JP3053368B2 - Cosmetic and method for producing the same - Google Patents
Cosmetic and method for producing the sameInfo
- Publication number
- JP3053368B2 JP3053368B2 JP8168324A JP16832496A JP3053368B2 JP 3053368 B2 JP3053368 B2 JP 3053368B2 JP 8168324 A JP8168324 A JP 8168324A JP 16832496 A JP16832496 A JP 16832496A JP 3053368 B2 JP3053368 B2 JP 3053368B2
- Authority
- JP
- Japan
- Prior art keywords
- yucca
- saponin
- extract
- resveratrol
- 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
Links
Landscapes
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、化粧料及びその製
造方法に関し、更に詳しくは、抗菌性及び紫外線吸収性
等に優れ、肌荒れや艶消しを防ぎ、美しい肌を保つ化粧
料及びその製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cosmetic and a method for producing the same, and more particularly, to a cosmetic which is excellent in antibacterial properties and ultraviolet absorption, prevents roughening and matting, and maintains beautiful skin, and a method for producing the same. About.
【0002】[0002]
【従来の技術】従来の化粧料には、種々の薬効の目的で
薬剤が配合されているが、その薬効を発揮する最低量を
添加しても副作用を伴うものが多い。その対策として
は、天然の動植物、特に植物の抽出物が配合されている
(例えば、特公平5−17206号公報に開示されたビ
ワ抽出物等)が、抗菌性及び紫外線吸収性等に優れるも
のはまだ見出されていない。2. Description of the Related Art Conventional cosmetics are formulated with various drugs for the purpose of various medicinal effects, but many of them have side effects even if a minimum amount of the medicinal effect is added. As a countermeasure, natural flora and fauna, especially plant extracts are blended (for example, loquat extract disclosed in Japanese Examined Patent Publication No. 5-17206), but those which are excellent in antibacterial properties, ultraviolet absorption properties, etc. Has not yet been found.
【0003】[0003]
【発明が解決しようとする課題】本発明は、上記従来技
術の問題点を解決するものであり、抗菌性及び紫外線吸
収性等に優れ、肌荒れや艶消しを防ぎ、美しい肌を保つ
化粧料及びその製造方法を提供することを目的とする。SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems of the prior art, and has excellent antibacterial properties and ultraviolet absorption, prevents roughening and matting, and maintains a beautiful skin. It is an object of the present invention to provide a manufacturing method thereof.
【0004】[0004]
【課題を解決するための手段】本発明者は、上記目的を
達成するため、植物抽出物の成分の特性について鋭意検
討した結果、ユッカ(Yucca)抽出物に含まれてい
るサポニンが抗菌性に優れ、特に酵母に対する抗菌性を
も有すること、上記ユッカ抽出物に含まれているポリフ
ェノ−ル、特にレスベラトロ−ル(3、4’、5 −ト
リヒドロキシスチルベン)が酵素に対し生活性を阻害す
ること、また、上記ユッカ抽出物に含まれているサポニ
ン、フラボン及びレスベラトロ−ルがいずれも紫外線吸
収性に優れることを活かし、サポニン、フラボン及びレ
スベラトロ−ルを化粧料に配合し、肌荒れや艶消しを防
ぎ、美しい肌を保つ化粧料が得られることを見出して本
発明を完成するに至ったのである。Means for Solving the Problems In order to achieve the above object, the present inventors have conducted intensive studies on the characteristics of the components of the plant extract, and as a result, the saponin contained in the Yucca extract has been found to have antibacterial properties. It has excellent antibacterial properties, especially against yeast, and polyphenols, especially resveratrol (3,4 ', 5-trihydroxystilbene) contained in the Yucca extract, inhibit the viability of enzymes. In addition, taking advantage of the fact that saponin, flavone and resveratrol contained in the above-mentioned yucca extract are all excellent in ultraviolet ray absorbability, saponin, flavone and resveratrol are blended in cosmetics to make the skin rough and matte. The present inventors have found that a cosmetic that can prevent blemishes and maintain beautiful skin can be obtained, thereby completing the present invention.
【0005】本発明は、本発明者が、ユッカ抽出液を含
有する化粧料が肌荒れ防止、老化防止に優れているこ
と、及びこの抽出液中にサポニン、フラボン及びレスベ
ラトロ−ルが含有されることを見出して、完成されたも
のである。According to the present invention, the present inventors have determined that a cosmetic containing a yucca extract is excellent in preventing rough skin and aging, and that the extract contains saponin, flavone and resveratrol. Was found and completed.
【0006】即ち、本第1発明の化粧料は、ユッカ(Y
ucca)抽出物を含有することを特徴とする。上記
「ユッカ」としては、ユッカシディゲラ(Yucca
schidigera)、アツバキミガヨラン(Yuc
ca gloriosa Linn)、キミガヨラン
(Yucca recurvifolia Salis
b)、イトラン(Yucca smalliana F
ernald)、センジュラン(Yucca aloi
folia Linn)等を使用できる。また、これら
の1種を用いてもよいし、これらの2種以上を用いても
よい。上記「ユッカ抽出物」は、原料ユッカから所定の
抽出溶媒にて抽出させて得た抽出液そのものでもよい
し、この抽出液を濃縮して得られる濃縮液でもよいし、
これらを乾燥して得られる固形物(粉末、果粒品等の形
状は問わない。)でもよい。That is, the cosmetic of the first aspect of the present invention is
ucca) characterized by containing an extract. The above-mentioned “Yucca” includes Yucca Sidigera (Yucca)
schidigera), Atsubakimigayoran (Yuc
ca gloriosa Linn), Kimigayoran (Yucca recurvifolia Salis)
b), Itran (Yucca smalliana F
ernald), Senjuran (Yucca aloi)
folin Linn) can be used. One of these may be used, or two or more of these may be used. The above-mentioned "Yucca extract" may be an extract itself obtained by extracting from a raw Yucca with a predetermined extraction solvent, or a concentrated solution obtained by concentrating this extract,
Solids obtained by drying these (the shapes of powders, granules, etc. do not matter) may be used.
【0007】上記ユッカ抽出物にはサポニン、フラボン
及びレスベラトロ−ルが含有されているものとすること
ができる。そして、上記サポニン、上記フラボン又は上
記レスベラトロ−ルとしては、この成分を含有するユッ
カ抽出液としてもよいし、この抽出液から分画されたも
のでもよい。また、これらを混合してもよいし、複数成
分の含有物を混合してもよい。[0007] The yucca extract may contain saponin, flavone and resveratrol. The saponin, the flavone or the resveratrol may be a Yucca extract containing this component, or may be a fraction obtained from this extract. Further, these may be mixed, or the content of a plurality of components may be mixed.
