JPH06219934A - Skin-whitening cosmetic - Google Patents

Skin-whitening cosmetic

Info

Publication number
JPH06219934A
JPH06219934A JP4353445A JP35344592A JPH06219934A JP H06219934 A JPH06219934 A JP H06219934A JP 4353445 A JP4353445 A JP 4353445A JP 35344592 A JP35344592 A JP 35344592A JP H06219934 A JPH06219934 A JP H06219934A
Authority
JP
Japan
Prior art keywords
skin
extract
radix
whitening
trichosanthis
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
JP4353445A
Other languages
Japanese (ja)
Inventor
Masayuki Suzuki
雅之 鈴木
Takashi Kurokawa
隆史 黒川
Kazunari Shigematsu
一成 重松
Giyokuban Chin
玉盤 陳
Masao Takahashi
雅夫 高橋
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.)
Dowa Holdings Co Ltd
Original Assignee
Dowa Mining 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 Dowa Mining Co Ltd filed Critical Dowa Mining Co Ltd
Priority to JP4353445A priority Critical patent/JPH06219934A/en
Publication of JPH06219934A publication Critical patent/JPH06219934A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a skin-whitening cosmetic having excellent skin whitening effect and sufficient storage stability and high safety. CONSTITUTION:The skin-whitening cosmetic is obtained by blending at least one extract of galenical drug selected from the group consisting of Pinellie Tuber, Trichosanthis Fructus, Trichosanthis Radix and Dioscoreae radix. Concretely, about 100g of dried material of Pinellie Tuber which is a galenical drug is pulverized by a mixer and pulverized material thereof and 500ml 50% ethyl alcohol are put in flask and the pulverized material is subjected to reflux extraction at 50 deg.C for 1hr while stirring. After extraction, this solution is filtered with suction and the resultant filtrate is concentrated under reduced pressure at 50 deg.C using an evaporator. Then the resultant concentrate is dried under reduced pressure to provide 3.6g brawn crystal. 14.5g, 6.2 g and 3.2g extracts are obtained from about 100g dried material of Trichosanthis Fructus, trichosanthis Radix and Dioscoreae radix which are galenical drugs as similarly as mentioned above, respectively. The resultant extract is blended as an active ingredient in amount of 0.01-5.0% based on the cosmetic.

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、皮膚美白効果を有する
美白化粧料に関し、さらに詳しくはメラニン生成抑制作
用に基づく美白効果を有する生薬抽出物を有効成分とし
て配合し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 a skin whitening effect, and more particularly to a whitening cosmetic composition containing, as an active ingredient, a crude drug extract having a whitening effect based on a melanin production inhibitory effect.

【0002】[0002]

【従来の技術】一般に、日焼けによる色黒、シミ、ソバ
カス等は、黒褐色無定形の色素であるメラニンの生成に
より生じるものと考えられており、このメラニンは、皮
膚が紫外線などの外的刺激を受けると皮膚のメラニン細
胞中に存在するチロシナーゼ(チロシン酸化酵素)が活
性化し、タンパク質構成アミノ酸の一種であるチロシン
が酸化されて生成する。このことから、メラニン細胞の
不活化や、チロシナーゼ活性の抑制、阻害といったメラ
ニン生成抑制作用を有する成分の化粧料への配合が提唱
されていた。
2. Description of the Related Art Generally, it is believed that dark skin, spots, freckles, etc. due to sunburn are caused by the production of melanin, which is a dark brown amorphous pigment, and this melanin causes the skin to receive external stimuli such as ultraviolet rays. Upon receiving it, tyrosinase (tyrosine oxidase) present in the melanocytes of the skin is activated, and tyrosine, which is one of the protein-constituting amino acids, is oxidized and produced. For this reason, it has been proposed to incorporate a component having a melanin production suppressing action such as inactivation of melanocytes and suppression or inhibition of tyrosinase activity into cosmetics.

