JPH0495012A - Beautifying and whitening cosmetic - Google Patents

Beautifying and whitening cosmetic

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Publication number
JPH0495012A
JPH0495012A JP2208003A JP20800390A JPH0495012A JP H0495012 A JPH0495012 A JP H0495012A JP 2208003 A JP2208003 A JP 2208003A JP 20800390 A JP20800390 A JP 20800390A JP H0495012 A JPH0495012 A JP H0495012A
Authority
JP
Japan
Prior art keywords
beautifying
whitening
seaweeds
extract
whitening 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.)
Granted
Application number
JP2208003A
Other languages
Japanese (ja)
Other versions
JP2970767B2 (en
Inventor
Masaki Takabayashi
高林 政樹
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.)
Mikimoto Pharmaceutical Co Ltd
Original Assignee
Mikimoto Pharmaceutical 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 Mikimoto Pharmaceutical Co Ltd filed Critical Mikimoto Pharmaceutical Co Ltd
Priority to JP2208003A priority Critical patent/JP2970767B2/en
Publication of JPH0495012A publication Critical patent/JPH0495012A/en
Application granted granted Critical
Publication of JP2970767B2 publication Critical patent/JP2970767B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain a safe beautifying and whitening cosmetic, containing an extract separated from seaweeds of the family Ishigeaceae with water or a hydrophilic organic solvent and having powerful beautifying and whitening action. CONSTITUTION:A beautifying and whitening cosmetic containing an extract separated from Ishige okamurai Yendo or Ishige foliacea Okamura with water or a hydrophilic organic solvent as an active ingredient. The aforementioned extract has stronger inhibitory effects on tyrosinase activity, i.e., beautifying and whitening action than that of brown algae such as especially Hizikia fusiforme Okamura, WAKAME seaweed or Eisenia bicyclis Setchell. Since the seaweeds partially used for foods are employed as a raw material, there is no problem in safety and the beautifying and whitening cosmetic has sufficient value of utilization even from the viewpoint of even both safety and beautifying whitening effects.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は特定の海藻の抽出物を有効成分とする美白化粧
料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a whitening cosmetic containing an extract of a specific seaweed as an active ingredient.

〔従来の技術〕[Conventional technology]

従来、チロシナーゼ活性阻害効果をもったものは、肌を
白くするという効果が期待でき、この作用をもった各種
の美白作用を有する物質を配合した化粧料が使用されて
いる。
Conventionally, products that have the effect of inhibiting tyrosinase activity can be expected to have the effect of whitening the skin, and cosmetics containing various whitening substances that have this effect have been used.

その代表的なものとしては、L−アスコルビン酸または
その脂肪酸誘導体、あるいはリン酸化アスコルビン酸ま
たはその塩などがよく知られている。
As representative examples thereof, L-ascorbic acid or its fatty acid derivatives, phosphorylated ascorbic acid or its salts, etc. are well known.

しかしながら、美白剤物質としてのし一アスコルビン酸
またはその脂肪酸誘導体は、熱や光に弱く、水溶液中で
の安定性が悪く、分解や着色を起こすなどの欠点があっ
た。
However, ascorbic acid or its fatty acid derivative as a skin whitening agent has drawbacks such as being sensitive to heat and light, having poor stability in an aqueous solution, and causing decomposition and discoloration.

またリン酸化アスコルビン酸またはその塩は安定性では
優れるものの、化粧水等に配合した場合に、経時′的に
沈殿を発生するなどの問題がある。
Furthermore, although phosphorylated ascorbic acid or its salts have excellent stability, they have problems such as precipitation over time when added to lotions and the like.

その他、コウジ酸やアルブチン等が美白剤物質として知
られているが、コウジ酸は配合物によっては着色を起こ
すなど、従来の美白剤物質は安定性や安全性に問題があ
った。
Other whitening agents such as kojic acid and arbutin are known, but kojic acid can cause coloration depending on the formulation, and conventional skin whitening agents have had problems with stability and safety.

海藻抽出物を配合する美白化粧料ないしメラニン形成阻
害物質としては、特開平1− 224308号公報、特開平2−88592号公報、特
開平2−124810号公報がある。
Examples of whitening cosmetics or melanin formation inhibitors containing seaweed extracts include JP-A-1-224308, JP-A-2-88592, and JP-A-2-124810.

特開平1−224308号公報は褐藻類ひばまた、こん
ぶ、くろめ、あらな、はんだわら等から抽出されたフェ
ノール性化合物を含有し、ゲル形成能を有しない水溶性
抽出物からなる化粧品配合液である。
JP-A-1-224308 discloses a cosmetic formulation containing phenolic compounds extracted from brown algae Hibamata, kelp, Kurome, Arana, solder straw, etc., and consisting of a water-soluble extract without gel-forming ability. be.

