JP3449759B2 - Whitening cosmetics - Google Patents

Whitening cosmetics

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Publication number
JP3449759B2
JP3449759B2 JP28438293A JP28438293A JP3449759B2 JP 3449759 B2 JP3449759 B2 JP 3449759B2 JP 28438293 A JP28438293 A JP 28438293A JP 28438293 A JP28438293 A JP 28438293A JP 3449759 B2 JP3449759 B2 JP 3449759B2
Authority
JP
Japan
Prior art keywords
whitening
extract
cells
present
buffalo
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
Application number
JP28438293A
Other languages
Japanese (ja)
Other versions
JPH07118138A (en
Inventor
雅之 鈴木
真樹子 柳沢
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 Holdings Co Ltd
Dowa Mining Co Ltd
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Filing date
Publication date
Application filed by Dowa Holdings Co Ltd, Dowa Mining Co Ltd filed Critical Dowa Holdings Co Ltd
Priority to JP28438293A priority Critical patent/JP3449759B2/en
Publication of JPH07118138A publication Critical patent/JPH07118138A/en
Application granted granted Critical
Publication of JP3449759B2 publication Critical patent/JP3449759B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Cosmetics (AREA)
  • Medicines Containing Plant Substances (AREA)

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は、皮膚美白効果を有する
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植物抽出物を有効成分として配
合した美白化粧料に関する。 【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1種であるチロシ
ンが酸化されて生成する。 【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。 【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、アルブチンを配合した皮膚外用材
(特開昭60−16906号)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)または動物成分(特開昭63−8
312号)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。 【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。 【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。 【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結果、中米産の植物でア
モール、穂ビユ、バッファローウリ、アチョテおよびグ
アコールから得られる植物抽出物がメラノーマ細胞にお
けるメラニン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。 【0008】すなわち本発明は、アモール、穂ビユ、バ
ッファローウリ、アチョテおよびグアコールからなる群
より選ばれる少なくとも1種の植物から得られた抽出物
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。 【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、中米産であるアモール(学
名:Stegnosperma halimifolium )、穂ビユ(学名:Am
aranthus candatus )、バッファローウリ(学名:Cucu
rbita foetidissima)、アチョテ(学名:Bixa orellaa
na)およびグアユール(学名:Parthenium argentatum
)の乾燥物あるいは乾燥粉砕物を、抽出溶媒を用いて
加熱抽出する。 【0010】この場合、抽出溶媒としては、メタノー
ル、エタノール、プロー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またはこれらの混合溶液
を用いることができるが、例えば、アルコール濃度が2
0〜70%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ことを確認している。 【0011】抽出後、抽出液を濾別して抽出エキスを得
た後、さらに抽出エキスを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
化粧料に配合するが、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構わない。 【0012】このようにして得た植物(アモール、穂ビ
ユ、バッファローウリ、アチョテおよびグアコール)の
抽出物は、従来より用いられている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き
る。 【0013】尚、本発明で用いることのできる植物の乾
燥物としては、これら植物の実、葉、茎、根等の各部分
が使用できる。 【0014】以下実施例をもって詳細に説明するが、本
発明の範囲はこれらに限定されるものではない。 【0015】 【実施例1】本実施例では、穂ビユの抽出方法の一例を
示す。まず、穂ビユの乾燥物約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
流抽出を行なった。 【0016】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℃で減圧濃縮し、次
いで得られた濃縮液を減圧乾燥し、7.2gの褐色粉末
を得た。 【0017】また、上記と同様にアモール、バッファロ
ーウリ、アチョテおよびグアコールの乾燥物を各自10
0gを粉砕したものから抽出物としてそれぞれ14.4
g、15.3g、7.2gおよび8.4gを得た。 【0018】 【実施例2】本実施例では、実施例1で得たアモール、
穂ビユ、バッファローウリ、アチョテおよびグアコール
の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、ウシ胎児血清を終濃度1
0%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、CO2 インキュベーター(5%CO2 、3
7℃)内で5日間培養した。 【0019】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。 【0020】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)に移して、遠心分離(1,000×g、15分間)
した。 【0021】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他、細胞の白色化を
比較するためん実験区として、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)1
50μl、(c)300μl添加し、上記同様の試験を
行った。 【0022】次に、ペレットとなった細胞の白色度の度
合を目視で比較し、メラニン生成抑制効果の判定を行な
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比
較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、
−、+、++、+++のどれに対応するかを目視で判断
し、試料溶液のメラニン生成抑制効果の強さとして4段
階の判定を行ない、その結果を表1に示した。 【0023】 【表1】 【0024】表1示す結果から明らかなように、穂ビ
ユ、バッファローウリ、アチョテおよびグアユールの各
抽出物は200μg/mlの濃度でL−アスコルビン酸5
00μg/mlと同等のメラニン生成抑制作用を示した。 【0025】また、アモールの抽出物は50μg/mlの
低濃度でL−アスコルビン酸1000μg/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。 【0026】 【実施例3】本実施例では、実施例1で得た穂ビユの抽
出物の美白化粧料への配合例を示す。 【0027】 (重量%) 穂ビユ 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 【0028】 【発明の効果】上述のように中米産の植物であるアモー
ル、穂ビユ、バッファローウリ、アチョテおよびグアユ
ールの抽出物は、メラノーマ細胞におけるメラニン生成
抑制作用を有しており、これらの抽出物のうち少なくと
も1種を配合した本発明の美白化粧料は、優れた皮膚美
白効果を有する他、これらの抽出物は、少量で優れた皮
膚美白効果を発揮し、細胞への毒性も低いため安全性の
高いものである。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cosmetic having a skin whitening effect, and more particularly to a plant extract having a whitening effect based on an inhibitory action on melanin production as an active ingredient. It relates to blended whitening cosmetics. 2. Description of the Related Art Generally, it is considered that darkening, spots, freckles, etc. due to sunburn are caused by the formation of melanin which is a black-brown amorphous pigment. When stimulated, 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] 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. Conventionally, as whitening cosmetics having a whitening effect, as disclosed in JP-B-55-43443, "Whitening cosmetics" and JP-B-54-974, "Composition of crude drug extraction", ascorbic acid or In addition to those containing a derivative thereof, an external skin material containing arbutin (Japanese Patent Application Laid-Open No. 60-16906), a bleaching cosmetic containing kojic acid (Japanese Patent Publication No. 32-8100), a plant component ( JP-A-63-2913) or an animal component (JP-A-63-8913).
