CN110448687A - A kind of whitening lozenge containing SOD component - Google Patents
A kind of whitening lozenge containing SOD component Download PDFInfo
- Publication number
- CN110448687A CN110448687A CN201910898242.XA CN201910898242A CN110448687A CN 110448687 A CN110448687 A CN 110448687A CN 201910898242 A CN201910898242 A CN 201910898242A CN 110448687 A CN110448687 A CN 110448687A
- Authority
- CN
- China
- Prior art keywords
- whitening
- sod
- melanin
- lozenge containing
- component according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 230000002087 whitening effect Effects 0.000 title claims abstract description 32
- 239000007937 lozenge Substances 0.000 title claims abstract description 29
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 49
- QNVSXXGDAPORNA-UHFFFAOYSA-N Resveratrol Natural products OC1=CC=CC(C=CC=2C=C(O)C(O)=CC=2)=C1 QNVSXXGDAPORNA-UHFFFAOYSA-N 0.000 claims abstract description 27
- LUKBXSAWLPMMSZ-OWOJBTEDSA-N Trans-resveratrol Chemical compound C1=CC(O)=CC=C1\C=C\C1=CC(O)=CC(O)=C1 LUKBXSAWLPMMSZ-OWOJBTEDSA-N 0.000 claims abstract description 27
- 235000021283 resveratrol Nutrition 0.000 claims abstract description 27
- 229940016667 resveratrol Drugs 0.000 claims abstract description 27
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims abstract description 26
- 235000005152 nicotinamide Nutrition 0.000 claims abstract description 26
- 229960003966 nicotinamide Drugs 0.000 claims abstract description 26
- 239000011570 nicotinamide Substances 0.000 claims abstract description 26
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229930003268 Vitamin C Natural products 0.000 claims abstract description 24
- 235000019154 vitamin C Nutrition 0.000 claims abstract description 24
- 239000011718 vitamin C Substances 0.000 claims abstract description 24
- 230000000694 effects Effects 0.000 claims abstract description 18
- 229920002472 Starch Polymers 0.000 claims abstract description 17
- 239000002002 slurry Substances 0.000 claims abstract description 17
- 239000008107 starch Substances 0.000 claims abstract description 17
- 235000019698 starch Nutrition 0.000 claims abstract description 17
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims abstract description 16
- 239000008108 microcrystalline cellulose Substances 0.000 claims abstract description 16
- 229940016286 microcrystalline cellulose Drugs 0.000 claims abstract description 16
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims abstract description 15
- 239000000314 lubricant Substances 0.000 claims abstract description 7
- 235000020985 whole grains Nutrition 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 13
- 102000004190 Enzymes Human genes 0.000 claims description 12
- 108090000790 Enzymes Proteins 0.000 claims description 12
- -1 One of sorbierite Chemical compound 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 8
- 238000005469 granulation Methods 0.000 claims description 8
- 230000003179 granulation Effects 0.000 claims description 8
- 238000004806 packaging method and process Methods 0.000 claims description 8
- 239000011122 softwood Substances 0.000 claims description 8
- 230000001954 sterilising effect Effects 0.000 claims description 8
- 239000003826 tablet Substances 0.000 claims description 8
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 6
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 claims description 6
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 6
- 229940057838 polyethylene glycol 4000 Drugs 0.000 claims description 6
- 229930195725 Mannitol Natural products 0.000 claims description 5
- 239000000594 mannitol Substances 0.000 claims description 5
- 235000010355 mannitol Nutrition 0.000 claims description 5
- 241000196324 Embryophyta Species 0.000 claims description 4
- 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 claims description 4
- 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 claims description 4
- 239000008103 glucose Substances 0.000 claims description 4
- 239000008101 lactose Substances 0.000 claims description 4
- 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 claims description 2
- 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 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- 235000009754 Vitis X bourquina Nutrition 0.000 claims 1
- 235000012333 Vitis X labruscana Nutrition 0.000 claims 1
- 235000014787 Vitis vinifera Nutrition 0.000 claims 1
- 240000006365 Vitis vinifera Species 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical group CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 239000008117 stearic acid Substances 0.000 claims 1
- 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 abstract description 72
- 239000003963 antioxidant agent Substances 0.000 abstract description 14
- 230000003078 antioxidant effect Effects 0.000 abstract description 14
- 235000006708 antioxidants Nutrition 0.000 abstract description 13
- 230000002829 reductive effect Effects 0.000 abstract description 8
- 102000003425 Tyrosinase Human genes 0.000 abstract description 7
- 108060008724 Tyrosinase Proteins 0.000 abstract description 7
- 235000010980 cellulose Nutrition 0.000 abstract description 7
- 229920002678 cellulose Polymers 0.000 abstract description 7
- 239000001913 cellulose Substances 0.000 abstract description 7
- 238000004090 dissolution Methods 0.000 abstract description 6
- 239000008187 granular material Substances 0.000 abstract description 6
