JPH08283137A - Skin lightening cosmetic - Google Patents

Skin lightening cosmetic

Info

Publication number
JPH08283137A
JPH08283137A JP8661595A JP8661595A JPH08283137A JP H08283137 A JPH08283137 A JP H08283137A JP 8661595 A JP8661595 A JP 8661595A JP 8661595 A JP8661595 A JP 8661595A JP H08283137 A JPH08283137 A JP H08283137A
Authority
JP
Japan
Prior art keywords
group
pigmentation
skin lightening
cosmetic
acid ester
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
Application number
JP8661595A
Other languages
Japanese (ja)
Inventor
Tadashi Hase
正 長谷
Takatoshi Murase
孝利 村瀬
Yusuke Shibuya
祐輔 渋谷
Ichirou Tokimitsu
一郎 時光
Yoshinori Nishizawa
義則 西澤
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.)
Kao Corp
Original Assignee
Kao 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 Kao Corp filed Critical Kao Corp
Priority to JP8661595A priority Critical patent/JPH08283137A/en
Publication of JPH08283137A publication Critical patent/JPH08283137A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: To obtain a skin lightening cosmetic containing a gallic acid ester as an active ingredient, excellent in suppressing effect on wrinkles and on the formation of a pigmentation caused by the irradiation of ultraviolet rays and useful for preventing the pigmentation. CONSTITUTION: This skin lightening cosmetic contains a gallic acid ester expressed by the formula (R is a 1-2C or a 10-20C alkyl or alkenyl which may be substituted with a hydroxyl group) as an active ingredient, and is blended in a cosmetic by 0.0001-20wt.%, preferably by 0.01-5wt.%. It is possible to aim at the improvement of suppressing effect on the formation of wrinkles and spots by adding an antiinflammatory agent, etc., such as allantoin, glycyrrhetinic acid, etc. Furthermore, by blending commonly used cosmetic components suitably, the cosmetics such as O/W type and W/O type emulsified cosmetics, a cream, a milky lotion, a pack, a detergent, a foundation, etc., are prepared.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、皮膚の色素沈着を抑制
・改善する作用に優れた美白化粧料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a whitening cosmetic composition having an excellent action of suppressing and improving pigmentation of skin.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】近年、
健康で美しい肌を保つことが老若男女を問わず重大な関
心事となっている。ところが、肌は温度、湿度、紫外
線、加齢、疾病、ストレス、食習慣等により微妙な影響
を受け、そのため肌の諸機能の減退、肌の老化等の種々
のトラブルが発生する。
2. Description of the Related Art In recent years,
Maintaining healthy and beautiful skin has become a serious concern for people of all ages. However, the skin is subtly affected by temperature, humidity, ultraviolet rays, aging, illness, stress, eating habits, etc. Therefore, various troubles such as deterioration of various functions of the skin and aging of the skin occur.

【0003】しみ、そばかす及び日焼け後の肌への色素
沈着は、メラノサイトにより表皮内で合成されるメラニ
ン色素が増加することによって発生するものであり、そ
の発症機序については紫外線、女性ホルモン、遺伝的要
因などの関与が指摘されているが、未だ十分には解明さ
れていない。そのため、これまでにメラニンの生成抑制
や既成メラニンの還元などを目的とした薬剤が美白剤と
して研究されてきており、アルブチンやコウジ酸、ビタ
ミンC、カンゾウエキス(特開昭63−23809号、
特開平1−149706号公報)、カッコン(特開昭6
4−16709号公報)、ヒドロキシスチルベン(特開
昭64−38009号公報)、3−ヒドロキシクロモン
(特開昭55−111410号、特開昭55−1439
08号公報)、イソフラボン(特開昭58−22500
4号公報)などが提案されている。しかし、現状におい
ては実際の化粧品への配合性に優れ、かつ色素沈着抑制
効果の高い物質はほとんど無く、また、従来の美白剤は
その効果が十分ではなかった。
[0003] Stain, freckles and pigmentation on the skin after sunburn are caused by an increase in melanin pigment synthesized in the epidermis by melanocytes, and the pathogenic mechanism thereof is ultraviolet rays, female hormones and inheritance. Although it has been pointed out that the social factors are involved, it has not been fully clarified yet. Therefore, drugs for the purpose of suppressing the production of melanin or reducing existing melanin have been studied as whitening agents, and arbutin, kojic acid, vitamin C, licorice extract (JP-A-63-23809,
Japanese Unexamined Patent Publication No. 1-149706), and parentheses (Japanese Unexamined Patent Publication No. Sho 6-6)
4-16709), hydroxystilbene (JP-A-64-38009), 3-hydroxychromone (JP-A-55-111410, JP-A-55-1439).
08), isoflavones (JP-A-58-22500).
No. 4) is proposed. However, under the present circumstances, there are almost no substances that have excellent blending properties in actual cosmetics and have a high pigmentation-inhibiting effect, and conventional whitening agents are not sufficiently effective.

