WO2015141926A1 - Composition pour inhiber ou atténuer un vieillissement cutané causé par une stimulation de stress, contenant de la trapa japonica comme principe actif - Google Patents
Composition pour inhiber ou atténuer un vieillissement cutané causé par une stimulation de stress, contenant de la trapa japonica comme principe actif Download PDFInfo
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- WO2015141926A1 WO2015141926A1 PCT/KR2014/011418 KR2014011418W WO2015141926A1 WO 2015141926 A1 WO2015141926 A1 WO 2015141926A1 KR 2014011418 W KR2014011418 W KR 2014011418W WO 2015141926 A1 WO2015141926 A1 WO 2015141926A1
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- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000002018 overexpression Effects 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 210000004927 skin cell Anatomy 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 230000037394 skin elasticity Effects 0.000 description 1
- 229950011392 sorbitan stearate Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000194 supercritical-fluid extraction Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- 238000002137 ultrasound extraction Methods 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
- 235000013343 vitamin Nutrition 0.000 description 1
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- 229930003231 vitamin Natural products 0.000 description 1
- 238000003809 water extraction 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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- 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
- A61K8/0216—Solid or semisolid forms
-
- 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
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
- A61Q19/08—Anti-ageing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
- A61K2800/522—Antioxidants; Radical scavengers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
Definitions
- composition for inhibiting or improving skin aging due to stress stimulation containing twill extract as an active ingredient
- the present invention is made by the task number HN12C0061 in support of the Ministry of Health and Welfare, the research management professional organization of the task is a global cosmetic research and development project,
- the present invention relates to a composition for inhibiting or improving skin aging due to stress stimulation containing a twill extract as an active ingredient, and more specifically for inhibiting or improving skin aging due to stress stimulation containing a twill extract or a twill fraction as an active ingredient. It relates to a cosmetic composition or a topical skin composition.
- Aging refers to the gradual decline in physiological function of normal function as a result of complex human mechanisms.
- the skin contains keratinocytes, melanocytes, islets of Langerhans, fibroblasts and adipocytes. These cells undergo aging and change in physiological function, shape, and structure.
- Skin aging is divided into two types: intr ic aging and photoaging. Endogenous aging is irrelevant to the external environment with the passage of time. It refers to the aging phenomenon that occurs naturally depending on the genetic factors. On the other hand, photoaging is a phenomenon caused by external environmental factors and can be avoided because it can be artificially controlled. The representative factor of photoaging is ultraviolet light, which leads to the activation of proteolytic enzymes, chain breakage of substrate proteins and damage of biological components of abnormal cross-links, and repetition of this mechanism leads to apparent skin aging. .
- Wrinkles, decreased skin elasticity, sagging and dryness in aged skin are mostly due to changes in matrix proteins present in the dermis.
- the dermis is located directly below the epidermis and determines the strength and shape of the skin. Therefore, when aging progresses, morphological changes occur in this area, which leads to a change in elasticity.
- Ps Moatr ix metal loproteinases
- ⁇ P activity is increased in the skin even with a single UV irradiation, and it significantly degrades collagen and other substrate proteins in the skin to promote skin aging. It acts as a major factor.
- Intracellular reactions by stress are reactions of glucocorticoids acting as stress hormones and are regulated by secretion of active cortisol and ⁇ ⁇ -HSDl (11 ⁇ -hydroxysteroid dehydrogenasel) activity.
- ⁇ ⁇ -HSDl converts inactive glucocorticoids into active glucocorticoids, thereby playing an important role in regulating the concentration of cellular agents and activating corticosteroid receptors in target tissues.
- ⁇ ⁇ -HSDl converts inactive glucocorticoids into active glucocorticoids, thereby playing an important role in regulating the concentration of cellular agents and activating corticosteroid receptors in target tissues.
- the present inventors have made diligent research efforts to overcome the problems of the prior art, to discover that the role of ⁇ -HSDl activated by ultraviolet light is related to photoaging and to find a substance that improves the efficacy of anti-aging Based on the plant extracts reported to have been compared and selected, among them, the extracts of the filth extract or its fractions, ⁇ ⁇ -HSDl and ⁇ Ps, the expression of inflammatory factors and the thickness of the dermis . It has been confirmed that the inhibition of skin aging, the improvement and treatment of aging skin can be suppressed, and the present invention has been completed.
- the main object of the present invention is to inhibit the skin aging by inhibiting the expression of ⁇ -HSDl and ⁇ Ps, the expression of inflammatory factors and the thickness of the dermis, which has the effect of improving the aging skin. It is to provide a composition for inhibiting or improving skin aging due to stress stimulation containing a twill extract or a twill fraction as an active ingredient.
