KR20210056984A - Composition for improving skin - Google Patents
Composition for improving skin Download PDFInfo
- Publication number
- KR20210056984A KR20210056984A KR1020210060710A KR20210060710A KR20210056984A KR 20210056984 A KR20210056984 A KR 20210056984A KR 1020210060710 A KR1020210060710 A KR 1020210060710A KR 20210060710 A KR20210060710 A KR 20210060710A KR 20210056984 A KR20210056984 A KR 20210056984A
- Authority
- KR
- South Korea
- Prior art keywords
- stem cell
- skin
- promoting
- cell activity
- extract
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 72
- 210000000130 stem cell Anatomy 0.000 claims abstract description 93
- 230000000694 effects Effects 0.000 claims abstract description 92
- 230000001737 promoting effect Effects 0.000 claims abstract description 36
- 206010003645 Atopy Diseases 0.000 claims abstract description 35
- 239000002537 cosmetic Substances 0.000 claims abstract description 31
- 235000013305 food Nutrition 0.000 claims abstract description 22
- 230000004663 cell proliferation Effects 0.000 claims abstract description 12
- 239000000284 extract Substances 0.000 claims description 79
- 239000004480 active ingredient Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 19
- 238000002360 preparation method Methods 0.000 claims description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 108010076876 Keratins Proteins 0.000 claims description 12
- 102000011782 Keratins Human genes 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000012046 mixed solvent Substances 0.000 claims description 2
- 238000004299 exfoliation Methods 0.000 claims 2
- RQXXCWHCUOJQGR-UHFFFAOYSA-N 1,1-dichlorohexane Chemical compound CCCCCC(Cl)Cl RQXXCWHCUOJQGR-UHFFFAOYSA-N 0.000 claims 1
- 239000012454 non-polar solvent Substances 0.000 claims 1
- 239000002798 polar solvent Substances 0.000 claims 1
- 230000006872 improvement Effects 0.000 abstract description 52
- 230000003110 anti-inflammatory effect Effects 0.000 abstract description 30
- 230000036548 skin texture Effects 0.000 abstract description 28
- 230000003020 moisturizing effect Effects 0.000 abstract description 26
- 230000036560 skin regeneration Effects 0.000 abstract description 19
- 102000023984 PPAR alpha Human genes 0.000 abstract description 15
- 108010028924 PPAR alpha Proteins 0.000 abstract description 15
- 238000004519 manufacturing process Methods 0.000 abstract description 14
- 230000002401 inhibitory effect Effects 0.000 abstract description 10
- 230000035755 proliferation Effects 0.000 abstract description 8
- 102100028314 Filaggrin Human genes 0.000 abstract description 7
- 101710088660 Filaggrin Proteins 0.000 abstract description 7
- 239000003814 drug Substances 0.000 abstract description 7
- 230000001965 increasing effect Effects 0.000 abstract description 5
- 241000180649 Panax notoginseng Species 0.000 abstract description 3
- 235000003143 Panax notoginseng Nutrition 0.000 abstract 1
- 230000023895 stem cell maintenance Effects 0.000 abstract 1
- 210000003491 skin Anatomy 0.000 description 116
- 210000004027 cell Anatomy 0.000 description 29
- 238000009472 formulation Methods 0.000 description 26
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 16
- 239000004615 ingredient Substances 0.000 description 13
- 206010061218 Inflammation Diseases 0.000 description 12
- 239000006071 cream Substances 0.000 description 12
- 230000004054 inflammatory process Effects 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 11
- 210000002615 epidermis Anatomy 0.000 description 10
- 239000002609 medium Substances 0.000 description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000000306 component Substances 0.000 description 9
- 210000002510 keratinocyte Anatomy 0.000 description 9
- 241000282414 Homo sapiens Species 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 235000013361 beverage Nutrition 0.000 description 7
- -1 etc. Substances 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 239000006210 lotion Substances 0.000 description 7
- 230000008591 skin barrier function Effects 0.000 description 7
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 6
- 238000002835 absorbance Methods 0.000 description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
- 239000003755 preservative agent Substances 0.000 description 6
- 208000024891 symptom Diseases 0.000 description 6
- 210000001519 tissue Anatomy 0.000 description 6
- 206010052428 Wound Diseases 0.000 description 5
- 208000027418 Wounds and injury Diseases 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 238000010609 cell counting kit-8 assay Methods 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 239000003826 tablet Substances 0.000 description 5
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 4
- 206010012438 Dermatitis atopic Diseases 0.000 description 4
- NTNWOCRCBQPEKQ-YFKPBYRVSA-N N(omega)-methyl-L-arginine Chemical compound CN=C(N)NCCC[C@H](N)C(O)=O NTNWOCRCBQPEKQ-YFKPBYRVSA-N 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 230000032683 aging Effects 0.000 description 4
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 4
- 201000008937 atopic dermatitis Diseases 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 230000002757 inflammatory effect Effects 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000002674 ointment Substances 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 239000003495 polar organic solvent Substances 0.000 description 4
- 239000013641 positive control Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 229930003231 vitamin Natural products 0.000 description 4
- 239000011782 vitamin Substances 0.000 description 4
- 235000013343 vitamin Nutrition 0.000 description 4
- 229940088594 vitamin Drugs 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- 230000037303 wrinkles Effects 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 206010013786 Dry skin Diseases 0.000 description 3
- 108060001084 Luciferase Proteins 0.000 description 3
- 239000005089 Luciferase Substances 0.000 description 3
- 241000124008 Mammalia Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- 102000003425 Tyrosinase Human genes 0.000 description 3
- 108060008724 Tyrosinase Proteins 0.000 description 3
- 230000002159 abnormal effect Effects 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 235000014633 carbohydrates Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000009508 confectionery Nutrition 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 230000004069 differentiation Effects 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 230000037336 dry skin Effects 0.000 description 3
- 235000003599 food sweetener Nutrition 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 210000003780 hair follicle Anatomy 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 150000002632 lipids Chemical class 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- 238000012423 maintenance Methods 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- 244000052769 pathogen Species 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 230000009759 skin aging Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 210000000434 stratum corneum Anatomy 0.000 description 3
- 230000035882 stress Effects 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000003765 sweetening agent Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
- 229920002498 Beta-glucan Polymers 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 2
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 2
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 2
- 102000004127 Cytokines Human genes 0.000 description 2
- 108090000695 Cytokines Proteins 0.000 description 2
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 2
- 206010015150 Erythema Diseases 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- 102000004889 Interleukin-6 Human genes 0.000 description 2
- 108090001005 Interleukin-6 Proteins 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 description 2
- 244000131316 Panax pseudoginseng Species 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 102000040945 Transcription factor Human genes 0.000 description 2
- 108091023040 Transcription factor Proteins 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 229930003268 Vitamin C Natural products 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- 230000007815 allergy Effects 0.000 description 2
- 239000002260 anti-inflammatory agent Substances 0.000 description 2
- 229940114079 arachidonic acid Drugs 0.000 description 2
- 235000021342 arachidonic acid Nutrition 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzydamine Chemical compound C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 229940106189 ceramide Drugs 0.000 description 2
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol 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)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 239000002299 complementary DNA Substances 0.000 description 2
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 210000003981 ectoderm Anatomy 0.000 description 2
- 239000003974 emollient agent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000002158 endotoxin Substances 0.000 description 2
- 210000002514 epidermal stem cell Anatomy 0.000 description 2
- 210000000981 epithelium Anatomy 0.000 description 2
- 231100000321 erythema Toxicity 0.000 description 2
- 239000000686 essence Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 210000002950 fibroblast Anatomy 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 235000013355 food flavoring agent Nutrition 0.000 description 2
- 235000015203 fruit juice Nutrition 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000003349 gelling agent Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000013632 homeostatic process Effects 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- BJRNKVDFDLYUGJ-RMPHRYRLSA-N hydroquinone O-beta-D-glucopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-RMPHRYRLSA-N 0.000 description 2
- 230000028993 immune response Effects 0.000 description 2
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 2
- 230000028709 inflammatory response Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 230000015788 innate immune response Effects 0.000 description 2
- 229940100601 interleukin-6 Drugs 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 230000003780 keratinization Effects 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 108020001756 ligand binding domains Proteins 0.000 description 2
- 229920006008 lipopolysaccharide Polymers 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 210000002752 melanocyte Anatomy 0.000 description 2
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 2
- 239000013642 negative control Substances 0.000 description 2
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 230000037361 pathway Effects 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 2
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 229940113124 polysorbate 60 Drugs 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000009993 protective function Effects 0.000 description 2
- 238000003753 real-time PCR Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000001172 regenerating effect Effects 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 108020004418 ribosomal RNA Proteins 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- 208000017520 skin disease Diseases 0.000 description 2
- 230000036620 skin dryness Effects 0.000 description 2
- 230000036559 skin health Effects 0.000 description 2
- 229940032094 squalane Drugs 0.000 description 2
- 239000000829 suppository Substances 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 235000013616 tea Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 2
- 235000019154 vitamin C Nutrition 0.000 description 2
- 239000011718 vitamin C Substances 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- DMASLKHVQRHNES-UPOGUZCLSA-N (3R)-beta,beta-caroten-3-ol Chemical compound C([C@H](O)CC=1C)C(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C DMASLKHVQRHNES-UPOGUZCLSA-N 0.000 description 1
- HBOQXIRUPVQLKX-BBWANDEASA-N 1,2,3-trilinoleoylglycerol Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC HBOQXIRUPVQLKX-BBWANDEASA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- RQTTXGQDIROLTQ-FASGCTRLSA-N 2''-O-(beta-D-glucosyl)isovitexin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@H]1[C@H](C=2C(=C3C(=O)C=C(OC3=CC=2O)C=2C=CC(O)=CC=2)O)O[C@H](CO)[C@@H](O)[C@@H]1O RQTTXGQDIROLTQ-FASGCTRLSA-N 0.000 description 1
- QGJZLNKBHJESQX-UHFFFAOYSA-N 3-Epi-Betulin-Saeure Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C(=C)C)C5C4CCC3C21C QGJZLNKBHJESQX-UHFFFAOYSA-N 0.000 description 1
- CLOUCVRNYSHRCF-UHFFFAOYSA-N 3beta-Hydroxy-20(29)-Lupen-3,27-oic acid Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C(O)=O)CCC5(C)CCC(C(=C)C)C5C4CCC3C21C CLOUCVRNYSHRCF-UHFFFAOYSA-N 0.000 description 1
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 1
- 201000004384 Alopecia Diseases 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- DIZWSDNSTNAYHK-XGWVBXMLSA-N Betulinic acid Natural products CC(=C)[C@@H]1C[C@H]([C@H]2CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12)C(=O)O DIZWSDNSTNAYHK-XGWVBXMLSA-N 0.000 description 1
- 241000282817 Bovidae Species 0.000 description 1
- 101100297347 Caenorhabditis elegans pgl-3 gene Proteins 0.000 description 1
- 241000700199 Cavia porcellus Species 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 241000195649 Chlorella <Chlorellales> Species 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 108020004414 DNA Proteins 0.000 description 1
- 230000004568 DNA-binding Effects 0.000 description 1
- 101710088194 Dehydrogenase Proteins 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- AHMIDUVKSGCHAU-UHFFFAOYSA-N Dopaquinone Natural products OC(=O)C(N)CC1=CC(=O)C(=O)C=C1 AHMIDUVKSGCHAU-UHFFFAOYSA-N 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- 102000016942 Elastin Human genes 0.000 description 1
- 108010014258 Elastin Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241000283073 Equus caballus Species 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 102000002464 Galactosidases Human genes 0.000 description 1
- 108010093031 Galactosidases Proteins 0.000 description 1
- 102100039556 Galectin-4 Human genes 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000608765 Homo sapiens Galectin-4 Proteins 0.000 description 1
- 101000741788 Homo sapiens Peroxisome proliferator-activated receptor alpha Proteins 0.000 description 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
- 102000000426 Integrin alpha6 Human genes 0.000 description 1
- 108010041100 Integrin alpha6 Proteins 0.000 description 1
- 102000012355 Integrin beta1 Human genes 0.000 description 1
- 108010022222 Integrin beta1 Proteins 0.000 description 1
- 102000002397 Kinins Human genes 0.000 description 1
- 108010093008 Kinins Proteins 0.000 description 1
- WTDRDQBEARUVNC-LURJTMIESA-N L-DOPA Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-LURJTMIESA-N 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- AHMIDUVKSGCHAU-LURJTMIESA-N L-dopaquinone Chemical compound [O-]C(=O)[C@@H]([NH3+])CC1=CC(=O)C(=O)C=C1 AHMIDUVKSGCHAU-LURJTMIESA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- 102000008072 Lymphokines Human genes 0.000 description 1
- 108010074338 Lymphokines Proteins 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- RQTTXGQDIROLTQ-FRMBBQOESA-N Meloside A Natural products O([C@@H]1[C@@H](O)[C@H](O)[C@H](CO)O[C@H]1c1c(O)c2C(=O)C=C(c3ccc(O)cc3)Oc2cc1O)[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1 RQTTXGQDIROLTQ-FRMBBQOESA-N 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 235000002789 Panax ginseng Nutrition 0.000 description 1
- 235000003181 Panax pseudoginseng Nutrition 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 229920002230 Pectic acid Polymers 0.000 description 1
- 201000011152 Pemphigus Diseases 0.000 description 1
- 102000012141 Peroxisome proliferator-activated receptor alpha Human genes 0.000 description 1
- 241000009328 Perro Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 1
