WO1993005755A1 - Cosmetic composition and emulsion composition - Google Patents
Cosmetic composition and emulsion composition Download PDFInfo
- Publication number
- WO1993005755A1 WO1993005755A1 PCT/JP1992/001229 JP9201229W WO9305755A1 WO 1993005755 A1 WO1993005755 A1 WO 1993005755A1 JP 9201229 W JP9201229 W JP 9201229W WO 9305755 A1 WO9305755 A1 WO 9305755A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cis
- acid
- derivative
- purity
- oily
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 77
- 239000000839 emulsion Substances 0.000 title claims abstract description 41
- 239000002537 cosmetic Substances 0.000 title claims abstract description 34
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 32
- 239000000194 fatty acid Substances 0.000 claims abstract description 32
- 229930195729 fatty acid Natural products 0.000 claims abstract description 32
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 32
- 239000004094 surface-active agent Substances 0.000 claims description 66
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 59
- 239000000126 substance Substances 0.000 claims description 57
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- 239000002253 acid Substances 0.000 claims description 23
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- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 3
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- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 1
- 235000015500 sitosterol Nutrition 0.000 description 1
- 229950005143 sitosterol Drugs 0.000 description 1
- NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- KKDONKAYVYTWGY-UHFFFAOYSA-M sodium;2-(methylamino)ethanesulfonate Chemical compound [Na+].CNCCS([O-])(=O)=O KKDONKAYVYTWGY-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- WRPMUZXHQKAAIC-ZZEZOPTASA-N stearyl oleate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC WRPMUZXHQKAAIC-ZZEZOPTASA-N 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229950009883 tocopheryl nicotinate Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Classifications
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- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
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- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
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- 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
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
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- 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
- A61K8/37—Esters of carboxylic acids
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- A—HUMAN NECESSITIES
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- 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
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
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- 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
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4993—Derivatives containing from 2 to 10 oxyalkylene groups
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- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
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- A—HUMAN NECESSITIES
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- 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
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61Q5/00—Preparations for care of the hair
Definitions
- the present invention relates to a cosmetic composition and an emulsion composition containing cis- ⁇ 9-octadedecenoic acid or a derivative thereof at a high concentration in an oily component.
- Japanese Patent Application Laid-Open No. Sho 61-297 discloses a method for producing high-purity oleic acid.
- Japanese Unexamined Patent Publication (Kokai) No. 62-13832 / 41 discloses a method for producing glycerin monoolate
- Japanese Unexamined Patent Publication (Kokai) No. 62-138485 / 1991 discloses a method for producing propylene glycol monoolate.
- Japanese Patent Application Laid-Open No. Sho 62-1384852 describes a method for producing a polyalkylene alcohol monohydrate
- Japanese Patent Application Laid-Open No. 62-142421 discloses a method for producing a sorbitan monolate.
- Japanese Patent Application Laid-Open No. Sho 62-153,250 discloses a method for producing a polyalkylene glycol alkyl ether oleate
- Japanese Patent Application Laid-Open No. Sho 62-153,251 discloses a polyoxyalkylene polyol
- Japanese Patent Application Laid-Open No. Sho 62-1533252 discloses a method for producing polyoxyalkylene polyhydric alcoholate.
- Oleic acid Japanese Patent Application Laid-Open No. Sho 62-153,254 discloses a method for producing a polyalkylene glycololate.
- a method for producing serine monoolate is disclosed in Japanese Patent Application Laid-Open No.
- the present invention provides a chemical composition and an emulsion composition containing a high concentration of cis- ⁇ 9-agectadecenoic acid or a derivative thereof in an oily component, and has an unprecedented excellent feeling in use and excellent aging.
- An object of the present invention is to provide a cosmetic composition exhibiting stability and an emulsion composition exhibiting excellent emulsion stability. Disclosure of the invention
- the present invention comprises: 0.1 to 99% by weight of an oily component and 99.9 to 1% by weight of an aqueous component, wherein 85% by weight or more of cis-1- ⁇ 9-octadedecenoic acid or a derivative thereof in the oily component, and Cosmetics in which the content of cis- ⁇ 9-unsaturated fatty acids or derivatives thereof is 90% by weight or more, and the content of fatty acids other than cis- ⁇ 9-unsaturated fatty acids, derivatives or other oily components is 10% by weight or less.
