JPS583631A - Water-in-oil type emulsion - Google Patents

Water-in-oil type emulsion

Info

Publication number
JPS583631A
JPS583631A JP56101043A JP10104381A JPS583631A JP S583631 A JPS583631 A JP S583631A JP 56101043 A JP56101043 A JP 56101043A JP 10104381 A JP10104381 A JP 10104381A JP S583631 A JPS583631 A JP S583631A
Authority
JP
Japan
Prior art keywords
water
oil
emulsion
acid
parts
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
JP56101043A
Other languages
Japanese (ja)
Inventor
Yoji Tomioka
富岡 庸次
Kyoken Usuba
恭謙 薄羽
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.)
Kawaken Fine Chemicals Co Ltd
Original Assignee
Kawaken Fine Chemicals 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 Kawaken Fine Chemicals Co Ltd filed Critical Kawaken Fine Chemicals Co Ltd
Priority to JP56101043A priority Critical patent/JPS583631A/en
Publication of JPS583631A publication Critical patent/JPS583631A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/064Water-in-oil emulsions, e.g. Water-in-silicone emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Abstract

PURPOSE:To obtain a water-in-oil type emulsion having shelf life stability, dynamic stability and good feeling, by compounding a specific fatty acid ester of a trihydric alcohol and a carboxyvinyl polymer as emulsifiers in a specific ratio. CONSTITUTION:As emulsifiers, 1pt.wts monoester of a trihydric alcohol with an 8C or higher fatty acid, which is a liquid or a flowable paste at a room temp., such as glycerol monooleate, and 0.03-1pt.wt. carboxyvinyl polymer are compounded. A water-in-oil type emulsion prepared by using the obtained emulsifier composition has good shelf life stability and dynamic stability as well as is rich in compatibility with skin and shows a refreshing effect to skin.

Description

【発明の詳細な説明】 本発明は、油中水型エマルジ璽ンに関し、特(化粧品及
び薬用製剤分野において有用な安定した油中水堰ヱマル
ジ嘗ン系に係す、エマルシロy系において予想されない
ほどの安定性を与える独特の乳化剤の組合せを用いて、
IIJ9 s sKも及ぶ高率の内水相を外泊相中に分
散させることを可能とする油中水型エマルジ璽ンに関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to water-in-oil emulsions, and in particular to stable water-in-oil emulsion systems useful in the cosmetic and pharmaceutical formulation fields, which are unexpected in emulsion systems. Using a unique combination of emulsifiers that provides a degree of stability,
IIJ9 s This relates to a water-in-oil emulsion bottle that makes it possible to disperse a high percentage of the internal water phase in the external phase.

従来、クリーム等の基剤としては、一般の油の中和水の
粒子が含まれた、いわゆる油中水型エマルジ璽ンの方が
、水の中に油の粒子が含まれている、いわゆる水中油型
エマルジ冒ンに比較して。
Conventionally, as a base for creams, etc., so-called water-in-oil emulsions, which contain water particles neutralized with general oil, have been used as bases for creams, etc. Compared to oil-in-water emulsion.

皮膚の保−や柔軟性の賦与など多くの点ですぐれている
ことは、一般に認められているところである。しかし、
油中水型エマルジw7F1品質の安定性において幾つか
の問題点があり、その安定性を向上させるために、油分
の量を増やしたり、粘度を高める等の手段で、安定性を
改良する努力がなされてきたが、その結果、エマルジヨ
ンの使用感を損ね、必要以上のべとつきヤ油っぽさを与
え、消費者に嫌われる傾向があった。これらの点を改良
する念めに、油肴分を少なくしたり、油っぽさの少ない
油成分を使用するなどの改良が試みられているが、いず
れも安定性や外観的上品さ、使用感の点で問題が残り、
満足すべき結果が得られていないのが現状である。
It is generally recognized that it is excellent in many respects, such as providing skin protection and flexibility. but,
There are several problems with the stability of the water-in-oil emulsion W7F1, and efforts are being made to improve the stability by increasing the amount of oil and increasing the viscosity. However, as a result, the feel of the emulsion is impaired and the emulsion becomes unnecessarily sticky or oily, which tends to be disliked by consumers. In order to improve these points, attempts have been made to reduce the amount of oil used in the seasonings and to use oil components that are less oily, but all of these methods have problems with stability, elegance of appearance, and use. There remains a problem with the sense of
At present, satisfactory results have not been obtained.

