JPH08268833A - W/o-type emulsion composition - Google Patents

W/o-type emulsion composition

Info

Publication number
JPH08268833A
JPH08268833A JP10045895A JP10045895A JPH08268833A JP H08268833 A JPH08268833 A JP H08268833A JP 10045895 A JP10045895 A JP 10045895A JP 10045895 A JP10045895 A JP 10045895A JP H08268833 A JPH08268833 A JP H08268833A
Authority
JP
Japan
Prior art keywords
phase
composition
water
soluble polymer
emulsion composition
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.)
Withdrawn
Application number
JP10045895A
Other languages
Japanese (ja)
Inventor
Fumiaki Matsuzaki
文昭 松崎
Toshio Hariki
利男 梁木
Michihiro Yamaguchi
道広 山口
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.)
Shiseido Co Ltd
Original Assignee
Shiseido 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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP10045895A priority Critical patent/JPH08268833A/en
Publication of JPH08268833A publication Critical patent/JPH08268833A/en
Withdrawn legal-status Critical Current

Links

Landscapes

  • Cosmetics (AREA)

Abstract

PURPOSE: To obtain an emulsion composition good in emulsion stability, safety and usability, by incorporating an oily phase with ethylhydroxyethyl cellulose. CONSTITUTION: This composition is obtained by incorporating an oily phase with 0.1-20wt.% of ethylhydroxyethyl cellulose as a liposoluble polymer and incorporating an aqueous phase with 0.01-10wt.% of a water-soluble polymer (e.g. carboxymethylcellulose). Besides, the composition is also incorporated, as necessary, with a humectant, a medicine, a UV absorber, an antiseptic agent and an antioxidant. This emulsified composition is prepared by dissolving the ethylhydroxyethyl cellulose in the oily phase and adding the aqueous phase portion to the resultant mixture under agitation followed by dispersing treatment. It is preferable that the weight ratio of the oily phase/the aqueous phase be (5-40%)/(95-60%).

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、W/O型乳化組成物に
関し、詳細には、従来の界面活性剤を使用せず、安定
性、安全性および使用性の良好なW/O型乳化組成物に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a W / O type emulsified composition, and more particularly, to a W / O type emulsified composition which does not use a conventional surfactant and has good stability, safety and usability. It relates to a composition.

【0002】[0002]

【従来の技術】従来、化粧品または医薬品の調製を目的
とし、乳化に関する数多くの研究がなされ、多数の乳化
剤が開発された。また、乳化技術の進歩もめざましく、
非常に安定なエマルションがあらゆる工業で広く利用さ
れて来ている。しかしながら、その多くは、ポリオキシ
エチレン鎖を含有する非イオン界面活性剤、脂肪酸石け
んで代表されるアニオン性界面活性剤、両性界面活性剤
を乳化剤として使用しており、特に一般消費者の間で安
全性に不安を抱くものが多い。
2. Description of the Related Art Hitherto, many studies have been conducted on emulsification for the purpose of preparing cosmetics or pharmaceuticals, and many emulsifiers have been developed. In addition, the progress of emulsification technology is remarkable,
Very stable emulsions have been widely used in all industries. However, most of them use nonionic surfactants containing polyoxyethylene chains, anionic surfactants represented by fatty acid soaps, and amphoteric surfactants as emulsifiers, and especially among general consumers. Many are concerned about safety.

【0003】このようなことから、近年特に、安全性が
高いと考えられる水溶性高分子を乳化剤として使用する
試みがなされている。しかし、上記の非イオン界面活性
剤等のいわゆる「界面活性剤」に比較して、水溶性高分
子は界面張力低下能が小さいため、乳化力は相対的に小
さく、乳化安定性が悪い。また、塗布時に乳化系が容易
に破壊されるため、肌への馴染みが悪く、いわゆる「は
じき」が認められるものであった。
Under these circumstances, attempts have recently been made to use a water-soluble polymer, which is considered to be highly safe, as an emulsifier. However, compared with the so-called "surfactants" such as the above-mentioned nonionic surfactants, the water-soluble polymer has a smaller interfacial tension lowering ability, so the emulsifying power is relatively small and the emulsion stability is poor. Further, since the emulsion system was easily destroyed during application, it was not so familiar with the skin and so-called "repellency" was observed.

