JP2000290131A - Bleaching preparation - Google Patents

Bleaching preparation

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Publication number
JP2000290131A
JP2000290131A JP11099820A JP9982099A JP2000290131A JP 2000290131 A JP2000290131 A JP 2000290131A JP 11099820 A JP11099820 A JP 11099820A JP 9982099 A JP9982099 A JP 9982099A JP 2000290131 A JP2000290131 A JP 2000290131A
Authority
JP
Japan
Prior art keywords
extract
component
present
linne var
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.)
Granted
Application number
JP11099820A
Other languages
Japanese (ja)
Other versions
JP4063443B2 (en
Inventor
Toshio Hikima
俊雄 引間
Taiji Nakagawa
泰治 中川
Shigeru Igarashi
滋 五十嵐
Toshio Horikoshi
俊雄 堀越
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.)
Kanebo Ltd
Original Assignee
Kanebo 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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP09982099A priority Critical patent/JP4063443B2/en
Publication of JP2000290131A publication Critical patent/JP2000290131A/en
Application granted granted Critical
Publication of JP4063443B2 publication Critical patent/JP4063443B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain the subject bleaching preparation exhibiting an inhibitory effect on melanization, etc., developing a bleaching effect in a short time by including one or more kinds selected from extracts of Glycyrrhiza glaba Linne Var, Silybum marianum Gaertn., Prunus persica Batsch and an extract of wheat embryo bud. SOLUTION: This bleaching preparation contains (A) one or more kinds selected from extracts of (i) Glycyrrhiza glaba Linne Var., (ii) Silybum marianum Gaertn. and (iii) Prunus persica Batsch and (B) an extract of wheat embryo bud. Preferably the preparation contains 0.0001-10 wt.% calculated as a dried solid content of the compound A and 0.0001-10 wt.% content of the component B. For example, oil-soluble Glycyrrhiza glaba Linne Var. essence PT (40) (trade name) and glabridin extract from Glycyrrhiza glaba Linne Var., can be used as the component (i), an extract obtained from the fruit or the whole plant of Silybum marianum Gaertn. with acetone as the component (ii) and an extract obtained from leaves, fruits, seeds, etc., of Prunus persica Batsch with ethanol as the component (iii). A substance obtained by extracting wheat embryo bud with water, concentrating and filtering can be used as the composition B.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は化粧品及び医薬部外
品に関する。
The present invention relates to cosmetics and quasi-drugs.

【0002】[0002]

【従来の技術】従来より、肌のしみやそばかす等の予防
や治療を目的とする美白化粧料には、L−アスコルビン
酸及びその誘導体、ハイドロキノン誘導体、コウジ酸の
ピロン類、プラセンターエキスの胎盤抽出物等が配合さ
れている。
2. Description of the Related Art Conventionally, whitening cosmetics for the purpose of preventing and treating skin spots and freckles include L-ascorbic acid and its derivatives, hydroquinone derivatives, pyrones of kojic acid, and placenta of placenta extract. Extracts and the like are blended.

【0003】これらは、メラニン生成の抑制、生成した
メラニンの淡色漂白作用等の効果を有し、美白効果を有
する物質として広く知られている。しかし、これらの物
質を単独で使用した場合、例えばL−アスコルビン酸及
びその誘導体は保存安定性が十分ではなくその効果が十
分に発揮されなかったり、またハイドロキノン誘導体は
安全性に問題があるなど十分なものではなかった。
[0003] These substances have effects such as suppression of melanin production and light-color bleaching action of the produced melanin, and are widely known as substances having a whitening effect. However, when these substances are used alone, for example, L-ascorbic acid and its derivatives have insufficient storage stability and their effects are not sufficiently exerted, and hydroquinone derivatives have insufficient safety, for example, they have a problem in safety. It was not something.

