JPH0672851A - Skin cosmetic - Google Patents

Skin cosmetic

Info

Publication number
JPH0672851A
JPH0672851A JP15734293A JP15734293A JPH0672851A JP H0672851 A JPH0672851 A JP H0672851A JP 15734293 A JP15734293 A JP 15734293A JP 15734293 A JP15734293 A JP 15734293A JP H0672851 A JPH0672851 A JP H0672851A
Authority
JP
Japan
Prior art keywords
skin
water
formula
alkyl
feeling
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.)
Granted
Application number
JP15734293A
Other languages
Japanese (ja)
Other versions
JP3251719B2 (en
Inventor
Eishin Takanabe
英信 高鍋
Ichirou Tokimitsu
一郎 時光
Yoshihiro Minematsu
義博 峰松
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP15734293A priority Critical patent/JP3251719B2/en
Publication of JPH0672851A publication Critical patent/JPH0672851A/en
Application granted granted Critical
Publication of JP3251719B2 publication Critical patent/JP3251719B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To obtain skin cosmetics having excellent moisture retention, no irritation and no greasy feeling, thus giving good application feeling with high durability, by using an amphiphilic lipid and a specific organopolysiloxane. CONSTITUTION:The objective cosmetics contain 1 to 40wt.% of an amphiphilic lipid such as phospholipid and 0.01 to 40wt.% of a compound of formula I and formula II (R<1>, R<2> are 1 to 4C alkyl; R<3> is 1 to 40C alkyl, alkenyl, fluoroalkyl; R<4> is 7 to 40C alkyl, alkenyl, fluoroalkyl; l is 2 or more; m is 3 or more and l+m is 5 to 6,000). In addition, the additives used in usual cosmetics such as salts, oil, emulsion, powder, ultraviolet scattering agent, pH adjuster, thickener, pigments, preservative, antioxidant, fungicidal or water-soluble solvents are suitably used to produce emulsion, dispersion, double-layered or solubilized preparations. Since the humectant is not flown off by sweat or water, the preparation can stay on the application site to sustain the moisture retention effect for hours.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は保湿性に優れ、刺激性や
べたつきがなく、使用感が良好で持続性の高い皮膚化粧
料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a skin cosmetic having excellent moisturizing properties, non-irritating properties, non-greasiness, good feeling on use and high durability.

【0002】[0002]

【従来の技術】従来、水仕事、乾燥、摩擦等による肌荒
れから皮膚を保護する目的で化粧水、乳液、クリーム等
が汎用されている。これらの化粧水の乳液、クリーム等
は水仕事、乾燥、摩擦等によって失なわれた皮脂を補給
し、更に保湿剤の配合により、皮膚に適度な水分を補給
するなどの働きにより皮膚を保護するものである。
2. Description of the Related Art Conventionally, lotions, emulsions, creams and the like have been widely used for the purpose of protecting the skin from rough skin caused by water work, drying, rubbing and the like. These lotion emulsions, creams, etc. replenish the skin oil lost by water work, drying, rubbing, etc., and the addition of a moisturizing agent protects the skin by the action of replenishing the skin with an appropriate amount of water. It is a thing.

【0003】しかしながら、従来の化粧水、乳液、クリ
ームは汗や水によって容易に洗い流されてしまうため、
皮膚に補給した保湿成分も皮脂成分とともに汗や水で流
れてしまうなど経時的に保湿効果が減少してしまうもの
が多かった。また、保湿効果を上げようとして保湿成分
を多量に配合するとべたついた使用感がでる等、必ずし
も満足できるものではなかった。現に、炊事、洗濯など
の水仕事を頻度高く行なうために手荒れで悩んでいる主
婦は多い。また、美容師などの中にも、度重なるシャン
プーによる手荒れに加え、染毛剤、パーマ液等による乾
燥、炎症を訴える人が少なくない。
However, conventional lotions, emulsions and creams are easily washed away by sweat and water,
In many cases, the moisturizing component replenished to the skin was also washed away with sweat and water along with the sebum component, and the moisturizing effect was reduced over time. Further, when a large amount of a moisturizing component is added in an attempt to enhance the moisturizing effect, a sticky feeling is produced, which is not always satisfactory. In fact, many housewives suffer from rough hands because they frequently do water work such as cooking and washing. Also, many beauticians complain of dryness and inflammation caused by hair dye, perm solution, etc. in addition to rough hands caused by repeated shampooing.