【0004】[0004]

【発明が解決しようとする課題】上述の事情を鑑み、本
発明は、乳化安定性、安全性および使用性の良好な乳化
組成物を提供することを目的とする。
SUMMARY OF THE INVENTION In view of the above circumstances, an object of the present invention is to provide an emulsion composition having good emulsion stability, safety and usability.

【0005】[0005]

【課題を解決するための手段】本発明者は鋭意探求の結
果、油相にエチルヒドロキシエチルセルロースを配合す
ることで上記目的を達成できることを見い出し、本発明
を完成するに至った。
As a result of earnest research, the present inventor has found that the above object can be achieved by blending ethylhydroxyethyl cellulose in the oil phase, and has completed the present invention.

【0006】すなわち、本発明は油相に油溶性高分子と
して、エチルヒドロキシエチルセルロースを配合するこ
とを特徴とするW/O型乳化組成物である。また、本発
明においては、連続相に対して0.1〜20重量%配合
することが好ましい。
That is, the present invention is a W / O type emulsion composition characterized by containing ethylhydroxyethyl cellulose as an oil-soluble polymer in the oil phase. Further, in the present invention, it is preferable to add 0.1 to 20% by weight to the continuous phase.

【0007】さらに、本発明は、前記W/O型乳化組成
物において、水相に水溶性高分子を配合することを特徴
とする。また、非連続相に対して0.01〜10重量%
配合することが好ましい。
Further, the present invention is characterized in that, in the W / O type emulsion composition, a water-soluble polymer is blended in an aqueous phase. Moreover, 0.01 to 10% by weight relative to the discontinuous phase
It is preferable to mix them.

【0008】[0008]

【作用】次に本発明の構成について詳細に説明する。Next, the structure of the present invention will be described in detail.

【0009】本発明において用いられる油溶性高分子で
あるエチルヒドロキシエチルセルロース(以下EHEC
と略す)はセルロースの3個の水酸基中多くのものがエ
トキシル基またはエチルヒドロキシル基で置換されてい
るものである。EHECは通常、化粧品、医薬品、食品
等の分野で使用される油分に溶解または膨潤させて使用
する。配合量としては、W/O型乳化組成物の連続相を
形成する油相に対して0.1〜20重量%が好ましく、
1〜10重量%がより好ましい。また、溶解剤としてメ
チルフェニルポリシロキサンが好ましい。
Ethyl hydroxyethyl cellulose (hereinafter referred to as EHEC) which is an oil-soluble polymer used in the present invention.
Is abbreviated), in which most of the three hydroxyl groups of cellulose are substituted with ethoxyl groups or ethylhydroxyl groups. EHEC is usually used by dissolving or swelling it in an oil component used in the fields of cosmetics, pharmaceuticals, foods and the like. The blending amount is preferably 0.1 to 20% by weight with respect to the oil phase forming the continuous phase of the W / O type emulsion composition,
1 to 10% by weight is more preferable. Further, methylphenyl polysiloxane is preferable as the dissolving agent.

【0010】なお、本発明に用いられる油分としては、
例えば、牛脂、スクワラン、オリーブ油等の動植物油
脂、ミツロウ、ラノリン、キャンデリラワックス等のワ
ックス類および炭化水素、流動パラフィン、ワセリン等
の鉱物油、エステル油、シリコン油、高級アルコール、
脂肪酸等である。
As the oil component used in the present invention,
For example, beef tallow, squalane, animal and vegetable oils and fats such as olive oil, beeswax, lanolin, waxes such as candelilla wax and hydrocarbons, liquid paraffin, mineral oils such as vaseline, ester oils, silicone oils, higher alcohols,
Fatty acids and the like.

【0011】次に、本発明において用いられる水溶性高
分子としては、従来より増粘剤、乳化安定剤として利用
されている水溶性高分子であればよいが、塩による影響
を受けにくいものが好ましい。例えば、カルボキシメチ
ルセルロース(以下CMCと略す)が好ましい。配合量
としては、W/O型乳化組成物の非連続相を形成する水
相に対して0.01〜10重量%が好ましく、0.01
〜5重量%がより好ましい。
Next, the water-soluble polymer used in the present invention may be any water-soluble polymer which has been conventionally used as a thickener or an emulsion stabilizer, but one which is not easily influenced by salts. preferable. For example, carboxymethyl cellulose (hereinafter abbreviated as CMC) is preferable. The blending amount is preferably 0.01 to 10% by weight, based on the aqueous phase forming the discontinuous phase of the W / O type emulsion composition, and 0.01
-5% by weight is more preferred.

【0012】本発明に係る前記乳化組成物には前記の必
須成分の他に使用目的に合わせて保湿剤、薬剤、紫外線
吸収剤、防腐剤、酸化防止剤を添加してもよい。
In addition to the above-mentioned essential components, a moisturizing agent, a drug, an ultraviolet absorber, an antiseptic and an antioxidant may be added to the emulsified composition according to the present invention.

【0013】また、油相と水相の比率は広範囲に選択で
きるが、油相5〜40%に対して水相95〜60%が好
ましい。
The ratio of the oil phase to the water phase can be selected within a wide range, but the oil phase is preferably 5 to 40% and the water phase is preferably 95 to 60%.

【0014】本発明の乳化組成物を得る方法としては、
例えば、油分にEHECを溶解し、これに攪拌しなが
ら、水相部を添加することにより得られる。この場合、
ホモミキサー、ディスパー処理を行うことが望ましい。
The method for obtaining the emulsified composition of the present invention includes:
For example, it can be obtained by dissolving EHEC in an oil component and adding the aqueous phase portion thereto while stirring. in this case,
It is desirable to carry out a homomixer and disper treatment.

【0015】[0015]

【実施例】以下、本発明を実施例および比較例によって
さらに詳細に説明する。本発明は本実施例により限定さ
れるものではない。
EXAMPLES The present invention will be described in more detail with reference to Examples and Comparative Examples. The present invention is not limited to this embodiment.

【0016】(実施例1〜6、比較例1,2) (調製法)EHEC、油分、精製水、CMCおよびカル
ボキシビニルポリマー等を下記表1に示す配合組成およ
び量で配合し、70℃に加温し、ディスパー処理して、
乳化組成物を調製した。
(Examples 1 to 6, Comparative Examples 1 and 2) (Preparation Method) EHEC, oil, purified water, CMC, carboxyvinyl polymer, etc. were compounded in the composition and amount shown in Table 1 below, and the mixture was heated to 70 ° C. Heat, disperse,
An emulsified composition was prepared.

【0017】調製した乳化組成物は状態を観察した後、
ガラス瓶に充填し、50℃、2週間放置後、評価を行っ
た。安定性は下記の3段階にて評価した。
After observing the condition of the prepared emulsion composition,
It was filled in a glass bottle, left at 50 ° C. for 2 weeks, and then evaluated. The stability was evaluated according to the following three grades.

【0018】○:まったく分離が見られない △:油相もしくは水相のわずかな分離が見られる ×:油相もしくは水相がかなり分離している 結果を表1に示す。なお、表中の数字は重量%である。◯: No separation was observed at all Δ: Slight separation of the oil phase or the water phase was observed ×: Significant separation of the oil phase or the water phase is shown in Table 1. The numbers in the table are% by weight.

【0019】[0019]

