JPH09143091A - Composition having active oxygen-scavenging ability - Google Patents

Composition having active oxygen-scavenging ability

Info

Publication number
JPH09143091A
JPH09143091A JP7329473A JP32947395A JPH09143091A JP H09143091 A JPH09143091 A JP H09143091A JP 7329473 A JP7329473 A JP 7329473A JP 32947395 A JP32947395 A JP 32947395A JP H09143091 A JPH09143091 A JP H09143091A
Authority
JP
Japan
Prior art keywords
extract
scavenging ability
active oxygen
composition
water
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
JP7329473A
Other languages
Japanese (ja)
Other versions
JP3128727B2 (en
Inventor
Noriko Takagi
紀子 高木
Toshinari Houjiyou
俊成 寳城
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.)
ARUSOA OUSHIYOU KK
Original Assignee
ARUSOA OUSHIYOU KK
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Priority to JP07329473A priority Critical patent/JP3128727B2/en
Publication of JPH09143091A publication Critical patent/JPH09143091A/en
Application granted granted Critical
Publication of JP3128727B2 publication Critical patent/JP3128727B2/en
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Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a composition having excellent oxygen-scavenging ability, useful for maintaining and recovering human health and capable of being expected to have a wide uses as a raw material for cosmetics, medicines and foods by containing an extract of Rhinacanthus nasuta (L.) Kurz) with water or an organic solvent. SOLUTION: This composition having active oxygen-scavenging ability contains an extract (A) of Rhinacanthus nasuta (L.) Kurz with water or an organic solvent as an effective ingredient. E.g. the component A is obtained by extracting any one of the total plant, leaves, stems, branches, roots of Rhinacanthus nasuta (L.) Kurz or their mixture by using an organic solvent such as ethanol, dimethyl ether, acetone or hexane in normal temperature or in a heated state to obtain an extract, which is purified by filtration, centrifugal precipitation, etc., and distilled off to dryness, lyophilized, etc.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は活性酸素消去能を有する
植物由来の組成物に関する。
FIELD OF THE INVENTION The present invention relates to a plant-derived composition having an active oxygen scavenging ability.

【0002】[0002]

【従来の技術】従来より活性酸素は生体組織に有害な毒
性を有するとされ、皮膚の老化や癌、脳卒中、リュウマ
チその他の様々な疾病を引き起こす重要な原因の一つに
挙げられている(生化学辞典第2版、第699頁、19
91年2月5日、東京化学同人、岩波理化学辞典第3版
増補版、第749頁、1986年2月20日、米国特許
第4022224号公報、特開昭63−79834号公
報)。この活性酸素は、superoxide dis
mutase(SOD)の作用により、その毒性が消去
されることが知られている[Misra,H.P.およ
びFridovich,I.,(1972)J.Bio
l.Chem.247,3170〜3175;Frid
ovich,I.,Advan.Enzymol.4
1,35〜97(1975)]。米国特許第40222
24号公報は、オルゴタイン中にこのSODが含まれて
いることを開示し、さらに特公昭61−29711号公
報は、玄米粉、黄粉(大豆粉)および緑茶粉の混合物に
麹菌を添加したものから、ごま油および大豆油よりなる
植物性混合油にスーパーオキサイド・ディスムターゼを
含有する成分を抽出する方法を提案している。さらに特
公平5−19531号公報は、遠赤外線で焙煎した植物
種子または胚芽に微生物を加えて醗酵させたものに、焙
煎した植物からの植物油を添加してなる活性酸素抑制組
成物を提案している。なお、本公報で例示されている植
物は米、小麦、大麦等の穀物および大豆、とうもろこし
等の豆類である。このように活性酸素の作用を抑制する
ものの提案は種々なされているが、白鶴霊芝の溶媒抽出
物が活性酸素消去能を有することについて開示した例は
見当たらない。
2. Description of the Related Art Conventionally, active oxygen is considered to have harmful toxicity to living tissues, and is one of the important causes of skin aging and cancer, stroke, rheumatism and various other diseases (raw Chemical Dictionary 2nd Edition, page 699, 19
February 5, 1991, Tokyo Kagaku Dojin, Iwanami Physics and Chemistry 3rd Edition, Supplement, page 749, February 20, 1986, U.S. Pat. No. 4,022,224, JP-A-63-79834). This active oxygen is superoxide dis
It is known that its toxicity is eliminated by the action of mutase (SOD) [Misra, H. et al. P. And Fridovich, I .; , (1972) J. Bio
l. Chem. 247, 3170-3175; Frid
ovich, I.D. , Advan. Enzymol. 4
1, 35-97 (1975)]. U.S. Pat. No. 40222
Japanese Patent Publication No. 24 discloses that SOD is contained in orgotine, and Japanese Patent Publication No. 61-29711 discloses a mixture of brown rice flour, yellow flour (soybean flour) and green tea flour to which koji mold is added. , A method of extracting a component containing superoxide dismutase from a vegetable mixed oil consisting of sesame oil and soybean oil has been proposed. Further, JP-B-5-19531 proposes an active oxygen suppressing composition obtained by adding plant oil from a roasted plant to fermented plant seeds or germs roasted by far infrared rays and fermenting them. doing. The plants exemplified in this publication are grains such as rice, wheat, barley and soybeans, and legumes such as corn. Although various proposals have been made to suppress the action of active oxygen as described above, no example has been found which discloses that the solvent extract of Shiratsuru Reishi has the ability to eliminate active oxygen.