【0004】[0004]

【発明が解決しようとする課題】本発明者らは、上記の
欠点を解消すべく鋭意検討を行った結果、後記の美白化
粧料が、紫外線による炎症を防ぎ紫外線障害によるメラ
ニン産生を抑制するとともに優れたメラニン生成抑制効
果を示すだけではなく、肌を整えることによりメラニン
色素の排泄を促し、短期間で優れた美白効果を発現する
ことを見出し、本発明を完成した。
SUMMARY OF THE INVENTION The present inventors have conducted intensive studies to solve the above-mentioned drawbacks. As a result, the whitening cosmetics described below prevent inflammation caused by ultraviolet rays, suppress melanin production due to ultraviolet damage, and The present invention has been found not only to exhibit an excellent melanin production inhibitory effect, but also to promote excretion of melanin pigments by conditioning the skin and to exhibit an excellent whitening effect in a short period of time.

【0005】すなわち、本発明の目的は、紫外線による
炎症を防ぎ紫外線障害によるメラニン産生を抑制すると
ともに優れたメラニン生成抑制効果を示すだけではな
く、肌を整えることによりメラニン色素の排泄を促し、
短期間で優れた美白効果を発現する発現する美白化粧料
を提供することにある。
[0005] That is, an object of the present invention is not only to prevent inflammation due to ultraviolet rays, to suppress melanin production due to ultraviolet damage and to show an excellent inhibitory effect on melanin production, but also to promote excretion of melanin pigments by adjusting skin,
An object of the present invention is to provide a whitening cosmetic which expresses an excellent whitening effect in a short period of time.

【0006】[0006]

【課題を解決するための手段】上記の目的を達成する本
発明は、甘草(Glycyrrhiza glabaL
inne Var.)、マリアアザミ(Silybum
marianum Gaertn.)、モモ(Prun
us persica Batsch)の抽出物から選ば
れる一種以上と小麦胚芽の抽出物を含有する美白化粧料
である。
According to the present invention, which achieves the above objects, there is provided licorice (Glycyrrhiza glabaL).
inne Var. ), Maria Thistle (Silybum)
marianum Gaertn. ), Peach (Prun
us persica Batsch) and a whitening cosmetic containing an extract of wheat germ.

【0007】[0007]

【発明の実施の形態】本発明の実施の形態は美白化粧料
である。以下、本発明の構成について詳述する。
BEST MODE FOR CARRYING OUT THE INVENTION An embodiment of the present invention is a whitening cosmetic. Hereinafter, the configuration of the present invention will be described in detail.

【0008】本発明に用いられる小麦胚芽の抽出物は、
例えば水にて抽出し、これを濃縮した後、ろ過して得る
ことができる。但しこの製造方法に限られるものではな
い。
[0008] The wheat germ extract used in the present invention comprises:
For example, it can be obtained by extracting with water, concentrating this, and then filtering. However, it is not limited to this manufacturing method.

【0009】小麦胚芽の抽出物の本発明の美白化粧料中
への配合量は抽出物の乾燥固形分に換算して0.000
1〜10.0重量%が好ましいが、これに限られない。
The amount of the wheat germ extract in the whitening cosmetic composition of the present invention is 0.000 in terms of the dry solid content of the extract.
The content is preferably, but not limited to, 1 to 10.0% by weight.

【0010】本発明に用いられる甘草及びマリアアザミ
の抽出物は、水またはメタノール、エタノール、プロパ
ノール、1,3ブチレングリコール等の低級アルコー
ル、ベンゼン、エチルエーテル、クロロホルム、酢酸エ
チル、酢酸ブチル、アセトンまたはそれらの混液により
抽出される。抽出液はそのまま化粧料に配合することも
可能であるが、これを凍結乾燥法やスプレ−ドライ法等
で粉末化して使用するほうが望ましい。また、抽出液を
液液分配、吸着クロマトグラフィー等の手段で精製し
て、液状のものあるいは粉末化したものを配合すること
も可能である。
The extract of licorice and Maria thistle used in the present invention may be water or a lower alcohol such as methanol, ethanol, propanol or 1,3 butylene glycol, benzene, ethyl ether, chloroform, ethyl acetate, butyl acetate, acetone or It is extracted by their mixture. The extract may be directly incorporated into cosmetics, but it is preferable to use the extract in the form of a powder by freeze-drying or spray-drying. It is also possible to purify the extract by means of liquid-liquid distribution, adsorption chromatography or the like, and to mix it in a liquid form or a powdered form.