【0008】上記サポニン、フラボン及びレスベラトロ
−ルの含有量は、第3発明に示すように、化粧料を10
0重量%とした場合に、0.001〜5重量%、(好ま
しくは0.01〜1重量%)とすることができる。上記
物質の含有量が0.001重量%未満ではその物質の効
果が十分発揮されず、含有量が5重量%を越えると、着
色したり、微臭などの欠点が現れるからである。また、
上記サポニン、フラボン及びレスベラトロ−ルの3成分
を含む場合には、このサポニンを10重量部とする場
合、フラボンは3〜5重量部、レスベラトロ−ルは0.
5〜2重量部とするのが好ましい。The contents of the above-mentioned saponin, flavone and resveratrol are, as shown in the third invention, 10% of cosmetics.
When it is 0% by weight, it can be 0.001 to 5% by weight (preferably 0.01 to 1% by weight). The content of the material is not sufficiently exhibited the effect of the substance is less than 0.001 wt%, the content is more than 5 wt%, colored or because the defects such as fine odor appears. Also,
When the saponin, flavone and resveratrol are contained, the saponin is 10 parts by weight, the flavones are 3 to 5 parts by weight, and the resveratrol is 0.1 part by weight.
It is preferable to use 5 to 2 parts by weight.
【0009】本第4発明の化粧料の製造方法は、ユッカ
(Yucca)の根及び茎の中の少なくとも一方をチッ
プにし乾燥した後、若しくは乾燥しチップにした後、粉
砕して粉末を製造し、その後、該粉末をエタノ−ルと水
の混合溶媒に浸漬し抽出してユッカ抽出物を得、次い
で、該ユッカ抽出物を配合することを特徴とする。上記
「ユッカ」は前記と同様の意味に用いられる。そして、
このユッカ原料としては、通常は、根又は茎を用いるこ
ともできるが、通常、その両方を用いる。上記エタノ−
ルと水の上記混合溶媒は、第5発明に示すようにその混
合比率がエタノ−ル75〜95重量%とすることができ
る。エタノ−ルが75重量%未満では、抽出成分が糖を
多量に含みサポニン成分の比率が低くなり、また、ユッ
カの抽出に時間が掛かり過ぎて不能率であり、エタノ−
ルが95重量%を越えると、サポニン成分の含有量が低
下するからである。また、上記「ユッカ抽出物」の形態
としては、前記に示すように、抽出液でも、濃縮液で
も、固形物でもよい。The method for producing a cosmetic according to the fourth aspect of the present invention is a method for producing a powder after at least one of the roots and stems of Yucca is made into chips and dried, or dried into chips, and then crushed to produce powder. Thereafter, the powder is immersed and extracted in a mixed solvent of ethanol and water to obtain a Yucca extract, and then the Yucca extract is blended. The above “Yucca” is used in the same meaning as described above. And
As the Yucca raw material, usually, roots or stems can be used, but usually both are used. Etano-
The mixed solvent of water and water may have a mixing ratio of 75 to 95% by weight of ethanol as shown in the fifth invention. If the ethanol content is less than 75% by weight, the extraction component contains a large amount of sugar and the ratio of the saponin component becomes low, and the extraction of yucca takes too much time, resulting in an impossible rate.
When the content exceeds 95% by weight, the content of the saponin component decreases. As described above, the form of the “Yucca extract” may be an extract, a concentrate, or a solid.
【0010】本発明の化粧料及び本発明の製造方法で製
造された化粧料の形態は、特に限定されず、例えば、液
状体(化粧水、乳液等)、クリ−ム若しくは軟膏状体等
とすることができる。また、必要に応じて、化粧品に一
般に用いられ各種添加剤、例えば、低級アルコ−ル、多
価アルコ−ル等の水性成分、酸化チタン、ホウ砂等の粉
末成分、油分、更には界面活性剤、増粘剤、酸化防止
剤、香料、包剤、薬剤等を配合することができる。The form of the cosmetic of the present invention and the cosmetic produced by the production method of the present invention are not particularly limited, and examples thereof include liquids (lotions, emulsions, etc.), creams and ointments. can do. If necessary, various additives commonly used in cosmetics, for example, aqueous components such as lower alcohols and polyhydric alcohols, powder components such as titanium oxide and borax, oils, and surfactants , A thickener, an antioxidant, a fragrance, a wrapping agent, a drug, and the like.
【0011】[0011]
【発明の実施の形態】以下、本発明を、実施例及び比較
例により更に詳細に説明する。ユッカ抽出物の調製、化
粧料の調製及びその性能評価は以下の方法で行った。 (1)ユッカ抽出物の調製 (その1)ユッカシディゲラ(Yucca schid
igera)の根及び茎をチップにし、天日乾燥した
後、粉砕して原末を得た。この原末500gを5倍量の
90%エタノ−ルに浸漬し、24時間常温放置した後、
濾過して90%エタノ−ル抽出液を得た。この90%エ
タノ−ル抽出液を常圧で加熱し、エタノ−ルを留去して
有効成分30〜40重量%の濃縮液を得た。これらの濃
縮液に5倍量の蒸留水を加え12時間放置した。その
後、上層の水溶液と下層の水不溶物を、デカンテ−ショ
ンで分け、残量が少なくなった後に濾過した。この水溶
液を減圧下で加熱して水分を留去して濃縮し、水分が5
0%程度になったところで蒸留を止め、真空、凍結或い
は噴霧乾燥によって褐色の粉末(「ユッカ抽出物1」と
いう。)35gを得た。この粉末の主成分は、サポニン
(乾燥粉末中60〜70重量%)と糖(乾燥粉末中30
〜40重量%)である。尚、このサポニンと糖の重量比
は、約2:1である。その後、水不溶物を濾別した後、
真空乾燥して褐色粉末(「ユッカ抽出物1A」とい
う。)15gを得た。この粉末の主成分は、フラボン
(乾燥粉末中75〜85重量%)とレスベラトロ−ル
(乾燥粉末中15〜25重量%)である。尚、このフラ
ボンとレスベラトロ−ルとの重量比は約4:1である。DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples. Preparation of Yucca extract, preparation of cosmetics and evaluation of its performance were performed by the following methods. (1) Preparation of Yucca Extract (Part 1) Yucca schidella
igera) was made into chips, dried in the sun, and ground to obtain a raw powder. 500 g of this bulk powder was immersed in five times the amount of 90% ethanol and left at room temperature for 24 hours.
