JPS63284109A - Beautifying cosmetic - Google Patents

Beautifying cosmetic

Info

Publication number
JPS63284109A
JPS63284109A JP11968487A JP11968487A JPS63284109A JP S63284109 A JPS63284109 A JP S63284109A JP 11968487 A JP11968487 A JP 11968487A JP 11968487 A JP11968487 A JP 11968487A JP S63284109 A JPS63284109 A JP S63284109A
Authority
JP
Japan
Prior art keywords
acid
salt
skin
cosmetic
beautifying
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
JP11968487A
Other languages
Japanese (ja)
Other versions
JPH0567125B2 (en
Inventor
Hideya Ando
秀哉 安藤
Akira Hashimoto
晃 橋本
Akira Takeuchi
明 竹内
Yoshiji Ozasa
小笹 祥次
Mitsuaki Shimizu
清水 満章
Kozo Masamoto
政本 幸三
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.)
Sunstar Inc
Original Assignee
Sunstar Inc
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 Sunstar Inc filed Critical Sunstar Inc
Priority to JP11968487A priority Critical patent/JPS63284109A/en
Publication of JPS63284109A publication Critical patent/JPS63284109A/en
Publication of JPH0567125B2 publication Critical patent/JPH0567125B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/67Vitamins

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain a beautifying agent eliminating or preventing blackening of skin by ultraviolet rays, stain or freckle, containing a liberated fatty acid having limited numbers of carbons and unsaturated bonds, a salt thereof or an ester with an alcohol as an active ingredient. CONSTITUTION:A beautifying cosmetic containing 0.1-10wt.% fatty acid (e.g. linoleic acid, gamma-linolenic acid, arachidonic acid or eicosapentaenoic acid) having 18-22C and two or more unsaturated bonds in the molecular structure, salt (e.g. Na salt, arginine salt or triethanolamine salt) or ester (e.g. methyl ester). The cosmetic can eliminate or prevent blackening of skin by ultraviolet rays, skin chromatosis such as stain or freckle and can show excellent beautifying effects without causing side effects. The purified liberated fatty acid of raw material is preferably used.

Description

【発明の詳細な説明】 東!直へ帆且立」 本発明は特定の脂肪酸またはその誘導体を化粧料基剤に
配合し、紫外線による皮膚の黒化あるいはシミ、ソバカ
スなどの皮膚の色素沈着を消失もしくは予防する美白化
粧料に関する。
[Detailed description of the invention] East! TECHNICAL FIELD The present invention relates to whitening cosmetics that contain specific fatty acids or derivatives thereof in a cosmetic base to eliminate or prevent darkening of the skin or skin pigmentation such as spots and freckles caused by ultraviolet rays.

従来の技 および問題点 従来、美白化粧料組成物としてはビタミンCおよびその
誘導体など、還元剤や胎盤エキスなどのチロシナーゼ活
性阻害剤を配合したものが知られている。しかしながら
、これら従来の美白化粧料は培養細胞によるin vi
troの実験ではメラニン産生抑制作用などを示すもの
の、実際に皮膚に適用した場合、充分な色素沈着の消失
もしくは予防効果は得られていない。
Conventional Techniques and Problems Conventionally, whitening cosmetic compositions containing vitamin C and its derivatives, reducing agents, and tyrosinase activity inhibitors such as placenta extract are known. However, these conventional whitening cosmetics are in vitro using cultured cells.
Although TRO's experiment shows that it has an effect of inhibiting melanin production, when it is actually applied to the skin, it has not been able to sufficiently eliminate or prevent pigmentation.

本発明は実際に皮膚に適用した場合、副作用がなく優れ
た美白効果を奏しうる化粧料を提供することを目的とす
る。
An object of the present invention is to provide a cosmetic that exhibits excellent whitening effects without side effects when actually applied to the skin.

