JP2011079771A - Skin care preparation - Google Patents

Skin care preparation Download PDF

Info

Publication number
JP2011079771A
JP2011079771A JP2009232932A JP2009232932A JP2011079771A JP 2011079771 A JP2011079771 A JP 2011079771A JP 2009232932 A JP2009232932 A JP 2009232932A JP 2009232932 A JP2009232932 A JP 2009232932A JP 2011079771 A JP2011079771 A JP 2011079771A
Authority
JP
Japan
Prior art keywords
skin
trehalose
mass
external preparation
maltitol
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.)
Pending
Application number
JP2009232932A
Other languages
Japanese (ja)
Inventor
Toru Koike
徹 小池
Azusa Tsukamoto
梓 塚本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Noevir Co Ltd
Original Assignee
Noevir Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Noevir Co Ltd filed Critical Noevir Co Ltd
Priority to JP2009232932A priority Critical patent/JP2011079771A/en
Publication of JP2011079771A publication Critical patent/JP2011079771A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Cosmetics (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide an excellent skin care preparation having an anti-aging effect by solving a problem wherein although various natural origin components have so far been applied, some natural origin components are not effective, and development of a better component has been required. <P>SOLUTION: A skin care preparation having a synergistically excellent horny layer-softening effect has been found by combining four types of sugar comprising sorbitol, glucosyl trehalose, maltitol, and trehalose. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、ソルビトール、グリコシルトレハロース、マルチトール、及びトレハロースを組み合わせて用いることにより、優れた角層柔軟効果を有する皮膚外用剤に関する。     The present invention relates to a skin external preparation having an excellent stratum corneum softening effect by using a combination of sorbitol, glycosyl trehalose, maltitol, and trehalose.

皮膚に触れたときに感じる触感は、美容上大変重要な因子であり、これまで皮膚に柔らかさを与える報告が多数なされている。特に皮膚の最外部である角層の柔軟性には水分が大きな影響を与えており、そのメカニズムとして水分が角層のケラチン繊維の凝集状態をコントロールすることで柔軟性を保っているというものである(非特許文献1参照)。一方、水のみではなく、液状油を塗布した際に「肌が柔らかくなった」と感じたという経験は多くの人が持つものであるが、これらが皮膚に与える柔軟化メカニズムは曖昧である。     The tactile sensation that is felt when touching the skin is a very important factor in cosmetics, and there have been many reports that give skin softness. In particular, moisture has a major effect on the flexibility of the stratum corneum, which is the outermost part of the skin, and its mechanism is that the moisture maintains flexibility by controlling the aggregation state of the keratin fibers in the stratum corneum. Yes (see Non-Patent Document 1). On the other hand, many people have the experience of feeling that “the skin has become softer” when applying not only water but also liquid oil, but the softening mechanism that these give to the skin is vague.

糖類は単独で、又は2種以上で保湿剤として用いることは知られている(特許文献1参照)。しかしながら、糖類を単独で用いた場合、べたつき感という点で満足のいくものではなかった。     It is known that saccharides are used alone or in combination of two or more as moisturizers (see Patent Document 1). However, when sugars were used alone, they were not satisfactory in terms of stickiness.

特開平9−77650号公報JP-A-9-77650

川田:角層ケラチンタンパクの状態と物性 フレグランスジャーナル2004-9:53-58,2004Kawada: State and physical properties of stratum corneum keratin protein Fragrance journal 2004-9: 53-58,2004 日本機械学会 情報・知能・精密機器部門講演会講演論文集(2004)Proceedings of the Japan Society of Mechanical Engineers, Information, Intelligence and Precision Instruments (2004)

従来より、化粧品が皮膚に対して柔軟効果を発揮することは良く知られているものの、柔軟化のメカニズムや効果的な成分は、よくわかっていない。そこで、より効果的に皮膚角層に柔軟性を与える成分を提供することを課題とした。     Conventionally, it is well known that cosmetics exert a softening effect on the skin, but the softening mechanism and effective ingredients are not well understood. Then, it made it the subject to provide the component which gives a softness | flexibility to a skin stratum corneum more effectively.

