JP4912593B2 - 重合可能な複合材料 - Google Patents
重合可能な複合材料 Download PDFInfo
- Publication number
- JP4912593B2 JP4912593B2 JP2004566618A JP2004566618A JP4912593B2 JP 4912593 B2 JP4912593 B2 JP 4912593B2 JP 2004566618 A JP2004566618 A JP 2004566618A JP 2004566618 A JP2004566618 A JP 2004566618A JP 4912593 B2 JP4912593 B2 JP 4912593B2
- Authority
- JP
- Japan
- Prior art keywords
- composite material
- concentration range
- polymerizable composite
- weight
- water
- 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.)
- Expired - Lifetime
Links
- 239000002131 composite material Substances 0.000 title claims description 42
- 230000002378 acidificating effect Effects 0.000 claims description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 38
- 239000000945 filler Substances 0.000 claims description 33
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 claims description 28
- 238000006116 polymerization reaction Methods 0.000 claims description 23
- 235000013024 sodium fluoride Nutrition 0.000 claims description 14
- 239000011775 sodium fluoride Substances 0.000 claims description 14
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000003999 initiator Substances 0.000 claims description 8
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 7
- UUEYEUDSRFNIQJ-UHFFFAOYSA-N CCOC(N)=O.CCOC(N)=O.CC(=C)C(O)=O.CC(=C)C(O)=O Chemical compound CCOC(N)=O.CCOC(N)=O.CC(=C)C(O)=O.CC(=C)C(O)=O UUEYEUDSRFNIQJ-UHFFFAOYSA-N 0.000 claims description 5
- 229930006711 bornane-2,3-dione Natural products 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 claims description 4
- 150000008040 ionic compounds Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical group COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 239000003178 glass ionomer cement Substances 0.000 claims 2
- 125000002362 bornane-2,3-dione group Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 description 94
- 239000000178 monomer Substances 0.000 description 42
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 14
- 238000001723 curing Methods 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 230000035515 penetration Effects 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000011347 resin Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000000565 sealant Substances 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 230000008439 repair process Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 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 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- NEHAWKFCIACDQI-UHFFFAOYSA-N [1,6-dihydroxy-6-(2-methylprop-2-enoyloxy)hexyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(O)CCCCC(O)OC(=O)C(C)=C NEHAWKFCIACDQI-UHFFFAOYSA-N 0.000 description 4
- 239000005548 dental material Substances 0.000 description 4
- -1 sodium fluoride Chemical class 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229920000554 ionomer Polymers 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000000016 photochemical curing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 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 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 239000003479 dental cement Substances 0.000 description 2
- 239000011350 dental composite resin Substances 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- GQKZBCPTCWJTAS-UHFFFAOYSA-N methoxymethylbenzene Chemical compound COCC1=CC=CC=C1 GQKZBCPTCWJTAS-UHFFFAOYSA-N 0.000 description 2
- FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- FOWLFMDRZGRPAG-UHFFFAOYSA-N 2-(dimethylamino)-4-ethylbenzoic acid Chemical compound CCC1=CC=C(C(O)=O)C(N(C)C)=C1 FOWLFMDRZGRPAG-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- DILXLMRYFWFBGR-UHFFFAOYSA-N 2-formylbenzene-1,4-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(S(O)(=O)=O)C(C=O)=C1 DILXLMRYFWFBGR-UHFFFAOYSA-N 0.000 description 1
- VSAOBTTWOMTTKB-UHFFFAOYSA-N 4-methyl-n,n-bis(methylamino)aniline Chemical compound CNN(NC)C1=CC=C(C)C=C1 VSAOBTTWOMTTKB-UHFFFAOYSA-N 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminum fluoride Inorganic materials F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 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
