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JPH0415763B2 - - Google Patents

Info

Publication number
JPH0415763B2
JPH0415763B2 JP60048034A JP4803485A JPH0415763B2 JP H0415763 B2 JPH0415763 B2 JP H0415763B2 JP 60048034 A JP60048034 A JP 60048034A JP 4803485 A JP4803485 A JP 4803485A JP H0415763 B2 JPH0415763 B2 JP H0415763B2
Authority
JP
Japan
Prior art keywords
arbutin
skin
mucopolysaccharide
present
sticky
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.)
Expired - Lifetime
Application number
JP60048034A
Other languages
Japanese (ja)
Other versions
JPS61207310A (en
Inventor
Tomohisa Asahara
Shinji Tobe
Shintaro Abe
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 JP4803485A priority Critical patent/JPS61207310A/en
Publication of JPS61207310A publication Critical patent/JPS61207310A/en
Publication of JPH0415763B2 publication Critical patent/JPH0415763B2/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
    • A61K8/72Cosmetics 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
    • 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
    • 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)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

[産業上の利用分野] 本発明は保湿効果に優れ、かつべたつきのない
使用感触を有する皮膚外用剤に関する。 [従来の技術] 皮膚の水分を適正な範囲に保つことは皮膚の健
康の面から非常に大切なことであり、保湿を目的
とした化粧料は多くみられる。また、医薬品にも
保湿成分が配合されて、主剤の効果をより高めて
いる例が見受けられる。 皮膚の保湿に関与する物質についての研究も進
んでおり、現在ではプロピレングリコールやソル
ビトールなどの多価アルコールをはじめとして数
多くの保湿剤が使用されるに至つている。 このような状況のもとで、とくに最近、注目を
集めているのがムコ多糖である。ムコ多糖は皮膚
の天然湿因子でもあり、その保湿作用は強力であ
る。 しかしながら、ムコ多糖は保湿作用の優秀さと
は裏腹にべたつきの強い使用感触をもつており、
皮膚外用剤、とくに化粧料に配合するには難点と
なつていた。 [発明が解決しようとする問題点] 本発明者らはこのような事情にかんがみてムコ
多糖のべたつきをおさえることを目的に鋭意検討
した結果、ムコ多糖とともに特定のハイドロキノ
ンの配糖体を配合すると、上記問題が解決するこ
とを見いだし、本発明を完成するに至つた。 [問題点を解決するための手段] すなわち、本発明はムコ多糖の一種又は二種以
上と、アルブチン(ハイドロキノン−β−D−グ
ルコース)0.1〜30重量%とを含有することを特
徴とする皮膚外用剤である。 本発明で用いるムコ多糖はヒアルロン酸、コン
ドロイチン−4−硫酸、コンドロイチン−6−硫
酸、デルマタン硫酸、ケラタン硫酸、ヘパリンな
どのムコ多糖およびそれらの塩であり、これらの
なかから一種又は二種以上が適宜選ばれて用いら
れる。 配合量は皮膚外用剤全量中の0.001〜10重量%、
好ましくは0.01〜3重量%ある。0.001重量%未
満では保湿効果に乏しく、また、べたつきも少な
い。10重量%を越えると本発明のハイドロキノン
の配糖体を併用してもべたつきをおさえることが
困難となる。 本発明において、ムコ多糖とともに皮膚外用剤
中に配合され、ムコ多糖のべたつきをおさえるア
ルブチンの配合量は皮膚外用剤全量中の0.1〜30
重量%、好ましくは6〜20重量%である。 ムコ多糖および上記アルブチンを配合できる皮
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、どのような基剤
でもよく、用途も化粧水、乳液、クリーム、パツ
クなどの基礎化粧料、口紅、フアンデーシヨンな
どのメーキヤツプ化粧料、シヤンプー、リンス、
ヘアトニツクなどの頭髪化粧料などの化粧料、医
薬部外品など多岐にわたるが、なかでも、透明ま
たは半透明の化粧水に応用したときにとくに真価
を発揮する。化粧水は一般に水−アルコールベー
スであるので、使用後のべたつきがとくに感じら
れるからである。 本発明の皮膚外用剤には必要に応じて、本発明
の効果を損なわない範囲で、保湿剤、増粘剤、防
腐剤、乳化剤、酸化防止剤、金属イオン封鎖剤、
紫外線吸収剤、粉末、顔料、薬剤、色素、香料な
どを配合できる。 [発明の効果] 本発明の皮膚外用剤は、ムコ多糖を配合して保
湿効果に優れているにもかかわらず、ムコ多糖特
有のべたつきがなく、かつ安定性、安全性も良好
で優れた皮膚外用剤である。 [実施例] つぎに実施例により本発明をさらに詳細に説明
する。本発明は、これによつて何ら限定されるも
のではない。 実施例1 化粧水 エタノール 20.0 1,3−ブチレングリコール 5.0 ヒアルロン酸ナトリウム 0.3 POE(ポリオキシエチレン、以下同じ、15モ
ル)オレイルエーテル 0.8 エチルパラベン 0.1 アルブチン 6.0 精製水 残余 (製法) エタノールの一部にPOEオレイルエ
ーテルおよびエチルパラベンを溶解する。べつ
に精製水とエタノールの残部に1,3−ブチレ
ングリコール、ヒアルロン酸ナトリウムおよび
アルブチンを溶解する。エタノール相を水相中
に添加、可溶化して化粧水を得た。 実施例 2 実施例1のアルブチンを1.0重量%に減量した
他は実施例1に準じて、実施例2を得た。 比較例 1 実施例1のアルブチンを除いた他は実施例1に
準じて、比較例1を得た。 実施例1〜2、比較例1の使用性(べたつき)
を、女性美容専門パネルの実使用試験によつて判
定、評価した。 (判定) A;べたつかない。 B;わずかにべたつくが、使用性上問題のない範
囲である。 C;べたつく。 D;著しくべたつく。 結果を表−1に示す。 アルブチンが、ムコ多糖のべたつきを防止して
いることが明らかである。
[Industrial Field of Application] The present invention relates to an external preparation for skin that has an excellent moisturizing effect and a non-sticky feeling when used. [Prior Art] Maintaining skin moisture within an appropriate range is extremely important from the perspective of skin health, and many cosmetics are available for the purpose of moisturizing. In addition, there are cases in which moisturizing ingredients are added to pharmaceutical products to further enhance the effectiveness of the main ingredient. Research into substances involved in skin moisturization is progressing, and many moisturizers are now in use, including polyhydric alcohols such as propylene glycol and sorbitol. Under these circumstances, mucopolysaccharides have been attracting particular attention recently. Mucopolysaccharide is also a natural moisturizing factor for the skin, and its moisturizing effect is strong. However, despite its excellent moisturizing effect, mucopolysaccharides have a strong sticky feel when used.