ソルビトール、グルコシルトレハロース、マルチトール、及びトレハロースからなる4種の糖を組み合わせることにより、相乗的に優れた角層柔軟効果を有する皮膚外用剤を見出した。     A skin external preparation having a synergistically superior stratum corneum softening effect has been found by combining four sugars consisting of sorbitol, glucosyl trehalose, maltitol, and trehalose.

本発明によれば、4種の糖を組み合わせて用いることにより、べたつきを抑えつつ、より高い角層柔軟効果を付与する皮膚外用剤を提供できる。     ADVANTAGE OF THE INVENTION According to this invention, the skin external preparation which provides a higher stratum corneum softening effect can be provided, suppressing stickiness by using combining 4 types of saccharides.

図1は、陰圧付加過程の吸引圧(mbar)−変位(mm)曲線である。FIG. 1 is a suction pressure (mbar) -displacement (mm) curve in the negative pressure application process. 図2は、実施例1および比較例1−5における、柔軟性増加率を示したグラフである。FIG. 2 is a graph showing the flexibility increase rate in Example 1 and Comparative Example 1-5.

本発明で用いるソルビトールは、特に限定されず市販品を用いることができるが、好ましくはソルビトール水溶液(ソルビット液)である。     Although the sorbitol used by this invention is not specifically limited, A commercial item can be used, However, Preferably it is a sorbitol aqueous solution (sorbite liquid).

本発明で用いるグルコシルトレハロースは、特に限定されないが、林原生物科学研究所製のトルナーレ(登録商標)を用いるのが好ましい。     The glucosyl trehalose used in the present invention is not particularly limited, but it is preferable to use Torunare (registered trademark) manufactured by Hayashibara Bioscience Institute.

本発明で用いるマルチトールは、特に限定されず市販品を用いることができるが、好ましくはマルチトール液である。     The maltitol used in the present invention is not particularly limited, and a commercially available product can be used, but a maltitol solution is preferable.

本発明で用いるトレハロースは、特に限定されず市販品を用いることができる。     The trehalose used in the present invention is not particularly limited, and a commercially available product can be used.

4種の糖を組み合わせて用いることにより、べたつきを抑えつつ、優れた角層柔軟効果を発揮する。     By using a combination of four types of sugars, it exhibits excellent stratum corneum softening effects while suppressing stickiness.

4種の糖を組み合わせて用いることにより、べたつきを抑えつつ、優れた角層柔軟効果を発揮する皮膚外用剤を提供することができる。     By using a combination of four kinds of sugars, it is possible to provide a skin external preparation that exhibits an excellent horny layer softening effect while suppressing stickiness.

この皮膚外用剤は4種の糖を含む限り、その形態およびその他成分の配合の有無等については、何ら制限されない。形態については、液状、ペースト状、ゲル状、固体状または粉末状等の任意の形態を、その用途等に応じて選択でき、その形態とするために必要なビヒクル(賦形剤)、溶剤、またはその他の一般的な添加剤(酸化防止剤、着色剤または分散剤等)を任意に含むことができる。     As long as this external preparation for skin contains four kinds of sugars, the form and presence / absence of addition of other components are not limited at all. As for the form, any form such as liquid, paste, gel, solid or powder can be selected according to its use and the like, vehicle (excipient), solvent, Or other general additives (an antioxidant, a coloring agent, a dispersing agent etc.) can be included arbitrarily.

皮膚外用剤の剤型は任意であり、例えば、ローション等の可溶化系、カラミンローション等の分散系、またはクリームや乳液等の乳化系として提供することができる。さらに、噴射剤と共に充填するエアゾール形態、軟膏剤またはパップ剤等の種々の剤型で提供することもできる。     The dosage form of the external preparation for skin is arbitrary, and can be provided, for example, as a solubilization system such as lotion, a dispersion system such as calamine lotion, or an emulsification system such as cream or emulsion. Furthermore, it can also be provided in various dosage forms such as aerosol form, ointment or poultice filled with propellant.