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 206010039793 Seborrhoeic dermatitis Diseases 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 206010072170 Skin wound Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 244000228451 Stevia rebaudiana Species 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- 208000031673 T-Cell Cutaneous Lymphoma Diseases 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
- 241001135917 Vitellaria paradoxa Species 0.000 description 1
- 206010069055 Vulvovaginal pain Diseases 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 235000013334 alcoholic beverage Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 description 1
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 description 1
- 229960000458 allantoin Drugs 0.000 description 1
- 208000004631 alopecia areata Diseases 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 229960000271 arbutin Drugs 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 238000003149 assay kit Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910000063 azene Inorganic materials 0.000 description 1
- 208000002479 balanitis Diseases 0.000 description 1
- 210000000270 basal cell Anatomy 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 229960000333 benzydamine Drugs 0.000 description 1
- WQZGKKKJIJFFOK-FPRJBGLDSA-N beta-D-galactose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-FPRJBGLDSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 102000005936 beta-Galactosidase Human genes 0.000 description 1
- 108010005774 beta-Galactosidase Proteins 0.000 description 1
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 1
- 235000013734 beta-carotene Nutrition 0.000 description 1
- 239000011648 beta-carotene Substances 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 229960002747 betacarotene Drugs 0.000 description 1
- QGJZLNKBHJESQX-FZFNOLFKSA-N betulinic acid Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C(=C)C)[C@@H]5[C@H]4CC[C@@H]3[C@]21C QGJZLNKBHJESQX-FZFNOLFKSA-N 0.000 description 1
- 230000027455 binding Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 208000019748 bullous skin disease Diseases 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 235000001046 cacaotero Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 230000032677 cell aging Effects 0.000 description 1
- 230000024245 cell differentiation Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000035605 chemotaxis Effects 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- KNHUKKLJHYUCFP-UHFFFAOYSA-N clofibrate Chemical compound CCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1 KNHUKKLJHYUCFP-UHFFFAOYSA-N 0.000 description 1
- 229960001214 clofibrate Drugs 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 201000007241 cutaneous T cell lymphoma Diseases 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 230000004665 defense response Effects 0.000 description 1
- 210000004207 dermis Anatomy 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229960003957 dexamethasone Drugs 0.000 description 1
- UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- PZXJOHSZQAEJFE-UHFFFAOYSA-N dihydrobetulinic acid Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C(C)C)C5C4CCC3C21C PZXJOHSZQAEJFE-UHFFFAOYSA-N 0.000 description 1
- 229940120503 dihydroxyacetone Drugs 0.000 description 1
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 229920002549 elastin Polymers 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 210000001671 embryonic stem cell Anatomy 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 230000009786 epithelial differentiation Effects 0.000 description 1
- 230000008202 epithelial morphogenesis Effects 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012091 fetal bovine serum Substances 0.000 description 1
- 239000012894 fetal calf serum Substances 0.000 description 1
- 244000144992 flock Species 0.000 description 1
- 229960004369 flufenamic acid Drugs 0.000 description 1
- LPEPZBJOKDYZAD-UHFFFAOYSA-N flufenamic acid Chemical compound OC(=O)C1=CC=CC=C1NC1=CC=CC(C(F)(F)F)=C1 LPEPZBJOKDYZAD-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 230000003779 hair growth Effects 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 230000003660 hair regeneration Effects 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 238000001794 hormone therapy Methods 0.000 description 1
- 102000054223 human PPARA Human genes 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 229960001680 ibuprofen Drugs 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 239000000367 immunologic factor Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229960000905 indomethacin Drugs 0.000 description 1
- 239000012678 infectious agent Substances 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 description 1
- WZNJWVWKTVETCG-UHFFFAOYSA-N kojic acid Natural products OC(=O)C(N)CN1C=CC(=O)C(O)=C1 WZNJWVWKTVETCG-UHFFFAOYSA-N 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- VMPHSYLJUKZBJJ-UHFFFAOYSA-N lauric acid triglyceride Natural products CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- HBOQXIRUPVQLKX-UHFFFAOYSA-N linoleic acid triglyceride Natural products CCCCCC=CCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCC=CCCCCC)COC(=O)CCCCCCCC=CCC=CCCCCC HBOQXIRUPVQLKX-UHFFFAOYSA-N 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000003670 luciferase enzyme activity assay Methods 0.000 description 1
- 239000012139 lysis buffer Substances 0.000 description 1
- 229960003511 macrogol Drugs 0.000 description 1
- 210000002540 macrophage Anatomy 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000012533 medium component Substances 0.000 description 1
- 230000008099 melanin synthesis Effects 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 210000003716 mesoderm Anatomy 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 201000005962 mycosis fungoides Diseases 0.000 description 1
- 210000003098 myoblast Anatomy 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 235000021096 natural sweeteners Nutrition 0.000 description 1
- MQYXUWHLBZFQQO-UHFFFAOYSA-N nepehinol Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C)CCC(C(=C)C)C5C4CCC3C21C MQYXUWHLBZFQQO-UHFFFAOYSA-N 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 210000001020 neural plate Anatomy 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000036542 oxidative stress Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- BJRNKVDFDLYUGJ-UHFFFAOYSA-N p-hydroxyphenyl beta-D-alloside Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=C(O)C=C1 BJRNKVDFDLYUGJ-UHFFFAOYSA-N 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000006201 parenteral dosage form Substances 0.000 description 1
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 1
- 201000001976 pemphigus vulgaris Diseases 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 108091008725 peroxisome proliferator-activated receptors alpha Proteins 0.000 description 1
- 210000001539 phagocyte Anatomy 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 230000001817 pituitary effect Effects 0.000 description 1
- 235000013550 pizza Nutrition 0.000 description 1
- 210000002826 placenta Anatomy 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 229940012957 plasmin Drugs 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000010318 polygalacturonic acid Substances 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 229950008882 polysorbate Drugs 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 229960005205 prednisolone Drugs 0.000 description 1
- OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 description 1
- 208000025638 primary cutaneous T-cell non-Hodgkin lymphoma Diseases 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000001959 radiotherapy Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HELXLJCILKEWJH-NCGAPWICSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 108091008146 restriction endonucleases Proteins 0.000 description 1
- 229930002330 retinoic acid Natural products 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 208000008742 seborrheic dermatitis Diseases 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 235000011649 selenium Nutrition 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229940091258 selenium supplement Drugs 0.000 description 1
- 210000002265 sensory receptor cell Anatomy 0.000 description 1
- 102000027509 sensory receptors Human genes 0.000 description 1
- 108091008691 sensory receptors Proteins 0.000 description 1
- 239000012679 serum free medium Substances 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 235000011888 snacks Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 230000004037 social stress Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008227 sterile water for injection Substances 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 210000000438 stratum basale Anatomy 0.000 description 1
- 210000004003 subcutaneous fat Anatomy 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 210000000106 sweat gland Anatomy 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 229960001727 tretinoin Drugs 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 229940081852 trilinolein Drugs 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 230000002227 vasoactive effect Effects 0.000 description 1
- 230000024883 vasodilation Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 208000002003 vulvitis Diseases 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/25—Araliaceae (Ginseng family), e.g. ivy, aralia, schefflera or tetrapanax
- A61K36/258—Panax (ginseng)
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/318—Foods, ingredients or supplements having a functional effect on health having an effect on skin health and hair or coat
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Mycology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Botany (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Medical Informatics (AREA)
- Alternative & Traditional Medicine (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
본 발명은 피부 재생, 항염증, 아토피 개선, 피부 보습, 피부결 개선, 줄기세포 활성 촉진 효과를 나타내는 피부 개선용 조성물에 관한 것이다. The present invention relates to a composition for improving skin that exhibits skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing, skin texture improvement, and stem cell activity promoting effects.
염증은 상처나 질병에 반응하는 인체의 면역 반응으로, 자외선이나 활성산소, 자유라디칼 등의 산화적 스트레스 등이 염증성 인자를 활성화시켜 각종 질병 및 피부의 노화를 일으킨다. 혈관 활성 폴리펩타이드인 키닌(kinin), 플라스민(plasmin), 보체(complement) 등이 혈관 확장과 수축 및 주화성(chemotaxis) 작용을 하고, 그 외에 인터루킨-6(IL-6) 등과 같은 림포카인과 아라키돈산(arachidonic acid) 등이 염증 반응을 담당한다. 아라키돈산은 싸이클로옥시게나아제(cyclooxygenase) 혹은 리포옥시게 나아제(lipooxygenase)의 2가지 경로를 거쳐 염증 매개체인 프로스타글란딘(prostaglandin), 류코트리엔(lukotriene)들로 대사되어 다양한 염증 반응을 매개한다. Inflammation is the body's immune response in response to wounds or diseases, and oxidative stress such as ultraviolet rays, free radicals, etc. activates inflammatory factors, causing various diseases and aging of the skin. Vasoactive polypeptides such as kinin, plasmin, and complement act as vasodilation, contraction and chemotaxis, and other lymphokines such as interleukin-6 (IL-6). Phosphorus and arachidonic acid are responsible for the inflammatory response. Arachidonic acid is metabolized to prostaglandin and lukotriene, which are inflammatory mediators through two pathways of cyclooxygenase or lipooxygenase, mediating various inflammatory reactions.
한편, 염증을 소실시키기 위해 염증원의 제거, 생체 반응 및 증상을 감소시키는 작용을 하는 것을 항염제라 한다. 현재까지 항염의 목적으로 이용되고 있는 물질로는 비스테로이드계로 플루폐나믹산(flufenamic acid), 이부프로펜(ibuprofen), 벤지다민(benzydamine), 인도메타신(indomethacin) 등이 있고 스테로이드계통으로 프레드니솔론(prednisolone), 덱사메타손 (dexamethasone) 등이 있다. 또한, 알란토인, 아즈엔, 하이드로코티손 등이 항염증에 효과가 있는 것으로 알려져 있으나, 이들 물질은 피부에 대한 안전성의 문제로 사용량의 제한이 있거나, 효과가 미미하여 실질적으로 염증 완화 효과를 기대할 수 없는 문제점이 있다.On the other hand, in order to eliminate inflammation, it is called an anti-inflammatory agent that acts to remove inflammatory sources, reduce biological reactions, and symptoms. Substances used for anti-inflammatory purposes to date include flufenamic acid, ibuprofen, benzydamine, indomethacin, etc. as non-steroids, and prednisolone as a steroidal system , Dexamethasone, and the like. In addition, allantoin, azene, hydrocortisone, etc. are known to have anti-inflammatory effects, but these substances are limited in use due to safety issues on the skin, or the effect is insignificant, so the effect of substantially reducing inflammation cannot be expected. There is this.
또한, 피부의 최외각에 위치하고 있는 표피(epidermis)는 외부의 다양한 물리적, 화학적 및 기계적 자극에 대한 방어와 피부를 통한 체내 수분의 과도한 발산을 막는 보호 기능을 수행하고 있다. 이러한 보호 기능은 각질형성세포로 구성된 각질층이 정상적으로 형성되고 유지됨으로써 가능하다. 각질형성세포는 표피최하층(stratum basale)에서 지속적으로 증식하던 기저세포(basal cell)가 각질층(stratum corneum)으로 이동하면서, 단계적으로 형태 및 기능상의 변화를 거치며 형성된 세포이며, 일정 기간이 지나면 오래된 각질형성세포는 피부에서 탈락되고, 표피 최하층으로부터 올라온 새로운 각질형성세포가 그 기능을 대신하는 표피 분화(epidermis differentiation) 또는 각화(keratinization)의 과정을 반복하게 된다. 이러한 각화과정에서 각질형성세포는 천연보습인자(Natural Moisturizing Factor; NMF)와 세라마이드, 콜레스테롤 및 지방산과 같은 세포 간 지질을 생성하여, 각질층이 외부와의 차단층 역할을 하게 됨으로써 피부장벽(skin barrier)로서의 기능을 보유하게 된다.In addition, the epidermis located at the outermost part of the skin performs a protective function of protecting against various external physical, chemical, and mechanical stimuli and preventing excessive dissipation of moisture in the body through the skin. This protective function is possible when the stratum corneum composed of keratinocytes is normally formed and maintained. Keratinocytes are cells that are formed through phased morphological and functional changes as the basal cells that continuously proliferate in the stratum basale move to the stratum corneum. The forming cells are eliminated from the skin, and the process of epidermis differentiation or keratinization is repeated in which new keratinocytes raised from the lowermost layer of the epidermis take over their function. In this keratinization process, keratinocytes produce natural moisturizing factor (NMF) and intercellular lipids such as ceramide, cholesterol, and fatty acids, and the stratum corneum acts as a barrier to the outside, thereby creating a skin barrier. It will retain its function.
또한, 현대 사회의 주요 질환의 하나로 여겨지는 피부 건조증은 피부 장벽 기능 이상에 의해 야기되는 증상의 하나로, 최근, 환경 오염, 아파트, 고층 건물과 같은 건조한 환경의 증가, 사회적 스트레스의 증가, 우리 나라 특유의 과도한 목욕 문화, 피부 노화 등과 같은 여러 가지 요인에 의해 점점 더 증가하고 있으며, 증세가 심하여 치료를 필요로 하는 경우 또한 지속적으로 증가하고 있다.In addition, skin dryness, which is considered one of the major diseases in the modern society, is one of the symptoms caused by abnormal skin barrier function. Recently, environmental pollution, an increase in dry environments such as apartments and high-rise buildings, an increase in social stress, and uniqueness of Korea It is increasing more and more due to various factors such as excessive bathing culture, skin aging, etc., and cases in need of treatment due to severe symptoms are also continuously increasing.
최근 소아의 10%에서 발병하는 아토피성 피부염 역시 피부 건조증, 보다 근본적으로는 피부 장벽 기능의 이상을 주요 원인으로 하는 것으로 알려져 있다. 이러한 아토피성 피부염을 치료하기 위하여, 종래에는 피부 내 적절한 수분 유지에 중점을 두어 외부로부터 수분을 공급하거나 체내로부터의 수분 손실을 최소화하기 위한 연구가 많이 진행되어 왔으며, 실제로 수분 보유 능력이 있는 세라마이드(ceramide) 또는 그의 유도체와 같은 보습제가 개발되어 제약 또는 화장품 영역에서 많이 사용되고 있다.Recently, atopic dermatitis, which occurs in 10% of children, is also known to be a major cause of dry skin, more fundamentally, abnormal skin barrier function. In order to treat such atopic dermatitis, studies have been conducted to supply moisture from the outside or minimize moisture loss from the body by focusing on maintaining adequate moisture in the skin. ceramide) or a derivative thereof has been developed and is widely used in the pharmaceutical or cosmetic field.
그러나, 이와 같은 보습제의 사용은 그 대부분이 근본적인 치료이기보다는 일시적인 증상의 완화에 불과하여, 아토피성 피부염을 포함하는 피부 건조증 및 피부 장벽 기능 이상의 치료에 대한 충분한 효과를 나타내지 못하고 있다. 이에, 손상된 피부 장벽을 근원적으로 재생시켜주는 물질의 개발이 시급한 실정이다.However, the use of such a moisturizing agent is only a temporary relief of symptoms rather than a fundamental treatment, and has not exhibited a sufficient effect on the treatment of skin dryness and abnormal skin barrier function including atopic dermatitis. Accordingly, there is an urgent need to develop a substance that fundamentally regenerates the damaged skin barrier.
