JPS591404A - Emulsifiable composition - Google Patents

Emulsifiable composition

Info

Publication number
JPS591404A
JPS591404A JP57111169A JP11116982A JPS591404A JP S591404 A JPS591404 A JP S591404A JP 57111169 A JP57111169 A JP 57111169A JP 11116982 A JP11116982 A JP 11116982A JP S591404 A JPS591404 A JP S591404A
Authority
JP
Japan
Prior art keywords
water
oil
salts
composition
emulsion
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
JP57111169A
Other languages
Japanese (ja)
Other versions
JPH0356777B2 (en
Inventor
Masahiro Tajima
正裕 田島
Hisayuki Komazaki
駒崎 久幸
Yoshimaru Kumano
熊野 可丸
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 JP57111169A priority Critical patent/JPS591404A/en
Publication of JPS591404A publication Critical patent/JPS591404A/en
Publication of JPH0356777B2 publication Critical patent/JPH0356777B2/ja
Granted legal-status Critical Current

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
    • A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/65—Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/06—Emulsions
    • A61K8/062—Oil-in-water emulsions
    • 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
    • A61K8/55—Phosphorus compounds
    • A61K8/553—Phospholipids, e.g. lecithin
    • 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
    • A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
    • 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
    • A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/645—Proteins of vegetable origin; Derivatives or degradation products thereof
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Biophysics (AREA)
  • Dermatology (AREA)
  • Molecular Biology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Colloid Chemistry (AREA)

Abstract

PURPOSE:To provide an emulsifiable composition giving an emulsion having high safety to the human body, fine particle size, and excellent stability, by dissolving a protein together with a phospholipid or its salt in a polyhydric alcohol, and adding an oil to the solution. CONSTITUTION:The objective emulsifiable composition contains (A) an emulsifier consisting of (i) phospholipids or their salts (e.g. phosphatidic acid, lecithin, etc.) which are known as naturally existing high-safety amphoteric substances and (ii) proteins or their salts (e.g. soybean protein, collagen, etc.) which are known as natural water-soluble polymers, (B) water-soluble polyhydric alcohols having >=2 hydroxyl groups in the molecule (e.g. ethylene glycol, glycerol, etc.) and (C) an oil component (e.g. beef tallow, vaseline, etc.). The emulsifiable composition can be converted to an O/W-type emulsified composition by adding water thereto.

Description

【発明の詳細な説明】 本発明は天然に存在し、安全性の高い両親媒性物質とし
て知られているリン脂質またはその塩および、天然水溶
性高分子物質として知られる蛋白質またはその塩を乳化
剤として、これに分子内に2個以上の水酸基を有する水
溶性多価アルコール(以下、単に多価アルコールと称す
)と、油分を配合して得られる乳化組成物′、及びこの
乳化組成物にさらに水を加えて得られる水中油型乳化組
成物に関する。
Detailed Description of the Invention The present invention uses phospholipids or their salts, which are known as naturally occurring and highly safe amphiphilic substances, and proteins or their salts, which are known as natural water-soluble polymer substances, as emulsifiers. and an emulsified composition obtained by blending this with a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule (hereinafter simply referred to as polyhydric alcohol) and an oil component, and this emulsified composition further contains The present invention relates to an oil-in-water emulsion composition obtained by adding water.

(以下余白) 近年、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1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7利用され
てきている。しがし、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、脂肪酸層けんで代表
されるアニオン界面活性剤、カチオン界面活性剤、両性
界面活性剤を乳化剤として使用しでおり、とくに一般消
費者の間で安全性に不安を抱くものが多い。
(Left below) In recent years, much research has been conducted on emulsification, and a large number of emulsifiers have been developed.1 Also, emulsification technology has made remarkable progress, and extremely stable emulsions are now widely used in all industries. However, most of them use nonionic surfactants containing polyoxyethylene chains, anionic surfactants represented by fatty acid layer, cationic surfactants, and amphoteric surfactants as emulsifiers. In particular, many general consumers have concerns about safety.

このような事情から最近、安全性が高いと考えられる天
然高分子物質を乳化剤として使用することが研究されは
じめてきた。しかし、天然水溶性高分子物質は、前述の
非イオン界面活性剤等のいわゆ6る「界面活性剤」に比
較して為界面張力低下能が小さいため、乳化力は相対的
に小さく、一般的に乳化粒子径が10μ程度と粗くなり
、経時安定性が悪い。また、水溶性高分子物質を湿潤剤
濃厚水溶液系で使用すると乳化状態が良くなる傾向があ
ることが知られているが、この方法においては、使用で
きる油相成分および湿潤剤が制限され、工業的に応用範
囲が狭いという欠点が見られる。
Under these circumstances, research has recently begun on the use of natural polymeric substances, which are considered to be highly safe, as emulsifiers. However, natural water-soluble polymer substances have a smaller ability to reduce interfacial tension than the so-called ``surfactants'' such as the nonionic surfactants mentioned above, so their emulsifying power is relatively small, and In general, the emulsified particle size becomes coarse, about 10 μm, and the stability over time is poor. Furthermore, it is known that the emulsification state tends to improve when a water-soluble polymer substance is used in a concentrated aqueous solution system with a wetting agent, but this method limits the oil phase components and wetting agent that can be used, and The drawback is that the scope of application is narrow.

