Department Prosthodontics, Faculty of Dentistry, Istanbul University, Istanbul, Turkey.
J Appl Oral Sci. 2011 Aug;19(4):306-12. doi: 10.1590/s1678-77572011005000002. Epub 2011 May 27.
Residual methyl methacrylate (MMA) may leach from the acrylic resin denture bases and have adverse effects on the oral mucosa. This in vitro study evaluated and correlated the effect of the leaching residual MMA concentrations ([MMA]r) on in vitro cytotoxicity of L-929 fibroblasts.
A total of 144 heat-polymerized acrylic resin specimens were fabricated using 4 different polymerization cycles: (1) at 74ºC for 9 h, (2) at 74ºC for 9 h and terminal boiling (at 100ºC) for 30 min, (3) at 74ºC for 9 h and terminal boiling for 3 h, (4) at 74ºC for 30 min and terminal boiling for 30 min. Specimens were eluted in a complete cell culture medium at 37ºC for 1, 2, 5 and 7 days. [MMA]r in eluates was measured using high-performance liquid chromatography. In vitro cytotoxicity of eluates on L-929 fibroblasts was evaluated by means of cell proliferation using a tetrazolium salt XTT (sodium 3´-[1-phenyl-aminocarbonyl)-3,4-tetrazolium]bis(4-methoxy-6-nitro)benzenesulphonic acid) assay. Differences in [MMA]r of eluates and cell proliferation values between polymerization cycles were statistically analyzed by Kruskal-Wallis, Friedman and Dunn's multiple comparison tests. The correlation between [MMA]r of eluates and cell proliferation was analyzed by Pearson's correlation test (p<0.05).
[MMA]r was significantly (p<0.001) higher in eluates of specimens polymerized with cycle without terminal boiling after elution of 1 and 2 days. Cell proliferation values for all cycles were significantly (p<0.01) lower in eluates of 1 day than those of 2 days. The correlation between [MMA]r and cell proliferation values was negative after all elution periods, showing significance (p<0.05) for elution of 1 and 2 days. MMA continued to leach from acrylic resin throughout 7 days and leaching concentrations markedly reduced after elution of 1 and 2 days.
Due to reduction of leaching residual MMA concentrations, use of terminal boiling in the polymerization process for at least 30 min and water storage of the heat-polymerized denture bases for at least 1 to 2 days before denture delivery is clinically recommended for minimizing the residual MMA and possible cytotoxic effects.
甲基丙烯酸甲酯(MMA)残留可能会从丙烯酸树脂义齿基托中浸出,并对口腔黏膜产生不良影响。本体外研究评估并关联了浸出残留 MMA 浓度([MMA]r)对 L-929 成纤维细胞体外细胞毒性的影响。
共制作了 144 个热聚合丙烯酸树脂标本,采用 4 种不同聚合周期:(1)74℃聚合 9 小时,(2)74℃聚合 9 小时后终端煮沸(100℃)30 分钟,(3)74℃聚合 9 小时后终端煮沸 3 小时,(4)74℃聚合 30 分钟后终端煮沸 30 分钟。将标本在 37℃下于完全细胞培养液中孵育 1、2、5 和 7 天,然后洗脱。采用高效液相色谱法测量洗脱液中的[MMA]r。通过使用四唑盐 XTT(三[(1-苯氨基甲酰基)-3,4-四唑基]双(4-甲氧基-6-硝基)苯磺酸)测定细胞增殖来评估洗脱液对 L-929 成纤维细胞的体外细胞毒性。通过 Kruskal-Wallis、Friedman 和 Dunn 多重比较检验分析洗脱液中 [MMA]r 和细胞增殖值在聚合周期之间的差异。通过 Pearson 相关检验分析洗脱液中 [MMA]r 与细胞增殖之间的相关性(p<0.05)。
在洗脱后 1 和 2 天,未进行终端煮沸的标本聚合周期的洗脱液中[MMA]r 显著更高(p<0.001)。所有周期的洗脱液在 1 天的细胞增殖值显著低于 2 天(p<0.01)。在所有洗脱期后,[MMA]r 与细胞增殖值之间呈负相关,在洗脱后 1 和 2 天呈显著相关(p<0.05)。MMA 在整个 7 天内持续从丙烯酸树脂中浸出,洗脱后 1 和 2 天,浸出浓度显著降低。
由于浸出残留 MMA 浓度降低,建议在聚合过程中使用终端煮沸至少 30 分钟,并在义齿交付前将热聚合义齿基托在水中储存至少 1 至 2 天,以尽量减少残留 MMA 和可能的细胞毒性影响。