KR20120062030A - Powder-type dentifrice composition contained gold particles and manufacturing method thereof - Google Patents
Powder-type dentifrice composition contained gold particles and manufacturing method thereof Download PDFInfo
- Publication number
- KR20120062030A KR20120062030A KR1020100069361A KR20100069361A KR20120062030A KR 20120062030 A KR20120062030 A KR 20120062030A KR 1020100069361 A KR1020100069361 A KR 1020100069361A KR 20100069361 A KR20100069361 A KR 20100069361A KR 20120062030 A KR20120062030 A KR 20120062030A
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- powder
- gold
- gold particles
- particles
- Prior art date
Links
- 239000010931 gold Substances 0.000 title claims abstract description 164
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 title claims abstract description 120
- 229910052737 gold Inorganic materials 0.000 title claims abstract description 115
- 239000000203 mixture Substances 0.000 title claims abstract description 113
- 239000002245 particle Substances 0.000 title claims abstract description 104
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 239000000551 dentifrice Substances 0.000 title description 3
- 239000000843 powder Substances 0.000 claims abstract description 186
- 239000000606 toothpaste Substances 0.000 claims abstract description 72
- 229940034610 toothpaste Drugs 0.000 claims abstract description 72
- 241000894006 Bacteria Species 0.000 claims abstract description 23
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 17
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 claims abstract description 16
- 235000003599 food sweetener Nutrition 0.000 claims abstract description 15
- 239000003765 sweetening agent Substances 0.000 claims abstract description 15
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims abstract description 14
- 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 abstract description 14
- 239000008101 lactose Substances 0.000 claims abstract description 14
- 239000000600 sorbitol Substances 0.000 claims abstract description 14
- 241000241413 Propolis Species 0.000 claims abstract description 13
- 229940069949 propolis Drugs 0.000 claims abstract description 13
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229960003500 triclosan Drugs 0.000 claims abstract description 12
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims abstract description 11
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000811 xylitol Substances 0.000 claims abstract description 11
- 235000010447 xylitol Nutrition 0.000 claims abstract description 11
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims abstract description 11
- 229960002675 xylitol Drugs 0.000 claims abstract description 11
- 239000013521 mastic Substances 0.000 claims abstract description 10
- 239000003921 oil Substances 0.000 claims abstract description 10
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 9
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 8
- 239000011775 sodium fluoride Substances 0.000 claims abstract description 8
- 235000013024 sodium fluoride Nutrition 0.000 claims abstract description 8
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 claims abstract description 7
- XGRSAFKZAGGXJV-UHFFFAOYSA-N 3-azaniumyl-3-cyclohexylpropanoate Chemical compound OC(=O)CC(N)C1CCCCC1 XGRSAFKZAGGXJV-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229960004711 sodium monofluorophosphate Drugs 0.000 claims abstract description 6
- 230000000844 anti-bacterial effect Effects 0.000 claims description 29
- 238000001035 drying Methods 0.000 claims description 21
- 239000012153 distilled water Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 229960001927 cetylpyridinium chloride Drugs 0.000 claims description 17
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 claims description 17
- 238000002156 mixing Methods 0.000 claims description 17
- 239000003086 colorant Substances 0.000 claims description 16
- 239000000796 flavoring agent Substances 0.000 claims description 15
- 210000000214 mouth Anatomy 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 14
- 238000000576 coating method Methods 0.000 claims description 14
- 235000013355 food flavoring agent Nutrition 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 240000002900 Arthrospira platensis Species 0.000 claims description 12
- 235000016425 Arthrospira platensis Nutrition 0.000 claims description 12
- 229940082787 spirulina Drugs 0.000 claims description 12
- 241001474374 Blennius Species 0.000 claims description 10
- 239000001055 blue pigment Substances 0.000 claims description 10
- 229910052588 hydroxylapatite Inorganic materials 0.000 claims description 9
- 239000004615 ingredient Substances 0.000 claims description 9
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 9
- 238000005868 electrolysis reaction Methods 0.000 claims description 7
- 230000000855 fungicidal effect Effects 0.000 claims description 7
- 239000000417 fungicide Substances 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 5
- 238000005507 spraying Methods 0.000 claims description 5
- FTLYMKDSHNWQKD-UHFFFAOYSA-N (2,4,5-trichlorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=C(Cl)C=C1Cl FTLYMKDSHNWQKD-UHFFFAOYSA-N 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 229940085605 saccharin sodium Drugs 0.000 claims description 3
- 235000011511 Diospyros Nutrition 0.000 claims description 2
- 244000236655 Diospyros kaki Species 0.000 claims description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 235000006679 Mentha X verticillata Nutrition 0.000 claims 1
- 244000246386 Mentha pulegium Species 0.000 claims 1
- 235000016257 Mentha pulegium Nutrition 0.000 claims 1
- 235000002899 Mentha suaveolens Nutrition 0.000 claims 1
- 235000004357 Mentha x piperita Nutrition 0.000 claims 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 claims 1
- 235000001050 hortel pimenta Nutrition 0.000 claims 1
- 239000001488 sodium phosphate Substances 0.000 claims 1
- 229910000162 sodium phosphate Inorganic materials 0.000 claims 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 21
- 208000002925 dental caries Diseases 0.000 abstract description 12
- 208000024693 gingival disease Diseases 0.000 abstract description 10
- 239000000645 desinfectant Substances 0.000 abstract description 2
- NEUSVAOJNUQRTM-UHFFFAOYSA-N cetylpyridinium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 NEUSVAOJNUQRTM-UHFFFAOYSA-N 0.000 abstract 1
- 229960004830 cetylpyridinium Drugs 0.000 abstract 1
- 229940081974 saccharin Drugs 0.000 abstract 1
- 235000019204 saccharin Nutrition 0.000 abstract 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 abstract 1
- 230000001954 sterilising effect Effects 0.000 description 34
- 239000000243 solution Substances 0.000 description 30
- 238000004659 sterilization and disinfection Methods 0.000 description 29
- 206010006326 Breath odour Diseases 0.000 description 10
- 230000001580 bacterial effect Effects 0.000 description 9
- 239000008368 mint flavor Substances 0.000 description 9
- 230000000845 anti-microbial effect Effects 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 7
- 239000003623 enhancer Substances 0.000 description 7
- 239000007967 peppermint flavor Substances 0.000 description 7
- 238000011081 inoculation Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 230000009471 action Effects 0.000 description 4
- 230000001680 brushing effect Effects 0.000 description 4
- 238000000338 in vitro Methods 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- ACTIUHUUMQJHFO-UHFFFAOYSA-N Coenzym Q10 Natural products COC1=C(OC)C(=O)C(CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)=C(C)C1=O ACTIUHUUMQJHFO-UHFFFAOYSA-N 0.000 description 2
- 241000192700 Cyanobacteria Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 208000025157 Oral disease Diseases 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- -1 brightener Substances 0.000 description 2
- 235000017471 coenzyme Q10 Nutrition 0.000 description 2
- ACTIUHUUMQJHFO-UPTCCGCDSA-N coenzyme Q10 Chemical compound COC1=C(OC)C(=O)C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)=C(C)C1=O ACTIUHUUMQJHFO-UPTCCGCDSA-N 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 238000003113 dilution method Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 208000030194 mouth disease Diseases 0.000 description 2
- 208000028169 periodontal disease Diseases 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- CLWAXFZCVYJLLM-UHFFFAOYSA-N 1-chlorohexadecane Chemical compound CCCCCCCCCCCCCCCCCl CLWAXFZCVYJLLM-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241000606749 Aggregatibacter actinomycetemcomitans Species 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
- 235000005827 Arthrocnemum glaucum Nutrition 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 241000190885 Capnocytophaga ochracea Species 0.000 description 1
- 241000871189 Chenopodiaceae Species 0.000 description 1
- 241000196222 Codium fragile Species 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- 241000605986 Fusobacterium nucleatum Species 0.000 description 1
- 241001101025 Lilaeopsis Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 235000003042 Salicornia europaea Nutrition 0.000 description 1
- 240000002625 Salsola soda Species 0.000 description 1
- 241000194019 Streptococcus mutans Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 239000011425 bamboo Chemical class 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229940110767 coenzyme Q10 Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 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 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000009088 enzymatic function Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- ZBKIUFWVEIBQRT-UHFFFAOYSA-N gold(1+) Chemical compound [Au+] ZBKIUFWVEIBQRT-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000008557 oxygen metabolism Effects 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 230000036559 skin health Effects 0.000 description 1
- BFDWBSRJQZPEEB-UHFFFAOYSA-L sodium fluorophosphate Chemical compound [Na+].[Na+].[O-]P([O-])(F)=O BFDWBSRJQZPEEB-UHFFFAOYSA-L 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229960004747 ubidecarenone Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/98—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of animal origin
- A61K8/987—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of animal origin of species other than mammals or birds
- A61K8/988—Honey; Royal jelly, Propolis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- 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
- A23V2250/00—Food ingredients
- A23V2250/60—Sugars, e.g. mono-, di-, tri-, tetra-saccharides
- A23V2250/64—Sugar alcohols
- A23V2250/6422—Xylitol
Abstract
Description
본 발명은 금 입자가 함유된 분말치약 조성물과 그 제조방법에 관한 것으로, 보다 상세하게는, 금(Au) 성분의 고유한 성질을 이용하여 구강 내에서 부작용 없이 살균작용을 수행하되 단시간 내에 살균작용을 수행할 수 있도록 함으로써 분말치약으로 적용하더라도 실질적인 살균작용을 수행할 수 있고, 충치예방과 잇몸질환을 예방하고 구취제거 효과를 향상시킬 수 있는 금 입자가 함유된 분말치약 조성물과 그 제조방법에 관한 것이다.The present invention relates to a powder toothpaste composition containing gold particles and a method for manufacturing the same, and more particularly, using a unique property of the gold (Au) component to perform sterilization without side effects in the oral cavity, but within a short time Even if applied as a powder toothpaste can be carried out by performing a practical bactericidal action, to prevent tooth decay and gum disease and to improve the effect of removing bad breath powder powder composition and a method for manufacturing the same will be.