- 150000003254 radicals Chemical class 0.000 abstract description 6
- 230000009467 reduction Effects 0.000 abstract description 4
- 230000002401 inhibitory effect Effects 0.000 abstract description 3
- 239000000543 intermediate Substances 0.000 abstract description 3
- 239000002994 raw material Substances 0.000 abstract description 3
- 230000007246 mechanism Effects 0.000 abstract description 2
- 210000004400 mucous membrane Anatomy 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 210000003491 skin Anatomy 0.000 description 21
- 238000000034 method Methods 0.000 description 11
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- 239000000284 extract Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000008859 change Effects 0.000 description 7
- 238000013459 approach Methods 0.000 description 6
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 description 5
- 210000004027 cell Anatomy 0.000 description 5
- 235000013339 cereals Nutrition 0.000 description 5
- 229960004502 levodopa Drugs 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 235000019359 magnesium stearate Nutrition 0.000 description 5
- 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 description 4
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 4
- 240000003768 Solanum lycopersicum Species 0.000 description 4
- 244000061458 Solanum melongena Species 0.000 description 4
- 235000002597 Solanum melongena Nutrition 0.000 description 4
- 240000008866 Ziziphus nummularia Species 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 235000013399 edible fruits Nutrition 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000004060 metabolic process Effects 0.000 description 4
- 229940100688 oral solution Drugs 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000006722 reduction reaction Methods 0.000 description 4
- 208000003351 Melanosis Diseases 0.000 description 3
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 3
- 208000012641 Pigmentation disease Diseases 0.000 description 3
- 102000019197 Superoxide Dismutase Human genes 0.000 description 3
- 108010012715 Superoxide dismutase Proteins 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- MHUWZNTUIIFHAS-CLFAGFIQSA-N dioleoyl phosphatidic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(O)=O)OC(=O)CCCCCCC\C=C/CCCCCCCC MHUWZNTUIIFHAS-CLFAGFIQSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000000855 fermentation Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000019612 pigmentation Effects 0.000 description 3
- OEGPRYNGFWGMMV-UHFFFAOYSA-N (3,4-dimethoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC OEGPRYNGFWGMMV-UHFFFAOYSA-N 0.000 description 2
- 244000144730 Amygdalus persica Species 0.000 description 2
- 241000756943 Codonopsis Species 0.000 description 2
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 235000006040 Prunus persica var persica Nutrition 0.000 description 2
- 241001295692 Pyracantha fortuneana Species 0.000 description 2
- 229930003427 Vitamin E Natural products 0.000 description 2
- 230000003796 beauty Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000002500 effect on skin Effects 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 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 description 2
- 230000036541 health Effects 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
- 230000006872 improvement Effects 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 210000002752 melanocyte Anatomy 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 230000009758 senescence Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 229940046009 vitamin E Drugs 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- WVXRAFOPTSTNLL-NKWVEPMBSA-N 2',3'-dideoxyadenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@H]1CC[C@@H](CO)O1 WVXRAFOPTSTNLL-NKWVEPMBSA-N 0.000 description 1
- 241001412627 Adenophora liliifolia Species 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 244000061520 Angelica archangelica Species 0.000 description 1
- PYIXHKGTJKCVBJ-UHFFFAOYSA-N Astraciceran Natural products C1OC2=CC(O)=CC=C2CC1C1=CC(OCO2)=C2C=C1OC PYIXHKGTJKCVBJ-UHFFFAOYSA-N 0.000 description 1
- NDVRQFZUJRMKKP-UHFFFAOYSA-N Betavulgarin Natural products O=C1C=2C(OC)=C3OCOC3=CC=2OC=C1C1=CC=CC=C1O NDVRQFZUJRMKKP-UHFFFAOYSA-N 0.000 description 1
- 244000020518 Carthamus tinctorius Species 0.000 description 1
- 235000003255 Carthamus tinctorius Nutrition 0.000 description 1
- 102100035882 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- 206010008570 Chloasma Diseases 0.000 description 1
- 241000007126 Codonopsis pilosula Species 0.000 description 1
- 235000009917 Crataegus X brevipes Nutrition 0.000 description 1
- 235000013204 Crataegus X haemacarpa Nutrition 0.000 description 1
- 235000009685 Crataegus X maligna Nutrition 0.000 description 1
- 235000009444 Crataegus X rubrocarnea Nutrition 0.000 description 1
- 235000009486 Crataegus bullatus Nutrition 0.000 description 1
- 235000017181 Crataegus chrysocarpa Nutrition 0.000 description 1
- 235000009682 Crataegus limnophila Nutrition 0.000 description 1
- 240000000171 Crataegus monogyna Species 0.000 description 1
- 235000004423 Crataegus monogyna Nutrition 0.000 description 1
- 235000002313 Crataegus paludosa Nutrition 0.000 description 1
- 235000009840 Crataegus x incaedua Nutrition 0.000 description 1
- 229920000832 Cutin Polymers 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- 240000001008 Dimocarpus longan Species 0.000 description 1
