JPH0669931B2 - External skin preparation - Google Patents
External skin preparationInfo
- Publication number
- JPH0669931B2 JPH0669931B2 JP16368387A JP16368387A JPH0669931B2 JP H0669931 B2 JPH0669931 B2 JP H0669931B2 JP 16368387 A JP16368387 A JP 16368387A JP 16368387 A JP16368387 A JP 16368387A JP H0669931 B2 JPH0669931 B2 JP H0669931B2
- Authority
- JP
- Japan
- Prior art keywords
- skin
- water
- external preparation
- emulsion
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/68—Sphingolipids, e.g. ceramides, cerebrosides, gangliosides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/007—Preparations for dry skin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Biophysics (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は皮膚外用剤、更に詳しくは、角質層の水分保持
力を高め、肌あれを改善することができる皮膚外用剤に
関する。TECHNICAL FIELD The present invention relates to a skin external preparation, and more particularly to a skin external preparation capable of enhancing the water-retaining power of the stratum corneum and improving skin roughness.
従来、肌にうるおいを与え、肌を柔軟にするには、角質
層の水分が重要であることが知られている。そして、当
該水分の保持は、角質層に含まれている水溶性成分、す
なわち遊離アミノ酸、有機酸、尿素又は無機イオンによ
るものであるとされ、これらの物質は単独であるいは組
合せて薬用皮膚外用剤あるいは化粧料に配合して、肌あ
れの改善又は予防の目的で使用されている。It has been known that moisture in the stratum corneum is important in order to moisturize and soften the skin. The retention of water is said to be due to the water-soluble components contained in the stratum corneum, that is, free amino acids, organic acids, urea or inorganic ions, and these substances may be used alone or in combination for the external preparation for medicated skin. Alternatively, it is used in cosmetics for the purpose of improving or preventing skin roughness.
また、これとは別に水と親和性が高い多くの保湿性物質
が開発され、同様の目的で使用されている。In addition to this, many moisturizing substances having high affinity with water have been developed and used for the same purpose.
しかしながら、これらの保湿性物質を皮膚に適用した場
合、その作用は、皮膚角質層上にあつて水分を角質に供
給するというもので、しかもその効果は一時的であり、
根本的に角質層の水分保持能力を改善し、肌あれを本質
的に予防あるいは治癒するというものではなかつた。However, when these moisturizing substances are applied to the skin, the action is to supply water to the stratum corneum on the stratum corneum of the skin, and the effect is temporary,
It does not fundamentally improve the water-retaining ability of the stratum corneum and essentially prevent or cure the rough skin.
斯かる実情において、本発明者らは上記問題点を解決す
べく鋭意研究を行なつたところ、次の一般式(I)、 (式中、R1およびR2は炭素数10〜26の直鎖若しくは分岐
鎖の飽和若しくは不飽和の炭化水素基を示す) で表わされる化合物又はその塩が角質層の水分保持能力
を根本的に改善する効果を奏すること、そしてこの化合
物又はその塩に界面活性剤を併用するとその効果を更に
増大できることを見出し、本発明を完成した。In such a situation, the inventors of the present invention have conducted diligent research to solve the above-mentioned problems, and found that the following general formula (I): (In the formula, R 1 and R 2 represent a linear or branched saturated or unsaturated hydrocarbon group having 10 to 26 carbon atoms) or a salt thereof is fundamental to the water retention ability of the stratum corneum. The present invention has been completed based on the finding that the effect of improving the compound is exhibited, and that the effect can be further increased by using a surfactant together with this compound or a salt thereof.
すなわち本発明は、前記式(I)で表わされる化合物又
はその塩を含有する皮膚外用剤、並びに前記式(I)で
表わされる化合物又はその塩及び界面活性剤を含有する
皮膚外用剤を提供するものである。That is, the present invention provides a skin external preparation containing the compound represented by the formula (I) or a salt thereof, and a skin external preparation containing the compound represented by the formula (I) or a salt thereof and a surfactant. It is a thing.
