JP4518959B2 - Cosmetics - Google Patents

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JP4518959B2
JP4518959B2 JP2005002656A JP2005002656A JP4518959B2 JP 4518959 B2 JP4518959 B2 JP 4518959B2 JP 2005002656 A JP2005002656 A JP 2005002656A JP 2005002656 A JP2005002656 A JP 2005002656A JP 4518959 B2 JP4518959 B2 JP 4518959B2
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八束 吉田
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株式会社武蔵野免疫研究所
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Description

本発明は安全性に優れ、しかも有効性の高い化粧品に関する。   The present invention relates to a cosmetic product having excellent safety and high effectiveness.

従来、養毛、育毛、低刺激、肌荒防止、保湿、美白、日焼け防止等の効果を目的とした化粧品には、種々の作用を有する合成薬剤又は天然物抽出エキスが使用されているが、これらはいずれも少量の添加では十分な効果が得られず、一方多量の添加では適応部位に不快な刺激感を与え、更に継続して使用した場合には皮膚炎が発生するといった欠点を有している。   Conventionally, synthetic drugs or extracts of natural products having various actions have been used in cosmetics aimed at effects such as hair growth, hair growth, low irritation, rough skin prevention, moisturizing, whitening, sun protection, etc. None of these has the disadvantage that sufficient effects cannot be obtained with a small amount of addition, while addition of a large amount gives an unpleasant irritation to the indication site and further causes dermatitis when used continuously. ing.

そこで、長期間にわたり安全性の高い、上記効果の優れた化粧品の開発が望まれていた。   Therefore, it has been desired to develop cosmetics that are highly safe for a long period of time and have the above effects.

本発明者は、かかる実情に鑑み鋭意検討した結果、センダングサ属植物の抽出物と従来の薬剤又は植物エキスを併用することにより、相乗作用により優れた上記の効果を示し、しかも長期にわたり安全性が高いことを見出し、本発明を完成するに至った。   As a result of intensive studies in view of such circumstances, the present inventor has demonstrated the above-mentioned effect superior in synergistic effect by combining the extract of the plant belonging to the genus Sendangsa and a conventional drug or plant extract, and has a long-term safety. As a result, the present invention has been completed.

すなわち本発明は、センダングサ属植物の抽出物と、更に血行促進剤、抗菌剤、抗炎症剤、保湿剤、美白剤、及び紫外線吸収剤又は散乱剤から選ばれる成分を含有することを特徴とする化粧品を提供するものである。   That is, the present invention is characterized in that it contains an extract of a plant belonging to the genus Sendanga and further contains a component selected from a blood circulation promoter, an antibacterial agent, an anti-inflammatory agent, a moisturizer, a whitening agent, and an ultraviolet absorber or a scattering agent. It provides cosmetics.