具体的には、乳液、クリーム、ローション、化粧水、パック、美容液、洗浄料またはメイクアップ化粧料等の各種化粧料;液剤、軟膏、粉末、顆粒、エアゾール剤、貼付剤またはパップ剤等の様々な形態の化粧料、医薬部外品または外用医薬品などが例示できる。     Specifically, various cosmetics such as emulsions, creams, lotions, lotions, packs, cosmetic liquids, cleaning agents or makeup cosmetics; liquids, ointments, powders, granules, aerosols, patches or poultices Various forms of cosmetics, quasi-drugs, or external medicines can be exemplified.

皮膚外用剤には、4種の糖の他に、その用途と必要に応じて、医薬品、医薬部外品、皮膚化粧料、毛髪用化粧料および洗浄料等に通常配合される任意の成分、例えば水、油性成分、保湿剤、粉体、色素、乳化剤、可溶化剤、ゲル化剤、洗浄剤、紫外線吸収剤、抗炎症剤、増粘剤、pH調整剤、キレート剤、薬剤(薬効成分)、香料、樹脂、防菌防かび剤、抗酸化剤、またはアルコール類等を適宜配合することができる。さらに本発明の効果を損なわない範囲において、他の糖類との併用も可能である。     In addition to the four types of sugar, the external preparation for skin optionally contains any component that is usually blended in pharmaceuticals, quasi-drugs, skin cosmetics, hair cosmetics and cleansing agents, etc. For example, water, oily ingredients, moisturizers, powders, pigments, emulsifiers, solubilizers, gelling agents, detergents, UV absorbers, anti-inflammatory agents, thickeners, pH adjusters, chelating agents, drugs (medicinal ingredients) ), A fragrance, a resin, a fungicide, a fungicide, an antioxidant, an alcohol, or the like can be appropriately mixed. Furthermore, in the range which does not impair the effect of this invention, combined use with other saccharides is also possible.

ソルビトールの皮膚外用剤への配合量は、種類や目的等によって調整することができるが、効果や安定性などの点から、全量に対して固形分換算で、好ましくは0.01〜20.0質量%であり、より好ましくは0.1〜20.0質量%であり、さらに好ましくは0.1〜10.0質量%である。     The amount of sorbitol to be added to the external preparation for skin can be adjusted depending on the type and purpose, but from the viewpoint of effect and stability, it is preferably 0.01 to 20.0 in terms of solid content with respect to the total amount. It is mass%, More preferably, it is 0.1-20.0 mass%, More preferably, it is 0.1-10.0 mass%.

グルコシルトレハロースの皮膚外用剤への配合量は、種類や目的等によって調整することができるが、効果や安定性などの点から、全量に対して固形分換算で、好ましくは0.01〜20.0質量%であり、より好ましくは0.1〜20.0質量%であり、さらに好ましくは0.1〜10.0質量%である。     The amount of glucosyl trehalose to be added to the external preparation for skin can be adjusted depending on the type and purpose, but from the viewpoint of effect and stability, the total amount is preferably 0.01 to 20 in terms of solid content. It is 0 mass%, More preferably, it is 0.1-20.0 mass%, More preferably, it is 0.1-10.0 mass%.

マルチトールの皮膚外用剤への配合量は、種類や目的等によって調整することができるが、効果や安定性などの点から、全量に対して固形分換算で、好ましくは0.01〜20.0質量%であり、より好ましくは0.1〜20.0質量%であり、さらに好ましくは0.1〜10.0質量%である。     The amount of maltitol to be added to the external preparation for skin can be adjusted depending on the type and purpose, but from the viewpoint of effect and stability, it is preferably 0.01 to 20. It is 0 mass%, More preferably, it is 0.1-20.0 mass%, More preferably, it is 0.1-10.0 mass%.