かかる事情に鑑み、本発明者らは人体安全性の高い天然
高分子物質のなかでも、とくに蛋白質に着目し鋭意研究
した結果、蛋白質を特定の成分−と組み合せて多価アル
コール中に溶解し、これに油分を添加したならば、微細
な粒子径を持つ安定性良好なエマルジョンを製造し得る
ことを見い出し1本発明を完成するに至った。
In view of these circumstances, the present inventors have conducted extensive research focusing on proteins among natural polymeric substances with high human safety.As a result, the present inventors have found that proteins are combined with specific components and dissolved in polyhydric alcohol. The present inventors have discovered that by adding an oil component to this, it is possible to produce an emulsion with fine particle size and good stability, leading to the completion of the present invention.

すなわち本発明は、リン脂質またはその塩の1種または
2種以上と、蛋白質またはその塩の1種または2種以上
と、分子内に2個以上の水酸基を有する多価アルコール
の1種または2種以上と、油分とを含有してなる・多価
アルコール中に油分が可溶化もしくはマイクロエマルジ
ョンとしテ均一に分散した乳化組成物、あるいはこの乳
化組成物にさらに水を加えて得られる均一で微細な乳化
粒子を有する安定な水中油型乳化組成物を提供するもの
である。
That is, the present invention provides one or more phospholipids or salts thereof, one or more proteins or salts thereof, and one or more polyhydric alcohols having two or more hydroxyl groups in the molecule. An emulsified composition containing seeds or more and an oil component; an emulsified composition in which the oil component is solubilized or uniformly dispersed in a polyhydric alcohol, or a homogeneous and fine emulsified composition obtained by further adding water to this emulsified composition. The present invention provides a stable oil-in-water emulsion composition having emulsified particles.

本発明により寸得られた乳化組成物は透明もし−くは半
透明の粘稠液体またはゲルであり、さらに水を加えた水
中油型乳化組成物は乳白色の微細粒子のエマルジョンで
ある。これらは、水に高分子を溶解した後、油分を乳化
混合する従来の高分子乳化法では到底達しえない粒径の
細かい安定性良好な乳化組成物である。
The emulsion composition obtained according to the present invention is a transparent or translucent viscous liquid or gel, and the oil-in-water emulsion composition to which water is added is an emulsion of milky white fine particles. These are emulsified compositions with fine particle size and good stability that cannot be achieved by the conventional polymer emulsification method of dissolving a polymer in water and then emulsifying and mixing an oil component.

この微粒子化の原因は・リン脂質またはその塩と蛋白質
とが、水〜油界面より界面張力の低い多価アルコール−
油界面にすみやかに配向し、相互作用するためと考えら
れる。
The cause of this microparticulation is that phospholipids or their salts and proteins have a lower interfacial tension than the water-oil interface, which is polyhydric alcohol.
This is thought to be due to the rapid orientation and interaction at the oil interface.

本発明において用いられる多価アルコールは、分子内に
水酸基を二個以上含有する水溶性多価ア/l/ :+ 
−ルT・例エバ、エチレングリコール、プロピレングリ
フール、L3−ブチレングリコール、1.4−ブチレン
グリコール、ジプロピレングリコール・グリセリン、及
びジグリセリン、トリグリセリン、テトラグリセリンな
どのポリグリセリン、グルコース、マルトース、マルチ
トール、蔗糖、フラクトース、キシリトール、ソルビト
ール、育ルトトリオース、スレイトール、エリスリトー
ル、澱粉分解軸、澱粉分解糖環元アルコールなどであり
これらのうち1種または2種以上が用いられる。
The polyhydric alcohol used in the present invention is a water-soluble polyhydric alcohol containing two or more hydroxyl groups in the molecule.
-ru T・Example Eva, ethylene glycol, propylene glycol, L3-butylene glycol, 1,4-butylene glycol, dipropylene glycol, glycerin, and polyglycerin such as diglycerin, triglycerin, and tetraglycerin, glucose, maltose, These include maltitol, sucrose, fructose, xylitol, sorbitol, oltotriose, threitol, erythritol, starch decomposition axis, starch decomposition sugar ring alcohol, and one or more of these may be used.

