KR20190041799A - Composition for prevention or treatment of oral disease comprising Alkannin - Google Patents
Composition for prevention or treatment of oral disease comprising Alkannin Download PDFInfo
- Publication number
- KR20190041799A KR20190041799A KR1020170133489A KR20170133489A KR20190041799A KR 20190041799 A KR20190041799 A KR 20190041799A KR 1020170133489 A KR1020170133489 A KR 1020170133489A KR 20170133489 A KR20170133489 A KR 20170133489A KR 20190041799 A KR20190041799 A KR 20190041799A
- Authority
- KR
- South Korea
- Prior art keywords
- oral
- quasi
- composition
- present
- alkanin
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 77
- 208000025157 Oral disease Diseases 0.000 title claims abstract description 34
- 208000030194 mouth disease Diseases 0.000 title claims abstract description 34
- UNNKKUDWEASWDN-UHFFFAOYSA-N alkannin Natural products CC(=CCC(O)c1cc(O)c2C(=O)C=CC(=O)c2c1O)C UNNKKUDWEASWDN-UHFFFAOYSA-N 0.000 title abstract description 24
- NEZONWMXZKDMKF-JTQLQIEISA-N Alkannin Chemical compound C1=CC(O)=C2C(=O)C([C@@H](O)CC=C(C)C)=CC(=O)C2=C1O NEZONWMXZKDMKF-JTQLQIEISA-N 0.000 title abstract description 5
- 239000004229 Alkannin Substances 0.000 title abstract description 4
- 235000019232 alkannin Nutrition 0.000 title abstract description 4
- 230000002265 prevention Effects 0.000 title description 11
- 208000028169 periodontal disease Diseases 0.000 claims abstract description 39
- 208000002925 dental caries Diseases 0.000 claims abstract description 37
- 239000003814 drug Substances 0.000 claims abstract description 34
- 206010006326 Breath odour Diseases 0.000 claims abstract description 32
- 229940079593 drug Drugs 0.000 claims abstract description 31
- 235000013305 food Nutrition 0.000 claims abstract description 22
- 208000007565 gingivitis Diseases 0.000 claims abstract description 17
- 208000004371 toothache Diseases 0.000 claims abstract description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 15
- 229940034610 toothpaste Drugs 0.000 claims description 33
- 239000000606 toothpaste Substances 0.000 claims description 33
- 239000004480 active ingredient Substances 0.000 claims description 24
- 150000003839 salts Chemical class 0.000 claims description 21
- 241000194019 Streptococcus mutans Species 0.000 claims description 11
- 238000009472 formulation Methods 0.000 claims description 10
- 201000001245 periodontitis Diseases 0.000 claims description 10
- 208000032139 Halitosis Diseases 0.000 claims description 9
- 239000002324 mouth wash Substances 0.000 claims description 7
- 229940051866 mouthwash Drugs 0.000 claims description 7
- 241000605862 Porphyromonas gingivalis Species 0.000 claims description 5
- 235000009508 confectionery Nutrition 0.000 claims description 4
- 229940042125 oral ointment Drugs 0.000 claims description 2
- 239000000668 oral spray Substances 0.000 claims description 2
- 229940041678 oral spray Drugs 0.000 claims description 2
- 201000004681 Psoriasis Diseases 0.000 claims 1
- 239000002966 varnish Substances 0.000 claims 1
- 241000894006 Bacteria Species 0.000 abstract description 23
- 230000000694 effects Effects 0.000 abstract description 20
- 208000002193 Pain Diseases 0.000 abstract description 18
- 230000002401 inhibitory effect Effects 0.000 abstract description 14
- XEYBRNLFEZDVAW-ARSRFYASSA-N dinoprostone Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1C\C=C/CCCC(O)=O XEYBRNLFEZDVAW-ARSRFYASSA-N 0.000 abstract description 11
- 229960002986 dinoprostone Drugs 0.000 abstract description 11
- XEYBRNLFEZDVAW-UHFFFAOYSA-N prostaglandin E2 Natural products CCCCCC(O)C=CC1C(O)CC(=O)C1CC=CCCCC(O)=O XEYBRNLFEZDVAW-UHFFFAOYSA-N 0.000 abstract description 11
- 206010061218 Inflammation Diseases 0.000 abstract description 9
- 230000004054 inflammatory process Effects 0.000 abstract description 9
- 230000000845 anti-microbial effect Effects 0.000 abstract description 7
- 201000002170 dentin sensitivity Diseases 0.000 abstract description 6
- 230000015572 biosynthetic process Effects 0.000 abstract description 5
- 239000003550 marker Substances 0.000 abstract description 4
- 230000001419 dependent effect Effects 0.000 abstract description 3
- 230000036347 tooth sensitivity Effects 0.000 abstract 3
- 210000000214 mouth Anatomy 0.000 description 20
- 238000012360 testing method Methods 0.000 description 15
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 11
- 235000013376 functional food Nutrition 0.000 description 11
- 230000036541 health Effects 0.000 description 11
- 201000010099 disease Diseases 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 210000004268 dentin Anatomy 0.000 description 9
- 208000024891 symptom Diseases 0.000 description 9
- 244000052769 pathogen Species 0.000 description 8
- 208000032843 Hemorrhage Diseases 0.000 description 7
- 239000000796 flavoring agent Substances 0.000 description 7
- 230000009036 growth inhibition Effects 0.000 description 7
- 210000001519 tissue Anatomy 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 230000000740 bleeding effect Effects 0.000 description 6
- 239000002158 endotoxin Substances 0.000 description 6
- 235000003599 food sweetener Nutrition 0.000 description 6
- 229920006008 lipopolysaccharide Polymers 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000003765 sweetening agent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 208000034619 Gingival inflammation Diseases 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 235000019634 flavors Nutrition 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000546 pharmaceutical excipient Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 230000003449 preventive effect Effects 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000000080 wetting agent Substances 0.000 description 5
- 206010033102 Otosalpingitis Diseases 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 230000003239 periodontal effect Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 4
- 208000002874 Acne Vulgaris Diseases 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 3
- 208000002064 Dental Plaque Diseases 0.000 description 3
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 206010020751 Hypersensitivity Diseases 0.000 description 3
- 241000605894 Porphyromonas Species 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 241000194017 Streptococcus Species 0.000 description 3
- 241000193987 Streptococcus sobrinus Species 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 206010000496 acne Diseases 0.000 description 3
- -1 and the like Substances 0.000 description 3
- 239000003242 anti bacterial agent Substances 0.000 description 3
- 229940088710 antibiotic agent Drugs 0.000 description 3
- 239000004599 antimicrobial Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 229960003260 chlorhexidine Drugs 0.000 description 3
- 210000003298 dental enamel Anatomy 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000004088 foaming agent Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000609 methyl cellulose Polymers 0.000 description 3
- 239000001923 methylcellulose Substances 0.000 description 3
- 235000010981 methylcellulose Nutrition 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 210000005036 nerve Anatomy 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 239000003002 pH adjusting agent Substances 0.000 description 3
- 210000002379 periodontal ligament Anatomy 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 210000003296 saliva Anatomy 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 229940032147 starch Drugs 0.000 description 3
- 150000003464 sulfur compounds Chemical class 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- 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 2
- 241000196324 Embryophyta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- MJVAVZPDRWSRRC-UHFFFAOYSA-N Menadione Chemical compound C1=CC=C2C(=O)C(C)=CC(=O)C2=C1 MJVAVZPDRWSRRC-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 244000184734 Pyrus japonica Species 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- 244000269722 Thea sinensis Species 0.000 description 2
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000001055 chewing effect Effects 0.000 description 2
- 235000021270 cold food Nutrition 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 229940088598 enzyme Drugs 0.000 description 2
- 235000013355 food flavoring agent Nutrition 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 210000004195 gingiva Anatomy 0.000 description 2
- 235000021268 hot food Nutrition 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 229960001375 lactose Drugs 0.000 description 2
- 229940076522 listerine Drugs 0.000 description 2
- 210000002540 macrophage Anatomy 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000006187 pill Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 229960003415 propylparaben Drugs 0.000 description 2
- LXNHXLLTXMVWPM-UHFFFAOYSA-N pyridoxine Chemical compound CC1=NC=C(CO)C(CO)=C1O LXNHXLLTXMVWPM-UHFFFAOYSA-N 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 229960002920 sorbitol Drugs 0.000 description 2
- 235000010356 sorbitol Nutrition 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 229960004793 sucrose Drugs 0.000 description 2
- 239000006188 syrup Substances 0.000 description 2
- 235000020357 syrup Nutrition 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229940033134 talc Drugs 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000000811 xylitol Substances 0.000 description 2
- 235000010447 xylitol Nutrition 0.000 description 2
- 229960002675 xylitol Drugs 0.000 description 2
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- ZZPQSQFQHIGCRC-OOFFSTKBSA-N (2s,3s,4s,5r,6r)-6-[(2s,3r,4s,5s,6s)-2-[[(3s,4ar,6ar,6bs,8as,11s,12ar,14ar,14bs)-11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1h-picen-3-yl]oxy]-6-carboxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-c Chemical compound [Zn].O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@H]1CC[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@](C)(CC[C@@]5(CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C)C)C(O)=O)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O ZZPQSQFQHIGCRC-OOFFSTKBSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 208000030507 AIDS Diseases 0.000 description 1
- 241000606749 Aggregatibacter actinomycetemcomitans Species 0.000 description 1
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 1
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 1
- 240000002234 Allium sativum 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
- 108010011485 Aspartame Proteins 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 241000282465 Canis Species 0.000 description 1
- 206010007269 Carcinogenicity Diseases 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 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 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 235000019739 Dicalciumphosphate Nutrition 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 1
- 238000012286 ELISA Assay Methods 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000605909 Fusobacterium Species 0.000 description 1
- 241000605986 Fusobacterium nucleatum Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 206010018276 Gingival bleeding Diseases 0.000 description 1
- 208000024283 Gingival haemorrhages Diseases 0.000 description 1
- 238000003794 Gram staining Methods 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 208000035154 Hyperesthesia Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 208000003941 Impacted Tooth Diseases 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- 241001071917 Lithospermum Species 0.000 description 1
- 208000002720 Malnutrition Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 241000718543 Ormosia krugii Species 0.000 description 1
- 206010033433 Pain in jaw Diseases 0.000 description 1
- 229920002230 Pectic acid Polymers 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 108010077895 Sarcosine Proteins 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 241000194043 Streptococcus criceti Species 0.000 description 1
- 241000194023 Streptococcus sanguinis Species 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 206010042566 Superinfection Diseases 0.000 description 1
- 241001135235 Tannerella forsythia Species 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 208000008312 Tooth Loss Diseases 0.000 description 1
- 241000589892 Treponema denticola Species 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229960003563 calcium carbonate Drugs 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 229920003123 carboxymethyl cellulose sodium Polymers 0.000 description 1
- 229940063834 carboxymethylcellulose sodium Drugs 0.000 description 1
- 231100000260 carcinogenicity Toxicity 0.000 description 1
- 230000007670 carcinogenicity Effects 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 229940075614 colloidal silicon dioxide Drugs 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000035597 cooling sensation Effects 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- 239000000551 dentifrice Substances 0.000 description 1
- 210000004513 dentition Anatomy 0.000 description 1
- NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 1
- 229910000390 dicalcium phosphate Inorganic materials 0.000 description 1
- 229940038472 dicalcium phosphate Drugs 0.000 description 1
- 235000021045 dietary change Nutrition 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 206010013781 dry mouth Diseases 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 210000002950 fibroblast Anatomy 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 235000004611 garlic Nutrition 0.000 description 1
- 229940029982 garlic powder Drugs 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 210000001648 gingival epithelial cell Anatomy 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 229940025294 hemin Drugs 0.000 description 1
- BTIJJDXEELBZFS-QDUVMHSLSA-K hemin Chemical compound CC1=C(CCC(O)=O)C(C=C2C(CCC(O)=O)=C(C)\C(N2[Fe](Cl)N23)=C\4)=N\C1=C/C2=C(C)C(C=C)=C3\C=C/1C(C)=C(C=C)C/4=N\1 BTIJJDXEELBZFS-QDUVMHSLSA-K 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229940057948 magnesium stearate Drugs 0.000 description 1
- 230000001071 malnutrition Effects 0.000 description 1
- 235000000824 malnutrition Nutrition 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 210000004373 mandible Anatomy 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229960001855 mannitol Drugs 0.000 description 1
- 210000002050 maxilla Anatomy 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 208000015380 nutritional deficiency disease Diseases 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 244000039328 opportunistic pathogen Species 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 210000003800 pharynx Anatomy 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 235000013550 pizza Nutrition 0.000 description 1
- 230000007505 plaque formation Effects 0.000 description 1
- 239000010318 polygalacturonic acid Substances 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 230000035935 pregnancy Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 235000008160 pyridoxine Nutrition 0.000 description 1
- 239000011677 pyridoxine Substances 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical group C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 150000000030 silines Chemical class 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 235000011888 snacks Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 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
- 229940079862 sodium lauryl sarcosinate Drugs 0.000 description 1
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
- 210000004872 soft tissue Anatomy 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 235000021147 sweet food Nutrition 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 230000036346 tooth eruption Effects 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
- 210000005239 tubule Anatomy 0.000 description 1
- 210000002438 upper gastrointestinal tract Anatomy 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000012711 vitamin K3 Nutrition 0.000 description 1
- 239000011652 vitamin K3 Substances 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 229940041603 vitamin k 3 Drugs 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Images
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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- A61K8/355—Quinones
-
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
-
- 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
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/312—Foods, ingredients or supplements having a functional effect on health having an effect on dental health
-
- Y10S514/8995—
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Polymers & Plastics (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Food Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Cosmetics (AREA)
Abstract
Description
본 발명은 알칸닌을 포함하는 구강질환 예방 또는 치료용 조성물에 관한 것으로서, 보다 상세하게는 치아 우식증, 치주질환, 치통, 시린이 및 구취를 예방 또는 개선하는 효과를 가지는 의약외품 조성물에 관한 것이다. 또한, 본 발명은 알칸닌을 포함하는 약학적 조성물, 식품 조성물 및 알칸닌을 포함하는 구강용 조성물에 관한 것이다.The present invention relates to a composition for preventing or treating oral diseases including alkanin, and more particularly, to a quasi-drug composition having an effect of preventing or ameliorating dental caries, periodontal diseases, toothache, acne and bad breath. The present invention also relates to a pharmaceutical composition comprising an alkanin, a food composition and an oral composition comprising an alkanin.
