JPS58194805A - Cosmetic - Google Patents
CosmeticInfo
- Publication number
- JPS58194805A JPS58194805A JP57077726A JP7772682A JPS58194805A JP S58194805 A JPS58194805 A JP S58194805A JP 57077726 A JP57077726 A JP 57077726A JP 7772682 A JP7772682 A JP 7772682A JP S58194805 A JPS58194805 A JP S58194805A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- glycyrrhizic acid
- lotion
- salt
- urea
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は透明ローションに関する。更に詳しくは、グリ
チルリチン酸塩と尿素の配合によって油性物質を水系の
中に透明に可溶化した皮膚安全性の高い、使用感触、流
動性に優れた透明ローションに関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to clear lotions. More specifically, the present invention relates to a transparent lotion that is highly safe for the skin, has excellent texture and fluidity, and has an oily substance that is transparently solubilized in an aqueous system by blending glycyrrhizinate and urea.
香料、油溶性ホルモン、合成エステル油等の油性物質を
水性の系中へ可溶化するためには、例えば、高級アルコ
ールのエチレンオキサイド付加物のような界面活性剤を
使用する方法が一般的である。しかし、界面活性剤は、
皮膚、眼等に刺激を与える場合があり、特に、敏感肌、
荒れた肌、日焼けした肌、にきび吹き出物のある肌に対
しての使用は好ましくない。In order to solubilize oily substances such as fragrances, oil-soluble hormones, and synthetic ester oils into aqueous systems, it is common to use surfactants such as ethylene oxide adducts of higher alcohols. . However, surfactants
It may irritate the skin and eyes, especially sensitive skin,
Not recommended for use on rough, sunburned, or acne-prone skin.
従来、界面活性剤を使用しない透明ローションとして、
特開昭52−151’736にグリチルリチン酸ジカリ
ウム塩を可溶化剤としたものが開示されている。しかし
ながら、グリチルリチン酸ジカリウムはその性質上酸性
領域において著しくゲル化し、また溶解度が低下し白濁
するという欠点を有しているため、皮膚のpl−15,
5に近い皮膚に温和に作用するローシフンや、さらにp
Hの低い収れんローンヨンの製造はできず、pH6,1
以上の可溶化化粧水に応用が限られてしまっている。Conventionally, as a transparent lotion that does not use surfactants,
JP-A-52-151'736 discloses a dipotassium glycyrrhizinate as a solubilizer. However, due to its nature, dipotassium glycyrrhizinate gels significantly in an acidic region and has the disadvantage of decreasing solubility and becoming cloudy.
Low-sihun that has a gentle effect on skin close to 5, and also p
It is not possible to produce astringent lawn yong with low H, and the pH is 6.1.
Applications to the above-mentioned solubilized lotions are limited.
本発明者らは、前記の難点をヤ服した透明ローションを
得るために鋭意研究を重ねた結果、グリチルリチン酸塩
と共に尿素を配合すると、いかなるρ11、特に6]以
下の酸性領域においてもゲル化を起させないようにする
だけでなく、グリチルリチン酸塩の溶解性を著しく向上
させ酊溶化能を高めることを見い出し本発明を完成する
に至った。The present inventors have conducted intensive research to obtain a transparent lotion that overcomes the above-mentioned drawbacks, and have found that when urea is blended with glycyrrhizinate, gelation occurs in any acidic region below ρ11, especially 6]. The present inventors have discovered that they can not only prevent this from occurring, but also significantly improve the solubility of glycyrrhizinate and enhance its solubilization ability, leading to the completion of the present invention.