- 235000002722 Dioscorea batatas Nutrition 0.000 description 1
- 235000006536 Dioscorea esculenta Nutrition 0.000 description 1
- 240000001811 Dioscorea oppositifolia Species 0.000 description 1
- 235000003416 Dioscorea oppositifolia Nutrition 0.000 description 1
- 240000002943 Elettaria cardamomum Species 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 235000000235 Euphoria longan Nutrition 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 241000628997 Flos Species 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 208000005232 Glossitis Diseases 0.000 description 1
- 235000001287 Guettarda speciosa Nutrition 0.000 description 1
- 240000000950 Hippophae rhamnoides Species 0.000 description 1
- 235000003145 Hippophae rhamnoides Nutrition 0.000 description 1
- 239000009636 Huang Qi Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004201 L-cysteine Substances 0.000 description 1
- 235000013878 L-cysteine Nutrition 0.000 description 1
- 241000234435 Lilium Species 0.000 description 1
- 240000003394 Malpighia glabra Species 0.000 description 1
- 235000014837 Malpighia glabra Nutrition 0.000 description 1
- 240000002624 Mespilus germanica Species 0.000 description 1
- 235000017784 Mespilus germanica Nutrition 0.000 description 1
- 235000000560 Mimusops elengi Nutrition 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 206010033546 Pallor Diseases 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- IHPVFYLOGNNZLA-UHFFFAOYSA-N Phytoalexin Natural products COC1=CC=CC=C1C1OC(C=C2C(OCO2)=C2OC)=C2C(=O)C1 IHPVFYLOGNNZLA-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 244000046146 Pueraria lobata Species 0.000 description 1
- 235000010575 Pueraria lobata Nutrition 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 240000002547 Rosa roxburghii Species 0.000 description 1
- 235000000640 Rosa roxburghii Nutrition 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 241000208292 Solanaceae Species 0.000 description 1
- 206010042496 Sunburn Diseases 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- 102000008221 Superoxide Dismutase-1 Human genes 0.000 description 1
- 108010021188 Superoxide Dismutase-1 Proteins 0.000 description 1
- 241001506047 Tremella Species 0.000 description 1
- 235000007837 Vangueria infausta Nutrition 0.000 description 1
- 241000489523 Veratrum Species 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229960000271 arbutin Drugs 0.000 description 1
- 239000000823 artificial membrane Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229940046011 buccal tablet Drugs 0.000 description 1
- 239000006189 buccal tablet Substances 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 235000005300 cardamomo Nutrition 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000005779 cell damage Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000000287 crude extract Substances 0.000 description 1
- NKQPRNDTEUZYKT-UHFFFAOYSA-N cyclohex-5-ene-1,2,3,4-tetrone Chemical group O=C1C=CC(=O)C(=O)C1=O NKQPRNDTEUZYKT-UHFFFAOYSA-N 0.000 description 1
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical compound OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 description 1
- 230000013872 defecation Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- VJNCICVKUHKIIV-UHFFFAOYSA-N dopachrome Chemical compound O=C1C(=O)C=C2NC(C(=O)O)CC2=C1 VJNCICVKUHKIIV-UHFFFAOYSA-N 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 235000018927 edible plant Nutrition 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 210000001339 epidermal cell Anatomy 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 231100000321 erythema Toxicity 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 231100000025 genetic toxicology Toxicity 0.000 description 1
- 230000001738 genotoxic effect Effects 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- 229940087603 grape seed extract Drugs 0.000 description 1
- 235000002532 grape seed extract Nutrition 0.000 description 1
- 230000000640 hydroxylating effect Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 230000008099 melanin synthesis Effects 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 150000002926 oxygen Chemical class 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
- 230000037361 pathway Effects 0.000 description 1
- 239000000280 phytoalexin Substances 0.000 description 1
- 150000001857 phytoalexin derivatives Chemical class 0.000 description 1
- 230000000291 postprandial effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229940119485 safflower extract Drugs 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000036259 sexual stimuli Effects 0.000 description 1
- 230000008326 skin blood flow Effects 0.000 description 1
- 210000004927 skin cell Anatomy 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 208000003265 stomatitis Diseases 0.000 description 1
- 230000007666 subchronic toxicity Effects 0.000 description 1
- 231100000195 subchronic toxicity Toxicity 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 238000009461 vacuum packaging Methods 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
- 239000011708 vitamin B3 Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000001717 vitis vinifera seed extract Substances 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- 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
-
- 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