本発明で使用される、前記式(I)で表わされる化合物
は公知の物質であり、例えば東独特許第92940号(197
3)の方法に従つて合成することができる。またその塩
としてはアルカリ金属塩等の化粧料に使用可能なものが
挙げられる。The compound represented by the formula (I) used in the present invention is a known substance, for example, East German Patent No. 92940 (197).
It can be synthesized according to the method of 3). Examples of the salt include those usable for cosmetics such as alkali metal salts.
前記式(I)で表わされる化合物又はその塩の本発明皮
膚外用剤への配合量は、特に制限されないが、通常乳化
型の皮膚外用剤の場合には全組成の0.001〜50重量%
(以下単に%で示す)、特に0.1〜20%が好ましく、ま
たスクワレン等の液状炭化水素を基剤とする油性の皮膚
外用剤の場合には1〜50%、特に5〜25%が好ましい。The amount of the compound represented by the formula (I) or a salt thereof to be added to the skin external preparation of the present invention is not particularly limited, but in the case of an emulsified skin external preparation, it is usually 0.001 to 50% by weight of the total composition.
(Hereinafter simply indicated by%), particularly 0.1 to 20% is preferable, and 1 to 50%, particularly 5 to 25% is preferable in the case of oily external preparation for skin based on liquid hydrocarbon such as squalene.
本発明皮膚外用剤に配合される界面活性剤としては、非
イオン界面活性剤、陰イオン界面活性剤、両性界面活性
剤の何れをも使用できるが、就中特に非イオン界面活性
剤が好適である。As the surfactant to be added to the skin external preparation of the present invention, any of a nonionic surfactant, an anionic surfactant, and an amphoteric surfactant can be used, among which a nonionic surfactant is particularly preferable. is there.
非イオン界面活性剤としては、例えばポリオキシエチレ
ンアルキルエーテル、ポリオキシエチレンアルキルフエ
ニルエーテル、ポリオキシエチレン脂肪酸エステル、ソ
ルビタン脂肪酸エステル、ポリオキシエチレンソルビタ
ン脂肪酸エステル、脂肪酸モノグリセライド、グリセリ
ルエーテル等が挙げられる。その中でも、次の一般式
(II) (式中、Rは炭素数8〜24のアルキル基を示す) で表わされるグリセリルエーテルが好ましく、更に式
(II)中のRが次式(III) (式中、pは4〜10の整数、qは5〜11の整数を示し、
p+q=11〜17でp=7、q=8を頂点とする分布を有
する) で表わされるものが特に好ましい。Examples of the nonionic surfactant include polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, polyoxyethylene fatty acid ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, fatty acid monoglyceride, glyceryl ether and the like. Among them, the following general formula (II) (Wherein R represents an alkyl group having 8 to 24 carbon atoms) is preferred, and R in the formula (II) is represented by the following formula (III) (In the formula, p represents an integer of 4 to 10, q represents an integer of 5 to 11,
and a distribution represented by p + q = 11 to 17 with p = 7 and q = 8 at the vertices) is particularly preferable.
界面活性剤の配合量は、全組成の0.01〜20%、特に0.1
〜5%が好ましい。The content of the surfactant is 0.01 to 20% of the total composition, especially 0.1%.
-5% is preferable.
本発明の皮膚外用剤は、その使用形態において、薬用皮
膚外用剤と化粧料に大別される。The external preparation for skin of the present invention is roughly classified into a medicated external preparation for skin and a cosmetic in its use form.
薬用皮膚外用剤としては、例えば薬効成分を含有する各
種軟膏剤を挙げることができる。軟膏剤としては、油性
基剤をベースとするもの、油/水、水/油型の乳化系基
剤をベースとするもののいずれであつてもよい。油性基
剤としては、特に制限はなく、例えば植物油、動物油、
合成油、脂肪酸、及び天然又は合成のグリセライド等が
挙げられる。また薬効成分としては、特に制限はなく、
例えば鎮痛消炎剤、鎮痒剤、殺菌消毒剤、収斂剤、皮膚
軟化剤、ホルモン剤等を必要に応じて適宜使用すること
ができる。Examples of the external medicated skin preparation include various ointments containing medicinal components. The ointment may be either one based on an oily base, one based on oil / water, or one based on an emulsion base of water / oil type. The oily base is not particularly limited, for example, vegetable oil, animal oil,
Examples include synthetic oils, fatty acids, and natural or synthetic glycerides. The medicinal component is not particularly limited,
For example, an analgesic anti-inflammatory agent, an antipruritic agent, a bactericidal disinfectant, an astringent agent, an emollient agent, a hormone agent and the like can be appropriately used as necessary.
