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Development of a new photocurable composite resin with reduced curing shrinkage

DC Field Value Language
dc.contributor.author김경남-
dc.contributor.author김광만-
dc.date.accessioned2016-05-16T10:57:37Z-
dc.date.available2016-05-16T10:57:37Z-
dc.date.issued2002-
dc.identifier.issn0109-5641-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/143483-
dc.description.abstractObjective: This study was conducted to evaluate the potential of a novel trifunctional methacrylate as a component of a photocurable composite resin with reduced curing shrinkage. Methods: Tris[4-(2′-hydroxy-3′-methacryloyloxypropoxy)phenyl]methane (TTEMA) was synthesized by reacting triphenylolmethane triglycidyl ether (TTE) with methacrylic acid in the presence of 4-(dimethylamino)pyridine. Photopolymerization reactivity and volumetric shrinkage of unfilled resins based on TTEMA were investigated by Fourier transform infrared spectroscopy and density measurements, respectively, and the results were compared with those for conventional dental monomers. A three-point bending test of the TTEMA-containing composite resin was carried out. Results: TTEMA was easily prepared in a good yield of 89%. Unfilled resins of TTEMA and bis-GMA, each containing 40% TEGDMA, showed similar photopolymerization reactivity. TTEMA exhibited a very low photopolymerization shrinkage of 2.09%, and 3:2 TTEMA–TEGDMA unfilled resin revealed 10% lower shrinkage than a conventional bis-GMA system containing the same amount of TEGDMA. The flexural strength of a light-activated composite resin formulated with TTEMA is comparable to that of a bis-GMA composite resin under the same conditions. Significance: TTEMA is promising for application as a photocurable dental monomer due to ease of synthesis, good polymerization reactivity, and relatively low curing shrinkage.-
dc.description.statementOfResponsibilityopen-
dc.format.extent174~178-
dc.relation.isPartOfDENTAL MATERIALS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESH4-Aminopyridine/analogs & derivatives*-
dc.subject.MESH4-Aminopyridine/chemistry-
dc.subject.MESHAlgorithms-
dc.subject.MESHBisphenol A-Glycidyl Methacrylate/chemistry-
dc.subject.MESHBisphenol A-Glycidyl Methacrylate/radiation effects-
dc.subject.MESHComposite Resins/chemical synthesis-
dc.subject.MESHComposite Resins/chemistry*-
dc.subject.MESHComposite Resins/radiation effects-
dc.subject.MESHDensitometry-
dc.subject.MESHGlyceryl Ethers/chemistry-
dc.subject.MESHHumans-
dc.subject.MESHLight-
dc.subject.MESHMaterials Testing-
dc.subject.MESHMethacrylates/chemical synthesis-
dc.subject.MESHMethacrylates/chemistry*-
dc.subject.MESHMethacrylates/radiation effects-
dc.subject.MESHPliability-
dc.subject.MESHPolyethylene Glycols/chemistry-
dc.subject.MESHPolyethylene Glycols/radiation effects-
dc.subject.MESHPolymers/chemistry-
dc.subject.MESHPolymers/radiation effects-
dc.subject.MESHPolymethacrylic Acids/chemistry-
dc.subject.MESHPolymethacrylic Acids/radiation effects-
dc.subject.MESHPolyurethanes/chemistry-
dc.subject.MESHSpectroscopy, Fourier Transform Infrared-
dc.subject.MESHStatistics, Nonparametric-
dc.subject.MESHSurface Properties-
dc.titleDevelopment of a new photocurable composite resin with reduced curing shrinkage-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Dental Engineering (치과생체재료공학)-
dc.contributor.googleauthorC.M. Chung-
dc.contributor.googleauthorJ.G. Kim-
dc.contributor.googleauthorM.S. Kim-
dc.contributor.googleauthorK.M. Kim-
dc.contributor.googleauthorK.N. Kim-
dc.identifier.doi10.1016/S0109-5641(01)00039-2-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00292-
dc.contributor.localIdA00312-
dc.relation.journalcodeJ00699-
dc.identifier.eissn1879-0097-
dc.identifier.pmid11755597-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0109564101000392-
dc.subject.keywordDental material-
dc.subject.keywordComposite resin-
dc.subject.keywordTrifunctional methacrylate-
dc.subject.keywordPolymerization shrinkage-
dc.subject.keywordPolymerization reactivity-
dc.contributor.alternativeNameKim, Kyoung Nam-
dc.contributor.alternativeNameKim, Kwang Mahn-
dc.contributor.affiliatedAuthorKim, Kyoung Nam-
dc.contributor.affiliatedAuthorKim, Kwang Mahn-
dc.rights.accessRightsnot free-
dc.citation.volume18-
dc.citation.number2-
dc.citation.startPage174-
dc.citation.endPage178-
dc.identifier.bibliographicCitationDENTAL MATERIALS, Vol.18(2) : 174-178, 2002-
dc.identifier.rimsid38194-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Dental Biomaterials and Bioengineering (치과생체재료공학교실) > 1. Journal Papers

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