本発明はさらに以下を提供する。
(1)(a)センダングサ属植物の抽出物と、更に(b)血行促進剤、抗菌剤、抗炎症剤、保湿剤、美白剤、及び紫外線吸収剤、又は紫外線散乱剤から選ばれる成分を含有することを特徴とする化粧品。
(2)(a)センダングサ属植物がビデンス・ピローサである上記(1)記載の化粧品。
(3)血行促進剤が、センブリエキス、ニンジンエキス、イチョウエキス、ビタミンE及びその誘導体、セファランチン、ミノキシジル、塩化カルプロニウム、トウガラシチンキ、並びにノニル酸バニリルアミドから選ばれる1種又は2種以上である上記(1)記載の化粧品。
(4)抗菌剤が、ビサボロール、感光素201号、グルコン酸クロルヘキシジン、サリチル酸、イソプロピルメチルフェノール、フェノキシエタノール、安息香酸塩、及びデヒドロ酢酸塩から選ばれる1種又は2種以上である上記(1)記載の化粧品。
(5)抗炎症剤が、アラントイン又はその誘導体、グリチルリチン、グリチルレチン酸又はその誘導体、パントテン酸並びにその誘導体から選ばれる1種又は2種以上である上記(1)記載の化粧品。
(6)保湿剤が、ヒアルロン酸、コンドロイチン硫酸、デルマタン硫酸、ヘパリン等のムコ多糖類及びその塩、そしてトレハロース、グリシン、セリン、シスチン、アラニン、スレオニン、システイン、バリン、フェニルアラニン、メチオニン、ロイシン、チロシン、プロリン、イソロイシン、トリプトファン、ヒドロキシプロリン、アスパラギン酸、グルタミン、グルタミン酸、アルギニン、ヒスチジン、リジン、並びに、アシルグルタミン酸及びその塩等から選ばれる1種又は2種以上である上記(1)記載の化粧品。
(7)美白剤が、アスコルビン酸又はその誘導体、カンゾウエキス、プラセンタエキス、グルタチオン、桑白皮エキス、ウワウルシエキス、並びにコケモモエキス等から選ばれる1種又は2種以上である上記(1)記載の化粧品。
(8)紫外線吸収剤又は紫外線散乱剤が、安息香酸系、アントラニル酸系、サリチル酸系、桂皮酸系、ベンゾフェノン系の紫外線吸収剤、酸化チタン、酸化亜鉛、カオリン、マイカ、タルク、セリサイト等の紫外線散乱剤から選ばれる1種又は2種以上である上記(1)記載の化粧品。
(9)センダングサ属植物の抽出物(濃縮乾燥純分換算として)が0.0001〜50.0重量%含有する上記(1)〜(8)のいずれかに記載の化粧品。
(10)センダングサ属植物の抽出物(乾燥させない場合)が、組成物の全重量に対して0.001〜100重量%含まれることを特徴とする上記(1)〜(9)のいずれかに記載の化粧品。
(11)血行促進剤0.0001〜2.0重量%、抗菌剤0.0001〜1.0重量%、抗炎症剤0.0001〜1.0重量%、保湿剤0.001〜20.0重量%、美白剤0.001〜5.0重量%、紫外線吸収剤(散乱剤)0.1〜30.0重量%含有する上記(3)〜(10)のいずれかに記載の化粧品。
The present invention further provides the following.
(1) (a) Sendangusa plant extract and further (b) blood circulation promoter, antibacterial agent, anti-inflammatory agent, moisturizer, whitening agent, ultraviolet absorber, or ultraviolet scattering agent Cosmetics characterized by
(2) (a) The cosmetic according to (1) above, wherein the plant belonging to the genus Sendangusa is a bidens pillow.
(3) The blood circulation promoter is one or more selected from the group consisting of a carrot extract, carrot extract, ginkgo biloba extract, vitamin E and its derivatives, cephalanthin, minoxidil, carpronium chloride, red pepper tincture, and nonyl acid vanillylamide. 1) Cosmetics as described.
(4) The above description (1), wherein the antibacterial agent is one or more selected from bisabolol, photosensitizer 201, chlorhexidine gluconate, salicylic acid, isopropylmethylphenol, phenoxyethanol, benzoate, and dehydroacetate. Cosmetics.
(5) The cosmetic according to (1), wherein the anti-inflammatory agent is one or more selected from allantoin or a derivative thereof, glycyrrhizin, glycyrrhetinic acid or a derivative thereof, pantothenic acid and a derivative thereof.
(6) The moisturizing agent is hyaluronic acid, chondroitin sulfate, dermatan sulfate, heparin and other mucopolysaccharides and salts thereof, and trehalose, glycine, serine, cystine, alanine, threonine, cysteine, valine, phenylalanine, methionine, leucine, tyrosine Cosmetics according to the above (1), which is one or more selected from: proline, isoleucine, tryptophan, hydroxyproline, aspartic acid, glutamine, glutamic acid, arginine, histidine, lysine, and acylglutamic acid and salts thereof.
(7) The whitening agent according to the above (1), wherein the whitening agent is one or more selected from ascorbic acid or a derivative thereof, licorice extract, placenta extract, glutathione, mulberry bark extract, walnut extract, and bilberry extract. Cosmetics.
(8) UV absorbers or UV scatterers are benzoic acid, anthranilic acid, salicylic acid, cinnamic acid, benzophenone UV absorbers, titanium oxide, zinc oxide, kaolin, mica, talc, sericite, etc. The cosmetic according to (1) above, which is one or more selected from ultraviolet scattering agents.
(9) The cosmetic according to any one of the above (1) to (8), wherein the extract of the genus Sendangusa (in terms of concentrated dry pure content) is contained in an amount of 0.0001 to 50.0% by weight.
(10) In any one of the above (1) to (9), the extract of Sendangusa plant (when not dried) is contained in an amount of 0.001 to 100% by weight based on the total weight of the composition. The cosmetics described.
(11) Blood circulation promoter 0.0001 to 2.0% by weight, antibacterial agent 0.0001 to 1.0% by weight, anti-inflammatory agent 0.0001 to 1.0% by weight, humectant 0.001 to 20.0 Cosmetics according to any one of the above (3) to (10), containing 10% by weight, 0.001 to 5.0% by weight of a whitening agent, and 0.1 to 30.0% by weight of an ultraviolet absorber (scattering agent).