また、化粧料として使用する場合は、上記必須成分の他
に化粧料成分として一般に使用されている油分、保湿
剤、紫外線吸収剤、アルコール類、キレート剤、pH調整
剤、防腐剤、増粘剤、色素、香料等を任意に組合せて配
合することができる。When used as a cosmetic, in addition to the above essential ingredients, oils, moisturizers, UV absorbers, alcohols, chelating agents, pH adjusters, preservatives, thickeners that are commonly used as cosmetic ingredients. , Dyes, fragrances and the like can be combined in any combination.
化粧料としては、種々の形態、例えば水/油、油/水型
乳化化粧料、クリーム、化粧乳液、化粧水、油性化粧
料、口紅、フアウンデーシヨン、皮膚洗浄剤、ヘアート
ニツク、整髪剤、養毛剤、育毛剤等の皮膚化粧料とする
ことができる。As the cosmetics, various forms such as water / oil, oil / water emulsion cosmetics, creams, lotions, lotions, oily cosmetics, lipsticks, foundations, skin cleansers, hair nicks, hair styling agents, It can be used as a skin cosmetic such as a hair nourishing agent or a hair restorer.
本発明皮膚外用剤における式(I)で示される化合物又
はその塩の作用機構の詳細は完全には解明されていない
が、これが角質細胞間に脂質膜を再構築して角質層の水
分保持機能を発揮するものと考えられる。The details of the mechanism of action of the compound represented by formula (I) or a salt thereof in the external preparation for skin of the present invention have not been completely elucidated, but this has the effect of reconstructing a lipid membrane between corneocytes to retain water in the stratum corneum. It is thought that it exerts.
本発明皮膚外用剤は、このような作用を有する化合物
(I)又はその塩を含有するものであるため、肌あれに
対して優れた改善及び予防効果を発揮することができ
る。Since the external preparation for skin of the present invention contains the compound (I) or a salt thereof having such an action, it can exert excellent improving and preventing effects on skin roughness.
次に実施例を挙げて説明する。 Next, examples will be described.
実施例1 化合物Ia〜Idを使用し、ワセリン/化合物(Ia〜Id)=
3/1(重量比)の混合物(本発明品1)とワセリン(比
較品1)の下記方法による皮膚コンダクタンス及び肌あ
れについて評価した。結果を第1表に示す。Example 1 Using Compounds Ia-Id, Vaseline / Compound (Ia-Id) =
The skin conductance and skin roughness of the 3/1 (weight ratio) mixture (invention product 1) and vaseline (comparative product 1) were evaluated by the following methods. The results are shown in Table 1.
(試験方法) 冬期に頬部に肌あれを起こしている20〜50才の女性10名
を被験者とし、左右の頬に異なる皮膚外用剤を2週間塗
布する。2週間の塗布が終了した翌日に次の項目につき
試験を行なつた。(Test method) Ten women aged 20 to 50 who have rough skin on the cheeks in winter are used as test subjects, and different skin external preparations are applied to the left and right cheeks for 2 weeks. On the day after the application for two weeks was completed, the following items were tested.
(1)皮膚コンダクタンス 37℃の温水にて洗顔後、温度20℃、湿度40%の部屋で20
分間安静にした後、角質層の水分含有量を皮膚コンダク
タンスメータ(IBS社製)にて測定した。コンダクタン
ス値は値が小さいほど皮膚は肌あれし、5以下ではひど
い肌あれである。一方この値が20以上であれば肌あれは
ほとんど認められない。(1) Skin conductance After washing the face with warm water of 37 ℃, in a room with temperature of 20 ℃ and humidity of 40%, 20
After resting for a minute, the water content of the stratum corneum was measured with a skin conductance meter (IBS). The smaller the conductance value is, the rougher the skin is, and when the conductance value is 5 or less, the skin is severely rough. On the other hand, if this value is 20 or more, almost no rough skin is observed.