최근 들어, 각질 형성 세포에 존재하는 PPAR 알파(Peroxisome Proliferator Activated Receptor-alpha)가 그 리간드(ligand)와 결합하여 활성화되면, 각질 형성 세포의 분화를 촉진시켜 손상된 피부 장벽을 재구성하는 효과가 있다고 알려졌다. 실제로 공지된 PPAR 알파의 작용제(agonist)인 클로파이브레이트(Clofibrate)[비특허문헌 1] 또는 WY14643[비특허문헌 2] 등을 피부 장벽이 손상된 피부에 도포하는 경우, 각질 형성 세포의 분화가 촉진되고 피부 장벽의 회복이 촉진됨이 확인된 바 있다.Recently, when PPAR alpha (Peroxisome Proliferator Activated Receptor-alpha) present in keratinocytes is activated by binding to its ligand, it has been known that it has the effect of reorganizing the damaged skin barrier by promoting the differentiation of keratinocytes. When a known PPAR alpha agonist such as Clofibrate [Non-Patent Literature 1] or WY14643 [Non-Patent Literature 2] is applied to damaged skin, the differentiation of keratinocytes is promoted. It has been confirmed that the recovery of the skin barrier is accelerated.
또한, 희고 고운 피부를 갖고자 하는 것은 모든 사람의 한결 같은 소망이다. 사람의 피부 내 멜라닌(melanin)의 농도와 분포에 따라 유전적으로 결정되나, 태양 자외선이나 피로, 스트레스 등의 환경적 또는 생리적 조건에 의해서도 영향을 받는다. 멜라닌은 아미노산의 일종인 티로신(tyrosine)에 티로시나제(tyrosinase)라는 효소가 작용하여 도파(DOPA), 도파퀴논(dopaquinone)으로 바뀐 후, 비효소적인 산화반응을 거쳐 만들어진다. 이와 같이 멜라닌이 만들어지는 경로는 알려져 있으나, 티로시나제가 작용하는 이전 단계인 멜라닌 합성을 유도하는 메커니즘이 무엇인지에 대해서는 아직도 자세히 밝혀지지 않고 있다. Also, it is everyone's constant desire to have white and fair skin. It is genetically determined according to the concentration and distribution of melanin in human skin, but it is also affected by environmental or physiological conditions such as solar ultraviolet rays, fatigue, and stress. Melanin is made through a non-enzymatic oxidation reaction after an enzyme called tyrosinase acts on tyrosine, a kind of amino acid, and is converted into dopa and dopaquinone. As such, the pathway by which melanin is produced is known, but the mechanism that induces melanin synthesis, which is the previous step in which tyrosinase acts, is still not elucidated in detail.
또한, 피부 표면의 형태인 피부결은 미세한 선에 의해 형성된 3차원 미세구조를 특징으로 하며 연령별·부위별로 유의하게 다르다. 피부결은 선의 깊이에 따라 1차(약 20-100 μm), 2차(약 5-40 μm), 3차(약 0.5 μm) 라인으로 구분되며, 좋은 피부일수록 각 라인들이 그물형태의 네트워크구조를 이루며 선들이 만나서 생기는 다각형과 별 모양(star formation)이 뚜렷하다는 특징을 지니고 있다[비특허문헌 3].In addition, the skin texture, which is the shape of the skin surface, is characterized by a three-dimensional microstructure formed by fine lines and differs significantly by age and area. Skin texture is divided into 1st (about 20-100 μm), 2nd (about 5-40 μm), and 3rd (about 0.5 μm) lines depending on the depth of the line, and the better the skin, the more each line is a network structure It has a distinctive feature of polygonal and star formation formed when lines meet (Non-Patent Document 3).
그러나 나이가 들어감에 따라 또는 피부가 손상됨에 따라 촘촘하던 미세라인의 네트워크 구조가 무너져 미세 라인(2차, 3차 등)은 사라지고 1차 라인은 더욱 깊어져 주름이 생성되는 것으로 알려져 있다[비특허문헌 4,5]. 즉, 피부가 노화됨에 따라 나타나는 대표적인 징후인 주름은 이미 장기간에 걸쳐 일어나는 미세한 변화의 축적이다.However, it is known that with age or as the skin is damaged, the network structure of the fine lines collapses, the fine lines (secondary, third, etc.) disappear, and the first lines become deeper and wrinkles are created [non-patented Documents 4,5]. In other words, wrinkles, a typical symptom of skin aging, are the accumulation of subtle changes that occur over a long period of time.
발생학적으로 사람 피부의 모든 구성성분은 외배엽이나 중배엽에서 유래되는 것으로 알려져 있다. 표피, 모낭, 피지선 및 땀샘선 등은 외배엽에서 기원하며, 멜라닌 세포, 신경 및 특수 감각 수용체는 신경외배엽에서 유래된다. 발생학적 시기에 따라 배아의 줄기세포는 분화를 거듭하여 각각의 조직 기능에 맞는 특성의 세포가 되고, 성체가 된 후에도 일정수의 줄기세포는 조직에 남게 되는데 피부에서는 주로 두 곳에 줄기세포들이 존재한다. 첫째는 모낭(hair follicle)에 존재한다. 이곳은 세포분화가 일어나기 전의 세포로 표피의 재생과 관련해 중요한 역할을 담당하는 것으로 알려져 있으며, 털의 재생과 성장에도 중요한 역할을 수행하고 있다. 둘째는 표피의 기저층(the basal layer of epidermis)이다. 이곳에 자리하고 있는 줄기세포는 표피는 물론 진피층의 섬유아세포까지 관장하여 피부 건강을 지키는 중요한 역할을 수행하고 있음이 밝혀졌다. 이곳의 줄기세포는 상대적으로 양이 많고 쉽게 얻을 수 있다는 장점이 있어 피부줄기세포 연구에 널리 사용되고 있다. 피부는 지속적으로 재생(renew)되며, 피부의 상피에 존재하는 줄기세포 즉, 피부의 상피줄기세포(epidermal stem cells)는 상처 후 상피의 복구에 관여한다[비특허문헌 6]. 상기 피부의 상피줄기세포는 피부줄기세포(skin stem cells)로도 칭해지며, 상기 피부줄기세포를 활성화시킬 경우, 외상 등의 피부상처를 치료하거나 상처 치료를 촉진할 수 있으며 피부의 주름완화 또한 기대할 수 있다. 피부줄기세포의 지표로는 인테그린β1(integrin β1) 및 인테그린 α6(integrin α6)이 사용되고 있고, 상피 형태 형성 및 분화에 필요한 피부줄기세포의 유지는 p63 단백질에 의해 조절된다고 보고되고 있다. It is known that all constituents of human skin are derived from ectoderm or mesoderm. The epidermis, hair follicles, sebaceous glands, and sweat glands originate from the ectoderm, and melanocytes, nerves, and special sensory receptors are derived from the neuroectoderm. Depending on the embryonic period, embryonic stem cells continue to differentiate into cells with characteristics suitable for each tissue function, and even after adulthood, a certain number of stem cells remain in the tissue. In the skin, stem cells mainly exist in two places. . The first is in the hair follicle. These cells are known to play an important role in the regeneration of the epidermis as cells before cell differentiation occur, and play an important role in hair regeneration and growth. The second is the basal layer of epidermis. It has been found that the stem cells located here play an important role in protecting skin health by managing not only the epidermis but also the fibroblasts of the dermal layer. Stem cells here are widely used in skin stem cell research because they are relatively large in quantity and can be easily obtained. The skin is continuously renewed, and stem cells present in the epithelium of the skin, that is, epithelial stem cells of the skin, are involved in the repair of the epithelium after a wound [Non-Patent Document 6]. The epithelial stem cells of the skin are also referred to as skin stem cells, and when the skin stem cells are activated, skin wounds such as trauma can be treated or wound healing can be promoted, and wrinkle relief of the skin can also be expected. have. Integrin β1 and integrin α6 are used as indicators of skin stem cells, and it is reported that the maintenance of skin stem cells required for epithelial morphogenesis and differentiation is regulated by the p63 protein.
피부줄기세포는 피부의 건강과 생리학적 및 생화학적인 항상성을 유지하는데 중요한 역할을 수행한다. 피부에 존재하는 줄기세포도 노화의 영향으로 인하여 기능에 이상이 발생하게 되고, 이에 따라 피부의 항상성이 깨지면서 여러 가지 문제가 발생된다. 따라서 이러한 줄기세포의 활성을 통하여 피부노화의 여러 현상을 개선할 수 있을 것이다[비특허문헌 7].Skin stem cells play an important role in maintaining skin health and physiological and biochemical homeostasis. Stem cells present in the skin also have functional abnormalities due to the effect of aging, and accordingly, various problems occur as the homeostasis of the skin is broken. Therefore, various phenomena of skin aging may be improved through the activation of these stem cells [Non-Patent Document 7].
또한, 생체에 안전하고, 유효성분이 안정하며, 무엇보다도 기존의 항염증, 아토피 개선, 피부 보습 및 피부결 개선 효과가 있는 물질보다 효과가 우수한 항염증, 아토피 개선, 피부 보습 및 피부결 개선 활성을 지닌 성분의 개발이 절실히 요망되고 있다.In addition, it is safe for the living body and has a stable active ingredient. Above all, it has excellent anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement activities, which are superior to those of existing anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement substances. There is an urgent need for the development of ingredients.
한편, 삼칠은 다년생 초본으로 오가과 식물 Panax pseudoginseng, P.notoginseng의 뿌리로서 그 성상은 원추형으로 길이 1-6cm, 지름 1-4cm이고, 주위에는 작은 혹 모양의 돌기가 있으며, 바깥면은 회갈색-회황색이며 세로주름과 가는 뿌리가 붙었던 자국이 있고, 절단면은 회록색-황록색 및 회백색으로 방사상의 무늬가 나타나며 질은 무겁고 단단하다. 동의보감에 의하면 각종 혈증, 질타종통, 심교통의 치료에 사용되어 왔으며, 심혈관계질환, 면역증강작용, 세포보호효과가 있다고 알려져 있다. 기존의 첨과 성분 동정 연구에 의하면 β-carotene,cry ptoxanthine, meloside A, L saponin, trilinolein 등의 화합물이 주요성분으로 보고되어 있다.On the other hand, Samchil is a perennial herb and is the root of the Oga family Panax pseudoginseng, P.notoginseng. Its appearance is conical, 1-6cm long, 1-4cm in diameter, has small hump-shaped protrusions around it, and the outer surface is grayish brown-grey. It is yellow and has vertical wrinkles and marks with thin roots, and the cut surface is gray-green-yellow-green and gray-white with radial patterns, and the quality is heavy and hard. According to Donguibogam, it has been used to treat various types of blood vessels, vaginal pain, and cardiovascular disease, and is known to have cardiovascular disease, immunity enhancement, and cell protection effects. According to existing studies on the identification of additives, compounds such as β-carotene, cry ptoxanthine, meloside A, L saponin, and trilinolein have been reported as major components.
그러나, 삼칠의 피부에 대한 기전에 대해서는 아직까지 알려져 있지 않으며, 이에 대한 연구도 전무한 상태이다.However, the mechanism of Samchil's skin is not yet known, and there is no research on this.
이에, 본 발명자들은 삼칠 추출물이 피부줄기세포의 증식을 촉진하여 피부 재생을 촉진시키고, NO 생성을 억제하여 항염증 효과가 있으며, PPAR 알파의 활성도 우수하여 아토피 개선 효과가 있으며, 필라그린 발현 증가로 인한 피부 보습 개선 효과를 나타내며, 피부 밝기 개선으로 인한 피부결 개선 효과와 더불어, 피부줄기세포의 증식을 촉진하고, 줄기세포성 유지 효과를 나타내고 있어 줄기세포 활성 촉진 효과를 확인함으로써 본 발명을 완성하게 되었다.Accordingly, the present inventors argued that the extract of Samchil promotes the proliferation of skin stem cells, promotes skin regeneration, suppresses NO production, has an anti-inflammatory effect, and has an excellent atopy improvement effect due to the excellent activity of PPAR alpha, and increases filaggrin expression. The present invention is completed by confirming the effect of promoting skin moisturization due to the effect of improving skin moisturization, promoting the proliferation of skin stem cells and maintaining stem cell properties, along with the effect of improving skin texture due to the improvement of skin brightness. Became.
따라서, 본 발명의 목적은 삼칠 추출물을 유효성분으로 포함하는 항염증, 아토피 개선, 피부 보습 및 피부결 개선용 조성물을 제공하는데 있다.Accordingly, an object of the present invention is to provide a composition for improving anti-inflammatory, atopy, skin moisturizing and skin texture, comprising a Samchil extract as an active ingredient.
또한, 본 발명의 다른 목적은 하기 삼칠 추출물을 유효성분으로 포함하는 줄기세포 활성 촉진용 조성물을 제공하는데 있다.In addition, another object of the present invention is to provide a composition for promoting stem cell activity comprising the following Samchil extract as an active ingredient.
상기 과제를 해결하기 위한 수단으로서, 본 발명은 의약, 화장료 또는 식품 제조를 위한, 삼칠 추출물을 유효성분으로 포함하는 항염증, 아토피 개선, 피부 보습 및 피부결 개선용 조성물을 제공한다.As a means for solving the above problems, the present invention provides a composition for anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement, comprising a Samchil extract as an active ingredient for the manufacture of medicines, cosmetics or food.
상기 과제를 해결하기 위한 다른 수단으로서, 본 발명은 화장료 제형 제조를 위한, 삼칠 추출물을 유효성분으로 포함하는 줄기세포 활성 촉진용 조성물을 제공한다.As another means for solving the above problems, the present invention provides a composition for promoting stem cell activity, comprising a Samchil extract as an active ingredient for preparing a cosmetic formulation.
