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JP6845392B2 - Cosmetic composition - Google Patents

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JP6845392B2
JP6845392B2 JP2015122416A JP2015122416A JP6845392B2 JP 6845392 B2 JP6845392 B2 JP 6845392B2 JP 2015122416 A JP2015122416 A JP 2015122416A JP 2015122416 A JP2015122416 A JP 2015122416A JP 6845392 B2 JP6845392 B2 JP 6845392B2
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JP2016222637A (en
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貴大 北野
貴大 北野
香織 山▲崎▼
香織 山▲崎▼
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株式会社ピカソ美化学研究所
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Description

本発明は、水相に油相を浮遊させた化粧料用組成物に関する。 The present invention relates to a cosmetic composition in which an oil phase is suspended in an aqueous phase.

水相と油相とからなる化粧料用組成物は、従来より使用されている。このような組成物(例えば、特許文献1、2)は、使用時に振とうすることにより水相と油相とを混合して使用する。このように、水相と油相とを共存させた場合、水相と油相とが分離し、水相上に油相が浮いた二層の組成物になる。 Cosmetic compositions consisting of an aqueous phase and an oil phase have been conventionally used. Such compositions (for example, Patent Documents 1 and 2) are used by mixing an aqueous phase and an oil phase by shaking at the time of use. When the aqueous phase and the oil phase coexist in this way, the aqueous phase and the oil phase are separated to form a two-layer composition in which the oil phase floats on the aqueous phase.

しかしながら、油剤に酸化され易い成分が含まれている場合には、油相が水相上に存在するために、空気と接触し、酸化の影響による品質の低下も問題となる。 However, when the oil agent contains a component that is easily oxidized, since the oil phase is present on the aqueous phase, it comes into contact with air, and deterioration of quality due to the influence of oxidation also becomes a problem.

特開2002−255739号公報JP-A-2002-255739 特開2004−196713号公報Japanese Unexamined Patent Publication No. 2004-196713

本発明は、酸化され易い油性成分を含む場合においても、酸化の影響を受けにくく、経時劣化を抑制することができる化粧料用組成物を提供することを目的とする。 An object of the present invention is to provide a cosmetic composition that is less susceptible to oxidation and can suppress deterioration over time even when it contains an oily component that is easily oxidized.

本発明の化粧料用組成物は、(カプリル酸/カプリン酸/コハク酸)トリグリセリルに相溶した油剤からなる油相と、水相と、含むことを特徴としている。このように特定の油剤である(カプリル酸/カプリン酸/コハク酸)トリグリセリルを使用することより、水相中に油相を球状に存在させることができる。 The cosmetic composition of the present invention is characterized by containing an oil phase composed of an oil agent compatible with triglyceryl (caprylic acid / capric acid / succinic acid) and an aqueous phase. By using triglyceryl (caprylic acid / capric acid / succinic acid) which is a specific oil agent in this way, the oil phase can be made to exist in a spherical shape in the aqueous phase.

本発明の化粧料用組成物によれば、油剤を水相中に球状で存在させられるため、空気との接触を低減させ、油剤の酸化劣化を防止することができる。 According to the cosmetic composition of the present invention, since the oil agent can be present in the aqueous phase in a spherical shape, contact with air can be reduced and oxidative deterioration of the oil agent can be prevented.

以下、本発明の実施形態について説明する。 Hereinafter, embodiments of the present invention will be described.

本発明の化粧料用組成物は、(カプリル酸/カプリン酸/コハク酸)トリグリセリルと相溶した油剤からなる油相と、水相と、を含んでいる。上記(カプリル酸/カプリン酸/コハク酸)トリグリセリルに油剤を相溶させることにより、油相を水相中に球状に存在させることができる。 The cosmetic composition of the present invention contains an oil phase composed of an oil agent compatible with triglyceryl (caprylic acid / capric acid / succinic acid) and an aqueous phase. By dissolving the oil agent in the above (caprylic acid / capric acid / succinic acid) triglyceryl, the oil phase can be made to exist in a spherical shape in the aqueous phase.