【0004】[0004]

【発明が解決しようとする課題】従って、本発明は、の
びが良く保湿性に優れべたつき感の少ない使用感の良好
な被膜を形成し、水仕事や石鹸を用いた皮膚洗浄過程な
どによっても容易に洗い流されず、長時間にわたって皮
膚に保湿作用を付与し得る皮膚化粧料を提供することを
目的とする。
Therefore, the present invention forms a film having good spreadability, excellent moisturizing properties, and less sticky feeling and a good feeling in use, and can be easily prepared by water work or a skin washing process using soap. It is an object of the present invention to provide a skin cosmetic which can be moisturized to the skin for a long time without being washed off.

【0005】[0005]

【課題を解決するための手段】かかる実情において、本
発明者らは鋭意研究を行なった結果、保湿成分としての
両親媒性脂質と特定のオルガノポリシロキサンとを組み
合わせて用いることにより、保湿性、その持続性及び使
用感のすべてに優れた皮膚化粧料が得られることを見出
し、本発明を完成するに至った。
Under the circumstances, as a result of intensive studies by the present inventors, as a result of using a combination of an amphipathic lipid as a moisturizing component and a specific organopolysiloxane, It was found that a skin cosmetic excellent in all of its durability and feeling of use can be obtained, and the present invention has been completed.

【0006】すなわち、本発明は次の成分(A)及び
(B): (A)両親媒性脂質、 (B)分子中に
That is, the present invention comprises the following components (A) and (B): (A) amphipathic lipid, (B) in the molecule

【0007】[0007]

【化2】 [Chemical 2]

【0008】(R1及びR2はそれぞれ炭素数1〜4のア
ルキル基を示し、R3は炭素数1〜40の直鎖、分岐鎖
又は環状のアルキル基、アルケニル基又はフルオロアル
キル基を示し、R4は炭素数7〜40の直鎖、分岐鎖又
は環状のアルキル基、アルケニル基又はフルオロアルキ
ル基を示し、lは2以上の数を示し、mは3以上の数を
示し、更にl+m=5〜6000である)を有するオル
ガノポリシロキサン、を含有することを特徴とする皮膚
化粧料を提供するものである。
(R 1 and R 2 each represent an alkyl group having 1 to 4 carbon atoms, and R 3 represents a linear, branched or cyclic alkyl group having 1 to 40 carbon atoms, an alkenyl group or a fluoroalkyl group. , R 4 represents a linear, branched or cyclic alkyl group, alkenyl group or fluoroalkyl group having 7 to 40 carbon atoms, l represents a number of 2 or more, m represents a number of 3 or more, and further l + m The present invention provides a skin cosmetic, comprising: an organopolysiloxane having a value of 5 to 6000).

【0009】本発明における両親媒性脂質(A)とは、
一分子中に疎水性部と親水性部を有する固体物質であ
り、具体的にはリン脂質、セラミド、糖セラミド、セラ
ミド類似構造物質等が挙げられる。ここでいうセラミド
類似構造物質とは、2本の長鎖炭化水素基とこれらの間
に0H基とアミド基とを有し、かつ当該分子が一平面上の
立体配座をとることのできる脂質誘導体を言う。かかる
化合物としては、例えば、特開昭62−228048号
公報記載の次の一般式(1)で表わされるものが挙げら
れる。
The amphipathic lipid (A) in the present invention is
It is a solid substance having a hydrophobic portion and a hydrophilic portion in one molecule, and specific examples thereof include phospholipids, ceramides, sugar ceramides, ceramide-like structural substances and the like. The ceramide-like structural material referred to here is a lipid that has two long-chain hydrocarbon groups and an OH group and an amide group between them, and that the molecule can have a one-dimensional conformation. Says a derivative. Examples of such compounds include those represented by the following general formula (1) described in JP-A-62-228048.