【0003】白鶴霊芝(Rhinacanthus nasuta (L.)Ku
rz)は、インド南部デカン高原の原産とされるリナカン
サス属きつねのまご科に属する常緑小低木であり、その
全草(リナカンツス草)は駆虫、消炎、皮膚真菌に対す
る抗菌作用のあることが知られ、主に中国、台湾等にお
いて、また最近では日本国においても漢方薬として用い
られている。なお、この白鶴霊芝はマンネンタケ属(C
anoderma)に属する菌類である霊芝とは全くこ
となる植物である。
White Crane Reishi (Rhinacanthus nasuta (L.) Ku
rz) is an evergreen small shrub belonging to the family Lynacanthus fox, which is said to be native to the Deccan Plateau in southern India, and its whole plant (Linacanthus grass) is known to have antibacterial action against anthelminths, anti-inflammatory and skin fungi. It is used as a Chinese medicine mainly in China, Taiwan, etc., and recently in Japan. In addition, this white crane Reishi is genus Ganoderma (C
Reishi, which is a fungus belonging to anodermma), is a completely different plant.

【0004】[0004]

【発明が解決しようとする課題】本発明者等は、人体に
有害な作用を及ぼす活性酸素に対して消去能を有する素
材につき鋭意研究を行った結果、白鶴霊芝の溶媒抽出物
が優れた活性酸素消去能を有することを見出し、これが
化粧料、医薬、食品等の原料として適用可能であるとの
結論に達して本発明を完成させた。
DISCLOSURE OF THE INVENTION The inventors of the present invention have conducted earnest research on a material having an ability to eliminate active oxygen, which has a harmful effect on the human body. The present invention has been completed by finding that it has an active oxygen scavenging ability and concluding that it can be applied as a raw material for cosmetics, medicines, foods and the like.

【0005】[0005]

【課題を解決するための手段】本発明は、白鶴霊芝の水
および/または有機溶媒抽出物を有効成分とする活性酸
素消去能を有する組成物である。
The present invention is a composition having active oxygen scavenging ability, which contains water and / or an organic solvent extract of Shiratsuru Reishi as an active ingredient.

【0006】本発明に使用する白鶴霊芝は、市販されて
いる生のものもしくは乾燥物で、全草(地上部)あるい
は葉、茎、枝、根の各部分を単独でまたはこれらの2種
以上を適宜混合したものを使用すればよい。
The white crane Reishi used in the present invention is a commercially available raw or dried product, and the whole grass (above ground part) or each part of leaves, stems, branches and roots, or two kinds thereof. A mixture of the above may be used.

