JPH0375523B2 - - Google Patents
Info
- Publication number
- JPH0375523B2 JPH0375523B2 JP57013428A JP1342882A JPH0375523B2 JP H0375523 B2 JPH0375523 B2 JP H0375523B2 JP 57013428 A JP57013428 A JP 57013428A JP 1342882 A JP1342882 A JP 1342882A JP H0375523 B2 JPH0375523 B2 JP H0375523B2
- Authority
- JP
- Japan
- Prior art keywords
- collagen
- cream
- present
- humectant
- 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.)
- Expired
Links
Classifications
-
- 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
-
- 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
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/14—Preparations for removing make-up
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Description
本発明は化粧料組成物又は医薬組成物に使用可
能な新規湿潤剤組成物に関する。
化粧料に、湿潤剤すなわち周囲の空気から湿分
を吸収することができしかも化粧料組成物の水分
を乾燥する傾向のないように保持できる吸湿性の
物質を用いることは日常行なわれていることであ
る。そのうえ湿潤剤フイルム(薄膜)の吸湿性は
皮膚に施用されるとき、皮膚のしなやかさ及び手
ざわりに有利な影響を及ぼし得る重要な因子を構
成する。
多数の湿潤剤物質で最も通常に用いられ湿潤剤
物質のうち、乳酸ナトリウム又はピロリドン・カ
ルボン酸ナトリウムなどのナトリウム塩、グリセ
リン、ソルビトール及びプロピレングリコールの
如きポリオールならびに尿素の如き他の物質をあ
げることができる。
またこれらの湿潤剤物質の混合物を用いる場合
とくに著しい相乗作用効果を確認できなかつたに
も拘わらずこれらの混合物を用いることも提案さ
れている。
これらの混合物のうち、特に英国特許第
1471679号明細書にはピロリドンカルボン酸又は
その吸湿性塩のうちの一つと炭素原子数2乃至5
個のα−ヒドロキシカルボン酸の塩、とくにグリ
コール酸又は乳酸のナトリウム塩と改質コラーゲ
ンのポリペプチド物質との組合せが記載してあ
る。
この英国特許によると“改質コラーゲンのポリ
ペプチド物質”とはハロゲンイオンのある第四級
アミノ基を備えしかも炭素原子数3乃至12個のア
ミノアルコールによりエステル化した末端カルボ
キシル基を備えたポリペプチド物質あるいは飽和
又は不飽和脂肪酸と反応した末端アミノ基を備え
しかもポリオールと反応した末端カルボキシル基
を備えたポリペプチド物質であり、各々の場合ポ
リペプチド物質はコラーゲンから誘導され、ジ−
トリ−又はテトラ−ペプチドに相当する平均分子
量を有すると解すべきである。
この英国特許によると、種々成分の比率はピロ
リドンカルボン酸又はその吸湿性塩については
0.75乃至1.25、炭素原子数2乃至5個のα−ヒド
ロキシカルボン酸の塩については0.75乃至1.25及
び改質コラーゲンのポリペプチド誘導体について
は3.75乃至6.25の重量比内で変動できる。
本発明は、湿潤剤物質の特定の組合せに関し、
組成物にすぐれた保存性(Conservation)を付
与しそのうえ皮膚に軟化性及び柔軟性を付与し得
る湿潤剤組成物に関する。
本発明は水溶液中に乳酸ナトリウム3乃至8重
量%とグリセリン12乃至24重量%と尿素30乃至48
重量%と天然コラーゲン0.5重量%未満とを含ん
でなる湿潤剤組成物に関する。
さまざまな試験を行なつて上記割合のこの組合
せのみが所望の性質をもたらし得ることを示すこ
とができた。
とくに天然コラーゲンが良好な湿潤性質を得る
目的に不可避であることが立証された。
本発明の湿潤剤組成物は水溶液中に乳酸ナトリ
ウム4乃至7重量%、グリセリン15.5乃至21重量
%、尿素33.5乃至39重量%及び天然コラーゲン
0.05〜0.2重量%を含んでいるのが更に好ましい。
天然コラーゲンとは下記の諸特性を示すコラー
ゲンと解する:
分子量がそれぞれ100000,200000及び300000で
あるα,β及びγ三つの螺旋形連鎖を含む三重コ
イルからなる。
α連鎖は分子量がそれぞれ100000の2つの副単
位α1及びα2からなり両者はそれを構成するアミノ
酸の性質により僅かに相違している。
β連鎖は副単位α12個からなる副単位β11と副単
位α1及び副単位α2からなる副単位β12とから構成
される。
副単位β11及びβ12はそれぞれ分子量200000であ
