JPH0977655A - Skin preparation for external use - Google Patents
Skin preparation for external useInfo
- Publication number
- JPH0977655A JPH0977655A JP27335795A JP27335795A JPH0977655A JP H0977655 A JPH0977655 A JP H0977655A JP 27335795 A JP27335795 A JP 27335795A JP 27335795 A JP27335795 A JP 27335795A JP H0977655 A JPH0977655 A JP H0977655A
- Authority
- JP
- Japan
- Prior art keywords
- skin
- preparation
- external use
- aminophenol
- oil
- 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.)
- Pending
Links
Landscapes
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は美白に有効な物質に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a substance effective for whitening.
【0002】[0002]
【従来の技術】美白作用をもった物質はすでに多くのも
のが知られている。製品化されたものにはコウジ酸、ア
ルブチンなどがある。しかし、効果が弱い等問題があっ
た。2. Description of the Related Art Many substances having a whitening effect are already known. Commercialized products include kojic acid and arbutin. However, there were problems such as a weak effect.
【0003】[0003]
【発明が解決しようとする課題】本発明の目的は、皮膚
に適用して安全であると共に、美白作用が大きい皮膚外
用剤を提供することである。SUMMARY OF THE INVENTION An object of the present invention is to provide a skin external preparation which is safe when applied to the skin and has a large whitening effect.
【0004】[0004]
【課題を解決する手段】本発明者らは、前記の課題を解
決するため、種々の物質をスクリーニングして調べ、化
粧品として利用価値のあるものを検討した。その結果、
4−アミノフェノールに着目し各種の実験を行ったとこ
ろ、美白作用が強いことが判明した。[Means for Solving the Problems] In order to solve the above-mentioned problems, the present inventors have screened and examined various substances and examined those which are useful as cosmetics. as a result,
When various experiments were conducted focusing on 4-aminophenol, it was found that the whitening effect was strong.
【0005】すなわち、4−アミノフェノールを含む皮
膚外用剤である。That is, it is an external preparation for skin containing 4-aminophenol.
【0006】この物質を他の化粧品原料例えばスクワラ
ン、ホホバ油等の液状油、ミツロウ、セチルアルコール
等の固体油、各種の活性剤、グリセリン、1,3ブチレ
ングリコール等の保湿剤や各種薬剤等を添加してさまざ
まな剤形の皮膚外用剤を調整することができる。例えば
ローション、クリーム、乳液、パック等で目的に応じて
利用形態を考えればよい。配合量は製剤、用途によって
異なるが通常は0.005〜20%である。This substance is used as a raw material for other cosmetics such as liquid oils such as squalane and jojoba oil, solid oils such as beeswax and cetyl alcohol, various activators, humectants such as glycerin and 1,3 butylene glycol and various chemicals. It can be added to prepare various external forms of the skin external preparation. For example, a lotion, a cream, a milky lotion, a pack, or the like may be used depending on the purpose. The blending amount varies depending on the formulation and use, but is usually 0.005 to 20%.
【0007】[0007]
【実施例】以下に実際の利用方法である実施例を記載す
るが、本発明はこの実施例によって何ら限定されるもの
ではない。EXAMPLE An example of an actual usage will be described below, but the present invention is not limited to this example.
【0008】 実施例−1 ローション 重量部 オリーブ油 0.5 4−アミノフェノール 0.2 ポリオキシエチレン(20E.0)ソルビタンモノステアレート 2.0 ポリオキシエチレン(60E.0)硬化ヒマシ油 2.0 エタノール 10.0 1.0%ヒアルロン酸ナトリウム水溶液 5.0 精製水 80.0Example-1 Lotion parts by weight Olive oil 0.5 4-Aminophenol 0.2 Polyoxyethylene (20E.0) sorbitan monostearate 2.0 Polyoxyethylene (60E.0) hydrogenated castor oil 2.0 Ethanol 10.0 1.0% sodium hyaluronate aqueous solution 5.0 Purified water 80.0
【0009】 実施例−2 クリーム 重量部 A スクワラン 20.0 オリーブ油 2.0 ミンク油 1.0 ホホバ油 5.0 ミツロウ 5.0 セトステアリルアルコール 2.0 グリセリンモノステアレート 1.0 ソルビタンモノステアレート 2.0 4−アミノフェノール 0.1 B 精製水 47.9 ポリオキシエチレン(20E.0)ソルビタンモノステアレート 2.0 ポリオキシエチレン(60E.0)硬化ヒマシ油 1.0 グリセリン 5.0 1.0%ヒアルロン酸ナトリウム水溶液 5.0 パラオキシ安息香酸メチル 0.1 AとBをそれぞれ計量し、70℃まで加温し、BにAを攪拌しつつ徐々に加え たのち、ゆっくり攪拌しつつ30℃まで冷却した。Example-2 Cream parts by weight A Squalane 20.0 Olive oil 2.0 Mink oil 1.0 Jojoba oil 5.0 Beeswax 5.0 Cetostearyl alcohol 2.0 Glycerin monostearate 1.0 Sorbitan monostearate 2.0 4-Aminophenol 0.1 B Purified water 47.9 Polyoxyethylene (20E.0) sorbitan monostearate 2.0 Polyoxyethylene (60E.0) hydrogenated castor oil 1.0 Glycerin 5.01 0.0% aqueous solution of sodium hyaluronate 5.0 Methyl paraoxybenzoate 0.1 Weigh A and B respectively, warm to 70 ° C, slowly add A to B with stirring, then slowly stir 30 Cooled to ° C.
【0010】チロシナーゼ活性阻害 (試験方法)マックルバルン(Mcllvaln)緩衝
液0.9ml、1.66mMチロシン(Tyrosin
e)溶液1.0ml、検体のジメチルスルオキシド溶液
0.1ml、精製水0.9mlをスクリューバイアルに
とり、37℃恒温水槽中で5分以上加温した。チロシナ
ーゼ溶液(Sigma 社製、マッシュルーム由来、9
14ユニット/ml)0.1mlを加え、37℃恒温水
槽中で保温し、10分後に475nmで吸光度を測定し
た。対照として、上記試料液のかわりにジメチルスルオ
キシドを加え同様に測定した。 (計算式) チロシナーゼ活性阻害率(%)={B−(A−P)}/
B×100 但し A:試料検体の吸光度 B:対照の吸光度 P:試料検体の着色による吸光度(3倍希釈)Inhibition of tyrosinase activity (Test method) 0.9 ml of McClbaln buffer, 1.66 mM tyrosine (Tyrosin)
e) 1.0 ml of the solution, 0.1 ml of the sample dimethylsulfoxide solution, and 0.9 ml of purified water were placed in a screw vial and heated in a 37 ° C. constant temperature water bath for 5 minutes or more. Tyrosinase solution (manufactured by Sigma, mushroom-derived, 9
(14 units / ml), and the solution was kept warm in a constant temperature water bath at 37 ° C., and the absorbance was measured at 475 nm after 10 minutes. As a control, dimethylsulfoxide was added instead of the above sample solution, and the measurement was performed in the same manner. (Calculation formula) Tyrosinase activity inhibition rate (%) = {B- (AP)} /
B × 100 where A: Absorbance of sample specimen B: Absorbance of control P: Absorbance due to coloring of sample specimen (3 times dilution)
【0011】[0011]
【表1】 [Table 1]
【0012】使用テスト 女性8名の顔面を左右に分け、一方を実施例、もう一方
を比較例として毎日、1回以上使用してもらって、3月
後、アンケートした。なお、比較例は実施例より4−ア
ミノフェノールを水にかえたものである。(比較例1,
2) 判定基準は以下のようでアンケートの結果をまとめたの
が以下の表である。 実施例の方が非常によい 3 実施例の方がかなりよい 2 実施例の方がややよい 1 差がない 0 比較例の方がややよい −1 比較例の方がかなりよい −2 比較例の方が非常によい −3Use test Eight women's faces were divided into right and left sides, one of which was used as an example and the other of which was used as a comparative example once or more daily. Three months later, a questionnaire was given. In the comparative example, 4-aminophenol was replaced with water as compared with the examples. (Comparative Example 1,
2) The criteria are as follows, and the results of the questionnaire are summarized in the table below. Example is much better 3 Example is much better 2 Example is slightly better 1 No difference 0 Comparative example is slightly better -1 Comparative example is much better -2 Comparative example Is much better -3
【0013】 [0013]
【0014】[0014]
【効果】4−アミノフェノールはコウジ酸等に比較して
美白作用が強く、皮膚外用剤の有効成分として非常に有
効である。[Effect] 4-Aminophenol has a stronger whitening effect than kojic acid and the like, and is very effective as an active ingredient of a skin external preparation.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27335795A JPH0977655A (en) | 1995-09-14 | 1995-09-14 | Skin preparation for external use |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27335795A JPH0977655A (en) | 1995-09-14 | 1995-09-14 | Skin preparation for external use |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0977655A true JPH0977655A (en) | 1997-03-25 |
Family
ID=17526779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27335795A Pending JPH0977655A (en) | 1995-09-14 | 1995-09-14 | Skin preparation for external use |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0977655A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999010318A1 (en) * | 1997-08-27 | 1999-03-04 | L'oreal | Aminophenol derivatives and their use in cosmetics |
FR2802415A1 (en) * | 1999-12-20 | 2001-06-22 | Oreal | COSMETIC COMPOSITION COMPRISING N-ETHYLOXYCARBONYL-4-AMINO-PHENOL AND ARBUTIN OR ITS DERIVATIVES AND / OR ELLAGIC ACID OR DERIVATIVES THEREOF |
FR2802416A1 (en) * | 1999-12-20 | 2001-06-22 | Oreal | COSMETIC COMPOSITION COMPRISING AN AMINOPHENOL DERIVATIVE |
FR2804866A1 (en) * | 2000-02-16 | 2001-08-17 | Oreal | N-CHOLESTERYLOXYCARBONYL-4-PARA-AMINOPHENOL-BASED COMPOSITION AND HYDROQUINONE OR ONE OF ITS DERIVATIVES |
EP1205179A1 (en) * | 2000-11-10 | 2002-05-15 | L'oreal | Cosmetic composition comprising an aminophenol derivative and an isoflavonoid |
KR100546018B1 (en) * | 2001-06-26 | 2007-04-12 | 로레알 | Compositions comprising a compound of low solubility and a lipophilic amino acid derivative, uses thereof and process for dissolving a compound of low solubility |
WO2009007412A2 (en) * | 2007-07-09 | 2009-01-15 | Basf Beauty Care Solutions France Sas | Age deglycation |
-
1995
- 1995-09-14 JP JP27335795A patent/JPH0977655A/en active Pending
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999010318A1 (en) * | 1997-08-27 | 1999-03-04 | L'oreal | Aminophenol derivatives and their use in cosmetics |
FR2802415A1 (en) * | 1999-12-20 | 2001-06-22 | Oreal | COSMETIC COMPOSITION COMPRISING N-ETHYLOXYCARBONYL-4-AMINO-PHENOL AND ARBUTIN OR ITS DERIVATIVES AND / OR ELLAGIC ACID OR DERIVATIVES THEREOF |
FR2802416A1 (en) * | 1999-12-20 | 2001-06-22 | Oreal | COSMETIC COMPOSITION COMPRISING AN AMINOPHENOL DERIVATIVE |
EP1110538A3 (en) * | 1999-12-20 | 2004-01-02 | L'oreal | Cosmetic composition comprising an aminophenol derivative |
US7056498B2 (en) * | 1999-12-20 | 2006-06-06 | L'oreal | Composition containing aminophenol derivative, use thereof, and process for dissolving aminophenol derivative |
FR2804866A1 (en) * | 2000-02-16 | 2001-08-17 | Oreal | N-CHOLESTERYLOXYCARBONYL-4-PARA-AMINOPHENOL-BASED COMPOSITION AND HYDROQUINONE OR ONE OF ITS DERIVATIVES |
US6960347B2 (en) | 2000-02-16 | 2005-11-01 | L'oreal | Composition based on N-cholesteryloxycarbonyl-4-para-aminophenol and hydroquinone or one of its derivatives |
EP1205179A1 (en) * | 2000-11-10 | 2002-05-15 | L'oreal | Cosmetic composition comprising an aminophenol derivative and an isoflavonoid |
FR2816502A1 (en) * | 2000-11-10 | 2002-05-17 | Oreal | COSMETIC COMPOSITION CONSISTING OF AN AMINOPHENOL DERIVATIVE AND AN ISOFLAVONOIDE |
KR100546018B1 (en) * | 2001-06-26 | 2007-04-12 | 로레알 | Compositions comprising a compound of low solubility and a lipophilic amino acid derivative, uses thereof and process for dissolving a compound of low solubility |
WO2009007412A2 (en) * | 2007-07-09 | 2009-01-15 | Basf Beauty Care Solutions France Sas | Age deglycation |
WO2009007412A3 (en) * | 2007-07-09 | 2009-04-02 | Basf Beauty Care Solutions F | Age deglycation |
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