JPH10236941A - Skin lotion - Google Patents

Skin lotion

Info

Publication number
JPH10236941A
JPH10236941A JP9054190A JP5419097A JPH10236941A JP H10236941 A JPH10236941 A JP H10236941A JP 9054190 A JP9054190 A JP 9054190A JP 5419097 A JP5419097 A JP 5419097A JP H10236941 A JPH10236941 A JP H10236941A
Authority
JP
Japan
Prior art keywords
skin
extract
pearl
pinctada
ether
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.)
Pending
Application number
JP9054190A
Other languages
Japanese (ja)
Inventor
Hitoshi Masaki
仁 正木
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.)
Noevir Co Ltd
Original Assignee
Noevir 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 Noevir Co Ltd filed Critical Noevir Co Ltd
Priority to JP9054190A priority Critical patent/JPH10236941A/en
Publication of JPH10236941A publication Critical patent/JPH10236941A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a skin lotion that normalizes redox regulatory system in an organism, activates the intracellular peroxide deletion system and can effectively prevent skin disturbance and aging caused by oxidation stress due to ultraviolet rays and metabolism in vivo and can improve them. SOLUTION: This skin lotion contains extract from flesh of pearl shells such as Pinctada martensii, Pinctada margaritifera, Pinctada maxima, Hyriopsis schlegeli. As an extracting solvent, may be used a polar organic solvent, in addition to water, as a lower alcohol, for example, methanol, ethanol, propanol, isopropanol, as a polyhydric alcohol, for example, 1,3-butylene glycol, propylene glycol, dipropylene glycol, glycerol and the like, as an ether, for example, ethyl ether or propyl ether, as an ester, for example, ethyl acetate or butyl acetate, acetone or ethyl methyl ketone, or their mixture, physiological salt solution or phosphate buffer solution. The content of the extract is about 0.01-5.0wt.% in the skin preparation.

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、細胞内過酸化物消
去系を活性化し、紫外線や生体内代謝等に起因する酸化
ストレスによる皮膚の炎症や、しわ,しみの発生といっ
た皮膚老化症状の進展などの障害を防止或いは改善し得
る皮膚外用剤に関する。さらに詳しくは、真珠貝貝肉抽
出物を含有して成る皮膚外用剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention activates an intracellular peroxide scavenging system and promotes skin aging symptoms such as skin inflammation, wrinkles and spots caused by oxidative stress caused by ultraviolet rays and metabolism in the body. And a skin external preparation capable of preventing or improving such disorders. More specifically, the present invention relates to an external preparation for skin comprising a pearl shellfish meat extract.

【0002】[0002]

【従来の技術】紫外線,放射線,重金属等の外来刺激及
び生体内代謝により生じる活性酸素種は、動物の生体内
において様々な反応を惹き起こすが、皮膚組織において
も、これらの損傷や老化に深く関与することが知られて
いる。特に、紫外線等により活性酸素種のうち過酸化水
素が細胞内に蓄積されることが報告されている。この過
酸化水素から、皮膚組織内に微量存在する鉄イオンや銅
イオンによりフェントン反応が触媒され、最も組織傷害
性の高いヒドロキシラジカルが生成するといわれてい
る。
2. Description of the Related Art Reactive oxygen species generated by extraneous stimuli such as ultraviolet rays, radiation, heavy metals, and metabolism in a living body cause various reactions in the living body of an animal. It is known to be involved. In particular, it has been reported that hydrogen peroxide among reactive oxygen species is accumulated in cells due to ultraviolet rays or the like. It is said that the Fenton reaction is catalyzed from the hydrogen peroxide by iron ions or copper ions present in trace amounts in skin tissue, and a hydroxyl radical having the highest tissue damage is generated.

【0003】そこで近年、ヒドロキシラジカルをはじめ
とする活性酸素種に対して消去作用を有する物質のスク
リーニングが行われ、ビタミンE群化合物や茶タンニン
をはじめとする植物由来成分を皮膚外用剤に配合する試
みがなされてきた。また、ヒドロキシラジカルの生成を
阻害するべくキレート剤の配合も行われている。さらに
は、ヒドロキシラジカルの生成前駆体となる過酸化水素
を消去する物質が検索され、ボタン抽出物が知られてい
る(特願平7−191060)。
In recent years, substances having a scavenging effect on active oxygen species such as hydroxy radicals have been screened, and plant-derived components such as vitamin E group compounds and tea tannin are incorporated into an external preparation for skin. Attempts have been made. In addition, chelating agents have been added to inhibit the generation of hydroxy radicals. Furthermore, a substance that eliminates hydrogen peroxide, which is a precursor for the production of hydroxyl radicals, has been searched, and a button extract has been known (Japanese Patent Application No. 7-191060).

【0004】しかしながら、過酸化水素,ヒドロキシラ
ジカル等の活性酸素種は、連鎖的な酸化反応に関与し、
これらを個別に消去したとしても、生体内の一連の過酸
化反応を防止するには不十分である。一方、生体内には
チオレドキシンやグルタチオン等の関与するレドックス
制御機構が存在し、生体内の酸化還元状態を一定に保つ
働きをしている。
[0004] However, active oxygen species such as hydrogen peroxide and hydroxy radical are involved in a chain oxidation reaction,
Even if these are individually erased, they are not enough to prevent a series of peroxidation reactions in a living body. On the other hand, a redox control mechanism involving thioredoxin, glutathione, or the like exists in the living body, and functions to keep the oxidation-reduction state in the living body constant.

【0005】[0005]

【発明が解決しようとする課題】そこで本発明において
は、生体内のレドックス制御系を正常化し、生体の有す
る細胞内過酸化物消去系を活性化することにより、紫外
線や生体内代謝により生じる酸化ストレスに起因する皮
膚の傷害や老化を有効に防止し、改善し得る皮膚外用剤
を得ることを目的とした。
Therefore, in the present invention, the normalization of the redox control system in the living body and the activation of the intracellular peroxide scavenging system in the living body allow the oxidation caused by ultraviolet rays and metabolism in the living body to occur. An object of the present invention is to provide a skin external preparation that can effectively prevent and improve skin injuries and aging caused by stress.

