JP7750695B2 - topical skin preparations - Google Patents
topical skin preparationsInfo
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- JP7750695B2 JP7750695B2 JP2021145855A JP2021145855A JP7750695B2 JP 7750695 B2 JP7750695 B2 JP 7750695B2 JP 2021145855 A JP2021145855 A JP 2021145855A JP 2021145855 A JP2021145855 A JP 2021145855A JP 7750695 B2 JP7750695 B2 JP 7750695B2
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- topical skin
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- squalane
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Description
本発明は、皮膚外用剤に関する。 The present invention relates to an external skin preparation.
人間の皮膚は、加齢や紫外線等の外的ストレスによる影響で、しわやたるみが生じたり、その度合いが増加したりする。このような症状を改善するために様々な成分を組み合わせるなど技術開発が行われている(特許文献1)。
しかしながら、単に併用すれば効果が相乗的に向上するものではなく、相加的に効果が向上するもの、効果を相殺するものなど、その併用による効果は予測不可能な効果である。なかでもより少量で、より高い効果の得られる成分を皮膚外用剤へ配合することのニーズは非常に高い。
Human skin develops wrinkles and sagging due to aging and external stresses such as ultraviolet rays, and these conditions increase in severity. To improve these conditions, technological developments are being conducted, such as combining various ingredients (Patent Document 1).
However, simply using ingredients in combination does not synergistically improve the effect, but rather the effect of such combinations is unpredictable, with some ingredients additively improving the effect and others canceling out the other effects. In particular, there is a great need for ingredients that can provide greater effects in smaller amounts in topical skin preparations.
本発明は特定の成分を併用することにより、肌の粘弾性が相乗的に向上し、良好な使用感を有する皮膚外用剤を提供することを課題とする。 The objective of the present invention is to provide a topical skin preparation that synergistically improves skin viscoelasticity and has a pleasant feel when used in combination with specific ingredients.
本発明の課題を解決する手段は、下記(A)~(C)を含有する皮膚外用剤を提供することである。
(A)スクワラン
(B)ステアリン酸イソセチル、イソステアリン酸ヘキシルデシル、ミリスチン酸オクチルドデシル、イソステアリン酸イソステアリル、ミリスチン酸イソセチル、イソノナン酸イソトリデシル、エチルヘキサン酸セチル、パルミチン酸エチルヘキシル、ミリスチン酸イソプロピル、イソノナン酸イソノニル、ネオペンタン酸イソデシル、およびパルミチン酸イソプロピルからなる群より選択される1種または2種以上のエステル油
(C)HLBが5未満のポリグリセリン脂肪酸エステル
The means for solving the problems of the present invention is to provide an external skin preparation containing the following (A) to (C):
(A) Squalane; (B) One or more ester oils selected from the group consisting of isocetyl stearate, hexyldecyl isostearate, octyldodecyl myristate, isostearyl isostearate, isocetyl myristate, isotridecyl isononanoate, cetyl ethylhexanoate, ethylhexyl palmitate, isopropyl myristate, isononyl isononanoate, isodecyl neopentanoate, and isopropyl palmitate; and (C) a polyglycerin fatty acid ester having an HLB of less than 5.
本発明の皮膚外用剤は特定の成分を併用することにより、肌の粘弾性が相乗的に向上し、良好な使用感を有するという効果を発揮する。 By combining specific ingredients, the topical skin preparation of the present invention synergistically improves the viscoelasticity of the skin, providing a pleasant feel when used.
以下本発明を実施するための形態を説明する。 The following describes how to implement the present invention.