Filtration gave a 90% ethanol extract. This 90% ethanol extract was heated at normal pressure, and ethanol was distilled off to obtain a concentrate of 30 to 40% by weight of the active ingredient. A 5-fold amount of distilled water was added to these concentrated liquids and left for 12 hours. Thereafter, the aqueous solution in the upper layer and the water-insoluble matter in the lower layer were separated by decantation, and filtered after the remaining amount became small. This aqueous solution is heated under reduced pressure to distill off water and concentrate.
At about 0%, distillation was stopped, and 35 g of a brown powder (referred to as "Yucca extract 1") was obtained by vacuum, freezing or spray drying. The main components of this powder are saponin (60-70% by weight in dry powder) and sugar (30 in dry powder).
4040% by weight). The weight ratio between the saponin and the sugar is about 2: 1. Then, after filtering off the water-insoluble matter,
Vacuum drying was performed to obtain 15 g of a brown powder (referred to as “Yucca extract 1A”). The main components of this powder are flavone (75-85% by weight in dry powder) and resveratrol (15-25% by weight in dry powder). Incidentally, the weight ratio of this flavone to resveratrol is about 4: 1.
【0012】(その2)その1で得られた有効成分30
〜40%の濃縮液200gを、イオン交換樹脂(三菱化
学社製、商品名「ダイヤイオンHP20」)を充填した
カラムを用いて、水、30%エタノ−ル、80%エタノ
−ルで順次展開し分画した。水及び30%エタノ−ル抽
出物は、主として糖成分が、80%エタノ−ル抽出物
は、主としてサポニン、フラボン及びレスベラトロ−ル
が含有される。この80%エタノ−ル抽出液を初期段階
は常圧で、後半は減圧でそれぞれエタノ−ルを留去し、
有効成分が40〜50%の濃縮液を得た。更に、この濃
縮液を真空乾燥して褐色粉末(「ユッカ抽出物2」とい
う。)35gを得た。この粉末の主成分は、サポニン
(乾燥粉末中87〜90重量%)、フラボン(乾燥粉末
中10〜8重量%)及びレスベラトロ−ル(乾燥粉末中
3〜2重量%)である。尚、このサポニンとフラボンと
レスベラトロ−ルとの重量比は、10:4:1である。(Part 2) Active ingredient 30 obtained in Part 1
Using a column packed with an ion exchange resin (trade name "Diaion HP20", manufactured by Mitsubishi Chemical Corporation), 200 g of a concentrated solution of 40% to 40% is sequentially developed with water, 30% ethanol, and 80% ethanol. And fractionated. Water and 30% ethanol extract mainly contain sugar components, and 80% ethanol extract mainly contains saponin, flavone and resveratrol. Ethanol was distilled off from this 80% ethanol extract at normal pressure in the initial stage and at reduced pressure in the latter half.
A concentrate containing 40 to 50% of the active ingredient was obtained. Further, this concentrated liquid was dried under vacuum to obtain 35 g of a brown powder (referred to as "Yucca extract 2"). The main components of this powder are saponin (87-90% by weight in dry powder), flavone (10-8% by weight in dry powder) and resveratrol (3-2% by weight in dry powder). The weight ratio of saponin, flavone and resveratrol is 10: 4: 1.
【0013】(その3)その1で得られた有効成分30
〜40%の濃縮液100gに2〜3倍量の蒸留水を加
え、一夜常温で放置した後、水溶液部分をデカンテ−シ
ョンで分別した。この水溶液を上記と同様のカラムを用
いて、初期水洗い後、アセトン60%水混和液で抽出し
分画した。アセトン溶液を減圧蒸留にかけ、濃縮し放冷
した後、凍結、乾燥して粉末(「ユッカ抽出物3」とい
う。)27gを得た。この粉末の主成分は、サポニン
(乾燥粉末中90〜100重量%)である。(Part 3) Active ingredient 30 obtained in Part 1
Distilled water in an amount of 2 to 3 times was added to 100 g of the 4040% concentrated solution, and the mixture was allowed to stand at room temperature overnight. Then, the aqueous solution was separated by decantation. This aqueous solution was subjected to initial water washing using the same column as above, and then extracted and fractionated with a 60% water mixed solution of acetone. The acetone solution was subjected to distillation under reduced pressure, concentrated and allowed to cool, then frozen and dried to obtain 27 g of a powder (referred to as “Yucca extract 3”). The main component of this powder is saponin (90 to 100% by weight in the dry powder).
【0014】(2)化粧料の調製 実施例1の化粧料(化粧水) (組成)配合量は重量部(部という。以下も同じ。)で
表す。 1)グリセリン 1.0部 2)1,3−ブチレングリコ−ル 3.0部 3)ポリオキシエチレン(15モル付加)オレイル 0.3部 アルコ−ルエ−テル 4)ユッカ抽出物1;(サポニン:糖=2:1) 0.02部 5)クエン酸ナトリウム 0.1部 6)エタノ−ル 8.0部 7)香料 0.03部 8)精製水 87.55部 合計 100.0部(2) Preparation of Cosmetic The amount of the cosmetic (lotion) (composition) in Example 1 is expressed in parts by weight (hereinafter referred to as "parts"). 1) Glycerin 1.0 part 2) 1,3-butylene glycol 3.0 parts 3) Polyoxyethylene (15 mole addition) oleyl 0.3 parts alcohol ether 4) Yucca extract 1; (Saponin) : Sugar = 2: 1) 0.02 parts 5) Sodium citrate 0.1 parts 6) Ethanol 8.0 parts 7) Fragrance 0.03 parts 8) Purified water 87.55 parts Total 100.0 parts
【0015】(調製)グリセリン、1,3−ブチレング
リコ−ル及びクエン酸ナトリウムを精製水に加え、撹拌
して溶解する。別に、エタノ−ルにユッカ抽出物1、ポ
リオキシエチレンオレイルエ−テル及び香料を溶解し、
これを前記の精製水水溶液に加えて、均一に混合した
後、濾過して化粧水を得た。(Preparation) Glycerin, 1,3-butylene glycol and sodium citrate are added to purified water and dissolved by stirring. Separately, Yucca extract 1, polyoxyethylene oleyl ether and perfume are dissolved in ethanol,
This was added to the above purified water solution, mixed uniformly, and filtered to obtain a lotion.