【0011】本発明に用いられる甘草の抽出物は、たと
えば油溶性甘草エキスPT(40)(丸善製薬製)など
が市販されている。また甘草(Glycyrrhiza
glaba Linne Var.)から単離されるグ
ラブリジンを用いることもできる。
As the licorice extract used in the present invention, for example, an oil-soluble licorice extract PT (40) (manufactured by Maruzen Pharmaceutical Co., Ltd.) is commercially available. In addition, licorice (Glycyrrhiza)
Glaba Linne Var. ) Can also be used.

【0012】本発明に用いられるマリアアザミの抽出物
としては、マリアアザミ(Silybum maria
num Gaertn.)の実や全草からアセトンで抽
出したものなどが挙げられる。
[0012] The extract of Maria Thistle used in the present invention includes Maria Thistle (Silybum maria).
num Gaertn. ) And those extracted from whole plants with acetone.

【0013】本発明に用いられるモモ(Prunus
persica Batsch)の抽出物としては、葉、
実、種子などからエタノールで抽出したものなどが挙げ
られる。
The peach (Prunus) used in the present invention
persica Batsch) extracts include leaves,
Actually, there may be mentioned those extracted from seeds and the like with ethanol.

【0014】甘草、モモ及びマリアアザミの抽出物の本
発明の美白化粧料中への配合量は抽出物の乾燥固形分に
換算して0.0001〜10重量%が好ましいが、これ
に限られない。
The amount of the extract of licorice, peach and mari thistle in the whitening cosmetic composition of the present invention is preferably 0.0001 to 10% by weight in terms of the dry solid content of the extract, but is not limited thereto.

【0015】本発明の化粧料には上記の原料の他に一般
的に知られている色素、香料、防腐剤、界面活性剤、顔
料、抗酸化剤、保湿剤、紫外線吸収剤などの原料を本発
明の目的を達成する範囲内で適宜配合することができ
る。
In the cosmetic of the present invention, in addition to the above-mentioned raw materials, generally known raw materials such as dyes, fragrances, preservatives, surfactants, pigments, antioxidants, humectants, and ultraviolet absorbers are used. It can be appropriately compounded within a range that achieves the object of the present invention.

【0016】本発明の化粧料の剤型としてはクリーム、
乳液、化粧水、パックなど化粧料に一般に使用されてい
る剤型であればいずれでもよい。
The cosmetic of the present invention may be in the form of a cream,
Any dosage form commonly used in cosmetics such as emulsions, lotions, and packs may be used.

【0017】本発明の化粧料は、例えば化粧水の場合、
各成分を混合溶解するなど、通常の方法により製造する
ことができる。
The cosmetic of the present invention may be used, for example, in the case of a lotion.
It can be manufactured by an ordinary method such as mixing and dissolving each component.

【0018】[0018]

【実施例】以下、実施例および比較例に基づいて本発明
を詳述する。尚、実施例に示す配合%とは重量%であ
る。実施例に記載の皮膚色明度回復試験法、官能試験
(美白効果)は下記の通りである。また、以下実施例で
用いた小麦胚芽から得られる抽出物および他の本発明の
植物抽出物の調製方法は以下の通りであるが、本発明の
範囲はこれらのみに限定されるものではない。
The present invention will be described below in detail based on examples and comparative examples. In addition, the compounding% shown in the examples is% by weight. The skin color lightness recovery test method and sensory test (whitening effect) described in the examples are as follows. The methods for preparing the extract obtained from wheat germ and other plant extracts of the present invention used in the following Examples are as follows, but the scope of the present invention is not limited to these.

【0019】(小麦胚芽から得られる抽出物の調製法)
小麦胚芽50gを水1Lに浸漬して1昼夜攪拌しながら
放置する。得られた液を濃縮した後、ろ過した。これに
より小麦胚芽抽出物15.7g(固形物換算:0.16
g)を得た。
(Preparation method of extract obtained from wheat germ)
50 g of wheat germ is immersed in 1 L of water, and left stirring for 24 hours a day. The obtained liquid was concentrated and then filtered. Thereby, 15.7 g of wheat germ extract (solids conversion: 0.16
g) was obtained.