[スクワラン]
本発明の皮膚外用剤に配合するスクワランは、2,6,10,15,19,23-ヘキサメチルテトラコサンで、深海鮫の肝臓から抽出される動物由来のものとオリーブの果実又は米糠等から抽出される植物由来のものがある。いずれも抽出されたスクワレンに水素添加されたスクワランを用いることが好ましく、特に本発明においては植物由来のスクワランを用いることが好ましい。市販のNIKKOL シュガースクワラン(登録商標)(日本サーファクタント工業社製)、オリーブスクワラン(高級アルコール工業社製),オリザスクワラン(オリザ油化社製)、植物性スクワラン、スクワラン(いずれも岸本特殊肝油工業所社製)、スーパースクワラン、スクワラン(いずれもマルハニチロ社製)、スクワラン、精製オリーブスクワラン(日光ケミカルズ社製)、フィトスクワラン(ソフィーム社製)、プリピュア 3759-LQ(ユニケマ社製)等を用いることもできる。
[Squalane]
The squalane incorporated into the topical skin preparation of the present invention is 2,6,10,15,19,23-hexamethyltetracosane, and is available in animal-derived forms extracted from deep-sea shark liver, and plant-derived forms extracted from olive fruit, rice bran, etc. In either case, hydrogenated squalane is preferably used, and plant-derived squalane is particularly preferred in the present invention. Commercially available products such as NIKKOL Sugar Squalane (registered trademark) (manufactured by Nippon Surfactant Industries Co., Ltd.), Olive Squalane (manufactured by Kokyu Alcohol Kogyo Co., Ltd.), Oryza Squalane (manufactured by Oryza Oil & Fat Chemical Co., Ltd.), vegetable squalane, squalane (all manufactured by Kishimoto Tokushu Kanyu Kogyosho Co., Ltd.), super squalane, squalane (all manufactured by Maruha Nichiro Corporation), squalane, refined olive squalane (manufactured by Nikko Chemicals Co., Ltd.), phytosqualane (manufactured by Sophim Co., Ltd.), and Prepure 3759-LQ (manufactured by Uniqema Co., Ltd.) can also be used.
本発明におけるスクワランの配合量は、皮膚外用剤全量に対し、特に限定されないが、0.00001~40質量%が好ましく、さらに0.0001~30質量%が好ましい。 The amount of squalane in the present invention is not particularly limited to the total amount of the topical skin preparation, but is preferably 0.00001 to 40% by mass, and more preferably 0.0001 to 30% by mass.
[エステル油]
本発明の皮膚外用剤に配合するステアリン酸イソセチル、イソステアリン酸ヘキシルデシル、ミリスチン酸オクチルドデシル、イソステアリン酸イソステアリル、ミリスチン酸イソセチル、イソノナン酸イソトリデシル、エチルヘキサン酸セチル、パルミチン酸エチルヘキシル、ミリスチン酸イソプロピル、イソノナン酸イソノニル、ネオペンタン酸イソデシル、およびパルミチン酸イソプロピルからなる群より選択される1種または2種以上のエステル油は、通常皮膚外用剤等に用いられるものであれば、その原料、製造方法、精製方法等は特に限定されない。これらの中でもイソステアリン酸ヘキシルデシルを用いることが特に好ましい。
[Ester oil]
The one or more ester oils selected from the group consisting of isocetyl stearate, hexyldecyl isostearate, octyldodecyl myristate, isostearyl isostearate, isocetyl myristate, isotridecyl isononanoate, cetyl ethylhexanoate, ethylhexyl palmitate, isopropyl myristate, isononyl isononanoate, isodecyl neopentanoate, and isopropyl palmitate to be incorporated into the topical skin preparation of the present invention are not particularly limited in terms of raw materials, production method, purification method, etc., as long as they are those typically used in topical skin preparations, etc. Among these, hexyldecyl isostearate is particularly preferred.
市販のイソステアリン酸ヘキシルデシルとしては、EMALEX HIS-34(日本エマルジョン社製)、I.C.I.S(高級アルコール工業社製)等を挙げることができる。 Commercially available hexyldecyl isostearate includes EMALEX HIS-34 (manufactured by Nippon Emulsion Co., Ltd.) and I.C.I.S (manufactured by Kokyu Alcohol Kogyo Co., Ltd.).
本発明におけるイソステアリン酸ヘキシルデシルの配合量は、皮膚外用剤全量に対し、特に限定されないが、0.001~30質量%が好ましく、さらに0.001~20質量%が好ましい。 The amount of hexyldecyl isostearate used in the present invention is not particularly limited, but is preferably 0.001 to 30% by mass, and more preferably 0.001 to 20% by mass, based on the total amount of the topical skin preparation.
[HLBが5未満のポリグリセリン脂肪酸エステル]
本発明の皮膚外用剤に配合するポリグリセリン脂肪酸エステルは、HLBが5未満であれば、通常皮膚外用剤等に用いられるものを用いることができる。HLBが5未満のポリグリセリン脂肪酸エステルとしては、トリイソステアリン酸ポリグリセリル-2(HLB値:1.3)、イソステアリン酸ポリグリセリル-2(HLB値:4.6)、ペンタオレイン酸ポリグリセリル-10(HLB値:3.5)等が挙げられる。これらの中でも、トリイソステアリン酸ポリグリセリル-2を用いることが好ましい。
[Polyglycerol fatty acid ester having an HLB of less than 5]
The polyglycerol fatty acid ester to be incorporated into the topical skin preparation of the present invention can be one typically used in topical skin preparations, etc., as long as it has an HLB of less than 5. Examples of polyglycerol fatty acid esters having an HLB of less than 5 include polyglyceryl-2 triisostearate (HLB value: 1.3), polyglyceryl-2 isostearate (HLB value: 4.6), and polyglyceryl-10 pentaoleate (HLB value: 3.5). Of these, it is preferable to use polyglyceryl-2 triisostearate.