すなわち、本発明はグリチルリチン酸塩と尿素と油性物
質と水を含むことを特徴とする透明ロー属塩、グリチル
リヂン酸アンモニウノ\塩、グリチルリチン酸塩基性ア
ミノ酸塩のモノ、ジ、トリ塩であり、例えば、グリチル
リチン酸モノナトリウムルリチン酸モノアンモニウム塩
、グリチルリチン酸ジナトリウム塩、ゲリチルリチン酸
ンカリウム塩、グリチルリチン酸トリナI・リウム塩、
グリチルリチン酸モノLーアルギニン塩、グリチルリチ
ン酸モノLーリジン塩、グルチルリチン酸ジL −アル
ギニン塩、グリチルリチン酸ジLーリジン塩等である。That is, the present invention relates to transparent rho salts, glycyrrhizic acid ammonium salts, and mono-, di-, and tri-salts of glycyrrhizic acid basic amino acid salts, which are characterized by containing glycyrrhizinate, urea, an oily substance, and water, such as , monosodium glycyrrhizinate monoammonium ruritinate salt, disodium glycyrrhizinate salt, potassium gelycyrrhizate salt, trina I/rium glycyrrhizate salt,
These include glycyrrhizic acid mono-L-arginine salt, glycyrrhizic acid mono-L-lysine salt, glycyrrhizic acid di-L-arginine salt, glycyrrhizic acid di-L-lysine salt, and the like.
これらは、消炎作用、香料などによるアレルギー防止作
用等皮膚に対して優れた作用を有しており、しかも前記
界面活性剤のような皮膚、眼に対する刺激をり,えない
ものである。グリチルリチン酸塩の配合量は01〜]O
重量%である。01重量%より少ないと油性物質の可溶
化能枦゛十分でないため白濁するようになり、10重計
%より多いとべたつくため使用感触が悪くなる。These have excellent effects on the skin, such as anti-inflammatory effects and anti-allergy effects caused by fragrances, and are not irritating to the skin and eyes, unlike the surfactants mentioned above. The amount of glycyrrhizinate is 01~]O
Weight%. If it is less than 0.01% by weight, the solubilization of oily substances is not sufficient and it becomes cloudy, and if it is more than 10% by weight, it becomes sticky and feels bad when used.
本発明に使用する尿素はNMF(天然保湿因子)の主成
分の一つであり、尿素のもつ角質内水分保持作用、創傷
治癒作用、殺菌作用等の皮膚に対する優れた作用を有し
ている。尿素の配合Mけグリチルリチン酸塩に対して」
0重量%以−にである。]○を
重量%より少ないと酸性領域特にpH 6.1以下lの
ゲル化を防止できない。また該化粧料中には、00]〜
田重量%配合される。加重量%より多いとべたつくため
使用感触が悪くなる。 11本発明
に使用する油性物質としては透明ローションに通常用い
られる、天然および合成の香料、オリーブ油、ホホバ油
、ヒマシ油等の動植物油、イソプロピルミリステート、
セチルイソオクタノニー!・等(D 合fQエステル油
、オレイルアルコール、オクチルドデカノール等の高級
アルコール、副レイン酸、イソステアリン酸等の高級脂
肪酸、流動パラフィン・スクワラン等の炭化水素、エス
トラジオール、エチニルエストラジオール、ジエチルス
チルベストロール等の油溶性ホルモン、ビタミンAパル
ミテート、ビタミンEアセテート等の油溶性ビタミン、
タダン■、キニザリングリーンSS1テトラプロA”T
”/yオレ士イン等の油溶性色素等があげられ、これら
のうち1種または2種以上が配合される。その配合量は
1重量%以下で該油性物質の添加効果をもたらしめる量
以上である。]重量%より多いと可溶化が困難となるた
め白濁してしまう。Urea used in the present invention is one of the main components of NMF (natural moisturizing factor), and has excellent effects on the skin such as urea's ability to retain moisture in the stratum corneum, wound healing effect, and bactericidal effect. Contains urea for glycyrrhizinate
It is less than 0% by weight. ] If the content of ○ is less than % by weight, gelation cannot be prevented in an acidic region, particularly at a pH of 6.1 or lower. In addition, the cosmetics contain 00] to
% by weight. If it is more than the weighted amount %, it will be sticky and the feeling of use will be poor. 11 Oily substances used in the present invention include natural and synthetic fragrances commonly used in transparent lotions, animal and vegetable oils such as olive oil, jojoba oil, and castor oil, isopropyl myristate,
Cetyl isooctanony!・Etc. (D Synthetic fQ ester oil, oleyl alcohol, higher alcohols such as octyldodecanol, higher fatty acids such as secondary leic acid and isostearic acid, hydrocarbons such as liquid paraffin and squalane, estradiol, ethinyl estradiol, diethylstilbestrol, etc. oil-soluble hormones, oil-soluble vitamins such as vitamin A palmitate, vitamin E acetate,
Tadan ■, Quinizarin Green SS1 Tetrapro A”T
"/y Oil-soluble pigments such as olein, etc. are included, and one or more of these are blended. The blending amount is 1% by weight or less, an amount that can bring about the effect of adding the oil-based substance. If the amount is more than % by weight, it becomes difficult to solubilize, resulting in cloudiness.
