Da Silva Stephane, Da Silva Eduardo Moreira, Delphim Marcella Bruna Ferreira, Poskus Laiza Tatiana, Amaral Cristiane Mariote
Am J Dent. 2015 Dec;28(6):367-72.
To evaluate the repair bond strength after storage in water, lactic and propionic acid after 7 days and 6 months and the sorption and solubility of resin composites used.
Five cylinders of each resin composite (microhybrid, nanofilled and silorane-based composite) were prepared. Specimens were aged with thermocycling (5 and 55°C) 5,000 times. A repair procedure was performed using intraoral sandblasting with 50-µm aluminum oxide, application of an adhesive system and cylinder of composite was fabricated. Specimens were sectioned into beams and stored in three immersion media: water, propionic acid and lactic acid. The microtensile bond strength was measured after periods of 7 days and 6 months. Sorption and solubility were evaluated using 15 specimens (0 = 6 mm; h = 1 mm) of each resin composite, which were prepared and assigned into three groups (n = 5) according to the immersion media (water, propionic acid and lactic acid). Data were analyzed using one-way/two-way/three-way ANOVA and Tukey's test (α = 0.05).
The resin composites, immersion media and time of immersion did not affect the repair bond strength (microhybrid 38.3 to 40.9 MPa; nanofilled 38.7 to 42.2 MPa; silorane 41.2 to 51.1 MPa). Additionally, the immersion media did not affect the sorption and solubility. The silorane-based composite presented the lowest sorption (10.5 to 12.1 µg/mm3) and solubility (-2.4 to -2.7 µg/mm3), while the nanofilled methacrylate-based composite showed the highest sorption (32.1 to 33.6 µg/mm3). Regarding solubility, the nanofilled and microhybrid methacrylate-based composites did not present statistically significant differences.
评估在水、乳酸和丙酸中储存7天及6个月后的修复粘结强度,以及所用树脂复合材料的吸附性和溶解性。
制备每种树脂复合材料(微混合、纳米填充和硅氧烷基复合材料)的五个圆柱体。样本经5000次热循环(5和55°C)老化。采用50μm氧化铝进行口内喷砂、应用粘结系统并制作复合材料圆柱体进行修复操作。将样本切成梁状并储存在三种浸泡介质中:水、丙酸和乳酸。在7天和6个月后测量微拉伸粘结强度。使用每种树脂复合材料的15个样本(直径 = 6 mm;高度 = 1 mm)评估吸附性和溶解性,这些样本根据浸泡介质(水、丙酸和乳酸)制备并分为三组(n = 5)。数据采用单向/双向/三向方差分析和Tukey检验(α = 0.05)进行分析。
树脂复合材料、浸泡介质和浸泡时间均不影响修复粘结强度(微混合复合材料为38.3至40.9 MPa;纳米填充复合材料为38.7至42.2 MPa;硅氧烷复合材料为41.2至51.1 MPa)。此外,浸泡介质不影响吸附性和溶解性。硅氧烷基复合材料的吸附性最低(10.5至12.1 μg/mm³),溶解性最低(-2.4至-2.7 μg/mm³),而纳米填充甲基丙烯酸酯基复合材料的吸附性最高(32.1至33.6 μg/mm³)。关于溶解性,纳米填充和微混合甲基丙烯酸酯基复合材料无统计学显著差异。