NO311034B1 - Preparat for grunning av dentale og biologiske substrater, samt fremgangsmate for fremstilling av preparatet - Google Patents
Preparat for grunning av dentale og biologiske substrater, samt fremgangsmate for fremstilling av preparatet Download PDFInfo
- Publication number
- NO311034B1 NO311034B1 NO19974521A NO974521A NO311034B1 NO 311034 B1 NO311034 B1 NO 311034B1 NO 19974521 A NO19974521 A NO 19974521A NO 974521 A NO974521 A NO 974521A NO 311034 B1 NO311034 B1 NO 311034B1
- Authority
- NO
- Norway
- Prior art keywords
- primer
- polymerizable
- dentin
- group
- resin
- Prior art date
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims abstract description 33
- 230000037452 priming Effects 0.000 title claims abstract description 22
- 238000002360 preparation method Methods 0.000 title description 6
- 239000000203 mixture Substances 0.000 claims abstract description 57
- 239000011347 resin Substances 0.000 claims abstract description 56
- 229920005989 resin Polymers 0.000 claims abstract description 56
- 239000000025 natural resin Substances 0.000 claims abstract description 36
- 239000003505 polymerization initiator Substances 0.000 claims abstract description 32
- 239000002904 solvent Substances 0.000 claims abstract description 31
- 238000007789 sealing Methods 0.000 claims abstract description 16
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims abstract description 15
- 125000002843 carboxylic acid group Chemical group 0.000 claims abstract description 9
- -1 pontlanac Substances 0.000 claims description 30
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- 238000006116 polymerization reaction Methods 0.000 claims description 19
- 244000028419 Styrax benzoin Species 0.000 claims description 18
- 235000000126 Styrax benzoin Nutrition 0.000 claims description 18
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 18
- 235000007173 Abies balsamea Nutrition 0.000 claims description 13
- 239000004859 Copal Substances 0.000 claims description 11
- 241000782205 Guibourtia conjugata Species 0.000 claims description 11
- 241000717739 Boswellia sacra Species 0.000 claims description 9
- 240000005209 Canarium indicum Species 0.000 claims description 9
- 239000004863 Frankincense Substances 0.000 claims description 9
- 235000015511 Liquidambar orientalis Nutrition 0.000 claims description 9
- 235000008331 Pinus X rigitaeda Nutrition 0.000 claims description 9
- 235000011613 Pinus brutia Nutrition 0.000 claims description 9
- 241000018646 Pinus brutia Species 0.000 claims description 9
- 240000005428 Pistacia lentiscus Species 0.000 claims description 9
- 239000004870 Styrax Substances 0.000 claims description 9
- 235000008411 Sumatra benzointree Nutrition 0.000 claims description 9
- 241000736873 Tetraclinis articulata Species 0.000 claims description 9
- 229960002130 benzoin Drugs 0.000 claims description 9
- 239000004862 elemi Substances 0.000 claims description 9
- 235000019382 gum benzoic Nutrition 0.000 claims description 9
- 239000013521 mastic Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- 239000003760 tallow Substances 0.000 claims description 9
- 239000004857 Balsam Substances 0.000 claims description 8
- 230000002209 hydrophobic effect Effects 0.000 claims description 7
- 238000011065 in-situ storage Methods 0.000 claims description 6
- 230000000977 initiatory effect Effects 0.000 claims description 5
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 claims description 4
- 244000020998 Acacia farnesiana Species 0.000 claims description 4
- 235000003074 Acacia farnesiana Nutrition 0.000 claims description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- AMFGWXWBFGVCKG-UHFFFAOYSA-N Panavia opaque Chemical compound C1=CC(OCC(O)COC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCC(O)COC(=O)C(C)=C)C=C1 AMFGWXWBFGVCKG-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 3
- BGUAPYRHJPWVEM-UHFFFAOYSA-N 2,2-dimethyl-4-pentenoic acid Chemical compound OC(=O)C(C)(C)CC=C BGUAPYRHJPWVEM-UHFFFAOYSA-N 0.000 claims description 2
- FLYIRERUSAMCDQ-UHFFFAOYSA-N 2-azaniumyl-2-(2-methylphenyl)acetate Chemical compound CC1=CC=CC=C1C(N)C(O)=O FLYIRERUSAMCDQ-UHFFFAOYSA-N 0.000 claims description 2
- UKMBKKFLJMFCSA-UHFFFAOYSA-N [3-hydroxy-2-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)OC(=O)C(C)=C UKMBKKFLJMFCSA-UHFFFAOYSA-N 0.000 claims description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- HVAMZGADVCBITI-UHFFFAOYSA-N pent-4-enoic acid Chemical group OC(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-N 0.000 claims description 2
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 2
- 244000018716 Impatiens biflora Species 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical group [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims 2
- 150000005840 aryl radicals Chemical class 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 210000004268 dentin Anatomy 0.000 abstract description 147
- 239000012260 resinous material Substances 0.000 abstract description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 18
