JPS6042317A - Cosmetics - Google Patents

Cosmetics

Info

Publication number
JPS6042317A
JPS6042317A JP58149679A JP14967983A JPS6042317A JP S6042317 A JPS6042317 A JP S6042317A JP 58149679 A JP58149679 A JP 58149679A JP 14967983 A JP14967983 A JP 14967983A JP S6042317 A JPS6042317 A JP S6042317A
Authority
JP
Japan
Prior art keywords
oil
protein
cosmetic
cosmetics
powder
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
JP58149679A
Other languages
Japanese (ja)
Other versions
JPH0520406B2 (en
Inventor
Yuzo Higaki
桧垣 勇三
Toshihisa Okamura
岡村 敏尚
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.)
Nisshin Oillio Group Ltd
Original Assignee
Nisshin Oil Mills 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 Nisshin Oil Mills Ltd filed Critical Nisshin Oil Mills Ltd
Priority to JP58149679A priority Critical patent/JPS6042317A/en
Publication of JPS6042317A publication Critical patent/JPS6042317A/en
Publication of JPH0520406B2 publication Critical patent/JPH0520406B2/ja
Granted 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
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/062Oil-in-water 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • 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)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dermatology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To provide a cosmetic having excellent safety, comfortable feeling to the skin, and high emulsion stability, by using a protein or partially hydrolyzed protein as an emulsifier, emulsifying and dispersing a cosmetic oil and additive with the emulsifier, and spray-drying the emulsion. CONSTITUTION:The objective cosmetic containing powdery particles composed of the shell made of protein and the core made of oil and additive, is obtained by spray-drying an O/W-type emulsion composed of (A) an aqueous phase comprising an aqueous solution of a protein or a partially hydrolyzed protein obtained by hydrolyzing the protein with protease and (B) an oil phase comprising a cosmetic oil (e.g. mixed glyceride of octanoic acid and decanoic acid) and additives such as antioxidants, vitamins, hormones, preservatives, etc. The protein of the shell has high safety, is suitable as an emulsifier for cosmetics, and has extremely excellent feeling to the skin. Since the composition is emulsified by the user before use, a high emulsion stability is not necessary, and the agent can be stored for a long period.

Description

【発明の詳細な説明】 本発明は新規な化粧料に係る。[Detailed description of the invention] The present invention relates to a novel cosmetic.

一般に化粧品は化粧品用油剤に適当な添加剤を配合し、
乳化剤で乳化した水系タイプと、顔料に化粧品用油剤、
添加剤を加えて、混練した固形タイプに分類される。
Cosmetics are generally made by blending cosmetic oils with appropriate additives.
Water-based type emulsified with emulsifier, pigment and cosmetic oil,
It is classified as a solid type that is kneaded with additives.

これに用いられる化粧品用油剤として、従来多く使用さ
れているものは、ヒマシ油、木ろう、ラノリン、蜜ろう
、スクヮラン、オリーブ油、ホホバ油等の動植物油脂、
イソプロピルミリスタート、ミリスチン酸オクチルドデ
シル、オクタン酸・デカン酸混合グリセリド、イソオク
タン酸グリセリド、シリコーンオイル等の合成油、セレ
シン、流動パラフィン等の鉱物油がある。しかしながら
、これらは油性であるため、酸化安定性が悪かったり、
取扱いがめんどうな場合がある また従来使われている乳化剤は安全性、皮膚感、乳化安
定性等が必らずしも満足すべきものではないため化粧料
の製造上、種々の難点がある。
The most commonly used cosmetic oils are castor oil, wood wax, lanolin, beeswax, squalane, olive oil, jojoba oil, and other animal and vegetable oils.
There are synthetic oils such as isopropyl myristate, octyldodecyl myristate, octanoic acid/decanoic acid mixed glyceride, isooctanoic acid glyceride, silicone oil, and mineral oils such as ceresin and liquid paraffin. However, since these are oil-based, they have poor oxidation stability and
In addition, conventionally used emulsifiers are not always satisfactory in terms of safety, skin feel, emulsion stability, etc., and therefore have various difficulties in the production of cosmetics.

本発明の目的は、製造に際して上記のような欠点のない
化粧料を提供することを目的とする。
An object of the present invention is to provide a cosmetic that does not have the above-mentioned drawbacks during production.

本発明者らは鋭意研究の結果1.たん白またはこれをた
ん自分解酵素で加水分解処理した部分加水分解たん白を
乳化剤として用い、これに化粧品用油剤および添加剤を
乳化・分散させ、引続き噴霧乾燥することにより、上記
の目的が達成されることを見い出した。
As a result of intensive research by the present inventors, 1. The above purpose is achieved by using protein or partially hydrolyzed protein obtained by hydrolyzing it with a proteolytic enzyme as an emulsifier, emulsifying and dispersing cosmetic oils and additives therein, and then spray-drying. I found out that it can be done.

本発明は、かかる知見に基づいて完成されたもので、た
ん白またはこれをたん自分解酵素で加水分解した部分加
水分解たん白の水溶液を水相とし、化粧品用油剤および
抗酸化剤、ビタミン剤、ホルモン剤、薬剤、防腐・防菌
剤、香料等の添加剤を油相とする水中油型乳化物を噴霧
乾燥することにより得られる、外殻がたん白であり、内
部が油剤および添加剤である粉末を含有してなる化粧料
である。
The present invention was completed based on this knowledge, and uses an aqueous solution of protein or partially hydrolyzed protein obtained by hydrolyzing it with a protein autolytic enzyme as an aqueous phase, and uses a cosmetic oil, an antioxidant, and a vitamin preparation. , obtained by spray drying an oil-in-water emulsion containing additives such as hormones, drugs, preservatives and antibacterial agents, and fragrances as the oil phase.The outer shell is protein and the interior contains oil and additives. This is a cosmetic containing powder.

