JPS597106A - Emulsifiable composition - Google Patents
Emulsifiable compositionInfo
- Publication number
- JPS597106A JPS597106A JP57117494A JP11749482A JPS597106A JP S597106 A JPS597106 A JP S597106A JP 57117494 A JP57117494 A JP 57117494A JP 11749482 A JP11749482 A JP 11749482A JP S597106 A JPS597106 A JP S597106A
- Authority
- JP
- Japan
- Prior art keywords
- water
- oil
- polyhydric alcohol
- saponin
- 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.)
- Granted
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
- A61K8/02—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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- 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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- 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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9794—Liliopsida [monocotyledons]
-
- 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
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Botany (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Colloid Chemistry (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、天然に存在し、去痰、鎮咳、抗炎症、中枢抑
制、抗疲労、抗潰瘍、コレステロール代謝促進、脂質代
謝の促進、核酸、蛋白の合成促進、感染防御、抗腫瘍な
どの生理、薬理的効果が知られている生薬であるサポニ
ンまたはその塩を乳化剤として、化粧品、医薬品などに
有効に活用しようとするものである。Detailed Description of the Invention The present invention is naturally occurring, expectorant, antitussive, anti-inflammatory, centrally suppressing, anti-fatigue, anti-ulcer, promoting cholesterol metabolism, promoting lipid metabolism, promoting synthesis of nucleic acids and proteins, and preventing infection. The aim is to use saponin, a herbal medicine known for its antitumor and other physiological and pharmacological effects, or its salts as emulsifiers in cosmetics, pharmaceuticals, and the like.
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・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
きている。しかし1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や脂肪醗石けんで代表さ
れるアニオン界面活性剤あるいはカチオン界面活性剤や
両性界面活性剤が乳化剤として使用され、人体に対する
安全性に懸念が持たれているものが多い。In recent years, much research has been conducted on emulsification, a large number of emulsifiers have been developed, and emulsification technology has made remarkable progress, and extremely stable emulsions are now widely used in all industries. However, in most of them, nonionic surfactants containing polyoxyethylene chains, anionic surfactants such as fatty soaps, cationic surfactants, and amphoteric surfactants are used as emulsifiers, and they are not safe for the human body. There are many things that are of concern.
一方、安全性が高いとされる、レシチン、サポニンなど
の天然両親媒性物質や、ガム類などの水溶性高分子で代
表される天然物を乳化剤として利用する試みは近年盛ん
におこなわれているが、これらの天然物質は、上記の非
イオン界面活性剤等のいわゆるU界面活性剤Jに比較し
て、界面張力低下能が小さいため、乳化力は相対的に小
さく、天然物質を乳化剤とした乳化系では一般←乳化粒
子径がwμ程度と粗く〜良好な経時安定性を持つものは
得られなかった。On the other hand, in recent years there have been many attempts to use natural products, such as natural amphiphilic substances such as lecithin and saponin, and water-soluble polymers such as gums, as emulsifiers, which are considered to be highly safe. However, these natural substances have a lower interfacial tension lowering ability than the so-called U-surfactants J such as the above-mentioned nonionic surfactants, so their emulsifying power is relatively small, and it is difficult to use natural substances as emulsifiers. In the case of emulsion systems, emulsion particles generally have a rough emulsion particle diameter of approximately wμ and no emulsion with good stability over time was obtained.
そこで、本発明者らは、人体安全性の高い天然物質を乳
化剤として使用し、かつ均一で微細な粒子を持つ安定な
エマルションを開発すべく鋭意研。Therefore, the present inventors conducted extensive research to develop a stable emulsion with uniform and fine particles using a natural substance with high human safety as an emulsifier.
られることを見い出し・さらに、この乳化組成物と水と
を混合したならば、均一な微細粒子の分散した安定な水
中油型乳化組成物が得られることを見い出し、本発明を
完成するに至った。Furthermore, they discovered that if this emulsion composition and water are mixed, a stable oil-in-water emulsion composition in which fine particles are uniformly dispersed can be obtained, leading to the completion of the present invention. .