本発明に用いられる水の配合量は通常釦〜99,8重量
%程度である。The amount of water used in the present invention is usually about 99.8% by weight.
本発明の透明ローションには必要に応じて、アルコール
、保湿剤、防腐剤等が配合される。The transparent lotion of the present invention may contain alcohol, a humectant, a preservative, and the like, if necessary.
本発明の透明ローションは、いかなるpll(特に61
以下の酸性領域)においてもゲル化を起さず、長期間の
保存によっても透明性と安定性を保ち、皮膚安全性が高
く皮膚に対して優れた作用を有するものであり、柔軟化
粧水、収れん化粧水、アフターシェーブローション、ヘ
アー1・二,り、水性メイクア,ブベイスとして好適な
ものである。The transparent lotion of the present invention can be applied to any pll (especially 61
It does not gel even in the following acidic regions, maintains transparency and stability even after long-term storage, is highly safe for the skin, and has excellent effects on the skin. It is suitable for use as an astringent lotion, aftershave lotion, hair makeup, water-based makeup, and makeup.
(以下余白)
次に本発明の実施例を示す。本発明はこれにより限定さ
れるものではない。配合量は重滑%であるO
〔実施例−1収れん化粧水 比較例−1,2〕(製法)
■に■、■、■、■、■を溶解し、これに、■に■、■
を溶解したものを加え透明な収れん化粧水を得た。(The following is a blank space) Next, examples of the present invention will be shown. The present invention is not limited thereby. The blending amount is % O [Example-1 Astringent Lotion Comparative Examples-1, 2] (Production method) Dissolve ■, ■, ■, ■, ■ in ■, and add ■, ■ to ■.
A clear astringent lotion was obtained by adding the solution.
比較例−1,2も同様にして得た。Comparative Examples-1 and 2 were also obtained in the same manner.
表に示された特性から明らかなように、実施例−1は透
明性、状態、収れん効果とも良好であるのに対し、比較
例−1は収れん効果はあるがゲル化して濁っており、比
較例−2は透明性、状態は良好であるが、収れん効果に
欠けていることから・実施例−1は従来技術では得られ
なかった、皮膚安全性が高く、透明性、状態の良好な収
れん化粧1TJso 、ワ、下余白
)〔実施例−2柔軟化粧水 比較例−3〕(製造法)
■の一部に■を溶解したのち■を加え攪拌混合する。こ
れに■を加えて溶解したものに■を加えて可溶化する。As is clear from the characteristics shown in the table, Example-1 has good transparency, condition, and astringent effect, whereas Comparative Example-1 has an astringent effect but is gelatinized and cloudy, and compared to Example-2 has good transparency and condition, but lacks astringent effect.Example-1 has high skin safety, good transparency, and astringent condition that could not be obtained with conventional technology. Makeup 1 TJso, Wa, Bottom margin) [Example-2 Soft lotion Comparative example-3] (Manufacturing method) After dissolving ■ in a part of ■, add ■ and stir and mix. Add ■ to this and dissolve it, then add ■ to solubilize it.