【0006】[0006]

【課題を解決するための手段】上記の課題を解決するた
め、本発明者は過酸化水素による細胞傷害に対する防御
作用を指標として、生体の細胞内過酸化物消去系活性化
作用を有する物質のスクリーニングを行った。その結
果、真珠貝貝肉の抽出物に高い細胞内過酸化物消去系活
性化効果を見いだし、これを皮膚外用剤に含有させるこ
とにより本発明を完成するに至った。
Means for Solving the Problems To solve the above problems, the present inventor has determined that a substance having an activity of activating an intracellular peroxide scavenging system in a living body is used as an index of a protective action against cell injury caused by hydrogen peroxide. Screening was performed. As a result, a high intracellular peroxide scavenging activating effect was found in the pearl clam shell meat extract, and the present invention was completed by including this in a skin external preparation.

【0007】すなわち本発明は、皮膚外用剤基剤に真珠
貝貝肉より抽出して得た抽出物を含有させて成る。
That is, the present invention comprises a skin external preparation base containing an extract obtained from pearl shellfish meat.

【0008】[0008]

【作用】本発明において有効成分として含有させる真珠
貝貝肉抽出物について、過酸化水素による細胞傷害に対
する防御作用を以下に示す。
The protective effect of the pearl mussel shell meat extract contained as an active ingredient in the present invention against cell damage by hydrogen peroxide is shown below.

【0009】ヒト由来線維芽細胞を、1ウェル当たり
2.0×104個となるように96穴マイクロプレート
に播種し、24時間後に真珠貝貝肉の水抽出物をそれぞ
れ0,0.125,0.25,0.5及び1mg/ml
含有し、さらに1mMの過酸化水素1μlを添加したH
anks液を細胞に接触させ、37℃で2時間培養し
た。次いでニュートラルレッドを20μg/ml含有す
る培地に交換して37℃で2時間培養し、細胞に取り込
まれたニュートラルレッドを抽出して550nmにおけ
る吸光度(A1)を測定した。一方、真珠貝貝肉の水抽
出物のみを添加し、過酸化水素を添加しないで同様の処
理を行った場合の550nmにおける吸光度(A0)を
も測定した。真珠貝貝肉の水抽出物各添加濃度における
細胞の生存率は(1)式により求めた。細胞生存率の測
定は各添加濃度について6回ずつ行い、平均値を表1に
示した。
[0009] Human-derived fibroblasts are seeded in a 96-well microplate at 2.0 × 10 4 cells / well, and after 24 hours, an aqueous extract of pearl mussel is added to each of 0.1 and 0.125. , 0.25, 0.5 and 1 mg / ml
H containing 1 mM of 1 mM hydrogen peroxide
Anks solution was brought into contact with the cells and cultured at 37 ° C. for 2 hours. Next, the medium was replaced with a medium containing 20 μg / ml of neutral red and cultured at 37 ° C. for 2 hours. Neutral red incorporated in the cells was extracted and the absorbance at 550 nm (A 1 ) was measured. On the other hand, the absorbance (A 0 ) at 550 nm when only the water extract of the pearl mussel was added and the same treatment was carried out without adding hydrogen peroxide was also measured. The survival rate of the cells at each concentration of the water extract of the pearl mussel was determined by the formula (1). The cell viability was measured six times for each addition concentration, and the average value is shown in Table 1.

【数1】 (Equation 1)

【0010】[0010]

【表1】 表1より明らかなように、真珠貝貝肉の水抽出物を0.
125mg/ml以上添加した場合には有意な細胞生存
率の上昇が認められ、良好な細胞内過酸化物消去系活性
化作用を有することが示された。
[Table 1] As is evident from Table 1, the water extract of the pearl mussel was added to 0.1%.
When 125 mg / ml or more was added, a significant increase in cell viability was observed, indicating that the compound had a favorable intracellular peroxide scavenging system activating action.

【0011】[0011]

【発明の実施の形態】本発明において有効成分として皮
膚外用剤に含有させる真珠貝貝肉抽出物は、天然真珠の
採取や養殖真珠の養成に用いられるアコヤガイ,クロチ
ョウガイ,シロチョウガイ,イケチョウガイ等の貝肉よ
り、水の他、メタノール,エタノール,プロパノール,
イソプロパノール等の低級アルコール、1,3-ブチレング
リコール,プロピレングリコール,ジプロピレングリコ
ール,グリセリン等の多価アルコール、エチルエーテ
ル,プロピルエーテル等のエーテル類、酢酸エチル,酢
酸ブチル等のエステル類、アセトン,エチルメチルケト
ン等の極性有機溶媒、或いはこれらの混合物により抽出
して得られる。抽出溶媒としては、前記の他生理食塩水
やリン酸緩衝液等を用いてもよい。
BEST MODE FOR CARRYING OUT THE INVENTION The pearl shellfish meat extract contained in an external preparation for skin as an active ingredient in the present invention is used for collecting natural pearls and for cultivating cultured pearls such as pearl oysters, black mussels, white mussels, and mussels. Than meat, water, methanol, ethanol, propanol,
Lower alcohols such as isopropanol; polyhydric alcohols such as 1,3-butylene glycol, propylene glycol, dipropylene glycol and glycerin; ethers such as ethyl ether and propyl ether; esters such as ethyl acetate and butyl acetate; acetone and ethyl It is obtained by extraction with a polar organic solvent such as methyl ketone or a mixture thereof. As the extraction solvent, other than the above, physiological saline, phosphate buffer and the like may be used.

【0012】貝肉からの抽出には、貝肉をそのまま用い
てもよいが、細切,ホモジナイズ,乾燥,粉砕等の処理
を行った後に抽出を行うことが、抽出効率の点で好まし
い。抽出温度は0℃〜50℃程度が適切である。
For the extraction from the shell meat, the shell meat may be used as it is, but it is preferable to perform the extraction after processing such as shredding, homogenizing, drying, and pulverizing from the viewpoint of extraction efficiency. The extraction temperature is suitably about 0 ° C to 50 ° C.