It has been difficult to incorporate it into external skin preparations, especially cosmetics. [Problems to be Solved by the Invention] In view of the above circumstances, the inventors of the present invention conducted extensive studies with the aim of suppressing the stickiness of mucopolysaccharide, and found that when a specific hydroquinone glycoside is blended with mucopolysaccharide. The inventors have found that the above problem can be solved, and have completed the present invention. [Means for Solving the Problems] That is, the present invention provides a skin characterized by containing one or more mucopolysaccharides and 0.1 to 30% by weight of arbutin (hydroquinone-β-D-glucose). It is an external preparation. The mucopolysaccharides used in the present invention are mucopolysaccharides such as hyaluronic acid, chondroitin-4-sulfate, chondroitin-6-sulfate, dermatan sulfate, keratan sulfate, and heparin, and their salts, and one or more of these are mucopolysaccharides and salts thereof. It is selected and used as appropriate. The blending amount is 0.001 to 10% by weight of the total amount of the skin external preparation.
Preferably it is 0.01 to 3% by weight. If it is less than 0.001% by weight, it will have poor moisturizing effect and will also be less sticky. If the amount exceeds 10% by weight, it becomes difficult to suppress stickiness even when the hydroquinone glycoside of the present invention is used in combination. In the present invention, the amount of arbutin that is blended together with mucopolysaccharide in the skin external preparation to suppress the stickiness of the mucopolysaccharide is 0.1 to 30% of the total amount of the skin external preparation.
% by weight, preferably 6-20% by weight. The skin external preparations that can contain the mucopolysaccharide and the above-mentioned arbutin include the usual skin external preparations, such as aqueous solutions, solubilized systems, emulsified systems, powder dispersion systems, water-oil 2
Any type of base may be used, such as layer type, water-oil-powder three-layer type, etc., and can be used for basic cosmetics such as lotion, emulsion, cream, and pack, makeup cosmetics such as lipstick, foundation, shampoo, etc. rinse,
It is used in a wide variety of applications, including cosmetics such as hair tonics, and quasi-drugs, but its true value is particularly demonstrated when applied to transparent or translucent lotions. This is because lotions are generally water-alcohol based and feel particularly sticky after use. The skin external preparation of the present invention may contain, as necessary, a humectant, a thickener, a preservative, an emulsifier, an antioxidant, a sequestering agent, within a range that does not impair the effects of the present invention.
UV absorbers, powders, pigments, drugs, pigments, fragrances, etc. can be added. [Effects of the Invention] Although the skin external preparation of the present invention contains mucopolysaccharide and has an excellent moisturizing effect, it does not have the stickiness characteristic of mucopolysaccharide, and has good stability and safety, and is excellent for the skin. It is an external preparation. [Example] Next, the present invention will be explained in more detail with reference to Examples. The present invention is not limited to this in any way. Example 1 Lotion ethanol 20.0 1,3-butylene glycol 5.0 Sodium hyaluronate 0.3 POE (polyoxyethylene, the same hereinafter, 15 mol) oleyl ether 0.8 Ethylparaben 0.1 Arbutin 6.0 Purified water Remaining (manufacturing method) POE in part of the ethanol Dissolve oleyl ether and ethyl paraben. Separately, dissolve 1,3-butylene glycol, sodium hyaluronate, and arbutin in the remaining purified water and ethanol. The ethanol phase was added to the aqueous phase and solubilized to obtain a lotion. Example 2 Example 2 was obtained according to Example 1 except that the amount of arbutin in Example 1 was reduced to 1.0% by weight. Comparative Example 1 Comparative Example 1 was obtained according to Example 1 except that arbutin was used. Usability of Examples 1-2 and Comparative Example 1 (stickiness)
were judged and evaluated through actual use tests by a panel specializing in women's beauty. (Judgment) A: Not sticky. B: Slightly sticky, but within a range that poses no problem in terms of usability. C: Sticky. D: Significantly sticky. The results are shown in Table-1. It is clear that arbutin prevents mucopolysaccharide from becoming sticky.