【0003】従来、美白効果を有する美白化粧料とし
て、特公昭55−43443号「美白化粧料」や特公昭
54−974「生薬抽出配合組成物」に開示されるよう
に、アスコルビン酸またはその誘導体を配合したものが
知られている。他にも、アルブチンを配合した皮膚外用
剤や、コウジ酸を配合した漂白化粧料(特公昭32−8
100号)、植物成分(特開昭63−2913号他)ま
たは動物成分(特開昭63−3812)から抽出した化
粧料が美白効果を有するものとして公知である。
Conventionally, as a whitening cosmetic having a whitening effect, ascorbic acid or a derivative thereof, as disclosed in JP-B-55-43443 "Whitening cosmetic" and JP-B-54-974 "Crude drug extract-containing composition". It is known that a mixture of In addition, a skin external preparation containing arbutin and a bleaching cosmetic containing kojic acid (Japanese Patent Publication No. 32-8).
100), a plant component (JP-A-63-2913, etc.) or an animal component (JP-A-63-3812) is known to have a whitening effect.

【0004】しかしながら、上記従来の化粧料は、充分
な美白効果が認められないものが多く、また、保存安定
性が充分でなかったり、刺激性を有するなど皮膚に対す
る安全性に問題があるものも多かった。
However, many of the above-mentioned conventional cosmetics do not have a sufficient whitening effect, and also have some problems such as insufficient storage stability and irritation, which are problematic to the skin. There were many.

【0005】[0005]

【発明が解決しようとする課題】本発明は上述従来の問
題点を解消し、優れた美白効果を有し、かつ充分な保存
安定性及び高い安全性を有する美白化粧料を提供するこ
とを目的とする。
The object of the present invention is to provide a whitening cosmetic composition which solves the above-mentioned conventional problems, has an excellent whitening effect, and has sufficient storage stability and high safety. And

【0006】[0006]

【課題を解決するための手段】本発明は、かかる課題を
解決するため鋭意研究した結果、ハンゲ、カロジツ、カ
ロコン及びサンヤクの生薬抽出物がメラノーマ細胞にお
けるメラニン生成抑制作用を有することを見出し、本発
明を提供することができた。
Means for Solving the Problems As a result of intensive studies for solving the above problems, the present invention found that a crude drug extract of Hange, Karojitsu, Carocon and Sanyaku has an action of suppressing melanin production in melanoma cells. The invention could be provided.

【0007】すなわち本発明は、ハンゲ、カロジツ、カ
ロコン及びサンヤクからなる群より選ばれる少なくとも
1種の生薬の抽出物を配合したことを特徴とする美白化
粧料を提供するものである。
[0007] That is, the present invention provides a whitening cosmetic composition containing an extract of at least one crude drug selected from the group consisting of Hanghe, Karoditsu, Carocon and Sanyaku.

【0008】[0008]

【作用】本発明の化粧料は、次に示すような方法で製造
することができる。まず、ハンゲ、カロジツ、カロコン
及びサンヤクの乾燥物あるいは乾燥物粉砕物を、抽出溶
媒を用いて加熱抽出する。なお、抽出溶媒としては、ア
ルコール(メタノール、エタノール、プロパノールまた
はイソプロピルアルコール等)や水などを用いることが
でき、また、これらの混合溶媒を用いることもできる。
例えば、アルコール濃度が20〜70%の含水アルコー
ルを用い、50℃で1時間の抽出を行うと抽出効率が良
い。
The cosmetic of the present invention can be produced by the following method. First, a dried product or a dried product crushed product of Hange, Karoditsu, Carocon and Sanyaku is heated and extracted using an extraction solvent. As the extraction solvent, alcohol (methanol, ethanol, propanol, isopropyl alcohol, or the like), water, or the like can be used, or a mixed solvent thereof can also be used.
For example, extraction efficiency is good if hydrous alcohol having an alcohol concentration of 20 to 70% is used and extraction is performed at 50 ° C. for 1 hour.

【0009】抽出後、抽出液を濾別して抽出エキスを得
る。得られた抽出エキスは、さらに60℃以下の温度で
加熱しながら減圧濃縮して乾固させ、乾固した抽出物を
回収して化粧料に配合する。なお、上記抽出エキスをそ
のまま化粧料に配合しても良い。
After the extraction, the extract is filtered to obtain an extract. The obtained extract is further concentrated under reduced pressure while heating at a temperature of 60 ° C. or lower to dryness, and the dry extract is collected and blended in a cosmetic. In addition, you may mix | blend the said extract with cosmetics as it is.