본 발명에 따른 삼칠 추출물은 피부줄기세포의 증식을 촉진하여 피부 재생을 촉진시키고, NO 생성을 억제하여 항염증 효과가 있으며, PPAR 알파의 활성도 우수하여 아토피 개선 효과가 있으며, 필라그린 발현 증가로 인한 피부 보습 개선 효과와 더불어, 피부 밝기 개선으로 인한 피부결 개선 효과를 나타냄으로써, 의약, 화장료 또는 식품 제조에 사용할 수 있다. Samchil extract according to the present invention promotes skin regeneration by promoting the proliferation of skin stem cells, has an anti-inflammatory effect by inhibiting NO production, has excellent atopy improvement effect due to excellent PPAR alpha activity, and has an effect of improving atopy due to increased filaggrin expression. In addition to the skin moisturizing effect, it can be used in the manufacture of medicines, cosmetics, or foods by showing the effect of improving skin texture due to the improvement of skin brightness.
또한, 삼칠 추출물은 피부줄기세포의 증식을 촉진하고, 줄기세포성 유지 효과를 나타내고 있어 줄기세포 활성 촉진용 화장료 제형 제조에 사용할 수 있다. In addition, Samchil extract promotes the proliferation of skin stem cells and exhibits the effect of maintaining stem cell properties, and thus can be used to prepare a cosmetic formulation for promoting stem cell activity.
이하, 본 발명의 구성을 구체적으로 설명한다.Hereinafter, the configuration of the present invention will be described in detail.
피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 성분이 실제 피부에 적용 시 우수한 효과를 발휘하기 위해서는 저농도에서 고활성의 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 활성을 나타내고, 피부를 투과하여 흡수되는 능력이 우수하고, 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 효과를 나타내기에 충분한 시간 동안 머무를 수 있도록 휘발성이 낮고, 조성물이나 피부 상에서 활성 성분이 안정하게 유지되고, 의약, 화장료 또는 식품 등으로의 제조가 용이하며, 또한 피부에 안전한 것이 바람직하다. 그러나, 공지의 성분 중 상기 특성을 모두 만족시키는 성분은 흔치 않다. 예를 들어, 몇몇 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 성분들은 시험관 내 실험 시 저농도에서도 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 활성은 우수하나, 피부를 투과하여 흡수되는 능력이 떨어져 실제 피부에 적용하기엔 어렵다. 또 다른 활성 성분들은 친수성이 낮아 의약이나 화장품, 식품으로 제형화가 어렵다. 또한, 몇몇 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 성분들은 열, 광, 또는 산소에 노출되었을 때 상기 활성 성분이 분해되거나 다른 화합물로 변형되어 피부에 적용하기 전에 이미 효과가 사라지는 경우도 있다. Skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement ingredients are highly active at low concentrations in order to exert excellent effects when applied to the skin, anti-inflammatory, atopic improvement, skin moisturizing and skin texture improvement activities. It has low volatility so that it can stay for a sufficient time to exhibit skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing, and skin texture improvement effects, and the active ingredient is stable in the composition or on the skin. It is preferably maintained in a manner that is easy to manufacture as a medicine, cosmetic or food, and is safe for the skin. However, among known components, components that satisfy all of the above properties are not common. For example, some skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement ingredients are excellent in skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement activity even at low concentrations when tested in vitro. It is difficult to apply to actual skin due to its poor ability to penetrate and absorb. Other active ingredients have low hydrophilic properties, making it difficult to formulate into medicine, cosmetics, or food. In addition, some skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement ingredients are decomposed or transformed into other compounds when exposed to heat, light, or oxygen, and their effects already disappear before being applied to the skin. There are cases.
하기 실시예에서 확인할 수 있는 바와 같이, 삼칠 추출물은 저농도에서 월등히 우수한 피부 줄기세포의 증식 촉진 효과, 항염증 효과, PPAR 알파 활성 효과, 필라그린 발현 효과, 피부 밝기 개선 효과를 나타내므로 피부 재생. 항염증, 아토피 개선, 피부 보습 및 피부결 개선을 위한 의약, 화장료 또는 식품 조성물의 유효성분으로 사용할 수 있다.As can be seen in the following Examples, Samchil extract exhibits superior skin stem cell proliferation promoting effect, anti-inflammatory effect, PPAR alpha activity effect, filaggrin expression effect, and skin brightness improvement effect at low concentration, thus regenerating skin. It can be used as an active ingredient in medicine, cosmetics or food compositions for anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement.
따라서, 본 발명은 삼칠 추출물을 유효성분으로 포함하는 피부 재생. 항염증, 아토피 개선, 피부 보습 및 피부결 개선용 조성물을 제공한다.Therefore, the present invention regenerates the skin containing the Samchil extract as an active ingredient. It provides a composition for anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement.
본 발명에서 삼칠은 오가과 식물 Panax pseudoginseng, P.notoginseng의 뿌리로서, 일명 전칠(田七)이라고도 한다In the present invention, Samchil is the root of the Oga family plant Panax pseudoginseng, P.notoginseng, and is also referred to as Jeonchil (田七).
상기 삼칠 추출물은 당업계에 공지된 방법에 의해 추출될 수 있으며, 그 방법은 특별히 한정되지 않는다. 또는, 시판되고 있는 추출물을 이용할 수 있다.The Samchil extract may be extracted by a method known in the art, and the method is not particularly limited. Alternatively, a commercially available extract can be used.
바람직하기로는 상기 삼칠 추출물은 삼칠을 물 및/또는 유기용매로 추출하여 수득한 추출물을 사용할 수 있으며, 상기 유기용매는 극성 유기용매, 비극성 유기용매 또는 이들의 혼합용매일 수 있다. 상기 극성 유기용매는 탄소수 1 내지 5의 저급 알코올, 에틸아세테이트 또는 아세톤일 수 있으며, 비극성 유기용매는 에테르, 클로로포름, 벤젠, 헥산 또는 디클로로메탄일 수 있다. 예를 들어, 상기 탄소수 1 내지 5의 저급 알코올은 메탄올, 에탄올, 프로판올, 부탄올 또는 이소프로판올일 수 있다. Preferably, the Samchil extract may be an extract obtained by extracting Samchil with water and/or an organic solvent, and the organic solvent may be a polar organic solvent, a non-polar organic solvent, or a mixed solvent thereof. The polar organic solvent may be a lower alcohol having 1 to 5 carbon atoms, ethyl acetate or acetone, and the non-polar organic solvent may be ether, chloroform, benzene, hexane, or dichloromethane. For example, the lower alcohol having 1 to 5 carbon atoms may be methanol, ethanol, propanol, butanol or isopropanol.
한 구체예에서 상기 삼칠 추출물은 전술한 추출용매를 이용하여 추출된 1차 추출물을 극성이 다른 추출용매를 이용하여 분획한 분획물을 포함할 수 있다. 예를 들어, 삼칠 추출물은 탄소수 1 내지 5의 알코올로 추출한 후, 에테르, 벤젠, 헥산 등의 극성이 다른 용매로 다시 분획한 분획물 일 수 있다. 상기 분획 시 용매는 2종 이상 사용할 수 있으며, 용매의 극성에 따라 순차적으로 사용하거나 혼합하여 사용하여, 각 용매 추출물을 제조할 수 있다. In one embodiment, the Samchil extract may include a fraction obtained by fractionating the primary extract extracted using the extraction solvent described above using an extraction solvent having a different polarity. For example, the Samchil extract may be a fraction that is extracted with an alcohol having 1 to 5 carbon atoms and then fractionated again with a solvent having a different polarity such as ether, benzene, or hexane. In the fractionation, two or more solvents may be used, and each solvent extract may be prepared by sequentially using or mixing them according to the polarity of the solvent.
본 발명에서, 상기 제조된 추출물 또는 상기 분획과정을 수행하여 수득한 분획물에 대해 여과하거나 농축 또는 건조과정을 수행하여 용매를 제거할 수 있으며, 상기 여과, 농축 및 건조를 모두 수행할 수 있다. 구체적으로 상기 여과는 여과지를 이용하거나 감압여과기를 이용할 수 있고, 농축은 감압 농축기 등을 이용하여 감압 농축할 수 있으며, 건조는 동결건조법을 수행할 수 있다. In the present invention, the prepared extract or the fraction obtained by performing the fractionation process may be filtered, concentrated or dried to remove the solvent, and the filtration, concentration, and drying may all be performed. Specifically, the filtration may be performed using a filter paper or a reduced pressure filter, the concentration may be concentrated under reduced pressure using a reduced pressure concentrator or the like, and the drying may be performed by a freeze-drying method.
또한, 상기 제조된 추출물 또는 상기 분획과정을 수행하여 수득한 분획물에 대해 실리카겔 컬럼 크로마토그래피(silica gel column chromatography), 박층 크로마토그래피(thin layer chromatography) 또는 고성능 액체 크로마토그래피(high performance liquid chromatography) 등의 다양한 크로마토그래피를 이용하여 정제함으로써 추가로 정제된 분획을 얻을 수 있다. In addition, silica gel column chromatography, thin layer chromatography, or high performance liquid chromatography for the prepared extract or the fraction obtained by performing the fractionation process. Further purified fractions can be obtained by purification using various chromatography.
본 발명의 조성물은 의약 제형 제조를 위해 사용할 수 있다.The composition of the present invention can be used to prepare a pharmaceutical formulation.
상기 의약 제형은 오일 또는 수성 매질 중의 용액, 현탁액 또는 유화액의 형태이거나, 엑스제, 분말제, 과립제, 정제 또는 캅셀제의 형태일 수 있다.The pharmaceutical formulation may be in the form of a solution, suspension or emulsion in an oil or aqueous medium, or in the form of an extract, powder, granule, tablet or capsule.
또한, 상기 조성물은 추가로 동일 또는 유사한 기능을 나타내는 유효성분을 1종 이상 함유할 수 있다. 예컨대, 공지의 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 성분을 포함할 수 있을 것이다. 추가적인 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 성분을 포함하게 되면 본 발명의 조성물의 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 효과는 더욱 증진될 수 있을 것이다. 상기 성분 추가 시에는 복합 사용에 따른 피부 안전성, 제형화의 용이성, 유효성분들의 안정성을 고려할 수 있다. 본 발명의 한 구체예에서, 상기 조성물은 당업계에 공지된 피부 재생 성분으로서, 레티노산, TGF, 동물 태반 유래의 단백질, 베튤린산 및 클로렐라 추출물, 당업계에 공지된 항산화 성분으로서, 토코페롤, 셀레늄, 비타민 C 및 페놀성 화합물, 당업계에 공지된 미백 성분으로서, 코지산(Kojic acid), 알부틴(Arbutin) 등과 같은 티로시나제 효소활성을 억제하는 물질, 하이드로퀴논(Hydroquinone), 비타민-C(L-Ascorbic acid) 및 이들의 유도체와 각종 식물 추출물로 구성되는 군으로부터 선택되는 1종 또는 2종 이상의 성분을 추가로 포함할 수 있다. 추가의 성분은 전체 조성물 중량에 대하여 0.0001 중량% 내지 10 중량%로 포함될 수 있을 것이며, 상기 함량 범위는 피부 안전성, 상기 삼칠 추출물의 제형화 시의 용이성 등의 요건에 따라 조절될 수 있을 것이다.In addition, the composition may further contain one or more active ingredients exhibiting the same or similar functions. For example, known skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improving ingredients may be included. When additional skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement ingredients are included, the skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement effects of the composition of the present invention may be further enhanced. When the above ingredients are added, skin safety, ease of formulation, and stability of active ingredients can be considered in combination with use. In one embodiment of the present invention, the composition is a skin regeneration component known in the art, retinoic acid, TGF, protein derived from animal placenta, betulinic acid and chlorella extract, as an antioxidant component known in the art, tocopherol, selenium , Vitamin C and phenolic compounds, as whitening components known in the art, substances that inhibit tyrosinase enzyme activity such as Kojic acid, arbutin, hydroquinone, vitamin-C (L- Ascorbic acid) and derivatives thereof, and one or more components selected from the group consisting of various plant extracts may be further included. Additional ingredients may be included in an amount of 0.0001% to 10% by weight based on the total weight of the composition, and the content range may be adjusted according to requirements such as skin safety and ease of formulation of the Samchil extract.
또한, 본 발명의 조성물은 약학적으로 허용 가능한 담체를 더 포함할 수 있다.In addition, the composition of the present invention may further include a pharmaceutically acceptable carrier.
약학적으로 허용 가능한 담체는 완충액, 주사용 멸균수, 일반 식염수 또는 인산염 완충 식염수, 슈크로스, 히스티딘, 염 및 폴리솔베이트 등과 같은 여러 성분을 함유할 수 있다.The pharmaceutically acceptable carrier may contain various components such as a buffer solution, sterile water for injection, general saline or phosphate buffered saline, sucrose, histidine, salt, and polysorbate.
본 발명의 조성물은 경구 또는 비경구로 투여할 수 있으며, 일반 약학 제제의 형태, 예를 들어, 임상 투여 시 경구 및 비경구의 여러 가지 제형으로 투여될 수 있는데, 제제화할 경우에는 보통 사용하는 충진제, 증량제, 결합제, 습윤제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용하여 조제될 수 있다.The composition of the present invention may be administered orally or parenterally, and may be administered in the form of a general pharmaceutical preparation, for example, in various oral and parenteral dosage forms during clinical administration. , A binder, a wetting agent, a disintegrant, and a diluent or excipient such as a surfactant.
경구 투여를 위한 고형제제에는 정제, 환제, 산제, 과립제, 캡슐제 등이 포함되며, 이러한 고형제제는 본 발명의 의약 조성물에 적어도 하나 이상의 부형제 예를 들면, 전분, 칼슘 카보네이트(Calcium carbonate), 수크로스(Sucrose) 또는 락토오스(Lactose), 젤라틴 등을 섞어 조제될 수 있다.Solid preparations for oral administration include tablets, pills, powders, granules, capsules, and the like, and these solid preparations include at least one excipient in the pharmaceutical composition of the present invention, such as starch, calcium carbonate, and water. It can be prepared by mixing sucrose or lactose, gelatin, and the like.