高水相含量の油中水型エマルジヨンの必要性はクリーム
中ローシ嘗ン等の化粧品や、トイレタリー製品、薬用製
剤t−目的としてその必要性が望まれていたが、水相が
50憾を超える油中水型の工マルジw 7ベース、又は
キャリアーとなるものFiこれ壕でのところWStが非
常(困難であっ九。特に水溶性活性成分や薬物成分を含
む化粧品や薬用製剤を目的とする油中水屋エマルジヨン
等に高水相含量を与える仁とは、多くの利点があるにも
かかわらず、こたらの商品寿命や安定性Kll影響を及
ぼさないで、このようなエマルジヨンに約5゜嘔以上の
水分を配合することは不可能であった。
The need for water-in-oil emulsions with high aqueous phase content has been desired for cosmetics such as lotions in creams, toiletry products, and medicinal preparations. Water-in-oil type industrial multiw7 Base or carrier WSt is extremely difficult (9).Especially oils intended for cosmetics and medicinal preparations containing water-soluble active ingredients and drug ingredients. Although it has many advantages, the kernels that give high aqueous phase content to Nakamizuya emulsions etc. can be added to such emulsions by approximately 5° without affecting the shelf life or stability of the product. It was impossible to incorporate more water.

この点く関しては、製品の製造と販売の時点には大きな
時間の隔たりがある故、特に輸送時や貯蔵中に遭遇する
恐れのある高温や低温に暴露された時に、短時日の関に
系が破壊してしまうようなエマルジョンペースを用いる
ことは好オしくない。
In this regard, because there is a large time lag between product manufacture and sale, short-term interactions may be a problem, especially when exposed to high or low temperatures that may be encountered during transportation or storage. It is not a good idea to use an emulsion pace that would destroy the emulsion.

ことなく安定を保たねばならない。We must maintain stability without any problems.

皮膚Wiを薄い油膜で覆うためのバリヤー製品や皮膚開
口部閉塞用薬用製剤には油中水型エマルジョン基剤が用
いられる。エマルジ璽ン中の水の含有量が増すに従つて
、処方の全体としての有用性を損わずに、油っぽい感触
が軽減され、この高水分含量が蒸発を昂進し、その結果
クリームやローンロンの清涼効果を高める点で使用者に
対するよ抄好ましい魅力を持ってhる0本発明による乳
化剤組成物により処方され食製品は従来の製品に比して
嶺布時の感触が油っぽくなく、清涼感にすぐれてお抄面
もこのタイプの製品(要求されるエヘモ゛′リエント特
性や皮膚閉塞性は保有している。
Water-in-oil emulsion bases are used in barrier products to cover the skin Wi with a thin oil film and medicinal preparations for closing skin openings. As the water content in the emulsion increases, the oily feel is reduced without compromising the overall usefulness of the formulation, and this high water content accelerates evaporation, resulting in cream and Food products formulated with the emulsifier composition according to the present invention have a less greasy feel when applied than conventional products, which has a more favorable appeal to users in terms of enhancing the cooling effect of the roan ron. This type of product has an excellent cooling sensation and has the required emollient properties and skin occlusive properties.

今′回、・油中水型エマルジ茸ンを得るに必要な所要)
ILB!有する親油性乳化剤↓秒選ばれた特定の乳化剤
と相対的な調和性を具え九ある種の水溶性吸水性高分子
物質を使用することにより、予想以上に多量の水分を油
中水型工!ルジ冒ン中に配合出来ることが分りた。
This time, the requirements required to obtain water-in-oil emulsion mushrooms)
ILB! By using nine types of water-soluble water-absorbing polymeric substances with relative compatibility with the lipophilic emulsifier ↓ seconds selected, water-in-oil molding can absorb a larger amount of water than expected! It turns out that it can be added to Luji's diet.

本発明による油中水種エマルジ璽ンは化粧品基剤として
有用であるのみならず、特に局所用軟膏の如き薬用製剤
組成物に有効に利用することが出来る。例えば、高水分
含量を利用して食塩、尿素、その他機々の水溶性薬効成
分を、基剤の安定性を損わすに配合添加することが出来
る。
The water-in-oil emulsion according to the present invention is not only useful as a cosmetic base, but can also be particularly effectively used in medicinal formulation compositions such as topical ointments. For example, taking advantage of the high water content, salt, urea, and other water-soluble medicinal ingredients can be added without compromising the stability of the base.

以上述べたように、本発明によれば、保存安定性差びに
動的安定性を有し、且つ皮膚に対する同質性に富み、使
用時にさっばりした触感を与える油中水型エマルジヨン
が提供される。
As described above, the present invention provides a water-in-oil emulsion that has storage stability and dynamic stability, is highly homogeneous to the skin, and provides a light texture upon use.