(以下余白)
すなわち本発明は、サポニンまたはその塩の一種または
二種以上と、分子内に二個以」二の水酸基を有する水溶
性多価アルコールと、油相成分を含有することを特徴と
する乳化組成物、及び該乳化組成物と水とを混合するこ
とによって得られる水中油型乳化組成物を提供するもの
である。(Hereinafter in the margin) That is, the present invention is characterized by containing one or more saponins or salts thereof, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, and an oil phase component. The present invention provides an emulsified composition that contains the present invention, and an oil-in-water emulsified composition obtained by mixing the emulsified composition and water.
本発明により得られた上記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、水を加えた上記水中
油型乳化組成物は乳白色の微細粒子のエマルションであ
る。これらの微粒子乳化物は、水に天然ゾ物質を溶解し
た後、油相成分を乳化混合する従来の乳化法では、到底
達しえない粒径の細かいもの−t=e−ある・
この微粒子化の原因は、サポニンまたはその塩と蛋白質
とが、水−油相成分界面より界面張力の低い、多価アル
コール−油相成分界面にすみやかに配向し、相互作用す
るためと考えられjる・本発明において用いられる水溶
性多価アルコールは、分子内に水酸基を二個以上含百す
る水溶性多価アルコールで、例えば、エチレングリコー
ル、プロピレングリコール、1.3−ブチレングリコー
ル、1.4−7’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、マルヂトール、蔗糖、フラクトース、
キシリトール、ソルビトール、マルトトリオース、スレ
イトール、エリスリトール、澱粉分解糖、澱粉分解糖還
元アルコールなどである。これらのうち、一種または二
種基」二が選ばれて用いられる。配合量は上記乳化組成
物の2〜95 爪、1ff1%(以下、単に%と称す)
が好ましし)。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 with water added is an emulsion of milky white fine particles. These fine particle emulsions have particle sizes so small that they cannot be achieved using the conventional emulsification method of dissolving natural substances in water and then emulsifying and mixing the oil phase components. The reason is thought to be that saponin or its salt and protein quickly align and interact at the polyhydric alcohol-oil phase component interface, which has a lower interfacial tension than the water-oil phase component interface. The water-soluble polyhydric alcohol used in this is a water-soluble polyhydric alcohol containing two or more hydroxyl groups in the molecule, such as ethylene glycol, propylene glycol, 1.3-butylene glycol, 1.4-7' tylene, etc. Glycol, dipropylene glycol, glycerin, and polyglycerin such as diglycerin, triglycerin, and tetraglycerin, glucose, maltose, malditol, sucrose, fructose,
These include xylitol, sorbitol, maltotriose, threitol, erythritol, starch-degrading sugar, and starch-degrading sugar-reduced alcohol. Among these, one or two groups are selected and used. The blending amount is 2 to 95 nails, 1ff1% (hereinafter simply referred to as %) of the emulsified composition.
is preferred).
本発明において用いられるサポニンは、動植物から得た
抽出物である。The saponins used in the present invention are extracts obtained from plants and animals.
サポニンは本質的にザボゲニンと糖とからなる。Saponins essentially consist of zabogenin and sugars.
づボゲニンは、ステロイド系またはトリテルペン系であ
り、糖はグルコース、グルコン酸キシロース1ラムノー
ス・アラビノース、バナザトリ、t −ル等を構成糖と
した単糖類、三糖類、オリゴ糖のいずれでも良い。Zubogenin is steroid-based or triterpene-based, and the sugar may be any of monosaccharides, trisaccharides, and oligosaccharides whose constituent sugars include glucose, xylose gluconate, rhamnose, arabinose, vanazatri, and t-ru.
サポニンを抽出する動植物を次に示す。The plants and animals from which saponins are extracted are shown below.
