Bacchi Atais, Nelson Morgan, Pfeifer Carmem S
Oregon Health and Science University, Biomaterials and Biomechanics, 2730 SW Moody Ave., Portland, OR 97201, United States; Meridional Faculty - IMED, School of Dentistry, Prosthodontics and Dental Materials, Av. Senador Pinheiro, 304, 99070-220 Passo Fundo, RS, Brazil.
Oregon Health and Science University, Biomaterials and Biomechanics, 2730 SW Moody Ave., Portland, OR 97201, United States.
Dent Mater. 2016 Feb;32(2):233-9. doi: 10.1016/j.dental.2015.11.022. Epub 2016 Jan 4.
To evaluate the ability of thio-urethane oligomers to improve the properties of restorative composite resins.
Oligomers were synthesized by combining 1,6-hexanediol-diissocyante (aliphatic) with pentaerythritol tetra-3-mercaptopropionate (PETMP) or 1,3-bis(1-isocyanato-1-methylethyl)benzene (aromatic) with trimethylol-tris-3-mercaptopropionate (TMP), at 1:2 isocyanate:thiol, leaving pendant thiols. Oligomers were added at 0-20 wt% to BisGMA-TEGDMA (70-30 wt%). Silanated inorganic fillers were added (70 wt%). Materials were photoactivated at 800 mW/cm(2) filtered to 320-500 nm. Near-IR was used to follow degree of methacrylate conversion (DC). Mechanical properties were evaluated in three-point bending with 2 mm × 2 mm × 25 mm bars for flexural strength/modulus and toughness (FS/E, and T) according to ISO 4049, and 2 mm × 5 mm × 25 mm notched specimens for fracture toughness (KIC). Polymerization stress (PS) was measured on the Bioman. Results were analyzed with ANOVA/Tukey's test (α=5%).
Significant increase in DC was observed in thio-urethane-containing materials especially for the group with 20 wt% of aliphatic version. Materials composed by oligomers also promoted higher FS, E, and KIC in comparison to controls irrespective of thio-urethane type. A significant increase in toughness was detected by ANOVA, but not distinguished in the groups. The PS was significantly reduced by the presence of thio-urethane for almost all groups.
The use of thio-urethane oligomer to compose methacrylate-based restorative composite promote increase in DC, FS, E and KIC while significant reduces PS.
A simple additive was shown to reduce stress while increasing convrersion and mechanical properties, mainly fracture toughness. This has he potential of increasing the service life of dental composites, without changing current operatory procedures.
评估硫代聚氨酯低聚物改善复合树脂修复材料性能的能力。
通过将1,6 - 己二醇二异氰酸酯(脂肪族)与季戊四醇四 - 3 - 巯基丙酸酯(PETMP)或1,3 - 双(1 - 异氰酸酯 - 1 - 甲基乙基)苯(芳香族)与三羟甲基三 - 3 - 巯基丙酸酯(TMP)以异氰酸酯:硫醇1:2的比例混合来合成低聚物,保留端基硫醇。将低聚物以0 - 20 wt%的比例添加到双酚A - 二甲基丙烯酸酯(BisGMA) - 三乙二醇二甲基丙烯酸酯(TEGDMA)(70 - 30 wt%)中。添加硅烷化无机填料(70 wt%)。材料在800 mW/cm²且过滤至320 - 500 nm的条件下进行光固化。使用近红外光谱跟踪甲基丙烯酸酯的转化率(DC)。根据ISO 4049标准,使用2 mm×2 mm×25 mm的条形试样进行三点弯曲试验以评估弯曲强度/模量和韧性(FS/E和T),使用2 mm×5 mm×25 mm的缺口试样评估断裂韧性(KIC)。在Bioman上测量聚合应力(PS)。结果采用方差分析/ Tukey检验(α = 5%)进行分析。
含硫代聚氨酯的材料中观察到DC显著增加,尤其是含20 wt%脂肪族版本的组。与对照组相比,由低聚物组成的材料无论硫代聚氨酯类型如何,均能提高FS、E和KIC。通过方差分析检测到韧性显著增加,但各实验组之间无显著差异。几乎所有组中硫代聚氨酯的存在均使PS显著降低。
使用硫代聚氨酯低聚物组成基于甲基丙烯酸酯的复合树脂修复材料可促进DC、FS、E和KIC的增加,同时显著降低PS。
一种简单的添加剂被证明在增加转化率和机械性能(主要是断裂韧性)的同时能降低应力。这有可能在不改变现有操作程序的情况下延长牙科复合材料的使用寿命。