- Another object of the present invention is to provide a method for use in the preparation of a composition for inhibiting or improving skin aging due to stress stimulation of the stalk extract or stalk fraction or a method for inhibiting or improving skin aging using such a composition.
- the present invention provides a composition for inhibiting or improving skin aging due to stress stimulation, which contains an extract of the stalk extract or the stalk fraction as an active ingredient.
- the composition is characterized in that it is used as a cosmetic or skin external preparation.
- Thunsil is a yearly grass that grows in water and has elongated stems. Each node floats in the shape of a feather-shaped water root. This insufficiency is effective in nourishing and tonic, so the body is a good nutritional to the weak, it is known to detoxify and act as a detoxification.
- Korean Patent No. 10-0927970 discloses that the extract of twill is effective in inhibiting sebum secretion and acne.
- the present inventors have found that the twill extract has an effect of suppressing skin photoaging due to stress stimulation, in particular, stress stimulation by ultraviolet rays, and thus, the present invention has been completed.
- the term 'stress stimulus' of the present invention means that harmful stimuli from the external environment increase the stress hormone (glucocorticoid) in the skin and cause skin aging or skin atrophy. In the present invention, it means specifically by stress stimulation by ultraviolet rays.
- the skin aging may be photoaging by ultraviolet rays, moreover.
- it is characterized by photoaging by UVB Jl travi olet B).
- the term 'photo-aging (Phhtoagipg)' of the present invention is a phenomenon caused by external environmental factors, and the most representative factor is ultraviolet rays. This ultraviolet light causes damage to biological components such as protease activation, substrate protein chain breakdown and abnormal crosslinking, and the repetition of this mechanism leads to apparent skin aging. That is, in the present invention, unlike endogenous aging caused by genetic factors regardless of the external environment, a composition for inhibiting or improving skin aging caused by photoaging caused by ultraviolet rays, in particular a cosmetic composition, or It relates to an external preparation composition for skin.
- the twill extract can be extracted with any solvent conventionally used .
- water, lower alcohol having 1 to 4 carbon atoms, polyhydric alcohol having 3 to 6 carbon atoms, glycerin, propylene glycol or butylene glycol is characterized in that the extraction with one or more solvents selected from the group consisting of.
- the lysyl fraction can be fractionated by any solvent used in the conventional systematic fractionation method, preferably a low polar organic solvent, more preferably nucleic acid, methylene chloride, ethyl acetate or n -Fractionate with at least one solvent selected from the group consisting of butanol.
- a low polar organic solvent more preferably nucleic acid, methylene chloride, ethyl acetate or n -Fractionate with at least one solvent selected from the group consisting of butanol.
- the twill extract or the twill fraction may be used as it is, characterized in that it can be used in the form of a concentrated lyophilized or lyophilized after filtration.
- the skin aging is 11 beta-HSD 1 (11 ⁇ _ It is characterized by inhibiting or improving skin aging by inhibiting the expression of hydroxysteroid dehydrogenasel).
- 11beta-HSD1 (11 ⁇ -hydroxysteroid dehydrogenasel, ⁇ -HSDl) regulates the reaction of glucocorticoids to act as stress hormones.
- ⁇ -HSDl increases Î ⁇ -HSDl activity in the skin with age (Tiganescu A et al, 2013; 123 (7): 3051-3060).
- the researchers found that the activity of ⁇ -HSDl at the site where photoaging occurred was about 4 times higher than the site where endogenous aging occurred. Reported (Tiganescu A et al, 2011; 131, 30-36).
- the skin aging is characterized by inhibiting or improving skin aging by inhibiting the expression of ⁇ Ps and inflammatory factors.
- ⁇ Ps (Matrix metal loproteinases) is increased ⁇ P activity in the skin in a single UV irradiation Representative enzymes that break down matrix proteins and i to to significantly decompose collagen and other matrix proteins in the skin, it promotes skin aging increases important factor Acts as.
- the skin aging is characterized in that to suppress or improve the skin aging by inhibiting the reduction of the dermal layer thickness.
- the twill extract or the twill fraction is characterized in that it comprises 0.01 to 90% by weight relative to the total weight of the composition. If it is outside the above range, the formulation is not easy and is not preferable.
- the composition may be prepared in any formulation commonly prepared in the art, for example, emulsion, cream, lotion, pack, foundation, lotion, essence, hair cosmetics, etc. .
- Cosmetic compositions of the present invention may include other auxiliaries in addition to the carrier, for example, may include preservatives, antioxidants, stabilizers, solubilizers, vitamins, pigments and flavors.