- A23L33/17—Amino acids, peptides or proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P10/00—Shaping or working of foodstuffs characterised by the products
- A23P10/20—Agglomerating; Granulating; Tabletting
- A23P10/28—Tabletting; Making food bars by compression of a dry powdered mixture
-
- 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
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
-
- 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
- A61K31/365—Lactones
- A61K31/375—Ascorbic acid, i.e. vitamin C; Salts thereof
-
- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/455—Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/44—Oxidoreductases (1)
- A61K38/446—Superoxide dismutase (1.15)
-
- 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
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2059—Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/18—Antioxidants, e.g. antiradicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y115/00—Oxidoreductases acting on superoxide as acceptor (1.15)
- C12Y115/01—Oxidoreductases acting on superoxide as acceptor (1.15) with NAD or NADP as acceptor (1.15.1)
- C12Y115/01001—Superoxide dismutase (1.15.1.1)
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Polymers & Plastics (AREA)
- Biochemistry (AREA)
- Nutrition Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Food Science & Technology (AREA)
- Zoology (AREA)
- Mycology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Dermatology (AREA)
- Toxicology (AREA)
- Physiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention provides a kind of whitening lozenge containing SOD component, is made of the raw material of following parts by weight: SOD 0.5-1%, resveratrol 5-10%, niacinamide 5-10%, vitamin C 5-10%, starch slurry 10-12%, lubricant 1-2%, microcrystalline cellulose cellulose content 30-40%, corrigent 20-32%.Free radical is removed by addition SOD, melanin is reduced and is formed;Mechanism of resveratrol inhibiting tyrosinase activity is added, melanin is reduced and is formed;Niacinamide is added to inhibit melanin granule to horn cell transmitting, accelerate skin renewal speed;Add vitamin C reduction melanin intermediates and melanin polymer, number of ways skin whitening, significant effect, and component safety.Dissolution time can not only guarantee soak time of the antioxidant by mucous membrane of mouth between 18.53-22.60min, but will not the time too long, it is inconvenient to use.
Description
Technical field
The invention belongs to field of health care products, and in particular to a kind of whitening lozenge for adding SOD component.
Background technique
As the saying goes: " a white screening three is ugly ", current mainstream is aesthetic or pursues pale skin.The variation of skin color is
One complicated dynamic process, is influenced by many factors, such as pigment, epidermis and thickness of corium in skin etc..Whitening
Method have very much, such as:
(1) B16 cell is prevented
Tyrosinase, dopachrome interconvertible enzyme, 5,6- dihydroindole -2- carboxylic oxidase are main in melanin forming process
Biological enzyme, wherein tyrosinase is the rate-limiting enzyme of the process, and tyrosinase major catalytic monohydric phenol hydroxylating generates dihydroxy
Compound and catechol oxidation generate adjacent benzene diquinone, and these two types reaction has oxygen radical participation, and scavenging activated oxygen can also
To destroy tyrosinase activity.Analog of the resveratrol as DOPA, the active site with substrate competitive desmoenzyme are reduced
Melanin generates.
(2) melanin is prevented to transmit
Azelaic acid, niacinamide (VB3) etc. can inhibit melanin granule from melanocyte to keratoprotein cell shift, therefore
With white-skinned face function.
(3) accelerate melanin metabolism
Oxidation state melanin granule can be reduced to the reduction-state melanin of white by vitamin e, vitamin c and its derivative
Grain, to achieve the effect that whitening.
(4) anti-oxidant whitening
After being irradiated with ultraviolet radiation, active oxygen can be generated, causes the destruction of immobilized artificial membrane, so as to cause the destruction of skin histology, into
And the problems such as generating erythema, pigmentation, carry out pressure to skin tape, more melanin is caused to generate.Superoxide dismutase
(Superoxide dismutase, SOD) is the important composition member of Antioxidant Enzymes in biosystem, is widely distributed in micro-
In biology, plant and animal body.It can efficiently remove intracorporal free radical.Internal extra free radical can cause cellular damage with
And pigmentation, human senility are the consequences due to free radical accumulation and removing obstacles.Supplemented with exogenous SOD can with skin whitening,
It delays senescence.
Patent relevant to research contents of the present invention is as follows:
CN110192994A discloses a kind of white tomato whitening piece and preparation method thereof, and the white tomato whitening piece is mainly by white tomato
Freeze-dried powder 200mg-900mg, acerola concentrate extract 10mg-280mg, kudzu-vine root powder 1mg-120mg, grape seed extract 1mg-
200mg and Fructus piperis nigrum extract 1mg-15mg are made by way of tabletting after mixed in equal amounts, in order to which improvement effect can also be
Increase L-cysteine 90mg-500mg or yeast extract 90mg-500mg and seabuckthorn fruit powder 1mg-180mg in formula.Change
Lozenge passes through anti-oxidant approach whitening.
