JPH11269066A - Skin-bleaching agent for peroral administration and skin-bleaching food - Google Patents
Skin-bleaching agent for peroral administration and skin-bleaching foodInfo
- Publication number
- JPH11269066A JPH11269066A JP10072100A JP7210098A JPH11269066A JP H11269066 A JPH11269066 A JP H11269066A JP 10072100 A JP10072100 A JP 10072100A JP 7210098 A JP7210098 A JP 7210098A JP H11269066 A JPH11269066 A JP H11269066A
- Authority
- JP
- Japan
- Prior art keywords
- skin
- isoflavone
- isoflavones
- group
- bleaching
- 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
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- Saccharide Compounds (AREA)
- Pyrane Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、経口で美白効果を
有する美白剤及び美白用食品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a whitening agent and a whitening food having an oral whitening effect.
【0002】[0002]
【従来の技術】女性にとって美容上最も多い悩みの一つ
に皮膚のしみ、そばかすがある。かかるしみ、そばかす
は、一般に紫外線による刺激やホルモン異常等によって
メラノサイトが刺激され、そこで生合成されたメラニン
色素が皮膚に沈着して発生するものと考えられている。
従来このようなしみ、そばかすに対しては、アスコルビ
ン酸類、ハイドロキノン誘導体、コウジ酸類、イソフラ
ボン配糖体、胎盤抽出物等のメラニン抑制剤を化粧品に
配合し、これを皮膚に塗布することによって治療する方
法が主に用いられてきた。2. Description of the Related Art One of the most cosmetic concerns for women is skin spots and freckles. It is considered that such spots and freckles are generally generated by stimulating melanocytes due to stimulation by ultraviolet rays, hormonal abnormalities, etc., and depositing the melanin pigment biosynthesized there on the skin.
Conventionally, such spots and freckles are treated by adding a melanin inhibitor such as ascorbic acid, hydroquinone derivative, kojic acid, isoflavone glycoside, placenta extract to cosmetics and applying it to the skin. The method has been mainly used.
【0003】また紫外線を浴びた皮膚には、淡色メラニ
ンが一次的に酸化して黒く見える一次黒化、メラノサイ
トの機能が亢進し、表皮細胞中のメラニン量が増加して
黒化する二次黒化が生じる(日焼け)。黒化が進行した
皮膚は、元の色にもどるまで数ヶ月以上を要する。この
ため過度の日焼けから回復させるため、サンスクリーン
等が用いられてきた。[0003] In addition, on the skin exposed to ultraviolet light, primary melanin, which is primarily oxidized by light-colored melanin, becomes black, and the function of melanocytes is enhanced, and the amount of melanin in epidermal cells increases, resulting in secondary black. The formation occurs (sunburn). It takes several months or more for the skin with advanced darkening to return to its original color. For this reason, sunscreens and the like have been used to recover from excessive sunburn.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、アスコ
ルビン酸類、ハイドロキノン誘導体、コウジ酸類、胎盤
抽出物等はメラニン抑制効果が弱く、化粧品に配合して
も十分な美白効果を発現することができなかった。また
イソフラボン配糖体は優れた美白効果を有するが、全身
にしみ、そばかすが生じた場合に、イソフラボン配糖体
含有化粧品を全身に塗布することは容易ではなく、使用
者の負担が大きかった。またサンスクリーン等では日焼
け等により生じた皮膚の黒化を回復させることは困難で
あった。さらに上記アスコルビン酸類やサンスクリーン
等ではしみ、そばかすの発生や日焼けを予防することは
困難であった。However, ascorbic acids, hydroquinone derivatives, kojic acids, placental extracts, and the like have a weak melanin-suppressing effect and cannot exhibit a sufficient whitening effect even when incorporated into cosmetics. In addition, isoflavone glycosides have an excellent whitening effect, but it is not easy to apply isoflavone glycoside-containing cosmetics to the whole body when spots and freckles occur on the whole body, and the burden on the user is large. In addition, it was difficult to recover the blackening of the skin caused by sunburn or the like with sunscreen or the like. Furthermore, it has been difficult to prevent the occurrence of freckles and sunburn with the ascorbic acids and sunscreens.
