JPH108049A - Antioxidant composition - Google Patents

Antioxidant composition

Info

Publication number
JPH108049A
JPH108049A JP8164934A JP16493496A JPH108049A JP H108049 A JPH108049 A JP H108049A JP 8164934 A JP8164934 A JP 8164934A JP 16493496 A JP16493496 A JP 16493496A JP H108049 A JPH108049 A JP H108049A
Authority
JP
Japan
Prior art keywords
extract
antioxidant
water
present
antioxidant composition
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.)
Withdrawn
Application number
JP8164934A
Other languages
Japanese (ja)
Inventor
Yoshihiro Yokogawa
佳浩 横川
Kunihiko Yoshida
邦彦 吉田
Norihisa Maeda
憲寿 前田
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.)
Shiseido Co Ltd
Original Assignee
Shiseido 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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP8164934A priority Critical patent/JPH108049A/en
Publication of JPH108049A publication Critical patent/JPH108049A/en
Withdrawn legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain the subject new composition useful as a raw material for foods, cosmetics, medicines, etc., high in effects as antioxidant and safety, free from problems of toxicity, comprising an extract of a specific natural substance. SOLUTION: This composition comprises preferably 0.005-20.0wt.%, calculated as a dried substance in the whole amount of external preparation, of an extract of one or more of Houttuynia cordata Thunb., peppermint, Cassia tora and Lentinus edodes. The extract is obtained, for example, by immersing the whole plant of one or more of Houttuynia cordata Thusnb., pappermint, Cassia tora and Lentinus edodes in an extracting solvent such as water or methanol or heating under reflux, filtering and concentrating, 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、新規にして、かつ優れ
た抗酸化作用を有する天然系の抗酸化剤組成物に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel antioxidant composition having a novel and excellent antioxidant action.

【0002】[0002]

【従来の技術】従来、油脂を含む食品や化粧品の抗酸化
剤としてジブチルヒドロキシトルエン(BHT)、ブチ
ルヒドロキシアニソール(BHA)、トコフェロールな
どが使用されている。しかしながら、BHT、BHAな
どの合成抗酸化剤は、安全性上の問題があり、添加量等
が制限されている。そのため天然系の抗酸化剤が望まれ
ていた。
2. Description of the Related Art Hitherto, dibutylhydroxytoluene (BHT), butylhydroxyanisole (BHA), tocopherol and the like have been used as antioxidants for foods and cosmetics containing oils and fats. However, synthetic antioxidants such as BHT and BHA have safety problems, and the amount added is limited. Therefore, natural antioxidants have been desired.

【0003】[0003]

【発明が解決しようとする課題】本発明はこのような従
来の事情に対処してなされたもので、抗酸化剤としての
効果が高く、かつ毒性上の問題がなく、食品や化粧品、
医薬品原料等としても用いることのできる安全性の高い
抗酸化剤組成物を提供することを目的とする。
DISCLOSURE OF THE INVENTION The present invention has been made in view of such a conventional situation, and has a high effect as an antioxidant and has no toxicity problem.
It is an object of the present invention to provide a highly safe antioxidant composition that can be used as a raw material for pharmaceuticals and the like.

【0004】[0004]

【課題を解決するための手段】本発明は、上記目的を達
成するため、天然物の抗酸化活性剤を鋭意検討した結
果、ジュウヤク(学術名:Houttuynia cordata)、ハッ
カ、ケツメイシ(学術名:Cassia tora 又は Cassia ob
tusifolia)、シイタケのいずれか1種もしくは2種以
上の抽出物を配合した組成物が抗酸化剤として有効であ
り、効果的であることを見いだした。
Means for Solving the Problems In order to achieve the above object, the present invention has made intensive studies on antioxidant activators of natural products. As a result, Juyak (scientific name: Houttuynia cordata), mentha, and beetle (scientific name: Cassia) tora or Cassia ob
tusifolia) and a composition containing one or more extracts of shiitake mushrooms were found to be effective and effective as antioxidants.

【0005】即ち、本発明は、ジュウヤク、ハッカ、ケ
ツメイシ、シイタケのいずれか1種もしくは2種以上の
抽出物を配合してなることを特徴とする抗酸化剤組成物
である。
[0005] That is, the present invention is an antioxidant composition comprising an extract of one or more of at least one of the following:

【0006】[0006]

【発明の実施の形態】以下、本発明の構成について詳述
する。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The configuration of the present invention will be described below in detail.

