JP2015020949A - HAIR COSMETIC AND SKIN COSMETIC CONTAINING PGD2 PRODUCTION INHIBITOR AND 5α-REDUCTASE ACTIVITY INHIBITOR - Google Patents

HAIR COSMETIC AND SKIN COSMETIC CONTAINING PGD2 PRODUCTION INHIBITOR AND 5α-REDUCTASE ACTIVITY INHIBITOR Download PDF

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JP2015020949A
JP2015020949A JP2013147341A JP2013147341A JP2015020949A JP 2015020949 A JP2015020949 A JP 2015020949A JP 2013147341 A JP2013147341 A JP 2013147341A JP 2013147341 A JP2013147341 A JP 2013147341A JP 2015020949 A JP2015020949 A JP 2015020949A
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JP6322368B2 (en
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文香 高崎
Ayaka Takasaki
文香 高崎
優子 猪爪
Yuko Inotsume
優子 猪爪
杉山 清
Kiyoshi Sugiyama
清 杉山
和 落合
Wataru Ochiai
和 落合
信智 五十嵐
Nobutomo Igarashi
信智 五十嵐
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Nicca Chemical Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a hair cosmetic and a skin cosmetic having a prostaglandin D(PGD) production inhibitory effect, and an excellent hair loss inhibitory and skin conditioning action.SOLUTION: The invention provides a hair cosmetic and a skin cosmetic containing a PGDproduction inhibitor and a 5α-reductase activity inhibitor containing at least one kind of plant extract selected from the group consisting of Rosemary extract, Time extract, Rumput roman extract, Scutellaria root extract, and Eucalyptus extract. As the 5α-reductase activity inhibitor, it is preferable to be at least one kind of plant extract selected from the group consisting of Pomegranate extract, Caryophylli flos extract, Guttiferae extract, Guava extract, and Sage extract.

Description

本発明は、PGD2産生抑制剤と5α−リダクターゼ活性阻害剤とを含有し、優れた脱毛抑制作用及び整肌作用を有する頭髪化粧料及び皮膚化粧料に関する。 The present invention relates to a hair cosmetic and a skin cosmetic that contain a PGD 2 production inhibitor and a 5α-reductase activity inhibitor and have an excellent hair loss inhibiting action and skin conditioning action.

脱毛や薄毛は、性ホルモン、ストレス、遺伝、加齢等のさまざまな原因が複雑に関与しているといわれている。なかでも男性ホルモンの影響による男性型脱毛症(以下、AGAとする)は広く知られており、加齢等により女性ホルモンの分泌が減少することで、相対的に男性ホルモンが優位になること等により、男性だけではなく女性にも生じる。   It is said that a variety of causes such as sex hormones, stress, heredity, and aging are involved in hair loss and thinning hair in a complex manner. In particular, male pattern baldness (hereinafter referred to as AGA) due to the effects of male hormones is widely known, and the secretion of female hormones decreases due to aging, etc., and male hormones are relatively dominant. This occurs not only for men but also for women.

AGAの発症には男性ホルモンの1種であるテストステロンが関与していると言われている。テストステロンは、還元酵素であるテストステロン5α−リダクターゼにより還元され、ジヒドロテストステロン(以下、DHTとする)に変化し、アンドロゲンレセプターに結合する。その結果、毛周期の退行期が誘導され成長期が通常より短くなることにより軟毛化し、頭頂部や前頭部の毛髪が薄くなったり脱毛すると言われている。   It is said that testosterone, a type of male hormone, is involved in the development of AGA. Testosterone is reduced by the reductase testosterone 5α-reductase, converted to dihydrotestosterone (hereinafter referred to as DHT), and binds to the androgen receptor. As a result, it is said that the regression period of the hair cycle is induced and the growth period becomes shorter than usual, so that the hair becomes soft and the hair on the top of the head or the frontal region becomes thinner or loses hair.

よって、5α−リダクターゼ活性を阻害することはAGAの抑制に有効であり、5α−リダクターゼ活性阻害効果を高めるための様々な方法が提案されている(特許文献1、特許文献2)。
しかしながら、これらの方法をもってしても薄毛や脱毛の改善は十分なものではなかった。
Therefore, inhibiting 5α-reductase activity is effective in suppressing AGA, and various methods for enhancing the 5α-reductase activity inhibitory effect have been proposed (Patent Documents 1 and 2).
However, even with these methods, improvement in thinning and hair loss has not been sufficient.

ところで近年、生理活性物質のプロスタグランジンD2(以下、PGD2とする)の発現量がAGA発症部位で高くなっていることが発見され(非特許文献1)、AGAとPGD2産生に関係があることが示唆されている。PGD2は、一般的なアレルギー炎症であるI型アレルギー反応においてマスト細胞から分泌されるものである。PGD2産生を抑制することによりAGAの抑制を図ることが考えられており、PGD2産生抑制成分として例えば特許文献3にシナモン成分等が記載されている。
しかしながら、これらの成分によるAGA抑制は未だ不十分であり、AGA抑制に有効なPGD2産生抑制物質はほとんど知られていない。
Recently, it has been discovered that the expression level of the bioactive substance prostaglandin D 2 (hereinafter referred to as PGD 2 ) is high at the AGA onset site (Non-Patent Document 1), and is related to AGA and PGD 2 production. It is suggested that there is. PGD 2 is secreted from mast cells in the type I allergic reaction, which is a general allergic inflammation. It is thought it possible to AGA suppression by inhibiting PGD 2 production, cinnamon component such as for example, Patent Document 3 as PGD 2 production inhibitory ingredients.
However, AGA suppression by these components is still insufficient, and almost no PGD 2 production inhibitor effective for AGA suppression is known.

また、今日では社会環境や食生活の変化を背景に、生活パターンが著しく変化し、これに起因する生活ストレスが急増していると言われている。かかるストレスが背景となって、皮膚のかぶれや湿疹等アレルギーによる皮膚の各種炎症や、原因不明の肌荒れに悩む人が急増している。このような肌荒れの改善方法として、上述のPGD2産生抑制成分を含む組成物(特許文献3)や抗炎症作用を有する植物抽出物を含有する皮膚外用剤(特許文献4)が提案されている。
しかしながら、原因が複雑化した今日の肌荒れの改善には未だ不十分であり、より優れた整肌作用を有する皮膚化粧料が望まれていた。
In addition, today, it is said that life patterns have changed remarkably against the background of changes in the social environment and dietary habits, and life stress resulting from this has increased rapidly. Against this background, the number of people suffering from various skin irritation caused by skin allergies such as skin irritation and eczema and rough skin for unknown causes is increasing rapidly. As a method for improving such rough skin, a composition containing the above-described PGD 2 production inhibitor (Patent Document 3) and an external preparation for skin containing a plant extract having an anti-inflammatory action (Patent Document 4) have been proposed. .
However, it is still insufficient for the improvement of today's rough skin whose causes are complicated, and a skin cosmetic having a better skin conditioning action has been desired.

特開平4−18026号公報JP-A-4-18026 特開平10−265350号公報JP-A-10-265350 特表2007−520545号公報Special table 2007-520545 gazette 特開2008−280317号公報JP 2008-280317 A

Sci.Transl.Med.(2012).4,126Sci. Transl. Med. (2012). 4,126

本発明は、上記課題に鑑みてなされたものであり、AGAとの関係が示唆され、加えて炎症時に発現量が高くなるPGD2の産生を抑制することにより、優れた脱毛抑制作用及び整肌作用を達成するPGD2産生抑制剤並びにこれと5α−リダクターゼ活性阻害剤とを含有する頭髪化粧料及び皮膚化粧料を提供することを目的とする。 The present invention has been made in view of the above problems, suggests a relationship with AGA, and in addition, suppresses the production of PGD 2 whose expression level is high during inflammation, thereby providing an excellent hair loss inhibiting action and skin conditioning. It is an object of the present invention to provide a hair cosmetic and a skin cosmetic containing a PGD 2 production inhibitor that achieves the action, and a 5α-reductase activity inhibitor.

