JPS58216109A - Dried film cosmetic and laminated film cosmetic - Google Patents
Dried film cosmetic and laminated film cosmeticInfo
- Publication number
- JPS58216109A JPS58216109A JP9964382A JP9964382A JPS58216109A JP S58216109 A JPS58216109 A JP S58216109A JP 9964382 A JP9964382 A JP 9964382A JP 9964382 A JP9964382 A JP 9964382A JP S58216109 A JPS58216109 A JP S58216109A
- Authority
- JP
- Japan
- Prior art keywords
- film
- cosmetic
- water
- dried
- thickness
- 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
- 239000002537 cosmetic Substances 0.000 title claims abstract description 47
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 24
- 102000004190 Enzymes Human genes 0.000 claims abstract description 23
- 108090000790 Enzymes Proteins 0.000 claims abstract description 23
- 239000010408 film Substances 0.000 claims abstract description 23
- 239000000203 mixture Substances 0.000 claims abstract description 16
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 12
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 12
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 11
- 239000010409 thin film Substances 0.000 claims abstract description 10
- 239000004615 ingredient Substances 0.000 claims description 12
- 238000001035 drying Methods 0.000 claims description 11
- 238000000354 decomposition reaction Methods 0.000 abstract description 4
- 230000009849 deactivation Effects 0.000 abstract description 3
- 238000005266 casting Methods 0.000 abstract description 2
- 235000011837 pasties Nutrition 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract description 2
- 229940079593 drug Drugs 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 239000012467 final product Substances 0.000 abstract 1
- 239000005001 laminate film Substances 0.000 abstract 1
- 150000000996 L-ascorbic acids Chemical class 0.000 description 17
- 239000000546 pharmaceutical excipient Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004367 Lipase Substances 0.000 description 3
- 102000004882 Lipase Human genes 0.000 description 3
- 108090001060 Lipase Proteins 0.000 description 3
- 108091005804 Peptidases Proteins 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 235000019421 lipase Nutrition 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 235000010378 sodium ascorbate Nutrition 0.000 description 2
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 2
- 229960005055 sodium ascorbate Drugs 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- DBTMGCOVALSLOR-UHFFFAOYSA-N 32-alpha-galactosyl-3-alpha-galactosyl-galactose Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(OC2C(C(CO)OC(O)C2O)O)OC(CO)C1O DBTMGCOVALSLOR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- RXVWSYJTUUKTEA-UHFFFAOYSA-N D-maltotriose Natural products OC1C(O)C(OC(C(O)CO)C(O)C(O)C=O)OC(CO)C1OC1C(O)C(O)C(O)C(CO)O1 RXVWSYJTUUKTEA-UHFFFAOYSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical class [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000057 Mannan Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000269851 Sarda sarda Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 229940081735 acetylcellulose Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- -1 etc. Chemical class 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- FYGDTMLNYKFZSV-UHFFFAOYSA-N mannotriose Natural products OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(OC2C(OC(O)C(O)C2O)CO)C(O)C1O FYGDTMLNYKFZSV-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- 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
- A61K8/0208—Tissues; Wipes; Patches
-
- 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
- A61Q19/10—Washing or bathing 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)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は新規な化粧料、史に詳しくは、アスコルビン′
rtR類、酵素等の条用成分又は美肌成分を安定化した
状態で配合してなる乾燥性膜状化粧料及び積層膜状化粧
料に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel cosmetic, specifically ascorbic
The present invention relates to a drying film-like cosmetic and a laminated film-like cosmetic that are formulated with rtRs, enzymes, and other treatment ingredients or skin-beautifying ingredients in a stabilized state.
