JPS61225106A - Dermatic agent for external use - Google Patents

Dermatic agent for external use

Info

Publication number
JPS61225106A
JPS61225106A JP6420885A JP6420885A JPS61225106A JP S61225106 A JPS61225106 A JP S61225106A JP 6420885 A JP6420885 A JP 6420885A JP 6420885 A JP6420885 A JP 6420885A JP S61225106 A JPS61225106 A JP S61225106A
Authority
JP
Japan
Prior art keywords
residue
skin
hydroquinone
acid
agent
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
JP6420885A
Other languages
Japanese (ja)
Other versions
JPH0481965B2 (en
Inventor
Yoshimori Fujinuma
好守 藤沼
Seiichi Kita
誠一 喜多
Shintaro Abe
慎太郎 阿部
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.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP6420885A priority Critical patent/JPS61225106A/en
Publication of JPS61225106A publication Critical patent/JPS61225106A/en
Publication of JPH0481965B2 publication Critical patent/JPH0481965B2/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
    • A61K8/18Cosmetics 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
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; 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
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • 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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning 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
    • A61K2800/74Biological properties of particular ingredients
    • A61K2800/75Anti-irritant

Abstract

PURPOSE:To provide an external agent for skin, containing an anionic surfactant in combination with a specific hydroquinone glucoside, having suppressed skin irritation of anionic surfactant in the external agent for skin, and useful as cosmetic, medicinal drug, quasi-drug, etc. CONSTITUTION:The objective external agent for skin contains (A) one or more aniotic surfactants such as lauric acid slat, cocoylsulfuric acid slat, casein salt, etc., and (B) one or more hydroquinone glucosides of formula (R is pentose residue, hexose residue, amino sugar residue, uronic acid residue and their methylated group) (especially preferably hydroquinone-beta-D-glucoxide). The sum of the components A and B in the agent is preferably 0.1-30wt%, especially 6-20wt%.

Description

【発明の詳細な説明】 [産業上の利用分野コ 本発明は、系中に配合されるアニオン界面活性剤の皮膚
刺激が緩和されてなる組成物に関し、化粧品、医薬品、
医薬部外品などの分野に有用な皮膚外用剤を提供するこ
とを目的とする。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Fields of Application] The present invention relates to a composition in which the skin irritation of an anionic surfactant contained in the system is alleviated, and is applicable to cosmetics, pharmaceuticals,
The aim is to provide external skin preparations that are useful in the field of quasi-drugs.

[従来の技術] 皮膚外用剤基剤中には、乳化剤、可溶化剤、分散剤、洗
浄剤などとして界面活性剤が配合されることが多い。ア
ニオン界面活性剤はその中でも乳化力、可溶化力、分散
力、洗浄力が強く、また、代表的なアニオン界面活性剤
である脂肪酸アルカリ七つけんば最も古くから使用され
ている界面活性剤でかつ使用感触もよいことから、とく
に化粧料分野では頻繁に使用されている。
[Prior Art] Surfactants are often blended into the base of external skin preparations as emulsifiers, solubilizers, dispersants, detergents, and the like. Among them, anionic surfactants have strong emulsifying power, solubilizing power, dispersing power, and detergent power.Furthermore, fatty acid alkali 7, which is a representative anionic surfactant, is the surfactant that has been used for the longest time. Because it feels good when used, it is frequently used, especially in the cosmetics field.

しかしながら、アニオン界面活性剤は皮膚刺激性を有し
ており、人によっては皮膚障害を起こすことがある。皮
膚外用剤中における界面活性剤の配合量は洗浄剤を除い
ては、比較的低濃度ではあるが、皮膚外用剤の皮膚安全
性が全体的に高まっている現在では、アニオン界面活性
剤の皮膚刺激性についてもより改善されることが望まれ
ている。
However, anionic surfactants have skin irritation properties and may cause skin disorders in some people. The concentration of surfactants in external skin preparations is relatively low, except for detergents, but now that the overall skin safety of external skin preparations has improved, anionic surfactants are It is also desired that the irritation properties be further improved.

