KR20180013056A - Cosmetic composition comprising extract from curcuma and oenothera laciniata hill - Google Patents

Abstract

The present invention relates to a cosmetic composition. More particularly, the present invention relates to a cosmetic composition which comprises extract from curcuma and Oenothera laciniata Hill and has an anti-inflammatory effect.

Description

(Cosmetic composition containing extract from curcuma and oenothera laciniata hill)

The present invention relates to a cosmetic composition, and more particularly, to a cosmetic composition having an anti-inflammatory effect by containing a ganoderma extract and an evening primrose oil extract.

Cosmetics are not only the traditional functions of cleansing and beautifying the human body by attracting and changing the appearance, but also due to external factors such as pollutants, stress and ultraviolet rays, internal factors such as impaired immune cell function and cell activity It has a skin protection function that removes or suppresses the causes of skin aging such as free radicals, free radicals, proteins, nucleic acids, and cell membrane lipid breakdown caused by peroxides and the like. In addition, cosmetics having skin inflammation and atopic treatment, whitening, skin wrinkle improvement and suppression, and ultraviolet shielding function to satisfy consumers' desire for high-performance cosmetics are continuously being developed. In particular, anti-inflammatory products are of great interest to consumers. Accordingly, various cosmetic compositions have been developed as shown in the following patent documents in order to alleviate the inflammatory reaction and minimize skin damage.

<Patent Literature>

Patent Publication No. 10-1077824 (Announcement of Oct. 28, 2011) "Cosmetic composition for improving atopy containing sunlight extract and preparation method thereof"

However, the conventional cosmetic composition is not satisfactory in the irritation-reducing effect, and there is a problem that stability is not ensured by using minerals or the like in a composition using ilite which is a mica-group mineral belonging to monoclinic system.

SUMMARY OF THE INVENTION The present invention has been made to solve the above problems,

It is an object of the present invention to provide a cosmetic composition containing Ulgum and Evening Primrose Oil extract having improved antioxidant and anti-inflammatory effects.

It is also an object of the present invention to provide a cosmetic composition containing an ingame and evening primrose extract which can improve skin wrinkles without inhibiting the anti-inflammatory effect.

In order to achieve the above object, the present invention is implemented by the following embodiments.

According to one embodiment of the present invention, the cosmetic composition according to the present invention is characterized in that it contains Ulgum extract and Evening Primrose oil extract.

According to another embodiment of the present invention, in the cosmetic composition according to the present invention, the baby's evening primrose oil extract is used in an amount of 50 parts by weight per 100 parts by weight of the extract.

According to another embodiment of the present invention, the cosmetic composition according to the present invention is characterized in that the extract is contained in an amount of 0.1 to 5% by weight based on the total weight of the cosmetic composition.

According to another embodiment of the present invention, the cosmetic composition according to the present invention may further comprise at least one selected from the group consisting of purified water, disodium edetate, trehalose, glycerin, butyleneglycol, carbomer, potassium hydroxide, essential oil, Dried extract, green tea extract, ginkgo leaf extract, petal extract, and natural preservative.

According to another embodiment of the present invention, in the cosmetic composition according to the present invention, the essential oil is made of Bergham berries oil, lavender oil, milk oil and sentenced geranium flower oil, and the petal extract is a peach tree flower extract, Extract, a lotus flower extract, and a magnolia tree flower extract, wherein the natural preservative is characterized by comprising an extract of Acerola japonica and an extract of Asniera.

According to another embodiment of the present invention, the cosmetic composition according to the present invention further comprises a pakira extract.

According to another embodiment of the present invention, in the cosmetic composition according to the present invention, the pakira extract is used in an amount of 50 parts by weight per 100 parts by weight of the extract.

According to another embodiment of the present invention, in the cosmetic composition according to the present invention, the cosmetic composition has an anti-inflammatory effect.

According to still another embodiment of the present invention, the cosmetic composition according to the present invention is characterized by having an anti-inflammatory effect and a wrinkle-reducing effect.

According to another embodiment of the present invention, the cosmetic composition according to the present invention is characterized by having a formulation of any one of a skin, a lotion, a cream, and a mask pack.

According to the present invention, the following effects can be obtained by this embodiment.

The present invention provides improved antioxidant, anti-inflammation, and wrinkle-improving effects, including Ulgum extract and Evening Primrose oil extract.

Hereinafter, the cosmetic composition containing Ulgum and Pygmyum evenpox extract according to the present invention will be described in detail. Unless defined otherwise, all terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs and, if conflict with the meaning of the terms used herein, It follows the definition used in the specification. Further, the detailed description of known functions and configurations that may unnecessarily obscure the subject matter of the present invention will be omitted. Throughout the specification, when an element is referred to as "including " an element, it is understood that the element may include other elements as well, without departing from the other elements unless specifically stated otherwise.

Meanwhile, the 'extract' referred to in the present invention is a concept including both general hot water extract and ethanol extract as a concept including all common extracts. Particularly, 'hot water extract' is extracted by hot water extraction method using distilled water or purified water Ethanol extract "refers to an extract obtained by using a polar solvent selected from lower alcohols having 1 to 4 carbon atoms or a mixed solvent thereof, preferably ethanol.

