JP4290841B2 - Melanocyte dendrite elongation inhibitor and cosmetics containing the same - Google Patents
Melanocyte dendrite elongation inhibitor and cosmetics containing the same Download PDFInfo
- Publication number
- JP4290841B2 JP4290841B2 JP2000013608A JP2000013608A JP4290841B2 JP 4290841 B2 JP4290841 B2 JP 4290841B2 JP 2000013608 A JP2000013608 A JP 2000013608A JP 2000013608 A JP2000013608 A JP 2000013608A JP 4290841 B2 JP4290841 B2 JP 4290841B2
- Authority
- JP
- Japan
- Prior art keywords
- skin
- melanocytes
- melanocyte
- elongation inhibitor
- dendrite elongation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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Images
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- Cosmetics (AREA)
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Description
【0001】
【発明の属する技術分野】
本発明は、メラノサイトのデンドライト伸長抑制剤及び化粧料などの皮膚外用剤に関し、更に詳細には、メラノサイトのデンドライト伸長抑制剤により、メラノサイトとマクロファージの相互作用を抑制するのに好適な、メラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤に関する。
【0002】
【従来の技術】
メラノサイトは動物において、色素に係わる生命現象の主役となっていることは既に知られていることであるが、かかる色素であるメラニンがメラノサイトで産生され、どの様な経緯で表皮細胞に移動していくかについては、未だ詳細には知られておらず、かかるメラニン顆粒の移動には、マクロファージが関与している場合が少なくないことのみが知られているにすぎない。かかるマクロファージの関与については、メラノサイトのデンドライトの伸長因子(DEF)を産生することにより為されていることが指摘されているが、この様な伸長因子の働きを抑制する試みや、抑制することによりメラノサイトのデンドライトの伸長を抑制すること、該デンドライトの伸長抑制により、メラニン顆粒の移動を抑制し、皮膚が黒化するのを防ぐ試みは全く為されていない。更に、バラ科の植物であるモモのエッセンスにこの様なメラノサイトの伸長抑制作用が有ることも全く知られていない。
【0003】
他方、メラノサイトによって産生されるメラニン顆粒の異常によって生じる色素異常の解決は、美しい白い肌を具現化するための人類永年の解決課題であり、この為、種々の努力が為され、多くの成果が得られてきており、そのメカニズムについても様々なものが得られているが、メラノサイトのデンドライトの伸長抑制に着目したものはなく、この様なメカニズムにより、光の関与する色素異常であって、炎症を伴う色素異常症の予防や改善などの対応に有用であることは全く知られていない。又、炎症を伴った色素異常やソバカスなどの色素異常に対して、従来良く知られているアスコルビン酸などのメラニン生成阻害剤の効果が今ひとつであり、この様な色素異常の予防或いは改善手段の開発が望まれていた。
【0004】
更に、バラ科モモのエッセンスは、抗菌作用や抗炎症作用を有していることは既に知られていることであるが、このものがメラノサイトのデンドライト伸長を抑制する作用を有していることは全く知られておらず、従って、このものを含有する化粧料などの皮膚外用剤がメラノサイトのデンドライト伸長を抑制し、以て、色素異常、取り分け、光が関与し、炎症を伴って起こる色素異常の予防と改善に有用であることは全く知られていないことであった。
【0005】
【発明が解決しようとする課題】
本発明は、この様な状況下為されたものであり、炎症を伴った色素異常やソバカスなどの色素異常に対して有効な予防或いは改善手段を提供することを課題とする。