(2)肌あれスコア 肌あれは肉眼で観測し、下記基準により判定した。スコ
アは平均値で示した。(2) Skin Roughness Score Rough skin was visually observed and judged according to the following criteria. The score is shown as an average value.
実施例2 化合物Ia〜Idを用いて下記第2表に示す組成の皮膚外用
剤(乳化化粧料)を製造し、その肌あれ改善効果を実施
例1と同様の方法により評価した。結果を第3表に示
す。 Example 2 Compounds Ia to Id were used to produce a skin external preparation (emulsion cosmetic) having the composition shown in Table 2 below, and the skin roughening improving effect was evaluated by the same method as in Example 1. The results are shown in Table 3.
実施例3 乳液 上記処方に従い、油相成分を混合し加熱溶解して70℃に
保つ。上記水相成分も同様に70℃で加熱混合し、この水
相部に前述の油相部を加えて乳化機にて乳化する。乳化
物を熱交換機にて終温30℃まで冷却して乳液を調製し
た。 Example 3 Emulsion According to the above formulation, the oil phase components are mixed, dissolved by heating and kept at 70 ° C. Similarly, the above water phase components are heated and mixed at 70 ° C., and the above oil phase part is added to this water phase part and emulsified by an emulsifying machine. The emulsion was cooled with a heat exchanger to a final temperature of 30 ° C. to prepare an emulsion.
この乳液は荒れ肌改善効果が高く、優れた保湿能を示し
た。This emulsion had a high effect of improving rough skin and showed excellent moisturizing ability.
実施例4 乳化型フアンデーシヨン 上記処方に従い、油相成分を混合し加熱溶解して70℃に
保つ。上記水相成分に粉末成分を加え分散させた後70℃
に加熱する。この水相部に前述の油相部を加えて乳化機
にて乳化、分散する。この乳化物を熱交換機にて終温30
℃まで冷却したのち充填を行なうことにより、乳化型フ
アンデーシヨンを調製した。Example 4 Emulsion type emulsion According to the above formulation, the oil phase components are mixed, dissolved by heating and kept at 70 ° C. After the powder component is added to the above aqueous phase component and dispersed, 70 ° C
Heat to. The above oil phase portion is added to this water phase portion and emulsified and dispersed by an emulsifying machine. Heat the emulsion to a final temperature of 30.
An emulsion type emulsion was prepared by cooling the mixture to 0 ° C. and then filling it.
この乳化型フアンデーシヨンは、荒れ肌改善効果が高
く、優れた保湿能を示した。This emulsion type foundation had a high effect of improving rough skin and showed excellent moisturizing ability.
実施例5 口紅 上記処方に従い、マイクロクリスタリンワツクス、キヤ
ンデリラロウ、ヒマシ油、化合物(Ia)、ホホバ油、オ
リーブ油、ラノリンを90°〜100℃にて加熱溶解した
後、顔料を加えてよく攪拌分散し脱気した後これに香料
を加えて口紅成型器に流し込み、15°〜20℃に冷却後、
型から取り出してステイツク状口紅を調製した。Example 5 Lipstick According to the above formulation, microcrystalline wax, candelilla wax, castor oil, compound (Ia), jojoba oil, olive oil, and lanolin are heated and dissolved at 90 ° to 100 ° C., after which pigments are added and well stirred and dispersed to deaerate. Add the fragrance to it and pour into a lipstick molding machine, cool to 15 ° -20 ° C,
A sticky lipstick was prepared by removing from the mold.
この口紅は荒れ肌改善効果が高く、優れた保湿能を示し
た。This lipstick had a high effect of improving rough skin and showed an excellent moisturizing ability.
実施例6 W/O型マツサージクリーム 上記処方に従い、精製水に石けん粉末を加えて加熱し70
℃に保つ。油相成分を混合し、加熱して70℃にする。こ
の油相部に前述の水相部を加えて予備乳化を行つた後、
ホモミキサーで均一に乳化し、熱交換器により室温付近
まで冷却する。Example 6 W / O type pine surge cream According to the above prescription, add soap powder to purified water and heat.