【0004】従って、本発明の目的は、肌への色素沈着
の予防・改善に有効な美白化粧料を提供することにあ
る。
Therefore, an object of the present invention is to provide a whitening cosmetic composition which is effective in preventing and improving pigmentation on the skin.

【0005】[0005]

【課題を解決するための手段】このような実情におい
て、本発明者は鋭意検討を行った結果、没食子酸エステ
ルが優れた色素沈着抑制作用を有することを見出し、本
発明を完成するに至った。
Under such circumstances, the present inventor has conducted diligent studies, and as a result, found that gallic acid ester has an excellent pigmentation-inhibiting action, and completed the present invention. .

【0006】すなわち、本発明は、次の一般式(1):That is, the present invention provides the following general formula (1):

【0007】[0007]

【化2】 Embedded image

【0008】〔式中、Rはヒドロキシ基が置換していて
もよい炭素数1、2又は10〜20の直鎖又は分岐鎖の
アルキル基又はアルケニル基を示す〕で表される没食子
酸エステルを有効成分として含有する美白化粧料を提供
するものである。
A gallic acid ester represented by the formula [wherein R represents a linear or branched alkyl or alkenyl group having 1, 2 or 10 to 20 carbon atoms which may be substituted by a hydroxy group] The present invention provides a whitening cosmetic composition containing an active ingredient.

【0009】一般式(1)で表される没食子酸エステル
において、Rはヒドロキシ基が置換していてもよい炭素
数1、2又は10〜20の直鎖又は分岐鎖のアルキル基
又はアルケニル基を示すが、その炭素数は1、2、10
〜15が好ましい。Rとして具体的にはメチル基、エチ
ル基、デシル基、ウンデシル基、ドデシル基、トリデシ
ル基、テトラデシル基、ペンタデシル基、ヘキサデシル
基、ヘプタデシル基、オクタデシル基、ノナデシル基、
イソヘキシル基、2−エチルヘキシル基、プロペニル
基、ブテニル基、ペンテニル基、オレイル基、リノレイ
ニル基、3,5,5−トリメチルヘキシル基、3,7−
ジメチルオクチル基、3,7,11−トリメチルドデシ
ル基、3−メチル−2−ブテニル基、3,7−ジメチル
−2,6−オクタジエニル基、シクロヘキシルメチル
基、シクロヘキシルエチル基、2−ヒドロキシプロピル
基、8−ヒドロキシオクチル基、10−ヒドロキシデシ
ル基、11−ヒドロキシウンデシル基、12−ヒドロキ
シデシル基、12−ヒドロキシオクタデシル基等を挙げ
ることができる。本発明においては、このうち直鎖アル
キル基が好ましい。すなわち没食子酸エステルとしては
没食子酸メチル、没食子酸エチル、没食子酸デシル、没
食子酸ウンデシル、没食子酸トリデシル等が好ましい。
In the gallic acid ester represented by the general formula (1), R represents a linear or branched alkyl group or alkenyl group having 1, 2 or 10 to 20 carbon atoms which may be substituted with a hydroxy group. The carbon number is 1, 2, 10
-15 are preferable. Specific examples of R include methyl group, ethyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group,
Isohexyl group, 2-ethylhexyl group, propenyl group, butenyl group, pentenyl group, oleyl group, linoleinyl group, 3,5,5-trimethylhexyl group, 3,7-
Dimethyloctyl group, 3,7,11-trimethyldodecyl group, 3-methyl-2-butenyl group, 3,7-dimethyl-2,6-octadienyl group, cyclohexylmethyl group, cyclohexylethyl group, 2-hydroxypropyl group, Examples thereof include 8-hydroxyoctyl group, 10-hydroxydecyl group, 11-hydroxyundecyl group, 12-hydroxydecyl group, and 12-hydroxyoctadecyl group. In the present invention, the linear alkyl group is preferable among them. That is, as the gallate ester, methyl gallate, ethyl gallate, decyl gallate, undecyl gallate, tridecyl gallate and the like are preferable.

【0010】式(1)の没食子酸エステルの配合量は特
に制限されるものではないが、配合時の色等の観点から
本発明の美白化粧料中に0.0001〜20重量%とす
ることが好ましく、0.01〜5重量%とすることが特
に好ましい。
The amount of gallic acid ester of the formula (1) is not particularly limited, but it is 0.0001 to 20% by weight in the whitening cosmetic composition of the present invention from the viewpoint of color and the like at the time of compounding. Is preferable, and it is particularly preferable to set it to 0.01 to 5% by weight.