問題点を解決するための手段 本発明者らは、前記目的を達成すべく鋭意研究を重ねた
結果、特定の脂肪酸およびその誘導体が皮膚の色素沈着
を消失、もしくは予防に対し優れた作用を示すことを見
いだし、本発明を完成するに至った。
Means for Solving the Problems As a result of extensive research to achieve the above object, the present inventors have found that certain fatty acids and their derivatives have an excellent effect on eliminating or preventing skin pigmentation. This discovery led to the completion of the present invention.

すなわち本発明は、炭素数!8〜22かつ分子構造中の
不飽和数が2以上の遊離脂肪酸、その塩、あるいは一価
または二価アルコールとのエステルを活性成分として含
有する美白化粧料を提供するものである。
In other words, the present invention is based on the number of carbon atoms! The present invention provides a whitening cosmetic containing as an active ingredient a free fatty acid having 8 to 22 unsaturations and 2 or more unsaturations in its molecular structure, a salt thereof, or an ester with a monohydric or dihydric alcohol.

本発明組成物に配合されるリノール酸、γ−リルン酸な
ど炭素数18〜22を有し、かつ分子構造中の不飽和数
が2以上の脂肪酸は、植物油脂および動物油脂に含まれ
ている。しかし、これら脂肪酸は遊離の状態で存在する
ことは少なく、そのほとんどはトリグリセリドの状態で
存在する。
The fatty acids having 18 to 22 carbon atoms and having 2 or more unsaturations in the molecular structure, such as linoleic acid and γ-lylunic acid, which are blended into the composition of the present invention, are contained in vegetable oils and animal fats. . However, these fatty acids rarely exist in a free state, and most of them exist in the form of triglycerides.

このようなトリグリセリドは、遊離の脂肪酸もしくはそ
のアルキルエステルのごとく動物試験等において優れた
色素沈着抑制作用は認められない。
Such triglycerides, unlike free fatty acids or their alkyl esters, have not been found to have an excellent pigmentation suppressing effect in animal tests.

また、バルミチン酸、ステアリン酸などの飽和脂肪酸に
あっても同様に色素沈着抑制効果は認められず、場合に
よっては逆にメラニン産生を先進する。かかる飽和脂肪
酸は、植物油脂および動物油脂に多量にふくまれている
ため、本発明化粧料に 。
Similarly, saturated fatty acids such as valmitic acid and stearic acid do not have the same effect on suppressing pigmentation, and in some cases may even promote melanin production. Since such saturated fatty acids are contained in large amounts in vegetable oils and animal fats, they can be used in the cosmetics of the present invention.

おけるリノール酸などの配合にあたっては精製したもの
を用いることが好ましい。
When blending linoleic acid, etc., it is preferable to use purified linoleic acid.

本発明の美白化粧料に配合される炭素数18〜22かつ
分子構造中の不飽和数が2以上の遊離脂肪酸の代表的な
ものとしては、リノール酸、リノエライジン酸、α−リ
ルン酸、γ−リルン酸、ジホモ−γ−リルン酸、アラキ
ドン酸、エイコサペンクエン酸などが挙げられ、これら
の1種また2種以上が用いられる。
Typical free fatty acids with 18 to 22 carbon atoms and 2 or more unsaturations in the molecular structure that are blended into the whitening cosmetics of the present invention include linoleic acid, linoleaidic acid, α-lilunic acid, and γ-linoleic acid. -lyllunic acid, dihomo-γ-lyllunic acid, arachidonic acid, eicosapencitric acid, etc., and one or more of these may be used.

また、これら遊離脂肪酸の塩としては、ナトリウム塩、
カリウム塩などの金属塩、アルギニン塩、リジン塩など
のアミノ酸塩、トリエタノールアミン塩、モノエタノー
ルアミン塩等のアミン塩などが挙げられる。
In addition, as salts of these free fatty acids, sodium salts,
Examples include metal salts such as potassium salts, amino acid salts such as arginine salts and lysine salts, and amine salts such as triethanolamine salts and monoethanolamine salts.

さらに、前記遊離脂肪酸のアルキルエステルとしては、
メタノール、エタノール、イソプロピルアルコールなど
のm個アルコールとのエステル、エチレングリコール、
プロピレングリコール、1.3−ブチレングリコールな
どの二価のアルコールとのエステルなどが挙げられる。
Furthermore, as the alkyl ester of the free fatty acid,
Esters with m alcohols such as methanol, ethanol, isopropyl alcohol, ethylene glycol,
Examples include esters with dihydric alcohols such as propylene glycol and 1,3-butylene glycol.