- the present invention comprises 0.1 to 99% by weight of an oily component and 99.9 to 1% by weight of an aqueous component, and 85% by weight of systemic 9-octadedecenoic acid or a derivative thereof in the oily component.
- the amount of cis-1- ⁇ 9-unsaturated fatty acid or derivative thereof is 90% by weight or more, and the content of fatty acids other than cis-1 ⁇ 9-unsaturated fatty acid, derivative or other oily component is 10% by weight or less
- the present invention further provides an emulsion composition comprising an oily substance in which an oily component is insoluble in an aqueous component and a surfactant which dissolves or emulsifies in the aqueous component.
- the ratio of the oily component to the aqueous component is 0.1 to 99% by weight: 99.9 to 1% by weight, and this ratio is the ratio used in ordinary cosmetic compositions, and is the ratio of the desired cosmetic composition.
- This ratio is, for example, 5 to 20% by weight for a lotion: 99.5 to 80% by weight, 10 to 85% by weight for a cream: 90 to 15% by weight, 3 to 5% for an emulsion.
- the cis-1 ⁇ 9-unsaturated fatty acid includes cis-1 ⁇ 9-octadecenoic acid (common name: oleic acid), cis-1 ⁇ 9-hexadecenoic acid (common name: palmitoleic acid) and the like. Is a fatty acid with one cis-unsaturated bond at position 9.
- Derivatives of cis- ⁇ 9-unsaturated fatty acids include the following.
- Salts Alkali metal salts such as sodium and potassium; ammonium salts; morpholine salts; alkylamines such as methylamine, ethylamine, butylamine, etc .; monoethanolamine, diethanolamine, triethanolamine, Alkanolamine salts such as triisopropanolamine, 2-amino-12-methyl-11-propanol, 2-amino-12-methyl-11,3-propanediol; basic amino acid salts such as arginine (2) Amid
- Amides (this amide is cis- ⁇ 9-unsaturated fatty acid amide); amides with alkyl or alkenylamines such as methylamine, ethylamine, butyramine, cis- ⁇ 9-unsaturated amines.
- Amino acids such as monoethanolamine, diethanolamine, isopropanolamine, 2-amino-2-methyl-11-propanol, and 2-amino-2-methyl-1,3-propanediol
- Ester methanol, ethanol, propanol, isopropanol, butanol, neopentyl alcohol, hexanol, octanol, 2-ethylhexanol, nonanol, isononanol, decanol, dodecanol, isotridecanol, tetra Decanol, Hexadecanol, Isopalmityl alcohol, Hexyldecyl alcohol, Octadecanol, Isostearyl alcohol, Eicosanol, 2-octyldodecanol, Docosanol, Octacosanol, Triacontanol, Aryl alcohol, Hexadecenyl Alcohol, cis- ⁇ 9-octadecenyl alcohol, docosenol, cyclohexanol, lanolin alcohol, terpene alcohol, benzyl alcohol, etc.
- Chole or their esters with voroxyxethylenate or polyoxypropylene ethylene glycol, propylene glycol, butylene glycol, glycerol, polyglycerol, trimethylolpropane, pentaerythritol, sorbitol, mannitol, sorbitan, etc.
- cis-1 ⁇ 9-unsaturated alcohol derivative cis-1 ⁇ 9-unsaturated alcohol derived from cis-1 ⁇ 9-unsaturated fatty acid, its phosphate ester, sulfate ester, polyoxyethylenate, polyoxy Propylene, Polyoxyethylenated Phosphate, Polyoxyethylenated Sulfate, Polyoxypropylene phosphate ester, polyoxypropylene sulfate ester or a salt thereof; cis-1 ⁇ 9-unsaturated alcohol and acetic acid, butyric acid, 2-ethylhexanoic acid, lauric acid, stearic acid, cis-1 ⁇ 9 —Saturated, unsaturated, linear, branched, mono- or polyvalent carboxylic acids such as decenoic acid, succinic acid, adipic acid, sebacic acid, maleic acid, oxalic acid, citric acid, malic acid Or
- cis-1 ⁇ 9-unsaturated amine derivative cis-1 ⁇ 9-unsaturated amine derived from cis-1 ⁇ 9-unsaturated fatty acid and acid such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, acetic acid, etc. Salts with cis-1 ⁇ 9-unsaturated groups, quaternary ammonium salts with cis-1- ⁇ 9-unsaturated groups, etc.