従来アスコルビン酸は熱や光に対して極めて、不安定で
、酸化され易く、化粧料の基剤成分に使用しても経時で
vo活性を失ない、本来的な効果を発揮し得々い。特に
水分を多量に含有する化粧料において、その傾向は著し
く、分解による異変や異臭を生じ製品として望ましいも
のではない。この為、高級脂肪酸やリン酸等の各種誘導
体化による安定化が試みられているものの未だ充分に目
的を達し得ていないのが現状である。また一部には粉末
分包化され安定化を図る試みも見られるが、これも使用
時に、水、化粧水との混ぜ合わせの動作を必要とし、甚
だ繁雑であシ好適なものとは言い難い、また酵素につい
ても同様に、熱に対する安定性、pH領域の制限等がろ
υ、通常の化粧料中において容易に失活し易い。′この
改良として一部マイクロカプセル化した形態があるが、
これとても他の化粧品原料の存在丁では失活し易くとて
も化粧料に使える状態では未だない。Conventionally, ascorbic acid is extremely unstable to heat and light and easily oxidized, and even when used as a base component of cosmetics, it does not lose its VO activity over time and cannot exert its original effects. This tendency is particularly noticeable in cosmetics containing a large amount of water, which causes abnormal changes and unpleasant odors due to decomposition, making them undesirable as products. For this reason, attempts have been made to stabilize it by various derivatizations such as higher fatty acids and phosphoric acid, but at present the objective has not yet been fully achieved. In addition, some attempts have been made to stabilize the product by packaging it in powder form, but this also requires mixing with water and lotion before use, which is extremely complicated and is not ideal. Similarly, enzymes have low stability against heat, limited pH range, etc., and are easily deactivated in ordinary cosmetics. 'As an improvement on this, there is a form in which some microcapsules are used.
This substance is easily deactivated in the presence of other cosmetic raw materials, so it is not yet in a state where it can be used in cosmetics.
本発明者は、上記の如き、アスコルビン酸類や#素の安
定性における欠点を解決すると共に、使い易い形態を具
備した新規な乾燥性膜状化粧料及び積層膜状化粧料を完
成するに至った。The present inventor has solved the above-mentioned drawbacks in the stability of ascorbic acids and # elements, and has completed a novel drying film-like cosmetic and a laminated film-like cosmetic that has an easy-to-use form. .
すなわち、本発明は、皮膜形成能を有する水浴性高分子
と水とを主剤とする基剤中に、薬用成分又は美肌成分の
うち少なくとも一種あるいは二種以上を配合したペース
ト状組成物を薄膜化し、乾燥させてなる皮膜の厚さが1
0μ〜1闘である乾燥性膜状化粧料に関するものである
。That is, the present invention provides a thin film of a paste composition in which at least one or more of medicinal ingredients or skin-beautifying ingredients are blended into a base mainly consisting of water and a water bathable polymer having film-forming ability. , the thickness of the dried film is 1
The present invention relates to a drying film-like cosmetic having a particle size of 0 μm to 1 μm.
さらに本発明は、皮膜形成能を有する水溶性高分子と水
とを主剤とする基剤中に、アスコルビン酸類もしくは酵
素から選択される薬用成分又は美肌成分のうち少なくと
も一種あるいは二種以上を配合したペースト状組成物を
保持体に薄膜を形成せしめるように均一塗布し、乾燥さ
せてなる厚さ50μ〜20〔]μの積層体とすることを
%徴とする積層膜状化粧料に関するものでもある。Furthermore, the present invention is characterized in that at least one or two or more medicinal ingredients or skin-beautifying ingredients selected from ascorbic acids or enzymes are blended into a base mainly consisting of water and a water-soluble polymer having film-forming ability. It also relates to a laminated film-like cosmetic product characterized by uniformly applying a paste composition to a holder to form a thin film and drying it to form a laminate with a thickness of 50μ to 20μ. .
本発明に適用される水溶性高分子である賦形剤としては
、デンプン類、マンナン、ガラクタン、アルギン酸ソー
ダ、デキストラン(α−1,6−グリコシド)、α−1
,6−マルトトリオース、ゼラチン、カセイン等に代表
される天然水溶性高分子、メチルセルロース、エチルセ
ルロース、ヒドロキシエチルセルロース、カルボキシメ
チルセルロース等に代表される半合成水溶性高分子、ポ
リビニルアルコール、ポリアクリル酸ソーダ、ポリエチ
レンオキサイドに代表される合成水浴性高分子があるが
、賦形剤自身の水への低温での溶解性、基剤中でのアス
コルビン酸類、酵素の分散安定性、賦形剤自体の安全性
及び薄膜化時の皮膜形成能h4を考慮してα−1,6−
マルトトリオースが好適である。Excipients that are water-soluble polymers that can be applied to the present invention include starches, mannan, galactan, sodium alginate, dextran (α-1,6-glycoside), α-1
, 6-maltotriose, gelatin, casein, etc., natural water-soluble polymers, methylcellulose, ethylcellulose, hydroxyethylcellulose, carboxymethylcellulose, etc., and other semisynthetic water-soluble polymers, polyvinyl alcohol, sodium polyacrylate, There are synthetic water bathable polymers such as polyethylene oxide, but the solubility of the excipient itself in water at low temperatures, ascorbic acids in the base, the dispersion stability of enzymes, and the safety of the excipient itself are important. and considering the film forming ability h4 during thinning, α-1,6-
Maltotriose is preferred.