本発明者らは、上記課題を解決するために鋭意研究を重ねた結果、特定の植物抽出物を用いることにより優れたPGD2産生抑制効果が得られることを見出した。また、そのPGD2産生抑制効果により得られる脱毛抑制作用及び整肌作用が、5α−リダクターゼ活性阻害剤を併用することにより非常に向上することを見出し、これらの知見に基づき本発明を完成させた。 As a result of intensive studies to solve the above problems, the present inventors have found that an excellent PGD 2 production inhibitory effect can be obtained by using a specific plant extract. In addition, it has been found that the hair loss inhibitory action and skin conditioning action obtained by the PGD 2 production inhibitory effect are greatly improved by using a 5α-reductase activity inhibitor in combination, and the present invention has been completed based on these findings. .

すなわち、本発明は、ローズマリー抽出物、タイム抽出物、カワラヨモギ抽出物、オウゴン抽出物、ユーカリ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有することを特徴とするPGD2産生抑制剤を提供するものである。
また本発明は、前記PGD2産生抑制剤と5α−リダクターゼ活性阻害剤とを含有することを特徴とする頭髪化粧料及び皮膚化粧料を提供するものである。
That is, the present invention contains PGD 2 production characterized in that it contains at least one plant extract selected from the group consisting of rosemary extract, thyme extract, kawara mugi extract, ougon extract, eucalyptus extract. An inhibitor is provided.
The present invention is to provide a hair cosmetic and skin cosmetic which is characterized by containing said PGD 2 production inhibitor and 5α- reductase activity inhibitors.

また、前記頭髪化粧料及び皮膚化粧料においては、前記5α−リダクターゼ活性阻害剤が、ザクロ抽出物、チョウジ抽出物、オトギリソウ抽出物、グアバ抽出物、セージ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有していることが好ましい。   In the hair cosmetics and skin cosmetics, the 5α-reductase activity inhibitor is at least one selected from the group consisting of pomegranate extract, clove extract, hypericum extract, guava extract, and sage extract. It is preferable that the plant extract is contained.

本発明のPGD2産生抑制剤は、AGAとの関係が示唆されているPGD2産生を抑制するため、これを用いて脱毛や薄毛、特にAGAの改善を図ることができる。また、これを配合することにより、優れた脱毛作用を有する頭髪化粧料を提供することができる。 PGD 2 production inhibitor of the present invention, in order to suppress the PGD 2 production relationship between AGA has been suggested, hair loss and thinning hair by using this, it is possible to particularly improve the AGA. Moreover, the hair cosmetics which have the outstanding hair removal action can be provided by mix | blending this.

また、本発明のPGD2産生抑制剤は、炎症時に発現量が高くなるPGD2の産生を抑制することもできるため、これを用いて肌荒れの改善を図ることができる。また、これを配合することにより優れた整肌作用を有する皮膚化粧料を提供することができる。 Further, PGD 2 production inhibitor of the present invention, since it is also possible to suppress the production of PGD 2 expression level during inflammation increases, it is possible to improve the skin roughness by using this. Moreover, the skin cosmetics which have the outstanding skin conditioning effect | action by mix | blending this can be provided.

本発明のPGD2産生抑制剤は、ローズマリー抽出物、タイム抽出物、カワラヨモギ抽出物、オウゴン抽出物、ユーカリ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有する。 The PGD 2 production inhibitor of the present invention contains at least one plant extract selected from the group consisting of a rosemary extract, a thyme extract, a Chinese mugwort extract, an ogon extract, and a eucalyptus extract.

これらの植物抽出物は、いずれも医薬又は民間薬、食品、化粧品の成分として一般的に用いられているものである。
中でも、PGD2産生抑制効果がより優れているという観点から、ローズマリー抽出物、タイム抽出物及びカワラヨモギ抽出物の1種または2種以上を含有することが好ましい。
All of these plant extracts are commonly used as components of medicines or folk medicines, foods, and cosmetics.
Among them, from the viewpoint of PGD 2 production inhibitory effect is better, rosemary extract, preferably contains one or more thyme extract and Artemisia capillaris extract.

本発明におけるローズマリー抽出物とは、シソ科ロスマリヌス属ローズマリー(Ros
marinus Officinalis)から抽出されて得られる抽出物を言う。抽出には全草、または地上部、茎や葉等の地上部の各部位を使用してもよいが、葉を使用することが好ましい。
The rosemary extract in the present invention is a rosinus genus rosemary (Ros).
The extract obtained by extracting from Marinus Officinalis). For extraction, the whole plant, or each part of the above-ground part such as the above-ground part, stem, and leaf may be used, but it is preferable to use the leaf.

本発明におけるタイム抽出物とは、タイム(Thymu)から抽出されて得られる抽出物を言う。タイムとはシソ科イブキジャコウソウ属の植物の総称であり、そのような植物としては、例えば、タチジャコウソウ(Thymus vulgaris、別名:コモンタイム)、イブキジャコウソウ(Thymus serpyllum ssp.quinquecostatus)、ヨウシュイブキジャコウソウ(Thymus serpyllum、別名:ワイルドタイム、クリーピングタイム)、シトラスタイム(Thymus
x citriodorus、別名:レモンタイム)等がある。中でも、タチジャコウソウが好ましい。
The thyme extract in the present invention refers to an extract obtained by extraction from thyme. Thyme is a collective term for plants belonging to the genus Lamiaceae, and examples of such plants include Thymus vulgaris (also known as common time), Thymus serpylum ssp. Quinquecostatus, (Thymus serpylum, aka: Wild Time, Creeping Time), Citrus Time (Thymus
x citriodorus, also known as: lemon thyme). Of these, Tachijasou is preferable.

抽出には全草、またはその地上部、茎や葉等地上部の各部位を使用してもよいが、花、茎、葉を使用することが好ましい。
本発明におけるカワラヨモギ抽出物とは、キク科ヨモギ属の植物の一種であるカワラヨモギ(Artemisia capillaris Thunb.)から得られる抽出物を言う。
For the extraction, the whole plant or each part of the above-ground part such as the above-ground part, stem and leaf may be used, but it is preferable to use flowers, stems and leaves.
The Kawara mugwort extract in the present invention refers to an extract obtained from Artemisia capillaris chumb. Which is a kind of plant belonging to the genus Artemisia.

抽出には全草、またはその地上部、茎、葉、花、花蕾等地上部の各部位を使用してもよいが、中でも花を使用することが好ましい。また、生薬「インチンコウ」を用いても良い。さらに、同属植物を用いることもできる。   For the extraction, the whole plant, or each part of the above-ground part such as the above-ground part, stem, leaf, flower, and floret may be used, but among them, it is preferable to use a flower. Alternatively, the herbal medicine “Inchinkou” may be used. Furthermore, plants belonging to the same genus can also be used.

本発明におけるオウゴン抽出物とは、シソ科タツナミソウ属の植物の一種であるコガネバナ(Scutellaria baicalensis Georgi)の根から抽出されて得られる抽出物を言う。   The Ogon extract in the present invention refers to an extract obtained by extraction from the roots of Scutellaria baicalensis Georgi, which is a kind of plant belonging to the genus Lamiaceae.

本発明におけるユーカリ抽出物とは、ユーカリから抽出されて得られる抽出物を言う。ユーカリとはフトモモ科ユーカリ属の植物の総称であり、そのような植物としては、例えば、ユーカリ・グロブラス(Eucalyptus globulus、別名:ユーカリノキ)、ユーカリ・シトリオドラ(Eucalyptus Citriodora、別名:レモンユーカリ)等がある。中でもユーカリ・グロブラスが好ましい。抽出には全草、またはその地上部、茎や葉等地上部の各部位を使用してもよいが、葉を使用することが好ましい。   The eucalyptus extract in the present invention refers to an extract obtained by extraction from eucalyptus. Eucalyptus is a general term for plants belonging to the genus Eucalyptus, and examples of such plants include Eucalyptus globulus (aka Eucalyptus), Eucalyptus Citriodora (aka Lemon Eucalyptus) and the like. . Of these, eucalyptus and globulas are preferred. For the extraction, the whole plant or each part of the above-ground part such as the above-ground part, stem and leaf may be used, but it is preferable to use the leaf.