トレハロースの皮膚外用剤への配合量は、種類や目的等によって調整することができるが、効果や安定性などの点から、全量に対して固形分換算で、好ましくは0.01〜20.0質量%であり、より好ましくは0.1〜20.0質量%であり、さらに好ましくは0.1〜10.0質量%である。     The amount of trehalose to be added to the external preparation for skin can be adjusted depending on the type and purpose, but from the viewpoint of effect and stability, it is preferably 0.01 to 20.0 in terms of solid content with respect to the total amount. It is mass%, More preferably, it is 0.1-20.0 mass%, More preferably, it is 0.1-10.0 mass%.

以下に4種の糖を含む皮膚外用剤の調製例、4種の糖を含む皮膚外用剤を用いる角層柔軟効果の試験方法についてさらに詳細に説明するが、本発明の技術的範囲はこれらによってなんら限定されるものではない。     Hereinafter, preparation examples of skin external preparations containing four kinds of sugars will be described in more detail with respect to the test method for the horny layer softening effect using the skin external preparations containing four kinds of sugars, but the technical scope of the present invention is based on these. It is not limited at all.

[実施例1]
使用したサンプルは、表1のとおり調製した。
[Example 1]
The samples used were prepared as shown in Table 1.

Figure 2011079771
Figure 2011079771

[実施例2]
<角層柔軟効果測定方法>
角層の柔軟効果は、非特許文献2の手法に従い、Cutometer SEM575(C+K,Germany)を用いて行った。Cutometerでは被検部位を吸引した時の皮膚の変位を光センサで検出する。今回はピペット吸引法の原理に基づき、吸引圧を一定速度(150mbar/s)で10秒間上昇させ、陰圧付加過程の吸引圧(mbar)−変位(mm)曲線の初期勾配(t=1s〜5s)を皮膚の柔軟性指標として算出した。(図1参照)
角層柔軟性=皮膚の伸び(mm)/吸引圧力(mbar)
洗浄後15分間鎮静させた前腕部に対して、サンプルを5μL/cm塗布した。その塗布前と塗布5分後の角層の柔軟性を、前述の手法により測定した。
柔軟性増加率(%)=(塗布5分後の角質柔軟性−塗布前の角質柔軟性)/塗布前の角質柔軟性×100
[Example 2]
<Measuring method of stratum corneum flexibility effect>
The softening effect of the stratum corneum was performed using Cutometer SEM575 (C + K, Germany) according to the method of Non-Patent Document 2. Cutometer detects the displacement of the skin when the test site is aspirated with an optical sensor. This time, based on the principle of the pipette suction method, the suction pressure is increased at a constant speed (150 mbar / s) for 10 seconds, and the initial gradient of the suction pressure (mbar) -displacement (mm) curve in the negative pressure application process (t = 1 s to 5s) was calculated as a skin softness index. (See Figure 1)
Stratum corneum flexibility = skin elongation (mm) / suction pressure (mbar)
5 μL / cm 2 of the sample was applied to the forearm that was sedated for 15 minutes after washing. The flexibility of the stratum corneum before application and 5 minutes after application was measured by the method described above.
Flexibility increase rate (%) = (Keratin flexibility after 5 minutes of application−Keratin flexibility before application) / Keratin flexibility before application × 100

実施例1と比較例1−5について、測定した角層柔軟性増加率の結果を図2に示した。     The measured results of the increase in the stratum corneum flexibility for Example 1 and Comparative Example 1-5 are shown in FIG.

以上の結果から、4種の糖を組み合わせて用いることにより、べたつきを抑えながら、相乗的に優れた角層柔軟効果を示した。     From the above results, the combination of four sugars showed a synergistically superior stratum corneum softening effect while suppressing stickiness.

続いて、4種の糖を含む皮膚外用剤の処方例を示す。     Then, the example of formulation of the skin external preparation containing 4 types of sugars is shown.

