Novel urethane-based polymer for dental applications with decreased monomer leaching

被引:28
作者
Martim, Gedalias C. [1 ]
Pfeifer, Carmem S. [2 ]
Girotto, Emerson M. [1 ]
机构
[1] Univ Estadual Maringa, Dept Chem, Mat Chem & Sensors Labs, Ave Colombo 5790, BR-87020900 Maringa, Parana, Brazil
[2] Oregon Hlth & Sci Univ, Biomat & Biomech, 611 SW Campus Dr, Portland, OR 97239 USA
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 72卷
关键词
Bisphenol A-glycidyl methacrylate; Bisphenol A; Methacrylates; Urethane; Composite resin; Physicochemical phenomena; BIS-GMA; RESIN-COMPOSITES; RESTORATIVE COMPOSITES; DIMETHACRYLATE RESINS; SHRINKAGE-STRESS; CONVERSION; KINETICS; TEGDMA; SPECTROSCOPY; DEGRADATION;
D O I
10.1016/j.msec.2016.11.050
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The aim of this study was to synthesize and characterize new multifunctional-urethane-methacrylate monomers to be used as the organic matrix in restorative dental composites, and evaluate the main physical-chemical properties of the resulting material. Bis-GMA (bisphenol-A-diglycidylmethacrylate) and GDMA (glycerol dimethacrylate) were modified by reacting the hydroxyl groups with isocyanate groups of urethane-methacrylate precursors to result in the new monomeric systems U-(bis-GMA)-Mod and U-(GDMA)-Mod, U = Urethane and Mod = Modified. The modifications were characterized by FUR and H-1 NMR. The final monomeric synthesized system was used to prepare dental resins and composites. The physical-chemical properties were evaluated and compared with those of bis-GMA composites with varying filler contents or unfilled resins. U-(bis-GMA)Mod and U-(GDMA)-Mod can be used to prepare dental restorative composites, with some foreseeable advantages compared with bis-GMA composites. One significant advantage is that these composites have the potential to be less toxic, once they presented a reduction of 50% in leaching of unreacted monomers extracted by solvent. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:192 / 201
页数:10
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