【0010】このようにして得たハンゲ、カロジツ、カ
ロコン及びサンヤクの生薬抽出物は、従来より用いられ
てきたアスコルビン酸と比較して、低濃度で優れたメラ
ニン生成抑制作用を発揮することが本発明者等によって
確認されており、この抽出物を有効成分として0.01
〜5.0%配合することにより、美白効果を有する美白
化粧料を得ることがでさる。
The herbal medicine extracts of Hange, Karoditsu, Carocon and Sanyaku obtained in this manner are expected to exert an excellent melanin production inhibitory effect at a low concentration, as compared with conventionally used ascorbic acid. It has been confirmed by the inventors that this extract is 0.01% as an active ingredient.
By blending up to 5.0%, a whitening cosmetic having a whitening effect can be obtained.

【0011】以下、実施例により本発明をさらに詳細に
説明にする。しかし本発明の範囲は以下の実施例により
制限されるものではない。
Hereinafter, the present invention will be described in more detail with reference to examples. However, the scope of the present invention is not limited by the following examples.

【0012】[0012]

【実施例1】本実施例では、生薬の抽出方法の一例を示
す。まず、生薬であるハンゲの乾燥物約100gをミキ
サーで粉砕し、その粉砕物および500mlの50%エ
チルアルコールをフラスコに入れ、攪拌しながら50℃
で1時間還流抽出を行った。抽出後、この溶液を吸引濾
過し、得られた濾液をエバポレーターを用いて50℃に
て減圧濃縮した。次いで得られた濃縮液を減圧乾燥し、
3.6gの褐色結晶体を得た。
Example 1 In this example, an example of a method for extracting a crude drug will be described. First, about 100 g of the dried product of Hange, which is a crude drug, was crushed with a mixer, and the crushed product and 500 ml of 50% ethyl alcohol were placed in a flask and stirred at 50 ° C.
Reflux extraction was performed for 1 hour. After extraction, this solution was suction filtered, and the obtained filtrate was concentrated under reduced pressure at 50 ° C. using an evaporator. Then, the obtained concentrated liquid is dried under reduced pressure,
3.6 g of brown crystals were obtained.

【0013】また、上記と同様に生薬であるカロジツ、
カロコン及びサンヤクの乾燥物約100gから、それぞ
れ14.5g、6.2g及び3.2gの抽出物を得た。
[0013] Further, as in the above, the herbal medicine Carodizu,
Approximately 100 g of calocon and sanyaku dried products yielded 14.5 g, 6.2 g and 3.2 g of extract, respectively.

【0014】[0014]

【実施例2】本実施例では、実施例1で得たハンゲ、カ
ロジツ、カロコン及びサンヤクの各生薬抽出物のメラニ
ン生成抑制作用の測定を行った。まず、メラニンを生産
するマウス由来の悪性黒色腫細胞であるB16メラノー
マ細胞(B16−FO、ATCC No.CRL−63
22)を、ウシ胎児血清を終濃度10%となるように添
加したイーグルMEN培地で培養し、6ウェルプレート
(FALCON社製)の各ウェルに、該細胞を3×10
Cell/mlの濃度で含む上記培地を6ml入れ、
COインキュベーター(5%CO、37℃)内で5
日間培養した。
Example 2 In this example, the melanin production inhibitory action of each of the herbal medicine extracts of Hange, Karoditsu, Carocon and Sanyaku obtained in Example 1 was measured. First, B16 melanoma cells (B16-FO, ATCC No. CRL-63), which are melanin-producing mouse-derived malignant melanoma cells.
22) was cultured in Eagle MEN medium supplemented with fetal bovine serum to a final concentration of 10%, and 3 × 10 6 of the cells was placed in each well of a 6-well plate (FALCON).
Add 6 ml of the above medium containing 3 Cell / ml concentration,
5 in a CO 2 incubator (5% CO 2 , 37 ° C)
Cultured for a day.