[実施例3]
アクネ用皮膚外用剤(ローションタイプ)
(1)エタノール 5.0(質量%)
(2)サリチル酸 0.1
(3)濃グリセリン 3.0
(4)1,3−ブチレングリコール 7.0
(5)トリメチルグリシン 1.0
(6)ソルビトール 1.0
(7)グルコシルトレハロース 1.0
(8)マルチトール 1.0
(9)トレハロース 1.0
(10)クエン酸 0.1
(11)精製水 100.0とする残部
製法:(1)〜(3)を均一に溶解しアルコール相とする。これを、あらかじめ(11)に(4)〜(10)を添加して均一にした水相に撹拌しながら均一に混合する。
[Example 3]
Skin preparation for acne (lotion type)
(1) Ethanol 5.0 (mass%)
(2) Salicylic acid 0.1
(3) Concentrated glycerin 3.0
(4) 1,3-butylene glycol 7.0
(5) Trimethylglycine 1.0
(6) Sorbitol 1.0
(7) Glucosyl trehalose 1.0
(8) Maltitol 1.0
(9) Trehalose 1.0
(10) Citric acid 0.1
(11) Purified water 100.0 The remaining manufacturing method: (1) to (3) are uniformly dissolved to obtain an alcohol phase. The mixture is uniformly mixed with stirring in an aqueous phase obtained by adding (4) to (10) to (11) in advance.

[実施例4]
アクネ用皮膚外用剤(乳液タイプ)
(1)トリ−2−エチルヘキサン酸グリセリル 8.0(質量%)
(2)自己乳化型モノステアリン酸グリセリン 2.5
(3)ベヘニルアルコール 0.5
(4)濃グリセリン 5.0
(5)精製水 100.0とする残部
(6)キサンタンガム(1重量%水溶液) 20.0
(7)1,3−ブチレングリコール 7.0
(8)トリメチルグリシン 1.0
(9)ソルビトール 1.0
(10)グルコシルトレハロース 1.0
(11)マルチトール 1.0
(12)トレハロース 1.0
(13)クエン酸 0.1
(14)エタノール 4.0
(15)サリチル酸 0.1
製法:(1)〜(3)の油相と(4)〜(6)の水相をそれぞれ80℃まで加熱溶解する。両相を混合し、ホモミキサーを用いて均一に乳化する。45℃まで冷却後(7)〜(13)の水相と(14)、(15)を併せたアルコール相を各々加え、均一に撹拌する。
[Example 4]
Acne skin external preparation (milky lotion type)
(1) Glyceryl tri-2-ethylhexanoate 8.0 (mass%)
(2) Self-emulsifying glyceryl monostearate 2.5
(3) Behenyl alcohol 0.5
(4) Concentrated glycerin 5.0
(5) Purified water 100.0 The remainder (6) Xanthan gum (1 wt% aqueous solution) 20.0
(7) 1,3-butylene glycol 7.0
(8) Trimethylglycine 1.0
(9) Sorbitol 1.0
(10) Glucosyl trehalose 1.0
(11) Maltitol 1.0
(12) Trehalose 1.0
(13) Citric acid 0.1
(14) Ethanol 4.0
(15) Salicylic acid 0.1
Production method: The oil phases (1) to (3) and the aqueous phases (4) to (6) are dissolved by heating up to 80 ° C., respectively. Both phases are mixed and uniformly emulsified using a homomixer. After cooling to 45 ° C., the aqueous phases (7) to (13) and the alcohol phase obtained by combining (14) and (15) are added and stirred uniformly.