단순한 부형제 이외에 마그네슘 스티레이트 탈크 같은 윤활제들도 사용된다. 경구를 위한 액상 제제로는 현탁제, 내용액제, 유제, 시럽제 등이 해당되는데 흔히 사용되는 단순희석제인 물, 리퀴드 파라핀 이외에 여러가지 부형제, 예를 들면 습윤제, 감미제, 방향제, 보존제 등이 포함될 수 있다.In addition to simple excipients, lubricants such as magnesium stearate and talc are also used. Liquid preparations for oral use include suspensions, liquid solutions, emulsions, syrups, etc., and various excipients, such as wetting agents, sweeteners, fragrances, and preservatives, in addition to water and liquid paraffin, which are commonly used simple diluents, may be included.
비경구 투여를 위한 제제에는 멸균된 수용액, 비수성용제, 현탁제, 유제, 동결건조제제, 좌제가 포함된다. 비수성용제, 현탁용제로는 프로필렌 글리콜(Propylene glycol), 폴리에틸렌 글리콜, 올리브 오일과 같은 식물성 기름, 에틸올레이트와 같은 주사 가능한 에스테르 등이 사용될 수 있다. 좌제의 기제로는 위텝솔(witepsol), 마크로골, 트윈(tween) 61, 카카오지, 라우린지, 글리세로제라틴 등이 사용될 수 있다.Preparations for parenteral administration include sterilized aqueous solutions, non-aqueous solutions, suspensions, emulsions, lyophilized preparations, and suppositories. As the non-aqueous solvent and the suspension solvent, propylene glycol, polyethylene glycol, vegetable oil such as olive oil, and injectable ester such as ethyl oleate may be used. As a base for suppositories, witepsol, macrogol, tween 61, cacao butter, laurin paper, glycerogelatin, and the like may be used.
본 발명에 있어서, '피부 재생 효과'라 함은 피부줄기세포의 활성이 촉진 됨에 따라, 피부 외부 및 내부 원인에 의한 손상에 대하여 피부 조직이 회복되는 것을 말한다. 이때, 상기 외부 원인에 의한 손상은 자외선, 외부 오염 물질, 창상 또는 외상 등을 들 수 있으며, 상기 내부 원인에 의한 손상은 스트레스 등을 들 수 있다.In the present invention, the term'skin regeneration effect' refers to the recovery of skin tissue against damage caused by external and internal causes as the activity of skin stem cells is promoted. In this case, the damage caused by the external cause may include ultraviolet rays, external pollutants, wounds or trauma, and the damage caused by the internal cause may include stress.
본 발명에 있어서, '항염증 효과'라 함은 염증을 억제하는 것을 말하며, 상기 염증은 어떤 자극에 대한 생체조직의 방어반응의 하나로, 조직 변질, 순환 장애와 삼출, 조직 증식의 세가지를 병발하는 복잡한 병변을 말한다. 보다 구체적으로 염증은 선천성 면역의 일부이며 다른 동물에서처럼 인간의 선천성 면역은 병원체에 특이적으로 존재하는 세포 표면의 패턴을 인식한다. 식세포는 그런 표면을 가진 세포를 비자기로 인식하고 병원체를 공격한다. 만일 병원균이 신체의 물리적 장벽을 깨고 들어온다면 염증반응이 일어난다. 염증반응은 상처부위에 침입한 미생물들에 대한 적대 환경을 만드는 비특이적인 방어작용이다. 염증반응에서, 상처가 나거나 외부 감염체가 체내로 들어왔을 때, 초기단계 면역반응을 맡고 있는 백혈구들이 몰려들어 사이토카인을 발현한다. 따라서 세포 내 사이토카인의 발현양이 염증반응 활성화의 지표가 된다. 염증과 관련된 피부질환의 예로는 아토피 피부염, 건선, 방사선, 화학물질, 화상 등에 의해 촉발되는 홍반성 질환, 산 화상, 수포성 피부병, 태선 모양 종류 질환, 알레르기에 기한 가려움증, 지루성 습진, 장미 여드름, 심상성 천포창, 다형 삼출성 홍반, 결절 홍반, 귀두염, 음문염, 원형 탈모증과 같은 염증성 모발 손실, 피부 T-세포 림프종 등이 있으나 이에 제한되는 것은 아니다.In the present invention, the term'anti-inflammatory effect' refers to suppressing inflammation, and the inflammation is one of the defense responses of living tissues against a certain stimulus, which causes tissue deterioration, circulatory disorders and effusion, and tissue proliferation. Refers to a complex lesion. More specifically, inflammation is part of innate immunity, and, as in other animals, innate immunity in humans recognizes patterns on the cell surface that are specific to pathogens. Phagocytes recognize cells with such surfaces as non-magnetic and attack pathogens. If pathogens break through the body's physical barriers, an inflammatory reaction occurs. The inflammatory reaction is a non-specific defense action that creates a hostile environment for microorganisms invading the wound. In the inflammatory reaction, when a wound or an external infectious agent enters the body, the white blood cells responsible for the initial stage immune response flock to express cytokines. Therefore, the amount of expression of cytokines in cells becomes an indicator of activation of the inflammatory response. Examples of skin diseases related to inflammation include atopic dermatitis, psoriasis, erythematous disease triggered by radiation, chemicals, burns, acid burns, bullous skin disease, lichen shape type disease, itching due to allergies, seborrheic eczema, rose acne, Pemphigus vulgaris, polymorphic exudative erythema, nodular erythema, balanitis, vulvitis, inflammatory hair loss such as alopecia areata, cutaneous T-cell lymphoma, and the like, but are not limited thereto.
본 발명에 있어서, '아토피 개선 효과'라 함은 아토피, 피부건조증과 같은 피부질환 예방 및 치료 효과를 나타내는 것으로, 아토피 증상을 억제 또는 저해하거나, 완화시키는 것을 말한다. In the present invention, the term'atopy improvement effect' refers to a prevention and treatment effect of skin diseases such as atopy and dry skin, and refers to suppressing, inhibiting, or alleviating atopic symptoms.
본 발명에 있어서, '보습 효과'라 함은 피부의 수분이 감소되는 것을 저해 또는 억제하거나 피부의 수분 함유량을 증가시켜 피부 표면을 매끄럽게 하며, 윤기를 부여하는 것을 말한다.In the present invention, the term'moisturizing effect' refers to inhibiting or inhibiting the reduction of moisture in the skin or increasing the moisture content of the skin to smooth the skin surface and impart gloss.
본 발명에 있어서, '피부결 개선 효과'라 함은 노화, 스트레스 등의 영향으로 피부 표면이 거칠어지는 것을 억제 또는 저해함으로써 피부 표면을 매끄럽게 하고, 광택을 부여하며, 피부 톤을 밝게 개선하는 것을 말한다.In the present invention, the term'skin texture improvement effect' refers to smoothing the skin surface, imparting gloss, and brightening the skin tone by inhibiting or inhibiting the roughening of the skin surface due to the effects of aging and stress. .
본 발명에 있어서, '유효량'이라 함은 손상된 피부의 재생을 촉진하거나, 염증을 억제하거나, 아토피와 같은 피부건조증을 개선하거나, 보습 효과나, 피부결을 개선할 수 있는 추출물의 양을 의미한다. 본 발명의 조성물이 유효량의 상기 삼칠 추출물을 포함할 때 바람직한 피부 재생 효과, 항염증 효과, 아토피 개선 효과, 보습 효과 및 피부결 개선 효과를 제공할 수 있다. 본 발명의 조성물에 포함되는 상기 삼칠 추출물의 유효량은 조성물이 제품화되는 형태, 상기 화합물이 피부에 적용되는 방법 및 피부에 머무르는 시간 등에 따라 달라질 것이다. 예컨대, 상기 조성물이 약학 제형으로 제품화되는 경우에는 일상적으로 피부에 적용하게 되는 화장품으로 제품화되는 경우에 비해 높은 농도로 상기 삼칠 추출물을 포함할 수 있을 것이다. 따라서, 일일 투여량은 상기 삼칠 추출물의 양을 기준으로 0.1 내지 100 ㎎/㎏이고, 바람직하게는 30 내지 80 ㎎/㎏이고, 더욱 바람직하게는 50 내지 60 mg/kg이며, 하루 1 ∼ 6 회 투여될 수 있다. In the present invention, the term'effective amount' means an amount of an extract capable of promoting regeneration of damaged skin, suppressing inflammation, improving dry skin such as atopy, moisturizing effect, or improving skin texture. . When the composition of the present invention contains an effective amount of the Samchil extract, it can provide a desirable skin regeneration effect, anti-inflammatory effect, atopy improvement effect, moisturizing effect, and skin texture improvement effect. The effective amount of the Samchil extract contained in the composition of the present invention will vary depending on the form in which the composition is commercialized, the method in which the compound is applied to the skin, and the time it stays on the skin. For example, when the composition is commercialized as a pharmaceutical formulation, it may contain the Samchil extract at a higher concentration than when it is commercialized as a cosmetic product that is routinely applied to the skin. Therefore, the daily dose is 0.1 to 100 mg/kg, preferably 30 to 80 mg/kg, more preferably 50 to 60 mg/kg, and 1 to 6 times a day based on the amount of the Samchil extract. Can be administered.
본 발명의 조성물은 단독으로, 또는 수술, 방사선 치료, 호르몬 치료, 화학 치료 및 생물학적 반응조절제를 사용하는 방법들과 병용하여 사용할 수 있다.The composition of the present invention may be used alone or in combination with surgery, radiation therapy, hormone therapy, chemotherapy, and methods using biological response modifiers.
본 발명의 의약 제형은 피부 외용제 제형을 포함할 수 있다. The pharmaceutical formulation of the present invention may include a formulation for external application for skin.
상기 삼칠 추출물을 피부외용제로 사용하는 경우, 추가로 지방 물질, 유기 용매, 용해제, 농축제 및 겔화제, 연화제, 항산화제, 현탁화제, 안정화제, 발포제(foaming agent), 방향제, 계면활성제, 물, 이온형 또는 비이온형 유화제, 충전제, 금속이온봉쇄제 및 킬레이트화제, 보존제, 비타민, 차단제, 습윤화제, 필수 오일, 염료, 안료, 친수성 또는 친유성 활성제, 지질 소낭 또는 피부용 외용제에 통상적으로 사용되는 임의의 다른 성분과 같은 피부 과학 분야에서 통상적으로 사용되는 보조제를 함유할 수 있다. 또한 상기 성분들은 피부 과학 분야에서 일반적으로 사용되는 양으로 도입될 수 있다. When using the Samchil extract as an external preparation for skin, additionally fatty substances, organic solvents, solubilizers, thickening and gelling agents, emollients, antioxidants, suspending agents, stabilizers, foaming agents, fragrances, surfactants, water , Ionic or nonionic emulsifiers, fillers, sequestering and chelating agents, preservatives, vitamins, blockers, wetting agents, essential oils, dyes, pigments, hydrophilic or lipophilic activators, lipid vesicles or external preparations for skin. It may contain adjuvants commonly used in the field of dermatology, such as any other ingredients that are made. In addition, the above ingredients may be introduced in an amount generally used in the field of dermatology.
상기 삼칠 추출물이 피부 외용제 제형으로 제공될 경우, 이에 제한되는 것은 아니나, 연고, 패취, 겔, 크림 또는 분무제와 같은 제형을 가질 수 있다.When the Samchil extract is provided in a formulation for external application for skin, it is not limited thereto, but may have a formulation such as an ointment, patch, gel, cream, or spray.
또한, 본 발명의 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선용 조성물은 화장료 제형 제조를 위해 사용될 수 있다.In addition, the composition for skin regeneration, anti-inflammatory, atopy improvement, skin moisturization, and skin texture improvement of the present invention may be used for preparing a cosmetic formulation.
상기 화장료 제형은 일반적인 유화 제형 및 가용화 제형의 형태일 수 있다. 예컨대, 유연 화장수 또는 영양 화장수 등과 같은 화장수, 훼이셜 로션, 바디로션 등과 같은 유액, 영양 크림, 수분 크림, 아이 크림 등과 같은 크림, 에센스, 화장연고, 스프레이, 젤, 팩, 선 스크린, 메이크업 베이스, 액체 타입, 고체 타입 또는 스프레이 타입 등의 파운데이션, 파우더, 클렌징 크림, 클렌징 로션, 클렌징 오일과 같은 메이크업 제거제, 클렌징 폼, 비누, 바디 워쉬 등과 같은 세정제 등의 제형을 가질 수 있다. The cosmetic formulation may be in the form of a general emulsifying formulation and a solubilizing formulation. For example, a lotion such as a flexible lotion or a nutrient lotion, an emulsion such as a facial lotion, a body lotion, a cream such as a nutritional cream, a moisture cream, an eye cream, an essence, a cosmetic ointment, a spray, a gel, a pack, a sunscreen, a makeup base, a liquid It may have a formulation such as a foundation such as a type, a solid type, or a spray type, a powder, a cleansing cream, a cleansing lotion, a makeup remover such as a cleansing oil, a cleansing foam, a soap, a body wash, and the like.
또한, 상기 화장품은 삼칠 추출물에 추가로 지방 물질, 유기 용매, 용해제, 농축제 및 겔화제, 연화제, 항산화제, 현탁화제, 안정화제, 발포제(foaming agent), 방향제, 계면활성제, 물, 이온형 또는 비이온형 유화제, 충전제, 금속이온봉쇄제 및 킬레이트화제, 보존제, 비타민, 차단제, 습윤화제, 필수 오일, 염료, 안료, 친수성 또는 친유성 활성제, 지질 소낭 또는 화장품에 통상적으로 사용되는 임의의 다른 성분과 같은 화장품학 분야에서 통상적으로 사용되는 보조제를 함유할 수 있다.In addition, the cosmetics are fatty substances, organic solvents, solubilizers, thickeners and gelling agents, emollients, antioxidants, suspending agents, stabilizers, foaming agents, fragrances, surfactants, water, ionic substances in addition to Samchil extract. Or nonionic emulsifiers, fillers, sequestering and chelating agents, preservatives, vitamins, blockers, wetting agents, essential oils, dyes, pigments, hydrophilic or lipophilic actives, lipid vesicles or any other commonly used in cosmetics. It may contain adjuvants commonly used in the field of cosmetics, such as ingredients.