【0010】[0010]

【化3】 [Chemical 3]

【0011】(式中、R5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、R6
は炭素数9〜25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)
(In the formula, R 5 is a linear or branched saturated or unsaturated hydrocarbon group having 10 to 26 carbon atoms, and R 6 is
Represents a linear or branched saturated or unsaturated hydrocarbon group having 9 to 25 carbon atoms)

【0012】これらの両親媒性脂質(A)は、単独又は
2種以上を組み合わせて用いることができ、本発明皮膚
化粧料全組成中に1.0〜40.0重量%(以下、単に
%で示す)、特に3.0〜20.0%配合するのが好ま
しい。
These amphipathic lipids (A) can be used alone or in combination of two or more, and are contained in 1.0 to 40.0% by weight (hereinafter simply referred to as% by weight) in the total composition of the skin cosmetic of the present invention. It is preferable to add 3.0 to 20.0%.

【0013】本発明において、(B)成分のオルガノポ
リシロキサンは、(A)成分の両親媒性脂質の保湿作用
を持続させる作用を有するとともに、べたつき感、洗浄
後の皮膚の感触等の使用感を改善する作用を有するもの
である。
In the present invention, the organopolysiloxane as the component (B) has a function of maintaining the moisturizing action of the amphipathic lipid as the component (A), and has a feeling of use such as stickiness and skin feel after washing. It has the effect of improving.

【0014】本発明に使用される(B)成分のオルガノ
ポリシロキサンは、1分子中に少なくとも3個の炭素数
7〜40の炭化水素基を有するものである。オルガノポ
リシロキサンの分子形態は直鎖状、分岐鎖状及び環状の
いずれであってもよい。
The component (B) organopolysiloxane used in the present invention has at least 3 hydrocarbon groups having 7 to 40 carbon atoms in one molecule. The molecular form of the organopolysiloxane may be linear, branched or cyclic.

【0015】オルガノポリシロキサン(B)が有するR
1及びR2で示されるアルキル基としては、メチル基、エ
チル基、n−プロピル基、イソプロピル基、n−ブチル
基等が挙げられるが、就中メチル基が好ましい。また、
3及びR4で示されるアルキル、アルケニル又はフルオ
ロアルキル基は、直鎖状、分岐鎖状及び環状のいずれで
あってもよいが、R3が炭素数1〜4のアルキル基であ
り、かつR4が炭素数7〜40(より好ましくは12〜
22、特に好ましくは16〜18)のアルキル基、アル
ケニル基又はフルオロアルキル基であることが好まし
い。R4の具体例としてはオクチル、ノニル、デシル、
ウンデシル、ドデシル、トリデシル、テトラデシル、ペ
ンタデシル、ヘキサデシル、ヘプタデシル、オクタデシ
ル、ノナデシル、エイコシル、ヘンエイコシル、ドコシ
ル、テトラコシル、ペンタコシル、ヘキサコシル、ヘプ
タコシル、オクタコシル、トリアコンチル、テトラトリ
アコンチル、オクタトリアコンチル、テトラコンチル、
2−ヘプチルウンデシル、2−ウンデシルペンタデシ
ル、2−デシルテトラデシル、2−デシルペンタデシ
ル、2−エチルヘキシル、2−オクチルドデシル、2−
ウンデシルテトラデシル、メチル分岐イソステアリル、
メチル分岐ドデシル(プロピレンテトラマー)、メチル
分岐ノニル(プロピレントリマー)基等が挙げられる。
また、l+mは5〜6000であるが、200〜300
0であることが好ましく、更には、l=m=150〜7
50でl+mが300〜1500であることが好まし
い。ここでl、mは重量平均分子量から算出した平均重
合度として求められる。
R contained in the organopolysiloxane (B)
Examples of the alkyl group represented by 1 and R 2 include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group, but a methyl group is preferable. Also,
The alkyl, alkenyl or fluoroalkyl group represented by R 3 and R 4 may be linear, branched or cyclic, but R 3 is an alkyl group having 1 to 4 carbon atoms, and R 4 has 7 to 40 carbon atoms (more preferably 12 to
22 and particularly preferably 16 to 18) alkyl group, alkenyl group or fluoroalkyl group. Specific examples of R 4 include octyl, nonyl, decyl,
Undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl, docosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, triacontyl, tetratriacontyl, octatriacontyl, tetracontyl,
2-heptyl undecyl, 2-undecyl pentadecyl, 2-decyl tetradecyl, 2-decyl pentadecyl, 2-ethylhexyl, 2-octyl dodecyl, 2-
Undecyl tetradecyl, methyl-branched isostearyl,
Examples thereof include methyl-branched dodecyl (propylene tetramer) and methyl-branched nonyl (propylene trimer) groups.
Also, l + m is 5 to 6000, but 200 to 300
0 is preferable, and further, l = m = 150 to 7
It is preferable that 1 + m is 50 to 300 and 1500. Here, l and m are obtained as an average degree of polymerization calculated from the weight average molecular weight.

