JPH06256151A - Skin cosmetic - Google Patents

Skin cosmetic

Info

Publication number
JPH06256151A
JPH06256151A JP5062520A JP6252093A JPH06256151A JP H06256151 A JPH06256151 A JP H06256151A JP 5062520 A JP5062520 A JP 5062520A JP 6252093 A JP6252093 A JP 6252093A JP H06256151 A JPH06256151 A JP H06256151A
Authority
JP
Japan
Prior art keywords
skin
glabridin
formulation
animal
action
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP5062520A
Other languages
Japanese (ja)
Other versions
JP3195683B2 (en
Inventor
Katsuki Ogawa
克樹 小川
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Maruzen Pharmaceutical Co Ltd
Original Assignee
Maruzen Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Maruzen Pharmaceutical Co Ltd filed Critical Maruzen Pharmaceutical Co Ltd
Priority to JP06252093A priority Critical patent/JP3195683B2/en
Publication of JPH06256151A publication Critical patent/JPH06256151A/en
Application granted granted Critical
Publication of JP3195683B2 publication Critical patent/JP3195683B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To provide a novel skin cosmetic capable of effectively preventing the blacking of skins and excellent also on the point of safety. CONSTITUTION:A skin cosmetic contains glabridin and an animal ingredient (e.g. collagen, placenta extract, conchiolin hydrolysate, elastin, fibronectin, vitronectin) and prevents the generation of inflammations and the production and deposition of skin melanin caused by external irritations such as UV rays due to the synergistic action of the essential ingredients.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、紫外線等の外的刺激で
生じる炎症や皮膚メラニンの生成もしくは沈着を抑制
し、紅斑(日焼け)、皮膚黒化、シミ、ソバカス等を防
止することができる皮膚化粧料に関するものである。
INDUSTRIAL APPLICABILITY The present invention can suppress inflammation caused by external stimuli such as ultraviolet rays and the production or deposition of skin melanin, and prevent erythema (sunburn), skin blackening, spots, freckles and the like. It relates to skin cosmetics.

【0002】[0002]

【従来の技術】皮膚の色が黒くなる過程の最終段階にお
いては、アミノ酸の一種であるチロシンがチロシナーゼ
の作用を受けることによって黒色色素・メラニンを生成
する。そこで、チロシナーゼの働きを阻害する作用を有
する種々の薬剤、たとえばグルタチオン、ビタミンCま
たはその誘導体等を皮膚に塗布することにより、色素の
沈着を防止しようとする試みが従来なされてきた。しか
しながら、これらの薬剤は局所適用における安定性や有
効性の点で、必ずしも満足できるものではない。
2. Description of the Related Art In the final stage of the process of darkening the skin color, tyrosine, which is one of the amino acids, produces the black pigment melanin by the action of tyrosinase. Therefore, it has been conventionally attempted to prevent pigment deposition by applying various agents having an action of inhibiting the action of tyrosinase, such as glutathione, vitamin C or its derivatives, to the skin. However, these drugs are not always satisfactory in terms of stability and effectiveness in topical application.

【0003】これは、チロシナーゼ以外にもメラニンを
生成させる原因や引き金となるもの、たとえば紫外線に
よるメラノサイトの活性化や炎症による種々のケミカル
メディエーターの関与、紫外線により生成する活性酸素
類の関与、更には皮脂過酸化物等の関与が報告されてい
るように、単にチロシナーゼの働きを阻害するだけの薬
剤を塗布してもメラニンの沈着を十分防止することは困
難なためである。
Other than tyrosinase, this causes or triggers the production of melanin, for example, activation of melanocytes by ultraviolet rays, involvement of various chemical mediators due to inflammation, involvement of active oxygen species produced by ultraviolet rays, and further. This is because it is difficult to sufficiently prevent the deposition of melanin even by applying a drug that merely inhibits the action of tyrosinase, as reported in the involvement of sebum peroxide and the like.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的は、上述
のように多くの要因が関与している皮膚黒色化を効果的
に防止することができ、しかも安全性の点でも優れてい
る、新しい皮膚化粧料を提供することにある。
DISCLOSURE OF THE INVENTION The object of the present invention is to effectively prevent skin blackening, which is associated with many factors as described above, and is also excellent in safety. To provide new skin cosmetics.