[発明が解決しようとする問題点] そこで、本発明者らは、皮膚外用剤中におけるアニオン
界面活性剤の皮膚刺激をより低減することを目的に鋭意
検討を加えた結果、驚くべきことに、アニオン界面活性
剤とともに特定のハイドロキノンの配糖体を配合したな
らば、この目的が達成されることを見いだし、本発明を
完成するに至った。
[Problems to be Solved by the Invention] Therefore, the present inventors conducted intensive studies with the aim of further reducing the skin irritation caused by anionic surfactants in external skin preparations, and surprisingly found that The present inventors have discovered that this objective can be achieved by blending a specific hydroquinone glycoside with an anionic surfactant, and have completed the present invention.

[問題点を解決するための手段] すなわち、本発明はアニオン界面活性剤の一種又は二種
以上と下記一般式(1)で表されるハイドロキノンの配
糖体から選ばれる一種又は二種以上とを含有することを
特徴とする皮膚外用剤である。
[Means for Solving the Problems] That is, the present invention uses one or more anionic surfactants and one or more hydroquinone glycosides represented by the following general formula (1). It is a skin external preparation characterized by containing.

(式(1)中、Rは五炭糖残基、六炭糖残基、十ミノ糖
残基、ウロン酸残基またはそれらのメチル化物を示す。
(In formula (1), R represents a pentose residue, a hexose residue, a deminosaccharide residue, a uronic acid residue, or a methylated product thereof.

) 以下、本発明について詳述する。) The present invention will be explained in detail below.

本発明で用いられるアニオン界面活性剤は皮膚外用剤に
おいて一般的に用いられるアニオン界面活性剤を全て包
含する。具体例をあげるならば、ラウリン酸塩、パルミ
チン酸塩、オレイン酸塩、ステアリン酸塩、イソステア
リン酸塩、ヘヘニン酸塩、アビエチン酸塩などの脂肪酸
塩、ラウリル硫酸塩、ココイル硫酸塩などのアルキル硫
酸エステル塩、POEラウリル硫酸塩、POEココイル
硫酸塩などのアルキルエーテル硫酸エステル塩、ラウロ
イル男ルコシン塩なとのN−アシルザルコシン塩、N−
ミリストイル−N−メチルクラリン塩、ココイルメチル
タウリノ「塩、ラウリルメチルタウソノl−塩などの脂
肪酸アミドコハク酸塩、POEオレイルエーテルリン酸
塩、POEステアリルエーテルリン酸塩などのリン酸エ
ステル塩、ジー2−エチルへキンルスルホコハク酸塩、
モノラウロイルモノエタノールアミドポリオキシエチレ
ンスルホコハク酸塩、ラウリルポリプロピレングリコー
ルスルホコハク酸塩などのスルホコハク酸塩、リニアト
デシルヘンゼンスルホン酸塩などのアルキルヘンゼンス
ルホン酸塩、N−ラウロイルグルタミン酸塩、N−ステ
アロイルグルタミン酸塩、N−ミリストイルグルタミン
酸塩、N−バルミトイルアスパラギン酸塩などのN−ア
シルアミノ酸塩、ロート油などの硫酸化油、ラウロイル
モノエタノールアミドコハク酸塩などのアミドコハク酸
塩、あるいはPOEアルキルエーテルカルボン酸塩、P
OEアルキルアリルエーテルカルボン酸塩、α−オレフ
ィンスルホン酸塩、脂肪酸エステルスルホン酸塩、二級
アルコール硫酸エステル塩、脂肪酸アルキロールアミド
硫酸エステル塩、カゼイン塩などが例示される。
The anionic surfactants used in the present invention include all anionic surfactants commonly used in external skin preparations. Specific examples include fatty acid salts such as laurate, palmitate, oleate, stearate, isostearate, hehenate, abietate, and alkyl sulfates such as lauryl sulfate and cocoyl sulfate. Ester salts, alkyl ether sulfate ester salts such as POE lauryl sulfate and POE cocoyl sulfate, N-acyl sarcosine salts such as lauroyl male lucosine salts, N-
Fatty acid amide succinates such as myristoyl-N-methyl clarine salt, cocoyl methyl taurino salt, lauryl methyl tausonol salt, phosphate ester salts such as POE oleyl ether phosphate, POE stearyl ether phosphate, 2-ethyl hequinyl sulfosuccinate,
Sulfosuccinates such as monolauroyl monoethanolamide polyoxyethylene sulfosuccinate, lauryl polypropylene glycol sulfosuccinate, alkyl hanzene sulfonates such as linear todecyl hanzene sulfonate, N-lauroyl glutamate, N-stearoyl N-acyl amino acid salts such as glutamate, N-myristoyl glutamate, N-balmitoyl aspartate, sulfated oils such as funnel oil, amidosuccinates such as lauroyl monoethanolamide succinate, or POE alkyl ethers. Carboxylate, P
Examples include OE alkyl allyl ether carboxylate, α-olefin sulfonate, fatty acid ester sulfonate, secondary alcohol sulfate ester salt, fatty acid alkylolamide sulfate ester salt, and caseinate.