配合量はリン脂質またはその塩の一種または二種以上と
多価アルコールと油相からなる乳化組成物の2〜95重
量%(以下、単に%と称す)である。
The blending amount is 2 to 95% by weight (hereinafter simply referred to as %) of the emulsified composition comprising one or more phospholipids or salts thereof, a polyhydric alcohol, and an oil phase.

(以下余白) 本発明において用いられるリン脂質は・大豆・トウモロ
コシ、落花生、ナタネ、麦等の植物・卵黄・牛等の動物
および大腸菌等の微生物から抽出されるリン脂質であり
、ホスファチジン酸、ホスファチジルグリセリン、ホス
ファチジルイノシトール、ホスファチジルエタノールア
ミン、ホスファチジルモノメチルエタノールアミン、ホ
スファチジルジメチルエタノールアミン、ホスファチジ
ルコリン(レシチン)、ホス7アチジルセリン、ビスホ
スファチジン酸、ジホスフ′7チジルグリセリン(カル
シオリピン)などのグリセロリン脂質、スフィンゴミエ
リンなどのスフィンゴリン脂質ヲ含み・さらに、これら
を水素添加処理したものも用いられる。
(The following is a blank space) The phospholipids used in the present invention are phospholipids extracted from plants such as soybeans, corn, peanuts, rapeseed, and wheat, egg yolks, animals such as cows, and microorganisms such as Escherichia coli, and include phosphatidic acid, phosphatidyl Glycerophospholipids such as glycerin, phosphatidylinositol, phosphatidylethanolamine, phosphatidylmonomethylethanolamine, phosphatidyldimethylethanolamine, phosphatidylcholine (lecithin), phos-7 atidylserine, bisphosphatidic acid, diphosph'7tidylglycerin (calciolipin), sphingomyelin, etc. Contains sphingophospholipids, and hydrogenated products of these are also used.

(以下余白) また本発明で用いられる蛋白質は、通常自然界より得ら
れる蛋白質またはそれらの分解物で、分子量が5000
ダルトン以上のものである。これらの例としては、例え
ば・大豆蛋白・小麦蛋白、グルテリン、ホエー粉末、大
豆カゼイン、大豆粉・フィブロイン、グルカゴン、コラ
ーゲン、ゼラチン、エラスチン、卵白リゾチーム、アミ
ラーゼ、フィブリノーゲン、ミオシン、エノラーゼ、キ
モトリブシ/−ゲン、ヒストン、アクチン、ナラチン1
ヘモグロビン、アビジン、ペプシン′、グリアジ八生長
ホルモン、アルブミン、グロブリン、ミオグロビン、カ
ゼイン1パパイン、β−ガラクトシダーゼ、インシュリ
ン、リゾチーム、カタラーゼを挙げることができる。同
様に、これらの酸、アルカリ、酵素分解物を使用するこ
とも可能である。
(Hereinafter, blank spaces) The proteins used in the present invention are usually proteins obtained from nature or their decomposition products, and have a molecular weight of 5000.
It's more than Dalton. Examples of these include: Soybean protein/wheat protein, glutelin, whey powder, soybean casein, soybean flour/fibroin, glucagon, collagen, gelatin, elastin, egg white lysozyme, amylase, fibrinogen, myosin, enolase, chymotrybium/gen , histone, actin, naratin 1
Mention may be made of hemoglobin, avidin, pepsin', growth hormone, albumin, globulin, myoglobin, casein-1-papain, β-galactosidase, insulin, lysozyme, and catalase. Similarly, it is also possible to use these acids, alkalis, and enzymatic decomposition products.

リン脂質 および蛋白質を塩として使用する場合の塩を
形成する物質としては、水酸化リチウム、水酸化ナトリ
ウム・         水酸化カリウム、水酸化セシ
ウム、水酸化アンモニウムなどの無機塩基1アルギ、ニ
ン、リジンへヒスチジン、オルニチンなどの塩基性アミ
ノ酸及びそれらを残基として有する塩基性オリゴペプチ
ド、モノエタノールアミン・ジェタノールアミン、トリ
エタノールアミンなどの塩基性アミン等の塩基、及び塩
酸、硫酸などの無機酸、酢酸、クエン酸、マレイン酸・
フマール酸などの有機酸、グルタミン酸、アスパラギン
酸などの酸性アミノ酸及びそれらを残基として有する酸
性オリゴペプチド等の酸が用いられる。塩はあらかじめ
反応させて塩にしてか)添加しても良いし・別々に添加
して、乳化組成物の製造工程中で反応させて塩にしても
良い。
Substances that form salts when phospholipids and proteins are used as salts include inorganic bases such as lithium hydroxide, sodium hydroxide/potassium hydroxide, cesium hydroxide, and ammonium hydroxide; , basic amino acids such as ornithine and basic oligopeptides having them as residues, bases such as basic amines such as monoethanolamine, jetanolamine, and triethanolamine, inorganic acids such as hydrochloric acid and sulfuric acid, acetic acid, Citric acid, maleic acid
Organic acids such as fumaric acid, acidic amino acids such as glutamic acid and aspartic acid, and acidic oligopeptides having these as residues are used. The salt may be added in advance (by reacting to form a salt) or may be added separately and reacted during the manufacturing process of the emulsion composition to form a salt.