【0005】[0005]

【課題を解決するための手段】本発明による皮膚化粧料
は、コラーゲン、プラセンターエキス、コンキオリン加
水分解物、エラスチン、フィブロネクチン、およびビト
ロネクチンからなる群から選ばれた動物成分およびグラ
ブリジンを必須の成分として含有することを特徴とし、
これら必須成分の相乗作用により、紫外線等の外的刺激
で生じる炎症や皮膚メラニンの生成・沈着を抑制するも
のである。本発明の皮膚化粧料を構成する有効成分の一
つであるグラブリジンは下記化1の構造式を有する化合
物であって、天然には、甘草の一種である Glycyrrhiza
glabra Linne var. (通称ロシア・アフガン・トルコカ
ンゾウ)に微量含まれている。
Means for Solving the Problems The skin cosmetic according to the present invention has an essential component of animal components selected from the group consisting of collagen, placenta extract, conchiolin hydrolyzate, elastin, fibronectin, and vitronectin and glabridin. Characterized by containing,
The synergistic action of these essential components suppresses inflammation caused by external stimuli such as ultraviolet rays and the production and deposition of skin melanin. Glabridin, which is one of the active ingredients constituting the skin cosmetic of the present invention, is a compound having the structural formula of the following chemical formula 1, and is naturally a kind of licorice Glycyrrhiza
It is contained in a small amount in glabra Linne var. (commonly known as Russian, Afghan and Turkish liquorice).

【0006】[0006]

【化1】 [Chemical 1]

【0007】グラブリジンについては抗菌作用、抗酸化
作用、抗う蝕作用、抗プラスミン作用等の薬理作用を有
することが確認されており、さらに、メラニン生成抑制
作用を有することも知られている(特開平1−3110
11号公報)。しかしながら、従来確認されていたグラ
ブリジンのメラニン生成抑制作用はグラブリジンを単用
した場合のものであって、それを動物成分その他の生理
活性物質と併用した場合の効果は知られていなかった。
It has been confirmed that glabridin has a pharmacological action such as an antibacterial action, an antioxidative action, an anticarious action and an antiplasmin action, and it is also known that it has a melanin production inhibiting action (Japanese Patent Laid-Open No. Hei 10 (1999) -29242) 1-3110
11 publication). However, the previously confirmed melanin production inhibitory action of glabridine is that of glabridine alone, and the effect of using it in combination with animal components and other physiologically active substances has not been known.

【0008】グラブリジンを甘草から抽出して本発明の
化粧料製造原料とする場合は、まず甘草の根部またはそ
の水抽出残渣(たとえばグリチルリチンを抽出した残
渣)を有機溶媒で抽出する。抽出溶媒としては、メタノ
ール、エタノール等の低級脂肪族アルコール;アセトン
等の低級脂肪族ケトン;ジオキサン、エチルエーテル等
のエーテル類;塩化メチレン、クロロホルム等のハロゲ
ン化炭化水素類;酢酸エチル、酢酸プロピル、酢酸ブチ
ル等のエステル類;ヘキサン、ベンゼン等の炭化水素
類;およびこれらの有機溶媒の2種以上の混合物を使用
することができる。
When glabridin is extracted from licorice to be used as a raw material for producing cosmetics of the present invention, first, the root portion of licorice or its water extraction residue (for example, the residue obtained by extracting glycyrrhizin) is extracted with an organic solvent. As the extraction solvent, lower aliphatic alcohols such as methanol and ethanol; lower aliphatic ketones such as acetone; ethers such as dioxane and ethyl ether; halogenated hydrocarbons such as methylene chloride and chloroform; ethyl acetate, propyl acetate, etc. Esters such as butyl acetate; hydrocarbons such as hexane and benzene; and mixtures of two or more of these organic solvents can be used.

【0009】抽出処理する甘草は、約5〜15倍量の上
記溶媒に浸漬し、常温で静置するか還流下に加熱する。
抽出液から溶媒を留去して得られる抽出物は、通常5〜
10%程度のグラブリジンを含有しており、そのまま本
発明の化粧料に使用することもできるが、精製して純度
を高めたものを用いることにより、より使用効果に優れ
且つ着色も少ない化粧料を得ることができる。精製は、
たとえば順相シリカゲルクロマトグラフィーおよび逆相
クロマトグラフィーにより処理したのちアセトンから結
晶化させる方法により行うことができ、この方法によれ
ば、比較的容易にグラブリジンの純品を得ることができ
る。精製は、ほかにも合成吸着体によるカラムクロマト
グラフィーや液−液向流抽出等、任意の有機化合物精製
手段を採用して行うことができる。
The licorice to be extracted is dipped in about 5 to 15 times the amount of the above solvent, and allowed to stand at room temperature or heated under reflux.
The extract obtained by distilling the solvent from the extract is usually 5 to
Although it contains about 10% of glabridin and can be used as it is in the cosmetic of the present invention, the use of a purified and highly purified cosmetic produces a cosmetic with more excellent use effect and less coloring. Obtainable. Purification
For example, it can be carried out by a method in which it is treated by normal phase silica gel chromatography and reverse phase chromatography and then crystallized from acetone. According to this method, a pure product of glabridin can be obtained relatively easily. In addition, the purification can be performed by employing any organic compound purification means such as column chromatography using a synthetic adsorbent or liquid-liquid countercurrent extraction.