本発明で使用するたん白としては、大豆、ひまわり等か
ら得られる植物性たん白、ゼラチン、カゼイン等の動物
性たん白を挙げることができる。
Examples of the protein used in the present invention include vegetable proteins obtained from soybeans, sunflowers, etc., and animal proteins such as gelatin and casein.

また上記たん白をたん自分解酵素で加水分解処理した部
分加水分解たん白も使用できる。部分加水分解たん白は
常法によって得られるたん白を塩酸などの酸やペプシン
、パパインなどのたん自分解酵素で部分加水分解したも
のを用いる。
Partially hydrolyzed proteins obtained by hydrolyzing the above-mentioned proteins with protein hydrolytic enzymes can also be used. Partially hydrolyzed protein is obtained by partially hydrolyzing protein obtained by conventional methods with an acid such as hydrochloric acid or a protein hydrolytic enzyme such as pepsin or papain.

カゼインやセラヂンはそれ自体の感触が重く、またこれ
らを用いた乳化液は高い粘性を示し、噴霧乾燥するため
には水分を70〜90%程度に高め、粘性を下げる必要
がある。このため噴霧乾燥するときのエネルギー費用も
大きくなるが、感触的に重く、被膜感を出す化粧料とす
る場合には、カゼインやゼラチンが好ましい。一般的に
は原料、色相、臭気、感触等の面からはたん白として大
豆たん白が良好である。さらには乳化性、分散性、化粧
品としての感触等の面から、常法によって得られる抽出
大豆たん白、濃縮大豆たん白及び分離大豆たん白を部分
加水分解したものが良好である。
Casein and celadin themselves have a heavy feel, and emulsions made of them exhibit high viscosity, and in order to spray dry them, it is necessary to increase the water content to about 70 to 90% and lower the viscosity. For this reason, the energy cost during spray drying increases, but casein and gelatin are preferable for cosmetics that are heavy to the touch and have a filmy feel. Generally, soybean protein is a good protein in terms of raw material, color, odor, texture, etc. Furthermore, from the viewpoint of emulsifying properties, dispersibility, feel as a cosmetic, etc., it is preferable to use partially hydrolyzed extracted soy protein, concentrated soy protein, and isolated soy protein obtained by conventional methods.

ここで部分加水分解の条件は、塩酸の場合、1〜5%の
たん自分散溶液を用い塩素濃度0.3〜3%、分解温度
75〜95°Cの範囲に1〜50時間程度保つものであ
る。またたん自分解酵素の場合は1〜5%のたん自分数
溶液を用い、酵素量は固形分に対し0.03〜0.3%
とし当該酵素の最適pHおよび最適温度で1〜50時間
に保つ。
In the case of hydrochloric acid, the conditions for partial hydrolysis are to use a 1 to 5% phlegm dispersion solution, maintain the chlorine concentration at 0.3 to 3%, and the decomposition temperature in the range of 75 to 95°C for about 1 to 50 hours. It is. In addition, in the case of protein hydrolytic enzyme, a 1 to 5% protein solution is used, and the enzyme amount is 0.03 to 0.3% based on the solid content.
and keep at the optimum pH and temperature for the enzyme for 1 to 50 hours.

部分加水分解の程度は20%の三塩化酢酸水溶液に対す
るたん白質の溶解率(以下TCA可溶率と言う)で示し
、本発明においてはTCA可溶率が10〜60重量%の
ものが好ましい。TCA可溶率が60%以上になると、
乳化性が減少し、包接機能も低下する。
The degree of partial hydrolysis is indicated by the solubility of the protein in a 20% trichloroacetic acid aqueous solution (hereinafter referred to as TCA solubility), and in the present invention, it is preferable that the TCA solubility is 10 to 60% by weight. When the TCA solubility is 60% or more,
The emulsifying property is reduced and the inclusion function is also reduced.

部分加水分解大豆たん白の乳化力は大きく、少量の部分
加水分解大豆たん白で水と油剤を乳化させることが可能
である。すなわち部分加水分解大豆たん白を用いた場合
は油分含量を90〜92%程度(被覆物質:油分−1:
9〜12)にまで高めることが可能である。
Partially hydrolyzed soy protein has a large emulsifying power, and it is possible to emulsify water and oil with a small amount of partially hydrolyzed soy protein. In other words, when partially hydrolyzed soybean protein is used, the oil content is approximately 90 to 92% (coating material: oil -1:
9 to 12).

また常法の大豆たん白は、一般ににおいや色調が劣るが
、本発明者らはさらに含水アルコールを用いて有臭成分
や色素を除いた大豆たん白を原料として部分加水分解を
行った大豆たん白は、これらの問題点をも解決すること
を見い出した。含水アルコールの好ましい濃度は50〜
90W/W%である。
In addition, conventional soy protein is generally inferior in odor and color, but the present inventors have further developed a soy protein that has been partially hydrolyzed using hydroalcohol to remove odor components and pigments. White has found a solution to these problems as well. The preferred concentration of hydroalcohol is 50~
It is 90W/W%.

