KR20130098038A - Composition for promoting circulation of blood and improving skin disease - Google Patents
Composition for promoting circulation of blood and improving skin disease Download PDFInfo
- Publication number
- KR20130098038A KR20130098038A KR1020120019827A KR20120019827A KR20130098038A KR 20130098038 A KR20130098038 A KR 20130098038A KR 1020120019827 A KR1020120019827 A KR 1020120019827A KR 20120019827 A KR20120019827 A KR 20120019827A KR 20130098038 A KR20130098038 A KR 20130098038A
- Authority
- KR
- South Korea
- Prior art keywords
- composition
- blood circulation
- weight
- skin diseases
- promoting blood
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 208000017520 skin disease Diseases 0.000 title claims abstract description 51
- 230000001737 promoting effect Effects 0.000 title claims abstract description 35
- 210000004369 blood Anatomy 0.000 title description 8
- 239000008280 blood Substances 0.000 title description 8
- 230000017531 blood circulation Effects 0.000 claims abstract description 52
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims abstract description 45
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 claims abstract description 41
- 235000020673 eicosapentaenoic acid Nutrition 0.000 claims abstract description 41
- 229960005135 eicosapentaenoic acid Drugs 0.000 claims abstract description 41
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 claims abstract description 41
- 235000020669 docosahexaenoic acid Nutrition 0.000 claims abstract description 29
- 235000019165 vitamin E Nutrition 0.000 claims abstract description 23
- 239000011709 vitamin E Substances 0.000 claims abstract description 23
- 229930003427 Vitamin E Natural products 0.000 claims abstract description 22
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229940046009 vitamin E Drugs 0.000 claims abstract description 22
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims abstract description 22
- 229960001763 zinc sulfate Drugs 0.000 claims abstract description 22
- 229910000368 zinc sulfate Inorganic materials 0.000 claims abstract description 22
- 241001465754 Metazoa Species 0.000 claims abstract description 15
- DVSZKTAMJJTWFG-SKCDLICFSA-N (2e,4e,6e,8e,10e,12e)-docosa-2,4,6,8,10,12-hexaenoic acid Chemical compound CCCCCCCCC\C=C\C=C\C=C\C=C\C=C\C=C\C(O)=O DVSZKTAMJJTWFG-SKCDLICFSA-N 0.000 claims abstract description 9
- GZJLLYHBALOKEX-UHFFFAOYSA-N 6-Ketone, O18-Me-Ussuriedine Natural products CC=CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O GZJLLYHBALOKEX-UHFFFAOYSA-N 0.000 claims abstract description 9
- KAUVQQXNCKESLC-UHFFFAOYSA-N docosahexaenoic acid (DHA) Natural products COC(=O)C(C)NOCC1=CC=CC=C1 KAUVQQXNCKESLC-UHFFFAOYSA-N 0.000 claims abstract description 9
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 claims description 40
- 229940090949 docosahexaenoic acid Drugs 0.000 claims description 20
- 235000013305 food Nutrition 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 230000006872 improvement Effects 0.000 claims description 6
- 230000000052 comparative effect Effects 0.000 description 19
- 230000000694 effects Effects 0.000 description 16
- 241000282472 Canis lupus familiaris Species 0.000 description 13
- 206010061218 Inflammation Diseases 0.000 description 10
- 208000003251 Pruritus Diseases 0.000 description 10
- 230000004054 inflammatory process Effects 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 230000007803 itching Effects 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 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 6
- 239000000470 constituent Substances 0.000 description 6
- 239000002674 ointment Substances 0.000 description 6
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000008213 purified water Substances 0.000 description 5
- 239000006071 cream Substances 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 208000015181 infectious disease Diseases 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
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 201000004624 Dermatitis Diseases 0.000 description 3
- 206010015150 Erythema Diseases 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 206010052428 Wound Diseases 0.000 description 3
- 208000027418 Wounds and injury Diseases 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 231100000321 erythema Toxicity 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000003020 moisturizing effect Effects 0.000 description 3
- 210000000056 organ Anatomy 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 208000024891 symptom Diseases 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- 201000004384 Alopecia Diseases 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-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
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000023555 blood coagulation Effects 0.000 description 2
- 210000004204 blood vessel Anatomy 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- CYQFCXCEBYINGO-IAGOWNOFSA-N delta1-THC Chemical class C1=C(C)CC[C@H]2C(C)(C)OC3=CC(CCCCC)=CC(O)=C3[C@@H]21 CYQFCXCEBYINGO-IAGOWNOFSA-N 0.000 description 2
- 230000001079 digestive effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 235000004626 essential fatty acids Nutrition 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- -1 impregnation pad Substances 0.000 description 2
- 230000007794 irritation Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- 231100000956 nontoxicity Toxicity 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 210000004623 platelet-rich plasma Anatomy 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
- 206010040872 skin infection Diseases 0.000 description 2
- 235000011888 snacks Nutrition 0.000 description 2
- 235000013599 spices Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- SKIIKRJAQOSWFT-UHFFFAOYSA-N 2-[3-[1-(2,2-difluoroethyl)piperidin-4-yl]oxy-4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound FC(CN1CCC(CC1)OC1=NN(C=C1C=1C=NC(=NC=1)NC1CC2=CC=CC=C2C1)CC(=O)N1CC2=C(CC1)NN=N2)F SKIIKRJAQOSWFT-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 102000015081 Blood Coagulation Factors Human genes 0.000 description 1
- 108010039209 Blood Coagulation Factors Proteins 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 241000282465 Canis Species 0.000 description 1
- 208000032544 Cicatrix Diseases 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 206010012434 Dermatitis allergic Diseases 0.000 description 1
- 208000007163 Dermatomycoses Diseases 0.000 description 1
- 206010012504 Dermatophytosis Diseases 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 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 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005913 Maltodextrin Substances 0.000 description 1
- 229920002774 Maltodextrin Polymers 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 208000006311 Pyoderma Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 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 1
- 229930006000 Sucrose Natural products 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 231100000360 alopecia Toxicity 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 201000008937 atopic dermatitis Diseases 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 239000000022 bacteriostatic agent Substances 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 239000003114 blood coagulation factor Substances 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000007975 buffered saline Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 210000001736 capillary Anatomy 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 210000003372 endocrine gland Anatomy 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 239000003205 fragrance Substances 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
- 229960005150 glycerol Drugs 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 208000024963 hair loss Diseases 0.000 description 1
- 230000003676 hair loss Effects 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 229940035034 maltodextrin Drugs 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000000668 oral spray Substances 0.000 description 1
- 239000007935 oral tablet Substances 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 235000017924 poor diet Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 230000037387 scars Effects 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 230000008591 skin barrier function Effects 0.000 description 1
- 230000036560 skin regeneration Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
-
- 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
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
- A23L33/12—Fatty acids or derivatives thereof
-
- 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
- A23L33/15—Vitamins
-
- 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
- A23L33/16—Inorganic salts, minerals or trace elements
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/202—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
- A61K31/355—Tocopherols, e.g. vitamin E
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
- A61K33/30—Zinc; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- 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
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Abstract
Description
본 발명은 혈액 순환 촉진 및 피부 질환 개선용 조성물에 대한 것으로, 보다 구체적으로 혈액 순환을 촉진시키는 동시에 피부 질환을 개선하는 인간 및 동물용 조성물에 대한 것이다.The present invention relates to a composition for promoting blood circulation and improving skin diseases, and more particularly, for a composition for humans and animals that promotes blood circulation and improves skin diseases.