【表1】 表1に示すように、本発明に係るEHECを用いた実施
例1〜6は、比較例1,2に比べ安定性が向上している
ことがわかる。また、水溶性高分子を併用したものはさ
らに安定していることがわかる。 (実施例7) モイスチャークリーム 重量% (A)EHEC 0.5 メチルフェニルポリシロキサン 5.0 ジイソステアリン酸グリセリル 2.0 ホホバ油 2.0 イソステアリルアルコール 0.5 ビタミンEアセテート 0.5 防腐剤 0.1 香料 0.1 (B)グリセリン 10.0 1,3ブチレングリコール 5.0 CMC−Na 1.0 ハイビスワコー105(和光純薬) 0.05 精製水 残余 (製法)(A)相を70℃で均一に溶解した。これに水
溶性高分子を均一に溶解し、水酸化ナトリウムでpH
6.8にした(B)相を70℃に加温して、ディスパー
攪拌下で徐々に添加し、添加終了後、6000rpmで
2分間ディスパー処理を行い、攪拌冷却して実施例7を
得た。得られたモイスチュアクリームは経時安定性に優
れ、皮膚に塗布したとき、非常にのびがよく、「はじ
き」も認められない使用特性を有していた。また、安全
性上問題のないことを確認した。 (実施例8) ナイトクリーム 重量% (A)EHEC 1.0 流動パラフィン 2.0 ワセリン 1.0 メチルフェニルポリシロキサン 7.0 トリオクタン酸グリセリル 5.0 オリーブ油 5.0 セチルアルコール 0.5 ビタミンEアセテート 0.5 防腐剤 0.1 香料 0.1 (B)グリセリン 5.0 1,3ブチレングリコール 5.0 CMC−Na 2.0 精製水 残余 (製法)(A)相を70℃で均一に溶解した。これに水
溶性高分子を均一に溶解し、70℃に加温した(B)相
をディスパー攪拌下で徐々に添加し、添加終了後、60
00rpmで2分間ディスパー処理を行い、攪拌冷却し
て実施例8を得た。得られたナイトクリームは経時安定
性に優れ、皮膚に塗布したとき、非常にのびがよく、
「はじき」も認められない使用特性を有していた。ま
た、安全性上問題のないことを確認した。 (実施例9) サンケアクリーム 重量% (A)EHEC 3.0 流動パラフィン 3.0 ワセリン 1.0 メチルフェニルポリシロキサン 10.0 ホホバ油 5.0 オクチルメトキシシンナメ−ト 10.0 ビタミンEアセテート 0.5 防腐剤 0.1 香料 0.1 (B)グリセリン 5.0 1,3ブチレングリコール 5.0 CMC−Na 1.0 PEMULEN TR−1(日光ケミカルズ) 0.05 精製水 残余 調製方法は実施例7と同様とした。得られたサンケアク
リームは経時安定性に優れ、皮膚に塗布したとき、非常
にのびがよく、「はじき」も認められない使用特性を有
していた。また、耐水性にも優れており、紫外線吸収剤
の効果を充分に発揮しうる処方系であった。
[Table 1] As shown in Table 1, it can be seen that Examples 1 to 6 using the EHEC according to the present invention have improved stability as compared with Comparative Examples 1 and 2. Further, it can be seen that the one using the water-soluble polymer together is more stable. (Example 7) Moisture cream wt% (A) EHEC 0.5 Methylphenylpolysiloxane 5.0 Glyceryl diisostearate 2.0 Jojoba oil 2.0 Isostearyl alcohol 0.5 Vitamin E acetate 0.5 Preservative 0. 1 Fragrance 0.1 (B) Glycerin 10.0 1,3 Butylene glycol 5.0 CMC-Na 1.0 Hibiswako 105 (Wako Pure Chemical Industries) 0.05 Purified water Residual (production method) (A) phase at 70 ° C It melted uniformly with. Dissolve the water-soluble polymer uniformly in this, and adjust the pH with sodium hydroxide.
The (B) phase adjusted to 6.8 was heated to 70 ° C., gradually added under stirring with a disper, after completion of the addition, a disper treatment was performed at 6000 rpm for 2 minutes, and the mixture was cooled with stirring to obtain Example 7. . The obtained moisture cream had excellent stability over time, had very good spreadability when applied to the skin, and had use characteristics in which "repellency" was not observed. In addition, it was confirmed that there were no safety problems. (Example 8) Night cream wt% (A) EHEC 1.0 Liquid paraffin 2.0 Vaseline 1.0 Methylphenylpolysiloxane 7.0 Glyceryl trioctanoate 5.0 Olive oil 5.0 Cetyl alcohol 0.5 Vitamin E acetate 0.5 Preservative 0.1 Perfume 0.1 (B) Glycerin 5.0 1,3 Butylene glycol 5.0 CMC-Na 2.0 Purified water Residual (production method) (A) phase is uniformly dissolved at 70 ° C. did. A water-soluble polymer was uniformly dissolved in this, and phase (B) heated to 70 ° C. was gradually added under stirring with a disper.
Example 8 was obtained by performing a disper treatment at 00 rpm for 2 minutes and stirring and cooling. The obtained night cream has excellent stability over time, and when applied to the skin, spreads very well,
It had a usage characteristic that "repellency" was not recognized. In addition, it was confirmed that there were no safety problems. (Example 9) Suncare cream wt% (A) EHEC 3.0 Liquid paraffin 3.0 Vaseline 1.0 Methylphenyl polysiloxane 10.0 Jojoba oil 5.0 Octyl methoxycinnamate 10.0 Vitamin E acetate 0 .5 Preservative 0.1 Perfume 0.1 (B) Glycerin 5.0 1,3 Butylene glycol 5.0 CMC-Na 1.0 PEMULEN TR-1 (Nikko Chemicals) 0.05 Purified water Residual Same as Example 7. The obtained sun care cream had excellent stability over time, had very good spreadability when applied to the skin, and had use characteristics in which "repellency" was not observed. In addition, the formulation was also excellent in water resistance and was able to sufficiently exert the effect of the ultraviolet absorber.