リン脂質と蛋白質の塩水溶液のpHはいくつでも良いが
、できれば、蛋白質の等電点を避けた方が好ましい。
The pH of the phospholipid and protein salt aqueous solution may be any value, but it is preferable to avoid the isoelectric point of the protein if possible.

リン脂質またはその塩と蛋白質の配合量は、重量比2−
8〜8:2の範囲で・それぞれ単独に使用した場合より
飛躍的に良好な乳化組成物が得られる。リン脂質または
その塩および蛋白質またはその塩と、分子内に二個以上
の水酸基を有する多価アルコールの配合量は、重量比で
1=1〜1000の範囲である。多価アルコールの配合
量がリン脂質またはその塩および蛋白質またはその塩の
総量に対し1未満であるとリン脂質またはその塩と蛋白
質が完全に溶解しなくなり、1o00を超えると乳化安
定性が悪くなる。
The blending amount of phospholipid or its salt and protein is 2-
In the range of 8 to 8:2, a significantly better emulsified composition can be obtained than when each is used alone. The weight ratio of the phospholipid or its salt, the protein or its salt, and the polyhydric alcohol having two or more hydroxyl groups in the molecule is in the range of 1=1 to 1000. If the amount of polyhydric alcohol is less than 1 to the total amount of phospholipid or its salt and protein or its salt, the phospholipid or its salt and protein will not be completely dissolved, and if it exceeds 1000, emulsion stability will deteriorate. .

本発明で用いられる油分は・牛脂、スクワラン・オリー
ブ油、コメヌカ油などの動植物油脂および炭化水素、流
動パラフィン、ワセリンなどの鉱物油、イソプロピルミ
リステート、ペンタエリスリバ トール−テトラ−2−エチルヘキサネート、ビタミンA
バネルミテート・ビタミンEアセテートなどのエステル
油、メチルフェニルシリコン、ジメチルシリコンなどの
シリコン油等の、化粧品、医薬品、食品等の業界で一般
に利用される油分である。
Oils used in the present invention include animal and vegetable oils and fats such as beef tallow, squalane, olive oil, and rice bran oil; hydrocarbons; mineral oils such as liquid paraffin and petrolatum; isopropyl myristate; pentaerythribatol-tetra-2-ethylhexanate; Vitamin A
These oils are commonly used in the cosmetics, pharmaceutical, and food industries, such as ester oils such as banermitate and vitamin E acetate, and silicone oils such as methylphenyl silicone and dimethyl silicone.

油分に対して、多価アルコールとリン脂質またはその塩
と蛋白質またはその塩との合計量が20%以上になるよ
うに調整することが望ましい。
It is desirable to adjust the total amount of polyhydric alcohol, phospholipid or its salt, and protein or its salt to 20% or more based on the oil content.

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、非イオン界面活性剤、アニオン界
面活性剤、カチオン界面活性剤、両性界面活性剤、薬剤
、紫外線吸収剤、防腐剤、酸化防止剤等を混合添加して
も良い。また、均質安定化、粘度調整の目的で、アルコ
ール、脂肪酸、他の水溶性高分子などを添加しても良い
。
In addition to the above-mentioned essential components, the emulsified composition according to the present invention may include nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, drugs, ultraviolet absorbers, Preservatives, antioxidants, etc. may be mixed and added. Furthermore, alcohol, fatty acids, other water-soluble polymers, etc. may be added for the purpose of homogeneity stabilization and viscosity adjustment.

本発明の乳化組成物は多価アルコールまたはそノ水溶液
中にリン脂質またはその塩 と蛋白質またはその塩を溶
解し、攪拌しながら油分を徐々に添加することにより得
られる。この場合、ホモミキサー処理を行なうことが好
ましいが、手攪拌等の弱い攪拌力でも良好な乳化組成物
を得ることができる。
The emulsified composition of the present invention can be obtained by dissolving a phospholipid or its salt and a protein or its salt in a polyhydric alcohol or its aqueous solution, and gradually adding an oil component while stirring. In this case, it is preferable to perform a homomixer treatment, but a good emulsified composition can be obtained even with a weak stirring force such as manual stirring.