【0020】(甘草抽出物の調製法)甘草の根5.00g
にエタノール500mlを加え、還流下で3時間抽出を
行った。この後、濾過し、得られた抽出液をダイヤイオ
ンHP−20(三菱化成工業(株)製)のカラム(Φ3
cm×11cm,Vt=80ml)に負荷後、800m
lの10%エタノ−ル水溶液で洗浄した。ついで、40
0mlの70%エタノ−ル水溶液で溶出し、溶出液を減
圧濃縮した後、凍結乾燥してグラブリジン0.04gを
得た。
(Method for Preparing Licorice Extract) 5.00 g of licorice root
To the mixture was added 500 ml of ethanol, and the mixture was extracted under reflux for 3 hours. Thereafter, the mixture was filtered, and the obtained extract was applied to a column (Φ3) of Diaion HP-20 (manufactured by Mitsubishi Kasei Kogyo Co., Ltd.).
cm × 11cm, Vt = 80ml), then 800m
Washed with 1 l of a 10% aqueous ethanol solution. Then, 40
The eluate was eluted with 0 ml of 70% aqueous ethanol, and the eluate was concentrated under reduced pressure and freeze-dried to obtain 0.04 g of glabridine.

【0021】(マリアアザミ抽出物の調製法)マリアアザ
ミの種5.00gにアセトン500mlを加え、還流下
で3時間抽出を行った。この後、濾過し、得られた抽出
液をダイヤイオンHP−20(三菱化成工業(株)製)
のカラム(Φ3cm×11cm,Vt=80ml)に負
荷後、500mlの精製水で洗浄した。ついで、500
mlの40%エタノ−ル水溶液で溶出し、溶出液を減圧
濃縮した後、凍結乾燥して乾燥粉末2.68gを得た。
(Preparation Method of Maria Thistle Extract) 500 ml of acetone was added to 5.00 g of thistle seeds, and the mixture was extracted under reflux for 3 hours. Thereafter, the mixture is filtered, and the obtained extract is subjected to Diaion HP-20 (manufactured by Mitsubishi Chemical Industry Co., Ltd.)
Was loaded onto a column (Φ3 cm × 11 cm, Vt = 80 ml), and washed with 500 ml of purified water. Then, 500
The elute was eluted with 40 ml of a 40% aqueous ethanol solution, and the eluate was concentrated under reduced pressure and freeze-dried to obtain 2.68 g of a dry powder.

【0022】(モモ抽出物の調製法)モモの種(桃仁)1
0.0gにエタノール500mlを加え、還流下で3時
間抽出を行った。この後、濾過し、得られた抽出液をダ
イヤイオンHP−20(三菱化成工業(株)製)のカラ
ム(Φ3cm×11cm,Vt=80ml)に負荷後、
800mlの10%エタノ−ル水溶液で洗浄した。つい
で、400mlの70%エタノ−ル水溶液で溶出し、溶
出液を減圧濃縮した後、凍結乾燥して乾燥粉末1.04
gを得た。
(Preparation method of peach extract) Peach seeds (peach kernel) 1
500 ml of ethanol was added to 0.0 g, and extraction was performed for 3 hours under reflux. Thereafter, the mixture was filtered, and the obtained extract was loaded on a column (Φ3 cm × 11 cm, Vt = 80 ml) of Diaion HP-20 (manufactured by Mitsubishi Kasei Kogyo Co., Ltd.).
It was washed with 800 ml of a 10% aqueous ethanol solution. The eluate was then eluted with 400 ml of 70% aqueous ethanol, and the eluate was concentrated under reduced pressure and lyophilized to give a dry powder of 1.04%.
g was obtained.