【0016】また、オルガノポリシロキサン(B)は、
その融点が10〜50℃、特に20〜40℃であるもの
が好ましい。なお、当該オルガノポリシロキサンの融点
は、示差走査熱量計(DSC)を用いて測定した。
The organopolysiloxane (B) is
Those having a melting point of 10 to 50 ° C, particularly 20 to 40 ° C are preferable. The melting point of the organopolysiloxane was measured using a differential scanning calorimeter (DSC).

【0017】オルガノポリシロキサン(B)は、前記両
ポリシロキサン単位を分子中のいずれの位置に有してい
る構造であってもよいが、製造の容易性の観点からは、
両単位1ブロックずつが直接に結合しており、これに両
末端残基が結合した単純な構造であるのが好ましい。ま
た、この両末端残基は−OSiR7R8R9 (R7〜R9は炭素数
1〜4のアルキル基を示す)であることが好ましい。
The organopolysiloxane (B) may have a structure having both the polysiloxane units at any position in the molecule, but from the viewpoint of easy production,
It is preferable that each unit is directly bonded to each one block, and both terminal residues are bonded to the unit to have a simple structure. Further, it is preferable that the both-terminal residues -OSiR 7 R 8 R 9 in which (R 7 to R 9 is an alkyl group having 1 to 4 carbon atoms) is.

【0018】オルガノポリシロキサン(B)の具体例と
しては、次の一般式(2)で表わされるものが挙げられ
る。
Specific examples of the organopolysiloxane (B) include those represented by the following general formula (2).

【0019】[0019]

【化4】 [Chemical 4]

【0020】オルガノポリシロキサン(B)の市販品と
しては、XF42−A7154、XF42−A504
8、XF42−A5047〔東芝シリコーン(株)製〕
等を使用することができる。
Commercially available products of the organopolysiloxane (B) include XF42-A7154 and XF42-A504.
8, XF42-A5047 [manufactured by Toshiba Silicone Co., Ltd.]
Etc. can be used.

【0021】かかるオルガノポリシロキサン(B)は単
独で、又は2種以上組み合わせて使用することができ、
本発明皮膚化粧料への配合量は両親媒性脂質(A)の配
合量によっても異なるが通常0.01%〜40.0%、
特に2〜20%であることが望ましい。
The above organopolysiloxane (B) can be used alone or in combination of two or more kinds,
The blending amount in the skin cosmetic of the present invention varies depending on the blending amount of the amphipathic lipid (A), but is usually 0.01% to 40.0%,
It is particularly preferable that the amount is 2 to 20%.

【0022】本発明の皮膚化粧料においては、前記必須
成分の他、通常化粧料に用いられる塩、油剤、乳化剤、
粉体、紫外線散乱剤、pH調整剤、増粘剤、色素、防腐
剤、酸化防止剤、紫外線吸収剤、香料、キレート剤、収
れん剤、殺菌剤、賦活剤等の薬効剤、エタノール、グリ
セリン等の水溶性溶剤を本発明の効果を損なわない範囲
で配合することができる。更に本発明皮膚化粧料は常法
により製造することができ、その剤型には、乳化型、分
散型、二層型、可溶化型等どのような剤型のものをも含
まれる。
In the skin cosmetic of the present invention, in addition to the above-mentioned essential components, salts, oils, emulsifiers, which are usually used in cosmetics,
Powders, UV scattering agents, pH adjusters, thickeners, pigments, preservatives, antioxidants, UV absorbers, fragrances, chelating agents, astringents, bactericides, activators, etc., ethanol, glycerin, etc. The water-soluble solvent can be added within a range that does not impair the effects of the present invention. Furthermore, the skin cosmetic of the present invention can be produced by a conventional method, and its dosage form includes any dosage form such as an emulsion type, a dispersion type, a two-layer type and a solubilizing type.