The cosmetic composition according to one embodiment of the present invention includes curcuma extract and oenothera laciniata hill extract. The evening primrose oil extract is preferably used in an amount of 30 to 250 parts by weight, more preferably 50 parts by weight, per 100 parts by weight of the extract. The extract is preferably contained in an amount of 0.1 to 5% by weight based on the total weight of the cosmetic composition. The cosmetic composition according to one embodiment of the present invention is characterized in that the uroguanthoid extract and the evening primrose oil extract are mixed at a specific ratio (in particular, a weight ratio of 2: 1), so that the antioxidant and antiinflammatory effect (A mixture of Ulgum extract and Pygmyum sinensis extract at a weight ratio of 2: 1 is highly effective against inflammation).

The cosmetic composition may be selected from the group consisting of purified water, disodium edetate, trehalose, glycerin, butyleneglycol, carbohydrate, potassium hydroxide, essential oil, phage-60 hydrogenated castor oil, green tea extract, Petal extract, natural preservative, and the like. Wherein the petroleum-derived extract is composed of a peach tree flower extract, a plum extract, a lotus flower extract, and a magnolia tree flower extract, wherein the natural preservative is selected from the group consisting of persimmon Pine fruit extract and earthy extract.

The cosmetic composition may further include a pachira extract so as not to deteriorate the anti-inflammatory effect and improve the wrinkle-improving effect. The cosmetic composition comprising the extract of Eugyol and the evening primrose may have an improved antioxidant and anti-inflammatory effect. However, since the cosmetic composition has a wrinkle-reducing effect that is lower than that of the Eugen extract and the evening primrose extract, The cosmetic composition according to the present invention further includes a pakira extract to provide an improved wrinkle-reducing effect without deteriorating antioxidant and anti-inflammatory effects. The pakira extract is preferably used in an amount of 30 to 150 parts by weight based on 100 parts by weight of the extract.

The cosmetic composition of the present invention may further comprise a composition selected from the group consisting of water-soluble vitamins, oiliness vitamins, polymer peptides, polymeric polysaccharides, sphingolipids and seaweed extracts.

As the water-soluble vitamin, any of vitamin B1, vitamin B2, vitamin B6, pyridoxine, pyridoxine hydrochloride, vitamin B12, pantothenic acid, nicotinic acid, nicotinic acid amide, folic acid, vitamin C and vitamin H can be used, And salts thereof (thiamine hydrochloride, sodium ascorbate, etc.) or derivatives (sodium ascorbic acid-2-phosphate, magnesium ascorbic acid-2-phosphate etc.) can also be used as water-soluble vitamins . The water-soluble vitamin can be obtained by a conventional method such as a microorganism conversion method, a purification method from a culture of a microorganism, an enzymatic method, or a chemical synthesis method.

As the above-mentioned useful vitamins, any vitamins A, carotene, vitamin D2, vitamin D3, vitamin E (d1-alpha tocopherol, d-alpha tocopherol, d-alpha tocopherol) , And derivatives thereof (such as palmitic acid ascorbin, stearic acid ascorbic acid, dipalmitic acid ascorbic acid, dl-alpha tocopheryl acetate, dl-alpha tocopherol nicotinic acid vitamin E, DL-pantothenyl alcohol, D-pantothenyl alcohol, Ethyl ether, etc.) and the like are also included in the usable vitamins used in the present invention. The usable vitamin can be obtained by a conventional method such as a microorganism conversion method, a purification method from a culture of a microorganism, an enzyme or a chemical synthesis method.

The polymeric peptide may be any compound as long as it can be compounded in a cosmetic, and preferably collagen, hydrolyzed collagen, gelatin, elastin, hydrolyzed elastin, keratin and the like. The polymeric peptide can be obtained by a conventional method such as purification from a culture broth of a microorganism, an enzymatic method, or a chemical synthesis method, or purified from natural products such as ducks such as pigs and cows and silk fiber of silkworms .

The polymeric polysaccharide may be any compound as long as it can be compounded in cosmetics, and examples thereof include hydroxyethylcellulose, xanthan gum, sodium hyaluronate, chondroitin sulfate or a salt thereof (sodium salt, etc.). For example, chondroitin sulfate or a salt thereof can be usually purified from mammals or fish.

The sphingogly lipid may be any as long as it can be compounded in cosmetics, and preferable examples thereof include ceramides, phytosphingosine and sphingoglycolipids. The sphingogly lipids can be purified from ordinary mammals, fish, shellfish, yeast or plants by a conventional method or can be obtained by chemical synthesis.

The seaweed extract may be any of those which can be compounded in cosmetics, but preferably include algae extract, red tiger extract, green algae extract and the like, and furthermore, coloring guanine, arginic acid, sodium alginate , Potassium alginate, and the like are also included in the seaweed extract used in the present invention. The seaweed extract can be obtained from seaweed by a conventional method.

The cosmetic composition of the present invention may contain other ingredients usually added to the cosmetic composition. For example, it is possible to use various additives such as a preservative, a moisturizer, an emollient, a surfactant, an organic and inorganic pigment, an organic powder, an ultraviolet absorber, an antiseptic, a bactericide, an antioxidant, a plant extract, a pH adjuster, Cold agents, antiperspirants, purified water, and the like.