【0013】さらに本発明に係る皮膚外用剤には、他の
活性酸素消去剤,抗炎症剤,美白剤,皮膚細胞賦活剤,
殺菌剤の他、油類,界面活性剤,保湿剤,紫外線吸収
剤,粉体,香料,防腐剤等、一般的な外用剤及び化粧料
原料をも含有させることができる。
The external preparation for skin according to the present invention further comprises other active oxygen scavengers, anti-inflammatory agents, whitening agents, skin cell activators,
In addition to the bactericide, general external preparations such as oils, surfactants, humectants, ultraviolet absorbers, powders, fragrances, preservatives, and raw materials for cosmetics can be contained.

【0014】本発明に係る皮膚外用剤は、ローション
剤,乳剤,ゲル剤,クリーム剤,軟膏等の剤型で提供す
ることができ、さらに化粧水,乳液,クリーム,パック
等の皮膚化粧料、メイクアップベースローション,メイ
クアップベースクリーム,液状又はクリーム状或いは軟
膏型のファンデーション,アイカラー,チークカラーと
いったメイクアップ化粧料、ハンドクリーム,レッグク
リーム,ボディローション等の身体用化粧料などとして
も提供することができる。皮膚外用剤中の真珠貝貝肉抽
出物の含有量としては、外用剤基剤中でのバイオアベイ
ラビリティ等を考慮して、0.01〜5.0重量%程度
が適当である。
The external preparation for skin according to the present invention can be provided in the form of lotions, emulsions, gels, creams, ointments and the like, and skin cosmetics such as lotions, emulsions, creams, packs and the like. Also provided as makeup base lotion, makeup base cream, liquid or creamy or ointment type foundation, makeup cosmetics such as eye color, cheek color, body cosmetics such as hand cream, leg cream, body lotion, etc. be able to. The content of the pearl shellfish extract in the external preparation for skin is suitably about 0.01 to 5.0% by weight in consideration of bioavailability in the external preparation base.

【0015】[0015]

【実施例】さらに本発明の特徴について、実施例により
詳細に説明する。まず、本発明において有効成分として
含有させる真珠貝貝肉抽出物の製造例について示す。
EXAMPLES Further, the features of the present invention will be described in detail with reference to examples. First, a production example of a pearl clam shell meat extract to be contained as an active ingredient in the present invention will be described.

【0016】[製造例1] アコヤガイ貝肉抽出物1 アコヤガイ貝肉1kgを10℃にて精製水2.0l中で
ホモジネートし、24時間攪拌抽出した後、ろ過してろ
液を回収した。
[Preparation Example 1] Pearl oyster shellfish extract 1 1 kg of pearl oyster shell meat was homogenized in 2.0 l of purified water at 10 ° C, extracted with stirring for 24 hours, and filtered to collect a filtrate.

【0017】[製造例2] アコヤガイ貝肉抽出物2 アコヤガイ貝肉1kgを10℃にて生理食塩水2.0l
中でホモジネートし、24時間攪拌抽出した後、ろ過し
てろ液を回収した。
[Preparation Example 2] Pearl oyster shell meat extract 2 1 kg of pearl oyster shell meat was extracted at 10 ° C. with 2.0 L of physiological saline.
The mixture was homogenized in water, extracted with stirring for 24 hours, and then filtered to collect the filtrate.

【0018】[製造例3] アコヤガイ貝肉抽出物3 アコヤガイ貝肉1kgを15℃にて0.05Mリン酸緩
衝液(pH7.0)2.0l中でホモジネートし、24
時間攪拌抽出した後、ろ過してろ液を回収した。
[Preparation Example 3] Pearl oyster shellfish extract 3 1 kg of pearl oyster shell meat was homogenized in 2.0 l of 0.05M phosphate buffer (pH 7.0) at 15 ° C.
After stirring and extracting for a time, the filtrate was collected by filtration.

【0019】[製造例4] クロチョウガイ貝肉抽出物 クロチョウガイ貝肉1kgを細切後、20℃にて50容
量%エタノール水溶液2.0l中に浸漬し、5日間静置
した後上清を回収した。
[Preparation Example 4] Black mussel shell meat extract 1 kg of black mussel shell meat was cut into small pieces, immersed in 2.0 liters of a 50% by volume aqueous ethanol solution at 20 ° C., allowed to stand for 5 days, and the supernatant was recovered. .

【0020】[製造例5] シロチョウガイ貝肉抽出物 シロチョウガイ貝肉1kgを細切後、20℃にて50容
量%1,3-ブチレングリコール水溶液2.0l中に浸漬
し、5日間静置した後上清を回収した。
[Production Example 5] White mussels shellfish extract 1 kg of white mussels were cut into small pieces, immersed in 2.0 l of a 50% by volume aqueous 1,3-butylene glycol solution at 20 ° C., and allowed to stand for 5 days After that, the supernatant was recovered.

【0021】[製造例6] イケチョウガイ貝肉抽出物 イケチョウガイ貝肉1kgを15℃にてグリセリン,ジ
プロピレングリコール,イソプロパノール混合溶媒(容
量比=2:2:1)1.5l中でホモジネートし、48
時間攪拌抽出した後ろ過して、ろ液を回収した。
[Preparation Example 6] Extract of mussel shellfish extract 1 kg of mussel shellfish was homogenized in 1.5 liter of a mixed solvent of glycerin, dipropylene glycol and isopropanol (volume ratio = 2: 2: 1) at 15 ° C., and 48
After extraction with stirring for a period of time, the mixture was filtered to recover the filtrate.

【0022】続いて本発明に係る皮膚外用剤の処方を示
す。なお以下の実施例においては、真珠貝貝肉抽出物と
して上記製造例のものを用いた。
Next, the formulation of the external preparation for skin according to the present invention will be described. In the following examples, the pearl mussel extract of the above-mentioned production example was used.

