿剤は、他の保湿剤はもちろん、ヒアルロン酸よ
り優れた保湿効果を有していることが分る。
Tables 1 and 2 clearly show that the moisturizing agent stabilized with hyaluronic acid of the present invention has a moisturizing effect superior to that of hyaluronic acid as well as other moisturizing agents. .

実施例2 市販のブタの皮を縦、横2cm角に切ったものを用意し
た。
Example 2 Commercially available pig skin was cut into 2 cm square pieces lengthwise and widthwise.

このブタの皮2枚を、参考例2で調製した保湿剤水溶液
(固形分5%)、コラーゲン5%水溶液及び水の中に浸
漬したのち、相対湿度50%のデシケータ−中に6時間
放置して、実施例1と同様にインピーダンス測定によシ
、ブタの皮表面の水分量をめた。
Two pieces of this pig skin were immersed in the moisturizer aqueous solution (solid content 5%) prepared in Reference Example 2, the collagen 5% aqueous solution, and water, and then left in a desiccator at a relative humidity of 50% for 6 hours. Then, as in Example 1, the amount of moisture on the surface of the pig's skin was determined by impedance measurement.

その結果、参考例2で得た本発明の保湿剤では水分量が
75%であったのに対し、コラーゲン5チ水溶液では5
5%、水のみでは5%であった。
As a result, the moisture content of the moisturizer of the present invention obtained in Reference Example 2 was 75%, whereas the moisture content of the collagen 5-ti aqueous solution was 5%.
5%, and water alone was 5%.

実施例3 参考例2と同様にして、保湿剤としてジメチルシランジ
オール−コンドロイチン硫酸B(重量比1:4)の5q
b水溶液を調製し、これを用いて、次に示すような組成
の化粧水を調製した。
Example 3 In the same manner as in Reference Example 2, 5q of dimethylsilanediol-chondroitin sulfate B (weight ratio 1:4) was added as a humectant.
An aqueous solution b was prepared and used to prepare a lotion having the composition shown below.

ジメチルシランジオール−コンドロイチン硫酸B5プロ
ピレングリコール 1 エタノール 6 メチルp−ヒドロキシベンゾエート0.1リン酸水素二
ナトリウム 0.06 香料 0.2 精製水 バランス この化粧水を女性20名に使用させたところ、肌のしつ
と多感、なめらかさについて1%の危険率で改善効果が
認められた。
Dimethylsilanediol-chondroitin sulfate B5 Propylene glycol 1 Ethanol 6 Methyl p-hydroxybenzoate 0.1 Disodium hydrogen phosphate 0.06 Fragrance 0.2 Purified water Balance When 20 women used this lotion, it was found that the skin Improvement effects were observed with a 1% risk rate for firmness, sensitivity, and smoothness.

実施例4 参考例1と同様にして、保湿剤としてエチルシラントリ
オ−ルーヒアルロン酸(重量比1:1〕1%水溶液を調
製し、これを用いて次の組成を有するエモリエントクリ
ームを調製した。
Example 4 In the same manner as in Reference Example 1, a 1% aqueous solution of ethylsilane trio-hyaluronic acid (weight ratio 1:1) was prepared as a moisturizer, and an emollient cream having the following composition was prepared using this.

成分 含有量(重量%) エチルシラントリオ−ルーヒアルロン酸1流動パラフイ
ン 6 スクアラン 3 セチルパルミテート 2 セタノール 2 ステアリン酸 2 酸化防止剤 3 精製水 バランス このクリームを女性20名に使用させたところ、肌のし
つと夛感、なめらかさについて、1%の危険率で改善効
果が認められた。
Ingredients Content (wt%) Ethylsilane trio-hyaluronic acid 1 liquid paraffin 6 squalane 3 cetyl palmitate 2 cetanol 2 stearic acid 2 antioxidant 3 purified water Balance When 20 women used this cream, it was found that the skin Improvement effects were observed with a 1% risk rate for stiffness, stiffness, and smoothness.

実施例5 参考例1と同様にして、保湿剤としてフェニルシラント
リオ−ルーヒアルロン酸(重量比1:1)1%水溶液を
調製し、これを用いて次に示すような組成のシャングー
を調製して使用したところ、毛髪に対して優れた保湿効
果を示した。
Example 5 In the same manner as in Reference Example 1, a 1% aqueous solution of phenylsilane trio-hyaluronic acid (weight ratio 1:1) was prepared as a humectant, and using this, a shanggu with the following composition was prepared. When used, it showed an excellent moisturizing effect on hair.

成分 含有量(重量%〕 フェニルシラントリオールーヒアルロン酸10□4−α
−オレフィンスルホン酸ナトリウム 1゜ラウリル硫酸
トリエタノールアミン 5香料 0.1 精製水 バランス 実施例6 参考例2と同様にしてトリメチルシラノール−コラーゲ
ン(重量比i : i、s ) 2%水溶液を調製し、
これを用いて次に示すような組成のリンスを調製して使
用したところ、毛髪に対して優れた保湿効果を示した。
Component Content (wt%) Phenylsilane triol-hyaluronic acid 10□4-α
- Sodium olefin sulfonate 1゜triethanolamine lauryl sulfate 5 Fragrance 0.1 Purified water Balance Example 6 A 2% aqueous solution of trimethylsilanol-collagen (weight ratio i: i, s) was prepared in the same manner as in Reference Example 2.
When this was used to prepare a rinse having the composition shown below, it showed an excellent moisturizing effect on hair.