本発明に用いる油剤としては、(カプリル酸/カプリン酸/コハク酸)トリグリセリルに相溶するものであれば特に限定されない。このような油剤としては、ミリスチン酸イソプロピル、オクタン酸セチル、ミリスチン酸オクチルドデシル、パルミチン酸イソプロピル、ステアリン酸ブチル、ラウリン酸ヘキシル、ミリスチン酸ミリスチル、オレイン酸デシル、ジメチルオクタン酸ヘキシルデシル、乳酸セチル、乳酸ミリスチル、乳酸オクチルドデシル、酢酸ラノリン、ステアリン酸イソセチル、イソステアリン酸イソセチル、12−ヒドロキシステアリン酸コレステリル、ジ−2−エチルヘキサン酸エチレングリコール、ジペンタエリスリトール脂肪酸エステル、モノイソステアリン酸N−アルキルグリコール、ジカプリン酸ネオペンチルグリコール、リンゴ酸ジイソステアリル、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エリスリトール、トリ−2−エチルヘキサン酸グリセリル、トリ(カプリル・カプリン・ミリスチン・ステアリン酸)グリセリド、トリイソステアリン酸トリメチロールプロパン、セチル2−エチルヘキサノエート、2−エチルヘキシルパルミテート、トリミリスチン酸グリセリン、トリ−2−ヘプチルウンデカン酸グリセライド、ヒマシ油脂肪酸メチルエステル、オレイン酸オレイル、アセトグリセライド、パルミチン酸2−ヘプチルウンデシル、アジピン酸ジイソブチル、(アジピン酸・2−エチルヘキサン酸・ステアリン酸)グリセリンオリゴエステル、(2−ヘキシルデカン酸・セバシン酸)ジグリセリルオリゴエステル、N−ラウロイル−L−グルタミン酸−2−オクチルドデシルエステル、アジピン酸ジ−2−ヘプチルウンデシル、エチルラウレート、セバシン酸ジ−2−エチルヘキシル、ミリスチン酸2−ヘキシルデシル、パルミチン酸2−ヘキシルデシル、アジピン酸2−ヘキシルデシル、セバシン酸ジイソプロピル、コハク酸2−エチルヘキシル、アボガド油、ツバキ油、タートル油、マカデミアナッツ油、トウモロコシ油、ヒマワリ油、ミンク油、オリーブ油、ナタネ油、卵黄油、ゴマ油、パーシック油、小麦胚芽油、サザンカ油、ヒマシ油、アマニ油、サフラワー油、グレープシード油、綿実油、エノ油、大豆油、落花生油、茶実油、カヤ油、コメヌカ油、シナギリ油、日本キリ油、ホホバ油、胚芽油、月見草油、トリオクタン酸グリセリン、トリイソパルミチン酸グリセリン、酢酸エチル、酢酸ブチル、クエン酸トリエチル等のエステル油や、酢酸トコフェロール、パルミチン酸レチノール、ユビキノン、アスコルビン酸、テトラヘキシルデカン酸アスコルビル等が挙げられる。
中でも、酢酸トコフェロール、パルミチン酸レチノール、ユビキノン、アスコルビン酸、テトラヘキシルデカン酸アスコルビル等の酸化されやすい油性成分が特に好ましい。
The oil agent used in the present invention is not particularly limited as long as it is compatible with triglyceryl (caprylic acid / capric acid / succinic acid). Examples of such oils include isopropyl myristate, cetyl octanoate, octyldodecyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, myristyl myristate, decyl oleate, hexyl decyl dimethyl octanate, cetyl lactate, and lactic acid. Myristic, octyldodecyl lactate, lanolin acetate, isosetyl stearate, isosetyl isostearate, cholesteryl 12-hydroxystearate, ethylene glycol di-2-ethylhexanoate, dipentaerythritol fatty acid ester, N-alkylglycol monoisostearate, dicapric acid Neopentylglycol, diisostearyl malate, glycerin di-2-heptylundecanoate, trimethylolpropane tri-2-ethylhexanoate, trimethylrolpropane triisostearate, pentaerythritol tetra-2-ethylhexanoate, tri-2 -Glyceryl ethylhexanoate, tri (capril, caprin, myristic, stearic acid) glyceride, trimethyl propane triisostearate, cetyl 2-ethylhexanoate, 2-ethylhexyl palmitate, glycerin trimyristate, tri-2-heptyl Glyceride undecanoate, methyl ester of castor oil fatty acid, oleyl oleate, acetoglyceride, 2-heptyl undecyl palmitate, diisobutyl adipate, glycerin oligoester (adipic acid, 2-ethylhexanoic acid, stearic acid), (2-hexyldecane) Acid / Sevacinic acid) Diglyceryl oligoester, N-lauroyl-L-glutamic acid-2-octyldodecyl ester, di-2-heptylundecyl adipate, ethyllaurate, di-2-ethylhexyl sebacate, myristic acid 2- Hexyldecyl, 2-hexyldecyl palmitate, 2-hexyldecyl adipate, diisopropyl sebacate, 2-ethylhexyl succinate, avocado oil, camellia oil, turtle oil, macadamia nut oil, corn oil, sunflower oil, mink oil, olive oil, Rapeseed oil, egg yolk oil, sesame oil, persic oil, wheat germ oil, southern ka oil, castor oil, flaxseed oil, saflower oil, grape seed oil, cotton seed oil, eno oil, soybean oil, peanut oil, tea seed oil, kaya oil, Rice bran oil, stearic acid oil, Japanese kiri oil, jojoba oil, germ oil, evening primrose oil, glycerin trioctanoate, triisopalmichi Examples thereof include ester oils such as glycerin acid, ethyl acetate, butyl acetate and triethyl citrate, tocopherol acetate, retinol palmitate, ubiquinone, ascorbic acid and ascorbic tetrahexyldecanoate.
Of these, oily components that are easily oxidized, such as tocopherol acetate, retinol palmitate, ubiquinone, ascorbic acid, and ascorbic tetrahexyl decanoate, are particularly preferable.