건강한 치아는 오복 중 하나라 일컬을 정도로 삶의 질을 결정하는 중요한 요소이다. 구강질환 중 치아 우식증(dental cavities, 충치)과 치주질환(periodontal disease, 풍치)은 세계적으로 발병률이 높은 질환으로서, 통증, 저작기능 장애, 치주조직의 파괴, 구취 및 시린이와 같은 다양한 임상적인 증상을 유발하고 치아상실을 초래하는 주된 요인으로 알려져 있으며 식생활의 변화로 구강질환의 원인요소는 더 증가하고 있는 실정이다.Healthy teeth are one of the most important factors that determine the quality of life. Among oral diseases, dental cavities and periodontal diseases are diseases with high incidence worldwide and they have various clinical symptoms such as pain, chewing dysfunction, destruction of periodontal tissue, bad breath, And is known to be the main cause of tooth loss. The causes of oral diseases are increasing due to dietary changes.
사람의 구강에는 대략 600 내지 800종 이상의 미생물이 존재하는 것으로 알려져 있는데 이러한 미생물들은 타액이 분비하는 리소자임(lysozyme)과 같은 효소에 의해 제어되고 있다. 그러나 영양분과 수분이 풍부한 구강환경은 미생물이 성장하기 좋은 조건이며, 혀나 치태(dental plaque)는 미생물의 훌륭한 서식처를 제공한다. 이러한 미생물 중 일부는 기회병원성 균으로서 치아우식, 치주질환 및 시린이(상아질 지각과민증)과 같은 질환 및 구취의 원인이 된다.It is known that about 600 to 800 or more microorganisms exist in human oral cavity, and these microorganisms are controlled by enzymes such as lysozyme secreted by saliva. However, nutrients and water-rich oral environments are good conditions for microbial growth, and dental plaques provide excellent microbial habits. Some of these microorganisms are opportunistic pathogens, causing diseases such as dental caries, periodontal disease, and acin (dentin hypersensitivity) and bad breath.
치태 내에 서식하면서 치아우식, 치주질환, 구취 및 시린이를 유발하는 구강병원균 증식을 억제하는 방법으로 항균제가 있으며, 구강병원균에 대한 살균 및 정균 작용을 갖는 항생제를 포함하는 다양한 종류의 항균제제가 충치, 치주질환, 치수 및 치근단 감염의 억제 및 치료제로써 개발되어 왔다. There are antimicrobial agents that inhibit the growth of oral pathogens that induce dental caries, periodontal disease, bad breath, and acinar infestation, and various kinds of antimicrobial agents including antibiotics that have a sterilizing and bacteriostatic action against oral pathogens, Have been developed as inhibitors and remedies for periodontal disease, dental and periapical infections.
그런데, 항생제는 우리 몸에 대한 전신적인 부작용과 함께 구강내 내성균의 출현 및 균교대증(superinfection)을 유발할 수 있기 때문에 장기적인 사용이 곤란하여 단지 치료제로만 이용될 수 있는 단점이 있다. 또한, 구강청정제에 사용되고 있는 항균제제로는 생구이나린(Sangquinarine), 리스테린(Listerine), 피록사이드(Peroxide), 클로르헥시딘(Chlorhexidine) 등이 있는데, 생구이나린은 구강 내에서 세균에 대한 효과가 불분명하고 치주질환에 대한 치료 효과가 더욱 불분명할 뿐만 아니라 가격도 비싼 단점이 있고, 리스테린은 알코올이 주성분으로 약간의 정균 작용이 있으나 실제 구강 내에서는 일시적인 효과를 나타낼 뿐, 장기간 사용 시 조직에 대해 위해 작용도 나타날 수 있는 단점이 있다. 아울러, 최근 미백 효과를 위해 첨가되고 있는 피록사이드는 세균에 대한 독성이 있으나 동시에 인체 조직에도 독성을 나타내어 안전성에 문제가 있을 뿐 아니라 간혹 세균에서 피록사이드에 대한 내성균이 출현하기도 한다. 또한 클로르헥시딘은 치태 형성 억제와 더불어 치주질환 예방 및 치료제로써 현재까지 알려진 제제 중에서 가장 우수한 것으로 알려져 있으나, 조직에 대한 자극, 조직의 착색 및 변성을 유발하고, 특히 자극적인 맛이 강하고 냄새가 심한 부작용을 나타내는 문제점이 있을 뿐 아니라, 균교대증이 유발될 수 있고, 발암성이 있어 임신부의 경우 사용이 제한되는 등 치료나 특히 예방의 목적으로 장기간 사용할 수 없는 단점이 있다.However, since antibiotics can cause systemic adverse effects on our bodies and induce resistance to oral bacteria and superinfection, they are difficult to use for a long time and can only be used as therapeutic agents. The antimicrobial agents used in mouthwash are Sangquinarine, Listerine, Peroxide, and Chlorhexidine. The effect of bacteria on oral bacteria is unclear in the oral cavity The treatment effect of periodontal disease is more unclear, and the price is also high. Listerine is a major ingredient of alcohol and has a slight bacteriostatic effect. However, it has a temporary effect only in the oral cavity. There are drawbacks that can appear. In addition, the recently added pyridoxine for the whitening effect is toxic to bacteria but at the same time toxic to human tissues, which is not only problematic in safety but also resistant to bacterial fungi in bacteria. In addition, chlorhexidine is known to be one of the best known agents for the prevention and treatment of periodontal disease as well as suppression of plaque formation. However, chlorhexidine induces irritation of tissues, pigmentation and degeneration of tissues, and especially stimulant taste and odor In addition, there is a disadvantage in that it can not be used for a long time for the purpose of treatment or especially prevention, such as the occurrence of bacterial diabetes, carcinogenicity and limited use in pregnant women.
한편, 알칸닌(Alkannin)는 분자식 C16H16O5, 분자량 288.3를 가지며 적갈색 바늘 모양 결정(벤젠에서 재결정)으로서, 수산화알칼리와 작용하여 청색을 나타내고 탄산수소알칼리에 잘 녹지 않는다.On the other hand, Alkannin has a molecular formula of C 16 H 16 O 5 , molecular weight of 288.3 and is a reddish brown needle crystal (recrystallized in benzene). It acts on alkali hydroxide to exhibit blue color and is insoluble in alkali hydrogencarbonate.
이러한 배경하에, 본 발명자들은 상기와 같은 부작용에 대한 우려가 없으면서도 치아우식, 치주질환, 치통, 시린이, 구취와 같은 구강질환 예방 및 개선에 효과가 뛰어난 천연소재를 도출하기 위해 연구를 수행하였다. 그 결과, 체내에 안전하여 안심하고 사용할 수 있는 천연 유래 조성물로서 알칸닌이 치아 우식증 및 치주질환 유발세균에 대한 항균 효과, PGE2 억제 효과, 치은염 형성 억제 효과, 시린이 억제 효과 및 구취 제거 효과를 나타냄을 규명하여, 이를 활용한 의약외품 조성물, 약학적 조성물, 식품 조성물 및 구강용 조성물을 완성하기에 이르렀다.Under these circumstances, the present inventors have conducted studies to derive natural materials excellent in prevention and improvement of oral diseases such as dental caries, periodontal disease, toothache, syringe and bad breath without fear of side effects as described above . As a result, as a naturally-occurring composition which can be used safely and safely in the body, alkanin exhibits antibacterial effect, PGE2 inhibitory effect, gingivitis formation inhibitory effect, siline inhibitory effect, and bad breath removing effect on dental caries and periodontal disease-causing bacteria And has completed the preparation of a quasi-drug composition, a pharmaceutical composition, a food composition and an oral composition using the same.
본 발명의 목적은 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 개선용 의약외품 조성물을 제공하는 것이다.It is an object of the present invention to provide a quasi-drug composition for preventing or ameliorating oral diseases, which comprises an alkanine or a pharmaceutically acceptable salt thereof as an active ingredient.
본 발명의 다른 목적은 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 치료용 약학적 조성물을 제공하는 것이다.Another object of the present invention is to provide a pharmaceutical composition for preventing or treating oral diseases comprising alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
본 발명의 또 다른 목적은 알칸닌 또는 이의 식품학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 개선용 식품 조성물을 제공하는 것이다.It is still another object of the present invention to provide a food composition for preventing or improving oral diseases, which comprises alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
본 발명의 또 다른 목적은 알칸닌 또는 이의 허용 가능한 염을 유효성분으로 포함하는 구강용 조성물을 제공하는 것이다.It is still another object of the present invention to provide an oral composition comprising alkanine or an acceptable salt thereof as an active ingredient.
본 발명은 상기와 같은 과제들을 해결하고, 본 발명의 목적을 달성하기 위하여 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 개선용 의약외품 조성물을 제공한다.The present invention provides a quasi-drug composition for preventing or ameliorating oral diseases, which comprises the alkanin or a pharmaceutically acceptable salt thereof as an active ingredient to solve the above-mentioned problems and to achieve the object of the present invention.
본 발명의 다른 양태로서, 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 치료용 약학적 조성물을 제공한다.As another aspect of the present invention, there is provided a pharmaceutical composition for preventing or treating oral diseases comprising alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
본 발명의 또 다른 양태로서, 알칸닌 또는 이의 식품학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 개선용 식품 조성물을 제공한다.As another embodiment of the present invention, there is provided a food composition for preventing or improving oral diseases comprising alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
본 발명의 또 다른 양태로서, 알칸닌 또는 이의 허용 가능한 염을 유효성분으로 포함하는 구강용 조성물을 제공한다.As another embodiment of the present invention, there is provided an oral composition comprising an alkanine or an acceptable salt thereof as an active ingredient.