本発明で使用される化粧品用油剤は、一般に使用されて
いる動植物油脂であるヒマシ油、木ろう、ジノリン、蜜
ろう、スクヮラン、オリーブ油、ホホバ油等、合成油で
あるイソプロピルミリスタート、ミリスチン酸オクチル
ドデシル、オクタン酸・デカン酸混合グリセリド、イソ
オクタン酸グリセリド、ジイソステアリン酸ジグリセリ
ド、トリイソステアリン酸ジグリセリド、リンゴ酸ジイ
ソステアリル、シリコーンオイル等、鉱物性であるセレ
シン、m動パラフィン、固形パラフィン等がある。また
これらの2種以上の混合物でもかまわない。
The cosmetic oils used in the present invention include commonly used animal and vegetable oils such as castor oil, wood wax, dinoline, beeswax, squalane, olive oil, and jojoba oil, and synthetic oils such as isopropyl myristate and octyl myristate. Examples include dodecyl, octanoic acid/decanoic acid mixed glyceride, isooctanoic acid glyceride, diisostearic acid diglyceride, triisostearic acid diglyceride, diisostearyl malate, silicone oil, mineral ceresin, m-dynamic paraffin, solid paraffin, and the like. Also, a mixture of two or more of these may be used.

本発明で使用される化粧品用添加剤はビタミンA1ビタ
ミンE1ビタミンEアセテート、ビタミンCステアラー
ド、ビタミンCパルミテート等のビタミン顧およびその
誘導体、BHA、BHT。
Cosmetic additives used in the present invention include vitamins such as vitamin A, vitamin E, vitamin E acetate, vitamin C stearard, vitamin C palmitate, and derivatives thereof, BHA, and BHT.

トコフェロール等の抗酸化剤、P−メトキシ桂皮酸オク
チル、オリザノール、グリチルリチン誘導体、各種植物
抽出物等の薬剤、卵胞ホルモン、プレグネノロン、副腎
皮質ホルモン等のホルモン類、パラオキシ安息香酸エス
テル等の防腐・防菌剤、各種香料等である。
Antioxidants such as tocopherol, drugs such as octyl P-methoxycinnamate, oryzanol, glycyrrhizin derivatives, various plant extracts, hormones such as follicle hormone, pregnenolone, and adrenal corticosteroid, and antiseptic and antibacterial agents such as paraoxybenzoic acid ester. agents, various fragrances, etc.

これらの各種添加剤は必要に応じて、化粧品用油剤に溶
解させるか、またばたん白の水溶液に化粧品用油剤と同
様に添加して用いる。同様にしてタルク、カオリン、ベ
ントナイト、マイカ、チタン等の無機顔料および各種有
機顔料を配合することも可能である。
These various additives are used by being dissolved in a cosmetic oil or added to an aqueous protein solution in the same manner as a cosmetic oil. Similarly, it is also possible to blend inorganic pigments such as talc, kaolin, bentonite, mica, titanium, and various organic pigments.

本発明は、以上の原料から次のように実施される。すな
わ、まずたん白を5〜10倍の水にとかして、たん白質
水溶液をつくる。この水溶液1部に対し0.5〜2部の
化粧品用油剤、各種添加剤を徐々に加え、ホモミキサー
などの撹拌機を用いて乳化させ水中油型乳化液をつくる
。また必要に応じてコロイドミル、高圧ホモジナイザー
などを用いて均質化を図ることも可能である。この水中
油型乳化液を噴霧乾燥することにより、外殻がたん白で
あり、内部が油剤および添加剤である粉末(以下、粉末
状カプセルという)を得る。噴霧乾燥は通常の方法によ
り、送風温度100〜130℃、排風温度60〜90℃
、品温5o〜80”cの条件で行う。
The present invention is carried out using the above raw materials as follows. In other words, first, dissolve the protein in 5 to 10 times the amount of water to create an aqueous protein solution. To 1 part of this aqueous solution, 0.5 to 2 parts of a cosmetic oil and various additives are gradually added and emulsified using a stirrer such as a homomixer to prepare an oil-in-water emulsion. Further, if necessary, it is also possible to achieve homogenization using a colloid mill, a high-pressure homogenizer, or the like. By spray-drying this oil-in-water emulsion, a powder (hereinafter referred to as powder capsule) whose outer shell is protein and whose interior is oil and additives is obtained. Spray drying is carried out using a normal method, with a blowing temperature of 100 to 130°C and an exhaust temperature of 60 to 90°C.
, and the product temperature is 5o~80''c.

本発明はこの粉末状カプセルを含有してなる化粧料であ
る。
The present invention is a cosmetic containing this powdered capsule.

本発明で得られた粉末状カプセルは外殻がたん白でおお
われ、内部に化粧品用油剤および添加剤を分散させたも
のであり、圧力をかけることにより、内部にある油剤が
流出し、液状となり、またさらに水を加えることにより
、外殻のたん白が乳化剤として働き自己乳化するもので
ある。従ってこのカプセルから自由に、何時でも乳化型
化粧料を得ることができる。そのため、基礎化粧品の・
クリーム、乳液、化粧水等を手軽に自由に水で希釈して
調合することができる。。
The powdered capsule obtained by the present invention has an outer shell covered with protein and a cosmetic oil and additives dispersed inside. When pressure is applied, the oil inside flows out and becomes liquid. Furthermore, by adding water, the protein in the outer shell acts as an emulsifier and self-emulsifies. Therefore, emulsified cosmetics can be obtained freely from these capsules at any time. Therefore, basic cosmetics
Creams, milky lotions, lotions, etc. can be easily and freely diluted with water and prepared. .