【0023】 [実施例1] 皮膚用ローション剤 (1)エタノール 10.0(重量%) (2)ヒドロキシエチルセルロース 1.0 (3)アコヤガイ貝肉抽出物1 0.5 (4)パラオキシ安息香酸メチル 0.1 (5)精製水 88.4 製法:(1)〜(5)を混合し均一とする。[Example 1] Lotion for skin (1) Ethanol 10.0 (wt%) (2) Hydroxyethylcellulose 1.0 (3) Pearl oyster shell meat extract 10.5 (4) Methyl paraoxybenzoate 0.1 (5) Purified water 88.4 Production method: (1) to (5) are mixed and made uniform.

【0024】 [実施例2] 皮膚用乳剤 (1)ステアリン酸 0.2(重量%) (2)セタノール 1.5 (3)ワセリン 3.0 (4)流動パラフィン 7.0 (5)ポリオキシエチレン(10E.O.)モノオレイン酸 1.5 エステル (6)酢酸トコフェロール 5.0 (7)グリセリン 5.0 (8)パラオキシ安息香酸メチル 0.1 (9)トリエタノールアミン 1.0 (10)精製水 74.7 (11)アコヤガイ貝肉抽出物2 1.0 製法:(1)〜(6)の油相成分を混合,加熱して均一に溶解
し、70℃に保つ。一方、(7)〜(10)の水相成分を混
合,加熱して均一とし、70℃とする。この水相成分に
前記油相成分を攪拌しながら徐々に添加して乳化し、冷
却した後40℃にて(11)を添加,混合する。
Example 2 Emulsion for skin (1) Stearic acid 0.2 (% by weight) (2) Cetanol 1.5 (3) Vaseline 3.0 (4) Liquid paraffin 7.0 (5) Polyoxy Ethylene (10E.O.) monooleic acid 1.5 ester (6) Tocopherol acetate 5.0 (7) Glycerin 5.0 (8) Methyl parahydroxybenzoate 0.1 (9) Triethanolamine 1.0 (10 ) Purified water 74.7 (11) Pearl oyster shell meat extract 21.0 Production method: The oil phase components of (1) to (6) are mixed, heated and uniformly dissolved, and kept at 70 ° C. On the other hand, the aqueous phase components (7) to (10) are mixed and heated to be uniform, and the temperature is set to 70 ° C. The oil phase component is gradually added to the aqueous phase component while stirring to emulsify, and after cooling, (11) is added and mixed at 40 ° C.

【0025】 [実施例3] 皮膚用ゲル剤 (1)ジプロピレングリコール 10.0(重量%) (2)カルボキシビニルポリマー 0.5 (3)水酸化カリウム 0.1 (4)パラオキシ安息香酸メチル 0.1 (5)精製水 87.8 (6)アコヤガイ貝肉抽出物3 1.5 製法:(5)に(2)を均一に溶解した後、(1)に(4)を溶解し
て添加し、次いで(3)を加えて増粘させ、(6)を添加す
る。
Example 3 Skin Gel (1) Dipropylene glycol 10.0 (% by weight) (2) Carboxyvinyl polymer 0.5 (3) Potassium hydroxide 0.1 (4) Methyl paraoxybenzoate 0.1 (5) Purified water 87.8 (6) Pearl oyster shell meat extract 3 1.5 Production method: After dissolving (2) uniformly in (5), dissolve (4) in (1) Add, then add (3) to thicken and add (6).

【0026】 [実施例4] 皮膚用クリーム (1)ミツロウ 6.0(重量%) (2)セタノール 5.0 (3)還元ラノリン 8.0 (4)スクワラン 27.5 (5)グリセリル脂肪酸エステル 4.0 (6)親油型グリセリルモノステアリン酸エステル 2.0 (7)ポリオキシエチレン(20E.O.)ソルビタン 5.0 モノラウリン酸エステル (8)プロピレングリコール 5.0 (9)パラオキシ安息香酸メチル 0.1 (10)精製水 35.4 (11)アコヤガイ貝肉抽出物1 1.0 (12)クロチョウガイ貝肉抽出物 1.0 製法:(1)〜(7)の油相成分を混合,溶解して75℃に加
熱する。一方、(8)〜(10)の水相成分を混合,溶解して
75℃に加熱する。次いで、上記水相成分に油相成分を
添加して予備乳化した後、ホモミキサーにて均一に乳化
し、冷却後40℃にて(11),(12)を添加,混合する。
Example 4 Skin Cream (1) Beeswax 6.0 (% by weight) (2) Cetanol 5.0 (3) Reduced Lanolin 8.0 (4) Squalane 27.5 (5) Glyceryl fatty acid ester 4.0 (6) Lipophilic glyceryl monostearate 2.0 (7) Polyoxyethylene (20E.O.) sorbitan 5.0 Monolaurate (8) Propylene glycol 5.0 (9) Paraoxybenzoic acid Methyl 0.1 (10) Purified water 35.4 (11) Pearl oyster shell meat extract 1 1.0 (12) Black mussel shell meat extract 1.0 Manufacturing method: Mix oil phase components of (1) to (7) Dissolve and heat to 75 ° C. On the other hand, the aqueous phase components (8) to (10) are mixed and dissolved, and heated to 75 ° C. Next, the oil phase component is added to the water phase component and pre-emulsified, then uniformly emulsified by a homomixer, and after cooling, (11) and (12) are added and mixed at 40 ° C.

