KR20010101153A - 의치 접착제 - Google Patents
의치 접착제 Download PDFInfo
- Publication number
- KR20010101153A KR20010101153A KR1020017007166A KR20017007166A KR20010101153A KR 20010101153 A KR20010101153 A KR 20010101153A KR 1020017007166 A KR1020017007166 A KR 1020017007166A KR 20017007166 A KR20017007166 A KR 20017007166A KR 20010101153 A KR20010101153 A KR 20010101153A
- Authority
- KR
- South Korea
- Prior art keywords
- copolymer
- lysine
- denture adhesive
- arginine
- histidine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 62
- 239000000853 adhesive Substances 0.000 title claims abstract description 61
- 229920001577 copolymer Chemical class 0.000 claims abstract description 89
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims abstract description 56
- 239000004472 Lysine Substances 0.000 claims abstract description 54
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims abstract description 53
- 150000003839 salts Chemical class 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 30
- 239000004475 Arginine Substances 0.000 claims abstract description 16
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims abstract description 16
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims abstract description 16
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims abstract description 16
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920000642 polymer Polymers 0.000 claims description 25
- 239000002253 acid Substances 0.000 claims description 12
- 150000008064 anhydrides Chemical class 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 11
- -1 alkyl vinyl ether Chemical compound 0.000 claims description 9
- 239000006071 cream Substances 0.000 claims description 9
- 150000008065 acid anhydrides Chemical class 0.000 claims description 7
- 150000001768 cations Chemical class 0.000 claims description 7
- 239000000499 gel Substances 0.000 claims description 7
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical group COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims description 7
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 231100000252 nontoxic Toxicity 0.000 claims description 5
- 230000003000 nontoxic effect Effects 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- 239000011701 zinc Substances 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- 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 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 230000003472 neutralizing effect Effects 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 229910052712 strontium Inorganic materials 0.000 claims description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 2
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims 1
- 125000002843 carboxylic acid group Chemical group 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000006072 paste Substances 0.000 claims 1
- 229910052718 tin Inorganic materials 0.000 claims 1
- 239000011135 tin Substances 0.000 claims 1
- 229960003646 lysine Drugs 0.000 description 45
- 235000018977 lysine Nutrition 0.000 description 45
- 238000004132 cross linking Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 235000009697 arginine Nutrition 0.000 description 8
- 235000014304 histidine Nutrition 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 7
- 210000000214 mouth Anatomy 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 229920001477 hydrophilic polymer Polymers 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 239000003446 ligand Substances 0.000 description 5
- 239000004971 Cross linker Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 229920006037 cross link polymer Polymers 0.000 description 4
- HZRUTVAFDWTKGD-JEDNCBNOSA-N (2s)-2,6-diaminohexanoic acid;hydrate Chemical compound O.NCCCC[C@H](N)C(O)=O HZRUTVAFDWTKGD-JEDNCBNOSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- 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 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-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
- 125000004018 acid anhydride group Chemical group 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229920005603 alternating copolymer Polymers 0.000 description 2