【0006】
【課題の解決手段】
この様な状況に鑑みて、本発明者らは、炎症を伴った色素異常やソバカスなどの色素異常に対して有効な予防或いは改善手段を求めて、鋭意研究を重ねた結果、バラ科モモのエッセンスに優れたメラノサイトのデンドライトの伸長抑制作用を見出し、かかる作用を有す
る物質を皮膚外用剤に含有させることにより、この様な皮膚外用剤により、炎症を伴った色素異常やソバカスなどの色素異常の予防・改善に有用であることを見出し、発明を完成させるに至った。即ち、本発明は次に示す技術に関するものである。
(1)バラ科モモの花弁の極性溶媒による抽出物からなる、メラノサイトのデンドライトの伸長抑制剤。
(2)デンドライトの伸長抑制が、マクロファージ由来のデンドライト伸長促進因子の抑制作用に起因することを特徴とする、(1)に記載のメラノサイトの伸長抑制剤。
(3)(1)〜(2)何れか1項に記載のメラノサイトの伸長抑制剤を含有することを特徴とする、メラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤。
(4)化粧料であることを特徴とする、(3)に記載のメラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤。
(5)メラノサイトとマクロファージが関与する皮膚現象が、光による炎症を伴った、皮膚の黒化現象或いはソバカスである、(3)又は(4)に記載のメラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤。
(6)バラ科モモの花弁の抽出物及び/又は抽出物の溶媒除去物を含有することを特徴とする、美白用の化粧料。
以下、本発明について、実施の形態を中心に詳細に説明を加える。
【0007】
【発明の実施の形態】
(1)本発明のメラノサイトのデンドライトの伸長抑制剤
本発明のメラノサイトのデンドライトの伸長抑制剤は、バラ科モモのエッセンスからなる。ここで、エッセンスとは、かかる植物の植物体それ自身、植物体を乾燥或いは細切、粉砕など加工した加工物、植物体乃至はその加工物を溶媒で抽出した抽出物、抽出物の溶媒を除去した、溶媒除去物、抽出物乃至はその溶媒除去物をカラムクロマトグラフィーや液液抽出で精製した精製分画物などの総称を意味する。これらの内、本発明のメラノサイトのデンドライトの伸長抑制剤としては、溶媒抽出物乃至はその溶媒除去物が好ましく例示でき、かかる溶媒としては、極性溶媒が特に好ましく例示できる。この様な極性溶媒としては、例えば、水、エタノール、メタノール、1,3−ブタンジオール、プロピレングリコールなどのアルコール類、酢酸エチルや蟻酸メチルなどのエステル類、アセトンやメチルエチルケトンなどのケトン類、クロロホルムや塩化メチレン等のハロゲン化炭化水素類、アセトニトリル等のニトリル類、ジエチルエーテルやテトラヒドロフランなどのエーテル類から選ばれる1種乃至は2種以上が好ましく例示できる。これらの内、特に好ましいものは、水及び/又はアルコール類である。この様な抽出物を作成するには、植物体乃至はその加工物に1〜10倍量の溶媒を加え、室温であれば数日、沸点付近の温度であれば数時間浸漬すればよい。しかる後に、不溶物を濾過などで除去し、必要に応じて減圧濃縮や凍結乾燥により溶媒除去することが出来る。この様な溶媒抽出に用いる植物体の部位としては、有効な物質が植物体全体に分布しているため特段の限定はないが、木部以外の部分が好ましく例示でき、中でも花弁の部分が、この様な成分が多く含まれており、特に好ましい。かくして得られた、本発明のメラノサイトのデンドライトの伸長抑制剤である、バラ科モモのエッセンスは、メラノサイトがデンドライトを伸長するのを抑制する作用に優れ、以て、メラノサイトより皮膚組織へメラニン顆粒が移動するのを抑制し、この様なメラニン顆粒の移動をメカニズムとする、光照射時に生じる、炎症を伴った黒化やソバカスなどの色素異常を予防或いは改善する作用を有する。この様な作用は、マクロファージが放出するメラノサイトのデンドライトの伸長因子がメラノサイトに働きかけるのを阻害することを機序としていると考えられる。勿論、色素異常が、メラニン顆粒の産生にあたってこの様なルートをとることから、本発明のメラノサイトのデンドライト伸長抑制剤は、光照射による炎症を伴った黒化やソバカス以外の色素異常も抑制するが、この様な色素異常は他の手段でも予防や改善が可能であるため、本発明の効果の特徴は前記の光照射時に生じる、炎症を伴った黒化やソバカスなどの色素異常を予防或いは改善する作用と言える。
【0008】
(2)本発明のメラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤
本発明のメラノサイトのデンドライト伸長抑制剤は、マクロファージが放出するメラノサイトのデンドライトの伸長因子がメラノサイトに働きかけるのを阻害することを機序としているので、メラノサイトとマクロファージとが協調的に働く生命現象を抑制することが出来、この様なメラノサイトのデンドライト伸長抑制剤を、皮膚外用剤に含有させることにより、メラノサイトとマクロファージが関与する皮膚現象へ対応する事が出来る。即ち、本発明の皮膚外用剤は、メラノサイトとマクロファージが関与する皮膚現象対応用であって、本発明のメラノサイトのデンドライト伸長抑制剤を含有することを特徴とする。ここで、本発明で言う皮膚外用剤とは、皮膚に外用で適用される組成物の総称であって、貼付剤を含む皮膚外用医薬や洗浄剤を含む化粧料が好ましく例示でき、これらの内では、化粧料であることが特に好ましい。これは、本発明のメラノサイトのデンドライト伸長抑制剤の安全性が高く、作用が穏やかであるためである。メラノサイトとマクロファージが関与する皮膚現象としては、特に好ましくは前述の光照射による炎症を伴った黒化やソバカスなどの色素異常がまず一番重要な課題として挙げられるが、その他炎症反応なども含まれる。本発明のメラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤に於ける、メラノサイトのデンドライト伸長抑制剤の好ましい含有量は、皮膚外用剤全量に対して、0.001重量%〜10重量%であり、更に好ましくは0.01重量%〜5重量%である。これは、少なすぎるとデンドライトの伸長抑制作用が発揮されない場合があり、多すぎても効果が頭打ちになり他の処方成分の自由度を損なうことがあるからである。
【0009】
本発明のメラノサイトとマクロファージが関与する皮膚現象対応用の皮膚外用剤は、上記必須成分以外に、通常化粧料や皮膚外用医薬で使用される任意の成分を含有することが出来る。かかる任意成分としては、例えば、スクワラン、ワセリン、マイクロクリスタリンワックス等の炭化水素類、ホホバ油、カルナウバワックス,オレイン酸オクチルドデシル等のエステル類、オリーブ油、牛脂、椰子油等のトリグリセライド類、ステアリン酸、オレイン酸、リチノレイン酸等の脂肪酸、オレイルアルコール、ステアリルアルコール、オクチルドデカノール等の高級アルコール、スルホコハク酸エステルやポリオキシエチレンアルキル硫酸ナトリウム等のアニオン界面活性剤類、アルキルベタイン塩等の両性界面活性剤類、ジアルキルアンモニウム塩等のカチオン界面活性剤類、ソルビタン脂肪酸エステル、脂肪酸モノグリセライド、これらのポリオキシエチレン付加物、ポリオキシエチレンアルキルエーテル、ポリオキシエチレン脂肪酸エステル等の非イオン界面活性剤類、ポリエチレングリコール、グリセリン、1,3−ブタンジオール等の多価アルコール類、増粘・ゲル化剤、酸化防止剤、紫外線吸収剤、色剤、防腐剤、粉体等を含有することができる。勿論、従来のメラニン産生抑制剤である、アスコルビン酸類やアルブチンなどのハイドロキノン類を含有することも相乗的な効果を発揮する場合があり、有利である。
【0010】
【実施例】
以下に実施例を挙げて更に詳細に本発明について説明を加えるが、本発明がこれら実施例にのみ、限定を受けないことは言うまでもない。
【0011】
<実施例1>
バラ科モモの花弁500gに5lの水を加え、攪拌しながら2時間、90℃で加熱し、室温まで冷却した後、濾過して不溶物を取り除き、本発明のメラノサイトのデンドライト伸長抑制剤1を得た。
【0012】
<実施例2>上記実施例1のメラノサイトのデンドライト伸長抑制剤1を用いて、デンドライト伸長抑制作用を調べた。即ち、予め常法に従い、マウス腹腔より、マクロファージを回収し、10%FBS加イーグルの最少培地で希釈し、2×10 6 セル/mlの濃度のマクロファージ液を調整しておいた。このものを90μlずつ35mmシャーレに分注し、これに0.05mW/cm 2 で20分間の紫外線照射を行った。これらにメラノサイトのデンドライト伸長抑制剤を溶媒に溶かして加え37℃で1晩培養した。又、他方マウスの尾を切り、尾の表皮を細かく刻みシャーレに入れ0.5%トリプシンにて37℃で一晩処理し、ピンセットを用いて、表皮と真皮に分離し、表皮のみを回収し、0.5%トリプシンにて37℃で20分間処理し、フィルター濾過でメラノサイトのみを濾液として集めた。このメラノサイトを含む濾液を、イーグルの最少培地に10%FBS、10 -4 MのIBMX及び10ng/mlのTPAを加えた培地で、37℃、48時間培養した。これを同培地で懸濁させ、96穴ウェルに1000セル/ウェルずつ分注し、37℃で一晩培養した。メラノサイトの培地を捨て、PBSで3回洗浄した後、10%FBS加イーグルの最少培地35μlに置換した。これに前記検体を含むマクロファージの培養上清35μlずつ添加し、37℃で二晩培養し、光学顕微鏡下写真撮影を行い、この写真よりデンドライトの長さを測定した。結果を図1に示す。これより、本発明のメラノサイトのデンドライト伸長抑制剤はデンドライト伸長の抑制作用に優れることが分かる。
