JP3547155B2 - Active oxygen suppressant - Google Patents
Active oxygen suppressant Download PDFInfo
- Publication number
- JP3547155B2 JP3547155B2 JP28500393A JP28500393A JP3547155B2 JP 3547155 B2 JP3547155 B2 JP 3547155B2 JP 28500393 A JP28500393 A JP 28500393A JP 28500393 A JP28500393 A JP 28500393A JP 3547155 B2 JP3547155 B2 JP 3547155B2
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- JP
- Japan
- Prior art keywords
- active oxygen
- extract
- production example
- water
- ethanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- Coloring Foods And Improving Nutritive Qualities (AREA)
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Description
【0001】
【産業上の利用分野】
本発明は化粧品、医薬品、食品等に応用され得る植物由来の人体に安全性のある活性酸素抑制剤に関する。
【0002】
【従来の技術】
トラギア インボルクラタ(Tragia involucrata)は、双子葉植物網、離弁花亜網、ドウダイグサ科の植物でインド、スリランカ、ミャンマー、中国に分布し、スリランカでは低地の荒れ地によく分布する。インドでは発汗、喉頭炎、気管支炎、肺炎、癩病などに利用されている。
【0003】
【発明が解決しようとする課題】
本発明の目的は、天然物で人体に安全であることが分かっており、しかも強い活性酸素抑制作用のある物質で、できれば活性酸素抑制作用以外の効果も発揮するような活性酸素抑制剤を提供することにある。
【0004】
【課題を解決するための手段】
本発明者らは、前記の課題を解決するため、すでに多年にわたって食用に供され、人体に対する安全性が確認されている植物をスクリーニングして調べ、活性酸素抑制剤として利用価値のあるものを検討した。その結果、トラギア インボルクラタの溶媒抽出物が化粧品原料として、或いは医薬部外品として、非常に活性酸素抑制に有効性を有することを見い出した。
【0005】
すなわち、本発明はトラギア インボルクラタ(Tragia involucrata)の溶媒抽出物を含む活性酸素抑制剤である。
【0006】
これらの植物の利用方法としては、水或いは親水性有機溶媒例えば、エタノール、メタノール、アセトン等で抽出する。しかしながら、化粧品、医薬品、食品等の原料の抽出であるから、水或いはエタノール或いはこれの混合溶媒での抽出が好ましいのは当然である。また、場合によっては、グリセリン、1,3ブチレングリコール、プロピレングリコール、等の多価アルコール又は多価アルコールと水との混液も抽出に利用できる。またさらに凍結乾燥して粉体として利用することも利用方法によっては有効である。
【0007】
この物質を他の化粧品原料例えばスクワラン、ホホバ油等の液状油、ミツロウ、セチルアルコール等の固体油、各種の活性剤、グリセリン、1,3ブチレングリコール等の保湿剤や各種薬剤等を添加してさまざまな剤形の化粧料を調製することができる。例えばローション、クリーム、乳液、パック等で目的に応じて利用形態を考えればよい。
【0008】
空気中には酸素があり、これがないと生物(嫌気性のものを除く)は存在しえない。しかし酸素は紫外線や酵素等の影響を受けて活性酸素になる。活性酸素は脂肪酸を酸化し過酸化物を生成させる。生体の生体膜のリン脂質も酸化させ、障害を与える。その上、生成した過酸化物と活性酸素はDNAに損傷を与え、老化を促進するといわれている。この活性酸素は、チロシンからメラニンを作る機構にも影響を与え皮膚の黒化にも関与している。この活性酸素を抑制することは皮膚にとって重要な、言い換えれば化粧料に求められる重要な要素である。
【0009】
【実施例】
以下に実際の利用方法である実施例を記載するが、本発明はこの実施例によって何ら限定されるものではない。本発明及び参考例で使用したアザディラクト インディカ(Azadirachdt indica)、トラギア インボルクラタ(Tragia involucrata)の抽出物の製造例を次に示す。
【0010】
(参考製造例1)