特開平2−88592号公報は、褐藻類、緑藻類、紅藻
類から抽出したメラニン形成阻害物質であるが、褐藻の
活性を中心としたものである。即ち、わかめ、こんぶ、
かしめ、おおばもくを中心とした海藻からの抽出物であ
る。
JP-A-2-88592 discloses melanin formation inhibitors extracted from brown algae, green algae, and red algae, and focuses on the activity of brown algae. Namely, wakame, konbu,
It is an extract from seaweeds, mainly Kakime and Obamoku.

特開平2−124810号公報は、褐藻綱特にヒバマタ
目またはコンブ目に属する海藻の親水性溶媒抽出物を含
有する化粧料である。ひじき、わかめ、あらめの抽出物
が例示されている。
JP-A-2-124810 discloses a cosmetic containing a hydrophilic solvent extract of a seaweed belonging to the Phaeophyceae, particularly the order Fucus or Laminata. Extracts of hijiki, wakame, and arame are exemplified.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

本発明者らが実験したところ、前記公報に示されている
海藻抽出物のチロシナーゼ活性阻害作用はさほど強くな
く、また海藻の種によって大きくその作用が異なること
がわかった。
Through experiments conducted by the present inventors, it was found that the tyrosinase activity inhibiting effect of the seaweed extract shown in the above-mentioned publication is not very strong, and that the effect varies greatly depending on the species of seaweed.

本発明の目的は、チロシナーゼ活性阻害作用か強く、且
つ安全てあり、実際に利用し易い美白剤物質を検索し、
これを用いて美白作用の強い安全な美白化粧料を提供す
ることである。
The purpose of the present invention is to search for skin whitening substances that have a strong tyrosinase activity inhibitory effect, are safe, and are easy to use in practice.
The object of the present invention is to provide a safe whitening cosmetic with strong whitening effect using this.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは、前記の課題を解決するため、後記のよう
な各種の海藻を用いて、そのチロシナー活性阻害率の測
定を試みた。その結果、驚くへきことに、同じ褐藻類に
属していても、前記公開公報に最も効果のあるものとし
て記載されているホンダワラ科のひしき、チガイソ科の
わかめ、コンブ科のあらめ等より、はるかにチロシナー
ゼ活性阻害効果の大きい海藻を見い出し本発明を完成し
た。
In order to solve the above problems, the present inventors attempted to measure the inhibition rate of tyrosiner activity using various seaweeds as described below. As a result, surprisingly, even though they belong to the same brown algae, they are listed as the most effective in the published publication, such as sargassum, wakame, and laminaria, which are listed as the most effective. We have discovered a seaweed that has a far greater effect on inhibiting tyrosinase activity and have completed the present invention.

即ち本発明はイシゲ科の海藻の水または親水性有機溶媒
による抽出物を含む美白化粧料である。
That is, the present invention is a skin-whitening cosmetic containing an extract of seaweed belonging to the family Polyaceae in water or a hydrophilic organic solvent.

本発明者らは、次のように褐藻類の海藻のチロシナーゼ
活性阻害を測定してみた。
The present inventors measured inhibition of tyrosinase activity of brown algae and seaweed as follows.

海藻の9倍量のリン酸ナトリウム緩衝液(lomM、 
p HI3.8 )を加えて、充分ホモジナイズした。
9 times the volume of seaweed sodium phosphate buffer (lomM,
pHI3.8) was added and thoroughly homogenized.

これを遠心分離し、不溶物を取り除き、さらに0.45
μのフィルターてi濾過した。これをサンプルとして以
下の実験を行った。
This was centrifuged to remove insoluble matter, and then 0.45
It was filtered using a μ filter. The following experiment was conducted using this as a sample.

リン酸ナトリウム緩衝液(30mM、 pH6,8)(
1,9ml、1.8BmM  チロシン 溶液1.0m
l、試料溶液1.0mlをスクリューバイアルにとり、
37℃恒温水槽中で5分以上加温した。
Sodium phosphate buffer (30mM, pH 6,8) (
1.9ml, 1.8BmM tyrosine solution 1.0m
l. Take 1.0ml of the sample solution into a screw vial,
It was heated for 5 minutes or more in a constant temperature water bath at 37°C.