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920004943 Delrin® Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- IPCRBOOJBPETMF-UHFFFAOYSA-N N-acetylthiourea Chemical compound CC(=O)NC(N)=S IPCRBOOJBPETMF-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- COHCXWLRUISKOO-UHFFFAOYSA-N [AlH3].[Ba] Chemical compound [AlH3].[Ba] COHCXWLRUISKOO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 210000004268 dentin Anatomy 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- SHXXPRJOPFJRHA-UHFFFAOYSA-K iron(iii) fluoride Chemical compound F[Fe](F)F SHXXPRJOPFJRHA-UHFFFAOYSA-K 0.000 description 1
- 230000018984 mastication Effects 0.000 description 1
- 238000010077 mastication Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012812 sealant material Substances 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 125000000626 sulfinic acid group Chemical group 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YUOWTJMRMWQJDA-UHFFFAOYSA-J tin(iv) fluoride Chemical compound [F-].[F-].[F-].[F-].[Sn+4] YUOWTJMRMWQJDA-UHFFFAOYSA-J 0.000 description 1
Images
Classifications
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/891—Compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- A61K6/893—Polyurethanes
-
- 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
- C08F30/00—Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
- C08F30/02—Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing phosphorus
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dental Preparations (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/336,255 | 2003-01-03 | ||
| US10/336,255 US6797767B2 (en) | 2003-01-03 | 2003-01-03 | Polymerizable composite material |
| PCT/US2003/041523 WO2004063274A1 (en) | 2003-01-03 | 2003-12-31 | Polymerizable composite material |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006512466A JP2006512466A (ja) | 2006-04-13 |
| JP2006512466A5 JP2006512466A5 (enExample) | 2007-02-22 |
| JP4912593B2 true JP4912593B2 (ja) | 2012-04-11 |
Family
ID=32680972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004566618A Expired - Lifetime JP4912593B2 (ja) | 2003-01-03 | 2003-12-31 | 重合可能な複合材料 |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US6797767B2 (enExample) |
| EP (1) | EP1578865B1 (enExample) |
| JP (1) | JP4912593B2 (enExample) |
| AU (1) | AU2003303679A1 (enExample) |
| WO (1) | WO2004063274A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1695685B2 (en) † | 2003-12-19 | 2016-12-28 | Kuraray Noritake Dental Inc. | One-part dental adhesive composition |
| EP1790323B1 (en) * | 2004-09-16 | 2016-03-23 | Kuraray Noritake Dental Inc. | Dental polymerizable core build-up material of separately packed type |
| WO2006058162A2 (en) * | 2004-11-23 | 2006-06-01 | Ormco Corporation | Orthodontic brackets having different adhesives and methods and appliances therewith |
| JP2007231174A (ja) * | 2006-03-01 | 2007-09-13 | Shinnakamura Kagaku Kogyo Kk | 紫外線硬化型コーティング剤 |
| US8753120B2 (en) * | 2006-03-06 | 2014-06-17 | Heraeus Kulzer Gmbh | Endodontic procedure using self-adhesive resin cements and sealers or self etching adhesives and chemically bondable obturators |
| WO2008140800A2 (en) * | 2007-05-11 | 2008-11-20 | Dentsply International Inc. | Dental compositions for coating restorations and tooth surfaces |
| JP5276916B2 (ja) | 2008-07-08 | 2013-08-28 | 株式会社松風 | 歯科用ツーペースト型自己接着性レジンセメント |
| EP2548546A1 (de) * | 2008-08-13 | 2013-01-23 | Ernst Mühlbauer GmbH & Co.KG | Röntgenopaker Infiltrant |
| US8292625B2 (en) | 2010-07-23 | 2012-10-23 | Pulpdent Corporation | Radically curable urethane dimethacrylates and compositions thereof for tougher dental prosthetics |
| EP2444052A1 (en) | 2010-10-19 | 2012-04-25 | Dentsply DeTrey GmbH | Dental composition |
| EP2444054A1 (en) | 2010-10-19 | 2012-04-25 | Dentsply DeTrey GmbH | Dental composition |
| EP2444053B1 (en) | 2010-10-19 | 2020-05-06 | Dentsply DeTrey GmbH | Dental cement composition |
| EP2497454A1 (en) | 2011-03-10 | 2012-09-12 | Dentsply DeTrey GmbH | Dental composition |
| DE102012212429A1 (de) | 2012-07-16 | 2014-01-16 | Voco Gmbh | Dentalhandgerät, Verfahren und Verwendung desselben zum Aushärten lichthärtbaren Materials |
| US8986003B2 (en) | 2012-09-13 | 2015-03-24 | Orthoaccel Technologies, Inc. | Pearlescent white aligners |
| WO2015191436A1 (en) * | 2014-06-13 | 2015-12-17 | 3M Innovative Properties Company | Curable compositions and methods for isolating a working area |
| US10219986B2 (en) | 2015-03-04 | 2019-03-05 | Modern Ideas LLC | Stabilized calcium phosphate and methods of forming same |
| KR102861380B1 (ko) | 2019-03-26 | 2025-09-17 | 소후 인코포레이티드 | 분액형 치과용 레진 강화형 글래스 아이오노머 시멘트 조성물 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02302409A (ja) * | 1989-04-27 | 1990-12-14 | Natl Res Dev Corp | 指示硬化可能な組成物 |
| JPH08231330A (ja) * | 1994-12-23 | 1996-09-10 | Heraeus Kulzer Gmbh | 重合性歯科材料 |
| JPH10236912A (ja) * | 1997-02-27 | 1998-09-08 | Tokuyama Corp | 接着性組成物 |
| JPH11140383A (ja) * | 1997-11-07 | 1999-05-25 | Tokuyama Corp | 接着性組成物 |
| JPH11209213A (ja) * | 1998-01-16 | 1999-08-03 | Kuraray Co Ltd | フッ素徐放性歯科用接着性組成物 |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1569021A (en) | 1976-03-17 | 1980-06-11 | Kuraray Co | Adhesive cementing agents containing partial phosphonic orphosphonic acid esters |
| US5304585A (en) | 1981-02-13 | 1994-04-19 | Minnesota Mining And Manufacturing | Dentin and enamel adhesive |
| JPS60197609A (ja) | 1984-03-16 | 1985-10-07 | Kuraray Co Ltd | 歯科用組成物 |
| DE3414164A1 (de) | 1984-04-14 | 1985-10-17 | Kulzer & Co GmbH, 6393 Wehrheim | Photopolymerisierbarer dentaler haftvermittler-lack |
| DE3414163A1 (de) | 1984-04-14 | 1985-10-17 | Kulzer & Co GmbH, 6393 Wehrheim | Photopolymerisierbarer phosphathaltiger dentaler haftvermittler-lack |
| US4657941A (en) * | 1984-11-29 | 1987-04-14 | Dentsply Research & Development Corp. | Biologically compatible adhesive containing a phosphorus adhesion promoter and a sulfinic accelerator |
| JPH024891A (ja) * | 1988-06-21 | 1990-01-09 | Mitsubishi Rayon Co Ltd | 歯科用接着剤組成物 |
| EP0356868A3 (en) | 1988-09-01 | 1991-03-20 | Dentsply International, Inc. | A method of treating a tooth with adhesive dental cavity basing composition |
| EP0423430B1 (de) | 1989-10-19 | 1993-04-21 | Heraeus Kulzer GmbH | Dentales Haftmittel |
| JP2634276B2 (ja) | 1990-02-15 | 1997-07-23 | 株式会社松風 | プライマー組成物 |
| US5204383A (en) | 1990-03-28 | 1993-04-20 | Kuraray Co., Ltd. | Dental adhesives |
| JPH05132409A (ja) * | 1991-04-17 | 1993-05-28 | Sankin Kogyo Kk | 光硬化性歯科用修復材組成物 |
| EP0537774B1 (en) | 1991-10-18 | 1998-01-07 | Kuraray Co., Ltd. | Antimicrobial polymerizable composition, the polymer and article obtained from the same |
| US5525648A (en) | 1991-12-31 | 1996-06-11 | Minnesota Mining And Manufacturing Company | Method for adhering to hard tissue |
| US5756559A (en) | 1992-02-06 | 1998-05-26 | Dentsply Research & Development | Method and composition for adhering to tooth structure |
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2003
- 2003-01-03 US US10/336,255 patent/US6797767B2/en not_active Expired - Lifetime
- 2003-12-31 EP EP03815251.8A patent/EP1578865B1/en not_active Revoked
- 2003-12-31 WO PCT/US2003/041523 patent/WO2004063274A1/en not_active Ceased
- 2003-12-31 AU AU2003303679A patent/AU2003303679A1/en not_active Abandoned
- 2003-12-31 JP JP2004566618A patent/JP4912593B2/ja not_active Expired - Lifetime
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2004
- 2004-08-23 US US10/923,944 patent/US7371782B2/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH02302409A (ja) * | 1989-04-27 | 1990-12-14 | Natl Res Dev Corp | 指示硬化可能な組成物 |
| JPH08231330A (ja) * | 1994-12-23 | 1996-09-10 | Heraeus Kulzer Gmbh | 重合性歯科材料 |
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| JPH11209213A (ja) * | 1998-01-16 | 1999-08-03 | Kuraray Co Ltd | フッ素徐放性歯科用接着性組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20050020721A1 (en) | 2005-01-27 |
| EP1578865B1 (en) | 2013-11-20 |
| AU2003303679A1 (en) | 2004-08-10 |
| US7371782B2 (en) | 2008-05-13 |
| US6797767B2 (en) | 2004-09-28 |
| WO2004063274A1 (en) | 2004-07-29 |
| EP1578865A4 (en) | 2006-06-07 |
| JP2006512466A (ja) | 2006-04-13 |
| US20040132937A1 (en) | 2004-07-08 |
| EP1578865A1 (en) | 2005-09-28 |
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