る。
他方各コイルの末端にはコラーゲンの抽出形式
に応じて長さ約50Åのポリペプチド直鎖いわゆる
テロペプチドが存在するか又は存在しない。
本発明による湿潤剤組成物に用いられるコラー
ゲンにはテロペプチドがあつてもなくてもよい。
この天然コラーゲンは英国特許第1471679号明
細書において用いられる改質コラーゲンのポリペ
プチド物質とは本発明によると天然コラーゲンが
若い動物とくに若い仔牛の皮膚から冷間抽出した
天然コラーゲンであることによつて全く相違して
いる。
従つてこの天然コラーゲンはその抽出の特定条
件から改質されず且つ変性してもいない構造であ
る。
本発明の湿潤剤組成物は一般に組成物の保存性
をよくするためにせよ皮膚の外見すなわち様子を
改良するためにせよ湿潤剤の存在を必要とするあ
らゆる組成物に使用できる。
本発明の湿潤剤組成物が使用できる組成物のう
ちとくにローシヨン、顔面手入クリーム、ボデー
用乳液、化粧落し用乳液又はクリーム、日焼けど
め乳液又はクリーム、フアンデーシヨン、着色ク
リーム、しわとりクリーム又は眼の輪郭用のクリ
ームをあげることができるがこれらに限定するも
のではない。
一般に良い結果を得る目的で本発明の湿潤剤組
成物を5乃至60重量%の割合で用いる。
同様に本発明の湿潤剤組成物は医薬組成物とく
に皮膚薬組成物中に同じ割合で使用できる。
以下に本発明の湿潤剤組成物の数例を実施例A
〜実施例Dに示し、またこれらを含んでいる化粧
料組成物又は医薬組成物の実施例1〜実施例8に
示す。さらに、また、本発明の湿潤組成物の湿潤
効果を試験例に示す。
実施例 A
乳酸ナトリウム(60%水溶液) 9g
グリセリン 18.5g
尿素 36g
コラーゲン(0.3%水溶液) 36.5g
実施例 B
乳酸ナトリウム(60%水溶液) 10g
グリセリン 17g
尿素 35g
コラーゲン(0.3%水溶液) 38g
実施例 C
乳酸ナトリウム(60%水溶液) 8g
グリセリン 20g
尿素 39g
コラーゲン(0.3%水溶液) 33g
実施例 D
乳酸ナトリウム(60%水溶液) 8g
グリセリン 16g
尿素 36g
コラーゲン(0.3%水溶液) 40g
実施例 1
本発明により下記の成分を混合して油中水型エ
マルジヨンの形の顔面用クリームを調製する:
ラノリン酸 13.5g
アルギニン 1.5g
水素添加ラノリン 15.0g
パラフイン油 35.0g
実施例Aの湿潤剤組成物 22g
防腐剤 0.15g
香料 0.10g
水 全体を100gとするに必要な量
実施例 2
本発明により下記の成分を混合して水中油型エ
マルジヨンの形の顔面用クリームを調製する:
Dynamit Nobel社から“MIGLYOL812”の名
称で市販されている飽和脂肪酸のトリグリセリド
4.0g
セチルアルコール 0.5g
オレイン酸デシルエステル 5.0g
ワセリン油 13.0g
エチレンオキシド10モルによりオキシエチレン
化したセチルアルコールのポリグリコールエーテ
ル 4.0g
ポリエチレン粉末 4.0g
実施例Aの湿潤剤組成物 27.5g
水及び防腐剤 全体を100gとする必要量
実施例 3
本発明により下記の成分を混合して化粧落し乳
液を調製する:
パラフイン油 10.0g
エチレンオキシド10モルでポリオキシエチレン
化したステアリルエーテル 2.0g
エチレンオキシド10モルでポリオキシエチレン
化したセチルエーテル 2.0g
モノステアリン酸グリセリン 4.0g
セチルアルコール 1.0g
ステアリルアルコール 1.0g
MiranolC2Mの名称で市販されている1−2
「ココイル」即ち1−(ナトリウムカルボキシメチ
ル)−2−〔2−(ナトリウムカルボキシメトキシ)
エチル〕・イミダゾリニウムヒドロキシド 2.0g
ヒドロキシ−プロピルメチルセルロース 0.3g
p−ヒドロキシ安息香酸メチル 0.2g
カオリナイト型粘土 5.0g
実施例Bの湿潤剤組成物 17g
香料 0.05g
水 全体を100gにする必要量
実施例 4
下記の成分を混合してボデー用乳液を調製す
る:
パルミチン酸イソプロピル 5.0g
パラフイン油 10.0g
American Cholesterol Products社から
Amerchol L101の名称で市販されているラノリ
ン化合物のアルコールとステロールとの混合物
0.3g
ステアリン酸 1.4g
自己乳化性モノステアリン酸グリセロール
2.0g
セチルアルコール 0.2g
トリエタノールアミン 0.75g
ヒドロキシメチルセルロース 0.5g
プロピレングリコール 2.0g
p−ヒドロキシ安息香酸メチル 0.35g
実施例Bの湿潤剤組成物 35g
香料 0.1g
水 全体を100gにする必要量
実施例 5
本発明により下記の成分を混合して日焼け用ク
リームを調製する:
ラノリン酸マグネシウム 2.85g
ラノリンアルコール 6.65g
パルミチン酸イソプロピル 22.20g
パラフイン油 26.00g
オゾケライト 2.00g
実施例Dの湿潤剤組成物 22g
Givaudan社からParsol Ultraの名称で市販さ
れている太陽光線フイルタ 5.00g
水及び防腐剤 全体を100gとする必要量
実施例 6