【0010】グラブリジンと共に本発明の皮膚化粧料に
含有させる動物成分について説明すると、コラーゲンは
動物の結合組織の主タンパク質であって、通常、牛の皮
や真皮層から製造される。市販されているものには、酸
可溶性コラーゲンおよび加水分解コラーゲンがある。プ
ラセンターエキスは、妊娠早期の牛胎盤の水抽出物を精
製したものであって、核酸関連物質、酵素、アミノ酸、
タンパク質、ビタミン、ミネラル、ムコ多糖などを含有
する。コンキオリン加水分解物は、アコヤ貝の真珠層か
ら得られるタンパク質を酸加水分解したものである。エ
ラスチン、フイブロネクチン、およびビトロネクチン
も、動物の結合組織、繊維芽細胞、体液等より調製され
たタンパク質または糖タンパク質である。これらの動物
成分は、2種以上を本発明の化粧料に含有させてもよ
い。
[0012] Explaining animal components to be contained in the skin cosmetic of the present invention together with glabridin, collagen is a main protein of connective tissue of animals and is usually produced from bovine hide or dermis layer. Commercially available are acid soluble collagen and hydrolyzed collagen. Placenta extract is a purified water extract of bovine placenta in early pregnancy, which contains nucleic acid-related substances, enzymes, amino acids,
Contains proteins, vitamins, minerals, mucopolysaccharides, etc. Conchiolin hydrolyzate is an acid hydrolyzed protein obtained from the pearl layer of pearl oysters. Elastin, fibronectin, and vitronectin are also proteins or glycoproteins prepared from animal connective tissue, fibroblasts, body fluids and the like. Two or more kinds of these animal components may be contained in the cosmetic of the present invention.

【0011】上記動物成分は皮膚保護作用と保湿作用に
優れており、皮膚との生体適合性もきわめて良い。動物
成分の上記作用はグラブリジンの作用と相乗的に作用し
て、好ましい皮膚の維持・形成に役立つ。本発明の皮膚
化粧料におけるグラブリジンの好適配合量は、化粧料の
種類によっても異なるが、通常、約0.001〜10重
量%であり、特に好ましくは約0.01〜1.0重量%で
ある。また、動物成分の好適配合量は約0.0001〜
5重量%であり、特に好ましくは約0.01〜0.5重量
%である。動物成分は、さらにグラブリジンに対して約
1〜500重量%になるように配合することが望まし
い。
The above-mentioned animal components are excellent in skin-protecting action and moisturizing action, and have very good biocompatibility with skin. The above-mentioned action of the animal component acts synergistically with that of glabridin to help maintain and form favorable skin. The suitable blending amount of glabridin in the skin cosmetic of the present invention varies depending on the kind of the cosmetic, but is usually about 0.001 to 10% by weight, particularly preferably about 0.01 to 1.0% by weight. is there. In addition, a suitable amount of animal components is about 0.0001-
It is 5% by weight, particularly preferably about 0.01 to 0.5% by weight. It is desirable that the animal component is further compounded in an amount of about 1 to 500% by weight based on glabridin.

【0012】本発明の化粧料は、グラブリジンと動物成
分の併用によるメラニン生成抑制作用を有利に利用する
ことのできる任意の化粧料、たとえば化粧水、乳液、ク
リーム、パック、石鹸、ボディーシャンプー等の形態を
とることができる。グラブリジンと動物成分以外の化粧
料構成成分、たとえば油脂類、界面活性剤、増粘剤、色
素、香料、防腐剤、エタノール、多価アルコール等は、
その化粧料の種類に応じて、必須2成分の作用を損なわ
ない範囲で任意に選択することができる。
The cosmetics of the present invention include any cosmetics that can advantageously utilize the melanin production-inhibiting action by the combined use of glabridin and animal ingredients, such as lotions, emulsions, creams, packs, soaps, body shampoos and the like. It can take the form. Cosmetic constituents other than glabridine and animal ingredients, such as oils and fats, surfactants, thickeners, pigments, fragrances, preservatives, ethanol, polyhydric alcohols, etc.
Depending on the kind of the cosmetic, it can be arbitrarily selected within a range that does not impair the action of the two essential components.