本発明の油中水型皿iルジ冒ンを調製するに際し、用り
られる乳化剤は (1)常温にて液状もしくけ、液状に近いペースト状を
呈する3価アルコールの脂肪酸エステルと (b)カル−キシビニルポリマー及び/又けその塩とを
必須成分とし、かつ、二つの成分(1)と(b)の使成
分(1)は常温にて液状もしくに液状に近いペースト状
t1iAする3価アルコールの脂肪酸エステルでアル、
ここで常温で液状もし、〈は液状に近いペースト状であ
ることが非常に重要である。何故なら常温において固体
を呈する高融点脂肪酸モノエステルを含む乳化剤組成物
を用いて油中水型エマルジヨンを調整する時は、エマル
ジ1ンの油/水界rMにおいて、時間と共【結晶相が転
移する固体界面膜を生じ、粘弾性に欠け、エマルジヨン
の保存安定性を損なうからである。
In preparing the water-in-oil dishwashing liquid of the present invention, the emulsifiers used are (1) a fatty acid ester of a trihydric alcohol that is liquid at room temperature and exhibits a pasty state close to liquid; - The xyvinyl polymer and/or its salt are essential components, and the two components (1) and (b) are used to form a liquid or near-liquid paste at room temperature. Al is a fatty acid ester of a hydric alcohol,
If it is liquid at room temperature, it is very important that it be a paste close to liquid. This is because when preparing a water-in-oil emulsion using an emulsifier composition containing a high-melting fatty acid monoester that is solid at room temperature, the crystalline phase transitions over time at the oil/water interface rM in emulsion 1. This is because a solid interfacial film is formed, which lacks viscoelasticity and impairs the storage stability of the emulsion.

本発明(於て用いられる乳化剤の成分(altia価了
ルジールと震肪蒙とのモノエステルで、3価アルコール
は、グリセリン及び/又はトリメチロールプロパンが好
ましく、脂肪酸としては、カプリン酸、ラウリン酸、オ
レイン酸、リノール酸、リシノール酸、イソオクタン酸
、インパルミチンi#、おヨヒイソステアリン酸などの
炭素数8ないし和暦肪酸から選ばれる少なく七も1種で
1%にオレイン酸、およびインステアリン酸が好ましい
Components of the emulsifier used in the present invention (monoester of altia triglycerol and zhen fat men), the trihydric alcohol is preferably glycerin and/or trimethylolpropane, and the fatty acids are capric acid, lauric acid, Oleic acid and instearic acid at least 1 type selected from 8-carbon or Japanese fatty acids such as oleic acid, linoleic acid, ricinoleic acid, isooctanoic acid, impalmitin i#, and oyohiisostearic acid. is preferred.

好ましい成分−)としては、グリセリルモノオレエート
、グリセリルモノインステアレート、トリメチロールプ
ロパンモノオレエート、およびトリメチロールプロパン
モノイソステアレートを挙げることが出来る。
Preferred components (-) include glyceryl monooleate, glyceryl monoinstearate, trimethylolpropane monooleate, and trimethylolpropane monoisostearate.

本発明のエマルジ冒ンにおいて用いる成分(bl t!
、カルボキシビニルポリマー、及び/又はその塩で塩を
形成させる塩基としては、ナトリウム、カリウム、アン
モニア、アルカノ−ルアiン及び塩基性アミノ酸などが
あげられる。このカルボキシビニルポリマーの代表的な
ものとしてはアクリル酸を重合したもので、例えば化粧
品原料基準追補注解(薬事日報社発行)の第59頁から
66員に述べられている。現在市販されているものとし
ては。
Ingredients used in the emulsion treatment of the present invention (bl t!
Examples of the base for forming a salt with the carboxyvinyl polymer and/or its salt include sodium, potassium, ammonia, alkanolamines, and basic amino acids. A typical carboxyvinyl polymer is one obtained by polymerizing acrylic acid, and is described, for example, in Cosmetic Raw Materials Standard Supplementary Commentary (published by Yakuji Nippo Co., Ltd.), pages 59 to 66. As for what is currently on the market.

米国グツドリッチ−ケミカル社製カーボボール(商標名
)及、び和光紬薬工場■製ノ・イビスワコ−(b)成分
t0.03ないし1.0重量部用いる。
Carboball (trade name) manufactured by Gutdrich Chemical Co., USA, and Ibis Wako manufactured by Wako Tsumugi Kogyo Co., Ltd. (b) component (t) 0.03 to 1.0 parts by weight are used.

本発明の乳化剤組成物が優れてい−るのはカルボキシビ
ニルポリマーが、カルボキシル基を多数に有する高分子
構造であり、そして吸水性の強いことが特長であり、そ
の高分子構造と吸水性は1本発明の油中水型エマルジ璽
ンにおいて水粒子を油相中に安定に分散させるうえに大
切な役割を果たしている。このことは脂肪酸モノエステ
ルとカルボ中ジビニルポリマー水溶液を混合した時、極
めて強固なゲルを形成し、水相゛を一見固体状に保持さ
せる能力があることからも明らかである・本発明におけ
る油中水臘工マルジ璽ンにおいてに1種々異なる極性を
有する油性物質を基本成分として使用することが出来る
。たとえばiネラルオイル、ペトロラタム、ノくラフイ
ン、スクアランの如き脂肪族炭化水素、イソプロピルミ
IJステートやインプロピルパルiデート、2−エチル
ヘキすン酸セチル及び2−エチルヘキサン酸ト11グI
Jセライトの如き合成エステル油、オII−フ油、#ホ
バ油、小麦胚芽油や2ンク油の如き天然油、会ろう1本
ろう、カルナラ/<ろう、硬化とマシ油の如き天然ワッ
クス中硬化油などを使用して曳好な基本エマルジ冒ンを
調製することができる。油性媒体中に分散させるべき水
性成分の主成分は水であるが、全体の凍結温度を下げる
など他の機能的性質を賦与するえめの水溶性添加物を添
加することができ、この目的のための例としては、プロ
ピレングリコール、ブチレングリコール、グ17セ1」
ン、ソルビトール、マルチトール、ヘキシレングリコー
ルの如き、水溶性ポリオールや食塩、塩イヒカリウム等
の水溶性無機塩があげられる。
The emulsifier composition of the present invention is superior because the carboxyvinyl polymer has a polymer structure having a large number of carboxyl groups, and is characterized by strong water absorption. In the water-in-oil emulsion bottle of the present invention, it plays an important role in stably dispersing water particles in the oil phase. This is clear from the fact that when a fatty acid monoester is mixed with an aqueous solution of divinyl polymer in a carboxylic acid, an extremely strong gel is formed, and the aqueous phase has the ability to maintain a seemingly solid state. Oily substances with different polarities can be used as the basic component in the water bottle. For example, aliphatic hydrocarbons such as mineral oil, petrolatum, nocturnal oil, squalane, isopropyl mi-state and inpropyl paldate, cetyl 2-ethylhexanoate and triglyceride 2-ethylhexanoate.
Synthetic ester oils such as J-Celite, OII-F oil, #joba oil, natural oils such as wheat germ oil and 2-ink oil, natural waxes such as Airou 1-wax, Karnara/< wax, hardened and mustard oil. Easy base emulsion solvents can be prepared using hydrogenated oils and the like. Although the main component of the aqueous component to be dispersed in the oily medium is water, water-soluble additives can be added that impart other functional properties, such as lowering the overall freezing temperature, and for this purpose. Examples include propylene glycol, butylene glycol,
Examples include water-soluble polyols such as salt, sorbitol, maltitol, and hexylene glycol, and water-soluble inorganic salts such as common salt and potassium salt.

同様に薬用製剤としては、全組成物の乳剤特性を変えな
いで局所製剤中に治療薬を配合出来なければならない。
Similarly, for pharmaceutical formulations, it must be possible to incorporate therapeutic agents into topical formulations without altering the emulsion properties of the overall composition.

・その他にも薬・用エマルジ冒ンは、乳化を破壊せずに
、約3.5〜9.0の比較的巾広いpHg囲で有効でな
ければならない。この点に関しては本発明の油中水型エ
マルジ璽ンは尿素、乳酸その他種々の水溶性薬効成分を
水相中に多量(添加配食出来ることもその特徴の一つで
ある。
- In addition, pharmaceutical emulsions must be effective over a relatively wide pHg range of about 3.5 to 9.0 without destroying the emulsification. In this regard, one of the features of the water-in-oil emulsion of the present invention is that it can contain large amounts of various water-soluble medicinal ingredients such as urea, lactic acid, and others in the aqueous phase.

本発明のエマルジ盲ンを調製するに際しては前記の乳化
剤以外に他の乳化剤を使用しなくても充分乳化が可能で
あるが、他の乳化剤を補助的に使用することを妨げるも
のではなく、たとえばHLBの低い他のいわゆる親油性
乳化剤を油相中に加えてもよい。
When preparing the emulsion blind of the present invention, it is possible to emulsify sufficiently without using any other emulsifier other than the above-mentioned emulsifier, but this does not preclude the use of other emulsifiers as an auxiliary, such as Other so-called lipophilic emulsifiers with low HLB may also be added to the oil phase.