혈액 순환이란 혈액이 동물의 체내를 일정한 방향으로 유동하는 현상을 말하는 것으로 산소를 체내 각 조직에 공급하고 탄산가스를 방출하고, 영양소를 보급하고 대사 산물을 방출하며, 여러 내분비선에서 호르몬을 운반하여 특정 기관이 기능을 조절하며 그 밖에 병원균 조절작용과 체온 조절, 삼투압 조절, 수분 조절 등의 기능을 수행하는 과정이다. 혈액 순환 장애란 심장에서 펌프되어 나온 혈액이 동맥, 모세혈관, 정맥을 거쳐 다시 심장으로 돌아오는데 혈관이 탄력을 잃고 내벽에 콜레스테롤 등이 침착되어 혈관 내강이 좁아져 혈액 순환이 원활히 이루어지지 못하는 것을 말한다. 현대사회가 서구화되면서 잘못된 식생활과 스트레스, 운동부족 등으로 인해 혈액순환장애는 다양한 연령층에서 다양한 질병과 증상을 만들어 내고 있다. Blood circulation refers to the phenomenon in which blood flows in an animal's body in a certain direction. It supplies oxygen to each tissue in the body, releases carbon dioxide, supplies nutrients, releases metabolites, and carries hormones from various endocrine glands. The organ regulates the function, and in addition, it is the process of controlling pathogens, controlling body temperature, controlling osmotic pressure, and controlling water. Blood circulation disorder means that blood pumped from the heart returns to the heart through arteries, capillaries, and veins, and blood vessels lose elasticity and cholesterol is deposited on the inner wall, resulting in narrowing of the lumen of the vessels. As modern society has become westernized, blood circulation disorders have caused various diseases and symptoms in various age groups due to poor diet, stress and lack of exercise.
한편, 피부는 신체의 표면을 덮고 있으므로 피부 사상균, 칸디다 등의 여러 병원체에 접촉할 기회가 많아 감염되기 쉽고, 특히 동물의 피부 및 털에는 각종 세균, 곰팡이 및 효모균 등이 기생하여 피부 질환이 발생하기 쉽다. 실제 동물병원에서 자주 접하게 되는 증례가 피부 질환이며, 피부 질환의 치료를 위해 고가의 연고, 경구제제나 주사약제를 투약하는 실정이나 치료효과가 일시적이며 장기간 과다사용으로 인해 다른 장기 조직의 손상을 유발하기도 한다. On the other hand, since the skin covers the surface of the body, there are many opportunities for contact with various pathogens such as skin filamentous fungi, Candida, and the like, and are susceptible to infection. easy. Skin disease is a case often encountered in veterinary clinics. Expensive ointments, oral or injectable medications are used for the treatment of skin diseases, and the effects of treatment are temporary and long-term overuse causes damage to other organ tissues. Sometimes.
본 발명이 해결하고자 하는 과제는 혈액순환을 촉진시킬 뿐만 아니라 피부 질환의 개선에도 효과가 있고 인체 및 동물의 모두에 적용될 수 있는 혈액 순환 촉진 및 피부 질환 개선용 조성물을 제공하는 것이다. The problem to be solved by the present invention is to provide a composition for promoting blood circulation and improving skin diseases, which is effective not only to promote blood circulation but also to improve skin diseases and can be applied to both humans and animals.
본 발명이 해결하려는 다른 과제는 혈액순환을 촉진시킬 뿐만 아니라 피부 질환의 개선에도 효과가 있고 인체 및 동물의 모두에 적용될 수 있는 혈액 순환 촉진 및 피부 질환 개선용 식품을 제공하는 것이다. Another problem to be solved by the present invention is to provide a food for promoting blood circulation and improving skin diseases, which is effective in improving skin diseases as well as promoting blood circulation and applicable to both humans and animals.
본 발명의 기술적 과제들은 이상에서 언급한 기술적 과제로 제한되지 않으며, 언급되지 않은 또 다른 기술적 과제들은 아래의 기재로부터 당업자에게 명확하게 이해될 수 있을 것이다.The technical objects of the present invention are not limited to the technical matters mentioned above, and other technical subjects not mentioned can be clearly understood by those skilled in the art from the following description.
상기 과제를 해결하기 위해, 본 발명의 일 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 에이코사펜타엔산(EPA), 도코사헥사엔산(DHA), 비타민 E 및 황산 아연을 포함한다. In order to solve the above problems, the composition for promoting blood circulation and skin disease improvement according to an embodiment of the present invention comprises eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), vitamin E and zinc sulfate do.
상기 다른 과제를 해결하기 위해, 본 발명의 다른 실시예에 따른 혈액 순환의 촉진 및 피부 질환 개선용 식품은 에이코사펜타엔산 30 내지 70중량%, 도코사헥사엔산 20 내지 60 중량%, 비타민 E 2 내지 30 중량% 및 황산 아연 0.1 내지 10 중량%를 포함한다. In order to solve the other problem, food for promoting blood circulation and improving skin diseases according to another embodiment of the present invention 30 to 70% by weight of eicosapentaenoic acid, 20 to 60% by weight of docosahexaenoic acid, vitamins E 2-30 wt% and zinc sulfate 0.1-10 wt%.
기타 실시예들의 구체적인 사항들은 상세한 설명에 포함되어 있다.The details of other embodiments are included in the detailed description.
본 발명의 일 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 동물 및 인간에 대해 혈액 순환 촉진 능력이 우수할 뿐만 아니라 피부 질환의 치료에도 효과를 나타낸다. The composition for promoting blood circulation and improving skin diseases according to an embodiment of the present invention not only has an excellent ability to promote blood circulation in animals and humans but also has an effect on the treatment of skin diseases.