일반적으로, 일반적으로 구강 및 치아의 세정을 위해 사용되는 치약으로는 페이스트 치약이 널리 사용되고 있으나, 장시간 사용하거나 튜브의 뚜껑을 열어둔 채 일정시간이 경과하게 되면 튜브의 앞부분이 고화되어 쉽게 짜지지 않거나 사용할 수 없게 되는 경우가 많았다. 또한 사용과정에서 튜브 내부에 잔류되는 치약을 완벽하게 사용할 수 없고, 치약이 주입되는 튜브는 일회용으로서 매번 버려야하므로 낭비가 심하고, 환경오염을 유발하는 문제점이 있었다.In general, paste toothpaste is widely used as a toothpaste used for cleaning mouth and teeth, but if a long time is used or a certain time elapses with the lid of the tube open, the front part of the tube is hardened and not easily squeezed. It often became unusable. In addition, the toothpaste remaining inside the tube in the process of use can not be used completely, because the tube in which the toothpaste is injected as a single disposable, wasteful, causing environmental pollution.
이와 같은 문제점을 해결하기 위하여 비교적 치약을 알뜰이 사용할 수 있고, 용기의 재사용이 가능한 액상치약이 제안되어 있다. 그러나 이와 같은 액상치약은 그 사용시에 액상의 치약 조성물이 쉽게 흘러내려 사용이 매우 불편하고 낭비가 심한 문제점으로 인해 현실적으로 사용되고 있지 않다.In order to solve such a problem, a toothpaste can be used relatively, and a liquid toothpaste has been proposed. However, such a liquid toothpaste is not actually used due to the problem that the liquid toothpaste composition flows easily during use and is very inconvenient and wasteful.
한편, 상기와 같은 페이스트 치약 및 액상치약의 문제점을 해결하기 위한 방안으로 최근에는 분말치약이 제안되고 있다. 이와 같은 분말치약으로는 대한민국 등록특허공보 등록번호 제10-0614685호의 "산화게르마늄 분말을 포함하는 치약조성물"에 나타난 바와 같이 순도 99% 이상의 산화게르마늄 분말을 포함시켜 산화게르마늄 특유의 다공성의 공극들에 의해 치아 표면의 치석을 제거하는 스케일효과를 높일 수 있는 치약조성물이 제시되어 있다.On the other hand, powder toothpaste has recently been proposed as a solution to the problems of the paste toothpaste and liquid toothpaste as described above. Such powder toothpaste includes germanium oxide powder having a purity of 99% or more, as shown in "Toothpaste Composition containing Germanium Oxide Powder" of Korean Patent Publication No. 10-0614685, to pores having a specific porosity unique to germanium oxide. Toothpaste composition has been proposed that can increase the scale effect of removing tartar on the surface of the tooth.
그리고, 대한민국 공개특허공보 공개번호 제10-2006-0102681호의 "분말한방치약"에 나타난 바와 같이 분말 소금과 죽염, 활석분, 맥만석, 한약재를 분말화하여 플라그 제거나 구강보호의 효능을 발휘하며, 치아 사기질의 보호할 수 있도록 한 분말치약이 제시되어 있고, 대한민국 공개특허공보 제10-2006-0008509호의 "원적외선 방사원으로 맥반석을 함유한 분말치약"과 같이 맥반석에서 방사되는 원적외선의 유효한 효과가 발휘되는 분말치약이 제시되어 있다.In addition, as shown in the "powdered herbal toothpaste" of the Republic of Korea Patent Publication No. 10-2006-0102681, powdered salt and bamboo salt, talc powder, McManseok, herbal medicines to exert the effect of plaque removal or oral protection , Powdered toothpaste has been proposed to protect tooth enamel, and the effective effect of far-infrared radiation emitted from elvanite, such as "powdery toothpaste containing ganbanite as far-infrared radiation source" of Korean Patent Publication No. 10-2006-0008509 Powder toothpaste is presented.
그 외에도, 대한민국 공개특허공보 공개번호 특1997-0069019호의 "풍치, 충치, 치근염 등을 예방 및 치료하는 분말치약의 제조방법"에 나타난 바와 같이 소금분말, 볶은 조각자분말, 송진가루 등을 혼합하여 이나 잇몸질환, 특히 풍치, 충치 치근염 등을 예방 및 치료하고자 하는 분말치약이 제시되어 있다.In addition, as shown in the "Preparation method of powdered toothpaste for preventing and treating cavities, tooth decay, tooth rootitis, etc." of the Republic of Korea Patent Publication No. 1997-0069019, by mixing salt powder, roasted flake powder, rosin powder, etc. Powder toothpaste is also proposed to prevent and treat gum disease, especially flavor, tooth decay root tooth.
그러나 전술한 바와 같은 종래 분말치약들은 스케일의 제거효과, 플라그 제 거효과, 및 잇몸질환 등 나름대로 일정한 효과를 발휘할 수 있으나, 살균력이 약하여 구강내 프라그의 제거 및 구강균제거에 충분한 효과를 기대할 수 없었다.However, the conventional powder toothpaste as described above may have a certain effect in its own way, such as the removal effect of the scale, plaque removal effect, and gum disease, but the sterilizing power is weak and could not be expected to be effective enough to remove oral plaque and oral bacteria.
이에 따라 살균작용을 수행하기 위한 화학첨가물을 투입하여야 하므로 예민한 구강의 피부를 자극하거나 악영향을 초래하는 문제점이 발생되었다. 예컨대 치약에서 살균작용을 위해 널리 사용되고 있는 불소제제는 치아의 충치 예방이나 세균을 억제하는 기능을 효과적으로 수행할 수 있었으나 치아를 지탱하는 잇몸이나 구강 내부의 피부에는 상대적으로 적절한 살균효과를 발휘할 수 없었고, 치아에 반점을 유발시키거나 약품 냄새로 인해 소비자에게 불쾌감을 초래하는 문제점이 있었다.Accordingly, the chemical additives to perform the sterilization action has to be added, causing problems or irritating the skin of the sensitive oral cavity. For example, fluorides, which are widely used for toothpaste in toothpaste, could effectively prevent tooth decay and inhibit bacteria, but they could not exert relatively appropriate sterilizing effect on the gums or the skin inside the mouth. There is a problem that causes a spot on the teeth or cause discomfort to the consumer due to the smell of the drug.
전술한 문제점을 해결하기 위하여 본 출원인은 대한민국 특허출원 제2007-0048135호로 개시된 금 입자가 함유된 분말치약 조성물을 제안하게 되었다.In order to solve the above problems, the applicant has proposed a powder toothpaste composition containing the gold particles disclosed in Korean Patent Application No. 2007-0048135.
대한민국 특허출원 제2007-0048135호에 의해 제안된 금 입자가 함유된 분말치약 조성물은 금 입자 0.0005 ~ 1중량%; 염화세틸피리디늄 분말 0.1 ~ 5중량%; 유비데카레논(코엔자임Q10) 분말 0.0001 ~ 2중량%; 프로폴리스 추출물 분말 0.1 ~ 5중량%; 하이드록시아파타이트 분말 0.5 ~ 2중량%; 솔비톨 분말 2.0 ~ 30중량%; 및 부형제로서 이산화규소, 함수규산, 유당, 산화티탄으로 이루어진 군으로부터 선택된 하나 이상의 부형제 분말 10 ~ 80중량%를 포함하여 구성된 것이다.Powder toothpaste composition containing gold particles proposed by the Republic of Korea Patent Application No. 2007-0048135 is 0.0005 ~ 1% by weight of gold particles; Cetylpyridinium chloride powder 0.1 to 5% by weight; Ubide carenone (coenzyme Q10) powder 0.0001 to 2% by weight; 0.1-5% by weight of propolis extract powder; 0.5-2% by weight of hydroxyapatite powder; Sorbitol powder 2.0-30 wt%; And 10 to 80 wt% of one or more excipient powders selected from the group consisting of silicon dioxide, hydrous silicic acid, lactose and titanium oxide as excipients.
이러한, 금 입자가 함유된 분말치약 조성물은 금 성분의 고유한 살균작용에 의해 구강내에서의 살균력이 강화되므로 충치 및 잇몸질환의 예방되는 효과가 기대되었다. 그리고, 전술한 분말치약 조성물을 멸균증류수에 동일한 양으로 풀어 용해 시킨 다음, 시험균주에 부어 1분의 시간이 경과한 후 잔존 균수를 측정한 결과 우수한 살균력 및 항균력을 갖는 것으로 측정되었다.Since the powdered toothpaste composition containing the gold particles is enhanced by the inherent bactericidal action of the gold component, the sterilization power in the oral cavity is strengthened, and thus the effect of preventing tooth decay and gum disease was expected. Then, the above-described powder dentifrice composition was dissolved in sterile distilled water in the same amount, dissolved, and then poured into the test strain. After 1 minute of elapsed time, the remaining bacterial count was measured to have excellent sterilizing and antibacterial activity.
하지만, 전술한 살균 및 항균력 테스트는 사전에 분말치약 조성물을 용매(멸균 증류수)에 비교적 장시간 녹인 다음 살균력을 측정한 것이므로 금 입자가 함유된 분말치약 조성물의 사용상의 특성을 고려하지 않아서 실제로 치약의 용도로 사용했을 때와는 상당한 살균력의 차이점을 갖고 있음을 알 수 있었다. 즉, 금 입자가 함유된 분말치약 조성물을 사전에 용매에 녹이지 않은 상태에서 동일한 방법으로 살균 테스트를 시행한 결과, 살균 및 항균력은 사전에 녹인 것에 비해 현저히 저하됨을 알 수 있었고, 이로 인해 양치질시에 충분한 살균효과를 기대할 수 없었다.However, the above-described sterilization and antimicrobial test was performed by dissolving the powder toothpaste composition in a solvent (sterile distilled water) for a relatively long time and then measuring the sterilization power. Therefore, the use of the toothpaste actually did not take into account the characteristics of the powder toothpaste composition containing gold particles. When used as it was found to have a significant difference in sterilization power. That is, as a result of the sterilization test performed in the same manner in the powder toothpaste composition containing the gold particles in the solvent beforehand, it can be seen that the sterilization and antimicrobial activity is significantly reduced compared to the pre-dissolved, because of this Sufficient bactericidal effect could not be expected.