【0013】[0013]

【実施例】【Example】

〔グラブリジン製造例〕甘草の根部の細切物500gを
5リットルの酢酸エチルに浸漬し、還流下に2時間加熱
して酢酸エチル可溶成分を抽出した。抽出液を分離した
抽出残渣について同様の操作を繰り返し、合計9リット
ルの抽出液を得た。抽出液の溶媒を減圧下に留去し、グ
ラブリジンを含有する抽出物13.1gを得た。次いで
抽出物をクロロホルムに溶解し、シリカゲルにまぶした
のち乾燥した。この乾燥物を、あらかじめシリカゲル
(ワコーゲルC-300,和光純薬工業株式会社製品)1kg
を充填したカラム上に積層充填し、クロロホルム/メタ
ノール混合液(30:1)で溶出し、グラブリジン含有画
分を採取した。この画分の溶媒を減圧下に留去して固形
物5.8gを得たのち、少量のメタノールに溶解し、逆
相シリカゲル(ODSG-3,水戸化学技術研究所製品)にま
ぶして乾燥し、あらかじめ逆相シリカゲル800gを充
填したカラム上に積層充填した。このカラムに、溶出溶
媒として水/アセトニトリル混合液(30/70)を流し、
グラブリジン含有画分を採取した。この画分から溶媒を
減圧下に留去し、得られた固形物(4.3g)をアセト
ン40mlに溶解し、5℃で3日間静置して、グラブリジ
ンの結晶3.8gを得た。以下の各実施例においては、
グラブリジンとして上記精製グラブリジンの結晶を用い
た。
[Preparation example of glabridin] 500 g of licorice root shredded pieces were immersed in 5 liters of ethyl acetate and heated under reflux for 2 hours to extract ethyl acetate-soluble components. The same operation was repeated for the extraction residue obtained by separating the extract, and a total of 9 liters of extract was obtained. The solvent of the extract was distilled off under reduced pressure to obtain 13.1 g of an extract containing glabridin. The extract was then dissolved in chloroform, sprinkled on silica gel and dried. 1 kg of this dried material was previously loaded with silica gel (Wakogel C-300, product of Wako Pure Chemical Industries, Ltd.)
Was stacked and packed on a column packed with, and eluted with a chloroform / methanol mixture (30: 1) to collect a glabridin-containing fraction. The solvent of this fraction was distilled off under reduced pressure to obtain 5.8 g of a solid substance, which was then dissolved in a small amount of methanol, sprinkled with reverse phase silica gel (ODSG-3, product of Mito Chemical Research Laboratory) and dried. , And stacked and packed on a column previously packed with 800 g of reverse phase silica gel. Pour water / acetonitrile mixture (30/70) into this column as elution solvent,
The fraction containing glabridine was collected. The solvent was distilled off from this fraction under reduced pressure, the obtained solid substance (4.3 g) was dissolved in 40 ml of acetone, and the mixture was allowed to stand at 5 ° C. for 3 days to obtain 3.8 g of crystals of glabridin. In each of the following examples,
Crystals of the above purified glabridin were used as glabridin.

【0014】実施例1 表1の処方により、化粧水を製造した。この場合、まず
エタノール/1,3-ブチレングリコール混合液に上記製造
例によるグラブリジン結晶を溶解し、さらに界面活性剤
(モノラウリン酸ポリオキシソルビタン;20EO)、
香料およびパラオキシ安息香酸エステルを加えて溶解し
た後、精製水およびその他の成分を加え、撹拌して均一
化した。
Example 1 A lotion was prepared according to the formulation shown in Table 1. In this case, the glabridin crystals according to the above-mentioned production example are first dissolved in an ethanol / 1,3-butylene glycol mixed solution, and then a surfactant (polyoxysorbitan monolaurate; 20EO),
A perfume and paraoxybenzoic acid ester were added and dissolved, and then purified water and other components were added and stirred to homogenize.

【0015】[0015]

【表1】化粧水処方(単位:重量%) 注:処方3は比較例[Table 1] Lotion formulation (unit:% by weight) Note: Prescription 3 is a comparative example

【0016】次に、上記各化粧水について下記の方法に
より使用効果の試験を行なった。 紅斑抑制効果試験法:褐色モルモットの背部を除毛して
そこにオクソラレンの0.1%溶液を塗布し、30分後
にUVA 1J/cm2を照射した。照射直後、照射部位につ
き2cm×2cm大の5区画を決め、各区画に、 A:上記化粧水そのまま B:上記化粧水の処方1,2からグラブリジンを除いた
化粧水 C:上記化粧水の処方1,2から動物成分を除いた化粧
水 D:上記化粧水の処方1,2からグラブリジンと動物成
分の両方を除いた化粧水 E:処方3の化粧水 のいずれかを塗布し、24時間後の紅斑抑制効果を肉眼
観察により判定した(PUVA処理しない皮膚の色を基
準色とする)。
Next, the use effect of each of the above lotions was tested by the following method. Test method for erythema suppressing effect: The back of a brown guinea pig was shaved, a 0.1% solution of oxsoralen was applied thereto, and after 30 minutes, UVA 1 J / cm 2 was irradiated. Immediately after irradiation, 5 sections of 2 cm × 2 cm size were determined for each irradiation site, and in each section: A: the above lotion as it was B: lotion excluding glabridin from the above lotion formulations 1 and 2 C: above lotion formulation Lotion without animal ingredients from 1, 2 D: Lotion with both glabridin and animal ingredients removed from prescriptions 1 and 2 above E: Apply any of prescription 3 lotions, and after 24 hours The erythema-suppressing effect of was determined by visual observation (using the color of the skin not treated with PUVA as the reference color).