チロシナーゼ溶液(Sigma社製、マツシュルーム由
来、914 Units / ml ) [1,1ml
を加え、37℃恒温水槽中で保温し、10分後に475
nmで吸光度を測定した。
Tyrosinase solution (manufactured by Sigma, derived from pine mushroom, 914 Units/ml) [1.1ml
was added, kept warm in a constant temperature water bath at 37℃, and after 10 minutes, 475℃ was added.
Absorbance was measured at nm.

又、対照として、試料溶液のがわりに純水を加え同様に
測定した。
In addition, as a control, pure water was added instead of the sample solution and measurements were made in the same manner.

チロシナーゼaNIH*(%)−1B−(A−P)l/
BXIOI)但し、A;試験検体の吸光度 B:対照の吸光度 P:試験検体の着色による吸光度 (3倍希釈) 結果は第1表のごとくになった。
Tyrosinase aNIH*(%)-1B-(A-P)l/
BXIOI) However, A: Absorbance of test specimen B: Absorbance of control P: Absorbance of colored test specimen (3-fold dilution) The results are as shown in Table 1.

第  1  表 このような結果となり、先行特許に示されているように
褐藻類のすべてに効果かあるわけてはなく、また先行特
許の最も効果のあるものを記載すべき実施例のものも、
弱い作用のものが多かった。
Table 1 The results are as shown above, and as shown in the prior patent, it is not effective for all brown algae, and the most effective example of the prior patent should also be described.
Many had weak effects.

本発明者らが行った実験によれば、一般にチロシナーゼ
活性阻害かあるといわれているひしき、あらめ、かじめ
等より、さらにイシゲ科の海藻はチロシナーゼ活性阻害
が強いことが判明した。
According to experiments conducted by the present inventors, it was found that seaweeds belonging to the family Iridaceae have a stronger inhibition of tyrosinase activity than seaweeds such as Hishiki, Arame, and Kajime, which are generally said to inhibit tyrosinase activity.

さらに、かしめ、あらめは他の海藻に比べれば、若干チ
ロシナーゼ活性阻害はあるが、以下の実験によってイシ
ゲ科の海藻は千ロジンかメラニンに変化する各段階に作
用し、より有効であることか確認できた。
Furthermore, although Kashima and Arame inhibit tyrosinase activity slightly compared to other seaweeds, the following experiment shows that seaweeds of the family Ishigamiaceae are more effective as they act on each stage of the transformation into rosin or melanin. It could be confirmed.

次のように気質にドーパを用いて、チロシナーゼのドー
パ酸化活性に対する阻害について試験した。即ちリン酸
ナトリウム緩衝液(30mM、pH64) 0.9 m
l 1.66mMドーパ溶液1 、0 ml s試料溶
液1.Omlをスクリューバイアルにとり37℃恒温水
槽中で5分以上加温した。チロシナーゼ溶液(Sigm
a製、マツシュルーム由来、914 Units /m
l) 0.1 mlを加え、37℃恒温水槽中で保温し
、2分後に475nmで吸光度を測定した。又対照とし
て試料溶液のかわりに純水を加え同様に測定した。
Dopa was used to test for inhibition of tyrosinase oxidation activity of dopa as follows. Sodium phosphate buffer (30mM, pH 64) 0.9m
l 1.66mM dopa solution 1, 0 ml s sample solution 1. Oml was placed in a screw vial and heated in a constant temperature water bath at 37° C. for 5 minutes or more. Tyrosinase solution (Sigma
Made by a, derived from pine mushrooms, 914 Units/m
l) 0.1 ml was added, kept warm in a constant temperature water bath at 37°C, and absorbance was measured at 475 nm after 2 minutes. As a control, pure water was added instead of the sample solution and the same measurements were performed.

チロシナーゼ活性阻害率(%)−1B−(A−P)l/
BX100但し、A:試験検体の吸光度 B:対照の吸光度 P:試験検体の着色による吸光度 (3倍希釈) 結果は第2表のようになった。
Tyrosinase activity inhibition rate (%) -1B-(A-P)l/
BX100 However, A: Absorbance of test specimen B: Absorbance of control P: Absorbance of colored test specimen (3-fold dilution) The results are as shown in Table 2.

第  2  表 〔メラニン生成抑制試験〕 Eagle  MEM培地に牛胎児血清10%および試
料を加え、検体とする。
Table 2 [Melanin production suppression test] 10% fetal bovine serum and a sample were added to Eagle MEM medium to serve as a sample.

↓ 6cmシャーレに検体を入れ、B−16細胞1×105
Cell/ 0. 1 m lを加える。
↓ Place the sample in a 6cm petri dish and add 1 x 105 B-16 cells.
Cell/0. Add 1 ml.