【0007】本発明に用いられる抽出物は上記、葉、茎
または果実等、ジュウヤク、ハッカ、ケツメイシ、シイ
タケのいずれか1種もしくは2種以上の全草を抽出溶媒
と共に浸漬または加熱還流した後、濾過し、濃縮して得
られる。
[0007] The extract used in the present invention is prepared by immersing or heating the above-mentioned leaves, stems or fruits, etc., of one or more whole plants of jujuya, mentha, katsumeishi and shiitake mushrooms together with an extraction solvent, or heating and refluxing. It is obtained by filtration and concentration.

【0008】本発明に用いられる抽出溶媒は、通常抽出
に用いられる溶媒であれば何でもよく、特に、水、メタ
ノール、エタノール等の含水アルコール類、アセトン、
酢酸エチルエステル等の有機溶媒を単独あるいは組み合
わせて用いることができる。
[0008] The extraction solvent used in the present invention may be any solvent as long as it is a solvent usually used for extraction. In particular, water, aqueous alcohols such as methanol and ethanol, acetone, and the like.
Organic solvents such as ethyl acetate can be used alone or in combination.

【0009】本発明におけるジュウヤク、ハッカ、ケツ
メイシ、シイタケのいずれか1種もしくは2種以上の配
合量は、外用剤全量中、乾燥物として、0.001〜2
0.0重量%が好ましい。
[0009] In the present invention, the amount of any one or more of jujuya, peppermint, beetroot, and shiitake mushroom is 0.001 to 2 as a dry matter in the total amount of the external preparation.
0.0% by weight is preferred.

【0010】0.001重量%未満とすると、抗酸化力
が不十分となることがあり、また、20.0重量%を越
えると、臭いが生じて使用性が悪くなることがある。
If the amount is less than 0.001% by weight, the antioxidant power may be insufficient, and if it exceeds 20.0% by weight, odor may be generated and the usability may be deteriorated.

【0011】また、本発明の抗酸化剤組成物は、上記必
須成分以外に、通常化粧品や医薬品等の皮膚外用剤に用
いられる成分、例えば、その他の美白剤、保湿剤、酸化
防止剤、油性成分、紫外線吸収剤、界面活性剤、増粘
剤、アルコール類、粉末成分、色材、水性成分、水、各
種皮膚栄養剤等を必要に応じて適宜配合することができ
る。
The antioxidant composition of the present invention may contain, in addition to the above essential components, components usually used for external preparations for skin such as cosmetics and pharmaceuticals, for example, other whitening agents, moisturizing agents, antioxidants, and oily agents. Components, ultraviolet absorbers, surfactants, thickeners, alcohols, powder components, coloring materials, aqueous components, water, various skin nutrients, and the like can be appropriately added as necessary.

【0012】その他、エデト酸二ナトリウム、エデト酸
三ナトリウム、クエン酸ナトリウム、ポリリン酸ナトリ
ウム、メタリン酸ナトリウム、グルコン酸等の金属封鎖
剤、カフェイン、タンニン、ベラパミル、トラネキサム
酸およびその誘導体、甘草抽出物、グラブリジン、火朿
の果実の熱水抽出物、各種生薬、酢酸トコフェロール、
グリチルリチン酸およびその誘導体またはその塩等の薬
剤、ビタミンC、アスコルビン酸リン酸マグネシウム、
アスコルビン酸グリコシド、アルブチン、コウジ酸等の
美白剤、グルコース、フルトース、マンノース、ショ
糖、トレハロース等の糖類等も適宜配合することができ
る。
In addition, sequestering agents such as disodium edetate, trisodium edetate, sodium citrate, sodium polyphosphate, sodium metaphosphate, gluconic acid, caffeine, tannin, verapamil, tranexamic acid and derivatives thereof, and licorice extract Products, glabridine, hot water extract of Hikaru fruit, various crude drugs, tocopherol acetate,
Drugs such as glycyrrhizic acid and its derivatives or salts thereof, vitamin C, magnesium ascorbate phosphate,
Whitening agents such as ascorbic acid glycoside, arbutin and kojic acid, and sugars such as glucose, fructose, mannose, sucrose, trehalose and the like can also be appropriately blended.

【0013】本発明の抗酸化剤組成物は皮膚外用剤とし
て用いることができるが、例えば、軟膏、クリーム、乳
液、ローション、パック、浴用剤等、従来皮膚外用剤に
用いるものであればいずれでもよく、剤型は特に制限し
ない。
The antioxidant composition of the present invention can be used as an external preparation for skin. For example, any antioxidant composition which is conventionally used for external preparations such as ointments, creams, emulsions, lotions, packs and bath preparations can be used. The dosage form is not particularly limited.