그 이유를 검토하여 본 결과, 입자가 함유된 분말치약 조성물은 분말 형태의 치약이므로 양치질을 할 경우 페이스트 치약이나 액상치약과는 달리 살균력을 발휘하는 물질들이 용해되는 시간이 필요하지만 양치질은 대개 3분 이내에 완료되므로 적절한 살균력을 발휘할 수 없었다. 특히, 살균력을 발휘하는 주요 성분으로 포함되는 금 입자는 부작용이 없는 천연 물질이므로 예민한 구강의 피부를 자극하거나 악영향을 초래하지 않고 살균을 위해 별도로 첨가되던 화학물질이 배제되어 약품 냄새가 발생되지 않는 장점을 있지만, 쉽게 용해되지 않은 고상의 알갱이로서 살균작용에는 일정한 한계점을 가지고 있으므로 이를 보완할 필요가 있었다.As a result of examining the reason, the powdered toothpaste composition containing particles is a toothpaste in powder form, so when brushing teeth, it takes time to dissolve the substances that exhibit sterilizing power, unlike paste toothpaste or liquid toothpaste, but it usually takes 3 minutes Since it was completed within a short time, it could not exhibit proper sterilizing power. Particularly, since gold particles, which are included as the main ingredient to exert bactericidal power, are natural substances with no side effects, they do not irritate or adversely affect the skin of sensitive oral skin and exclude chemicals added separately for sterilization so that no chemical smell occurs. However, it is a solid granule that is not easily dissolved, and since it has a certain limit in sterilization, it was necessary to supplement it.
본 발명은 상기와 같은 종래 문제점을 해결하기 위해 착안한 것으로, 금(Au) 성분의 고유한 성질을 이용하여 구강 내에서 부작용 없이 살균작용을 수행하되 단시간 내에 살균작용을 수행할 수 있도록 함으로써 분말치약으로 적용하더라도 실질적인 살균작용을 수행할 수 있고, 충치예방과 잇몸질환을 예방하고 구취제거 효과가 향상되도록 한 금 입자가 함유된 분말치약 조성물을 제공하는 것을 목적으로 한다.The present invention has been conceived to solve the conventional problems as described above, by using the inherent properties of gold (Au) to perform the sterilization without side effects in the oral cavity, so as to perform the sterilization in a short time to powder toothpaste Even if applied as a practical sterilization effect, to prevent tooth decay and gum disease, and to provide a powder toothpaste composition containing gold particles to improve the effect of removing bad breath.
상기한 바와 같은 본 발명의 목적을 달성하기 위한 금 입자가 함유된 분말치약 조성물은, 금 입자를 필수성분으로 하는 분말치약 조성물에 있어서, 구강내 세균을 억제해주는 살균제로서 입경이 10 내지 200(㎛) 범위이고 0.0005 ~ 1.0 중량% 범위로 함유되는 금 입자; 염화세틸피리디늄 0.1 ~ 0.5중량%, 불화나트륨 0.01 ~ 0.05중량%, 일불소인산나트륨 0.1 ~ 0.7중량% 중에서 1종의 또는 2종이 선택되어 함유되는 프라그 제거제; 트리클로산 0.01 ~ 0.5중량%, 매스틱오일 0.01 ~ 0.5중량%, 프로폴리스추출물 분말 0.1 ~ 5중량% 중에서 1종 이상이 선택되어 함유되는 살균력 증강 보조제; 자일리톨 분말 1.0 ~ 10중량%, 사카린나트륨 0.01 ~ 1.0중량%, 솔비톨 분말 2.0 ~ 30중량% 중에서 1종 이상이 선택되어 함유되는 감미제; 유당 50.0 ~ 86.0중량%, 이산화규소 19.0 ~ 75.0중량% 중에서 1종 이상 선택되어 함유되는 부형제; 및 상기 각 성분들의 잔량 중량%로 함유되는 착향제, 증백제, 착색제;로 이루어진 상기 각각의 성분을 혼합기에 투입하여 분말 혼합체를 형성하고, 상기 분말 혼합체를 교반, 혼합하면서 상기 분말 혼합체의 중량에 대해 3 내지 10 중량%이고 금(Au) 입자의 농도가 25 내지 55ppm인 금(Au) 입자 콜로이드 용액을 고르게 분사하여 코팅하고, 건조하여 형성한 것을 특징으로 한다.Powdered toothpaste composition containing gold particles for achieving the object of the present invention as described above, in the powdered toothpaste composition containing gold particles as an essential component, as a fungicide to suppress bacteria in the oral cavity 10 to 200 (㎛ ) And gold particles contained in the range 0.0005 to 1.0% by weight; A plaque remover containing one or two selected from 0.1 to 0.5% by weight of cetylpyridinium chloride, 0.01 to 0.05% by weight of sodium fluoride, and 0.1 to 0.7% by weight of sodium monofluorophosphate; Bactericidal power-enhancing adjuvant containing one or more selected from 0.01 to 0.5% by weight of triclosan, 0.01 to 0.5% by weight of mastic oil, and 0.1 to 5% by weight of propolis extract powder; Sweeteners containing at least one selected from 1.0 to 10% by weight of xylitol powder, 0.01 to 1.0% by weight of sodium saccharin, and 2.0 to 30% by weight of sorbitol powder; Excipients containing at least one selected from 50.0 to 86.0% by weight of lactose and 19.0 to 75.0% by weight of silicon dioxide; And a flavoring agent, a brightener, and a coloring agent, each of which is contained in the remaining weight% of each of the components, into a mixer to form a powder mixture, and stirring and mixing the powder mixture to the weight of the powder mixture. 3 to 10% by weight of gold (Au) is a gold (Au) particles colloidal solution having a concentration of 25 to 55ppm is sprayed evenly coated, characterized in that formed by drying.
그리고, 상기 착향제는 박하향 분말 1.0 ~ 5중량%, 민트향 분말 1.0 ~ 5.0중량% 중에서 1종 이상을 선택하여 함유하고, 상기 증백제는 하이드록시아파타이트를 0.5 ~ 2중량% 범위로 포함하고, 상기 착색제는 스피룰리나 청색소를 0.001 ~ 1.0중량% 범위로 함유할 수 있다.In addition, the flavoring agent is selected by containing at least one selected from 1.0 to 5% by weight of peppermint flavor powder, 1.0 to 5.0% by weight of mint flavor, the brightener comprises hydroxyapatite in the range of 0.5 to 2% by weight, The colorant may contain spirulina or blue pigment in a range of 0.001 to 1.0% by weight.
한편, 상기 금(Au) 입자 콜로이드 용액은 증류수에 99.9% 금(Au) 막대를 전기분해 과정을 통해 이온화하여 증류수내에 0.001 내지 0.015 마이크로미터(㎛) 정도의 금(Au) 소립자가 포함되도록 형성한 것을 특징으로 한다.On the other hand, the gold (Au) colloidal solution is formed by ionizing 99.9% gold (Au) rod in distilled water through an electrolysis process to form a small amount of gold (Au) particles of 0.001 to 0.015 micrometers (㎛) in distilled water. It is characterized by.
그리고, 상기 금(Au) 입자 콜로이드 용액을 코팅, 건조한 후, 상기 분말 혼합체의 전체 중량에 대해 1 내지 10 중량% 범위가 되도록 함초(鹹草) 분말을 더 포함할 수 있다.In addition, after coating and drying the gold (Au) particle colloidal solution, the grasswort powder may be further included to be in a range of 1 to 10% by weight based on the total weight of the powder mixture.
상기한 바와 같은 본 발명의 목적을 달성하기 위한 금 입자가 함유된 분말치약 조성물의 제조방법은, 입자를 필수성분으로 하는 분말치약 조성물의 제조방법에 있어서, 구강내 세균을 억제해주는 살균제로서 입경이 10 내지 200(㎛) 범위이고 0.0005 ~ 1.0 중량% 범위로 함유되는 금 입자, 염화세틸피리디늄 0.1 ~ 0.5중량%, 불화나트륨 0.01 ~ 0.05중량%, 일불소인산나트륨 0.1 ~ 0.7중량% 중에서 1종의 또는 2종이 선택되어 함유되는 프라그 제거제, 트리클로산 0.01 ~ 0.5중량%, 매스틱오일 0.01 ~ 0.5중량%, 프로폴리스추출물 분말 0.1 ~ 5중량% 중에서 1종 이상이 선택되어 함유되는 살균력 증강 보조제, 자일리톨 분말 1.0 ~ 10중량%, 사카린나트륨 0.01 ~ 1.0중량%, 솔비톨 분말 2.0 ~ 30중량% 중에서 1종 이상이 선택되어 함유되는 감미제, 유당 50.0 ~ 86.0중량%, 이산화규소 19.0 ~ 75.0중량% 중에서 1종 이상 선택되어 함유되는 부형제, 및 상기 각 성분들의 잔량 중량%로 함유되는 착향제, 증백제, 착색제를 각각 준비하는 분말성분 준비단계를 구비한다.The method for producing a powdered toothpaste composition containing gold particles for achieving the object of the present invention as described above, in the method for producing a powdered toothpaste composition containing the particles as an essential component, the particle size as a fungicide to suppress oral bacteria Gold particles contained in the range of 10 to 200 (μm) and in the range of 0.0005 to 1.0% by weight, 0.1 to 0.5% by weight of cetylpyridinium chloride, 0.01 to 0.05% by weight of sodium fluoride, and 0.1 to 0.7% by weight of sodium monofluorophosphate A bactericidal enhancer, xylitol, in which at least one of two or more selected is contained and selected from 0.01 to 0.5% by weight of triclosan, 0.01 to 0.5% by weight of mastic oil, and 0.1 to 5% by weight of propolis extract powder. A sweetener containing at least one selected from 1.0 to 10% by weight of powder, 0.01 to 1.0% by weight of sodium saccharin, and 2.0 to 30% by weight of sorbitol powder, lactose 50.0 to 86.0% by weight, And at least one excipient selected from among 19.0 to 75.0 wt% of silicon oxide, and a powder component preparation step of preparing a flavoring agent, a brightening agent, and a coloring agent, respectively, which are contained in the remaining weight% of the respective components.