【0016】比較例1の化粧料(化粧水) ユッカ抽出物1を配合しないこと以外は実施例1と同様
の組成及び調製で化粧水を得た。Cosmetic (Lotion) of Comparative Example 1 A lotion was obtained in the same composition and preparation as in Example 1 except that Yucca Extract 1 was not blended.
【0017】 実施例2の化粧料(乳液) (組成) 1)精製ホホバ油 2.0部 2)ステアリン酸 1.5部 3)セチルアルコ−ル 0.3部 4)ポリオキシエチレン(8モル付加)モノオレイン酸 1.0部 エステル 5)ソルビタンモノステアレ−ト 6.5部 6)ユッカ抽出物2; 0.05部 (サポニン:フラボン:レスベラトロ−ル=10:4:1) 7)プロピレングリコ−ル 3.0部 8)エタノ−ル 3.0部 9)香料 0.01部 10)精製水 82.64部 合計 100.0部[0017] Cosmetic of Example 2 (Emulsion) (Composition) 1) Refined jojoba oil 2.0 parts 2) Stearic acid 1.5 parts 3) Cetyl alcohol 0.3 parts 4) Polyoxyethylene (8 mol addition) ) Monooleic acid 1.0 part Ester 5) Sorbitan monostearate 6.5 parts 6) Yucca extract 2; 0.05 part (Saponin: flavone: resveratrol = 10: 4: 1) 7) Propylene Glycol 3.0 parts 8) Ethanol 3.0 parts 9) Fragrance 0.01 parts 10) Purified water 82.64 parts Total 100.0 parts
【0018】(調製)エタノ−ルにユッカ抽出物2と香
料を溶解し、エタノ−ル溶液を得る。精製水にプロピレ
ングリコ−ルを加えて得られる精製水溶液を70〜80
℃に保つ。他の成分同士を混合して加熱溶解し、得られ
る溶液を70〜80℃に保ち、撹拌しながら上記精製水
溶液の中へ加えて乳化し、均一になった後、ホモミキサ
−で更に撹拌し、上記エタノ−ル溶液を加えて仕上げ
る。更に、この液を熱交換機(混合練り機能付きオンレ
−タ−)により30℃に冷却し乳液を得た。(Preparation) Yucca extract 2 and a fragrance are dissolved in ethanol to obtain an ethanol solution. A purified aqueous solution obtained by adding propylene glycol to purified water is 70-80.
Keep at ° C. The other components are mixed together and dissolved by heating.The resulting solution is kept at 70 to 80 ° C., and added to the purified aqueous solution while stirring to emulsify the mixture. After the mixture becomes homogeneous, the mixture is further stirred with a homomixer. Finish by adding the above ethanol solution. Further, this liquid was cooled to 30 ° C. by a heat exchanger (an on-liner having a mixing and kneading function) to obtain an emulsion.
【0019】 実施例3の化粧料(クリ−ム) (組成) 1)精製ホホバ油 10.0部 2)スクワラン 35.0部 3)ステアリルアルコ−ル 3.0部 4)ポリオキシエチレン(15モル付加)パルミチン酸 3.0部 エステル 5)ソルビタンモノステアレ−ト 1.0部 6)ユッカ抽出物1;(サポニン:糖=2:1) 0.1部 7)プロピレングリコ−ル 8.0部 8)香料 0.01部 9)精製水 39.89部 合計 100.0部Cosmetic (cream) of Example 3 (Composition) 1) Refined jojoba oil 10.0 parts 2) Squalane 35.0 parts 3) Stearyl alcohol 3.0 parts 4) Polyoxyethylene (15) Mole addition) palmitic acid 3.0 parts ester 5) sorbitan monostearate 1.0 part 6) yucca extract 1; (saponin: sugar = 2: 1) 0.1 part 7) propylene glycol 8. 0 parts 8) Perfume 0.01 parts 9) Purified water 39.89 parts Total 100.0 parts
【0020】(調製)1)〜5)の原料を70〜80℃
に加熱し溶解したものを、75℃に加熱した原料6)、
7)及び9の水溶液に撹拌しながら加え、予備乳化す
る。次いで、原料8)を加えてホモミキサ−で撹拌し乳
化粒子を細かくして均一にした後、急冷して30℃に
し、クリ−ムを得た。(Preparation) The raw materials of 1) to 5) are heated at 70 to 80 ° C.
The raw material 6) heated to 75 ° C.
7. Add to the aqueous solutions of 7) and 9 with stirring and pre-emulsify. Next, the raw material 8) was added, and the mixture was stirred with a homomixer to make the emulsified particles fine and uniform, and then rapidly cooled to 30 ° C. to obtain a cream.
【0021】 実施例4の化粧料(軟膏) (組成) 1)ユッカ抽出物3 0.5部 2)ステアリルアルコ−ル 15.0部 3)密ロウ 20.0部 4)ポリオキシエチレン(5モル付加)ソルビタンモノ 0.3部 ステアレ−ト 5)ポリオキシエチレン(15モル付加)モノオレイン酸 0.2部 エステル 6)ワセリン 35.0部 7)グリセリン 5.0部 8)精製水 24.0部 合計 100.0部Cosmetic (Ointment) of Example 4 (Composition) 1) Yucca extract 3 0.5 part 2) Stearyl alcohol 15.0 parts 3) Beeswax 20.0 parts 4) Polyoxyethylene (5) Molar addition) sorbitan mono 0.3 part stearate 5) Polyoxyethylene (15 mole addition) monooleic acid 0.2 part ester 6) Vaseline 35.0 parts 7) Glycerin 5.0 parts 8) Purified water 24. 0 parts Total 100.0 parts
【0022】(調製)原料1)〜7)を75℃で加熱溶
解し70℃に保った精製水の中に加え、ホモミキサ−で
乳化した後、冷却して軟膏を得た。(Preparation) Raw materials 1) to 7) were heated and dissolved at 75 ° C., added to purified water kept at 70 ° C., emulsified by a homomixer, and then cooled to obtain an ointment.