本発明に使用されるセンダングサ属植物は、特願2000−105559に詳述したが、コシロノセンダングサ又はコセンダングサ、別名ビデンス・ピローサともいわれるものが主体で種類も多い。即ち、Bidens pilosa L.var.minor(Bl.)Sherff、Bidens pilosa L.var.radiata Sch.Bip.等と呼ばれるものもあり互いに交配する。中国・台湾では咸豊草と呼ばれるが異名が多く、同治草、鬼針草、三葉鬼針草、三葉刺針草、刺針草、婆婆針草、白花婆婆針、蝦箝草、符因草、符因頭、赤査某、金盞銀盤、含風草、南風草、蝦公鋏、羞査某仔等の名がある。日本名コバノセンダングサ(Bidens bipinnata L.)や、センダングサ(Bidens biternataあるいはBidens biternata(Lour.)Merrillet Sherff)、ホソバノセンダングサ(Bidens parviflora Willd)もセンダングサ属で、ほぼ同様に用いられる。更に北米原産の帰化植物というアメリカセンダングサ(Bidens frndosa L.)は養蜂家によく利用されている。植物学上も混乱が見られ、和名、漢名、学名の対応も交錯している。本発明で用いられるビデンス・ピローサはこれらのものを包含する。 The plant of the genus Sendangusa used in the present invention has been described in detail in Japanese Patent Application No. 2000-105559, but there are many types mainly called Koshirono Sendangsa or Kosendangusa, also known as Bidence Pilosa. That is, Bidens pilosa L. var. minor (Bl.) Sherff, Bidens pilosa L. var. radiata Sch. Bip. Some of them are called "etc." In China / Taiwan, it is called 咸咸 草, but it has many synonyms. There are names such as signhead, red check, gilding silver board, wind-containing grass, south wind grass, 蝦 公 鋏, 羞 测 某 子. Japan name Koba Roh Bidens (Bidens bipinnata L.) and, Bidens (Bidens biternata or Bidens biternata (Lour.) Merrillet Sherff ), e buckwheat Roh Bidens (Bidens parviflora Willd) in Bidens, used much the same way. In addition, the naturalized plant native to North America, Bidens frondasa L., is often used by beekeepers. There is confusion in botany, and the correspondence between Japanese names, Han names, and scientific names is also mixed. The evidence pillow used in the present invention includes these.

センダングサ属植物の抽出物は、センダングサ属植物の根又は地上部又は全草を乾燥し、又は蒸気で蒸したものを、常温又は加温下に、溶媒により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により得ることができる。   The extract of the plant belonging to the genus Sendungusa is obtained by drying the root or the above-ground part or whole grass of the plant of the genus Sendangsa or steaming it with steam at room temperature or under heating with a solvent or extracting it with a Soxhlet extractor, etc. It can be obtained by extraction using an instrument.

ここで使用される溶媒としては、水又はメタノール、エタノール、プロパノール、ブタノール、エチレングリコール、プロパンジオール、ブタンジオール、グリセリン等のアルコール類、並びにこれらの含水物が用いられるほか、アセトン、エチルメチルケトン、クロロホルム、塩化メチレン、酢酸エチル、並びにそれらの含水物を用いてもよい。抽出液は必要により溶媒留去濃縮し、濃度調整後そのまま用いてもよいし、脱色、不溶物除去、沈殿生成防止のため活性炭処理、HP20等の樹脂処理、瀘過、低温放置不溶物の除去等の処理を施してから用いてもよい。   As the solvent used here, water or alcohols such as methanol, ethanol, propanol, butanol, ethylene glycol, propanediol, butanediol, glycerin, and the like, as well as hydrates thereof, acetone, ethyl methyl ketone, You may use chloroform, a methylene chloride, ethyl acetate, and those hydrates. The extract may be concentrated by distilling off the solvent if necessary, and may be used as it is after the concentration adjustment, or it may be used as it is, decolorization, insoluble matter removal, activated carbon treatment to prevent precipitation, resin treatment such as HP20, filtration, removal of insoluble matter left at low temperature. You may use it, after processing such as.

抽出物は、そのままで本発明化粧品の有効成分として用いることもできるが、当該抽出物を更に、適当な分離手段、例えばゲル瀘過法やシリカゲルカラムクロマト法、又は逆相若しくは順相の高速液体クロマト法により活性の高い画分を分画して用いることもできる。   Although the extract can be used as it is as an active ingredient of the cosmetic product of the present invention, the extract is further subjected to an appropriate separation means such as a gel filtration method or a silica gel column chromatography method, or a reversed-phase or normal-phase high-speed liquid. A highly active fraction can also be fractionated and used by the chromatographic method.

かくして得られるセンダングサ属植物エキス(a)は、通常水又は水−低級アルコール等の溶媒に溶解して使用することが好ましい。センダングサ属植物エキスは、化粧品中に乾燥重量換算で0.0001〜50重量%、特に0.001〜6.0重量%含まれることが望ましい。最も望ましくは乾燥重量換算で0.001〜3.0重量%が好ましい。乾燥させない場合は、組成物の全重量に対して0.001〜100重量%、特に0.05〜50重量%含まれることが望ましい。最も望ましくは0.1〜10重量%の範囲で用いるのが好ましい。   The Sendangusa plant extract (a) thus obtained is preferably used usually dissolved in a solvent such as water or water-lower alcohol. It is desirable that the plant extract of the genus Sendangusa is contained in the cosmetic product in an amount of 0.0001 to 50% by weight, particularly 0.001 to 6.0% by weight in terms of dry weight. Most preferably, 0.001 to 3.0% by weight in terms of dry weight is preferable. When not drying, it is desirable to contain 0.001 to 100% by weight, particularly 0.05 to 50% by weight, based on the total weight of the composition. Most desirably, it is used in the range of 0.1 to 10% by weight.