また本発明の特長のひとつは、化粧品用油剤中に、抗酸
化剤、ビタミン剤、ホルモン剤、薬剤、防腐・防菌剤、
香料等の添加剤を混合できるため粉末状の状態で、これ
らを含有した化粧料を得られることである。また本発明
の特長のひとつは、たん白を粉末状カプセルの外殻とし
て用いておりかつ、そのたん白が乳化剤として作用する
ものであることから、従来一般的に使われている乳化剤
の欠点である安全性、皮膜感等も改良できる。
In addition, one of the features of the present invention is that cosmetic oils contain antioxidants, vitamins, hormones, drugs, preservatives and antibacterial agents,
Since additives such as fragrances can be mixed in, cosmetics containing these can be obtained in powder form. Another feature of the present invention is that protein is used as the outer shell of the powdered capsule, and the protein acts as an emulsifier, which eliminates the drawbacks of conventionally commonly used emulsifiers. Certain safety, film feel, etc. can also be improved.

すなわち外殻のたん白はそれ自体安全性が高く、化粧料
用乳化剤としても最適であり、感触的にも非常に良好で
ある。またさらに使用時に自由に乳化して使用すること
から、乳化安定性はそれほど必要とせず、手のひらに本
発明の粉末状カプセルと適当量の水を添加して、手で攪
拌混練するだけで、目的の化粧料を得ることができる。
That is, the protein in the outer shell itself is highly safe, is optimal as an emulsifier for cosmetics, and has a very good texture. Furthermore, since it can be freely emulsified and used, emulsion stability is not so necessary, and the powdered capsules of the present invention and an appropriate amount of water can be added to the palm of the hand and stirred and kneaded by hand. cosmetics can be obtained.

またさらに粉末状カプセルであるため、1回の使用量を
分包することが容易であり、またたん白で被覆されてい
ることから、空気、光等の遮断がし易く長期保存も可能
となる特長も有している。従ってまた安定性の悪い化粧
品用油剤、添加剤も使用できる。
Furthermore, since it is a powder capsule, it is easy to package the amount for one time use, and since it is coated with protein, it is easy to block air and light, making it possible to store it for a long time. It also has some features. Therefore, cosmetic oils and additives with poor stability can also be used.

一方メイクアソプ化粧品においては、使用時に本発明の
粉末状カプセルを破壊させて使用することにより、従来
にない新しいジイソの化粧料が得られる。例えば、顔料
と本発明粉末状カプセルを混練することにより、自由に
色調、濃度、油性感を調整することができる。そのため
、使用者は好みの色相、好みの感触のものを使用時の好
みで調合できる。
On the other hand, in the case of make-up cosmetics, by destroying the powdered capsules of the present invention before use, a new diiso cosmetic that has never existed before can be obtained. For example, by kneading the pigment and the powdered capsule of the present invention, the color tone, density, and oiliness can be freely adjusted. Therefore, the user can mix the desired hue and feel according to their preference at the time of use.

また本発明の粉末状カプセルを一般の化粧品原料として
使用することも可能である。その場合には通常の処方で
使用でき、たん白の乳化性と用いた油剤等の特徴を利用
して、多くの化粧料が得られる。
It is also possible to use the powdered capsules of the present invention as raw materials for general cosmetics. In that case, it can be used in a normal formulation, and many cosmetics can be obtained by taking advantage of the emulsifying properties of the protein and the characteristics of the oil used.

以下に実施例を示す。Examples are shown below.

実施例1 ゼラチン(@ニソピ製、ゼラチンPBF)300gに温
水41を加え、ホモミキサーで分散させた。
Example 1 Warm water 41 was added to 300 g of gelatin (Gelatin PBF, manufactured by Nisopi) and dispersed using a homomixer.

一方ビタミンCステアラード40gをジイソステアリン
酸ジグソセリン800gで加熱溶解させた。
On the other hand, 40 g of vitamin C stearard was heated and dissolved in 800 g of jigsoserine diisostearate.

ゼラチン水溶液に前記ビタミンCステアラード溶解油剤
をホモミキサーを用いて5000 r、p、m テ攪拌
しながら添加し、水中油型乳化液を得、さらに高圧ホモ
ジナイザー(圧力ニ 100 kg/cffl)で均質
化した。次いでこれを噴霧乾燥機(蒸発水分量50kg
/h)にかけ、送風温度120℃、排風a度90℃、溶
液処理量100 kg / hの条件で粉末状カプセル
を得た。このものは直径20〜60μの均一な粉体で油
のにじみは全く見られなかった。
The vitamin C stearard-dissolved oil was added to the gelatin aqueous solution while stirring at 5000 r, p, m using a homomixer to obtain an oil-in-water emulsion, which was further homogenized using a high-pressure homogenizer (pressure: 100 kg/cffl). did. This was then dried in a spray dryer (evaporated water content: 50 kg).
/h) to obtain powder capsules under conditions of a blowing temperature of 120°C, an exhaust air temperature of 90°C, and a solution throughput of 100 kg/h. This powder was a uniform powder with a diameter of 20 to 60 μm, and no oil bleed was observed at all.

上記粉末状カプセルは水を添加するだけで手のひらで簡
単に乳化物が出来、簡便な粉末状の栄養クリームが得ら
れた。
The above powdered capsules could be easily emulsified in the palm of the hand by simply adding water, resulting in a convenient powdered nutritional cream.