アザディラクト インディカ(Azadirachdt indica)の樹皮(乾燥品)を10gに精製水300mlを加えて3時間加熱する。これを放冷した後濾過後凍結乾燥した。
【0011】
(製造例1)
トラギア インボルクラタ(Tragia involucrata)の全草(乾燥品)を10gにエタノール300mlを加えて時々撹拌しつつ5日間放置した。これを濾過後凍結乾燥した。
【0012】
(製造例2)
トラギア インボルクラタ(Tragia involucrata)の全草(乾燥品)を10gに50%エタノール水溶液300mlを加えて時々撹拌しつつ5日間放置した。これを濾過後凍結乾燥した。
【0013】
(製造例3)
トラギア インボルクラタ(Tragia involucrata)の全草(乾燥品)を10gに精製水300mlを加えて3時間加熱する。これを放冷した後濾過後凍結乾燥した。
【0014】
(実施例1)クリーム (重量%)
A スクワラン 20.0
オリーブ油 2.0
ミンク油 1.0
ホホバ油 5.0
ミツロウ 5.0
セトステアリルアルコール 2.0
グリセリンモノステアレート 1.0
ソルビタンモノステアレート 2.0
製造例1抽出物 1.0
B 精製水 47.9
ポリオキシエチレン(20E.O.)ソルビタンモノステアレート 2.0
ポリオキシエチレン(60E.O.)硬化ヒマシ油 1.0
グリセリン 5.0
1.0%ヒアルロン酸ナトリウム水溶液 5.0
パラオキシ安息香酸メチル 0.1
AとBをそれぞれ計量し、70℃まで加温し、BにAを撹拌しつつ徐々に加えたのち、ゆっくり撹拌しつつ30℃まで冷却した。
【0015】
(実施例2)ローション (重量%)
オリーブ油 0.5
製造例2抽出物 0.5
ポリオキシエチレン(20E.O.)ソルビタンモノステアレート 2.0
ポリオキシエチレン(60E.O.)硬化ヒマシ油 2.0
エタノール 10.0
1.0%ヒアルロン酸ナトリウム水溶液 5.0
精製水 80.0
【0016】
(実施例3)
実施例3は実施例1の製造例1の抽出物を製造例3の抽出物に変え作成したクリーム。
【0017】
(参考例1)
参考例1は実施例2の製造例2の抽出物を参考製造例1の抽出物に変え作成したローション。
【0018】
(活性酸素抑制試験)
活性酸素を抑制する効果を測定する方法は各種あるが、今回以下の方法を利用した。
上の試薬の混合物を2.4ml、検体を0.3ml加えて、キサンチンオキシナーゼ(予め検体を水とし、実験するとき、吸光度が1分当たり0.02前後上昇するように上記のリン酸カリウム緩衝液で調整しておく)液を0.3ml加えて直ちに吸光度(560nm)を測定する。(測定は2分位し、直線性を確認する。)
試算式 阻害率=((A−B)/A)×100
A:検体を水としたときの1分当たりの吸光度の変化
B:検体の1分当たりの吸光度の変化
濃度段階を数段階行い、50%活性酸素生成阻害濃度を探した。検体の作成方法は前記製造例(凍結乾燥品)を適当な濃度の水溶液(溶解しにくい場合はエタノールを加えて溶解したのち精製水を加えて、エバポレートし、エタノールを除去したのち適当な濃度%になるように調製した)とした。その結果を表1に示す。
【0019】
【表1】
【0020】
(使用テスト)
女性4名づつの顔面を左右に分け、一方を実施例、もう一方を比較例として毎日、1回以上使用してもらって、3月後、アンケートした。なお、比較例は実施例より製造例の各種の抽出物を水にかえたものである。(比較例1,2)なお、20名を5班にわけ、下記の表2の試料を使って実験した。
【0021】
【表2】
判定基準は以下のようでこの評点の合計値をもって評価し、その結果をまとめたのが以下の表3である。
実施例の方が非常によい 3
実施例の方がかなりよい 2
実施例の方がややよい 1
差がない 0
比較例の方がややよい −1
比較例の方がかなりよい −2
比較例の方が非常によい −3
【0022】
【表3】
【0023】
【発明の効果】
本発明のトラギア インボルクラタのアルコール、水等の溶媒による抽出物は活性酸素抑制試験、使用テストの結果より明らかなように、極く微量でも活性酸素抑制効果が大きく、化粧品に配合した場合、肌荒れを防止し、肌のつや、肌のはりを保持する効果が大きい。長期にわたり、医薬品として使用されてきており、人体に対する安全性が保証されている。[0001]
[Industrial applications]
TECHNICAL FIELD The present invention relates to a plant-derived active oxygen inhibitor that is safe for the human body and can be applied to cosmetics, pharmaceuticals, foods, and the like.
[0002]
[Prior art]
Tragia involculata is a plant belonging to the dicotyledonous net, the leaf-flowering sub-net and the Euphorbiaceae family in India, Sri Lanka, Myanmar and China. In Sri Lanka, it is widely distributed in lowland wasteland. In India, it is used for sweating, laryngitis, bronchitis, pneumonia, leprosy, etc.
[0003]
[Problems to be solved by the invention]
An object of the present invention is to provide an active oxygen inhibitor which is a natural product, which is known to be safe for the human body, and which has a strong active oxygen suppressing effect, and preferably exerts an effect other than the active oxygen suppressing effect. Is to do.
[0004]
[Means for Solving the Problems]
The present inventors have screened and examined plants that have been used for food for many years and have been confirmed to be safe for the human body to solve the above-mentioned problems, and examined those that are useful as active oxygen inhibitors. did. As a result, the solvent extract of preparative Ragia Inborukura data as a cosmetic raw material, or as a quasi-drug, was found to have efficacy in the very active oxygen inhibited.
[0005]
That is, the present invention is an active oxygen inhibitor containing a solvent extract of preparative Ragia Inborukurata (Tragia involucrata).
[0006]
As a method for utilizing these plants, extraction is performed with water or a hydrophilic organic solvent such as ethanol, methanol, or acetone. However, it is natural that extraction with water, ethanol, or a mixed solvent thereof is preferable because the extraction of raw materials for cosmetics, pharmaceuticals, foods, and the like is performed. In some cases, a polyhydric alcohol such as glycerin, 1,3 butylene glycol, propylene glycol, or a mixture of polyhydric alcohol and water can also be used for extraction. It is also effective to freeze-dry and use it as a powder depending on the method of use.
[0007]
This material is added with other cosmetic ingredients such as liquid oils such as squalane and jojoba oil, solid oils such as beeswax and cetyl alcohol, various activators, humectants such as glycerin and 1,3 butylene glycol, and various chemicals. Various dosage forms of cosmetics can be prepared. For example, a use form may be considered depending on the purpose, such as a lotion, a cream, a milky lotion, and a pack.
[0008]
There is oxygen in the air, without which organisms (except anaerobic ones) cannot exist. However, oxygen becomes active oxygen under the influence of ultraviolet rays and enzymes. Active oxygen oxidizes fatty acids to form peroxides. Phospholipids in biological membranes of living organisms also oxidize and cause damage. In addition, it is said that the generated peroxide and active oxygen damage DNA and accelerate aging. This active oxygen affects the mechanism of producing melanin from tyrosine and is also involved in skin darkening. Suppressing this active oxygen is important for the skin, in other words, an important factor required for cosmetics.
[0009]
【Example】
An embodiment which is an actual use method will be described below, but the present invention is not limited to the embodiment. Production examples of extracts of Azadirachdt indica and Tragia involclata used in the present invention and Reference Examples are shown below.
[0010]
(Reference Production Example 1)
300 g of purified water is added to 10 g of the bark of Azadirachdt indica (dry product), and the mixture is heated for 3 hours. This was allowed to cool, filtered, and lyophilized.
[0011]
(Production Example 1 )
300 ml of ethanol was added to 10 g of the whole plant (dried product) of Tragia involculata, and the mixture was allowed to stand for 5 days with occasional stirring. This was filtered and freeze-dried.
[0012]
(Production Example 2 )
To 10 g of a whole plant (dried product) of Tragia involclata was added 300 ml of a 50% aqueous ethanol solution, and the mixture was allowed to stand for 5 days with occasional stirring. This was filtered and freeze-dried.
[0013]
(Production Example 3 )
300 ml of purified water is added to 10 g of the whole plant (dried product) of Tragia involculata, and the mixture is heated for 3 hours. This was allowed to cool, filtered, and lyophilized.
[0014]
(Example 1 ) Cream (% by weight)
A squalane 20.0
Olive oil 2.0
Mink oil 1.0
Jojoba oil 5.0
Beeswax 5.0
Cetostearyl alcohol 2.0
Glycerin monostearate 1.0
Sorbitan monostearate 2.0
Production Example 1 Extract 1.0
B Purified water 47.9
Polyoxyethylene (20EO) sorbitan monostearate 2.0
Polyoxyethylene (60EO) hydrogenated castor oil 1.0
Glycerin 5.0
1.0% aqueous sodium hyaluronate solution 5.0
Methyl paraoxybenzoate 0.1
A and B were each weighed and heated to 70 ° C., A was gradually added to B with stirring, and then cooled to 30 ° C. with slow stirring.
[0015]
(Example 2 ) Lotion (% by weight)
Olive oil 0.5
Production Example 2 Extract 0.5
Polyoxyethylene (20EO) sorbitan monostearate 2.0
Polyoxyethylene (60EO) hydrogenated castor oil 2.0
Ethanol 10.0
1.0% aqueous sodium hyaluronate solution 5.0
Purified water 80.0
[0016]
(Example 3)
Example 3 is a cream prepared by changing the extract of Production Example 1 of Example 1 to the extract of Production Example 3.
[0017]
(Reference Example 1)
Reference Example 1 is a lotion prepared by changing the extract of Production Example 2 of Example 2 to the extract of Reference Production Example 1.
[0018]
(Active oxygen suppression test)
There are various methods for measuring the effect of suppressing active oxygen, but the following method was used this time.
Add 2.4 ml of the mixture of the above reagents and 0.3 ml of the sample, and add xanthine oxynase (the above-mentioned potassium phosphate so that the absorbance increases by about 0.02 per minute when the sample is made into water before the experiment). Add 0.3 ml of the solution (adjusted with a buffer solution) and immediately measure the absorbance (560 nm). (Measurement is divided into two and linearity is confirmed.)
Trial calculation formula Inhibition rate = ((AB) / A) × 100
A: Change in absorbance per minute when the sample was water B: Change in absorbance per minute of the sample Several steps were performed to find the 50% active oxygen production inhibitory concentration. A sample was prepared by dissolving the above-mentioned production example (freeze-dried product) in an aqueous solution having an appropriate concentration (if it was difficult to dissolve, adding ethanol to the solution, adding purified water, evaporating the solution, removing the ethanol, and then removing an appropriate concentration of Was prepared so that Table 1 shows the results.
[0019]
[Table 1]
[0020]
(Use test)
The face of each of four women was divided into left and right, one was used as an example and the other was used as a comparative example, and used once or more every day. In the comparative examples, various extracts of the production examples were replaced with water from the examples. (Comparative Examples 1 and 2) Twenty people were divided into five groups, and experiments were performed using the samples shown in Table 2 below.
[0021]
[Table 2]
The criterion is as follows, and the evaluation was made based on the total value of the scores, and the results are summarized in Table 3 below.
Example is much better 3
Example is considerably better 2
Example is slightly better 1
No difference 0
Comparative example is slightly better -1
Comparative example is much better -2
Comparative example is much better -3
[0022]
[Table 3]
[0023]
【The invention's effect】
DOO Ragia Inborukura other alcohols, extract with solvents such as water of the present invention the active oxygen inhibition test, as is clear from the results of use tests, large active oxygen inhibitory effect in trace amount, when incorporated in cosmetics, It has a great effect of preventing rough skin and keeping skin shine and skin scalp. It has been used as a pharmaceutical for a long time, and its safety to the human body is guaranteed.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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JP28500393A JP3547155B2 (en) | 1993-11-15 | 1993-11-15 | Active oxygen suppressant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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JP28500393A JP3547155B2 (en) | 1993-11-15 | 1993-11-15 | Active oxygen suppressant |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH07138174A JPH07138174A (en) | 1995-05-30 |
JP3547155B2 true JP3547155B2 (en) | 2004-07-28 |
Family
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Application Number | Title | Priority Date | Filing Date |
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JP28500393A Expired - Fee Related JP3547155B2 (en) | 1993-11-15 | 1993-11-15 | Active oxygen suppressant |
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JP (1) | JP3547155B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP3487619B2 (en) * | 1993-11-17 | 2004-01-19 | 御木本製薬株式会社 | 5α-reductase inhibitor |
US20090181113A1 (en) | 2005-11-28 | 2009-07-16 | Apptec, Inc. | Compositions for the reversal of stratum granulosum in keratinization disorders |
US7666450B2 (en) * | 2007-12-04 | 2010-02-23 | Apptec, Inc. | Herbal compositions for the regression of chronic inflammatory skin disorders |
-
1993
- 1993-11-15 JP JP28500393A patent/JP3547155B2/en not_active Expired - Fee Related
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JPH07138174A (en) | 1995-05-30 |
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