↓5%CO□、37℃で培養 培養3日目に検体を交換する。↓Culture at 37℃ with 5% CO□ Replace the specimen on the third day of culture.

第3表 ↓ 培養6日目に細胞を剥離しく付着性であるので物理的に
剥離)遠心分離して、白色化度を観察する。
Table 3 ↓ On the 6th day of culture, the cells are detached (physically detached as they are adherent) and centrifuged to observe the degree of whitening.

(判定基準)白色度による判定 core −:白色化なし +:わずかに白色化 ++:明らかに白色化 ++十二強い白色化 ++はメラニン生成抑制能力があることを表わし、十が
多い程、メラニン生成抑制能力が強いことを示す。
(Judgment criteria) Judgment based on whiteness core -: No whitening +: Slight whitening ++: Obviously whitening ++ 12 Strong whitening ++ indicates the ability to suppress melanin production; Indicates strong ability to suppress production.

本発明の海藻(いしげ、いろろ)抽出物について、前記
メラニン生成抑制試験を行った結果を第3表に示す。
Table 3 shows the results of the melanin production inhibition test performed on the seaweed (Ishige, Iroro) extract of the present invention.

いしげ(Ishige okag+urai Yend
o)、いろろ(Ishige 5inicola Ch
ihara)等のイシゲ科の海藻が他の海藻、特に褐藻
類の海藻と比較して有用なことがわかった。
Ishige okag+urai Yend
o), Iroro (Ishige 5inicola Ch)
It has been found that seaweeds of the family Ishigaceae, such as A. ihara), are more useful than other seaweeds, especially seaweeds of the brown algae family.

いしげ科の海藻は、一部で食用にされている事実から、
安全性に関しても問題ないことは勿論である。
Due to the fact that some seaweeds of the Shigeidae family are eaten as food,
Of course, there are no problems with safety.

〔実施例〕〔Example〕

以下に実施例により、本発明を更に具体的に説明するが
、本発明はこの実施例により同等限定されるものでない
ことは勿論である。
The present invention will be explained in more detail below with reference to Examples, but it goes without saying that the present invention is not limited to the same extent by these Examples.

(実施例1) 化粧水処方          重量%エタノール  
         101.3ブチレングリコール  
 10 いしげ抽出物(固形物)     1 水                       7
9(実施例2) 実施例1において、いしげ抽出物(固形物)をいろろ抽
出物(固形物)に置き換えたもの。
(Example 1) Lotion formulation Weight% ethanol
101.3 Butylene glycol
10 Shigege extract (solid) 1 Water 7
9 (Example 2) Example 1 except that the Shigeki extract (solid substance) was replaced with the Iroro extract (solid substance).

(比較例1) 実施例1において、いしげ抽出物(固形物)を水に置き
換えたもの。
(Comparative Example 1) Example 1 except that the Shigege extract (solid substance) was replaced with water.

(比較例2) 実施例1において、いしげ抽出物(固形物)をあらめ抽
出物(固形物)に置き換えたもの。
(Comparative Example 2) Example 1 except that the Shigege extract (solid substance) was replaced with Arame extract (solid substance).

(比較例3) 実施例1において、いしげ抽出物(固形物)をかじき抽
出物(固形物)に置き換えたもの。
(Comparative Example 3) Example 1 except that the Shigeki extract (solid substance) was replaced with the Marlin extract (solid substance).

官能評価 女性20名、男性9名に対して、2ケ月間使用し、アン
ケートを取った。
Sensory evaluation 20 women and 9 men used the product for two months and completed a questionnaire.

評価は5段階評価で、以下のように記載してもらった。The evaluation was on a five-point scale and was written as follows.

+5 実施例の方か非常によい。+5 The example is very good.

+4 実施例の方かかなりよい。+4 The example is considerably better.

+3 実施例の方かよい。+3 The example is better.

+2 実施例の方かややよい。+2 The example is slightly better.

+1 実施例の方が若干よい。+1 Example is slightly better.

0 差がない。0 There is no difference.

1 比較例の方が若干よい。1 Comparative example is slightly better.

2 比較例の方がややよい。2 Comparative example is slightly better.

3 比較例の方がよい。3 Comparative example is better.

4 比較例の方がかなりよい。4 Comparative example is much better.

5 比較例の方か非常によい。5 Comparative example is very good.

比較例はすべて、比較例1と行った。All comparative examples were conducted with Comparative Example 1.

この合計値を第4表に示す。This total value is shown in Table 4.