【0023】[0023]

【発明の効果】本発明皮膚化粧料は、保湿性に優れ、刺
激やべたつきがなく使用感が良好で保湿成分も汗や水で
流されてしまうことなく、長時間塗布部位に残存し保湿
効果が持続する。
EFFECTS OF THE INVENTION The skin cosmetics of the present invention have excellent moisturizing properties, good feeling of use without irritation or stickiness, and moisturizing ingredients remain on the application site for a long time without being washed away by sweat or water, and have a moisturizing effect. Persists.

【0024】[0024]

【実施例】次に実施例を挙げて本発明を更に詳細に説明
するが、これらは本発明を何ら限定するものではない。
The present invention will be described in more detail with reference to the following examples, which are not intended to limit the present invention.

【0025】実施例1 表1〜表4に示す組成のうち精製水及び水溶性溶剤を除
く全成分を70〜80℃で攪拌溶解後、攪拌下70〜8
0℃の精製水及び水溶性溶剤を添加し攪拌を続けながら
冷却して各クリームを得た。得られたクリームについて
以下の試験方法に基づいて実用テスト及び皮膚保湿効果
試験を行なった。
Example 1 Of the compositions shown in Tables 1 to 4, all components except purified water and a water-soluble solvent were dissolved by stirring at 70 to 80 ° C. and then stirred at 70 to 8
Purified water at 0 ° C. and a water-soluble solvent were added and cooled with continuous stirring to obtain each cream. The obtained cream was subjected to a practical test and a skin moisturizing effect test based on the following test methods.

【0026】(1)実用テスト(パネルテスト) 女性パネラー10名に洗浄後の皮膚に使用してもらい、
下記の基準より使用感を評価した。評価項目は、塗布時
のべたつきの少なさ及び石鹸洗浄後の手肌のしっとり感
の2項目である。評価結果は次の3段階の基準に従い、
表1〜表4に示す。 ◎:良好と回答した者が10名中9名以上。 ○:良好と回答した者が10名中6〜8名。 △:良好と回答した者が10名中3〜5名。 ×:良好と回答した者が10名中3名未満。
(1) Practical test (panel test) We asked 10 female panelists to use it on the skin after washing,
The feeling of use was evaluated based on the following criteria. The evaluation items are two items, namely, the degree of stickiness during application and the moist feeling of the hand skin after soap washing. The evaluation results are based on the following three criteria
It shows in Table 1-4. ⊚: 9 or more out of 10 people answered good. ◯: 6 to 8 out of 10 respondents answered good. Δ: 3 to 5 out of 10 people answered good. X: Less than 3 out of 10 people answered good.

【0027】(2)皮膚保湿効果試験 人前腕内側にアセトン/エーテル(体積比1:1)を入
れたガラス製カップ(内径2cm)を装着し、10分間脱
脂処理を行ない、荒れ肌を誘発させた。荒れ肌部に表1
に示す5種のサンプルを均一に塗布(20μl/3.1
4cm2)し10分間かけて乾燥させた。乾燥直後、及び
20℃40%RHで24時間保持後に皮表コンダクタンス
を測定し、水分保持能を評価した。なお皮表コンダクタ
ンス値が高いほど水分保持量が高く、ひいては保湿効果
が高いことを示す。評価結果は次の3段階の基準に従い
表1〜表4に示す。 ○:健常肌の皮表コンダクタンス値と比して同等以上。 △:健常肌の皮表コンダクタンス値と比してやや低い。 ×:健常肌の皮表コンダクタンス値より著しく低い。
(2) Skin moisturizing effect test A glass cup (inner diameter 2 cm) containing acetone / ether (volume ratio 1: 1) was attached to the inside of the forearm, and degreasing treatment was performed for 10 minutes to induce rough skin. . Table 1 on rough skin
The 5 kinds of samples shown in (1) are uniformly applied (20 μl / 3.1).
4 cm 2 ) and dried for 10 minutes. Immediately after drying and after being kept at 20 ° C. and 40% RH for 24 hours, the skin surface conductance was measured to evaluate the water retention ability. It should be noted that the higher the skin surface conductance value, the higher the water retention amount, and thus the higher the moisturizing effect. The evaluation results are shown in Tables 1 to 4 according to the following three-stage criteria. ◯: Equal to or higher than the skin surface conductance value of normal skin. Δ: Slightly lower than the skin surface conductance value of normal skin. X: Remarkably lower than the skin surface conductance value of normal skin.