【表】 実施例3 フアンデーシヨン (A) セタノール 3.5 ステアリン酸 2.0 脱臭ラノリン 5.0 ワセリン 2.0 スクワラン 8.0 グリセリルモノオレート 2.5 POE(10)ベヘニルアルコール 0.5 エチルパラベン 0.2 ブチルパラベン 0.2 (B) コンドロイチン−6−硫酸ナトリウム 5.0 アルブチン 0.5 1,3−ブチレングリコール 2.0 調合粉末* 15.0 トリエタノールアミン 0.25 精製水 残余 調合粉末*……酸化チタン5.0、カオリン3.0、
タルク5.0、酸化鉄2.0よりなる粉末。 (製法) (A)の油相部と(B)の水相部を別々に加熱
撹拌する。油相部を水相部に添加し、乳化、冷
却してフアンデーシヨンを得た。 実施例4 化粧水 (A) 精製水 全体が100になる量 グリセリン 2.0 ヒアルロン酸ナトリウム 0.5 アルブチン 15.0 1,3−ブチレングリコール 2.0 (B) エタノール 15.0 精製レシチン 0.02 POE(60)硬化ヒマシ油 1.0 香 料 0.05 メチルパラベン 0.1 (製法) (A)の水相部および(B)のアルコール部を
それぞれ均一溶解した後、水相部にアルコール
部を加えて可溶化し、化粧水を得た。 実施例5 水性エツセンス (A) 精製水 全体が100になる量 1,3−ブチレングリコール 10.0 マルチトール 2.0 ヒアルロン酸ナトリウム 0.2 コンドロイチン−4−硫酸ナトリウム 0.1 アルブチン 1.0 ジプロピレングリコール 5.0 カルボキシメチル(セルロース) 0.2 (B) エタノール 5.0 POE(60)硬化ヒマシ油 1.0 ビタミンEアセテート 0.1 香 料 0.05 オレイルアルコール 0.2 メチルパラベン 0.2 (C)水酸化カリリウム 0.1 (製法) (A)の水相部および(B)のアルコール部を
それぞれ均一溶解した後、水相部にアルコール
部を加えて混合可溶化し、ついで(C)の水酸化カ
リウムを加えてエツセンスを得た。
[Table] Example 3 Foundation (A) Setanol 3.5 Stearic acid 2.0 Deodorized lanolin 5.0 Vaseline 2.0 Squalane 8.0 Glyceryl monooleate 2.5 POE(10) behenyl alcohol 0.5 Ethylparaben 0.2 Butylparaben 0.2 (B) Sodium chondroitin-6-sulfate 5.0 Arbutin 0.5 1,3-butylene glycol 2.0 Preparation powder* 15.0 Triethanolamine 0.25 Purified water Remaining Preparation powder*...Titanium oxide 5.0, Kaolin 3.0,
Powder consisting of talc 5.0 and iron oxide 2.0. (Production method) Heat and stir the oil phase (A) and the water phase (B) separately. The oil phase was added to the water phase, emulsified, and cooled to obtain a foundation. Example 4 Lotion (A) Purified water Amount to make the total 100 Glycerin 2.0 Sodium hyaluronate 0.5 Arbutin 15.0 1,3-butylene glycol 2.0 (B) Ethanol 15.0 Purified lecithin 0.02 POE (60) Hydrogenated castor oil 1.0 Fragrance 0.05 Methylparaben 0.1 (Production method) After uniformly dissolving the water phase (A) and the alcohol part (B), the alcohol part was added to the water phase for solubilization to obtain a lotion. Example 5 Aqueous essence (A) Purified water 1,3-butylene glycol 10.0 Maltitol 2.0 Sodium hyaluronate 0.2 Sodium chondroitin-4-sulfate 0.1 Arbutin 1.0 Dipropylene glycol 5.0 Carboxymethyl (cellulose) 0.2 ( B) Ethanol 5.0 POE (60) Hydrogenated castor oil 1.0 Vitamin E acetate 0.1 Fragrance 0.05 Oleyl alcohol 0.2 Methyl paraben 0.2 (C) Potassium hydroxide 0.1 (Production method) The aqueous phase part of (A) and the alcohol part of (B), respectively. After homogeneous dissolution, an alcohol part was added to the aqueous phase to mix and solubilize, and then potassium hydroxide (C) was added to obtain essence.