ここに得られた乳化組成物は、均一で透明または半透明
のゲルまたは粘稠な液体であるのでこのままで、例えば
、サンケアゼリー、美容液、食用本発明に係る他の水中
油型乳化組成物を得るには、前述した乳化組成物と水と
を混合すれば得らtel。  この場合、ホモミキサー
処理を行なうことが好ましい。ここに得られる水中油型
乳化組成物は極めて安定性に優れたものである。
The emulsified composition obtained here is a homogeneous transparent or translucent gel or viscous liquid, so it can be used as it is, for example, in sun care jelly, beauty serum, and other oil-in-water emulsified compositions according to the present invention. can be obtained by mixing the emulsion composition described above and water. In this case, it is preferable to perform homomixer treatment. The oil-in-water emulsion composition obtained here has extremely excellent stability.

水には、目的に応じて湿潤剤、水溶性ビタミン、水溶性
防腐剤、水溶性薬剤、水溶性高分子など、化粧品、医薬
品、食品などの業界で一般に汎用される水相成分を添加
することもできる。
Depending on the purpose, water phase components commonly used in the cosmetics, pharmaceutical, food, and other industries may be added to the water, such as humectants, water-soluble vitamins, water-soluble preservatives, water-soluble drugs, and water-soluble polymers. You can also do it.

上記乳化組成物と水相成分の量的関係については、極め
て広範囲に選択できるが、通常乳化組成物0.5〜80
部、水995〜2D部程度である。
The quantitative relationship between the emulsion composition and the aqueous phase components can be selected from a very wide range, but usually the emulsion composition is 0.5 to 80%
parts, and about 995 to 2D parts of water.

ここに得られた水中油型乳化組成物は、均一な微細粒子
を分散した乳白色の粘稠あるいは低粘度の液体であるた
め、このままの形態でも乳液、クリ二ム、ファウンデイ
ションなどの化粧品、シャンプー、リンスなどのトイレ
タリー製品、尿素クリーム、アクネクリームなどの医薬
品、マヨネーズなどの食品等あらゆる分野で好適に使用
することができる。
The oil-in-water emulsion composition obtained here is a milky white viscous or low-viscosity liquid in which uniform fine particles are dispersed, so it can be used in cosmetics such as emulsions, creams, foundations, etc. even in its original form. It can be suitably used in all fields such as toiletry products such as shampoo and conditioner, pharmaceuticals such as urea cream and acne cream, and food products such as mayonnaise.

また、均質安定化、粘性調整あるいは薬効を持たせるた
めに、他の水溶性高分子、薬剤、界面活性剤、粉末、な
どを添加することも一向に差支えないO 以下、本発明を実施例及び比較例によってさらに詳細に
説明する。本発明はこれにより限定されるものではない
。
In addition, there is no problem in adding other water-soluble polymers, drugs, surfactants, powders, etc. in order to stabilize homogeneity, adjust viscosity, or impart medicinal efficacy.Hereinafter, the present invention will be described in Examples and Comparisons. This will be explained in more detail by way of example. The present invention is not limited thereby.

実施例1〜9.比較例1〜7 蛋白質、リ ン 脂 質 多価アルコール、イオン交換
水、および油分を表−1に示す配合組成及び量で配合し
、70°Cホモミキサー処理して、乳化組成物を作った
、。さらに、この乳化組成物に、それに対して10倍量
の水を常温で攪拌しながら加えて、水中油型乳化組成物
を作った。乳化組成物と水中油型乳化組成物の状態を観
察し、特性値を測定しそれらの結果を表−1に示した。
Examples 1-9. Comparative Examples 1 to 7 Protein, phospholipid, polyhydric alcohol, ion-exchanged water, and oil were blended in the composition and amounts shown in Table 1, and treated with a homomixer at 70°C to make an emulsified composition. ,. Further, 10 times the amount of water was added to this emulsified composition while stirring at room temperature to prepare an oil-in-water emulsified composition. The states of the emulsified composition and oil-in-water emulsified composition were observed, and their characteristic values were measured, and the results are shown in Table 1.

なお、各成分の数字は重量%である。Note that the numbers for each component are weight %.

表−1から明らかなように、蛋白質またはリン脂質を乳
化剤として単一使用した場合、(比較例]〜3.5〜7
)、安定な乳゛化物は得らず、乳化物が得られた比較例
5.6でも、乳化粒子径は10μ以上であり、水中油型
乳化組成物は分離した。さらに、蛋白質と リ ン脂質
 を組み合せて乳化剤としても、多価アルコール量が少
ないと(比較例4)、安定な乳化組成物は得られなかっ
た。
As is clear from Table 1, when protein or phospholipid is used alone as an emulsifier, (comparative example) ~3.5~7
), a stable emulsion was not obtained, and even in Comparative Example 5.6 where an emulsion was obtained, the emulsion particle size was 10 μm or more and the oil-in-water emulsion composition was separated. Furthermore, even when a combination of protein and phospholipid was used as an emulsifier, a stable emulsified composition could not be obtained if the amount of polyhydric alcohol was small (Comparative Example 4).