また、基剤中に配合される薬用成分又は美肌成分として
は、アスコルビン酸類、更に詳しくはアスコルビン厳、
アスコルビン酸のナトリウム、カリウム、カルシウム、
マグネシウム等の塩、アスコルビン酸の2位または3位
水酸基のリン酸、酢酸、ラウリル酸、ノソルミチン酸、
ステアリン酸等の各ニス゛チル誘導体が挙げられ、溶解
・もしくは分散と言う形で配合され、また酵素について
は、タン自分解酵素としてのプロテアーゼ、加水分解酵
素としてのす・ソーゼ等が挙げられる。In addition, medicinal ingredients or skin-beautifying ingredients that are blended into the base include ascorbic acids, more specifically ascorbic acids,
Ascorbic acid sodium, potassium, calcium,
Salts of magnesium, etc., phosphoric acid of the 2- or 3-position hydroxyl group of ascorbic acid, acetic acid, lauric acid, nosorumitic acid,
Examples include various Nisthyl derivatives such as stearic acid, which are blended in the form of solution or dispersion, and examples of enzymes include protease as a protein enzyme, and souse as a hydrolytic enzyme.
・前記選択されたアスコルビン酸類または1[Rは、ア
スコルビン酸類の1aまたは2種以上単独もしく、は、
酵素の1種ま゛たけ2種以上単独でも良・く、又はアス
コルビン酸類の1種または2種以上と酵素の1種または
2種以上との組合せによっても配合し得る。配合量とし
ては、最終的な含有量が、アスコルビン酸類については
、効果面を考慮′して乾燥皮膜□に対しα1〜10チの
範囲で可能であるが、最適効果発現tを勘案す 5−
れは乾燥皮膜に対【7て、0.5〜2%の範囲が無駄が
なく、且つ効果的であり好ましいものであ不。- The selected ascorbic acids or 1 [R is 1a or two or more of ascorbic acids alone or,
One or more enzymes may be used alone, or one or more ascorbic acids and one or more enzymes may be combined. As for the blending amount, the final content of ascorbic acids can be in the range of α1 to 10 for the dry film □, taking into account the effectiveness, but taking into consideration the optimal effect expression 5- This is preferably in the range of 0.5 to 2% based on the dry film, as it is efficient and effective.
また#Iについては同様に乾燥皮膜に対して0,01〜
6チが効果を有する範囲として西゛己合可能であるが、
通常化粧料)・しては乾燥皮膜に対して102〜t1.
5%の範囲が好筐しい。Similarly, #I is 0.01 to 0.01 to the dry film.
Although it is possible to combine the west as the effective range of 6chi,
Normal cosmetics) and dry film are 102~t1.
A range of 5% is ideal.
前記選択された1、アスコルビン酸類、及び酵素の適用
Iけ、回l二<前記水溶性高分子群から選択された賦形
剤と水とを主剤とする基剤中に、溶解もしくけ分散され
、ペースト状組成物を得る。この時、賦形剤と水との配
合比率は、賦形剤1〜50%に対1.水99〜50%が
可能であるが、粘度、皮膜形成時の取扱い易さ等を考慮
して、賦形剤5〜25%に対12、水95〜75チの比
率が好まL7い。祠られた−2−ス]・状組成物は、流
延法等によ漫薄膜化され、約40℃以下で、減圧上乾燥
される。ここで得られる薄膜の厚みは、屈伸性を維持1
−1々おかつ膜一度を考慮して10μ〜111Ill+
のものが好ましい。同様にバースト状組成物を、紙、グ
ラシイ1,15す゛エチレン、ポリプロピ−6−
レン、ポリエステル、箒雫苓テ呼苓アセチルセルロース
等のいずれかを素材とする柔軟な保持体上に、ペーパー
キャスト法、ディプコータ法、ロールコータ法、ナイフ
コーター法等に代表される塗布法によシ、均一塗布し約
40℃以下で減圧上乾燥し、薄膜を形成させる。この時
保持体の厚みとしては、柔軟性を維持させ、また膜強度
を考慮して、50μ〜200μのものが好ましく、さら
に塗布薄膜の厚みとしては10μ〜針μが最適である。Application of the selected ascorbic acids and enzymes is dissolved or dispersed in a base mainly consisting of an excipient selected from the water-soluble polymer group and water. , a pasty composition is obtained. At this time, the mixing ratio of excipient and water is 1 to 50% excipient to 1. Although 99 to 50% water is possible, in consideration of viscosity, ease of handling during film formation, etc., a ratio of 12 to 25% excipient and 95 to 75% water is preferred. The polished -2-su]-like composition is formed into a thin film by a casting method or the like, and dried under reduced pressure at about 40° C. or lower. The thickness of the thin film obtained here maintains flexibility and extensibility.