ビデンス・ピローサ抽出物は単独でもよいが、更に化粧品効果を増強する目的で(b)血行促進剤、抗菌剤、抗炎症剤、保湿剤、美白剤、及び紫外線吸収剤又は紫外線散乱剤等と併用すると、更に効果が高まる。これはビデンス・ピローサ抽出物の持つ美肌効果、保湿効果、抗炎症効果、美白効果、防腐効果等が更に増強したものである。   The Bidence / Pirosa extract may be used alone, but it is also used in combination with (b) blood circulation promoters, antibacterial agents, anti-inflammatory agents, moisturizers, whitening agents, and UV absorbers or UV scattering agents for the purpose of further enhancing cosmetic effects. Then, the effect is further increased. This is a further enhancement of the skin beautifying effect, moisturizing effect, anti-inflammatory effect, whitening effect, antiseptic effect, etc. possessed by the Bidence Pirosa extract.

これらの成分のうち血行促進剤としては、アセチルコリン、センブリエキス、ニンジンエキス、イチョウエキス、塩化カルプロニウム、塩酸ジフェンヒドラミン、γ−オリザノール、l−メントール、セファランチン、ビタミンE、ビタミンEニコチネート等のビタミンE誘導体、ミノキシジル、キナエキス、スギナエキス、ショウブ根エキス、トウヒエキス、当薬エキス、トウガラシチンキ、ノニル酸バニリルアミド、イチョウエキス、ユズ抽出物が挙げられ、特にセンブリエキス、ニンジンエキス、イチョウエキス、ビタミンE又はビタミンE誘導体、セファランチン、ミノキシジル、トウガラシチンキ、ノニル酸バニリルアミドが好ましい。   Among these components, blood circulation promoters include vitamin E derivatives such as acetylcholine, assembly extract, carrot extract, ginkgo biloba extract, carpronium chloride, diphenhydramine hydrochloride, γ-oryzanol, l-menthol, cephalanthin, vitamin E, vitamin E nicotinate, Examples include minoxidil, quina extract, horsetail extract, ginger root extract, spruce extract, medicinal extract, capsicum tincture, nonylic acid vanillyl amide, ginkgo biloba extract, yuzu extract, especially assembly extract, carrot extract, ginkgo biloba extract, vitamin E or vitamin E Derivatives, cephalanthin, minoxidil, chili pepper, nonyl acid vanillylamide are preferred.

抗菌剤としては、ビサボロール、感光素201号、グルコン酸クロルヘキシジン、サリチル酸、イソプロピルメチルフェノール、フェノキシエタノール、安息香酸塩、デヒドロ酢酸塩、ソルビン酸カリウム、ヒノキチオール等が挙げられる。   Examples of the antibacterial agent include bisabolol, photosensitizer 201, chlorhexidine gluconate, salicylic acid, isopropylmethylphenol, phenoxyethanol, benzoate, dehydroacetate, potassium sorbate, hinokitiol and the like.

抗炎症剤としては、アラントイン又はその誘導体、グリチルリチン酸又はその誘導体、グリチルレチン酸又はその誘導体、パントテン酸並びにその誘導体、アズレン、グアイアズレン、ビワ葉エキス等が挙げられる。   Examples of the anti-inflammatory agent include allantoin or a derivative thereof, glycyrrhizic acid or a derivative thereof, glycyrrhetinic acid or a derivative thereof, pantothenic acid and a derivative thereof, azulene, guaiazulene, loquat leaf extract and the like.

保湿剤としては、ヒアルロン酸、コンドロイチン硫酸、デルマタン硫酸、ヘパリン等のムコ多糖類及びその塩、そしてトレハロース、グリシン、セリン、メチオニン、ロイシン、チロシン、プロリン、イソロイシン、トリプトファン、ヒドロキシプロリン、アスパラギン酸、グルタミン、グルタミン酸、アルギニン、ヒスチジン、リジン、アシルグルタミン酸又はその塩、可溶性コラーゲン、グリセリン、ピロリドンカルボン酸ナトリウム、1,3−ブチレングリコール、プロピレングリコール、ソルビトール、マルチトール、海藻エキス等が挙げられる。   Moisturizers include mucopolysaccharides such as hyaluronic acid, chondroitin sulfate, dermatan sulfate, heparin and their salts, and trehalose, glycine, serine, methionine, leucine, tyrosine, proline, isoleucine, tryptophan, hydroxyproline, aspartic acid, glutamine , Glutamic acid, arginine, histidine, lysine, acyl glutamic acid or a salt thereof, soluble collagen, glycerin, sodium pyrrolidonecarboxylate, 1,3-butylene glycol, propylene glycol, sorbitol, maltitol, seaweed extract and the like.

美白剤としては、アスコルビン酸又はその誘導体、カンゾウエキス、プラセンタエキス、グルタチオン、桑白皮エキス、ウワウルシエキス、コケモモエキス、イオウ、ジュウヤクエキス等が挙げられる。   Examples of the whitening agent include ascorbic acid or a derivative thereof, licorice extract, placenta extract, glutathione, mulberry bark extract, walnut extract, bilberry extract, sulfur, and jujube extract.