(検体)
1)メラノサイトのデンドライト伸長抑制剤1のジメチルスルホキシド溶液(0.0005%)
2)ジメチルスルホキシド(ポジティブコントロール)
3)マクロファージ上清を加えない(ネガティブコントロール)
【0013】
<実施例3>
上記メラノサイトのデンドライト伸長抑制剤1のメラノサイトに対する毒性を、細胞数計測にて、スクリーニングしたが、ベヒクルである、ジメチルスルホキサイドと同等であり、メラノサイトに対する毒性は認められなかった。
【0014】
<実施例4>
上記メラノサイトのデンドライト伸長抑制剤1のマクロファージに対する毒性を、MTTアッセイにて、スクリーニングしたが、ベヒクルである、ジメチルスルホキサイドと同等であり、マクロファージに対する毒性は認められなかった。
【0015】
<実施例5>
下記に示す処方に従って化粧水を作成した。即ち、処方成分を80℃で加熱、溶解させ、攪拌冷却して、化粧水を得た。この化粧水を用いて、紫外線照射に起因する、炎症を伴った黒化の改善作用を調べた。即ち、人の上腕内側部に2cm×4cmの部位を4つ設け、2日間にわたって、最少紅斑量の1.5倍の紫外線照射をこれらの部位に行い炎症を伴った黒化を起こさせた。これらの部位の標準白色板に対するΔL値を測定し、これらのそれぞれの部位に下記化粧水、下記化粧水中のデンドライト伸長抑制剤1を水に置換したもの(対照品)、同じくデンドライト伸長抑制剤1をアスコルビン酸ナトリウムに置換したもの(比較品1)、デンドライト伸長抑制剤1をグルタチオンに置換したもの(比較品2)で、1日1回28日間連日処理し、再び標準白色板に対するΔL値を測定し、これらより、(処置後のΔL値)−(処置前のΔL値)を算出したところ、対照品が0.5、本発明の化粧水が1.3、比較品1が0.7、比較品2が0.6であり、本発明の皮膚外用剤である化粧水が、紫外線照射によって生じた、炎症を伴った黒化に対して優れた改善効果があることがわかった。
メラノサイトのデンドライト伸長抑制剤1 0.1重量部
グリセリン 5 重量部
硫酸化トレハロースナトリウム 0.1重量部
ヘパリン類似物質 0.1重量部
エタノール 5 重量部
1,3−ブタンジオール 5 重量部
メチルパラベン 0.1重量部
水 84.6重量部
【0016】
<実施例6>下記に示す処方に従って乳液を作成した。即ち、処方成分イ、ロ、ハを80℃で加熱、溶解させ、イにロを徐々に加え乳化した後、ハを徐々に加え中和し、ホモジナイザーで乳化粒子を整え、攪拌冷却して、乳液を得た。このものはソバカスの抑制作用に優れていた。
イ)
スクワラン 10 重量部
セタノール 1.5重量部
イソステアリン酸トリグリセライド 5 重量部
ステアリン酸 1 重量部
ソルビタンセスキステアレート 1.5重量部
ポリオキシエチレンベヘニルエーテル 1 重量部
ブチルパラベン 0.1重量部
ロ)
メラノサイトのデンドライト伸長抑制剤1 0.5重量部
硫酸化トレハロースナトリウム 0.1重量部
ヘパリン類似物質 0.1重量部
1,3−ブタンジオール 5 重量部
メチルパラベン 0.1重量部
カルボキシビニルポリマー 0.3重量部
水 40 重量部
ハ)
水酸化カリウム 0.2重量部
水 33.6重量部
【0017】
【発明の効果】
本発明によれば、炎症を伴った色素異常やソバカスなどの色素異常に対して有効な予防或いは改善手段を提供することができる。
【図面の簡単な説明】
【図1】 実施例2の結果を示す図である。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a melanocyte dendrite elongation inhibitor and an external preparation for cosmetics and the like, and more specifically, a melanocyte and macrophage suitable for suppressing the interaction between melanocytes and macrophages with a melanocyte dendrite elongation inhibitor. The present invention relates to an external preparation for skin for dealing with skin phenomena.