【0007】このような白鶴霊芝を溶媒抽出して抽出液
を得るが、抽出に使用する溶媒としては水および有機溶
媒が挙げられ、これらを単独であるいは適当割合で混合
して用いる。これらの水および有機溶媒は常温または加
熱した状態で、もしくは冷却した状態で使用する。使用
する有機溶媒としては、エタノール、メタノール、プロ
パノール、1,3−ブチレングリコール等のアルコール
類、ジメチルエーテル、ジエチルエーテル、メチルエチ
ルエーテル等のエーテル類、アセトン等のケトン類、ベ
ンゼン等のフェノール類、ヘキサン、ヘプタン、流動パ
ラフィン、スクワラン等の炭化水素類、その他が挙げら
れ、これらを単独または2種以上混合して使用すること
ができる。
[0007] The extract of Shiratsuru Reishi as described above is obtained by solvent extraction, and the solvent used for extraction includes water and an organic solvent, which may be used alone or as a mixture in an appropriate ratio. These water and organic solvent are used at room temperature or in a heated state or in a cooled state. Examples of the organic solvent used include alcohols such as ethanol, methanol, propanol and 1,3-butylene glycol, ethers such as dimethyl ether, diethyl ether and methyl ethyl ether, ketones such as acetone, phenols such as benzene and hexane. , Hydrocarbons such as heptane, liquid paraffin, and squalane, and the like, and these can be used alone or in combination of two or more.

【0008】得られる白鶴霊芝の抽出液は、無臭乃至僅
かな芳香、独特のコクのある味を帯びた透明で緑褐色乃
至深い緑色の液体であり、これをそのまま使用してよい
が、好ましくは濾過、遠沈、その他の方法で精製し、さ
らには蒸留等の手段により適度に濃縮して用いる。また
この抽出液をさらに蒸留乾固、凍結乾燥等の手段で処理
して得られる無臭乃至僅かな芳香、独特のコクのある味
を帯びた緑褐色〜深緑色の微粉末として用いることも可
能である。このようにして得られる白鶴霊芝の溶媒抽出
物は、優れた活性酸素消去能を有しているので、皮膚の
老化防止目的で化粧品、活性酸素に起因する各種疾病の
予防、治療のための医薬あるいは健康維持のための食品
等の原料として好適である。 なお、この白鶴霊芝の溶
媒抽出物は、活性酸素消去能を有していることから酸化
防止能をも併せ有することが示唆され、この点でも化粧
品、医薬、食品等への使用に好適である。
[0008] The obtained white crane Reishi extract is a clear, greenish brown to deep green liquid having an odorless or slight fragrance and a unique rich taste, which may be used as it is, but is preferable. Is purified by filtration, centrifugation, or any other method, and is further appropriately concentrated by a means such as distillation before use. It is also possible to use this extract as a fine powder of greenish brown to dark green color which has an odorless to slight aroma and a unique rich taste obtained by further processing by means of distillation to dryness, freeze-drying and the like. is there. Since the solvent extract of Shiratsuru Reishi obtained in this manner has an excellent ability to eliminate active oxygen, cosmetics for the purpose of preventing skin aging, for the prevention and treatment of various diseases caused by active oxygen. It is suitable as a raw material for medicines and foods for maintaining health. It is suggested that the solvent extract of Shiratsuru Reishi has an active oxygen scavenging ability and thus also has an antioxidant ability. In this respect, it is also suitable for use in cosmetics, pharmaceuticals, foods, etc. is there.

【0009】次に本発明の実施例、試験例および応用例
を順に挙げて説明するが、これらは本発明の技術的範囲
を限定するものではない。
Next, examples, test examples and application examples of the present invention will be described in order, but these do not limit the technical scope of the present invention.

【実施例】実施例1 乾燥白鶴霊芝(大協物産有限会社、以下白鶴霊芝の入手
先は全て同じ)の葉および枝3gを100℃の熱水50
0mlに2分間浸漬し、500mlに定容して独特の味
と芳香とを有する透明で緑褐色の抽出液を得た。
Example 1 Dried Hakutsuru Reishi (Daikyo Bussan Co., Ltd., all the same obtainable from White Crane Reishi) leaves and branches (3 g) in hot water at 100 ° C. 50
It was immersed in 0 ml for 2 minutes and adjusted to a volume of 500 ml to obtain a transparent green-brown extract having a unique taste and aroma.

【0010】実施例2 乾燥白鶴霊芝の茎、枝および葉の混合物(全草)3gを
水500mlに浸漬し、100℃に加熱して60分間保
持した後濾過し、得られた濾液を500mlに定容して
独特の味と芳香とを有する透明で緑褐色の抽出液を得
た。
Example 2 3 g of a mixture of dried stems, branches and leaves (whole grass) of dried white crane Reishi was immersed in 500 ml of water, heated at 100 ° C. and kept for 60 minutes and then filtered, and the resulting filtrate was 500 ml. A clear, green-brown extract having a unique taste and aroma was obtained.