紫外線吸収剤又は紫外線散乱剤としては、安息香酸系、アントラニル酸系、サリチル酸系、桂皮酸系、ベンゾフェノン系、酸化チタン、酸化亜鉛、カオリン、タルク、マイカ、セリサイト等が挙げられる。   Examples of the ultraviolet absorber or ultraviolet scattering agent include benzoic acid, anthranilic acid, salicylic acid, cinnamic acid, benzophenone, titanium oxide, zinc oxide, kaolin, talc, mica, and sericite.

上記成分(b)は、1種又は2種以上を混合して用いるのが好ましい。   The component (b) is preferably used alone or in combination of two or more.

成分(b)は、成分(a)との相乗効果によるものであるが、成分(b)の配合量は、血行促進剤としては0.0001〜2重量%、特に0.001〜1重量%が好ましい。抗菌剤としては0.0001〜1.0重量%、特に0.001〜0.3重量%が好ましい。抗炎症剤としては0.0001〜1.0重量%、特に0.001〜0.5重量%が好ましい。保湿剤としては0.001〜20重量%、特に0.01〜10重量%が好ましい。美白剤としては0.001〜5重量%、特に0.1〜3重量%が好ましい。紫外線吸収剤又は散乱剤としては0.1〜30重量%、特に1.0〜20重量%が好ましい。   Component (b) is due to a synergistic effect with component (a), but the amount of component (b) is 0.0001 to 2% by weight, particularly 0.001 to 1% by weight as a blood circulation promoter. Is preferred. The antibacterial agent is preferably 0.0001 to 1.0% by weight, particularly 0.001 to 0.3% by weight. The anti-inflammatory agent is preferably 0.0001 to 1.0% by weight, particularly 0.001 to 0.5% by weight. The humectant is preferably 0.001 to 20% by weight, particularly 0.01 to 10% by weight. The whitening agent is preferably 0.001 to 5% by weight, particularly 0.1 to 3% by weight. As an ultraviolet absorber or a scattering agent, 0.1 to 30 weight%, especially 1.0 to 20 weight% are preferable.

以下実施例により本発明を具体的に説明するが、本発明はこれらに限定されるものではない。
[製造例1]ビデンス・ピローサ熱水抽出物
ビデンス・ピローサの全草の乾燥物100gに水2,000gを加え、90〜100℃で5時間抽出した後瀘過し、その瀘液を濃縮乾固してビデンス・ピローサ熱水抽出物23.1gを得た。
EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to these examples.
[Production Example 1] Hot water extract of Bidence pilosa 2,000 g of water was added to 100 g of dried vegetative pirosa whole plant, extracted at 90-100 ° C for 5 hours, filtered, and the filtrate was concentrated to dryness. Solidified to obtain 23.1 g of a Vidence Pilosa hot water extract.

[製造例2]ビデンス・ピローサのエタノール抽出物
ビデンス・ピローサの全草の乾燥物100gにエタノール2,000gを加え、常温で7日間抽出した後瀘過し、その瀘液を濃縮乾固してビデンス・ピローサのエタノール抽出物8.0gを得た。
[Production Example 2] Ethanol extract of Bidence pilosa 2,000 g of ethanol was added to 100 g of dried vegetation pirosa whole plant, extracted for 7 days at room temperature, filtered, and the filtrate was concentrated to dryness. 8.0 g of ethanol extract of Bidence Pilosa was obtained.

[製造例3]ビデンス・ピローサの1,3−ブチレングリコール抽出物
ビデンス・ピローサの全草の乾燥物50gに1,3−ブチレングリコール1,000gを加え、常温で10日間抽出した後瀘過し、ビデンス・ピローサの1,3−プチレングリコール抽出物800gを得た。
[Production Example 3] 1,3-Butylene Glycol Extract of Bidence Pyrrosa 1,000 g of 1,3-Butylene Glycol was added to 50 g of dried dried whole Bidence Pyrrhosa and extracted for 10 days at room temperature and filtered. 800 g of 1,3-butylene glycol extract of Bidence Pilosa was obtained.

[製造例4]ビデンス・ピローサの酢酸エチル及びメタノール抽出物
ビデンス・ピローサの地上部108kgを水で洗って蒸煮し、茎を潰すようにほぐしてから熱風乾燥して13.5kgの乾燥物を得た。その4kgに、9Lの酢酸エチルを加えて3時間加熱還流抽出して瀘過することを3回繰り返し、溶媒を蒸発させて89gの抽出物を得た。その残渣をメタノールで同様に抽出して185gの抽出物を得た。
[Production Example 4] Ethyl acetate and methanol extract of Bidence pillowa 108 kg above ground part of Bidence pillowa was washed with water, boiled and loosened to crush the stem, then dried with hot air to obtain 13.5 kg of dried product It was. 9 kg of ethyl acetate was added to 4 kg of the mixture, and the mixture was heated and refluxed for 3 hours and filtered three times, and the solvent was evaporated to obtain 89 g of an extract. The residue was similarly extracted with methanol to obtain 185 g of extract.