これら遊離脂肪酸、塩、またはエステルの化粧料中にお
ける配合量は、0.1〜lO重量%であるのが好ましい
。かかる配合量が、0.1重量%未満であると、色素沈
着の抑制効果がなく、一方、10重量%を越えると、刺
激性が強い。
The amount of these free fatty acids, salts, or esters in cosmetics is preferably 0.1 to 10% by weight. If the amount is less than 0.1% by weight, there will be no effect of suppressing pigmentation, while if it exceeds 10% by weight, it will be highly irritating.

つぎに各種活性成分についてその色素沈着抑制作用を評
価した結果を示す。
Next, the results of evaluating the pigmentation suppressing effects of various active ingredients are shown.

試験方法: English系茶色モルモットの背部を刺毛し、紫外
線(UV8強度:IJ/cmりを照射した。
Test method: The back of an English brown guinea pig was pricked with hair and irradiated with ultraviolet light (UV8 intensity: IJ/cm).

この操作を3日間繰り返し、その間リノール酸をはじめ
とする脂肪酸、あるいは他の成分を1(w/V)%でエ
タノールに溶解した検体を紫外線照射部位に塗布した。
This operation was repeated for 3 days, during which time a sample prepared by dissolving fatty acids such as linoleic acid or other components in ethanol at 1 (w/v)% was applied to the ultraviolet irradiated area.

10日間放置後、以下に示す判定基準に従い、色素沈着
度を肉眼判定した。
After standing for 10 days, the degree of pigmentation was visually judged according to the criteria shown below.

判定基準ニ ー  色素沈着なし ±  わずかな色素沈着 土  中等度の色素沈着 +十  強度の色素沈着 結果を次の第1表に示す。Judgment criteria d - No pigmentation ± Slight pigmentation Soil, moderate pigmentation +10 Intense pigmentation The results are shown in Table 1 below.

第1表 エタノール                  ++
リノール酸        1       −リノー
ル酸ナトリウム塩  l         −リノール
酸メチル     l        −リノール酸エ
チル     1       −リノール酸イソプロ
ピル  l        −γ−リルン酸     
 1        −α−リルン酸      1 
      −アラキドン酸        l   
      −パルミチン酸       1    
     ++ステアリン酸       1    
     ++オレイン酸         1   
      ++リノール酸トリグリセリド l   
     +リルン酸トリグリセリド 1      
   +サフラワー油       1       
  ++アマニ油         1       
 ++ビタミンC!         ++ 胎盤エキス        l         ++
リノール酸        0.01       +
+リノール酸        0.1        
±リノール酸        1       −リノ
ール酸       10        −第1表よ
り明らかなごとく、炭素数!8〜22かつ分子構造中の
不飽和数が2以上の遊離脂肪酸、その塩あるいはアルキ
ルエステルを配合した場合は、色素沈着の抑制作用が認
められるが、同様の炭素数を存していても飽和脂肪酸で
はかかる作用はない。
Table 1 Ethanol ++
Linoleic acid 1 -Linoleic acid sodium salt l -Methyl linoleate l -Ethyl linoleate 1 -Isopropyl linoleate l -γ-Lilunic acid
1 -α-lylunic acid 1
-Arachidonic acid l
-Palmitic acid 1
++Stearic acid 1
++Oleic acid 1
++Linoleic acid triglyceride l
+Ryrunic acid triglyceride 1
+Safflower oil 1
++ Linseed oil 1
++ Vitamin C! ++ Placenta extract l ++
Linoleic acid 0.01 +
+linoleic acid 0.1
±Linoleic acid 1 -Linoleic acid 10 -As is clear from Table 1, the number of carbons! When a free fatty acid, its salt, or alkyl ester with a molecular structure of 8 to 22 and 2 or more unsaturations is blended, an inhibitory effect on pigmentation is observed. Fatty acids have no such effect.