【0028】[0028]

【表1】 [Table 1]

【0029】[0029]

【表2】 [Table 2]

【0030】[0030]

【表3】 [Table 3]

【0031】[0031]

【表4】 [Table 4]

【0032】1):オクタデシル変性シリコーン〔式
(2)中、l=750、m=750、R4=C1837〕 2):オクタデシル変性シリコーン〔式(2)中、l=
500、m=500、R4=C1837〕 3):オクタデシル変性シリコーン〔式(2)中、l=
50、m=50、R4=C1837〕 4):ヘキサデシル変性シリコーン〔式(2)中、l=
500、m=500、R4=C1633〕 5):ヘキサデシル変性シリコーン〔式(2)中、l=
75、m=75、R4=C1633〕 6):オクチル変性シリコーン〔式(2)中、l=75
0、m=750、R4=C817〕 7):ドコシル変性シリコーン〔式(2)中、l=50
0、m=500、R4=C2245〕 8):特開昭62−228048号公報の実施例1のア
ミド誘導体 9):ジメチルシロキサン・メチル(ポリオキシエチレ
ン・ポリオキシプロピレン)シロキサン共重合体(東レ
・ダウ・コーニング・シリコーン社製、BY−22−0
12)
1): Octadecyl-modified silicone [in the formula (2), l = 750, m = 750, R 4 = C 18 H 37 ] 2): Octadecyl-modified silicone [in the formula (2), l =
500, m = 500, R 4 = C 18 H 37 ] 3): During octadecyl-modified silicone [formula (2), l =
50, m = 50, R 4 = C 18 H 37 ] 4): Hexadecyl-modified silicone [in the formula (2), l =
500, m = 500, R 4 = C 16 H 33 ] 5): in hexadecyl-modified silicone [formula (2), l =
75, m = 75, R 4 = C 16 H 33 ] 6): octyl-modified silicone [in the formula (2), l = 75]
0, m = 750, R 4 = C 8 H 17 ] 7): docosyl-modified silicone [in the formula (2), 1 = 50]
0, m = 500, R 4 = C 22 H 45 ] 8): amide derivatives 9 of Example 1 of JP 62-228048 JP): dimethylsiloxane-methyl (polyoxyethylene-polyoxypropylene) siloxane copolymer Polymer (Toray Dow Corning Silicone, BY-22-0
12)

【0033】表1〜表4から明らかなように本発明の皮
膚化粧料は比較品に比して使用感が良く、かつ保湿効果
の持続性にも優れていることがわかる。
As can be seen from Tables 1 to 4, the skin cosmetics of the present invention have a better feeling in use and a longer lasting moisturizing effect than the comparative products.

【0034】実施例2(乳液)Example 2 (milky lotion)

【0035】[0035]