【0014】本発明の組成物を用いれば、酸化安定性が
悪く配合が困難とされていた物質であっても安定に系中
に配合できる。例えば、化粧品に応用するとエモリエン
ト効果等が期待される、タートル油、ミンク油等は酸化
安定性が悪く、その利用には制限があったが、これらの
油脂を配合した化粧品に、本発明のジュウヤク、ハッ
カ、ケツメイシ、シイタケのいずれか1種もしくは2種
以上の抽出物を配合した組成物を添加することによっ
て、油脂を酸化から防ぐことができ、これらの油脂を化
粧品中に有効に配合することができる。
By using the composition of the present invention, even a substance which has been considered difficult to be compounded due to poor oxidation stability can be stably compounded in the system. For example, turtle oil, mink oil, and the like, which are expected to have an emollient effect when applied to cosmetics, have poor oxidative stability, and their use is restricted. By adding a composition containing one or two or more extracts of mint, mint, shiitake mushroom, oils and fats can be prevented from being oxidized, and these oils and fats can be effectively incorporated into cosmetics. Can be.

【0015】また、最近は生体系における脂質過酸化防
止を目的として、抗酸化剤適用の提案もされているが、
本発明の組成物も当然のことながら生体系への利用が可
能である。
[0015] Recently, application of antioxidants has been proposed for the purpose of preventing lipid peroxidation in biological systems.
The composition of the present invention can of course be used for biological systems.

【0016】(実験例1)ヒドロキシラジカルの消去活
性 本発明の組成物及び比較サンプルをヒドロキシラジカル
の消去活性により抗酸化性の評価試験を行った。試験方
法は以下の通りである。
(Experimental Example 1) Hydroxyl Radical Scavenging Activity The composition of the present invention and a comparative sample were subjected to an antioxidant evaluation test based on hydroxy radical scavenging activity. The test method is as follows.

【0017】1mMの硫酸鉄(II)(FeSO4)5
0μlと試料75μlの混合液に、5,5−ジメチル−
1−ピロリン−オキサイド(DMPO)の10%水溶液
20μlを加え、続いて1mM過酸化水素(H22)7
5μlを加え攪拌した。H22を添加してから75秒後
に発生したヒドロキシラジカル(・OH)のラジカル付
加体(DMPO−OH)を電子スピン共鳴装置(ES
R)を用いて測定した。なお、ヒドロキシラジカルの消
去活性は、蒸留水のヒドロキシラジカルの消去活性を0
%として求めた。
1 mM iron (II) sulfate (FeSO 4 ) 5
In a mixture of 0 μl and 75 μl of sample, 5,5-dimethyl-
20 μl of a 10% aqueous solution of 1-pyrroline-oxide (DMPO) was added, followed by 1 mM hydrogen peroxide (H 2 O 2 ) 7.
5 μl was added and stirred. A radical adduct (DMPO-OH) of a hydroxy radical (.OH) generated 75 seconds after the addition of H 2 O 2 was analyzed by an electron spin resonance apparatus (ES).
R). In addition, the elimination activity of the hydroxy radical is 0.
%.

【0018】[0018]

【表1】 ヒドロキシラジカル消去活性 (1)サンプル コントロール(水) 0% カノコソウの水抽出物 (10mg/ml) 8% ギムネマの水抽出物 (10mg/ml) 23% (2)本発明 ジュウヤクの水抽出物 (10mg/ml) 87% ハッカの水抽出物 (10mg/ml) 82% ケツメイシの水抽出物 (10mg/ml) 77% シイタケの水抽出物 (10mg/ml) 77% 上記の通り本発明に係る(2)ジュウヤク、ハッカ、ケ
ツメイシ、シイタケの抽出物は、(1)サンプルと比較
しヒドロキシラジカル消去活性に優れており、抗酸化力
が強いことがわかった。
Table 1 Hydroxy radical scavenging activity (1) Sample control (water) 0% Aqueous extract of valerian (10 mg / ml) 8% Aqueous extract of gymnema (10 mg / ml) 23% (2) Water of the present invention Extract (10 mg / ml) 87% Water extract of mentha (10 mg / ml) 82% Water extract of Katsumeishi (10 mg / ml) 77% Water extract of shiitake mushroom (10 mg / ml) 77% As described above, the present invention It was found that the extract of (2) Jujuya, mentha, beetroot, and shiitake mushrooms according to (1) had excellent hydroxy radical scavenging activity and strong antioxidant power as compared with (1) the sample.