- the composition may be used in the form of powders, granules, tablets, capsules, suspensions, emulsions, syrups, aerosols, and other external preparations and sterile injectable solutions, respectively, according to a conventional method. May have a cream, gel, patch, spray, ointment, warning, lotion, liniment pasta or cataplasma formulation.
- Carriers, excipients, and diluents that may be included in the composition include lactose, dextrose, sucrose, oligosaccharides, sorbbi, manny, xili, and erythritol. Malty, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, microcrystalline cellulose, polyvinyl pyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, Talc, magnesium stearate and mineral oil.
- diluents or excipients such as fillers, extenders, binders, wetting agents, disintegrating agents and surfactants are usually used.
- Solid preparations for oral administration include tablets, pills, powders, granules, capsules, and the like. Such solid preparations may contain at least one excipient such as starch, calcium carbonate, water, or the like. Prepared with a mixture of sucrose or lactose, gelatin and the like. In addition to simple excipients, lubricants such as magnesium styrate talc are also used. Oral liquid preparations include suspending agents, liquid solutions, emulsions, and syrups, and may include various excipients, such as wetting agents, sweeteners, fragrances, and preservatives, in addition to commonly used simple diluents such as water and liquid paraffin. .
- Formulations for parenteral administration include sterile aqueous solutions, non-aqueous solvents, suspensions, emulsions, lyophilized preparations, suppositories.
- non-aqueous solvent and suspending agent propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate and the like can be used.
- base of the suppository wi tepsol, macrogol, tween 61, cacao butter, laurin butter, glycerogelatin and the like can be used.
- the preferred dosage of the composition also depends on the condition and weight of the patient, the extent of the disease, the form of the drug, the route of administration and the duration, and may be appropriately selected by those skilled in the art. However, for the desired effect, the composition of the present invention is preferably administered at 0.0001 to 100mg / kg, preferably 0.001 to 10mg / kg per day. Topical administration may be administered once a day or may be divided several times. The dosage does not limit the scope of the invention in any aspect.
- the filth extract or fraction extract of the present invention inhibits the expression of ⁇ ⁇ -HSDl, MMPs and inflammatory factors overexpressed by UV light.
- the filth extract or fraction extract of the present invention inhibits the expression of ⁇ ⁇ -HSDl, MMPs and inflammatory factors overexpressed by UV light.
- Figure 1 is a picture of the results of Experimental Example 1 measuring the effect on the expression of ⁇ ⁇ -HSDl protein 'in the treatment of the extract and fractions in human fibroblasts.
- Figure 2 is a graph of the results of Experimental Example 2 measuring the effect on the P-1 protein expression in the treatment of the extract and fractions in human fibroblasts.
- Figure 3 is a graph of the results of Experimental Example 3 measuring the effect on ⁇ P-3 messenger RNA expression in the treatment of the extract and fractions in human fibroblasts.
- FIG. 4 is a graph showing the results of Experimental Example 3, which measured the effect of fflP-9 messenger R A expression upon treatment of filth extract and fraction on human fibroblasts.
- Figure 5 is a graph of the results of Experimental Example 4 measuring the effect on the C0X-2 messenger RNA expression when treatment with the extract and fractions in human keratinocytes.
- Figure 6 is a graph of the results of Experimental Example 4 measuring the effect on the expression of iNOS messenger R A in the treatment of extracts and fractions in human keratinocytes.
- Figure 7 is a graph of the results of Experimental Example 5 measuring the effect on the P-1 protein expression in the treatment of the extract and fractions in the three-dimensional artificial skin.
- Figure 8 is a graph of the results of Experimental Example 6 measuring the effect on the change in the thickness of the dermis layer during the treatment of the sample containing the twill extract in the photo-aging skin animal model.
- Tungsil used in the present invention was purchased from the herbal medicine of Gyeongdong market, Seoul, Korea.
- Electrophoresis using SDS-PAGE Sod i umdodecy 1 su 1 f at e-po 1 yacry 1 am i de gel electrophoresis
- transfer protein bands to PVDF Polyvinyl idene fluoride, Bio-rad, USA
- Enhanced chemi luminescence, ThermoScient if ic, USA was confirmed the amount of protein expression.
- RT-PCR was performed using a PCR machine (Step One Plus, Applied Biosystems, USA) and assayed by the addition of cyberrin (SYBRGreen supermix, Applied Biosystems, USA) with P-3 and P-9 primers and cDNA.
- the primer and reaction conditions were shown in Table 1 below, and the expression levels of ⁇ P-3 and ⁇ P-9 were expressed by correcting the ⁇ -actin gene.