本発明のエマルジ璽ンt−l1i1する方法において3
価アルコールモノエステルとカルボキシビニルポリマー
を乳化させた乳化剤組成物tm造し、これに基剤の油性
成分と水性成分を加えてエマルジ曹ンを得る方法と、油
性成分中にモノエステルを加え水性成分中にカルボキシ
ビニルポリ?−1に7jOえておいて両成分を混合して
乳化させる方法のいずれを選択しても、完全に乳化が行
われ目的のエマルジ璽ンを得ることができる。
In the method of emulsion sealing t-l1i1 of the present invention, 3
A method of preparing an emulsifier composition tm by emulsifying a monoester of alcohol and a carboxyvinyl polymer, and adding a base oil component and an aqueous component to this to obtain an emulsion carbonate, and a method of adding a monoester to the oil component to obtain an aqueous component. Carboxyvinyl poly inside? No matter which method is selected, in which the two components are mixed and emulsified with a difference of 7jO to -1, the emulsification is completed completely and the desired emulsion can be obtained.

本発明のエマルジ1ンは、クリーム等の化粧品や軟膏等
の薬用製剤の基剤として使用できる。このものの特徴は
後述する実施例で示すごとく、相対的に油性成分に対し
水性成分の割合が高い油中水垂エマルジ璽ンを開発した
ものであって、このものは皮膚に対する同質性に富み、
使用時にさっばりとした感触と保湿性のすぐれた製品を
得ることができる。
The emulsion of the present invention can be used as a base for cosmetics such as creams and medicinal preparations such as ointments. As shown in the examples below, the characteristics of this product are that we have developed a water-in-oil emulsion with a relatively high ratio of aqueous components to oily components, and this product is highly homogeneous to the skin.
When used, a product with a light feel and excellent moisturizing properties can be obtained.

本発明の油中水腫エマルジ璽ンは、他の種々のam剤1
例えば防腐剤、酸化防止剤、殺菌剤、香料、顔料、薬効
剤などを添加することができる。
The edema-in-oil emulsion of the present invention can be used with various other am preparations 1
For example, preservatives, antioxidants, bactericidal agents, fragrances, pigments, medicinal agents, etc. can be added.

以下実施例について本発明の詳細な説明する。The present invention will be described in detail with reference to Examples below.

実施例中部とあるは重量St示す。The middle part of the example indicates the weight St.

実施例1 VWlollに保−クダームの調製 グリセリルモノオレエート1.0部をよくかきオぜなが
ら、この中ヘカルポ中ジビニルポリマーとしてカーボボ
ール934(米国、グツドリッチケミカル社製:商品名
(以下同じ))のIIG水溶液20部を少量宛加えてい
った。水溶液を加える(従って生成物は硬さを増し、ゲ
ル状の乳化剤組成物を得た。この組成物に流動パラフィ
ン4.0部。
Example 1 Preparation of Cuderm stored in a VWroll 1.0 part of glyceryl monooleate was stirred well, and divinyl polymer in Hecarpo was prepared as Carboball 934 (manufactured by Gutdrich Chemical Co., USA; trade name (hereinafter the same). 20 parts of IIG aqueous solution of )) was added in small amounts. Add an aqueous solution (thus, the product increases in hardness and a gel-like emulsifier composition is obtained. 4.0 parts of liquid paraffin is added to this composition.

セレシン2.0部、シリコン油・2.0部及び2−エチ
ルヘキサン酸セチルエステル2.0部を加えよくかきま
ぜながら70Cまで昇温した。一方水64.4部、70
嘔ソルビト一ル水溶液5部に防腐剤(メチルパラベン(
以下同じ))0.1部を加えて加温して70Cとした。
2.0 parts of ceresin, 2.0 parts of silicone oil, and 2.0 parts of cetyl 2-ethylhexanoate were added, and the temperature was raised to 70C while stirring well. Meanwhile, 64.4 parts of water, 70
5 parts of sorbitol aqueous solution plus preservative (methylparaben)
The same applies hereinafter)) 0.1 part was added and heated to 70C.

後者の水相を前者の油相Kかきまぜながら少量ずつ加え
、加え終って5分間70Cで攪拌し、その後攪拌しなが
ら室温まで放冷して保護クリームを得た。
The latter aqueous phase was added little by little to the former oil phase while stirring, and after the addition was completed, the mixture was stirred at 70C for 5 minutes, and then allowed to cool to room temperature while stirring to obtain a protective cream.

の このも^気抵抗値を測定したところ、無限大を示し、水
が連続相を成していないことが証明され、W/ell工
脅ルジ1ンを形成していることが認められえ、この本の
を三分しQC,20C。
When the air resistance value was measured, it showed infinity, proving that water did not form a continuous phase, and it was recognized that it formed a W/ell structure. Divide this book into three parts: QC, 20C.