- 10 μ to 111 Ill+ considering each bonito membrane once
Preferably. Similarly, the burst composition is paper-cast onto a flexible holder made of paper, glassy 1,15-ethylene, polypropylene-6-ethylene, polyester, acetyl cellulose, etc. The composition is uniformly coated by a coating method such as a dip coater method, a roll coater method, a knife coater method, etc., and dried under reduced pressure at about 40° C. or lower to form a thin film. At this time, the thickness of the holder is preferably 50 to 200 microns in order to maintain flexibility and film strength, and the optimal thickness of the coated thin film is 10 to needle micro.
前記の様にして得られた乾燥性膜状化粧料、及び積層膜
状化粧料中には、程んど水分を含まず、従って水系にお
いて非常に不安定なアスコルビン酸類や酵素は、経時に
よっても程んど分解、失活などせず安定に存在し得るも
のである。The dry film-like cosmetics and laminated film-like cosmetics obtained as described above do not contain much water, and therefore ascorbic acids and enzymes, which are extremely unstable in aqueous systems, may deteriorate over time. It can exist stably without being decomposed or deactivated.
また使用時においては、顔面等に、水または化粧水等を
塗布後、前記膜状化粧料、普たは積層膜状化粧料を必要
に応じて任意の形に分割し、顔面等に貼シ付ける。この
時、水または化粧水中の水分によシ、アスコルビン酸類
または酵素を含む薄膜部が溶解し、配合されていたアス
コルビン酸類または酵素が所望の効果を発揮する。In addition, during use, after applying water or lotion to the face, etc., divide the film-like cosmetic, normal film-like cosmetic, or laminated film-like cosmetic into arbitrary shapes as needed, and paste it on the face, etc. wear. At this time, the water or the water in the lotion dissolves the thin film containing ascorbic acids or enzymes, and the ascorbic acids or enzymes contained therein exhibit the desired effect.
次に本発明の代表的配装置及び方法の実施例を示す。Next, examples of representative arrangement devices and methods of the present invention will be shown.
実施例1.7スコルビン#Rを含有する乾燥性膜状化粧
料
α−1,6−マルトトリオース20部を水80部に分散
し、これを60℃まで加熱、完全に溶解し、これをゆっ
くりと40℃以下まで冷却維持した。これとは別にアス
コルビン酸0.2部を水20部に攪拌溶解し九溶液を調
製し、これを前記基剤中に少量づつ混合し、は−スト状
組成物を得た。次にこのは−ス′ト状組成物をステンレ
スのベルトtたけドラム上に流し、次いで約40℃以下
で減圧上乾燥し、乾燥性膜状化粧料を得た。ここで得ら
れた乾燥性膜状化粧料中には、アスコルビン酸が乾燥皮
膜に対して1パーセントの割合で含′まれる。また膜厚
の調節は、基剤中の樹脂分含有率、及び樹脂自体の分子
量に由来する粘度刺部によりコントロールされる。Example 1.7 Dry membranous cosmetic containing Scorbine #R 20 parts of α-1,6-maltotriose was dispersed in 80 parts of water, and the mixture was heated to 60°C to completely dissolve it. Cooling was maintained slowly to below 40°C. Separately, 0.2 part of ascorbic acid was stirred and dissolved in 20 parts of water to prepare a solution, which was mixed little by little into the base to obtain a starch composition. Next, this cast composition was poured onto a stainless steel belt-tall drum, and then dried under reduced pressure at a temperature below about 40 DEG C. to obtain a dry film-like cosmetic. The dry filmy cosmetic obtained here contains ascorbic acid at a ratio of 1% to the dry film. Further, the film thickness is controlled by the resin content in the base and the viscosity derived from the molecular weight of the resin itself.