【0023】(3)肌荒れ改善性能評価 上記の化粧料の性能を明らかにするため、以下の性能試
験を行った。実施例1で得た化粧水と比較例1で得た化
粧水を用いて人体パネルで肌荒れの改善効果試験を行っ
た。即ち、ミリスン樹脂によるレプリカ法を用いて、女
性健常人の顔面の皮膚表面形態のレプリカを取り、顕微
鏡(17倍)にて観察した。皮紋の状態及び角膜の剥離
状態から表1に示す基準に従って肌荒れ評価1,2と判
断された者(肌荒れパネル)25名を用い、顔面左右半
々に、上記各化粧水を1日1回づつ2週間塗布した。2
週間後、再び上記のレプリカ法によって顔面の皮膚表面
形態を観察し、表1の判定基準に従って評価した。結果
を表2に示す。(3) Evaluation of Skin Roughness Improvement Performance The following performance tests were conducted to clarify the performance of the above cosmetics. Using the lotion obtained in Example 1 and the lotion obtained in Comparative Example 1, a skin roughness improvement effect test was performed on a human body panel. That is, a replica of the skin surface morphology of the face of a healthy female was taken using a replica method using a Myrison resin and observed with a microscope (17 ×). Each of the lotions was applied once a day to the left and right half of the face using 25 people (rough panel) whose skin roughness was judged to be 1 or 2 according to the criteria shown in Table 1 based on the state of the skin pattern and the peeled state of the cornea. It was applied for two weeks. 2
After one week, the skin surface morphology of the face was observed again by the replica method described above, and evaluated according to the criteria shown in Table 1. Table 2 shows the results.
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【表2】 [Table 2]
【0026】表2から次のことが分かる。即ち、ユッカ
抽出物1を配合した化粧水(実施例1)を使用した顔面
の場合は、「皮溝、皮丘の消失、広範囲の角層のめく
れ」が0名、「皮溝、皮丘が不鮮明、角層のめくれ」が
0名、「皮溝、皮丘が鮮明」が11名、「皮溝、皮丘が
鮮明で整っている」が12名であったのに対して、ユッ
カ抽出物1を配合しない化粧水(比較例1)を使用した
顔面の場合は、「皮溝、皮丘の消失、広範囲の角層のめ
くれ」が10名、「皮溝、皮丘が不鮮明、角層のめく
れ」が8名、「皮溝、皮丘が鮮明」が0名、「皮溝、皮
丘が鮮明で整っている」が0名であった。従って、ユッ
カ抽出物1を配合した化粧水は、ユッカ抽出物1を配合
しない化粧水と比較し、肌荒れや艶消しを防ぎ、美しい
肌を保つ効果が顕著である。The following can be seen from Table 2. In other words, in the case of the face using the lotion containing Yucca extract 1 (Example 1), no “skins, disappearance of skin ridges, and widespread turning of the stratum corneum” were 0, and “skins, skin hills” Were unclear, the horny layer was turned up ", 11 were" skins and ridges were sharp, "and 12 were" skins and ridges were sharp and tidy. " In the case of the face using the lotion not containing the extract 1 (Comparative Example 1), 10 persons “skin folds, disappearance of skin ridges, turning over of a wide range of stratum corneum”, “skin ridges and skin hills are unclear, There were 8 people who turned up the stratum corneum, 0 people who had clear skin and ridges, and 0 people who had clear skin and ridges. Therefore, the lotion containing the Yucca extract 1 has a remarkable effect of preventing skin roughness and matting and maintaining beautiful skin, as compared with the lotion not containing the Yucca extract 1.
【0027】(4)紫外線吸収性能評価 サポニン、フラボン及びレスベラトロ−ルの紫外線吸収
性能を、図1(サポニン)、図2(フラボン及びレスベ
ラトロ−ル)及び図3(レスベラトロ−ル)に示す。こ
れらの結果から、いずれの物質も優れた紫外線吸収性能
を示すことが分かる。特に、サポニンは260〜340
nmにて、フラボンは260〜320nm程度にて、レ
スベラトロ−ルは280〜340nmにて優れた紫外線
吸収性能を示している。従って、サポニン及び/又はフ
ラボンとレスベラトロ−ルとを含むものとすれば、広い
範囲にて紫外線吸収性能を示すことが分かる。尚、この
試験に用いたレスベラトロ−ルは、有機合成品(純度9
8重量%)を用いた。(4) Evaluation of ultraviolet absorption performance The ultraviolet absorption performance of saponin, flavone and resveratrol is shown in FIG. 1 (saponin), FIG. 2 (flavone and resveratrol) and FIG. 3 (resveratrol). From these results, it can be seen that all the substances show excellent ultraviolet absorption performance. In particular, saponin is 260-340
In nm, flavone shows excellent ultraviolet absorption performance at about 260-320 nm, and resveratrol shows excellent ultraviolet absorption performance at 280-340 nm. Therefore, it can be seen that, if it contains saponin and / or flavone and resveratrol, it exhibits ultraviolet absorption performance in a wide range. The resveratrol used in this test was an organic synthetic product (purity 9
8% by weight).
【0028】(5)レスベラトロ−ルの美白作用評価 レスベラトロ−ルの美白作用効果を見るため、メラニン
産生能を有するB16メラノ−マ細胞に対するレスベラ
トロ−ルの影響を調べた。尚、この試験に用いたレスベ
ラトロ−ルは、有機合成品(純度98重量%)を用い
た。 (試験方法) 1)細胞培養 B16メラノ−マ細胞溶液を培養フラスコ25cm2 に
移し、培養液(FBSを10%含むDMEM)4ml加
え、37℃、5%−CO2 /95%−airの条件下で
培養した。細胞がセミコンフルエントな状態になった
ら、トリプシン処理にて細胞を集め、5×104 個/1
00μlになるように96wellマルチプレ−トに播
種し、再び37℃、5%−CO2 /95%−airの条
件下で24時間培養した。(5) Evaluation of Whitening Effect of Resveratrol In order to observe the whitening effect of resveratrol, the effect of resveratrol on B16 melanoma cells having melanin-producing ability was examined. The resveratrol used in this test was an organic synthetic product (purity: 98% by weight). (Test method) 1) Cell culture Transfer the B16 melanoma cell solution to a culture flask 25 cm 2 , add 4 ml of a culture solution (DMEM containing 10% FBS), and condition at 37 ° C., 5% -CO 2 /95% -air. Cultured underneath. When the cells became semi-confluent, the cells were collected by trypsin treatment and 5 × 10 4 cells / 1
The seeds were inoculated to a 96-well multiplet so as to have a volume of 00 μl, and cultured again at 37 ° C. for 24 hours under the conditions of 5% -CO 2 /95% -air.