Examples of the above-mentioned fat-soluble ingredients include ester-based fats, hydrocarbon-based fats, silicon-based fats, fluorine-based fats, animal fats and plant fats and the like. Examples of the ester-based oil include glyceryl tri-2-ethylhexanoate, cetyl 2-ethylhexanoate, isopropyl myristate, butyl myristate, isopropyl palmitate, ethyl stearate, octyl palmitate, isostearyl isostearate, But are not limited to, ethylbutyl, butylbutyl, ethylbutylbutyl, butylbutyl, isobutylbutyl, isobutylbutyl, isobutylisobutyl, isobutylisobutyl, isobutylisobutyl, Trimethylol propane, triisostearic acid trimethylol propane, tetra-2-ethylhexanoic acid pentaerythritol tri (2-ethylhexanoic acid) But are not limited to, tallow, caprylic estersyl, decyl laurate, hexyl laurate, decyl myristate, myristyl myristate, myristine sasyl, stearyl stearate, decyl oleate, Examples of the isocyanates include isophorone diisostearate, isophorone diisostearate, isophorone diisostearate, isophorone diisostearate, isophorone diisostearate, isophorone diisostearate, isophorone diisostearate, Ethylhexanoate, stearyl 2-ethylhexanoate, hexyl isostearate, ethylene glycol dioctanoate, ethylene glycol dioleate, propylene glycol dicaprate, di (capryl, capric acid) propylene glycol , Propylene glycol dicaprylylate, dicapric acid neopentyl glycol, dioctanoic acid neopentyl glycol, tricarboxylic acid glyceryl, triunsaturated acid glyceryl, triisopalmitic acid glyceryl, triisostearic acid glyceryl, neopentanoic acid octyl Dodecylsuccinic acid, octadecanoic acid, octadecanoic acid, octadecanoic acid, octadecanoic acid, octadecanoic acid, octadecanoic acid, Polyglycerin isostearic acid ester, triisocetyl citrate, triisoalkyl citrate, triisooctyl citrate, lauryl lactate, myristyl lactate, cetyl lactate, octyldecyl lactate, octyldecyl lactate, octyldecyl isostearate, polyglycerin oleic acid ester, But are not limited to, triethyl citrate, acetyl triethyl citrate, acetyl tributyl citrate, trioctyl citrate, diisostearyl malate, 2-ethylhexyl hydroxystearate, di-2-ethylhexyl succinate, diisobutyl adipate, Propyl stearate, propyl stearate, propyl stearate, stearyl stearate, stearyl stearate, propyl stearate, stearyl stearate, Stearyl hydroxystearate, stearyl 12-stearoyl hydroxystearate, 12-stearoyl hydroxystearic acid, Allo one hydroxy stearic acid and the like esters such as cetearyl source. Examples of the hydrocarbonaceous oil include hydrocarbons such as squalene, liquid paraffin, alpha-olefin oligomer, isoparaffin, ceresin, paraffin, floating isoparaffin, polybutene, microcrystalline wax and vaseline. Examples of the silicone-based oil include polymethyl silicone, methylphenyl silicone, methyl cyclopolysiloxane, octamethyl polysiloxane, decamethyl polysiloxane, dodecamethyl cyclosiloxane, dimethyl siloxane methyl cetyloxysiloxane copolymer, dimethyl siloxane methyl stearoxysiloxane copolymer, Alkyl-modified silicone oil, and amino-modified silicone oil. Examples of the fluorine-based oil include perfluoropolyether and the like. Examples of the animal or plant oil include avocado oil, almond oil, olive oil, sesame oil, rice bran oil, new flower oil, soybean oil, corn oil, rape oil, apricot kernel oil, palm kernel oil, palm oil, castor oil, The present invention relates to a process for producing a starch-containing starch, which is selected from the group consisting of seed oil, cottonseed oil, palm oil, palm oil, cucumber nut oil, wheat germ oil, rice germ oil, Animal or vegetable fats such as oil, can-pick wax, carnauba wax, liquid lanolin, and hardened castor oil.

Examples of the moisturizing agent include water-soluble low-molecular moisturizing agents, oil-soluble molecular moisturizing agents, water-soluble polymers, and oil-soluble polymers. Examples of the water-soluble low molecular weight moisturizing agent include serine, glutamine, sorbitol, mannitol, sodium pyrrolidone-carboxylate, glycerin, propylene glycol, 1,3-butylene glycol, ethylene glycol, polyethylene glycol B Propylene glycol (polymerization degree n = 2 or more), polyglycerin B (polymerization degree n = 2 or more), lactic acid, lactic acid salt and the like. Examples of the lipid-soluble low-molecular moisturizing agent include cholesterol, cholesterol ester and the like. Examples of the water-soluble polymer include carboxyvinyl polymer, polyaspartic acid salt, tragacanth, xanthan gum, methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, water-soluble chitin, chitosan, dextrin, . Examples of the oil-soluble polymer include polyvinylpyrrolidone / eicosene copolymer, polyvinylpyrrolidone / hexadecene copolymer, nitrocellulose, dextrin fatty acid ester, and polymer silicone.

Examples of the molient agent include long chain acyl glutamic acid cholesteryl ester, hydroxystearic acid cholesteryl, 12-hydroxystearic acid, stearic acid, rosin acid and lanolin fatty acid cholesteryl ester.