- the derivative of cis-1- ⁇ 9-unsaturated fatty acid which is an oily component in the present invention
- the cosmetic composition of the present invention is a composition separated into two layers composed of an oily substance and an aqueous component, a uniform composition composed of a surfactant and an aqueous component, There are homogeneous, clear or cloudy compositions that are solubilized, emulsified, or dispersed in the components.
- oily substances such as ethanol, isopropanol, cis-1 ⁇ 9-hexadecenyl alcohol, cis-1 ⁇ 9-octadecenyl alcohol, isostearyl.
- oily substances such as ethanol, isopropanol, cis-1 ⁇ 9-hexadecenyl alcohol, cis-1 ⁇ 9-octadecenyl alcohol, isostearyl.
- Glycerol or polyglycerol as a surfactant 9-octadecenoic acid ester, sorbitan mono- or sesquisium 9-octadecenoic acid ester, polyoxyethylene sorbitan monocis-1- ⁇ 9-octadecenoic acid ester, tri- or tetracis-ammonium polyoxyethylene sorbitol ether 9 —Octadecenoic acid ester, polyoxyethylene monocis 9-octadecenoic acid ester, polyoxyshethylen cis-1 ⁇ 9-octadecenyl ether, etc., and particularly preferred are cis-1 ⁇ both for oily substances and surfactants.
- 9 Examples of esters of kutadecenoic acid.
- a surfactant which is a cis-1-unsaturated fatty acid derivative for emulsifying or solubilizing cis-1- ⁇ 9-unsaturated fatty acid and a derivative thereof, which is an oily substance insoluble in an aqueous component, in an aqueous component is used.
- emulsification or solubilization is performed more easily than when other surfactants are used, and the stability is very excellent.
- the weight ratio of the oily substance to the surfactant at this time varies depending on the type of the oily component or aqueous component, the ratio thereof, other added components, etc., but it is 99 to 1: 1 to 99, preferably 97 to 99. 3: 3 to 97.
- the other oily components include all oily components other than cis-1- ⁇ 9-unsaturated fatty acids and derivatives thereof. That is, in addition to fatty acids other than cis- ⁇ 9-unsaturated fatty acids or derivatives thereof, paraffin, kerosene, squalane, vegetable oil, animal oil, lanolin, wood wax, hexadenosol, isostearyl alcohol, silicone oil, fluorinated carbonized It contains natural or synthetic oily substances such as hydrogen, polyoxypropylene ether, cholesterol, and tocopherol, and surfactants derived from fatty acids other than system 9-unsaturated fatty acids such as lauric acid diethanolamide. Other surfactants, such as polyoxyethylene phenyl ether, are also included.
- the aqueous component acts as a humectant and can be any compound that mixes with water as well as water, such as ethanol, isopropanol, ethylene glycol, propylene glycol, and 1,3-butylene glycol.
- Alcohols such as glycerol, polyethylene glycol, glycerol, sorbitol, polyglycerol, and polyvinyl alcohol; sugars such as gnorecose and sucrose; mucopolysaccharides such as hyaluronic acid; amino acids such as glutamate; proteins such as collagen and so on.
- cis-1 ⁇ 9-unsaturated fatty acids such as palmitreic acid
- cis-1 ⁇ 9-octadecenoic acid this shows the same effect as cis-1 ⁇ 9-octadecenoic acid.
- the content of the system 9 in the oily component is 85% by weight or more, and the content of the cis- ⁇ 9-unsaturated fatty acid is 90% by weight or more, and preferably 10% by weight or more.
- —Octadecenoic acid is 90% by weight or more
- cis— ⁇ 9—Unsaturated fatty acid is 93% by weight or more, more preferably 95% by weight of cis- ⁇ 9-octadecenoic acid, 95% by weight of cis- ⁇ 9—
- Saturated fatty acids are at least 97% by weight, most preferably cis- ⁇ 9-octadecenoic acid is at least 99% by weight. If the amount of cis- ⁇ 9-butadecatenoic acid is less than 8.5% by weight or the amount of cis- ⁇ 9-unsaturated fatty acid is less than 90% by weight, the feeling of use of the cosmetic composition is insufficient.