본 발명의 조성물은 동물 및 사람의 피부에 생긴 염증 완화에 효과를 나타내며 피부에 대한 독성이 작다. The composition of the present invention has an effect on relieving inflammation in the skin of animals and humans and has low toxicity to the skin.
본 발명의 조성물은 피부 감염에 따른 가려움증을 완화시키고 피부에 보습력을 제공할 뿐만 아니라 재생 능력이 우수하여 빠른 치료효과를 나타낸다. The composition of the present invention not only relieves the itch caused by skin infection and provides moisturizing power to the skin, but also exhibits a rapid therapeutic effect due to its excellent regenerative ability.
본 발명의 조성물은 제형화에 구애받지 않고 다양한 제형으로 제조될 수 있으며, 경구용으로 사용가능하므로 다양한 식품에 첨가물처럼 활용하는 것도 가능하며, 애완동물의 간식 등으로 제조할 수도 있다. The composition of the present invention can be prepared in a variety of formulations, regardless of the formulation, and can be used orally, so it can be used as an additive to a variety of food, it can also be prepared as a snack for pets.
본 발명에 따른 효과는 이상에서 예시된 내용으로 제한되지 않으며, 더욱 다양한 효과들이 본 명세서 내에 포함되어 있다.The effects according to the present invention are not limited to the contents exemplified above, and more various effects are included in the specification.
본 발명의 이점 및 특징, 그리고 그것들을 달성하는 방법은 상세하게 후술되어 있는 실시예들을 참조하면 명확해질 것이다. 그러나 본 발명은 이하에서 개시되는 실시예들에 한정되는 것이 아니라 서로 다른 다양한 형태로 구현될 수 있으며, 단지 본 실시예들은 본 발명의 개시가 완전하도록 하고, 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 발명의 범주를 완전하게 알려주기 위해 제공되는 것이며, 본 발명은 청구항의 범주에 의해 정의될 뿐이다.Advantages and features of the present invention and methods of achieving them will become apparent with reference to the embodiments described in detail below. The present invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. To fully disclose the scope of the invention to those skilled in the art, and the invention is only defined by the scope of the claims.
본 명세서에서, 단수형은 문구에서 특별히 언급하지 않는 한 복수형도 포함하며, "포함한다(comprises)" 및/또는 "포함하는(comprising)" 은 하나 이상의 다른 구성요소의 존재 또는 추가를 배제하지 않는다. In the present specification, the singular forms include plural forms unless the context clearly dictates otherwise, and "comprises" and / or "comprising" do not exclude the presence or addition of one or more other constituents.
이하, 당업자가 명확하게 이해할 수 있도록 본 발명을 상세하게 설명한다. Hereinafter, the present invention will be described in detail so that those skilled in the art can clearly understand.
본 발명의 일 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 에이코사펜타엔산(Eicosapentaenoic acid, EPA)(A)를 포함한다. 에이코사펜타엔산(A)은 생체 내에서 프로스타글란딘(prostaglandin) 및 류코트리엔(leukotrien)의 전구체가 될 수 있는 필수 지방산으로 불포화 ω-3 지방산의 일종이다. 에이코사펜타엔산(A)은 혈중 콜레스테롤 수치를 낮추고 혈액 순환을 촉진하는 역할을 한다. 또한, 에이코사펜타엔산(A)은 피부 질환, 예를 들어, 건선, 가려움증, 염증 및 다양한 피부 질환의 치료에 효과를 나타낸다. 구체적으로, 상기 피부 질환은 동물에게 나타나는 진균성 피부 질환, 개선충성 피부 질환, 지루성 피부 질환, 화농성 질환인 농피증, 알러지성 피부염 등을 포함한다. 에이코사펜타엔산(A)은 피부에 보습력을 제공하고 재생력을 향상시킴으로써 가려움증을 완화하고 염증을 개선한다. 구체적으로, 사람이 아닌 개나 고양이 등의 애완동물의 경우 피부가 털로 덮여 있어 다양한 병원성 세균, 진균, 효모균 등의 미생물 및 기생충에 감염될 확률이 높다. 미생물이나 기생충에 감염되는 경우 가려움증이 유발되고 이로 인해 피부 장벽이 손상되어 탈수가 가속화되는데, 에이코사펜타엔산(A)은 피부를 재생시켜 탈수를 억제시키고 가려움증을 완화하는 역할을 한다.Composition for promoting blood circulation and improving skin diseases according to an embodiment of the present invention includes Eicosapentaenoic acid (EPA) (A). Eicosapentaenoic acid (A) is an essential fatty acid that can be a precursor of prostaglandin and leukotrien in vivo and is a type of unsaturated ω-3 fatty acid. Eicosapentaenoic acid (A) lowers blood cholesterol levels and promotes blood circulation. In addition, eicosapentaenoic acid (A) is effective in the treatment of skin diseases such as psoriasis, itching, inflammation and various skin diseases. Specifically, the skin diseases include fungal skin diseases, ameliorative skin diseases, seborrheic skin diseases, pyoderma, purulent diseases, allergic dermatitis, and the like, which appear in animals. Eicosapentaenoic acid (A) relieves itching and improves inflammation by providing moisture to the skin and improving regeneration. Specifically, pets such as dogs or cats, which are not humans, are covered with hairs, and thus are highly likely to be infected with microorganisms and parasites such as various pathogenic bacteria, fungi and yeasts. Infection with microorganisms or parasites causes itching and damages the skin barrier resulting in accelerated dehydration. Eicosapentaenoic acid (A) regenerates the skin to inhibit dehydration and relieve itching.
에이코사펜타엔산(A)은 조성물에 대해 30 내지 70 중량부로 포함될 수 있으며, 구체적으로, 40 내지 60 중량부로 포함될 수 있다. 에이코사펜타엔산(A)이 30 중량부 미만으로 포함되는 경우 혈액 순환의 촉진 및 피부 질환의 개선 효과가 우수하며, 70 중량부를 초과하는 경우 오히려 혈중 지질 및 응고 인자가 상승하여 혈액 순환 효과가 감소하는 경향을 나타낼 수 있다.Eicosapentaenoic acid (A) may be included in an amount of 30 to 70 parts by weight, and specifically, 40 to 60 parts by weight of the composition. When eicosapentaenoic acid (A) is included in an amount less than 30 parts by weight, the effect of promoting blood circulation and improving skin diseases is excellent. If it exceeds 70 parts by weight, blood lipids and coagulation factors are increased to increase blood circulation effects. It may show a tendency to decrease.