【0005】したがって本発明は、労力を要することな
くしみ、そばかすや日焼け等の皮膚の黒化等を予防また
は回復させて簡単に美白効果を得ることができる美白用
組成物を提供することを目的とする。Accordingly, an object of the present invention is to provide a whitening composition which can easily obtain a whitening effect by preventing or restoring blackening of skin such as freckles and sunburn without labor. And
【0006】[0006]
【課題を解決するための手段】本発明者らは上記目的を
達成すべく鋭意研究した結果、全く意外にもイソフラボ
ン類が経口投与においてそばかすや日焼け等の黒化等を
予防または回復させ、優れた美白効果を有することを見
出し、本発明を完成させた。Means for Solving the Problems The present inventors have conducted intensive studies in order to achieve the above object, and as a result, surprisingly, isoflavones can prevent or recover freckles and blackening such as sunburn when administered orally, and provide excellent results. The present invention has been found to have a whitening effect.
【0007】すなわち本発明は、イソフラボン類を有効
成分とする経口用美白剤を提供するものである。また本
発明はイソフラボン類を配合した美白用食品を提供する
ものである。That is, the present invention provides an oral whitening agent containing isoflavones as an active ingredient. The present invention also provides a whitening food containing isoflavones.
【0008】[0008]
【発明の実施の形態】本発明において用いられるイソフ
ラボン類とは、イソフラボン及びその誘導体であり、イ
ソフラボン誘導体としては次の一般式(1)BEST MODE FOR CARRYING OUT THE INVENTION The isoflavones used in the present invention are isoflavones and derivatives thereof, and the isoflavone derivatives represented by the following general formula (1)
【0009】[0009]
【化1】 Embedded image
【0010】(式中、R1 は水素原子またはヒドロキシ
ル基を示し、R2 は水素原子、ヒドロキシル基または炭
素数1〜6のアルコキシル基を示し、R3 は水素原子ま
たは次の一般式(2)(Wherein, R 1 represents a hydrogen atom or a hydroxyl group, R 2 represents a hydrogen atom, a hydroxyl group or an alkoxyl group having 1 to 6 carbon atoms, and R 3 represents a hydrogen atom or the following general formula (2) )
【0011】[0011]
【化2】 Embedded image
【0012】(式中、R4 は水素原子、またはCO(C
H2)n R5 (式中nは1〜5の整数を示し、R5 は水
素原子またはCOOHを示す。)を示す。)で表される
基を示す。)で表されるものが好ましい。このうちR2
は水素原子及びメトキシ基が特に好ましい。またR3 は
水素原子または一般式(2)においてR4 が水素原子、
アセチル基、2−カルボキシエタノイル基もしくは3−
カルボキシプロパノイル基であることが特に好ましい。
最も好ましいイソフラボン類としては、イソフラボン、
ダイジン、グリシチン、ゲニスチン、6’−O−アセチ
ルダイジン、6’−O−アセチルグリシチン、6’−O
−アセチルゲニスチン、6’−O−マロニルダイジン、
6’−O−マロニルグリシチン、6’−O−マロニルゲ
ニスチン、6’−O−スクシニルダイジン、6’−O−
スクシニルグリシチン、6’−O−スクシニルゲニスチ
ン、ダイゼイン、グリシテイン、ゲニステインが挙げら
れる。本発明においてはこれらのイソフラボンまたはイ
ソフラボン誘導体を1種または2種以上用いることがで
きる。(Wherein R 4 is a hydrogen atom or CO (C
H2) n R 5 (wherein n represents an integer of 1 to 5, and R 5 represents a hydrogen atom or COOH). ). ) Are preferred. R 2
Is particularly preferably a hydrogen atom or a methoxy group. R 3 is a hydrogen atom or R 4 in the general formula (2) is a hydrogen atom;
Acetyl group, 2-carboxyethanoyl group or 3-
Particularly preferred is a carboxypropanoyl group.
As the most preferred isoflavones, isoflavones,
Daidzin, glycitin, genistin, 6'-O-acetyldaididine, 6'-O-acetylglycitin, 6'-O
-Acetylgenistin, 6'-O-malonyl daidzin,
6'-O-malonylglycitin, 6'-O-malonylgenistin, 6'-O-succinyl daidzin, 6'-O-
Succinylglycitin, 6'-O-succinylgenistin, daidzein, glycitein, genistein. In the present invention, one or more of these isoflavones or isoflavone derivatives can be used.