本発明における上記植物抽出物としては、従来の抽出方法により抽出したものを用いてもよいし、市販のものを用いてもよい。
抽出方法としては例えば、適当な溶媒を用いて抽出する方法が挙げられる。
抽出の際は、使用する植物をそのまま用いてもよいし、粉砕や乾燥等を施して用いてもよいが、粉砕して用いることが好ましく、乾燥させたものを用いることがより好ましい。
As said plant extract in this invention, what was extracted by the conventional extraction method may be used, and a commercially available thing may be used.
Examples of the extraction method include a method of extraction using an appropriate solvent.
At the time of extraction, the plant to be used may be used as it is, or may be used after being pulverized or dried, but is preferably used after being pulverized, and more preferably dried.

抽出に使用する溶媒に特に制限はなく、水、低級1価アルコール類(例えばメタノール、エタノール、プロパノール、ブタノール等)、多価アルコール類(例えばプロピレングリコール、ジプロピレングリコール、ブチレングリコール、グリセリン等)、エステル類(例えば酢酸メチル、酢酸エチル等)、ケトン類(例えばアセトン、メチルエチルケトン等)、エーテル類(ジエチルエーテル、テトラヒドロフラン等)等の極性溶媒や、ハロゲン化炭化水素類(例えばクロロホルム、四塩化炭素等)、炭化水素類(例えばヘキサン、ヘプタン、シクロヘキサン等)等を用いることができる。またこれらのうちの1種を単独で用いても、2種以上からなる混合溶媒を用いてもよい。特に、極性溶媒を用いることが好ましい。   There is no particular limitation on the solvent used for extraction, water, lower monohydric alcohols (eg, methanol, ethanol, propanol, butanol, etc.), polyhydric alcohols (eg, propylene glycol, dipropylene glycol, butylene glycol, glycerin, etc.), Polar solvents such as esters (such as methyl acetate and ethyl acetate), ketones (such as acetone and methyl ethyl ketone), ethers (such as diethyl ether and tetrahydrofuran), and halogenated hydrocarbons (such as chloroform and carbon tetrachloride) ), Hydrocarbons (eg, hexane, heptane, cyclohexane, etc.) and the like can be used. One of these may be used alone, or a mixed solvent composed of two or more may be used. In particular, it is preferable to use a polar solvent.

抽出手順に特に制限はなく、例えば、抽出に使用する植物を20〜40℃の前記溶媒中に1時間〜7日間浸漬し、濾過する手順が挙げられる。
また、得られた抽出液を希釈、濃縮、凍結乾燥、精製等することにより抽出液の希釈液や濃縮液、乾燥物、精製物を得、これらを本発明に係る植物抽出物として用いることもできる。
There is no restriction | limiting in particular in an extraction procedure, For example, the procedure which immerses the plant used for extraction in the said solvent of 20-40 degreeC for 1 hour-7 days, and filters is mentioned.
In addition, by diluting, concentrating, lyophilizing, purifying, etc. the obtained extract, a diluted solution, concentrated solution, dried product, or purified product of the extract solution can be obtained, and these can be used as the plant extract according to the present invention. it can.

本発明においては、上記植物抽出物をそのまま本発明のPGD2産生抑制剤としてもよいし、以下に示す他の成分をさらに含んでいてもよい。 In the present invention, the plant extract may be used as the PGD 2 production inhibitor of the present invention as it is, or may further contain other components shown below.

本発明のPGD2産生抑制剤における上記植物抽出物の総含有量は、例えば乾燥物の質量で0.000001〜10質量%という量が挙げられる。総含有量が前記下限未満であると本発明の作用が得られない恐れがあり、前記上限を超えると含有量に見合った作用が得られない傾向があり、コスト的に不利である。 The total content of the plant extract in PGD 2 production inhibitor of the present invention, for example an amount of from 0.000001 to 10% by weight by weight of dry matter and the like. If the total content is less than the lower limit, the action of the present invention may not be obtained, and if it exceeds the upper limit, the action corresponding to the content tends to be not obtained, which is disadvantageous in terms of cost.

本発明のPGD2産生抑制剤に使用可能な他の成分としては、例えば賦形剤、増粘剤、溶剤、分散剤、溶解補助剤、緩衝剤、防腐剤、抗酸化剤、着色剤等が挙げられる。 Examples of other components that can be used in the PGD 2 production inhibitor of the present invention include excipients, thickeners, solvents, dispersants, solubilizers, buffers, preservatives, antioxidants, and colorants. Can be mentioned.

具体的には、乳糖、白糖等の賦形剤;天然ガム類、セルロース誘導体、アクリル酸重合体等の増粘剤;注射用水、アルコール、プロピレングリコール、マルクゴール、ゴマ油、トウモロコシ油等の溶剤;ポリオキシエチレンソルビタンモノオレアート、ポリオキシエチレン硬化ヒマシ油、ポリエチレングリコール等の分散剤;D−マンニトール、安息香酸ベンジル、エタノール等の溶解補助剤;リン酸塩、酢酸塩、炭酸塩等の緩衝剤;パラオキシ安息香酸エステル類、クロロブタノール、ベンジルアルコール等の防腐剤;亜流酸塩、アスコルビン酸等の抗酸化剤等が挙げられる。   Specifically, excipients such as lactose and sucrose; thickeners such as natural gums, cellulose derivatives, and acrylic acid polymers; solvents such as water for injection, alcohol, propylene glycol, markgol, sesame oil, and corn oil; Dispersing agents such as polyoxyethylene sorbitan monooleate, polyoxyethylene hydrogenated castor oil, polyethylene glycol; solubilizing agents such as D-mannitol, benzyl benzoate, ethanol; buffering agents such as phosphate, acetate, carbonate A preservative such as paraoxybenzoates, chlorobutanol and benzyl alcohol; and an antioxidant such as sulfite and ascorbic acid.

本発明のPGD2産生抑制剤は、医薬品、医薬部外品、薬用又は化粧用の製剤類をはじめとする各種の外用剤に配合することが可能であるが、その優れたPGD2産生抑制効果により優れた脱毛抑制作用及び整肌作用が得られるため、頭髪(頭皮)又は皮膚に適用する頭髪化粧料又は皮膚化粧料に配合することが好適である。 The PGD 2 production inhibitor of the present invention can be blended in various external preparations including pharmaceuticals, quasi drugs, medicinal or cosmetic preparations, and has an excellent PGD 2 production inhibitory effect. Therefore, it is preferable to blend in hair cosmetics or skin cosmetics to be applied to the hair (scalp) or skin.

本発明の頭髪化粧料及び皮膚化粧料は、上記本発明のPGD2産生抑制剤と5α−リダクターゼ活性阻害剤とを含有するものである。上記本発明のPGD2産生抑制剤と5α−リダクターゼ活性阻害剤とを併用することにより、脱毛抑制作用及び整肌作用の向上効果が非常に優れたものとなる。 The hair cosmetics and skin cosmetics of the present invention contain the PGD 2 production inhibitor of the present invention and a 5α-reductase activity inhibitor. By using the PGD 2 production inhibitor of the present invention and the 5α-reductase activity inhibitor in combination, the effect of improving the hair loss inhibiting action and the skin conditioning action becomes very excellent.

5α−リダクターゼ活性阻害剤としては従来公知のものを特に制限なく使用することができ、例えば、ザクロ抽出物、チョウジ抽出物、グアバ抽出物、オトギリソウ抽出物、セージ抽出物、センキュウ抽出物、ハッカ抽出物、セイヨウハッカ抽出物、カミツレ抽出物、アルニカ抽出物等の植物抽出物を含有するものが挙げられる。   As the 5α-reductase activity inhibitor, conventionally known ones can be used without particular limitation. For example, pomegranate extract, clove extract, guava extract, hypericum extract, sage extract, sensu extract, mint extract And those containing plant extracts such as mint extract, chamomile extract, arnica extract.