実施例2 Zカゼインソーダ300gに温水5βを加え、ホモミキ
サーで分散させ、これとは別に、蜜ろう50g1ラノリ
ン50g1流動パラフィン300g、イソオクタン酸ト
リグ、ソセリド400g、ビタミンE10g、エチルパ
ラベン2g1香料適量を混合溶解した油相を5000 
r、p、m i?攪拌しながらカゼインソーダ溶液に添
加し、水中油型乳化液を得、さらに高圧ホモジナイザー
(圧力ニ 50kg / cJ )で均質化した。次い
でこれを噴霧乾燥機(蒸発水分量50kg / h )
にかけ、送風温度110℃、排風温度70°C1溶液処
理’! 100kg/ hの条件で粉末状カプセルを得
た。このものは直径20〜50μの均一な粉体で、油の
にじみは全く見られなかった。
Example 2 Add 5β of warm water to 300 g of Z casein soda and disperse with a homomixer. Separately, 50 g of beeswax, 50 g of lanolin, 300 g of liquid paraffin, 400 g of isooctanoic acid trig, Socerid, 10 g of vitamin E, 2 g of ethyl paraben, and an appropriate amount of fragrance were mixed. 5000 ml of dissolved oil phase
r, p, m i? It was added to the casein soda solution while stirring to obtain an oil-in-water emulsion, which was further homogenized using a high-pressure homogenizer (pressure: 50 kg/cJ). This was then dried in a spray dryer (evaporated water content: 50 kg/h).
1 solution treatment'! Powdered capsules were obtained under the condition of 100 kg/h. This product was a uniform powder with a diameter of 20 to 50 μm, and no oil bleed was observed at all.

上記粉末状カプセルは水を添加するだけで手のひらで簡
単に乳化物ができ、感触も良好なりリームが得られた。
The above powdered capsules could be easily emulsified in the palm of the hand just by adding water, and had a good texture and a creamy texture.

実施例3 濃縮大豆たん白(粗たん内含量68%)500gに温水
71を加え、ホモミキサーで分散させ、一方、ラノリン
100g、流動パラフィン400g、スクヮラン400
 g、ミリスチン酸イソステアリル600g・ビタミン
Cステアラード20g、ビタミンEアセテート20g、
グリセリン20g。
Example 3 71 g of warm water was added to 500 g of concentrated soy protein (crude protein content 68%) and dispersed with a homomixer, while 100 g of lanolin, 400 g of liquid paraffin, and 400 g of squalane were added.
g, isostearyl myristate 600g, vitamin C stearard 20g, vitamin E acetate 20g,
20g of glycerin.

メチルパラベン3g、香料適量を混合溶解した油相を5
00 Or、p、mで攪拌しながら濃縮大豆たん自溶液
に添加し、水中油型乳化液を得、さらに高圧ホモジナイ
ザー(圧力50 kg/cJ)で均質化した。次いでこ
れを噴霧乾燥機(蒸発水分量50kg/h)にかけ、送
風温度110 ”c、排風温度70’C。
Mix and dissolve 3 g of methylparaben and an appropriate amount of fragrance into the oil phase.
The mixture was added to a concentrated soybean protein solution while stirring at 00 Or, p, m to obtain an oil-in-water emulsion, which was further homogenized using a high-pressure homogenizer (pressure 50 kg/cJ). Next, this was applied to a spray dryer (evaporated water content: 50 kg/h), with an air blowing temperature of 110'C and an exhaust air temperature of 70'C.

溶液処理量100kg/hの条件で粉末状カプセルを得
た。このものは直径20〜50μの均一な粉体(たん内
含量は約16%)で油のにじみは全く見られなかった。
Powdered capsules were obtained under conditions of a solution throughput of 100 kg/h. This product was a uniform powder with a diameter of 20 to 50 μm (sputum content was approximately 16%), and no oil ooze was observed at all.

上記粉末状カプセルは水を添加するだけで、手のひらで
簡単に乳化物ができ、感触も良好なりリームが得られた
The above powdered capsules could be easily emulsified in the palm of the hand by simply adding water, and had a good texture and a creamy texture.

実施例4 常法により得られる分離大豆たん白(粗たん内含量92
%)の5%水溶液100部に対し、o、005部の精製
ペプシンを加え、塩酸でpHを2.0に調整した後、液
温を50 ”cに1時間保持した。この溶液を超高温短
時間殺菌法(UHT法)で 135℃、5秒間の殺菌を
行った後、たん白濃度が10%になるよう減圧濃縮した
。得られた部分加水分解大豆たん白のTCA可溶率は2
5%であった。
Example 4 Isolated soybean protein obtained by a conventional method (crude protein content: 92
After adding 0.005 parts of purified pepsin to 100 parts of a 5% aqueous solution of 1.0%) and adjusting the pH to 2.0 with hydrochloric acid, the solution temperature was maintained at 50"C for 1 hour. This solution was heated to an ultra-high temperature. After sterilization at 135°C for 5 seconds using the short-time sterilization method (UHT method), it was concentrated under reduced pressure so that the protein concentration was 10%.The TCA solubility of the obtained partially hydrolyzed soybean protein was 2.
It was 5%.

この濃縮液1o7!をホモミキサーを用いて5000r
、p、mで攪拌を続けながら、ジメヂルシリコン(信越
化学工業O1l製、KF96−50) 5.0kgを徐
々に添加し、水中油型乳化液を得、さらに高圧ホモジナ
イザー(圧力ニ 100 kg/ci)で均質化した。
This concentrate is 1o7! 5000r using a homomixer
While continuing to stir at , p, and m, 5.0 kg of dimedyl silicone (manufactured by Shin-Etsu Chemical O1l, KF96-50) was gradually added to obtain an oil-in-water emulsion. It was homogenized with

次゛いでこれを噴霧乾燥8M (蒸発水分t100kg
/ h ) ニカ4:t、送風温度120’c、排風温
度90’C1溶液処理量100kg/h)の条件で粉末
状カプセルを得た。このものは直径30〜70μの均一
な粉体で、油のにじみは全く見られなかった。得らレタ
粉末状カプセルを使用して以下の配合でコンディショニ
ングリンスを作った。
Next, spray-dry this 8M (evaporated water t100kg)
/h) Powdered capsules were obtained under the following conditions: Nika 4:t, air blowing temperature 120'C, exhaust air temperature 90'C1 solution throughput 100 kg/h). This product was a uniform powder with a diameter of 30 to 70 μm, and no oil bleed was observed at all. A conditioning rinse was made using the obtained Reta powder capsules with the following formulation.