これらの油剤は、(カプリル酸/カプリン酸/コハク酸)トリグリセリルに対して、0.01〜30質量%、好ましくは、0.1〜20質量%の割合で混合する。油剤の割合が0.01質量%未満では、油剤としての効果が得られず、30質量%を超えると、製剤中でのバランスが崩れ、分離する可能性がある。 These oils are mixed in a proportion of 0.01 to 30% by mass, preferably 0.1 to 20% by mass, based on triglyceryl (caprylic acid / capric acid / succinic acid). If the proportion of the oil agent is less than 0.01% by mass, the effect as an oil agent cannot be obtained, and if it exceeds 30% by mass, the balance in the preparation may be lost and separation may occur.

また、水相には、各種エキス等、水溶性の成分を複数添加してもよい。 Further, a plurality of water-soluble components such as various extracts may be added to the aqueous phase.

本発明の化粧料用組成物においては、水相と、油相との重量比は、1:0.01〜1:1程度が好ましい。油相が少ないと、油剤の効果を得ることが難しくなり、多すぎると水相と油相とのバランスが崩れ、油相を水相に球状で存在させることが難しくなる。 In the cosmetic composition of the present invention, the weight ratio of the aqueous phase to the oil phase is preferably about 1: 0.01 to 1: 1. If the amount of the oil phase is small, it becomes difficult to obtain the effect of the oil agent, and if it is too large, the balance between the water phase and the oil phase is lost, and it becomes difficult for the oil phase to exist in the water phase in a spherical shape.

さらに本発明の化粧料用組成物は、上記成分以外に他の成分として化粧品や医薬部外品などで配合成分として一般的に用いられる、界面活性剤、油脂類、pH調整剤、保湿剤、溶剤、防腐剤、植物抽出物、抗炎症剤、色素、香料などを適宜配合することができる。しかしながら、界面活性剤を添加することなく、安定に油剤を球状に保つことが出来るため、不要な界面活性剤等の成分はなるべく添加しないことが好ましい。 Further, the cosmetic composition of the present invention contains surfactants, oils and fats, pH adjusters, moisturizers, which are generally used as compounding ingredients in cosmetics and quasi-drugs as other ingredients in addition to the above ingredients. Solvents, preservatives, plant extracts, anti-inflammatory agents, pigments, fragrances and the like can be appropriately added. However, since the oil agent can be stably kept in a spherical shape without adding a surfactant, it is preferable not to add unnecessary components such as a surfactant as much as possible.