【0017】色素沈着抑制効果試験法:紅斑抑制効果試
験法に準じてPUVA処理した褐色モルモットにつき、
1週間後、色素の沈着が認められた部位を2cm×2cmの
5区画に分け、各区画に、先に示したA〜Eの化粧水の
いずれかを朝夕各1回、10日間連続で塗布し、10日
後の色素沈着抑制効果を肉眼観察により判定した(PU
VA処理しない皮膚の色を基準色とする)。
Pigmentation inhibitory effect test method: According to the erythema inhibitory effect test method, the brown guinea pigs treated with PUVA were tested.
After 1 week, the area where pigmentation was observed was divided into 5 sections of 2 cm x 2 cm, and one of the above-mentioned lotions A to E was applied to each section once every morning and evening for 10 consecutive days. After 10 days, the effect of suppressing pigmentation was judged by visual observation (PU
The standard color is the color of the skin that is not VA-treated).

【0018】その結果を表2および表3に示す。グラブ
リジンおよび動物成分の両方を含有する化粧水を塗布し
た場合をグラブリジンまたは動物成分を除いた化粧水の
塗布例と比較すると、前者は紫外線による紅斑を抑制す
る効果および色素沈着抑制効果のいずれにおいて後者よ
り優れていることがわかった。また、炎症その他の皮膚
障害は観察されなかった。さらに、グラブリジンと動物
成分の代わりにL-アスコルビン酸リン酸マグネシウムの
みを含有させた処方3の化粧水は、本発明の化粧水と比
べて明らかに使用効果が劣っていた。
The results are shown in Tables 2 and 3. Comparing the case of applying lotion containing both glaburidine and animal components with the application example of lotion excluding glabridin or animal components, the former is the latter in both the effect of suppressing erythema due to ultraviolet rays and the effect of suppressing pigmentation. Turns out to be better. In addition, no inflammation or other skin disorders were observed. Furthermore, the lotion of Formulation 3 containing only L-magnesium ascorbate phosphate in place of glabridin and the animal component was obviously inferior in use effect to the lotion of the present invention.

【0019】[0019]

【表2】 化粧水基本処方 紅斑抑制効果 処方1 PUVA処理しない皮膚=A≫C=B>D=E 処方2 PUVA処理しない皮膚=A≫C=B>D=E[Table 2] Skin lotion basic prescription Erythema suppressing effect Prescription 1 Skin not treated with PUVA = A >> C = B> D = E Prescription 2 Skin not treated with PUVA = A >> C = B> D = E

【0020】[0020]

【表3】 化粧水基本処方 色素沈着抑制効果 処方1 PUVA処理しない皮膚=A≫C>B>D 処方2 PUVA処理しない皮膚=A≫C>B≧D[Table 3] Basic lotion formulation Pigmentation suppression effect formulation 1 Skin not treated with PUVA = A >>C>B> D Formula 2 Skin not treated with PUVA = A >>C> B ≧ D

【0021】実施例2 表4の処方によりクリームを製造した。製造に際して
は、まず同表群の原料を70℃で溶解し、原料と混
合した後、78℃にした。次いでこれを、75℃に加熱
した原料へ撹拌しながら徐々に加え、予備乳化を行っ
た。その後ホモジナイザーにかけて乳化を完全に行い、
50℃に冷却後、を添加し、30℃まで冷却した。な
お、処方7は比較例である。
Example 2 A cream was prepared according to the formulation shown in Table 4. At the time of production, the raw materials in the same table group were first melted at 70 ° C., mixed with the raw materials, and then heated to 78 ° C. Next, this was gradually added to the raw material heated to 75 ° C. with stirring to carry out preliminary emulsification. After that, apply a homogenizer to completely emulsify,
After cooling to 50 ° C, was added and cooled to 30 ° C. In addition, the prescription 7 is a comparative example.