【0011】本発明の美白化粧料は上記必須成分の他、
アラントイン、グリチルリチン酸等の公知の抗炎症剤な
どを添加することにより、しわやしみの形成抑制効果の
向上を図ることができる。また、化粧料成分として一般
に使用されている油分、ヒアルロン酸やセラミド等の保
湿剤、紫外線吸収剤、アルコール類、キレート剤、pH
調整剤、防腐剤、増粘剤、色素、香料等を任意に組み合
わせて配合することができる。
The whitening cosmetic composition of the present invention contains, in addition to the above essential components,
By adding known anti-inflammatory agents such as allantoin and glycyrrhizic acid, the effect of suppressing the formation of wrinkles and spots can be improved. In addition, oils commonly used as cosmetic ingredients, moisturizers such as hyaluronic acid and ceramide, ultraviolet absorbers, alcohols, chelating agents, pH
A regulator, an antiseptic, a thickener, a pigment, a fragrance and the like can be combined in any combination.

【0012】本発明の美白化粧料は一般美白化粧料に限
定されるものではなく、医薬部外品、薬用化粧料等を包
含するものである。本発明の美白化粧料は種々の形態及
び用途、例えば油/水型、水/油型の乳化化粧料、クリ
ーム、化粧乳液、化粧水、油性化粧料、パック剤、ファ
ンデーション等として用いることができる。
The whitening cosmetic of the present invention is not limited to general whitening cosmetics, but includes quasi drugs, medicated cosmetics and the like. The whitening cosmetic composition of the present invention can be used in various forms and applications, for example, oil / water type, water / oil type emulsified cosmetics, creams, lotions, lotions, oily cosmetics, packs, foundations and the like. .

【0013】[0013]

【発明の効果】本発明の美白化粧料は、紫外線の照射に
よって生じるしわや色素沈着形成抑制作用に優れてお
り、このため色素沈着予防用化粧料として有用である。
The whitening cosmetic composition of the present invention is excellent in the effect of suppressing the formation of wrinkles and pigmentation caused by the irradiation of ultraviolet rays, and is therefore useful as a cosmetic composition for preventing pigmentation.

【0014】[0014]

【実施例】次に実施例を挙げて説明するが、本発明はこ
れらの実施例に限定されるものではない。
The present invention will be described below with reference to examples, but the present invention is not limited to these examples.

【0015】試験例1 褐色モルモットの背部のUV−
Bによる色素沈着に対する効果:褐色モルモットの背部
毛をバリカンとシェーバーにて丁寧に剃毛した後、1.
5cm四方に8分割した。各々の部位に評価試料(2%
エタノール溶液、20μl)を塗布し、2時間後、塗布
した試料をエタノールで拭き取り、UV−B領域の紫外
線を最小紅斑量(MED)の2倍量を照射した。UV照
射後、再度評価試料を塗布した。以上の操作を3日間繰
り返した。それ以降は試料(2%エタノール溶液、10
μl)のみ1週間連続して塗布し、2週間後に色素沈着
量を調べた。また、コントロールとしてエタノールのみ
を塗布したものを試料と同様に試験した。
Test Example 1 UV-on the back of a brown guinea pig
Effect of B on pigmentation: After brown hair of a guinea pig was shaved carefully with a hair clipper and a shaver, 1.
It was divided into eight 5 cm squares. Evaluation sample (2%
An ethanol solution (20 μl) was applied, and after 2 hours, the applied sample was wiped with ethanol and irradiated with ultraviolet rays in the UV-B region at twice the minimum erythema dose (MED). After UV irradiation, the evaluation sample was applied again. The above operation was repeated for 3 days. After that, samples (2% ethanol solution, 10
μl) was applied continuously for 1 week, and after 2 weeks, the amount of pigmentation was examined. As a control, a sample coated with only ethanol was tested in the same manner as the sample.

【0016】評価は色差計(村上色彩製、CMS−12
00)を用いて測定を行い、得られたマンセル値からL
*値を算出し、下記式に従ってΔL*を求め、色素沈着の
程度を比較した。−ΔL*の値が大きいほど色素沈着の
程度が強いことを示す。結果を表1に示す。
A color difference meter (CMS-12, manufactured by Murakami Color Co., Ltd.) was used for evaluation.
00) was used for measurement, and L was calculated from the obtained Munsell value.
* The value was calculated, ΔL * was calculated according to the following formula, and the degree of pigmentation was compared. The larger the value of −ΔL *, the stronger the degree of pigmentation. The results are shown in Table 1.

【0017】[0017]

【数1】ΔL*=(UV−B照射2週間後のL*値)−
(UV−B照射前のL*値)
[Formula 1] ΔL * = (L * value 2 weeks after UV-B irradiation) −
(L * value before UV-B irradiation)

【0018】[0018]

【表1】 [Table 1]

【0019】表1から、没食子酸エステルは優れた色素
沈着抑制作用を有することがわかる。
From Table 1, it can be seen that gallic acid ester has an excellent pigmentation suppressing effect.