【0011】実施例3 乾燥白鶴霊芝の枝3gを水500mlに浸漬し、100
℃に加熱して90分間保持した後濾過し、得られた濾液
を250mlに定容して独特の味と芳香とを有する透明
で緑褐色の抽出液を得た。
Example 3 3 g of dried white crane Reishi twigs were soaked in 500 ml of water to obtain 100
The mixture was heated to 90 ° C. and kept for 90 minutes and then filtered, and the obtained filtrate was adjusted to 250 ml to obtain a transparent green-brown extract having a unique taste and aroma.

【0012】実施例4 抽出例1の抽出残渣を水500mlに浸漬し、100℃
に加熱して60分間保持した後、250mlに定容して
独特の味と芳香とを有する透明で緑褐色の抽出液を得
た。
Example 4 Extraction residue of Extraction Example 1 was immersed in 500 ml of water and heated at 100 ° C.
After heating to 60 ° C. and holding for 60 minutes, the volume was adjusted to 250 ml to obtain a transparent green-brown extract having a unique taste and aroma.

【0013】実施例5 白鶴霊芝全草および根の乾燥混合物を、下記表1に記載
したように調製した検体を各々ティーバックに入れ、熱
湯600mlを注入して1分間振盪し、独特の味と芳香
とを有する透明で緑褐色の抽出液を得た。各原料の配合形態 サンプルNo. 白鶴霊芝(2.0g) A 全原料固形のままブレンドB 全原料グラインド後ブレンド
Example 5 The dried mixture of white shiratsuru ganoderma lucidum and root was prepared in the manner described in Table 1 below and placed in a tea bag. 600 ml of boiling water was poured into the tea bag and shaken for 1 minute to give a unique taste. A transparent, green-brown extract having aroma and aroma was obtained. Mixing form of each raw material Sample No. Shiratsuru Reishi (2.0g) A Blend of all raw materials as solid B Blend of all raw materials after grinding

【0014】実施例6 乾燥白鶴霊芝全草を粉砕機にかけて粉砕し、得られた粉
砕物をアセトン、ベンゼン、1,3−ブチレングリコー
ル、エタノール、エーテルに各々1.00g/50ml
の割合で約24時間浸漬した。次いでこのものを濾過し
て独特の味と芳香とを有する透明で深い緑色の抽出液を
得た。
Example 6 Dried Shiratsuru Reishi grass was crushed by a crusher, and the obtained crushed product was added to acetone, benzene, 1,3-butylene glycol, ethanol and ether, respectively, at 1.00 g / 50 ml.
Was soaked for about 24 hours. It was then filtered to give a clear deep green extract with a unique taste and aroma.

【0015】試験例1 実施例1〜4の方法で抽出した各抽出液を、各々100
%および蒸留水希釈10%濃度としたものをサンプルと
して用いた。スーパーオキサイドは、ヒポキサンチン−
キサンチンオキシダーゼ(hypoxanthin-xanthin oxidas
e) 系により発生させたO を5,5−ジメチル−1
−ピロリン−1−オキシド[5,5-dimethyl-1-pyrroline-
N-oxide(DMPO)]でアダクトし、電子スピン共鳴装
置(ESR)を用いラジカル強度を測定した。コントロ
ールは蒸留水または緩衝液を使用し、これの値を基準に
ラジカル強度の割合と標準偏差(SD)を求めた。試験
結果を表1に示す。白鶴霊芝の溶媒抽出物には高いスー
パーオキサイド消去能があることが明らかである。
Test Example 1 100% of each extract extracted by the method of Examples 1 to 4
% And distilled water diluted to 10% were used as samples. Superoxide is hypoxanthine-
Xanthine oxidas (hypoxanthin-xanthin oxidas
e) O 2 generated by the system is converted to 5,5-dimethyl-1
-Pyrroline-1-oxide [5,5-dimethyl-1-pyrroline-
N-oxide (DMPO)] was adducted, and the radical intensity was measured using an electron spin resonance device (ESR). As a control, distilled water or a buffer solution was used, and the ratio of the radical strength and the standard deviation (SD) were determined based on this value. Table 1 shows the test results. It is clear that the solvent extract of Shiratsuru Reishi has a high superoxide scavenging ability.