Examples of the surfactant include nonionic surfactants, anionic surfactants, cationic surfactants, and amphoteric surfactants. Examples of the nonionic surfactant include self emulsifying monostearic acid glycerin, propylene glycol fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, sorbitan fatty acid ester, POE (polyoxyethylene), sorbitan fatty acid ester, POE sorbit fatty acid ester POE glycerin fatty acid ester, POE alkyl ether, POE fatty acid ester, POE hardened castor oil, POE castor oil, POEPOP (polyoxyethylene polyoxypropylene) copolymer, POEPOP alkyl ether, polyether modified silicone, lauric acid alkanolamide , Alkylamine oxides, hydrogenated soybean phospholipids, and the like. Examples of the anionic surfactant include fatty acid soap, alpha-acylsulfonate, alkylsulfonate, alkylallylsulfonate, alkylnaphthalenesulfonate, alkylsulfate, POE alkyl ether sulfate, alkylamide sulfate, alkyl phosphate, POE alkyl ginseng salt, alkyl Amide phosphate, alkyloyl taurine salt, N-acyl amino acid salt, POE alkyl ether carboxylate, alkylsulfosuccinate, sodium alkylsulfoacetate, acylated hydrolyzed collagen peptide salt, perfluoroalkyl phosphate ester and the like . Examples of the cationic surfactant include alkyl trimethyl ammonium chloride, stearyl trimethyl ammonium chloride, stearyl trimethyl ammonium bromide, cetostearyl trimethyl ammonium chloride, distearyl dimethyl ammonium chloride, stearyl dimethyl benzyl ammonium chloride, behenyl trimethyl ammonium bromide, Benzalkonium chloride, diethylaminoethylamide stearate, dimethylaminopropylamide stearate, quaternary ammonium salts of lanolin derivatives, and the like. Examples of the amphoteric surfactant include carboxybetaine, amidebetaine, sulfobetaine, hydroxysulfobetaine, amidosulfobetaine, phosphobetaine, aminocarboxylate, imidazoline derivative, amideamine, etc. , And the like.

Examples of the organic and inorganic pigments include silicic acid, anhydrous silicic acid, magnesium silicate, talc, sericite, mica, kaolin, spinach, clay, bentonite, titanium coated mica, bismuth oxychloride, zirconium oxide, magnesium oxide, Inorganic pigments such as aluminum, calcium sulfate, barium sulfate, magnesium sulfate, calcium carbonate, magnesium carbonate, iron oxide, chromium oxide, chromium oxide, chromium oxide, But are not limited to, polyamide, polyester, polypropylene, polystyrene, polyurethane, vinyl resin, urea resin, phenol resin, fluororesin, silicon resin, acrylic resin, melamine resin, epoxy resin, polycarbonate resin, Silk powder, cellulose, CI Pigment Yellow, CI Pigment Orange, and composite pigments of inorganic pigments and organic pigments thereof.

Examples of the organic powder include metal soaps such as calcium stearate; Metal salts of alkyl phosphates such as sodium zinc cetylate, zinc laurylate and calcium lauryl laurate; Acylamino acid polyvalent metal salts such as N-lauroyl-beta-alanine calcium, N-lauroyl-beta-alanine zinc and N-lauroylglycine calcium; Amidosulfonic acid multivalent metal salts such as N-lauroyl-taurine calcium and N-palmitoyl-taurine calcium; Such as N-epsilon-lauroyl-L-lysine, N-epsilon-palmitoylidene, N-alpha-paratyylnitine, N-alpha-lauroyl arginine, Acyl basic amino acids; N-acylpolypeptides such as N-lauroylglycylglycine; Alpha-amino fatty acids such as alpha-aminocaprylic acid, alpha-aminoaurauric acid, and the like; Polyethylene, polypropylene, nylon, polymethylmethacrylate, polystyrene, divinylbenzene-styrene copolymer, ethylene tetrafluoride, and the like.

Examples of the ultraviolet absorber include ultraviolet absorbers such as p-aminobenzoic acid, ethyl p-aminobenzoate, amyl paranobenzoate, octyl p-aminobenzoate, ethylene glycol salicylate, phenyl salicylate, benzyl salicylate, benzyl salicylate, butylphenyl salicylate, homomenthyl salicylate, Benzyl, 2-ethoxyethyl methoxycinnamate, octyl methoxycinnamate, mono-2-ethylhexane glyceryl dipyrromethoxycinnamate, isopropyl methoxycinnamate, diisopropyl-diisopropyl cinnamate ester mixture, Dihydroxymethoxybenzophenone sulfonic acid, dihydroxybenzophenone sulfonic acid, dihydroxybenzophenone sulfonic acid and its salt, dihydroxymethoxybenzophenone, sodium dihydroxymethoxybenzophenone disulfonate, dihydroxybenzo Phenanone, tetrahydroxybenzophenone, 4-tert-butyl-4'-methoxydibenzoylmethane, 2,4,6-trianylino-p- (carbo-2'-ethylhexyl- 1,3,5-triazine, 2- (2- And the like can be de-hydroxy-5-methylphenyl) benzotriazole.

Examples of the bactericide include antibiotics such as hinokitiol, trichloroacid, trichlorohydroxydiphenyl ether, crohexidine gluconate, phenoxyethanol, resorcin, isopropylmethylphenol, azulene, salicylic acid, No. 301, mononitro and eicoll sodium, undecylenic acid, and the like.

Examples of the antioxidant include butylhydroxyanisole, gallic acid propyl, and eicosorbic acid.

Examples of the pH adjuster include citric acid, sodium citrate, malic acid, sodium malate, fumaric acid, sodium fumarate, succinic acid, sodium succinate, sodium hydroxide, sodium monohydrogenphosphate and the like.

Examples of the alcohol include higher alcohols such as cetyl alcohol.