市販のトリイソステアリン酸ポリグリセリル-2としては、コスモール 43V、コスモール 43N(いずれも日清オイリオグループ社製)、EMALEX TISG-2(日本エマルジョン社製)、リソレックス PGIS23(高級アルコール工業社製)、NIKKOL DGTIS(日光ケミカルズ社製)等を挙げることができる。 Commercially available polyglyceryl-2 triisostearate includes Cosmol 43V and Cosmol 43N (both manufactured by The Nisshin Oillio Group, Ltd.), EMALEX TISG-2 (manufactured by Nippon Emulsion Co., Ltd.), Lysolex PGIS23 (manufactured by Kokyu Alcohol Kogyo Co., Ltd.), and NIKKOL DGTIS (manufactured by Nikko Chemicals Co., Ltd.).
本発明におけるHLBが5未満のポリグリセリン脂肪酸エステルの配合量は、皮膚外用剤全量に対し、特に限定されないが、0.001~30質量%が好ましく、さらに0.01~10質量%が好ましい。 The amount of polyglycerol fatty acid ester with an HLB of less than 5 in the present invention is not particularly limited, but is preferably 0.001 to 30% by mass, and more preferably 0.01 to 10% by mass, based on the total amount of the topical skin preparation.
本発明の皮膚外用剤には、上述の成分の他に、通常の化粧料、医薬部外品に用いられる任意成分を、本発明の効果を阻害しない程度に配合することができる。具体的には、油剤、界面活性剤、増粘剤、防腐剤、香料、保湿剤、抗酸化剤、抗炎症剤、抗菌剤等を挙げることができる。 In addition to the above-mentioned ingredients, the topical skin preparation of the present invention can contain optional ingredients commonly used in cosmetics and quasi-drugs to the extent that they do not impair the effects of the present invention. Specific examples include oils, surfactants, thickeners, preservatives, fragrances, moisturizers, antioxidants, anti-inflammatory agents, and antibacterial agents.
本発明の皮膚外用剤の剤型は、特に限定されず、油系、乳化型等いずれの剤型でもよい。 The formulation of the topical skin preparation of the present invention is not particularly limited, and may be any formulation, such as an oil-based or emulsion-based formulation.
本発明の皮膚外用剤は定法により調製することができる。 The topical skin preparation of the present invention can be prepared by standard methods.
本発明の皮膚外用剤は、例えば、ローション剤、乳剤、軟膏の剤型で用いることができる。 The topical skin preparation of the present invention can be used in the form of, for example, a lotion, emulsion, or ointment.
以下、実施例により本発明を具体的に説明するが、これにより本発明の範囲が限定されるものではない。なお、配合量は特に断りのない限り質量%である。 The present invention will be explained in more detail below using examples, but the scope of the present invention is not limited by these examples. Unless otherwise specified, blend amounts are in mass %.
[粘弾性試験方法]
表1および表2に示した試料を調製し、粘弾性の測定を行った。
[Viscoelasticity test method]
The samples shown in Tables 1 and 2 were prepared and subjected to viscoelasticity measurements.
[測定方法]
(1)馴化
被験者は左右前腕内側部を洗浄後、水分をふき取り、温度21±0.5℃、湿度50±5%に調整された室内で15分間安静にし、馴化を行った。
(2)塗布
左右前腕内側部に3cm×3cmの領域を記し、ピペットを用いて9μLを滴下し、指サックをした指で均一に塗布した。
(3)測定
塗布前および塗布15分後の粘弾性をCutometer MPA580を用いて測定した。キュートメーターによる皮膚粘弾性の測定は、吸引口2ミリのプローブを用い150mb吸引圧で1秒間吸引し、その後開放したときの皮膚の変位を解析した。本試験では皮膚の粘弾性指標として用いられるパラメータ(R1)を解析したが、これは「一定時間皮膚を吸い、決められた時間内に皮膚がどれくらい戻るか」を示す値であり、粘弾性が低いほど皮膚の戻りが悪くなり値が大きくなる。塗布前を1とした場合の相対値を算出し、表1および表2に示した。
[Measurement method]
(1) Acclimatization After washing the inside of the left and right forearms of each subject, the subject wiped off the moisture and rested for 15 minutes in a room adjusted to a temperature of 21±0.5° C. and a humidity of 50±5% for acclimation.