【0016】[0016]

【表1】 [Table 1]

【0017】試験例2 実施例1〜4の方法で抽出した各抽出液を凍結乾燥し、
得られた粉末を蒸留水にて適宜希釈したものをサンプル
として用いた他は、試験例1と同様に処理した。 3回
行った試験結果の平均値を表2に示す。試験結果から加
熱抽出法が効率的であることが示唆された。
Test Example 2 Each extract extracted by the method of Examples 1 to 4 was freeze-dried,
The same treatment as in Test Example 1 was performed except that the obtained powder was appropriately diluted with distilled water and used as a sample. Table 2 shows the average values of the results of the tests conducted three times. The test results suggest that the heat extraction method is efficient.

【0018】[0018]

【表2】 [Table 2]

【0019】試験例3 実施例5の方法で抽出したサンプルAおよびBを用い
た。スーパーオキサイドは、ヒポキサンチン−キサンチ
ンオキシダーゼ(hypoxanthin-xanthin oxidase) 系に
より発生させたO を5,5−ジメチル−1−ピロリ
ン−1−オキシド[5,5-dimethyl-1-pyrroline-N-oxide
(DMPO)]でアダクトし、電子スピン共鳴装置(E
SR)を用いラジカル強度を測定した。また、ヒドロキ
シルラジカルはフェントン反応系により発生させた・O
HをDMPOでアダクトし、ESRを用いてラジカル強
度を測定した。コントロールは超純水または緩衝液を使
用し、これの値を基準にラジカル強度の割合と標準偏差
(SD)を求めた。試験結果を表3に示す。スーパーオ
キサイドの消去能では形態の違いによる差は3%程度で
しかなく、60%以上のラジカル消去能を持つため、ど
のサンプルでも強い消去能を持つといえる。またヒドロ
キシラジカルにおいても有効なラジカル消去能を示し
た。
Test Example 3 Samples A and B extracted by the method of Example 5 were used. Superoxide is an O 2 generated by a hypoxanthin-xanthin oxidase system and is capable of generating O 2 5,5-dimethyl-1-pyrroline-1-oxide [5,5-dimethyl-1-pyrroline-N- oxide
(DMPO)] and electron spin resonance device (E
The radical intensity was measured using SR). The hydroxyl radical was generated by the Fenton reaction system.
H was adducted with DMPO, and the radical strength was measured using ESR. As a control, ultrapure water or a buffer solution was used, and the ratio of the radical strength and the standard deviation (SD) were determined based on this value. The test results are shown in Table 3. With respect to the scavenging ability of superoxide, the difference due to the difference in form is only about 3%, and since it has a radical scavenging ability of 60% or more, it can be said that any sample has a strong scavenging ability. It also showed an effective radical scavenging ability for hydroxy radicals.

【0020】[0020]

【表3】 [Table 3]

【0021】試験例4 実施例6の方法で抽出したアセトン、エタノールおよび
エーテルの各抽出液を100%原液とし、これら原液の
他に各溶媒で適宜稀釈したものをサンプルとして1,1
−Diphenyl−2−picrylhydrazy
l(DPPH)ラジカル消去能を測定した。試験はDP
PH0.0012gをエタノール100mlに溶解さ
せ、得られたDPPH溶液0.1mlとサンプル0.1
mlとを反応させたものをESRを用いてラジカル強度
を測定することにより行った。なお、コントロールとし
ては各抽出に用いた溶媒と同じものをそれぞれ使用し
た。試験結果を表4に示す。いずれのサンプルも優れた
DPPHラジカル消去能を有することが明らかである。
Test Example 4 Each of the acetone, ethanol and ether extracts extracted by the method of Example 6 was used as a 100% stock solution, and samples prepared by appropriately diluting these stock solutions with each solvent were 1,1.
-Diphenyl-2-picrylhydrazy
l (DPPH) radical scavenging ability was measured. The test is DP
0.0012 g of PH was dissolved in 100 ml of ethanol, and 0.1 ml of the obtained DPPH solution and sample 0.1
The reaction with ml was carried out by measuring the radical intensity using ESR. The same solvent as that used for each extraction was used as a control. Table 4 shows the test results. It is apparent that all the samples have excellent DPPH radical scavenging ability.

