JP3231908B2 - Whitening cosmetics - Google Patents
Whitening cosmeticsInfo
- Publication number
- JP3231908B2 JP3231908B2 JP19543793A JP19543793A JP3231908B2 JP 3231908 B2 JP3231908 B2 JP 3231908B2 JP 19543793 A JP19543793 A JP 19543793A JP 19543793 A JP19543793 A JP 19543793A JP 3231908 B2 JP3231908 B2 JP 3231908B2
- Authority
- JP
- Japan
- Prior art keywords
- whitening
- extract
- cells
- melanin production
- cosmetic
- 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 - Fee Related
Links
Landscapes
- Cosmetics (AREA)
Description
【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 having a skin whitening effect, and more particularly to a whitening cosmetic in which a crude drug extract having a whitening effect based on a melanin production inhibitory action is blended as an active ingredient.
【0002】[0002]
【従来の技術】一般に、日焼けによる色黒、シミ、そば
かす等は、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。2. Description of the Related Art In general, it is considered that darkening, spots, freckles, and the like due to sunburn are caused by the production of melanin, which is a black-brown amorphous pigment. This melanin causes external stimuli such as ultraviolet rays on the skin. When it is received, tyrosinase (tyrosine oxidase) present in the melanocytes of the skin is activated, and tyrosine, one of the amino acids constituting the protein, is oxidized and produced.
【0003】したがって、メラニン生成に関与するチロ
シナーゼの活性を抑制することにより肌を白くする効果
が期待されるために、チロシナーゼ活性抑制成分の化粧
料への配合が提唱されていた。[0003] Accordingly, since an effect of whitening skin is expected by suppressing the activity of tyrosinase involved in melanin production, it has been proposed to add a tyrosinase activity-inhibiting component to cosmetics.
【0004】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号「生薬抽出物配合組成物」に開示され
ているように、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、アルブチンを配合した皮膚
外用剤(特開昭60−16906号等)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63−8312号他)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, as disclosed in JP-B-55-43443, "Whitening cosmetic" and JP-B-54-974, "Composition of crude drug extract", ascorbin Known are those containing an acid or a derivative thereof, an external preparation for skin containing arbutin (JP-A-60-16906, etc.), a bleaching cosmetic containing kojic acid (Japanese Patent Publication No. 32-8100), Cosmetics extracted from plant components (JP-A-63-2913 and others) or animal components (JP-A-63-8312 and others) are known to have a whitening effect.
【0005】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が多かった。However, many of the above-mentioned conventional cosmetics do not have a sufficient whitening effect, and also have problems in safety to the skin such as insufficient storage stability and irritation. There were many.
【0006】[0006]
【発明が解決しようとする課題】本発明は、上記従来の
技術の問題点を解決し、優れた皮膚美白効果を有し、且
つ充分な保存安定性および高い安全性を有する新規な美
白化粧料を提供することを目的とする。DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems of the prior art, and has a novel skin whitening effect having an excellent skin whitening effect, sufficient storage stability and high safety. The purpose is to provide.
【0007】[0007]
【課題を解決するための手段】 本発明者等は斯かる課
題を解決するために鋭意研究したところ、蒼朮および抗
菊花の生薬抽出物が、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いだし、本発明を提供す
ることができた。Means for Solving the Problems The present inventors have conducted intensive studies in order to solve such problems, and found that crude drug extracts of Soju and anti-Chrysanthemum have an inhibitory effect on melanin production in melanoma cells, The present invention could be provided.
【0008】 すなわち本発明は、蒼朮および抗菊花か
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に関するものであ
る。[0008] That is, the present invention relates to a whitening cosmetic comprising an extract of at least one crude drug selected from the group consisting of Soju and anti-Chrysanthemum.
【0009】[0009]
【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。先ず、蒼朮および抗菊花の粉砕物
を抽出溶媒を用いて加熱抽出する。The cosmetic of the present invention can be manufactured by the following method. First, pulverized products of Sojuju and anti-Chrysanthemum flower are extracted by heating using an extraction solvent.
【0010】この場合、抽出溶媒としては、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
コール等のアルコール類や水などを単独で、またはこれ
らの混合溶液として用いることができるが、一例として
アルコール濃度が20〜70%の含水アルコールを用
い、50℃で1時間の抽出を行なうと抽出効率が良い。In this case, as the extraction solvent, alcohols such as methanol, ethanol, propanol or isopropyl alcohol, water and the like can be used alone or as a mixed solution thereof. Extraction at 50 ° C. for 1 hour using 50% aqueous alcohol improves the extraction efficiency.