[0002]
[Prior art]
It is already known that melanocytes are the leading role of life phenomena related to pigments in animals, but melanin, which is such a pigment, is produced in melanocytes and how it moves to epidermal cells. It is not yet known in detail, but it is only known that macrophages are often involved in the movement of such melanin granules. It has been pointed out that the involvement of such macrophages is caused by producing melanocyte dendrite elongation factor (DEF). No attempt has been made to suppress the growth of melanocytes and to suppress the movement of melanin granules to prevent the skin from becoming darkened by suppressing the extension of dendrites. Furthermore, it is not known at all that the essence of peach, which is a plant of the Rosaceae family, has such a melanocyte elongation-inhibiting action.
[0003]
On the other hand, resolving pigment abnormalities caused by abnormalities in melanin granules produced by melanocytes is a long-standing problem for humankind to embody beautiful white skin. Various mechanisms have been obtained, but none has focused on the suppression of melanocyte dendrite elongation. It is not known at all that it is useful for the prevention and improvement of pigmented dysfunctions associated with. In addition, melanin production inhibitors such as ascorbic acid, which are well known in the art, are not yet effective against pigment abnormalities associated with inflammation and pigment abnormalities such as buckwheat, and a means for preventing or improving such pigment abnormalities. Development was desired.
[0004]
In addition, it is already known that the essence of rosaceae peach has antibacterial and anti-inflammatory effects, but this has the effect of suppressing the dendritic extension of melanocytes. It is not known at all, and therefore, a topical skin preparation such as cosmetics containing this suppresses dendrite elongation of melanocytes, and therefore, abnormal pigmentation, particularly, abnormal pigmentation caused by inflammation involving light. It is not known at all to be useful in the prevention and improvement of the disease.
[0005]
[Problems to be solved by the invention]
The present invention has been made under such circumstances, and it is an object of the present invention to provide an effective preventive or ameliorating means for pigment abnormalities such as pigment abnormalities accompanied by inflammation and buckwheat.
[0006]
[Means for solving problems]
In view of such a situation, the present inventors have sought for effective preventive or remedy measures for pigment abnormalities such as inflammation and pigment abnormalities such as buckwheat. By finding an excellent essence of melanocyte dendrite elongation-inhibiting action and adding a substance having such action to an external preparation for skin, such an external preparation for skin causes abnormalities in pigmentation such as inflammation and pigmentation such as buckwheat. They found it useful for prevention and improvement, and completed the invention. That is, the present invention relates to the following technique.
(1) A melanocyte dendrite elongation inhibitor comprising an extract of a petal of a Rosaceae peach petal with a polar solvent .
(2) The melanocyte elongation inhibitor according to (1 ), wherein dendrite elongation inhibition is caused by an inhibitory action of a macrophage-derived dendrite elongation promoting factor.
( 3 ) A skin external preparation for dealing with skin phenomena involving melanocytes and macrophages, comprising the melanocyte elongation inhibitor according to any one of (1) to (2).
( 4 ) A skin external preparation for dealing with skin phenomena involving melanocytes and macrophages according to ( 3 ), which is a cosmetic.
( 5 ) The skin phenomenon involving melanocytes and macrophages is skin darkening or buckwheat accompanied by light-induced inflammation. ( 3 ) or ( 4 ) For dealing with skin phenomena involving melanocytes and macrophages. Topical skin preparation.
( 6 ) A cosmetic for whitening, characterized by containing an extract of petals of rosaceae peaches and / or a solvent-removed product of the extract .