No. 312) is known as having a whitening effect. 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. SUMMARY OF THE INVENTION [0006] The present invention solves the above-mentioned problems of the prior art, and has a novel skin whitening effect, and has a sufficient storage stability and high safety. The purpose is to provide whitening cosmetics. Means for Solving the Problems The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems, and as a result, a plant obtained from Amor, Panicle, Buffalo Uri, Achote, and Guacol is a plant produced in Central America. The present inventors have found that the extract has a melanin-suppressing effect on melanoma cells, and have provided the present invention. [0008] That is, the present invention relates to a whitening cosmetic comprising an extract obtained from at least one plant selected from the group consisting of amor, spikelet, buffalo uri, achote and guacol. is there. The cosmetic of the present invention can be produced by the following method. First, Amor (scientific name: Stegnosperma halimifolium), Hobiyu (scientific name: Am)
aranthus candatus), buffalo cucumber (scientific name: Cucu)
rbita foetidissima), Achote (scientific name: Bixa orellaa)
na) and guayule (scientific name: Parthenium argentatum)
) Is dried by heating using an extraction solvent. In this case, as the extraction solvent, alcohols such as methanol, ethanol, propanol or isopropyl alcohol, water or a mixed solution thereof can be used.
It has been confirmed that an extraction efficiency of 1 hour at 50 ° C. using 0-70% aqueous alcohol is good. After the extraction, the extract is filtered to obtain an extract, and the extract is further concentrated under reduced pressure while heating at a temperature of 60 ° C. or less to dryness. In this case, the above-mentioned extract may be directly blended with the cosmetic. The extracts of the plants (amol, spikelet, buffalo uli, achote and guacol) thus obtained have a superior melanin production inhibitory activity at a lower concentration than the conventionally used ascorbic acid. It has been confirmed by the present inventors and others that a whitening cosmetic having a whitening effect can be obtained by incorporating this extract as an active ingredient in an amount of 0.01 to 5.0%. [0013] As the dried product of the plant that can be used in the present invention, each part of these plants such as fruit, leaves, stems and roots can be used. Hereinafter, the present invention will be described in detail with reference to Examples, but the scope of the present invention is not limited thereto. Embodiment 1 In this embodiment, an example of a method for extracting ear panicles will be described. First, about 100 g of the dried panicle was pulverized with a mixer, and the pulverized substance and 500 ml of 50% ethyl alcohol were placed in a flask and subjected to reflux extraction at 50 ° C. for 1 hour with stirring. 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. Then, the obtained concentrated liquid was dried under reduced pressure to obtain 7.2 g of a brown powder. In the same manner as described above, dried amol, buffalo uri, achote, and guaco
14.4 g each as an extract from pulverized 0 g.
g, 15.3 g, 7.2 g and 8.4 g. Example 2 In this example, the amor obtained in Example 1
The melanin production inhibitory effect of each of the extract of panicle bilberry, buffalo uli, acochate, and guacol was measured.
First, B16 melanoma cells (B16FO, ATCC) which are malignant melanoma cells derived from mice that produce melanin
No. CRL-6322) and fetal bovine serum at a final concentration of 1
Were cultured in 0% and comprising as the added Eagle's MEM medium, to each well of a 6-well plate (FALCON Corp.), the culture medium was placed 6ml containing the cells at a concentration of 3 × 10 3 cell / ml, CO 2 Incubator (5% CO 2 , 3
(7 ° C) for 5 days. 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, 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 to scrape the cells. Next, the cell suspension was transferred to a microcentrifuge tube (1.5 ml, manufactured by Eppendorf) using a pipette, and centrifuged (1,000 × g, 15 minutes).
did. On the other hand, as a control, sterilized water was added in place of the sample solution, and the same test was performed. In addition, 2% instead of the sample solution was used as an experimental group for comparing the whitening of cells.
L-ascorbic acid aqueous solution (a) 60 μl, (b) 1
50 μl and (c) 300 μl were added, and the same test was performed. Next, the degree of whiteness of the pelleted cells was visually compared to determine the melanin production inhibitory effect. 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 comparative group to which L-ascorbic acid was added was (a):
“+”, (B): “++”, (c): “++”, the degree of whiteness of the cells when the sample solution was added,
Which one of-, +, ++, and +++ it corresponds to was visually determined, and the strength of the melanin production inhibitory effect of the sample solution was determined in four steps, and the results are shown in Table 1. [Table 1] As is evident from the results shown in Table 1, each of the extract of panicle bilberry, buffalo uri, achote and guayule was L-ascorbic acid 5 at a concentration of 200 μg / ml.
A melanin production inhibitory action equivalent to 00 μg / ml was shown. Also, it was confirmed that the amor extract exhibited a melanin production inhibitory effect at a low concentration of 50 μg / ml equivalent to that of 1000 μg / ml L-ascorbic acid, and inhibited melanin production at a lower concentration than L-ascorbic acid. Was done. Example 3 In this example, an example of blending the extract of panicle biloba obtained in Example 1 with a whitening cosmetic will be described. (% By weight) Panicle 1.0 Glycerin 5.0 Polyoxyethylene sorbitan monolaurate 1.5 Ethanol 10.0 Appropriate amount of preservative, antioxidant Appropriate amount of dye Appropriate amount of purified water Remainder of the present invention EFFECTS As described above, the extracts of Central American plants Amol, Panicle, Buffalo Uri, Achote and Guayule have an inhibitory effect on melanin production in melanoma cells, and at least one of these extracts In addition to having an excellent skin whitening effect, the extracts of the present invention exhibit excellent skin whitening effect in a small amount and are highly safe because of low toxicity to cells. is there.