本発明の美白化粧料は、公知の方法により、化粧水、化
粧用油、クリーム、乳液、パック、パウダーなどの形態
に製造される。
The whitening cosmetic of the present invention is manufactured in the form of lotion, cosmetic oil, cream, milky lotion, pack, powder, etc. by a known method.

さらに本発明の化粧料には、その種類に応じ性能を損な
わない範囲において、適宜公知の成分を配合することが
できる。
Further, the cosmetic composition of the present invention may contain any known ingredients as appropriate, depending on the type thereof, within a range that does not impair performance.

なお、従来から使用されているメラニン産生抑制剤(ビ
タミンC1胎盤抽出物)、紫外線吸収剤、紫外線散乱剤
、抗炎症剤、抗酸化剤などを配合しても良い。
Note that conventionally used melanin production inhibitors (vitamin C1 placenta extract), ultraviolet absorbers, ultraviolet scattering agents, anti-inflammatory agents, antioxidants, and the like may be added.

寒胤鳳 つぎに本発明を実施例によりさらに具体的に説明する。Kantaneho Next, the present invention will be explained in more detail with reference to Examples.

実施例1(化粧水) 成 分             配合!(重量%)リ
ノール酸             0゜5グリセリン
            6.0エタノール     
         8.0ポリオキシエチレン硬化ヒマ
シ油   0.8パラオキシ安息香酸メチル     
 0.05クエン酸                
0.05クエン酸ナトリウム          0.
07香料                0.1水溶
性プラセンタエキス       2.0精製水   
            残部精製水にグリセリン、ク
エン酸、クエン酸ナトリウム、水溶性プラセンタエキス
を溶解する。別個にエタノールにリノール酸、ポリオキ
シエチレン硬化ヒマシ油(60E、O,)、メチルパラ
ベン、香料を溶解し、前記の精製水溶液に加えて可溶化
し、ろ過して化粧水を得た。
Example 1 (Lotion) Ingredients Formula! (Weight%) Linoleic acid 0゜5 Glycerin 6.0 Ethanol
8.0 Polyoxyethylene hydrogenated castor oil 0.8 Methyl paraoxybenzoate
0.05 citric acid
0.05 Sodium citrate 0.
07 Fragrance 0.1 Water-soluble placenta extract 2.0 Purified water
Dissolve glycerin, citric acid, sodium citrate, and water-soluble placenta extract in the remaining purified water. Separately, linoleic acid, polyoxyethylene hydrogenated castor oil (60E, O,), methylparaben, and fragrance were dissolved in ethanol, added to the purified aqueous solution, solubilized, and filtered to obtain a lotion.

実施例2(化粧用油) 成  分              配合量(重量%
)リノール酸エチル           1.0パル
ミチン酸アスコルビル       0.2酢酸レチノ
ール            0,3ステアリン酸コレ
ステリル       1.0オリーブ油      
         2.0スクワラン        
      残部スクワランに他の成分を均一に溶解し
て化粧用油を得た。
Example 2 (cosmetic oil) Ingredients Amount (wt%)
) Ethyl linoleate 1.0 Ascorbyl palmitate 0.2 Retinol acetate 0.3 Cholesteryl stearate 1.0 Olive oil
2.0 squalane
A cosmetic oil was obtained by uniformly dissolving other ingredients in the remaining squalane.