본 발명의 일 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 도코사헥사엔산(Docosahexaenoic acid, DHA)(B)을 포함한다. 도코사헥사엔산(B)도 에이코사펜타엔산(A)과 마찬가지로 필수 지방산으로 불포화 ω-3 지방산의 일종이다. 도코사헥사엔산(B)은 혈액 응고를 억제하고 혈관을 확장하여 혈압을 낮출 뿐만 아니라 혈액 응고를 억제하는 역할을 하므로, 결과적으로 혈액 순환을 개선시킨다. 또한, 도코사헥사엔산(B)은 피부의 보습력 및 재생력을 향상시켜 피부 질환의 개선에 효과를 나타낸다. 즉, 피부에 보습력을 제공하므로 가려움증이 완화되고, 재생력을 향상시켜 염증 및 상처의 치료에 효과적이다. Composition for promoting blood circulation and improving skin diseases according to an embodiment of the present invention includes docosahexaenoic acid (Docosahexaenoic acid, DHA) (B). Docosahexaenoic acid (B), like eicosapentaenoic acid (A), is an essential fatty acid and is a type of unsaturated ω-3 fatty acid. Docosahexaenoic acid (B) inhibits blood coagulation and dilates blood vessels, thereby lowering blood pressure as well as inhibiting blood coagulation, thereby improving blood circulation. In addition, docosahexaenoic acid (B) is effective in improving skin diseases by improving the moisturizing and regenerating power of the skin. That is, because it provides moisture to the skin, itching is alleviated, and regeneration is improved, which is effective in treating inflammation and wounds.
도코사헥사엔산(B)은 조성물에 대하여 20 내지 60 중량부, 구체적으로 30 내지 50 중량부로 포함될 수 있다. 도코사헥사엔산(B)이 20 중량부 미만으로 포함되는 경우 혈액 순환 촉진 및 피부 질환 개선 효과가 나타나지 않을 수 있으며, 60 중량부를 초과하는 경우 혈액 순환 효과가 감소할 수 있으며, 피부에 자극을 초래할 수 있다.Docosahexaenoic acid (B) may be included in 20 to 60 parts by weight, specifically 30 to 50 parts by weight based on the composition. When docosahexaenoic acid (B) is included in less than 20 parts by weight may not exhibit the effect of promoting blood circulation and improving skin diseases, and in excess of 60 parts by weight may reduce the blood circulation effect, irritating the skin Can cause.
본 발명의 일 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 비타민 E(C)를 포함한다. 비타민 E vitamin E)(C)는 지용성 비타민의 일종으로 일반적으로 토코페롤(tocopherol)로 부른다. 비타민 E(C)는 에이코사펜타엔산(A) 및 도코사헥사엔산(B)이 산화되는 것을 막으며, 에이코사펜타엔산(A) 및 도코사헥사엔산(B)과 함께 사용시 혈액 순환을 더욱 촉진시킨다. 또한, 피부 재생력을 향상시켜 상처의 치유를 빠르게 하며 염증을 감소시키고 흉터를 남지 않게 하는 효과가 있다. 따라서, 비타민 E(C)를 에이코사펜타엔산(A) 및 도코사헥사엔산(B)과 병용하는 경우 동물이나 사람의 피부 질환 개선 효과를 증가시킨다. Composition for promoting blood circulation and skin disease improvement according to an embodiment of the present invention includes vitamin E (C). Vitamin E vitamin E) (C) is a type of fat-soluble vitamin, commonly referred to as tocopherol. Vitamin E (C) prevents the oxidation of eicosapentaenoic acid (A) and docosahexaenoic acid (B), and when used with eicosapentaenoic acid (A) and docosahexaenoic acid (B) Further promote blood circulation. In addition, it improves the skin regeneration ability to speed up the healing of wounds, reduce inflammation and leave no scars. Therefore, when vitamin E (C) is used in combination with eicosapentaenoic acid (A) and docosahexaenoic acid (B), the effect of improving skin diseases in animals or humans is increased.
비타민 E(C)는 조성물에 대하여 2 내지 30 중량부, 구체적으로 10 내지 20 중량부로 포함될 수 있다. 비타민 E(C)가 2 중량부 미만으로 포함되는 경우 혈액 순환 촉진 및 피부 질환 개선 효과가 미미하며 30 중량부로 포함되는 경우 두통 또는 소화기능 장애 등을 유발할 수 있다. Vitamin E (C) may be included in 2 to 30 parts by weight, specifically 10 to 20 parts by weight based on the composition. If the vitamin E (C) is included in less than 2 parts by weight of the blood circulation and skin disease improvement effects are insignificant, and when included in 30 parts by weight can cause headaches or digestive problems.
본 발명의 일 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 황산 아연(Zinc sulfate, ZnSO4)(D)을 포함한다. 황산 아연(D)은 생체 내에 콜레스테롤의 축적을 감소시켜 혈류 개선에 효과를 가져올 수 있으며, 피부에 생긴 상처 치유에 도움을 준다. 또한, 황산 아연(D)은 에이코사펜타엔산(A) 및 도코사헥사엔산(B)과 함께 사용되는 경우 이들의 혈액 순환 촉진 및 피부 질환 개선 효능을 상승시키는 역할을 한다. Composition for promoting blood circulation and improving skin diseases according to an embodiment of the present invention comprises zinc sulfate (Zinc sulfate, ZnSO 4 ) (D). Zinc sulfate (D) can reduce the accumulation of cholesterol in the body, thereby improving blood flow, and helps to heal wounds on the skin. In addition, zinc sulfate (D) when used in conjunction with eicosapentaenoic acid (A) and docosahexaenoic acid (B) serves to promote their blood circulation and skin disease improvement efficacy.
황산 아연(D)은 조성물에 대하여 0.1 내지 10 중량부로 포함될 수 있으며, 구체적으로 1 내지 5 중량부로 포함될 수 있다. 황산 아연(D)이 0.1 중량부 미만으로 포함되는 경우 혈액 순환 촉진 및 피부 질환 개선 효과가 미미할 수 있으며, 10 중량부를 초과하여 포함되는 경우 피부에 자극을 초래하거나 장기간 복용하는 경우 소화장애를 일으킬 수 있다.Zinc sulfate (D) may be included in an amount of 0.1 to 10 parts by weight, and specifically 1 to 5 parts by weight, based on the composition. If it contains less than 0.1 parts by weight of zinc sulfate (D) may be less effective in promoting blood circulation and improving skin diseases, if contained in more than 10 parts by weight may cause irritation to the skin or digestive problems if taken for a long time have.
