Ayaz Elif Aydogan, Durkan Rukiye, Koroglu Ayşegul, Bagis Bora
1 Department of Prosthodontics, Faculty of Dentistry, Karadeniz Technical University, Trabzon - Turkey.
J Appl Biomater Funct Mater. 2014 Dec 30;12(3):228-33. doi: 10.5301/jabfm.5000199.
The aim of this study was to compare the residual monomer and microhardness of poly(methyl methacrylate) (PMMA)-based denture resins processed by using autoclave and conventional water bath techniques.
To determine the amount of residual methyl methacrylate (MMA) monomer, disk-shaped specimens (n=5) were prepared from 3 different acrylic resins (Meliodent, Paladent and Qc-20). Control groups were polymerized in water bath for 30 minutes at 100°C. The study groups were prepared in an autoclave device for 60°C/30 min followed 130°C/10 min and the other group for 60°C/30 min followed by 130°C/20 min. According to standard calibration curves, ultraviolet spectrophotometry at 230 nm was used to determine the residual monomer. For the Vickers hardness measurements, disk-shaped specimens (n=5) were prepared for each test group. Hardness measurements were performed with a Vickers hardness tester under a 4.91-N press load for a 30 seconds, after immersion in distilled water at 37ºC for 48 hours. The data were analyzed by ANOVA and Tukey HSD test (p<0.05).
Autoclave polymerization produced a significant decrease in the amount of residual monomers for all resin groups (p<0.05). This procedure also showed a significant increase in hardness for all resin groups (p<0.05). For the 3 resin groups, no significant differences were found between autoclave polymerization for 10 minutes and for 20 minutes (p>0.05).
The autoclave polymerization technique exhibited significantly lower residual monomer content and greater hardness than conventional heat polymerization.
本研究旨在比较采用高压釜和传统水浴技术加工的聚甲基丙烯酸甲酯(PMMA)基义齿树脂的残留单体和显微硬度。
为测定残留甲基丙烯酸甲酯(MMA)单体的含量,从3种不同的丙烯酸树脂(Meliodent、Paladent和Qc - 20)制备圆盘形试样(n = 5)。对照组在100°C水浴中聚合30分钟。研究组在高压釜装置中于60°C/30分钟后再于130°C/10分钟制备,另一组于60°C/30分钟后再于130°C/20分钟制备。根据标准校准曲线,使用230 nm处的紫外分光光度法测定残留单体。对于维氏硬度测量,为每个测试组制备圆盘形试样(n = 5)。在37ºC蒸馏水中浸泡48小时后,使用维氏硬度测试仪在4.91 - N的压力载荷下进行30秒的硬度测量。数据采用方差分析和Tukey HSD检验进行分析(p < 0.05)。
高压釜聚合使所有树脂组的残留单体量显著降低(p < 0.05)。该方法还使所有树脂组的硬度显著增加(p < 0.05)。对于这3种树脂组,在10分钟和20分钟的高压釜聚合之间未发现显著差异(p > 0.05)。
与传统热聚合相比,高压釜聚合技术表现出显著更低的残留单体含量和更高的硬度。