中でも、脱毛抑制作用及び整肌作用の向上がより優れるという観点から、5α−リダクターゼ活性阻害剤としてはザクロ抽出物、チョウジ抽出物、グアバ抽出物、オトギリソウ抽出物、セージ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有するものが好ましく、ザクロ抽出物、チョウジ抽出物及びグアバ抽出物の1種または2種以上を含有するものがより好ましい。   Among them, from the viewpoint of better hair loss inhibiting action and skin conditioning action, the 5α-reductase activity inhibitor is selected from the group consisting of pomegranate extract, clove extract, guava extract, hypericum extract, and sage extract In particular, those containing at least one plant extract are preferred, and those containing one or more of pomegranate extract, clove extract and guava extract are more preferred.

上記ザクロ抽出物とは、ザクロ科ザクロ属ザクロ(Punica granatum)から抽出されて得られる抽出物を言う。抽出には、全草、または果実、果皮、樹皮等の地上部の各部位を使用してもよいが、中でも果皮を使用することが好ましい。また、生薬の「柘榴皮」を用いてもよい。   The pomegranate extract refers to an extract obtained by extraction from a pomegranate family, Punica granatum. For extraction, the whole plant or each part of the above-ground part such as fruit, pericarp and bark may be used, but among these, pericarp is preferred. Alternatively, a herbal “skin” may be used.

上記チョウジ抽出物とは、フトモモ科フトモモ属チョウジノキ(Eugenia caryophyllus)から抽出されて得られる抽出物を言う。抽出には、全草、または葉、花、蕾、茎等地上部の各部位を使用してもよいが、中でも蕾を使用することが好ましい。また、同属植物を用いることができ、例えばフトモモ(Syzygium jambos)等が挙げられる。   The above-mentioned clove extract refers to an extract obtained by extraction from Eugenia caryophyllus. For the extraction, the whole plant or each part of the above-ground part such as leaves, flowers, buds and stems may be used. In addition, plants belonging to the same genus can be used, and examples thereof include yellow peach (Syzygium jambos).

上記グアバ抽出物とは、フトモモ科バンジロウ属グアバ(Psidium guajava)から抽出されて得られる抽出物を言う。抽出には、全草、または葉、花、茎等の地上部の各部位を使用してもよいが、中でも葉を使用することが好ましい。   The guava extract refers to an extract obtained by extraction from Psidium guajava. For extraction, the whole plant or each part of the above-ground part such as a leaf, a flower, and a stem may be used, but it is preferable to use a leaf among them.

上記オトギリソウ抽出物とは、オトギリソウ科オトギリソウ属オトギリソウ(Hypericum erectum)から抽出されて得られる抽出物を言う。抽出には、全草、または葉、花、茎等の地上部の各部位を使用してもよいが、中でも地上部を使用することが好ましい。   The above-mentioned Hypericum extract refers to an extract obtained by extraction from Hypericum electum. For the extraction, the whole plant or each part of the above-ground part such as a leaf, a flower, and a stem may be used, but it is preferable to use the above-ground part.

上記セージ抽出物とは、シソ科アオギリ属セージ(Salvia officinalis)から抽出されて得られる抽出物を言う。抽出には、全草、または葉、花、茎等の地上部の各部位を使用してもよいが、中でも全草または葉を使用することが好ましい。   The above sage extract refers to an extract obtained by extraction from a sage family Salvia officinalis. For the extraction, the whole grass or each part of the above-ground part such as a leaf, a flower, and a stem may be used, but it is particularly preferable to use the whole grass or the leaf.

上記植物抽出物としては、例えば上述の方法で抽出したものを用いてもよいし、市販のものを用いてもよい。また、得られた抽出液の希釈液や濃縮液、乾燥物、精製物を用いてもよい。   As said plant extract, what was extracted by the above-mentioned method may be used, for example, and a commercially available thing may be used. Moreover, you may use the dilution liquid of the obtained extract, a concentrated liquid, a dried product, and a purified product.

本発明の頭髪化粧料又は皮膚化粧料における、PGD2産生抑制剤と5α−リダクターゼ活性阻害剤との質量比は、脱毛抑制作用及び整肌作用の向上がより優れるという観点から、植物抽出物の乾燥物の質量で5:95〜60:40が好ましい。 The mass ratio of the PGD 2 production inhibitor and the 5α-reductase activity inhibitor in the hair cosmetic composition or skin cosmetic composition of the present invention is such that the plant hair extract is more excellent in hair loss inhibiting action and skin conditioning action. 5: 95-60: 40 is preferable by the mass of a dried material.

本発明の頭髪化粧料又は皮膚化粧料における上記本発明のPGD2産生抑制剤及び5α−リダクターゼ活性阻害剤の各含有量は、頭髪化粧料又は皮膚化粧料の剤型によって適宜調節され得るが、例えば植物抽出物の乾燥物の質量でそれぞれ0.000001〜10質量%という量が挙げられる。各含有量が前記下限未満であると本発明の作用が得られない恐れがあり、前記上限を超えると含有量に見合った作用が得られない傾向があり、コスト的に不利である。 The contents of the PGD 2 production inhibitor and the 5α-reductase activity inhibitor of the present invention in the hair cosmetic or skin cosmetic of the present invention can be appropriately adjusted depending on the form of the hair cosmetic or skin cosmetic, For example, the quantity of 0.000001-10 mass% is mentioned by the mass of the dried material of a plant extract, respectively. If each content is less than the lower limit, the action of the present invention may not be obtained, and if it exceeds the upper limit, an action corresponding to the content tends to be not obtained, which is disadvantageous in terms of cost.

本発明の頭髪用化粧料としては、例えば、整髪料、ヘアトニック等の頭皮用化粧料、洗髪料、ヘアリンス、養毛剤、育毛剤等が挙げられ、また、皮膚用化粧料としては、例えば、化粧水、乳液、ボディローション、ボディクリーム、パック、軟膏、ファンデーション等が挙げられる。   Examples of the cosmetics for hair of the present invention include, for example, cosmetics for scalp such as hair styling and hair tonics, hair shampoos, hair rinses, hair nourishing agents, hair restorers and the like. Examples of skin cosmetics include cosmetics. Water, emulsion, body lotion, body cream, pack, ointment, foundation and the like can be mentioned.

本発明の頭髪化粧料及び皮膚化粧料には、本発明の効果を損なわない範囲で、頭髪化粧料及び皮膚化粧料に従来から使用される成分を配合することもできる。そのような成分としては例えば、保湿剤、エモリエント剤、血行促進剤、細胞賦活化剤、抗酸化剤、抗炎症剤、抗菌剤、過酸化物抑制剤、育毛、養毛効果を有する成分、上記以外の植物や動物、微生物由来の各種抽出物等が挙げられる。   In the hair cosmetic composition and skin cosmetic composition of the present invention, ingredients conventionally used in the hair cosmetic composition and skin cosmetic composition can be blended within a range not impairing the effects of the present invention. Such components include, for example, moisturizers, emollients, blood circulation promoters, cell activators, antioxidants, anti-inflammatory agents, antibacterial agents, peroxide inhibitors, hair growth, hair restoration effects, the above And various extracts derived from plants, animals, and microorganisms.

より具体的にはグリセリン、尿素、アミノ酸、ヒアルロン酸類等の保湿剤;スクワラン、マカデミアナッツ油、オリーブ油、ホホバ油、シリコン油等のエモリエント剤;ビタミンE類、トウガラシチンキ等の血行促進剤;核酸等の細胞賦活化剤、ジブチルヒドロキシ
トルエン(BHT)、ジブチルヒドロキシアニソール(BHA)、酢酸トコフェロール等の抗酸化剤;グリチルリチン、アラントイン等の抗炎症剤;ヒノキチオール、塩化ベンザルコニウム、クロルヘキシジン塩、パラヒドロキシ安息香酸エステル等の抗菌剤;スーパーオキシドジスムターゼ(SOD)等の過酸化物抑制剤;チンピ、アロエ、ショウキョウ、ソウハクヒ等の生薬及びこれらの抽出物やパントテニルエチルエーテル、酢酸トコフェロール、フォルスコリン等の化合物等の育毛、養毛効果を有する成分;イチョウエキス、胎盤抽出物、乳酸菌培養抽出物等の上記以外の植物、動物、微生物由来の各種抽出物等が挙げられる。
More specifically, humectants such as glycerin, urea, amino acids and hyaluronic acids; emollients such as squalane, macadamia nut oil, olive oil, jojoba oil, and silicone oil; blood circulation promoters such as vitamin E and red pepper tincture; Cell activating agents, dibutylhydroxytoluene (BHT), dibutylhydroxyanisole (BHA), antioxidants such as tocopherol acetate; anti-inflammatory agents such as glycyrrhizin, allantoin; hinokitiol, benzalkonium chloride, chlorhexidine salt, parahydroxybenzoic acid Antibacterial agents such as esters; Peroxide inhibitors such as superoxide dismutase (SOD); Herbal medicines such as chimpi, aloe, ginger, sohakhi, etc., and extracts thereof, pantothenyl ethyl ether, tocopherol acetate, forskolin, etc. Hair growth, such as goods, components having a hair revitalizing effect, ginkgo extract, placenta extract, the other plants such as lactic acid bacteria culture extracts, animal, various extracts, etc. derived from microorganisms can be mentioned.

また、本発明の頭髪化粧料及び皮膚化粧料には、本発明の効果を損なわない範囲で、その剤型化のために界面活性剤、油脂類等の基材成分や、必要に応じて増粘剤、防腐剤、等張化剤、酸化防止剤、紫外線吸収剤、キレート剤、香料、着色料等の種々の添加物を併用することができる。   In addition, the hair cosmetics and skin cosmetics of the present invention may be added to base ingredients such as surfactants and fats and oils as needed for formulation, within the range that does not impair the effects of the present invention. Various additives such as a sticking agent, an antiseptic, an isotonic agent, an antioxidant, an ultraviolet absorber, a chelating agent, a fragrance, and a coloring agent can be used in combination.

以下、本発明を更に詳しく説明するために実施例によって説明するが、本発明はこれらの実施例により何ら限定されるものではない。
(1)製造方法
(1−1)PGD2産生抑制剤
Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to these examples.
(1) Production method (1-1) PGD 2 production inhibitor

(実施例1)
ローズマリーの葉を50g採取し、375mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しローズマリー抽出物3.1gを得た。これをPGD2産生抑制剤とした。
Example 1
50 g of rosemary leaves were collected and immersed in 375 ml of 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 3.1 g of a rosemary extract. This was used as a PGD 2 production inhibitor.

(実施例2)
タチジャコウソウの花、葉、茎を50g採取し、375mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しタイム抽出物9.0gを得た。これをPGD2産生抑制剤とした。
(Example 2)
50 g of flowers, leaves and stems were collected and immersed in 375 ml of a 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by freeze-drying to obtain 9.0 g of a thyme extract. This was used as a PGD 2 production inhibitor.

(実施例3)
カワラヨモギの花を50g採取し、375mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しカワラヨモギ抽出物9.3gを得た。これをPGD2産生抑制剤とした。
Example 3
50 g of Kawara mugwort flowers were collected and immersed in 375 ml of 50% by mass aqueous ethanol at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 9.3 g of the extract of Kawamomogi. This was used as a PGD 2 production inhibitor.

(実施例4)
コガネバナの根を50g採取し、375mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しオウゴン抽出物14.1gを得た。これをPGD2産生抑制剤とした。
Example 4
50 g of roots of Koganebana were collected and immersed in 375 ml of 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 14.1 g of an orgone extract. This was used as a PGD 2 production inhibitor.

(実施例5)
ユーカリの葉を50g採取し、375mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しユーカリ抽出物11.1gを得た。これをPGD2産生抑制剤とした。
(Example 5)
50 g of eucalyptus leaves were collected and immersed in 375 ml of a 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 11.1 g of an eucalyptus extract. This was used as a PGD 2 production inhibitor.

(1−2)5α−リダクターゼ活性阻害剤
(製造例1)
ザクロの果皮を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しザクロ抽出物14.7gを得た。これを5α−リダクターゼ活性阻害剤とした。
(1-2) 5α-reductase activity inhibitor (Production Example 1)
50 g of pomegranate peels were collected and immersed in 275 ml of a 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 14.7 g of a pomegranate extract. This was used as a 5α-reductase activity inhibitor.

(製造例2)
チョウジの花蕾を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しチョウジエキス9.3gを得た。これを5α−リダクターゼ活性阻害剤とした。
(Production Example 2)
50 g of clove flower buds were collected and immersed in 275 ml of 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 9.3 g of clove extract. This was used as a 5α-reductase activity inhibitor.

(製造例3)
グアバの葉を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しグアバ抽出物7.4gを得た。これを5α−リダクターゼ活性阻害剤とした。
(Production Example 3)
50 g of guava leaves were collected and immersed in 275 ml of a 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 7.4 g of guava extract. This was used as a 5α-reductase activity inhibitor.

(製造例4)
オトギリソウの地上部を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しオトギリソウ抽出物4.5gを得た。これを5α−リダクターゼ活性阻害剤とした。
(Production Example 4)
50 g of the above-ground part of hypericum was collected and immersed in 275 ml of a 50% by mass aqueous ethanol solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by freeze-drying to obtain 4.5 g of Hypericum extract. This was used as a 5α-reductase activity inhibitor.

(製造例5)
セージの全草を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しセージ抽出物10.3gを得た。これを5α−リダクターゼ活性阻害剤とした。
(Production Example 5)
50 g of whole sage grass was collected and immersed in 275 ml of 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 10.3 g of a sage extract. This was used as a 5α-reductase activity inhibitor.

(製造例6)
センキュウの根茎を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しセンキュウ抽出物16.2gを得た。これを5α−リダクターゼ活性阻害剤とした。
(Production Example 6)
50 g of rhizome of senkyu were collected and immersed in 275 ml of a 50% by mass aqueous ethanol solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 16.2 g of a Senkyu extract. This was used as a 5α-reductase activity inhibitor.

(1−3)比較成分
(比較例1)
シナモンの樹皮を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しシナモン抽出物9.5gを得た。これを比較成分とした。
(1-3) Comparative component (Comparative Example 1)
50 g of cinnamon bark was collected and immersed in 275 ml of a 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 9.5 g of a cinnamon extract. This was used as a comparative component.

(比較例2)
チャノキの葉を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃)下で浸漬した。24時間後これをろ過し、得られた抽出液から水、エタノールを減圧留去後、凍結乾燥しチャノキ抽出物6.3gを得た。これを比較成分とした。
(Comparative Example 2)
50 g of chanoki leaves were collected and immersed in 275 ml of 50% by mass ethanol aqueous solution at room temperature (about 25 ° C.). After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 6.3 g of a chanoki extract. This was used as a comparative component.

(比較例3)
ユリの根を50g採取し、275mlの50質量%エタノール水溶液に室温(約25℃
)下で浸漬した。24時間後これをろ過し、得られた抽出物から水、エタノールを減圧留去後、凍結乾燥し抽出物8.7gを得た。これを比較成分とした。
(Comparative Example 3)
50 g of lily roots were collected and placed in 275 ml of 50% by weight ethanol aqueous solution at room temperature (about 25 ° C.
) Dipped under. After 24 hours, this was filtered, and water and ethanol were distilled off from the resulting extract under reduced pressure, followed by lyophilization to obtain 8.7 g of the extract. This was used as a comparative component.