【0023】(1)皮膚色明度回復試験法 被験者20名の背部皮膚にUV−B領域の紫外線を最小
紅斑量の2倍照射し、試料塗布部位と非塗布部位を設定
して各々の皮膚の基準明度(V0値,V0’値)を測定
した。引きつづいて塗布部位には試料を1日2回ずつ1
5週間連続塗布した後、3,6,9,12,15週間後
の塗布部位及び非塗布部位の皮膚の明度(Vn値,V
n’値)を測定し、下記の判断基準にしたがって皮膚色
の回復を評価した。尚、皮膚の明度(マンセル表色系V
値)は高速分光色彩計で測定して得られたX,Y,Z値
より算出した。また評価は被験者20名について、3週
間後の評価点の平均値で示した。
(1) Skin Color Brightness Recovery Test Method The ultraviolet light in the UV-B region was irradiated twice as much as the minimum erythema dose to the back skin of 20 subjects, and the sample application site and non-application site were set, and each skin was examined. The reference lightness (V0 value, V0 'value) was measured. Then, apply the sample twice a day to the application site.
After continuous application for 5 weeks, the lightness (Vn value, Vn) of the skin at the application site and the non-application site after 3, 6, 9, 12, and 15 weeks
n ′ value), and the recovery of skin color was evaluated according to the following criteria. The lightness of the skin (Munsell color system V
Value) was calculated from the X, Y, and Z values obtained by measuring with a high-speed spectral colorimeter. In addition, the evaluation was shown as an average value of the evaluation points after 3 weeks for 20 subjects.

【0024】[0024]

【表1】 [Table 1]

【0025】(2)官能試験 被験者20名が試料を10日間連用した後、試料の特性
を評価した。評価は、美白効果のアンケート項目に対
し、「美白効果が感じられた」と回答した人数で示し
た。
(2) Sensory test Twenty test subjects continuously used the sample for 10 days, and then evaluated the characteristics of the sample. The evaluation was shown by the number of respondents who answered that "the whitening effect was felt" to the questionnaire item of the whitening effect.

【0026】実施例1〜3,比較例1〜5 小麦胚芽から得られる抽出物、甘草及びマリアアザミの
抽出物をそれぞれ表2の組成において配合し、下記の調
製方法に基づいてスキンクリームを調製した。各々につ
いて前記の試験を実施し、その結果を表3に示した。
Examples 1 to 3 and Comparative Examples 1 to 5 Extracts obtained from wheat germ, licorice and Maria Thistle extracts were each blended in the composition shown in Table 2, and a skin cream was prepared according to the following preparation method. did. The above test was performed for each, and the results are shown in Table 3.

【0027】[0027]

【表2】 [Table 2]

【0028】[0028]

【表3】 [Table 3]

【0029】調製方法:(A)(B)を70℃にて均一
に溶解し、(A)を攪拌しながら(B)を(A)に注入
して乳化分散した後、攪拌しながら温度30℃まで冷却
して調製した。
Preparation method: (A) and (B) are uniformly dissolved at 70 ° C., (B) is poured into (A) while stirring (A), emulsified and dispersed, and then stirred to a temperature of 30 ° C. Prepared by cooling to ° C.

【0030】表3の結果から本発明の実施例1〜3のス
キンクリームは、前記諸試験において良好な特性を示す
ことがわかる。一方、比較例1〜5のスキンクリーム
は、十分な効果が認められず、本発明の実施例に比べて
劣ることがわかる。
From the results shown in Table 3, it can be seen that the skin creams of Examples 1 to 3 of the present invention show good characteristics in the above-mentioned tests. On the other hand, the skin creams of Comparative Examples 1 to 5 did not show a sufficient effect, indicating that they were inferior to the examples of the present invention.

【0031】実施例4(スキンローション) 表4の組成により本発明のスキンローションを通常の製
法によって調製した。
Example 4 (Skin Lotion) The skin lotion of the present invention was prepared according to the composition shown in Table 4 by a conventional method.

【0032】[0032]

【表4】 [Table 4]

【0033】実施例4のスキンローションは前記諸試験
において良好な結果を示した。
The skin lotion of Example 4 showed good results in the above tests.

【0034】実施例5(デイエッセンス) 表5の組成により本発明のデイエッセンス(日中用美容
液)を下記の製法によって調製した。
Example 5 (Day Essence) The day essence (daytime serum) of the present invention was prepared according to the composition shown in Table 5 by the following method.