상기 화장료 제형은 유효성분이 단기간 내에 피부에 머무르게 되는 메이크업 제거제, 세정제 등과 같은 워쉬-오프(wash-off) 타입의 화장품의 경우에는 비교적 높은 농도의 상기 삼칠 추출물을 포함할 수 있을 것이다. 반면, 유효성분이 장기간 동안 피부에 머무르게 되는 화장수, 유액, 크림, 에센스 등의 리브-온(leave-on) 타입의 화장품의 경우에는 워쉬-오프 타입의 화장품에 비해 낮은 농도의 상기 삼칠 추출물을 포함해도 무방할 것이다. 이에 제한되는 것은 아니나, 본 발명의 한 구체예에서, 상기 조성물은 상기 삼칠 추출물을 전체 조성물 중량에 대하여 0.0001 중량% 내지 10 중량%(바람직하게는 0.0001 중량% 내지 1 중량%)로 포함할 수 있다. 본 발명의 조성물이 상기 삼칠 추출물을 0.0001 중량% 미만으로 포함할 경우에는 충분한 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 효과를 기대할 수 없고, 10 중량%를 초과하여 포함할 경우에는 알러지 등 원치 않는 반응이 발생하거나 피부 안전성에 문제가 있을 수 있으므로 이를 방지하기 위한 것이다.The cosmetic formulation may contain a relatively high concentration of the Samchil extract in the case of a wash-off type cosmetic such as a makeup remover or detergent in which the active ingredient stays on the skin within a short period of time. On the other hand, in the case of leave-on-type cosmetics such as lotions, emulsions, creams, and essences in which the active ingredient stays on the skin for a long period of time, even if it contains a lower concentration of the Samchil extract compared to the wash-off type cosmetics. It would be okay. Although not limited thereto, in one embodiment of the present invention, the composition may include 0.0001 wt% to 10 wt% (preferably 0.0001 wt% to 1 wt%) of the Samchil extract based on the total weight of the composition. . When the composition of the present invention contains less than 0.0001% by weight of the Samchil extract, sufficient skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement effects cannot be expected, and when it contains more than 10% by weight This is to prevent unwanted reactions such as allergies or skin safety problems.
또한, 본 발명의 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선용 조성물은 식품 제형 제조를 위해 사용될 수 있다.In addition, the composition for skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement of the present invention may be used for preparing a food formulation.
상기 식품 제형은 상기 삼칠 추출물을 음료, 차류, 향신료, 껌, 과자류 등의 식품 소재에 첨가하거나, 캡슐화, 분말화, 현탁액 등으로 제조한 식품을 의미한다. The food formulation refers to a food prepared by adding the Samchil extract to food materials such as beverages, teas, spices, gums, confectionery, or the like, encapsulated, powdered, or suspended.
상기 식품 제형은 일상적으로 섭취하는 것이 가능하기 때문에 높은 피부 재생, 항염증, 아토피 개선, 피부 보습 및 피부결 개선 효과를 기대할 수 있어 매우 유용하다.Since the above food formulation can be consumed on a daily basis, it is very useful because it can expect high skin regeneration, anti-inflammatory, atopy improvement, skin moisturizing and skin texture improvement effects.
상기 삼칠 추출물을 식품첨가물로 사용하는 경우, 상기 삼칠 추출물을 그대로 첨가하거나 다른 식품 또는 식품 성분과 함께 사용될 수 있고, 통상적인 방법에 따라 적절하게 사용될 수 있다. 유효성분의 혼합양은 그의 사용 목적(예방, 건강 또는 치료적 처치)에 따라 적합하게 결정될 수 있다. 일반적으로, 식품 또는 음료의 제조시에 본 발명의 조성물은 원료에 대하여 15 중량부 이하, 바람직하게는 10 중량부 이하의 양으로 첨가된다. 그러나, 건강 및 위생을 목적으로 하거나 또는 건강 조절을 목적으로 하는 장기간의 섭취의 경우에는 상기 양은 상기 범위 이하일 수 있으며, 안전성 면에서 아무런 문제가 없기 때문에 유효성분은 상기 범위 이상의 양으로도 사용될 수 있다.When using the Samchil extract as a food additive, the Samchil extract may be added as it is or may be used with other foods or food ingredients, and may be appropriately used according to a conventional method. The mixing amount of the active ingredient may be appropriately determined according to the purpose of use (prevention, health or therapeutic treatment). In general, when preparing food or beverage, the composition of the present invention is added in an amount of 15 parts by weight or less, preferably 10 parts by weight or less based on the raw material. However, in the case of long-term intake for the purpose of health and hygiene or for the purpose of health control, the amount may be less than the above range, and there is no problem in terms of safety, so the active ingredient may be used in an amount above the above range. .
상기 식품의 종류에는 특별한 제한은 없다. 상기 물질을 첨가할 수 있는 식품의 예로는 육류, 소세지, 빵, 초콜릿, 캔디류, 스넥류, 과자류, 피자, 라면, 기타 면류, 껌류, 아이스크림류를 포함한 낙농제품, 각종 스프, 음료수, 차, 드링크제, 알코올 음료 및 비타민 복합제 등이 있으며, 통상적인 의미에서의 건강식품을 모두 포함한다.There is no particular limitation on the type of the food. Examples of foods to which the above substances can be added include meat, sausage, bread, chocolate, candy, snacks, confectionery, pizza, ramen, other noodles, gum, dairy products including ice cream, various soups, beverages, tea, drinks, There are alcoholic beverages and vitamin complexes, and all health foods in the usual sense are included.
식품 제형이 음료인 경우, 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다. 상술한 천연 탄수화물은 포도당, 과당과 같은 모노사카라이드, 말토스, 슈크로스와 같은 디사카라이드, 및 덱스트린, 사이클로덱스트린과 같은 폴리사카라이드, 자일리톨, 소르비톨, 에리트리톨 등의 당알코올이다. 감미제로서는 타우마틴, 스테비아 추출물과 같은 천연 감미제나, 사카린, 아스파르탐과 같은 합성 감미제 등을 사용할 수 있다. 상기 천연 탄수화물의 비율은 본 발명의 조성물 100 mL당 일반적으로 약 0.01 ∼ 0.04 g, 바람직하게는 약 0.02 ∼ 0.03 g이다.When the food formulation is a beverage, it may contain various flavoring agents or natural carbohydrates as an additional component, like a conventional beverage. The natural carbohydrates described above are monosaccharides such as glucose and fructose, disaccharides such as maltose and sucrose, and polysaccharides such as dextrin and cyclodextrin, and sugar alcohols such as xylitol, sorbitol, and erythritol. As the sweetener, natural sweeteners such as taumatin and stevia extract, and synthetic sweeteners such as saccharin and aspartame can be used. The proportion of the natural carbohydrate is generally about 0.01 to 0.04 g, preferably about 0.02 to 0.03 g per 100 mL of the composition of the present invention.
상기 외에 식품 제형은 여러 가지 영양제, 비타민, 전해질, 풍미제, 착색제, 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알코올, 탄산 음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 식품 제형은 천연 과일주스, 과일주스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 혼합하여 사용할 수 있다. 이러한 첨가제의 비율은 크게 중요하진 않지만 본 발명의 조성물 100 중량부당 0.01 ~ 0.1 중량부의 범위에서 선택되는 것이 일반적이다.In addition to the above, food formulations include various nutrients, vitamins, electrolytes, flavoring agents, coloring agents, pectic acid and salts thereof, alginic acid and salts thereof, organic acids, protective colloidal thickeners, pH adjusters, stabilizers, preservatives, glycerin, alcohols, carbonated beverages. It may contain a carbonation agent and the like used in the. In addition, the food formulation may contain pulp for the manufacture of natural fruit juice, fruit juice beverage and vegetable beverage. These ingredients may be used independently or in combination. Although the proportion of these additives is not very important, it is generally selected from 0.01 to 0.1 parts by weight per 100 parts by weight of the composition of the present invention.
본 발명은 또한, 상기 삼칠 추출물을 유효성분으로 포함하는 줄기세포 활성 촉진용 조성물을 제공한다.The present invention also provides a composition for promoting stem cell activity comprising the Samchil extract as an active ingredient.
본 발명에서 용어 ‘줄기세포’는 스스로 세포 분열을 할 수 있고, 매우 다양한 형태의 특이 세포 타입(specific cell type)으로 분화할 수 있는 능력을 갖는 세포이다. 이러한 줄기세포의 종류는 특별히 제한되지 않으며, 한 구체예에서, 상기 줄기세포는 피부줄기세포일 수 있다. 상기 ‘피부줄기세포’는 피부(표피, 진피 및 피하지방층)를 이루는 세포로 분화될 수 있는 줄기세포를 의미한다. 상기 피부를 이루는 세포는 표피에 존재하는 케라티노사이트(keratinocyte), 멜라노사이트(melanocyte) 및 진피에 존재하는 섬유아세포(콜라겐 및 엘라스틴의 생합성을 주로 담당)를 포함한다. In the present invention, the term'stem cell' refers to a cell that can divide cells by itself and has the ability to differentiate into a wide variety of specific cell types. The type of stem cells is not particularly limited, and in one embodiment, the stem cells may be skin stem cells. The “skin stem cells” refer to stem cells that can differentiate into cells that make up the skin (epidermis, dermis, and subcutaneous fat layer). The cells constituting the skin include keratinocytes, melanocytes, and fibroblasts (mainly responsible for the biosynthesis of collagen and elastin) present in the epidermis.
상기 피부줄기세포의 종류는 특별히 제한되지 않는다. 본 발명에서 사용되는 피부줄기세포는 그것이 어디로부터 유래한 것인지 관계없이 이용될 수 있다. 예를 들어, 피부줄기세포는 공지의 피부줄기세포 공급원, 예를 들어, 모낭 또는 표피의 기저층에서 얻을 수 있으며, 채취 대상인 동물은 포유동물일 수 있다. 한 구체예에서, 포유동물은 인간, 마우스, 랫트, 기니어 피그, 토끼, 원숭이, 돼지, 말, 소, 양, 영양, 개 또는 고양이를 포함할 수 있지만, 이에 한정되는 것은 아니다. 바람직하게 포유동물은 인간일 수 있다. 이러한, 피부줄기세포 공급원으로부터 피부줄기세포를 수득하는 방법에 대해서는 당업계에서 잘 알려져 있다.The type of skin stem cells is not particularly limited. The skin stem cells used in the present invention can be used regardless of where they originate from. For example, skin stem cells can be obtained from a known source of skin stem cells, such as hair follicles or the basal layer of the epidermis, and the animal to be collected may be a mammal. In one embodiment, the mammal may include, but is not limited to, a human, mouse, rat, guinea pig, rabbit, monkey, pig, horse, cow, sheep, antelope, dog, or cat. Preferably, the mammal may be a human. Such, a method of obtaining skin stem cells from a source of skin stem cells is well known in the art.
본 발명에 있어서, '줄기세포 활성 촉진 효과'라 함은 줄기세포 증식 촉진 효과, 및/또는 줄기세포의 특이적 지표 분자 및 자가 분열적 성질인 줄기세포성을 유지하는 효과를 포함하는 것을 말한다.In the present invention, the term'stem cell activity promoting effect' refers to a stem cell proliferation promoting effect and/or a specific indicator molecule of stem cells and an effect of maintaining stem cell properties, which are self-dividing properties.
또한, 본 발명의 조성물은 화장료 제형 제조를 위해 사용될 수 있다. 이러한 화장료 제형에 대해서는 앞서 삼칠 추출물을 포함하는 화장료 제형에 관한 설명에 기재된 내용과 동일하다. In addition, the composition of the present invention can be used to prepare a cosmetic formulation. These cosmetic formulations are the same as those described in the description of the cosmetic formulation containing the Samchil extract.
이하, 본 발명을 실시예에 의해 상세히 설명한다. 단, 하기 실시예는 본 발명을 예시하는 것일 뿐, 본 발명의 내용이 하기 실시예에 한정되는 것은 아니다. Hereinafter, the present invention will be described in detail by examples. However, the following examples are merely illustrative of the present invention, and the contents of the present invention are not limited to the following examples.
제조예 1: 삼칠 추출물의 제조Preparation Example 1: Preparation of Samchil extract
삼칠을 세척하고, 분말화한 뒤, 10 배량의 에탄올 용매에서 5일간 냉침한 후 추출 원액을 여과, 농축한 엑기스를 얻었다. 여기에 정제수 및 에탄올의 혼합용액을 첨가하여 용해시킨 다음 여과하여 최종 추출물을 제조하였다.Samchil was washed, powdered, and then cooled for 5 days in a 10-fold amount of ethanol solvent, and the extracted stock solution was filtered to obtain concentrated extract. A mixed solution of purified water and ethanol was added thereto, dissolved, and filtered to prepare a final extract.
제조예 2: 무혈청 배지조건에서 피부줄기세포의 배양Preparation Example 2: Culture of skin stem cells in serum-free medium conditions
Cellntec 사에서 구입한 인간 피부줄기세포(Human epidermal stem cell)를 48-웰 플레이트(6×103 cells/well)에, 소태아혈청(fetal bovine serum)과 유사한 BPE(Bovine pituitary extract)가 첨가된 CNT-57 배지(Cellntec사)를 이용하여 24 시간 동안 5% CO2 및 37℃ 조건에서 배양하였다. 그 후, 배양액을 흡입관을 통하여 제거한 다음, PBS 용액(GibcoBRL 사)을 이용하여 배지 성분을 제거하고, BPE가 포함되지 않은 CNT-57 배지에 삼칠 추출물 0.0005 중량%을 처리하여 5% CO2 및 37℃ 조건에서 72 시간 동안 배양하였다.Human epidermal stem cells purchased from Cellntec were added to a 48-well plate (6×10 3 cells/well) and bovine pituitary extract (BPE) similar to fetal bovine serum was added. CNT-57 medium (Cellntec) was used for 24 hours at 5% CO 2 and 37°C. Thereafter, the culture solution was removed through a suction tube, and then the medium component was removed using a PBS solution (GibcoBRL), and 0.0005% by weight of the Samchil extract was treated in CNT-57 medium without BPE to 5% CO 2 and 37 Incubated for 72 hours at ℃ conditions.