これに対して、本発明に係る実施例1〜9については、
いずれの水準においても非常に良好な透明あるいは半透
明の粘稠な液体またはゲルが得ら汽さらに、水を加えて
得られた水中油型乳化組成物は、非常に微細な粒子の分
散した安定なエマルジョ表−14の■ 水中油型乳化組成物状態は、1日放置後以下の基準にて
判定した。
On the other hand, for Examples 1 to 9 according to the present invention,
At any level, a very good transparent or translucent viscous liquid or gel is obtained.Furthermore, the oil-in-water emulsion composition obtained by adding water is stable with very fine particles dispersed. Emulsion Table 14 (■) The condition of the oil-in-water emulsion composition was evaluated based on the following criteria after being left for one day.

◎ 乳化粒子径1μ以下 Ol〜5μ △      5〜10μ ×      wμ以上 (以下余白) 重量% (A)  大豆レシチン            &0
カゼインナトリウム         1.0マルチト
ール(50%水溶液)200 1.3 −ブチレングリコール     lα0ヒアル
ロン酸ナトリウム       01(B)  流動パ
ラフィン           4αOオリーブ油  
            2Z5グリセリルトリステア
レート     3.0ビタミンEアセテート    
    α5防腐剤               0
.5香  料                   
       α4(A)相を70°Cで充分攪拌し、
(B)相を70℃で溶解したものを(A)相に攪拌しな
がら添加した・このものをホモミキサー処理し、攪拌冷
却して水性美容ゼリーを得た。この美容ゼリーは、粘稠
でやや流動感のある透明ゲル状を呈°し、皮膚安全性が
高く、かつ経時安定性の優れた乳化物で、皮膚に塗布し
たとき、非常にのびが良く、小量にて広範囲に拡がる使
用特性を有していた0 (以下余白) 実施例■ 栄養乳液 重量% □L)局方グリセリン         2001.3
−ブチレングリコール     5.0大豆蛋白分解物
(分子量10000 )   b。
◎ Emulsified particle size 1μ or less Ol~5μ △ 5~10μ × wμ or more (hereinafter margin) Weight% (A) Soybean lecithin &0
Sodium caseinate 1.0 Maltitol (50% aqueous solution) 200 1.3 -Butylene glycol lα0 Sodium hyaluronate 01(B) Liquid paraffin 4αO olive oil
2Z5 Glyceryl Tristearate 3.0 Vitamin E Acetate
α5 preservative 0
.. 5 fragrances
Stir α4(A) phase thoroughly at 70°C,
A solution of phase (B) at 70° C. was added to phase (A) with stirring. This mixture was treated with a homomixer and cooled with stirring to obtain an aqueous cosmetic jelly. This beauty jelly is a viscous, slightly fluid, transparent gel-like emulsion that is highly safe for the skin and has excellent stability over time.When applied to the skin, it spreads very easily. It had the characteristic of being used over a wide range in small amounts.
-Butylene glycol 5.0 soybean protein decomposition product (molecular weight 10,000) b.

水溶性フラーゲン         1.0卵黄レシチ
ン水素添加物      05カルシオリピン    
      0.5アラントイン          
 02水酸化ナトリウム         0.05(
B)  流動パラフィン         1α0ホホ
バ油             5.0ペンタエリスリ
トール−テトラ− 2−エチルヘキサノエート      5.0ワセリン
             5.0エチニルエストラジ
オール     α1防腐剤            
  。4香料               α3(0
)精製水             45.75アルギ
ン酸ナトリウム       α1キサンチンガム  
        α1実施例1oの製造法に準じて、(
A)相、(B)相より乳化組成物を得、70°Cとし、
別に調整し70°C番こ保っておいた増粘剤水溶液(0
)相で希釈分散した後、冷却し水中油型エマルションの
栄養乳液を得た。この乳液の粘度は30’Cで 4″L
IQOPsであり、乳化粒子径1〜3μ程度の安定でか
つなじみの良い感触を有していた0 実施例圧 サンケアクリーム 重量% (A)  ジグリセリン          20.0
ソルビトール(70%水溶液)    a。
Water-soluble flagen 1.0 Egg yolk lecithin hydrogenated product 05 Calciolipin
0.5 allantoin
02 Sodium hydroxide 0.05 (
B) Liquid paraffin 1α0 Jojoba oil 5.0 Pentaerythritol-tetra-2-ethylhexanoate 5.0 Vaseline 5.0 Ethinyl estradiol α1 Preservative
. 4 Fragrance α3 (0
) Purified water 45.75 Sodium alginate α1 xanthine gum
According to the manufacturing method of α1 Example 1o, (
An emulsion composition was obtained from the A) phase and the (B) phase, and the temperature was set at 70°C.
Aqueous thickener solution prepared separately and kept at 70°C (0
) phase and then cooled to obtain a nutritional emulsion of oil-in-water emulsion. The viscosity of this emulsion is 4"L at 30'C.
IQOPs, with emulsified particle size of about 1 to 3 μm, stable and familiar feel 0 Example Pressure Suncare Cream Weight % (A) Diglycerin 20.0
Sorbitol (70% aqueous solution) a.