Below, the present invention will be described in detail focusing on embodiments.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
(1) Melanocyte Dendrite Elongation Inhibitor of the Present Invention The melanocyte dendrite elongation inhibitor of the present invention comprises the essence of a rose family peach. Here, the essence refers to a plant body of the plant itself, a processed product obtained by drying, chopping, pulverizing the plant body, an extract obtained by extracting the plant body or the processed product with a solvent, and a solvent of the extract. It means a general term for the removed solvent-removed product, the extract or the purified fraction obtained by purifying the solvent-removed product by column chromatography or liquid-liquid extraction. Among these, as the dendrite elongation inhibitor of the melanocyte of the present invention, a solvent extract or a solvent removed product thereof can be preferably exemplified, and a polar solvent can be particularly preferably exemplified as such a solvent. Examples of such polar solvents include alcohols such as water, ethanol, methanol, 1,3-butanediol, and propylene glycol, esters such as ethyl acetate and methyl formate, ketones such as acetone and methyl ethyl ketone, chloroform, and the like. Preferred examples include one or more selected from halogenated hydrocarbons such as methylene chloride, nitriles such as acetonitrile, and ethers such as diethyl ether and tetrahydrofuran. Of these, water and / or alcohols are particularly preferable. In order to prepare such an extract, a 1 to 10-fold amount of a solvent is added to a plant body or a processed product, and it is immersed for several days at room temperature or for several hours at a temperature near the boiling point. Thereafter, the insoluble matter is removed by filtration or the like, and the solvent can be removed by vacuum concentration or lyophilization as necessary. As a part of the plant body used for such solvent extraction, there is no particular limitation because an effective substance is distributed throughout the plant body, but a part other than the xylem can be preferably exemplified, and among them the petal part, Many such components are contained, which is particularly preferable. The essence of rosaceae peach, which is the melanocyte dendrite elongation inhibitor of the present invention thus obtained, is excellent in the action of inhibiting melanocytes from stretching dendrite, so that melanin granules are transferred from melanocytes to the skin tissue. It has the action of preventing or improving pigment abnormalities such as blackening and buckwheat accompanied by inflammation, which occurs at the time of light irradiation, which suppresses movement and has such a mechanism of movement of melanin granules. Such an action is considered to be based on the mechanism by which the dendritic elongation factor of melanocytes released by macrophages inhibits melanocytes from acting. Of course, since pigment abnormalities take such a route in the production of melanin granules, the dendritic elongation inhibitor of melanocytes of the present invention also suppresses pigment abnormalities other than blackening and buckwheat accompanied by inflammation caused by light irradiation. Since such pigment abnormalities can be prevented or ameliorated by other means, the effect of the present invention is characterized by preventing or improving pigment abnormalities such as blackening or buckwheat accompanied by inflammation caused by the light irradiation. It can be said that it works.
[0008]
(2) Skin external preparation for dealing with skin phenomenon involving melanocytes and macrophages of the present invention The dendritic elongation inhibitor of melanocytes of the present invention inhibits melanocyte dendritic elongation factor released from macrophages from acting on melanocytes. Therefore, it is possible to suppress the life phenomenon in which melanocytes and macrophages work in a coordinated manner. By including such a dendritic elongation inhibitor of melanocytes in a topical skin preparation, melanocytes and macrophages are involved. Can cope with skin phenomenon. That is, the external preparation for skin of the present invention is for dealing with skin phenomena involving melanocytes and macrophages, and is characterized by containing the dendrite elongation inhibitor of melanocytes of the present invention. Here, the topical skin preparation as used in the present invention is a general term for compositions applied externally to the skin, and can be preferably exemplified by a skin external medicine containing a patch and a cosmetic containing a cleansing agent. Then, it is especially preferable that it is cosmetics. This is because the melanocyte dendrite elongation inhibitor of the present invention has high safety and mild action. As the skin phenomenon involving melanocytes and macrophages, particularly preferably, the above-mentioned pigmentation abnormality such as blackening or buckwheat accompanied by inflammation caused by light irradiation is mentioned as the most important problem, but other inflammatory reactions are also included. . In the skin external preparation for dealing with skin phenomena involving melanocytes and macrophages of the present invention, the preferred content of the dendritic elongation inhibitor for melanocytes is 0.001% by weight to 10% by weight with respect to the total amount of the external preparation for skin. More preferably, it is 0.01% by weight to 5% by weight. This may outgrowth inhibition effect of too small dendrites not exhibited, because the effect is too large, it may undermine the freedom of the other ingredients become plateaued.