本発明により下記の成分を混合して油中水型日
焼クリームを調製する:
自己乳化性モノステアリン酸グリセロール
5.00g
ミリスチン酸イソプロピル 16.00g
ペルヒドロスクアレン 10.00g
p−ヒドロキシ安息香酸メチル 0.3g
ヒドロキシメチルセルロース 0.5g
p−メトキシ桂皮酸2−エトキシエチル 5.0g
実施例Cの湿潤剤組成物 26g
香料 0.1g
水 全体を100gとする必要量
実施例 7
本発明により下記の成分を混合して水中油型エ
マルジヨンの形の着色フアンデーシヨンを調製す
る:
ラノリン酸イソプロピル 4.0g
ステアリン酸 2.6g
自己乳化性ステアリン酸グリセロール 5.0g
パラフイン油 10.0g
ワセリン 10.0g
トリエタノールアミン 1.2g
ラウリル硫酸ナトリウム 1.1g
ベントナイト 2.5g
実施例Aの湿潤剤組成物 16g
赤色酸化鉄 0.7g
黄色酸化鉄 0.9g
酸化チタン 2.0g
香料 0.1g
水及び防腐剤 全体を100gにする必要量
実施例 8
本発明により下記の成分を混合して水中油型エ
マルジヨンの形の眼輪郭用クリームを調製する:
自己乳化性モノステアリン酸グリセロール
3.0g
American Cholesterol Products社から
Amerchol L101の名称で市販されたラノリンの
アルコールとステロールとの混合物 3.0g
ペルヒドロスクアレン 10.0g
パルミチン酸イソプロピル 1.0g
セチルアルコール 2.0g
大豆レシチン 0.5g
ヒドロキシメチルセルロース 0.5g
胎盤エキス 2.0g
アミノ・血清(amino−serique)エキス 1.0g
実施例Bの湿潤剤組成物 28g
香料 0.5g
水及び防腐剤 全体を100gとする必要量
試験例
本発明の湿潤剤組成物を使用してクリームを調
製し、その湿潤効果を以下に示した方法により測
定した。また、比較用として本発明の湿潤剤組成
物の成分である乳酸ナトリウムと尿素とを有効成
分として配合したクリーム、コラーゲンを有効成
分として配合したクリーム、及び尿素を有効成分
として配合したクリームを同様に調製し、その湿
潤効果を同様の方法により測定した。
1 クリームの調製
下記の第1表に示した成分を混合して4種類の
クリームすなわちクリームA,P,Q及びRを調
製した。クリームAは本発明の実施例Aの湿潤剤
組成物27.5gを有効成分として配合したものであ
る。クリームP,Q及びRは比較試験用のクリー
ムである。クリームPは本発明の湿潤剤組成物の
成分である乳酸ナトリウムと尿素とを有効成分と
して配合したものであり、クリームQは本発明の
湿潤剤組成物の成分であるコラーゲンのみを有効
成分として配合したものであり、またクリームR
は本発明の湿潤剤組成物の成分である尿素のみを
有効成分として配合したものであり、それらの有
効成分量は下記の第1表に示した通りである。
The present invention relates to novel humectant compositions that can be used in cosmetic or pharmaceutical compositions. It is common practice in cosmetics to use humectants, ie hygroscopic substances capable of absorbing moisture from the surrounding air and retaining the moisture in the cosmetic composition without a tendency to dry it out. It is. Moreover, the hygroscopicity of humectant films constitutes an important factor that can favorably influence the suppleness and texture of the skin when applied to the skin. Among the many humectant substances most commonly used are sodium salts such as sodium lactate or sodium pyrrolidone carboxylate, polyols such as glycerin, sorbitol and propylene glycol, and other substances such as urea. can. It has also been proposed to use mixtures of these humectant substances, although no particularly significant synergistic effects could be observed when using mixtures of these humectant substances. Among these mixtures, in particular British patent no.