40CK6ケ月間保存したが油分と水分の分離はなく、
エマルジ冒ンが安定に保たれていた。
40CK was stored for 6 months, but there was no separation of oil and water.
The emulsion was kept stable.

実施例2 W1011保鏝クリームの調製 実施例1におけるグリセリルモノオレエートに代えトリ
メチロールプロノ(ンイソステ丁レートを用いて乳化剤
組成物を得、さらに同様に操作して実施例1のクリーム
と同様のものを得た。
Example 2 Preparation of W1011 trowel cream An emulsifier composition was obtained by using trimethylolpronoisostelate in place of glyceryl monooleate in Example 1, and a cream similar to that of Example 1 was prepared by the same procedure. I got it.

実施例3 ゛ w7o*クレンジングタリームの調製 ゛グリセリルモノイソステアレー)LOIS、スフ讐う
ンao部、流動ノ(ラフイン20.0s、セレンンLo
11.白色ワセリン!LO部を混合して加熱溶解して?
Orとした。一方、)゛0嘔ソルビトール6.01B、
カーボボー3140(米国、グツド1Jツチケミ力ル社
II:商品名(以下同じ))の14水溶1[14,0部
、水417部、肪腐剤0.2部を72cvcして均−K
l!解し、これを餉記油性成分中に攪拌しながら添加し
て乳化させた。)OCで5分攪拌し先後放冷して4SC
Kなつ゛たとき香料を加え、さらvcsocになるまで
攪拌を行りた。
Example 3 Preparation of w7o* cleansing cream Glyceryl monoisostearate LOIS, sulfate ao part, fluidity (rough-in 20.0s, selenium LOIS)
11. White Vaseline! Mix the LO part and heat and dissolve?
Or. On the other hand, )゛0 sorbitol 6.01B,
14 water solution 1 [14.0 parts of Carbobo 3140 (U.S., Gutsud 1J Tsuchi Chemiru Co., Ltd. II: trade name (the same applies hereinafter)), 417 parts of water, and 0.2 parts of fat preservative in 72 cvc and uniformly
l! This was added to the oily component while stirring to emulsify it. ) Stir in OC for 5 minutes, then let it cool for 4SC.
When the temperature reached K, the flavoring agent was added and stirring was continued until the temperature reached vcsoc.

このものは外観上きめ細かく光沢のあるり11−ムであ
った。電気抵抗値を測定したところ1000MΩ以上無
限大を示し、W10型エマルジ寧ン管形成していること
が認められ・た。このものf OC。
This product had a fine and glossy appearance. When the electrical resistance value was measured, it showed infinity of 1000 MΩ or more, and it was confirmed that a W10 type emulsion tube was formed. This thing f OC.

2oC%40Cでそれぞれ6ケ月及び−20Cと20で
の隔週交互による冷凍−融堺サイクルの3回繰返しによ
る乳化安定性を求めたが、いずれも乳化がこわれること
はなかつ九。また使用感についてもベトツ命がなく、さ
つば9とした感触であることが認められた。
Emulsion stability was determined by repeating the freezing-thawing Sakai cycle three times, alternating every other week at -20C and -20C for 6 months at 2oC% and 40C, but the emulsion did not break in either case. In addition, regarding the feeling of use, it was found that there was no stickiness and the feel was rated at 9.

実施例4 油性成分 グリセリルモノオレエート     1□0IB2−エ
チルヘキサン置場チルエステル!Lollジグリセリン
ジオレエード     10部流動パラフィン    
 °    to、oIl白色9セリ/z、 o s 水性成分 グリセリン           !L011カーボポ
ール94o 1嘔水溶液 10.0部防腐M     
          O,1部水          
    60.9部を用い実施例3に準じて乳化を用い
スキンクリ−五を得た。このものの電気抵抗値からW2
O型であることが認められ、実施例3と同様に乳化安定
性を試験したところ、いずれの方法でも安定であった。
Example 4 Oil component glyceryl monooleate 1□0IB2-Ethylhexane storage ester! Loll diglycerine dioleade 10 parts liquid paraffin
° to, oIl white 9 seri/z, o s aqueous component glycerin! L011 Carbopol 94o 1 Vomit Solution 10.0 parts Preservative M
O, 1 part water
Using 60.9 parts, Skin Cree-5 was obtained using emulsification according to Example 3. From the electrical resistance value of this thing, W2
It was found to be type O, and when the emulsion stability was tested in the same manner as in Example 3, it was stable by all methods.