実施例2. リi#−ゼを含有する乾燥性膜状化粧料
α−1,6−マルトトリオース5部を水95部に溶解し
た。これとは別に[1005部のリパーゼを水10部に
溶解した溶液を調製し、これを前記基剤中に少量づつ混
合し、は−スト状組成物を得た。以後実施例1と同様の
方法にて乾燥性膜状化粧料を得た。得られた乾燥性膜状
化粧料中には、乾燥皮膜に対し7て0.1パーセントの
割合でリパーゼを含む。Example 2. EXAMPLE 1 A drying film-like cosmetic containing lysate 5 parts of α-1,6-maltotriose was dissolved in 95 parts of water. Separately, a solution of 1,005 parts of lipase dissolved in 10 parts of water was prepared, and this was mixed into the base little by little to obtain a starch composition. Thereafter, a dry film-like cosmetic was obtained in the same manner as in Example 1. The resulting dry film cosmetic contains lipase at a ratio of 0.1% to the dry film.
実施例6. アスコルビン酸ナトリウム及びプロテアー
ゼを含有する積層膜状化粧料
α−1.6−マルトトリオース15部を水85部に分散
し、60℃に加熱、完全に溶解し2、これを40℃以下
に冷却維持した。これとは別に、アスコルビン酸ナトリ
ウム0.1部及びプロテアーゼ0.02部を水20部に
溶解した溶液を調製し、これを前記基剤中に少量づつ混
合し、バースト状組成°物を得た。次にこのペースト状
朝成物を、厚さ80μ、少量のシリコーン系剥離剤 9
−
を塗布したポリエステル保持膜−ヒに、ナイフコーター
、またはロールコータ−を用いて均一に塗布した。次い
で40“C以下、減圧下、ゆっくりと乾燥され、MJi
l膜状11″、粧料f得た。Example 6. Disperse 15 parts of α-1,6-maltotriose, a laminated film cosmetic containing sodium ascorbate and protease, in 85 parts of water, heat to 60°C to completely dissolve 2, and cool to 40°C or below. Maintained. Separately, a solution was prepared in which 0.1 part of sodium ascorbate and 0.02 part of protease were dissolved in 20 parts of water, and this was mixed into the base little by little to obtain a burst-like composition. . Next, this paste-like as-prepared product was coated with a thickness of 80 μm and a small amount of silicone release agent 9
A knife coater or a roll coater was used to uniformly coat the polyester retention film coated with -. Then, it was slowly dried under reduced pressure below 40"C to obtain MJi
1 film-like 11'', cosmetic f was obtained.
本発明によって傳られる乾燥性膜状化粧料または積層膜
状化粧料は水分を程んど含まない水溶性高分子素手4中
に、水に対1.て不安定なアスコルビン酸類や酵Xを閉
じ込める方法である為、安定性が極めてA < 、i
fL Cd!用時においては任意の大きさと1,7て使
用し得る為、極めて簡便である。The drying film-like cosmetic or laminated film-like cosmetic according to the present invention is prepared by adding 1.0% to water to a water-soluble polymer bare hand 4 that does not contain much water. Since this method confines unstable ascorbic acids and enzyme X, the stability is extremely high.
fL Cd! When in use, it is extremely convenient because it can be used in any size.
次に本発明に係るアスコルビン酸類または酵素配合の乾
燥性膜状化粧料とアスコルビン酸類ま次は酵素単独での
安定性の比較データを示す。Next, comparative data will be shown regarding the stability of the dry film cosmetic containing ascorbic acids or enzymes according to the present invention and ascorbic acids or enzymes alone.
試験方法とし7て、′rスコルビン酸類については、同
一1(1%^度)で配合された乾燥性膜状化粧料(実施
例1)及び水溶液、酵素については、四fit ([1
,1% 濃度)で配合され急乾燥性膜状化粧料(実施I
J’lJ 2 )及び水溶液について、40℃、2週間
数ff1tJのアスコルビン酸分解率及びリバ10−
−ゼ失活率について比較し友。ここでアスコルビン酸分
解率については高速液体クロマトグラフィーを用いたア
スコルビン酸残存量の測定、またリパーゼ失活率につい
ては、オリーブ油を基質として得られる遊離脂肪酸量を
ガスクロマトグラフィーを用いて測定し、得られた測定
値よシ逆算出した。結果を表1に示す。As a test method 7, for scorbic acids, dry film cosmetics (Example 1) and aqueous solutions formulated at the same concentration (1%), and for enzymes, 4fit ([1%
, 1% concentration) and rapidly drying film-like cosmetics (Implementation I
The ascorbic acid decomposition rate and the liver-10-ase deactivation rate were compared for several ff1tJ at 40°C for 2 weeks for J'lJ2) and aqueous solutions. Here, the ascorbic acid decomposition rate is determined by measuring the residual amount of ascorbic acid using high performance liquid chromatography, and the lipase deactivation rate is determined by measuring the amount of free fatty acids obtained using olive oil as a substrate using gas chromatography. The measured values were back calculated. The results are shown in Table 1.