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract description 7
- 235000010654 Melissa officinalis Nutrition 0.000 abstract description 2
- 239000000865 liniment Substances 0.000 abstract description 2
- 241000021559 Dicerandra Species 0.000 abstract 1
- 239000000463 material Substances 0.000 description 21
- 210000003298 dental enamel Anatomy 0.000 description 20
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 18
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 16
- 208000002599 Smear Layer Diseases 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- 230000001143 conditioned effect Effects 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 239000003999 initiator Substances 0.000 description 11
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 9
- 244000283070 Abies balsamea Species 0.000 description 9
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 9
- 239000004568 cement Substances 0.000 description 9
- 239000003178 glass ionomer cement Substances 0.000 description 9
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 8
- 239000005770 Eugenol Substances 0.000 description 8
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 8
- 125000001931 aliphatic group Chemical group 0.000 description 8
- 230000003750 conditioning effect Effects 0.000 description 8
- 229960002217 eugenol Drugs 0.000 description 8
- 239000012530 fluid Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229930006711 bornane-2,3-dione Natural products 0.000 description 7
- 239000004851 dental resin Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 229910052573 porcelain Inorganic materials 0.000 description 7
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000002562 thickening agent Substances 0.000 description 6
- 239000011260 aqueous acid Substances 0.000 description 5
- 238000007664 blowing Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 239000004858 Canada balsam Substances 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 210000004262 dental pulp cavity Anatomy 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- RMCCONIRBZIDTH-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 1,3-dioxo-2-benzofuran-5-carboxylate Chemical compound CC(=C)C(=O)OCCOC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 RMCCONIRBZIDTH-UHFFFAOYSA-N 0.000 description 3
- NPKSPKHJBVJUKB-UHFFFAOYSA-N N-phenylglycine Chemical compound OC(=O)CNC1=CC=CC=C1 NPKSPKHJBVJUKB-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000005548 dental material Substances 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- 239000000573 polycarboxylate cement Substances 0.000 description 3
- GPLACOONWGSIIP-UHFFFAOYSA-N 2-(n-[2-hydroxy-3-(2-methylprop-2-enoyloxy)propyl]anilino)acetic acid Chemical compound CC(=C)C(=O)OCC(O)CN(CC(O)=O)C1=CC=CC=C1 GPLACOONWGSIIP-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000003929 acidic solution Substances 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- 239000007767 bonding agent Substances 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002810 dentin bonding agent Substances 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000002452 interceptive effect Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007788 roughening Methods 0.000 description 2
- 238000005488 sandblasting Methods 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- UEKHZPDUBLCUHN-UHFFFAOYSA-N 2-[[3,5,5-trimethyl-6-[2-(2-methylprop-2-enoyloxy)ethoxycarbonylamino]hexyl]carbamoyloxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOC(=O)NCCC(C)CC(C)(C)CNC(=O)OCCOC(=O)C(C)=C UEKHZPDUBLCUHN-UHFFFAOYSA-N 0.000 description 1
- JUVSRZCUMWZBFK-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-methylanilino]ethanol Chemical compound CC1=CC=C(N(CCO)CCO)C=C1 JUVSRZCUMWZBFK-UHFFFAOYSA-N 0.000 description 1
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000002362 bornane-2,3-dione group Chemical group 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000010634 clove oil Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 201000002170 dentin sensitivity Diseases 0.000 description 1
- 229940079920 digestives acid preparations Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- MHCLJIVVJQQNKQ-UHFFFAOYSA-N ethyl carbamate;2-methylprop-2-enoic acid Chemical compound CCOC(N)=O.CC(=C)C(O)=O MHCLJIVVJQQNKQ-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 102000034240 fibrous proteins Human genes 0.000 description 1
- 108091005899 fibrous proteins Proteins 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 210000004905 finger nail Anatomy 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 230000005660 hydrophilic surface Effects 0.000 description 1
- 230000005661 hydrophobic surface Effects 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 239000003211 polymerization photoinitiator Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000036347 tooth sensitivity Effects 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/20—Protective coatings for natural or artificial teeth, e.g. sealings, dye coatings or varnish
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dental Preparations (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/418,764 US5534562A (en) | 1995-04-07 | 1995-04-07 | Compositions and methods for priming and sealing dental and biological substrates |
| PCT/US1996/000052 WO1996031559A1 (en) | 1995-04-07 | 1996-01-11 | Composition for priming dental and biological substrates |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO974521D0 NO974521D0 (no) | 1997-09-30 |
| NO974521L NO974521L (no) | 1997-11-19 |
| NO311034B1 true NO311034B1 (no) | 2001-10-01 |
Family
ID=23659481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19974521A NO311034B1 (no) | 1995-04-07 | 1997-09-30 | Preparat for grunning av dentale og biologiske substrater, samt fremgangsmate for fremstilling av preparatet |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US5534562A (ja) |
| EP (2) | EP0820484A4 (ja) |
| JP (1) | JPH11503150A (ja) |
| KR (1) | KR100312906B1 (ja) |
| AU (1) | AU711874B2 (ja) |
| BR (1) | BR9604832A (ja) |
| CA (1) | CA2217490A1 (ja) |
| MX (1) | MX9707690A (ja) |
| NO (1) | NO311034B1 (ja) |
| WO (1) | WO1996031559A1 (ja) |
Families Citing this family (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5534562A (en) * | 1995-04-07 | 1996-07-09 | Ultradent Products, Inc. | Compositions and methods for priming and sealing dental and biological substrates |
| US5730601A (en) * | 1996-03-11 | 1998-03-24 | The Regents Of The University Of Colorado | Method and material for use with dental composites for improving conversion of monomers to polymers and reducing volume shrinkage |
| US5927983A (en) * | 1996-07-29 | 1999-07-27 | Hughes; Michael F. | Intracoronal bristle brush |
| US6458454B1 (en) | 1996-10-07 | 2002-10-01 | 3M Innovative Properties Company | Holding device |
| EP0891195B1 (en) * | 1996-12-30 | 2005-06-15 | Xenon Research Inc. | Improved bone connective prosthesis and method of forming same |
| USRE38722E1 (en) | 1997-02-19 | 2005-04-12 | Ultradent Products, Inc. | Polymerizable isolation barriers containing reflective materials and methods for forming and using such barriers |
| US6305936B1 (en) | 1997-02-19 | 2001-10-23 | Ultradent Products, Inc. | Polymerizable isolation barriers with reduced polymerization strength and methods for forming and using such barriers |
| US6004390A (en) * | 1997-04-14 | 1999-12-21 | Dentsply Detrey Gmbh | Tooth surface treatment composition and methods |
| US6008264A (en) | 1997-04-30 | 1999-12-28 | Laser Med, Inc. | Method for curing polymeric materials, such as those used in dentistry, and for tailoring the post-cure properties of polymeric materials through the use of light source power modulation |
| US6282013B1 (en) | 1997-04-30 | 2001-08-28 | Lasermed, Inc. | System for curing polymeric materials, such as those used in dentistry, and for tailoring the post-cure properties of polymeric materials through the use of light source power modulation |
| US6096328A (en) * | 1997-06-06 | 2000-08-01 | The Procter & Gamble Company | Delivery system for an oral care substance using a strip of material having low flexural stiffness |
| US20020018754A1 (en) * | 1999-03-15 | 2002-02-14 | Paul Albert Sagel | Shapes for tooth whitening strips |
| JPH1180593A (ja) * | 1997-09-12 | 1999-03-26 | Sankin Kogyo Kk | プラスチック製ブラケット用プライマー組成物および該組成物の使用方法 |
| WO1999021505A1 (en) | 1997-10-29 | 1999-05-06 | Bisco, Inc. | Dental composite light curing system |
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1996
- 1996-01-11 AU AU46518/96A patent/AU711874B2/en not_active Ceased
- 1996-01-11 MX MX9707690A patent/MX9707690A/es unknown
- 1996-01-11 EP EP96902065A patent/EP0820484A4/en not_active Withdrawn
- 1996-01-11 BR BR9604832A patent/BR9604832A/pt not_active Application Discontinuation
- 1996-01-11 CA CA002217490A patent/CA2217490A1/en not_active Abandoned
- 1996-01-11 WO PCT/US1996/000052 patent/WO1996031559A1/en not_active Application Discontinuation
- 1996-01-11 EP EP01130013A patent/EP1213005A1/en not_active Withdrawn
- 1996-01-11 JP JP8530271A patent/JPH11503150A/ja not_active Ceased
- 1996-01-11 KR KR1019970707070A patent/KR100312906B1/ko not_active IP Right Cessation
- 1996-07-08 US US08/676,957 patent/US5708052A/en not_active Expired - Lifetime
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- 1997-09-30 NO NO19974521A patent/NO311034B1/no not_active IP Right Cessation
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|---|---|
| MX9707690A (es) | 1997-12-31 |
| CA2217490A1 (en) | 1996-10-10 |
| BR9604832A (pt) | 1999-01-05 |
| JPH11503150A (ja) | 1999-03-23 |
| EP0820484A1 (en) | 1998-01-28 |
| EP1213005A1 (en) | 2002-06-12 |
| NO974521D0 (no) | 1997-09-30 |
| KR100312906B1 (ko) | 2001-12-12 |
| KR19980703671A (ko) | 1998-12-05 |
| US5534562A (en) | 1996-07-09 |
| EP0820484A4 (en) | 1998-08-26 |
| WO1996031559A1 (en) | 1996-10-10 |
| AU4651896A (en) | 1996-10-23 |
| US5708052A (en) | 1998-01-13 |
| NO974521L (no) | 1997-11-19 |
| AU711874B2 (en) | 1999-10-21 |
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