これに■の残部に■、■を溶解したものを加えて柔軟化
粧水を得た。To this, a solution of ■ and ■ was added to the remaining part of ■ to obtain a softening lotion.
比較例3も同様の製法で得た。Comparative Example 3 was also obtained by the same manufacturing method.
表に示された特性から明らかなように、実施例−2は透
明性、状態とも良好であるのに対し・比較例−3はグリ
チルリチン酸モノアンモニウムの溶解性が悪く、濁って
いるうえゲル化も起していることから、実施例−2は従
来技術では得られなかった、皮膚安全性が高く、透明性
、状態の良好な皮膚に温和に作用する柔軟化粧水である
。As is clear from the characteristics shown in the table, Example 2 has good transparency and condition, while Comparative Example 3 has poor solubility of monoammonium glycyrrhizinate and is cloudy and gelatinous. Therefore, Example-2 is a softening lotion that has high skin safety, transparency, and a mild effect on skin that is in good condition, which could not be obtained using conventional techniques.
〔実施例−3〜6 薬用化粧水 比較例−45〕■に■
、■、■、■を溶解し、これに、■に■、■、■を溶解
したものを加えて透明な薬用化粧水を得た。[Example-3 to 6 Medicinal lotion Comparative example-45] ■■
, ■, ■, and ■ were dissolved, and a solution of ■, ■, and ■ dissolved in ■ was added to this to obtain a transparent medicated lotion.
表より明らかなように、尿素の配合量がグリチルリチン
酸塩に対して]0重量%以上であれば透明性、状態とも
良好であるのに対し、10重量%より少ないと透明性に
欠けるうえゲル化を起す。As is clear from the table, if the blending amount of urea is 0% by weight or more based on glycyrrhizinate, the transparency and condition are good, whereas if it is less than 10% by weight, the transparency and gelation are poor. cause a change.
また、尿素の配合量が加重量%より多いとべ!たつくよ
うになり使用感触が悪くなる。Also, if the blended amount of urea is greater than the weighted amount%! It becomes stiff and feels uncomfortable when used.
実施例3.4.5.6は皮膚安全性が高く、透明性、状
態とも良好な皮膚に温和に作用する薬用1実施例−7,
8,9アフターシェーブローション比較例−6,7〕
(製法)
実施例−1と同様にして透明なアフターシェーブローシ
ョンを得た。Example 3.4.5.6 is a medicinal example 1 example-7 that has high skin safety and has a mild effect on the skin with good transparency and condition.
8,9 Aftershave Lotion Comparative Examples-6,7] (Manufacturing method) A transparent aftershave lotion was obtained in the same manner as in Example-1.
表より明らかなように、グリチルリチン酸塩が01〜1
0市量%では透明性、状態、使用感触とも、良好である
のに対し、01重量%未満では濁りが生3
じ、]00重量より多いとべたつくようになり使用感触
が悪くなる。As is clear from the table, glycyrrhizinate is 01-1
At 0% by weight, the transparency, condition, and feeling in use are good, whereas at less than 01% by weight, turbidity occurs, and when it exceeds 00% by weight, it becomes sticky and feels bad in use.
(以下余白) (製法) 実施例−1と同様にして透明なヘアートニックを得た。(Margin below) (Manufacturing method) A transparent hair tonic was obtained in the same manner as in Example-1.
このヘアートニックはPH4,6で透明性、状態の良好
なものであった。This hair tonic had a pH of 4.6 and was transparent and in good condition.