본 발명에서는 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 의약외품 조성물을 제공한다.The present invention provides a quasi-drug composition comprising an alkanine or a pharmaceutically acceptable salt thereof as an active ingredient.
본 발명에 있어서, "알칸닌(Alkannin)"은 상기 화학식 1로 표시되고, 분자식 C16H16O5, 분자량 288.3을 가지며, 식물 색소의 하나인 시코닌의 광학 이성질체이다.In the present invention, " Alkannin " is an optically isomer of a shikonin having the molecular formula C 16 H 16 O 5 and a molecular weight of 288.3, which is one of plant pigment.
본 발명은 알칸닌의 획득 방법에 특별히 한정되지 않으며, 당업계에 공지된 방법으로 화학적으로 합성하거나, 시판되는 물질을 사용할 수 있다.The present invention is not particularly limited to the method for obtaining an alkanine, and may be chemically synthesized by a method known in the art, or a commercially available material may be used.
본 발명의 알칸닌은 용매화된 형태뿐만 아니라 비-용매화된(unsolvated) 형태로 존재할 수도 있다. 본 발명의 알칸닌은 결정형 또는 무정형 형태로 존재할 수 있으며, 이러한 모든 물리적 형태는 본 발명의 범위에 포함된다.The alkanines of the present invention may exist in solvated as well as unsolvated forms. The alkanines of the present invention may exist in crystalline or amorphous form, and all such physical forms are included within the scope of the present invention.
본 발명은 상기 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 구강질환 예방 또는 개선용 의약외품 조성물을 제공한다. The present invention provides a quasi-drug composition for preventing or improving oral diseases, which comprises the alkanine or a pharmaceutically acceptable salt thereof as an active ingredient.
또한, 구체적으로, 본 발명은 상기 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 치아 우식증, 치주질환(치주염 또는 치은염), 치통, 시린이 및 구취로 이루어진 군으로부터 선택된 1 이상의 구강질환 예방 또는 개선용 의약외품 조성물을 제공할 수 있다.More specifically, the present invention relates to a pharmaceutical composition comprising at least one oral cavity selected from the group consisting of dental caries, periodontal disease (periodontitis or gingivitis), toothache, syringitis and bad breath comprising the alkanin or a pharmaceutically acceptable salt thereof as an active ingredient A quasi-product composition for preventing or ameliorating a disease can be provided.
본 발명에 있어서, "구강질환"이란 구강영역에서 발생하는 여러 가지 질환을 말하며, 상기 구강영역은 앞쪽 입술부터 뒤쪽 구협에서 인두와 연결되는 입 안의 공간을 의미한다. 본 발명에서 상기 구강질환은 구강에 발생하는 질환이라면 그 병증에 관계없이 모두 포함하는 개념이며, 상기 구강질환의 비제한적인 예로는 치아 우식증, 치주질환(치주염 또는 치은염), 치통, 시린이, 구취 등을 들 수 있다.In the present invention, " oral disease " refers to various diseases occurring in the oral cavity region, and the oral cavity region refers to a space in the mouth which is connected to the pharynx from the front lip to the rear mouth. In the present invention, the oral disease refers to a disease that occurs in the oral cavity, regardless of its pathology. Examples of the oral disease include dental caries, periodontal disease (periodontitis or gingivitis), toothache, And the like.
본 발명에 있어서, "치아 우식증(dental cavities)"이란 치아면에 서식하는 세균으로 인한 감염성 질환으로서, 충치라고도 하며, 치아의 경조직이 침식되어 결손하는 증세를 보인다. 구체적으로 치아의 머리 부분 표면을 덮고 있고, 치아 상아질을 보호하는 유백색의 반투명하고 단단한 물질을 치아 법랑질 또는 에나멜질이라고 하는데, 입 안에 서식하는 구강병원균에 의해 설탕, 전분 등이 분해되면서 생기는 산에 의해 치아의 법랑질이 손상되어 충치가 생기는 것을 말한다. 치아 우식증을 일으키는 주요 원인으로는 치아 표면에 생성된 세균막인 치태(dental plaque, 플라크)를 들 수 있는데, 타액이 치아에 얇고 끈적한 막을 형성하고, 그 위에 연쇄상구균의 일종인 스트렙토코쿠스 소브리누스(Streptococcus sobrinus)균 및 스트렙토코쿠스 뮤탄스(Streptococcus mutans) 등의 구강 미생물이 부착해 바이오 필름(biofilm)을 형성함으로써 치태(dental plaque, 플라크)가 만들어지고 푸조박테리움(Fusobacterium)에 의해 더욱 두꺼워진다. 본 발명의 치아 우식증은 치아 우식증을 일으키는 원인균이라면 그 종류에 관계없이 모두 포함되나, 구체적으로는 스트렙토코쿠스 뮤탄스(Streptococcus mutans), 스트렙토코커스 산구이니스(Streptococcus sanguinis), 스트렙토코커스 소브리누스(Streptococcus sobrinus), 스트렙토코커스 라티(Streptococcus ratti), 스트렙토코커스 크리세티(Streptococcus criceti), 스트렙토코커스 안지노서스(Streptococcus anginosus) 및 유산균으로 이루어진 군에서 선택된 1종 이상의 균일 수 있으며, 보다 구체적으로는 스트렙토코쿠스 뮤탄스일 수 있다.In the present invention, " dental cavities " is an infectious disease caused by bacteria in the tooth surface, which is also called tooth decay. Specifically, a milky translucent and hard material that covers the surface of the head of a tooth and protects the tooth dentin is called tooth enamel or enamel. By the acid generated by decomposition of sugar and starch by the oral pathogenic bacteria in the mouth It means that tooth enamel is damaged and tooth decay occurs. The main cause of dental caries is dental plaque (plaque), which is a bacterial membrane formed on the surface of the teeth. The saliva forms a thin and sticky film on the tooth, and on top of it, Streptococcus sobrinus ( Streptococcus sobrinus ) and Streptococcus mutans mutans and the like attach themselves to biofilms to form dental plaques and become thicker by Fusobacterium . The dental caries of the present invention includes all kinds of dental caries causing dental caries irrespective of its kind, but specifically includes Streptococcus mutans mutans , Streptococcus sanguinis , Streptococcus sobrinus , Streptococcus spp. ratti , Streptococcus criceti , Streptococcus spp. anginosus , and lactic acid bacteria. More specifically, it may be Streptococcus mutans.
상기 스트렙토코쿠스 뮤탄스는 연쇄상구균의 일종으로 그람양성균이며 충치균이라도 불린다. 상기 스트렙토코쿠스 뮤탄스는 치아의 표면에서만 증식하는데, 생후 30개월 전후까지는 유치가 완성되지 않는다. 따라서 이 시기까지는 유아기 이후처럼 뮤탄스 균이 증식하기 어렵다. 유아기 동안 어른들의 입으로부터 뮤탄스 균에 감염되지 않아 입 안에 다른 구강 세균이 자리를 잡게 되면 이미 균형이 잡힌 구강 내의 생태계에 뮤탄스 균이 새로이 진입하기 어려워져 유아기 이후 일생동안 충치에 걸릴 확률이 현저히 낮아지게 된다. 이미 어른들의 입을 통해 원인균에 전염되었을 경우에는 양치질을 자주하고 입 안을 청결하게 유지하는 것이 충치 예방에 도움이 된다. 다만, 일단 뮤탄스 균이 구강 내에 자리잡았다면 뮤탄스 균 박멸은 불가능하다. The Streptococcus mutans is a type of streptococcus, Gram-positive bacteria, and is also referred to as carnivorous. Streptococcus mutans proliferate only on the surface of the teeth, but not until 30 months after birth. Therefore, it is difficult for Mythans to multiply until after this period. When other oral bacteria in the mouth are not infected by the mutans bacteria from the mouths of adults during infancy, it is difficult for the mutans bacteria to enter the already balanced ecosystem in the oral cavity. . If you are already infected with causative organisms through adults' mouths, brush your teeth frequently and keep your mouth clean to help prevent tooth decay. However, once mutans bacteria are in the oral cavity, it is impossible to eradicate mutans.
본 발명의 일 실시예에서는, 스트렙토코쿠스 뮤탄스를 도말한 배지에 알칸닌이 포함된 디스크를 접종한 후 생육저지환의 크기를 측정한 결과, 상기 알칸닌을 포함한 실험군의 경우 생육저지환 직경이 11.0 mm 이상으로 스트렙토코커스 뮤탄스에 대한 상당히 우수한 항균 활성을 나타내어, 알칸닌을 포함하는 조성물은 치아우식증 예방 또는 개선 용도로 사용될 수 있음을 확인하였다(표 2).In one embodiment of the present invention, the size of the growth inhibition circle after inoculation of a disk containing alkanin in the medium coated with Streptococcus mutans was measured. As a result, in the case of the experimental group containing the alkanin, the growth inhibition diameter The antimicrobial activity against Streptococcus mutans was more than 11.0 mm, and it was confirmed that the composition containing alkanin could be used for prevention or improvement of dental caries (Table 2).
본 발명에 있어서, "치주질환(periodontal disease)"은 치아를 받치고 있는 치은과 치주인대 및 골조직에 염증이 생기는 질환으로서, 흔히 풍치라고도 하는데, 병의 정도에 따라 치은염(gingivitis)과 치주염(periodontitis)으로 나뉜다. 비교적 가볍고 회복이 빠른 형태의 치주질환으로 잇몸 즉, 연조직에만 국한된 형태를 치은염이라고 하고, 이러한 염증이 잇몸과 잇몸뼈 주변까지 진행된 경우를 치주염이라고 한다. 치은(잇몸)과 치아 사이에는 V자 모양의 틈이 있는데, 이 홈(sulcus)의 잇몸 선 아래 부분을 구강병원균이 공격하면서 염증 자극원인 리포폴리사카라이드(Lipopolysaccharide, LPS)를 방출하고, 이로 인해 잇몸이 붓고 출혈이 일어나는 등 염증이 생성되며, 이로써 치주인대와 인접조직이 손상된다. 치주염이 진행되면 치주인대, 더 나아가 치조골까지 손상시키고 결국 치아가 손실된다. 단백질, 비타민 등의 영양부족, 임신한 경우나 당뇨병 등과 같은 호르몬 장애, 흡연, 후천성면역결핍증(AIDS) 등이 질환을 악화시킬 수 있다. 또한, 치주질환의 다른 원인으로 치태 및 치석을 들 수 있다. 본 발명의 치주질환은 치주질환을 일으키는 원인균이라면 그 종류에 관계없이 모두 포함되나, 구체적으로는 악티노바실루스 악티노마이세템코미탄스(Actinobacillus actinomycetemcomitans), 포피로모나스 진지발리스(Porphyromonas gingivalis), 타네렐라 포르시시아(Tannerella forsythia), 트레포네마 덴티콜라(Treponema denticola) 및 푸소박테리움 누클리아툼(Fusobacterium nucleatum)으로 이루어진 군으로부터 선택된 1종 이상의 균일 수 있으며, 보다 구체적으로는 포피로모나스 진지발리스일 수 있다.In the present invention, " periodontal disease " refers to a disease in which gingiva, periodontal ligament, and bone tissue injure the teeth, and is often referred to as a style. Depending on the severity of the disease, gingivitis and periodontitis, . It is a relatively light and fast-acting periodontal disease called gingivitis that is limited to gingiva or soft tissue, and it is called periodontitis when the inflammation progresses to the gums and the gums. There is a V-shaped gap between the gum (gums) and the teeth, where oral pathogens attack the area under the gum line of the sulcus to release the inflammatory stimulant Lipopolysaccharide (LPS) Inflammation occurs, such as swelling of the gums and bleeding, which can damage the periodontal ligament and adjacent tissue. If periodontal disease progresses, the periodontal ligament, and even the alveolar bone, will be damaged and eventually the teeth will be lost. Malnutrition such as protein and vitamins, hormonal disorders such as pregnancy and diabetes, smoking, AIDS and the like can aggravate the disease. Other causes of periodontal disease include plaque and calculus. The periodontal disease of the present invention includes all kinds of periodontal disease causing irregular periodontal disease, but specifically includes Actinobacillus actinomycetemcomitans , Porphyromonas gingivalis , Tannerella forsythia , Treponema denticola , and Fusobacterium nucleatum . More specifically, it may be Poppyromonas japonica varis.