【0013】かかるイソフラボン類はすべて公知の化合
物である。イソフラボンは天然には存在せず、例えば塩
基の存在下ジヒドロキシフェニルベンジルケトンとオル
トギ酸メチルエステルから7−ヒドロキシイソフラボン
が合成できる。イソフラボン誘導体はイソフラボンから
合成することもできるが、マメ科、バラ科、アヤメ科等
の植物に含まれており、例えばマメ科植物、好ましくは
大豆、特に好ましくは粉砕脱脂大豆からメタノール等の
低級アルコール等を用いて抽出することもできる。本発
明に用いるイソフラボン誘導体は粗抽出物でも精製物で
もよい。また市販品を用いることもできる。市販品とし
ては、例えばフジフラボンP40(フジッコ社製)等が
挙げられる。All such isoflavones are known compounds. Isoflavone does not exist in nature, and for example, 7-hydroxyisoflavone can be synthesized from dihydroxyphenylbenzylketone and methyl orthoformate in the presence of a base. Isoflavone derivatives can also be synthesized from isoflavones, but are included in plants such as legumes, roses, and irises; for example, legumes, preferably soybeans, and particularly preferably lower alcohols such as methanol from ground defatted soybeans. Can be used for extraction. The isoflavone derivative used in the present invention may be a crude extract or a purified product. Also, commercially available products can be used. Examples of commercially available products include Fujiflavone P40 (manufactured by Fujikko).
【0014】本発明の経口用美白剤は、かかるイソフラ
ボン類を散剤、顆粒剤、カプセル剤、丸剤、錠剤等の固
形製剤、または水剤、懸濁剤、乳剤等の液剤等に製剤化
して得られる。製剤化にあたっては、経口投与剤に一般
に用いられる、賦形剤、結合剤、崩壊剤、滑沢剤、コー
ティング剤、基剤、懸濁化剤、乳化剤、保湿剤、保存
剤、安定剤、界面活性剤、矯味剤等を添加し、常法にし
たがって製造することができる。The oral whitening agent of the present invention is prepared by formulating such isoflavones into solid preparations such as powders, granules, capsules, pills and tablets, or liquids such as solutions, suspensions and emulsions. can get. Upon formulation, excipients, binders, disintegrants, lubricants, coatings, bases, suspending agents, emulsifiers, humectants, preservatives, stabilizers, and surfactants commonly used for oral administration Activators, flavoring agents and the like can be added to produce the composition according to a conventional method.
【0015】またかかるイソフラボン類を食品に配合す
ることもできる。これによりイソフラボン類を無理なく
摂取することができる。イソフラボン類を配合する食品
には特に制限はなく、ジュース、牛乳、カレー等の液状
またはペースト状食品、ガム、豆腐等の固形状食品、あ
るいは粉末状の保存食品等その形態は問わない。イソフ
ラボン類は、食品製造時に原料の一部として添加しても
よく、また食品製造終了後に添加してもよい。[0015] Such isoflavones can also be incorporated into foods. Thereby, isoflavones can be taken without difficulty. The food containing the isoflavones is not particularly limited, and may be in any form such as liquid or paste food such as juice, milk, curry, solid food such as gum, tofu, or powdered preserved food. The isoflavones may be added as a part of the raw material at the time of producing the food, or may be added after the production of the food.
【0016】イソフラボン類の経口用美白剤及び美白用
食品中の配合量は、例えば0.002重量%以上、特に
0.02〜40重量%であることが好ましい。この範囲
であれば製剤化が容易であり、また効率よくイソフラボ
ン類を摂取することができる。The compounding amount of the isoflavones in the oral whitening agent and the whitening food is, for example, preferably 0.002% by weight or more, particularly preferably 0.02 to 40% by weight. Within this range, formulation is easy and isoflavones can be ingested efficiently.
【0017】またイソフラボン類の成人一人当たりの1
日の摂取量は、年齢、健康状態、体重等にもよるが、日
焼け等の予防または回復の場合には一般に1〜120,
000mg、特に10〜12,000mgであることが
好ましく、かかる摂取を10日間以上、特に20日間以
上続けることが好ましい。The isoflavones per adult person
The daily intake depends on the age, health condition, weight, etc., but is generally 1 to 120, in the case of prevention or recovery of sunburn.
Preferably, the dose is 2,000 mg, especially 10 to 12,000 mg, and such intake is preferably continued for at least 10 days, especially at least 20 days.
【0018】[0018]
【実施例】次に実施例を挙げて本発明をさらに詳細に説
明するが、本発明は以下の実施例に限定されるものでは
ない。EXAMPLES Next, the present invention will be described in more detail by way of examples, but the present invention is not limited to the following examples.