CN103655446B provides a kind of product and preparation method thereof with skin beauty health-care function;The system
Each component in product are as follows: lotus seeds, lily, the root of straight ladybell, Chinese yam, hawthorn, fructus lycii, tremella each water extract be 1-3 parts, radix polygonati officinalis water extract 1-
4 parts, it is 2-4 parts that the root of Dahurain angelica, Amomum cardamomum water, which mention volatile oil respectively, 3-5 parts of Flos Rosae Rugosae extract, 0.05-0.1 parts of water soluble pearl powder,
0.01-0.05 parts of vitamin C, 0.001-0.005 parts of vitamin E, 50-90 parts of auxiliary material;The form of the product is granule
Or buccal tablet.Combination is optimized with the homologous article of tender skin, the medicine of white-skinned face function, food, then with vitamin C and vitamin
E prevents skin oxidative as antioxidant.Change lozenge and two approach whitenings are metabolized by anti-oxidant and reinforcement melanin.
CN105267435A discloses a kind of three eggplant piece of compound and the preparation method and application thereof of speckle removing, antisenescence.It is described multiple
Three eggplant pieces of side are mainly made by the following raw material by weight: 10-20 parts of eggplant powder, 10-20 parts of tomato meal, pyracantha fortuneana fruit powder
10-20 parts, 10-20 parts of red date powder, 0.5-1 parts of medlar powder, 0.5-1 parts of codonopsis pilosula powder and 0.5-1 parts of peach kernel powder.Of the invention answers
Solanaceae Triratna in conjunction with the advantage of pyracantha fortuneana fruit, jujube, Radix Codonopsis and peach kernel, is formed characteristic by three eggplant pieces of side, has reduction skin black
Pigment generates and deposition, improvement skin blood circulation, removing free radical, anti-oxidant, adjustment endocrine, relax bowel and defecation and enhancing are exempted from
The effects of epidemic disease, play significant nti-freckle and improve the colour of skin and other effects, it can be used for preventing and treating the pigmentations such as freckle, chloasma, sunburn
Skin blackening caused by skin disease, it may also be used for anti-aging etc., effect is obvious, and without any side effects.Change lozenge by resisting
Oxidative pathway whitening.
CN107865423A discloses a kind of SOD oral solution of anti-enteron aisle oxidation, is mainly main former with marine low temperature SOD
Material, addition safflower extract, Fructus lycii P.E, Rhizoma Chuanxiong extract, jujube concentrate stir evenly vacuum packaging to get,
Specific proportion are as follows: the anti-enteron aisle of the present invention aoxidizes SOD oral solution, directly takes in postprandial half an hour.The features of the present invention exists
In: marine low temperature SOD:2 ~ 3 part, crude extract from carthamus tinctorius L. with water: 1 ~ 2 part, fructus lycii water extract: 1 ~ 2 part, Rhizoma Chuanxiong water extract: 1 ~ 2
Part, 3 ~ 4 parts of jujube concentrate.Change lozenge and passes through anti-oxidant approach whitening.
CN107541502A, which is disclosed, a kind of prepares SOD multienzyme alkalinity oral solution with rich in the cereal crops of SOD multienzyme
Pulvis is mixed with water, is mixed this method comprises: pulvis is made after crushing in the cereal crops that 1) will be enriched in SOD multienzyme by method
Close liquid A;2) amylase and activator are added into mixed liquor A, 25~35min is digested at 60 DEG C~85 DEG C, obtains mixed liquor
B;The pH value for adjusting mixed liquid B is 8~12, and alkali cellulose enzyme and protease is added, 4h~5h is digested at 40~50 DEG C, is obtained
To mixed liquor C;Beer complex enzyme, distiller's yeast are added into mixed liquor C, carries out anaerobic fermentation under conditions of 30~40 DEG C, obtains
Fermentation liquid;Alkaline pectase is added into fermentation liquid, is stirred to react at 35~50 DEG C, filtering to get.This method maintains grain
The activity of the primitive environment of the multienzyme such as SOD in food crop, each function factor is high, and healthcare function is good.Change lozenge and passes through anti-oxidant way
Diameter whitening.
CN108835630A discloses a kind of oral solution and preparation method thereof with high SOD enzyme activity, including will be edible
Plant material is squeezed the juice, and is then centrifuged (1000-4000rpm, 0-30min) removal bulky grain, uses twice ultrafiltration membrane
It is separated and (is separated for the first time using tubular membrane, aperture 60-120kD;Second is separated into rolled film, aperture 8-30kD);It
Afterwards, ultra high pressure treatment, pressure 200-600MPa, time 1-20min are carried out then.It is had activated after the method for the present invention is handled
SOD enzyme, enzyme activity have been increased to 10000U/ml or more, efficiently solve the problems, such as that SOD enzyme activity is low in product.Through this hair
Product made from bright method is relatively beneficial to human health.Change lozenge and passes through anti-oxidant approach whitening.
