JP4913487B2 - Cosmetics characterized by a feeling of use - Google Patents
Cosmetics characterized by a feeling of use Download PDFInfo
- Publication number
- JP4913487B2 JP4913487B2 JP2006188147A JP2006188147A JP4913487B2 JP 4913487 B2 JP4913487 B2 JP 4913487B2 JP 2006188147 A JP2006188147 A JP 2006188147A JP 2006188147 A JP2006188147 A JP 2006188147A JP 4913487 B2 JP4913487 B2 JP 4913487B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- skin
- external preparation
- clay mineral
- modified
- 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.)
- Active
Links
- 239000002537 cosmetic Substances 0.000 title description 33
- 238000002360 preparation method Methods 0.000 claims description 37
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
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- 230000000052 comparative effect Effects 0.000 description 4
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- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
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- 239000004386 Erythritol Substances 0.000 description 2
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- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
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Landscapes
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Description
本発明は、皮膚外用剤に関し、更に詳細には、化粧料に好適な油中水中油乳化剤形の皮膚外用剤に関する。 The present invention relates to an external preparation for skin, and more particularly to an external preparation for skin in the form of an oil-in-water-in-oil emulsifier suitable for cosmetics.
化粧料の効果は、薬事法によれば、肌を整え、清潔に、健やかに保つことであり、その為の保湿成分、美白成分、抗炎症成分などが開発され、配合されている。しかしながら、化粧料の機能としては、この様な機能に留まるものではなく、それを使用することによる
心地よさに誘起される好ましい効果も存することも確かである。又、この反面として、ストレスの過負荷のような心理的な状態が、肌荒れを誘起することも知られており、化粧料を使用することは、肌に直接的に改善作用を及ぼすと同時に、使用感の心地よさを介して、心理的な面でのリラクゼーションを誘起し、以て、内面より間接的に肌状態の改善作用も奏しているものと考えられる(例えば、特許文献1、特許文献2、特許文献3、特許文献4、特許文献5、特許文献6、特許文献7を参照)。更に、この様な心理的な面に作用する要素としては、使用感という触覚刺激に止まらず、視覚刺激によっても奏されることが知られている(例えば、特許文献8を参照)。斯くの如くに、化粧料のような、敏感な感覚器官である皮膚に投与される皮膚外用剤においては、使用時における、その触感刺激を好ましい状態に調整することが望まれていると言える。
The effect of cosmetics is to keep the skin clean and healthy according to the Pharmaceutical Affairs Law, and moisturizing ingredients, whitening ingredients, anti-inflammatory ingredients, etc. have been developed and formulated. However, the function of cosmetics is not limited to such a function, and it is also certain that there is a favorable effect induced by comfort by using the cosmetic. On the other hand, psychological conditions such as stress overload are also known to induce rough skin, and the use of cosmetics has a direct effect on the skin, It is considered that the relaxation in the psychological aspect is induced through the comfortable feeling of use, and thus the skin condition is also improved indirectly from the inner surface (for example, Patent Document 1, Patent Document). 2, Patent Document 3, Patent Document 4, Patent Document 5, Patent Document 6, and Patent Document 7). Furthermore, it is known that such an element that acts on a psychological aspect is not limited to a tactile stimulus such as a feeling of use but is also played by a visual stimulus (see, for example, Patent Document 8). As described above, it can be said that it is desired to adjust the tactile sensation to a preferable state in use in a skin external preparation administered to the skin which is a sensitive sensory organ such as cosmetics.
皮膚外用剤について、触感刺激という点で、製剤形との関係について考察を加えると、ローション剤形においては、使用時、溶剤である水性担体の揮散とともに擦過における摩擦抵抗値が急上昇することから、有効成分の投与剤形としては好適であっても、好適な触覚刺激付与の剤形としては、改善するべき点を有するものである。乳化剤形の内、水中油乳化剤形においては、皮膚上で塗布擦過する過程に於いて、外相の水性成分の揮散とともに油中水乳化剤形へ反転し、それに伴い摩擦係数が急上昇する、当初ののびが軽すぎて心地よさが足りないなどの短所が存し、この剤形においても改善すべき点を有するものである。油中水乳化剤形においては、反転による摩擦係数の急上昇は存しないメリットが存するが、のびそのものが非常に重い、塗布後に脂っぽさを感じる等の欠点が存するために、この剤形においても改善すべき点を有するものである。単純オイル系においては、使用時の摩擦感のない擦過の心地よさは存するものの、使用後にオイル分が過剰に皮膚に残る、水性有効成分の投与剤形としては適していないなどの短所が存し、この剤形においても改善すべき点を有するものである。即ち、皮膚外用剤としての基本的な直接作用を奏しながら、使用感における間接作用を高めた剤形の開発が望まれていると言える。 Regarding the topical skin preparation, when considering the relationship with the formulation in terms of tactile stimulation, in the lotion dosage form, the friction resistance value in rubbing rapidly increases with the volatilization of the aqueous carrier as a solvent during use. Even if it is suitable as a dosage form of the active ingredient, a suitable tactile stimulation imparting dosage form has a point to be improved. Among the emulsifier forms, the oil-in-water emulsifier form reverses to the water-in-oil emulsifier form along with volatilization of the aqueous component in the external phase in the process of applying and rubbing on the skin. However, there are disadvantages such as being too light and not comfortable, and this dosage form also has a point to be improved. In the water-in-oil emulsifier form, there is a merit that the friction coefficient does not rise rapidly due to reversal, but because the spread itself is very heavy and there are drawbacks such as feeling greasy after application, this dosage form also has It has points to be improved. In the case of simple oil systems, although there is a feeling of rubbing without a feeling of friction during use, excessive oil remains on the skin after use, and there are disadvantages such as being unsuitable as a dosage form of an aqueous active ingredient. This dosage form also has a point to be improved. That is, it can be said that there is a demand for development of a dosage form that has a basic direct action as an external preparation for skin and has an enhanced indirect action in use feeling.