- 229960003121 arginine Drugs 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229940032007 methylethyl ketone Drugs 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 210000003296 saliva Anatomy 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 235000013599 spices Nutrition 0.000 description 2
- ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical compound CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 description 1
- YIWGJFPJRAEKMK-UHFFFAOYSA-N 1-(2H-benzotriazol-5-yl)-3-methyl-8-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carbonyl]-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound CN1C(=O)N(c2ccc3n[nH]nc3c2)C2(CCN(CC2)C(=O)c2cnc(NCc3cccc(OC(F)(F)F)c3)nc2)C1=O YIWGJFPJRAEKMK-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- LEVWYRKDKASIDU-QWWZWVQMSA-N D-cystine Chemical compound OC(=O)[C@H](N)CSSC[C@@H](N)C(O)=O LEVWYRKDKASIDU-QWWZWVQMSA-N 0.000 description 1
- 238000006021 Dakin-West synthesis reaction Methods 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000569 Gum karaya Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000934878 Sterculia Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001370 alpha-amino acid derivatives Chemical class 0.000 description 1
- 235000008206 alpha-amino acids Nutrition 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000001483 arginine derivatives Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000227 bioadhesive Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 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
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 235000020965 cold beverage Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 239000008266 hair spray Substances 0.000 description 1
- 229960002885 histidine Drugs 0.000 description 1
- 235000012171 hot beverage Nutrition 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000010494 karaya gum Nutrition 0.000 description 1
- 239000000231 karaya gum Substances 0.000 description 1
- 229940039371 karaya gum Drugs 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000002680 magnesium Chemical class 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 210000003097 mucus Anatomy 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 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
- 238000004064 recycling Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/60—Preparations for dentistry comprising organic or organo-metallic additives
- A61K6/65—Dyes
- A61K6/66—Photochromic dyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/60—Preparations for dentistry comprising organic or organo-metallic additives
- A61K6/69—Medicaments
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J135/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least another carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J135/08—Copolymers with vinyl ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/28—Non-macromolecular organic substances
- C08L2666/36—Nitrogen-containing compounds
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dental Preparations (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/207,309 | 1998-12-08 | ||
| US09/207,309 US6166102A (en) | 1998-12-08 | 1998-12-08 | Denture adhesive |
| PCT/GB1999/004122 WO2000033792A1 (en) | 1998-12-08 | 1999-12-08 | Denture adhesive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20010101153A true KR20010101153A (ko) | 2001-11-14 |
Family
ID=22769991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020017007166A Withdrawn KR20010101153A (ko) | 1998-12-08 | 1999-12-08 | 의치 접착제 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6166102A (enExample) |
| EP (1) | EP1137388A1 (enExample) |
| JP (1) | JP2002531475A (enExample) |
| KR (1) | KR20010101153A (enExample) |
| CN (1) | CN1334714A (enExample) |
| AU (1) | AU1667800A (enExample) |
| BR (1) | BR9916070A (enExample) |
| CA (1) | CA2354038A1 (enExample) |
| CZ (1) | CZ20012040A3 (enExample) |
| HK (1) | HK1043044A1 (enExample) |
| HU (1) | HUP0104744A2 (enExample) |
| MX (1) | MXPA01005812A (enExample) |
| NZ (1) | NZ512746A (enExample) |
| PL (1) | PL348832A1 (enExample) |
| UA (1) | UA72485C2 (enExample) |
| WO (1) | WO2000033792A1 (enExample) |
| ZA (1) | ZA200105545B (enExample) |
Families Citing this family (28)
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| IL145672A0 (en) * | 1999-04-14 | 2002-06-30 | Procter & Gamble | Denture adhesive compositions |
| US6617374B1 (en) | 1999-04-14 | 2003-09-09 | The Procter & Gamble Company | Denture adhesives with mixed salts of alkyl vinyl ether-maleic copolymer or terpolymer |
| AU765259B2 (en) * | 1999-04-14 | 2003-09-11 | Procter & Gamble Company, The | Denture adhesive compositions |
| US6355706B1 (en) * | 1999-04-14 | 2002-03-12 | The Procter & Gamble Company | Denture adhesives with mixed salt copolymers of terpolymers |
| US6475497B1 (en) | 1999-12-08 | 2002-11-05 | The Procter & Gamble Company | Tartar control denture adhesive compositions |
| US6905672B2 (en) | 1999-12-08 | 2005-06-14 | The Procter & Gamble Company | Compositions and methods to inhibit tartar and microbes using denture adhesive compositions with colorants |
| US6475498B1 (en) | 1999-12-08 | 2002-11-05 | The Procter & Gamble Company | Method to inhibit tartar and stain using denture adhesive compositions |
| CA2510316A1 (en) * | 2002-12-20 | 2004-07-15 | Smithkline Beecham Corporation | Denture adhesive |
| JP3847736B2 (ja) * | 2003-08-04 | 2006-11-22 | 株式会社ジーシー | ジェル状の歯牙用漂白材組成物 |
| US7834066B2 (en) * | 2005-11-09 | 2010-11-16 | The Procter & Gamble Company | Denture adhesive articles |
| US20090238776A1 (en) * | 2005-11-09 | 2009-09-24 | Arif Ali Baig | Oral Care Compositions and Methods |
| US20090239972A1 (en) * | 2005-11-09 | 2009-09-24 | Jayanth Rajaiah | Denture Adhesive Compositions and Methods |
| US20070149642A1 (en) | 2005-12-28 | 2007-06-28 | Sunstar, Inc. | Denture fixative composition |
| CA2711262C (en) * | 2008-02-08 | 2015-06-23 | Colgate-Palmolive Company | Dental composition comprising a basic amino acid for alleviating tooth sensitivity |
| AU2009212333C1 (en) | 2008-02-08 | 2012-07-19 | Colgate-Palmolive Company | Compositions and devices |
| SG191691A1 (en) | 2008-02-08 | 2013-07-31 | Colgate Palmolive Co | Dental floss |
| CN101938985A (zh) | 2008-02-08 | 2011-01-05 | 高露洁-棕榄公司 | 组合物和装置 |
| MY155564A (en) * | 2008-02-08 | 2015-10-30 | Colgate Palmolive Co | Arginine salts and their uses for the treatment of illnesses in the oral cavity |
| RU2423966C2 (ru) * | 2009-07-10 | 2011-07-20 | Феликс Аркадьевич Ерусалимов | Биоактивная бондинговая система |
| WO2011112664A2 (en) | 2010-03-10 | 2011-09-15 | The Procter & Gamble Company | Denture adhesive compositions |
| US9089730B2 (en) * | 2010-11-25 | 2015-07-28 | Zzakey Technologies Ltd | Biodegradable fire-fighting formulation |
| CN104856890A (zh) * | 2015-06-01 | 2015-08-26 | 吴迪 | 一种义齿粘合剂组合物及其制备方法 |
| EP3310867B1 (en) | 2015-06-22 | 2021-04-21 | 3M Innovative Properties Company | Pressure sensitive adhesive comprising (meth)acrylic polymer and amino acid crosslinker |
| CA3003938A1 (en) * | 2015-10-29 | 2017-05-04 | Bimeda Research & Development Limited | A teat seal formulation |
| KR101929321B1 (ko) * | 2017-03-21 | 2019-03-14 | 씨제이제일제당 주식회사 | 점착 조성물, 및 이의 제조방법 |
| KR102190916B1 (ko) | 2018-08-31 | 2020-12-15 | 씨제이제일제당 주식회사 | 점착 조성물, 및 이의 제조방법 |
| KR102280739B1 (ko) | 2018-08-31 | 2021-07-27 | 씨제이제일제당 주식회사 | 라벨용 점착 조성물, 이의 제조 방법, 이를 포함하는 점착 시트 및 물품 |
| KR102284844B1 (ko) | 2018-08-31 | 2021-08-03 | 씨제이제일제당 주식회사 | 먼지 생성을 억제하는 방법, 토양안정제 조성물, 및 이를 포함하는 분무 장치 |
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| US2313565A (en) * | 1939-10-31 | 1943-03-09 | Eastman Kodak Co | Resin and its preparation |
| US3121043A (en) * | 1960-05-11 | 1964-02-11 | Scient Associates Inc | Sustained release pharmaceutical preparation and methods for making same |
| US3878151A (en) * | 1968-05-28 | 1975-04-15 | Basf Ag | Thickeners for print pastes composed of cross-linked maleic anhydride-alkyl vinyl ether polymers |
| US3729452A (en) * | 1968-07-26 | 1973-04-24 | Mobil Oil Corp | Reaction products of an amine and a methyl vinyl ether-maleic anhydride copolymer |
| US3684776A (en) * | 1970-03-20 | 1972-08-15 | Nathan D Field | Novel interpolymers useful as thickening agents |
| US3974128A (en) * | 1972-05-08 | 1976-08-10 | The Gillette Company | Esters of maleic anhydride interpolymers |
| US4182800A (en) * | 1977-07-16 | 1980-01-08 | Hercules Incorporated | Methotrexate-divinyl ether--maleic anhydride copolymer reaction product |
| US5330746A (en) * | 1988-05-03 | 1994-07-19 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Dental varnish composition, and method of use |
| US5438076A (en) * | 1988-05-03 | 1995-08-01 | Perio Products, Ltd. | Liquid polymer composition, and method of use |
| US4874604A (en) * | 1988-06-23 | 1989-10-17 | S. C. Johnson & Son, Inc. | Hairspray with improved adhesion/removability upon washing |
| GB2228488B (en) * | 1989-02-27 | 1992-03-25 | Du Pont Canada | Coextrudable adhesives |
| US5066709A (en) * | 1990-09-20 | 1991-11-19 | Gaf Chemicals Corporation | Bioadhesive composition |
| US5178143A (en) * | 1991-07-24 | 1993-01-12 | Isp Investments Inc. | Electrically conductive gel composition |
| US5298568A (en) * | 1992-01-31 | 1994-03-29 | Toyo Ink Manufacturing Co., Ltd. | Modified olefin resin and resin composition |
| FR2688788B1 (fr) * | 1992-03-17 | 1994-05-13 | Bio Merieux | Composes hydrosolubles derives d'un homopolymere ou copolymere de l'anhydride maleique, et applications desdits composes au support de molecules biologiques. |
| US5534597A (en) * | 1992-03-20 | 1996-07-09 | Affinity Technology, Inc. | Water insoluble cross-linked acid compositions |
| US5294681A (en) * | 1992-03-20 | 1994-03-15 | Affinity Technology, Inc. | Water insoluble cross-linked acid compositions |
| FR2706126B1 (fr) * | 1993-06-08 | 1995-07-21 | Oreal | Composition cosmétique contenant un pseudo-latex ayant des propriétés de rémanence. |
| US5578661A (en) * | 1994-03-31 | 1996-11-26 | Nepera, Inc. | Gel forming system for use as wound dressings |
| US5521256A (en) * | 1995-05-16 | 1996-05-28 | Isp Investments Inc. | Process for hydrolyzing and neutralizing a crosslinked polymer of maleic anhydride and a C1 -C5 alkyl vinyl ether, optionally with a hydrophobic monomer, substantially instantly at room temperature |
| US5696181A (en) * | 1995-09-22 | 1997-12-09 | The Block Drug Company, Inc. | Denture fixative |
| JP2001517125A (ja) * | 1997-03-27 | 2001-10-02 | ザ、プロクター、エンド、ギャンブル、カンパニー | 義歯安定化組成物 |
-
1998
- 1998-12-08 US US09/207,309 patent/US6166102A/en not_active Expired - Lifetime
-
1999
- 1999-08-12 UA UA2001074708A patent/UA72485C2/uk unknown
- 1999-12-08 HU HU0104744A patent/HUP0104744A2/hu unknown
- 1999-12-08 AU AU16678/00A patent/AU1667800A/en not_active Abandoned
- 1999-12-08 WO PCT/GB1999/004122 patent/WO2000033792A1/en not_active Ceased
- 1999-12-08 EP EP99959537A patent/EP1137388A1/en not_active Withdrawn
- 1999-12-08 NZ NZ512746A patent/NZ512746A/en unknown
- 1999-12-08 BR BR9916070-6A patent/BR9916070A/pt not_active IP Right Cessation
- 1999-12-08 CN CN99816076A patent/CN1334714A/zh active Pending
- 1999-12-08 JP JP2000586287A patent/JP2002531475A/ja not_active Withdrawn
- 1999-12-08 MX MXPA01005812A patent/MXPA01005812A/es unknown
- 1999-12-08 KR KR1020017007166A patent/KR20010101153A/ko not_active Withdrawn
- 1999-12-08 CA CA002354038A patent/CA2354038A1/en not_active Abandoned
- 1999-12-08 CZ CZ20012040A patent/CZ20012040A3/cs unknown
- 1999-12-08 HK HK02102562.2A patent/HK1043044A1/zh unknown
- 1999-12-08 PL PL99348832A patent/PL348832A1/xx not_active Application Discontinuation
-
2001
- 2001-07-05 ZA ZA200105545A patent/ZA200105545B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HK1043044A1 (zh) | 2002-09-06 |
| MXPA01005812A (es) | 2002-04-24 |
| HUP0104744A2 (hu) | 2002-04-29 |
| WO2000033792A1 (en) | 2000-06-15 |
| CZ20012040A3 (cs) | 2001-12-12 |
| JP2002531475A (ja) | 2002-09-24 |
| NZ512746A (en) | 2003-08-29 |
| CA2354038A1 (en) | 2000-06-15 |
| AU1667800A (en) | 2000-06-26 |
| UA72485C2 (en) | 2005-03-15 |
| EP1137388A1 (en) | 2001-10-04 |
| US6166102A (en) | 2000-12-26 |
| CN1334714A (zh) | 2002-02-06 |
| BR9916070A (pt) | 2001-09-04 |
| PL348832A1 (en) | 2002-06-17 |
| ZA200105545B (en) | 2002-06-14 |
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| PA0105 | International application |
Patent event date: 20010608 Patent event code: PA01051R01D Comment text: International Patent Application |
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| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |