BR112013005887B1 - Compostos de sacarídeo substituído e composições dentais - Google Patents
Compostos de sacarídeo substituído e composições dentais Download PDFInfo
- Publication number
- BR112013005887B1 BR112013005887B1 BR112013005887-0A BR112013005887A BR112013005887B1 BR 112013005887 B1 BR112013005887 B1 BR 112013005887B1 BR 112013005887 A BR112013005887 A BR 112013005887A BR 112013005887 B1 BR112013005887 B1 BR 112013005887B1
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- Prior art keywords
- group
- saccharide
- fact
- dental
- polymerizable
- Prior art date
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- 230000004140 ketosis Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 150000002632 lipids 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000001906 matrix-assisted laser desorption--ionisation mass spectrometry Methods 0.000 description 1
- 238000000074 matrix-assisted laser desorption--ionisation tandem time-of-flight detection Methods 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 239000005300 metallic glass Substances 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 229940124561 microbicide Drugs 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GCRLIVCNZWDCDE-SJXGUFTOSA-N n-methyl-n-[(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl]nonanamide Chemical compound CCCCCCCCC(=O)N(C)C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO GCRLIVCNZWDCDE-SJXGUFTOSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002972 pentoses Chemical class 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000005365 phosphate glass Substances 0.000 description 1
- WDHYRUBXLGOLKR-UHFFFAOYSA-N phosphoric acid;prop-2-enoic acid Chemical class OC(=O)C=C.OP(O)(O)=O WDHYRUBXLGOLKR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 125000000075 primary alcohol group Chemical group 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- MUYIJHPQJTXCJE-UHFFFAOYSA-N propoxy dihydrogen phosphate Chemical compound CCCOOP(O)(O)=O MUYIJHPQJTXCJE-UHFFFAOYSA-N 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000000395 remineralizing effect Effects 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 210000004872 soft tissue Anatomy 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003538 tetroses Chemical class 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000036347 tooth sensitivity Effects 0.000 description 1
- 125000005590 trimellitic acid group Chemical group 0.000 description 1
- 150000003641 trioses Chemical class 0.000 description 1
- XREXPQGDOPQPAH-QKUPJAQQSA-K trisodium;[(z)-18-[1,3-bis[[(z)-12-sulfonatooxyoctadec-9-enoyl]oxy]propan-2-yloxy]-18-oxooctadec-9-en-7-yl] sulfate Chemical compound [Na+].[Na+].[Na+].CCCCCCC(OS([O-])(=O)=O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(CCCCCC)OS([O-])(=O)=O)COC(=O)CCCCCCC\C=C/CC(CCCCCC)OS([O-])(=O)=O XREXPQGDOPQPAH-QKUPJAQQSA-K 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
- C07H13/12—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by acids having the group -X-C(=X)-X-, or halides thereof, in which each X means nitrogen, oxygen, sulfur, selenium or tellurium, e.g. carbonic acid, carbamic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C5/00—Filling or capping teeth
- A61C5/70—Tooth crowns; Making thereof
- A61C5/77—Methods or devices for making crowns
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/30—Compositions for temporarily or permanently fixing teeth or palates, e.g. primers for dental adhesives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/40—Primers
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Dentistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Dental Preparations (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Crystallography & Structural Chemistry (AREA)
- Ceramic Engineering (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38308010P | 2010-09-15 | 2010-09-15 | |
| US61/383,080 | 2010-09-15 | ||
| PCT/US2011/048383 WO2012036838A2 (en) | 2010-09-15 | 2011-08-19 | Substituted saccharide compounds and dental compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR112013005887A2 BR112013005887A2 (pt) | 2016-05-10 |