그리고, 전해조에 멸균 증류수를 주입하고 순도 99.9% 금(Au) 막대를 설치하여 전기분해 과정을 통해 금(Au) 입자의 농도가 25 내지 55ppm인 금(Au) 입자 콜로이드 용액을 준비하는 용액 준비단계; 상기 분말 준비단계에서 준비된 상기 각각의 분말성분을 20 ~ 30 메시의 채를 통과하도록 하면서 혼합기에 투입하여 분말 혼합체를 형성하는 혼합체 형성단계; 상기 분말 혼합체를 교반, 혼합하면서 상기 금(Au) 입자 콜로이드 용액을 상기 분말 혼합체의 중량에 대해 3 내지 10 중량% 범위로 분사하여 상기 각각의 분말 성분의 표면에 코팅하는 코팅단계; 및 상기 코팅단계에서 상기 금(Au) 입자 콜로이드 용액이 코팅된 분말 혼합체를 건조하는 건조단계를 포함하는 것을 특징으로 한다.In addition, a solution preparation step of preparing a gold (Au) particle colloidal solution having a concentration of 25 to 55 ppm of gold (Au) particles through electrolysis by injecting sterile distilled water into an electrolytic cell and installing a 99.9% pure gold (Au) rod. ; A mixture formation step of forming a powder mixture by introducing each powder component prepared in the powder preparation step into a mixer while passing through 20 to 30 mesh; Coating the surface of each powder component by spraying the gold (Au) particle colloidal solution in a range of 3 to 10% by weight based on the weight of the powder mixture while stirring and mixing the powder mixture; And a drying step of drying the powder mixture coated with the gold (Au) particle colloidal solution in the coating step.
아울러, 상기 건조단계의 시행 후에 상기 분말 혼합체의 전체 중량에 대해 1 내지 10 중량% 범위가 되도록 함초(鹹草) 분말을 투입하여 고르게 혼합하는 함초분말 혼합단계를 더 포함할 수 있다.In addition, after performing the drying step may further include a mixing step to mix evenly by putting the persimmon (鹹 草) powder to be in a range of 1 to 10% by weight relative to the total weight of the powder mixture.
상기와 같은 본 발명에 따른 금 입자가 함유된 분말치약 조성물에 의하면, 금 성분의 고유한 살균작용에 의해 구강내에서의 살균력이 강화되므로 충치 및 잇 몸질환의 예방효과가 향상되고, 염화세틸피리디늄이 첨가로 인해 살균력과 구취제거 효과가 보다 더 향상된다.According to the powdered toothpaste composition containing the gold particles according to the present invention as described above, by the inherent bactericidal action of the gold component is strengthened in the oral disinfection, the effect of preventing tooth decay and gum disease is improved, cetyl chloride The addition of dinium improves sterilization and bad breath.
특히, 본 발명에 따른 금 입자가 함유된 분말치약 조성물은 살균작용이 우수하고 충치 및 잇몸질환의 예방효과가 향상되도록 분말 혼합체를 조성한 후 단시간 내에 살균작용을 수행할 수 있도록 금(Au) 입자의 농도가 25 내지 55ppm 정도 범위이고, 입자의 크기가 0.001 내지 0.015 마이크로미터(㎛) 정도인 금(Au) 입자 콜로이드 용액을 각 분말성분에 코팅, 건조함으로써, 분말치약으로 적용하더라도 실질적인 살균작용을 수행할 수 있는 효과가 있다.In particular, the powder toothpaste composition containing the gold particles according to the present invention has excellent sterilization effect and after the composition of the powder mixture to improve the prevention effect of caries and gum disease after the gold (Au) particles to perform the sterilization action within a short time By coating and drying the gold (Au) particle colloidal solution having a concentration in the range of about 25 to 55 ppm and the particle size of about 0.001 to 0.015 micrometers (μm) to each powder component, practical sterilization is performed even when applied as a powder toothpaste. It can work.
이하, 본 발명에 따른 금 입자가 함유된 분말치약 조성물을 분말치약의 제조기술에 의거하여 상세히 설명하고, 종래 일반적인 기술로부터 이 분야의 종사자들이 용이하게 알 수 있는 구성과 그에 대한 작용 및 효과에 대한 상세한 설명은 간략히 하거나 생략하고 본 발명과 관련된 부분들을 중심으로 설명하였다.Hereinafter, the powdered toothpaste composition containing the gold particles according to the present invention will be described in detail based on the manufacturing technology of the powdered toothpaste, and the composition and operation and effects thereof can be easily understood by those skilled in the art from the related art. The detailed description is briefly omitted or omitted and described based on the parts related to the present invention.
본 발명에 따른 금 입자가 함유된 분말치약 조성물은 구강내 세균을 억제해주는 살균제로서 함유되는 금 입자, 프라그 제거제, 살균력 증강 보조제, 감미제, 부형제, 착향제, 증백제, 및 착색제로 이루어진 모든 성분을 혼합기에 투입하여 분말 혼합체를 형성하고, 이 분말 혼합체를 교반, 혼합하면서 분말 혼합체의 중량에 대해 3 내지 10 중량%이고 금(Au) 입자의 농도가 25 내지 55ppm인 금(Au) 입자 콜로이드 용액을 고르게 분사하여 코팅하고, 건조하여 형성한다.Powdered toothpaste composition containing gold particles according to the present invention contains all the ingredients consisting of gold particles, plaque remover, bactericidal enhancer, sweetener, excipient, flavoring agent, brightener, and coloring agent contained as a fungicide to inhibit oral bacteria. It was put in a mixer to form a powder mixture, while stirring and mixing the powder mixture, a gold (Au) particle colloidal solution having a concentration of 3 to 10% by weight based on the weight of the powder mixture and 25 to 55 ppm of gold (Au) particles. Spray evenly to coat, dry to form.
이하, 분말 혼합체를 형성하는 각각의 성분에 대해 구체적으로 살펴본다.Hereinafter, each component forming the powder mixture will be described in detail.
상기 금 입자는 금(Au) 성분이 가지고 있는 성질로 인해 구강내에서의 살균력을 강화시켜 세균증식을 억제하여 프라그제거와 구강내 질환을 예방하는 작용을 수행하게 되는데, 이와 같은 금 입자의 살균작용은 금속 금이 방출하는 금 이온이 세균의 호흡, 소화 등을 하는 신진대사에 작용하여 살균작용을 수행하게 된다.The gold particles act to prevent the growth of plaque and prevent diseases in the oral cavity by inhibiting bacterial growth by enhancing the bactericidal power in the oral cavity due to the properties of the gold (Au) component, such as the sterilization of gold particles The gold ions emitted by the silver metal gold act on the metabolism, which causes the bacteria to breathe and digest.
그리고, 상기 금입자는 금(Au) 성분이 가지고 있는 성질로 인해 구강내에서의 살균력을 강화시켜 충치예방과 잇몸질환을 예방하는 작용을 수행하게 되는데, 금입자는 널리 알려진 바와 같이 인체의 피부나 세포에 쉽게 침투하여 박테리아나 균류, 바이러스 등이 산소대사를 할 때 필요한 효소의 기능을 정지시키는 촉매의 역할을 하여 빠른 시간내에 상기 병원체 등을 살균하므로 부작용이 없는 천연 살균제의 기능을 수행하고, 또한 피부 생리 기능과 세포 재생 기능을 활성화해 손상된 잇몸 세포의 회복을 해독작용을 수행하게 되며, 금에서 나오는 양이온이 호르몬의 분비를 원활하게 수행하여 피부건강을 유지시키는 작용을 하게 된다.In addition, the gold particles are due to the properties of the gold (Au) component to enhance the bactericidal power in the oral cavity to prevent tooth decay and prevent gum disease. It penetrates easily into cells and acts as a catalyst to stop the function of enzymes required for oxygen metabolism by bacteria, fungi, viruses, etc., and sterilizes the pathogens in a short time, thus functioning as a natural fungicide without side effects. The skin's physiological function and cell regeneration function are activated to detoxify damaged gum cells and detoxification is performed. The cations from gold smoothly release hormones to maintain skin health.
바람직하게, 금 입자는 순도 99.9%의 금속 금(Au)을 입경이 10 ~ 200㎛가 되도록 형성한 금박을 첨가한다.Preferably, gold particle | grains add the gold foil which formed metallic gold (Au) of purity 99.9% so that a particle diameter might be 10-200 micrometers.
또한, 금 입자의 함량은 상기 분말 혼합체의 전체 중량에 대해 0.0005 ~ 1중량%가 바람직한데, 그 이유는 0.0005중량% 이하이면 살균력이 현저히 약하여 프라제거 와 구강내 질환의 예방효과가 발휘될 수 없고, 그 중량이 1중량%를 초과하게 될 경우에는 그 함량이 추가되더라도 더 이상 살균효과가 증대되지 않음을 실험적으로 알 수 있었다.In addition, the content of gold particles is preferably 0.0005 to 1% by weight relative to the total weight of the powder mixture, because if the amount is less than 0.0005% by weight of the bactericidal power is remarkably weak can not exert the effect of preventing the removal of plastics and oral diseases When the weight exceeds 1% by weight, it can be seen experimentally that the sterilization effect is no longer increased even if the content is added.
프라그 제거제는 염화세틸피리디늄(CPC), 불화나트륨, 일불소인산나트륨과 같이 구강내 세균을 억제하여 프라그를 제거 해주고 구강 내 질환예방과 구취제거의 효과를 발휘하는 성분을 적용할 수 있다. 그 함량은 상기 분말 혼합체의 전체 중량에 대해 염화세틸피리디늄(CPC) 0.1 ~ 0.5중량%, 불화나트륨 0.01 ~ 0.05증량%, 일불소인산나트륨 0.1 ~ 0.7중량% 중에서 1종 또는 2종이 이상을 함유 하는 것이 바람직하다.Plaque remover can be applied to ingredients such as cetylpyridinium chloride (CPC), sodium fluoride, sodium monofluorophosphate to remove plaque by inhibiting oral bacteria and to prevent oral disease and remove bad breath. The content contains one or two or more of cetylpyridinium chloride (CPC) 0.1 to 0.5% by weight, sodium fluoride 0.01 to 0.05% by weight and 0.1 to 0.7% by weight sodium monofluorophosphate relative to the total weight of the powder mixture. It is desirable to.
살균력 증강 보조제는 트리클로산, 매스틱오일, 프로폴리스추출물과 같은 천연 항생물질을 적용할 수 있다. 이때, 상기 분말 혼합체의 전체 중량에 대해 트리클로산 0.01 ~ 0.5중량%, 매스틱오일 0.01 ~ 0.5중량%, 프로폴리스추출물 분말 0.1 ~ 5중량% 중에서 1종 이상을 혼합하는 것이 바람직하다.Antibacterial aids may be applied to natural antibiotics such as triclosan, mastic oil, propolis extract. At this time, it is preferable to mix 1 or more types from 0.01 to 0.5 weight% of triclosan, 0.01 to 0.5 weight% of mastic oil, and 0.1 to 5 weight% of propolis extract powder with respect to the total weight of the said powder mixture.
감미제는 충치예방을 할 수 있는 자일리톨, 사카린나트륨, 및 솔비톨 분말 중에서 선택, 함유하되, 자일리톨 분말 1.0 ~ 10중량%, 사카린나트륨 0.01 ~ 1.0중량%, 솔비톨 분말 2.0 ~ 30중량% 중에서 1종 이상을 함유하는 것이 바람직하다.The sweetener is selected from xylitol, sodium saccharin, and sorbitol powder to prevent tooth decay, and contains at least one of xylitol powder 1.0-10 wt%, saccharin sodium 0.01-1.0 wt%, and sorbitol powder 2.0-30 wt%. It is preferable to contain.
부형제는 분말치약을 일정한 형태로 형성하기 위해 첨가하는 물질로서 유당 50.0 ~ 86.0중량%, 이산화규소 19.0 ~ 75.0중량% 중에서 1종 이상을 함유 하는 것이 바람직하다.The excipient is a substance added to form a powder toothpaste in a certain form, it is preferable to contain at least one of lactose 50.0 ~ 86.0% by weight, silicon dioxide 19.0 ~ 75.0% by weight.
착향제는 박하향 분말 1.0 ~ 5중량%, 민트향 분말 1.0 ~ 5.0중량% 중에서 1종을 선택하여 함유한다.A flavoring agent selects and contains 1 type from 1.0 to 5 weight% of mint flavor powder, and 1.0 to 5.0 weight% of mint flavor powder.
증백제는 인체의 뼈 및 치아 에나멜을 구성하는 주성분인 하이드록시아파타이트(Hydroxyapatite)를 적용하여 치아의 미세한 결손 부분을 메워 치아를 매끄럽 고 광택 있게 만들어 주는 기능을 수행하는 것으로, 그 함량의 범위는 0.5 ~ 2중량% 범위가 되도록 한다.Brightener is a hydroxyapatite, the main component of human bone and tooth enamel, which fills minute defects of teeth and makes the teeth smooth and glossy. The range is 0.5 to 2% by weight.
착색제는 스피룰리나(spirulina)로부터 추출한 스피룰리나 청색소를 0.001 ~ 1.0중량% 범위로 함유하도록 구성한다. 스피룰리나는 청녹색의 남조류로서 사이아노 박테리아의 일종으로 세포벽이 없는 스프링 모양의 나선형 원핵 미생물로서 비타민이 많이 함유되어 있어 황산화작용이 뛰어나며 구강내 세균 감염에 저항력을 높여 면역력을 향상시켜 구강내의 잇몸질환을 예방하고 엽록소인 크로로필은 강력한 살균작용이 있어 구강내 세균증식을 억제시켜주는 물질이다.The colorant is configured to contain spirulina blue pigment extracted from spirulina in the range of 0.001 to 1.0% by weight. Spirulina is a blue-green cyanobacteria, a type of cyano bacteria, a spring-shaped spiral prokaryotic microorganism without cell walls, which contains a lot of vitamins, which is highly sulfated, improves immunity by increasing resistance to bacterial infections in the oral cavity, and improves gum disease in the oral cavity. Chrorophyll, a chlorophyll, is a substance that has a strong bactericidal action and inhibits bacterial growth in the oral cavity.
상기 금(Au) 입자 콜로이드 용액은 증류수에 99.9% 금(Au) 막대를 전기분해 과정을 통해 이온화하여 증류수내에 0.001 내지 0.015 마이크로미터(㎛) 정도의 금(Au) 소립자가 포함되도록 형성한 것이다.The gold (Au) colloidal solution is formed by ionizing a 99.9% gold (Au) rod in distilled water through an electrolysis process to include gold (Au) small particles of about 0.001 to 0.015 micrometers (µm) in distilled water.
한편, 본 발명에 따른 금 입자가 함유된 분말치약 조성물은 함초(鹹草) 분말을 더 포함할 수 있다. 함초 분말은 1 중량% 미만의 미량으로 함유할 경우 유효한 성분의 이용에 한계가 있고, 10 중량% 이상일 경우에는 치약으로서 상쾌감이나 사용감을 해치게 되므로 분말 혼합체의 전체 중량에 대해 1 내지 10 중량% 범위가 되도록 한다.On the other hand, the powdered toothpaste composition containing the gold particles according to the present invention may further comprise a glasswort (鹹 草) powder. When contained in a trace amount of less than 1% by weight of the seaweed powder, there is a limit to the use of the effective ingredients, if more than 10% by weight as a toothpaste impairs the feeling of freshness or feel as a range of 1 to 10% by weight relative to the total weight of the powder mixture Be sure to
함초는 우리나라 해안이나 섬지방의 바닷물이 닿는 해안이나 개펄, 염전 주위에 무리지어 자라고, 퉁퉁하고 마디마다 튀어나온 풀이라 해서 " 퉁퉁마디" 라고 불리우기도 하며, 식물학적 분류로는 명주아과(chenopodiaceae)에 속하는 1년초 식물로서, 육상 식물로서 바닷물에 녹아있는 소금을 비롯하여 칼슘, 마그네슘, 칼륨, 철, 인 등 갖가지 미네랄이 풍부하게 함유하고 있어 치아나 잇몸에 유효한 작용을 수행한다.The seaweed grows in groups around the coast, Gaepul, and salt fields that the seawater of Korea's coast or island region touches, and is called the 'Tung node' because it is a big and protruding grass. The botanical classification is chenopodiaceae. It is a plant belonging to the beginning of the year, which is a land plant, which contains abundant minerals such as calcium, magnesium, potassium, iron and phosphorus, including salt dissolved in seawater, and performs effective action on teeth and gums.
그리고, 함초(鹹草) 분말은 가열 추출방식에 의해 추출하여 분말화한 후 투입할 수도 있지만, 본 실시예에서는 함초에 포함된 유효한 생약성분이 파괴되지 않도록 수집한 함초를 세정하고 냉동 건조하여 파쇄한 후 분말화한 것을 투입한다.In addition, the seaweed powder may be added after extraction and powdering by heating extraction method, but in the present embodiment, the collected seaweeds are washed and freeze-dried so as not to destroy the effective herbal ingredients contained in the seaweed. After that, the powdered one is added.
특히, 함초에 포함된 유효한 생약성분이 파괴되지 않도록 하기 위해서는 이하에서 설명하는 바와 같이 열기에 노출되지 않도록 건조단계 후에 별도로 투입하는 것이 매우 중요하다.In particular, in order not to destroy the effective herbal ingredients contained in the seaweed as described below it is very important to add separately after the drying step to avoid exposure to heat.
그리고, 분말 혼합체를 형성하는 각각의 분말 성분은 20 ~ 50 메시의 체(여과망)를 통과하는 정도의 입도가 바람직하다.And the particle size of the grade which each powder component which forms a powder mixture passes through the sieve (filtration net) of 20-50 mesh is preferable.
이하, 본 발명의 바람직한 실시예에 따른 금 입자가 함유된 분말치약 조성물의 제조방법을 설명한다.Hereinafter, a method for preparing a powder dentifrice composition containing gold particles according to a preferred embodiment of the present invention.
본 발명에 따른 금 입자가 함유된 분말치약 조성물의 제조방법은, 금 입자, 프라그 제거제, 살균력 증강 보조제, 감미제, 부형제, 및 상기 각각의 분말성분들의 잔량 중량%로 함유되는 착향제, 증백제, 착색제를 준비하는 분말성분 준비단계와, 금(Au) 입자 콜로이드 용액을 준비하는 용액 준비단계와, 분말 혼합체를 형성하는 혼합체 형성단계와, 분말 성분의 표면에 금(Au) 입자 콜로이드 용액을 코팅하는 코팅단계와, 분말 혼합체를 건조하는 건조단계를 순차적으로 시행한다.Method for producing a powder toothpaste composition containing gold particles according to the present invention, gold particles, plaque remover, bactericidal enhancer, sweeteners, excipients, flavoring agent, brightener, contained in the remaining weight% of each powder component, A powder component preparation step of preparing a colorant, a solution preparation step of preparing a gold (Au) particle colloidal solution, a mixture formation step of forming a powder mixture, and coating a gold (Au) particle colloidal solution on the surface of the powder component The coating step and the drying step of drying the powder mixture are carried out sequentially.
먼저, 분말성분 준비단계는 전술한 바와 같이 구강내 세균을 억제해주는 살균제로서 0.0005 ~ 1.0 중량% 범위로 함유되는 금 입자, 염화세틸피리디늄 0.1 ~ 0.5중량%, 불화나트륨 0.01 ~ 0.05중량%, 일불소인산나트륨 0.1 ~ 0.7중량% 중에서 1종의 또는 2종이 선택되어 함유되는 프라그 제거제, 트리클로산 0.01 ~ 0.5중량%, 매스틱오일 0.01 ~ 0.5중량%, 프로폴리스추출물 분말 0.1 ~ 5중량% 중에서 1종 이상의 살균력 증강 보조제, 자일리톨 분말 1.0 ~ 10중량%, 사카린나트륨 0.01 ~ 1.0 중량%, 솔비톨 분말 2.0 ~ 30중량% 중에서 1종 이상이 선택되어 함유되는 감미제, 유당 50.0 ~ 86.0중량%, 이산화규소 19.0 ~ 75.0중량% 중에서 1종 이상 선택되어 함유되는 부형제, 및 상기 각각의 분말성분들의 잔량 중량%로 함유되는 착향제, 증백제, 착색제를 각각 준비한다.First, the powder component preparation step is a fungicide for inhibiting oral bacteria as described above, gold particles contained in the range of 0.0005 to 1.0% by weight, 0.1 to 0.5% by weight of cetylpyridinium chloride, 0.01 to 0.05% by weight of sodium fluoride, and One or two types of plaque remover selected from among 0.1 to 0.7% by weight of sodium fluorophosphate, 0.01 to 0.5% by weight of triclosan, 0.01 to 0.5% by weight of mastic oil, and 0.1 to 5% by weight of propolis extract powder The above-mentioned bactericidal enhancer, xylitol powder 1.0 to 10% by weight, saccharin sodium 0.01 to 1.0% by weight, sorbitol powder 2.0 to 30% by weight, one or more selected sweeteners contained, lactose 50.0 to 86.0% by weight, silicon dioxide 19.0 to One or more excipients selected from 75.0 wt%, and flavoring agents, brighteners and coloring agents, which are contained in the remaining wt% of the respective powder components, are prepared. .
용액 준비단계는 전해조에 증류수를 주입하고 순도 99.9% 금(Au) 막대를 설치하여 전기분해 과정을 통해 금(Au) 입자의 농도가 25 내지 55ppm인 금(Au) 입자 콜로이드 용액을 준비하는 단계로서, 순도 99.9% 금(Au) 막대를 전해조에 설치하여 전기분해를 실시하면 금(Au) 막대의 금 성분이 이온화된 후 입자화 되어 증류수상에 존재하게 된다. 이때, 금은 은(Ag)에 비해 이온화 경향이 빨라 그 농도가 대략 25ppm 정도가 되면 입자화 되어 증류수상에 존재하면서 콜로이드 용액으로 형성되기 시작하고 55ppm를 넘어서게 되면 금 입자가 침전될 뿐만 아니라 입자가 서로 결합되면서 그 크기가 증가됨을 알 수 있었다.Solution preparation step is to prepare a gold (Au) particle colloidal solution having a concentration of 25 to 55ppm of gold (Au) particles by injecting distilled water into the electrolytic cell and installing a 99.9% purity gold rod. When electrolysis is performed by installing a 99.9% pure gold (Au) rod in an electrolytic cell, the gold component of the gold (Au) rod is ionized and then granulated to exist in distilled water. In this case, gold has a tendency to ionize faster than silver (Ag), and when the concentration reaches about 25 ppm, the particles are granulated and present in distilled water and start to form a colloidal solution. Combined with each other, the size was found to increase.
그리고, 본 실시예에서 금(Au) 입자의 농도가 25 내지 55ppm 정도 범위에 있도록 전기분해하게 되면 멸균 증류수에 포함되는 금 입자의 크기가 0.001 내지 0.015 마이크로미터(㎛) 정도가 되는데, 이와 같이 입경이 작은 금 소립자를 사용함으로써, 양치질시에 보다 신속하게 살균작용을 수행할 수 있도록 구성한 것이다.In addition, in the present embodiment, when the electrolysis is performed such that the concentration of Au particles is in the range of about 25 to 55 ppm, the size of the gold particles included in the sterile distilled water is about 0.001 to 0.015 micrometers (μm). By using these small gold particles, it is configured to perform sterilization more quickly when brushing teeth.
혼합체 형성단계는 상기 분말성분 준비단계에서 준비된 각각의 분말성분을 채를 통과하도록 하면서 혼합기에 투입하여 분말 혼합체를 형성하는 단계로서, 먼저, 프라그 제거제, 살균력 증강 보조제, 감미제, 및 부형제를 30메시 정도의 여과망으로 여과하면서 투입, 혼합하고, 2차로 박하향 분말, 민트향 분말 중에서 1종과 스피룰리나 청색소를 30메시로 여과하여 혼합기에 투입한 다음 15 ~ 25rpm으로 90분에서 120분간 혼합을 하게 되면 각 성분들이 점차적으로 등분포하게 된다.Mixture forming step is a step of forming a powder mixture by passing each powder ingredient prepared in the powder ingredient preparation step to the mixer while first, the plaque remover, bactericidal enhancer, sweetener, and excipient about 30 mesh After filtering and filtering with a filter network of 2, peppermint flavor powder, mint flavor powder and one of the spirulina blue pigment filtered through 30 mesh and put into the mixer and then mixed at 90 minutes to 15 minutes at 15-25 rpm each The components are gradually distributed equally.
코팅단계는 상기 분말 혼합체를 교반, 혼합하면서 용액 준비단계에서 준비된 금(Au) 입자 콜로이드 용액을 분말 혼합체의 중량에 대해 3 내지 10 중량% 범위로 분사하여 각각의 분말 성분의 표면에 코팅하는 단계로서, 정해진 양을 분무할 수 있는 자동 분무기를 이용하여 교반, 혼합되는 분말 혼합체의 표면으로 금(Au) 입자 콜로이드 용액을 분사하는 방식으로 시행한다.The coating step is a step of coating the surface of each powder component by spraying the gold (Au) particle colloidal solution prepared in the solution preparation step while stirring and mixing the powder mixture in a range of 3 to 10% by weight based on the weight of the powder mixture. In this case, a gold (Au) particle colloidal solution is sprayed onto the surface of the powder mixture to be stirred and mixed by using an automatic sprayer capable of spraying a predetermined amount.
그리고, 금(Au) 입자 콜로이드 용액의 투입 중량이 3 내지 10 중량% 범위로 정해진 이유는, 그 중량이 분말 혼합체의 중량에 대해 10 중량% 넘어서게 되면 분말 혼합체를 형성하는 각 분말 성분이 서로 엉켜 붙어 덩어리 형태가 되므로 별도의 파쇄공정을 다시 한 번 거쳐야 할 뿐만 아니라 건조에 지나치게 많은 시간이 소요되어 각 분말 성분이 서로 반응하는 등의 문제점을 초래하게 된다. 그리고, 금(Au) 입자 콜로이드 용액의 투입 중량이 3 중량% 미만일 경우에는 그 양이 너무 작아서 분말 혼합체에 전체적으로 고르게 분포되게 분사할 수 없으므로 유효한 작용을 기대할 수 없었다.The reason why the input weight of the gold (Au) particle colloidal solution is set in the range of 3 to 10% by weight is that when the weight exceeds 10% by weight relative to the weight of the powder mixture, the respective powder components forming the powder mixture are entangled with each other. Since it becomes a lump form, not only has to go through a separate crushing process once again, it takes too much time for drying, which causes problems such as each powder component reacting with each other. In addition, when the input weight of the gold (Au) particle colloidal solution was less than 3% by weight, the amount thereof was too small to be evenly distributed in the powder mixture so that an effective action could not be expected.
건조단계는 코팅단계에서 금(Au) 입자 콜로이드 용액이 코팅된 분말 혼합체 를 건조하는 단계로서, 이 건조단계는 혼합기에 열을 가하여 시행하는 가열건조, 또는 열풍을 분사하여 시행하는 열풍건조 중에서 선택하여 시행할 수 있다.The drying step is a step of drying the powder mixture coated with the gold (Au) particle colloid solution in the coating step. This drying step is selected from heat drying performed by applying heat to the mixer, or hot air drying performed by spraying hot air. Can be implemented.
이러한 건조단계가 완료되면 금(Au) 입자 콜로이드 용액 중에 포함된 증류수는 모두 증발하고 미세한 금(Au) 소립자가 분말 혼합체를 구성하는 각 분말입자에 잔류하게 된다.When the drying step is completed, all distilled water contained in the gold (Au) particle colloid solution is evaporated and fine gold (Au) small particles remain in each powder particle constituting the powder mixture.
전술한 건조단계가 완료되면, 조성된 분말 조성물을 소정 용기에 충전하여 포장하여 본 발명에 따른 분말치약 조성물의 제조과정이 완료된다.When the drying step described above is completed, the powder powder composition is packed in a predetermined container, and then the manufacturing process of the powder toothpaste composition according to the present invention is completed.
한편, 함초 분말을 포함하는 경우에는 함초분말 혼합단계를 더 시행한다. 함초분말 혼합단계는 분말성분 준비단계를 통해 준비된 함초(鹹草) 분말을 건조단계를 시행한 분말 혼합체에 투입하여 고르게 분포되도록 다시 한번 교반 및 혼합하는 단계로서, 이때, 투입되는 함초분말은 분말 혼합체의 전체 중량에 대해 1 내지 10 중량% 범위가 되도록 한다.On the other hand, when it contains a seaweed powder, the seaweed powder mixing step is further performed. The mixing of the seaweed powder is a step of stirring and mixing the green seaweed powder prepared through the powder component preparation step into the powder mixture subjected to the drying step to distribute the powder evenly. To 1 to 10% by weight relative to the total weight of the.
한편, 상기와 같은 제조과정을 통해 조제된 본 발명에 따른 금 입자가 함유된 분말치약 조성물의 사용방법을 간략하게 설명한다.On the other hand, it will be described briefly how to use the powdered toothpaste composition containing the gold particles according to the present invention prepared through the manufacturing process as described above.
본 발명에 따른 금 입자가 함유된 분말치약 조성물의 성상은 엷은 회색이나 엷은 청색의 분말상으로서 종래에는 반드시 페이스트상의 치약에 부착하여 사용하였지만, 단시간의 양치질 시간에도 충분하게 살균작용을 수행하므로 본 실시예에 따른 분말상의 조성물은 단독으로도 사용할 수 있다.The powder toothpaste composition containing the gold particles according to the present invention is a light gray or light blue powder, which is conventionally used by being attached to a paste-like toothpaste, but it performs sterilization sufficiently even for a short time brushing time. The powdery composition according to the present invention can be used alone.
이하, 본 발명에 따른 바람직한 실시예를 나타내는 것으로, 이와 같은 실시예들은 본 발명의 이해를 돕기 위해 예시한 것으로 본 발명의 범위가 하기 실시예 에 의해 한정되는 것은 아니다. 그리고, 먼저, 분말 혼합체에 대해 유해균에 대한 생체 외 항균력을 실험하고, 구취제거성, 프라그 제거 능력, 및 사용감을 실험하고, 금(Au) 입자 콜로이드 용액를 코팅한 후의 유해균에 대한 생체 외 항균력을 실험하였다.Hereinafter, preferred embodiments according to the present invention, these examples are illustrated to help the understanding of the present invention and the scope of the present invention is not limited by the following examples. First, the in vitro antimicrobial activity against harmful bacteria was tested on the powder mixture, bad breath removal ability, plaque removal ability, and feeling test were performed, and the in vitro antimicrobial activity against harmful bacteria after coating the gold (Au) particle colloidal solution was tested. It was.
이하, 구체적인 실시예에 대해 설명한다.Hereinafter, specific examples will be described.
(분말 혼합체1)(Powder mixture 1)
하기의 표1에 나타난 바와 같이 살균제로서 금 입자(금박) 0.0005중량%, 살균력 증강 보조제로서 트리클로산 0.1중량%, 매스틱오일 0.1중량%, 프로폴리스추출물 1.0중량%, 프라그제거제로 염화세틸피리디늄 0.1중량%, 감미제로서 자일리톨 5중량%, 사카린나트륨 0.002중량%, 부형제로서 유당 85.98중량%, 착향제로서 박하향분말 5.0중량%, 민트향분말 2.0중량%, 증백제로서 하이드록시아파타이트 0.3중량%, 착색제로서 스피룰리나 청색소 0.4중량를 혼합하여 분말치약 조성물을 제조하였다.As shown in Table 1 below, 0.0005% by weight of gold particles (gold leaf) as a bactericide, 0.1% by weight of triclosan, 0.1% by weight of mastic oil, 1.0% by weight of propolis extract, and 0.1% of cetylpyridinium chloride as a plaque remover. 5% by weight xylitol as a sweetener, 0.002% by weight sodium saccharin, 85.98% by weight lactose as excipient, 5.0% by weight mint flavor powder as flavoring agent, 2.0% by weight mint flavor powder, 0.3% by weight hydroxyapatite as brightener, colorant As a powder toothpaste composition was prepared by mixing 0.4 wt% of spirulina and blue pigment.
(분말 혼합체2)(Powder mixture 2)
하기의 표1에 나타난 바와 같이 살균제로서 금 입자(금박) 0.5중량%, 살균력 증강 보조제로서 트리클로산 0.2중량%, 프로폴리스추출물 1.5중량%, 프라그 제거제로 염화세틸피리디늄 0.2중량%, 감미제로서 자일리톨 3중량%, 솔비톨 분말 20중량%, 부형제로서 유당 67.90중량%, 착향제로서 박하향분말 5.0중량%, 민트향분말 1.0중량%, 증백제로서 하이드록시아파타이트 0.5중량%, 착색제로서 스피룰리나 청색소 0.4중량를 혼합하여 분말치약 조성물을 제조하였다.As shown in Table 1 below, 0.5% by weight of gold particles (gold leaf) as a disinfectant, 0.2% by weight of triclosan as a bactericidal enhancer, 1.5% by weight of propolis extract, 0.2% by weight of cetylpyridinium chloride as a plaque remover, and xylitol as a sweetener 3 20 wt% sorbitol powder, 67.90 wt% lactose as excipient, 5.0 wt% peppermint flavor powder as flavoring agent, 1.0 wt% mint flavor powder, 0.5 wt% hydroxyapatite as brightener, 0.4 wt% spirulina and blue pigment as colorant To powder powder composition was prepared.
(분말 혼합체3)(Powder mixture 3)
하기의 표1에 나타난 바와 같이 살균제로서 금 입자(금박) 1.0중량%, 살균력 증강 보조제로서 트리클로산 0.3중량%, 프로폴리스추출물 3중량%, 프라그 제거제로 염화세틸피리디늄 0.4중량%, 감미제로서 사카린나트륨 0.03중량%, 솔비톨 분말 20중량%, 부형제로서 유당 49.17중량%, 이산화규소 20.0중량%, 착향제로서 박하향분말 5.0중량%, 증백제로서 하이드록시아파타이트 0.7중량%, 착색제로서 스피룰리나 청색소 0.4중량를 혼합하여 분말치약 조성물을 제조하였다.As shown in Table 1 below, 1.0% by weight of gold particles (gold leaf) as a bactericide, 0.3% by weight of triclosan as a bactericidal enhancer, 3% by weight of propolis extract, 0.4% by weight of cetylpyridinium chloride as a plaque remover, sodium saccharin as a sweetener 0.03% by weight, 20% by weight of sorbitol powder, 49.17% by weight of lactose as excipient, 20.0% by weight of silicon dioxide, 5.0% by weight of peppermint flavor powder as flavoring agent, 0.7% by weight of hydroxyapatite as brightener, 0.4% by weight of spirulina or blue pigment as colorant To powder powder composition was prepared.
(분말 혼합체4)(Powder mixture 4)
하기의 표1에 나타난 바와 같이 살균제로서 금 입자(금박) 1.2중량%, 살균력 증강 보조제로서 트리클로산 0.5중량%, 매스틱오일 0.4중량%, 프로폴리스추출물 4중량%, 프라그 제거제로 염화세틸피리디늄 0.5중량%, 감미제로서 자일리톨 10중량%, 솔비톨 분말 20중량%, 부형제로서 유당 55.00중량%, 착향제로서 박하향분말 2.0중량%, 민트향분말 5중량%, 증백제로서 하이드록시아파타이트 1.0중량%, 착색제로서 스피룰리나 청색소 0.4중량를 혼합하여 분말치약 조성물을 제조하였다.As shown in Table 1 below, 1.2% by weight of gold particles (gold leaf) as a bactericide, 0.5% by weight of triclosan, 0.4% by weight of mastic oil, 4% by weight of propolis extract, and 0.5% cetylpyridinium chloride as a plaque remover Wt%, xylitol 10% by weight, sorbitol powder 20% by weight, lactose 55.00% as excipient, peppermint flavor powder 2.0% by weight, mint flavor powder 5% by weight, hydroxyapatite 1.0% by weight, colorant As a powder toothpaste composition was prepared by mixing 0.4 wt% of spirulina and blue pigment.
(분말 혼합체5)(Powder mixture 5)
하기의 표1에 나타난 바와 같이 감미제로서 솔비톨 분말 20중량%, 부형제로서 유당 73.10중량%, 착향제로서 박하향분말 1.0중량%, 민트향분말 5.0중량%, 증백제로서 하이드록시아파타이트 0.5중량%, 착색제로서 스피룰리나 청색소 0.4중량%를 혼합하여 분말치약 조성물을 제조하였다.As shown in Table 1 below, 20% by weight of sorbitol powder as a sweetening agent, 73.10% by weight of lactose as excipient, 1.0% by weight of peppermint flavor powder, 5.0% by weight of mint flavor powder, 0.5% by weight of hydroxyapatite as brightener, colorant As a powder toothpaste composition was prepared by mixing 0.4% by weight of spirulina and blue pigment.
(분말 혼합체6)(Powder mixture 6)
하기의 표1에 나타난 바와 같이 감미제로서 솔비톨 분말 20중량%, 부형제로서 유당 74.10중량%, 착향제로서 박하향분말 5.0중량%, 증벡제로서 하이드록시아파타이트 0.5중량%, 착색제로서 스피룰리나 청색소 0.4중량%를 혼합하여 분말치약 제조하였다.As shown in Table 1 below, 20% by weight of sorbitol powder as a sweetener, 74.10% by weight of lactose as excipient, 5.0% by weight of peppermint flavor powder as a flavoring agent, 0.5% by weight of hydroxyapatite as an additive, and 0.4% by weight of spirulina or blue pigment as colorant Powder Toothpaste was prepared by mixing.
[실험예1]Experimental Example 1
이하의 실험예1은 표1의 각 분말 혼합체의 구강 유해균에 대한 생체 외 항균력을 실험한 것으로, 이때 사용되는 시험균주는 치아에 충치를 발생시키는 스트렙토코커스 뮤탄스(Streptococcus mutans;NCTC 10449)와, 치주질환을 발생시키는 악티노바실러스 악티노마이세템코미탄스(Actinobacillus actinomycetemcomitans;ATCC 29522) 및 캡노시토파자 오크라시아(Capnocytophaga ochracea;ATCC 27827)와, 치주질환 및 구취를 발생시키는 푸조박테리움 뉴클레아텀(Fusobacterium nucleatum;ATCC 25586)이 적용되었다.Experimental Example 1 below is to test the in vitro antimicrobial activity of the oral harmful bacteria of each powder mixture of Table 1, the test strain used at this time Streptococcus mutans (NCTC 10449) and the caries generated tooth, Actinobacillus actinomycetemcomitans (ATCC 29522) and Capnocytophaga ochracea (ATCC 27827), which cause periodontal disease, and Peugeot bacterium nucleatum, which cause periodontal disease and bad breath (Fusobacterium nucleatum; ATCC 25586) was applied.
상기한 시험균주를 동결보관상태에서 꺼내어 누트리언트 브로스(Nutrient broth)에 접종한 후 37℃의 배양기에서 48시간 동안 배양하고, 이와 같이 전 배양된 각 시험균액을 100㎖의 누트리언트 브로스에 1%(v/v) 접종 후 배양기에서 다시 12-20 시간 동안 배양한 것을 실험에 사용하였다.The test strains were taken out of the frozen storage state, inoculated in Nutrient broth, and then incubated for 48 hours in a 37 ° C. incubator. Incubation for 12-20 hours in the incubator after 1% (v / v) inoculation was used for the experiment.
시험을 위해 적절한 세균수(bacterial suspension number)의 초기값은 106 ~ 107 cell/㎖이며 이를 위해 전배양한 균액으로부터 1 ㎖ 씩을 미리 살균한 100 ㎖의 멸균증류수에 넣고, 이것을 원액으로 하여 단계희석법으로 희석한 후 각각을 고체배지에 도말하고 이를 24시간 배양하여 재생된 집락을 계수하여 초기 접종농도를 구하였다.The initial bacterial suspension number for the test is 106 ~ 107 cell / ml. To this end, 1 ml of pre-cultivated bacterial solution is added to 100 ml of sterile distilled water, which is pre-sterilized. After dilution, each was plated in a solid medium and cultured for 24 hours to count the regenerated colonies to determine the initial inoculation concentration.
한편, 시험액의 조제는, 전술한 분말 혼합체1 내지 6과 같이 조제된 조성물을 멸균증류수에 동일한 양으로 풀어 장시간 용해시켜서 준비하였다.On the other hand, the preparation of the test solution was prepared by dissolving the composition prepared in the same manner as the powder mixtures 1 to 6 described above in sterile distilled water and dissolving it for a long time.
그리고, 상기와 준비된 각 시험액 1㎖ 씩을 초기 접종농도가 맞추어진 각각의 시험균주에 부어 1분의 시간이 경과한 후 잔존 균수를 측정하였다. 균수의 측정은 회수한 원액을 단계희석법으로 희석하고 각 희석배수별로 평판배지에 도말하여 배양기에 배양한 후 각 평판배지의 군락을 계수하여 잔존 균수에 따른 균수의 감소여부를 확인함으로써 항균력을 측정하였다. 이와 같은 방법으로 초기 접종농도에 대한 잔존 균수의 농도에 의해 백분율로 구해지는 감균율(%)로서 항균력(살균력)을 정리하면 하기의 표2에 나타난 바와 같다.Then, 1 ml of each test solution prepared as described above was poured into each of the test strains at which the initial inoculation concentration was adjusted, and after 1 minute of elapsed time, the remaining bacterial count was measured. The bacterial count was measured by diluting the recovered stock solution by the step dilution method, spreading it on a plate medium for each dilution fold, incubating in the incubator, and counting the colonies of each plate medium to determine whether the number of bacteria was reduced according to the number of remaining bacteria. . In this way, the antimicrobial activity (sterilization power) is summarized as Table 2 below, as a percentage of the microbial fungi obtained as a percentage by the concentration of the remaining bacteria to the initial inoculation concentration.
실험예1을 통해서 알 수 있는 사실은 표2에 나타난 바와 같이, 금 입자의 함량이 0.0005중량% 이하인 비교예1에서는 모든 시험균주에서 살균력이 현저히 낮다는 사실은 알 수 있고, 금 입자의 함량을 0.0005중량%에서 1중량% 까지 증가시킬 경우에는 점차적으로 살균력이 증가되다가 1중량%를 초과하게 될 경우에는 살균력에 변화가 없음을 알 수 있다. 또한 염화세틸피리디늄이 전혀 함유되지 않은 분말 혼합체5 및 6은 살균력이 현저히 낮다는 사실을 알 수 있다.As can be seen from Experimental Example 1, as shown in Table 2, in Comparative Example 1 in which the content of gold particles is 0.0005% by weight or less, the bactericidal power is significantly lower in all test strains. When the amount is increased from 0.0005% by weight to 1% by weight, the sterilization power gradually increases, but when it exceeds 1% by weight, it can be seen that there is no change in the sterilization power. It can also be seen that powder mixtures 5 and 6, which contain no cetylpyridinium chloride at all, have a significantly lower bactericidal power.
결국, 금 입자의 함량이 0.0005중량% 내지 1중량%이고, 염화세틸피리디늄이 함유된 경우에는 살균력이 뛰어나다는 사실을 확인할 수 있다.As a result, when the content of gold particles is 0.0005% by weight to 1% by weight, and it contains cetylpyridinium chloride, it can be confirmed that the bactericidal power is excellent.
[실험예2]Experimental Example 2
이하의 실험예2은 상기의 표1에 나타난 조성비에 따라 제조한 분말 혼합체1 내지 6의 조성물에 대하여 각각 성인 남녀 10명씩을 대상으로 사용하도록 하고, 구취제거, 프라그제거, 사용감을 5점 척도법에 따라 관능검사를 실시하여 그 평균값을 하기의 표3에 나타낸 것이다.Experimental Example 2 below is to use the composition of the powder mixtures 1 to 6 prepared in accordance with the composition ratio shown in Table 1 to each adult 10 men and women, and to remove the bad breath, plaque, feeling in a five-point scale method According to the sensory test, the average value is shown in Table 3 below.
상기와 같은 실험예3을 통해서 알 수 있는 사실은 표3에 나타난 바와 같이, 금 입자의 함량이 증가할수록 프라그제거 와 구취제거는 향상되지만 사용감은 점차적으로 저하된다는 사실을 알 수 있고, 특히 염화세틸피리디늄이 첨가되지 않은 분말 혼합체5 및 6에서는 구취제거와 프라그제거 효과가 현저한 낮다는 사실을 알 수 있다.As can be seen from the above Experimental Example 3, as shown in Table 3, it can be seen that as the content of the gold particles increases, the removal of plaque and the bad breath are improved, but the feeling gradually decreases. It can be seen that in the powder mixtures 5 and 6 without pyridinium addition, the bad breath removal and plaque removal effects are remarkably low.
결국, 실험예3을 통해서는 금 입자의 함량이 0.0005중량% 내지 1중량%이고, 염화세틸피리디늄이 함유된 경우에 구취제거, 프라그제거, 및 사용감을 모두 만족할 수 있다는 사실을 확인할 수 있다.As a result, it can be confirmed from Experimental Example 3 that the content of gold particles is 0.0005% by weight to 1% by weight, and when the cetylpyridinium chloride is contained, all of bad breath removal, plaque removal, and usability can be satisfied.
[실험예3]Experimental Example 3
이하의 실험예3은 표1의 각 분말 혼합체 중에서 항균력이 뛰어난 것으로 확인된 시료 중에서 분말 혼합체2를 선택하고 농도가 서로 다른 금 콜로이드 용액(20ppm,25ppm,45ppm,55ppm,70ppm)을 분말 혼합체2의 중량에 대해 3중량%의 양으로 코팅하여 준비한 후, 구강 유해균에 대한 생체 외 살균력을 실험한 결과 표4와 같은 결과를 얻었다. 실험예3은 전술한 실험예1과 동일한 방법으로 시행하지만, 실질적인 양치질시에 살균력을 확인할 수 있도록 조제된 분말치약 조성물을 멸균증류수에 동일한 양으로 투입하되 실험예1에서와 같이 완전히 용해될 때 기다리지 않고 교반한 후 즉시 준비된 각 시험액 1㎖ 씩을 초기 접종농도가 맞추어진 각각의 시험균주에 부어 1분의 시간이 경과한 후 잔존 균수를 측정하였다. 균수의 측정은 회수한 원액을 단계희석법으로 희석하고 각 희석배수별로 평판배지에 도말하여 배양기에 배양한 후 각 평판배지의 군락을 계수하여 잔존 균수에 따른 균수의 감소여부를 확인함으로써 항균력을 측정하였다. 이와 같은 방법으로 초기 접종농도에 대한 잔존 균수의 농도에 의해 백분율로 구해지는 감균율(%)로서 항균력(살균력)을 정리하였다.Experimental Example 3 below selects powder mixture 2 from among the powder mixtures of Table 1, which are found to have excellent antimicrobial activity, and selects gold colloidal solutions having different concentrations (20ppm, 25ppm, 45ppm, 55ppm, 70ppm) of powder mixture 2. After coating and preparing in an amount of 3% by weight based on the weight, the in vitro bactericidal power against oral harmful bacteria was tested, and the results as shown in Table 4 were obtained. Experimental Example 3 was carried out in the same manner as Experimental Example 1 described above, but in the same amount of the powdered toothpaste composition prepared in sterile distilled water so as to confirm the bactericidal power during substantial brushing, but wait until completely dissolved as in Experimental Example 1 After stirring without stirring, 1 ml of each test solution prepared immediately was poured into each test strain at which the initial inoculation concentration was adjusted, and after 1 minute elapsed, the remaining bacterial count was measured. The bacterial count was measured by diluting the recovered stock solution by the step dilution method, spreading it on a plate medium for each dilution fold, incubating in the incubator, and counting the colonies of each plate medium to determine whether the number of bacteria was reduced according to the number of remaining bacteria. . In this way, the antimicrobial activity (sterilization power) was summarized as the percentage of microbial fungi obtained as a percentage by the concentration of the remaining bacteria to the initial inoculation concentration.
실험예3을 통해서 알 수 있는 사실은 표4에 나타난 바와 같이, 금 입자 콜로이드 용액이 코팅된 경우 비율에 관계없이 상대적으로 단시간 내에 효과적인 살균작용을 수행함을 알 수 있다.As can be seen from Experiment 3, it can be seen that, as shown in Table 4, when the gold particle colloidal solution is coated, effective sterilization is performed within a relatively short time regardless of the ratio.
하지만, 금 입자 콜로이드 용액의 농도가 25ppm 이하이거나 55ppm 이상인 경우 모든 시험균주에서 살균력이 떨어진다는 사실은 알 수 있다. 그 이유는 금 입자 콜로이드 용액의 농도가 25ppm 이하일 경우 살균작용을 위한 농도가 너무 낮아서 충분한 살균작용을 수행할 수 없는 것으로 판단되고, 금 입자 콜로이드 용액의 농도가 55ppm 이상인 경우는 금 미립자의 크기가 상대적으로 커짐에 따라 시험균주와의 접촉 면적이 작아서 살균력이 저하되는 것으로 판단된다.However, it can be seen that the bactericidal power of all test strains is poor when the concentration of the colloidal gold particles is less than 25ppm or more than 55ppm. The reason is that when the concentration of the gold particle colloidal solution is 25ppm or less, the concentration for sterilization is too low to perform sufficient sterilization, and when the concentration of the gold particle colloidal solution is 55ppm or more, the size of the gold fine particles is relatively high. As it becomes larger, the contact area with the test strain becomes smaller, so that the sterilizing power is deteriorated.
상술한 바와 같은, 본 발명의 바람직한 실시예에 따른 금 입자가 함유된 분말치약 조성물과 그 제조방법을 상기한 설명 및 도면에 따라 도시하였지만, 이는 예를 들어 설명한 것에 불과하며 본 발명의 기술적 사상을 벗어나지 않는 범위 내에서 다양한 변화 및 변경이 가능하다는 것을 이 분야의 통상적인 기술자들은 잘 이해할 수 있을 것이다.As described above, the powder toothpaste composition containing the gold particles according to a preferred embodiment of the present invention and a manufacturing method thereof are shown in accordance with the above description and drawings, but this is merely described for example and the technical spirit of the present invention. Those skilled in the art will appreciate that various changes and modifications can be made without departing.
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