상기 포피로모나스 진지발리스는 박테로이드(Bacteroide) 유연균의 일종으로 그람음성균이고, 혐기성균이다. 상기 포피로모나스 진지발리스는 치주질환이 발생한 구강 내에서 발견되며, 그 외에도 위장관 상부, 호흡기 및 결장에서도 발견된다. 만성 치주질환 환자는 상기 균의 콜라게네이즈 효소에 의해 콜라겐이 분해되며, 상기 균은 치은 섬유아세포에 침입할 수 있으며, 상당한 농도의 항생제 하에서도 생존할 수 있다. 또한, 상기 균은 치은 상피세포에 침입하여 장시간 생존할 수 있다. The Poppyromonas jinx valis is a kind of Bacteroide-type bacteria and is gram-negative bacteria and anaerobic bacteria. The Poppyromonas jinx valis is found in the oral cavity with periodontal disease, as well as in the upper gastrointestinal tract, respiratory tract and colon. In patients with chronic periodontal disease, collagen is degraded by the collagenase enzyme of the bacterium, and the bacterium can enter the gingival fibroblast, and can survive even at a considerable concentration of antibiotics. In addition, the bacterium can enter the gingival epithelial cells and survive for a long time.
본 발명의 일 실시예에서는, 포피로모나스 진지발리스를 도말한 배지에 알칸닌이 포함된 디스크를 접종한 후 생육저지환의 크기를 측정한 결과, 상기 알칸닌을 포함한 실험군의 경우 생육저지환 직경이 11.0 mm 이상으로 포피로모나스 진지발리스에 대한 상당히 우수한 항균 활성을 나타내어, 알칸닌을 포함하는 조성물은 치주질환 예방 또는 개선 용도로 사용될 수 있음을 확인하였다(표 2).In one embodiment of the present invention, the size of the growth inhibition ring was measured after inoculating a disk containing the alkanin in the medium coated with Poppyromonas japonica, and as a result, in the experimental group containing the alkanin, the growth inhibition diameter Showed a remarkably excellent antimicrobial activity against Porphyromonas japonicus var. At 11.0 mm or more. It was confirmed that a composition containing alkanin could be used for prevention or improvement of periodontal disease (Table 2).
또한, 본 발명의 일 실시예에서는, 치은염증을 갖는 실험 대상자를 선별하여 임상실험을 수행한 결과, 상기 알칸닌을 포함하는 실험군 치약을 사용한 실험군의 경우 치은염증 억제 효과가 우수하며 6개월이 경과했음에도 정상출혈 상태를 유지하여 치은염증 억제 효과가 지속되어, 알칸닌을 포함하는 조성물은 치은염을 포함하는 치주질환 예방 또는 개선 용도로 사용될 수 있음을 확인하였다(표 4).In addition, in an embodiment of the present invention, a test subject having gingival inflammation was selected and subjected to clinical tests. As a result, in the experimental group using the alkanin-containing toothpaste, the gingival inflammation suppression effect was excellent. It was confirmed that the composition containing alkanin could be used for prevention or improvement of periodontal disease including gingivitis (Table 4).
본 발명에 있어서, "치통"이란 단 음식, 또는 아주 차갑거나 뜨거운 음식 등을 먹을 때 치아에 통증이 오는 것을 말하는데, 일반적으로는 치아 자체의 통증뿐만 아니라, 치아를 턱뼈에 지탱시키고 있는 치주조직의 통증도 포함된다. 보통 씹을 때 통증이 발생하며, 잇몸이 붓고 역한 냄새의 분비물이 나온다. 치통은 원인 질병에 따라 조금씩 다른 통증을 보이는데, 구체적으로 치아 우식증에 의한 통증은 초기에는 통증이 없으나 점차 진행되어 치아 속 신경까지 깊이 썩은 경우에 통증이 나타나고, 매복치가 있는 경우 치아 주변 조직의 염증으로 통증이 유발되며, 치아가 부서지거나 금이 간 경우, 찬 음식에 닿거나 강하게 깨물었을 때 치아가 갈라지면서 신경에 자극을 주어 통증이 생긴다. 치수염에 의한 경우, 초기에는 찬 음식이 닿을 때 통증을 느끼고 더 진행된 경우에는 뜨거운 음식에 통증을 느끼게 되며, 염증이 진행되어 치수 조직이 죽으면 찬 것, 더운 것에 대한 반응은 없고 치근단(치아 뿌리 끝)의 염증에 의한 통증이 생기게 된다.In the present invention, " toothache " refers to a pain in a tooth when eating a sweet food or a very cold or hot food. In general, not only the pain of the tooth itself, but also the periodontal tissue supporting the tooth on the jaw Pain is also included. It usually causes pain when chewing, and the gums are swollen and emit a strong odor. Toothache is slightly different according to the cause disease. Specifically, pain caused by dental caries is not pain at first, but gradually progresses to pain in the deep tooth nerve. When there is impacted tooth, If the tooth is broken or cracked, when it touches cold food or when it bites strongly, the tooth is split and the nerve is stimulated to cause pain. In the case of dental infection, it is painful when cold food is initially exposed, and pain is felt in hot food when it is advanced. When inflammation progresses and dental tissue is dying, there is no cold reaction, no reaction to hot, Of the pain caused by inflammation.
본 발명의 일 실시예에서는, 통증 및 염증 마커로 알려진 PGE2 억제 효과를 확인한 결과, 상기 알칸닌을 포함한 실험군의 경우 농도 의존적으로 PGE2를 억제하는 효과를 나타내어, 알칸닌을 포함하는 조성물은 치통 예방 또는 개선 용도로 사용될 수 있음을 확인하였다(도 1).In one embodiment of the present invention, the PGE2 inhibitory effect, known as pain and inflammation markers, was examined. As a result, the test group containing the alkanin showed a concentration-dependent inhibitory effect on PGE2, It can be used for improvement purposes (FIG. 1).
본 발명에 있어서, "시린이"란 상아질과민증 치아(hypersensitive dentine)를 말하며, 시린이 증상이란 상아질 지각과민증(dentine hyperesthesia)을 말한다. 시린이 증상은 노출된 치아의 상아질 부분이 찬 공기나 자극적인 음식물 등에 접촉되었을 때 민감하게 느껴지는 것으로써, 치주질환을 가진 성인의 60 ~ 98%에서 증상을 보이고 있다. 시린이 증상은 잘못된 양치 습관이나 과도한 교합력, 산에 의한 용해에 의해 잇몸쪽에 이가 패이는 경우, 구강 위생 상태가 불량한 경우, 치주 치료 후, 수복 치료를 받은 후, 산성화에 의한 치아가 용해된 경우에 나타날 수 있다. 시린이 증상의 근본적인 원인으로 치아의 상아질에 존재하는 많은 세관이 외부로 노출되면서 나타나는데, 노출에 의해 모든 자극을 그대로 치수 내 신경으로 전달하여 똑같은 자극에 대해서도 평소보다 민감하게 반응하게 되며 통증을 유발할 수 있다. 시린이 증상은 가벼운 증상에서 격렬하고 지속적인 통증까지 다양하게 나타날 수 있으며, 치아의 특성상 재생이 되지 않기 때문에 진통제나 소염제 등의 복용은 시린 현상의 근본적인 해결책이 되지 못한다. 시린이 증상은 치아 전체에 전반적으로 나타나기도 하며, 상악이나 하악, 또는 오른쪽이나 왼쪽 등 특정 부위에 한정되어 나타나기도 한다. 많이 발병하는 부위는 원인에 따라 다르나, 주로 송곳니, 작은 어금니 부위이며 가장 심하게 통증이 나타나는 부위는 90% 이상이 잇몸과 치아의 경계부분인 치경부이다. In the present invention, " syringe " refers to dentin hypersensitive dentine, and silent refers to dentine hyperesthesia. This symptom is felt when the dentin part of the exposed tooth touches cold air or irritating food or the like, and it shows symptoms in 60 ~ 98% of adults with periodontal disease. This symptom may be caused by incorrect brushing habits, excessive occlusal force, dissolution of the tooth due to acid dissolution, gum breakage, poor oral hygiene, periodontal treatment, restorative treatment, . As the root cause of the symptoms is acne, many tubules present in the dentin of the teeth are exposed to the outside. By exposure, all the stimuli are transmitted to the nerve in the dentine as they are, and they react more sensitively to the same stimuli than usual. have. Symptoms can range from mild symptoms to intense and persistent pain, and due to the nature of teeth, the use of painkillers and anti-inflammatory agents is not a fundamental solution to the symptoms. Symptoms may occur throughout the tooth, either in the maxilla or mandible, or even in certain areas, such as the right or left side. The most common site is the canine, the small molar area, and the most severe pain area is the cervical area where more than 90% is the boundary between the gum and the tooth.
본 발명의 일 실시예에서는, 상아질과민증 치아를 갖는 실험 대상자를 선별하여 임상실험을 수행한 결과, 상기 알칸닌을 포함하는 실험군 치약을 사용한 실험군의 경우 시린이 증상 억제 효과가 우수하여, 알칸닌을 포함하는 조성물은 시린이 예방 또는 개선 용도로 사용될 수 있음을 확인하였다(표 6).In one embodiment of the present invention, the subjects who had dentin hypersensitive teeth were selected and subjected to clinical tests. As a result, in the experimental group using the alkanin-containing toothpaste, (Table 6). ≪ tb > < TABLE >
본 발명에 있어서, "구취"란 구강 및 인접기관으로부터 유래되는 냄새로 구취의 85 ~ 90%가 구강에서 유래하며, 특히, 혀의 뒷쪽에서 유래하고 있다. 구취의 주요 성분은 휘발성 황화합물인데, 휘발성 황화합물의 전체량 중 90%가 시스테인으로부터 만들어지는 황화수소(hydrogen sulfide)와 메티오닌으로부터 만들어지는 메틸머캡탄(methyl mercaptan)및 디메틸설파이드(dimethyl sulfide)이다. 이러한 성분들은 주로 혐기성 세균이 분비하는 단백질 효소에 의해서 생성되며, 혀의 뒷쪽이 가장 중요한 서식지가 된다. 이 부위는 타액에 의해 세정작용이 잘 되지 않고, 많은 작은 함몰이 있어 세균이 지속적으로 살아가는 장소가 된다. 혐기성 세균에 의한 휘발성 황화합물 생성이 구취의 원인으로 가장 중요하지만, 그 외 치아 우식증, 치주염, 구강 건조증 등과 같은 구강질환에 의해서도 발생한다. 구취를 발생시키는데 많은 종류의 혐기성 세균이 관여하며, 구취 발생 원인균의 비제한적인 예로 많은 종류와 많은 양의 효소를 분비하는 포르피로모나스 진지발리스(Porphyromonas gingivalis)를 들 수 있다.In the present invention, " bad breath " refers to the odor derived from the oral cavity and adjacent organs, and 85 to 90% of the bad breath is originated from the oral cavity, in particular from the back of the tongue. The major component of halitosis is volatile sulfur compounds, in which 90% of total volatile sulfur compounds are methyl mercaptan and dimethyl sulfide produced from hydrogen sulfide and methionine produced from cysteine. These components are produced mainly by protein enzymes secreted by anaerobic bacteria, and the back of the tongue is the most important habitat. This area is not well cleansed by saliva, and there are many small depressions, making it a place where bacteria live on. The formation of volatile sulfur compounds by anaerobic bacteria is the most important cause of halitosis, but it is also caused by oral diseases such as dental caries, periodontitis and dry mouth. Many types of anaerobic bacteria are involved in generating bad breath, and a non-limiting example of causative organisms of halitosis is Porphyromonas gingivalis , which secretes many species and large amounts of enzymes.
본 발명의 일 실시예에서는, 치아 우식증이 없는 실험 대상자를 대상으로 임상실험을 수행한 결과, 상기 알칸닌을 포함하는 실험군 치약을 사용한 실험군의 경우 구취 제거 효과가 우수하여, 알칸닌을 포함하는 조성물은 구취 예방 또는 개선 용도로 사용될 수 있음을 확인하였다(표 7).In an embodiment of the present invention, clinical trials were conducted on subjects who did not have dental caries, and as a result, the test group using the dental caries containing the alkanin showed excellent odor removal effect and the composition containing alkanin Can be used for preventing or improving bad breath (Table 7).
본 발명의 의약외품 조성물은 구강용 의약외품을 포함할 수 있다. 본 발명의 의약외품 조성물에 포함되는 성분은 유효성분으로서 상기 유효성분 이외에 구강용 의약외품 조성물에 통상적으로 이용되는 성분들을 포함할 수 있으며, 예컨대 연마제, 습윤제, 결합제, 기포제, 감미제, 방부제, 약효성분, 향미제, 색소, 용제, 증백제, 가용화제 또는 pH 조정제를 포함할 수 있다.The quasi-drug composition of the present invention may include quasi-drugs for oral use. The components contained in the quasi-drug composition of the present invention may contain, as an active ingredient, the components commonly used in oral quasi-drug compositions in addition to the above-mentioned effective ingredients, and examples thereof include abrasives, wetting agents, binders, foaming agents, sweeteners, preservatives, A coloring agent, a solvent, a brightener, a solubilizing agent or a pH adjusting agent.
본 발명의 구강용 의약외품 조성물은 당업계에서 통상적으로 제조되는 어떠한 제형으로도 제조될 수 있으며, 예를 들어, 치약, 구강세정제, 구강청정제, 껌, 캔디류, 구강스프레이, 구강용 연고제, 구강용 바니쉬, 구강양치액 및 잇몸 마사지 크림 등의 제형을 가질 수 있으나 이에 제한되는 것은 아니다.The oral quasi-drug composition of the present invention may be prepared in any form conventionally produced in the art, and examples thereof include toothpaste, mouthwash, mouthwash, gum, candy, oral spray, oral ointment, , Mouthwash and gum massage cream, but are not limited thereto.
하나의 예로서, 본 발명의 구강용 의약외품 조성물이 치약의 제형일 경우, 습윤제, 연마제, 결합제, 기포제, 향미제, 감미제, 착색제, 보존제, 약효성분, 용제, pH 조절제 등을 포함할 수 있다.As one example, when the quasi-drug composition for oral use of the present invention is a toothpaste formulation, it may contain a wetting agent, an abrasive, a binder, a foaming agent, a flavoring agent, a sweetening agent, a coloring agent, a preservative, a pharmaceutical composition, a solvent and a pH adjusting agent.
상기 습윤제는 치약제 성분 중 분말이 페이스트상이 되게 하고 치약제가 공기 중에 굳는 것을 방지하기 위한 것으로 글리세린, 솔비트액, 프로필렌글리콜, 폴리에틸렌 글리콜 등을 단독 또는 2종 이상 혼합하여 조성물 총 중량 중 1 ~ 60 중량%, 구체적으로는 10 ~ 50 중량%를 사용할 수 있다.The wetting agent is used to prevent the toothpaste from hardening in the air and to make the powder of the toothpaste composition paste-like and prevent the toothpaste from hardening in the air. The wetting agent may be used alone or in combination of two or more kinds of glycerin, sorbitol, propylene glycol, polyethylene glycol, %, Specifically 10 to 50% by weight.
상기 기포제는 치약제를 구강 중에 확산시켜 청소효과를 높이고, 계면활성제로서 작용하여 구강 오염을 세정하는 것으로 라우릴황산나트륨, 라우릴 사르코신산 나트륨, 알킬 설포호박산 나트륨, 자당 지방산 에스테르 등의 계면활성제를 단독 혹은 2종 이상 혼합하여 조성물 총 중량 중 0.5 ~ 10 중량%, 구체적으로는 0.5 ~ 5 중량%를 사용할 수 있다.The foaming agent is a surfactant which diffuses the toothpaste into the oral cavity to enhance the cleaning effect and acts as a surfactant to clean the oral contamination. It is also possible to use a surfactant such as sodium lauryl sulfate, sodium lauryl sarcosinate, sodium alkylsulfosuccinate, Or 0.5 to 10% by weight, specifically 0.5 to 5% by weight, based on the total weight of the composition.
상기 결합제는 치약제중의 분말과 액체 성분 간의 분리를 방지하는 것으로 카복시메틸셀룰로오스나트륨, 메틸셀룰로오스, 하이드록시 프로필셀룰로오스 등의 셀룰로오스 유도체와 알긴산나트륨, 카라기난, 잔탄검 등을 단독 혹은 2종 이상 혼합하여 조성물 총 중량 중 0.1 ~ 5 중량%, 구체적으로는 0.3 ~ 2 중량%를 사용할 수 있다.The binder is to prevent the separation of the powder and the liquid component in the dentifrice, and may be a combination of a cellulose derivative such as sodium carboxymethylcellulose, methylcellulose or hydroxypropylcellulose, sodium alginate, carrageenan or xanthan gum alone or in combination 0.1 to 5% by weight, specifically 0.3 to 2% by weight, of the total weight of the composition may be used.
상기 연마제는 치아표면을 상처내지 않고 치아표면의 부착물을 제거하고 치아 본래의 광택이 나도록 하는 것으로 탄산칼슘(CaCO3), 제2인산칼슘(CaHPO4, CaHPO42H2O), 무수규산(SiO22H2O), 수산화알루미늄(Al(OH)3), 피로인산카륨, 탄산마그네슘 등을 단독 혹은 2종 이상 혼합하여 조성물 총 중량 중 1 ~ 60 중량%, 구체적으로는 10 ~ 50 중량%를 사용할 수 있다.The abrasive is used to remove calcium oxide (CaCO 3 ), dicalcium phosphate (CaHPO 4 , CaHPO 4 2H 2 O), silicic anhydride (SiO 2 ) 2 H 2 O), aluminum hydroxide (Al (OH) 3 ), potassium pyrophosphate, magnesium carbonate, etc., in an amount of 1 to 60% by weight, specifically 10 to 50% by weight, Can be used.
상기 향미제는 치약에 상쾌감과 냄새를 부여하여 사용감을 증진시키기 위한 것으로 페퍼민트오일, 스피아민트오일, 멘톨 등을 단독 혹은 2종 이상 혼합하여 조성물 총 중량 중 1 ~ 60 중량%, 구체적으로는 0.01 ~ 5 중량%를 사용할 수 있다.The flavor agent is used for imparting an exhilarating feeling and smell to the toothpaste to improve the sensation of use. The flavor agent is selected from the group consisting of peppermint oil, spearmint oil, menthol, etc. in an amount of 1 to 60% by weight, 5% by weight can be used.
상기 감미제는 치약제 원료에 의한 불쾌한 맛이나 제거하고 청량감을 좋게 하기 위한 것으로 사카린산, 아스파탐, 자일리톨, 감초산 등을 단독 혹은 2종 이상 혼합하여 조성물 총 중량 중 1 ~ 60 중량%, 구체적으로는 0.01 ~ 5 중량%를 사용할 수 있다.The sweetener is used to remove an unpleasant taste or raw material from a toothpaste raw material and to improve a cooling sensation. The sweetener is used in an amount of 1 to 60% by weight of the total composition of saccharin acid, aspartame, xylitol, licorice acid, 0.01 to 5% by weight can be used.
약효성분은 치우 우식증 예방, 치주질환 예방, 치통 예방, 시린이 예방, 구취 제거 등의 효과를 위한 것으로 불화물, 염화아연, 클로르헥시딘, 아미노카프론산, 트라넥사민산, 염화세틸피리디움, 염화피리독신, 트리클로산, 초산토코페롤, 일불소인산나트륨 등을 단독 혹은 2종 이상 혼합하여 사용할 수 있다. 본 발명에서는 알칸닌을 추가적인 약효성분으로 사용할 수 있다.The active ingredient is for the prevention of periodontal disease, prevention of periodontal disease, prevention of toothache, prevention of acne, removal of bad breath, and the like. Triclosanic acid, tocopherol acetate, sodium fluorophosphate, and the like, or a mixture of two or more thereof. In the present invention, alkanine may be used as an additional active ingredient.
본 발명의 구강용 의약외품 조성물은 단독 또는 중복하여 사용하거나, 본 발명 이외의 다른 구강용 의약외품 조성물과 중복하여 사용할 수 있다.The oral quasi-drug composition of the present invention may be used singly or in combination, or may be used in combination with other oral quasi drug compositions other than the present invention.
본 발명의 다른 하나의 양태로서, 상기 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 약학적 조성물을 제공한다. 또한, 구체적으로, 본 발명은 상기 알칸닌을 유효성분으로 포함하는 치아 우식증, 치주질환(치주염 또는 치은염), 치통, 시린이 및 구취로 이루어진 군으로부터 선택된 1 이상의 구강질환 예방 또는 치료용 약학적 조성물을 제공할 수 있다. 알칸닌, 구강질환, 치아 우식증, 치주질환, 치통, 시린이 및 구취는 상기에서 설명한 바와 같다.In another aspect of the present invention, there is provided a pharmaceutical composition comprising the alkanine or a pharmaceutically acceptable salt thereof as an active ingredient. More specifically, the present invention relates to a pharmaceutical composition for preventing or treating at least one oral disease selected from the group consisting of dental caries, periodontal disease (periodontitis or gingivitis), toothache, syrinite and bad breath containing the alkanin as an active ingredient Can be provided. Alkaline, oral disease, dental caries, periodontal disease, toothache, syringitis and halitosis are as described above.
본 발명의 약학적 조성물은 구강질환을 예방하고 치료하기 위한 통상의 방법에 따라 정제, 환제, 산제, 과립제, 캡슐제, 현탁제, 내용액제, 유제, 시럽제, 에어로졸, 멸균 주사용액 등의 형태로 제형화가 가능하다.The pharmaceutical composition of the present invention may be in the form of tablets, pills, powders, granules, capsules, suspensions, solutions, emulsions, syrups, aerosols, sterilized injection solutions or the like in accordance with a conventional method for preventing and treating oral diseases Formulation is possible.
경구투여를 위한 고형제제에는 정제, 환제, 산제, 과립제, 캡슐제 등이 포함되며, 이러한 고형제제는 적어도 하나 이상의 부형제, 예를 들면, 전분, 탄산칼슘, 수크로스, 락토오스, 젤라틴 등을 섞어 조제될 수 있다. 또한, 단순한 부형제 이외에 마그네슘 스테아레이트, 탈크 같은 윤활제도 사용될 수 있다. 경구투여를 위한 액상제제로는 현탁제, 내용액제, 유제, 시럽제 등이 포함되며, 흔히 사용되는 단순 희석제인 물, 리퀴드 파라핀 이외에 여러 가지 부형제, 예를 들면, 습윤제, 감미제, 방향제, 보존제 등이 사용될 수 있다.Solid formulations for oral administration include tablets, pills, powders, granules, capsules, etc. These solid preparations are prepared by mixing at least one excipient, for example, starch, calcium carbonate, sucrose, lactose, . In addition to simple excipients, lubricants such as magnesium stearate and talc may also be used. Liquid preparations for oral administration include suspensions, solutions, emulsions, syrups and the like. In addition to water and liquid paraffin which are commonly used simple diluents, various excipients such as wetting agents, sweeteners, fragrances, Can be used.
비경구투여를 위한 제제는 멸균된 수용액, 비수성용제, 현탁제, 유제, 동결건조 제제, 좌제 등을 포함할 수 있다. 비수성용제와 현탁용제로는 프로필렌글리콜, 폴리에틸렌 글리콜, 올리브 오일 등과 같은 식물성 기름, 에틸올레이트와 같은 주사 가능한 에스테르 등이 사용될 수 있다.Formulations for parenteral administration may include sterilized aqueous solutions, non-aqueous solutions, suspensions, emulsions, freeze-dried preparations, suppositories, and the like. Examples of the non-aqueous solvent and the suspending agent include vegetable oils such as propylene glycol, polyethylene glycol and olive oil, injectable esters such as ethyl oleate, and the like.