[0009]
The skin external preparation for dealing with skin phenomena involving melanocytes and macrophages according to the present invention can contain any components that are usually used in cosmetics and external skin medicines in addition to the above essential components. Such optional components include, for example, hydrocarbons such as squalane, petrolatum, microcrystalline wax, esters such as jojoba oil, carnauba wax, octyldodecyl oleate, triglycerides such as olive oil, beef tallow, coconut oil, stearic acid, etc. , Fatty acids such as oleic acid, lithinoleic acid, higher alcohols such as oleyl alcohol, stearyl alcohol, octyldodecanol, anionic surfactants such as sulfosuccinic acid ester and sodium polyoxyethylene alkylsulfate, and amphoteric surfactants such as alkylbetaine salts Agents, cationic surfactants such as dialkylammonium salts, sorbitan fatty acid esters, fatty acid monoglycerides, polyoxyethylene adducts thereof, polyoxyethylene alkyl ethers, polyoxyethylenes Nonionic surfactants such as fatty acid esters, polyhydric alcohols such as polyethylene glycol, glycerin, 1,3-butanediol, thickening / gelling agents, antioxidants, ultraviolet absorbers, colorants, preservatives , Powder and the like can be contained. Of course, the inclusion of hydroquinones such as ascorbic acids and arbutin, which are conventional melanin production inhibitors, may also exhibit a synergistic effect and is advantageous.
[0010]
【Example】
Hereinafter, the present invention will be described in more detail with reference to examples, but it is needless to say that the present invention is not limited to these examples.
[0011]
<Example 1>
Add 5 liters of water to 500 g of rose petal petals, heat at 90 ° C. with stirring for 2 hours, cool to room temperature, filter to remove insoluble matter, and remove the dendrite elongation inhibitor 1 for melanocytes of the present invention. Obtained.
[0012]
<Example 2> Using the dendrite elongation inhibitor 1 for melanocytes of Example 1, the dendrite elongation inhibitory action was examined. That is, according to a conventional method, macrophages were collected from the mouse abdominal cavity and diluted with a minimal medium containing 10% FBS-added eagle to prepare a macrophage solution at a concentration of 2 × 10 6 cells / ml. 90 μl of this was dispensed into a 35 mm petri dish and irradiated with ultraviolet rays at 0.05 mW / cm 2 for 20 minutes. These dendrites elongation inhibitor for melanocytes were cultured overnight at added 37 ° C. dissolved in a solvent. Also, cut the tail of the other mouse, finely cut the tail epidermis into a petri dish, treat with 0.5% trypsin at 37 ° C overnight, separate it into epidermis and dermis using tweezers, and collect only the epidermis. The solution was treated with 0.5% trypsin at 37 ° C. for 20 minutes, and only melanocytes were collected as a filtrate by filtration. The filtrate containing this melanocyte was cultured at 37 ° C. for 48 hours in a medium in which 10% FBS, 10 −4 M IBMX and 10 ng / ml TPA were added to Eagle's minimal medium. This was suspended in the same medium, dispensed at 1000 cells / well into 96-wells, and cultured overnight at 37 ° C. The melanocyte medium was discarded, washed 3 times with PBS, and replaced with 35 μl of minimal medium with 10% FBS-added eagle. To this was added 35 μl each of the culture supernatant of macrophages containing the specimen, cultured at 37 ° C. overnight, photographed under an optical microscope, and the length of dendrites was measured from this photograph. The results are shown in FIG. From this, it can be seen that the dendrite elongation inhibitor of melanocytes of the present invention is excellent in dendrite elongation-inhibiting action.
(Sample)
1) Dimethyl sulfoxide solution of melanocyte dendrite elongation inhibitor 1 (0.0005%)
2) Dimethyl sulfoxide (positive control)
3) Do not add macrophage supernatant (negative control)
[0013]
<Example 3>
Toxicity of the melanocyte dendrite elongation inhibitor 1 to melanocytes was screened by counting the number of cells, but it was equivalent to the vehicle, dimethyl sulfoxide, and no toxicity to melanocytes was observed.
[0014]
<Example 4>
Toxicity of the melanocyte dendrite elongation inhibitor 1 to macrophages was screened by MTT assay, but it was equivalent to the vehicle, dimethyl sulfoxide, and no toxicity to macrophages was observed.