- the cosmetic composition of the present invention may further include, in addition to the oily component and the aqueous component, medicines such as vitamins and antibiotics, nutrients, ultraviolet absorbers, carbon black, titanium oxide, iron oxide, metal stones, It can contain components normally added to cosmetics, such as calcium carbonate, silica, talc, dyes, and fragrances.
- the cosmetic composition of the present invention may be in the form of a liquid, cream, gel, or solid depending on the composition thereof, such as lotion, cosmetic oil, emulsion, lipstick, hair liquid, hair cream, hair restorer, foundation. Used as various creams.
- the emulsion composition of the present invention can contain various additives which are added to the usual emulsion composition 'composition.
- the method for preparing the cosmetic composition and the emulsion composition of the present invention can be carried out by combining the above components.
- the order of addition of each component is particularly limited However, it can be appropriately selected and added.
- the blended components are appropriately mixed by various mixers, various dispersers, various emulsifiers and the like to prepare the cosmetic composition and the emulsion composition of the present invention.
- the cosmetic composition containing a high concentration of 9-year-old cutadecenoic acid or a derivative thereof in the oily component of the present invention has a very good feeling in use, and a low concentration of cis- ⁇ 9-octadecenoic acid or a derivative thereof. The results are remarkably superior to those of a cosmetic composition containing the same.
- cosmetics made from commercially available oleic acid or a derivative thereof having a low content of cis-1 ⁇ 9-octadecenoic acid cause coloring and odor generation over time, but the cosmetic composition of the present invention There is no such problem.
- the emulsion composition of the present invention which contains a high concentration of 9-year-old kutadecenoic acid or a derivative thereof in the oily component, has extremely excellent emulsification stability.
- oleic acid or oleic acid derivatives containing various cis- ⁇ 9-octadecenoic acids and derivatives thereof were used as the oily components.
- concentration of the system is 9-octadecenoic acid in oleic acid or Is represented by the purity of cis-1 ⁇ 9-unsaturated fatty acid.
- each oleic acid or oleic acid derivative to be mixed has the same purity as that of cis-acid having the same purity.
- Oleic acid or a oleic acid derivative containing ⁇ 9 -octadecenoic acid was used.
- the percentages in the examples are% by weight, and the oleic acid or its derivative in the comparative example having a purity of 57% cis-1- ⁇ 9-butadecenoic acid and 66% by weight of cis-1- ⁇ unsaturated fatty acid is as follows: Commercially available oleic acid or a derivative thereof.
- the method for evaluating the cosmetic composition the method for evaluating the emulsification stability, and the method for analyzing the purity of cis-1 ⁇ 9-unsaturated fatty acid containing systemic 9-year-old kutadecenoic acid are as follows.
- the oily component (oily substance and surfactant) and the aqueous component were mixed by light shaking, and the mixture was homogenized using a homogenizer [DX-3, manufactured by Hon Seiki Seisakusho Co., Ltd.] at 10,000 rpm. Emulsified for minutes. After visually observing the state of the emulsion, its standing stability was evaluated according to the following criteria.
- a lotion containing oleoylglutamic acid, a derivative of oleic acid having a different purity shown in Table 1, as a surfactant was prepared by the following formulation, and its usability was evaluated. Table 1 shows the results.
- Cis-1 ⁇ 9 octa cis-1 ⁇ 9—unsaturated Usability evaluation Decenoic acid purity () Fatty acid purity (%) (number) Example 6 99.9 100 20
- a lotion using glycerol monoolate, a derivative of oleic acid with different purity, shown in Table 3, and polyoxyethylene (25 mol) oleyl ether, a derivative of oleic acid with a corresponding purity, as surfactants was prepared according to the following formulation, and its usability was evaluated. Table 3 shows the results.
- Dioleoylphosphatidylcholine which is a derivative of oleic acid with different purity shown in Table 4
- polyoxyethylene (20 mol) sorbitan monoolate which is a derivative of oleic acid with corresponding purity
- a lotion to be used was prepared according to the following formulation, and its usability was evaluated. Table 4 shows the results.