또한, 본 발명의 약학적 조성물은 담체, 부형제 또는 희석제를 추가로 포함할 수 있다. 담체, 부형제 또는 희석제로는 락토즈, 텍스트로즈, 수크로스, 솔비톨, 만니톨, 자일리톨, 에리스리톨, 말티톨, 전분, 아카시아 고무, 알지네이트, 젤라틴, 칼슘 포스페이트, 칼슘 실리케이트, 셀룰로오즈, 메틸 셀루로오즈, 하이드록시 프로필 메틸 셀룰로오즈, 미정질 셀룰로오즈, 폴리비닐 피롤리돈, 물, 메틸히드록시벤조에이트, 플로필히드록시벤조에이트, 프로필히드록시벤조에이트, 탈크, 마그네슘 스테아레이트, 이산화규소 등의 광물유 등이 사용될 수 있다.In addition, the pharmaceutical composition of the present invention may further comprise a carrier, an excipient or a diluent. Examples of the carrier, excipient or diluent include lactose, textol, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, cellulose, methylcellulose, Mineral oil such as propyl methylcellulose, microcrystalline cellulose, polyvinylpyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate and silicon dioxide can be used have.
본 발명에 따른 약학적 조성물의 구체적인 투여량은 제제화 방법, 환자의 상태 및 체중, 환자의 성별, 연령, 질병의 정도, 약물형태, 투여경로 및 기간, 배설 속도, 반응 감응성 등과 같은 요인들에 따라 당업자에 의해 다양하게 선택될 수 있으며, 투여량 및 횟수는 어떠한 면에서든 본 발명의 범위를 제한하는 것은 아니다.The specific dosage of the pharmaceutical composition according to the present invention depends on factors such as the formulation method, the patient's condition and body weight, the patient's sex, age, degree of disease, drug type, administration route and period, excretion rate, May be variously selected by those skilled in the art, and the dosage and the number of times do not limit the scope of the present invention in any way.
본 발명의 약학적 조성물은 쥐, 생쥐, 가축, 인간 등의 포유동물에 다양한 경로를 통해 투여될 수 있다. 투여의 모든 방식은 예상될 수 있으며, 예를 들어 경구, 정맥, 근육 또는 피하 주사에 의해 투여될 수 있다.The pharmaceutical composition of the present invention can be administered to mammals such as rats, mice, livestock, humans, and the like through various routes. All modes of administration may be expected and may be administered, for example, by oral, intravenous, intramuscular or subcutaneous injection.
본 발명의 또 다른 하나의 양태로서, 본 발명은 상기 알칸닌 또는 이의 식품학적으로 허용 가능한 염을 유효성분으로 포함하는 식품 조성물을 제공한다. 또한, 구체적으로, 본 발명은 상기 알칸닌을 유효성분으로 포함하는 치아 우식증, 치주질환(치주염 또는 치은염), 치통, 시린이 및 구취로 이루어진 군으로부터 선택된 1 이상의 구강질환 예방 또는 개선용 식품 조성물을 제공할 수 있다. 알칸닌, 구강질환, 치아 우식증, 치주질환, 치통, 시린이 및 구취는 상기에서 설명한 바와 같다. 상기 식품 조성물은 건강기능식품의 형태로 사용될 수 있으나, 이에 제한되는 것은 아니다.In another aspect of the present invention, there is provided a food composition comprising the alkanine or a pharmaceutically acceptable salt thereof as an active ingredient. More specifically, the present invention relates to a food composition for preventing or ameliorating at least one oral disease selected from the group consisting of dental caries, periodontal disease (periodontitis or gingivitis), toothache, syrinite and bad breath containing the alkanin as an active ingredient . Alkaline, oral disease, dental caries, periodontal disease, toothache, syringitis and halitosis are as described above. The food composition may be used in the form of a health functional food, but is not limited thereto.
본 발명의 식품 조성물에 포함된 상기 알칸닌 또는 이의 식품학적으로 허용 가능한 염은 알칸닌을 포함하는 동식물, 이의 추출물, 이의 분획물 또는 이의 가공물의 형태로 포함될 수 있다. 또한 상기 조성물은 유효성분 이외에 식품학적으로 허용 가능한 식품보조첨가제를 포함할 수 있다.The alkanine or a pharmaceutically acceptable salt thereof contained in the food composition of the present invention may be contained in the form of an animal or plant including an alkanin, an extract thereof, a fraction thereof or a processed product thereof. The composition may also include a food-acceptable food-aid additive in addition to the active ingredient.
본 발명에 있어서, "식품보조첨가제"란 식품에 보조적으로 첨가될 수 있는 구성요소를 의미하며, 각 제형의 건강기능식품을 제조하는데 첨가되는 것으로서 당업자가 적절히 선택하여 사용할 수 있다. 식품보조첨가제의 예로는 여러 가지 영양제, 비타민, 광물(전해질), 합성 풍미제 및 천연 풍미제 등의 풍미제, 착색제 및 충진제, 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알콜, 탄산음료에 사용되는 탄산화제 등이 포함되지만, 상기 예들에 의해 본 발명의 식품보조첨가제의 종류가 제한되는 것은 아니다.In the present invention, the term " food-aid additive " means a component that can be added to foods in a supplementary manner, and is appropriately selected and used by those skilled in the art as added to produce health functional foods of each formulation. Examples of food-aid additives include flavors such as various nutrients, vitamins, minerals (electrolytes), synthetic flavors and natural flavors, colorants and fillers, pectic acid and its salts, alginic acid and its salts, organic acids, , a pH adjusting agent, a stabilizer, a preservative, a glycerin, an alcohol, and a carbonating agent used in a carbonated drink. However, the types of the food auxiliary additives of the present invention are not limited by these examples.
본 발명의 식품 조성물에는 건강기능식품이 포함될 수 있다. 본 발명에 있어서, "건강기능식품"이란 인체에 유용한 기능성을 가진 원료나 성분을 사용하여 정제, 캅셀, 분말, 과립, 액상 및 환 등의 형태로 제조 및 가공한 식품을 말한다. 여기서 “기능성”이라 함은 인체의 구조 및 기능에 대하여 영양소를 조절하거나 생리학적 작용 등과 같은 보건용도에 유용한 효과를 얻는 것을 의미한다. 본 발명의 건강기능식품은 당업계에서 통상적으로 사용되는 방법에 의하여 제조 가능하며, 상기 제조시에는 당업계에서 통상적으로 첨가하는 원료 및 성분을 첨가하여 제조할 수 있다. 또한 상기 건강기능식품의 제형 또한 건강기능식품으로 인정되는 제형이면 제한 없이 제조될 수 있다. 본 발명의 식품 조성물은 다양한 형태의 제형으로 제조될 수 있으며, 일반 약품과는 달리 식품을 원료로 하여 약품의 장기 복용 시 발생할 수 있는 부작용 등이 없는 장점이 있고, 휴대성이 뛰어나, 본 발명의 건강기능식품은 구강질환을 예방 또는 개선시키기 위한 보조제로 섭취가 가능하다.A health functional food may be included in the food composition of the present invention. In the present invention, the term " health functional food " refers to a food prepared and processed in the form of tablets, capsules, powders, granules, liquids and rings using raw materials and components having useful functions in the human body. The term "functional" as used herein means that the structure and function of the human body have a beneficial effect on health uses such as controlling nutrients or physiological actions. The health functional food of the present invention can be prepared by a method commonly used in the art and can be prepared by adding raw materials and ingredients that are conventionally added in the art. In addition, the formulations of the above health functional foods may also be manufactured without limitations as long as they are acceptable as health functional foods. The food composition of the present invention can be manufactured in various formulations, and unlike general pharmaceuticals, it has an advantage of being free from side effects that may occur when a food is used as a raw material for a long period of time, and is excellent in portability. Health functional foods can be ingested as an adjunct to prevent or improve oral diseases.
본 발명의 건강기능식품이 취할 수 있는 형태에는 제한이 없으며, 통상적인 의미의 식품을 모두 포함할 수 있고, 기능성 식품 등 당업계에 알려진 용어와 혼용 가능하다. 아울러 본 발명의 건강기능식품은 당업자의 선택에 따라 식품에 포함될 수 있는 적절한 기타 보조성분과 공지의 첨가제를 혼합하여 제조할 수 있다. 첨가할 수 있는 식품의 예로는 육류, 소세지, 빵, 쵸코렛, 캔디류, 스낵류, 과자류, 피자, 라면, 기타 면류, 껌류, 아이스크림류를 포함한 낙농제품, 각종 스프, 음료수, 차, 드링크제, 알콜 음료 및 비타민 복합제 등이 있으며, 본 발명에 따른 알칸닌을 주성분으로 하여 제조한 즙, 차, 젤리 및 주스 등에 첨가하여 제조할 수 있다. 또한 동물을 위한 사료로 이용되는 식품도 포함한다.The form of the health functional food of the present invention is not limited, and may include all foods in the conventional meaning, and may be used in combination with terms known in the art such as functional foods. In addition, the health functional food of the present invention can be prepared by mixing other suitable auxiliary ingredients, which may be included in food, according to the selection of a person skilled in the art, and known additives. Examples of foods that can be added include dairy products, such as meat, sausage, bread, chocolates, candies, snacks, confectionery, pizza, ramen, other noodles, gums, ice cream, various soups, drinks, tea, Vitamin complex, and the like, and can be prepared by adding to the juice, tea, jelly, and juice prepared from the alkanin according to the present invention as a main component. It also includes foods used as feed for animals.
본 발명의 알칸닌 또는 이의 약학적으로 허용 가능한 염을 유효성분으로 포함하는 의약외품 조성물은 구강질환 예방 또는 개선 효과가 우수하다. 구체적으로 본 발명의 조성물은 치아우식증 및 치주질환 유발세균에 대한 항균활성이 우수하며, 통증 및 염증 마커인 PGE2를 농도 의존적으로 억제하고, 치은염 형성 억제 효과, 시린이 증상 억제 효과 및 구취 제거 효과가 우수하여 치아 우식증, 치주질환, 치통, 시린이 및 구취로 이루어진 군으로부터 선택된 1 이상의 구강질환 예방 또는 개선용 의약외품 조성물로서의 활용도가 높다. 또한, 본 발명의 알칸닌을 포함하는 조성물은 약학적 조성물 및 식품 조성물로서 사용할 수 있다.The quasi-drug composition containing the alkanine of the present invention or a pharmaceutically acceptable salt thereof as an active ingredient is excellent in preventing or improving oral diseases. Specifically, the composition of the present invention is excellent in antimicrobial activity against dental caries and periodontal disease-causing bacteria, and inhibits the pain and inflammation marker PGE2 in a concentration-dependent manner, and has a gingivitis formation inhibitory effect, And is highly utilized as a quasi-drug composition for preventing or ameliorating at least one oral disease selected from the group consisting of dental caries, periodontal diseases, toothache, syringitis and bad breath. In addition, the composition containing the alkanine of the present invention can be used as a pharmaceutical composition and a food composition.
본 명세서에 첨부되는 다음의 도면들은 본 발명의 바람직한 실시예를 예시하는 것이며, 전술한 발명의 내용과 함께 본 발명의 기술사상을 더욱 이해시키는 역할을 하는 것이므로, 본 발명은 그러한 도면에 기재된 사항에만 한정되어 해석되어서는 아니 된다.
도 1은 대식세포에 각각 염증 자극원인 LPS(대조군)와 LPS 및 알칸닌(실험군)를 처리하여 PGE2 억제 효과를 확인한 결과를 나타낸다.BRIEF DESCRIPTION OF THE DRAWINGS The accompanying drawings, which are incorporated in and constitute a part of the specification, illustrate exemplary embodiments of the invention and, together with the description of the invention, It should not be construed as limited.
FIG. 1 shows the results of confirming the inhibitory effect of PGE2 by treating LPS (control group), LPS and alkanin (experimental group), which are inflammatory stimuli, on macrophages.