セネガ・オンジ、キキョウ、ゴシツ、サイコチクセツニ
ンジン、ニンジン、バクモンドウ、モクツク、サルサ、
アスパラガス、ユッカ、ルスクス、ディスコレア、ヒガ
ン花、キラヤア号ボナリア・トチツギ、グアヤカム、カ
ンゾウ、ナデシコ、キズタ、ヒメハギ、サピンダス、サ
ボナリアなどの浸漬法、消化法、煎出法、浸出法または
、圧搾法によって得られる。Senega onji, Bellflower, Goshitsu, Saikochikusetsu Carrot, Carrot, Bakumodo, Mokutsuku, Salsa,
Soaking, digestion, decoction, infusion, or pressing of asparagus, yucca, ruscus, discorea, higan flower, Killayaa Bonaria, guaiacum, licorice, dianthus, icus, sapindus, sabonaria, etc. obtained by.
サポニンは塩を形成するものと形成しないものがあるが
、塩として使用する場合、塩を形成する物質としては次
のような物質が使用される。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、アルギニン、リグノ、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であり、塩はあらかしめ
製造されるものだけでなく、乳化組成物の製造工程中で
製造されても良い。塩水溶液の州は2〜11の広範囲で
好適に使用できる。Some saponins form salts while others do not. When used as salts, the following substances are used as salt-forming substances. Inorganic bases such as lithium hydroxide, sodium hydroxide/potassium hydroxide, cesium hydroxide, ammonium hydroxide, basic amino acids such as arginine, ligno, histidine, ornithine, and basic oligopeptide monomers containing these as residues. The salt is a base such as a basic amine such as ethanolamine, jetanolamine, or triethanolamine, and the salt may be produced not only in advance but also during the production process of the emulsified composition. The state of the salt aqueous solution can be suitably used in a wide range of 2 to 11.
サポニンまたはその塩と、分子内に二個以上の水酸基を
有する多価アルコールの使用量は、重は比l:l〜1.
000の範囲が好ましい。サポニンまたはその塩が、多
価アルコール1に対し1より多いとサホ゛ニンの溶解が
困難となり、1 / 1.000より少ないと乳化安定
性が悪くなる。The amounts of saponin or its salt and the polyhydric alcohol having two or more hydroxyl groups in the molecule are in the ratio of 1:1 to 1.
A range of 000 is preferred. If the ratio of saponin or its salt is more than 1 part to 1 part of polyhydric alcohol, it will be difficult to dissolve saponin, and if it is less than 1/1.000, emulsion stability will deteriorate.
本発明で用いられる油相成分としては、牛脂、スクヮラ
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・ワセリンナトの鉱物MI+
、イソプロピルミリステート、ペンタエリスリトール−
テトラ−2−エチルへギサネート、ビタミンAパルミテ
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、油溶性薬剤を挙げることができる、にすること
が望ましい。The oil phase components used in the present invention include beef tallow, squalane, animal and vegetable oils such as olive oil and rice bran oil, and hydrocarbons, liquid paraffin, and the mineral MI+ of petrolatum.
, isopropyl myristate, pentaerythritol
Oils and oil-soluble oils commonly used in the cosmetics, pharmaceutical, and food industries, such as ester oils such as tetra-2-ethyl hegisanate, vitamin A palmitate, and vitamin E acetate, and silicone oils such as methylphenyl silicone and dimethyl silicone. It is desirable to be able to list drugs.
本発明による前記乳化組成物には、上記の必須構成成分
の他、使用]」的に合わせて、非イオン界面活性剤、ア
ニAン界面活性剤、カヂオン界面活性剤、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 includes a nonionic surfactant, an anionic surfactant, a cationic surfactant, an amphoteric surfactant, and a drug. , 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.