실험예 1: CCK-8 평가법을 통한 피부줄기세포 증식 촉진 효과Experimental Example 1: Effect of promoting skin stem cell proliferation through CCK-8 evaluation method
상기 참조예 2에서 배양된 피부줄기세포에 CCK-8(Cell counting kit-8) 평가를 실시하였다. CCK-8 평가는 세포 내 전자전달계 내의 탈수소효소(Dehydrogenase)가 테트라졸리움 염(Tetrazolium Salt)를 분해하여 생성하는 포르마잔(Formazan)의 흡광도를 측정하여 살아있는 세포의 밀도를 간접적으로 나타내는 분석방법이다. The skin stem cells cultured in Reference Example 2 were evaluated for CCK-8 (Cell Counting Kit-8). The CCK-8 evaluation is an analysis method that indirectly indicates the density of living cells by measuring the absorbance of Formazan, which is produced by decomposing Tetrazolium Salt by dehydrogenase in the intracellular electron transport system.
세포에 CCK-8 용액(배지부피의 1/10을 처리)을 37℃에서 2 시간 동안 처리한 후, 파장 450 nm에서의 흡광도를 측정함으로써 분광학적으로 측정하였다. 삼칠 추출물의 피부줄기세포의 증식 촉진 효과는 측정된 흡광도 값으로부터 대조군(BPE 첨가한 CNT-57 배지) 대비 하기 수학식 1에 따라 증식율(%)을 구하고, 그 값을 하기 표 1에 나타냈다.Cells were treated with a CCK-8 solution (1/10 of the medium volume was treated) at 37° C. for 2 hours, and then measured spectroscopically by measuring the absorbance at a wavelength of 450 nm. The proliferation promoting effect of skin stem cells of Samchil extract was obtained from the measured absorbance value in accordance with Equation 1 below compared to the control (CNT-57 medium with BPE), and the values are shown in Table 1 below.
[수학식 1][Equation 1]
증식율(%) = (시료처리군의 흡광도/대조군의 흡광도) × 100Growth rate (%) = (absorbance of sample treatment group/absorbance of control group) × 100
표 1에 나타난 바와 같이, 삼칠 추출물을 처리한 배지조건에서의 피부줄기세포는 우수한 증식 촉진 효과를 나타내었다. As shown in Table 1, skin stem cells in the medium condition treated with Samchil extract showed excellent proliferation promoting effect.
실험예 2: 피부줄기세포의 줄기세포성(stemness) 유지 효과 확인Experimental Example 2: Confirmation of the effect of maintaining stemness of skin stem cells
상기 참조예 2에서 배양된 피부줄기세포의 줄기세포성 유지 효과 확인을 위해 p63 발현 정도를 평가하였다. p63은 세포 내 전사인자로서 피부줄기세포의 유지 마커로 잘 알려져 있다. 세포의 RNA를 분리하여 cDNA를 합성한 다음, Taqman 염색액으로 실시간-PCR을 수행하여 p63의 발현 정도를 측정하였다. 본 실험에서 RNA의 농도는 S16 리보솜 RNA로 표준화하였다.In order to confirm the effect of maintaining stem cell properties of the skin stem cells cultured in Reference Example 2, the level of p63 expression was evaluated. p63 is an intracellular transcription factor and is well known as a maintenance marker for skin stem cells. After separating RNA from cells, cDNA was synthesized, and then real-time-PCR was performed with Taqman's stain solution to measure the level of p63 expression. In this experiment, the concentration of RNA was normalized to S16 ribosomal RNA.
상기 실험 결과는 하기 표 2에 나타내었다. 하기 표 2에서 p63 증가 배수의 수치는 대조군(BPE 첨가한 CNT-57 배지) 대비 배수를 의미한다.The experimental results are shown in Table 2 below. In Table 2 below, the value of the p63 increase fold refers to the fold compared to the control (CNT-57 medium added with BPE).
표 2에 나타난 바와 같이, 삼칠 추출물을 처리한 배지 조건은 피부줄기세포의 p63 발현을 촉진하여 줄기세포성 유지 효과가 우수하다.As shown in Table 2, the medium condition treated with Samchil extract promotes the expression of p63 in skin stem cells, thereby exhibiting excellent stem cell properties.
실시예 1: 항염증 효과-NO 생성 억제 효과 Example 1: Anti-inflammatory effect-NO production inhibitory effect
삼칠 추출물의 항염증 효과 및 피부트러블 완화 효과를 확인하기 위하여, RAW264.7 세포주(ATCC number: CRL-2278)를 이용한 GRIESS 법으로 nitric oxide(NO) 형성 억제력 실험을 실시하였다.In order to confirm the anti-inflammatory effect and skin trouble relief effect of Samchil extract, nitric oxide (NO) formation inhibition ability was tested by the GRIESS method using RAW264.7 cell line (ATCC number: CRL-2278).
구체적으로, 생쥐의 대식세포인 RAW264.7 세포를 수 차례 계대 배양하고, 웰 하나에 3×105 개씩 들어가도록 24-웰 프레이트에 넣은 후, 24 시간 동안 배양시켰다. 이어서, 하기 표 6에 나타난 농도로 삼칠 추출물을 희석하여 함유한 세포 배지로 교체하였다. 이때, NO-생성 억제 물질인 L-NMMA(L-NG-Monomethylarginine) 20 ㎍/mL을 양성 대조군으로 함께 처리하여 30분 동안 배양하였고, 자극원으로 LPS(Lipopolysaccharide)를 1 ㎍씩 처리하여 24시간 동안 배양하였다. 상층액을 100 ㎕씩 취해 96-웰 프레이트에 옮기고, GRIESS 용액을 100 ㎕씩 가해 상온에서 10분간 반응시키고, 540 nm에서의 흡광도를 측정함으로써 화합물 1의 NO 억제 효과를 판단하고, 그 결과를 하기 표 3에 나타내었다.Specifically, RAW264.7 cells, which are mouse macrophages, were passaged several times, placed in a 24-well plate so as to enter each of 3×10 5 cells in each well, and cultured for 24 hours. Subsequently, the Samchil extract was diluted to the concentration shown in Table 6 and replaced with a cell medium containing. At this time, 20 µg/mL of L-NG-Monomethylarginine (L-NMMA), a substance that inhibits NO-production, was treated together as a positive control and incubated for 30 minutes, and 1 µg of LPS (Lipopolysaccharide) was treated as a stimulating source for 24 hours. During incubation. 100 µl of the supernatant is taken and transferred to a 96-well plate, 100 µl of the GRIESS solution is added at a time, reacted at room temperature for 10 minutes, and the absorbance at 540 nm is measured to determine the NO inhibitory effect of Compound 1, and the results are as follows. It is shown in Table 3.
표 3에 나타난 바와 같이, 삼칠 추출물은 기존에 알려진 항염 물질인 L-NMMA와 동등 수준의 NO 생성 억제능이 있음을 알 수 있다.As shown in Table 3, it can be seen that the Samchil extract has the ability to inhibit NO generation at the same level as L-NMMA, an anti-inflammatory substance known in the past.
실시예 2 : PPAR 알파 활성화 촉진 효과 검증Example 2: PPAR alpha activation promoting effect verification
삼칠 추출물의 PPAR 알파 활성화 촉진 효과를 확인하기 위하여, 삼칠 추출물을 이용하여 하기와 같은 실험을 수행하였다. 마우스 유래의 근아세포(myoblast) 세포주인 C2C12 세포(ATCC CRL-1772)를 10% 우태아 혈청을 포함하는 DMEM(Dulbeco's Modified Eagle's Medium) 배지에 계대 배양하였다. 여기서 사용된 벡터로는, In order to confirm the PPAR alpha activation promoting effect of the Samchil extract, the following experiment was performed using the Samchil extract. C2C12 cells (ATCC CRL-1772), a mouse-derived myoblast cell line, were subcultured in DMEM (Dulbeco's Modified Eagle's Medium) medium containing 10% fetal calf serum. As the vector used here,
1) pZEO 벡터 (Invitrogen)의 SV40 프로모터에 효모의 전사 인자인 GAL4-DBD(DNA Binding Domain)과 인간 PPAR 알파 LBD(Ligand Binding Domain)에서 Ser167 내지 Tyr468을 암호화하는 DNA 단편(유전자 은행 정보, NM 005036)을 포함하는 벡터; 1) DNA fragment encoding Ser 167 to Tyr 468 in the yeast transcription factor GAL4-DBD (DNA Binding Domain) and human PPAR alpha LBD (Ligand Binding Domain) in the SV40 promoter of the pZEO vector (Invitrogen) (gene bank information, NM 005036);
2) GAL4 응답 서열을 루시퍼라이제 (Luciferase)를 발현하는 pGL3 벡터(Promega)의 다중 제한 효소 인지 부위에 삽입된 벡터, 및 3) 트랜스팩션 대조군(transfection internal control)으로 β-갈락토시다아제(β-galactodisase)를 발현하는 벡터를 사용하였다.2) a vector in which the GAL4 response sequence was inserted into the multiple restriction enzyme recognition site of the pGL3 vector (Promega) expressing luciferase, and 3) β-galactosidase as a transfection internal control ( β-galactodisase) was used.
상기 배양한 세포를 4×104의 농도로 24웰 플레이트에 도말한 후, 12 시간 동안 배양하고, 상기 세 종류의 플라스미드 유전자를 일시적인 리포팩타민(Lipopectamine)을 이용하여 트랜스팩션(transient transfection)하였다. 8시간 후, 삼칠 추출물을 처리하고 12 시간 동안 배양한 다음, 1×PBS로 세척하고 1×리포터 용해 버퍼(reporter lysis buffer)로 세포를 용해시킨 후, 루시퍼라아제 분석 키트(Promega) 및 β-갈락토시다아제 분석 키트(Promega)를 사용하여 루시퍼라아제의 활성을 측정하였다. 즉, PPAR 알파 활성도는 '루시퍼라아제 활성/β-갈락토오스 활성'으로 측정하였다.The cultured cells were plated on a 24-well plate at a concentration of 4×10 4 and then cultured for 12 hours, and the three types of plasmid genes were transiently transfected using Lipopectamine. . After 8 hours, the Samchil extract was treated and incubated for 12 hours, washed with 1×PBS, and lysed with 1×reporter lysis buffer, followed by luciferase assay kit (Promega) and β- The activity of luciferase was measured using a galactosidase assay kit (Promega). That is, PPAR alpha activity was measured as'luciferase activity/β-galactose activity'.
본 실험에서 양성 대조군으로는 PPAR 알파의 리간드 중 가장 강력한 것으로 알려진 Wy-14,643(Calbiochem)을 사용하였고, 음성 대조군으로는 시료를 녹일 때 사용한 DMSO 0.05%를 사용하였다.In this experiment, Wy-14,643 (Calbiochem), which is known to be the most potent PPAR alpha ligand, was used as a positive control, and DMSO 0.05% used when dissolving the sample was used as a negative control.
상기 실험 방법에 따라, 삼칠 추출물을 C2C12 세포에 처리하여 농도 변화에 따른 PPAR 알파의 활성을 측정하였으며, 그 결과를 하기 표 7에 나타내었다. 하기 표 4에서 PPAR 알파 활성도의 수치는 음성 대조군(DMSO 0.05%) 대비 백분율을 의미한다.According to the above experimental method, the activity of PPAR alpha according to the concentration change was measured by treating the Samchil extract to C2C12 cells, and the results are shown in Table 7 below. In Table 4 below, the value of PPAR alpha activity refers to a percentage compared to the negative control (DMSO 0.05%).
표 4에 나타난 바와 같이, 양성 대조군과 비교하여, 삼칠추출물은 매우 강력한 PPAR 알파 활성능을 나타낸다는 것을 확인할 수 있었다.As shown in Table 4, compared to the positive control, it was confirmed that the Samchil extract showed very strong PPAR alpha activity.
실시예 3: 필라그린(Filaggrin)의 발현 촉진 효과Example 3: Effect of promoting the expression of Filaggrin
삼칠 추출물을 5 ㎍/mL, 10 ㎍/mL가 되도록 하여 각각 인간 각질세포주 HaCaT 세포의 배양배지에 첨가하여 1일간 배양한 후, 세포의 RNA를 분리하고 cDNA를 합성한 뒤 Taqman 염색액으로 Real-time PCR을 수행하였다. RNA농도는 S16 리보솜 RNA로 표준화시켰다.Samchil extract was added to the culture medium of the human keratin cell line HaCaT cells to be 5 μg/mL and 10 μg/mL, and cultured for 1 day. After separating RNA from the cells, synthesizing cDNA, and using Taqman's stain solution, Real- Time PCR was performed. RNA concentration was normalized to S16 ribosomal RNA.
표 5에 나타난 바와 같이, 삼칠 추출물은 인간 각질세포주 HaCaT 세포의 필라그린 발현 촉진능이 있다.As shown in Table 5, Samchil extract has the ability to promote filaggrin expression in human keratinocyte line HaCaT cells.
실시예 4: 각질 박리(turn-over) 개선에 대한 효능성Example 4: Efficacy in improving turn-over
하기 제제예 2의 영양크림에 대해서 건강한 20대에서 50대의 여성을 대상으로 각질 박리 개선 효과를 다음과 같이 시험하였다.For the nutritional cream of Formulation Example 2 below, the effect of improving keratin peeling was tested for women in their 20s to 50s who were healthy.
20세에서 50세까지의 여성 20명의 시험 부위에 DHA(Dihydroxyacetone, Sigma Aldrich, USA) 1.5% 용액을 8시간 동안 폐쇄첩포하여 침착시킨 후 제조예 영양크림을 매일 2회 시험 부위에 도포하였다. 도포 4일 후, 도포 8일 후, 도포 12일 후에 Chromameter CR-400(Minolta, Japan)을 이용하여 침착 부위의 피부 밝기에 대한 기기측정과 DSLR을 이용하여 사진 촬영을 실시하였다. 측정값은 최대값과 최소값을 제외한 3회의 평균값을 구하여 평가하였으며, 침착 부위의 피부 밝기 개선이 높을수록 각질 박리 개선 효과가 있음을 나타낸다. 결과는 하기 표 6에 나타내었다.A 1.5% solution of DHA (Dihydroxyacetone, Sigma Aldrich, USA) was deposited on the test site of 20 women between the ages of 20 and 50 with a closed patch for 8 hours, and then the prepared nourishing cream was applied to the test site twice daily. After 4 days of application, 8 days after application, and 12 days after application, an instrument measurement of the skin brightness of the deposited area was measured using a Chromameter CR-400 (Minolta, Japan) and a photo was taken using a DSLR. The measured value was evaluated by obtaining an average value of three times excluding the maximum and minimum values, and the higher the skin brightness improvement at the deposited area, the better the keratin peeling improvement effect. The results are shown in Table 6 below.