【表5】 (組成) (%) (1)ジメチルシロキサン・メチル(ポリオキシエチレン・ ポリオキシプロピレン)共重合体 0.5 (2)オクタデシル変性シリコーン1) 3.0 (3)オクタメチルシクロテトラシロキサン 10.0 (4)セレブロシド(ナカライテスク社製) 2.0 (5)グリセリルモノオレート 1.5 (6)グリセリルモノステアレート 1.0 (7)ポリオキシエチレン(20)ソルビタンモノステアレート 1.5 (8)1,3−ブチレングリコール 10.0 (9)精製水 バランス 1):オクタデシル変性シリコーン〔式(2)中、l=7
50、m=750、R4 =C1837
[Table 5] (Composition) (%) (1) Dimethylsiloxane-methyl (polyoxyethylene-polyoxypropylene) copolymer 0.5 (2) Octadecyl-modified silicone 1) 3.0 (3) Octamethylcyclotetra Siloxane 10.0 (4) Cerebroside (manufactured by Nacalai Tesque) 2.0 (5) Glyceryl monooleate 1.5 (6) Glyceryl monostearate 1.0 (7) Polyoxyethylene (20) sorbitan monostearate 1 .5 (8) 1,3-butylene glycol 10.0 (9) Purified water balance 1): octadecyl-modified silicone [in the formula (2), l = 7
50, m = 750, R 4 = C 18 H 37 ]

【0036】(製法)(1)〜(6)を混合し、加熱溶
解して70℃に保ち油相部とする。別に(7)〜(9)
を加熱溶解して70℃に保ち水相部とする。この水相部
に油相部を添加して乳化機により十分に乳化する。乳化
後かきまぜながら冷却し製品とする。
(Production method) (1) to (6) are mixed, heated and dissolved to maintain an oil phase of 70 ° C. Separately (7)-(9)
Is melted by heating and kept at 70 ° C. to form an aqueous phase. The oil phase portion is added to this water phase portion and sufficiently emulsified by an emulsifying machine. After emulsification, cool while stirring to obtain a product.

【0037】本乳液はさっぱりとした使用感触を有する
ものであった。
The milky lotion had a refreshing feeling of use.

【0038】実施例3(エッセンス)Example 3 (essence)

【0039】[0039]

【表6】 (組成) (%) (1)エタノール 10.0 (2)オクタデシル変性シリコーン1) 2.0 (3)カルボキシビニルポリマー(カーボポール) 0.3 (4)L−アルギニン 0.3 (5)大豆レシチン(LS−60,日清製油社製) 1.0 (6)リノール酸 0.3 (7)グリセリン 10.0 (8)ジプロピレングリコール 25.0 (9)オレイルアルコール 0.2 (10)L−アスコルビン酸 0.5 (11)精製水 バランス 1):オクタデシル変性シリコーン〔式(2)中、l=7
50、m=750、R4 =C1837
[Table 6] (Composition) (%) (1) Ethanol 10.0 (2) Octadecyl-modified silicone 1) 2.0 (3) Carboxyvinyl polymer (Carbopol) 0.3 (4) L-arginine 0.3 (5) Soybean lecithin (LS-60, manufactured by Nisshin Oil Co., Ltd.) 1.0 (6) Linoleic acid 0.3 (7) Glycerin 10.0 (8) Dipropylene glycol 25.0 (9) Oleyl alcohol 0. 2 (10) L-ascorbic acid 0.5 (11) Purified water balance 1): Octadecyl-modified silicone [in the formula (2), l = 7
50, m = 750, R 4 = C 18 H 37 ]

【0040】(製法)(1)〜(11)を70℃にて加
温溶解させる。本エッセンスはさっぱり、しっとりとし
た使用感を有するものであった。
(Production method) (1) to (11) are dissolved by heating at 70 ° C. This essence had a refreshing and moisturizing feel.

【0041】実施例4(栄養クリーム)Example 4 (nutrition cream)

【0042】[0042]

【表7】 (組成) (%) (1)ジメチルシロキサン・メチル(ポリオキシエチレン・ ポリオキシプロピレン)共重合体 3.0 (2)ステアリン酸 3.0 (3)スクワラン 10.0 (4)オクタデシル変性シリコーン1) 10.0 (5)イソプロピルミリステート 2.0 (6)グリセリルモノステアレート 2.0 (7)グルタミン酸誘導体(エルデュウ CL−301 味の素社製) 5.0 (8)ジプロピレングリコール 3.0 (9)ポリオキシエチレンメチルグルコシドエーテル (EO10モル) 1.0 (10)精製水 バランス 1):オクタデシル変性シリコーン〔式(2)中、l=7
50、m=750、R4 =C1837
[Table 7] (Composition) (%) (1) Dimethylsiloxane / methyl (polyoxyethylene / polyoxypropylene) copolymer 3.0 (2) Stearic acid 3.0 (3) Squalane 10.0 (4) Octadecyl-modified silicone 1) 10.0 (5) Isopropyl myristate 2.0 (6) Glyceryl monostearate 2.0 (7) Glutamic acid derivative (Eldew CL-301 manufactured by Ajinomoto Co., Inc.) 5.0 (8) Dipropylene glycol 3.0 (9) Polyoxyethylene methyl glucoside ether (EO 10 mol) 1.0 (10) Purified water balance 1): Octadecyl-modified silicone [in the formula (2), l = 7
50, m = 750, R 4 = C 18 H 37 ]