【0027】 [実施例5] 水中油型乳剤性軟膏 (1)白色ワセリン 25.0(重量%) (2)ステアリルアルコール 25.0 (3)グリセリン 12.0 (4)ラウリル硫酸ナトリウム 1.0 (5)パラオキシ安息香酸メチル 0.1 (6)精製水 35.4 (7)アコヤガイ貝肉抽出物2 0.5 (8)シロチョウガイ貝肉抽出物 0.5 (9)イケチョウガイ貝肉抽出物 0.5 製法:(1)〜(4)の油相成分を混合,溶解して均一とし、
75℃に加熱する。一方、(5)を(6)に溶解して75℃に
加熱し、これに前記油相成分を添加して乳化し、冷却後
40℃にて(7)〜(9)を添加,混合する。
Example 5 Oil-in-water emulsion ointment (1) White petrolatum 25.0 (% by weight) (2) Stearyl alcohol 25.0 (3) Glycerin 12.0 (4) Sodium lauryl sulfate 1.0 (5) Methyl paraoxybenzoate 0.1 (6) Purified water 35.4 (7) Pearl oyster shell meat extract 2 0.5 (8) White pearl mussel shell meat extract 0.5 (9) Ikecho mussel shell meat extract 0.5 Production method: Mix and dissolve the oil phase components (1) to (4)
Heat to 75 ° C. On the other hand, dissolve (5) in (6), heat to 75 ° C, add the oil phase component to this, emulsify, and after cooling, add (7) to (9) at 40 ° C and mix. .

【0028】 [実施例6] 化粧水 (1)エタノール 10.00(重量%) (2)1,3-ブチレングリコール 5.00 (3)クロチョウガイ貝肉抽出物 0.01 (4)シロチョウガイ貝肉抽出物 0.01 (5)香料 0.10 (6)精製水 84.88 製法:(1)〜(5)を順次(6)に添加して均一に混合,溶解
する。
Example 6 Lotion (1) Ethanol 10.00 (% by weight) (2) 1,3-butylene glycol 5.00 (3) Black mussel shellfish extract 0.01 (4) White mussel Meat extract 0.01 (5) Fragrance 0.10 (6) Purified water 84.88 Production method: (1) to (5) are sequentially added to (6) and uniformly mixed and dissolved.

【0029】 [実施例7] エモリエントクリーム(油中水型) (1)流動パラフィン 30.00(重量%) (2)マイクロクリスタリンワックス 2.00 (3)ワセリン 5.00 (4)ジグリセリルジオレイン酸エステル 5.00 (5)L-グルタミン酸ナトリウム 1.60 (6)L-セリン 0.40 (7)プロピレングリコール 3.00 (8)パラオキシ安息香酸メチル 0.10 (9)精製水 52.75 (10)香料 0.10 (11)シロチョウガイ貝肉抽出物 0.05 製法:(5),(6)を(9)の一部に溶解して50℃とし、5
0℃に加熱した(4)に攪拌しながら徐々に添加する。こ
れをあらかじめ混合し70℃に加熱溶解した(1)〜(3)に
均一に分散し、これに(7),(8)を(9)の残部に溶解して
70℃に加熱したものを攪拌しながら添加し、ホモミキ
サーにて乳化する。冷却後、40℃にて(10),(11)を添
加,混合する。
[Example 7] Emollient cream (water-in-oil type) (1) Liquid paraffin 30.00 (% by weight) (2) Microcrystalline wax 2.00 (3) Vaseline 5.00 (4) Diglyceryl geo Leic acid ester 5.00 (5) Sodium L-glutamate 1.60 (6) L-serine 0.40 (7) Propylene glycol 3.00 (8) Methyl parahydroxybenzoate 0.10 (9) Purified water 52. 75 (10) Fragrance 0.10 (11) White mussel shellfish extract 0.05 Manufacturing method: (5) and (6) are dissolved in a part of (9) to 50 ° C and 5 ° C.
Add slowly to (4) heated to 0 ° C. with stirring. This was previously mixed and uniformly dispersed in (1) to (3), which were heated and dissolved at 70 ° C., and (7) and (8) were dissolved in the remainder of (9) and heated to 70 ° C. Add while stirring and emulsify with a homomixer. After cooling, (10) and (11) are added and mixed at 40 ° C.

【0030】 [実施例8] メイクアップベースクリーム (1)ステアリン酸 12.00(重量%) (2)セタノール 2.00 (3)グリセリルトリ2-エチルヘキサン酸エステル 2.50 (4)自己乳化型グリセリルモノステアリン酸エステル 2.00 (5)プロピレングリコール 10.00 (6)水酸化カリウム 0.30 (7)精製水 69.56 (8)酸化チタン 1.00 (9)ベンガラ 0.10 (10)黄酸化鉄 0.40 (11)香料 0.10 (12)アコヤガイ貝肉抽出物1 0.02 (13)クロチョウガイ貝肉抽出物 0.02 製法:(1)〜(4)の油相成分を混合し、75℃に加熱して
均一とする。一方(5)〜(7)の水相成分を混合し、75℃
に加熱,溶解して均一とし、これに(8)〜(10)の顔料を
添加し、ホモミキサーにて均一に分散させる。この水相
成分に前記油相成分を添加し、ホモミキサーにて乳化し
た後冷却し、40℃にて(11)〜(13)を添加,混合する。
Example 8 Makeup Base Cream (1) Stearic acid 12.00 (% by weight) (2) Cetanol 2.00 (3) Glyceryl tri-2-ethylhexanoate 2.50 (4) Self-emulsification Type glyceryl monostearate 2.00 (5) Propylene glycol 10.00 (6) Potassium hydroxide 0.30 (7) Purified water 69.56 (8) Titanium oxide 1.00 (9) Bengala 0.10 ( 10) Yellow iron oxide 0.40 (11) Fragrance 0.10 (12) Pearl oyster shell meat extract 1 0.02 (13) Black mussel shell meat extract 0.02 Production method: Oil phase of (1) to (4) The ingredients are mixed and heated to 75 ° C. to homogeneity. On the other hand, mix the aqueous phase components (5) to (7)
The mixture is heated and dissolved to make the mixture uniform, and the pigments (8) to (10) are added to the mixture and uniformly dispersed by a homomixer. The oil phase component is added to the aqueous phase component, emulsified by a homomixer, cooled, and (11) to (13) are added and mixed at 40 ° C.