[実施例5]
アクネ用皮膚外用剤(クリームタイプ)
(1)スクワラン 10.0(質量%)
(2)ステアリン酸 2.0
(3)水素添加パーム核油 0.5
(4)水素添加大豆リン脂質 0.1
(5)セタノール 3.6
(6)親油型モノステアリン酸グリセリン 2.0
(7)グリセリン 10.0
(8)サリチル酸 0.1
(9)1重量%カルボキシビニルポリマー水溶液 15.0
(10)精製水 100.0とする残部
(11)10重量%L−アルギニン水溶液 3.0
(12)1,3−ブチレングリコール 7.0
(13)トリメチルグリシン 1.0
(14)ソルビトール 1.0
(15)グルコシルトレハロース 1.0
(16)マルチトール 1.0
(17)トレハロース 1.0
(18)クエン酸 0.1
製法:(1)〜(6)の油相成分を加熱溶解し、80℃とする。一方(7)〜(10)を加熱溶解し、80℃とする。これに前記油相を撹拌しながら加えたあと、(11)を加えて、ホモジナイザーにより均一に乳化し45℃まで冷却後(12)〜(18)を加え、均一に撹拌する。
[Example 5]
Skin preparation for acne (cream type)
(1) Squalane 10.0 (mass%)
(2) Stearic acid 2.0
(3) Hydrogenated palm kernel oil 0.5
(4) Hydrogenated soybean phospholipid 0.1
(5) Cetanol 3.6
(6) Lipophilic glyceryl monostearate 2.0
(7) Glycerin 10.0
(8) Salicylic acid 0.1
(9) 1% by weight carboxyvinyl polymer aqueous solution 15.0
(10) Purified water 100.0 The remainder (11) 10 wt% L-arginine aqueous solution 3.0
(12) 1,3-butylene glycol 7.0
(13) Trimethylglycine 1.0
(14) Sorbitol 1.0
(15) Glucosyl trehalose 1.0
(16) Maltitol 1.0
(17) Trehalose 1.0
(18) Citric acid 0.1
Production method: The oil phase components (1) to (6) are dissolved by heating to 80 ° C. On the other hand, (7) to (10) are dissolved by heating to 80 ° C. The oil phase is added to this while stirring, then (11) is added, and the mixture is uniformly emulsified with a homogenizer, cooled to 45 ° C., (12) to (18) are added, and the mixture is stirred uniformly.

[実施例6]
クレンジング料
(1)スクワラン 70.0(質量%)
(2)イソステアリン酸ポリオキシエチレングリセリル 8.0
(3)精製水 100.0とする残部
(4)1,3−ブチレングリコール 7.0
(5)トリメチルグリシン 1.0
(6)ソルビトール 1.0
(7)グルコシルトレハロース 1.0
(8)マルチトール 1.0
(9)トレハロース 1.0
(10)クエン酸 0.1
(11)サリチル酸 0.1
製法:(1)と(2)を均一に溶解する。これに、(3)〜(11)を順次加え、均一に混合する。
[Example 6]
Cleansing fee (1) Squalane 70.0 (mass%)
(2) Polyoxyethylene glyceryl isostearate 8.0
(3) Purified water 100.0 The remainder (4) 1,3-butylene glycol 7.0
(5) Trimethylglycine 1.0
(6) Sorbitol 1.0
(7) Glucosyl trehalose 1.0
(8) Maltitol 1.0
(9) Trehalose 1.0
(10) Citric acid 0.1
(11) Salicylic acid 0.1
Manufacturing method: (1) and (2) are uniformly dissolved. To this, (3) to (11) are sequentially added and mixed uniformly.