ジメチルジステアリルアンモニウム変性ヘクトライトなどの有機変性粘土鉱物は、油性成分とゲルを形成し、このゲル中に水を取り込む性質が存し、この性質を利用して、乳化成分として使用されている(例えば、特許文献9、特許文献10を参照)。又、N−ラウロイル−L−グルタミン酸ジ(コレステリル/ベヘニル/オクチルドデシル)、N−ラウロイル−L−グルタミン酸ジ(コレステリル/オクチルドデシル)、N−ラウロイル−L−グルタミン酸ジ(フィトステリル/ベヘニル/オクチルドデシル)、N−ラウロイル−L−グルタミン酸ジ(フィトステリル/オクチルドデシル)等のアシル化グルタミン酸ジエステルは難溶性の有効成分の担体として有用な油性のアミノ酸誘導体として化粧料に配合されることが知られている(例えば、特許文献11を参照)。更に、油中水乳化剤形にアシル化グルタミン酸ジエステルを含有させる技術も既に知られている(例えば、特許文献12、特許文献13を参照)。しかしながら、1)有機変性粘土鉱物と、2)N−アシル(炭素数10〜30)グルタミン酸ジアルキル(炭素数1〜30)エステルとを含有する油中水中油乳化剤形の皮膚外用剤は知られておらず、この様な構成を取ることにより、ストレス緩和に好適な触覚刺激を使用時に誘起する使用感を有する皮膚外用剤とすることが出来ることも全く知られていない。 Organically modified clay minerals such as dimethyl distearyl ammonium-modified hectorite form a gel with an oily component and have the property of incorporating water into the gel, and this property is used as an emulsifying component ( For example, see Patent Document 9 and Patent Document 10.) Further, N-lauroyl-L-glutamate di (cholesteryl / behenyl / octyldodecyl), N-lauroyl-L-glutamate di (cholesteryl / octyldodecyl), N-lauroyl-L-glutamate di (phytosteryl / behenyl / octyldodecyl) It is known that acylated glutamic acid diesters such as N-lauroyl-L-glutamic acid di (phytosteryl / octyldodecyl) are blended in cosmetics as oily amino acid derivatives useful as carriers for sparingly soluble active ingredients ( For example, see Patent Document 11). Furthermore, a technique for incorporating an acylated glutamic acid diester into a water-in-oil emulsifier form is already known (see, for example, Patent Document 12 and Patent Document 13). However, a skin external preparation in the form of an oil-in-water-in-oil emulsifier containing 1) an organically modified clay mineral and 2) an N-acyl (10 to 30 carbon atoms) dialkyl glutamate (1 to 30 carbon atoms) ester is known. In addition, it is not known at all that it is possible to obtain a skin external preparation having a feeling of use that induces tactile stimulation suitable for stress relaxation at the time of use by adopting such a configuration.
本発明は、この様な状況下為されたものであり、その使用感において、心地よい剤形を提供することを課題とする。 The present invention has been made under such circumstances, and an object of the present invention is to provide a dosage form that is comfortable in use feeling.
この様な状況に鑑みて、本発明者らは、こころを安定させ、ストレス緩和に好適な、その使用感において、心地よい剤形を求めて、鋭意研究努力を重ねた結果、1)有機変性粘土鉱物と、2)ポリエーテル変性メチルポリシロキサンと、3)N−アシル(炭素数10〜30)グルタミン酸ジアルキル(炭素数1〜30)エステルと、4)特定の保湿性高分子とを含有する油中水中油乳化剤形の皮膚外用剤が、その様な特性を具備していることを見出し、発明を完成させるに至った。即ち、本発明は次に示すとおりである。
(1)油中水中油乳化剤形の皮膚外用剤であって、外相油中に、1)有機変性粘土鉱物と、2)ポリエーテル変性メチルポリシロキサンと、3)N−アシル(炭素数10〜30)グルタミン酸ジアルキル(炭素数1〜30)エステルとを含有し、水相中に、4)ポリメタクリロイルリジン、ポリグルコシルエチルメタクリレート及びポリメタクリロイルオキシエチルホスホリルコリンから選択される保湿性高分子を含有することを特徴とする、皮膚外用剤。
(2)前記N−アシル(炭素数10〜30)グルタミン酸ジアルキル(炭素数1〜30)エステルが、N−ラウロイルグルタミン酸ジ(フィトステリル/オクチルドデシル)であることを特徴とする、(1)に記載の皮膚外用剤。
(3)前記ポリエーテル変性メチルポリシロキサンを構成するポリエーテル部分がポリエチレングリコールであることを特徴とする、(1)又は(2)に記載の皮膚外用剤。
In view of such circumstances, the present inventors have found that heart stabilizes and suitable stress relaxation in its feeling, seeking pleasant dosage form, the results of extensive research efforts, 1) Organic-modified clay Oil containing mineral, 2) polyether-modified methylpolysiloxane, 3) N-acyl (C10-30) dialkyl glutamate (C1-30) ester, and 4) specific moisturizing polymer It has been found that a skin external preparation in the form of an oil-in-water emulsifier has such characteristics, and has completed the invention. That is, the present invention is as follows.
(1) A skin external preparation in the form of an oil-in-water oil-in-oil emulsifier, comprising: 1) an organically modified clay mineral, 2) a polyether-modified methylpolysiloxane, 3 ) N-acyl (10 to 10 carbon atoms) 30) containing a dialkyl glutamate (1-30 carbon atoms) ester, and containing a moisturizing polymer selected from 4) polymethacryloyllysine, polyglucosylethyl methacrylate and polymethacryloyloxyethyl phosphorylcholine in the aqueous phase. and wherein, skin Hadagaiyo agent.
(2) The N-acyl (10 to 30 carbon atoms) dialkyl glutamic acid (1 to 30 carbon atoms) ester is N-lauroyl glutamate di (phytosteryl / octyldodecyl), described in (1) Topical skin preparation.
(3), wherein the polyether portion constituting the port Rieteru modified methylpolysiloxane is a polyethylene glycol, a skin external preparation as described in (1) or (2).
本発明によれば、その使用感において、心地よい剤形を提供することができる。 According to the present invention, it is possible to provide a dosage form that is comfortable to use.
(1)本発明の皮膚外用剤の必須成分である有機変性粘土鉱物
本発明の皮膚外用剤は有機変性粘土鉱物を必須成分として含有することを特徴とする。ここで有機変性とは、粘土鉱物の一部に有機化合物の一部を共有結合乃至はイオン結合を介して強固乃至は緩やかな結合を生ぜしめ、有機化合物の性質の一部乃至は全部を粘土鉱物に付与させることを意味し、この様な変性としては4級アミン基と粘土鉱物のアニオン部分を結合させる方法、カルボキシル基と粘土鉱物のカチオン部分を結合させる方法等が例示でき、4級アミン基と粘土鉱物のアニオン部分を結合させる方法が特に好ましく例示できる。
(1) Organically modified clay mineral which is an essential component of the external preparation for skin of the present invention The external preparation for skin of the present invention is characterized by containing an organically modified clay mineral as an essential component. Here, organic modification means that a part or all of the properties of an organic compound is made into a clay mineral by causing a part of the organic compound to form a strong or loose bond via a covalent bond or an ionic bond. This means that it is imparted to minerals. Examples of such modifications include a method of binding a quaternary amine group and an anion portion of a clay mineral, and a method of binding a carboxyl group and a cation portion of a clay mineral. A method of combining the group and the anion portion of the clay mineral is particularly preferable.