多価アルコール中にサポニンまたはその塩を溶解し、攪
拌しながら、油相成分を徐々に添加すれば乳化組成物が
得られる。この場合、ホモミキサー処理を行うことが好
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。An emulsified composition can be obtained by dissolving saponin or its salt in a polyhydric alcohol and gradually adding the oil phase components 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、 先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、食用ゼリー、薬用ゼ
リー・マツサージ′ゼリー・潤滑油などとして、食品、
化粧品、薬品、飼料などあらゆる分野において好適に使
用することができる。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, it can be used as sun care jelly, serum, edible jelly, medicated jelly, pine surge jelly, lubricating oil, etc.
It can be suitably used in all fields such as cosmetics, medicine, and feed.
次に、上記サポニンまたはその塩の一種または二種以上
と、分子内に二個以上の水酸基を有する乳化組成物が得
られる。この場合、ホモミキサー処理を行うことが好ま
しい。Next, an emulsified composition containing one or more of the saponins or their salts and two or more hydroxyl groups in the molecule is obtained. In this case, it is preferable to perform homomixer treatment.
(以下余白)
上記乳化組成物と水の量的関係につい−では・極めで広
範囲な割合でエマルションを生成することが可能である
が、一般的には乳化組成物5〜80部水95〜20部で
ある。(Left below) Regarding the quantitative relationship between the emulsifying composition and water, it is possible to produce an emulsion in an extremely wide range of proportions, but generally the emulsifying composition is 5 to 80 parts water, 95 to 20 parts. Department.
上記の水には必要に応じて湿潤剤、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
溶解することができる。The above water may contain moisturizing agents, water-soluble vitamins, water-soluble preservatives, water-soluble drugs, water-soluble polymers, etc. as necessary for cosmetics,
It can dissolve aqueous phase components commonly used in the pharmaceutical, food, and other industries.
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、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、界面活性剤などを添加する口とによっても、乳液、
クリーム、ファウンデイションなどあ化粧品、シャンプ
ー、すI)
ンスなどのトイレター−製品、尿素クリーム、アタネク
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ととができる。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 its original form as well as having homogeneity stabilization, viscosity adjustment, or medicinal effects. In addition, other water-soluble polymers, drugs, surfactants, etc. can be added to make emulsions,
It can be suitably used in all fields such as cosmetics such as creams and foundations, toilet products such as shampoos and soaps, pharmaceuticals such as urea cream and oilseed cream, and foods such as mayonnaise.
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。Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples. The present invention is not limited to this.
実施例1〜9、比較例1〜3、
サポニン、多価アルコール、および油相成分を表−1に
示す配合組成及び量で配合し、70℃でホモミキサー処
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、評価し、
それらの結果を表−1に示した。なお、各成分の数字は
重量%である。Examples 1 to 9, Comparative Examples 1 to 3, saponin, polyhydric alcohol, and oil phase components were blended in the composition and amount 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. Observe the state of the emulsified composition and oil-in-water emulsified composition, measure and evaluate the characteristic values,
The results are shown in Table-1. Note that the numbers for each component are weight %.
多価アルコールを含まない、比較例1.3や大量の水に
多価アルコールを溶解し、これに油分を乳化する通常の
乳化法である比較例2では、良い乳化が見られなかった
。これに対して、本発明に係る実施例1〜9では、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れ、さらに、水を加えて得
られた水中油型乳化組成物は、非常に微細粒子の油滴の
分散した安定なエマルションであった。Good emulsification was not observed in Comparative Example 1.3, which does not contain polyhydric alcohol, and Comparative Example 2, which is a conventional emulsification method in which polyhydric alcohol is dissolved in a large amount of water and oil is emulsified therein. On the other hand, in Examples 1 to 9 according to the present invention, very good transparent or translucent viscous liquids or gels were obtained at all levels, and furthermore, the The oil emulsion composition was a stable emulsion with very fine oil droplets dispersed therein.