[0015]
<Example 5>
A lotion was prepared according to the formulation shown below. That is, the prescription ingredients were heated and dissolved at 80 ° C., stirred and cooled to obtain a lotion. Using this lotion, the effect of improving blackening accompanied by inflammation caused by ultraviolet irradiation was investigated. That is, four sites of 2 cm × 4 cm were provided on the inner side of the upper arm of the person, and ultraviolet irradiation of 1.5 times the minimum amount of erythema was applied to these sites for 2 days to cause blackening accompanied by inflammation. ΔL values of these parts with respect to the standard white plate were measured, and the following lotion and the dendrite elongation inhibitor 1 in the following lotion were replaced with water (control product), and the dendrite elongation inhibitor 1 Was replaced with sodium ascorbate (Comparative product 1) and dendrite elongation inhibitor 1 was replaced with glutathione (Comparative product 2). Measured, and from these, (ΔL value after treatment) − (ΔL value before treatment) was calculated. The control product was 0.5, the lotion of the present invention was 1.3, and the comparative product 1 was 0.7. The comparative product 2 was 0.6, and it was found that the skin lotion which is an external preparation for skin of the present invention has an excellent improvement effect on blackening accompanied by inflammation caused by ultraviolet irradiation.
Melanocyte dendrite elongation inhibitor 1 0.1 parts by weight glycerin 5 parts by weight sulfated trehalose sodium 0.1 part by weight heparin analog 0.1 part by weight ethanol 5 parts by weight 1,3-butanediol 5 parts by weight methylparaben 0.1 Parts by weight water 84.6 parts by weight
<Example 6 > An emulsion was prepared according to the formulation shown below. That is, the prescription ingredients A, B, and C are heated and dissolved at 80 ° C., and after gradually adding and emulsifying B, the mixture is gradually added and neutralized, and the emulsified particles are prepared with a homogenizer, stirred and cooled, An emulsion was obtained. This thing was excellent in the suppression effect of buckwheat.
I)
Squalane 10 parts by weight cetanol 1.5 parts by weight isostearic acid triglyceride 5 parts by weight stearic acid 1 part by weight sorbitan sesquistearate 1.5 parts by weight polyoxyethylene behenyl ether 1 part by weight butylparaben 0.1 part by weight
B )
Melanocyte dendrite elongation inhibitor 1 0.5 part by weight sulfated trehalose sodium 0.1 part by weight heparin analog 0.1 part by weight 1,3-butanediol 5 part by weight methylparaben 0.1 part by weight carboxyvinyl polymer 0.3 Parts by
Potassium hydroxide 0.2 parts by weight Water 33.6 parts by weight
【The invention's effect】
ADVANTAGE OF THE INVENTION According to this invention, the effective prevention or improvement means can be provided with respect to pigment abnormalities accompanying inflammation, pigment abnormalities, such as buckwheat.
[Brief description of the drawings]
FIG. 1 is a diagram showing the results of Example 2. FIG.
Claims (5)
該皮膚現象が、光による炎症を伴った、皮膚の黒化現象或いはソバカスである、皮膚外用剤。 A skin external preparation for dealing with skin phenomena involving melanocytes and macrophages, comprising the melanocyte elongation inhibitor according to any one of claims 1 to 2 ,
A skin external preparation, wherein the skin phenomenon is a skin blackening phenomenon or buckwheat accompanied by light-induced inflammation.
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JP2003081748A (en) * | 2001-09-12 | 2003-03-19 | Pola Chem Ind Inc | Extension inhibitor of dendrite of melanocyte and cosmetic containing the same |
JP2003081807A (en) * | 2001-09-12 | 2003-03-19 | Pola Chem Ind Inc | Extension inhibitor of dendrite of melanocyte and cosmetic comprising the same |
JP2003081747A (en) * | 2001-09-12 | 2003-03-19 | Pola Chem Ind Inc | Extension inhibitor of dendrite of melanocyte and cosmetic containing the same |
JP2003081746A (en) * | 2001-09-12 | 2003-03-19 | Pola Chem Ind Inc | Extension inhibitor of dendrite of melanocyte and cosmetic containing the same |
EP1570837B1 (en) * | 2002-12-02 | 2013-09-11 | Pola Chemical Industries, Inc. | Dendrite elongation inhibitor for melanocyte and skin preparation for external use containing the same |
JP2005015450A (en) * | 2003-06-30 | 2005-01-20 | Kanebo Cosmetics Inc | Skin cosmetic |
JP2006056845A (en) * | 2004-08-23 | 2006-03-02 | Teikoku Seiyaku Co Ltd | Plaster agent containing extract of plant of rose family |
JP5951173B2 (en) * | 2009-01-09 | 2016-07-13 | ロート製薬株式会社 | Method for inhibiting discoloration of composition for external use containing diphenhydramine or salt thereof and ascorbic acid or salt thereof |
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