粘土鉱物を変性させる4級アミノ基を有する化合物としては、特に限定されるわけではないが、クオタニウムと称される化合物が例示される。クオタニウムとは、低分子の置換第4級アンモニウム塩であって、国際基準化粧品原材料(INCI)に登録された化粧料原料が好ましい。さらに、粘土鉱物を変性させる4級アミノ基を有する化合物は、クオタニウム化合物のなかでも、従来の皮膚外用剤に含有されるクオタニウム化合物であることが好ましい。従来の皮膚外用剤で使用されているクオタニウム化合物としては、ステアリルトリメチルアンモニウムクロリド、ジメチルジステアリルアンモニウムクロリド等が好
ましく例示される。ステアリルトリメチルアンモニウムクロリド、ジメチルジステアリルアンモニウムクロリド等は、粘土鉱物とともに安定な油中水性成分乳化構造を形成することができるので好ましい。特に、水性成分が水中油乳化物であった場合には、前記水中油乳化物にあまり影響を与えずに連続相を油相とする乳化物を形成できるので、油中水中油乳化剤形には好ましい。
Although it does not necessarily limit as a compound which has a quaternary amino group which modifies a clay mineral, The compound called quaternium is illustrated. Quotanium is a low molecular weight substituted quaternary ammonium salt, and is preferably a cosmetic raw material registered in International Standard Cosmetic Ingredients (INCI). Furthermore, the compound having a quaternary amino group that modifies the clay mineral is preferably a quaternium compound contained in a conventional external skin preparation among quaternium compounds. Preferred examples of the quaternium compound used in conventional external preparations for skin include stearyl trimethyl ammonium chloride and dimethyl distearyl ammonium chloride. Stearyl trimethyl ammonium chloride, dimethyl distearyl ammonium chloride, and the like are preferable because they can form a stable aqueous oil-in-water component emulsion structure together with clay minerals. In particular, when the aqueous component is an oil-in-water emulsion, an emulsion having a continuous phase as an oil phase can be formed without significantly affecting the oil-in-water emulsion. preferable.
一方、4級アミノ基を有する化合物で変性される粘土鉱物(未変性粘土鉱物)としては、従来の皮膚外用剤に含有される粘土鉱物であれば特段の限定無く使用することができる。従来の皮膚外用剤に含有される粘土鉱物としては、スメクタイト系のヘクトライト、ベントナイトやモンモリロナイト;カオリナイト;イライト;マリーン粘土鉱物(海泥);デザートローズ粘土鉱物;パスカライトなどが好ましく挙げられる。これらのうち、油中水乳化構造を安定化させることができるベントナイト、ヘクトライト、モンモリロナイト又はカオリナイトが好ましく例示される。 On the other hand, as a clay mineral (unmodified clay mineral) modified with a compound having a quaternary amino group, any clay mineral contained in a conventional external preparation for skin can be used without particular limitation. Preferred clay minerals contained in conventional skin external preparations include smectite-type hectorite, bentonite and montmorillonite; kaolinite; illite; marine clay mineral (sea mud); desert rose clay mineral; Among these, bentonite, hectorite, montmorillonite or kaolinite which can stabilize the water-in-oil emulsion structure is preferably exemplified.
本発明の皮膚外用剤に含有される4級アミノ基を有する化合物で変性された粘土鉱物の製造方法の一例を以下に説明する。
前記未変性粘土鉱物を分散媒に分散させる。該分散剤は水系の溶媒であることが好ましく、水であってもよい。分散未変性粘土鉱物を含む分散液に、さらに4級アミノ基を有する化合物を加え、よく撹拌する。4級アミノ基を有する化合物は、水に溶解されて加えられてもよい。加えられる4級アミノ基を有する化合物の量は、分散未変性粘土鉱物の量に対して0.1〜20質量%であることが好ましく、0.5〜15質量%であることがより好ましい。この様な構成を取ることにより、乳化系において、好ましい使用感を呈するためである。撹拌後、分散質を濾取し、脱水、乾固することにより本発明における変性粘土鉱物を得ることができる。あるいは、分散質を濾取することなく、減圧濃縮することにより分散剤を除去して乾固させることにより、本発明における変性粘土鉱物を得ることもできる。得られた変性粘土鉱物は、好ましくは所望のサイズ(粒径が1〜1000μmであることが好ましい)に粉砕され、本発明の皮膚外用剤に含有される。
An example of a method for producing a clay mineral modified with a compound having a quaternary amino group contained in the external preparation for skin of the present invention will be described below.
The unmodified clay mineral is dispersed in a dispersion medium. The dispersant is preferably an aqueous solvent, and may be water. A compound having a quaternary amino group is further added to the dispersion containing the dispersed unmodified clay mineral and stirred well. The compound having a quaternary amino group may be added after being dissolved in water. The amount of the compound having a quaternary amino group to be added is preferably 0.1 to 20% by mass, and more preferably 0.5 to 15% by mass with respect to the amount of the dispersed unmodified clay mineral. This is because by taking such a configuration, a preferable feeling of use is exhibited in the emulsification system. After stirring, the dispersoid is filtered, dehydrated and dried to obtain the modified clay mineral in the present invention. Or the modified clay mineral in this invention can also be obtained by removing a dispersing agent by concentrating under reduced pressure without filtering a dispersoid, and making it dry. The obtained modified clay mineral is preferably pulverized to a desired size (preferably having a particle size of 1 to 1000 μm) and contained in the skin external preparation of the present invention.
本発明における変性粘土鉱物は、前述したように調製して使用されることもできるが、市販されているものを使用することもできる。市販されている変性粘土鉱物には、化粧料などの皮膚外用剤などとして用いられているものもある。市販されている変性粘土鉱物としては、例えば、エレメンティス社より「ベントン38V」の名称で販売されている、ジメチルジステアリルアンモニウム変性ヘクトライトなどが好ましく例示される。 The modified clay mineral in the present invention can be prepared and used as described above, but a commercially available one can also be used. Some modified clay minerals on the market are used as external preparations for skin such as cosmetics. Preferable examples of commercially available modified clay minerals include dimethyl distearyl ammonium modified hectorite sold under the name “Benton 38V” by Elementis.