| BR112013005887B1 true BR112013005887B1 (pt) | 2018-05-22 |
Family
ID=44543859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112013005887-0A BR112013005887B1 (pt) | 2010-09-15 | 2011-08-19 | Compostos de sacarídeo substituído e composições dentais |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8557893B2 (https=) |
| EP (1) | EP2616476A2 (https=) |
| JP (2) | JP6272029B2 (https=) |
| CN (1) | CN103119050B (https=) |
| BR (1) | BR112013005887B1 (https=) |
| RU (1) | RU2605097C2 (https=) |
| WO (1) | WO2012036838A2 (https=) |
Families Citing this family (7)
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|---|---|---|---|---|
| CN103119050B (zh) * | 2010-09-15 | 2016-08-24 | 3M创新有限公司 | 取代的糖类化合物和牙科用组合物 |
| EP2803691B1 (en) | 2013-05-17 | 2016-04-20 | 3M Innovative Properties Company | Fluoropolymer compositions containing a polyhydroxy surfactant |
| EP2868674B1 (en) | 2013-10-30 | 2019-11-20 | 3M Innovative Properties Company | Peroxide curable fluoropolymers obtainable by polymerization using non-fluorinated polyhydroxy emulsifiers |
| TWI515255B (zh) * | 2014-12-31 | 2016-01-01 | 財團法人工業技術研究院 | 可固化樹脂及應用其之可固化組成物 |
| CN107709388B (zh) * | 2015-06-26 | 2020-07-07 | 日产化学工业株式会社 | 光固化性树脂组合物 |
| EP3246002A1 (en) | 2016-05-20 | 2017-11-22 | DENTSPLY DETREY GmbH | Dental composition |
| WO2018043342A1 (ja) * | 2016-08-30 | 2018-03-08 | 日産化学工業株式会社 | 感光性接着剤組成物 |
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| US2776951A (en) | 1954-12-08 | 1957-01-08 | Rohm & Haas | Amides of vinyl ethers containing hydroxyl groups and polymers thereof |
| JPS59135272A (ja) * | 1983-01-21 | 1984-08-03 | Kuraray Co Ltd | 接着剤 |
| US4503169A (en) | 1984-04-19 | 1985-03-05 | Minnesota Mining And Manufacturing Company | Radiopaque, low visual opacity dental composites containing non-vitreous microparticles |
| US4642126A (en) | 1985-02-11 | 1987-02-10 | Norton Company | Coated abrasives with rapidly curable adhesives and controllable curvature |
| DE3506020A1 (de) | 1985-02-21 | 1986-08-21 | Etablissement Dentaire Ivoclar, Schaan | Verfahren zur herstellung von kuenstlichen zaehnen oder zahnteilen und dafuer geeigneter lagerfaehiger dentalwerkstoff |
| JPS61268192A (ja) | 1985-05-24 | 1986-11-27 | Meito Sangyo Kk | 糖類脂肪酸エステル化合物の製造法 |
| US4652274A (en) | 1985-08-07 | 1987-03-24 | Minnesota Mining And Manufacturing Company | Coated abrasive product having radiation curable binder |
| CA1323949C (en) | 1987-04-02 | 1993-11-02 | Michael C. Palazzotto | Ternary photoinitiator system for addition polymerization |
| AU618772B2 (en) | 1987-12-30 | 1992-01-09 | Minnesota Mining And Manufacturing Company | Photocurable ionomer cement systems |
| EP0367886B1 (en) | 1988-10-19 | 1995-04-19 | Guest Elchrom Scientific AG | Hydrophilic monomers, polymers thereof and their applications |
| US5278270A (en) | 1990-04-20 | 1994-01-11 | Branko Kozulic | Hydrophilic and amphiphatic monomers, their polymers and gels and hydrophobic electrophoresis |
| US5185466A (en) * | 1989-01-05 | 1993-02-09 | Branko Kozulic | Hydrophilic and amphiphatic monomers, their polymers and gels and hydrophobic electrophoresis |
| GB2246127B (en) * | 1990-04-20 | 1994-06-08 | Branko Kozulic | Improvements in or relating to acrylic monomers |
| DE3904246A1 (de) * | 1989-02-13 | 1990-08-16 | Suedzucker Ag | Polymerisierbare n'-polyhydroxy-n'-alkylharnstoffderivate, verfahren zu ihrer herstellung, deren verwendung und daraus erhaeltliche homo- oder copolymeren |
| DE4011084A1 (de) * | 1990-04-05 | 1991-10-10 | Boehringer Mannheim Gmbh | Saccharid-modifizierte, wasserloesliche proteine |
| JPH0565159A (ja) | 1991-08-29 | 1993-03-19 | Dainippon Printing Co Ltd | 押しつぶし可能なギフト箱の製造方法 |
| JPH06242532A (ja) | 1993-02-15 | 1994-09-02 | Konica Corp | ハロゲン化銀写真感光材料 |
| EP0650974A1 (en) * | 1993-10-28 | 1995-05-03 | Tanabe Seiyaku Co., Ltd. | Acylaminosaccharide derivative and process for preparing the same |
| JPH07316098A (ja) | 1994-05-23 | 1995-12-05 | San Medical Kk | アクリレート化合物および歯科用接着剤 |
| FR2726279B1 (fr) * | 1994-10-28 | 1997-01-17 | Prolabo Sa | Particule de latex ou d'oxyde mineral glucosylee, procede de preparation d'une telle particule et utilisation de celle-ci en tant qu'agent de detection biologique ou de chromatographie d'affinite |