【0011】抽出後、抽出液を濾別して抽出エキスを
得、次いで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。この場合、上記抽出
エキスをそのまま化粧料に配合しても同等の効果を有す
るものである。After extraction, the extract is filtered to obtain an extract, and the extract is concentrated under reduced pressure while heating at a temperature of 60 ° C. or lower to dryness. And blend it into cosmetics. In this case, the same effect can be obtained even if the above-mentioned extract is directly added to the cosmetic.
【0012】 このようにして得た蒼朮および抗菊花の
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の試験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
ができるものである。[0012] The inventors of the present invention have found that the crude drug extracts of sojujutsu and anti-chrysanthemum flowers thus obtained exhibit excellent melanin production inhibitory action at a low concentration as compared with conventionally used ascorbic acid. Has been confirmed by testing,
By blending this extract as an active ingredient in an amount of 0.01 to 5.0%, a whitening cosmetic having a whitening effect can be obtained.
【0013】以下、実施例により本発明をさらに詳細に
説明するが、本発明の範囲はこれらに限定されるもので
はない。Hereinafter, the present invention will be described in more detail by way of examples, but the scope of the present invention is not limited thereto.
【0014】[0014]
【実施例1】本実施例では、生薬の抽出方法の一例を示
す。先ず、生薬である蒼朮約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
抽出を行なった。Embodiment 1 In this embodiment, an example of a method for extracting crude drugs will be described. First, about 100 g of crude drug, Soju, was pulverized with a mixer, and the pulverized product and 500 ml of 50% ethyl alcohol were placed in a flask and refluxed at 50 ° C. for 1 hour with stirring.
【0015】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、
次いで該濃縮液を減圧乾燥し、17.9gの褐色結晶体
を得た。After the extraction, this solution was subjected to suction filtration, and the obtained filtrate was concentrated under reduced pressure at 50 ° C. using an evaporator.
Next, the concentrated liquid was dried under reduced pressure to obtain 17.9 g of brown crystals.
【0016】 また、上記と同様に生薬である抗菊花約
100gから13.8gの抽出物を得た。In the same manner as above, 13.8 g of an extract was obtained from about 100 g of anti-chrysanthemum as a crude drug.
【0017】[0017]
【実施例2】本実施例では、実施例1で得た各抽出物の
メラニン生成抑制作用の測定を行なった。先ず、メラニ
ンを生成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(B16Fo、ATCC No.CRL
−6322)を、ウシ胎児血清で終濃度10%となるよ
うに添加したイーグルMEM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
×103 cell/ml の濃度で含む上記培地を6ml入れ、C
O2 インキュベーター(5%CO2 、37℃)内で5日
間培養した。Example 2 In this example, the melanin production inhibitory effect of each extract obtained in Example 1 was measured. First, B16, a malignant melanoma cell derived from a mouse that produces melanin,
Melanoma cells (B16Fo, ATCC No. CRL)
-6322) was cultured in Eagle's MEM medium supplemented with fetal bovine serum to a final concentration of 10%, and the cells were added to each well of a 6-well plate (manufactured by FALCON).
Add 6 ml of the above medium containing a concentration of × 10 3 cell / ml,
The cells were cultured in an O 2 incubator (5% CO 2 , 37 ° C.) for 5 days.
【0018】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、該培養液から培地を捨て
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、次いで、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(1,000×g、15分間)
した。Next, 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 (the extract obtained in Example 1) was added to each well. Was further cultured for 3 days. After completion of the culture, the medium was discarded from the culture solution, 1 ml of physiological saline was added to each well, and the cells adhered to the bottom of the well were suspended using a scraper, and then suspended using a pipette. The cell suspension was transferred to a microcentrifuge tube (1.5 ml volume, manufactured by Eppendorf) and centrifuged (1,000 × g, 15 minutes).
did.
【0019】一方、対照として試料溶液の代りに滅菌水
を添加して上記同様の試験を行った。また、細胞の白色
化を比較するための実験区として、試料溶液の代りに2
%L−アスコルビン酸水溶液を(a)60μl、(b)
150μl、(c)300μl添加し、上記同様の試験
を行った。On the other hand, as a control, the same test as above was conducted by adding sterile water instead of the sample solution. In addition, as an experimental group for comparing the whitening of the cells, instead of the sample solution, 2
% (L) -ascorbic acid aqueous solution (a) 60 μl, (b)
150 μl and (c) 300 μl were added, and the same test was performed.
【0020】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なった。
この場合、対照実験区(滅菌水添加区)の細胞の白色の
度合を「−」、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が、これらのどれに相当す
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段階の判定を行ない、その結果を表1に
示した。Next, the whiteness of the pelleted cells was visually compared to determine the melanin production inhibitory action.
In this case, the degree of whiteness of the cells in the control group (sterilized water-added group) was "-", and the degree of whiteness of the cells in the experimental group 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 visually judged to determine which of these, and the strength of the melanin production inhibitory effect of the sample solution. , And the results are shown in Table 1.