【0035】[0035]

【表5】 [Table 5]

【0036】調製方法:(A)(B)を70℃にて各成
分をそれぞれ混合溶解し、(B)を(A)に加えて混合
攪拌し、30℃まで冷却して調製した。
Preparation method: (A) and (B) were mixed and dissolved at 70 ° C. for each component, and (B) was added to (A), mixed, stirred and cooled to 30 ° C.

【0037】この実施例4のデイエッセンスは前記諸試
験において良好な結果を示した。
The day essence of Example 4 showed good results in the above tests.

【0038】[0038]

【発明の効果】以上記載のごとく、本発明が、短期間で
美白効果を発現する優れた美白化粧料を提供することは
明らかである。
As described above, it is apparent that the present invention provides an excellent whitening cosmetic which exhibits a whitening effect in a short period of time.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 堀越 俊雄 神奈川県小田原市寿町5丁目3番28号 鐘 紡株式会社基礎科学研究所内 Fターム(参考) 4C083 AA082 AA111 AA112 AB242 AC012 AC022 AC102 AC122 AC212 AC242 AC422 AC442 AC482 AC662 AD352 AD572 CC01 CC04 CC05 DD23 DD31 EE16 FF01 FF05  ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Toshio Horikoshi 5-28, Kotobukicho, Odawara-shi, Kanagawa Kanebo Co., Ltd. Basic Research Laboratory F-term (reference) 4C083 AA082 AA111 AA112 AB242 AC012 AC022 AC102 AC122 AC212 AC242 AC422 AC442 AC482 AC662 AD352 AD572 CC01 CC04 CC05 DD23 DD31 EE16 FF01 FF05

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 甘草(Glycyrrhiza glab
a Linne Var.)、マリアアザミ(Silyb
um marianum Gaertn.)、モモ(Pr
unus persica Batsch)の抽出物から
選ばれる一種以上と小麦胚芽の抽出物を含有することを
特徴とする美白化粧料。
[Claim 1] Glycyrrhiza glab
a Linne Var. ), Maria Thistle (Silyb
um marianum Gaertn. ), Peach (Pr
A whitening cosmetic comprising: an extract of unus persica Batsch) and an extract of wheat germ.
JP09982099A 1999-04-07 1999-04-07 Whitening cosmetics Expired - Fee Related JP4063443B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP09982099A JP4063443B2 (en) 1999-04-07 1999-04-07 Whitening cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP09982099A JP4063443B2 (en) 1999-04-07 1999-04-07 Whitening cosmetics

Publications (2)

Publication Number Publication Date
JP2000290131A true JP2000290131A (en) 2000-10-17
JP4063443B2 JP4063443B2 (en) 2008-03-19

Family

ID=14257480

Family Applications (1)

Application Number Title Priority Date Filing Date
JP09982099A Expired - Fee Related JP4063443B2 (en) 1999-04-07 1999-04-07 Whitening cosmetics

Country Status (1)

Country Link
JP (1) JP4063443B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6645514B1 (en) 2002-12-19 2003-11-11 Access Business Group International, Llc Increasing skin cell renewal with water-soluble Vitamin E
JP2008530062A (en) * 2005-02-11 2008-08-07 グリーンファーマ Use of silymarin and / or silymarin constituents as skin or hair pigmentation stimulants
CN102178629A (en) * 2011-04-19 2011-09-14 窦建国 Silybum marianum essential oil skin-care cream and preparation method thereof
CN109793685A (en) * 2019-03-25 2019-05-24 丹东欣时代生物医药科技有限公司 A kind of production method of functions of removing chloasma facial mask

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6645514B1 (en) 2002-12-19 2003-11-11 Access Business Group International, Llc Increasing skin cell renewal with water-soluble Vitamin E
JP2008530062A (en) * 2005-02-11 2008-08-07 グリーンファーマ Use of silymarin and / or silymarin constituents as skin or hair pigmentation stimulants
CN102178629A (en) * 2011-04-19 2011-09-14 窦建国 Silybum marianum essential oil skin-care cream and preparation method thereof
CN109793685A (en) * 2019-03-25 2019-05-24 丹东欣时代生物医药科技有限公司 A kind of production method of functions of removing chloasma facial mask

Also Published As

Publication number Publication date
JP4063443B2 (en) 2008-03-19

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