前記シリコン配合粉末状カプセル 2.5重量%ポリオ
キシエチレンコレステロール 1.0〃グリセリールモ
ノステアラード 2.0〃香料、防腐剤 適 量 実施例5 常法により得られる濃縮大豆たん白(粗たん内含量67
%)の5%水溶液に濃塩酸を加え塩酸濃度が1%となる
よう調整し、液温を85℃に10時間保持した。次に2
0%水酸化ナトリウム溶液で中和した後、実施例4と同
様に加熱殺菌・減圧濃縮した。得られた部分加水分解大
豆たん白のTCA可溶率は40%であった。この濃縮液
lOlをホモミキサーを用いて5000 r、p、mで
攪拌する。一方、オクタン酸・デカン酸混合グリセリド
6.0kg、アスコルビン酸ステアラード600 g。
Said silicon-containing powder capsule 2.5% by weight Polyoxyethylene cholesterol 1.0 Glyceryl monostearard 2.0 Flavoring agent, preservative Appropriate amount Example 5 Concentrated soy protein obtained by a conventional method (in crude protein) Content 67
%) was added to a 5% aqueous solution to adjust the hydrochloric acid concentration to 1%, and the liquid temperature was maintained at 85° C. for 10 hours. Next 2
After neutralizing with 0% sodium hydroxide solution, the mixture was heat sterilized and concentrated under reduced pressure in the same manner as in Example 4. The TCA solubility of the obtained partially hydrolyzed soybean protein was 40%. This concentrated solution 1Ol is stirred at 5000 r, p, m using a homomixer. On the other hand, 6.0 kg of octanoic acid/decanoic acid mixed glyceride and 600 g of ascorbic acid stearard.

ビタミンE300gを加熱溶融したペースト状油剤を攪
拌しながら前記濃縮液に徐々に添加し、水中油型乳化液
を得、さらに高圧ホモジナイザー(圧力ニ 100 k
g/cnl)で均質化した。次いで実施例4と同様に噴
霧乾燥し、粉末状カプセルを得た。
A paste-like oil solution prepared by heating and melting 300 g of vitamin E was gradually added to the concentrated solution while stirring to obtain an oil-in-water emulsion, and then heated using a high-pressure homogenizer (pressure 100 k).
(g/cnl). Next, spray drying was carried out in the same manner as in Example 4 to obtain powdered capsules.

このものは直径20〜60μの均一な粉体で、油のにじ
みは全く見られなかった。この粉末状カプセルは水を添
加するだけで、手のひらで簡単に乳化物ができ、感触も
良好なりリームが得られた。
This powder was a uniform powder with a diameter of 20 to 60 μm, and no oil bleed was observed at all. This powdered capsule could be easily emulsified in the palm of the hand by simply adding water, and had a good texture and a creamy texture.

実施例6 常法により得られた分離大豆たん白(粗たん内含量92
%)を5倍量の80%エタノール溶液に分散し、50℃
で1時間洗浄した。遠心分離により沈渣を得たのち、こ
れを減圧乾燥して大豆たん白粉末を得た。次にこの大豆
たん白粉末の5%水溶液100部に対し、0.01部の
ビオプラーゼ(長瀬産業側製)を加え、アンモニア水で
pl+を9.0に調整し、液温を55℃に2時間保持し
た。この溶液を実施例4と同様に加熱殺菌、減圧し、た
ん白濃度10%に濃縮した。得られた部分加水分解大豆
たん白のTCA可溶率は35%であった。この濃縮液1
o1!をホモミキサーを用いて5000r、p、IIl
で攪拌した。一方、蜜ろう300g、セタノール300
 g、ラノリン400g、スクヮラン1000g、イソ
オクタン酸トリグリセリド1500g、プロピレングリ
コール300 g、タルク200g、マイカ200g、
着色剤適量、香料適量、抗酸化剤・防腐剤適量を攪拌し
ながら前記濃縮液に加えて、水中油型乳化液を得た。次
いで実施例4と同様に噴霧乾燥し、粉末体カプセルを得
た。このものは直径20〜60μの均一な粉体で油のに
じみは全くみられなかった。化粧品用油剤の食残量は約
60%である。この粉末状カプセルは水を添加するだけ
で、手のひらで簡単に乳化物ができ、感触も良好であっ
た。
Example 6 Isolated soybean protein obtained by a conventional method (crude protein content: 92
%) in 5 times the amount of 80% ethanol solution, and heated at 50°C.
Washed for 1 hour. After obtaining a precipitate by centrifugation, this was dried under reduced pressure to obtain soybean protein powder. Next, 0.01 part of bioplase (manufactured by Nagase Sangyo) was added to 100 parts of a 5% aqueous solution of this soy protein powder, the pl+ was adjusted to 9.0 with ammonia water, and the temperature of the solution was raised to 55°C for 2 hours. Holds time. This solution was heat sterilized and depressurized in the same manner as in Example 4, and concentrated to a protein concentration of 10%. The TCA solubility of the obtained partially hydrolyzed soybean protein was 35%. This concentrate 1
o1! using a homomixer at 5000r, p, IIl
It was stirred with Meanwhile, 300g of beeswax, 300g of cetanol
g, lanolin 400g, squalane 1000g, isooctanoic acid triglyceride 1500g, propylene glycol 300g, talc 200g, mica 200g,
An appropriate amount of a coloring agent, an appropriate amount of a fragrance, and an appropriate amount of an antioxidant/preservative were added to the concentrate while stirring to obtain an oil-in-water emulsion. Next, spray drying was carried out in the same manner as in Example 4 to obtain powder capsules. This product was a uniform powder with a diameter of 20 to 60 μm, and no oil bleed was observed at all. The remaining amount of cosmetic oils is about 60%. This powdered capsule could be easily emulsified in the palm of the hand by simply adding water, and had a good feel.

実施例7 実施例6でえたTCA可溶率35%の濃縮液1゜lをホ
モミキサーを用いて5000 r、p、mで攪拌する。
Example 7 1 ml of the concentrated solution with a TCA solubility of 35% obtained in Example 6 was stirred at 5000 r, p, m using a homomixer.

攪拌しながら、イソオクタン酸トリグリセリド4kgを
徐々に添加し、水中油型乳化液を得、さらに高圧ホモジ
ナイザー(圧力ニ 100 kg/cIa)で均質化し
た。次いで実施例4と同様に噴霧乾燥し、粉末状カプセ
ルを得た。このものは直径20〜60μの均一な粉体で
、油のにじみは全(見られなかった。上記粉末状カプセ
ルを用いて以下の配合例でエモリエントクリームを得た
While stirring, 4 kg of isooctanoic acid triglyceride was gradually added to obtain an oil-in-water emulsion, which was further homogenized using a high-pressure homogenizer (pressure: 100 kg/cIa). Next, spray drying was carried out in the same manner as in Example 4 to obtain powdered capsules. This product was a uniform powder with a diameter of 20 to 60 μm, and no oil bleed was observed. Using the above powdered capsule, an emollient cream was obtained according to the following formulation example.

実施例7の粉末状カプセル 40.0重量%蜜ろう 6
.0〃 ラノリン 8.ON Nツタール 5.0〃 モノステアリン酸グリセリン 2.0〃香料、防腐剤、
酸化防止剤 適 量 特許出願人 日清製油株式会社
Powder capsule of Example 7 40.0% by weight beeswax 6
.. 0〃 Lanolin 8. ON N Tutar 5.0〃 Glycerin monostearate 2.0〃Fragrance, preservative,
Antioxidant Appropriate Amount Patent Applicant Nisshin Oil Co., Ltd.

Claims (8)

【特許請求の範囲】[Claims] (1)′ たん白またはこれをたん自分前酵素で加水分
解した部分加水分解たん白の水溶液を水相とし、化粧品
用油、剤および抗酸化剤、ビタミン剤、ホルモン剤、薬
剤、防腐・防殺菌剤、香料等の添加剤を油相とする水中
油型乳化物を噴霧乾燥することにより、得られる外殻が
たん白であり、内部が油剤および添加剤である粉末を含
有してなる化粧料。
(1) The aqueous phase is an aqueous solution of protein or partially hydrolyzed protein obtained by hydrolyzing it with proprotein enzymes, and is used to produce cosmetic oils, agents, antioxidants, vitamins, hormones, drugs, and preservatives. Cosmetics whose outer shell is protein and whose inner shell contains oil and additive powder by spray-drying an oil-in-water emulsion containing additives such as disinfectants and fragrances as the oil phase. fee.
(2)たん白が大豆たん白である特許請求の範囲第1項
記載の化粧料。
(2) The cosmetic according to claim 1, wherein the protein is soybean protein.
(3)部分加水分解した大豆たん白の原料が含水アルコ
ールを用いて色素、有臭成分などを除去した大豆たん白
である特許請求の範囲第1項記載の化粧料。
(3) The cosmetic according to claim 1, wherein the raw material of partially hydrolyzed soybean protein is soybean protein from which pigments, odorous components, etc. have been removed using hydroalcohol.
(4)粉体中のたん内含有量が10〜50重量%である
特許請求の範囲第1項記載の化粧料。
(4) The cosmetic according to claim 1, wherein the sputum content in the powder is 10 to 50% by weight.
(5) 化粧品用油剤として、流動パラフィン、オクタ
ン酸・デカン酸混合グリセリド、イソオクタン酸トリグ
リセリド、ジグリセリンイソステアリン酸エステル、ス
クアラン、オリーブ油、シリコーンオイルのうちの1種
または2種以上を用いる特許請求の範囲第1項記載の化
粧料。
(5) Claims that use one or more of liquid paraffin, octanoic acid/decanoic acid mixed glyceride, isooctanoic acid triglyceride, diglycerin isostearate, squalane, olive oil, and silicone oil as a cosmetic oil agent. Cosmetics according to item 1.
(6) 粉末中の化粧品用油剤の含有量が50〜90重
景%である特許請求の範囲第1項記載の化粧料。
(6) The cosmetic composition according to claim 1, wherein the content of the cosmetic oil in the powder is 50 to 90% by weight.
(7)化粧品用油剤としてオクタン酸・デカン酸混合グ
リセリド、イソオクタン酵グリセリド、ジグリセリンイ
ソステアリン酸エステルのいずれかからなり、かつ添加
剤としてアスコルビン酸脂肪酸エステルを添加し、粉末
中のたん内含量が10〜50重量パーセント、化粧品用
油剤の含量が50〜90重itパーセント、アスコルビ
ン酸エステル含量が1.0〜15.0重量パーセントで
ある特許請求のl1IIIIlF!1項記載の化粧料。
(7) The oil agent for cosmetics is made of octanoic acid/decanoic acid mixed glyceride, isooctane-fermented glyceride, or diglycerin isostearate, and ascorbic acid fatty acid ester is added as an additive, and the phlegm content in the powder is 10. ~50 weight percent, the cosmetic oil content is 50-90 weight percent, and the ascorbic acid ester content is 1.0-15.0 weight percent! Cosmetics according to item 1.
(8)水中油型乳化物に□マイカ、タルク、カオリン等
の顔料を分散させてなる特許請求の@間第1項記載の化
粧料。
(8) The cosmetic according to claim 1, wherein a pigment such as mica, talc, kaolin, etc. is dispersed in an oil-in-water emulsion.
JP58149679A 1983-08-18 1983-08-18 Cosmetics Granted JPS6042317A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58149679A JPS6042317A (en) 1983-08-18 1983-08-18 Cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58149679A JPS6042317A (en) 1983-08-18 1983-08-18 Cosmetics