- Example 17 9 9 9 9.5.2 0
- Example 18 9 5 9 7 1 8
- a lotion using N-oleoyl daltamic acid, a derivative of oleic acid with different purity, and hexaglycerol monooleate, a derivative of oleic acid with the corresponding purity, as surfactants was prepared by the following method, and its usability was evaluated. Table 5 shows the results.
- the isoleic acid derivatives of oleic acid with different purities shown in Table 6 were used as oily substances, and the corresponding oleic acid derivatives of polyoxyethylene (20 mol) sorbitan tetraoleate were used as the oily substances.
- a skin lotion used as an activator and separated into two layers was prepared according to the following formulation, and its usability was evaluated. Table 6 shows the results.
- Hexadecenyl oleate which is a derivative of oleic acid with different purity shown in Table 7, is used as an oily substance, and polyoxyethylene (10 mol) oleyl ether, which is a derivative of oleic acid with the corresponding purity, is used as a surfactant.
- the used skin cream was prepared according to the following formulation, and its usability was evaluated. Table 7 shows the results.
- Aqueous component Purified water 22%
- Example 32 99 99.5 20
- Example 33 95 97 19
- the skin creams shown in Table 8 using ethyleolate, a derivative of oleic acid of different purity, as an oily substance and diglycerol monooleate, a derivative of oleic acid of a corresponding purity, as a surfactant were prepared as follows. It was prepared according to the formulation and its usability was evaluated. Table 8 shows the results.
- Aqueous component purified water 30% Table 8
- Oleic acids having different purities shown in Table 9 were esterified with oleyl alcohols obtained by reducing the respective oleic acids, and oleyl alcohols having different purities were prepared.
- Oily substance Oleylolate 40%
- Sucrose monoolate 1.5% Aqueous component: Purified water 53%
- Example 42 99 99.5 19
- Example 43 95 97 18
- Example 44 90 93 16
- Example 45 85
- 90 13 Comparative example 25
- 80 86 8 Comparative example 26
- 70 78 0
- Glycerol triolate a derivative of oleic acid with different purity shown in Table 10, was used as an oily substance.
- a skin cream used as an activator was prepared according to the following formulation, and its usability was evaluated. Table 10 shows the results.
- Aqueous component Purified water 17%
- Cis-1 ⁇ 9-octa cis-1 ⁇ 9 unsaturated Usability evaluation Decenoic acid availability (%) Fatty acid purity (%) (number of people)
- Oily material 2-year-old cutildodecylolate 20%
- Aqueous component Purified water 72%
- An emulsion comprising oleic acid having different purity and cholesterol oleate as a derivative thereof as an oily substance and dioleoylphosphatidylcholine as a derivative of oleic acid having a corresponding purity as a surfactant, as shown in Table 12, were used. It was prepared according to the following formulation and its usability was evaluated. Table 12 shows the results.
- Oily substance Oleic acid. 2%
- Cis-1 ⁇ 9 stable cis-1 ⁇ 9—unsaturated Usability evaluation Decenoic acid Purity (%) Fatty acid Purity (%) (Number) Example 56 99.9 100 20
- Aqueous component purified water 84% Table 13
- Aqueous component purified water 84%
- Cis- ⁇ 9 Aged cis— ⁇ 9—Unsaturated Usability evaluation Decenoic acid Purity (%) Fatty acid purity (%) (Number) Example 66 99.9 100 20
- the oleic acid derivatives of oleic acid with different purity shown in Table 15 were used as the oily substances, and the corresponding oleic acid derivatives of oleic acid, polyoxyethylene (20 mol) oleyl ether and polyoxyethylene, were used as the oily substances.
- (5 mol) A cleansing cream using sorbitan monoolate as a surfactant was prepared according to the following formulation, and its usability was evaluated. Table 15 shows the results.
- Oily substance Isopropylate 80%
- Sorbitan monoolate 2% Aqueous component Purified water 15% Table 15 System 9 1 year old Kuta cis 1 ⁇ 9-unsaturated Usability evaluation Decenoic acid purity (%) Fatty acid purity (%) (Number) Example 71 99.9 100 20
- a cleansing foam using oleyl alcohol, a derivative of oleic acid with different purity, shown in Table 16 as an oily substance, and permoleate, a derivative of oleic acid with a corresponding purity, as a surfactant was prepared as follows. It was prepared according to the following formulation and its usability was evaluated. Table 16 shows the results.