(2)PGD2産生抑制剤
(2−1)PGD2産生抑制率試験
細胞はラット由来マスト細胞(RBL−2H3細胞)を使用した。サブコンフルエント状態のRBL−2H3細胞をトリプシン処理で剥離し、48ウェルプレートの各ウェルに80,000cellsずつ播種し、10%胎仔ウシ血清(以下、FBSとする)含有ダルベッコ改変イーグル培地(以下、DMEMとする)で24時間、37℃、5%CO2条件下で培養した。実施例1〜5のPGD2産生抑制剤、比較例1及び比較例2の比較成分をそれぞれジメチルスルホキシド(以下、DMSOとする)に溶解させたものを用いて、PGD2産生抑制剤又は比較成分濃度が表1に記載の濃度でありDMSO濃度が0.1質量%である0.5%FBS含有DMEMに培地を調整し、培地をこれに交換し、1時間培養した。その後、PGD2産生促進剤として、A23187(カルシウムイオノフォア)を0.5μMとなるように添加し、30分後に培養上清を回収した。
(2) PGD 2 production inhibitor (2-1) PGD 2 production inhibition rate test Rat-derived mast cells (RBL-2H3 cells) were used as the cells. Subconfluent RBL-2H3 cells are detached by trypsin treatment, seeded with 80,000 cells in each well of a 48-well plate, and Dulbecco's modified Eagle's medium (hereinafter DMEM) containing 10% fetal calf serum (hereinafter referred to as FBS). And 24 hours at 37 ° C. and 5% CO 2 . The PGD 2 production inhibitor of Examples 1 to 5, the comparative component of Comparative Examples 1 and 2 were dissolved in dimethyl sulfoxide (hereinafter referred to as DMSO), and the PGD 2 production inhibitor or comparative component was used. The medium was adjusted to 0.5% FBS-containing DMEM having a concentration shown in Table 1 and a DMSO concentration of 0.1% by mass, and the medium was changed to this and cultured for 1 hour. Thereafter, A23187 (calcium ionophore) was added as a PGD 2 production promoter to a concentration of 0.5 μM, and the culture supernatant was recovered after 30 minutes.

また、PGD2産生抑制剤、比較成分をDMSOに溶解させたものの代わりにDMSO水溶液を用いたこと以外は上述と同様の方法で培養したものを陰性対照とした。
回収した培養上清に含まれるPGD2の定量には、「PGD2−MOX EIA kits」(Cayman Chemical社)を使用し、ELISA法により測定した。PGD2産生抑制率は、陰性対照に対しての抑制率を計算した。計算式は下記の通りである。この結果を表1に示す。
PGD2産生抑制率(%)=(1−Y/X)×100
X:陰性対照のPGD2
Y:PGD2産生抑制剤又は比較成分添加時のPGD2
A negative control was prepared by culturing in the same manner as described above except that an aqueous solution of DMSO was used instead of the PGD 2 production inhibitor and the comparative component dissolved in DMSO.
For the quantification of PGD 2 contained in the collected culture supernatant, “PGD2-MOX EIA kits” (Cayman Chemical Co.) was used and measured by ELISA. For the PGD 2 production inhibition rate, the inhibition rate relative to the negative control was calculated. The calculation formula is as follows. The results are shown in Table 1.
PGD 2 production inhibition rate (%) = (1−Y / X) × 100
X: PGD 2 amount of negative control Y: PGD 2 production inhibitor or PGD 2 amount when compared components added

(2−2)脱毛抑制作用試験
実施例1〜5のPGD2産生抑制剤及び比較例1の比較成分を用いて、試験用頭髪化粧料として、ヘアトニック、シャンプー及びコンディショナーを以下の組成で調整した。なお、配合量の単位は質量部で、精製水の「残量」とは全量を100質量部とする量である。また、シャンプーにおける、クエン酸25質量%水溶液の適量とはpHを約5.5に調整するのに要する量、塩化ナトリウム10質量%水溶液の適量とは粘度を約1500mPa・sに調整するのに要する量である。
(2-2) Hair loss inhibitory action test Using the PGD 2 production inhibitor of Examples 1 to 5 and the comparative component of Comparative Example 1, hair tonic, shampoo and conditioner were prepared with the following composition as test hair cosmetics. did. The unit of the blending amount is parts by mass, and the “remaining amount” of purified water is an amount that makes the total amount 100 parts by mass. In addition, the appropriate amount of 25% by weight citric acid aqueous solution in shampoo is the amount required to adjust the pH to about 5.5, and the proper amount of 10% sodium chloride aqueous solution is to adjust the viscosity to about 1500 mPa · s. It is a necessary amount.

ヘアトニックの試験を被験者5名で行い、シャンプー及びコンディショナーの試験を被験者5名で行った。被験者は30〜50歳のAGAを発症している男性とした。
3ヶ月間の試験中、ヘアトニックの試験については毎日の入浴後及び朝に頭皮に適量使用してもらい、シャンプー及びコンディショナーの試験については、毎日の入浴時に頭髪に適量使用してもらった。
A hair tonic test was conducted with 5 subjects, and a shampoo and conditioner test was conducted with 5 subjects. The test subject was a male who developed AGA 30 to 50 years old.
During the 3-month study, the hair tonic test was used on the scalp after daily bathing and in the morning, and the shampoo and conditioner test was used on the hair at the daily bathing time.

試験開始前と終了後の3日において、1日1回の洗髪時の抜け毛数を数えた。1日当たりの抜け毛数を3日分の抜け毛数の平均値として算出し、試験開始前の平均抜け毛数に対する終了後の平均抜け毛数の減少率を算出し、下記の評価点基準に従って点数をつけた。次に、各試験の被験者5名の評価点を合計し、以下の判定基準により判定した。その結果を表1に示す。
なお、試験中に皮膚の異常を訴えた者はいなかった。
Three days before and after the start of the test, the number of hair loss at the time of washing once a day was counted. The number of hair loss per day was calculated as the average value of the number of hair loss for 3 days, the reduction rate of the average number of hair loss after the end relative to the average number of hair loss before the start of the test was calculated, and the score was given according to the following evaluation point criteria . Next, the evaluation points of five test subjects in each test were summed up and determined according to the following criteria. The results are shown in Table 1.
No one complained of skin abnormalities during the study.

(i)ヘアトニック
エタノール 40
オレイン酸エチル 1
ポリオキシエチレン(40モル)硬化ヒマシ油 2
メチルパラベン 0.2
精製水 残量
PGD2産生抑制剤又は比較成分 0.01
合計 100

(ii)シャンプー
ポリクオタニウム−7 0.05
ラウリル硫酸ナトリウム 10
ポリオキシエチレン(3モル)ラウリル硫酸ナトリウム 10
コカミドプロピルベタイン 3
コカミドジエタノールアミド 1
精製水 残量
クエン酸25%水溶液 適量
塩化ナトリウム10%水溶液 適量
エタノール 10
プロピレングリコール 3
メチルパラベン 0.2
PGD2産生抑制剤又は比較成分 0.01
合計 100

(iii)コンディショナー
メチルポリシロキサン 3
セタノール 4
ポリオキシエチレン(40モル)モノステアレート 0.3
ベヘニルトリメチルアンモニウムクロリド 2.5
カチオン化グァーガム 0.4
パンテニルヒドロキシプロピルステアルジモニウムクロリド 0.3
メチルパラベン 0.2
精製水 残量
水酸化ナトリウム10%水溶液 0.2
エタノール 10
プロピレングリコール 3
PGD2産生抑制剤又は比較成分 0.01
合計 100
(I) Hair tonic ethanol 40
Ethyl oleate 1
Polyoxyethylene (40 mol) hydrogenated castor oil 2
Methylparaben 0.2
Purified water remaining amount PGD 2 production inhibitor or comparative component 0.01
Total 100

(Ii) Shampoo Polyquaternium-7 0.05
Sodium lauryl sulfate 10
Polyoxyethylene (3 mol) sodium lauryl sulfate 10
Cocamidopropyl betaine 3
Cocamide diethanolamide 1
Purified water Remaining 25% aqueous solution of citric acid Appropriate amount 10% aqueous solution of sodium chloride Appropriate amount Ethanol 10
Propylene glycol 3
Methylparaben 0.2
PGD 2 production inhibitor or comparative component 0.01
Total 100

(Iii) Conditioner Methylpolysiloxane 3
Cetanol 4
Polyoxyethylene (40 mol) monostearate 0.3
Behenyltrimethylammonium chloride 2.5
Cationized guar gum 0.4
Panthenyl hydroxypropyl stearidimonium chloride 0.3
Methylparaben 0.2
Purified water Residual amount Sodium hydroxide 10% aqueous solution 0.2
Ethanol 10
Propylene glycol 3
PGD 2 production inhibitor or comparative component 0.01
Total 100