【0019】試験例1 黒化した皮膚の美白効果の確認 メス6週齢の有色モルモットの背の半分を除毛し、該除
毛した部分に1日目はUVランプ1.2mWを5分間、
2及び3日目は1.0mWを5分間照射した。2週間後
から、これらのモルモットを紫外線誘導色素沈着の程度
に差が生じないように4群に分け(各群5〜6頭)、市
販の固形飼料(オリエンタル社製RC4)に大豆由来の
イソフラボン誘導体含有飼料(フジフラボンP40(フ
ジッコ社製))をイソフラボン誘導体がそれぞれ0重量
%(第1群)、0.02重量%(第2群)、0.2重量
%(第3群)及び2重量%(第4群)となるように配合
した飼料の給餌を開始した。各群の一匹の一日当たりの
飼料摂取量は50g/日であった。給餌開始日及び開始
6週間後までの1週間毎に色差計(日本電色工業社製1
001DP)を用いて色差を測定した。すなわち同一点
を5点色差測定し、その平均のL値をその固体のL値と
し、各群の平均のL値を求めた。次いで給餌開始日のL
値(L0 値)との差dLを算出した。結果を図1に示
す。図1は各測定日における各群のdLを示したもので
あり、dLが高いほど、皮膚の紫外線による色素沈着
(黒化)の回復が大きいことを示す。Test Example 1 Confirmation of Whitening Effect of Darkened Skin Half of the back of a female 6-week-old colored guinea pig was shaved, and a 1.2 mW UV lamp was applied to the shaved portion on the first day for 5 minutes.
On the second and third days, 1.0 mW was irradiated for 5 minutes. After two weeks, these guinea pigs were divided into four groups (5 to 6 animals per group) so that there was no difference in the degree of ultraviolet-induced pigmentation, and soybean-derived isoflavones were added to commercially available solid feed (RC4, manufactured by Oriental). Derivative-containing feed (Fujiflavone P40 (manufactured by Fujico)) is 0% by weight (Group 1), 0.02% by weight (Group 2), 0.2% by weight (Group 3) and 2% by weight of isoflavone derivatives. % (Group 4) was started. The daily feed intake per animal in each group was 50 g / day. Color difference meter (Nippon Denshoku Industries Co., Ltd. 1)
001DP). That is, the same point was subjected to color difference measurement at five points, the average L value was taken as the L value of the solid, and the average L value of each group was determined. Next, L on the feeding start date
The difference dL from the value (L 0 value) was calculated. The results are shown in FIG. FIG. 1 shows the dL of each group on each measurement day, and shows that the higher the dL, the greater the recovery of pigmentation (darkening) due to ultraviolet rays on the skin.
【0020】図1より、イソフラボン誘導体含有飼料を
摂取していない第1群は、3週間目までは黒化が進行
し、その後の回復も遅いことが確認された。一方イソフ
ラボン誘導体含有飼料を摂取した第2群〜第4群は、2
週間目から回復が速やかで、その傾向は特に第4群で著
しく、イソフラボン誘導体が美白効果を有することが確
認された。From FIG. 1, it was confirmed that in the first group which did not take the isoflavone derivative-containing feed, the blackening progressed until the third week, and the recovery thereafter was slow. On the other hand, the 2nd to 4th groups that took the isoflavone derivative-containing feed were 2
The recovery was rapid from the week, and the tendency was remarkable especially in the fourth group, and it was confirmed that the isoflavone derivative had a whitening effect.
【0021】試験例2 試験例1で用いた第1群、第3群及び第4群のモルモッ
トについて、試験例1における給餌開始日から3週間後
に背の残りの半分を除毛し、UVランプ1.2mWを5
分間、その1日後及び2日後には1.0mWを5分間照
射した。なお照射にあたっては、試験例1で除毛、UV
照射した部分に再度UVが照射されないように、該部分
をカバーした。次いで除毛日から2週間後(給餌開始日
から5週間後)に試験例1と同様にして各群のL値を求
め、L0 値との差dLを算出した。結果を図2に示す。Test Example 2 With respect to the guinea pigs of Groups 1, 3 and 4 used in Test Example 1, the other half of the back was shaved three weeks after the start of feeding in Test Example 1, and a UV lamp was used. 1.2mW to 5
For 1 minute, 1 day and 2 days later, 1.0 mW was irradiated for 5 minutes. In irradiation, hair removal and UV irradiation were performed in Test Example 1.
The irradiated part was covered so that UV was not irradiated again. Then obtains the L value of each group in the same manner as in Test Example 1 after two weeks depilatory date (5 weeks after feeding start date), and calculates the difference dL between the L 0 value. The results are shown in FIG.