【0021】[0021]

【表4】クリーム処方(単位:重量%) (注)界面活性剤A:自己乳化型モノステアリン酸グリ
セリン 界面活性剤B:モノステアリン酸ソルビタン カルボキシビニルポリマー:1%水溶液
[Table 4] Cream prescription (unit:% by weight) (Note) Surfactant A: Self-emulsifying glycerin monostearate Surfactant B: Sorbitan monostearate Carboxyvinyl polymer: 1% aqueous solution

【0022】次に、上記各クリームについて下記の方法
により使用効果の試験を行なった。 色素沈着抑制効果試験法:褐色モルモットの背部を除毛
し、除毛部位を2cm×2cmの区画4区画に分割し、そこ
に、1日当たりUVBを1J/cm2で2日間照射した。4
日後に色素の沈着が認められたので、各区画に A:上記クリームそのまま B:上記クリームの処方からグラブリジンのみを除いた
クリーム C:上記クリームの処方から動物成分を除いたクリーム D:処方7のクリーム のいずれかを、1日1回、10日間連続で塗布し、10
日後に色素沈着抑制効果を肉眼観察により判定した(U
VB処理しない皮膚の色を基準色とする)。
Next, the effect of use of each of the above creams was tested by the following method. Pigmentation suppression effect test method: The back of a brown guinea pig was shaved, and the shaved site was divided into 4 sections of 2 cm x 2 cm, and UVB was irradiated at 1 J / cm 2 for 2 days per day. Four
Since pigment deposition was observed after a day, A: the above cream as it was in each compartment B: a cream obtained by removing only glabridin from the above cream formulation C: a cream obtained by removing animal components from the above cream formulation D: formulation 7 Apply one of the creams once a day for 10 consecutive days and
After a day, the effect of suppressing pigmentation was judged by visual observation (U
The standard color is the color of the skin that is not VB treated).

【0023】紅斑抑制効果試験法:色素沈着抑制効果試
験法に準じてUVB処理した褐色モルモットの背部の各
区画に、先に示したA〜Dのクリームを塗布し、24時
間後に紅斑の抑制効果を肉眼観察により判定した(UV
B処理しない皮膚の色を基準色とする)。その結果を表
5および表6に示す。グラブリジンと動物成分を含有す
るクリームを塗布した場合をグラブリジンまたは動物成
分を除いたクリームの塗布例と比較すると、前者は紫外
線による紅斑抑制効果および色素沈着抑制効果のいずれ
においても後者より優れていることがわかった。また、
炎症その他の皮膚障害は観察されなかった。
Test method for erythema inhibitory effect: According to the test method for pigmentation inhibitory effect, the above-mentioned creams A to D were applied to the respective compartments on the back of UVB-treated brown guinea pigs, and after 24 hours, erythema inhibitory effect. Was judged by visual observation (UV
B: The color of the skin not treated is the standard color). The results are shown in Tables 5 and 6. Comparing the case of applying cream containing glaburidine and animal ingredients to the application example of cream excluding glaburidine or animal ingredients, the former is superior to the latter in both erythema suppressing effect and pigmentation suppressing effect by ultraviolet rays. I understood. Also,
No inflammation or other skin disorders were observed.

【0024】[0024]

【表5】 クリーム基本処方 色素沈着抑制効果 処方4 UVB処理しない皮膚=A≫C>B=D 処方5 UVB処理しない皮膚≧A≫C>B=D 処方6 UVB処理しない皮膚=A≫C>B≧D[Table 5] Cream basic formulation Pigmentation suppressing effect Formulation 4 UVB-untreated skin = A >>C> B = D Formulation 5 UVB-untreated skin ≧ A >>C> B = D Formulation 6 UVB-untreated skin = A >>C> B ≧ D

【0025】[0025]

【表6】 クリーム基本処方 紅斑抑制効果 処方4 UVB処理しない皮膚≧A≫C≧B≫D 処方5 UVB処理しない皮膚≧A≫C≧B≫D 処方6 UVB処理しない皮膚≧A≫C≧B≫D[Table 6] Cream basic formulation Erythema suppressing effect Formulation 4 UVB-untreated skin ≧ A >> C ≧ B >> D Formulation 5 UVB-untreated skin ≧ A >> C ≧ B >> D Formulation 6 UVB-untreated skin ≧ A >> C ≧ B ≫ D

【0026】[0026]

【発明の効果】上述のように、グラブリジンと動物成分
を含有する本発明の化粧料は紫外線による皮膚の炎症お
よび色素沈着を効果的に防止するとともに適度の保湿作
用により肌荒れを防止することができ、好ましくない副
作用も認められない。
As described above, the cosmetic composition of the present invention containing glabridin and animal ingredients can effectively prevent skin inflammation and pigmentation due to ultraviolet rays and can also prevent rough skin due to an appropriate moisturizing effect. No adverse side effects were observed.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 //(A61K 31/35 37:02) 8314−4C ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area // (A61K 31/35 37:02) 8314-4C

