JP2007277121A - Keratinocyte contractile agent - Google Patents

Keratinocyte contractile agent Download PDF

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JP2007277121A
JP2007277121A JP2006103180A JP2006103180A JP2007277121A JP 2007277121 A JP2007277121 A JP 2007277121A JP 2006103180 A JP2006103180 A JP 2006103180A JP 2006103180 A JP2006103180 A JP 2006103180A JP 2007277121 A JP2007277121 A JP 2007277121A
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keratinocyte
extract
yellowfin
agent
pores
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Yoriko Nakagiri
頼子 中桐
Akiyo Kameyama
明代 亀山
Megumi Mori
めぐみ 森
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Kao Corp
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Kao Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a keratinocyte contraction-accelerating agent excellent in safety. <P>SOLUTION: The keratinocyte contractile agent contains Phellodendron amurense Bark or an extract of the same as an active ingredient. The keratinocyte contractile agent can make the pores inconspicuous or improve the pores, since the agent strongly contract epidermis keratinocyte by acting on epidermic cells of the skin. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、皮膚の表皮細胞に作用し、表皮ケラチノサイトを収縮させるケラチノサイト収縮剤に関する。   The present invention relates to a keratinocyte contracting agent that acts on epidermal cells of the skin and contracts epidermal keratinocytes.

多くの女性は常に若く又は健康的に見せるために、毛穴の目立ちを目立たなくする又は改善するよう様々なスキンケアを日々行っている。かかる成分としては、個人差やその日の体調によって肌の状態が異なり易いため、スキンケアに際して安全性の高いものが望まれている。
毛穴の目立ちを目立たなくしたり又は改善したりするためのスキンケア剤の成分として、皮膚を構成する表皮ケラチノサイトを収縮させる作用を有する成分を用いることが知られている(特許文献1)。また、毛穴を目立たなくさせる方法としては、肌の表皮と真皮を双方から相乗的に収縮させることを目的とし、ケラチノサイト収縮剤と真皮引締め剤を配合することが知られている(特許文献2)。しかし、キハダの植物エキスがケラチノサイトの収縮を引き起こすことについては全く知られていなかった。
特開2002−187817号公報 特開2005−298403号公報
Many women take various skin care daily to make the pores less noticeable or improve to always look younger or healthier. As such a component, since the skin condition is likely to vary depending on individual differences and physical condition of the day, a highly safe component is desired for skin care.
As a component of a skin care agent for making pores less noticeable or improving, it is known to use a component having an action of contracting epidermal keratinocytes constituting the skin (Patent Document 1). Further, as a method for making pores inconspicuous, it is known to combine a keratinocyte contracting agent and a dermal tightening agent for the purpose of synergistically contracting the skin epidermis and dermis from both sides (Patent Document 2). . However, it was not known at all that yellowfin plant extracts cause keratinocyte contraction.
JP 2002-187817 A JP 2005-298403 A

本発明は、安全性に優れた、ケラチノサイト収縮剤を提供することを目的とする。   An object of the present invention is to provide a keratinocyte contraction agent having excellent safety.

本発明者らは、ケラチノサイトを収縮させる植物成分について、さらに探索したところ、ミカン科のキハダの抽出物に優れたケラチノサイト収縮作用があることを見出した。   As a result of further searching for plant components that contract keratinocytes, the present inventors have found that an extract of the citrus family yellowfin has an excellent keratinocyte contracting action.

すなわち、本発明は、キハダ又はその抽出物を有効成分とするケラチノサイト収縮剤を提供するものである。   That is, this invention provides the keratinocyte contraction agent which uses yellowfin or its extract as an active ingredient.

本発明のケラチノサイト収縮剤は、皮膚の表皮細胞に作用して表皮ケラチノサイトを強く収縮するので、毛穴の目立ちを目立たなくしたり又は改善したりすることができる。   The keratinocyte contracting agent of the present invention acts on the epidermal cells of the skin and strongly contracts the epidermal keratinocytes, so that the conspicuous pores can be made inconspicuous or improved.