No. 1471679 discloses that pyrrolidonecarboxylic acid or one of its hygroscopic salts and carbon atoms of 2 to 5
Combinations of salts of α-hydroxycarboxylic acids, particularly the sodium salts of glycolic or lactic acid, with polypeptide materials of modified collagen have been described. According to this British patent, a "modified collagen polypeptide substance" is a polypeptide having a quaternary amino group with a halogen ion and a terminal carboxyl group esterified with an amino alcohol having 3 to 12 carbon atoms. substances or polypeptide substances with terminal amino groups reacted with saturated or unsaturated fatty acids and with terminal carboxyl groups reacted with polyols, in each case the polypeptide substances are derived from collagen and di-
It is to be understood that it has an average molecular weight corresponding to a tri- or tetra-peptide. According to this British patent, the proportions of the various ingredients are:
The weight ratio can vary within a weight ratio of 0.75 to 1.25, 0.75 to 1.25 for salts of α-hydroxycarboxylic acids having 2 to 5 carbon atoms, and 3.75 to 6.25 for polypeptide derivatives of modified collagen. The present invention relates to a particular combination of humectant substances,
The present invention relates to a humectant composition capable of imparting excellent preservation to the composition and also imparting softening and suppleness to the skin. The present invention contains 3 to 8% by weight of sodium lactate, 12 to 24% by weight of glycerin, and 30 to 48% of urea in an aqueous solution.
% by weight and less than 0.5% by weight of natural collagen. Various tests have been carried out and it has been possible to show that only this combination of the above proportions can provide the desired properties. In particular, natural collagen has proven to be essential for the purpose of obtaining good wetting properties. The wetting agent composition of the present invention contains 4 to 7% by weight of sodium lactate, 15.5 to 21% by weight of glycerin, 33.5 to 39% by weight of urea and natural collagen in an aqueous solution.
More preferably, it contains 0.05 to 0.2% by weight. Natural collagen is understood to be collagen which exhibits the following properties: It consists of a triple coil containing three helical chains α, β and γ with molecular weights of 100,000, 200,000 and 300,000, respectively. The α-linkage consists of two subunits α 1 and α 2 each having a molecular weight of 100,000, and both subunits differ slightly depending on the properties of the amino acids that constitute them. The β chain is composed of a subunit β 11 consisting of two subunits α 1 and a subunit β 12 consisting of a subunit α 1 and a subunit α 2 . Subunits β 11 and β 12 each have a molecular weight of 200,000. On the other hand, at the end of each coil, depending on the type of collagen extraction, a linear polypeptide chain, so-called telopeptide, about 50 Å in length is present or absent. The collagen used in the humectant composition according to the invention may or may not have telopeptides. This natural collagen is the modified collagen polypeptide material used in British Patent No. 1471679. According to the present invention, the natural collagen is natural collagen cold extracted from the skin of young animals, especially young calves. They are completely different. Therefore, this natural collagen has a structure that has not been modified or denatured due to the specific conditions of its extraction. The humectant compositions of the present invention can generally be used in any composition requiring the presence of a humectant, whether to improve the shelf life of the composition or to improve the appearance or appearance of the skin. Among the compositions in which the humectant composition of the present invention can be used, particularly lotions, facial care creams, body emulsions, make-up remover emulsions or creams, sunscreen emulsions or creams, foundations, coloring creams, anti-wrinkle creams. or eye contour creams, but are not limited thereto. Generally, the wetting agent compositions of the present invention are used in proportions of 5 to 60% by weight to obtain good results. Similarly, the humectant compositions of the invention can be used in the same proportions in pharmaceutical compositions, especially dermatological compositions. Examples of wetting agent compositions of the present invention are shown below in Example A.