[実施例7]
洗顔フォーム
(1)ステアリン酸 16.0(質量%)
(2)ミリスチン酸 16.0
(3)親油型モノステアリン酸グリセリン 2.0
(4)グリセリン 25.0
(5)水酸化ナトリウム 7.5
(6)ヤシ油脂肪酸アミドプロピルベタイン 1.0
(7)精製水 100.0とする残部
(8)サリチル酸 0.1
(9)1,3−ブチレングリコール 7.0
(10)トリメチルグリシン 1.0
(11)ソルビトール 1.0
(12)グルコシルトレハロース 1.0
(13)マルチトール 1.0
(14)トレハロース 1.0
(15)クエン酸 0.1
製法:(1)〜(4)の油相成分を80℃にて加熱溶解する。一方(5)〜(7)の水相成分を80℃にて加熱溶解し、油相成分と均一に混合撹拌する。冷却後40℃にて(8)〜(15)を順次加え、均一に混合する。
[Example 7]
Facial cleansing foam (1) Stearic acid 16.0 (mass%)
(2) Myristic acid 16.0
(3) Lipophilic glyceryl monostearate 2.0
(4) Glycerin 25.0
(5) Sodium hydroxide 7.5
(6) Palm oil fatty acid amidopropyl betaine 1.0
(7) Purified water 100.0 balance (8) Salicylic acid 0.1
(9) 1,3-butylene glycol 7.0
(10) Trimethylglycine 1.0
(11) Sorbitol 1.0
(12) Glucosyl trehalose 1.0
(13) Maltitol 1.0
(14) Trehalose 1.0
(15) Citric acid 0.1
Production method: The oil phase components (1) to (4) are heated and dissolved at 80 ° C. On the other hand, the aqueous phase components (5) to (7) are heated and dissolved at 80 ° C., and mixed and stirred uniformly with the oil phase components. After cooling, (8) to (15) are sequentially added at 40 ° C. and mixed uniformly.

[実施例8]
パック
(1)精製水 100.0とする残部(質量%)
(2)ポリビニルアルコール 12.0
(3)エタノール 17.0
(4)グリセリン 9.0
(5)ポリエチレングリコール(平均分子量1000) 2.0
(6)サリチル酸 0.1
(7)1,3−ブチレングリコール 7.0
(8)トリメチルグリシン 1.0
(9)ソルビトール 1.0
(10)グルコシルトレハロース 1.0
(11)マルチトール 1.0
(12)トレハロース 1.0
(13)クエン酸 0.1
(14)香料 0.1
製法:(2)と(3)を混合し、80℃に加温した後、80℃に加温した(1)に溶解する。均一に溶解した後、(4)と(5)を加え、攪拌しながら冷却する。40℃にて(6)〜(14)を順次加え、均一に混合する。
[Example 8]
Pack (1) Purified water 100.0 The remainder (mass%)
(2) Polyvinyl alcohol 12.0
(3) Ethanol 17.0
(4) Glycerin 9.0
(5) Polyethylene glycol (average molecular weight 1000) 2.0
(6) Salicylic acid 0.1
(7) 1,3-butylene glycol 7.0
(8) Trimethylglycine 1.0
(9) Sorbitol 1.0
(10) Glucosyl trehalose 1.0
(11) Maltitol 1.0
(12) Trehalose 1.0
(13) Citric acid 0.1
(14) Fragrance 0.1
Production method: (2) and (3) are mixed, heated to 80 ° C, and then dissolved in (1) heated to 80 ° C. After evenly dissolving, add (4) and (5) and cool with stirring. (6) to (14) are sequentially added at 40 ° C. and mixed uniformly.

本発明の4種の糖を含有する組成物は、べたつきを抑えつつ、優れた角層柔軟効果を発揮し、皮膚外用剤として有用である。     The composition containing the four types of sugars of the present invention exhibits an excellent stratum corneum softening effect while suppressing stickiness and is useful as a skin external preparation.

Claims (3)

4種の糖を含むことを特徴とする、皮膚外用剤。   An external preparation for skin, comprising four kinds of sugars. 4種の糖が、ソルビトール、グルコシルトレハロース、マルチトール、及びトレハロースである、請求項1に記載の皮膚外用剤。   The skin external preparation according to claim 1, wherein the four sugars are sorbitol, glucosyl trehalose, maltitol, and trehalose. 角層柔軟効果を有する、請求項1に記載の皮膚外用剤。   The skin external preparation of Claim 1 which has a stratum corneum softening effect.
JP2009232932A 2009-10-07 2009-10-07 Skin care preparation Pending JP2011079771A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009232932A JP2011079771A (en) 2009-10-07 2009-10-07 Skin care preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2009232932A JP2011079771A (en) 2009-10-07 2009-10-07 Skin care preparation

Publications (1)