【0031】 [実施例9] 乳液状ファンデーション (1)ステアリン酸 2.00(重量%) (2)スクワラン 5.00 (3)ミリスチン酸オクチルドデシル 5.00 (4)セタノール 1.00 (5)デカグリセリルモノイソパルミチン酸エステル 9.00 (6)1,3-ブチレングリコール 6.00 (7)水酸化カリウム 0.10 (8)パラオキシ安息香酸メチル 0.10 (9)精製水 53.52 (10)酸化チタン 9.00 (11)タルク 7.40 (12)ベンガラ 0.50 (13)黄酸化鉄 1.10 (14)黒酸化鉄 0.10 (15)香料 0.15 (16)イケチョウガイ貝肉抽出物 0.03 製法:(1)〜(5)の油相成分を混合し、75℃に加熱して
均一とする。一方(6)〜(9)の水相成分を混合し、75℃
に加熱,溶解して均一とし、これに(10)〜(14)の顔料を
添加し、ホモミキサーにて均一に分散させる。この水相
成分に前記油相成分を添加し、ホモミキサーにて均一に
乳化した後冷却し、40℃にて(15),(16)を添加,混合
する。
Example 9 Emulsion Foundation (1) Stearic acid 2.00 (% by weight) (2) Squalane 5.00 (3) Octyldodecyl myristate 5.00 (4) Cetanol 1.00 (5) Decaglyceryl monoisopalmitate 9.00 (6) 1,3-butylene glycol 6.00 (7) Potassium hydroxide 0.10 (8) Methyl parahydroxybenzoate 0.10 (9) Purified water 53.52 ( 10) Titanium oxide 9.00 (11) Talc 7.40 (12) Bengala 0.50 (13) Yellow iron oxide 1.10 (14) Black iron oxide 0.10 (15) Fragrance 0.15 (16) Shellfish extract 0.03 Production method: Mix oil phase components (1) to (5) and heat to 75 ° C to make uniform. On the other hand, the aqueous phase components of (6) to (9) were mixed and
The mixture is heated and dissolved to make the mixture uniform, and the pigments (10) to (14) are added to the mixture and uniformly dispersed by a homomixer. The oil phase component is added to the water phase component, and the mixture is uniformly emulsified by a homomixer, then cooled, and (15) and (16) are added and mixed at 40 ° C.

【0032】 [実施例10] ハンドクリーム (1)セタノール 4.0(重量%) (2)ワセリン 2.0 (3)流動パラフィン 10.0 (4)グリセリルモノステアリン酸エステル 1.5 (5)ポリオキシエチレン(60E.O.)グリセリル 2.5 イソステアリン酸エステル (6)酢酸トコフェロール 0.5 (7)グリセリン 20.0 (8)パラオキシ安息香酸メチル 0.1 (9)精製水 59.0 (10)アコヤガイ貝肉抽出物2 0.2 (11)シロチョウガイ貝肉抽出物 0.2 製法:(1)〜(6)の油相成分を混合,溶解して75℃に加
熱する。一方、(7)〜(9)の水相成分を混合,溶解して7
5℃に加熱する。次いで、上記水相成分に油相成分を添
加して予備乳化した後、ホモミキサーにて均一に乳化し
て冷却し、40℃にて(10),(11)を添加,混合する。
Example 10 Hand cream (1) Cetanol 4.0 (% by weight) (2) Vaseline 2.0 (3) Liquid paraffin 10.0 (4) Glyceryl monostearate 1.5 (5) Polyoxyethylene (60E.O.) glyceryl 2.5 isostearate (6) Tocopherol acetate 0.5 (7) Glycerin 20.0 (8) Methyl paraoxybenzoate 0.1 (9) Purified water 59.0 ( 10) Pearl oyster shell meat extract 2 0.2 (11) White pearl oyster shell meat extract 0.2 Production method: Mix and dissolve the oil phase components of (1) to (6) and heat to 75 ° C. On the other hand, the aqueous phase components (7) to (9)
Heat to 5 ° C. Next, the oil phase component is added to the water phase component and pre-emulsified, then uniformly emulsified and cooled with a homomixer, and (10) and (11) are added and mixed at 40 ° C.

【0033】上記本発明の実施例のうち実施例1〜実施
例5について、紫外線によるしわの発生に対する防止効
果を評価した。なお、各実施例において配合した真珠貝
貝肉抽出物を、各抽出物の調製に用いた抽出溶媒に代替
したものを比較例とした。しわ発生防止効果は、ヘアレ
スマウス5匹を1群とし、各群について実施例及び比較
例をそれぞれ1日1回背部に塗布し、1J/cm2/週
の長波長紫外線(UVA)を50週間照射し、ヘアレス
マウスにおけるしわの発生状況を観察し、表2に示す判
定基準に従って点数化して行った。この際、精製水のみ
を塗布した群を対照とした。結果は各群の平均値を算出
し、UVA照射日数との関係により表3に示した。
In Examples 1 to 5 among the above Examples of the present invention, the effect of preventing wrinkles caused by ultraviolet rays was evaluated. In addition, what replaced the pearl mussel shell meat extract compounded in each Example with the extraction solvent used for preparation of each extract was made into the comparative example. The wrinkle-preventing effect was obtained by applying five hairless mice to one group, applying Examples and Comparative Examples to the back once a day for each group, and applying 1 J / cm 2 / week long-wave ultraviolet light (UVA) for 50 weeks. Irradiation was performed to observe the occurrence of wrinkles in hairless mice, and scored according to the criteria shown in Table 2. At this time, a group to which only purified water was applied was used as a control. The results were calculated as the average value of each group, and are shown in Table 3 in relation to the number of UVA irradiation days.