- Aqueous component Purified water 57% Table 16
- Cis-1 ⁇ 9 stable cis-1 ⁇ 9—unsaturated Usability evaluation Decenoic acid Purity (%) Fatty acid Purity (%) (People)
- Ethylene dalicol monooleate a derivative of oleic acid with different purity shown in Table 17, was used as an oily substance, and sodium-N-oleoyl glutamate, which is a derivative of oleic acid of the corresponding purity, was used for each.
- a cleanser foam was prepared according to the following formulation, and the usability was evaluated. The results are shown in Table 17.
- Oily substance ethylene glycol monoolate 5%
- Surfactant sodium mono-N-oleoyl glutamate 40%
- Aqueous component purified water 50%
- Oily substance Isostearyl acrylate 18%
- Aqueous component purified water 64.9%
- oleic acid derivatives dococenyl cholate and octacosyl cholate, which are derivatives of oleic acid with different purities, were used as oily substances, and glycerol monooleate, a derivative of oleic acid with corresponding purity, was used as a surfactant.
- a lipstick was prepared according to the following formulation, and its usability was evaluated. Table of results
- Aqueous component glycerol 3%
- Coloring material Titanium oxide 1%
- Cis-1 ⁇ 9 stable cis-1 ⁇ 9—unsaturated Usability evaluation Decenoic acid purity (%) Fatty acid purity (%) (number)
- Example 101 99.9 100 20
- Example 103 95 97 19
- Example 104 90 93 18
- Example 105 85
- Comparative Example 61 80 86 7 Comparative Example 62 70 78 1
- Palmitoylolate a derivative of oleic acid of different purity shown in Table 22, was used as an oily substance, and sodium polyoxyethylene (10 mol) oleyl ether phosphate, a derivative of oleic acid of the corresponding purity, was used as the oily substance.
- a hair nourisher used as a surfactant was prepared according to the following formulation, and its usability was evaluated. The results are shown in Table 22.
- Glycerol triolate a derivative of oleic acid with different purity shown in Table 23, was used as an oily substance, and sorbitan sesquiolate and polyoxyethylene (20 mol)
- An emulsified liquid was prepared according to the following formulation using bitane monoolate as a surfactant.
- Oily substance glycerol triolate 50%
- Aqueous component Purified water 40% Table 23
- Example 111 Good Stable Stable Stable Stable Stable Stable Stable Stable Example 112 Good Stable Stable Stable Stable Stable Example 113 Good Stable Stable Stable Stable Stable Stable Example 114 Stable Stable Stable Stable Stable Slightly Example 115 Good Stable Stable Stable Stable Stable Stable
- Emulsification Stability stability 30 minutes 1 hour 5 hours 24 hours Comparative Example 70 Poor Separation Separation Slightly slight
- Ethylolate a derivative of oleic acid with a different purity shown in Table 26, was used as an oily substance, and sorbitan sesquiolate and polyoxyethylene (20 mol) sorbitan monoolate, which are the corresponding oleic acid derivatives, were used as surfactants. Then, prepare an emulsion according to the following formulation and formulate
- Aqueous component Purified water 40% Table 26
- Comparative Example 75 57 66 The emulsion stability thus prepared was evaluated for its emulsion stability. The results of the emulsified state and the stability of standing are shown in Table 27 below.
- oleyl alcohol a derivative of oleic acid of different purity, was used as an oily substance.
- An emulsified liquid was prepared according to the following formulation, using as an activator.
- Oily substance Oleyl alcohol 50%
- Aqueous component Purified water 40% Table 28
- the cosmetic composition according to the present invention is useful as various cosmetics such as lotions, creams, emulsions, and foams for cleaning, and has a very good feeling in use.
- the emulsion composition of the present invention can provide an emulsion having excellent emulsion stability, this emulsion is used as a pharmaceutical base other than cosmetics, or used for emulsification of hard-to-emulsify oily substances. can do.