Publication Number Publication Date
JP2011079771A true JP2011079771A (en) 2011-04-21

Family

ID=44074220

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009232932A Pending JP2011079771A (en) 2009-10-07 2009-10-07 Skin care preparation

Country Status (1)

Country Link
JP (1) JP2011079771A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011093835A (en) * 2009-10-29 2011-05-12 Noevir Co Ltd Skin care preparation
JP2013155161A (en) * 2012-01-31 2013-08-15 Mandom Corp Liquid cleanser
JP2014076964A (en) * 2012-10-10 2014-05-01 Naris Cosmetics Co Ltd Skin external agent

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0977650A (en) * 1995-09-14 1997-03-25 Ajinomoto Co Inc Cosmetic
WO2004071472A1 (en) * 2003-02-13 2004-08-26 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo SKIN PREPARATION FOR EXTERNAL USE CHARACTERIZED BY CONTAINING SUGAR DERIVATIVE OF α,α-TREHALOSE

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0977650A (en) * 1995-09-14 1997-03-25 Ajinomoto Co Inc Cosmetic
WO2004071472A1 (en) * 2003-02-13 2004-08-26 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo SKIN PREPARATION FOR EXTERNAL USE CHARACTERIZED BY CONTAINING SUGAR DERIVATIVE OF α,α-TREHALOSE

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
化学大辞典6 縮刷版, vol. 第16刷, JPN6013048912, 10 March 1974 (1974-03-10), pages 306 - 307, ISSN: 0002645347 *
新化粧品学, JPN6013048913, 18 January 2001 (2001-01-18), pages 20 - 21, ISSN: 0002645348 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011093835A (en) * 2009-10-29 2011-05-12 Noevir Co Ltd Skin care preparation
JP2013155161A (en) * 2012-01-31 2013-08-15 Mandom Corp Liquid cleanser
JP2014076964A (en) * 2012-10-10 2014-05-01 Naris Cosmetics Co Ltd Skin external agent

Similar Documents

Publication Publication Date Title
RU2722783C2 (en) Compositions and methods of increasing efficiency of local application of an alkaline beneficial agent
BR112016022159B1 (en) POWDER AND METHOD TO IMPROVE THE TOPICAL APPLICATION OF AN ACID BENEFIT AGENT
KR101665756B1 (en) oil-in-water emulsified cosmetic composition with low viscosity comprising high content silicone derivatives for skin moisturing effect
MX2011005082A (en) Personal care composition containing a volatile and a terpene alcohol.
WO2007039974A1 (en) Emulsion lotion
WO2020064843A1 (en) Pharmaceutical composition in the form of a water-in-oil emulsion (w/o) and its uses
JP2011079771A (en) Skin care preparation
JP5125122B2 (en) Adapalene-containing external preparation composition
JP5061984B2 (en) Adapalene-containing external preparation composition
JP6260111B2 (en) Anti-wrinkle composition and cosmetic
JP5233149B2 (en) Adapalene-containing external preparation composition
JP5338030B2 (en) Adapalene-containing external preparation composition
JP5670008B2 (en) Adapalene-containing external preparation composition
JP2013129638A (en) Cosmetic material
JP5109382B2 (en) Adapalene-containing external preparation composition
JP7256624B2 (en) Gel-form external preparation for skin or skin cosmetics
JP2013133303A (en) Advanced glycation end product production inhibitor
JP5632310B2 (en) Cosmetic or external preparation for skin
TW201934115A (en) Method for improving stickiness of adenosine-phosphate-containing composition
JP5980171B2 (en) Adapalene-containing external preparation composition
JP2011162518A (en) Humectant and skin care preparation for external use
JP5646129B2 (en) Adapalene-containing external preparation composition
JP2011201826A (en) Emulsion composition
EP4173612A1 (en) Compositions suitable for use in skin care
KR20140087905A (en) Oil-in-water emulsified cosmetic composition comprising high content of silicone derivatives for skin moisturing effect

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20120802

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20130821

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20131001

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20131127

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20140617