~Example D and examples 1 to 8 of cosmetic compositions or pharmaceutical compositions containing these. Furthermore, the wetting effect of the wetting composition of the present invention is also shown in the test examples. Example A Sodium lactate (60% aqueous solution) 9g Glycerin 18.5g Urea 36g Collagen (0.3% aqueous solution) 36.5g Example B Sodium lactate (60% aqueous solution) 10g Glycerin 17g Urea 35g Collagen (0.3% aqueous solution) 38g Example C Lactic acid Sodium (60% aqueous solution) 8g Glycerin 20g Urea 39g Collagen (0.3% aqueous solution) 33g Example D Sodium lactate (60% aqueous solution) 8g Glycerin 16g Urea 36g Collagen (0.3% aqueous solution) 40g Example 1 The following ingredients were prepared according to the present invention. A facial cream in the form of a water-in-oil emulsion is prepared by mixing: Lanolinic acid 13.5g Arginine 1.5g Hydrogenated lanolin 15.0g Paraffin oil 35.0g Humectant composition of Example A 22g Preservative 0.15g Perfume 0.10g Water Required amount for 100 g total Example 2 A facial cream in the form of an oil-in-water emulsion is prepared according to the invention by mixing the following ingredients: Commercially available from Dynamit Nobel under the name "MIGLYOL812" Triglycerides of saturated fatty acids
4.0 g Cetyl alcohol 0.5 g Decyl oleate 5.0 g Vaseline oil 13.0 g Polyglycol ether of cetyl alcohol oxyethylated with 10 moles of ethylene oxide 4.0 g Polyethylene powder 4.0 g Wetting agent composition of Example A 27.5 g Water and preservatives Required amount Example 3 According to the present invention, the following ingredients are mixed to prepare a makeup remover emulsion: Paraffin oil 10.0 g Stearyl ether polyoxyethylated with 10 moles of ethylene oxide 2.0 g Polyoxyethylene with 10 moles of ethylene oxide Ethylated cetyl ether 2.0g Glyceryl monostearate 4.0g Cetyl alcohol 1.0g Stearyl alcohol 1.0g 1-2, commercially available under the name MiranolC2M
"Cocoyl" i.e. 1-(sodium carboxymethyl)-2-[2-(sodium carboxymethoxy)
[Ethyl]imidazolinium hydroxide 2.0g Hydroxy-propyl methylcellulose 0.3g Methyl p-hydroxybenzoate 0.2g Kaolinite clay 5.0g Wetting agent composition of Example B 17g Fragrance 0.05g Water Required amount to make the total amount to 100g Example 4 A body emulsion is prepared by mixing the following ingredients: Isopropyl palmitate 5.0 g Paraffin oil 10.0 g From American Cholesterol Products.
A mixture of lanolin compounds with alcohol and sterols, marketed under the name Amerchol L101
0.3g Stearic acid 1.4g Self-emulsifying glycerol monostearate
2.0g Cetyl alcohol 0.2g Triethanolamine 0.75g Hydroxymethyl cellulose 0.5g Propylene glycol 2.0g Methyl p-hydroxybenzoate 0.35g Wetting agent composition of Example B 35g Fragrance 0.1g Water Required amount to make the total 100g Example 5 A tanning cream is prepared according to the invention by mixing the following ingredients: Magnesium lanophosphate 2.85 g Lanolin alcohol 6.65 g Isopropyl palmitate 22.20 g Paraffin oil 26.00 g Ozokerite 2.00 g Wetting agent composition of Example D 22 g From the company Givaudan Sun filter commercially available under the name Parsol Ultra 5.00 g Water and preservative Required amount for a total of 100 g Example 6 A water-in-oil suntan cream is prepared according to the invention by mixing the following ingredients: Self Emulsifying glycerol monostearate
5.00 g Isopropyl myristate 16.00 g Perhydrosqualene 10.00 g Methyl p-hydroxybenzoate 0.3 g Hydroxymethyl cellulose 0.5 g 2-ethoxyethyl p-methoxycinnamate 5.0 g Humectant composition of Example C 26 g Fragrance 0.1 g Water Requirements for 100 g Example 7 A pigmented foundation in the form of an oil-in-water emulsion is prepared according to the invention by mixing the following ingredients: Isopropyl lanophosphate 4.0 g Stearic acid 2.6 g Self-emulsifying glycerol stearate 5.0 g Paraffin oil 10.0g Petrolatum 10.0g Triethanolamine 1.2g Sodium lauryl sulfate 1.1g Bentonite 2.5g Wetting agent composition of Example A 16g Red iron oxide 0.7g Yellow iron oxide 0.9g Titanium oxide 2.0g Fragrance 0.1g Water and preservatives Requirements for a total of 100 g Example 8 An eye contour cream in the form of an oil-in-water emulsion is prepared according to the invention by mixing the following ingredients: Self-emulsifying glycerol monostearate
3.0g from American Cholesterol Products
A mixture of lanolin and sterols sold under the name Amerchol L101 3.0g Perhydrosqualene 10.0g Isopropyl palmitate 1.0g Cetyl alcohol 2.0g Soybean lecithin 0.5g Hydroxymethylcellulose 0.5g Placenta extract 2.0g Amino-serum serique) extract 1.0g Humectant composition of Example B 28g Fragrance 0.5g Water and preservative Required amount test example using a total of 100g A cream was prepared using the humectant composition of the present invention, and its moisturizing effect was evaluated. It was measured by the method shown below. For comparison, a cream containing sodium lactate and urea as active ingredients, which are components of the humectant composition of the present invention, a cream containing collagen as an active ingredient, and a cream containing urea as an active ingredient were similarly prepared. were prepared and their wetting effect was determined by a similar method. 1. Preparation of creams Four types of creams, namely creams A, P, Q and R, were prepared by mixing the ingredients shown in Table 1 below. Cream A contains 27.5 g of the humectant composition of Example A of the present invention as an active ingredient. Creams P, Q and R are creams for comparative testing. Cream P is formulated with sodium lactate and urea, which are components of the humectant composition of the present invention, as active ingredients, and Cream Q is formulated only with collagen, which is a component of the humectant composition of the present invention, as an active ingredient. Cream R
These are formulations containing only urea, which is a component of the wetting agent composition of the present invention, as an active ingredient, and the amounts of their active ingredients are as shown in Table 1 below.