표 6에 나타난 바와 같이, 본 발명에 따른 영양크림을 사용한 경우 각질 박리 개선 효과가 있는 것으로 나타났다.As shown in Table 6, when the nutritional cream according to the present invention was used, it was found that there is an effect of improving keratin peeling.
제제예 1: 의약 제제의 제조Formulation Example 1: Preparation of pharmaceutical formulation
1. 정제의 제조1. Preparation of tablets
삼칠 추출물 0.2㎎Samchil extract 0.2mg
옥수수전분 100㎎Corn starch 100mg
유 당 100㎎100mg lactose
스테아린산 마그네슘 2㎎ Magnesium stearate 2mg
상기의 성분을 혼합한 후, 통상의 정제의 제조방법에 따라서 타정하여 정제를 제조하였다.After mixing the above ingredients, tablets were prepared by tableting according to a conventional tablet preparation method.
제제예 2: 화장품의 제조Formulation Example 2: Preparation of cosmetics
1. 영양크림의 제조1. Manufacture of nourishing cream
하기 조성과 같이, 삼칠 추출물을 유효성분으로 포함하는 영양크림을 통상의 방법에 따라 제조하였다.As shown in the following composition, a nutrient cream containing Samchil extract as an active ingredient was prepared according to a conventional method.
삼칠 추출물 0.2중량%0.2% by weight of Samchil extract
베타-1,3-글루칸 5.0 중량%5.0% by weight of beta-1,3-glucan
밀납 10.0 중량%10.0 wt% beeswax
폴리솔베이트60 1.5 중량%1.5% by weight of polysorbate 60
피이지 60 경화피마자유 2.0 중량%Sebum 60 hydrogenated castor oil 2.0% by weight
솔비탄세스퀴올레이트 0.5 중량%0.5% by weight of sorbitansquioleate
유동파라핀 10.0 중량%Liquid paraffin 10.0% by weight
스쿠알란 5.0 중량%5.0% by weight of squalane
카프릴릭/카프릭트리글리세라이드 5.0 중량%Caprylic/Capric Triglyceride 5.0% by weight
글리세린 5.0 중량%5.0% by weight of glycerin
부틸렌글리콜 3.0 중량%3.0% by weight of butylene glycol
프로필렌글리콜 3.0 중량%Propylene glycol 3.0% by weight
트리에탄올아민 0.2 중량%0.2% by weight of triethanolamine
방부제 0.05 중량%0.05% by weight of preservative
색소 0.05 중량%0.05% by weight of pigment
향료 0.05 중량%Perfume 0.05% by weight
정제수 to 100 중량%Purified water to 100% by weight
제제예 3: 피부 외용제의 제조Formulation Example 3: Preparation of external preparation for skin
1. 연고의 제조1. Preparation of ointment
하기 조성과 같이, 삼칠 추출물을 유효성분으로 포함하는 연고를 통상의 방법에 따라 제조하였다.As shown in the following composition, an ointment containing Samchil extract as an active ingredient was prepared according to a conventional method.
삼칠 추출물 0.5 중량%0.5% by weight of Samchil extract
베타-1,3-글루칸 10.0 중량%Beta-1,3-glucan 10.0% by weight
밀납 10.0 중량%10.0 wt% beeswax
폴리솔베이트60 5.0 중량%5.0% by weight of polysorbate 60
피이지 60 경화피마자유 2.0 중량%PEG 60 hydrogenated castor oil 2.0% by weight
솔비탄세스퀴올레이트 0.5 중량%0.5% by weight of sorbitansquioleate
바셀린 5.0 중량%Vaseline 5.0% by weight
유동파라핀 10.0 중량%Liquid paraffin 10.0% by weight
스쿠알란 5.0 중량%5.0% by weight of squalane
쉐어버터 3.0 중량%Shea butter 3.0% by weight
카프릴릭/카프릭트리글리세라이드 5.0 중량%Caprylic/Capric Triglyceride 5.0% by weight
글리세린 10.0 중량%Glycerin 10.0% by weight
프로필렌글리콜 10.2 중량%10.2% by weight of propylene glycol
트리에탄올아민 0.2 중량%0.2% by weight of triethanolamine
방부제 0.05 중량%0.05% by weight of preservative
색소 0.05 중량%0.05% by weight of pigment
향료 0.05 중량%Perfume 0.05% by weight
정제수 to 100 중량%Purified water to 100% by weight
Claims (14)
A cosmetic composition for improving keratin peeling by promoting stem cell activity, comprising a Samchil extract as an active ingredient.
삼칠 추출물은 삼칠을 물 및 유기용매로 이루어진 군에서 선택된 하나 이상으로 추출하여 얻은 추출물인 줄기세포 활성 촉진에 따른 각질 박리 개선용 화장료 조성물.
The method of claim 1,
Samchil extract is an extract obtained by extracting Samchil with one or more selected from the group consisting of water and an organic solvent, and a cosmetic composition for improving keratin peeling by promoting stem cell activity.
유기 용매는 탄소수 1 내지 5의 저급 알코올, 에틸아세테이트, 또는 아세톤을 포함하는 극성용매; 에테르, 클로로포름, 벤젠, 헥산 또는 디클로로헥산을 포함하는 비극성용매; 또는 이들의 혼합용매인 줄기세포 활성 촉진에 따른 각질 박리 개선용 화장료 조성물.
The method of claim 2,
The organic solvent is a polar solvent including a lower alcohol having 1 to 5 carbon atoms, ethyl acetate, or acetone; A non-polar solvent including ether, chloroform, benzene, hexane or dichlorohexane; Or a cosmetic composition for improving keratin peeling by promoting stem cell activity, which is a mixed solvent thereof.
상기 줄기세포 활성은 줄기세포 증식 촉진 또는 줄기세포성 유지를 특징으로 하는 줄기세포 활성 촉진에 따른 각질 박리 개선용 화장료 조성물.
The method of claim 1,
The stem cell activity is a cosmetic composition for improving keratin exfoliation according to the promotion of stem cell activity, characterized by promoting stem cell proliferation or maintaining stem cell properties.
Skin external preparation for promoting keratin peeling by promoting stem cell activity containing Samchil extract as an active ingredient.
상기 줄기세포 활성은 줄기세포 증식 촉진 또는 줄기세포성 유지를 특징으로 하는 줄기세포 활성 촉진에 따른 각질 박리 촉진용 피부 외용제.
The method of claim 5,
The stem cell activity is a skin external preparation for promoting keratin peeling according to the promotion of stem cell activity, characterized by promoting stem cell proliferation or maintaining stem cell properties.
A food composition for improving keratin exfoliation by promoting stem cell activity comprising Samchil extract as an active ingredient.
상기 줄기세포 활성은 줄기세포 증식 촉진 또는 줄기세포성 유지를 특징으로 하는 줄기세포 활성 촉진에 따른 각질 박리 개선용 식품 조성물.
The method of claim 7,
The stem cell activity is a food composition for improving keratin peeling according to the promotion of stem cell activity, characterized by promoting stem cell proliferation or maintaining stem cell properties.
A pharmaceutical composition for the treatment of atopy according to the promotion of stem cell activity comprising a Samchil extract as an active ingredient.
상기 줄기세포 활성은 줄기세포 증식 촉진 또는 줄기세포성 유지를 특징으로 하는 줄기세포 활성 촉진에 따른 아토피 치료용 약학적 조성물.
The method of claim 9,
The stem cell activity is a pharmaceutical composition for the treatment of atopy according to the promotion of stem cell activity, characterized by promoting stem cell proliferation or maintaining stem cell properties.
A cosmetic composition for improving atopy by promoting stem cell activity comprising a Samchil extract as an active ingredient.
상기 줄기세포 활성은 줄기세포 증식 촉진 또는 줄기세포성 유지를 특징으로 하는 줄기세포 활성 촉진에 따른 아토피 개선용 화장료 조성물.
The method of claim 11,
The stem cell activity is a cosmetic composition for improving atopy by promoting stem cell activity, characterized by promoting stem cell proliferation or maintaining stem cell properties.
A food composition for improving atopy according to the promotion of stem cell activity, comprising Samchil extract as an active ingredient.
상기 줄기세포 활성은 줄기세포 증식 촉진 또는 줄기세포성 유지를 특징으로 하는 줄기세포 활성 촉진에 따른 아토피 개선용 식품 조성물.The method of claim 13,
The stem cell activity is a food composition for improving atopy according to the promotion of stem cell activity, characterized by promoting stem cell proliferation or maintaining stem cell properties.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020210060710A KR102360881B1 (en) | 2020-05-11 | 2021-05-11 | Composition for improving skin |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020200055714A KR102260961B1 (en) | 2015-08-28 | 2020-05-11 | Composition for improving skin |
KR1020210060710A KR102360881B1 (en) | 2020-05-11 | 2021-05-11 | Composition for improving skin |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020200055714A Division KR102260961B1 (en) | 2015-08-28 | 2020-05-11 | Composition for improving skin |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20210056984A true KR20210056984A (en) | 2021-05-20 |
KR102360881B1 KR102360881B1 (en) | 2022-02-09 |
Family
ID=70913337
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020200055714A KR102260961B1 (en) | 2015-08-28 | 2020-05-11 | Composition for improving skin |
KR1020210060710A KR102360881B1 (en) | 2020-05-11 | 2021-05-11 | Composition for improving skin |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020200055714A KR102260961B1 (en) | 2015-08-28 | 2020-05-11 | Composition for improving skin |
Country Status (1)
Country | Link |
---|---|
KR (2) | KR102260961B1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20230080033A (en) | 2021-11-29 | 2023-06-07 | 충북대학교 산학협력단 | Pharmaceutical composition comprising green tea extract extracted with natural eutectic solvents as an active ingredient |
KR20230114486A (en) | 2022-01-25 | 2023-08-01 | 충북대학교 산학협력단 | Cosmetic composition comprising camellia oleifera extract as an active ingredient |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030009454A (en) * | 2000-05-31 | 2003-01-29 | 카가쿠키쥬쯔 신코지교단 | SKIN TISSUE REGENERATION PROMOTERS COMPRISING GINSENOSIDE Rb1 |
KR20150022248A (en) * | 2013-08-22 | 2015-03-04 | 주식회사 아데나 | Composition for preventing, improving or treating of th2-mediated immune disease comprising extracts from panax notoginseug, saponaria officinalis l. , glycine max l., phaseolus radiatus l., phaseolus vulgaris l. |
-
2020
- 2020-05-11 KR KR1020200055714A patent/KR102260961B1/en active IP Right Grant
-
2021
- 2021-05-11 KR KR1020210060710A patent/KR102360881B1/en active IP Right Grant
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030009454A (en) * | 2000-05-31 | 2003-01-29 | 카가쿠키쥬쯔 신코지교단 | SKIN TISSUE REGENERATION PROMOTERS COMPRISING GINSENOSIDE Rb1 |
KR20150022248A (en) * | 2013-08-22 | 2015-03-04 | 주식회사 아데나 | Composition for preventing, improving or treating of th2-mediated immune disease comprising extracts from panax notoginseug, saponaria officinalis l. , glycine max l., phaseolus radiatus l., phaseolus vulgaris l. |
Non-Patent Citations (7)
Title |
---|
Epidermal Stem Cells of the Skin, Cedric Blanpain, Elaine Fuchs, Annual Review of Cell and Developmental Biology, November 2006, Vol. 22, Pages 339-373 |
Feingold 외, J. Invest. Dermatol., 110, pp 368-375, 1998. |
Feingold 외, J. Invest. Dermatol., 115, pp 353-360, 2000. |
Human skin stem cells and the ageing process, Catherin Niemann, Stem Cell Aging and Regenerative Medicine, November 2008, Pages 986-997 |
Journal of the European Academy of Dermatology and Venereology. 12:103-114, 1999 |
Skin research and technology.5:189-194, 1999 |
The British journal of dermatology. 110: 129-138, 1984 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20230080033A (en) | 2021-11-29 | 2023-06-07 | 충북대학교 산학협력단 | Pharmaceutical composition comprising green tea extract extracted with natural eutectic solvents as an active ingredient |
KR20230114486A (en) | 2022-01-25 | 2023-08-01 | 충북대학교 산학협력단 | Cosmetic composition comprising camellia oleifera extract as an active ingredient |
Also Published As
Publication number | Publication date |
---|---|
KR102260961B1 (en) | 2021-06-04 |
KR20200054151A (en) | 2020-05-19 |
KR102360881B1 (en) | 2022-02-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR102360881B1 (en) | Composition for improving skin | |
KR20150087145A (en) | Composition for improving skin | |
KR102472978B1 (en) | Composition for improving skin | |
KR20150087146A (en) | Composition for improving skin | |
KR102275267B1 (en) | Composition for improving skin | |
KR102245188B1 (en) | Composition for improving skin | |
KR20210117247A (en) | Composition for improving skin comprising stevioside as active ingredient | |
KR20170025352A (en) | Composition for improving skin | |
KR101872919B1 (en) | Composition for improving skin | |
KR20180041108A (en) | Composition for improving skin | |
KR20170025355A (en) | Composition for improving skin | |
KR102013164B1 (en) | Composition for improving skin | |
KR102397926B1 (en) | Composition for improving skin | |
KR20170025371A (en) | Composition for improving skin | |
KR20170025353A (en) | Composition for improving skin | |
KR20170025364A (en) | Composition for improving skin | |
KR20170025373A (en) | Composition for improving skin | |
KR20170025356A (en) | Composition for improving skin | |
KR20160128765A (en) | Composition for improving skin | |
KR20190096908A (en) | Composition for improving skin | |
KR20170025370A (en) | Composition for improving skin | |
KR20170035658A (en) | Composition for improving skin comprising cryptochlorogenic acid as active ingredient | |
KR102351478B1 (en) | Composition for improving skin | |
KR102308476B1 (en) | Composition for improving skin | |
KR102349947B1 (en) | Composition for improving skin |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A107 | Divisional application of patent | ||
E902 | Notification of reason for refusal | ||
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right |