Claims (1)

【特許請求の範囲】[Claims] 1 ムコ多糖の一種又は二種以上と、アルブチン
0.1〜30重量%とを含有することを特徴とする皮
膚外用剤。
1 One or more mucopolysaccharides and arbutin
A skin external preparation characterized by containing 0.1 to 30% by weight.
JP4803485A 1985-03-11 1985-03-11 External agent for skin Granted JPS61207310A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4803485A JPS61207310A (en) 1985-03-11 1985-03-11 External agent for skin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4803485A JPS61207310A (en) 1985-03-11 1985-03-11 External agent for skin

Publications (2)

Publication Number Publication Date
JPS61207310A JPS61207310A (en) 1986-09-13
JPH0415763B2 true JPH0415763B2 (en) 1992-03-19

Family

ID=12792026

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4803485A Granted JPS61207310A (en) 1985-03-11 1985-03-11 External agent for skin

Country Status (1)

Country Link
JP (1) JPS61207310A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01213227A (en) * 1988-02-23 1989-08-28 Tadashi Koyake Ointment and solution
JP3634113B2 (en) * 1997-03-31 2005-03-30 株式会社資生堂 Topical skin preparation
JP2005187354A (en) * 2003-12-25 2005-07-14 Lion Corp Aqueous external preparation composition
MX2009007048A (en) * 2006-12-26 2009-07-10 Romano Dev Inc Skin lightening composition for hyperpigmented skin.
CN108553321B (en) * 2018-05-09 2021-08-10 重庆医药高等专科学校 Pearlescent lipstick and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5781410A (en) * 1980-11-11 1982-05-21 Tokitaka Mori Remedy for skin pigmentation
JPS57183707A (en) * 1981-05-02 1982-11-12 Shiseido Co Ltd Cosmetic
JPS57185208A (en) * 1981-05-07 1982-11-15 Shiseido Co Ltd Skin cosmetic
JPS6016906A (en) * 1983-07-07 1985-01-28 Pola Chem Ind Inc External drug for skin

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5781410A (en) * 1980-11-11 1982-05-21 Tokitaka Mori Remedy for skin pigmentation
JPS57183707A (en) * 1981-05-02 1982-11-12 Shiseido Co Ltd Cosmetic
JPS57185208A (en) * 1981-05-07 1982-11-15 Shiseido Co Ltd Skin cosmetic
JPS6016906A (en) * 1983-07-07 1985-01-28 Pola Chem Ind Inc External drug for skin

Also Published As

Publication number Publication date
JPS61207310A (en) 1986-09-13

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