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

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) an...

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Veröffentlicht in:Materials Science & Engineering C 2017-03, Vol.72, p.192-201
Hauptverfasser: Martim, Gedalias C., Pfeifer, Carmem S., Girotto, Emerson M.
Format: Artikel
Sprache:eng
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Zusammenfassung: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 FTIR and 1H 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. [Display omitted] •New urethane monomers derived from bis-GMA and glycerol dimethacrylate.•Significantly greater resistance to leaching in organic solvents•BPA-free precursors when using a glycerol dimethacrylate derivative
ISSN:0928-4931
1873-0191
DOI:10.1016/j.msec.2016.11.050