実施例3(クリーム) 成  分             配合量(重量%)
成分(A) γ−リルン酸             2.0ステア
リン酸アスコルビル       1.0酢酸dJ2−
α−トコフェロール     0.2サラシミツロウ 
           4.0セタノール      
         2.0ステアリン酸       
      1.0ミリスチン酸イソプロピル    
   5.0ラノリン               
2.0流動パラフイン            9.0
自己乳化型モノステアリン酸グリセリル 3.0モノス
テアリン酸 ポリオキシエチレンソルビタン(20E、O,) 1.
5バラオキシ安息香酸プロピル      0.1成分
(B) パラオキシ安息香酸メチル       0.2プロピ
レングリコール         5.0香料    
             0,2成分(A)を加熱溶
解し、80℃に保持する。
Example 3 (cream) Ingredients Amount (wt%)
Component (A) γ-Lilunic acid 2.0 Ascorbyl stearate 1.0 Acetic acid dJ2-
α-tocopherol 0.2 white beeswax
4.0 cetanol
2.0 stearic acid
1.0 Isopropyl myristate
5.0 lanolin
2.0 Liquid paraffin 9.0
Self-emulsifying glyceryl monostearate 3.0 Polyoxyethylene sorbitan monostearate (20E, O,) 1.
5 Propyl paraoxybenzoate 0.1 Ingredient (B) Methyl paraoxybenzoate 0.2 Propylene glycol 5.0 Fragrance
0.2 component (A) is heated and dissolved and maintained at 80°C.

別に香料を除く成分(B)を加熱溶解して80℃に保ち
、これに前記成分(A)を撹拌しながら加え、充分混合
する。さらに撹拌しながら冷却を行い、香料を加え、さ
らに冷却してクリームを得た。
Separately, component (B) excluding perfume is dissolved by heating and maintained at 80° C., and component (A) is added to this with stirring and mixed thoroughly. The mixture was further cooled while stirring, a flavoring agent was added, and the mixture was further cooled to obtain a cream.

実施例4(乳液) 成分(A) リノール酸イソプロピル      2.0グリチルレ
チン酸ステアリル    0,1流動パラフイン   
       5.0ワセリン           
   2,0ミツロウ              1
.0セスキオレイン酸ソルビタン    2,0成分工
旦Σ パラオキシ安息香酸エチル     0.2プロピレン
グリコール       5.0カルボキシビニルポリ
マー     0.5水酸化カリウム        
  0.5香料               0.2
精製氷               残部成分(A)
を80℃にて加熱溶解し、別に加温(80℃)溶解した
香料を除く成分(B)に撹拌しながら加え、充分混合す
る。ついで、撹拌しながら冷却を行い、香料を加え、さ
らに冷却して乳液を得た。
Example 4 (Emulsion) Component (A) Isopropyl linoleate 2.0 Stearyl glycyrrhetinate 0.1 Liquid paraffin
5.0 Vaseline
2,0 beeswax 1
.. 0 Sorbitan sesquioleate 2,0 Ingredients Σ Ethyl paraoxybenzoate 0.2 Propylene glycol 5.0 Carboxyvinyl polymer 0.5 Potassium hydroxide
0.5 fragrance 0.2
Purified ice remaining component (A)
The mixture is heated and dissolved at 80°C, and added to component (B) other than the fragrance, which was separately heated (80°C) and dissolved, with stirring, and thoroughly mixed. Next, the mixture was cooled while stirring, perfume was added, and the mixture was further cooled to obtain a milky lotion.

実施例5(パック) 成  分           配合量(重量%)リノ
ール酸            380水溶性プラセン
タエキス      2.0酢酸ビニル・スチレン共重
合体  10.0ポリビニルアルコール      1
0.0ソルビツト            5.0酸化
チタン            8.0カオリン   
          7・0エタノール       
      5.0香料              
 2.0パラオキシ安息香酸エチル     0.2リ
ノール酸、香料およびエタノールを均一に溶解する。こ
れを酢酸ビニル・スチレン共重合体、ポリビニルアルコ
ニル、ソルビット、酸化チタンお上びカオリンを均一に
混和したものに加える。
Example 5 (Pack) Ingredients Amount (wt%) Linoleic acid 380 Water-soluble placenta extract 2.0 Vinyl acetate-styrene copolymer 10.0 Polyvinyl alcohol 1
0.0 Sorbit 5.0 Titanium oxide 8.0 Kaolin
7.0 ethanol
5.0 fragrance
2.0 Ethyl paraoxybenzoate 0.2 Uniformly dissolve linoleic acid, fragrance and ethanol. This is added to a uniform mixture of vinyl acetate/styrene copolymer, polyvinylalconyl, sorbitol, titanium oxide, and kaolin.