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 コラーゲン、プラセンターエキス、コン
キオリン加水分解物、エラスチン、フィブロネクチン、
およびビトロネクチンからなる群から選ばれた動物成分
およびグラブリジンを必須の成分として含有することを
特徴とする皮膚化粧料。
1. Collagen, placenta extract, conchiolin hydrolyzate, elastin, fibronectin,
A skin cosmetic comprising an animal component selected from the group consisting of and vitronectin and glabridin as essential components.
JP06252093A 1993-03-01 1993-03-01 Skin cosmetics Expired - Lifetime JP3195683B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06252093A JP3195683B2 (en) 1993-03-01 1993-03-01 Skin cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06252093A JP3195683B2 (en) 1993-03-01 1993-03-01 Skin cosmetics

Publications (2)

Publication Number Publication Date
JPH06256151A true JPH06256151A (en) 1994-09-13
JP3195683B2 JP3195683B2 (en) 2001-08-06

Family

ID=13202553

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06252093A Expired - Lifetime JP3195683B2 (en) 1993-03-01 1993-03-01 Skin cosmetics

Country Status (1)

Country Link
JP (1) JP3195683B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010105925A (en) * 2008-10-28 2010-05-13 Juntendo Skin keratinization-promoting agent
US8563054B2 (en) 2005-03-15 2013-10-22 Maruzen Pharmaceuticals Co., Ltd. Anti-inflammatory agent
JP2014009212A (en) * 2012-07-02 2014-01-20 Mikimoto Pharmaceut Co Ltd Collagen production promoter
JP2014074016A (en) * 2012-09-13 2014-04-24 Mikimoto Pharmaceut Co Ltd Metallothionein production promoter
JP2014074017A (en) * 2012-09-13 2014-04-24 Mikimoto Pharmaceut Co Ltd ENDOTHELIN-1 INHIBITOR, SCF INHIBITOR, bFGF INHIBITOR, HGF INHIBITOR, WHITENING AGENT AND WHITENING SKIN LOTION
JP2016011288A (en) * 2014-06-03 2016-01-21 御木本製薬株式会社 Pmel17 gene expression inhibitor
JP2016196430A (en) * 2015-04-03 2016-11-24 株式会社ダイセル Composition for external application comprising equol and humectant
JP2018507904A (en) * 2015-03-17 2018-03-22 欧詩漫生物股▲ふん▼有限公司Osm Biology Co., Ltd. A kind of cosmetic composition used for skin whitening and its preparation method

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5976007A (en) * 1982-10-22 1984-04-28 Shiseido Co Ltd Cosmetic
JPS60202806A (en) * 1984-03-26 1985-10-14 Sansho Seiyaku Kk Whitening cosmetic
JPS61155303A (en) * 1984-12-28 1986-07-15 Sansho Seiyaku Kk Skin color-lightening cosmetic
JPH01100113A (en) * 1987-10-12 1989-04-18 Sansho Seiyaku Co Ltd External preparation for skin
JPH01311011A (en) * 1988-06-09 1989-12-15 Maruzen Kasei Co Ltd Melanization inhibitory drug for external use
JPH03200707A (en) * 1989-12-28 1991-09-02 Max Fuakutaa Kk Dermal external agent
JPH0441409A (en) * 1990-06-06 1992-02-12 Nonogawa Shoji Kk Whitening cosmetic
JPH04368315A (en) * 1991-06-12 1992-12-21 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH0517318A (en) * 1991-07-11 1993-01-26 Sunstar Inc Skin beautifying cosmetic
JPH05139952A (en) * 1991-11-22 1993-06-08 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH05194176A (en) * 1992-01-20 1993-08-03 Sunstar Inc Skin-beautifying cosmetic
JPH05201847A (en) * 1992-01-28 1993-08-10 Sunstar Inc Skin-beautifying cosmetic
JPH06211640A (en) * 1993-01-22 1994-08-02 Mikimoto Pharmaceut Co Ltd Active oxygen suppressing agent
JPH06234624A (en) * 1993-02-12 1994-08-23 Maruzen Pharmaceut Co Ltd Skin care cosmetic
JPH06256152A (en) * 1993-03-01 1994-09-13 Maruzen Pharmaceut Co Ltd Skin cosmetic

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5976007A (en) * 1982-10-22 1984-04-28 Shiseido Co Ltd Cosmetic
JPS60202806A (en) * 1984-03-26 1985-10-14 Sansho Seiyaku Kk Whitening cosmetic
JPS61155303A (en) * 1984-12-28 1986-07-15 Sansho Seiyaku Kk Skin color-lightening cosmetic
JPH01100113A (en) * 1987-10-12 1989-04-18 Sansho Seiyaku Co Ltd External preparation for skin
JPH01311011A (en) * 1988-06-09 1989-12-15 Maruzen Kasei Co Ltd Melanization inhibitory drug for external use
JPH03200707A (en) * 1989-12-28 1991-09-02 Max Fuakutaa Kk Dermal external agent
JPH0441409A (en) * 1990-06-06 1992-02-12 Nonogawa Shoji Kk Whitening cosmetic
JPH04368315A (en) * 1991-06-12 1992-12-21 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH0517318A (en) * 1991-07-11 1993-01-26 Sunstar Inc Skin beautifying cosmetic
JPH05139952A (en) * 1991-11-22 1993-06-08 Mikimoto Pharmaceut Co Ltd Cosmetic
JPH05194176A (en) * 1992-01-20 1993-08-03 Sunstar Inc Skin-beautifying cosmetic
JPH05201847A (en) * 1992-01-28 1993-08-10 Sunstar Inc Skin-beautifying cosmetic
JPH06211640A (en) * 1993-01-22 1994-08-02 Mikimoto Pharmaceut Co Ltd Active oxygen suppressing agent
JPH06234624A (en) * 1993-02-12 1994-08-23 Maruzen Pharmaceut Co Ltd Skin care cosmetic
JPH06256152A (en) * 1993-03-01 1994-09-13 Maruzen Pharmaceut Co Ltd Skin cosmetic

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8563054B2 (en) 2005-03-15 2013-10-22 Maruzen Pharmaceuticals Co., Ltd. Anti-inflammatory agent
JP2010105925A (en) * 2008-10-28 2010-05-13 Juntendo Skin keratinization-promoting agent
JP2014009212A (en) * 2012-07-02 2014-01-20 Mikimoto Pharmaceut Co Ltd Collagen production promoter
JP2014074016A (en) * 2012-09-13 2014-04-24 Mikimoto Pharmaceut Co Ltd Metallothionein production promoter
JP2014074017A (en) * 2012-09-13 2014-04-24 Mikimoto Pharmaceut Co Ltd ENDOTHELIN-1 INHIBITOR, SCF INHIBITOR, bFGF INHIBITOR, HGF INHIBITOR, WHITENING AGENT AND WHITENING SKIN LOTION
JP2016011288A (en) * 2014-06-03 2016-01-21 御木本製薬株式会社 Pmel17 gene expression inhibitor
JP2018507904A (en) * 2015-03-17 2018-03-22 欧詩漫生物股▲ふん▼有限公司Osm Biology Co., Ltd. A kind of cosmetic composition used for skin whitening and its preparation method
JP2016196430A (en) * 2015-04-03 2016-11-24 株式会社ダイセル Composition for external application comprising equol and humectant

Also Published As

Publication number Publication date
JP3195683B2 (en) 2001-08-06

Similar Documents

Publication Publication Date Title
JP3195684B2 (en) Skin cosmetics
JP2008143784A (en) Cell growth promoter
JPH05306231A (en) Skin external preparation
JP3091045B2 (en) Skin cosmetics
DE10033717A1 (en) Cosmetic and dermatological preparation for removing sebum
JP2015155394A (en) photoaging inhibitor
JP3195683B2 (en) Skin cosmetics
JP3052104B2 (en) Skin cosmetics
JP3091040B2 (en) Skin cosmetics
JPH06336422A (en) External agent for skin
JP3188021B2 (en) Skin cosmetics
JP2000109417A (en) Cosmetic for improving somber color
WO2002051374A1 (en) Hair growth inhibitors and compositions containing the same
JP4235602B2 (en) Melanin production inhibitor and topical skin preparation
JP6723979B2 (en) Wrinkle improver
JP3317735B2 (en) Skin cosmetics for erythema control and pigmentation control
JPH0873340A (en) Skin external preparation
JP4222973B2 (en) Elastase activity inhibitors and cosmetics
JP3686394B2 (en) Anti-aging agent, Maillard reaction inhibitor, collagenase activity inhibitor and cosmetics for preventing skin aging containing these
JP5155543B2 (en) Endothelin-1 production inhibitor, hexosaminidase release inhibitor, anti-inflammatory / whitening skin preparation, endothelin-1 production inhibition method, and hexosaminidase release inhibition method
JPH07238010A (en) Skin cosmetic
JP3150841B2 (en) External preparation for skin
JP4173719B2 (en) New steroid saponin
JP4309190B2 (en) Topical skin preparation
JP5144048B2 (en) Radical scavenger, antioxidant skin external preparation, and radical scavenging method

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term