【0022】[0022]

【表4】 [Table 4]

【0023】試験例5 実施例6の方法で抽出したベンゼン抽出液を用い、試験
例1と同様の方法でスーパーオキサイドのラジカル強度
を測定した。なお、抽出に用いたベンゼンは水不溶性の
溶媒であるため、これが完全に除去されるまで放置して
自然蒸発させた後、20mlのエタノールで稀釈した。
このように処理した抽出液を100%原液とし、この原
液の他にエタノールで10%および1%液に稀釈したも
のをサンプルとして使用した。試験結果を表5に示す。
いずれのサンプルもスーパーオキサイド消去能を有する
ことが明らかである。
Test Example 5 Using the benzene extract extracted by the method of Example 6, the radical strength of superoxide was measured in the same manner as in Test Example 1. Since benzene used for extraction is a water-insoluble solvent, it was allowed to stand until it was completely removed and spontaneously evaporated, and then diluted with 20 ml of ethanol.
The extract treated in this way was used as a 100% stock solution, and in addition to this stock solution, a 10% and 1% solution diluted with ethanol was used as a sample. Table 5 shows the test results.
It is clear that all the samples have superoxide scavenging ability.

【0024】[0024]

【表5】 [Table 5]

【0025】試験例6 実施例6の方法で抽出した1,3−ブチレングリコール
の抽出液を用い、試験例1と同様の方法でスーパーオキ
サイドのラジカル強度を測定した。試験結果を表6に示
す。この抽出液もスーパーオキサイド消去能を有するこ
とが明らかである。
Test Example 6 Using the extract of 1,3-butylene glycol extracted by the method of Example 6, the radical strength of superoxide was measured by the same method as in Test Example 1. Table 6 shows the test results. It is clear that this extract also has superoxide scavenging ability.

【0026】[0026]

【表6】 [Table 6]

【0027】応用例1 固形石鹸 下記処方の石鹸用素材を充分混練りした後、口金を50
℃に維持た押出成型機に入れて押出し、型打ち成型機に
かけて固形石鹸を製造した。 処方(重量%) セタノール 10.00 ジブチルヒドロキシトルエン 0.02 実施例1の抽出液 20.0 着色料 微量 天然油脂石鹸ベース(牛脂40%、やし油20%、 NaOH30%、水分10%) 残量
Application Example 1 Solid soap After thoroughly kneading the soap material having the following formulation, the mouthpiece is 50
The solid soap was put into an extrusion molding machine maintained at 0 ° C., extruded, and then subjected to a stamping molding machine to produce solid soap. Formulation (% by weight) Cetanol 10.00 Dibutylhydroxytoluene 0.02 Extract of Example 1 20.0 Colorant Trace amount Natural oil and fat soap base (beef tallow 40%, coconut oil 20%, NaOH 30%, water 10%) Residual amount

【0028】応用例2 乳液 下記処方の乳液用素材を、加温溶解、撹拌乳化、冷却等
常法により処理して乳液を得た。 処方(重量%) モノステアリン酸ポリオキシエチレンソルビタン 1.00 ステアリン酸 0.50 テトラオレイン酸ポリオキシエチレンソルビット 0.50 ベヘニルアルコール 0.50 親油型モノステアリン酸グリセリン 1.00 トリオクタン酸グリセリル 4.00 アボガド油 4.00 アスコルビン酸 0.10 試験例5Bの抽出液 0.015 1,3−ブチレングリコール 5.00 パラオキシ安息香酸エステル 0.20 エデト酸2ナトリウム 0.01 キサンタンガム 0.14 精製水 残量
Application Example 2 Emulsion A milky lotion having the following formulation was treated by a conventional method such as heating dissolution, stirring emulsification and cooling to obtain an emulsion. Formulation (wt%) Polyoxyethylene sorbitan monostearate 1.00 Stearic acid 0.50 Polyoxyethylene sorbit tetraoleate 0.50 Behenyl alcohol 0.50 Lipophilic glyceryl monostearate 1.00 Glyceryl trioctanoate 4.00 Avocado oil 4.00 Ascorbic acid 0.10 Extract of Test Example 5B 0.015 1,3-Butylene glycol 5.00 Paraoxybenzoic acid ester 0.20 Disodium edetate 0.01 Xanthan gum 0.14 Purified water remaining

【0029】応用例3 オレンジジュース オレンジを搾って得た汁液95ccに、実施例6の方法
でエタノール溶媒を用いて得られた抽出液5ccを混合
してオレンジジュースを得た。
Application Example 3 Orange Juice 95 cc of juice obtained by squeezing orange was mixed with 5 cc of the extract obtained by using the ethanol solvent in the method of Example 6 to obtain orange juice.