(以下余白)
表−1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。(The following is a blank space) ■ The condition of the oil-in-water emulsion composition in Table 1 was judged based on the following criteria after being left for one day.
◎ 乳化粒子径1μ以下
0 1〜5μ
△ 5〜10 μX
10μ以上
(以下余白)
実施例10 美容ゼリー
(重量%)
(Δ)ニンジンサポニン 2
0ルスクス抽出物 f−
0グリセリン(局方) 45
.0フンドロイチン硫酸ナトリウム 0
.2アデノシン三リン酸 0・
2(B)ホホバ油
20・0ペンタエリスリトールテトラ2エチルヘキサネ
ート 2α6ワセリン
&0ビタミンAバルミテー)
LOα−トコフェロール
1.0防腐剤 0.5
香 料
0.5(A)相を70 °Cで充分攪拌し、(B)を
70℃で溶解したものを(A)相に攪拌しながら添加し
た。これをホモミキサー処理し、攪拌冷却し美容ゼリー
を得たコ日月
この美容ゼリーは粘稠でクリーム状の透電ゲルであり、
安全性が高くかつ経時安定性の優れた乳化組成物で、皮
膚に塗布したとき、非常にのびが良く、少量にて広範囲
に拡がる使用特性を有していた0
実施例11 エモリエント乳液
(重量%)
(A)ジグリセリン 10・
0マルチト一ル75%水溶液 10.01
.3ブチレングリコール 5・0チクセ
ツニンジン抽出物3.0
オンジ抽出物 LOビタミ
ンB6塩酸塩 0.2アラントイン
0.2水酸化カルシウム
0.06(E)オリーブ油
lα0(2−オクチル)
ドデシルパルミテート5.0ワセリン
&0エチニルエストラジオール
α1防腐剤 α4
香 料 0
3(0)精製水 5L44カルボキ
シビニルポリマー 02ヒアルロン酸ナ
トリウム α1実施例10の製造法に
準じて、(A) (E)より乳化組成物を得、70℃と
し、別に調整し70℃に保っておい・た増粘剤水溶液U
で希釈分散した後、冷却し水中油型エマルションのエモ
リエント乳液を得り。この乳液の粘度は、3:l”Cで
5180cp8であり、乳化粒子径1〜3μ程度の安定
でかつなじみの良い使用感触を有し・さらに・サポニン
の薬効をも期待できる乳液であった。◎ Emulsion particle size 1 μ or less 0 1-5 μ △ 5-10 μX
10 μ or more (blank below) Example 10 Beauty jelly (% by weight) (Δ) Carrot saponin 2
0Ruscus extract f-
0 Glycerin (pharmacopoeia) 45
.. 0 Fundroitin sulfate sodium 0
.. 2 Adenosine triphosphate 0.
2(B) Jojoba oil
20.0 Pentaerythritol Tetra 2 Ethyl Hexanate 2α6 Vaseline
&0 vitamin A balmite)
LOα-tocopherol
1.0 Preservative 0.5 Flavoring
0.5 Phase (A) was sufficiently stirred at 70°C, and (B) dissolved at 70°C was added to phase (A) while stirring. This was treated with a homomixer, stirred and cooled to obtain beauty jelly.This beauty jelly is a viscous, creamy, electrically conductive gel.
It was an emulsion composition that was highly safe and had excellent stability over time, and when applied to the skin, it spread very well and had the property of being used over a wide range with a small amount.Example 11 Emollient emulsion (wt%) ) (A) Diglycerin 10.