본 발명의 다른 실시예에 따른 혈액 순환 촉진 및 피부 질환 개선용 조성물은 에이코사펜타엔산 30 내지 70 중량%, 도코사헥사엔산 20 내지 60 중량%, 비타민 E 2 내지 30 중량% 및 황산 아연 0.1 내지 10 중량%를 포함할 수 있다. 상기 조성물은 혈액 순환 촉진 및 피부 질환 개선에 효과가 우수할 뿐만 아니라 장기간 복용하여도 다른 장기 조직에 이상이 발생하지 않으며 피부 또는 점막 등에 직접 적용하여도 자극이 적다. Composition for promoting blood circulation and skin disease improvement according to another embodiment of the present invention is eicosapentaenoic acid 30 to 70% by weight, docosahexaenoic acid 20 to 60% by weight, vitamin E 2 to 30% by weight and zinc sulfate 0.1 to 10% by weight. The composition is not only excellent in promoting blood circulation and improving skin diseases, but also does not cause abnormalities in other organ tissues even after long-term use, and has little irritation even when applied directly to skin or mucous membranes.
본 발명의 혈액 순환 촉진 및 피부 질환 개선용 조성물은 다양한 식품으로 제형화될 수 있으며, 구체적으로 음료, 껌, 정제, 환제, 캅셀, 과립제 초코렛, 캔디류, 스넥류, 아이스크림 등 경구 섭취를 위한 일반적인 건강 기능 식품의 형태로 제형화될 수 있다. 또한, 애완 동물용 경구용 제제, 구체적으로 애완 동물용 정제, 캡슐, 액체, 겔, 페이스트, 경구용 스프레이, 구강정, 산제 및 씹어먹는 트리트(chewable treat) 또는 동물 사료 등으로 제형화될 수 있으나 이에 한정되는 것은 아니다. 제형화시 일반적으로 사용하는 충진제, 증량제, 결합제, 수분제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용할 수 있으며, 부형제로 전분, 탄산 칼슘, 수크로스, 락토오스 또는 젤라틴 등을 사용할 수 있다. 이외에 마그네슘 스테아레이트 탈크 등의 윤활제를 사용할 수 있다. The composition for promoting blood circulation and improving skin diseases of the present invention may be formulated into various foods, and in particular, general health functions for oral intake such as beverages, gums, tablets, pills, capsules, granulated chocolates, candy, snacks, ice cream, etc. It may be formulated in the form of a food. It may also be formulated as an oral preparation for pets, specifically pet tablets, capsules, liquids, gels, pastes, oral sprays, oral tablets, powders and chewable treats or animal feeds. It is not limited to this. In formulating, diluents or excipients such as fillers, extenders, binders, moisture agents, disintegrants, surfactants, etc. which are generally used may be used, and starch, calcium carbonate, sucrose, lactose or gelatin may be used as excipients. In addition, lubricants, such as magnesium stearate talc, can be used.
본 발명의 혈액 순환 촉진 및 피부 질환 개선용 조성물은 피부 및 점막에 적용되는 연고, 크림, 유액, 고약, 파우더, 함침 패드, 용액, 겔, 스프레이, 로션 또는 현탁액 형태의 피부 외용제로 제형화될 수 있다. 이 때, 투여를 위해서 상술한 활성 성분 이외에 추가로 담체를 1종 이상 포함할 수 있다. 상기 담체로 식염수, 멸균수, 링거액, 완충 식염수, 덱스트로즈 용액, 말토 덱스트린 용액, 글리세롤 및 에탄올로 이루어진 군으로부터 선택된 단독 또는 이들의 혼합물을 사용할 수 있으며, 필요에 따라 항산화제, 완충액, 정균제 등 다른 통상의 첨가제를 첨가할 수 있다. 또한 희석제, 분산제, 계면활성제, 결합제 및 윤활제를 부가적으로 첨가하여 제제화할 수 있다. The composition for promoting blood circulation and improving skin diseases of the present invention may be formulated as an external preparation for skin in the form of an ointment, cream, emulsion, plaster, powder, impregnation pad, solution, gel, spray, lotion or suspension applied to the skin and mucous membranes. have. At this time, in addition to the above-mentioned active ingredient for administration may comprise at least one carrier. As the carrier, saline, sterile water, Ringer's solution, buffered saline, dextrose solution, maltodextrin solution, glycerol and ethanol alone or mixtures thereof may be used, and antioxidants, buffers, bacteriostatic agents, etc. may be used as necessary. Other conventional additives can be added. It may also be formulated by additionally adding diluents, dispersants, surfactants, binders and lubricants.
본 발명의 피부 감염의 치료 및 예방을 위한 조성물은 화장료 조성물로 제조될 수 있다. 본 발명의 화장료 조성물은 상기 성분 외에 본 발명의 목적을 해치지 않는 범위 내에서 통상 화장료에 사용되는 각종 성분을 배합할 수 있다. 구체적으로 예를 들어, 라놀린, 스쿠알렌 등의 천연 동식물 유지류, 스테아릴알코올, 이소스테아릴알콜 등의 고급 알콜류, 글리세린, 히알론산 등의 보습제, 비타민 C, 자외선 흡수제, 자외선 차폐제, 방부제, 점도 조정제, 안료, 향료 등을 당업자의 필요에 따라 임의의 함량으로 배합할 수 있다. 상기 화장료 조성물은 화장수, 크림, 클렌징 크림, 클렌징 폼, 클렌징 워터, 파우더, 에센스, 팩, 연고, 비누 또는 샴푸 등의 제형을 가질 수 있다. 이는 인간은 물론 동물에 적용되는 화장료 조성물로 제조될 수 있음은 물론이다. Compositions for the treatment and prevention of skin infections of the invention may be prepared as cosmetic compositions. The cosmetic composition of this invention can mix | blend the various components normally used for cosmetics in the range which does not impair the objective of this invention other than the said component. Specifically, For example, natural animal and vegetable oils, such as lanolin and squalene, higher alcohols, such as stearyl alcohol and isostearyl alcohol, moisturizing agents, such as glycerin and hyaluronic acid, vitamin C, a ultraviolet absorber, a ultraviolet shield, a preservative, a viscosity modifier, Pigments, fragrances and the like may be blended in any amount as required by those skilled in the art. The cosmetic composition may have a formulation such as lotion, cream, cleansing cream, cleansing foam, cleansing water, powder, essence, pack, ointment, soap or shampoo. Of course, it can be made of a cosmetic composition that is applied to humans as well as animals.