【表2】 [Table 2]

【0034】[0034]

【表3】 表3に示されるように、対照群においては、UVA照射
日数が40週を超える頃には形成されたしわの深さは中
程度にまで達し、50週後には深いしわの発生が認めら
れていた。これに対し、本発明の実施例塗布群ではいず
れにおいてもしわの発生は顕著に抑制されており、実施
例1塗布群で50週後に軽微なしわの発生が、実施例2
〜実施例5塗布群では微小なしわの発生が見られたに過
ぎなかった。一方比較例塗布群では、酢酸トコフェロー
ルを含有する比較例2塗布群でしわの発生の程度の軽減
が若干認められた他は、有意なしわの発生防止或いは軽
減は認められなかった。
[Table 3] As shown in Table 3, in the control group, when the number of days of UVA irradiation exceeded 40 weeks, the depth of wrinkles formed reached a moderate level, and after 50 weeks, deep wrinkles were observed. Was. On the other hand, the wrinkles were significantly suppressed in each of the application groups of the examples of the present invention, and the occurrence of minor wrinkles was observed in the application group of Example 1 after 50 weeks.
-Only the generation of fine wrinkles was observed in the application group of Example 5. On the other hand, in the group applied with the comparative example, the occurrence of wrinkles was slightly reduced in the group coated with the comparative example 2 containing tocopherol acetate, but no significant wrinkles were prevented or reduced.

【0035】次に、本発明の実施例1〜実施例10につ
いて、6カ月間の実使用試験を行った。パネラーとし
て、日常戸外で作業することが多く、しわや皮膚弾性の
低下といった皮膚症状を有する40才〜60才代の女性
を用い、1群20名とした。この使用試験においても、
上記と同様各実施例において配合した真珠貝貝肉抽出物
を、各貝肉抽出物の調製に用いた抽出溶媒に代替したも
のを比較例とした。使用試験は紫外線量の多い4月〜1
0月にわたって、各群に実施例及び比較例のそれぞれを
ブラインドにて使用させて行った。使用試験開始前及び
使用試験終了後に皮膚の状態を観察し、しわ及び皮膚弾
性の各改善状況について「改善」,「やや改善」,「変
化なし」の3段階にて評価した。なお、しわの程度につ
いては写真撮影及びレプリカにより、皮膚弾性について
はキュートメーターにより測定して評価した。結果は、
各評価を得たパネラー数にて表4に示した。
Next, a practical use test for six months was performed on Examples 1 to 10 of the present invention. As panelists, women in their 40s and 60s who often work outdoors and have skin symptoms such as wrinkles and decreased skin elasticity were used, and the number of panelists was 20. In this use test,
As a comparative example, the pearl mussel shell meat extract compounded in each example was replaced with the extraction solvent used for the preparation of each shell meat extract in the same manner as described above. Use test is from April to 1 with a lot of ultraviolet rays.
Over a period of 0 months, each group was blindly using each of the examples and comparative examples. Before the start of the use test and after the end of the use test, the condition of the skin was observed, and the wrinkle and skin elasticity were evaluated in three stages of "improvement", "slight improvement", and "no change". The degree of wrinkles was evaluated by taking a photograph and a replica, and the skin elasticity was measured and evaluated by a cute meter. Result is,
Table 4 shows the number of panelists who obtained each evaluation.

【0036】[0036]

【表4】 表4に示されるようにしわの改善状況については、本発
明の実施例6使用群で改善の見られなかったパネラーが
1名見られた他は、すべてにおいて改善傾向が認められ
ていた。特に、実施例1〜実施例5及び実施例10使用
群では、50%以上のパネラーにおいて明確な改善を認
めていた。皮膚弾性の改善状況については、実施例使用
群ではすべて改善傾向が認められており、実施例1〜実
施例5及び実施例10使用群では65%以上のパネラー
で明確な改善を認めていた。これに対し、比較例使用群
ではしわ及び皮膚弾性ともに明確な改善を認めたパネラ
ーは見られず、しわについては70%以上、皮膚弾性に
ついては60%以上のパネラーで症状の改善を認めなか
った。
[Table 4] As shown in Table 4, the improvement of wrinkles was observed in all the cases except that one paneler who did not show any improvement was observed in the group using Example 6 of the present invention. In particular, in the groups using Examples 1 to 5 and Example 10, a clear improvement was recognized in 50% or more of the panelists. Regarding the state of improvement of skin elasticity, improvement tendency was observed in all the groups using the examples, and clear improvement was recognized by 65% or more of the panelists in the groups using the examples 1 to 5 and the example 10. On the other hand, in the group using the comparative example, there were no panelists who observed a clear improvement in both wrinkles and skin elasticity, and no improvement was observed in 70% or more of wrinkles and 60% or more of skin elasticities. .

【0037】なお、本発明の実施例1〜実施例10につ
いては、上記の使用試験期間中に含有成分の析出,分
離,凝集、変色,変臭といった状態変化は全く見られな
かった。また、各実施例使用群において、皮膚刺激性反
応や皮膚感作性反応を示したパネラーも存在しなかっ
た。
In Examples 1 to 10 of the present invention, no change in state such as precipitation, separation, agglomeration, discoloration, and odor of the contained components was observed at all during the above use test period. In addition, in each group used in Examples, there was no paneler showing a skin irritating reaction or a skin sensitizing reaction.

【0038】[0038]

【発明の効果】以上詳述したように、本発明により、細
胞内過酸化物消去系を活性化し、紫外線や生体内代謝等
に起因する酸化ストレスによる皮膚の炎症や、しわ,し
みの発生といった皮膚老化症状の進展などの障害を防止
或いは改善し得る、安定且つ安全な皮膚外用剤を得るこ
とができた。
As described in detail above, according to the present invention, the intracellular peroxide scavenging system is activated, and skin inflammation due to oxidative stress caused by ultraviolet rays and metabolism in a living body, wrinkles and spots are generated. A stable and safe external preparation for skin which can prevent or improve disorders such as development of skin aging symptoms could be obtained.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 真珠貝貝肉抽出物を含有して成る、皮膚
外用剤。
1. An external preparation for skin comprising a pearl shellfish meat extract.
【請求項2】 真珠貝貝肉抽出物の含有量が、0.01
〜5.0重量%であることを特徴とする、請求項1に記
載の皮膚外用剤。
2. The pearl mussel extract has a content of 0.01%.
The external preparation for skin according to claim 1, wherein the amount is from 5.0 to 5.0% by weight.
【請求項3】 皮膚外用剤が化粧料であることを特徴と
する、請求項1又は請求項2に記載の皮膚外用剤。
3. The external preparation for skin according to claim 1, wherein the external preparation for skin is a cosmetic.
JP9054190A 1997-02-21 1997-02-21 Skin lotion Pending JPH10236941A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9054190A JPH10236941A (en) 1997-02-21 1997-02-21 Skin lotion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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Publications (1)