このように、イシゲ科の海藻はチロシナーゼ活性阻害効
果が強く、チロシーゼ活性阻害効果やパネルテストにお
いても、他の海藻に比較して、その作用が強いことが判
明した。
In this way, seaweeds belonging to the family Iridaceae have a strong tyrosinase activity inhibitory effect, and in tyrosinase activity inhibitory effects and panel tests, it has been found that this effect is stronger than that of other seaweeds.

〔発明の効果〕〔Effect of the invention〕

本発明によって、褐藻類の海藻すべてがチロシナーゼ活
性阻害効果即ち美白作用が強いわけてはなく、特にイシ
ゲ科の海藻が他の海藻特に他の褐藻類に比較してチロシ
ナーゼ活性阻害効果即ち美白作用が強く、パネルテスト
においても、その作用が実証された。
According to the present invention, not all brown algae have a strong tyrosinase activity inhibiting effect, that is, a whitening effect, and in particular, seaweeds of the family Iridaceae have a tyrosinase activity inhibiting effect, that is, a whitening effect, compared to other seaweeds, especially other brown algae. Its effectiveness was strongly demonstrated in panel tests.

イシゲ科の海藻は、一部で食用に供されていることから
安全性については問題なく、美白化粧料として、安全性
の面からも、その美白効果の面からも十分に利用価値が
あることが明白となった。
Since some seaweeds of the family Iridaceae are edible, there are no safety issues, and they have sufficient utility as skin-whitening cosmetics, both from the safety perspective and from the whitening effect. became clear.

出願人代理人  藤  本   博  光−9:Applicant's agent Hiroshi Fujimoto-9:

Claims (1)

【特許請求の範囲】[Claims] イシゲ科の海藻の水または親水性有機溶媒による抽出物
を含む美白化粧料。
A skin whitening cosmetic containing an extract of seaweed belonging to the family Porites in water or a hydrophilic organic solvent.
JP2208003A 1990-08-08 1990-08-08 Whitening cosmetics Expired - Lifetime JP2970767B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2208003A JP2970767B2 (en) 1990-08-08 1990-08-08 Whitening cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2208003A JP2970767B2 (en) 1990-08-08 1990-08-08 Whitening cosmetics

Publications (2)

Publication Number Publication Date
JPH0495012A true JPH0495012A (en) 1992-03-27
JP2970767B2 JP2970767B2 (en) 1999-11-02

Family

ID=16549061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2208003A Expired - Lifetime JP2970767B2 (en) 1990-08-08 1990-08-08 Whitening cosmetics

Country Status (1)

Country Link
JP (1) JP2970767B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030015536A (en) * 2001-08-16 2003-02-25 벤트리 주식회사 Whitening cosmetics containing extracts from Ishige sinicola
KR101132572B1 (en) * 2009-04-06 2012-04-05 재단법인 제주테크노파크 Skin Whitening Composition
KR101365822B1 (en) * 2012-02-10 2014-02-20 제주대학교 산학협력단 Skin whitening composition comprising octaphlorethol A compound
JP2014097959A (en) * 2012-11-15 2014-05-29 Mikimoto Pharmaceut Co Ltd Claudin production promoter, occludin production promoter, and enhancer for function of tight junction
JP2014101309A (en) * 2012-11-20 2014-06-05 Mikimoto Pharmaceut Co Ltd Cystatin a production promoter, skin barrier increasing agent, skin keratinization function increasing agent, and skin roughness preventing agent
JP2014133708A (en) * 2013-01-09 2014-07-24 Mikimoto Pharmaceut Co Ltd Dendrite growth inhibitor

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030015536A (en) * 2001-08-16 2003-02-25 벤트리 주식회사 Whitening cosmetics containing extracts from Ishige sinicola
KR101132572B1 (en) * 2009-04-06 2012-04-05 재단법인 제주테크노파크 Skin Whitening Composition
KR101365822B1 (en) * 2012-02-10 2014-02-20 제주대학교 산학협력단 Skin whitening composition comprising octaphlorethol A compound
JP2014097959A (en) * 2012-11-15 2014-05-29 Mikimoto Pharmaceut Co Ltd Claudin production promoter, occludin production promoter, and enhancer for function of tight junction
JP2014101309A (en) * 2012-11-20 2014-06-05 Mikimoto Pharmaceut Co Ltd Cystatin a production promoter, skin barrier increasing agent, skin keratinization function increasing agent, and skin roughness preventing agent
JP2014133708A (en) * 2013-01-09 2014-07-24 Mikimoto Pharmaceut Co Ltd Dendrite growth inhibitor

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