0 Multitol 75% aqueous solution 10.01
.. 3 Butylene glycol 5.0 Ginseng extract 3.0 Onji extract LO vitamin B6 hydrochloride 0.2 Allantoin 0.2 Calcium hydroxide 0.06 (E) Olive oil
lα0 (2-octyl)
dodecyl palmitate 5.0 vaseline
&0 ethinyl estradiol
α1 Preservative α4 Flavoring 0
3 (0) Purified water 5L44 carboxyvinyl polymer 02 Sodium hyaluronate α1 According to the manufacturing method of Example 10, an emulsion composition was obtained from (A) and (E), and the temperature was adjusted to 70°C, and the temperature was adjusted separately and kept at 70°C. Oi・ta thickener aqueous solution U
After diluting and dispersing, the mixture is cooled to obtain an emollient oil-in-water emulsion. The viscosity of this emulsion was 5180 cp8 at 3:1''C, and the emulsion had a stable emulsion particle size of about 1 to 3 μm and a familiar texture, and was also expected to have the medicinal effects of saponin.
実施例認 マツサージクリーム
(重量%)
(A)ソルビトール70%水溶液 22
.0グルコース 5,
0精製サポニン 5.0(
B)流動パラフィン 450グ
リセリルトリステアレート 5.
0グリセリルトリオレート 5.0
防腐剤 α5
香 料 0
.3(0)精製水 110アルギン
酸ナトリウム α2実施例11の製
造法に準じて・マツ1−ジクIJ−ムを得た。このマツ
サージクリームは、25℃硬度が8であり、やや透明感
があり、また乳化粒子径がQ、5〜3μの安定性の良い
水中油型乳化組成物で、かつ、皮膚をマツサージしたと
き、マツサージの回数によりのびの変化が少ない使用感
触をもっていた。Example pine surge cream (% by weight) (A) Sorbitol 70% aqueous solution 22
.. 0 glucose 5,
0 Purified Saponin 5.0 (
B) Liquid paraffin 450 glyceryl tristearate 5.
0 Glyceryl triolate 5.0
Preservative α5 Flavor 0
.. 3(0) Purified water 110 Sodium alginate α2 According to the manufacturing method of Example 11, Pine 1-diku IJ-me was obtained. This pine surge cream is a highly stable oil-in-water emulsion composition with a hardness of 8 at 25°C, a slightly transparent feeling, and an emulsion particle size of Q, 5 to 3μ, and when the skin is pine surged. It had a feeling of use with little change in spread depending on the number of pine surges.
特許出願人 株式会社 資 生 堂patent applicant Shiseido Co., Ltd.
Claims (2)
と、分子内に二個以上の水酸基を有する水溶性多価アル
コールと、油相成j分とを含有することを特徴とする乳
化組成物◇(1) An emulsified composition containing one or more saponins or salts thereof, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, and an oil phase component◇
と、分子内に二個以上の水酸基を有する水溶性多価アル
コールと、油相成夕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。(2) An emulsified composition containing one or more saponins or salts thereof, a water-soluble polyhydric alcohol having two or more hydroxyl groups in the molecule, an oil phase composition, and water. Characteristic oil-in-water emulsion composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57117494A JPS597106A (en) | 1982-07-06 | 1982-07-06 | Emulsifiable composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57117494A JPS597106A (en) | 1982-07-06 | 1982-07-06 | Emulsifiable composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS597106A true JPS597106A (en) | 1984-01-14 |
JPH0364185B2 JPH0364185B2 (en) | 1991-10-04 |
Family
ID=14713114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57117494A Granted JPS597106A (en) | 1982-07-06 | 1982-07-06 | Emulsifiable composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS597106A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61171406A (en) * | 1985-01-23 | 1986-08-02 | Kanebo Ltd | Emulsion type cosmetic |
JPS61194030A (en) * | 1985-02-25 | 1986-08-28 | Shiseido Co Ltd | Cosmetic |