本発明で使用されるキハダは、ミカン科のキハダ(Ephellodendron amurense Bark)である。   The yellowfin used in the present invention is Ephellodendron amurense Bark.

本発明におけるキハダは、葉、茎、芽、花、木質部、木皮部(樹皮)等の地上部及び根、塊茎等の地下部、種子、果実、樹脂等の部分が使用可能であるが、木皮部(樹皮)を用いるのが好ましい。また、市場で流通しているオウバクを用いてもよい。   The yellowfin in the present invention can be used in the above-ground parts such as leaves, stems, buds, flowers, woody parts, bark parts (bark), and underground parts such as roots and tubers, seeds, fruits, resins, etc. It is preferable to use a part (bark). Moreover, you may use the buckwheat currently distribute | circulated in the market.

本発明におけるキハダは、植物そのまま若しくはそれを圧搾することにより得られる搾汁、植物自身を乾燥させた乾燥物若しくはその粉砕物、さらに或いはこれらの抽出物として用いることができるが、これらの抽出物が好ましく、乾燥物若しくはその粉砕物からの抽出物がより好ましい。また、これらの抽出物は、市販品のオウバク抽出物を用いても良い。   The yellowfin in the present invention can be used as a plant as it is or by squeezing it, a dried product obtained by drying the plant itself, or a pulverized product thereof, or an extract thereof. Is preferable, and an extract from a dried product or a pulverized product thereof is more preferable. Moreover, you may use a commercially available agaric extract for these extracts.

抽出物としては、キハダを常温又は加温下にて抽出するか又はソックスレー抽出器等の抽出器具を用いて抽出すること等公知の抽出方法により得られる各種溶剤抽出液、その希釈液、その濃縮液、その乾燥末又はペースト状が挙げられる。
公知の抽出方法としては、例えば、浸漬、煎出、浸出、還流抽出、超臨界抽出、超音波抽出及びマイクロ波抽出等が挙げられる。
As an extract, various solvent extracts obtained by a known extraction method such as extracting yellowfin at room temperature or under heating or using an extraction device such as a Soxhlet extractor, diluted solutions thereof, and concentrated solutions thereof A liquid, its dry powder, or paste is mentioned.
Known extraction methods include, for example, immersion, decoction, leaching, reflux extraction, supercritical extraction, ultrasonic extraction, and microwave extraction.

当該抽出物を得るために用いられる抽出溶剤としては、極性溶剤、非極性溶剤のいずれをも使用することができる。例えば、水;メタノール、エタノール、プロパノール、ブタノール等のアルコール類;プロピレングリコール、ブチレングリコール等の多価アルコール類;アセトン、メチルエチルケトン等のケトン類;酢酸メチル、酢酸エチル等のエステル類;テトラヒドロフラン、ジエチルエーテル等の鎖状及び環状エーテル類;ポリエチレングリコール等のポリエーテル類;ジクロロメタン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類;ヘキサン、シクロヘキサン、石油エーテル等の炭化水素類;ベンゼン、トルエン等の芳香族炭化水素類;ピリジン類等が挙げられ、これらは単独又は混合物として用いることができる。このうち、極性溶剤を用いるのが好ましく、特に水−アルコール系溶剤(40%〜100%(v/v))を用いるのが好ましく、80〜100%(v/v)がより好ましい。ここで、アルコール系とは、上記アルコール類及び/又は多価アルコール類をいい、このうちアルコール類がより好ましく、メタノール、エタノール、プロパノール等がより好ましく、エタノールが特に好ましい。   As the extraction solvent used for obtaining the extract, either a polar solvent or a nonpolar solvent can be used. For example, water; alcohols such as methanol, ethanol, propanol and butanol; polyhydric alcohols such as propylene glycol and butylene glycol; ketones such as acetone and methyl ethyl ketone; esters such as methyl acetate and ethyl acetate; tetrahydrofuran and diethyl ether Linear and cyclic ethers such as polyethylene; polyethers such as polyethylene glycol; halogenated hydrocarbons such as dichloromethane, chloroform and carbon tetrachloride; hydrocarbons such as hexane, cyclohexane and petroleum ether; aroma such as benzene and toluene Group hydrocarbons; pyridines and the like, and these can be used alone or as a mixture. Among these, it is preferable to use a polar solvent, and it is particularly preferable to use a water-alcohol solvent (40% to 100% (v / v)), and more preferably 80 to 100% (v / v). Here, the alcohol type refers to the above alcohols and / or polyhydric alcohols, among which alcohols are more preferable, methanol, ethanol, propanol and the like are more preferable, and ethanol is particularly preferable.