- Human keratinocytes were cultured in the same manner as described in Experimental Example 3 above, the cells were inoculated into 6 we ll plates and irradiated with UVB 15mJ after 24 hours, and then each extract was added. After further incubation for 24 hours, real-t ime RT-PCR was carried out in the same manner as in Experiment 2 to measure messenger RNA expression levels of inflammatory factors C0X-2 ( C yc looxygenase_2) and iNOS (inducibl e NO synthase).
- C0X-2 C yc looxygenase_2
- iNOS inducibl e NO synthase
- Example 5 MMP-1 Inhibitory Activity of Twill Extract in Three-Dimensional Skin Tissues
- P-1 expression of the twill extract of Example 1 was confirmed using three-dimensional artificial skin tissue.
- Epi dermal ti ssue (Skin Ethi cs, Nikoderm Research Inc., France) was stabilized in growth medi a for 24 hours, and then irradiated with UVB 40mJ. Enzyme-linked immunosorbent assay (enzyme- l inked) to quantify the amount of protein secretion of ⁇ P-1 after incubation for 72 hours An immunosorbent assay (ELISA) was performed.
- the effect of the sample containing the twill extract of Example 1 on the photoaging skin animal model was evaluated. Dermal mice were irradiated with ultraviolet rays three times a week for a total of eight weeks, and the samples containing the twill methanol extract were mixed with the base and applied twice a day for a total of eight weeks to measure dermal thickness.
- the base was mixed with PG (propylene glycol): EtOH (ethane) at 7: 3 and treated with sham light to serve as a control.
- the toner agent containing the extract obtained in Example 1 was prepared in a conventional manner according to the composition components and composition ratios shown in Table 2 below.
- the cream containing the extract obtained in Example 1 was prepared in a conventional manner according to the composition components and composition ratios shown below.
- Example 1 ⁇ 1 1.0 Glyceryl Stearate / Sebum -1 00 Stearate 2.0 Fully Solate 60 0.5
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- General Health & Medical Sciences (AREA)
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- Birds (AREA)
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Abstract
La présente invention concerne une composition cosmétique ou une composition de préparation cutanée à usage externe pour inhiber ou atténuer un vieillissement cutané causé par une stimulation de stress, contenant un extrait deTrapa japonica ou une fraction de Trapa japonica comme principe actif. Selon la présente invention, l'extrait de Trapa japonica ou une fraction de celui-ci peut inhiber un vieillissement cutané, et atténuer et traiter le vieillissement cutané par l'inhibition de 11β-HSD1 et MMP, de l'expression de facteurs d'inflammation et de la diminution de l'épaisseur du derme.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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KR1020140030820A KR20150108088A (ko) | 2014-03-17 | 2014-03-17 | 능실 추출물을 유효성분으로 함유하는 스트레스 자극에 의한 피부노화 억제 또는 개선용 조성물 |
KR10-2014-0030820 | 2014-03-17 |
Publications (1)
Publication Number | Publication Date |
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WO2015141926A1 true WO2015141926A1 (fr) | 2015-09-24 |
Family
ID=54144856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/KR2014/011418 WO2015141926A1 (fr) | 2014-03-17 | 2014-11-26 | Composition pour inhiber ou atténuer un vieillissement cutané causé par une stimulation de stress, contenant de la trapa japonica comme principe actif |
Country Status (2)
Country | Link |
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KR (1) | KR20150108088A (fr) |
WO (1) | WO2015141926A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109431846A (zh) * | 2018-11-28 | 2019-03-08 | 邯郸学院 | 一种生物活性成分护肤品 |
CN115485338A (zh) * | 2020-05-04 | 2022-12-16 | Omya国际股份公司 | 化学和物理防晒用干组合物和/或乳液及其用途 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102344703B1 (ko) * | 2018-12-28 | 2021-12-30 | 에이앤펩주식회사 | 마름 발효물의 제조방법과 이로부터 제조된 마름 발효물이나 펩타이드를 유효성분으로 함유하는 피부 주름 개선, 항노화에 효과가 있는 조성물과 발효물로 이루어진 피부노화 개선용 조성물 |
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- 2014-03-17 KR KR1020140030820A patent/KR20150108088A/ko not_active Application Discontinuation
- 2014-11-26 WO PCT/KR2014/011418 patent/WO2015141926A1/fr active Application Filing
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Cited By (3)
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CN109431846A (zh) * | 2018-11-28 | 2019-03-08 | 邯郸学院 | 一种生物活性成分护肤品 |
CN109431846B (zh) * | 2018-11-28 | 2021-09-07 | 邯郸学院 | 一种生物活性成分护肤品 |
CN115485338A (zh) * | 2020-05-04 | 2022-12-16 | Omya国际股份公司 | 化学和物理防晒用干组合物和/或乳液及其用途 |
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