이하, 실시예 및 실험예를 통하여 본 발명의 구성 및 효과를 더욱 상세히 설명하고자 한다. 이들 실시예 및 실험예는 오로지 본 발명을 예시하기 위한 것일 뿐 본 발명의 범위가 이들 실시예 및 실험예에 의해 제한되는 것은 아니다.Hereinafter, the constitution and effects of the present invention will be described in more detail with reference to Examples and Experimental Examples. These Examples and Experimental Examples are only for illustrating the present invention, and the scope of the present invention is not limited by these Examples and Experimental Examples.
실험예Experimental Example 1 : One : 치아 우식증Dental caries 및 치주염 원인균에 대한 항균 효과 And antimicrobial effect against periodontitis causing bacteria
상기 알칸닌의 치아 우식증 및 치주염에 대한 예방 또는 치료 효과를 확인하기 위하여 항균 활성 실험을 수행하였다. 구강병원균 생육 억제 효과를 확인하고자 치아 우식증 대표유발 세균인 스트렙토코커스 뮤탄스(Streptococcus mutans)와 치주질환 대표유발 세균인 포피로모나스 진지발리스(Porphyromonas gingivalis)를 이용하여 페이퍼 디스크 검사법을 사용함으로써 항균력 테스트를 실시하였다.Antibacterial activity tests were performed to confirm the preventive or therapeutic effect of the alkanin on dental caries and periodontitis. Streptococcus mutans , a representative dental caries-inducing bacterium, and Porphyromonas , a representative bacterium for periodontal disease, gingivalis ) was used for the test of antimicrobial activity.
상기 각 구강병원균들을 하기 표 1의 최적 배양조건에서 활성을 증가시킨 후, 각 균의 최적배지에서 4 ~ 6시간 정도 배양하여 배양액의 탁도를 Macfarland turbidity No. 0.5 (1.5 X 108)가 되도록 맞추고, 상기 각 구강병원균 0.1ml를 평판배지에 골고루 도말하였다. 이후, 상기 멸균한 페이퍼 디스크에 상기 알칸닌을 10 mg/disc 농도로 접종하여 1시간 동안 흡수 건조시켰다. 그런 다음, 상기 각 구강병원균의 최적온도에서 24 ~ 48시간 배양한 후 생육저지환의 크기(직경 mm)를 측정하였으며, 그 결과를 하기 표 2에 나타내었다.Each of the oral pathogens was cultivated for 4 to 6 hours in an optimal medium after increasing the activity under the optimal culture conditions shown in Table 1 below. The turbidity of the culture was determined by Macfarland turbidity No. 1. 0.5 (1.5 x 10 8 ), and 0.1 ml of each of the oral pathogens was evenly plated on a plate medium. Then, the alkanin was inoculated on the sterilized paper disk at a concentration of 10 mg / disc and absorbed and dried for 1 hour. Then, after culturing at the optimal temperature of each of the oral pathogens for 24 to 48 hours, the size (diameter mm) of the growth inhibition rings was measured. The results are shown in Table 2 below.
(Gram staining)Gram stain
(Gram staining)
상기 표 2에 나타난 바와 같이, 알칸닌을 처리하지 않은 무처리군과 비교했을 때, 알칸닌을 처리한 군은 상기 2 종의 구강병원균에 대한 생육저지환 직경이 약 11.0 mm 정도로 스트렙토코커스 뮤탄스 및 포피로모나스 진지발리스에 대한 상당히 우수한 항균활성을 나타내었다. 따라서, 알칸닌은 치아 우식증 또는 치주질환을 예방 또는 치료하는 용도로 사용할 수 있음을 알 수 있었다.As shown in the above Table 2, the group treated with alkanin had a growth inhibition diameter of about 11.0 mm for the two oral pathogens, compared with the non-treated group not treated with alkanine, And < RTI ID = 0.0 > Porphyromonas jinx valis. ≪ / RTI > Therefore, it has been found that alkanin can be used for preventing or treating dental caries or periodontal disease.
실험예Experimental Example 2 : 치은염 형성 억제 효과 2: Gingivitis formation inhibitory effect
상기 알칸닌의 치은염 예방 또는 치료 효과를 확인하기 위하여 실험 대상군을 선별하여 임상실험을 수행하였다.In order to confirm the preventive or therapeutic effect of the alkanin in the gingivitis, the experimental group was selected and the clinical experiment was performed.
먼저, 치약 제조 시에 일반적으로 사용되는 카르복시메칠세룰로오스나트륨, 라우릴황산나트륨, 글리세린, 콜리이드성 이산화규소, 실리카류, 소디움코코일이세치온산나트륨, 도디신과 감미제, 방향제, 착색제 등을 이용하여 대조군 치약을 만들었고, 상기 대조군 치약에 상기 알칸닌이 0.01 중량% 함유하도록 하여 실험군 치약을 제조하였다. First, there are used carboxymethylcellulose sodium, sodium lauryl sulfate, glycerin, colloidal silicon dioxide, silica, sodium cocoyl sulfate, sodium dodecanoate, sweetener, flavoring agent, coloring agent, To prepare a control toothpaste. To the toothpaste of the control group, 0.01% by weight of the alkanine was contained to prepare an experimental toothpaste.
실험 대상자를 선별하기 위하여 치열이 고르고 결손 치아가 없는 치은염증 환자를 대상으로 연령별 30세부터 50세까지 10세 간격으로 성별에 따라 30명씩 정밀한 구강검진을 실시하였으며, 그런 다음 120명의 실험 대상군을 선별한 후 60명씩 나누어 치은염증 치료효과에 대한 임상실험을 하기와 같이 수행하였다. In order to select the subjects, a thorough oral examination was performed on 30 patients of gingival inflammation without dentition and between 30 and 50 years of age at 10-year intervals according to gender. After the screening, 60 patients were divided into two groups.
구체적으로, 실험 대상군을 대조군과 실험군으로 나누고 대조군은 식후 2시간 경과 후 잠자기 전에 하루 3회 상기 제조된 대조군 치약을 사용하도록 교육시키고, 실험군은 동일 시간에 하루 3회 상기 제조된 실험군 치약을 사용하도록 교육시켰다. 이후 치면세마를 실시하여 초기 치은염지수를 점수화하고 대조군은 상기 제조된 대조군 치약을, 실험군은 상기 제조된 실험군 치약을 사용하도록 하여 1주, 1개월, 3개월 및 6개월 경과 후 구강검진을 실시하여 치은염지수를 검사하였다. 치은염지수의 측정방법은 페리오덴탈 프로브(periodontal probe)를 치은열구 내에 삽입하여 힘을 가하지 않은 상태로 각 치아주위를 연소하여 탐침하고 30초가 지난 뒤에 출혈된 상태를 측정하여 하기 표 3에 나타난 기준에 따라 점수를 기록하였으며, 그 결과는 표 4에 나타내었다. Specifically, the test subjects were divided into a control group and an experimental group, and the control group was instructed to use the prepared control toothpaste three times a day before sleeping 2 hours after the meal, and the test group was used three times a day at the same time . Thereafter, the initial gingival index was scored and the oral gingivitis was scored at 1 week, 1 month, 3 months and 6 months after the control toothpaste was prepared and the experimental toothpaste was used in the experimental group. Gingivitis index was examined. The method of measuring the gingival index was performed by inserting a periodontal probe into the gingival fissure, burning the circumference of each tooth without applying any force, measuring the bleeding state after 30 seconds, The scores were recorded according to the results, and the results are shown in Table 4.
상기 표 4에 나타난 바와 같이, 대조군과 비교했을 때, 알칸닌이 포함된 치약을 사용한 실험군은 6개월이 경과했음에도 정상출혈 상태를 유지하여 치은염증 억제 효과가 지속되었다. 따라서, 알칸닌은 치은염을 예방 또는 치료하는 용도로 사용할 수 있음을 알 수 있었다.As shown in Table 4, the test group using alkanine-containing toothpaste maintained the normal bleeding state even after 6 months, and the gingival inflammation-suppressing effect was maintained as compared with the control group. Therefore, it was found that the alkanin can be used for preventing or treating gingivitis.
실험예Experimental Example 3 : 통증 및 염증 3: Pain and inflammation 마커인Marker Inn PGE2PGE2 억제 효과 Inhibitory effect
상기 알칸닌의 치통 예방 또는 치료 효과를 확인하기 위하여 통증 및 염증 마커로 알려진 PGE2 억제 효과를 확인하였다.In order to confirm the preventive or therapeutic effect of the alkanin on toothache, PGE2 inhibitory effect, known as pain and inflammation marker, was confirmed.
먼저, 대식세포를 10% FBS를 포함하는 DMEM 배지에서 1.5 X 105 cells/ml 농도로 접종하여 37℃, 5% CO2 조건으로 24 well plate에 24시간 동안 배양하였다. 그런 다음 염증 유도 자극원인 LPS 1㎍/ml와 알칸닌을 농도별로 처리하여 24시간 동안 추가 배양한 후, PGE2 ELISA assay kit(Thermo SCIENTIFIC)를 구입하여 상층액을 이용해 알칸닌 농도에 따른 PGE2 억제능을 분석하였다(도 1). First, macrophages were inoculated in DMEM medium containing 10% FBS at a concentration of 1.5 × 10 5 cells / ml and cultured in a 24-well plate at 37 ° C and 5% CO 2 for 24 hours. After incubation for 24 hours with 1 μg / ml LPS and alkaline phosphatase, the PGE2 ELISA assay kit (Thermo SCIENTIFIC) was purchased and the PGE2 inhibitory effect of alkanin concentration (Fig. 1).
도 1에 나타난 바와 같이, LPS만을 처리한 군과 비교했을 때, 2ppm 농도의 알칸닌은 약 80%까지, 20ppm 농도의 알칸닌은 약 95%까지 PGE2를 억제하는 효능이 있었다. 따라서, 알칸닌은 치통을 예방 또는 치료하는 용도로 사용할 수 있음을 알 수 있었다.As shown in Fig. 1, the alkanin concentration of 2 ppm was effective to suppress PGE2 up to about 80%, and the alkanol concentration of 20 ppm was inhibited to about 95% when compared to the group treated with LPS alone. Therefore, it was found that alkanin can be used for preventing or treating toothache.
실험예Experimental Example 4 : 4 : 시린이Cyrin 억제 효과 Inhibitory effect
상기 알칸닌의 시린이 예방 또는 치료 효과를 확인하기 위하여 실험 대상자를 선별하여 임상실험을 수행하였으며, 임상실험에서 사용된 대조군 치약 및 실험군 치약은 상기 실험예 2의 치약과 동일한 방법으로 각각 제조하였다.In order to confirm the preventive or therapeutic effect of the alkynin, the subjects were selected for clinical trials. The control toothpaste and the experimental toothpaste used in the clinical experiment were prepared in the same manner as the toothpaste of Experimental Example 2, respectively.
실험 대상자들은 상아질과민증 치아를 가진 사람으로서 이 실험에 참여하기를 동의한 지원자 40명이며, 총 실험 대상 치아는 80개였다. 또한, 실험 대상자들 중 남자는 20명, 여자는 20명이고, 연령은 20세에서 50세였다. 실험 대상자들이 치약 내용물을 알지 못하도록 하였으며, 총 실험기간은 2주로 하였다. The subjects were 40 volunteers who agreed to participate in this experiment as dentin hypersensitive teeth, and 80 teeth were used for the total test. Of the subjects, 20 were male and 20 were female and the ages ranged from 20 to 50 years. The subjects were not allowed to know the contents of toothpaste, and the total duration of the experiment was 2 weeks.