上記の塩を形成するカチオンとしては、ナ1−リウム、
カリウムなどのアルカリ金属、マグネシウム、カルシウ
ムなどのアルカリ土類金属、ジェタノールアミン、トリ
エタノールアミンなどのアミン、リジン、アルギニンな
どの塩基性アミノ酸のほか、2−アミノ−2−メチルプ
ロパツールあるいはアンモニアなどがあげられる。
The cations forming the above salts include sodium,
Alkali metals such as potassium, alkaline earth metals such as magnesium and calcium, amines such as jetanolamine and triethanolamine, basic amino acids such as lysine and arginine, as well as 2-amino-2-methylpropanol or ammonia, etc. can be given.

本発明においては、これらアニオン界面活性剤のうちの
任意の一種又は二種以上が選ばれて用いられる。配合量
はとくに限定されないが、一般的には、洗浄材で5〜1
00重量%、そのほかの場合で0.1〜2Ofi量%で
ある。
In the present invention, any one or more of these anionic surfactants may be selected and used. The amount of the cleaning agent is not particularly limited, but in general, the amount of cleaning material is 5 to 1.
00% by weight, and 0.1 to 2% by weight in other cases.

本発明で用いられるハイドロキノンの配糖体は、」二記
一般式(1)で表される。その具体例をあげるならば、
L−アラビノース、D−アラビノース、D−キシロース
、D−リボース、L−キシルロース、L−リキソース、
D−リブロースなどの五炭糖の残基、D−グルコース、
D−ガラクトース、L−ガラクトース、D−マンノース
、D−タロース、D−フルクトース、■、−ソルボース
、D−タガト−ス、D−プシコースなどの六炭糖の残基
、D−グルコサミン、D−ガラクトサミン、シアル酸、
アミノウロン酸、ムラミン酸などのアミノ糖の残基、D
−グルクロン酸、D−ガラクツロン酸、D−マンヌロン
酸、L−イズロン酸、■、−グルロン酸などのウロン酸
の残基またばそれらのメチル化物などが例示される。
The hydroquinone glycoside used in the present invention is represented by general formula (1). To give you a specific example,
L-arabinose, D-arabinose, D-xylose, D-ribose, L-xylulose, L-lyxose,
Residues of pentose sugars such as D-ribulose, D-glucose,
Residues of hexose sugars such as D-galactose, L-galactose, D-mannose, D-talose, D-fructose, -sorbose, D-tagatose, D-psicose, D-glucosamine, D-galactosamine , sialic acid,
Residues of amino sugars such as aminouronic acid and muramic acid, D
Examples include uronic acid residues such as -glucuronic acid, D-galacturonic acid, D-mannuronic acid, L-iduronic acid, -guluronic acid, and methylated products thereof.