【0043】(製法)(1)〜(7)を70℃にて加熱
溶解し油相部とする。別に(8)〜(10)を加熱溶解
して70℃に保ち水相部とする。この水相部に油相部を
添加して乳化機より十分に乳化する。乳化後かきまぜな
がら冷却し製品とする。本クリームはべたつかずしっと
りとした使用感触を有するものであった。
(Production method) (1) to (7) are heated and melted at 70 ° C. to form an oil phase part. Separately, (8) to (10) are dissolved by heating and kept at 70 ° C. to form an aqueous phase part. The oil phase part is added to this water phase part to be sufficiently emulsified by an emulsifying machine. After emulsification, cool while stirring to obtain a product. The cream had a non-greasy, moisturizing feel.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 次の成分(A)及び(B): (A)両親媒性脂質、 (B)分子中に 【化1】 (R1及びR2はそれぞれ炭素数1〜4のアルキル基を示
し、R3は炭素数1〜40の直鎖、分岐鎖又は環状のア
ルキル基、アルケニル基又はフルオロアルキル基を示
し、R4は炭素数7〜40の直鎖、分岐鎖又は環状のア
ルキル基、アルケニル基又はフルオロアルキル基を示
し、lは2以上の数を示し、mは3以上の数を示し、更
にl+m=5〜6000である)を有するオルガノポリ
シロキサン、を含有することを特徴とする皮膚化粧料。
1. The following components (A) and (B): (A) amphipathic lipid, (B) in the molecule: (R 1 and R 2 each represent an alkyl group having 1 to 4 carbon atoms, R 3 represents a linear, branched or cyclic alkyl group, alkenyl group or fluoroalkyl group having 1 to 40 carbon atoms, R 4 Represents a linear, branched or cyclic alkyl group, alkenyl group or fluoroalkyl group having 7 to 40 carbon atoms, l represents a number of 2 or more, m represents a number of 3 or more, and further l + m = 5 to 5 6000) is contained in the organopolysiloxane.
JP15734293A 1992-06-29 1993-06-28 Skin cosmetics Expired - Lifetime JP3251719B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15734293A JP3251719B2 (en) 1992-06-29 1993-06-28 Skin cosmetics

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP17091392 1992-06-29
JP4-170913 1992-06-29
JP15734293A JP3251719B2 (en) 1992-06-29 1993-06-28 Skin cosmetics

Publications (2)

Publication Number Publication Date
JPH0672851A true JPH0672851A (en) 1994-03-15
JP3251719B2 JP3251719B2 (en) 2002-01-28

Family

ID=26484831

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15734293A Expired - Lifetime JP3251719B2 (en) 1992-06-29 1993-06-28 Skin cosmetics

Country Status (1)

Country Link
JP (1) JP3251719B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0977653A (en) * 1995-09-14 1997-03-25 Advance Co Ltd Cosmetic
WO2007116999A1 (en) 2006-04-12 2007-10-18 Kao Corporation W/o/w type emulsified composition
US7511002B2 (en) 2004-04-27 2009-03-31 Kao Corporation Oil-in-water emulsion and process for producing the same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0977653A (en) * 1995-09-14 1997-03-25 Advance Co Ltd Cosmetic
US7511002B2 (en) 2004-04-27 2009-03-31 Kao Corporation Oil-in-water emulsion and process for producing the same
WO2007116999A1 (en) 2006-04-12 2007-10-18 Kao Corporation W/o/w type emulsified composition

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