In addition, any of the above components may be blended within the range not impairing the object and effect of the present invention, but is preferably 0.01 to 5% by weight based on the total weight, More preferably 0.01 to 3% by weight.

The cosmetic composition of the present invention may take the form of a solution, an emulsion, a viscous mixture or the like.

The ingredients contained in the cosmetic composition of the present invention may contain, as an active ingredient, the ingredients conventionally used in cosmetic compositions in addition to the above-mentioned compounds, for example, conventional additives such as stabilizers, solubilizers, vitamins, And a carrier.

The cosmetic composition of the present invention can be prepared in any formulations conventionally produced in the art, and examples thereof include emulsions, creams, foundations, lotions, essences, and hair cosmetic compositions. Specifically, the cosmetic composition of the present invention can be used as a skin lotion, a skin softener, a moisturizing lotion, a nutritional lotion, a massage cream, a nutrition cream, a hand cream, a moisturizing cream, an essence, a pack, a soap, a lotion, a milk lotion, A cleansing foam, a body cleanser, an astringent, a spray, and preferably a formulation of a mask pack. When the formulation of the present invention is a paste, cream or gel, animal fiber, plant fiber, wax, paraffin, starch, tracant, cellulose derivative, polyethylene glycol, silicone, bentonite, silica, talc or zinc oxide may be used as the carrier component . When the formulation of the present invention is a powder or a spray, lactose, talc, silica, aluminum hydroxide, calcium silicate or polyamide powder may be used as a carrier component. In the case of a spray, in particular, / Propane or dimethyl ether. In the case of the solution or emulsion of the present invention, a solvent, a solvent or an emulsifier is used as a carrier component, and examples thereof include water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, , 3-butyl glycol oil, glycerol aliphatic ester, polyethylene glycol or sorbitan fatty acid esters. When the formulation of the present invention is a suspension, a carrier such as water, a liquid diluent such as ethanol or propylene glycol, a suspending agent such as ethoxylated isostearyl alcohol, polyoxyethylene sorbitol ester and polyoxyethylene sorbitan ester, Cellulose, aluminum metahydroxide, bentonite, agar or tracant, etc. may be used. When the formulation of the present invention is an interfacial active agent-containing cleansing, the carrier component may include aliphatic alcohol sulfate, aliphatic alcohol ether sulfate, sulfosuccinic acid monoester, isethionate, imidazolinium derivative, methyltaurate, sarcosinate, fatty acid amide Ether sulfates, alkylamidobetaines, aliphatic alcohols, fatty acid glycerides, fatty acid diethanolamides, linolenic derivatives, or ethoxylated glycerol fatty acid esters.

Hereinafter, the present invention will be described in more detail with reference to Examples. However, these are only for the purpose of illustrating the present invention in more detail, but the scope of the present invention is not limited thereto.

&Lt; Example 1 > Preparation of sample

(1) 100 g of each dried and crushed corn, each evening primrose (leaves) and pakira (leaves) were immersed in 500 ml of 80% ethanol for 36 hours, and the extract was concentrated under reduced pressure. &Lt; / RTI &gt;

(2) Prepare a herbal extract as a sample 1, prepare a sample of the evening primrose extract, prepare a sample 2, and use a mixture of a herbal extract and a herbal evening primrose extract in a weight ratio of 1: 1 as a sample 3, The extracts prepared by mixing the extracts at a weight ratio of 1: 2 were prepared as Sample 4, and the extracts prepared by mixing the herbal extracts and the baby's evening primrose extracts at a weight ratio of 2: 1 were prepared as Sample 5, and the herbal extracts, the evening primrose extract, A sample 6 was prepared by mixing the extract at a weight ratio of 2: 1: 1.

&Lt; Example 2 > Cytotoxicity evaluation (MTT assay)

(1) Cell Culture (Cell Culture)

RAW 264.7 cells were cultured in a DMEM medium supplemented with 10% FBS and 100 units / ml penicillin-streptomycin in an incubator maintained at 37 ° C and 5% CO ₂ and subcultured.

(2) MTT assay was performed to determine the toxicity of the samples. Cultured RAW 264.7 cells were co-treated with LPS (1 ug / mL) and Samples 1-6, respectively, for 24 hours. After the incubation, 10 μl of MTT solution was added and cultured for 4 hours. The supernatant was removed, and DMSO was added. After shaking well using a plate mixer, absorbance was measured at 540 nm. The cytotoxicity was evaluated in comparison with the control group treated with the stimulant. As a result, it was confirmed that each of Samples 1 to 6 did not show cytotoxicity at a concentration of 60 μg / mL or less.

Example 3 Confirmation of Antioxidative Effect (DPPH radical scavenging activity)

(1) Antioxidant activity was measured by the Blois method, which measures the radical scavenging effect of 1,1-diphenyl-2-picrylhydrazyl (DPPH).