【0029】2)チロシナ−ゼ生合成抑制作用の測定 96wellマルチプレ−トで24時間培養後、培養液
を除去し、新しい培養液195μlと各濃度の試料溶液
5μlを添加し、37℃、5%−CO2 /95%−ai
rの条件下で24時間培養した。24時間後、試料を含
む培養液を除去、PBSで洗浄し、1%−トリトンX−
100/PBS溶液50μlを加え、30分間撹拌し、
10mM−DOPA/PBS溶液100μlを加え、3
7℃、5%−CO2 /95%−airの条件下で3時間
インキュベ−トし、波長475nmで吸光度を測定し
た。 チロシナ−ゼ生合成抑制率(%)=〔(A−B)/A〕
×100 A;試料無添加の吸光度 B;試料を添加したときの吸光度2) Measurement of tyrosinase biosynthesis inhibitory activity After culturing in a 96-well multiple plate for 24 hours, the culture solution was removed, 195 μl of a new culture solution and 5 μl of a sample solution of each concentration were added, and the mixture was added at 37 ° C., 5% -CO 2/95% -ai
Culture was performed for 24 hours under the conditions of r. After 24 hours, the culture solution containing the sample was removed, washed with PBS, and washed with 1% -Triton X-
Add 50 μl of 100 / PBS solution, stir for 30 minutes,
Add 100 μl of a 10 mM-DOPA / PBS solution, add 3
After incubating for 3 hours at 7 ° C. and 5% -CO 2 /95% -air, the absorbance was measured at a wavelength of 475 nm. Tyrosinase biosynthesis inhibition rate (%) = [(AB) / A]
× 100 A; Absorbance without sample added B: Absorbance when sample was added
【0030】3)細胞生存率の測定 96wellマルチプレ−トで24時間培養後、培養液
を除去し、新しい培養液195μlと各濃度の試料溶液
5μlを添加し、37℃、5%−CO2 /95%−ai
rの条件下で24時間培養した。24時間後、試料を含
む培養液を除去、PBSで洗浄し、MTT含有培地10
0μlを加え、4時間インキュベ−トした。4時間後、
培養液を除去、イソプロピルアルコ−ル200μlを加
え、30分放置後、波長570nmと655nmで吸光
度を測定した。 細胞生存率=〔Y/X〕×100 X;試料無添加の吸光度(570nm−655nm)の
値 Y;試料を添加したときの吸光度(570nm−655
nm)の値 試料溶液は、50%エタノ−ル水溶液を用いた。3) Measurement of cell viability After culturing in a 96-well multiple plate for 24 hours, the culture solution was removed, 195 μl of a new culture solution and 5 μl of a sample solution of each concentration were added, and the mixture was added at 37 ° C., 5% -CO 2 / 95% -ai
Culture was performed for 24 hours under the conditions of r. After 24 hours, the culture solution containing the sample was removed, washed with PBS, and the MTT-containing medium 10 was removed.
0 μl was added, and the mixture was incubated for 4 hours. Four hours later,
The culture solution was removed, 200 μl of isopropyl alcohol was added, and the mixture was allowed to stand for 30 minutes, and the absorbance was measured at wavelengths of 570 nm and 655 nm. Cell viability = [Y / X] × 100 X; value of absorbance without sample (570 nm-655 nm) Y; absorbance with sample added (570 nm-655)
(nm) value The sample solution used was a 50% aqueous ethanol solution.
【0031】(試験結果)これらの試験結果を表3に示
す。表3から次のことが分かる。即ち、レスベラトロ−
ルの濃度が10ppmでは、51.4%のチロシナ−ゼ
生合成抑制率が認められるとともに、細胞生存率が10
0.3%で細胞毒性が全く認められなかった。それが5
ppmにおいても、細胞毒性が全く認められないととも
に、22.1%と比較的優れたその抑制率を示した。一
方、それが50ppm以上においては、その優れた抑制
率を示すとともに、細胞生存率が32.3%である程度
の細胞毒性を示した。また、それが100ppm以上で
は、細胞生存率が8.4%と低く、そのため細胞毒性が
強く認められ、更に、それが1ppm以下ではその抑制
率が1.2%以下と低く、そのため優れた美白作用効果
を示さなかった。以上より、その濃度が5〜50ppm
においては、細胞毒性がある程度以上抑えられるととも
に、ある程度以上の優れた美白作用効果を示した。この
うち、特に、5〜10ppmにおいては、細胞毒性が全
く認められないとともに、ある程度の優れた美白作用効
果を示した。更に、以上の結果から、その濃度が3〜4
0ppmによれば、チロシナ−ゼ生合成抑制効果及び細
胞毒性低減性のバランスに優れたもとすることができ
る。(Test Results) The results of these tests are shown in Table 3. The following can be seen from Table 3. That is, resveratro-
At a concentration of 10 ppm, a tyrosinase biosynthesis inhibition rate of 51.4% was observed, and the cell viability was 10%.
No cytotoxicity was observed at 0.3%. That is 5
Even at ppm, no cytotoxicity was observed at all, and a relatively excellent inhibition rate of 22.1% was shown. On the other hand, when it was 50 ppm or more, it exhibited its excellent inhibition rate and exhibited a certain degree of cytotoxicity with a cell viability of 32.3%. When it is 100 ppm or more, the cell viability is as low as 8.4%, and therefore cytotoxicity is strongly observed. When it is 1 ppm or less, the inhibition rate is as low as 1.2% or less, and therefore, excellent whitening. No effect was shown. From the above, the concentration is 5 to 50 ppm
In the case of, cytotoxicity was suppressed to a certain extent or more, and an excellent whitening effect was exhibited to a certain extent or more. Among them, in particular, at 5 to 10 ppm, no cytotoxicity was observed at all, and some excellent whitening effect was exhibited. Further, from the above results, the concentration was 3 to 4
According to 0 ppm, the tyrosinase biosynthesis inhibitory effect and the cytotoxicity-reducing ability can be excellently balanced.
【0032】[0032]
【表3】 [Table 3]
【0033】(6)総合評価 ユッカ抽出物に含まれているサポニン、フラボン及びレ
スベラトロ−ルを化粧料に配合した場合の効果を総合す
る。上記サポニンが殆ど単独で含有される化粧料は、肌
荒れ改善効果があり、紫外線吸収効果も見られる。即
ち、サポニンは化粧料に使用の効果がある。上記レスベ
ラトロ−ルが単独では低濃度で顕著な美白作用効果があ
るが、この濃度調製が大変困難であるため、レスベラト
ロ−ルは単体で用いるよりも、サポニン、フラボンと併
用して用いた方が化粧料としての使用の効果がある。フ
ラボンは、紫外線吸収効果が見られる。従って、フラボ
ンも化粧料に使用の効果があると考えられる。(6) Comprehensive Evaluation The effects of adding saponin, flavone, and resveratrol contained in the yucca extract to cosmetics are summarized. Cosmetics containing the above-mentioned saponin almost solely have an effect of improving skin roughness and also have an ultraviolet absorbing effect. That is, saponin is effective for use in cosmetics. The above-mentioned resveratrol alone has a remarkable whitening effect at a low concentration, but it is very difficult to adjust the concentration. Therefore, it is better to use resveratrol in combination with saponin and flavone than in use alone. Useful as cosmetics. Flavone has an ultraviolet absorbing effect. Therefore, it is considered that flavone is also effective for use in cosmetics.