果糖               zO大豆レシチン
           2−0卵白アルブミン    
     3゜グロブリン           Lo
CB)  流動パラフィン          20.
0イソプロピルミリステート       100ワセ
リン              5.0ステアリルア
ルコール         5.OP A B A  
               2.0防  腐  剤
                    05香  
   料                    α
3(0)   精  製  水           
          IELOヒドロキシエチルセルロ
ース      α2(D)  調合粉末      
        LO二酸化チタン         
  20実施例uの製造法に準じて、サンケアクリーム
を得た。このとき(0)相は(D)相を70°Cにて分
散ホモミキサー処理した後、希釈相として使用した。こ
のサンケアクリームは、25°C硬度が摺であり、やや
透明感があり、また乳化粒子径が1〜3μ程度で安定性
の良い水中油型乳化組成物で、太陽光の下で好適に使用
できるものであった。
Fructose zO soy lecithin 2-0 egg albumin
3゜globulin Lo
CB) Liquid paraffin 20.
0 Isopropyl myristate 100 Vaseline 5.0 Stearyl alcohol 5. OP A B A
2.0 preservative 05 fragrance
Fee α
3(0) Purified water
IELO Hydroxyethyl Cellulose α2(D) Mixed Powder
LO titanium dioxide
A sun care cream was obtained according to the manufacturing method of Example 20. At this time, the (0) phase was used as a diluted phase after the (D) phase was subjected to a dispersion homomixer treatment at 70°C. This sun care cream has a 25°C hardness of Suri, is slightly transparent, and has a highly stable oil-in-water emulsion composition with an emulsion particle size of approximately 1 to 3 μm, making it suitable for use under sunlight. It was possible.

特許出願人 株式会社 資 生 堂Patent applicant Shiseido Co., Ltd.

Claims (1)

【特許請求の範囲】 1、リン脂質またはその塩の1種または2種以上と・蛋
白質またはその塩の1種または2種以上と、分子内に2
個以上の水酸基を有する水溶性多価アルコールの1種ま
たは2種以上と、油分とを含有することを特徴とする乳
化組成物 2−1〕ン脂質またはその塩の1種または2種以上と、
蛋白質またはその塩の1種または2種以上と、分生内に
2個以上の水酸基を有する水溶性多価アルフールの1種
または2種以上と、油分とを含む乳化組成物と、水とを
含有することを特徴とする水中油型乳化組成物。 (以下余白)
[Claims] 1. One or more phospholipids or salts thereof; one or more proteins or salts thereof;
Emulsified composition characterized by containing one or more water-soluble polyhydric alcohols having at least three hydroxyl groups, and an oil component 2-1] One or more types of lipids or salts thereof; ,
An emulsified composition containing one or more proteins or salts thereof, one or more water-soluble polyhydric alfurs having two or more hydroxyl groups in the conidia, and an oil component, and water. An oil-in-water emulsion composition comprising: (Margin below)
JP57111169A 1982-06-28 1982-06-28 Emulsifiable composition Granted JPS591404A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57111169A JPS591404A (en) 1982-06-28 1982-06-28 Emulsifiable composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57111169A JPS591404A (en) 1982-06-28 1982-06-28 Emulsifiable composition

Publications (2)

Publication Number Publication Date
JPS591404A true JPS591404A (en) 1984-01-06
JPH0356777B2 JPH0356777B2 (en) 1991-08-29

Family

ID=14554223

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57111169A Granted JPS591404A (en) 1982-06-28 1982-06-28 Emulsifiable composition

Country Status (1)

