Fugolin Ana Paula, Costa Ana Rosa, Kono Emilie, Quirk Eleanor, Ferracane Jack L, Pfeifer Carmem S
Department of Restorative Dentistry, Division of Biomaterials and Biomechanics - Oregon Health & Science University, Portland, OR, US.
Department of Restorative Dentistry, Division of Dental Materials - Piracicaba Dental School - UNICAMP, Piracicaba, SP, BRA.
Eur Polym J. 2020 May 5;130. doi: 10.1016/j.eurpolymj.2020.109664. Epub 2020 Apr 6.
The incorporation of thiourethane-based oligomeric additives into resin composite formulations leads to improvement in mechanical properties and reduction in polymerization stress, but may increase viscosity. The objective of this study was to functionalize filler particle surfaces with thiourethane silane molecules and determine the impact of the inorganic filler loading and surface treatment on the behavior of experimental resin composites with systematically-varied organic matrices.
Thiourethane oligomer was synthesized , and grafted to the surface of 0.7um barium glass. BisGMA and TEGDMA (BT) were combined (at 30:70, 50:50 or 70:30 wt%) to 50 or 75 wt% of methacrylate (MA-Sil - control) or thiourethane-silanized (TU-Sil) particles. Composites were made polymerizable by the addition of 0.2 wt% BAPO and 0.05 wt% BHT was added as inhibitor. A mercury arc lamp (320-500 nm) at 800 mW/cm was used for all curing procedures. Kinetics of polymerization was assessed by near-IR spectroscopy in real time. Polymerization stress was determined with a cantilever system in real time (Bioman). Flexural modulus and strength were determined in 3-point bending (25x2x2 mm). Water sorption and solubility and film thickness were tested according to ISO 4049. Polymeric network characteristics were analyzed by dynamic mechanical analysis (DMA). Data was analyzed with two-way ANOVA/Tukey's test (95%).
Viscosity increased with the increase in BisGMA and/or filler amounts. Overall, TU-Sil containing composites showed delayed vitrification and higher final DC. Filler concentration did not affect DC neither flexural strength. DC decreased with increasing BisGMA content. Polymerization stress reduced and flexural modulus increased for higher filler content, especially for formulations containing TU-Sil particles. The water stability was positively affected by the increase in amount of BisGMA and inorganic filler particles. In terms of polymeric network, the addition of TU-Sil particles increased the T and decreased the E' and cross-link density.
With the exception of flexural modulus, all tested properties were significantly impacted by the matrix viscosity and/or the addition of TU-Sil filler particles. In general, the use of thiourethane oligomers as a silane coupling agent was able to reinforce the materials and reduce the polymerization stress without negatively affecting the viscosity of the system.
将基于硫脲烷的低聚物添加剂加入树脂复合材料配方中可改善机械性能并降低聚合应力,但可能会增加粘度。本研究的目的是用硫脲烷硅烷分子对填料颗粒表面进行功能化,并确定无机填料负载量和表面处理对具有系统变化有机基质的实验性树脂复合材料性能的影响。
合成硫脲烷低聚物,并将其接枝到0.7μm钡玻璃表面。将双酚A双甲基丙烯酸缩水甘油酯(BisGMA)和三乙二醇二甲基丙烯酸酯(TEGDMA,BT)按30:70、50:50或70:30的重量比与50%或75%重量的甲基丙烯酸酯(MA - Sil - 对照)或硫脲烷硅烷化(TU - Sil)颗粒混合。通过添加0.2%重量的过氧化苯甲酰引发剂(BAPO)使复合材料可聚合,并添加0.05%重量的二叔丁基对甲酚(BHT)作为抑制剂。所有固化过程均使用功率为800 mW/cm²的汞弧灯(320 - 500 nm)。通过近红外光谱实时评估聚合动力学。使用悬臂系统实时测定聚合应力(Bioman)。通过三点弯曲(2×2×25 mm)测定弯曲模量和强度。根据ISO 4049测试吸水率、溶解度和膜厚度。通过动态力学分析(DMA)分析聚合物网络特性。数据采用双向方差分析/ Tukey检验(95%)进行分析。
粘度随BisGMA和/或填料量的增加而增加。总体而言,含TU - Sil的复合材料显示出玻璃化延迟和更高的最终转化率(DC)。填料浓度对转化率和弯曲强度均无影响。转化率随BisGMA含量的增加而降低。对于较高的填料含量,聚合应力降低,弯曲模量增加
,特别是对于含有TU - Sil颗粒的配方。BisGMA和无机填料颗粒量的增加对水稳定性有积极影响。在聚合物网络方面,添加TU - Sil颗粒增加了玻璃化转变温度(T),降低了储能模量(E')和交联密度。
除弯曲模量外,所有测试性能均受到基质粘度和/或TU - Sil填料颗粒添加的显著影响。一般来说,使用硫脲烷低聚物作为硅烷偶联剂能够增强材料并降低聚合应力,而不会对体系粘度产生负面影响。