Keep at ℃. Mix the oil phase ingredients and heat to 70 ° C. After performing the preliminary emulsification by adding the above-mentioned water phase part to this oil phase part,
Emulsify uniformly with a homomixer and cool to near room temperature with a heat exchanger.
このマツサージクリームは荒れ肌改善効果が高く、優れ
た保湿能を示した。This pine surge cream has a high effect of improving rough skin and has an excellent moisturizing effect.
実施例7 パツク(ピールオフタイプ) 上記処方に従い、水相成分を混合し加熱溶解して70℃に
保つ。上記油相成分も同様に70℃で加熱混合し前述の水
相部に加えて乳化機にて乳化する。この乳化物中に粉末
成分、皮膜剤を加え混合する。乳化物を熱交換機にて終
温30℃まで冷却したのち充填を行なうことによりパツク
を調製した。Example 7 Pack (peel-off type) According to the above formulation, the aqueous phase components are mixed, dissolved by heating and kept at 70 ° C. Similarly, the above oil phase components are heated and mixed at 70 ° C., added to the above water phase portion and emulsified by an emulsifying machine. A powder component and a film forming agent are added to this emulsion and mixed. A pack was prepared by cooling the emulsion to a final temperature of 30 ° C. with a heat exchanger and then filling it.
このパツクは荒れ肌改善効果が高く、優れた保湿能を示
した。This pack had a high effect of improving rough skin and showed an excellent moisturizing ability.
実施例8 ヘアトニツク 下記成分を70℃で加温溶解し、冷却してヘアトニツクを
得た。Example 8 Hair Tonic The following components were dissolved by heating at 70 ° C and cooled to obtain a hair tonic.
Claims (2)
鎖の飽和若しくは不飽和の炭化水素基を示す) で表わされる化合物又はその塩を含有する皮膚外用剤。1. The following general formula (I): (In the formula, R 1 and R 2 represent a linear or branched saturated or unsaturated hydrocarbon group having 10 to 26 carbon atoms) or a skin external preparation containing a salt thereof.
鎖の飽和若しくは不飽和の炭化水素基を示す) で表わされる化合物又はその塩及び界面活性剤を含有す
る皮膚外用剤。2. The following general formula (I): (Wherein, R 1 and R 2 represent a linear or branched saturated or unsaturated hydrocarbon group having 10 to 26 carbon atoms) or a salt thereof and a skin external preparation containing a surfactant. .
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16368387A JPH0669931B2 (en) | 1987-06-30 | 1987-06-30 | External skin preparation |
ES92115766T ES2077948T3 (en) | 1987-03-06 | 1988-03-02 | PREPARATION FOR EXTERNAL SKIN CARE. |
EP92115766A EP0534286B1 (en) | 1987-03-06 | 1988-03-02 | External skin care preparation |
EP88103177A EP0282816B1 (en) | 1987-03-06 | 1988-03-02 | External skin care preparation |
DE3854275T DE3854275T2 (en) | 1987-03-06 | 1988-03-02 | External skin care preparation. |
DE88103177T DE3884021T2 (en) | 1987-03-06 | 1988-03-02 | External skin care preparation. |
US07/163,835 US4985547A (en) | 1987-03-06 | 1988-03-03 | External skin care preparation |
US07/546,276 US5028416A (en) | 1987-03-06 | 1990-06-29 | External skin care preparation |
US07/584,739 US5071971A (en) | 1987-03-06 | 1990-09-19 | External skin care preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16368387A JPH0669931B2 (en) | 1987-06-30 | 1987-06-30 | External skin preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS649906A JPS649906A (en) | 1989-01-13 |
JPH0669931B2 true JPH0669931B2 (en) | 1994-09-07 |
Family
ID=15778615
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16368387A Expired - Lifetime JPH0669931B2 (en) | 1987-03-06 | 1987-06-30 | External skin preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0669931B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR19980034991A (en) | 1996-11-11 | 1998-08-05 | 안용찬 | Non-natural ceramide-related compounds and external skin preparations containing them |
-
1987
- 1987-06-30 JP JP16368387A patent/JPH0669931B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS649906A (en) | 1989-01-13 |
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