Country Link
JP (1) JPS591404A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5929606A (en) * 1982-08-10 1984-02-16 Iwasekenjirou Shoten:Kk Oil-in-water type emulsified composition for external skin use
JPS60146812A (en) * 1984-01-09 1985-08-02 Nonogawa Shoji:Kk Thickening and gelling composition
JPS61289018A (en) * 1985-06-17 1986-12-19 Pola Chem Ind Inc Skin external agent
JPS6293239A (en) * 1985-10-21 1987-04-28 Nippon Saafuakutanto Kogyo Kk Base material for external use
JPS62175414A (en) * 1986-01-28 1987-08-01 Pola Chem Ind Inc Emulsion cosmetic
JPS62209009A (en) * 1986-03-10 1987-09-14 Kobayashi Kooc:Kk Cosmetic
JPS62234535A (en) * 1986-03-14 1987-10-14 ア−・ナツタ−マン・ウント・コンパニ・ゲ−エムベ−ハ− Product containing phospholipid
FR2657525A1 (en) * 1990-01-26 1991-08-02 Dubois Jacques NEW DERMO-COSMETIC PRODUCTS FOR THE CLEANING AND CARE OF THE SKIN AND / OR HAIR.
WO1993014748A1 (en) * 1992-02-03 1993-08-05 Otsuka Pharmaceutical Co., Ltd. Remedy for dermatopathy and metallothionein inducer
JP2003342126A (en) * 2002-05-27 2003-12-03 Q P Corp Transparent cosmetics
JP2004269502A (en) * 2003-02-19 2004-09-30 Kose Corp Oil in water type emulsion cosmetic
JP2008290951A (en) * 2007-05-22 2008-12-04 Mikimoto Pharmaceut Co Ltd Emulsified composition
JP2017197452A (en) * 2016-04-26 2017-11-02 照屋 亮 Method for producing emulsion composition

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5670826A (en) * 1979-11-15 1981-06-13 Nippon Saafuakutanto Kogyo Kk Oil-in-polyhydric alcohol type emulsion composition
JPS5759628A (en) * 1980-09-25 1982-04-10 Asahi Denka Kogyo Kk Solubilizing method
JPS5759627A (en) * 1980-09-25 1982-04-10 Asahi Denka Kogyo Kk Solubilization
JPS5759629A (en) * 1980-09-25 1982-04-10 Asahi Denka Kogyo Kk Solubilizing method for nonaqueous substance
JPS5863750A (en) * 1981-10-12 1983-04-15 Asahi Denka Kogyo Kk Emulsified or solubilized silicone oil

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5670826A (en) * 1979-11-15 1981-06-13 Nippon Saafuakutanto Kogyo Kk Oil-in-polyhydric alcohol type emulsion composition
JPS5759628A (en) * 1980-09-25 1982-04-10 Asahi Denka Kogyo Kk Solubilizing method
JPS5759627A (en) * 1980-09-25 1982-04-10 Asahi Denka Kogyo Kk Solubilization
JPS5759629A (en) * 1980-09-25 1982-04-10 Asahi Denka Kogyo Kk Solubilizing method for nonaqueous substance
JPS5863750A (en) * 1981-10-12 1983-04-15 Asahi Denka Kogyo Kk Emulsified or solubilized silicone oil

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5929606A (en) * 1982-08-10 1984-02-16 Iwasekenjirou Shoten:Kk Oil-in-water type emulsified composition for external skin use
JPS60146812A (en) * 1984-01-09 1985-08-02 Nonogawa Shoji:Kk Thickening and gelling composition
JPS61289018A (en) * 1985-06-17 1986-12-19 Pola Chem Ind Inc Skin external agent
JPS6293239A (en) * 1985-10-21 1987-04-28 Nippon Saafuakutanto Kogyo Kk Base material for external use
JPS62175414A (en) * 1986-01-28 1987-08-01 Pola Chem Ind Inc Emulsion cosmetic
JPS62209009A (en) * 1986-03-10 1987-09-14 Kobayashi Kooc:Kk Cosmetic
JPS62234535A (en) * 1986-03-14 1987-10-14 ア−・ナツタ−マン・ウント・コンパニ・ゲ−エムベ−ハ− Product containing phospholipid
FR2657525A1 (en) * 1990-01-26 1991-08-02 Dubois Jacques NEW DERMO-COSMETIC PRODUCTS FOR THE CLEANING AND CARE OF THE SKIN AND / OR HAIR.
WO1991011170A1 (en) * 1990-01-26 1991-08-08 Jacques Dubois Cleansing cosmetics for skincare and/or haircare
WO1993014748A1 (en) * 1992-02-03 1993-08-05 Otsuka Pharmaceutical Co., Ltd. Remedy for dermatopathy and metallothionein inducer
JP2003342126A (en) * 2002-05-27 2003-12-03 Q P Corp Transparent cosmetics
JP2004269502A (en) * 2003-02-19 2004-09-30 Kose Corp Oil in water type emulsion cosmetic
JP2008290951A (en) * 2007-05-22 2008-12-04 Mikimoto Pharmaceut Co Ltd Emulsified composition
JP2017197452A (en) * 2016-04-26 2017-11-02 照屋 亮 Method for producing emulsion composition

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