【0034】(7)抽出条件 ユッカから得た原末を80%エタノ−ルで抽出すると、
サポニンが80%エタノ−ルに溶解するので、サポニン
の高濃度抽出液が得られる。従って、サポニンを主力成
分として含む場合には、これが適用できる。この結果か
ら見ると100%エタノ−ルでも同様の結果が得られ
る。上記原末を90%エタノ−ルに浸漬すると、サポニ
ン、フラボン及びレスベラトロ−ルの3成分を含む抽出
液が得られる。従って、上記3成分を含む化粧料を調製
したい場合には、これが適用できる。水単独、30%エ
タノ−ルでは、上記3成分が抽出されないので、40%
以上のエタノ−ルが必要と考えられる。従って、上記3
成分を含む抽出液を得るためには、40〜90%エタノ
−ル、好ましくは50〜90%エタノ−ル、更に好まし
くは70〜90%エタノ−ルが適用できる。(7) Extraction conditions When the bulk powder obtained from Yucca is extracted with 80% ethanol,
Since saponin is dissolved in 80% ethanol, a high-concentration extract of saponin can be obtained. Therefore, when saponin is contained as a main component, this can be applied. From these results, similar results can be obtained with 100% ethanol. By immersing the bulk powder in 90% ethanol, an extract containing three components of saponin, flavone and resveratrol can be obtained. Therefore, this can be applied when a cosmetic containing the above three components is to be prepared. With water alone and 30% ethanol, the above three components are not extracted.
The above ethanol is considered necessary. Therefore, the above 3
To obtain an extract containing the components, 40-90% ethanol, preferably 50-90% ethanol, more preferably 70-90% ethanol can be applied.
【0035】本発明においては、前記具体的実施例に示
すものに限られず、目的、用途に応じて本発明の範囲内
で種々変更した実施例とすることができる。即ち、抽出
原料としては、根及び茎のうちの一方を用いてもよい。
また上記実施例においては、そのチップから得た粉砕物
を用いて抽出しているが、これに限らず、チップをその
まま用いて抽出してもよいし、根及び/又は茎を直接粉
砕物としてこの粉砕粉末を用いてもよいし、更に、この
粉砕粉末の大きさも特に限定されない。抽出条件、特
に、抽出溶媒の種類及び抽出時間、その温度等も種々変
更できる。また、ユッカ抽出物から分画(分取)して得
られたサポニン、フラボン及びレスベラトロ−ルの配合
割合は適宜、目的に応じて変更してもよい。更に、この
ユッカ抽出物から分画(分取)して得られたサポニン、
フラボン及びレスベラトロ−ルのうちの1種又は2種を
適宜量配合してもよいし、分画せずに抽出条件により、
これらの1種又は2種を抽出して含有される抽出物(液
状、乾燥固体を問わない。)を用いることもできる。The present invention is not limited to the specific embodiments described above, but can be variously modified within the scope of the present invention according to the purpose and application. That is, one of the root and the stem may be used as the extraction raw material.
Further, in the above embodiment, the extraction is performed using the pulverized material obtained from the chip, but the present invention is not limited to this, and the chip may be extracted as it is, or the roots and / or stems may be directly pulverized as the pulverized material. This crushed powder may be used, and the size of the crushed powder is not particularly limited. The extraction conditions, in particular, the type of the extraction solvent, the extraction time, the temperature thereof, and the like can be variously changed. The mixing ratio of saponin, flavone, and resveratrol obtained by fractionation (fractionation) from the Yucca extract may be appropriately changed according to the purpose. Furthermore, saponin obtained by fractionation (fractionation) from this yucca extract,
One or two of flavone and resveratrol may be appropriately blended, or may be subjected to extraction conditions without fractionation.
An extract (whether liquid or dry solid) which is obtained by extracting one or two of these may be used.
【0036】[0036]
【発明の効果】本発明の化粧料及びその製造方法で得ら
れる化粧料は、サポニン、フラボン及びレスベラトロ−
ルを含有しているので、抗菌性及び紫外線吸収性等に優
れ、肌荒れや艶消しを防ぎ、美しい肌を保つ効果があ
る。EFFECTS OF THE INVENTION The cosmetics of the present invention and the cosmetics obtained by the method for producing the same are saponin, flavone and resveratro.
Since it contains phenol, it has excellent antibacterial properties and ultraviolet absorption properties, has the effect of preventing rough and matte skin and maintaining beautiful skin.
【図1】実施例にて得たユッカ抽出物3の紫外線吸収性
能を示すグラフである。FIG. 1 is a graph showing the UV absorption performance of Yucca extract 3 obtained in an example.
【図2】実施例にて得たユッカ抽出物1Aの紫外線吸収
性能を示すグラフである。FIG. 2 is a graph showing the ultraviolet absorption performance of Yucca extract 1A obtained in Example.
【図3】レスベラトロ−ルの紫外線吸収性能を示すグラ
フである。FIG. 3 is a graph showing the ultraviolet absorption performance of resveratrol.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI A61K 35/78 A61K 35/78 C09K 3/00 104 C09K 3/00 104Z // A61P 17/00 A61P 17/00 31/04 31/04 43/00 111 43/00 111 C12N 9/99 C12N 9/99 (58)調査した分野(Int.Cl.7,DB名) A61K 7/00 A61K 7/42 A61K 7/48 A61K 35/78 C09K 3/00 104 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI A61K 35/78 A61K 35/78 C09K 3/00 104 C09K 3/00 104Z // A61P 17/00 A61P 17/00 31/04 31 / 04 43/00 111 43/00 111 C12N 9/99 C12N 9/99 (58) Fields investigated (Int.Cl. 7 , DB name) A61K 7/00 A61K 7/42 A61K 7/48 A61K 35/78 C09K 3/00 104
Claims (5)
ことを特徴とする化粧料。1. A cosmetic comprising a Yucca extract.
ン及びレスベラトロ−ルが含有されている請求項1記載
の化粧料。2. The cosmetic according to claim 1, wherein said yucca extract contains saponin, flavone and resveratrol.