実施例5 油性成分 グリセリルモノインステアレート   2.0 部流動
パラフィン          10.0部鵞−エチル
ヘキサン酸トリグリセリド 7.0部セレシン    
          3.0部白色ワ竜リン     
        8.。部密ろう          
     2.0 %水性成分 7011ノルピトー/’          10部グ
リセリン            10部1’lカーボ
ボール934水溶液 (Na0HKてpH6,3とする)     1 !L
oll防腐剤               0.21
1ピロリドン−5−カルボ′シ酸ナトリウム1.5s水
                         
37.3部油性、水性両成分tl−75cとし、実施例
3に準じて乳化を行った。電気抵抗値からW10型エマ
ルジ嘗ンであることが認められ、実施例3と同様(乳化
安定性試験を行ったところ安定であることが認められた
。使用に際してもべとつきがなく。
Example 5 Oil component Glyceryl monoinstearate 2.0 parts Liquid paraffin 10.0 parts Ethylhexanoic acid triglyceride 7.0 parts Ceresin
3.0 part White Waryu Rin
8. . Secret talk
2.0% aqueous component 7011 norpitot/' 10 parts Glycerin 10 parts 1'l Carbobol 934 aqueous solution (adjusted to pH 6.3 with NaOH) 1! L
oll preservative 0.21
Sodium 1-pyrrolidone-5-carboxylate 1.5s water
Emulsification was carried out according to Example 3 using 37.3 parts of both oil-based and aqueous components TL-75c. It was confirmed that it was a W10 type emulsion from the electrical resistance value, and as in Example 3 (an emulsion stability test was performed, it was found to be stable. It was not sticky during use).

さっばりした感触にもかかわらず、皮膚にしっとりとし
た湿潤性を与えることが藺められた。
Despite its light feel, it was noted to provide moisturizing properties to the skin.

実施例6 W10型尿素軟膏の調製 油性成分 グリセリルモノインステアレート3.0il半硬化大豆
油(融、$37tl’)     18.0II硬化ヒ
マシ油            λos水性成分 1.3−ブチレングリコール      &0部1嗟カ
ーボボール9’34.’水溶液   40.0ml防腐
剤               0.2部水    
                       11
.811水性成分を80Cにて均一に溶解した後s 、
o c tで冷却して、原素20.0部を加えて均一に
溶解した。一方、油性成分を80Cに加熱して均−C@
解し、この中へ攪拌しながら前記水性成分を加え。
Example 6 Preparation of W10 type urea ointment Oil component glyceryl monoinstearate 3.0 il semi-hardened soybean oil (melted, $37 tl') 18.0 II hydrogenated castor oil λos aqueous component 1.3-butylene glycol &0 parts 1 hour carb Ball 9'34. 'Aqueous solution 40.0ml preservative 0.2 parts water
11
.. After uniformly dissolving the 811 aqueous component at 80C,
After cooling at oct, 20.0 parts of the element was added and uniformly dissolved. Meanwhile, heat the oily component to 80C and homogenize it.
Dissolve the mixture and add the aqueous component to the mixture while stirring.

放冷しながら30Cとなるまで・攪拌を行った。得られ
た生成物の電気抵抗値からW10型エマルジ冒ンである
ことが認められ、安定性試験においても実施例3と同様
の結果が得られた。
Stirring was performed while cooling until the temperature reached 30C. The electrical resistance value of the obtained product confirmed that it was a W10 type emulsion, and the same results as in Example 3 were obtained in the stability test.

Claims (1)