이하, 실시예를 통하여 본 발명을 보다 구체적으로 설명한다. 이는 본 발명의 설명을 위한 것일 뿐, 이로 인해 본 발명의 범위가 제한되지 않는다. Hereinafter, the present invention will be described more specifically by way of examples. This is for the purpose of illustrating the present invention, and thus the scope of the present invention is not limited thereto.
<< 실시예Example 1 내지 17> 혈액 순환 촉진 및 피부 질환 개선용 조성물의 제조 1 to 17> Preparation of a composition for promoting blood circulation and improving skin diseases
하기 표 1 및 2의 조성으로 혼합하여 혈액 순환 촉진 및 피부 질환 개선용 조성물을 제조하였다. 하기 표 1 및 2의 단위는 g이다. By mixing to the compositions of Tables 1 and 2 to prepare a composition for promoting blood circulation and improving skin diseases. The units of Tables 1 and 2 below are g.
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
100To
100
<< 비교예Comparative example 1 내지 4> 혈액 순환 촉진 및 피부 질환 개선용 조성물의 제조 1 to 4> Preparation of a composition for promoting blood circulation and improving skin diseases
하기 표 3의 조성으로 혼합하여 혈액 순환 촉진 및 피부 질환 개선용 조성물을 제조하였다. 하기 표 3의 단위는 g이다. By mixing to the composition of Table 3 to prepare a composition for promoting blood circulation and improving skin diseases. The unit of Table 3 below is g.
<< 제조예Manufacturing example 1> 1> 드링크의Drink 제조 Produce
하기 표 3의 조성을 혼합하고 병에 충진하여 드링크제를 제조하였다. 하기 표 4의 단위는 mg이다. The composition of Table 3 was mixed and filled into bottles to prepare a drink. The unit of Table 4 below is mg.
<< 제조예Manufacturing example 2> 정제의 제조 2> Preparation of tablets
하기 표 5의 조성을 혼합하여 30% 에탄올 40 mg을 첨가하여 과립을 형성한 후, 60 ℃에서 건조하고 타정기를 이용하여 정제하여 타정하였다. 하기 표 4의 단위는 mg이다. The composition of Table 5 was mixed to form granules by adding 40 mg of 30% ethanol, dried at 60 ° C., and purified by tableting. The unit of Table 4 below is mg.
<< 제조예Manufacturing example 3> 껌의 제조 3> Manufacture of gum
하기 표 6의 조성으로 혈액 순환 촉진 및 피부 질환 개선용 껌을 제조하였다. 하기 표 6의 단위는 mg이다.To prepare a gum for promoting blood circulation and improving skin diseases with the composition of Table 6. The unit of Table 6 below is mg.
<< 제조예Manufacturing example 3> 피부 외용 연고의 제조 3> Preparation of skin external ointment
하기 표 7의 조성으로 피부 외용 연고를 제조하였다. 구체적으로 하기 표 4와 같이 유성 성분, 수성 성분, 계면활성제 등이 포함된 크림 베이스에 구성 성분을 혼합하여 혼합기에서 잘 유화시키고, 탈기, 여과 및 냉각시킨 후, 첨가제로서 향료 및 색소를 첨가하고, 적은 양의 유성 성분이 존재하도록 수중유형(oil/water)으로 연고를 제조하였다. 하기 표 7의 단위는 mg이다.To the skin ointment was prepared in the composition of Table 7. Specifically, as shown in Table 4, after mixing the constituents in the cream base containing an oil component, an aqueous component, a surfactant, etc., emulsify well in a mixer, degassing, filtration and cooling, and then add flavoring and coloring as additives, Ointments were prepared in oil / water so that small amounts of oily components were present. The unit in Table 7 below is mg.
<< 실험예Experimental Example 1> 혈소판 응집 억제 활성의 측정 1> Determination of platelet aggregation inhibitory activity
비글견에 5일 동안 상기 실시예 1 내지 17 및 비교예 1 내지 4 에서 제조한 조성물을 경구 섭취하게 한 뒤, 투여 시간 별로 채혈하였다. 채혈한 혈액은 0.38% 소듐 시트레이트(sodium citrate)를 처리하여 혈액의 응고를 억제하였다. 혈액을 원심분리하여 얻어진 PRP (platelet rich plasma)층은 혈소판 응집능 분석기를 사용하여 agonist인 콜라겐을 넣고 4분간 빛 투과도를 tracing 하여 혈액의 응집을 관찰하였다. 조성물 투여 전 혈소판 응집율을 100%로 하여 혈소판 응집 억제 활성을 계산하였다. 그 결과는 하기 표 8과 같다. After beagle dogs were orally ingested the compositions prepared in Examples 1 to 17 and Comparative Examples 1 to 4 for 5 days, blood was collected for each administration time. Blood collected was treated with 0.38% sodium citrate to inhibit coagulation. The platelet rich plasma (PRP) layer obtained by centrifugation of blood was added to collagen as an agonist using a platelet aggregation ability analyzer and tracing the light transmittance for 4 minutes to observe the aggregation of blood. Platelet aggregation inhibitory activity was calculated by making platelet aggregation rate 100% before administration of a composition. The results are shown in Table 8 below.
표 8에 의하면, 에이코사펜타엔산 (EPA)과 도코헥사엔산 (DHA)을 모두 포함하는 실시예의 조성물은 이들 중 하나만을 사용하는 비교예 1 및 2의 조성물에 비해 혈소판 응집 활성이 우수하였다. 따라서, 에이코사펜타엔산 (EPA)과 도코헥사엔산 (DHA)을 모두 사용하는 경우 단독으로 사용하는 경우에 비해 혈액 순환 촉진 효과가 우수함을 알 수 있다. 또한, 비타민 E 를 포함하지 않거나 황산 아연을 포함하지 않는 비교예 3 및 4의 조성물도 실시예에 비해 혈소판 응집 활성이 열악하였다. 또한, 에이코사펜타엔산 (EPA)을 30 내지 70 중량%, 특히 40 내지 60 중량%로 포함하는 경우와 도코헥사엔산 (DHA)을 20 내지 60 중량%, 특히 30 내지 50 중량%로 포함하는 조성물의 경우 그 효과가 우수하였다. According to Table 8, the composition of the example containing both eicosapentaenoic acid (EPA) and docohexaenoic acid (DHA) had better platelet aggregation activity than the compositions of Comparative Examples 1 and 2 using only one of them. . Therefore, when both eicosapentaenoic acid (EPA) and docohexaenoic acid (DHA) are used, it can be seen that the effect of promoting blood circulation is superior to that of using alone. In addition, the compositions of Comparative Examples 3 and 4, which did not contain vitamin E or did not contain zinc sulfate, were also poor in platelet aggregation activity compared with Examples. In addition, it contains 30 to 70% by weight of eicosapentaenoic acid (EPA), especially 40 to 60% by weight, and 20 to 60% by weight of docohexaenoic acid (DHA), in particular 30 to 50% by weight. The composition was excellent in the effect.