なかでは、RがD−グルコースの残基、とくにハイドロ
キノンにD−グルコースがβ結合した、すなわち、ハイ
l−ロキノンーβ−D−グルコシド (−船名:アルブ
チン)が、もっとも好ましい。
Among these, the most preferred is where R is a residue of D-glucose, particularly hydroquinone with a β-bond of D-glucose, that is, hy-l-quinone-β-D-glucoside (-ship name: arbutin).

本発明においては上記ハイドロキノンの配糖体の一種又
は二種以」二が任意に選ばれて用いられ、その配合量は
皮膚外用剤全量中の0、i〜30市量%、好ましくは6
〜20重量%である。
In the present invention, one or more of the above hydroquinone glycosides are arbitrarily selected and used, and the blending amount is 0.1 to 30% by weight, preferably 6%, based on the total amount of the skin external preparation.
~20% by weight.

アニオン界面活性剤とハイl、”ロキノンの配糖体とを
配合できる皮膚外用剤は、通常の皮膚外用剤、たとえば
、水溶液系、可溶化系、乳化系、粉末分散系、水−油2
層系、水−油−粉末3層系などの広い範囲の基剤であり
、用途も化粧水、乳液、クリーム、パンク、クレンジン
グフオームなどの基礎化粧料、口紅、ファンデーション
などのメーキャンプ化粧料、シャンプー、リンス、ヘア
トニックなどの頭髪化粧料などの化粧料のほか、医薬品
、医薬部外品など多岐にわたる。
External skin preparations that can be formulated with anionic surfactants and glycosides of ``Hy-l'' and ``roquinone'' are common external skin preparations, such as aqueous solution systems, solubilized systems, emulsification systems, powder dispersion systems, water-oil 2
It has a wide range of bases such as layer type, water-oil-powder three-layer type, etc., and can be used in basic cosmetics such as lotion, emulsion, cream, blowout, cleansing foam, makeup cosmetics such as lipstick, foundation, etc. In addition to cosmetics such as hair cosmetics such as shampoos, conditioners, and hair tonics, our products range from pharmaceuticals to quasi-drugs.

本発明の皮膚外用剤には必要に応して、本発明の効果を
損なわない範囲で、保湿剤、増粘剤、油分、防腐剤、他
の界面活性剤、酸化防止剤、金属イオン封鎖剤、紫外線
吸収剤、粉末、薬剤、色剤、香料などを配合できる。
The skin external preparation of the present invention may contain humectants, thickeners, oils, preservatives, other surfactants, antioxidants, and sequestering agents, as necessary, to the extent that the effects of the present invention are not impaired. , ultraviolet absorbers, powders, drugs, colorants, fragrances, etc. can be added.

(以下余白) [発明の効果] 以下に、本発明に係るハイドロキノンの配糖体が有する
アニオン界面活性剤の皮膚刺激抑制効果を示す。
(The following is a blank space) [Effects of the Invention] Below, the skin irritation suppressing effect of the anionic surfactant possessed by the glycoside of hydroquinone according to the present invention will be shown.

実験は、アニオン界面活性剤としてドテシル硫酸ナトリ
ウム、ステアリン酸トリエタノールアミン、N−ラウロ
イルグルタミン酸モノナトリウムを用い、それぞれを単
独で水−エタノール溶液(水:エタノール−95:5)
中に下記濃度で熔解した試料と、さらにアルブチンを0
.5重量%または6重量%加えた試料とを用いて行った
In the experiment, sodium dotecyl sulfate, triethanolamine stearate, and monosodium N-lauroylglutamate were used as anionic surfactants, and each was individually dissolved in water-ethanol (water:ethanol-95:5).
A sample melted at the following concentration and 0 arbutin were added to the container.
.. The test was carried out using samples to which 5% by weight or 6% by weight had been added.