トリメチルシラノール−コラーゲン 2アーカード2H
T 、 、 2 セタノール 3 ステアリルエトキシレー) (KO5モル)1香料 o
、i 精製水 バランス
Trimethylsilanol-Collagen 2 Alucard 2H
T , , 2 Setanol 3 Stearyl ethoxyle) (KO5 mol) 1 Fragrance o
, i Purified water balance

Claims (1)

【特許請求の範囲】 1(A)分子中に少なくとも1個のシラノール基を有す
るケイ素化合物とΦ)水溶性高分子物質との組合せから
成る保湿剤。 2 ケイ素化合物が分子中にケイ素原子1〜3個を有す
るものである特許請求の範囲第1項記載の保湿剤。 6 水溶性高分子物質が分子中に少なくとも1個のヒド
ロキシル基又はアミノ基若しくはその両方を有するもの
である特許請求の範囲第1項記載の保湿剤。 4 水溶性高分子物質が水溶性生体高分子物質である特
許請求の範囲第1項記載の保湿剤。
[Scope of Claims] 1. A humectant comprising a combination of (A) a silicon compound having at least one silanol group in its molecule and Φ) a water-soluble polymeric substance. 2. The moisturizing agent according to claim 1, wherein the silicon compound has 1 to 3 silicon atoms in the molecule. 6. The moisturizing agent according to claim 1, wherein the water-soluble polymeric substance has at least one hydroxyl group, one amino group, or both in the molecule. 4. The moisturizer according to claim 1, wherein the water-soluble polymer substance is a water-soluble biopolymer substance.
JP6121684A 1984-03-30 1984-03-30 Humectant Granted JPS60204708A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP6121684A JPS60204708A (en) 1984-03-30 1984-03-30 Humectant
GB08506618A GB2159408B (en) 1984-03-30 1985-03-14 Humectant
DE19853511135 DE3511135C2 (en) 1984-03-30 1985-03-27 Humectants
FR8504702A FR2561915A1 (en) 1984-03-30 1985-03-28 MOISTURIZING PRODUCT

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6121684A JPS60204708A (en) 1984-03-30 1984-03-30 Humectant

Publications (2)

Publication Number Publication Date
JPS60204708A true JPS60204708A (en) 1985-10-16
JPH0557968B2 JPH0557968B2 (en) 1993-08-25

Family

ID=13164777

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6121684A Granted JPS60204708A (en) 1984-03-30 1984-03-30 Humectant

Country Status (4)

Country Link
JP (1) JPS60204708A (en)
DE (1) DE3511135C2 (en)
FR (1) FR2561915A1 (en)
GB (1) GB2159408B (en)

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JP2782207B2 (en) * 1988-10-24 1998-07-30 株式会社ナブコ Machine parts and hydraulic pressure control valves containing the parts
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US5753214A (en) * 1994-08-24 1998-05-19 Seiwa Kasei Co., Ltd. Base material for cosmetics and uses of the same
FR2761074B1 (en) * 1997-03-24 1999-05-28 Exsymol Sa BIOLOGICALLY ACTIVE SILICON COMPOUNDS IN SOLID FORM
FR2761607A1 (en) * 1997-04-04 1998-10-09 Boots Co Plc DERMATOLOGICAL COMPOSITION FOR THE TREATMENT OF SKIN AGING SYMPTOMS
FR2865935B1 (en) * 2004-02-05 2006-06-23 Exsymol Sa USE OF ORGANO-SILICY COMPOUNDS FOR CONSTRAINTING CONNECTIVE TISSUES FOUNDED THROUGH MECHANICAL ACTION
FR2936708B1 (en) 2008-10-03 2012-08-17 Exsymol Sa COMPLEX COMPRISING AN ORGANIC DERIVATIVE OF SILICON WITH CALIBER FRAGMENTS OF HYALURONIC ACID, WITH PREVENTIVE ACTION AND REPAIR OF SKIN DEGRADATION.
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FR2989891A1 (en) * 2012-04-26 2013-11-01 Oreal COSMETIC COMPOSITION COMPRISING SILANE AND SUGAR OR SUGAR DERIVATIVE
FR2989885A1 (en) * 2012-04-26 2013-11-01 Oreal COMPOSITION COMPRISING A SILANE AND A POLYSACCHARIDE WITH HYDROPHOBIC GROUPS
FR2989889B1 (en) * 2012-04-26 2016-12-30 Oreal COSMETIC COMPOSITION COMPRISING SILANE AND LIPOPHILIC THICKENER
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Also Published As

Publication number Publication date
FR2561915A1 (en) 1985-10-04
DE3511135A1 (en) 1985-10-10
GB2159408A (en) 1985-12-04
JPH0557968B2 (en) 1993-08-25
DE3511135C2 (en) 1987-03-12
GB8506618D0 (en) 1985-04-17
GB2159408B (en) 1988-01-27

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