Claims (1)

(57)【特許請求の範囲】 【請求項1】 アモール、穂ビユ、バッファローウリ、
アチョテおよびグアユールからなる群より選ばれる少な
くとも1種の植物から得られた抽出物を配合したことを
特徴とする美白化粧料。
(57) [Claims] [Claim 1] Amor, ear biyu, buffalo uri,
A whitening cosmetic comprising an extract obtained from at least one plant selected from the group consisting of achote and guayule.
JP28438293A 1993-10-19 1993-10-19 Whitening cosmetics Expired - Fee Related JP3449759B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28438293A JP3449759B2 (en) 1993-10-19 1993-10-19 Whitening cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28438293A JP3449759B2 (en) 1993-10-19 1993-10-19 Whitening cosmetics

Publications (2)

Publication Number Publication Date
JPH07118138A JPH07118138A (en) 1995-05-09
JP3449759B2 true JP3449759B2 (en) 2003-09-22

Family

ID=17677866

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Application Number Title Priority Date Filing Date
JP28438293A Expired - Fee Related JP3449759B2 (en) 1993-10-19 1993-10-19 Whitening cosmetics

Country Status (1)

Country Link
JP (1) JP3449759B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2746303B1 (en) * 1996-03-21 1998-06-12 Fabre Pierre Dermo Cosmetique AMARANTE SEED EXTRACT AND DERMO-COSMETIC COMPOSITION COMPRISING THE SAME
JP4553424B2 (en) * 1999-10-05 2010-09-29 一丸ファルコス株式会社 Cosmetic composition
BRPI0504797B1 (en) * 2005-10-27 2020-02-04 Pele Nova Biotecnologia S A topical formulation, cosmetic treatment method for skin rejuvenation, cosmetic treatment method and use of a formulation
CN105101938A (en) * 2013-04-02 2015-11-25 气体产品与化学公司 Compositions of delivery systems for personal care products
KR101591499B1 (en) * 2013-11-01 2016-02-03 가천대학교 산학협력단 Composition for skin whitening comprising amaranthus spp. l. extract or fraction thereof

Also Published As

Publication number Publication date
JPH07118138A (en) 1995-05-09

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