本発明の植物原体からの抽出は、例えば以下の様に行うことができる。すなわち、植物1質量部に対して1〜30質量部の溶剤を用いて、4〜100℃にて0.5時間〜30日間、好ましくは10〜70℃の温度で、0.5時間〜30日間、特に1〜15日間抽出すればよい。   Extraction from the plant material of the present invention can be performed, for example, as follows. That is, using 1 to 30 parts by mass of a solvent with respect to 1 part by mass of a plant, 0.5 to 30 days at 4 to 100 ° C, preferably 10 to 70 ° C, and 0.5 to 30 hours. It may be extracted for 1 day, especially 1 to 15 days.

また、上記キハダ抽出物は、液々分配、固液分配、濾過膜、活性炭、吸収樹脂、イオン交換樹脂等の公知の技術により不活性な夾雑物を除去して用いることが好ましい。このとき用いられる溶剤は上記抽出溶剤として例示のいたものを用いることができる。また、これらは、必要により公知の方法で脱臭、脱色等の処理を施してから用いてもよい。
また、本発明のキハダ抽出物は、上記溶剤抽出を組み合わせて行って得られる特定の抽出画分であってもよい。具体的には、例えば、キハダの水−エタノール系混合抽出物を、更にヘキサン、ジエチルエーテル、ベンゼン等疎水溶剤を用いて抽出して得られる疎水性画分が挙げられる。
The yellow extract is preferably used after removing inactive impurities by a known technique such as liquid-liquid distribution, solid-liquid distribution, filtration membrane, activated carbon, absorption resin, ion exchange resin and the like. As the solvent used at this time, those exemplified as the extraction solvent can be used. Moreover, you may use these, after giving processes, such as a deodorizing and a decoloring, by a well-known method as needed.
The yellow extract of the present invention may be a specific extract fraction obtained by combining the above solvent extractions. Specifically, for example, a hydrophobic fraction obtained by further extracting a water-ethanol mixed extract of yellowfin using a hydrophobic solvent such as hexane, diethyl ether, benzene and the like.

後記実施例で示すとおり、キハダ抽出物は、表皮細胞に作用し、ケラチノサイトを収縮させる。表皮ケラチノサイトを収縮させることにより毛穴が収縮するため、従ってキハダ又はその抽出物は毛穴を収縮させ、毛穴の目立ちを目立たなくする又は改善するための化粧品、医薬部外品、医薬品等として使用可能なケラチノサイト収縮剤として用いることができる。当該製剤は、通常の皮膚表面の他に、脱毛処理後、さらには角層除去後に使用してもよい。   As shown in Examples below, yellowfin extract acts on epidermal cells and contracts keratinocytes. Since the pores contract by contracting the epidermal keratinocytes, yellowfin or its extract can be used as cosmetics, quasi-drugs, pharmaceuticals, etc. to contract the pores and make the pores less noticeable or improved It can be used as a keratinocyte shrinking agent. In addition to the normal skin surface, the preparation may be used after depilation and further after removal of the stratum corneum.