に、上記サポニン、フラボン及びレスベラトロ−ルの含
有量は、0.001〜5重量%である請求項2記載の化
粧料。3. The cosmetic according to claim 2, wherein the content of said saponin, flavone and resveratrol is 0.001 to 5% by weight, based on 100% by weight of said cosmetic.
少なくとも一方をチップにし乾燥した後、若しくは乾燥
しチップにした後、粉砕して粉末を製造し、その後、該
粉末をエタノ−ルと水の混合溶媒に浸漬し抽出してユッ
カ抽出物を得、次いで、該ユッカ抽出物を配合すること
を特徴とする化粧料の製造方法。4. A method in which at least one of the roots and stems of Yucca (Yucca) is chipped and dried, or dried and chipped, and then crushed to produce a powder, and then the powder is mixed with ethanol. A method for producing cosmetics, comprising immersing and extracting in a mixed solvent of water to obtain a Yucca extract, and then blending the Yucca extract.
混合比率がエタノ−ル75〜95重量%である請求項4
記載の化粧料の製造方法。5. A mixed solvent of ethanol and water in a mixing ratio of 75 to 95% by weight of ethanol.
The method for producing the cosmetic according to the above.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8168324A JP3053368B2 (en) | 1996-06-06 | 1996-06-06 | Cosmetic and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8168324A JP3053368B2 (en) | 1996-06-06 | 1996-06-06 | Cosmetic and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH09328410A JPH09328410A (en) | 1997-12-22 |
JP3053368B2 true JP3053368B2 (en) | 2000-06-19 |
Family
ID=15865936
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8168324A Expired - Fee Related JP3053368B2 (en) | 1996-06-06 | 1996-06-06 | Cosmetic and method for producing the same |
Country Status (1)
Country | Link |
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JP (1) | JP3053368B2 (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6270780B1 (en) * | 1997-07-25 | 2001-08-07 | Chesebrough-Pond's Usa Co., Division Of Conopco | Cosmetic compositions containing resveratrol |
FR2777183B1 (en) * | 1998-04-10 | 2001-03-02 | Oreal | USE OF AT LEAST ONE HYDROXYSTILBENE IN A COMPOSITION FOR PROMOTING DEQUAMATION OF THE SKIN AND COMPOSITION COMPRISING SAME |
FR2777186B1 (en) * | 1998-04-10 | 2001-03-09 | Oreal | USE OF AT LEAST ONE HYDROXYSTILBENE IN A FIRMING COMPOSITION |
FR2777184B1 (en) * | 1998-04-10 | 2001-08-24 | Oreal | USE OF AT LEAST ONE HYDROXYSTILBENE AS AN AGENT FOR REDUCING THE ADHESION OF MICROORGANISMS |
FR2778337B1 (en) * | 1998-05-05 | 2001-08-31 | Inst Nat Sante Rech Med | ARYLHYDROCARBON RECEPTOR LIGAND ANTAGONISTS |
ES2237164T3 (en) * | 1998-10-09 | 2005-07-16 | Ciba Specialty Chemicals Holding Inc. | HYDROXIESTILBENE COMPOUND USED AS ACTIVE SUBSTANCES MICROBICIDES. |
FR2796278B1 (en) * | 1999-07-16 | 2002-05-03 | Oreal | USE OF AT LEAST ONE HYDROXYSTILBENE AS AN ANTI-GLYCATION AGENT |
AU7596100A (en) | 1999-09-21 | 2001-04-24 | Rutgers, The State University | Resveratrol analogs for prevention of disease |
IT1318425B1 (en) * | 2000-03-24 | 2003-08-25 | D B P Dev Biotechnological Pro | USE OF RESVERATROL FOR THE TREATMENT OF DESQUAMATIVE ECZEMA, ACNE AND PSORIASIS. |
ITNA20000037A1 (en) * | 2000-06-02 | 2001-12-02 | Dev Biotechnological Proces Se | INNOVATIVE MULTIFUNCTION SOLAR FILTER. |
FR2811568B1 (en) * | 2000-07-13 | 2003-01-17 | Oreal | COMPOSITION, ESPECIALLY COSMETIC, COMPRISING DHEA AND / OR A PRECURSOR OR DERIVATIVE THEREOF, IN ASSOCIATION WITH AT LEAST ONE ANTI-GLYCATION AGENT |
FR2817747B1 (en) * | 2000-12-11 | 2004-12-03 | Oreal | USE OF AT LEAST ONE SAPOGENIN, OR A NATURAL EXTRACT CONTAINING IT, TO PREVENT THE SIGNS OF SKIN AGING |
JP4934254B2 (en) * | 2001-09-25 | 2012-05-16 | 株式会社バスクリン | Weakly acidic detergent composition |
US7485110B2 (en) | 2001-12-20 | 2009-02-03 | Kimberly Clark Worldwide, Inc. | Wipe comprising a pathogen selective antimicrobial |
US6891079B2 (en) | 2001-12-20 | 2005-05-10 | Kimberly-Clark Worldwide, Inc. | Wipe |
US7154018B2 (en) | 2001-12-20 | 2006-12-26 | Kimberly-Clark Worldwide, Inc. | Absorbent article |
FR2871061B1 (en) * | 2004-06-04 | 2007-08-10 | Coletica Sa | ACTIVE PRINCIPLE CAPABLE OF INDUCING TRANSFORMATION FROM INACTIVE TGBF-LATENT TO ACTIVE TGFB |
KR100718345B1 (en) * | 2005-04-27 | 2007-05-14 | 계명대학교 산학협력단 | An antifungal composition comprising resveratrol having antifungal activity |
JP2009227619A (en) * | 2008-03-24 | 2009-10-08 | Maruzen Pharmaceut Co Ltd | ENDOTHELIN-1 mRNA EXPRESSION ELEVATION INHIBITOR, STEM CELL GROWTH FACTOR mRNA EXPRESSION ELEVATION INHIBITOR, BASIC FIBROBLAST GROWTH FACTOR mRNA EXPRESSION ELEVATION INHIBITOR, AND PROPIOMELANOCORTIN mRNA EXPRESSION ELEVATION INHIBITOR |
JP5918168B2 (en) * | 2012-04-27 | 2016-05-18 | 富士フイルム株式会社 | β-Glucocerebrosidase activity enhancer |
KR102466456B1 (en) * | 2020-11-30 | 2022-11-15 | 주식회사 미그림 | Composition comprising fermented cactus honey and its use for improving skin condition |
-
1996
- 1996-06-06 JP JP8168324A patent/JP3053368B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH09328410A (en) | 1997-12-22 |
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