Claims (3)
含むことを特徴とする透明ローンヨン〇州゛(1) Transparent lawn jellyfish characterized by containing glycyrrhizinate, urea, oily substance and water
カリ金属塩、グリチルリチン酸アンモニウム塩・グリチ
ルリチン酸塩基性アミノ酸塩である特許請求の範囲第1
項記載の透明ローション。(2) Glycyrrhizinate l Glycyrrhizic acid alkali metal salt, glycyrrhizic acid ammonium salt, glycyrrhizic acid basic amino acid salt Claim 1
Transparent lotion as described in section.
成エステル油、高級脂肪酸、高級アルコール、油溶性ホ
ルモン、油溶性ビタミン、油溶性色素の1種または2種
以上である特許請求の範囲第1項記載の透明ローション
。(3) The oily substance is one or more of the following: fragrances, animal and vegetable oils, hydrocarbons, synthetic ester oils, higher fatty acids, higher alcohols, oil-soluble hormones, oil-soluble vitamins, and oil-soluble pigments. The transparent lotion described in item 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57077726A JPS58194805A (en) | 1982-05-10 | 1982-05-10 | Cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57077726A JPS58194805A (en) | 1982-05-10 | 1982-05-10 | Cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58194805A true JPS58194805A (en) | 1983-11-12 |
Family
ID=13641896
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57077726A Pending JPS58194805A (en) | 1982-05-10 | 1982-05-10 | Cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58194805A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006001477A1 (en) * | 2004-06-29 | 2006-01-05 | Minophagen Pharmaceutical Co., Ltd. | Glycyrrhizin-containing suppository compositions for rectal infusion |
US10073104B2 (en) | 2013-03-14 | 2018-09-11 | Siemens Healthcare Diagnostics Inc. | Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions |
-
1982
- 1982-05-10 JP JP57077726A patent/JPS58194805A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006001477A1 (en) * | 2004-06-29 | 2006-01-05 | Minophagen Pharmaceutical Co., Ltd. | Glycyrrhizin-containing suppository compositions for rectal infusion |
US10073104B2 (en) | 2013-03-14 | 2018-09-11 | Siemens Healthcare Diagnostics Inc. | Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions |
US10921333B2 (en) | 2013-03-14 | 2021-02-16 | Siemens Healthcare Diagnostics Inc. | Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions |
US11921124B2 (en) | 2013-03-14 | 2024-03-05 | Siemens Healthcare Diagnostics Inc. | Control of pH in aqueous urea-containing solutions utilizing amino acid-containing compositions |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TW510801B (en) | Skin toning formulation | |
TW508246B (en) | Stabilization of an unstable retinoid in oil-in-water emulsions for skin care compositions | |
JPH1053510A (en) | Composition for external use | |
JPH0552806B2 (en) | ||
WO1997002803A1 (en) | External skin preparation | |
EP1216696A2 (en) | Method for reducing the appearance of dark circles under the eyes | |
US20040219125A1 (en) | Oily thickened gel-like composition, emulsified composition using the composition and preparation method thereof | |
JP2983311B2 (en) | External preparation for skin | |
JPH11139951A (en) | Cosmetic | |
EP0204586A2 (en) | Stabilizer for hair compositions and such compositions | |
JPH11255633A (en) | Mixture of procystein with polyol | |
US6284718B1 (en) | Composition for topical use containing an acetylenic diol, and use thereof for cleansing or removing make-up from the skin, mucous membranes and the hair | |
JP3657068B2 (en) | Anti-photoaging agent and external preparation for skin | |
JPS58194805A (en) | Cosmetic | |
JP3258801B2 (en) | Skin metabolism promoter | |
JP2854767B2 (en) | Thickening gelling agent | |
JPH0892062A (en) | External preparation | |
JP3280712B2 (en) | External preparation for skin | |
JPH0632710A (en) | Skin external preparation | |
JP3001121B2 (en) | External preparation for skin | |
JP3268504B2 (en) | Gel composition | |
JP3455553B2 (en) | External preparation for skin | |
JPH10287524A (en) | Solubilized cosmetic | |
JPS6111137A (en) | Water in oil type emulsion composition | |
JPH11106325A (en) | Skin lotion |