表 1 アスコルビン酸、酵素安定性比較データ表1よ
り明らかな様に5本発明において得られた膜状化粧料に
おいては、配合されたアスコルビン酸、酵素の安定性は
極めて高い。Table 1 Comparative Data on Ascorbic Acid and Enzyme Stability As is clear from Table 1, the stability of the ascorbic acid and enzyme blended in the film-like cosmetics obtained in the present invention is extremely high.
前記の如く、本発明による乾燥性膜状化粧料、積層膜状
化粧料においてはそこに配合されたアスコルビン酸類、
酵素の安定性は極めて高く、しかも使用時には充分に効
果を発揮し得る様に剤形化された化粧料であり、また使
用者が所望の大きさに分割して使用できる点で極めて簡
便性に優れた化粧料である。As mentioned above, in the drying film cosmetic and laminated film cosmetic according to the present invention, ascorbic acids,
The stability of the enzyme is extremely high, and the cosmetic is formulated in such a way that it can be fully effective when used, and it is extremely convenient as the user can divide it into the desired size and use it. It is an excellent cosmetic.
特許出願人 ポーラ化成工業株式会社Patent applicant: POLA CHEMICAL INDUSTRIES, INC.
Claims (1)
する基剤中に薬用成分又は美肌成分のうち少なくとも一
種あるいは二種以上を配合したペースト状組成物を薄膜
化し、乾燥させてなる皮膜の厚さが10μ〜1−である
乾燥性膜状化粧料。 2、 皮膜形成能を有する水溶性高分子と水とを主剤と
する基剤中に、アスコルビン酸li%しくけ酵素から選
択される薬用成分又は美肌成分のうち少なくとも一種あ
るいは二種以上を配合したペースト状組成物を保持体に
薄膜を形成せしめるように均一塗布し、乾燥させてなる
厚さ50μ〜200μの積層体とすることを%徴とする
積層膜状化粧料。 3、 水溶性高分子がα−1,6−マルトトリオースで
ある特許請求の範囲第1項記載の乾燥性膜状化粧料及び
%fFmf4求の範囲第2項記載の積層膜状化粧料。[Scope of Claims] 1. A paste composition containing at least one or two or more of medicinal ingredients or beautifying ingredients in a base mainly consisting of water and a water-soluble polymer having film-forming ability is made into a thin film. A drying film-like cosmetic having a film thickness of 10μ to 1−1 after drying. 2. At least one or two or more medicinal ingredients or skin-beautifying ingredients selected from ascorbic acid li% shikke enzyme are blended into a base mainly consisting of water and a water-soluble polymer with film-forming ability. A laminated film cosmetic comprising a paste composition uniformly applied to a holder to form a thin film and dried to form a laminate with a thickness of 50 μm to 200 μm. 3. The drying film-like cosmetic according to claim 1, wherein the water-soluble polymer is α-1,6-maltotriose, and the laminated film-like cosmetic according to claim 2, wherein the desired range is %fFmf4.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9964382A JPS58216109A (en) | 1982-06-10 | 1982-06-10 | Dried film cosmetic and laminated film cosmetic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9964382A JPS58216109A (en) | 1982-06-10 | 1982-06-10 | Dried film cosmetic and laminated film cosmetic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS58216109A true JPS58216109A (en) | 1983-12-15 |
Family
ID=14252731
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9964382A Pending JPS58216109A (en) | 1982-06-10 | 1982-06-10 | Dried film cosmetic and laminated film cosmetic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58216109A (en) |
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| US6042844A (en) * | 1996-03-04 | 2000-03-28 | Kao Corporation | Sheet pack |
| US6306382B1 (en) | 1991-05-15 | 2001-10-23 | Kao Corporation | Keratotic plug remover |
| US6602513B2 (en) | 1997-11-27 | 2003-08-05 | Shiseido Co., Ltd. | Face pack |
| US6942869B2 (en) | 1999-05-12 | 2005-09-13 | Kao Corporation | Keratotic plug remover |
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