실험은 온도 자극을 가한 후 실험 대상자의 반응을 측정하는 방법으로 수행되었다. 실험을 실시하기 전에 미리 각 실험 대상자의 상아질과민증 치아의 과민 부위를 체크하고, 치아의 시린 부위에 약 5℃의 차가운 물을 스포이드로 떨어뜨려 하기 표 5에 나타난 기준에 따라 평점을 한 후 대조군은 상기 대조군 치약을, 실험군은 상기 실험군 치약을 2주 동안 1일 3회 사용하게 하고, 2주가 지나 다시 약 5℃의 차가운 물을 스포이드로 떨어뜨려 평점을 하였다. 통계처리는 실험 실시 전과 2주 후의 자극 점수를 대응표본 T- 검정(paired Student-t test)로 검정하였으며, 온도 자극에 대한 2주 후의 반응 점수는 하기 표 6에 나타내었다.The experiment was performed by measuring the response of the subject after applying the temperature stimulus. Before the experiment, the dentin hypersensitivity areas of dentin hypersensitivity teeth of each subject were checked in advance, and cold water of about 5 ° C was dropped on the syringe area of the teeth with a syringe. The teeth were rated according to the criteria shown in Table 5, The control toothpaste was used in the experimental group, and the toothpaste of the test group was used three times a day for two weeks. After about two weeks, cold water of about 5 ° C was dropped on the syringe and evaluated. Statistical analysis was performed using a paired Student's t-test before and two weeks after the experiment, and the response score after two weeks to the temperature stimulation is shown in Table 6 below.
※ p>0.05: 95% 신뢰도, 통계적으로 유의한 차이가 없음. *p<0.05: 95% 신뢰도, 통계적으로 유의한 차이가 있음. ※ p> 0.05: 95% reliability, no statistically significant difference. * p <0.05: 95% confidence, statistically significant difference.
상기 표 6에 나타난 바와 같이, 대조군과 비교했을 때, 알칸닌이 포함된 치약을 사용한 실험군은 2주 경과 후 시린이 현상이 억제되었다. 따라서, 알칸닌은 시린이를 예방 또는 치료하는 용도로 사용할 수 있음을 알 수 있었다.As shown in Table 6, in the test group using the alkanine-containing toothpaste, the syringe phenomenon was suppressed after 2 weeks as compared with the control group. Therefore, it was found that the alkanine can be used as a preventive or therapeutic agent for acylin.
실험예Experimental Example 5 : 구취 제거 효과 5: Bad breath removal effect
상기 알칸닌의 구취 예방 또는 치료 효과를 확인하기 위하여 실험 대상자를 선별하여 임상실험을 수행하였으며, 임상실험에서 사용된 대조군 치약 및 실험군 치약은 상기 실험예 2의 치약과 동일한 방법으로 각각 제조하였다.In order to confirm the effect of preventing or treating bad breath of the alkanin, a subject was selected and a clinical experiment was conducted. The control toothpaste and the experimental toothpaste used in the clinical experiment were prepared in the same manner as the toothpaste of Experimental Example 2, respectively.
실험 대상자로 치아 우식증이 없는 남녀 50명을 선정하여 상기 대조군 치약 및 실험군 치약에 대하여 교차 반복 실험(Cross-over test)을 실시하였다. 시판하는 마늘분을 물에 분산시켜 24시간 방치한 후 희석하여 할리미터(Halimeter) 측정값이 700ppb 이상이 되도록 하고, 상기 희석액을 구취 유발원으로 사용하였다. 실험 대상자들은 마늘분 희석액 15ml로 30초간 가글을 하고, 1분 뒤에 할리미터로 구취 정도를 측정한 후, 대조군은 상기 대조군 치약을, 실험군은 상기 실험군 치약을 각각 사용하여 30초 ~ 1분간 양치질하였다. 양치질 후 1분, 5분, 30분 경과 후 할리미터로 구취 정도를 측정하여 구취억제의 지속여부를 측정하였으며, 그 결과는 하기 표 7에 나타내었다.Fifty men and women without dental caries were selected as subjects and cross-over tests were performed on the toothpaste of the control group and the toothpaste of the experimental group. The commercially available garlic powder was dispersed in water, allowed to stand for 24 hours, and diluted so that the measured value of halimeter was 700 ppb or more. The diluted solution was used as a source of bad breath. The subjects were gagged with 15 ml of garlic min diluted solution for 30 seconds and after 1 minute, the degree of halitosis was measured with a halimeter, then the control group was used the control toothpaste and the experimental group was used for 30 seconds to 1 minute using the test group toothpaste . After 1 minute, 5 minutes, and 30 minutes after brushing, the degree of halitosis was measured with a halimeter to measure the persistence of halitosis suppression. The results are shown in Table 7 below.
상기 표 7에 나타난 바와 같이, 대조군과 비교했을 때, 알칸닌이 포함된 치약을 사용한 실험군은 양치질 후 약 98% 정도로 구취가 제거되었으며, 양치질 후 30분이 경과하여도 구취 제거율이 93% 이상으로 구취 제거 효과가 대조군에 비해 월등히 우수하였다. 따라서, 알칸닌은 구취를 예방 또는 치료하는 용도로 사용할 수 있음을 알 수 있었다.As shown in Table 7, in the experiment group using the alkanine-containing toothpaste, about 98% of the odorant was removed after 30 minutes compared to the control group, and the odor removal rate was 93% The removal efficiency was much better than the control group. Therefore, it has been found that alkanin can be used for preventing or treating bad breath.
Claims (14)
A quasi-drug composition for preventing or ameliorating oral diseases, comprising an alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
The quasi-drug composition according to claim 1, wherein the oral disease is dental caries.
3. The quasi-drug composition according to claim 2, wherein the dental caries is caused by Streptococcus mutans .
The quasi-drug composition according to claim 1, wherein the oral disease is periodontal disease.
The quasi-drug composition according to claim 4, wherein the periodontal disease is periodontitis or gingivitis.
The quasi-drug composition according to claim 4, wherein the periodontal disease is caused by Porphyromonas gingivalis .
The quasi-drug composition according to claim 1, wherein the oral disease is toothache.
The quasi-drug composition according to claim 1, wherein the oral disease is psoriasis.
The quasi-drug composition according to claim 1, wherein the oral disease is halitosis.
The quasi-drug composition according to claim 1, wherein the quasi-drug is oral.
The composition according to claim 10, wherein the formulation of the quasi-drug composition is one or more formulations selected from the group consisting of toothpaste, mouthwash, mouthwash, gum, candy, oral spray, oral ointment, oral varnish, mouthwash, Lt; / RTI > composition.
A pharmaceutical composition for preventing or treating oral diseases, comprising an alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
A food composition for preventing or ameliorating an oral disease comprising alkanin or a pharmaceutically acceptable salt thereof as an active ingredient.
An oral composition comprising an alkanin or an acceptable salt thereof as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020170133489A KR102459936B1 (en) | 2017-10-13 | 2017-10-13 | Composition for prevention or treatment of oral disease comprising Alkannin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020170133489A KR102459936B1 (en) | 2017-10-13 | 2017-10-13 | Composition for prevention or treatment of oral disease comprising Alkannin |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20190041799A true KR20190041799A (en) | 2019-04-23 |
KR102459936B1 KR102459936B1 (en) | 2022-10-27 |
Family
ID=66285145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020170133489A KR102459936B1 (en) | 2017-10-13 | 2017-10-13 | Composition for prevention or treatment of oral disease comprising Alkannin |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR102459936B1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102438800B1 (en) * | 2022-02-11 | 2022-08-31 | (주)엔에스티바이오 | Composition comtaining lactic acid fermented noni extract as active ingredient for prevention or treatment of oral disease |
KR20230170836A (en) | 2022-06-11 | 2023-12-19 | 남호진 | an insect-killing spear |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR970005299A (en) * | 1995-07-20 | 1997-02-19 | 박동기 | Extraction Modifier for Acne Improvement from Natural Products |
JP2013043952A (en) * | 2011-08-25 | 2013-03-04 | Toyo Ink Sc Holdings Co Ltd | Photopolymerizable composition, and application thereof |
KR20140089337A (en) * | 2011-08-25 | 2014-07-14 | 토요잉크Sc홀딩스주식회사 | Photopolymerizable composition, photopolymerizable coating agent, laminate, and polarizing plate |
KR20150050239A (en) | 2013-10-31 | 2015-05-08 | 주식회사 엘지생활건강 | Composition for preventing or treating oral disease comprising toosendanin |
KR20180080189A (en) * | 2015-09-01 | 2018-07-11 | 퍼스트 웨이브 바이오, 인코포레이티드 | And compositions for treating diseases associated with abnormal inflammatory response |
-
2017
- 2017-10-13 KR KR1020170133489A patent/KR102459936B1/en active IP Right Grant
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR970005299A (en) * | 1995-07-20 | 1997-02-19 | 박동기 | Extraction Modifier for Acne Improvement from Natural Products |
JP2013043952A (en) * | 2011-08-25 | 2013-03-04 | Toyo Ink Sc Holdings Co Ltd | Photopolymerizable composition, and application thereof |
KR20140089337A (en) * | 2011-08-25 | 2014-07-14 | 토요잉크Sc홀딩스주식회사 | Photopolymerizable composition, photopolymerizable coating agent, laminate, and polarizing plate |
KR20150050239A (en) | 2013-10-31 | 2015-05-08 | 주식회사 엘지생활건강 | Composition for preventing or treating oral disease comprising toosendanin |
KR20180080189A (en) * | 2015-09-01 | 2018-07-11 | 퍼스트 웨이브 바이오, 인코포레이티드 | And compositions for treating diseases associated with abnormal inflammatory response |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102438800B1 (en) * | 2022-02-11 | 2022-08-31 | (주)엔에스티바이오 | Composition comtaining lactic acid fermented noni extract as active ingredient for prevention or treatment of oral disease |
KR20230170836A (en) | 2022-06-11 | 2023-12-19 | 남호진 | an insect-killing spear |
Also Published As
Publication number | Publication date |
---|---|
KR102459936B1 (en) | 2022-10-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR102470030B1 (en) | Composition for prevention or treatment or oral disease | |
KR102459936B1 (en) | Composition for prevention or treatment of oral disease comprising Alkannin | |
KR102700606B1 (en) | Composition for prevention or treatment of oral disease comprising icaritin | |
KR102687220B1 (en) | Composition for prevention or treatment of oral disease comprising d-tetrahydropalmatine | |
KR102665310B1 (en) | Composition for prevention or treatment of oral disease comprising Verbascoside | |
KR20190041801A (en) | Composition for prevention or treatment of oral disease comprising Ginkgolide C | |
KR20180055519A (en) | Composition for prevention or treatment of oral disease comprising salvianolic acid A | |
KR20180055520A (en) | Composition for prevention or treatment of oral disease comprising neferine | |
KR20180046250A (en) | Composition for prevention or treatment of oral disease comprising Astilbin | |
KR20180046244A (en) | Composition for prevention or treatment of oral disease comprising Cordycepin | |
KR102485968B1 (en) | Composition for prevention or treatment of oral disease comprising Casticin | |
KR20180047705A (en) | Composition for prevention or treatment of oral disease comprising Forsythiae Fructus extract | |
KR102687221B1 (en) | Composition for prevention or treatment of oral disease comprising dihydrotanshinone Ⅰ | |
KR102665306B1 (en) | Composition for prevention or treatment of oral disease comprising forsythoside B | |
KR102670487B1 (en) | Composition for prevention or treatment of oral disease comprising cynarin | |
KR102700607B1 (en) | Composition for prevention or treatment of oral disease comprising tiliroside | |
KR102626865B1 (en) | Composition for prevention or treatment of oral disease comprising Crotonoside | |
KR102626864B1 (en) | Composition for prevention or treatment of oral disease comprising Shikonin | |
KR102605700B1 (en) | Composition for prevention or treatment of oral disease comprising 1,2,4-Trihydroxyanthraquinone | |
KR102681673B1 (en) | Composition for prevention or treatment of oral disease comprising Nobiletin | |
KR20180055526A (en) | Composition for prevention or treatment of oral disease comprising salvianolic acid B | |
KR20180055524A (en) | Composition for prevention or treatment of oral disease comprising punicalagin | |
KR20180055527A (en) | Composition for prevention or treatment of oral disease comprising eriodictyol | |
KR20180055523A (en) | Composition for prevention or treatment of oral disease comprising nitidine chloride | |
KR20180046249A (en) | Composition for prevention or treatment of oral disease comprising lithospermic acid |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant |