Department of Operative Dentistry and Dental Materials, School of Dentistry, Federal University of Uberlândia, Uberlândia, Minas Gerais, Brazil.
Biomaterials and Biomechanics, Restorative Dentistry Department, School of Dentistry, Oregon Health & Science University, Portland, OR, USA.
Dent Mater. 2019 Nov;35(11):1523-1531. doi: 10.1016/j.dental.2019.07.015. Epub 2019 Aug 5.
Thiourethane oligomers have been shown to increase the fracture toughness and reduce the polymerization stress of methacrylate-based materials. However, network formation has not been elucidated in these materials yet. The aim of this study was to evaluate how the addition of a thiourethane oligomer (TU) influences the sol/gel composition and network structure of methacrylate-based materials using dynamic mechanical analysis and extraction methods.
BisGMA/TEGDMA at systematically varied mass ratios (20/80 to 80/20wt%) were mixed with pre-polymerized thiourethane oligomers at 0 (control) or 20wt%, synthesized by combining pentaerythritol tetra-3-mercaptopropionate with dicyclohexylmethane 4,4⿲-Diisocyanate, at 1:2 isocyanate:thiol. 0.1wt% of 2,2-Dimethoxy-2-phenylacetophenone was added as the photoinitiator and 0.3wt% of 2,6-di-tert-butyl-4-methylphenol was added as a free radical inhibitor. Disk specimens (0.8ÿ10mm in diameter, n=3) were photoactivated at 270mW/ (320500nm) for 1min. The degree of conversion (DC) was measured in near-IR (˿6165cm). Specimens were immersed in two different solvents (water for 7 days or dicholoromethane for 48h). Water sorption (WS) and solubility (SL) were obtained according to ISO 4049. The leachates for both solutions were analyzed with H-NMR (400MHz, CDCL). Bar specimens (1ÿ3ÿ25mm, photocured and then post-processed at 180°C for 8h to DC>95%) were subjected to dynamic mechanical analysis (30 to 230°C) to obtain glass transition temperature (Tg), tan delta curves and crosslinking density (ν). Data was analyzed with two-way ANOVA/Tukeys test (95%).
In general, the presence of TU increased the overall conversion. The WS was similar for all groups, but the SL decreased by 2-fold with the addition of the TU oligomer for all compositions, except BisGMA/TEGDMA 80/20. The BisGMA concentration of the leachates increased with increasing BisGMA in the initial mixture, and with the presence of thiourethane. This compositional drift of the gel with the presence of TU was attributed to the preferential dissolution of TEGDMA into the TU network. Tg and ν decreased with the addition of TU, as expected. The addition of TU produced more homogeneous networks, as evidenced by narrower breadth of the tan delta curve.
The addition of TU affected the composition of the sol/gel in crosslinked networks, which were more homogeneous and presented 2-fold less potentially toxic leachates than the methacrylate controls.
The addition of TU may produce less cytotoxic materials based on the increased conversion and reduced amount of unreacted extractables from its network after water storage.
已有研究表明硫代尿烷低聚物能提高甲基丙烯酸酯基材料的断裂韧性和降低聚合应力。然而,这些材料的网络形成尚未得到阐明。本研究旨在通过动态力学分析和萃取方法,评估添加硫代尿烷低聚物(TU)如何影响甲基丙烯酸酯基材料的溶胶/凝胶组成和网络结构。
以系统变化的质量比(20/80 至 80/20wt%)将 BisGMA/TEGDMA 混合,并以 0(对照)或 20wt%添加预聚合的硫代尿烷低聚物,该低聚物由五羟乙基季戊四醇三巯基丙酸酯与二环己基甲烷 4,4′-二异氰酸酯以 1:2 的异氰酸酯:巯基比例合成。添加 0.1wt%的 2,2-二甲氧基-2-苯乙酮作为光引发剂和 0.3wt%的 2,6-二叔丁基-4-甲基苯酚作为自由基抑制剂。用光(320 500nm 下 270mW/)在 1 分钟内对直径为 0.8ÿ10mm 的圆盘试件进行光激活。在近红外(˿6165cm)下测量转化率(DC)。将试件分别浸入两种不同的溶剂(水 7 天或二氯甲烷 48h)中。根据 ISO 4049 测定吸水率(WS)和溶解度(SL)。对两种溶液的浸提液进行 H-NMR(400MHz,CDCL)分析。用光固化后(然后在 180°C 下后处理 8 小时以达到转化率>95%)的棒试件(1ÿ3ÿ25mm)进行动态力学分析(˿30 至 230°C),以获得玻璃化转变温度(Tg)、tan δ 曲线和交联密度(ν)。使用双因素方差分析/Tukey 检验(95%)进行数据分析。
一般来说,TU 的存在增加了整体转化率。所有组的 WS 相似,但除了 BisGMA/TEGDMA 80/20 外,添加 TU 低聚物后所有组成的 SL 降低了 2 倍。随着初始混合物中 BisGMA 浓度的增加以及 TU 的存在,浸出物中的 BisGMA 浓度增加。TU 的存在导致凝胶的这种组成漂移归因于 TEGDMA 优先溶解到 TU 网络中。如预期的那样,Tg 和 ν 随着 TU 的添加而降低。添加 TU 产生了更均匀的网络,这从 tan δ 曲线的更窄的宽度得到证明。
TU 的添加影响了交联网络中溶胶/凝胶的组成,其网络更加均匀,并且在水储存后从其网络中提取的潜在毒性物质减少了 2 倍。
基于转化率的提高和水储存后未反应的萃取物数量减少,TU 的添加可能会产生毒性更小的材料。