【0015】次いで、この培地を0.03%のテオフィ
リン(SIGMA社製)を含む新しいイーグルMEM培
地(6ml)に交換し、各ウェルに適当な量の試料溶液
(実施例1で得た抽出物の水溶液)を添加した後さらに
3日間培養した。培養終了後、該培地を捨てて各ウェル
に1mlの生理食塩水を加え、スクレーパーを用いてウ
ェルの底面に付着している細胞をかきとるように懸濁さ
せた。次に、ピペットを用いて該細胞懸濁液をマイクロ
遠心チューブ(1.5ml容量、エッペンドルフ社製)
に移し、遠心分離(1000×g、15分間)した。
Then, this medium was replaced with a new Eagle MEM medium (6 ml) containing 0.03% theophylline (manufactured by SIGMA), and an appropriate amount of the sample solution (extract obtained in Example 1 was added to each well. After the addition of the aqueous solution), the cells were further cultured for 3 days. After the completion of the culture, the medium was discarded, 1 ml of physiological saline was added to each well, and the cells attached to the bottom of the well were suspended using a scraper so as to be scraped. Next, the cell suspension was pipetted into a microcentrifuge tube (1.5 ml volume, manufactured by Eppendorf).
And was centrifuged (1000 × g, 15 minutes).

【0016】一方、対照として試料溶液の代わりに滅菌
水を添加して上記同様の試験を行った。また、細胞の白
色度を比較するための実験区として、試料溶液の代わり
に2%L−アスコルビン酸水溶液を(a)60μl、
(b)150μl、(c)300μlを添加し、上記同
様の試験を行った。
On the other hand, as a control, sterilized water was added instead of the sample solution and the same test as above was conducted. In addition, as an experimental section for comparing the whiteness of cells, 60 μl of (a) 2% L-ascorbic acid aqueous solution was used instead of the sample solution.
(B) 150 μl and (c) 300 μl were added, and the same test as above was conducted.

【0017】次に、ペレットとなった細胞の白色度を目
視で比較し、メラニン生成抑制作用の判定を行った。そ
の際、対照実験区(滅菌水添加区)の細胞の白色の度合
いを「−」、L−アスコルビン酸を添加した実験区の細
胞の白色の度合いをそれぞれ(a):「+」、(b):
「++」、(c):「+++」として、試料溶液を添加
した場合の細胞の白色の度合いが−、+、++、+++
のどれに相当するかを目視で判断し、試料溶液のメラニ
ン生成抑制作用の強さとして、4段階の判定を行った。
なお、その結果は表1に示した。
Next, the whiteness of the pelletized cells was visually compared to determine the melanin production inhibitory effect. At that time, the degree of whiteness of cells in the control experimental section (sterile water-added section) was “−”, and the degree of whiteness of cells in the experimental section to which L-ascorbic acid was added was (a): “+”, (b ):
“++”, (c): As “++++”, the degree of whiteness of the cells when the sample solution was added was −, +, ++, ++++.
It was judged visually which of the above corresponds to the strength of the melanin production inhibitory effect of the sample solution, and the judgment was carried out in four steps.
The results are shown in Table 1.

【0018】[0018]

【表1】 [Table 1]

【0019】表1からもわかるようにハンゲ、カロジ
ツ、カロコン及びサンヤクの各抽出物は200μg/m
lの濃度でL−アスコルビン酸500μg/mlと同等
のメラニン生成抑制作用を示した。また、カロコンの抽
出物は50μg/mlの低濃度でL−アスコルビン酸1
000μg/mlと同等のメラニン生成抑制作用を示
し、L−アスコルビン酸より低濃度でメラニン生成を抑
制することが確認された。さらに各抽出物は800μg
/mlの高濃度であっても細胞に対する毒性はなかっ
た。
As can be seen from Table 1, each extract of Hange, Karojitsu, Carocon and Sanyaku is 200 μg / m 2.
At a concentration of 1 L, as much as 500 μg / ml of L-ascorbic acid showed a melanin production inhibitory action. In addition, the extract of carocon was L-ascorbic acid 1 at a low concentration of 50 μg / ml.
It was confirmed that it showed a melanin production inhibitory effect equivalent to 000 μg / ml and suppressed melanin production at a lower concentration than L-ascorbic acid. Furthermore, each extract is 800 μg
There was no toxicity to cells even at the high concentration of / ml.