本発明の皮膚外用剤においては、かかる成分は好ましくは0.5〜10質量%含有され、より好ましくは1〜5質量%含有される。かかる成分は、前記の含有量の範囲において、乳化剤として働くと同時に、その塗布時の使用感において、N−アシルグルタミン酸ジエステルとともに働き、塗布されている人に心地よさを感じせしめ、以て、リラックスさせ、ストレスを緩和する作用を有する。これにより、ストレスによる肌への悪影響を還元、緩和することが出来る。特に、油中水中油乳化剤形を取ることにより、揮散成分の揮散に伴う、系の変化などに起因して数回起こる摩擦係数の変化が適度に触感を刺激し、リラックス効果を増強する。 In the skin external preparation of the present invention, such components are preferably contained in an amount of 0.5 to 10% by mass, more preferably 1 to 5% by mass. Such an ingredient works as an emulsifier within the above-mentioned range of contents, and at the same time, works together with N-acyl glutamic acid diester in the feeling of use at the time of application, making the applied person feel comfortable and relaxing. And has the effect of relieving stress. Thereby, the bad influence to the skin by stress can be reduced and relieved. In particular, by taking the oil-in-water emulsifier form in oil, the change in the friction coefficient that occurs several times due to the change in the system due to the volatilization of the volatilization component moderately stimulates the tactile sensation and enhances the relaxation effect.
(2)本発明の皮膚外用剤の必須成分であるN−アシルグルタミン酸ジエステル
本発明の皮膚外用剤は、N−アシル(炭素数10〜30)グルタミン酸ジアルキル(炭素数1〜30)エステルを必須成分として含有する。かかる成分を構成するアシル基としては、飽和でも、不飽和でも良く、例えば、2−エチルヘキサノイル基、ラウロイル基、ミリストイル基、パルミトイル基、ステアロイル基、ベヘノイル基、オレオイル基、イソステアロイル基、リノレノイル基などが好適に例示でき、特に好ましいものはラウロイル基である。又、ジアルキルエステルを構成するアルキル基としては、分岐でも、直鎖でも
、環状構造を有するものでも良く、例えば、オクチル基、ラウリル基、セチル基、ステアリル基、イソステアリル基、ベヘニル基、オクチルドデシル基、カンペステリル基やシトステリル基等のフィトステリル基、コレステリル基などが好適に例示できる。具体的な化合物例としては、N−ラウロイル−L−グルタミン酸ジ(コレステリル/ベヘニル/オクチルドデシル)、N−ラウロイル−L−グルタミン酸ジ(コレステリル/オクチルドデシル)、N−ラウロイル−L−グルタミン酸ジ(フィトステリル/ベヘニル/オクチルドデシル)、N−ラウロイル−L−グルタミン酸ジ(フィトステリル/オクチルドデシル)等が好適に例示でき、N−ラウロイル−L−グルタミン酸ジ(コレステリル/オクチルドデシル)が特に好適に例示できる。かかるN−アシルグルタミン酸ジエステルは、グルタミン酸とアシルクロリドをアルカリ存在下縮合させ、N−アシルグルタミン酸と為し、しかる後、塩基又は酸の存在下、所望により溶剤を存在させ、対応するアルコールと脱水縮合せしめ製造することが出来る。N−アシルグルタミン酸ジエステルは、この様に合成したものを使用することも出来るが、既に化粧料原料などとして市販されているものも存し、この様な市販品を購入し利用することも出来る。特に好ましい市販品としては味の素株式会社より販売されている「エルデュウPS203」(N−ラウロイル−L−グルタミン酸ジ(フィトステリル/オクチルドデシル))が例示できる。かかる成分は唯一種含有させることも出来るし、二種以上を組み合わせて含有させることも出来る。好ましい含有量は、総量で、皮膚外用剤全量に対し、0.1〜10質量%であり、より好ましくは1〜5質量%である。かかる成分は、系に適度なのびと、延展時の指と皮膚との密着感を高める作用を有し、前記有機変性粘土鉱物とともに使用すると、塗布されている人に心地よさを感じせしめ、以て、リラックスさせ、こころを安定させて、ストレスを緩和する作用を有する。これにより、ストレスによる肌への悪影響を還元、緩和することが出来る。特に、油中水中油乳化剤形に於いて、油相(最外相)にこの成分が存在する場合にはこの効果は著しい。
(2) N-acyl glutamic acid diester which is an essential component of the external preparation for skin of the present invention The external preparation for skin of the present invention is an N-acyl (10 to 30 carbon atoms) dialkyl glutamic acid (1 to 30 carbon atoms) ester as an essential component. Contained as. The acyl group constituting the component may be saturated or unsaturated, for example, 2-ethylhexanoyl group, lauroyl group, myristoyl group, palmitoyl group, stearoyl group, behenoyl group, oleoyl group, isostearoyl group, A linolenoyl group etc. can be illustrated suitably, A lauroyl group is especially preferable. In addition, the alkyl group constituting the dialkyl ester may be branched, straight chain, or cyclic, for example, octyl group, lauryl group, cetyl group, stearyl group, isostearyl group, behenyl group, octyldodecyl. Preferred examples include phytosteryl groups such as campesteryl group and sitosteryl group, and cholesteryl group. Specific examples of the compound include N-lauroyl-L-glutamate di (cholesteryl / behenyl / octyldodecyl), N-lauroyl-L-glutamate di (cholesteryl / octyldodecyl), N-lauroyl-L-glutamate di (phytosteryl). / Behenyl / octyldodecyl), N-lauroyl-L-glutamate di (phytosteryl / octyldodecyl) and the like can be preferably exemplified, and N-lauroyl-L-glutamate di (cholesteryl / octyldodecyl) can be particularly suitably exemplified. Such an N-acyl glutamic acid diester is obtained by condensing glutamic acid and acyl chloride in the presence of an alkali to form N-acyl glutamic acid, and then in the presence of a base or acid, optionally in the presence of a solvent, and dehydrating condensation with the corresponding alcohol. Can be manufactured. As the N-acylglutamic acid diester, those synthesized in this way can be used, but there are those already marketed as cosmetic raw materials, and such commercial products can be purchased and used. A particularly preferred commercially available product is “Erudu PS203” (N-lauroyl-L-glutamate di ( phytosteryl / octyldodecyl)) sold by Ajinomoto Co., Inc. These components can be contained alone or in combination of two or more. The preferred content is 0.1 to 10% by mass, more preferably 1 to 5% by mass, based on the total amount of the external preparation for skin. Such an ingredient has an appropriate effect on the system and has an effect of enhancing the feeling of adhesion between the finger and the skin at the time of spreading, and when used together with the above organically modified clay mineral, makes the applied person feel comfortable, It has the action of relaxing, stabilizing the mind and relieving stress. Thereby, the bad influence to the skin by stress can be reduced and relieved. In particular, in the oil-in-water oil-in-water emulsifier form, this effect is remarkable when this component is present in the oil phase (outermost phase).