これに、さらに水溶性プラセンタエキス、パラオキシ安
息香酸エチルを精製水に均一に溶解した溶液を加え、均
一に混和しパックを得た。
To this, a solution in which water-soluble placenta extract and ethyl paraoxybenzoate were uniformly dissolved in purified water was added and mixed uniformly to obtain a pack.

実施例6(パウダー) 成  分        配合量(重量%)リノール酸
          2.0デキストリン      
  95.0タルク             2.0
ステアリン酸デカグリセリル  1.0リノール酸およ
びステアリン酸デカグリセリルを加熱溶解し、70℃に
保持し、これをデキストリンおよびタルクの混合物に撹
拌しながら徐々に加えてパウダーを得た。
Example 6 (powder) Ingredients Amount (wt%) Linoleic acid 2.0 Dextrin
95.0 talc 2.0
Decaglyceryl Stearate 1.0 Linoleic acid and decaglyceryl stearate were heated and dissolved, maintained at 70°C, and gradually added to a mixture of dextrin and talc with stirring to obtain a powder.

褒」Δ級果"Reward" Δ class result

Claims (2)

【特許請求の範囲】[Claims] (1)炭素数18〜22かつ分子構造中の不飽和数が2
以上の遊離脂肪酸、その塩、あるいは一価または二価ア
ルコールとのエステルを活性成分として含有する美白化
粧料。
(1) 18 to 22 carbon atoms and 2 unsaturations in the molecular structure
A whitening cosmetic containing the above free fatty acids, their salts, or esters with monohydric or dihydric alcohols as active ingredients.
(2)前記活性成分の配合量が組成物全体に対して0.
1〜10重量%である前記第(1)項の美白化粧料。
(2) The amount of the active ingredient added to the entire composition is 0.
The whitening cosmetic according to item (1) above, which contains 1 to 10% by weight.
JP11968487A 1987-05-15 1987-05-15 Beautifying cosmetic Granted JPS63284109A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11968487A JPS63284109A (en) 1987-05-15 1987-05-15 Beautifying cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11968487A JPS63284109A (en) 1987-05-15 1987-05-15 Beautifying cosmetic

Publications (2)

Publication Number Publication Date
JPS63284109A true JPS63284109A (en) 1988-11-21
JPH0567125B2 JPH0567125B2 (en) 1993-09-24

Family

ID=14767489

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11968487A Granted JPS63284109A (en) 1987-05-15 1987-05-15 Beautifying cosmetic

Country Status (1)

Country Link
JP (1) JPS63284109A (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0345082A2 (en) * 1988-06-02 1989-12-06 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Enzyme formation suppressing agent
EP0345081A2 (en) * 1988-06-02 1989-12-06 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Enzyme formation suppressing agent
EP0355842A2 (en) * 1988-08-26 1990-02-28 Sansho Seiyaku Co., Ltd. External preparation
JPH0320205A (en) * 1989-06-16 1991-01-29 Sunstar Inc Cosmetic
US5262153A (en) * 1989-09-20 1993-11-16 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkujo Skin-whitening agent
FR2765482A1 (en) * 1997-07-07 1999-01-08 Oreal USE OF Y-LINOLENIC ACID TO PREVENT OXIDATIVE STRESS
JP2004091351A (en) * 2002-08-30 2004-03-25 Kose Corp Skin preparation for external use
JP2005272444A (en) * 2004-02-25 2005-10-06 Kose Corp External preparation for skin
JP2006076997A (en) * 2004-08-09 2006-03-23 Kao Corp Liquid deodorant
JP2007063195A (en) * 2005-08-31 2007-03-15 Katakura Chikkarin Co Ltd Bleaching agent and external preparation for skin containing the same
WO2007105706A1 (en) * 2006-03-14 2007-09-20 Kose Corporation Skin-whitening agent for external application to the skin, and method for whitening the skin
JP2009256314A (en) * 2008-03-19 2009-11-05 Kose Corp Skin-lightening agent and external agent for skin
JP2013502380A (en) * 2009-08-17 2013-01-24 ナチュラ コスメティコス ソシエダッド アノニマ Skin refining complex, use of said complex, cosmetic or pharmaceutical composition comprising said complex and method for its application
JP2015523333A (en) * 2012-05-16 2015-08-13 コシードバイオファーム カンパニー リミテッド Cosmetic, pharmaceutical and food composition containing a crushed or extracted fish eyeball
JP2018090516A (en) * 2016-12-01 2018-06-14 日光ケミカルズ株式会社 Inhibitor of melanosome uptake into epidermal cells (keratinocytes), and promoter for excreting taken up melanosomes to outside body
CN108348422A (en) * 2015-09-24 2018-07-31 Elc 管理有限责任公司 Method and composition for handling skin