【0022】図2より、第1群ではUV照射により黒化
が進行していることが確認された。一方第2群及び第3
群では、UV照射にもかかわらずdLは正であり、イソ
フラボン誘導体がUV照射による黒化に対する予防効果
を有していることが確認された。From FIG. 2, it was confirmed that in the first group, the blackening progressed due to the UV irradiation. On the other hand, the second group and the third group
In the group, dL was positive despite UV irradiation, and it was confirmed that the isoflavone derivative has a preventive effect against blackening due to UV irradiation.
【0023】[0023]
【発明の効果】本発明の経口用美白剤または美白用食品
は、労力を要することなく、しみ、そばかすや日焼け等
による黒化を予防しまたは回復して皮膚を美白化するこ
とができる。EFFECTS OF THE INVENTION The oral whitening agent or whitening food of the present invention is capable of preventing or recovering from blackening due to spots, freckles, sunburn, etc., and lightening the skin without requiring labor.
【図1】イソフラボン類含有飼料の摂食期間に対する、
紫外線誘導色素沈着の消退促進効果をイソフラボン類の
含有率毎に表したものである。FIG. 1 shows the feeding period of isoflavone-containing feed.
1 shows the effect of promoting the extinction of ultraviolet-induced pigmentation for each content of isoflavones.
【図2】イソフラボン類を3週間給餌した後の、紫外線
誘導色素沈着予防効果をイソフラボン類の含有率毎に表
したものである。FIG. 2 shows the effect of preventing isoplavone-induced pigmentation after feeding isoflavones for 3 weeks for each content of isoflavones.
Claims (2)
美白剤。1. An oral whitening agent comprising isoflavones as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10072100A JPH11269066A (en) | 1998-03-20 | 1998-03-20 | Skin-bleaching agent for peroral administration and skin-bleaching food |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10072100A JPH11269066A (en) | 1998-03-20 | 1998-03-20 | Skin-bleaching agent for peroral administration and skin-bleaching food |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH11269066A true JPH11269066A (en) | 1999-10-05 |
Family
ID=13479663
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10072100A Pending JPH11269066A (en) | 1998-03-20 | 1998-03-20 | Skin-bleaching agent for peroral administration and skin-bleaching food |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH11269066A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1205179A1 (en) * | 2000-11-10 | 2002-05-15 | L'oreal | Cosmetic composition comprising an aminophenol derivative and an isoflavonoid |
EP1234572A1 (en) * | 2001-02-26 | 2002-08-28 | Mibelle AG Cosmetics | Skin treatment compositions containing isoflavone aglycones |
JP2002306129A (en) * | 2001-04-13 | 2002-10-22 | Noevir Co Ltd | Food having excellent beauty effect |
JP2010503728A (en) * | 2006-09-19 | 2010-02-04 | 株式會社アモーレパシフィック | Method for producing icariside II, cosmetic composition containing the same and use thereof for skin whitening |
KR101066676B1 (en) | 2005-05-20 | 2011-09-21 | (주)아모레퍼시픽 | A oral composition for improving beauty of skin |
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JPS58225003A (en) * | 1982-06-23 | 1983-12-27 | Ichimaru Fuarukosu Kk | Cosmetic containing extracted material for natto (fermented soybean) |
JPS5985265A (en) * | 1982-11-04 | 1984-05-17 | Naganoken Kooridoufu Kogyo Kyodo Kumiai | Preparation of nutrient enriched food raw material |
JPS63303910A (en) * | 1987-06-03 | 1988-12-12 | Kanebo Ltd | Beautifying cosmetic |
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JPH02154662A (en) * | 1988-12-05 | 1990-06-14 | Kiyourin Yobou Igaku Kenkyusho:Kk | Active oxygen supressing composition |
JPH02257852A (en) * | 1989-03-31 | 1990-10-18 | Kyodo Nyugyo Kk | Nonspecific free radical scavenger and production thereof |
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JPH05301823A (en) * | 1992-04-23 | 1993-11-16 | Soken Kk | Eliminator for active oxygen from rice |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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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 |
EP1234572A1 (en) * | 2001-02-26 | 2002-08-28 | Mibelle AG Cosmetics | Skin treatment compositions containing isoflavone aglycones |
JP2002306129A (en) * | 2001-04-13 | 2002-10-22 | Noevir Co Ltd | Food having excellent beauty effect |
KR101066676B1 (en) | 2005-05-20 | 2011-09-21 | (주)아모레퍼시픽 | A oral composition for improving beauty of skin |
JP2010503728A (en) * | 2006-09-19 | 2010-02-04 | 株式會社アモーレパシフィック | Method for producing icariside II, cosmetic composition containing the same and use thereof for skin whitening |
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