Publication Number Publication Date
JPH10236941A true JPH10236941A (en) 1998-09-08

Family

ID=12963637

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH10236941A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2798140A1 (en) * 1999-09-03 2001-03-09 Ifremer ENZYMATIC HYDROLYSATS OF OYSTERS AND THEIR APPLICATIONS
FR2850574A1 (en) * 2003-02-04 2004-08-06 Robert Wan Holding Regenerating cosmetic composition, useful for treatment of the skin, contains a lipid extract from pearl-bearing molluscs, particularly oysters
US6936280B1 (en) * 1999-10-05 2005-08-30 Centre National De La Recherche Scientifique (Cnrs) Method for preparing a composition by extraction of mother-of-pearl, composition obtained by said method and use thereof in cosmetics and dermatology
JP2014210766A (en) * 2013-04-05 2014-11-13 御木本製薬株式会社 Hyaluronic acid production promoter, and hyaluronic acid synthase gene production promoter
JP2015010081A (en) * 2013-07-02 2015-01-19 御木本製薬株式会社 Matrix metallo protease activity inhibitor, external preparation for skin, external preparation for skin for aging prevention, external preparation for skin for wrinkle prevention, and treatment or preventive agent for rheumatoid arthritis and other diseases

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59141511A (en) * 1983-02-03 1984-08-14 Tokyo Sankei Kagaku:Kk Mucopolysaccharide additive
JPS61285966A (en) * 1985-06-14 1986-12-16 Mikimoto Seiyaku Kk Nutrient agent composed of mucilage of japanese pearl oyster and production thereof
JPH0662383B2 (en) * 1988-11-11 1994-08-17 御木本製薬株式会社 Method for manufacturing cosmetic raw materials
JPH0782132A (en) * 1993-09-14 1995-03-28 Mikimoto Pharmaceut Co Ltd Active oxygen suppressing agent
JPH07102252A (en) * 1993-10-05 1995-04-18 Mikimoto Pharmaceut Co Ltd Antioxidant
JPH07285871A (en) * 1994-04-18 1995-10-31 Mikimoto Pharmaceut Co Ltd Agent for suppressing active oxygen
JPH0826971A (en) * 1994-07-21 1996-01-30 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH08143444A (en) * 1994-11-22 1996-06-04 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH0920633A (en) * 1995-07-03 1997-01-21 Noevir Co Ltd Anti-aging skin preparation for external use

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59141511A (en) * 1983-02-03 1984-08-14 Tokyo Sankei Kagaku:Kk Mucopolysaccharide additive
JPS61285966A (en) * 1985-06-14 1986-12-16 Mikimoto Seiyaku Kk Nutrient agent composed of mucilage of japanese pearl oyster and production thereof
JPH0662383B2 (en) * 1988-11-11 1994-08-17 御木本製薬株式会社 Method for manufacturing cosmetic raw materials
JPH0782132A (en) * 1993-09-14 1995-03-28 Mikimoto Pharmaceut Co Ltd Active oxygen suppressing agent
JPH07102252A (en) * 1993-10-05 1995-04-18 Mikimoto Pharmaceut Co Ltd Antioxidant
JPH07285871A (en) * 1994-04-18 1995-10-31 Mikimoto Pharmaceut Co Ltd Agent for suppressing active oxygen
JPH0826971A (en) * 1994-07-21 1996-01-30 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH08143444A (en) * 1994-11-22 1996-06-04 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH0920633A (en) * 1995-07-03 1997-01-21 Noevir Co Ltd Anti-aging skin preparation for external use

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FR2798140A1 (en) * 1999-09-03 2001-03-09 Ifremer ENZYMATIC HYDROLYSATS OF OYSTERS AND THEIR APPLICATIONS
WO2001017538A1 (en) * 1999-09-03 2001-03-15 Institut Français De Recherche Pour L'exploitation De La Mer (Ifremer) Use of oyster flesh enzymatic hydrolysates for preparing compositions eliminating free radicals
US6841171B1 (en) 1999-09-03 2005-01-11 Institut Francis De Recherche Pour L'exploitation De La Recherche Use of oyster flesh enzymatic hydrolysates for preparing compositions eliminating free radicals
US7270807B2 (en) 1999-09-03 2007-09-18 Institut Francais De Recherche Pour L'exploitation De La Mer (Ifremer) Cosmetic composition containing oyster flash enzymatic hydrolysates
US6936280B1 (en) * 1999-10-05 2005-08-30 Centre National De La Recherche Scientifique (Cnrs) Method for preparing a composition by extraction of mother-of-pearl, composition obtained by said method and use thereof in cosmetics and dermatology
FR2850574A1 (en) * 2003-02-04 2004-08-06 Robert Wan Holding Regenerating cosmetic composition, useful for treatment of the skin, contains a lipid extract from pearl-bearing molluscs, particularly oysters
JP2014210766A (en) * 2013-04-05 2014-11-13 御木本製薬株式会社 Hyaluronic acid production promoter, and hyaluronic acid synthase gene production promoter
JP2015010081A (en) * 2013-07-02 2015-01-19 御木本製薬株式会社 Matrix metallo protease activity inhibitor, external preparation for skin, external preparation for skin for aging prevention, external preparation for skin for wrinkle prevention, and treatment or preventive agent for rheumatoid arthritis and other diseases

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