(2) About 2 mg of DPPH was dissolved in 15 mL of ethanol to prepare a DPPH solution. To 10 mL of this solution was added 6.0 mL of DMSO, and UV-Vis of the control group was observed at 525 nm. Diluted with ethanol to an absorbance of 0.94-0.97 and shaken for 15 seconds. 0.4 ml of the sample solution (60 μg / ml of each of the samples 1 to 6) was added to 1.6 ml of the prepared DPPH and allowed to stand at room temperature for 10 minutes. After 48 hours, the absorbance was measured at 525 nm, Respectively. The elimination formula was calculated by the following method. Electron donating ability (%) = 100 - [(O.D. Of sample / O.D. of control)] 100

(3) As shown in Table 1 below, Samples 3 to 5, which were obtained by mixing Ulugum extract and evening primrose oil extract, and Sample 6, which is a mixture of Ulugum extract, Pygmaliae subsp. It was found that the antioxidant effect of the present invention was improved compared to the sample 2 of the present invention.

sample Scavenging ability (%) 1 (Ulgum extract) 28 2 (Evening Primrose Oil Extract) 32 3 (Ulgum extract + Evening primrose extract (weight ratio of 1: 1)) 40 4 (Ulgum extract + Evening primrose extract (weight ratio of 1: 2)) 58 5 (Ulugum extract + Evening primrose extract (weight ratio of 2: 1)) 46 6 (Ulgum extract + Pygmyum evening primrose extract + pakira extract (weight ratio of 1: 1: 1)) 54

Example 4 Confirmation of anti-inflammatory effect (suppression of nitric oxide formation)

(1) NO assay was performed to investigate the effect of nitric oxide production, which is one of the active oxygen species and plays an important role in inflammation induction. The cultured RAW 264.7 cells were adjusted to ^1.5 × 10 ⁵ cells / mL using DMEM medium, and then seeded in 96-well plates. New medium containing LPS (1 μg / mL) (The final concentration of each of Samples 1 to 6 was 60 μg / mL). The amount of NO produced was measured in the form of NO ₂ ^- present in cell culture medium using Griess reagent. 100 μL of the cell culture supernatant and 100 μL of the glycated reagent were mixed and reacted for 10 minutes, and the absorbance was measured at 540 nm using an ELISA reader. The amount of NO produced was compared with sodium nitrite (NaNO ₂ ) as a standard, and the results are shown in Table 2.

(1) As shown in Table 2, it can be seen that Samples 3 to 6 have lower NO production than Samples 1 and 2, and thus it has a further improved antiinflammatory effect as a result of the addition of the uroguanum extract and the evening primrose oil extract. In addition, it was found that the amount of NO produced was the lowest when mixed with the 2: 1 weight ratio of Ulgum extract and Pygmyum sinensis extract.

NO production rate (%) Untreated 0 LPS only processing 100 LPS + Sample 1 (Ulgum extract) 85 LPS + Sample 2 (Evening Primrose Oil Extract) 90 LPS + sample 3 (Ulugum extract + Evening primrose extract (weight ratio of 1: 1)) 70 LPS + Sample 4 (Ulgum extract + Evening primrose extract (weight ratio of 1: 2)) 75 LPS + Sample 5 (Ulugin Extract + Evening Primrose Oil Extract (weight ratio of 2: 1)) 61 LPS + sample 6 (Ulgum extract + Pygmyum evening primrose extract + pakira extract (weight ratio of 1: 1: 1)) 64

<Example 5> Confirmation of anti-inflammatory effect (inhibition of pro-inflammatory cytokines (TNF-α, IL-6)

(1) RAW 264.7 cells (1.5 × 10 ⁵ cells / mL) were inoculated into 96-well plates using DMEM medium and cultured in a 5% CO ₂ incubator for 24 hours. Subsequently, the medium was removed, and fresh medium containing each of Samples 1 to 6 and stimulant substance LPS (1 ug / mL) was simultaneously treated and cultured under the same conditions as the pre-culture (final concentration of each of Samples 1 to 6 was 60 μg / mL) . After 24 hours, the culture medium was centrifuged (12,000 rpm, 3 minutes) and the content of pro-inflammatory cytokines produced in the supernatant was measured. The results are shown in Table 3. Quantification of pro-inflammatory cytokines was quantitated using a mouse enzyme-linked immunosorbent assay (ELISA) kit (R & D Systems Inc., Minneapolis, MN, USA).

(2) Table 3 shows that samples 3 and 6 produced less TNF-α and IL-6 than samples 1 and 2. Therefore, the combination of Ulgum extract and Evening primrose extract resulted in better anti-inflammatory effect . In addition, TNF-α production was the lowest when Eulgum extract and Pygmyum sinensis extract were mixed at a weight ratio of 2: 1.

TNF-a
Generation rate (%) IL-6
Generation rate (%) Untreated 0 0 LPS only processing 100 100 LPS + Sample 1 (Ulgum extract) 93 88 LPS + Sample 2 (Evening Primrose Oil Extract) 87 84 LPS + sample 3 (Ulugum extract + Evening primrose extract (weight ratio of 1: 1)) 73 65 LPS + Sample 4 (Ulgum extract + Evening primrose extract (weight ratio of 1: 2)) 68 63 LPS + Sample 5 (Ulugin Extract + Evening Primrose Oil Extract (weight ratio of 2: 1)) 61 68 LPS + sample 6 (Ulgum extract + Pygmyum evening primrose extract + pakira extract (weight ratio of 1: 1: 1)) 68 65

Example 6 Evaluation of anti-inflammatory efficacy (Prostaglandin E ₂ (PGE ₂ ) production inhibition)

(1) RAW 264.7 cells were adjusted to 1.0 × 10 ⁵ cells / mL using DMEM medium and then inoculated into 96-well plates and cultured in a 5% CO ₂ incubator for 24 hours. Then, the medium was removed, and fresh medium containing each of Samples 1 to 6 and LPS (1 ug / mL) was simultaneously treated and cultured under the same conditions as the pre-culture (final concentration of each of Samples 1 to 6 was 60 μg / mL). After 24 hours, the supernatant was obtained by centrifuging the culture medium (12,000 rpm, 3 min) to measure prostaglandin E ₂ (PGE ₂ ). PGE ₂ was quantitated using a PGE ₂ ELISA kit (R & D Systems Inc., Minneapolis, MN, USA). The results are shown in Table 4, and the r 2 value of the standard curve for the standard was 0.99 or more.