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60181006A (en) * 1984-02-27 1985-09-14 Kanebo Ltd Skin cosmetic
JPS61176510A (en) * 1985-01-31 1986-08-08 Pola Chem Ind Inc Skin-beautifying cosmetic

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60181006A (en) * 1984-02-27 1985-09-14 Kanebo Ltd Skin cosmetic
JPS61176510A (en) * 1985-01-31 1986-08-08 Pola Chem Ind Inc Skin-beautifying cosmetic

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0345082A2 (en) * 1988-06-02 1989-12-06 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Enzyme formation suppressing agent
EP0345081A2 (en) * 1988-06-02 1989-12-06 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Enzyme formation suppressing agent
EP0355842A2 (en) * 1988-08-26 1990-02-28 Sansho Seiyaku Co., Ltd. External preparation
JPH0320205A (en) * 1989-06-16 1991-01-29 Sunstar Inc Cosmetic
US5262153A (en) * 1989-09-20 1993-11-16 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkujo Skin-whitening agent
FR2765482A1 (en) * 1997-07-07 1999-01-08 Oreal USE OF Y-LINOLENIC ACID TO PREVENT OXIDATIVE STRESS
EP0891773A1 (en) * 1997-07-07 1999-01-20 L'oreal Use of gamma-linolenic acid for preventing oxydative stress
JPH1171260A (en) * 1997-07-07 1999-03-16 L'oreal Sa Oxidation stress preventing agent comprising gamma-linolenic acid
JP2004091351A (en) * 2002-08-30 2004-03-25 Kose Corp Skin preparation for external use
JP2005272444A (en) * 2004-02-25 2005-10-06 Kose Corp External preparation for skin
JP2006076997A (en) * 2004-08-09 2006-03-23 Kao Corp Liquid deodorant
JP2007063195A (en) * 2005-08-31 2007-03-15 Katakura Chikkarin Co Ltd Bleaching agent and external preparation for skin containing the same
WO2007105706A1 (en) * 2006-03-14 2007-09-20 Kose Corporation Skin-whitening agent for external application to the skin, and method for whitening the skin
JP5399701B2 (en) * 2006-03-14 2014-01-29 株式会社コーセー Whitening skin external preparation and skin whitening method
JP2009256314A (en) * 2008-03-19 2009-11-05 Kose Corp Skin-lightening agent and external agent for skin
JP2013502380A (en) * 2009-08-17 2013-01-24 ナチュラ コスメティコス ソシエダッド アノニマ Skin refining complex, use of said complex, cosmetic or pharmaceutical composition comprising said complex and method for its application
JP2015523333A (en) * 2012-05-16 2015-08-13 コシードバイオファーム カンパニー リミテッド Cosmetic, pharmaceutical and food composition containing a crushed or extracted fish eyeball
CN108348422A (en) * 2015-09-24 2018-07-31 Elc 管理有限责任公司 Method and composition for handling skin
EP3352729A4 (en) * 2015-09-24 2019-06-19 ELC Management LLC Method and compositions for treating skin
CN108348422B (en) * 2015-09-24 2022-06-21 Elc 管理有限责任公司 Methods and compositions for treating skin
JP2018090516A (en) * 2016-12-01 2018-06-14 日光ケミカルズ株式会社 Inhibitor of melanosome uptake into epidermal cells (keratinocytes), and promoter for excreting taken up melanosomes to outside body

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