(評価点基準)
10点:40%以上の減少
8点 :30%以上から40%未満の減少
6点 :20%以上から30%未満の減少
4点 :10%以上から20%未満の減少
2点 :5%以上から10%未満の減少
0点 :5%未満の減少
(判定基準)
1級 :評価点の合計が 46〜50点
2級 :評価点の合計が 41〜45点
3級 :評価点の合計が 36〜40点
4級 :評価点の合計が 31〜35点
5級 :評価点の合計が 26〜30点
6級 :評価点の合計が 21〜25点
7級 :評価点の合計が 16〜20点
8級 :評価点の合計が 11〜15点
9級 :評価点の合計が 6〜11点
10級:評価点の合計が 5点以下
(Evaluation criteria)
10 points: Reduction of 40% or more 8 points: Reduction of 30% or more to less than 40% 6 points: Reduction of 20% or more to less than 30% 4 points: Reduction of 10% or more to less than 20% 2 points: 5% or more Reduction of less than 10% from 0 point: Reduction of less than 5%
1st grade: Total evaluation points 46-50 points 2nd grade: total evaluation points 41-45 points 3rd grade: total evaluation points 36-40 points 4th grade: total evaluation points 31-35 points 5th grade : Total evaluation points 26-30 points 6 grades: Total evaluation points 21-25 points 7 grades: Total evaluation points 16-20 points 8 grades: Total evaluation points 11-15 points 9 grades: Evaluation The total score is 6-11 points, 10th grade: the total score is 5 points or less

(2−3)整肌作用試験
実施例1〜5のPGD2産生抑制剤及び比較例2の比較成分を用いて、試験用皮膚化粧料として化粧水及び乳液を以下の組成で調整した。なお、配合量の単位は質量部で、精製水の「残量」とは全量を100質量部とする量である。
化粧水及び乳液の試験を、25〜50歳の肌荒れを呈する被験者10名(男女各5名)で行った。
(2-3) Skin conditioning effect test Using the PGD 2 production inhibitor of Examples 1 to 5 and the comparative component of Comparative Example 2, skin lotions and emulsions were prepared as test skin cosmetics with the following composition. The unit of the blending amount is parts by mass, and the “remaining amount” of purified water is an amount that makes the total amount 100 parts by mass.
The test of lotion and milky lotion was conducted with 10 subjects (5 men and women) who had rough skin of 25 to 50 years old.

1ヶ月の試験中、被験者に化粧水及び乳液を毎日、朝晩の洗顔後に顔に適量使用してもらい、試験開始前と終了後に被験者の肌を目視及び触感により観察し、開始前と比べ肌荒れが改善した人数を数えた。その結果を表1に示す。
なお、試験中に皮膚の異常を訴えた者はいなかった。
During the 1-month test, subjects were asked to use lotion and milk lotion every day, after morning and evening face washing, and the skin of the subject was visually and tactilely observed before and after the test. The number of people who improved was counted. The results are shown in Table 1.
No one complained of skin abnormalities during the study.

(i)化粧水
1,3−ブチレングリコール 1
グリセリン 2
ペンチレングリコール 1
メチルパラベン 0.2
精製水 残量
PGD2産生抑制剤又は比較成分 0.01
合計 100

(ii)乳液
メチルポリシロキサン 3
セタノール 5
ステアリン酸 3
ワセリン 5
1,3−ブチレングリコール 10
グリセリン 5
メチルパラベン 0.2
精製水 残量
PGD2産生抑制剤又は比較成分 0.01
合計 100
(I) Lotion 1,3-butylene glycol 1
Glycerin 2
Pentylene glycol 1
Methylparaben 0.2
Purified water remaining amount PGD 2 production inhibitor or comparative component 0.01
Total 100

(Ii) Latex Methylpolysiloxane 3
Cetanol 5
Stearic acid 3
Vaseline 5
1,3-butylene glycol 10
Glycerin 5
Methylparaben 0.2
Purified water remaining amount PGD 2 production inhibitor or comparative component 0.01
Total 100

Figure 2015020949
Figure 2015020949

表1に示すように、本発明のPGD2産生抑制剤は優れたPGD2産生抑制効果を示した。
また、表1に示すように、本発明のPGD2産生抑制剤を用いた頭髪化粧料及び皮膚化粧料は、優れた脱毛抑制作用及び整肌作用を有する。
As shown in Table 1, the PGD 2 production inhibitor of the present invention showed an excellent PGD 2 production inhibitory effect.
Moreover, as shown in Table 1, the hair cosmetics and skin cosmetics using the PGD 2 production inhibitor of the present invention have an excellent hair loss inhibiting action and skin conditioning action.

(3)頭髪化粧料
実施例1〜5のPGD2産生抑制剤、製造例1〜6の5α−リダクターゼ活性阻害剤及び比較例1及び比較例3の比較成分を用いて、試験用頭髪化粧料としてヘアトニック(実施例6〜23、比較例3〜12)、シャンプー及びコンディショナー(実施例24〜30)を以下の組成で調整した。各頭髪化粧料におけるPGD2産生抑制剤、5α−リダクターゼ活性阻害剤及び比較成分の配合量を表2〜5に示す。なお、配合量の単位は質量部で、精製水の「残量」とは全量を100質量部とする量である。また、シャンプーにおける、クエン酸25質量%水溶液の適量とはpHを約5.5に調整するのに要する量、塩化ナトリウム10質量%水溶液の適量とは粘度を約1500mPa・sに調整するのに要する量である。
(3) Hair cosmetics Test hair cosmetics using the PGD 2 production inhibitors of Examples 1 to 5, the 5α-reductase activity inhibitors of Production Examples 1 to 6 and the comparative components of Comparative Examples 1 and 3. As a hair tonic (Examples 6 to 23, Comparative Examples 3 to 12), shampoos and conditioners (Examples 24 to 30) were prepared with the following compositions. Tables 2 to 5 show the amounts of the PGD 2 production inhibitor, the 5α-reductase activity inhibitor, and the comparative component in each hair cosmetic composition. The unit of the blending amount is parts by mass, and the “remaining amount” of purified water is an amount that makes the total amount 100 parts by mass. In addition, the appropriate amount of 25% by weight citric acid aqueous solution in shampoo is the amount required to adjust the pH to about 5.5, and the proper amount of 10% sodium chloride aqueous solution is to adjust the viscosity to about 1500 mPa · s. It is a necessary amount.

得られた頭髪化粧料の脱毛抑制作用試験を上記と同様にして行った。その結果を表2〜5に示す。なお、試験中に皮膚の異常を訴えた者はいなかった。
(i)ヘアトニック
エタノール 40
オレイン酸エチル 1
ポリオキシエチレン(40モル)硬化ヒマシ油 2
メチルパラベン 0.2
精製水 残量
PGD2産生抑制剤 表2〜4に記載の量
5α−リダクターゼ活性阻害剤 表2〜4に記載の量
比較成分 表2〜4に記載の量
合計 100

(ii)シャンプー
ポリクオタニウム−7 0.05
ラウリル硫酸ナトリウム 10
ポリオキシエチレン(3モル)ラウリル硫酸ナトリウム 10
コカミドプロピルベタイン 3
コカミドジエタノールアミド 1
精製水 残量
クエン酸25質量%水溶液 適量
塩化ナトリウム10質量%水溶液 適量
エタノール 10
プロピレングリコール 3
メチルパラベン 0.2
PGD2産生抑制剤 表2〜4に記載の量
5α−リダクターゼ活性阻害剤 表2〜4に記載の量
比較成分 表2〜4に記載の量
合計 100

(iii)コンディショナー
メチルポリシロキサン 3
セタノール 4
ポリオキシエチレン(40モル)モノステアレート 0.3
ベヘニルトリメチルアンモニウムクロリド 2.5
カチオン化グァーガム 0.4
パンテニルヒドロキシプロピルステアルジモニウムクロリド 0.3
メチルパラベン 0.2
精製水 残量
水酸化ナトリウム10質量%水溶液 0.2
エタノール 10
プロピレングリコール 3
PGD2産生抑制剤 表5に記載の量
5α−リダクターゼ活性阻害剤 表5に記載の量
比較成分 表5に記載の量
合計 100
The hair loss inhibitory effect test of the obtained hair cosmetic was carried out in the same manner as described above. The results are shown in Tables 2-5. No one complained of skin abnormalities during the study.
(I) Hair tonic ethanol 40
Ethyl oleate 1
Polyoxyethylene (40 mol) hydrogenated castor oil 2
Methylparaben 0.2
Purified water remaining amount PGD 2 production inhibitor Amounts listed in Tables 2-4 5α-reductase activity inhibitors Amounts listed in Tables 2-4 Comparative components Amounts listed in Tables 2-4 Total 100