(2) As shown in Table 4, it can be seen that Samples 3 to 6 have a smaller amount of PGE ₂ than Samples 1 and 2, and thus it has a further improved anti-inflammatory effect . In addition, PGE ₂ production was the lowest when corynebacterium extract and corynebum extract were mixed at a weight ratio of 2: 1.

PGE ₂ release (%) Untreated 0 LPS only processing 100 LPS + Sample 1 (Ulgum extract) 85 LPS + Sample 2 (Evening Primrose Oil Extract) 87 LPS + sample 3 (Ulugum extract + Evening primrose extract (weight ratio of 1: 1)) 74 LPS + Sample 4 (Ulgum extract + Evening primrose extract (weight ratio of 1: 2)) 72 LPS + Sample 5 (Ulugin Extract + Evening Primrose Oil Extract (weight ratio of 2: 1)) 66 LPS + sample 6 (Ulgum extract + Pygmyum evening primrose extract + pakira extract (weight ratio of 1: 1: 1)) 70

<Example 7> Evaluation of anti-inflammatory effect (skin patch test)

(1) A cosmetic composition was prepared in the composition ratio shown in Table 5 below.

content(%) ingredient Cosmetic composition 1 Cosmetic composition 2 Cosmetic composition 3 Cosmetic composition 4 Sample 1 One 0 0 0 Sample 2 0 One 0 0 Sample 5 0 0 One 0 Sample 6 0 0 0 One Vitamin E 0.5 0.5 0.5 0.5 Propylene glycol 5.0 5.0 5.0 5.0 maintain 6.0 6.0 6.0 6.0 Ultraviolet absorber 2.0 2.0 2.0 2.0 Camellia oil 3.0 3.0 3.0 3.0 Flowing isoparaffin 2.0 2.0 2.0 2.0 antiseptic 0.01 0.01 0.01 0.01 Spices 0.5 0.5 0.5 0.5 Purified water Balance Balance Balance Balance Sum 100 100 100 100

(2) The anti-inflammatory effect was confirmed in 20 patients in their 10 to 20 years suffering from inflammatory skin diseases such as atopy and acne. Twenty persons were divided into four groups and each of the cosmetic compositions 1 to 4 was applied twice daily for 2 weeks to skin disease sites. Thereafter, the subjective evaluation of each participant in the skin condition was collected and shown in Table 6. Significant improvement, improvement, moderate, and worsening were used as evaluation items.

(3) From Table 6, it can be seen that the use of cosmetic compositions 3 and 4 significantly improved the skin condition as compared to the use of cosmetic compositions 1 and 2, It seems to be decided according to whether or not. That is, the anti-inflammatory effect is improved when mixed with the Ulgum extract and Evening primrose extract, respectively.

Percentage of responses (%) A significant improvement Improving usually worse Cosmetic composition 1 0 30 70 0 Cosmetic composition 2 0 40 50 10 Cosmetic composition 3 20 60 20 0 Cosmetic composition 4 30 50 20 0

<Example 8> Quantitative detection of type 1 collagen

(1) Cell Culture (Cell Culture)

10% FBS (fetal bovine serum) and 1% penicillin-streptomycin using DMEM culture medium is contained, Human fibroblast dermal cell of HDFn (American Type Culture Colletion (ATCC -CRL-2076) to 37 ℃, 5% CO ₂ conditions , And subcultured.

(2) The HDFn was inoculated into a 96-well plate at 1 × 10 ⁵ cells / ml, and then stabilized for 24 hours at 37 ° C. and 5% CO ₂ . Thereafter, after replacing with DMEM medium not containing FBS, Samples 1 to 6 were added and cultured for 48 hours (final concentration of each of Samples 1 to 6 was 60 μg / mL). Then, the supernatant was collected and the amount of procollagen was measured using a Procollagen type 1 C-peptide (PIP) EIA kit. The results are shown in Table 7.

(3) As shown in Table 7, it can be seen that sample 6 produced a larger amount of collagen 1 than samples 1 through 5, and samples 1 and 2 produced larger amounts of collagen 1 than samples 3 and 4. As a result, it was found that the wrinkle-improving effect was lowered when the uroguanum extract and the bilberry-evening primrose extract were mixed, and that the wrinkle-improving effect was improved when the wrinkle extract was added to the mixed extract.

collagen 1 content (%) Untreated 100 LPS + Sample 1 (Ulgum extract) 129 LPS + Sample 2 (Evening Primrose Oil Extract) 135 LPS + sample 3 (Ulugum extract + Evening primrose extract (weight ratio of 1: 1)) 117 LPS + Sample 4 (Ulgum extract + Evening primrose extract (weight ratio of 1: 2)) 108 LPS + Sample 5 (Ulugin Extract + Evening Primrose Oil Extract (weight ratio of 2: 1)) 119 LPS + sample 6 (Ulgum extract + Pygmyum evening primrose extract + pakira extract (weight ratio of 1: 1: 1)) 140

Example 9 Evaluation of wrinkle-improving effect (cell proliferation)