【0019】[0019]

【実施例】以下に実施例によって、本発明を更に具体的
に説明するが、本発明はこの実施例に限定されるもので
はない。
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples.

【0020】 (実施例1)乳液 ステアリン酸 2.5(重量%) セチルアルコール 1.5 ワセリン 5.0 流動パラフィン 7.0 タートル油 3.0 ポリオキシエチレン(10モル) モノオレイン酸エステル 2.0 ポリエチレングリコール1500 3.0 トリエタノールアミン 1.0 シイタケ水抽出物 0.01 香料 適量 防腐剤 適量 精製水 残余 (製法)イオン交換水にポリエチレングリコール150
0とトリエタノールアミンとを加え、加熱溶解して70
℃に保つ(水相)。他の成分を混合し、加熱融解して7
0℃に保つ(油相)。油相を撹拌しながらこれに水相を
徐々に加えホモミキサーで均一に乳化した。乳化後撹拌
しながら30℃まで冷却した。
(Example 1) Emulsion Stearic acid 2.5 (% by weight) Cetyl alcohol 1.5 Vaseline 5.0 Liquid paraffin 7.0 Turtle oil 3.0 Polyoxyethylene (10 mol) monooleate 0 Polyethylene glycol 1500 3.0 Triethanolamine 1.0 Shiitake mushroom water extract 0.01 Perfume proper amount Preservative proper amount Purified water residue (Production method) Polyethylene glycol 150 in ion exchange water
0 and triethanolamine, and heat and dissolve.
Keep at ° C (aqueous phase). Mix other ingredients, heat and melt.
Keep at 0 ° C. (oil phase). The aqueous phase was gradually added to the oil phase while stirring, and the mixture was uniformly emulsified with a homomixer. After the emulsification, the mixture was cooled to 30 ° C. while stirring.

【0021】 (実施例2)クリーム ミツロウ 10.0(重量%) セチルアルコール 5.0 水添ラノリン 5.0 スクワラン 37.5 ミンク油 3.0 グリセリルモノステアリン酸エステル 2.0 ポリオキシエチレン(20モル) ソルビタンモノラウリン酸エステル 2.0 プロピレングリコール 5.0 ケツメイシ水抽出物 0.01 香料 適量 防腐剤 適量 精製水 残余 (製法)イオン交換水にプロピレングリコールとケツメ
イシ水抽出物とを加え、加熱して70℃に保つ(水
相)。他の成分を混合し、加熱融解して70℃に保つ
(油相)。水相に油相を加え予備乳化を行い、ホモミキ
サーで均一に乳化した後、撹拌しながら30℃まで冷却
した。
Example 2 Cream Beeswax 10.0 (wt%) Cetyl Alcohol 5.0 Hydrogenated Lanolin 5.0 Squalane 37.5 Mink Oil 3.0 Glyceryl Monostearate 2.0 Polyoxyethylene (20 Mol) Sorbitan monolaurate 2.0 Propylene glycol 5.0 Water extract 0.01 Perfume Appropriate amount Preservative Appropriate amount Purified water residue (Production method) Add propylene glycol and water extract to ion-exchanged water and heat. Keep at 70 ° C. (aqueous phase). The other components are mixed, heated and melted and kept at 70 ° C. (oil phase). The oil phase was added to the water phase to carry out preliminary emulsification, and after uniform emulsification with a homomixer, the mixture was cooled to 30 ° C. with stirring.