【表】【table】
【表】
2 湿潤効果試験
J.Inv.Demr.75,500−507(1980)に記載の
Hachiro Tagamiらの方法に従つて測定装置と
してSKICON 200[I.B.S.Inc.社(浜松市)製の生
体内表皮角質層の水和状態測定装置の商品名]を
使用して、3.5MHzの周波数で皮膚表皮角質層の
電気抵抗を測定することによつて皮膚表面角質層
の湿潤状態を測定した。試験は次のようにして行
つた。
16人の女性の前腕の内側表面の2か所の部分を
試験区として各供試クリームを塗布した。尚、対
照区としてクリームを塗布しない部分を設けた。
クリーム塗布前の試験区及び対照区の湿潤状態を
上記装置により測定しこの測定値をT0とした。
また、クリーム塗布30分後の試験区の湿潤状態及
び30分後の対照区の湿潤状態を同様に測定しこの
測定値をT30とした。得られたT0及びT30の平均
値並びにそれらから求められた種々のパラメータ
及び湿潤効果値(E)を下記の第2表に示す。[Table] 2 Wetting effect test as described in J.Inv.Demr. 75 , 500-507 (1980)
The skin epidermis was measured at a frequency of 3.5 MHz using SKICON 200 [trade name of an in-vivo epidermal stratum corneum hydration state measuring device manufactured by IBS Inc. (Hamamatsu City)] as a measuring device according to the method of Hachiro Tagami et al. The moist state of the stratum corneum on the skin surface was measured by measuring the electrical resistance of the stratum corneum. The test was conducted as follows. Each test cream was applied to two areas on the inner surface of the forearms of 16 women as test areas. In addition, a part to which no cream was applied was provided as a control area.
The wet state of the test area and control area before application of the cream was measured using the above device, and this measured value was defined as T 0 .
In addition, the moist state of the test plot 30 minutes after applying the cream and the moist state of the control plot 30 minutes later were measured in the same manner, and this measured value was defined as T 30 . The average values of T 0 and T 30 obtained as well as the various parameters and wetting effect values (E) determined therefrom are shown in Table 2 below.
【表】
表中の有意差は、Keulの有意差検定法を用い
て評価した測定値の差(T30−T0)の有意差であ
り、NSは有意差なしを表わし、Sは有意差あり
を表わす。
表中のDは、試験区の各供試クリーム(X)の
測定値の差(T30−T0)と対照区(U)の測定値
の差(T30−T0)との差を表わす。すなわち、
D=[T(X)30−T(X)0]−[T(U)30−T
(U)
0]
[式中、X=A,P,Q及びRであり、T(U)
30−T(U)0=3.2である]を表わす。
また、表中のEは、各供試クリームの有効性す
なわちクリームを塗布しない未処理の皮膚と比べ
た湿潤効果を表わす。湿潤効果Eは次式に従つて
算出した。
E=T(X)30−T(X)0/T(X)0
−T(U)30−T(U)0/T(U)0
上記式中、
T(U)30−T(U)0/T(U)0=3.2/13.8
得られた結果は、本発明の湿潤剤組成物が、コ
ラーゲン単独、尿素単独又は乳酸ナトリウムと尿
素の混合物を有効成分として使用した湿潤剤組成
物に比べて顕著な湿潤効果を有することを示す。
すなわち、本発明の湿潤剤組成物は湿潤効果139
%を示し、本発明の湿潤剤組成物の個々の成分を
有効成分とした湿潤剤組成物それぞれが示す湿潤
効果の合計値よりも格段に優れており、本発明の
湿潤剤組成物は優れた相乗効果を有する。[Table] The significant difference in the table is the significant difference in the measured value difference (T 30 - T 0 ) evaluated using Keul's significance test method, where NS represents no significant difference and S represents a significant difference. Represents existence. D in the table is the difference between the measured value difference (T 30 - T 0 ) of each test cream (X) in the test area and the difference (T 30 - T 0 ) in the measured value of the control area (U). represent. That is, D=[T(X) 30 −T(X) 0 ]−[T(U) 30 −T
(U)
0 ] [wherein, X=A, P, Q and R, and T(U)
30 −T(U) 0 =3.2]. Further, E in the table represents the effectiveness of each test cream, that is, the moisturizing effect compared to untreated skin without cream application. Wetting effect E was calculated according to the following formula. E=T(X) 30 -T(X) 0 /T(X) 0 -T(U) 30 -T(U) 0 /T(U) 0In the above formula, T(U) 30 -T(U ) 0 /T(U) 0 = 3.2/13.8 The results obtained show that the wetting agent composition of the present invention is superior to the wetting agent composition using collagen alone, urea alone, or a mixture of sodium lactate and urea as active ingredients. It shows that it has a remarkable moisturizing effect compared to the above.
