Department of Conservative Dentistry, School of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
Oregon Health & Science University, Portland, OR, United States of America.
Mater Sci Eng C Mater Biol Appl. 2021 Jan;118:111535. doi: 10.1016/j.msec.2020.111535. Epub 2020 Sep 18.
The aim of this study was to modify the surface of fillers used in dental composites by the synthesis of two novel thiourethane oligomeric silanes, used to functionalize the silica-containing inorganic particles. Several thiourethane silane concentrations were tested during the silanization process to systematically assess the effect of silane coverage on experimental composite conversion, polymerization stress and fracture toughness.
Two different thiourethane silanes were synthesized based either on 1,6-hexanediol-diissocynate (HDDI), or 1,3-bis(1-isocyanato-1-methylethyl) benzene (BDI). Conventional 3-(Trimethoxysilyl)propyl methacrylate was used as the control. Glass fillers were silanized with 1, 2 or 4 wt% of each thiourethane silane, then evaluated by thermogravimetrical analysis. Photopolymerizable resin composites were prepared with Bis-GMA/UDMA/TEGDMA and 50 wt% silanized glass filler. Polymerization kinetics and degree of conversion were tested using Near-IR. Bioman was used to test polymerization stress. Data were analyzed with two-way ANOVA/Tukey's test (α = 5%).
The mass of silane coupled to the filler increased with the concentrations of thiourethane in the silanizing solution, as expected. Thiourethane-containing groups exhibited significantly higher degree of conversion compared to control groups, except for BDI 4%. HDDI 4%, BDI 2% and BDI 4% showed significantly lower polymerization stress than control groups. HDDI 4% exhibited significantly higher fracture toughness.
Novel filler functionalization with thiourethane silanes may be a promising alternative for improving dental composites properties by significantly increasing the degree of conversion, fracture toughness and reducing the polymerization stress.
本研究旨在通过合成两种新型硫脲寡聚硅烷来修饰牙科复合材料中使用的填充物,以对含硅无机颗粒进行功能化。在硅烷化过程中测试了几种硫脲硅烷浓度,以系统地评估硅烷覆盖率对实验性复合转化、聚合应力和断裂韧性的影响。
根据 1,6-己二醇二异氰酸酯 (HDDI) 或 1,3-双(1-异氰酸根合-1-甲基乙基)苯 (BDI) ,合成了两种不同的硫脲硅烷。传统的 3-(三甲氧基硅基)丙基甲基丙烯酸酯用作对照。玻璃填料用 1%、2%或 4%wt 的每种硫脲硅烷进行硅烷化,然后通过热重分析进行评估。用 Bis-GMA/UDMA/TEGDMA 和 50%wt 的硅烷化玻璃填料制备可光聚合树脂复合材料。使用近红外光测试聚合动力学和转化率。使用 Bioman 测试聚合应力。使用双因素方差分析/Tukey 检验(α=5%)对数据进行分析。
如预期的那样,与填料偶联的硅烷的质量随着硅烷化溶液中硫脲浓度的增加而增加。含硫脲基团的转化率明显高于对照组,除了 BDI 4%组。与对照组相比,HDDI 4%、BDI 2%和 BDI 4%的聚合应力显著降低。HDDI 4%的断裂韧性显著提高。
用硫脲硅烷对新型填料进行功能化可能是一种有前途的替代方法,可以通过显著提高转化率、断裂韧性和降低聚合应力来改善牙科复合材料的性能。