CN1072090 discloses a kind of preparation method of SOD oral liquid, is by natural crude drugs Rosa roxburghii Tratt through adding
Work separation and Extraction, protection processing, it is a variety of effectively to obtain erythrocuprein SOD, cat catalase, selenium, VC, VE, tannin etc.
Ingredient cooperates Radix Codonopsis, Radix Astragali, fructus lycii, longan, jujube percolate, is a kind of new oral liquid formulations containing SOD.Change lozenge
Pass through anti-oxidant approach whitening.
Summary of the invention
It is an object of the invention to for only by one or two kinds of approach come whitening, effect is not prominent enough currently on the market
Defect, provide a kind of from preventing melanin production, prevent melanin from transmitting, accelerate melanin metabolism, anti-oxidant multipath beauty
White lozenge.
Above-mentioned purpose to realize the present invention, using following technical scheme:
It is made of raw material from the following weight: SOD 0.5-1%, resveratrol 5-10%, niacinamide 5-10%, vitamin C 5-
10%, starch slurry 10-12%, lubricant 1-2%, microcrystalline cellulose cellulose content 30-40%, corrigent 20-32%.Corrigent be mannitol,
One of sorbierite, glucose, lactose.Lubricant is one of magnesium stearate, talcum powder, polyethylene glycol-4000.
Part material purchase information of the present invention is as follows:
SOD is purchased from the long-range development in science and technology Co., Ltd in Wuhan;
Resveratrol is purchased from Suzhou Fu Lu Biotechnology Co., Ltd;
Niacinamide is purchased from Wuhan Chu Fengyuan Science and Technology Ltd.;
Vitamin C is purchased from one hundred Xinda raw-food material Co., Ltd of Wuhan.
Preparation process the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, corrigent sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, and more easy mold release adds lubricant, are uniformly mixed, send
Enter tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Specifically, SOD can remove the ultra-oxygen anion free radical and hydroxyl radical free radical of organism metabolism generation, together
When, it also can be used as the substrate for induction enzyme of superoxide anion, protect body cell from the damage of aerobic metabolism object.SOD is as one
The good free radical scavenger of kind is improving immunity of organisms, and delay senescence etc. has fine effect.
Resveratrol is a kind of phytoalexin of polyatomic phenol, is plant in external source sexual stimulus such as ultraviolet light, machine
It generates, is widely distributed in root, stem, leaf and the fruit of plant under the action of tool damage or fungal infection, had anti-well
Oxidisability and tyrosinase inhibitory action, resveratrol can reach arbutin and ethyl Vc more highly concentrated under low concentration
Whitening effect under the conditions of degree.Williams etc. grinds the safety of the resveratrol of high-purity by animal experiment
Study carefully.Studies have shown that resveratrol to skin and eyes without irritation, and pass through micronucleus assay in vivo, it was demonstrated that resveratrol
There is no genetoxic.Found by 90 d subchronic toxicity tests, in maximum 700 mg/(kgd of study dosage) when white black false hellebore
Alcohol does not cause any adverse effect to body and does not have genotoxicity, so that preliminary proof resveratrol is nontoxic peace
Complete.
Niacinamide also known as niacinamide (NAA), vitamin B3, nicotinic acid, being widely used in clinic prevents rough skin
The treatment of disease, glossitis, stomatitis, dermatitis.It can inhibit the formation of melanin granule, it can also be inhibited to epidermal cell uplink
To cuticula, effectively melanin is inhibited to transmit to horn cell, after thering is part melanin inevitably to reach superficial skin,
Niacinamide again can be by with accelerating Skin Cell renewal speed to promote melanocyte to fall off.
Vitamin C is a kind of water-soluble powerful antioxidant, can combine with oxygen radical reduction reaction occurs in vivo,
Mitigate esters peroxidization, reduce the generation of lipid peroxide, protects SOD isoreactivity, moreover it is possible to aoxidize with preventing melanin
Process inhibits melanin to be formed, poly- by influencing multiple links such as reduction melanin intermediates and melanin that melanin is formed
Object is closed, DOPA is reduced and DOPA quinones substance is formed, inhibit the generation of melanin.
Compared with prior art, the invention has the benefit that removing free radical by addition SOD, melanin shape is reduced
At;Mechanism of resveratrol inhibiting tyrosinase activity is added, melanin is reduced and is formed;Adding niacinamide inhibits melanin granule to cutin
Skin renewal speed is accelerated in cell transmitting;Vitamin C reduction melanin intermediates and melanin polymer are added, DOPA is reduced
It is formed with DOPA quinones substance, number of ways skin whitening, significant effect, and component safety.Dissolution time is in 18.53-
Between 22.60min, can not only guarantee soak time of the antioxidant by mucous membrane of mouth, but will not the time too long, use not side
Just.
Detailed description of the invention
The variation of Fig. 1 skin brightness
The variation of Fig. 2 melanin.