【0020】[0020]

【実施例3】本実施例では、実施例1で得た生薬ハンゲ
の抽出物の美白化粧料への配合例を示す。 (重量%) ハンゲ抽出物 1.0 グリセリン 5.0 ポリオキシエチレンソルビタンモノラウレート 1.5 エタノール 10.0 香料 適量 防腐剤、酸化防止剤 適量 色素 適量 精製水 残部
Example 3 In this example, an example of blending the extract of the herbal medicine Hange obtained in Example 1 into a whitening cosmetic composition is shown. (Wt%) Hange extract 1.0 Glycerin 5.0 Polyoxyethylene sorbitan monolaurate 1.5 Ethanol 10.0 Fragrance Suitable amount Preservative, antioxidants Suitable amount Pigment Suitable amount Purified water Remainder

【0021】[0021]

【発明の効果】ハンゲ、カロジツ、カロコン及びサンヤ
クの抽出物は、メラノーマ細胞に対して優れたメラニン
生成抑制作用を発揮するため、これらの抽出物を一種又
は二種以上配合した美白化粧料は優れた皮膚美白効果を
発揮する。また、ハンゲ、カロジツ、カロコン及びサン
ヤクの各抽出物は、細胞への毒性も低いため、安全性の
高いものである。
EFFECTS OF THE INVENTION Since the extracts of Hangge, Caroditu, Carocon and Sanyaku exert excellent melanin production inhibitory action on melanoma cells, whitening cosmetics containing one or more of these extracts are excellent. Exhibits the skin whitening effect. In addition, the extracts of Hange, Karojitsu, Carocon and Sanyaku are highly safe because they have low toxicity to cells.

─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成6年1月17日[Submission date] January 17, 1994

【手続補正3】[Procedure 3]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0003[Name of item to be corrected] 0003

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0003】 従来、美白効果を有する美白化粧料とし
て、特公昭55−43443号「美白化粧料」や特公昭
54−974「生薬抽出配合組成物」に開示されるよ
うに、アスコルビン酸またはその誘導体を配合したもの
が知られている。他にも、アルブチンを配合した皮膚外
用剤や、コウジ酸を配合した漂白化粧料(特公昭32−
8100号)、植物成分(特開昭63−2913号他)
または動物成分(特開昭63−3812)から抽出し
た化粧料が美白効果を有するものとして公知である。
Conventionally, as a whitening cosmetic composition having a whitening effect, as disclosed in Japanese Patent Publication No. 55-43443 "whitening cosmetic" and JP-B-54-974 "herbal extract blend composition", ascorbic acid or a Those containing a derivative are known. In addition, a skin external preparation containing arbutin and a bleaching cosmetic containing kojic acid (Japanese Patent Publication No.
8100), plant components (JP-A-63-2913, etc.)
Alternatively, cosmetics extracted from animal components (Japanese Patent Laid-Open No. 63-3812) are known to have a whitening effect.

【手続補正4】[Procedure amendment 4]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0014[Correction target item name] 0014

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0014】[0014]

【実施例2】 本実施例では、実施例1で得たハンゲ、
カロジツ、カロコン及びサンヤクの各生薬抽出物のメラ
ニン生成抑制作用の測定を行った。まず、メラニンを生
産するマウス由来の悪性黒色腫細胞であるB16メラノ
ーマ細胞(B16−FO、ATCC No.CRL−6
322)を、ウシ胎児血清を終濃度10%となるように
添加したイーグルME培地で培養し、6ウェルプレー
ト(FALCON社製)の各ウェルに、該細胞を3×1
cell/mlの濃度で含む上記培地を6ml入
れ、COインキュベーター(5%CO、37℃)内
で5日間培養した。
Example 2 In this example, the hanger obtained in Example 1
The melanin production inhibitory action of each crude drug extract of Caroditu, Carocon and Sanyaku was measured. First, B16 melanoma cells (B16-FO, ATCC No. CRL-6), which are melanin-producing mouse-derived malignant melanoma cells.
322), were cultured in the added Eagle ME M medium to the fetal calf serum to a final concentration of 10% to each well of a 6 well plate (FALCON Corp.), the cells 3 × 1
6 ml of the above medium containing a concentration of 0 3 cell / ml was added and cultured in a CO 2 incubator (5% CO 2 , 37 ° C.) for 5 days.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 陳 玉盤 台湾台北市重慶南路3段116号 必安研究 所内 (72)発明者 高橋 雅夫 東京都中央区日本橋小舟町4番11号 順成 産業株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Chen Jingban, No. 116, 3rd dan, Chongqing South Road, Taipei City, Taiwan (72) Inventor Masao Takahashi 4-11 Nihonbashi Kobunecho, Chuo-ku, Tokyo Junsei Industrial Co., Ltd. In the company