表−1 アニオン界面活性剤の種類 熔解濃度(重量%)ドテシ
ル硫酸ナトリウム     0.2表−2 上記試料を用いて人体閉塞パンチテストを行った。被験
者は健康な成人女子54名で、貼付部位は前腕とし、以
下の判定基準に従って評価し、陽性率を算出した。
Table-1 Type of anionic surfactant Dissolved concentration (wt%) Sodium dotesyl sulfate 0.2 Table-2 A human body occlusion punch test was conducted using the above samples. The test subjects were 54 healthy adult women, and the application site was the forearm. Evaluations were made according to the following criteria, and the positive rate was calculated.

一判定基準− 反応が全くないもの     − わずかな紅斑        士 紅斑            士 紅斑に加えて浮腫、丘疹   +十 浮腫、丘疹に加えて小水泡  士士十 −陽性率一 上記判定基準の(+)、(十→−)、 (+ 十+)を陽性者として、合計数が54名中に占め
る割合をもって陽性率とした。
1 Judgment criteria - No reaction at all - Slight erythema erythema edema and papules in addition to edema + small blisters in addition to edema and papules →−), (+10+) were considered positive, and the percentage of the total number of 54 people was defined as the positive rate.

結果を表−3に示す。The results are shown in Table-3.

(以下余白) 表−3 試料No、  陽性率 1   31.5% 29.2 3   12.9 4   27.8 57.4 6   11.1 7   14.8 93.7 表−3の結果から、本発明に係るアルブチンがアニオン
界面活性剤の皮膚刺激を緩和することが明らかである。
(Left below) Table 3 Sample No., Positive rate 1 31.5% 29.2 3 12.9 4 27.8 57.4 6 11.1 7 14.8 93.7 From the results in Table 3, this It is clear that arbutin according to the invention alleviates the skin irritation of anionic surfactants.

し実施例コ つぎに、本発明の実施例を示す。本発明はこれによって
限定されるものではない。
EXAMPLES Next, examples of the present invention will be shown. The present invention is not limited thereby.

実施例1 乳液 A、ステアリン酸         2.5セタノール
          1.5ワセリン        
   5.0流動パラフイン        10.0
POE(10)オレエート    2.0プロピルパラ
ヘン       0.1酢酸トコフエロール    
  0.01香料             0.2B
、ポリエチレングリコール1500  3.0トリエタ
ノールアミン     1.0アルブチン      
    1.0へキサメタリン酸ナトリウム  0.0
5楕製氷            残余 (製法)Aに属する成分を加熱熔解する(油相)。別に
、Bに属する成分を混合熔解加熱する(水相)。水相中
に油相を添加して乳化後、冷却して乳液を得た。
Example 1 Emulsion A, stearic acid 2.5 cetanol 1.5 vaseline
5.0 Liquid paraffin 10.0
POE (10) Oleate 2.0 Propylparahen 0.1 Tocopheryl acetate
0.01 fragrance 0.2B
, polyethylene glycol 1500 3.0 triethanolamine 1.0 arbutin
1.0 Sodium hexametaphosphate 0.0
5 Oval ice making Heat and melt the components belonging to the remainder (manufacturing method) A (oil phase). Separately, the components belonging to B are mixed and melted and heated (aqueous phase). The oil phase was added to the water phase to emulsify it, and then cooled to obtain a milky lotion.

実施例2 クレンジングフオーム A、N−ラウロイルグルタミン酸 モノナトリウム 20.0 ココイルメチルタウリッド ナトリウム l04O POE(60)硬化ヒマシ油   4.0ラウリン酸 
          2.0香料          
    0.5B、アルブチン           
1.0槓製氷            残余 (製法)実施例1.に準じる。
Example 2 Cleansing Foam A, Monosodium N-Lauroylglutamate 20.0 Sodium Cocoyl Methyl Tauride 104O POE (60) Hydrogenated Castor Oil 4.0 Lauric Acid
2.0 fragrance
0.5B, arbutin
1.0 Ice making remainder (manufacturing method) Example 1. According to.