【0020】実施例1〜3示す化粧料を常法に従って調
製した。
The cosmetics shown in Examples 1 to 3 were prepared by a conventional method.

【0021】実施例1 クリーム:Example 1 Cream:

【表2】 (成分) (重量%) 没食子酸エチル 0.2 コレステロール 0.5 コレステロールイソステアレート 1 ポリエーテル変性シリコーン 1.5 環状シリコーン 20 メチルフェニルポリシロキサン 2 メチルポリシロキサン 2 硫酸マグネシウム 0.5 55%エタノール 5 カルボキシメチルキチン 0.5 セラミド 1 香料,色素 微量 精製水 残量 計 100.0Table 2 (Components) (wt%) Ethyl gallate 0.2 Cholesterol 0.5 Cholesterol isostearate 1 Polyether-modified silicone 1.5 Cyclic silicone 20 Methylphenylpolysiloxane 2 Methylpolysiloxane 2 Magnesium sulfate 0.5 55% Ethanol 5 Carboxymethyl chitin 0.5 Ceramide 1 Perfume, pigment Micro purified water Residual amount meter 100.0

【0022】実施例2 スキンローション:Example 2 Skin lotion:

【表3】 (成分) (重量%) 没食子酸エチル 2 グリセリンモノステアレート 1 エタノール 15 プロピレングリコール 4 イソプロピルパルミテート 3 ラノリン 1 セラミド 0.5 パラオキシ安息香酸メチル 0.1 ビタミンC 0.5 香料,色素 微量 精製水 残量 計 100.0[Table 3] (Components) (wt%) Ethyl gallate 2 Glycerin monostearate 1 Ethanol 15 Propylene glycol 4 Isopropyl palmitate 3 Lanolin 1 Ceramide 0.5 Methyl paraoxybenzoate 0.1 Vitamin C 0.5 Perfume, pigment Micro Purified Water Fuel Gauge 100.0

【0023】実施例3 パック剤:Example 3 Packing agent:

【表4】 (成分) (重量%) 没食子酸エチル 3 ポリビニルアルコール 20 グリセリン 5 エタノール 16 香料,色素 微量 精製水 残量 計 100[Table 4] (Components) (% by weight) Ethyl gallate 3 Polyvinyl alcohol 20 Glycerin 5 Ethanol 16 Perfume, pigment Micro purified water Residual amount meter 100

───────────────────────────────────────────────────── フロントページの続き (72)発明者 西澤 義則 栃木県宇都宮市清原台1−17−10 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yoshinori Nishizawa 1-17-10 Kiyoharadai, Utsunomiya City, Tochigi Prefecture

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 次の一般式(1): 【化1】 〔式中、Rはヒドロキシ基が置換していてもよい炭素数
1、2又は10〜20の直鎖又は分岐鎖のアルキル基又
はアルケニル基を示す〕で表される没食子酸エステルを
有効成分として含有する美白化粧料。
1. The following general formula (1): [Wherein R represents a linear or branched alkyl group or alkenyl group having 1, 2 or 10 to 20 carbon atoms which may be substituted by a hydroxy group] as a gallic acid ester Whitening cosmetics contained.
JP8661595A 1995-04-12 1995-04-12 Skin lightening cosmetic Pending JPH08283137A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8661595A JPH08283137A (en) 1995-04-12 1995-04-12 Skin lightening cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8661595A JPH08283137A (en) 1995-04-12 1995-04-12 Skin lightening cosmetic

Publications (1)

Publication Number Publication Date
JPH08283137A true JPH08283137A (en) 1996-10-29

Family

ID=13891934

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8661595A Pending JPH08283137A (en) 1995-04-12 1995-04-12 Skin lightening cosmetic

Country Status (1)

Country Link
JP (1) JPH08283137A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997035618A1 (en) * 1996-03-22 1997-10-02 Kao Corporation Dermatologic preparation
JP2001031580A (en) * 1999-05-19 2001-02-06 Kose Corp Preparation for external use for skin
WO2003027055A1 (en) * 2001-09-24 2003-04-03 Amorepacific Corporation 3,4,5-trimethoxy phenyl-based ester compound and preparation method thereof and whitening cosmetic composition containing the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997035618A1 (en) * 1996-03-22 1997-10-02 Kao Corporation Dermatologic preparation
JP2001031580A (en) * 1999-05-19 2001-02-06 Kose Corp Preparation for external use for skin
WO2003027055A1 (en) * 2001-09-24 2003-04-03 Amorepacific Corporation 3,4,5-trimethoxy phenyl-based ester compound and preparation method thereof and whitening cosmetic composition containing the same
US7517911B2 (en) 2001-09-24 2009-04-14 Amorepacific Corporation 3,4,5-trimethoxy phenyl-based ester compound and preparation method thereof and whitening cosmetic composition containing the same

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