<< 실험예Experimental Example 2> 무모 마우스를 이용한 피부 감염증 치료 시험 2> Skin Infectious Disease Treatment Test Using Hairless Mouse
무모 마우스(hairless mouse)를 Staphylococcus aureus, Candida albicans, Microsporium canis 및 효모균에 감염시켜 홍반 및 염증 등을 일어나게 하고, 감염된 부위에 상기 실시예 및 비교예에서 제조한 조성물을 경구 투여하였다. 경구 투여의 방법으로는 상기 실시예 및 비교예에서 제조한 조성물을 무모 마우스에 1일 3회 각 회마다 2 mg씩 섭취하게 하였다. 섭취 후 24 시간 경과 후마다 피부 상태를 관찰하였다. Staphylococcus hairless mouse aureus , Candida albicans , Microsporium canis And infection with yeast causing erythema and inflammation, and the compositions prepared in Examples and Comparative Examples were orally administered to the infected sites. In the method of oral administration, the compositions prepared in Examples and Comparative Examples were ingested with 2 mg of the hairless mice three times each day. The skin condition was observed every 24 hours after ingestion.
상기 실험 결과, 실시예의 조성물을 경구 투여한 마우스의 경우 24시간 경과 후부터 염증이 가라앉고 홍반이 완화되었다. 반면에, 비교예의 조성물을 경구 투여한 마우스의 경우 48시간 경과 후에야 홍반이 완화되는 듯한 경향을 보였으며, 120시간 경과 후에도 여전히 염증이 존재하였다. 또한, 상기 시험 동안 무모 마우스에 어떠한 독성도 나타나지 않았다. As a result of the experiment, in the case of the oral administration of the composition of the Example, inflammation subsided after 24 hours and erythema was alleviated. On the other hand, in the oral administration of the composition of the comparative example, the erythema tended to alleviate only after 48 hours, and there was still inflammation after 120 hours. In addition, no toxicity was seen in hairless mice during the test.
<< 실험예Experimental Example 3> 개에서의 피부염 치료 효과 측정 3> Determination of dermatitis treatment effect in dogs
동일한 가정의 6 마리의 가정용 개를 선택하여 실험을 수행하였다. 실험 시에 두 동물은 피부염의 다수의 임상 징후, 특히 강한 가려움증, 즉, 긁기, 물기, 꼬리에서 탈모증 등을 나타내었다. 6 마리의 개()에게 동일한 먹이를 주었고, 동일한 조건 하에 함께 살도록 하였다. 개에서 실시예 및 비교예에서 제조한 조성물을 각각 먹이와 함께 매 10 ml씩 공급하였다. 2 마리의 개에게는 각각 실시예 10 및 11의 조성물을 먹이와 함께 공급하고 나머지 4마리의 개에게는 각각 비교예 1 내지 4의 조성물을 먹이와 함께 공급하였다.. 24 시간 경과 후 마다 피부 상태를 관찰하였다. 상기 실험 결과, 실시예의 조성물을 경구 투여한 개의 경우 6시간 경과 후부터 염증이 가라앉고 가려움증이 완화되어 120시간 후에는 거의 완치에 가까운 피부 상태를 나타내었으며, 탈모 증상도 완화되었다. 반면에, 비교예의 조성물을 경구 투여한 한 개 4마리 모두의 경우 48시간 경과 후에야 가려움증이 완화되는 듯한 경향을 보였으며, 120시간 경과 후에도 여전히 염증이 존재하였다. 또한, 상기 시험 동안 개에 어떠한 독성도 나타나지 않았다.상술한 바와 같이 실시예의 조성물을 섭취한 개는 비교예의 조성물을 섭취한 개보다 빠른 시간 내에 가려움증이 완화되는 한편, 이외에 기타 피부염 증상 들이 완화되는 것을 볼 수 있다. Experiments were performed with six domestic dogs of the same household selected. In the experiment, both animals showed a number of clinical signs of dermatitis, especially strong itching, ie scratching, biting, alopecia in the tail, and the like. Six dogs () were fed the same food and were allowed to live together under the same conditions. In dogs, the compositions prepared in Examples and Comparative Examples were each fed with 10 ml each with food. Two dogs were fed with the compositions of Examples 10 and 11, respectively, with food, and the other four dogs were fed with the compositions of Comparative Examples 1-4, respectively, with food. Skin condition was observed every 24 hours. It was. As a result of the experiment, the dogs orally administered the composition of the example, the inflammation subsided after 6 hours, the itch was alleviated, and after 120 hours, the skin condition was almost completely cured, and the hair loss symptoms were also alleviated. On the other hand, all four dogs orally administered with the composition of Comparative Example tended to relieve itching after 48 hours, and there was still inflammation after 120 hours. In addition, there was no toxicity to the dogs during the test. As described above, dogs ingesting the composition of the Example relieved itching in less time than dogs ingesting the composition of the Comparative Example, while other dermatitis symptoms were alleviated. can see.
이상 첨부된 도면을 참조하여 본 발명의 실시예를 설명하였지만, 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자는 본 발명이 그 기술적 사상이나 필수적인 특징을 변경하지 않고서 다른 구체적인 형태로 실시될 수 있다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다.While the present invention has been described in connection with what is presently considered to be practical exemplary embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, You will understand. It is therefore to be understood that the above-described embodiments are illustrative in all aspects and not restrictive.
Claims (10)
상기 에이코사펜틴산이 조성물에 대해 30 내지 70 중량부로 포함되는 혈액순환 촉진 및 피부 질환 개선용 조성물.The method of claim 1,
A composition for promoting blood circulation and improving skin diseases, wherein the eicosapentanic acid is included in an amount of 30 to 70 parts by weight based on the composition.
상기 도코사헥사에노산이 조성물에 대해 20 내지 60 중량부로 포함되는 혈액순환 촉진 및 피부 질환 개선용 조성물.The method of claim 1,
The docosahexaenoic acid is 20 to 60 parts by weight based on the composition for promoting blood circulation and skin disease composition.