(3)本発明の皮膚外用剤
本発明の皮膚外用剤は前記必須成分及び後記するポリエーテル変性メチルポリシロキサンを最外油相に含有し、後記する保湿性高分子を水相中に含有する油中水中油乳化剤形であることを特徴とする。これはこの様な油中水中油乳化形態がより大きな使用感の心地よさを提供できるからである。本発明の皮膚外用剤としては、皮膚に外用で投与されるものであれば特段の限定はなく適用され、例えば、化粧料、皮膚外用医薬、皮膚外用雑貨などが好ましく例示できる。これらの内では、化粧料が特に好ましい。これは、本発明の皮膚外用剤の作用が緩和であるためである。又、化粧料としては、医薬部外品が好ましく、医薬部外品においてはグリチルリチン酸塩やグリチルレチン酸ステアリルなどの抗炎症成分を0.05〜0.1質量%有効成分として含有することが好ましい。特に、グリチルリチン酸塩は、界面活性作用を有するため、油相に分散させる水中油乳化物に界面活性剤として含有させることが好ましい。この様な界面活性作用のある有効成分としては、サポニン類を多く含有する、コウライニンジンエキス、ツボクサエキスなどが存し、これらを同様の目的で含有することも好ましい。かかる成分の好ましい含有量は、それぞれ0.05〜0.1質量%である。これは本発明の必須成分の組合せでは炎症そのものを抑制する作用が低いためである。本発明の皮膚外用剤においては、使用態様を的確に遵守することが効果と結びついているので、使用態様を遵守させるために、その使用感を介して、こころの安定感を付与する化粧料であることの旨の表示を有することが好ましい。
(3) Skin external preparation of the present invention The skin external preparation of the present invention contains the essential components and the polyether-modified methylpolysiloxane described later in the outermost oil phase, and the moisturizing polymer described later in the aqueous phase. It is characterized by being in the form of an oil-in-water oil emulsifier. This is because such an oil-in-water-in-oil emulsified form can provide greater comfort in use. The external preparation for skin of the present invention is not particularly limited as long as it is externally administered to the skin, and examples thereof include cosmetics, external preparations for skin, and sundry items. Of these, cosmetics are particularly preferred. This is because the action of the external preparation for skin of the present invention is mild. The cosmetic is preferably a quasi-drug, and the quasi-drug preferably contains an anti-inflammatory component such as glycyrrhizinate or stearyl glycyrrhetinate as an active ingredient in an amount of 0.05 to 0.1% by mass. . In particular, since glycyrrhizinate has a surface active action, it is preferable to contain it as a surfactant in an oil-in-water emulsion dispersed in an oil phase. As such an active ingredient having a surface-active action, there is a mulberry extract, a camellia extract, etc. containing a large amount of saponins, and it is also preferable to contain these for the same purpose. Preferable content of such a component is 0.05 to 0.1% by mass. This is because the combination of essential components of the present invention has a low effect of suppressing inflammation itself. In the preparation for external use of the skin of the present invention, it is associated with the effect that the usage mode is strictly observed. Therefore, in order to comply with the usage mode, a cosmetic that imparts a sense of stability to the mind through its usage feeling. It is preferable to have an indication to the effect.
本発明の皮膚外用剤においては、前記の必須成分以外に、通常化粧料などの皮膚外用剤で使用される任意成分を含有することが出来る。この様な任意成分としては、例えば、マカデミアナッツ油、アボガド油、トウモロコシ油、オリーブ油、ナタネ油、ゴマ油、ヒマシ油、サフラワー油、綿実油、ホホバ油、ヤシ油、パーム油、液状ラノリン、硬化ヤシ油、硬化油、モクロウ、硬化ヒマシ油、ミツロウ、キャンデリラロウ、カルナウバロウ、イボタロウ、ラノリン、還元ラノリン、硬質ラノリン、ホホバロウ等のオイル、ワックス類
;流動パラフィン、スクワラン、プリスタン、オゾケライト、パラフィン、セレシン、ワセリン、マイクロクリスタリンワックス等の炭化水素類;オレイン酸、イソステアリン酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、ベヘン酸、ウンデシレン酸等の高級脂肪酸類;セチルアルコール、ステアリルアルコール、イソステアリルアルコール、ベヘニルアルコール、オクチルドデカノール、ミリスチルアルコール、セトステアリルアルコール等の高級アルコール等;イソオクタン酸セチル、ミリスチン酸イソプロピル、イソステアリン酸ヘキシルデシル、アジピン酸ジイソプロピル、セバチン酸ジ−2−エチルヘキシル、乳酸セチル、リンゴ酸ジイソステアリル、ジ−2−エチルヘキサン酸エチレングリコール、ジカプリン酸ネオペンチルグリコール、ジ−2−ヘプチルウンデカン酸グリセリン、トリ−2−エチルヘキサン酸グリセリン、トリ−2−エチルヘキサン酸トリメチロールプロパン、トリイソステアリン酸トリメチロールプロパン、テトラ−2−エチルヘキサン酸ペンタンエリトリット等の合成エステル油類;ジメチルポリシロキサン、メチルフェニルポリシロキサン、ジフェニルポリシロキサン等の鎖状ポリシロキサン;オクタメチルシクロテトラシロキサン、デカメチルシクロペンタシロキサン、ドデカメチルシクロヘキサンシロキサン等の環状ポリシロキサン;アミノ変性メチルポリシロキサン、アルキル変性ポリシロキサン、フッ素変性ポリシロキサン等の変性ポリシロキサン等のシリコーン油等の油剤類;脂肪酸セッケン(ラウリン酸ナトリウム、パルミチン酸ナトリウム等)、ラウリル硫酸カリウム、アルキル硫酸トリエタノールアミンエーテル等のアニオン界面活性剤類;塩化ステアリルトリメチルアンモニウム、塩化ベンザルコニウム、ラウリルアミンオキサイド等のカチオン界面活性剤類;イミダゾリン系両性界面活性剤(2−ココイル−2−イミダゾリニウムヒドロキサイド−1−カルボキシエチロキシ2ナトリウム塩等)、ベタイン系界面活性剤(アルキルベタイン、アミドベタイン、スルホベタイン等)、アシルメチルタウリン等の両性界面活性剤類;ソルビタン脂肪酸エステル類(ソルビタンモノステアレート、セスキオレイン酸ソルビタン等)、グリセリン脂肪酸類(モノステアリン酸グリセリン等)、プロピレングリコール脂肪酸エステル類(モノステアリン酸プロピレングリコール等)、硬化ヒマシ油誘導体、グリセリンアルキルエーテル、POEソルビタン脂肪酸エステル類(POEソルビタンモノオレエート、モノステアリン酸ポリオキエチレンソルビタン等)、POEソルビット脂肪酸エステル類(POE−ソルビットモノラウレート等)、POEグリセリン脂肪酸エステル類(POE−グリセリンモノイソステアレート等)、POE脂肪酸エステル類(ポリエチレングリコールモノオレート、POEジステアレート等)、POEアルキルエーテル類(POE2−オクチルドデシルエーテル等)、POEアルキルフェニルエーテル類(POEノニルフェニルエーテル等)、プルロニック型類、POE・POPアルキルエーテル類(POE・POP2−デシルテトラデシルエーテル等)、テトロニック類、POEヒマシ油・硬化ヒマシ油誘導体(POEヒマシ油、POE硬化ヒマシ油等)、ショ糖脂肪酸エステル、アルキルグルコシド等の非イオン界面活性剤類;ポリエチレングリコール、グリセリン、1,3−ブチレングリコール、エリスリトール、ソルビトール、キシリトール、マルチトール、プロピレングリコール、ジプロピレングリコール、ジグリセリン、イソプレングリコール、1,2−ペンタンジオール、2,4−ヘキサンジオール、1,2−ヘキサンジオール、1,2−オクタンジオール等の多価アルコール類;ピロリドンカルボン酸ナトリウム、乳酸、乳酸ナトリウム等の保湿成分類;表面を処理されていても良い、マイカ、タルク、カオリン、合成雲母、炭酸カルシウム、炭酸マグネシウム、無水ケイ酸(シリカ)、酸化アルミニウム、硫酸バリウム等の粉体類;表面を処理されていても良い、ベンガラ、黄酸化鉄、黒酸化鉄、酸化コバルト、群青、紺青、酸化チタン、酸化亜鉛の無機顔料類;表面を処理されていても良い、雲母チタン、魚燐箔、オキシ塩化ビスマス等のパール剤類;レーキ化されていても良い赤色202号、赤色228号、赤色226号、黄色4号、青色404号、黄色5号、赤色505号、赤色230号、赤色223号、橙色201号、赤色213号、黄色204号、黄色203号、青色1号、緑色201号、紫色201号、赤色204号等の有機色素類;ポリエチレン末、ポリメタクリル酸メチル、ナイロン粉末、オルガノポリシロキサンエラストマー等の有機粉体類;パラアミノ安息香酸系紫外線吸収剤;アントラニル酸系紫外線