【特許請求の範囲】 1、油中水型エマルジ冒ンにおいて、乳化剤として (a)常温にて液状又は液状に近いペースト状を呈する
3価アルコールと炭素数8以上の脂肪酸のモノエステル
と 世)カルボ中ジビニルポリマー の二成分を必須成分とし、かつ、暑とbの使用割合が1
1.0重量llK対し、bを0.03ないし1.0重量
部用いて乳化させたことt特徴とする油中水種エマルジ
璽ン。 13偵アルコールと脂肪酸のモノエステルにおいて、構
成する3価アルコールがグリセリン及びトリメチロール
プロパンのいずれか又は両者混合物である特許請求の範
囲第1項記載のエマルジ1ン。 1.3価アルコールと脂肪酸のモノエステルにおいて、
構成する脂肪酸がオレイン酸及びイノステアリン酸のい
ずれか又は両者の混合物である特許請求の範囲第1項記
載のエマルジーン。 4、 カル〆キシピニルボI)゛マーにおいて、このカ
ルボ中ジビニルポリマーが遊離酸、ナトリウム塩、力I
Iウム塩、アンモニウム塩1丁ルカノールアミン塩及び
塩基性アミノ酸塩の少くとも一種である特許請求の範囲
第1項記載のエマルジーン。
[Scope of Claims] 1. In a water-in-oil emulsion, as an emulsifier (a) a monoester of a trihydric alcohol and a fatty acid having 8 or more carbon atoms, which exhibits a liquid or near-liquid paste form at room temperature; Two components of divinyl polymer in carbo are essential components, and the usage ratio of heat and b is 1
A water-in-oil emulsion, characterized in that it is emulsified using 0.03 to 1.0 parts by weight of b to 1.0 parts by weight. 2. The emulsion according to claim 1, wherein in the monoester of 13-alcohol and fatty acid, the constituting trihydric alcohol is either glycerin or trimethylolpropane, or a mixture of both. 1. In monoesters of trihydric alcohols and fatty acids,
The emulgene according to claim 1, wherein the constituent fatty acid is either oleic acid or inostearic acid, or a mixture of both. 4. In the carboxypinyl carbon I) polymer, the divinyl polymer in the carboxylic acid contains the free acid, sodium salt, and divinyl polymer.
The emulgene according to claim 1, which is at least one of a lium salt, an ammonium salt, an ethanolamine salt, and a basic amino acid salt.
JP56101043A 1981-06-29 1981-06-29 Water-in-oil type emulsion Pending JPS583631A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56101043A JPS583631A (en) 1981-06-29 1981-06-29 Water-in-oil type emulsion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56101043A JPS583631A (en) 1981-06-29 1981-06-29 Water-in-oil type emulsion

Publications (1)

Publication Number Publication Date
JPS583631A true JPS583631A (en) 1983-01-10

Family

ID=14290107

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56101043A Pending JPS583631A (en) 1981-06-29 1981-06-29 Water-in-oil type emulsion

Country Status (1)

Country Link
JP (1) JPS583631A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008024630A (en) * 2006-07-20 2008-02-07 Shiseido Co Ltd Water-in-oil type emulsion composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52117441A (en) * 1976-03-26 1977-10-01 Henkel & Cie Gmbh Waterrinnoil type cosmetic emulsion and its preparation
JPS52151305A (en) * 1976-06-11 1977-12-15 Kao Corp Emulsifying agents for water-in-oil type emulsion fuels
JPS5484883A (en) * 1977-11-22 1979-07-06 Peterson Puritan Inc Water in oil emulsion* its manufacture and liquid composition containing said emulsion

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52117441A (en) * 1976-03-26 1977-10-01 Henkel & Cie Gmbh Waterrinnoil type cosmetic emulsion and its preparation
JPS52151305A (en) * 1976-06-11 1977-12-15 Kao Corp Emulsifying agents for water-in-oil type emulsion fuels
JPS5484883A (en) * 1977-11-22 1979-07-06 Peterson Puritan Inc Water in oil emulsion* its manufacture and liquid composition containing said emulsion

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008024630A (en) * 2006-07-20 2008-02-07 Shiseido Co Ltd Water-in-oil type emulsion composition

Similar Documents

Publication Publication Date Title
EP0373661B1 (en) Water-in-oil type emulsion cosmetic
KR100690469B1 (en) Gelled Aqueous Cosmetic Composition
US4368187A (en) Sensitive-skin care regime
EP0331833A1 (en) Water-in-oil emulsion type cosmetics
US4776976A (en) O/W type emulsion composition
JPWO1997002803A1 (en) topical skin preparations
KR20100042254A (en) Liquid cosmetic preparation
WO2012012857A2 (en) Surfactant-free oil-in-water type emulsion, process for preparation thereof and its uses
JP2012067024A (en) Skin care preparation for external use
JP2003095956A (en) Microemulsion composition
JPS58183611A (en) Cosmetic of polyphase emulsification type
JPH0662385B2 (en) Emulsified composition
JP2944258B2 (en) Emulsion type cosmetic
JP6133618B2 (en) Water-in-oil emulsion composition
JP2549119B2 (en) Topical
CA2086689A1 (en) Cosmetic or dermatological composition containing a diol ester
JP2004059526A (en) Water-in-oil type emulsifying cosmetic
JPS6231975B2 (en)
JPS6186940A (en) Oil in water type emulsion composition
JP2854767B2 (en) Thickening gelling agent
JP2002145733A (en) Solid water-in-oil type emulsion cosmetic
JP3565332B2 (en) Emulsion type solid cosmetic
JP7459418B2 (en) Toner
JP3565320B2 (en) Oil-in-water emulsion composition containing inorganic salt
JPH0669532B2 (en) Oil-in-water emulsion composition