実施例3 シャンプー ラウリルエーテル硫酸 ナトリウム  10.0 ラウリルエーテル硫酸 トリエタノールアミン 10.0 ココイルジエタノールアミド   5.0ラウリルジメ
チルアミノ 酢酸ヘタイン   4.0 クエン酸              0.5エデト酸
三ナトリウム      0.1プロピルパラヘン  
      0.5香料              
0.3アルブチン          10.0精製水
            残余 (製法)各成分を加熱攪拌熔解後、冷却してシャンプー
を得た。
Example 3 Sodium shampoo lauryl ether sulfate 10.0 Triethanolamine lauryl ether sulfate 10.0 Cocoyl diethanolamide 5.0 Hetaine lauryl dimethylaminoacetate 4.0 Citric acid 0.5 Trisodium edetate 0.1 Propylparahen
0.5 fragrance
0.3 Arbutin 10.0 Purified water Remaining components (manufacturing method) After heating, stirring and melting each component, a shampoo was obtained by cooling.

実施例4 クリーム A、ステアリン酸         10.0ステアリ
ルアルコール      4.0ブチルステアレート 
      8.0グリセリルモノステアレート (自己乳化型)2.0 プロピレングリコール     3.0力セイカリ  
         0.2香料           
   0.2エチルパラヘン         0.0
5B、アルブチン           0.2ハイド
ロキノンβ−D− アラビノシト    0.5 精製水            残余 (製法)実施例1に準しる。
Example 4 Cream A, stearic acid 10.0 stearyl alcohol 4.0 butyl stearate
8.0 Glyceryl monostearate (self-emulsifying type) 2.0 Propylene glycol 3.0 Seikari
0.2 fragrance
0.2 Ethylparahen 0.0
5B, Arbutin 0.2 Hydroquinone β-D-arabinocyto 0.5 Purified water Remaining (manufacturing method) as in Example 1.

実施例1〜実施例4は、安全性良好で、経口安定性、使
用性にも優れていた。
Examples 1 to 4 had good safety, excellent oral stability, and usability.

Claims (1)

【特許請求の範囲】[Claims] (1)アニオン界面活性剤の一種又は二種以上と下記一
般式( I )で表されるハイドロキノンの配糖体から選
ばれる一種又は二種以上とを含有することを特徴とする
皮膚外用剤。 ▲数式、化学式、表等があります▼・・・・( I ) (式( I )中、Rは五炭糖残基、六炭糖残基、アミノ
糖残基、ウロン酸残基またはそれらのメチル化物を示す
。)
(1) An external preparation for skin, characterized by containing one or more anionic surfactants and one or more hydroquinone glycosides represented by the following general formula (I). ▲There are mathematical formulas, chemical formulas, tables, etc.▼・・・(I) (In formula (I), R is a pentose residue, a hexose residue, an amino sugar residue, a uronic acid residue, or their (Indicates methylated product.)
JP6420885A 1985-03-28 1985-03-28 Dermatic agent for external use Granted JPS61225106A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6420885A JPS61225106A (en) 1985-03-28 1985-03-28 Dermatic agent for external use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6420885A JPS61225106A (en) 1985-03-28 1985-03-28 Dermatic agent for external use

Publications (2)

Publication Number Publication Date
JPS61225106A true JPS61225106A (en) 1986-10-06
JPH0481965B2 JPH0481965B2 (en) 1992-12-25

Family

ID=13251427

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6420885A Granted JPS61225106A (en) 1985-03-28 1985-03-28 Dermatic agent for external use

Country Status (1)

Country Link
JP (1) JPS61225106A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002094211A1 (en) * 2001-05-19 2002-11-28 Beiersdorf Ag Cosmetic or dermatological preparations containing one or more ketohexoses

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6016906A (en) * 1983-07-07 1985-01-28 Pola Chem Ind Inc External drug for skin

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6016906A (en) * 1983-07-07 1985-01-28 Pola Chem Ind Inc External drug for skin

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002094211A1 (en) * 2001-05-19 2002-11-28 Beiersdorf Ag Cosmetic or dermatological preparations containing one or more ketohexoses

Also Published As

Publication number Publication date
JPH0481965B2 (en) 1992-12-25

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