なお、本発明の化粧料用組成物は、油剤成分を(カプリル酸/カプリン酸/コハク酸)トリグリセリルに相溶させた後、水に添加するだけで製造することができる。また、本発明の化粧料用組成物は、よく振とうした後、皮膚や髪に適用することより使用すればよい。 The cosmetic composition of the present invention can be produced simply by dissolving an oil component in triglyceryl (caprylic acid / capric acid / succinic acid) and then adding it to water. In addition, the cosmetic composition of the present invention may be used by applying it to the skin or hair after shaking it well.

つぎに、本発明の実施例を比較例と共に説明するが、本発明は、下記の実施例に限定されるものではない。
本発明の実施例および比較例の化粧料用組成物を表1に示す組成にて調製した。
具体的には、油相成分を相溶させた後、水に添加することにより調製した。調製後の状態も表1に示す。
Next, examples of the present invention will be described with comparative examples, but the present invention is not limited to the following examples.
The cosmetic compositions of Examples and Comparative Examples of the present invention were prepared with the compositions shown in Table 1.
Specifically, it was prepared by dissolving the oil phase components and then adding them to water. The state after preparation is also shown in Table 1.

Figure 0006845392
Figure 0006845392

調製した実施例1と比較例1の化粧料用組成物について、0℃および50℃で1ヶ月保存の後、パルミチン酸レチノールの定量をHPLCにて行った。その結果を表1に示す。表1より、実施例1より、比較例1のほうが、定量値が高く、パルミチン酸レチノールの減少が抑制されていることが明らかである。
よって、油相を水相中に球状で存在させることにより、油剤の劣化を防止することができることがわかる。
The prepared cosmetic compositions of Example 1 and Comparative Example 1 were stored at 0 ° C. and 50 ° C. for 1 month, and then quantification of retinol palmitate was performed by HPLC. The results are shown in Table 1. From Table 1, it is clear that Comparative Example 1 has a higher quantitative value than Example 1 and the decrease in retinol palmitate is suppressed.
Therefore, it can be seen that deterioration of the oil agent can be prevented by allowing the oil phase to exist in the aqueous phase in a spherical shape.

また、実施例2では、比較例1では上層となった油相に使用したオリーブ油を用いたが、(カプリル酸/カプリン酸/コハク酸)トリグリセリルに相溶させることにより水相中に球状で存在させることができた。 Further, in Example 2, the olive oil used for the upper oil phase was used in Comparative Example 1, but it became spherical in the aqueous phase by being compatible with triglyceryl (caprylic acid / capric acid / succinic acid). I was able to make it exist.

Claims (2)

(カプリル酸/カプリン酸/コハク酸)トリグリセリルを、パルミチン酸レチノールの酸化劣化防止剤の有効成分として含み、(カプリル酸/カプリン酸/コハク酸)トリグリセリルに相溶したパルミチン酸レチノールを含有する油相と、水相を含有し、界面活性剤を含有する事なく、水相中に油相を球状に浮遊させることを特徴とする化粧料用組成物(但し、(アクリレーツ/アクリル酸アルキル(C10−30))クロスポリマーを含有する化粧料用組成物を除く。)。Contains triglyceryl (caprylic acid / capric acid / succinic acid) as an active ingredient of an antioxidant for retinol palmitate, and contains retinol palmitate compatible with (caprylic acid / capric acid / succinic acid) triglyceryl. A cosmetic composition containing an oil phase and an aqueous phase and suspending the oil phase in a spherical shape in the aqueous phase without containing a surfactant (however, (Acrylate / alkyl acrylate (acrylate / alkyl acrylate) ( C10-30)) Cosmetic compositions containing cross-polymers are excluded). パルミチン酸レチノールは、(カプリル酸/カプリン酸/コハク酸)トリグリセリルに対して0.01〜30質量%の割合であることを特徴とする請求項1に記載の化粧料用組成物。 The cosmetic composition according to claim 1, wherein the retinol palmitate is in a proportion of 0.01 to 30% by mass with respect to triglyceryl (caprylic acid / capric acid / succinic acid).
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JP7510584B2 (en) * 2019-09-19 2024-07-04 株式会社コスメテックゲート Two-layered cosmetics
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