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| DE19860364C2 (de) | 1998-12-24 | 2001-12-13 | 3M Espe Ag | Polymerisierbare Dentalmassen auf der Basis von zur Aushärtung befähigten Siloxanverbindungen, deren Verwendung und Herstellung |
| DE19860361A1 (de) | 1998-12-24 | 2000-06-29 | Espe Dental Ag | Vernetzbare Monomere auf Cyclosiloxanbasis, deren Herstellung und deren Verwendung in polymerisierbaren Massen |
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| US6387981B1 (en) | 1999-10-28 | 2002-05-14 | 3M Innovative Properties Company | Radiopaque dental materials with nano-sized particles |
| US6572693B1 (en) | 1999-10-28 | 2003-06-03 | 3M Innovative Properties Company | Aesthetic dental materials |
| DE60042038D1 (de) | 1999-10-28 | 2009-05-28 | 3M Innovative Properties Co | Siliziumdioxid-Nanoteilchen in Form eines trockenen Pulvers |
| US6730156B1 (en) | 1999-10-28 | 2004-05-04 | 3M Innovative Properties Company | Clustered particle dental fillers |
| DE10026432A1 (de) | 2000-05-29 | 2002-02-14 | 3M Espe Ag | Präpolymere (Meth)acrylate mit polycyclischen oder aromatischen Segmenten |
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| US20070264509A1 (en) | 2006-05-11 | 2007-11-15 | Yu-Chin Lai | Copolymer and Medical Device with the Copolymer |
| US20080004410A1 (en) | 2006-06-30 | 2008-01-03 | Yu-Chin Lai | Hydrophilic macromonomers having alpha,beta-conjugated carboxylic terminal group and medical devices incorporating same |
| US20080003252A1 (en) | 2006-06-30 | 2008-01-03 | Yu-Chin Lai | Functionalized hydrophilic macromonomers and medical devices incorporating same |
| CN101516319B (zh) | 2006-09-13 | 2015-11-25 | 3M创新有限公司 | 包含有机凝胶因子的牙科用组合物、产品及方法 |
| WO2008047812A1 (fr) | 2006-10-20 | 2008-04-24 | Kuraray Medical Inc. | Procédé de fabrication d'un monomère hydrophile |
| WO2008087980A1 (ja) | 2007-01-17 | 2008-07-24 | Kuraray Medical Inc. | 親水性モノマー含有重合性組成物及び歯科用材料 |
| CN101677957A (zh) | 2007-02-05 | 2010-03-24 | 卡比兰生物外科公司 | 用于递送生物活性试剂的聚合物制剂 |
| US20080197324A1 (en) | 2007-02-20 | 2008-08-21 | Fang Zhao | Ophthalmic composition containing a polyol-acid copolymer |
| JP5416581B2 (ja) | 2007-03-20 | 2014-02-12 | クラレノリタケデンタル株式会社 | 重合性単量体、重合性組成物及び歯科用材料 |
| US8735463B2 (en) | 2007-05-31 | 2014-05-27 | Creighton University | Self-healing dental composites and related methods |
| US8329674B2 (en) | 2007-07-25 | 2012-12-11 | 3M Innovative Properties Company | Film forming dental compositions and related methods |
| JP5628031B2 (ja) | 2007-07-25 | 2014-11-19 | スリーエム イノベイティブ プロパティズ カンパニー | 治療用歯科用組成物及び関連する方法 |
| JP5552812B2 (ja) | 2007-10-25 | 2014-07-16 | ライオン株式会社 | モノフルオロリン酸化高分子化合物 |
| WO2011126647A2 (en) | 2010-03-31 | 2011-10-13 | 3M Innovative Properties Company | Polymerizable isocyanurate monomers and dental compositions |
| CN103119050B (zh) * | 2010-09-15 | 2016-08-24 | 3M创新有限公司 | 取代的糖类化合物和牙科用组合物 |
-
2011
- 2011-08-19 CN CN201180044152.6A patent/CN103119050B/zh not_active Expired - Fee Related
- 2011-08-19 BR BR112013005887-0A patent/BR112013005887B1/pt not_active IP Right Cessation
- 2011-08-19 WO PCT/US2011/048383 patent/WO2012036838A2/en not_active Ceased
- 2011-08-19 US US13/813,673 patent/US8557893B2/en not_active Expired - Fee Related
- 2011-08-19 JP JP2013529161A patent/JP6272029B2/ja not_active Expired - Fee Related
- 2011-08-19 RU RU2013110557/04A patent/RU2605097C2/ru not_active IP Right Cessation
- 2011-08-19 EP EP11751743.3A patent/EP2616476A2/en not_active Withdrawn
-
2016
- 2016-12-27 JP JP2016252377A patent/JP2017095478A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US20130164709A1 (en) | 2013-06-27 |
| JP2013541524A (ja) | 2013-11-14 |
| RU2605097C2 (ru) | 2016-12-20 |
| WO2012036838A2 (en) | 2012-03-22 |
| CN103119050B (zh) | 2016-08-24 |
| BR112013005887A2 (pt) | 2016-05-10 |
| EP2616476A2 (en) | 2013-07-24 |
| RU2013110557A (ru) | 2014-10-20 |
| CN103119050A (zh) | 2013-05-22 |
| WO2012036838A3 (en) | 2012-06-21 |
| US8557893B2 (en) | 2013-10-15 |
| JP2017095478A (ja) | 2017-06-01 |
| JP6272029B2 (ja) | 2018-01-31 |
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