(2) Application A 3 cm x 3 cm area was marked on the inside of each forearm, and 9 μL of the solution was dropped onto the area using a pipette, which was then evenly applied using a finger wearing a finger cot.
(3) Measurement The viscoelasticity was measured before application and 15 minutes after application using a Cutometer MPA580. The measurement of skin viscoelasticity using a Cutometer involved using a probe with a 2 mm suction port, suction at 150 mb suction pressure for 1 second, and then analyzing the displacement of the skin when released. In this test, a parameter (R1) used as an index of skin viscoelasticity was analyzed. This is a value indicating "how much the skin returns within a specified time after suctioning the skin for a certain period of time." The lower the viscoelasticity, the worse the skin's return, and the larger the value. The relative value was calculated, with the value before application set to 1, and is shown in Tables 1 and 2.
[使用感評価]
官能評価専門員21名が、実施例および比較例にかかる皮膚外用剤をそれぞれ独立して使用し、膜感、肌の柔らかさ、ハリ感、厚み、高級感、嗜好性それぞれについて1~7点の評価を行い、その平均値を算出し、下記4段階判定基準により判定した。結果を表2に示した。
5点以上:非常に良い「◎」
4.25点以上5点未満:良い「〇」
3.5点以上4.25点未満:少し悪い「△」
3.5点未満:悪い「×」
[Usage evaluation]
Twenty-one sensory evaluators independently used the topical skin preparations of the Examples and Comparative Examples, and rated the film-like feel, skin softness, firmness, thickness, luxurious feel, and palatability on a scale of 1 to 7. The average scores were calculated and the results were judged according to the following four-level rating scale. The results are shown in Table 2.
5 points or more: Very good "◎"
4.25 points or more but less than 5 points: Good "〇"
3.5 points or more but less than 4.25 points: slightly bad "△"
Less than 3.5 points: Poor "X"
表1に示した通り、各成分を単独で塗布した比較例1~3と比較し、実施例1では粘弾性の値が減少した。また、実施例1は各成分が比較例1~3の3分の1量であることから、相乗的に粘弾性の値が減少したことが分かる。 As shown in Table 1, the viscoelasticity value of Example 1 was reduced compared to Comparative Examples 1 to 3, in which each component was applied alone. Furthermore, since Example 1 used one-third the amount of each component compared to Comparative Examples 1 to 3, it can be seen that the viscoelasticity value was reduced synergistically.
表2に示した通り、比較例4~7と比較し、実施例2は粘弾性の値が減少し、良好な使用感を有した。したがって、本発明の皮膚外用剤は肌の粘弾性を向上させ、良好な使用感を有した。 As shown in Table 2, compared to Comparative Examples 4 to 7, Example 2 had a reduced viscoelasticity value and provided a good feel when used. Therefore, the topical skin preparation of the present invention improved the viscoelasticity of the skin and provided a good feel when used.
Claims (1)
(A)スクワラン 1.2~3質量%
(B)イソステアリン酸ヘキシルデシル 1.2~3質量%
(C)トリイソステアリン酸ポリグリセリル-2 0.6~3質量% A topical skin preparation containing the following (A) to (C):
(A) Squalane 1.2 to 3% by mass
(B ) Hexyldecyl isostearate 1.2 to 3 mass%
(C) Polyglyceryl-2 triisostearate 0.6 to 3 mass%
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021145855A JP7750695B2 (en) | 2021-09-08 | 2021-09-08 | topical skin preparations |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021145855A JP7750695B2 (en) | 2021-09-08 | 2021-09-08 | topical skin preparations |
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| Publication Number | Publication Date |
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| JP2023038966A JP2023038966A (en) | 2023-03-20 |
| JP7750695B2 true JP7750695B2 (en) | 2025-10-07 |
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| JP2021145855A Active JP7750695B2 (en) | 2021-09-08 | 2021-09-08 | topical skin preparations |
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Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2024190840A1 (en) | 2023-03-13 | 2024-09-19 | 三菱ケミカル株式会社 | Cured product, cured product-containing carbon material, negative electrode, and nonaqueous secondary battery |
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| JP2023038966A (en) | 2023-03-20 |
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