상기 비타민 E가 조성물에 대해 2 내지 30 중량부로 포함되는 혈액순환 촉진 및 피부 질환 개선용 조성물.The method of claim 1,
The vitamin E is a composition for promoting blood circulation and skin diseases comprising 2 to 30 parts by weight with respect to the composition.
상기 황산 아연이 조성물에 대해 0.1 내지 10 중량부로 포함되는 혈액순환 촉진 및 피부 질환 개선용 조성물. The method of claim 1,
The zinc sulfate is 0.1 to 10 parts by weight based on the composition for promoting blood circulation and improving skin diseases.
상기 에이코사펜틴산 30 내지 70 중량%, 상기 도코헥사에노산 20 내지 60 중량%, 상기 비타민 E 2 내지 30 중량%, 및 상기 황산 아연 0.1 내지 10 중량%를 포함하는 혈액순환 촉진 및 피부 질환 개선용 조성물.The method of claim 1,
30 to 70% by weight of the eicosapentanic acid, 20 to 60% by weight of the docohexaenoic acid, 2 to 30% by weight of the vitamin E, and 0.1 to 10% by weight of zinc sulfate to promote blood circulation and improve skin diseases Composition.
상기 조성물이 경구투여용 제제인 혈액순환 촉진 및 피부 질환 개선용 조성물. The method of claim 1,
Composition for promoting blood circulation and improving skin disease, wherein the composition is an oral preparation.
상기 조성물이 동물에게 투여되는 혈액순환 촉진 및 피부 질환 개선용 조성물. The method of claim 7, wherein
A composition for promoting blood circulation and improving skin diseases, wherein the composition is administered to an animal.
상기 식품이 동물용 식품인 혈액순환 촉진 및 피부 질환 개선용 식품. 10. The method of claim 9,
Food for promoting blood circulation and improving skin diseases wherein the food is an animal food.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020120019827A KR101681907B1 (en) | 2012-02-27 | 2012-02-27 | Composition for promoting circulation of blood and improving skin disease |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020120019827A KR101681907B1 (en) | 2012-02-27 | 2012-02-27 | Composition for promoting circulation of blood and improving skin disease |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20130098038A true KR20130098038A (en) | 2013-09-04 |
KR101681907B1 KR101681907B1 (en) | 2016-12-12 |
Family
ID=49450132
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020120019827A KR101681907B1 (en) | 2012-02-27 | 2012-02-27 | Composition for promoting circulation of blood and improving skin disease |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR101681907B1 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20070098954A (en) * | 1999-02-17 | 2007-10-05 | 파마시아 이탈리아 에스.피.에이. | A pharmaceutical composition containing essential fatty acids in the prevention of cardiovascular events |
JP2009504588A (en) * | 2005-08-10 | 2009-02-05 | ブルツツエーゼ,テイベリオ | Composition of n-3 fatty acids having a high concentration of EPA and / or DHA and containing n-6 fatty acids |
KR20120000109A (en) * | 2009-04-29 | 2012-01-03 | 아마린 파마, 인크. | Stable pharmaceutical composition and methods of using same |
-
2012
- 2012-02-27 KR KR1020120019827A patent/KR101681907B1/en active IP Right Grant
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20070098954A (en) * | 1999-02-17 | 2007-10-05 | 파마시아 이탈리아 에스.피.에이. | A pharmaceutical composition containing essential fatty acids in the prevention of cardiovascular events |
JP2009504588A (en) * | 2005-08-10 | 2009-02-05 | ブルツツエーゼ,テイベリオ | Composition of n-3 fatty acids having a high concentration of EPA and / or DHA and containing n-6 fatty acids |
KR20120000109A (en) * | 2009-04-29 | 2012-01-03 | 아마린 파마, 인크. | Stable pharmaceutical composition and methods of using same |
Also Published As
Publication number | Publication date |
---|---|
KR101681907B1 (en) | 2016-12-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP7242718B2 (en) | Formulations containing pomegranate seed oil, rosa canina fruit oil, and inula viscosa oleoresin or extract | |
CA1272450A (en) | Composition for the treatment of acne | |
CA3067924A1 (en) | Topical dermatologic acne treatment cream composition and method of manufacture | |
US20230338435A1 (en) | Topical composition comprised of cod li ver oil for treating wounds and skin disorders | |
US10463699B2 (en) | Fish oil topical composition | |
US20140199413A1 (en) | Melatonin and an antimicrobial or antibacterial agent for the treatment of acne | |
ES2249008T3 (en) | COMPOSITIONS FOR THE TREATMENT OF ACNE. | |
US10588979B1 (en) | Cannabinoid and terpene-infused topical cream | |
KR101681907B1 (en) | Composition for promoting circulation of blood and improving skin disease | |
KR20110138709A (en) | Composition for improving acne comprising 5-aminolevulinic acid or ester thereof | |
RU2405535C1 (en) | Foot care cream-gel | |
FR2558058A1 (en) | Metronidazole based dermatological compositions for external topical use, which are useful in the treatment of acne | |
RU2469704C1 (en) | Regenerin serum for external application with anti-inflammatory and regenerative effect | |
CN111700825B (en) | Oily composition for oral health care, preparation method and application thereof | |
RU2811227C1 (en) | Antibacterial hand spray | |
FI129488B (en) | Salve composition, method of manufacture and use of the composition | |
GB2481629A (en) | Anti-acne composition | |
RU2310435C1 (en) | Cosmetic cream | |
WO2023218391A1 (en) | Extracts in eutectic solvent of olive oil polyphenols, compositions, uses and methods of preparation thereof | |
KR20210034797A (en) | Cosmetic composition for improving acne of skin comprising quercetin, terpene and vitamin k | |
WO2019178658A2 (en) | Healing, moisturizing, humectant and emolient composition for topical administration in intertrigo skin lesions, skin lesions due to urinary and faecal incontinence and other related injuries. | |
KR20190132197A (en) | Cosmetic composition for use in the treatment and prevention of acne-prone skin | |
EA037232B1 (en) | Lotion for treatment of acne manifestations, such as comedones, seborrhea, acneiform rash, red spots on skin | |
JP2019011261A (en) | External composition | |
SK18652000A3 (en) | PHARMACEUTICAL COMPOSITION ON THE BASIS OF ERYTHROMYCIN FATTYì (54) ACID SALTS FOR THE TOPICAL TREATMENT OF SKIN DISEASES |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
FPAY | Annual fee payment |
Payment date: 20190916 Year of fee payment: 4 |