【0020】[0020]

【発明の効果】本発明によれば、乳化安定性、安全性お
よび使用性の優れたW/O型乳化組成物を提供できる。
According to the present invention, it is possible to provide a W / O type emulsion composition having excellent emulsion stability, safety and usability.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 エチルヒドロキシエチルセルロースを油
相に配合したことを特徴とするW/O型乳化組成物。
1. A W / O type emulsified composition comprising ethyl hydroxyethyl cellulose incorporated in an oil phase.
【請求項2】 水相に水溶性高分子を配合したことを特
徴とする請求項1に記載のW/O型乳化組成物。
2. The W / O type emulsion composition according to claim 1, wherein a water-soluble polymer is mixed in the aqueous phase.
【請求項3】 前記水溶性高分子がカルボキシメチルセ
ルロースであることを特徴とする請求項2に記載のW/
O型乳化組成物。
3. The W / according to claim 2, wherein the water-soluble polymer is carboxymethyl cellulose.
O-type emulsion composition.
JP10045895A 1995-03-31 1995-03-31 W/o-type emulsion composition Withdrawn JPH08268833A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10045895A JPH08268833A (en) 1995-03-31 1995-03-31 W/o-type emulsion composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10045895A JPH08268833A (en) 1995-03-31 1995-03-31 W/o-type emulsion composition

Publications (1)

Publication Number Publication Date
JPH08268833A true JPH08268833A (en) 1996-10-15

Family

ID=14274477

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10045895A Withdrawn JPH08268833A (en) 1995-03-31 1995-03-31 W/o-type emulsion composition

Country Status (1)

Country Link
JP (1) JPH08268833A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000219617A (en) * 1999-01-28 2000-08-08 Shiseido Co Ltd Skin preparation for external use
JP2001139452A (en) * 1999-11-18 2001-05-22 Fancl Corp Water-in-oil type emulsified cosmetic

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000219617A (en) * 1999-01-28 2000-08-08 Shiseido Co Ltd Skin preparation for external use
JP2001139452A (en) * 1999-11-18 2001-05-22 Fancl Corp Water-in-oil type emulsified cosmetic

Similar Documents

Publication Publication Date Title
US5015469A (en) Water-in-oil emulsion type cosmetics
JP2922176B2 (en) Gelled oil-in-water ultrafine emulsion stabilized with crosslinked poly (2-acrylamido-2-methylpropanesulfonic acid) neutralized by at least 90%, its preparation method and its application
EP0795318B1 (en) A w/o cosmetic emulsion containing ethylcellulose
JP3489703B2 (en) Fine emulsion composition
JPH09301824A (en) W/o type emulsion composition and cosmetic
JPH08283303A (en) Emulsifier comprising higher fatty acid dextrin, emulsion composition containing the same, and cosmetic
JPH09278644A (en) Cosmetic of o/w-type emulsion
JP2944258B2 (en) Emulsion type cosmetic
JPH09309813A (en) Preparation for external use for skin
JP2001002521A (en) Water-in-oil type emulsion cosmetic having excellent phase inversion feeling having high inner water phase ratio
JPS63151351A (en) Water in oil type emulsified composition
KR100570497B1 (en) Anti-wrinkle cosmetic composition and its manufacturing method containing a pure retinol stabilized with a nano size of multiple liquid crystal membrane capsule
JP2004307414A (en) W/o/w emulsion skin care preparation for external use and method for producing the same
JPH08268833A (en) W/o-type emulsion composition
JP2002145733A (en) Solid water-in-oil type emulsion cosmetic
JP2003212750A (en) Gel composition and emulsified composition
JPH07304629A (en) Water-in-oil type emulsion composition and its production
JPH08268834A (en) W/o-type emulsion composition
JP3444329B2 (en) Water-in-oil emulsion composition
JP2854767B2 (en) Thickening gelling agent
JPH09301823A (en) Water-in-oil type emulsion cosmetic
JPH0645534B2 (en) Emulsified cosmetics
JPH10316523A (en) Oil-in-water type emilsified composition
JP2001039851A (en) Massaging cosmetic for eye
JP2001158714A (en) High-internal aqueous phase water-in-oil type emulsified cosmetic

Legal Events

Date Code Title Description
A300 Withdrawal of application because of no request for examination

Free format text: JAPANESE INTERMEDIATE CODE: A300

Effective date: 20020604