Specific embodiment
The present invention is further described below by way of specific embodiment, but the present invention is not limited only to this.
Embodiment one
SOD 0.5%, resveratrol 5%, niacinamide 5%, vitamin C 5%, starch slurry 12%, magnesium stearate 2%, microcrystalline cellulose contain
Measure 40%, mannitol 30.5%.The present embodiment is dissolved as 15.30min.
Preparation the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, mannitol sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, and more easy mold release adds magnesium stearate, are uniformly mixed,
It is sent into tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Embodiment two
It is formulated SOD 0.6%, resveratrol 6%, niacinamide 6%, vitamin C 6%, starch slurry 11%, talcum powder 1.4%, microcrystalline cellulose
Cellulose content 37%, sorbierite 32%.The dissolution time of the present embodiment is 19.53min.
Preparation the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, sorbierite sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, and more easy mold release adds talcum powder, are uniformly mixed, send
Enter tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Embodiment three
Formula: SOD 0.7%, resveratrol 7%, niacinamide 7%, vitamin C 7%, starch slurry 10%, polyethylene glycol-4000 1%,
Microcrystalline cellulose cellulose content 38%, glucose 29.3%.The dissolution time of the present embodiment is 17.25min.
Preparation the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, glucose sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, more easy mold release, add polyethylene glycol-4000, mixing
Uniformly, it is sent into tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Example IV
Formula: SOD 0.8%, resveratrol 8%, niacinamide 8%, vitamin C 8%, starch slurry 12%, magnesium stearate 1%, crystallite are fine
Tie up cellulose content 32%, lactose 30.2%.The dissolution time of the present embodiment is 20.30min.
Preparation the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, lactose sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, and more easy mold release adds magnesium stearate, are uniformly mixed,
It is sent into tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Embodiment five
Formula: SOD 0.9%, resveratrol 9%, niacinamide 9%, vitamin C 9%, starch slurry 12%, talcum powder 2%, microcrystalline cellulose
Cellulose content 30%, sorbierite 28.1%.The dissolution time of the present embodiment is 18.93min.
Preparation the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, sorbierite sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, and more easy mold release adds talcum powder, are uniformly mixed, send
Enter tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Embodiment six
Formula: SOD 1%, veratryl alcohol 10%, niacinamide 10%, vitamin C 10%, starch slurry 12%, polyethylene glycol-4000 2%, micro-
Crystalline cellulose content 35%, mannitol 20%.
Preparation the following steps are included:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, mannitol sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, more easy mold release, add polyethylene glycol-4000, mixing
Uniformly, it is sent into tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
Whitening spot-removing experiment
Laboratory apparatus: Minolta company, Minolta Chromameter CM-700d(Japan), Mexameter MX18 skin
Melanin and ferroheme tester (German Courage+Khazak company).
Experimental method:
1. recruiting trial volunteer 100.
2. subject takes embodiment 61 daily.
3. before taking product, the 4th week, the 8th week, the 12nd week respectively use apparatus measures subject skin condition.Skin
Brightness measures skin brightness L value using Minolta Chromameter (CM-700d), is measured in parallel 3 times, is averaged every time,
The L value of all trial volunteers is averaged again.Dermal melanin value is measured with Mexameter MX18, is measured in parallel every time
It 3 times, is averaged, calculates melanin down ratio, all volunteer's melanin down ratios are averaged again.
4. experimental result is as shown in Figure 1, 2.
It can be seen from experimental result this product can bright color, reduce melanin whitening effect.
Claims (9)
1. a kind of whitening lozenge containing SOD component, which is characterized in that be made of the components of following parts: SOD 0.5-1%,
Resveratrol 5-10%, niacinamide 5-10%, vitamin C 5-10%, starch slurry 10-12%, lubricant 1-2%, microcrystalline cellulose contain
Measure 30-40%, corrigent 20-32%.
2. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that SOD is to mention from plant
It takes, the enzyme activity of SOD is 100000U/g.
3. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that resveratrol is from Portugal
It is extracted in grape skin, purity >=99%.
4. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that niacinamide purity >=
99%。
5. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that vitamin C >=99%.
6. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that lubricant is stearic acid
One of magnesium, talcum powder, polyethylene glycol-4000.
7. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that corrigent be mannitol,
One of sorbierite, glucose, lactose.
8. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that preparation process include with
Lower step:
Step 1: it weighs after SOD, resveratrol, niacinamide, vitamin C, microcrystalline cellulose, corrigent sieve with 100 mesh sieve and mixes;
Step 2: granulation is added starch slurry and softwood is made, is granulated by 20 meshes;
Step 3: it is dry, 30 DEG C of drying temperature;
Step 4: whole grain and tabletting keep lozenge surface smooth after whole grain, and more easy mold release adds lubricant, are uniformly mixed, send
Enter tabletting machine;
Step 4: tablet is irradiated 15min under ultraviolet light, carries out blister package by sterilizing and packaging.