【0022】 (実施例3)クリーム セトステアリルアルコール 3.5(重量%) スクワラン 40.0 ミツロウ 3.0 還元ラノリン 5.0 エチルパラベン 0.3 ポリオキシエチレン(20モル) ソルビタンモノパルミチン酸エステル 2.0 ステアリン酸モノグリコシド 2.0 ハッカ30%エタノール抽出物 0.01 香料 0.03 1,3−ブチレングリコール 5.0 グリセリン 5.0 ヒアルロン酸ナトリウム 0.05 精製水 残余 (製法)イオン交換水に1,3−ブチレングリコールを
加え加熱して70℃に保つ(水相)。他の成分を配合し
て加熱融解して70℃に保つ(油相)。水相に油相を加
え予備乳化を行い、ホモミキサーで均一に乳化した後、
撹拌しながら30℃まで冷却した。
Example 3 Cream Cetostearyl Alcohol 3.5 (wt%) Squalane 40.0 Beeswax 3.0 Reduced Lanolin 5.0 Ethyl Paraben 0.3 Polyoxyethylene (20 mol) Sorbitan Monopalmitate 2 2.0 Monoglycoside stearic acid 2.0 Mint extract 30% ethanol 0.01 0.01 Fragrance 0.03 1,3-butylene glycol 5.0 Glycerin 5.0 Sodium hyaluronate 0.05 Purified water Residue (Preparation method) Ion exchange water 1,3-butylene glycol is added to the mixture and heated to 70 ° C. (aqueous phase). The other components are blended, heated and melted and kept at 70 ° C. (oil phase). After adding the oil phase to the water phase and pre-emulsifying and homogenizing with a homomixer,
Cool to 30 ° C. with stirring.

【0023】 (実施例4)乳液 シイタケ50%エタノール抽出物 0.02(重量%) ジュウヤク水抽出物 0.01 ステアリン酸 1.5 セチルアルコール 0.5 ミツロウ 2.0 ポリオキシエチレン(10モル) モノオレイン酸エステル 1.0 ステアリン酸モノグリコシド 1.0 クインスシード抽出液(5%水溶液)20.0 プロピレングリコール 5.0 エタノール 3.0 エチルパラベン 0.3 メチルパラベン 0.05 香料 0.05 精製水 残余 (製法)イオン交換水にプロピレングリコールを加え、
加熱して70℃に保つ(水相)。他の成分を混合し、加
熱融解して70℃に保つ(油相)。油相を撹拌しながら
これに水相を徐々に加え、ホモミキサーで均一に乳化し
た。乳化後撹拌しながら30℃まで冷却した。
(Example 4) Emulsion Shiitake mushroom 50% ethanol extract 0.02 (% by weight) Jujube water extract 0.01 Stearic acid 1.5 Cetyl alcohol 0.5 Beeswax 2.0 Polyoxyethylene (10 mol) Monooleate 1.0 Monoglycoside stearate 1.0 Quince seed extract (5% aqueous solution) 20.0 Propylene glycol 5.0 Ethanol 3.0 Ethylparaben 0.3 Methylparaben 0.05 Perfume 0.05 Purified water Residue (Production method) Add propylene glycol to ion-exchanged water,
Heat and maintain at 70 ° C. (aqueous phase). The other components are mixed, heated and melted and kept at 70 ° C. (oil phase). While stirring the oil phase, the aqueous phase was gradually added thereto, and the mixture was uniformly emulsified with a homomixer. After the emulsification, the mixture was cooled to 30 ° C. while stirring.

【0024】[0024]

【発明の効果】以上説明したように、本発明によれば、
従来の抗酸化剤に比較して顕著な酸化防止効果を発現
し、かつ毒性の問題のない抗酸化剤組成物を提供でき
る。
As described above, according to the present invention,
An antioxidant composition exhibiting a remarkable antioxidant effect as compared with conventional antioxidants and having no toxicity problem can be provided.

【0025】さらに、本発明の組成物を用いれば、酸化
安定性が悪く配合が困難とされてきた物質であっても安
定に系中に配合できるようになり、化粧品や食品等、広
い範囲での利用が期待される。
Furthermore, the use of the composition of the present invention allows even a substance which has been considered difficult to be compounded due to poor oxidative stability to be stably compounded in a system. The use of is expected.

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A61K 35/78 ADA A61K 35/78 ADAQ ADD ADDC 35/84 35/84 A Continued on the front page (51) Int.Cl. 6 Identification code Agency reference number FI Technical display location A61K 35/78 ADA A61K 35/78 ADAQ ADD ADD ADDDC 35/84 35/84 A

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ジュウヤク、ハッカ、ケツメイシ、シイ
タケのいずれか1種もしくは2種以上の抽出物を配合し
てなることを特徴とする抗酸化剤組成物。
1. An antioxidant composition comprising an extract of at least one selected from the group consisting of jujube, peppermint, beetle, and shiitake mushroom.
【請求項2】 前記ジュウヤク、ハッカ、ケツメイシ、
シイタケのいずれか1種もしくは2種以上の抽出物を外
用剤全容量中乾燥物で0.005〜20.0重量%配合
することを特徴とする抗酸化剤組成物。
2. The method according to claim 2, wherein
An antioxidant composition comprising one or more extracts of Shiitake mushrooms in an amount of 0.005 to 20.0% by weight as a dry matter in the total volume of the external preparation.
JP8164934A 1996-06-25 1996-06-25 Antioxidant composition Withdrawn JPH108049A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8164934A JPH108049A (en) 1996-06-25 1996-06-25 Antioxidant composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8164934A JPH108049A (en) 1996-06-25 1996-06-25 Antioxidant composition