Publications (2)

Publication Number Publication Date
JPS6042317A true JPS6042317A (en) 1985-03-06
JPH0520406B2 JPH0520406B2 (en) 1993-03-19

Family

ID=15480451

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58149679A Granted JPS6042317A (en) 1983-08-18 1983-08-18 Cosmetics

Country Status (1)

Country Link
JP (1) JPS6042317A (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63254180A (en) * 1987-04-09 1988-10-20 Kobayashi Kooc:Kk Antioxidant composition
JPS6462373A (en) * 1987-09-01 1989-03-08 Osaka Printing Ink Mfg Ink composition for flexographic printing
JPH01175924A (en) * 1987-12-28 1989-07-12 Hoou Kk Hair treatment agent
WO1996001570A1 (en) * 1994-07-11 1996-01-25 Basf Aktiengesellschaft Cold water-dispersible compositions of fat-soluble active substances
JPH10291924A (en) * 1997-04-18 1998-11-04 Kao Corp Skin cosmetic for wet skin
US5928652A (en) * 1996-03-01 1999-07-27 L'oreal Binder compositions comprising an ester and their use
JP2002262824A (en) * 2000-12-21 2002-09-17 Basf Ag Method for producing dried powder of one or several oxygen-containing carotenoids
DE10254334A1 (en) * 2002-11-21 2004-06-03 Beiersdorf Ag cosmetics concentrate
USRE38952E1 (en) 1994-03-08 2006-01-31 Hale Nathan S Heat activated ink jet ink
US9302468B1 (en) 2014-11-14 2016-04-05 Ming Xu Digital customizer system and method
US9781307B2 (en) 2014-11-14 2017-10-03 Sawgrass Technologies, Inc. Networked digital imaging customization
US10419644B2 (en) 2014-11-14 2019-09-17 Sawgrass Technologies, Inc. Digital image processing network
US10827098B2 (en) 2015-11-02 2020-11-03 Sawgrass Technologies, Inc. Custom product imaging method
US10827097B2 (en) 2015-11-02 2020-11-03 Sawgrass Technologies, Inc. Product imaging

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5242483A (en) * 1975-10-02 1977-04-02 Idemitsu Kosan Co Ltd Emulsion stabilizing agent
JPS5244781A (en) * 1975-10-07 1977-04-08 Idemitsu Kosan Co Ltd Emulsion stabilizing agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5242483A (en) * 1975-10-02 1977-04-02 Idemitsu Kosan Co Ltd Emulsion stabilizing agent
JPS5244781A (en) * 1975-10-07 1977-04-08 Idemitsu Kosan Co Ltd Emulsion stabilizing agent

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0781139B2 (en) * 1987-04-09 1995-08-30 株式会社コーセー Antioxidant composition
JPS63254180A (en) * 1987-04-09 1988-10-20 Kobayashi Kooc:Kk Antioxidant composition
JPS6462373A (en) * 1987-09-01 1989-03-08 Osaka Printing Ink Mfg Ink composition for flexographic printing
JPH01175924A (en) * 1987-12-28 1989-07-12 Hoou Kk Hair treatment agent
JPH0460564B2 (en) * 1987-12-28 1992-09-28 Hoyu Kk
USRE38952E1 (en) 1994-03-08 2006-01-31 Hale Nathan S Heat activated ink jet ink
WO1996001570A1 (en) * 1994-07-11 1996-01-25 Basf Aktiengesellschaft Cold water-dispersible compositions of fat-soluble active substances
US5928652A (en) * 1996-03-01 1999-07-27 L'oreal Binder compositions comprising an ester and their use
JPH10291924A (en) * 1997-04-18 1998-11-04 Kao Corp Skin cosmetic for wet skin
JP2002262824A (en) * 2000-12-21 2002-09-17 Basf Ag Method for producing dried powder of one or several oxygen-containing carotenoids
DE10254334A1 (en) * 2002-11-21 2004-06-03 Beiersdorf Ag cosmetics concentrate
US9302468B1 (en) 2014-11-14 2016-04-05 Ming Xu Digital customizer system and method
US9781307B2 (en) 2014-11-14 2017-10-03 Sawgrass Technologies, Inc. Networked digital imaging customization
US10075619B2 (en) 2014-11-14 2018-09-11 Sawgrass Technologies, Inc. Networked digital imaging customization
US10419644B2 (en) 2014-11-14 2019-09-17 Sawgrass Technologies, Inc. Digital image processing network
US10827098B2 (en) 2015-11-02 2020-11-03 Sawgrass Technologies, Inc. Custom product imaging method
US10827097B2 (en) 2015-11-02 2020-11-03 Sawgrass Technologies, Inc. Product imaging
US11503187B2 (en) 2015-11-02 2022-11-15 Sawgrass Technologies, Inc. Custom product imaging method

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