本発明のケラチノサイト収縮剤は、軟膏等の薬用皮膚外用剤や化粧用皮膚外用剤の形態、具体的には、乳化化粧料、クリーム、乳液、ローション、ジェル等の種々の形態で用いることがとりわけ好ましい。斯かる上記製剤は、それぞれ一般的な製造法により、直接又は製剤上許容し得る担体とともに混合、分散した後、所望の形態に加工することによって得ることができる。この場合、本発明のキハダ抽出物の他に、かかる形態に一般的に用いられる植物油、動物油等の油性基剤、鎮痛消炎剤、鎮痛剤、殺菌消毒剤、収斂剤、皮膚軟化剤、ホルモン剤、ビタミン類、保湿剤、紫外線吸収剤、アルコール類、キレート剤、pH調整剤、防腐剤、増粘剤、色素、香料等を本発明の効果を妨害しない範囲で適宜配合することができる。
また、本発明の上記製剤は、化粧料に限定されず、医薬品、医薬部外品、薬用化粧料等をも包含するものである。
The keratinocyte shrinking agent of the present invention is used in various forms such as a medicinal skin external preparation such as an ointment and a cosmetic skin external preparation, specifically, emulsified cosmetics, creams, emulsions, lotions, gels and the like. preferable. Such a preparation can be obtained by mixing and dispersing directly or together with a pharmaceutically acceptable carrier and then processing into a desired form by a general production method. In this case, in addition to the yellowfin extract of the present invention, oily bases such as vegetable oils and animal oils commonly used in such forms, analgesic anti-inflammatory agents, analgesics, bactericidal disinfectants, astringents, emollients, hormone agents , Vitamins, humectants, ultraviolet absorbers, alcohols, chelating agents, pH adjusters, preservatives, thickeners, pigments, fragrances, and the like can be appropriately blended within a range that does not interfere with the effects of the present invention.
Moreover, the said formulation of this invention is not limited to cosmetics, A pharmaceutical, a quasi-drug, pharmaceutical cosmetics, etc. are included.

本発明の上記製剤のキハダ又はその抽出物の配合量は、乾燥物として通常全組成の0.0001〜20質量%、特に0.001〜5質量%が好ましい。   The blending amount of yellowfin or its extract of the above-mentioned preparation of the present invention is usually 0.0001 to 20% by mass, particularly preferably 0.001 to 5% by mass of the total composition as a dry product.

以下、実施例により本発明をさらに詳細に説明する。
製造例1 キハダ抽出物の製造
キハダの樹皮1.0kgに95%(v/v)エタノール水溶液10Lを加え、室温で7日間抽出後、濾過して抽出液を得た(蒸発残分:1.2(w/v)。これを減圧濃縮し、さらに減圧乾燥して、キハダ抽出物を得た。
Hereinafter, the present invention will be described in more detail with reference to examples.
Production Example 1 Production of yellowfin extract 10 L of 95% (v / v) ethanol aqueous solution was added to 1.0 kg of yellowfin bark, extracted for 7 days at room temperature, and filtered to obtain an extract (evaporation residue: 1. 2 (w / v) This was concentrated under reduced pressure and further dried under reduced pressure to obtain a yellow extract.

製造例2 キハダ抽出物疎水性画分の製造
キハダの樹皮1.0kgに95%(v/v)エタノール水溶液10Lを加え、室温で7日間抽出後、濾過して抽出液を得た。この抽出液を減圧濃縮後、更にヘキサン0.6Lで抽出し、濾過して抽出液を得た。これを減圧濃縮し、さらに減圧乾燥して、キハダエキス疎水性画分を得た(蒸発残分:1.0(w/v)。
Production Example 2 Production of hydrophobic fraction of yellowfin extract 10 kg of 95% (v / v) aqueous ethanol solution was added to 1.0 kg of yellowfin bark, extracted for 7 days at room temperature, and filtered to obtain an extract. The extract was concentrated under reduced pressure, further extracted with 0.6 L of hexane, and filtered to obtain an extract. This was concentrated under reduced pressure and further dried under reduced pressure to obtain a yellowfin extract hydrophobic fraction (evaporation residue: 1.0 (w / v)).

実施例1:ケラチノサイトゲル収縮作用
I型コラーゲン(セルマトリックスType-IA:新田ゼラチン)、MCDB153培地(SIGMA:5倍濃度)、20mM HEPES(DOJINDO)および精製水を氷冷しながらよく混合した後、24穴プレート(ファルコン)に各ウェル500μLずつ注入し、インキュベーターで37℃に加温しゲル化させた。得られたコラーゲンゲルにケラチノサイト用培地(Epi Life:クラボウ)を用いてケラチノサイト(HEKn:Cascade Biologics)を2×104 cells/cm2で1mLずつ播種し、24時間培養した後、スクレーパーを用いてコラーゲンゲルを培養皿から剥離した。その直後、キハダ抽出物及びキハダ疎水性画分を最終濃度(固形分濃度)0.001%、0.01%で添加した。添加1時間後にミノルタα707-siカメラ、50macroレンズを用い収縮の様子を撮影した。写真現像後、収縮環をOHPシート用紙に写し取り、画像解析ソフトImage-Pro PLUS (Media Cybanetics社)により収縮環内の面積を求めた。
コントロール(ゲル剥離のみ)ゲルの面積を100%とした時の収縮率(%)(ゲル面積比)を求めた。結果を表に示す。
Example 1: Keratinocyte gel contracting action
Type I collagen (Cell Matrix Type-IA: Nitta Gelatin), MCDB153 medium (SIGMA: 5-fold concentration), 20 mM HEPES (DOJINDO) and purified water were mixed well with ice cooling, and then added to a 24-well plate (Falcon). 500 μL of each well was injected and heated to 37 ° C. in an incubator for gelation. Keratinocytes (HEKn: Cascade Biologics) are seeded at 2 × 10 4 cells / cm 2 at 1 × L using the keratinocyte culture medium (Epi Life: Kurabo) on the obtained collagen gel, cultured for 24 hours, and then scrapered. The collagen gel was peeled from the culture dish. Immediately thereafter, yellowfin extract and yellowfin hydrophobic fraction were added at final concentrations (solids concentration) of 0.001% and 0.01%. One hour after the addition, the state of contraction was photographed using a Minolta α707-si camera and a 50 macro lens. After photo development, the shrink ring was copied onto OHP sheet paper, and the area inside the shrink ring was determined using image analysis software Image-Pro PLUS (Media Cybanetics).
Control (only gel peeling) The shrinkage rate (%) (gel area ratio) when the area of the gel was taken as 100% was determined. The results are shown in the table.

Figure 2007277121
Figure 2007277121

この結果から、キハダ抽出物は優れたケラチノサイト収縮活性を有し、疎水性画分ではより高いケラチノサイト収縮活性を有することがわかった。   From this result, it was found that the yellowfin extract has an excellent keratinocyte contractile activity and a higher keratinocyte contractile activity in the hydrophobic fraction.

Claims (1)

キハダ又はその抽出物を有効成分とするケラチノサイト収縮剤。   A keratinocyte contractor containing yellowfin or its extract as an active ingredient.
JP2006103180A 2006-04-04 2006-04-04 Keratinocyte contractile agent Pending JP2007277121A (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1072336A (en) * 1996-06-28 1998-03-17 Kao Corp Collagen gel contraction accelerator
JP2001019617A (en) * 1999-07-06 2001-01-23 Kanebo Ltd Skin pore astringent pack and usage thereof
JP2002187817A (en) * 2000-10-12 2002-07-05 Kao Corp Pore contractile agent
JP2005097250A (en) * 2003-09-05 2005-04-14 Kao Corp Phosphorylated glyceryl ether aluminum salt
JP2005298403A (en) * 2004-04-12 2005-10-27 Kao Corp Skin cosmetic

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1072336A (en) * 1996-06-28 1998-03-17 Kao Corp Collagen gel contraction accelerator
JP2001019617A (en) * 1999-07-06 2001-01-23 Kanebo Ltd Skin pore astringent pack and usage thereof
JP2002187817A (en) * 2000-10-12 2002-07-05 Kao Corp Pore contractile agent
JP2005097250A (en) * 2003-09-05 2005-04-14 Kao Corp Phosphorylated glyceryl ether aluminum salt
JP2005298403A (en) * 2004-04-12 2005-10-27 Kao Corp Skin cosmetic

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