吸収剤;サリチル酸系紫外線吸収剤;桂皮酸系紫外線吸収剤;ベンゾフェノン系紫外線吸収剤;糖系紫外線吸収剤;2−(2’−ヒドロキシ−5’−t−オクチルフェニル)ベンゾトリアゾール、4−メトキシ−4’−t−ブチルジベンゾイルメタン等の紫外線吸収剤類;エタノール、イソプロパノール等の低級アルコール類;ビタミンA又はその誘導体、ビタミンB6塩酸塩、ビタミンB6トリパルミテート、ビタミンB6ジオクタノエート、ビタミンB2又はその誘導体、ビタミンB12、ビタミンB15又はその誘導体等のビタミンB類;α−トコフェロール、β−トコフェロール、γ−トコフェロール、ビタミンEアセテート等のビタミンE類、ビタミンD類、ビタミンH、パントテン酸、パンテチン、ピロロキノリンキノン等のビタミン類等;フェノキシエタノール等の抗菌剤等が好ましく例示できる。
In the external preparation for skin of the present invention, in addition to the essential components described above, optional components that are usually used in external preparations for skin such as cosmetics can be contained. Examples of such optional ingredients include macadamia nut oil, avocado oil, corn oil, olive oil, rapeseed oil, sesame oil, castor oil, safflower oil, cottonseed oil, jojoba oil, coconut oil, palm oil, liquid lanolin, and hardened coconut oil. Oil, wax, oils such as beeswax, molasses, hydrogenated castor oil, beeswax, candelilla wax, carnauba wax, ibotarou, lanolin, reduced lanolin, hard lanolin, jojoba wax; , Hydrocarbons such as microcrystalline wax; higher fatty acids such as oleic acid, isostearic acid, lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, undecylenic acid; cetyl alcohol, stearyl alcohol, isostearyl Higher alcohols such as alcohol, behenyl alcohol, octyldodecanol, myristyl alcohol, cetostearyl alcohol; cetyl isooctanoate, isopropyl myristate, hexyldecyl isostearate, diisopropyl adipate, di-2-ethylhexyl sebacate, cetyl lactate, malic acid Diisostearyl, di-2-ethylhexanoic acid ethylene glycol, dicaprate neopentyl glycol, di-2-heptylundecanoic acid glycerin, tri-2-ethylhexanoic acid glycerin, tri-2-ethylhexanoic acid trimethylolpropane, tri Synthetic ester oils such as trimethylolpropane isostearate and pentane erythritol tetra-2-ethylhexanoate; dimethylpolysiloxane, methylphenylpoly Rokisan, linear polysiloxanes such as diphenyl polysiloxane; octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, cyclic polysiloxanes such as dodeca methylcyclohexane siloxane; amino-modified methylpolysiloxane, A alkyl-modified polysiloxane, fluorine-modified polysiloxane Oils such as silicone oil such as modified polysiloxane such as fatty acid soap (sodium laurate, sodium palmitate, etc.), anionic surfactants such as potassium lauryl sulfate, alkylsulfuric triethanolamine ether; stearyltrimethylammonium chloride, Cationic surfactants such as benzalkonium chloride and laurylamine oxide; imidazoline-based amphoteric surfactants (2-cocoyl-2-imidazolinium hydroxide) 1-carboxyethyloxy disodium salt, etc.), betaine surfactants (alkyl betaine, amide betaine, sulfobetaine, etc.), and amphoteric surfactants such as acylmethyltaurine; sorbitan fatty acid esters (sorbitan monostearate, sesquiskies) Sorbitan oleate, etc.), glycerin fatty acids (eg glyceryl monostearate), propylene glycol fatty acid esters (eg propylene glycol monostearate), hardened castor oil derivatives, glycerin alkyl ethers, POE sorbitan fatty acid esters (POE sorbitan monoole) Acid, polyoxyethylene sorbitan monostearate, etc.), POE sorbite fatty acid esters (POE-sorbitol monolaurate, etc.), POE glycerin fatty acid esters (POE-glycerin) Monoisostearate, etc.), POE fatty acid esters (polyethylene glycol monooleate, POE distearate, etc.), POE alkyl ethers (POE2-octyldodecyl ether, etc.), POE alkyl phenyl ethers (POE nonylphenyl ether, etc.), Pluronic type , POE / POP alkyl ethers (POE / POP2-decyltetradecyl ether, etc.), Tetronics, POE castor oil / hardened castor oil derivatives (POE castor oil, POE hardened castor oil, etc.), sucrose fatty acid ester, alkyl Nonionic surfactants such as glucoside; polyethylene glycol, glycerin, 1,3-butylene glycol, erythritol, sorbitol, xylitol, maltitol, propylene glycol, dipropylene glycol Polyhydric alcohols such as coal, diglycerin, isoprene glycol, 1,2-pentanediol, 2,4-hexanediol, 1,2-hexanediol, 1,2-octanediol; sodium pyrrolidonecarboxylate, lactic acid, lactic acid Moisturizing ingredients such as sodium; surface treated powders such as mica, talc, kaolin, synthetic mica, calcium carbonate, magnesium carbonate, silicic anhydride (silica), aluminum oxide, barium sulfate ; surface May be treated, inorganic pigments of bengara, yellow iron oxide, black