[製造例5]蒸煮溜液の分析
製造例4の原料を蒸煮した時に蒸煮缶に残った溜液は70Lあり、これを分析したところ、固形分は2.5%、その30%が灰分であった。
[Production Example 5] Analysis of Steamed Distillate When the raw material of Production Example 4 was steamed, 70 L of the liquid remaining in the steaming can was analyzed and analyzed to find that the solid content was 2.5% and 30% was ash. there were.

(実施例)ヘアトニック(血行促進剤との併用)
実施例1〜4、比較例1〜3
[表1]に示す組成のヘアトニックを調製し、その使用感及び効果について、下記の方法に従い評価を行なった。
[評価基準]
◎:20名中15名以上が明らかに抜け毛が減少したと回答した。カユミも同じ。
○:20名中10名〜15名未満が抜け毛が減少したと回答した。カユミも同じ。
△:20名中5名〜10名未満が抜け毛が減少したと回答した。カユミも同じ。
×:20名中5名未満が抜け毛が減少したと回答した。カユミも同じ。








(Example) Hair tonic (Combination with blood circulation promoter)
Examples 1-4, Comparative Examples 1-3
Hair tonics having the composition shown in [Table 1] were prepared, and the feeling of use and effects were evaluated according to the following methods.
[Evaluation criteria]
A: 15 or more of 20 responded that hair loss was clearly reduced. Kayumi is the same.
A: 10 to less than 15 out of 20 responded that hair loss decreased. Kayumi is the same.
Δ: 5 to less than 10 out of 20 responded that hair loss had decreased. Kayumi is the same.
X: Less than 5 out of 20 responded that hair loss had decreased. Kayumi is the same.








Figure 0004518959
[製造方法]
成分Aグループを混合溶解し、これに成分B(精製水)を加えて溶かし、瀘過して製品とする。
[表1]の結果より、本発明の実施例の方が、比較例に比べて顕著な抜け毛防止効果とカユミ防止効果の改善が認められた。
Figure 0004518959
[Production method]
The component A group is mixed and dissolved, and component B (purified water) is added and dissolved therein, followed by filtration to obtain a product.
From the results shown in [Table 1], the examples of the present invention showed a marked improvement in the hair loss prevention effect and the hair color prevention effect as compared with the comparative example.

(実施例)スキンクリーム(抗菌剤との併用)
実施例 5〜6、比較例4〜5
表−2に示す組成のスキンクリームを調製し、その使用感及び効果について、下記の方法に従い、評価を行った。
[評価基準]
抗菌力
◎:緑濃菌、大腸菌、黄色ブドウ状球菌を1×105ケ/g植菌し、10日間で100ケ/g以下になった。
△:10日間で103〜104ケ/gとなり、100ケ/g以下にならず。
×:10日間で1×105ケ/g以上となり増殖した。
美肌効果(各20名ずつテスト)
◎:皮膚がしっとりしたと回答75%以上。
○:皮膚がしっとりしたと回答50〜75%未満。
△:皮膚がしっとりしたと回答25〜50%未満。





(Example) Skin cream (in combination with antibacterial agent)
Examples 5-6, Comparative Examples 4-5
Skin creams having the compositions shown in Table-2 were prepared, and the feeling of use and effects were evaluated according to the following methods.
[Evaluation criteria]
Antibacterial activity A: 1 × 10 5 / g inoculated green-rich bacteria, Escherichia coli, and Staphylococcus aureus, and the number reached 10 or less in 10 days.
Δ: 10 3 to 10 4 / g in 10 days, not less than 100 / g
X: Growth increased to 1 × 10 5 units / g or more in 10 days.
Skin beautifying effect (20 people each test)
A: 75% or more responded that the skin was moist.
○: Response is less than 50 to 75% that the skin is moist.
Δ: Less than 25% to 50% responded that the skin was moist.





Figure 0004518959
[製造方法]
成分Aグループを加温溶解し80℃に保ち油相とする。
成分Bグループを加温溶解し80℃に保ち水相とする。
油相に水相を加えて乳化し、冷却して製品とする。
[表−2]の結果より、本発明の実施例の方が比較例に比べて顕著な抗菌性と、美肌効果の改善が認められた。
Figure 0004518959
[Production method]
Ingredient A group is dissolved by heating and kept at 80 ° C. to form an oil phase.
Ingredient B group is dissolved by heating and kept at 80 ° C. to form an aqueous phase.
A water phase is added to the oil phase to emulsify, and then cooled to obtain a product.
From the results of [Table-2], the antibacterial property and the improvement of the skin beautifying effect of the example of the present invention were recognized as compared with the comparative example.

(実施例)乳液(抗炎症剤との併用)
実施例7〜8、比較例6〜8
表−3に示す組成の乳液を調製し、その使用感及び効果について、下記の方法に従い、評価を行った。
[評価基準]
アトピー性皮膚炎者に使用消炎効果
◎:10名中7名以上が炎症が軽減した。
○:10名中4〜6名が炎症が軽減した。
△:10名中2〜3名が炎症が軽減した。
×:10名中1名以下が炎症が軽減した。
カユミ止め効果
◎:10名中7名以上がカユミが軽減した。
○:10名中4〜6名がカユミが軽減した。
△:10名中2〜3名がカユミが軽減した。
×:10名中1名以下がカユミが軽減した。
(Example) Emulsion (Combination with anti-inflammatory agent)
Examples 7-8, Comparative Examples 6-8
An emulsion having the composition shown in Table 3 was prepared, and its usability and effects were evaluated according to the following methods.
[Evaluation criteria]
Anti-inflammatory effect used for atopic dermatitis ◎: More than 7 out of 10 people had reduced inflammation.
○: In 4 to 10 out of 10, inflammation was reduced.
Δ: Inflammation was reduced in 2-3 persons out of 10 persons.
X: Inflammation was reduced in 1 or less of 10 people.
Kayumi stop effect ◎: More than 7 out of 10 people reduced Kayumi.
○: Kayumi was reduced in 4 to 6 of 10 people.
Δ: Kayumi was reduced in 2 to 3 of 10 people.
X: Kayumi reduced in 1 or less of 10 people.

Figure 0004518959
[製造方法]
成分Aグループを加温溶解して80℃に保ち油相とする。
成分Bグループを加温溶解して80℃に保ち水相とする。
油相に水相を加えて乳化し、冷却して製品とする。
[表−3]の結果より、本発明の実施例の方が比較例に比べて、顕著な消炎効果と、カユミ止め効果の改善が認められた。
Figure 0004518959
[Production method]
The component A group is dissolved by heating and kept at 80 ° C. to obtain an oil phase.
Ingredient B group is dissolved by heating and kept at 80 ° C. to form an aqueous phase.
A water phase is added to the oil phase to emulsify, and then cooled to obtain a product.
From the results of [Table-3], the examples of the present invention showed a remarkable anti-inflammatory effect and an improvement in anti-fogging effect as compared with the comparative example.

(実施例)化粧水(保湿剤との併用)
実施例9〜10、比較例9〜10
表−4に示す組成の化粧水を調製し、以下の方法に従い、使用感及び効果について評価を行った。
女性10名の専門パネルにより、使用テストを行い、塗布時ののび広がり、べたつきのなさ、保湿の持続性について、次の基準で評価を行い、その平均点で判定した。
[評価基準]
5点:非常に良好、4点:良好、3点:普通、2点:やや不良、1点:不良
[判定]
◎:平均点4.5以上。
○:平均点3.5以上4.5未満。
△:平均点2.5以上3.5未満。
×:平均点2.5未満。
(Example) lotion (combination with moisturizer)
Examples 9-10, Comparative Examples 9-10
A lotion having the composition shown in Table 4 was prepared, and the feel and effects were evaluated according to the following methods.
Using a panel of 10 women, a usage test was conducted, and the spread and spread at the time of application, non-stickiness, and sustainability of moisturizing were evaluated according to the following criteria, and the average score was determined.
[Evaluation criteria]
5 points: very good, 4 points: good, 3 points: normal, 2 points: slightly bad, 1 point: bad [judgment]
A: Average score of 4.5 or more.
A: Average score of 3.5 or more and less than 4.5.
Δ: Average score of 2.5 or more and less than 3.5.
X: Average point less than 2.5.

Figure 0004518959
[製造方法]
成分Aグループを混合溶解し、それに成分Bグループの混合溶解したものを加えて、濾過して製品とする。
[表−4]の結果より、本発明の実施例の方が比較例に比べて顕著な保湿持続性等の効果の改善が見られた。
Figure 0004518959
[Production method]
The component A group is mixed and dissolved, and the component B group mixed and dissolved is added thereto, followed by filtration to obtain a product.
From the result of [Table-4], the improvement of the effect of the moisture retention and the like was remarkable in the example of the present invention compared with the comparative example.

(実施例)日焼けによるシミ・ソバカス防止クリーム(美肌剤の併用)
実施例11〜13、比較例11〜13
[表−5]に示す組成のクリームを調製し、効果について以下の方法に従い、評価を行った。

Figure 0004518959
紫外線(UVB)の最少紅斑量(MED)の2倍量を、人の背部の10×10mmの面積に照射して皮膚の黒化を作り、その上に試料を毎日塗布して、黒化の消失期間の差により効果の判定をした。


(Example) Anti-smudge cream with sunburn (combination with skin cleanser)
Examples 11-13, Comparative Examples 11-13
Creams having the compositions shown in [Table-5] were prepared, and the effects were evaluated according to the following methods.
Figure 0004518959
Irradiate twice the amount of ultraviolet (UVB) erythema (MED) to a 10x10mm area on the back of a person to make the skin dark, and apply a sample daily on it to The effect was judged by the difference in disappearance period.


Figure 0004518959
[製造方法]
成分Aグループを加温溶解して80℃に保ち油相とする。
成分Bグループを加温溶解して80℃に保ち水相とする。
油相に水相を加えて乳化し、冷却して製品とする。
[表−5]の結果より、本発明の実施例の方が比較例に比べて顕著な日焼けによるシミ等の消失効果の改善が見られた。
Figure 0004518959
[Production method]
The component A group is dissolved by heating and kept at 80 ° C. to obtain an oil phase.
Ingredient B group is dissolved by heating and kept at 80 ° C. to form an aqueous phase.
A water phase is added to the oil phase to emulsify, and then cooled to obtain a product.
From the results of [Table-5], the examples of the present invention showed an improvement in the disappearance effect of spots and the like due to significant sunburn as compared with the comparative examples.

(実施例)日焼け止めクリーム(紫外線吸収剤、散乱剤の併用)
実施例14〜15、比較例14〜15
[表−6]に示す組成の日焼け止めクリームを調製し、効果について以下の方法に従い評価を行った。
人の背部に試料を塗布し、その上に紫外線UVBを照射し、日焼け防止効果SPFを算出した。日本化粧品工業会の測定法に準じた。

(Example) Sunscreen cream (combination of UV absorber and scattering agent)
Examples 14-15, Comparative Examples 14-15
Sunscreen creams having the composition shown in [Table-6] were prepared, and the effects were evaluated according to the following methods.
A sample was applied to the back of a person, and ultraviolet rays UVB were irradiated thereon, and the sun protection effect SPF was calculated. According to the measurement method of Japan Cosmetic Industry Association.

Figure 0004518959

[製造方法]
成分Aグループを混合加温均一にして80℃に保ち油相とする。
成分Bグループを混合加温溶解させて80℃に保ち水相とする。
油相に水相を加えて乳化し、冷却して製品とする。
[表−6]の結果により、比較例に比べて本発明の実施例の方が、顕著な日焼け防止効果の改善が見られた。
以上の通り、本発明は、表1〜表6の通り、化粧品改善効果が顕著に認められた。
Figure 0004518959

[Production method]
The component A group is mixed and heated uniformly, and kept at 80 ° C. to obtain an oil phase.
The component B group is mixed and dissolved by heating and kept at 80 ° C. to obtain an aqueous phase.
A water phase is added to the oil phase to emulsify, and then cooled to obtain a product.
As a result of [Table-6], the sunscreening effect was significantly improved in the example of the present invention compared to the comparative example.
As described above, according to the present invention, as shown in Tables 1 to 6, the cosmetic improvement effect was remarkably recognized.

Claims (2)

(a)センダングサ属植物の抽出物、及び(b)センブリエキス、ニンジンエキス、イチョウエキス、ビタミンE及びその誘導体、セファランチン、ミノキシジル、塩化カルプロニウム、トウガラシチンキ、並びにノニル酸バニリルアミドからなる群より選択される1種または2種以上である血行促進剤を含有する抜け毛防止剤。 (A) an extract of a plant belonging to the genus Sendangsa, and (b) selected from the group consisting of an extract of a carp extract, carrot extract, ginkgo biloba, vitamin E and its derivatives, cephalanthin, minoxidil, carpronium chloride, capsicum tincture, and nonyl acid vanillylamide A hair loss prevention agent containing one or more blood circulation promoters. 組成物の全重量に対して、(b)血行促進剤が0.0001〜2.0重量%含有される、請求項に記載の抜け毛防止剤。 Relative to the total weight of the composition, (b) blood circulation accelerator is contained 0.0001 to 2.0 wt%, hair loss prevention agent according to claim 1.
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04243834A (en) * 1991-01-09 1992-08-31 Youki Rin Pharmaceutical composition
JPH1150050A (en) * 1997-08-06 1999-02-23 Lion Corp Antioxidant
JPH11322574A (en) * 1998-03-16 1999-11-24 Asahi Chem Ind Co Ltd Skin cosmetic
JPH11335232A (en) * 1998-05-21 1999-12-07 Maruzen Seiyaku Kk Testosterone 5 alpha-reductase inhibitor
JPH11343226A (en) * 1998-03-31 1999-12-14 Shiseido Co Ltd Composition for activating skin

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04243834A (en) * 1991-01-09 1992-08-31 Youki Rin Pharmaceutical composition
JPH1150050A (en) * 1997-08-06 1999-02-23 Lion Corp Antioxidant
JPH11322574A (en) * 1998-03-16 1999-11-24 Asahi Chem Ind Co Ltd Skin cosmetic
JPH11343226A (en) * 1998-03-31 1999-12-14 Shiseido Co Ltd Composition for activating skin
JPH11335232A (en) * 1998-05-21 1999-12-07 Maruzen Seiyaku Kk Testosterone 5 alpha-reductase inhibitor

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