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ハンゲ、カロジツ、カロコン及びサンヤ
クからなる群より選ばれる少なくとも1種の生薬の抽出
物を配合したことを特徴とする美白化粧料。
1. A whitening cosmetic characterized in that it contains an extract of at least one herbal medicine selected from the group consisting of Hange, Karojitsu, Carocon and Sanyaku.
JP4353445A 1992-11-26 1992-11-26 Skin-whitening cosmetic Pending JPH06219934A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4353445A JPH06219934A (en) 1992-11-26 1992-11-26 Skin-whitening cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4353445A JPH06219934A (en) 1992-11-26 1992-11-26 Skin-whitening cosmetic

Publications (1)

Publication Number Publication Date
JPH06219934A true JPH06219934A (en) 1994-08-09

Family

ID=18430900

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4353445A Pending JPH06219934A (en) 1992-11-26 1992-11-26 Skin-whitening cosmetic

Country Status (1)

Country Link
JP (1) JPH06219934A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0811595A4 (en) * 1995-11-24 1998-05-06 Mitsui Toatsu Chemicals Hydrochalcone derivatives, comestic compositions containing the same, and processes for the preparation of both
JP2002284626A (en) * 2001-03-23 2002-10-03 Nippon Hypox Lab Inc External skin preparation
JP2002363057A (en) * 2001-06-08 2002-12-18 Ichimaru Pharcos Co Ltd Melanogenesis inhibitor or cosmetic composition
KR20030025716A (en) * 2001-09-22 2003-03-29 (주)대덕바이오 Melanin synthesis inhibition compound and its composition contaning Dioscorea rhizoma extract
KR20030061985A (en) * 2002-01-14 2003-07-23 (주)대덕바이오 Melanin synthesis inhibition compound and its composition containing stigmasterol
KR100416400B1 (en) * 2001-02-14 2004-01-31 우원홍 Composition containing extracts from dried roots of Trichosantes kirilowii maxim for external application and skin-whitening and process for preparation thereof
JP2010535758A (en) * 2008-01-04 2010-11-25 ビオスペクトルム,インコーポレイテッド Skin whitening composition containing diosgenin
JP2014118366A (en) * 2012-12-13 2014-06-30 Pola Chem Ind Inc Advanced glycation end product decomposer

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0811595A4 (en) * 1995-11-24 1998-05-06 Mitsui Toatsu Chemicals Hydrochalcone derivatives, comestic compositions containing the same, and processes for the preparation of both
US5880314A (en) * 1995-11-24 1999-03-09 Mitsui Chemicals, Inc. Hydrochalcone derivatives, cosmetic compositions containing said derivatives and methods of producing the same
KR100416400B1 (en) * 2001-02-14 2004-01-31 우원홍 Composition containing extracts from dried roots of Trichosantes kirilowii maxim for external application and skin-whitening and process for preparation thereof
JP2002284626A (en) * 2001-03-23 2002-10-03 Nippon Hypox Lab Inc External skin preparation
JP2002363057A (en) * 2001-06-08 2002-12-18 Ichimaru Pharcos Co Ltd Melanogenesis inhibitor or cosmetic composition
KR20030025716A (en) * 2001-09-22 2003-03-29 (주)대덕바이오 Melanin synthesis inhibition compound and its composition contaning Dioscorea rhizoma extract
KR20030061985A (en) * 2002-01-14 2003-07-23 (주)대덕바이오 Melanin synthesis inhibition compound and its composition containing stigmasterol
JP2010535758A (en) * 2008-01-04 2010-11-25 ビオスペクトルム,インコーポレイテッド Skin whitening composition containing diosgenin
JP2014118366A (en) * 2012-12-13 2014-06-30 Pola Chem Ind Inc Advanced glycation end product decomposer

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