Publications (1)

Publication Number Publication Date
JPH108049A true JPH108049A (en) 1998-01-13

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP8164934A Withdrawn JPH108049A (en) 1996-06-25 1996-06-25 Antioxidant composition

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JP (1) JPH108049A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000128728A (en) * 1998-10-20 2000-05-09 Ichimaru Pharcos Co Ltd Cosmetic composition
WO2002017938A1 (en) * 2000-08-29 2002-03-07 Cognis France S.A. Use of extracts of the cassia alata plant
WO2002065836A3 (en) * 2001-02-20 2003-11-13 Paul Stamets Delivery systems for mycotechnologies, mycofiltration and mycoremediation
WO2003101466A1 (en) * 2002-05-31 2003-12-11 Suntory Limited Rubrofusarin glycoside-containing composition
JP2005013227A (en) * 2003-06-06 2005-01-20 Hayashibara Biochem Lab Inc Method for keeping quality of processed product
WO2007004570A1 (en) * 2005-06-30 2007-01-11 Suntory Limited Composition having physical endurance improving effect and/or anti-fatigue effect
JP2008266177A (en) * 2007-04-19 2008-11-06 Noda Shokukin Kogyo Kk Brain-protective agent
KR100867202B1 (en) 2006-03-22 2008-11-06 한국화학연구원 A composition for external application for skinwhitening containing extract of seeds of cassia tora or emodin isolated therefrom
JP2009227654A (en) * 2008-03-24 2009-10-08 Republic Of Korea Management Rural Development Administration Composition for improvement of atopic dermatitis containing plant extracts
JP2016529206A (en) * 2013-05-10 2016-09-23 ザ プロクター アンド ギャンブル カンパニー Consumer products containing silane-modified oil
CN108576258A (en) * 2018-04-14 2018-09-28 长沙小新新能源科技有限公司 A kind of health care Radish seed compound oil and preparation method thereof

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000128728A (en) * 1998-10-20 2000-05-09 Ichimaru Pharcos Co Ltd Cosmetic composition
WO2002017938A1 (en) * 2000-08-29 2002-03-07 Cognis France S.A. Use of extracts of the cassia alata plant
US8535731B2 (en) 2000-08-29 2013-09-17 Basf Beauty Care Solutions France S.A.S. Use of extracts of the Cassia alata plant
WO2002065836A3 (en) * 2001-02-20 2003-11-13 Paul Stamets Delivery systems for mycotechnologies, mycofiltration and mycoremediation
JP4520089B2 (en) * 2002-05-31 2010-08-04 サントリーホールディングス株式会社 Rubrofusarin glycoside-containing composition
WO2003101466A1 (en) * 2002-05-31 2003-12-11 Suntory Limited Rubrofusarin glycoside-containing composition
JP2004002231A (en) * 2002-05-31 2004-01-08 Suntory Ltd Composition comprising rubrofusarin glycoside
JP2005013227A (en) * 2003-06-06 2005-01-20 Hayashibara Biochem Lab Inc Method for keeping quality of processed product
WO2007004570A1 (en) * 2005-06-30 2007-01-11 Suntory Limited Composition having physical endurance improving effect and/or anti-fatigue effect
KR100867202B1 (en) 2006-03-22 2008-11-06 한국화학연구원 A composition for external application for skinwhitening containing extract of seeds of cassia tora or emodin isolated therefrom
JP2008266177A (en) * 2007-04-19 2008-11-06 Noda Shokukin Kogyo Kk Brain-protective agent
JP2009227654A (en) * 2008-03-24 2009-10-08 Republic Of Korea Management Rural Development Administration Composition for improvement of atopic dermatitis containing plant extracts
JP2016529206A (en) * 2013-05-10 2016-09-23 ザ プロクター アンド ギャンブル カンパニー Consumer products containing silane-modified oil
CN108576258A (en) * 2018-04-14 2018-09-28 长沙小新新能源科技有限公司 A kind of health care Radish seed compound oil and preparation method thereof

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