JPS61210009A (en) * | 1985-03-14 | 1986-09-18 | Shiseido Co Ltd | External preparation for skin |
JPS61236732A (en) * | 1985-04-05 | 1986-10-22 | フイデイ−ア・ソシエタ・ペル・アチオニ | Novel local medicine |
JPS61289008A (en) * | 1985-06-14 | 1986-12-19 | Shiseido Co Ltd | Cosmetic |
JPS62209009A (en) * | 1986-03-10 | 1987-09-14 | Kobayashi Kooc:Kk | Cosmetic |
JP2004519411A (en) * | 2000-03-28 | 2004-07-02 | ビルケン ゲーエムベーハー | Emulsion containing plant extract, method for producing said emulsion and method for obtaining plant extract |
FR2945936A1 (en) * | 2009-05-26 | 2010-12-03 | Jean Claude Epiphani | Preparing aqueous emulsion of oily active substance, useful for e.g. cosmetic and food use, comprises mixing hydrophilic component (water and saponin emulsifier), mixing lipophilic components (substance and stabilizer) and homogenizing |
CN103655378A (en) * | 2013-12-25 | 2014-03-26 | 常熟市双平宠物用品厂 | Pet shampoo |
US11083733B2 (en) | 2018-01-04 | 2021-08-10 | Amryt Research Limited | Betulin-containing birch bark extracts and their formulation |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5488879A (en) * | 1977-12-26 | 1979-07-14 | Nippon Saafuakutanto Kougiyou | Selffemulsified oil composition |
JPS5742326A (en) * | 1980-07-25 | 1982-03-09 | Oreal | Stable o/w type emulsion |
-
1982
- 1982-07-06 JP JP57117494A patent/JPS597106A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5488879A (en) * | 1977-12-26 | 1979-07-14 | Nippon Saafuakutanto Kougiyou | Selffemulsified oil composition |
JPS5742326A (en) * | 1980-07-25 | 1982-03-09 | Oreal | Stable o/w type emulsion |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61171406A (en) * | 1985-01-23 | 1986-08-02 | Kanebo Ltd | Emulsion type cosmetic |
JPH0552287B2 (en) * | 1985-01-23 | 1993-08-05 | Kanebo Ltd | |
JPH0469615B2 (en) * | 1985-02-25 | 1992-11-06 | Shiseido Co Ltd | |
JPS61194030A (en) * | 1985-02-25 | 1986-08-28 | Shiseido Co Ltd | Cosmetic |
JPS61210009A (en) * | 1985-03-14 | 1986-09-18 | Shiseido Co Ltd | External preparation for skin |
JPS61236732A (en) * | 1985-04-05 | 1986-10-22 | フイデイ−ア・ソシエタ・ペル・アチオニ | Novel local medicine |
JPS61289008A (en) * | 1985-06-14 | 1986-12-19 | Shiseido Co Ltd | Cosmetic |
JPS62209009A (en) * | 1986-03-10 | 1987-09-14 | Kobayashi Kooc:Kk | Cosmetic |
JP2004519411A (en) * | 2000-03-28 | 2004-07-02 | ビルケン ゲーエムベーハー | Emulsion containing plant extract, method for producing said emulsion and method for obtaining plant extract |
FR2945936A1 (en) * | 2009-05-26 | 2010-12-03 | Jean Claude Epiphani | Preparing aqueous emulsion of oily active substance, useful for e.g. cosmetic and food use, comprises mixing hydrophilic component (water and saponin emulsifier), mixing lipophilic components (substance and stabilizer) and homogenizing |
CN103655378A (en) * | 2013-12-25 | 2014-03-26 | 常熟市双平宠物用品厂 | Pet shampoo |
US11083733B2 (en) | 2018-01-04 | 2021-08-10 | Amryt Research Limited | Betulin-containing birch bark extracts and their formulation |
US11266660B2 (en) | 2018-01-04 | 2022-03-08 | Amryt Research Limited | Betulin-containing birch bark extracts and their formulation |
US11826374B2 (en) | 2018-01-04 | 2023-11-28 | Amryt Research Limited | Betulin-containing birch bark extracts and their formulation |
Also Published As
Publication number | Publication date |
---|---|
JPH0364185B2 (en) | 1991-10-04 |
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