9. a kind of whitening lozenge containing SOD component according to claim 1, which is characterized in that in mouth when dissolving
Between be 15.30-20.30min.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910898242.XA CN110448687A (en) | 2019-09-23 | 2019-09-23 | A kind of whitening lozenge containing SOD component |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910898242.XA CN110448687A (en) | 2019-09-23 | 2019-09-23 | A kind of whitening lozenge containing SOD component |
Publications (1)
Publication Number | Publication Date |
---|---|
CN110448687A true CN110448687A (en) | 2019-11-15 |
Family
ID=68492514
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910898242.XA Withdrawn CN110448687A (en) | 2019-09-23 | 2019-09-23 | A kind of whitening lozenge containing SOD component |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110448687A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113632992A (en) * | 2021-09-07 | 2021-11-12 | 何泽剑 | Skin beautifying food formula and preparation method of buccal tablets thereof |
CN116616448A (en) * | 2023-05-08 | 2023-08-22 | 石药集团中诺药业(泰州)有限公司 | Vitamin C tablet containing organic selenium and production process thereof |
-
2019
- 2019-09-23 CN CN201910898242.XA patent/CN110448687A/en not_active Withdrawn
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113632992A (en) * | 2021-09-07 | 2021-11-12 | 何泽剑 | Skin beautifying food formula and preparation method of buccal tablets thereof |
CN116616448A (en) * | 2023-05-08 | 2023-08-22 | 石药集团中诺药业(泰州)有限公司 | Vitamin C tablet containing organic selenium and production process thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100962587B1 (en) | A method for fermentation of natural plants and herbal medicines, a fermented product prepared therefrom and a paharmaceutical composition, a cosmetic compositon and a food composition comprising the product | |
CN103025307B (en) | Chicoric acid and derivant are used for the purposes for adjusting cutaneous pigmentation | |
FR2604445A1 (en) | ANTIOXIDANT COMPOSITION OF NATURAL PRODUCTS AND PROCESS FOR PRODUCING THE SAME | |
CN107595737B (en) | Whitening and anti-wrinkle composition containing antrodia camphorata, essence containing composition and preparation method of essence | |
CN111032009B (en) | Skin whitening agent, external skin preparation for whitening skin, and method for whitening skin | |
JP4100911B2 (en) | Glutamate decarboxylase activator | |
KR20120010687A (en) | Composition for skin beauty food, drug and cosmetic use comprising an extract of fermented ginseng | |
KR101147541B1 (en) | A skin-care agent containing Arctii fructus extracts using microbial fermentation | |
CN110448687A (en) | A kind of whitening lozenge containing SOD component | |
CN103025309B (en) | Chicoric acid and lactobacillus in food supplement for the Pigmented purposes of regulation of skin | |
KR100843745B1 (en) | Fermented spirulina extract and method for preparing the same | |
KR20090111719A (en) | Cosmetic Compositions for whitening Skin containing jujube culture | |
WO2020054204A1 (en) | Antioxidant | |
WO2008029877A1 (en) | Anti-aging agent, skin-whitening agent, anti-oxidative agent, and anti-inflammatory agent | |
KR101180258B1 (en) | A skin-care agent containing Ophioglossum vulgatum extracts using microbial fermentation | |
CN114766679B (en) | Whitening and antioxidant composition, preparation process and application thereof | |
KR101803757B1 (en) | Cosmetic composition containing natural complex fermented extracts | |
KR100466623B1 (en) | The culture medium for Kombucha fermentation, that has functions of skin regeneration and anti-aging, and composition containing thereof | |
TWI767387B (en) | Use of red grape fermented liquid for manufacturing of a composition for improving skin condition and reducing skin pores | |
CN114128893A (en) | Composition containing nicotinamide and glutathione and application thereof | |
JP2000319122A (en) | Cell proliferation promoting cosmetic | |
KR100542446B1 (en) | A cosmetic composition containing an extract of capsosiphon fulvescens | |
KR20120081289A (en) | A skin-care agent containing fermented licorice extracts | |
JP2003267857A (en) | Skin care preparation and composition of skin care preparation | |
JP2001048768A (en) | Cosmetic, quasi-drug, drug and food |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
TA01 | Transfer of patent application right | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20210420 Address after: 417010 group 4, guanjiawei Committee, Changqing office, Louxing District, Loudi City, Hunan Province Applicant after: Liu Jianhui Address before: 510070 no.76-2, yard 81, Xianlie Middle Road, Yuexiu District, Guangzhou City, Guangdong Province 122c Applicant before: Guangzhou Yihui Biotechnology Co.,Ltd. |
|
WW01 | Invention patent application withdrawn after publication | ||
WW01 | Invention patent application withdrawn after publication |
Application publication date: 20191115 |