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- 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)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
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- Cosmetics (AREA)
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/066,017 US5589515A (en) | 1991-09-27 | 1992-09-25 | Cosmetic composition and an emulsion composition |
DE69228373T DE69228373T2 (de) | 1991-09-27 | 1992-09-25 | Kosmetikum und emulsion |
EP92920395A EP0564656B1 (en) | 1991-09-27 | 1992-09-25 | Cosmetic composition and emulsion composition |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP03276697A JP3089749B2 (ja) | 1991-09-27 | 1991-09-27 | 化粧料 |
JP3/276697 | 1991-09-27 | ||
JP3/351403 | 1991-12-11 | ||
JP35140391 | 1991-12-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993005755A1 true WO1993005755A1 (en) | 1993-04-01 |
Family
ID=26552065
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1992/001229 WO1993005755A1 (en) | 1991-09-27 | 1992-09-25 | Cosmetic composition and emulsion composition |
Country Status (4)
Country | Link |
---|---|
US (2) | US5589515A (ja) |
EP (1) | EP0564656B1 (ja) |
DE (1) | DE69228373T2 (ja) |
WO (1) | WO1993005755A1 (ja) |
Families Citing this family (40)
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WO1993005755A1 (en) * | 1991-09-27 | 1993-04-01 | Nof Corporation | Cosmetic composition and emulsion composition |
DE19635195C1 (de) * | 1996-08-30 | 1998-01-29 | Henkel Kgaa | Kosmetische Zubereitungen und Verfahren zu ihrer Herstellung |
US6677327B1 (en) | 1999-11-24 | 2004-01-13 | Archer-Daniels-Midland Company | Phytosterol and phytostanol compositions |
US8512718B2 (en) | 2000-07-03 | 2013-08-20 | Foamix Ltd. | Pharmaceutical composition for topical application |
US6515031B2 (en) * | 2001-02-13 | 2003-02-04 | Platte Chemical Company | Technique for emulsifying highly saturated hydroisomerized fluids |
IL152486A0 (en) | 2002-10-25 | 2003-05-29 | Meir Eini | Alcohol-free cosmetic and pharmaceutical foam carrier |
US20060140984A1 (en) | 2002-10-25 | 2006-06-29 | Foamix Ltd. | Cosmetic and pharmaceutical foam |
US10117812B2 (en) | 2002-10-25 | 2018-11-06 | Foamix Pharmaceuticals Ltd. | Foamable composition combining a polar solvent and a hydrophobic carrier |
US7704518B2 (en) | 2003-08-04 | 2010-04-27 | Foamix, Ltd. | Foamable vehicle and pharmaceutical compositions thereof |
US8119109B2 (en) | 2002-10-25 | 2012-02-21 | Foamix Ltd. | Foamable compositions, kits and methods for hyperhidrosis |
US7820145B2 (en) | 2003-08-04 | 2010-10-26 | Foamix Ltd. | Oleaginous pharmaceutical and cosmetic foam |
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US7700076B2 (en) | 2002-10-25 | 2010-04-20 | Foamix, Ltd. | Penetrating pharmaceutical foam |
US8900554B2 (en) | 2002-10-25 | 2014-12-02 | Foamix Pharmaceuticals Ltd. | Foamable composition and uses thereof |
US9265725B2 (en) | 2002-10-25 | 2016-02-23 | Foamix Pharmaceuticals Ltd. | Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof |
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US9211259B2 (en) | 2002-11-29 | 2015-12-15 | Foamix Pharmaceuticals Ltd. | Antibiotic kit and composition and uses thereof |
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US8486374B2 (en) | 2003-08-04 | 2013-07-16 | Foamix Ltd. | Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses |
US7416756B2 (en) | 2003-09-10 | 2008-08-26 | Eastman Chemical Company | Process for the recovery of a phytolipid composition |
CA2609953A1 (en) | 2005-05-09 | 2007-04-12 | Foamix Ltd. | Saccharide foamable compositions |
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US20080260655A1 (en) | 2006-11-14 | 2008-10-23 | Dov Tamarkin | Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses |
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WO2009069006A2 (en) | 2007-11-30 | 2009-06-04 | Foamix Ltd. | Foam containing benzoyl peroxide |
US8518376B2 (en) | 2007-12-07 | 2013-08-27 | Foamix Ltd. | Oil-based foamable carriers and formulations |
WO2009072007A2 (en) | 2007-12-07 | 2009-06-11 | Foamix Ltd. | Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof |
AU2009205314A1 (en) | 2008-01-14 | 2009-07-23 | Foamix Ltd. | Poloxamer foamable pharmaceutical compositions with active agents and/or therapeutic cells and uses |
US20120087872A1 (en) | 2009-04-28 | 2012-04-12 | Foamix Ltd. | Foamable Vehicles and Pharmaceutical Compositions Comprising Aprotic Polar Solvents and Uses Thereof |
WO2011013008A2 (en) | 2009-07-29 | 2011-02-03 | Foamix Ltd. | Non surface active agent non polymeric agent hydro-alcoholic foamable compositions, breakable foams and their uses |
WO2011013009A2 (en) | 2009-07-29 | 2011-02-03 | Foamix Ltd. | Non surfactant hydro-alcoholic foamable compositions, breakable foams and their uses |
US9849142B2 (en) | 2009-10-02 | 2017-12-26 | Foamix Pharmaceuticals Ltd. | Methods for accelerated return of skin integrity and for the treatment of impetigo |
CN102686205A (zh) | 2009-10-02 | 2012-09-19 | 弗艾米克斯有限公司 | 局部四环素组合物 |
US8174881B2 (en) | 2009-11-24 | 2012-05-08 | Micron Technology, Inc. | Techniques for reducing disturbance in a semiconductor device |
DE102013018158A1 (de) | 2013-12-05 | 2015-06-11 | Airbus Defence and Space GmbH | Verfahren zur Herstellung von verstärkten Materialien und Material erhältlich aus diesem Verfahren |
JP6620623B2 (ja) * | 2015-03-31 | 2019-12-18 | 日油株式会社 | 毛髪洗浄剤組成物 |
CA2978573A1 (en) | 2016-09-08 | 2018-03-08 | Foamix Pharmaceuticals Ltd. | Compositions and methods for treating rosacea and acne |
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JPS61297A (ja) * | 1984-06-12 | 1986-01-06 | 日本油脂株式会社 | オレイン酸の製造法 |
JPS63126543A (ja) * | 1986-11-18 | 1988-05-30 | Shiseido Co Ltd | マイクロエマルシヨン |
JPH03115208A (ja) * | 1989-09-28 | 1991-05-16 | Kobayashi Kose Co Ltd | 皮膚用油性化粧料 |
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Publication number | Priority date | Publication date | Assignee | Title |
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FR2474310A1 (fr) * | 1980-01-25 | 1981-07-31 | Oreal | Solution stable a l'oxydation de vitamine f et d'huile de jojoba et compositions cosmetiques la contenant |
EP0225946B1 (en) * | 1985-12-05 | 1991-03-06 | Nippon Oil And Fats Company, Limited | Method of producing oleic acid |
FR2584925B1 (fr) * | 1985-07-17 | 1987-11-27 | Bosserelle Micheline | Composition de corps gras d'origine vegetale pour usage cosmetique |
WO1993005755A1 (en) * | 1991-09-27 | 1993-04-01 | Nof Corporation | Cosmetic composition and emulsion composition |
-
1992
- 1992-09-25 WO PCT/JP1992/001229 patent/WO1993005755A1/ja active IP Right Grant
- 1992-09-25 EP EP92920395A patent/EP0564656B1/en not_active Expired - Lifetime
- 1992-09-25 DE DE69228373T patent/DE69228373T2/de not_active Expired - Lifetime
- 1992-09-25 US US08/066,017 patent/US5589515A/en not_active Expired - Lifetime
-
1996
- 1996-10-18 US US08/734,014 patent/US5700396A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61297A (ja) * | 1984-06-12 | 1986-01-06 | 日本油脂株式会社 | オレイン酸の製造法 |
JPS63126543A (ja) * | 1986-11-18 | 1988-05-30 | Shiseido Co Ltd | マイクロエマルシヨン |
JPH03115208A (ja) * | 1989-09-28 | 1991-05-16 | Kobayashi Kose Co Ltd | 皮膚用油性化粧料 |
Non-Patent Citations (1)
Title |
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See also references of EP0564656A4 * |
Also Published As
Publication number | Publication date |
---|---|
DE69228373D1 (de) | 1999-03-18 |
US5589515A (en) | 1996-12-31 |
DE69228373T2 (de) | 1999-06-17 |
US5700396A (en) | 1997-12-23 |
EP0564656A1 (en) | 1993-10-13 |
EP0564656A4 (en) | 1995-09-06 |
EP0564656B1 (en) | 1999-02-03 |
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