(1) 96 well plates were inoculated with HDFn at a concentration of 1 x 10 ⁵ cells / ml, and then stabilized for 24 hours at 37 ° C and 5% CO ₂ . Thereafter, after replacing with DMEM medium not containing FBS, Samples 1 to 6 were added and cultured for 24 hours (the final concentration of each of Samples 1 to 6 was 60 μg / mL). After culturing, 10 μl of MTT (3- (4,5-dimethyl-thiazol-2-yl) 2,5-diphenyl tetrazolium: 5 mg / ml) solution is added and reacted for 4 hours to remove the reaction solution. 100 쨉 l of DMSO was added to each well to dissolve the stained cells, and the absorbance at 570 nm was measured. Cell proliferation was calculated by the following method and is shown in Table 8. Cell proliferation (%) = (OD of sample - OD of control) / OD of control × 100

(2) From Table 8, it can be seen that Sample 6 has better cell proliferation power than Samples 1 to 5, and Samples 1 and 2 have better cell proliferation power than Samples 3 to 4. As a result, it was found that the wrinkle-improving effect was lowered when the uroguanum extract and the bilberry-evening primrose extract were mixed, and that the wrinkle-improving effect was improved when the wrinkle extract was added to the mixed extract.

Growth Potency (%) Untreated 0 LPS + Sample 1 (Ulgum extract) 38 LPS + Sample 2 (Evening Primrose Oil Extract) 45 LPS + sample 3 (Ulugum extract + Evening primrose extract (weight ratio of 1: 1)) 21 LPS + Sample 4 (Ulgum extract + Evening primrose extract (weight ratio of 1: 2)) 25 LPS + Sample 5 (Ulugin Extract + Evening Primrose Oil Extract (weight ratio of 2: 1)) 19 LPS + sample 6 (Ulgum extract + Pygmyum evening primrose extract + pakira extract (weight ratio of 1: 1: 1)) 57

Example 10 Evaluation of Wrinkle Reducing Effect (Skin Patch Test)

(1) The cosmetic composition having the composition ratio shown in Table 5 was confirmed to have an effect of improving wrinkles. Twenty women in their 40s or older were divided into 20 groups and divided into four groups. Each of the cosmetic compositions 1 to 4 was applied twice daily for 4 weeks around the eye area with wrinkles. Then, the skin wax- (Skin Visiometer SV 600 FireWire, CK Electronic GmbH). The results are shown in Table 9.

(2) In Table 9, the average depth of the wrinkles is divided into five equal parts of the specimen made by using the silicone rubber at the part to measure the wrinkles, and the average value of the difference between the highest point and the lowest point of the wrinkle height is shown at each of the five parts. The roughness average represents the mean value of the wrinkle depth differences at the individual measurement sites (the total is divided by 255 measurement site points) from the mean of the total wrinkle depth in the sample. The lower the average depth of the wrinkles and the roughness average, the less wrinkles are formed, which means that the degree of skin aging is small. Table 9 shows that the average depth and roughness average of the wrinkles were lower in the order of cosmetic compositions 4, 2, 1, and 3, respectively. This indicates that wrinkle improvement And the effect of improving the wrinkles can be improved when the extract is added to the mixed extract.

Wrinkle improvement effect Average depth of wrinkles (%) Roughness average (%) Cosmetic composition 1 T0 100.0 100.0 T4 75 72 Cosmetic composition 2 T0 100.0 100.0 T4 71 70 Cosmetic composition 3 T0 100.0 100.0 T4 85 81 Cosmetic composition 4 T0 100.0 100.0 T4 66 61

While the present invention has been described in connection with what is presently considered to be practical exemplary embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, Should be interpreted as belonging to the scope.

Claims (10)

A herbal extract, and a bilberry evening primrose extract. The method according to claim 1, wherein the evening primrose oil extract
50 parts by weight based on 100 parts by weight of the extract. 3. The method according to claim 2,
Wherein the cosmetic composition is contained in an amount of 0.1 to 5% by weight based on the total weight of the cosmetic composition. The cosmetic composition according to claim 1, wherein the cosmetic composition comprises
60 Hydrogenated Castor Oil, Green Tea Extract, Ginkgo Biloba Extract, Ginkgo Biloba Extract, Petal Extract, Natural Extracts, Natural Extracts, Natural Extracts, Wherein the cosmetic composition further comprises a preservative. 5. The method of claim 4,
The essential oil is composed of bergamot fruit oil, lavender oil, milk oil and sentenced geranium flower oil,
The petal extract is composed of peach tree flower extract, plum extract, lotus flower extract and magnolia tree flower extract,
Wherein the natural preservative is composed of an extract of Acerola japonica fruit and an extract of Earthia. The cosmetic composition according to claim 1, wherein the cosmetic composition comprises
Wherein the composition further comprises a pakira extract. 7. The method according to claim 6, wherein the pakira extract
50 parts by weight based on 100 parts by weight of the extract. The cosmetic composition according to claim 1, wherein the cosmetic composition comprises
Wherein the cosmetic composition has an anti-inflammatory effect. The cosmetic composition according to claim 6, wherein the cosmetic composition comprises
Wherein the cosmetic composition has an anti-inflammatory effect and a wrinkle-reducing effect. 10. The cosmetic composition according to any one of claims 1 to 9,
Wherein the cosmetic composition has any one of a skin, a lotion, a cream, and a mask pack.