CA2371204A1 - Easy-to-use and easy-to-handle dental materials having improved rheological properties - Google Patents
Easy-to-use and easy-to-handle dental materials having improved rheological properties Download PDFInfo
- Publication number
- CA2371204A1 CA2371204A1 CA002371204A CA2371204A CA2371204A1 CA 2371204 A1 CA2371204 A1 CA 2371204A1 CA 002371204 A CA002371204 A CA 002371204A CA 2371204 A CA2371204 A CA 2371204A CA 2371204 A1 CA2371204 A1 CA 2371204A1
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- CA
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- Prior art keywords
- hydrogen
- component
- bond
- dental material
- sites
- 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.)
- Abandoned
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- 239000000463 material Substances 0.000 claims abstract description 75
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- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- ULQMPOIOSDXIGC-UHFFFAOYSA-N [2,2-dimethyl-3-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)COC(=O)C(C)=C ULQMPOIOSDXIGC-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
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- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
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- HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
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- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 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
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- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- QUZSUMLPWDHKCJ-UHFFFAOYSA-N bisphenol A dimethacrylate Chemical compound C1=CC(OC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OC(=O)C(C)=C)C=C1 QUZSUMLPWDHKCJ-UHFFFAOYSA-N 0.000 description 1
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- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
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- 239000002738 chelating agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
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- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
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- 239000000834 fixative Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000003178 glass ionomer cement Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
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- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
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- 150000004767 nitrides Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
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- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 238000012858 packaging process Methods 0.000 description 1
- FZUGPQWGEGAKET-UHFFFAOYSA-N parbenate Chemical compound CCOC(=O)C1=CC=C(N(C)C)C=C1 FZUGPQWGEGAKET-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
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- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 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
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
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- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
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- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
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- 229910052718 tin Inorganic materials 0.000 description 1
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- HVYVMSPIJIWUNA-UHFFFAOYSA-N triphenylstibine Chemical compound C1=CC=CC=C1[Sb](C=1C=CC=CC=1)C1=CC=CC=C1 HVYVMSPIJIWUNA-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
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- 229910052725 zinc Inorganic materials 0.000 description 1
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- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/70—Preparations for dentistry comprising inorganic additives
- A61K6/71—Fillers
-
- 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
-
- 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
- A61K6/80—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
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Dental Preparations (AREA)
- Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/314,491 US6315566B1 (en) | 1999-05-18 | 1999-05-18 | Dental materials |
| US09/314,491 | 1999-05-18 | ||
| PCT/US2000/008045 WO2000069395A1 (en) | 1999-05-18 | 2000-03-24 | Dental materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2371204A1 true CA2371204A1 (en) | 2000-11-23 |
Family
ID=23220179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002371204A Abandoned CA2371204A1 (en) | 1999-05-18 | 2000-03-24 | Easy-to-use and easy-to-handle dental materials having improved rheological properties |