(Ii) Shampoo Polyquaternium-7 0.05
Sodium lauryl sulfate 10
Polyoxyethylene (3 mol) sodium lauryl sulfate 10
Cocamidopropyl betaine 3
Cocamide diethanolamide 1
Purified water Remaining amount 25% by weight citric acid aqueous solution Appropriate amount Sodium chloride 10% by weight aqueous solution Appropriate amount Ethanol 10
Propylene glycol 3
Methylparaben 0.2
PGD 2 production inhibitor Amounts listed in Tables 2-4 5α-reductase activity inhibitors Amounts listed in Tables 2-4 Comparative components Amounts listed in Tables 2-4 Total 100

(iii) Conditioner Methylpolysiloxane 3
Cetanol 4
Polyoxyethylene (40 mol) monostearate 0.3
Behenyltrimethylammonium chloride 2.5
Cationized guar gum 0.4
Panthenyl hydroxypropyl stearidimonium chloride 0.3
Methylparaben 0.2
Purified water remaining amount Sodium hydroxide 10 mass% aqueous solution 0.2
Ethanol 10
Propylene glycol 3
PGD 2 production inhibitor Amount described in Table 5 5α-reductase activity inhibitor Amount described in Table 5 Comparative component Amount described in Table 5 Total 100

Figure 2015020949
Figure 2015020949

Figure 2015020949
Figure 2015020949

Figure 2015020949
Figure 2015020949

Figure 2015020949
Figure 2015020949

表2〜5に示すように、本発明の頭髪化粧料は優れた脱毛抑制作用を有することが分かった。   As shown in Tables 2 to 5, it was found that the hair cosmetic composition of the present invention has an excellent hair loss inhibiting action.

(4)皮膚化粧料
実施例1〜5のPGD2産生抑制剤、製造例1〜6の5α−リダクターゼ活性阻害剤及び比較例1〜3の比較成分を用いて、試験用皮膚化粧料として、化粧水及び乳液(実施例31〜48、比較例13〜24)を以下の組成で調整した。各皮膚化粧料におけるPGD2産生抑制剤、5α−リダクターゼ活性阻害剤及び比較成分の配合量を表6〜8に示す。なお、配合量の単位は質量部で、精製水の「残量」とは全量を100質量部とする量である。
(4) Skin cosmetics Using the PGD 2 production inhibitors of Examples 1 to 5, the 5α-reductase activity inhibitors of Production Examples 1 to 6 and the comparative components of Comparative Examples 1 to 3, as test skin cosmetics, A lotion and emulsion (Examples 31 to 48, Comparative Examples 13 to 24) were prepared with the following compositions. Tables 6 to 8 show the blending amounts of the PGD 2 production inhibitor, the 5α-reductase activity inhibitor and the comparative component in each skin cosmetic. The unit of the blending amount is parts by mass, and the “remaining amount” of purified water is an amount that makes the total amount 100 parts by mass.

得られた皮膚化粧料の整肌作用試験を上記と同様にして行った。その結果を表6〜8に示す。なお、試験中に皮膚の異常を訴えた者はいなかった。
(i)化粧水
1,3−ブチレングリコール 1
グリセリン 2
ペンチレングリコール 1
メチルパラベン 0.2
精製水 残量
PGD2産生抑制剤 表6〜8に記載の量
5α−リダクターゼ活性阻害剤 表6〜8に記載の量
比較成分 表6〜8に記載の量
合計 100

(ii)乳液
メチルポリシロキサン 3
セタノール 5
ステアリン酸 3
ワセリン 5
1,3−ブチレングリコール 10
グリセリン 5
メチルパラベン 0.2
精製水 残量
PGD2産生抑制剤 表6〜8に記載の量
5α−リダクターゼ活性阻害剤 表6〜8に記載の量
比較成分 表6〜8に記載の量
合計 100
The skin conditioning test of the obtained skin cosmetic was performed in the same manner as described above. The results are shown in Tables 6-8. No one complained of skin abnormalities during the study.
(I) Lotion 1,3-butylene glycol 1
Glycerin 2
Pentylene glycol 1
Methylparaben 0.2
Purified water remaining amount PGD 2 production inhibitor Amounts listed in Tables 6-8 5α-reductase activity inhibitors Amounts listed in Tables 6-8 Comparative components Amounts listed in Tables 6-8 Total 100

(Ii) Latex Methylpolysiloxane 3
Cetanol 5
Stearic acid 3
Vaseline 5
1,3-butylene glycol 10
Glycerin 5
Methylparaben 0.2
Purified water remaining amount PGD 2 production inhibitor Amounts listed in Tables 6-8 5α-reductase activity inhibitors Amounts listed in Tables 6-8 Comparative components Amounts listed in Tables 6-8 Total 100

Figure 2015020949
Figure 2015020949

Figure 2015020949
Figure 2015020949

Figure 2015020949
表6〜8に示すように、本発明の皮膚化粧料は優れた整肌作用を有することが分かった。
Figure 2015020949
As shown to Tables 6-8, it turned out that the skin cosmetics of this invention have the outstanding skin-conditioning effect | action.

本発明のPGD2産生抑制剤は、優れた脱毛抑制作用及び整肌作用を有しており、脱毛や薄毛、中でも特にAGA、肌荒れの予防や改善を目的とした化粧品をはじめとする各種外用剤への利用が可能となる。
また、本発明の頭髪化粧料及び皮膚化粧料は、優れた脱毛抑制作用及び整肌作用を有しており、脱毛や薄毛、中でも特にAGA、肌荒れの予防や改善を図ることができる。
The PGD 2 production inhibitor of the present invention has an excellent hair removal inhibitory action and skin conditioning action, and various external preparations including hair removal and thin hair, especially AGA, cosmetics for the purpose of preventing and improving rough skin. Can be used.
Moreover, the hair cosmetics and skin cosmetics of the present invention have excellent hair removal inhibiting action and skin conditioning action, and can prevent and improve hair loss and thin hair, especially AGA and rough skin.

Claims (5)

ローズマリー抽出物、タイム抽出物、カワラヨモギ抽出物、オウゴン抽出物、ユーカリ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有することを特徴とするPGD2産生抑制剤。 A PGD 2 production inhibitor comprising at least one plant extract selected from the group consisting of a rosemary extract, a thyme extract, a cormorant mugwort extract, an ougon extract, and a eucalyptus extract. 請求項1に記載のPGD2産生抑制剤と5α−リダクターゼ活性阻害剤とを含有することを特徴とする頭髪化粧料。 A hair cosmetic comprising the PGD 2 production inhibitor according to claim 1 and a 5α-reductase activity inhibitor. 請求項1に記載のPGD2産生抑制剤と5α−リダクターゼ活性阻害剤とを含有することを特徴とする含有する皮膚化粧料。 A skin cosmetic composition containing the PGD 2 production inhibitor according to claim 1 and a 5α-reductase activity inhibitor. 前記5α−リダクターゼ活性阻害剤がザクロ抽出物、チョウジ抽出物、オトギリソウ抽出物、グアバ抽出物、セージ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有することを特徴とする請求項2に記載の頭髪化粧料。   The 5α-reductase activity inhibitor contains at least one plant extract selected from the group consisting of pomegranate extract, clove extract, hypericum extract, guava extract, and sage extract. 2. Hair cosmetics according to 2. 前記5α−リダクターゼ活性阻害剤がザクロ抽出物、チョウジ抽出物、オトギリソウ抽出物、グアバ抽出物、セージ抽出物からなる群より選ばれる少なくとも1種の植物抽出物を含有することを特徴とする請求項3に記載の皮膚化粧料。   The 5α-reductase activity inhibitor contains at least one plant extract selected from the group consisting of pomegranate extract, clove extract, hypericum extract, guava extract, and sage extract. 3. A skin cosmetic according to 3.
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