iron oxide, cobalt oxide, ultramarine, bitumen, titanium oxide, zinc oxide; surface may be treated, titanium mica, fish phosphorus foil Pearl agents such as bismuth oxychloride; red 202, red 228, red 226, yellow which may be raked Color No. 4, Blue No. 404, Yellow No. 5, Red No. 505, Red No. 230, Red No. 223, Orange No. 201, Red No. 213, Yellow No. 204, Yellow No. 203, Blue No. 1, Green No. 201, Purple 201 No., organic dyes such as red No. 204; organic powders such as polyethylene powder, polymethyl methacrylate, nylon powder, organopolysiloxane elastomer; paraaminobenzoic acid UV absorber; anthranilic acid UV absorber; salicylic acid UV absorber; cinnamic acid UV absorber; benzophenone UV absorber; sugar UV absorber; 2- (2′-hydroxy-5′-t-octylphenyl) benzotriazole, 4-methoxy-4′-t UV absorbers such as butyldibenzoylmethane; lower alcohols such as ethanol and isopropanol; vitamin A or its derivatives Body, vitamin B 6 hydrochloride, vitamin B 6 tripalmitate, vitamin B 6 dioctanoate, vitamin B 2 or derivatives thereof, vitamin B 12 such as vitamin B 12 , vitamin B 15 or derivatives thereof; α-tocopherol, β-tocopherol , .gamma.-tocopherol, vitamin E such as vitamin E acetate, vitamin D, vitamin H, pantothenic acid, pantethine, vitamins pyrroloquinoline quinone such like; antibacterial agents such as phenoxyethanol or the like can be preferably exemplified.
前記した如く、本発明の皮膚外用剤は、ポリエーテル変性メチルポリシロキサンを含有する。かかるポリエーテル変性メチルポリシロキサンを構成するポリエーテル構造としては、ポリエチレングリコール残基やポリプロピレングリコール残基が好ましく例示でき、ポリエチレングリコール残基が特に好ましい。この様なポリエーテル変性メチルポリシロキサンには市販品が存し、かかる市販品を購入して利用することが出来る。好ましい市販品としては、信越化学株式会社より販売されている「シリコーンKF6017」、「シリコーンKF6018」(ポリエチレングリコール変性メチルポリシロキサン)が好適に例示できる。かかる成分は、前記必須成分である有機変性粘土鉱物が作る乳化構造をより安定化し、塗布における皮膚上での擦過時に水相が漏出する使用感を軽減する作用を有し、以て使用感を向上せしめる。この様な効果を奏するためには、ポリエーテル変性メチルポリシロキサンは、1〜10質量%含有することが好ましく、より好ましくは、2〜7質量%がより好ましい。 As mentioned above, the external preparation for skin of the present invention contains a port Rieteru modified methylpolysiloxane. The polyether structure constituting or mow port Rieteru modified methylpolysiloxane, polyethylene glycol residue or a polypropylene glycol residue can be preferably exemplified, polyethylene glycol residues are particularly preferred. The such port Rieteru modified methyl polysiloxane commercially resides, it can be utilized to purchase such commercially. Preferred commercially available products sold by Shin-Etsu Chemical Co., Ltd. "Silicone KF6017", "Silicone KF6018" (Po triethylene glycol-modified methylpolysiloxane) can be suitably exemplified. This component has the effect of further stabilizing the emulsified structure formed by the organically modified clay mineral, which is the essential component, and reducing the feeling of use when the aqueous phase leaks out during rubbing on the skin during application. Improve. To achieve such a effect, positive Rieteru modified methylpolysiloxane preferably contains 1 to 10 wt%, more preferably, more preferably 2 to 7 wt%.
同様に、本発明の皮膚外用剤には、ゲル構造を高め、内相構造を強固にする意味で、ポリメタクリロイルリジン、ポリグルコシルエチルメタクリレート、ポリメタクリロイルオキシエチルホスホリルコリンから選択される保湿性高分子を含有させる。この様な作用を奏するためにはかかる保湿性高分子は総量で、皮膚外用剤全量に対して0.01〜0.1質量%含有させることが好ましい。かかる成分が多すぎても、少なすぎても安定性が損なわれる場合が存する。 Similarly, the skin external preparation of the present invention to enhance the gel structure in the sense that to strengthen the internal phase structure, polymethacryloylacetones Le lysine, poly-glucosyl ethyl methacrylate, moisturizing polymer selected from polymethacryloylacetones oxyethyl phosphorylcholine Containing . In order to exhibit such an effect, the moisturizing polymer is preferably added in a total amount of 0.01 to 0.1% by mass based on the total amount of the external preparation for skin. There are cases where the stability is impaired if there are too many or too few such components.
以下に、実施例を挙げて、本発明について、更に詳細に説明を加えるが、本発明が、かかる実施例にのみ限定されないことは言うまでもない。 Hereinafter, the present invention will be described in more detail with reference to examples, but it is needless to say that the present invention is not limited to such examples.
<参考例1>
以下に示す処方に従って、化粧料を作成した。即ち、イ、ロ、ハ、ニの成分を80℃に加熱し、イの成分とロの成分を良く混練りし、これにハを加えて希釈し、攪拌下これにニを徐々に加え、乳化し、攪拌冷却し、油中水乳化剤形の化粧料1(抗炎症医薬部外品)を得た。
<Reference Example 1>
A cosmetic was prepared according to the formulation shown below. That is, the ingredients (a), (b), (c), and (d) are heated to 80 ° C., the ingredients (a) and (b) are kneaded well, added to this to dilute, and gradually added to the mixture with stirring. The mixture was emulsified, cooled with stirring, and a water-in-oil emulsifier type cosmetic 1 (anti-inflammatory pharmaceutical quasi-drug) was obtained.