【0021】[0021]
【表1】 [Table 1]
【0022】 表1に示す結果からも分かるように、蒼
朮および抗菊花の各抽出物は200μg/ml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、L−アスコルビン酸よりはるかに
低濃度でメラニン生成を抑制することが確認された。ま
た、800μg/mlの高濃度のものであっても細胞に
対する毒性はなく、安全性が確認された。[0022] As can be seen from the results shown in Table 1, the extracts of Sophora autumatum and Anti-Chrysanthemum flower show a melanin production inhibitory action at a concentration of 200 µg / ml equivalent to 500 µg / ml of L-ascorbic acid. It was confirmed that melanin production was suppressed at a much lower concentration. In addition, even at a high concentration of 800 μg / ml, there was no toxicity to cells, and safety was confirmed.
【0023】[0023]
【実施例3】本実施例では、実施例1で得た蒼朮の抽出
物の美白化粧料への配合例を示す。Example 3 In this example, an example of blending the extract of Sophora jujuta obtained in Example 1 with a whitening cosmetic is shown.
【0024】 (重量%) 蒼朮抽出物 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(% By weight) Soju extract 1.0 Glycerin 5.0 Polyoxyethylene sorbitan monolaurate 1.5 Ethanol 10.0 Appropriate perfume Preservative, antioxidant Appropriate dye Appropriate purified water Remainder
【0025】[0025]
【発明の効果】 上述のように本発明で使用する蒼朮お
よび抗菊花の抽出物は、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1種または2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と共に、これらの抽出物は、細胞へ
の毒性も低いため安全性の高い製品を提供できるもので
ある。EFFECTS OF THE INVENTION As described above, the extracts of C. aureus and anti-chrysanthemum used in the present invention exhibit an excellent melanin production inhibitory effect on melanoma cells. Therefore, one or more of these extracts may be used. The formulated whitening cosmetics exhibit an excellent skin whitening effect, and these extracts can provide highly safe products because of their low toxicity to cells.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) A61K 7/00 - 7/035 A61K 7/32 - 7/48 ──────────────────────────────────────────────────続 き Continued on the front page (58) Fields surveyed (Int.Cl. 7 , DB name) A61K 7/ 00-7/035 A61K 7/ 32-7/48
Claims (1)
キッカ)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) Sojutsu and anti-chrysanthemum (Kou)
A whitening cosmetic comprising an extract of at least one crude drug selected from the group consisting of Kicca) .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19543793A JP3231908B2 (en) | 1993-07-13 | 1993-07-13 | Whitening cosmetics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19543793A JP3231908B2 (en) | 1993-07-13 | 1993-07-13 | Whitening cosmetics |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001221477A Division JP2002068958A (en) | 2001-07-23 | 2001-07-23 | Skin-whitening cosmetic |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0725745A JPH0725745A (en) | 1995-01-27 |
JP3231908B2 true JP3231908B2 (en) | 2001-11-26 |
Family
ID=16341051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19543793A Expired - Fee Related JP3231908B2 (en) | 1993-07-13 | 1993-07-13 | Whitening cosmetics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3231908B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6653375B2 (en) | 1998-01-28 | 2003-11-25 | Ivoclar Ag | Urethane di(meth)acrylate derivatives of 1,3-bis(1-isocyanato-1-methylethyl)benzene |
CN105560144A (en) * | 2015-12-15 | 2016-05-11 | 北京健旭康技术有限公司 | Cosmetic based on weekly change law of skin beauty index and production technology |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0725746A (en) * | 1993-07-13 | 1995-01-27 | Suntory Ltd | Whitening cosmetic composition |
JPH0977635A (en) * | 1995-09-14 | 1997-03-25 | Mikimoto Pharmaceut Co Ltd | Beautifying and whitening cosmetic |
JP3993936B2 (en) * | 1998-05-22 | 2007-10-17 | 一丸ファルコス株式会社 | Melanin production inhibitor and cosmetic composition |
WO2007083904A1 (en) * | 2006-01-18 | 2007-07-26 | Lg Household & Health Care Ltd. | C-kit activation inhibitor, skin whitening compound and composition for skin whitening containing the same |
-
1993
- 1993-07-13 JP JP19543793A patent/JP3231908B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6653375B2 (en) | 1998-01-28 | 2003-11-25 | Ivoclar Ag | Urethane di(meth)acrylate derivatives of 1,3-bis(1-isocyanato-1-methylethyl)benzene |
CN105560144A (en) * | 2015-12-15 | 2016-05-11 | 北京健旭康技术有限公司 | Cosmetic based on weekly change law of skin beauty index and production technology |
Also Published As
Publication number | Publication date |
---|---|
JPH0725745A (en) | 1995-01-27 |
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