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|---|---|
| US (1) | US6315566B1 (enExample) |
| EP (1) | EP1178770B1 (enExample) |
| JP (1) | JP4723096B2 (enExample) |
| AU (1) | AU3923700A (enExample) |
| CA (1) | CA2371204A1 (enExample) |
| DE (1) | DE60043058D1 (enExample) |
| WO (1) | WO2000069395A1 (enExample) |
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| CN1153775C (zh) * | 1999-03-31 | 2004-06-16 | 可乐丽股份有限公司 | 用在补齿可聚合组合物中的有机磷化合物 |
| US7217124B2 (en) * | 2002-04-18 | 2007-05-15 | 3M Innovative Properties Company | Orthodontic brackets including one part of an at least two-part adhesive on the base of the bracket |
| US6971874B2 (en) * | 2002-10-16 | 2005-12-06 | 3M Innovative Properties Company | Dental restorative formula selector and methods of use |
| US6797767B2 (en) * | 2003-01-03 | 2004-09-28 | Pulpdent Corporation | Polymerizable composite material |
| JP4663225B2 (ja) * | 2003-11-21 | 2011-04-06 | 株式会社ジーシー | 光重合型歯科用表面被覆材 |
| WO2005074546A2 (en) | 2004-02-02 | 2005-08-18 | Ambrx, Inc. | Modified human growth hormone polypeptides and their uses |
| US20090030109A1 (en) * | 2005-11-18 | 2009-01-29 | Hare Robert V | Dental composite restorative material |
| US20070183987A1 (en) * | 2006-02-08 | 2007-08-09 | Jensen Steven D | Peroxide Gel Compositions |
| US9295620B2 (en) | 2006-02-08 | 2016-03-29 | Cao Group, Inc. | Dental treatment compositions and conformable dental treatment trays using the same |
| CA2654814C (en) | 2006-06-09 | 2014-03-11 | Dentsply International Inc. | Photopolymerizable and photocleavable resins and low shrink and low stress composite and compositions |
| US20080076848A1 (en) * | 2006-06-09 | 2008-03-27 | Xiaoming Jin | Low stress flowable compositions |
| US20080064009A1 (en) | 2006-09-13 | 2008-03-13 | Clark David J | Dental Separator Rings And A Seamless, Single Load Cavity Preparation And Filling Technique |
| US20100167231A1 (en) * | 2006-11-24 | 2010-07-01 | Dubbe John W | Piston and handheld dispenser including a piston |
| US8393897B2 (en) * | 2007-11-07 | 2013-03-12 | David J. Clark | Methods and devices for diastema closure |
| US9414895B2 (en) | 2008-01-29 | 2016-08-16 | David J. Clark | Dental matrix devices specific to anterior teeth, and injection molded filling techniques and devices |
| WO2009148579A2 (en) * | 2008-06-03 | 2009-12-10 | Qlt Usa, Inc. | Dehydrated hydrogel inclusion complex of a bioactive agent with flowable drug delivery system |
| EP2133064A1 (en) * | 2008-06-10 | 2009-12-16 | 3M Innovative Properties Company | Initiator system containing a diarylalkylamine derivate, hardenable composition and use thereof |
| US8568696B2 (en) * | 2008-08-06 | 2013-10-29 | Indiana Nanotech Llc | Grinding method for the manipulation or preservation of calcium phosphate hybrid properties |
| RU2417068C2 (ru) * | 2009-12-10 | 2011-04-27 | Закрытое акционерное общество "Стоматология-Дентистри" (ЗАО "СтомаДент") | Материал для восстановления культи зуба |
| US9358080B2 (en) | 2012-03-26 | 2016-06-07 | David J. Clark | Dental separator ring |
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| US6126922A (en) | 1995-11-17 | 2000-10-03 | 3M Innovative Properties Company | Fluorid-releasing compositions and compositions with improved rheology |
| WO1997031614A1 (en) * | 1996-03-01 | 1997-09-04 | Sunstar Kabushiki Kaisha | Denture stabilizer composition |
| JP2001521501A (ja) | 1997-04-02 | 2001-11-06 | デンツプライ インターナショナル インコーポレーテッド | 歯科用修復材料および歯の修復方法 |
| US5965632A (en) * | 1997-06-20 | 1999-10-12 | Scientific Pharmaceuticals Inc. | Dental cement compositions |
| US6506816B1 (en) | 1997-07-17 | 2003-01-14 | 3M Innovative Properties Company | Dental resin cements having improved handling properties |
| JP2000197645A (ja) * | 1998-12-29 | 2000-07-18 | Sunstar Inc | 粉末エアゾ―ル式義歯安定剤 |
| SE9900935D0 (sv) * | 1999-03-16 | 1999-03-16 | Pharmacia & Upjohn Bv | Macromolecular compounds |
-
1999
- 1999-05-18 US US09/314,491 patent/US6315566B1/en not_active Expired - Lifetime
-
2000
- 2000-03-24 JP JP2000617854A patent/JP4723096B2/ja not_active Expired - Fee Related
- 2000-03-24 EP EP00918426A patent/EP1178770B1/en not_active Expired - Lifetime
- 2000-03-24 WO PCT/US2000/008045 patent/WO2000069395A1/en not_active Ceased
- 2000-03-24 DE DE60043058T patent/DE60043058D1/de not_active Expired - Lifetime
- 2000-03-24 CA CA002371204A patent/CA2371204A1/en not_active Abandoned
- 2000-03-24 AU AU39237/00A patent/AU3923700A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| JP4723096B2 (ja) | 2011-07-13 |
| DE60043058D1 (de) | 2009-11-12 |
| WO2000069395A1 (en) | 2000-11-23 |
| EP1178770B1 (en) | 2009-09-30 |
| EP1178770A1 (en) | 2002-02-13 |
| US6315566B1 (en) | 2001-11-13 |
| JP2002544214A (ja) | 2002-12-24 |
| AU3923700A (en) | 2000-12-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |