Effect of thiourethane filler surface functionalization on stress, conversion and mechanical properties of restorative dental composites

被引:22
作者
Faria-e-Silva, Andre L. [1 ]
dos Santos, Andressa [2 ]
Tang, Angela [3 ]
Girotto, Emerson M. [4 ]
Pfeifer, Carmem S. [5 ]
机构
[1] Univ Fed Sergipe, Dept Dent, Rua Claudio Batista S-N, BR-49060100 Aracaju, SE, Brazil
[2] Univ Estadual Maringa, Grad Program Chem, Av Colombo 5790,Jardim Univ, BR-87020900 Maringa, Parana, Brazil
[3] Phillips Acad, 180 Main St, Andover, MA USA
[4] Univ Estadual Maringa, Dept Chem, Av Colombo 5790,Jardim Univ, BR-87020900 Maringa, Parana, Brazil
[5] Oregon Hlth & Sci Univ, Dept Restorat Dent, Div Biomat & Biomech, 2730 SW Moody Ave, Portland, OR 97201 USA
关键词
Pre-polymerized additives; Resin composite; Polymerization; FAILED BONDED INTERFACES; POLYMERIZATION STRESS; THIOL-ENE; RESIN COMPOSITES; GLASS; LONGEVITY; BEHAVIOR; BRUSHES; IMPROVE; IMPACT;
D O I
10.1016/j.dental.2018.06.023
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives. This study evaluated the efficacy of a thiourethane(TU)-modified silane agent in improving properties in filled composites. Methods. The TU-silane agent was synthesized by combining 1,3-bis(1-isocyanato-1-methylethyl)benzene and 3-(triethoxysilyl)propyl isocyanate with trimethylol-tris-3-mercaptopropionate (TMP), at 1:2 isocyanate:thiol, leaving pendant thiol and alkoxy silane groups. Barium glass fillers (1 mu m average particle size) were functionalized with 5 wt% TU-silane in an acidic ethanol solution. Commercially available 3-(trimethoxysilyl)propyl methacrylate (MA-silane) and (3-mercaptopropyl)trimethoxysilane (SH-silane), as well as no silane treatment (NO-silane), were used as controls. Composites were made with BisGMA-UDMA-TEGDMA (5:3:2), camphorquinone/ethyl-4-dimethylaminobenzoate (0.2/0.8 wt%) and di-tert-butyl hydroxytoluene (0.3 wt%) and 70 wt% silanated inorganic fillers. Polymerization stress (PS) was measured using a cantilever beam apparatus (Bioman). Methacrylate conversion (DC) and rate of polymerization (RP) during photoactivation (800 mW/cm(2)) were followed in real-time with near-IR. Flexural strength/modulus (FS/FM) were evaluated in three-point bending with 2 x 2 x 25 mm. Statistical analysis: 2-way ANOVA/Tukey's test (alpha = 5%). Results. DC, Rp(max) and E were similar for all groups tested. FS was similar for the TU- and MA-silane, which were statistically higher than the untreated and SH-silane groups. Stress reductions in relation to the MA-silane were observed for all groups, but statistically more markedly for the TU-silane material. This is likely due to stress relaxation and/or toughening provided at the filler interface by the oligomeric TU structure. Significance. TU-silane oligomers favorably modified conventional dimethacrylate networks with minimal disruption to existing curing chemistry, in filled composites. For the same conversion values, stress reductions of up to 50% were observed, without compromise to mechanical properties or handling characteristics. (C) 2018 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1351 / 1358
页数:8
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