【0030】応用例4 ビタミン剤 ビタミンA、B、CおよびDの各粉末1kgおよ
びカルボキシメチルセルロース(CMC)500gに実
施例6の方法でエタノール溶媒を用いて得られた抽出液
を蒸発乾固させて得た粉末500gを混合したものを打
錠機にかけてビタミン剤を製造した。
Application Example 4 Vitamin A vitamin B, B 1 B 2 , C and D powder (1 kg) and carboxymethyl cellulose (CMC) (500 g) obtained by the method of Example 6 using the ethanol solvent were evaporated to dryness. A mixture of 500 g of the powder obtained by solidifying was put into a tableting machine to produce a vitamin preparation.

【0031】応用例5 注射液 実施例2で得られた抽出液の凍結乾燥粉末10mgを充
分にエタノールで洗浄、殺菌し、乾燥させた粉末を生理
食塩水1ccに混合して注射薬を製造した。
Application Example 5 Injectable Solution 10 mg of the freeze-dried powder of the extract obtained in Example 2 was thoroughly washed with ethanol, sterilized, and the dried powder was mixed with 1 cc of physiological saline to prepare an injectable drug. .

【0032】[0032]

【発明の効果】本発明組成物は優れた活性酸素消去能を
有しており、人の健康維持、回復に有用なものである。
従って本発明組成物は、化粧品、医薬および食品の原料
としての広範な用途が期待される汎用性の高い製品であ
る。
The composition of the present invention has an excellent ability to eliminate active oxygen and is useful for maintaining and recovering human health.
Therefore, the composition of the present invention is a highly versatile product that is expected to have a wide range of uses as a raw material for cosmetics, pharmaceuticals, and foods.

─────────────────────────────────────────────────────
────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成8年1月24日[Submission date] January 24, 1996

【手続補正1】[Procedure amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】特許請求の範囲[Correction target item name] Claims

【補正方法】変更[Correction method] Change

【補正内容】[Correction contents]

【特許請求の範囲】[Claims]

【手続補正2】[Procedure amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0005[Correction target item name] 0005

【補正方法】変更[Correction method] Change

【補正内容】[Correction contents]

【0005】[0005]

【課題を解決するための手段】本発明は、白鶴霊芝の水
および/または有機溶媒抽出物およびこれを有効成分と
する活性酸素消去能を有する組成物である。
The present invention is a water and / or organic solvent extract of Shiratsuru Reishi, and a composition having the active oxygen scavenging ability containing this extract as an active ingredient.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 白鶴霊芝の水および/または有機溶媒抽
出物を有効成分とする活性酸素消去能を有する組成物。
1. A composition having active oxygen scavenging ability, which comprises, as an active ingredient, a water and / or organic solvent extract of Shiratsuru Reishi.
JP07329473A 1995-11-27 1995-11-27 Active oxygen scavenger Expired - Fee Related JP3128727B2 (en)

Priority Applications (1)

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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP07329473A JP3128727B2 (en) 1995-11-27 1995-11-27 Active oxygen scavenger

Publications (2)

Publication Number Publication Date
JPH09143091A true JPH09143091A (en) 1997-06-03
JP3128727B2 JP3128727B2 (en) 2001-01-29

Family

ID=18221777

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3128727B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010090088A (en) * 2008-10-10 2010-04-22 Arsoa Honsya Corp Collagen production promoter, cosmetic having collagen production-promoting effect, and food and drink for cosmetological use
JP2023028872A (en) * 2021-08-20 2023-03-03 株式会社アルソア慧央グループ METHOD FOR PRODUCING AGING-RELATED IL-1β BLOOD CONCENTRATION RISE INHIBITOR FOR ORAL INGESTION

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11161642B2 (en) 2014-08-11 2021-11-02 Avery Dennison Retail Information Services, Llc Fastener assembly
US11465795B2 (en) 2017-04-14 2022-10-11 Avery Dennison Corporation Automation for plastic disc

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010090088A (en) * 2008-10-10 2010-04-22 Arsoa Honsya Corp Collagen production promoter, cosmetic having collagen production-promoting effect, and food and drink for cosmetological use
JP2023028872A (en) * 2021-08-20 2023-03-03 株式会社アルソア慧央グループ METHOD FOR PRODUCING AGING-RELATED IL-1β BLOOD CONCENTRATION RISE INHIBITOR FOR ORAL INGESTION

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