That is, the wetting agent composition of the present invention has a wetting effect of 139
%, which is much better than the total value of the moisturizing effect shown by each of the wetting agent compositions containing the individual components of the wetting agent composition of the present invention as active ingredients, and the wetting agent composition of the present invention has an excellent Has a synergistic effect.
Claims (1)
乳酸ナトリウム3乃至8%、グリセリン12乃至24
%、尿素30乃至42%及び天然コラーゲン0.5%未
満を含んでなることを特徴とする湿潤剤組成物。 2 水溶液中に乳酸ナトリウム4乃至7重量%、
グリセリン15.5乃至21重量%、尿素33.5乃至39重
量%及び天然コラーゲン0.05乃至0.2重量%を含
んでいる特許請求の範囲第1項記載の組成物。[Claims] 1. In an aqueous solution, 3 to 8% sodium lactate and 12 to 24% glycerin, based on the total weight of the wetting agent composition.
%, 30 to 42% urea and less than 0.5% natural collagen. 2 4 to 7% by weight of sodium lactate in aqueous solution,
A composition according to claim 1, comprising 15.5-21% by weight of glycerin, 33.5-39% by weight of urea and 0.05-0.2% by weight of natural collagen.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8101971A FR2498929A1 (en) | 1981-02-02 | 1981-02-02 | NOVEL HUMIDIZING COMPOSITION BASED ON SODIUM LACTATE, GLYCERIN, UREA AND NATIVE COLLAGEN |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57150608A JPS57150608A (en) | 1982-09-17 |
| JPH0375523B2 true JPH0375523B2 (en) | 1991-12-02 |
Family
ID=9254738
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57013428A Granted JPS57150608A (en) | 1981-02-02 | 1982-02-01 | Wetting agent composition |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS57150608A (en) |
| BE (1) | BE891972A (en) |
| CA (1) | CA1171265A (en) |
| CH (1) | CH651471A5 (en) |
| DE (1) | DE3203260A1 (en) |
| FR (1) | FR2498929A1 (en) |
| GB (1) | GB2092444B (en) |
| IT (1) | IT1150163B (en) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4454159A (en) * | 1981-12-28 | 1984-06-12 | Albert Musher | Dermatological treatment preparations |
| JPS6089410A (en) * | 1983-10-20 | 1985-05-20 | Shiseido Co Ltd | Cosmetic |
| JPS6133105A (en) * | 1984-07-24 | 1986-02-17 | Shiseido Co Ltd | Skin external preparation |
| JPS627A (en) * | 1985-03-04 | 1987-01-06 | Shiseido Co Ltd | Skin external agent containing incorporated urea |
| DE3538412A1 (en) * | 1985-10-29 | 1987-05-07 | Volker Dr Krainbring | Urea ointment |
| JPH0774144B2 (en) * | 1986-03-12 | 1995-08-09 | 久光製薬株式会社 | Skin composition containing urea |
| US5306289A (en) * | 1987-08-26 | 1994-04-26 | United States Surgical Corporation | Braided suture of improved characteristics |
| US5366081A (en) | 1987-08-26 | 1994-11-22 | United States Surgical Corporation | Packaged synthetic absorbable surgical elements |
| US5051272A (en) * | 1988-07-19 | 1991-09-24 | United States Surgical Corporation | Method for improving the storage stability of a polymeric article susceptible to hydrolytic degradation and resulting article |
| US5222978A (en) | 1987-08-26 | 1993-06-29 | United States Surgical Corporation | Packaged synthetic absorbable surgical elements |
| US5359831A (en) | 1989-08-01 | 1994-11-01 | United States Surgical Corporation | Molded suture retainer |
| JP2866114B2 (en) * | 1989-09-20 | 1999-03-08 | 株式会社資生堂 | Cosmetics |
| DE4322395C1 (en) * | 1993-07-01 | 1994-07-28 | Kuehnl Petzoldt Christa Dr Med | Shower lotion for the treatment and care of dry skin |