<実施例1>
化粧料1と同じ成分構成で、剤形を油中水中油乳化剤形に変えて、化粧料2を作製した。即ち、イ、ロ、ハ、ニ、ホの成分をそれぞれ80℃に加熱し、イの成分とロの成分を良く混練りし、これにハを加えて希釈し、攪拌下これに、ホにニを加えて作製した水中油乳化物を、徐々に添加し、油中水中油乳化剤形を形成させ、攪拌冷却して化粧料2を得た。
<Example 1>
Cosmetic 2 was prepared with the same composition as cosmetic 1 but with the dosage form changed to an oil-in-water oil-in-water emulsifier. That is, each of the ingredients i, b, c, d, and e is heated to 80 ° C., the ingredients a and b are kneaded well, added with c, diluted, and stirred, The oil-in-water emulsion prepared by adding 2 was gradually added to form an oil-in-water oil-in-water emulsifier form, and stirred and cooled to obtain a cosmetic 2.
<試験例1>
化粧料1、化粧料2を用いて、こころのいらいらストレスの関与した損傷皮膚モデルにおける作用を確かめた。化粧料1とともに、化粧料1のベントン−38VをシリコーンKF6017に置換した比較例1、エルデュウPS203をデカメチルシクロペンタシロキサンに置換した比較例2を用意し、パネラー10名を3畳に1時間詰め込み、その後、前腕部に設けた2cm×4cmの5つの部位を、各部位のTEWL(経皮的散逸水分量)を「テヴァメータ」(インテグラル社製)で測定し、粘着テープで10回ストリッピングし、それぞれの部位に化粧料1、化粧料2、比較例1、比較例2の40μlをのせ、5分間擦過を続けた。1部位はコントロールとして損傷のみを行った。5分後、化粧料を石鹸とお湯で洗い流し、15分静置し、再びTEWLを測定した。次に示す式に従って、TEWL抑制率を算出した。この結果を平均値として表3に示す。又、同時にパネラーにアンケートで擦過時の感じを気持ちがよい、特に何も感じない、不快である、の3者択一の形で調査した結果も表3に示す。化粧料1は、使用感の良さによって、過密ストレスと皮膚損傷が引き起こした肌のトラブルを抑制していることが判る。同じ成分構成でありながら、化粧料2は更にこの効果が増強していることもわかる。
(1−(処理後の部位のTEWL−試験前の部位のTEWL)/(処理後のコントロール部位のTEWL−試験前のコントロール部位のTEWL))*100
<Test Example 1>
Using the cosmetics 1 and 2, the effect on the damaged skin model in which mental stress was involved was confirmed. Along with cosmetic 1, a comparative example 1 in which Benton-38V of cosmetic 1 is replaced with silicone KF6017 and a comparative example 2 in which Erdeu PS203 is replaced with decamethylcyclopentasiloxane are prepared, and 10 panelists are packed into 3 tatami mats for 1 hour. Then, measure 5 parts of 2cm x 4cm provided on the forearm, TEWL (percutaneous dissipated moisture) of each part with "Tevameter" (manufactured by Integral), stripping 10 times with adhesive tape Then, 40 μl of Cosmetic 1, Cosmetic 2, Comparative Example 1, and Comparative Example 2 were put on each part, and rubbing was continued for 5 minutes. One site was damaged only as a control. After 5 minutes, the cosmetic was washed away with soap and hot water, allowed to stand for 15 minutes, and TEWL was measured again. The TEWL suppression rate was calculated according to the following equation. The results are shown in Table 3 as average values. At the same time, Table 3 also shows the results of a survey conducted by the panelists in a three-choice form of feeling pleasant when scratched, especially feeling nothing, and being uncomfortable. It can be seen that the cosmetic 1 suppresses skin troubles caused by overstress stress and skin damage due to good usability. It can also be seen that the cosmetic 2 further enhances this effect even though the composition is the same.
(1- (TEWL of site after treatment-TEWL of site before test) / (TEWL of control site after treatment-TEWL of control site before test)) * 100
<参考例2>
実施例1と同様に下記の処方に従って、化粧料3(抗炎症医薬部外品)を製造した。試験例1のTEWL抑制率は64.3%(n=1)であった。ポリエーテル変性メチルシロキサンを含有することが好ましいことが判る。
<Reference Example 2>
In the same manner as in Example 1, cosmetic 3 (anti-inflammatory quasi-drug) was produced according to the following formulation. The TEWL suppression rate of Test Example 1 was 64.3% (n = 1). It can be seen that preferably contains a port Rieteru modified siloxane.
<参考例3>
実施例1と同様に下記の処方に従って、化粧料4(抗炎症医薬部外品)を製造した。試験例1のTEWL抑制率は62.9%(n=1)であった。保湿性高分子を含有することが好ましいことが判る。
<Reference Example 3>
In the same manner as in Example 1, cosmetic 4 (anti-inflammatory pharmaceutical quasi-drug) was produced according to the following formulation. The TEWL suppression rate of Test Example 1 was 62.9% (n = 1). It can be seen that it is preferable to contain a moisturizing polymer.
<実施例2>
実施例1と同様に下記の処方に従って、化粧料5(抗炎症医薬部外品)を製造した。試験例1のTEWL抑制率は68.9%(n=1)であった。N−アシルグルタミン酸ジエステルが汎用できることが判る。又、中でもN−ラウロイルグルタミン酸ジ(フィトステリル/オクチルドデシル)が特に好ましいことも判る。
<Example 2>
In the same manner as in Example 1, cosmetic 5 (anti-inflammatory pharmaceutical quasi-drug) was produced according to the following formulation. The TEWL suppression rate of Test Example 1 was 68.9% (n = 1). It turns out that N-acyl glutamic acid diester can be used widely. It can also be seen that N-lauroyl glutamate di (phytosteryl / octyldodecyl) is particularly preferable.
本発明は化粧料に応用できる。 The present invention can be applied to cosmetics.
Claims (3)
外相油中に、1)有機変性粘土鉱物と、2)ポリエーテル変性メチルポリシロキサンと、3)N−アシル(炭素数10〜30)グルタミン酸ジアルキル(炭素数1〜30)エステルとを含有し、
水相中に、4)ポリメタクリロイルリジン、ポリグルコシルエチルメタクリレート及びポリメタクリロイルオキシエチルホスホリルコリンから選択される保湿性高分子を含有することを特徴とする、皮膚外用剤。 A skin external preparation in the form of an oil-in-water oil emulsifier,
The outer phase oil contains 1) an organically modified clay mineral, 2) a polyether-modified methylpolysiloxane, and 3 ) an N-acyl (10 to 30 carbon atoms) dialkyl glutamate (1 to 30 carbon atoms) ester ,
In the aqueous phase, 4) polymethacryloylacetones Le lysine, characterized in that it contains a moisturizing polymer selected from poly glucosyl methacrylate and polymethacryloylacetones oxyethyl phosphorylcholine, leather Hadagaiyo agent.
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