| DE4341001A1 (en) * | 1993-12-02 | 1995-06-08 | Beiersdorf Ag | Topical preparations containing L-arginine |
| JPH07300419A (en) * | 1993-12-06 | 1995-11-14 | Lansinoh Lab Inc | Composition of lanolin/lanolin acid ester for treating skin |
| FR2718639B1 (en) * | 1994-04-18 | 1996-05-15 | Oreal | Cosmetic and / or dermatological composition containing a tri (alpha-hydroxyacylate) of glycerol as the only precursor of glycerol. |
| DE19529773A1 (en) * | 1995-08-12 | 1997-02-13 | Beiersdorf Ag | Weak, water-soluble mono:carboxylic acids used in skin care prepns. - as active agent for regeneration and promotion of the natural protective and barrier function of healthy or diseased skin |
| JP2002167328A (en) * | 2000-11-29 | 2002-06-11 | Toyo Aerosol Ind Co Ltd | Composition and aerosol composition for external skin preparation |
| DE10133202A1 (en) * | 2001-07-07 | 2003-01-16 | Beiersdorf Ag | Topical compositions containing osmolytes, useful e.g. for treating or preventing dry skin or inflammatory conditions of the skin, e.g. eczema, polymorphic light dermatosis or psoriasis |
| DE10133201A1 (en) * | 2001-07-07 | 2003-01-23 | Beiersdorf Ag | Use of topical compositions containing electrolytes in combination with polyols and/or urea to, e.g. improve skin condition or to treat or prevent skin disorders |
| EP1475806A4 (en) * | 2002-01-23 | 2006-04-26 | Allmighty Co Ltd | Radiation protector and utilization thereof |
| DE10241541A1 (en) * | 2002-09-05 | 2004-03-18 | Nguyen-Petersen, Chanh-Dinh, Dr.med. | Urea is used in cosmetics, including fat-free and greasy cosmetics, used for treating scalp disorders accompanied by dandruff and/or itching, especially in shampoo |
| US20060216260A1 (en) * | 2003-04-24 | 2006-09-28 | L'oreal | Cosmetic peeling method using urea |
| FR2854070A1 (en) * | 2003-04-24 | 2004-10-29 | Oreal | COSMETIC PEELING METHOD |
| JP7336357B2 (en) * | 2019-11-05 | 2023-08-31 | 日本精化株式会社 | Lactic acid ester and cosmetics containing the same |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE325667B (en) * | 1968-03-06 | 1970-07-06 | Medisan Ab | |
| DE2064604C3 (en) * | 1970-12-30 | 1982-10-21 | Chemisches Laboratorium Dr. Kurt Richter Gmbh, 1000 Berlin | Skin care products |
| JPS5025741A (en) * | 1973-07-17 | 1975-03-18 | ||
| DE2514844A1 (en) * | 1975-04-04 | 1977-03-17 | Freudenberg Carl Fa | COSMETIC INGREDIENT |
-
1981
- 1981-02-02 FR FR8101971A patent/FR2498929A1/en active Granted
-
1982
- 1982-02-01 JP JP57013428A patent/JPS57150608A/en active Granted
- 1982-02-01 IT IT19388/82A patent/IT1150163B/en active
- 1982-02-01 BE BE0/207192A patent/BE891972A/en not_active IP Right Cessation
- 1982-02-01 CH CH600/82A patent/CH651471A5/en not_active IP Right Cessation
- 1982-02-01 DE DE19823203260 patent/DE3203260A1/en active Granted
- 1982-02-01 CA CA000395338A patent/CA1171265A/en not_active Expired
- 1982-02-01 GB GB8202754A patent/GB2092444B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2092444B (en) | 1985-11-13 |
| FR2498929A1 (en) | 1982-08-06 |
| IT8219388A0 (en) | 1982-02-01 |
| DE3203260C2 (en) | 1992-08-27 |
| IT1150163B (en) | 1986-12-10 |
| GB2092444A (en) | 1982-08-18 |
| JPS57150608A (en) | 1982-09-17 |
| FR2498929B1 (en) | 1984-04-13 |
| DE3203260A1 (en) | 1982-09-23 |
| CA1171265A (en) | 1984-07-24 |
| CH651471A5 (en) | 1985-09-30 |
| BE891972A (en) | 1982-08-02 |
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