Golkar Parisa, Ranjbar Omrani Ladan, Zohourinia Shide, Ahmadi Elham, Asadian Faeze
Department of Operative Dentistry, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.
Dental Materials Research Center, Department of Operative Dentistry, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.
Front Dent. 2021 May 17;18:17. doi: 10.18502/fid.v18i17.6248. eCollection 2021.
In this study we assessed the cytotoxic effect of nanohydroxyapatite (NHA) incorporated into resin modified and conventional glass ionomer cements (RMGICs and CGICs) on L929 murine fibroblasts. In this in vitro study, 0wt%, 1wt%, 2wt%, 5wt%, 7wt% and 10wt% concentrations of NHA were added to Fuji II LC RMGIC and Fuji IX CGIC powders. Eighteen samples (5×3mm) were fabricated from each type of glass ionomer, in six experimental groups (n=3): CG, CG, CG, CG, CG, CG RMG RMG, RMG, RMG, RMG, and RMG. Samples were incubated for 72h. The overlaying solution was removed and added to L929 fibroblasts. The methyl thiazolyl tetrazolium bromide (MTT) assay was performed at 24, 48 and 72h. The wavelength was read by a spectrophotometer. Data were analyzed by ANOVA and Tukey's test. There was no significant difference in cytotoxicity of the two types of glass ionomers, with and without NHA, except for CG and RMG groups after 72h. RMG group was significantly more cytotoxic than the CG group (P<0.05). In CG groups during the first 24h, the cytotoxicity of CG and CG groups was significantly higher than that of CG; while, there was no significant difference between the RMG groups. Cytotoxicity significantly decreased in all groups after 24h (P<0.05). Incorporation of NHA into Fuji II LC RMGIC and Fuji IX CGIC did not affect their biocompatibility and therefore its addition to these materials can provide favorable biological properties, especially considering its beneficial effects on the other properties of GICs.
在本研究中,我们评估了掺入树脂改性和传统玻璃离子水门汀(RMGICs和CGICs)中的纳米羟基磷灰石(NHA)对L929小鼠成纤维细胞的细胞毒性作用。在这项体外研究中,将0wt%、1wt%、2wt%、5wt%、7wt%和10wt%浓度的NHA添加到Fuji II LC RMGIC和Fuji IX CGIC粉末中。从每种类型的玻璃离子水门汀制备18个样本(5×3mm),分为六个实验组(n = 3):CG、CG、CG、CG、CG、CG、RMG、RMG、RMG、RMG、RMG。样本孵育72小时。去除上层溶液并添加到L929成纤维细胞中。在24、48和72小时进行甲基噻唑基四氮唑溴盐(MTT)测定。用分光光度计读取波长。数据通过方差分析和Tukey检验进行分析。两种类型的玻璃离子水门汀(含和不含NHA)的细胞毒性没有显著差异,但72小时后CG和RMG组除外。RMG组的细胞毒性显著高于CG组(P<0.05)。在CG组的前24小时内,CG和CG组的细胞毒性显著高于CG组;而RMG组之间没有显著差异。24小时后所有组的细胞毒性均显著降低(P<0.05)。将NHA掺入Fuji II LC RMGIC和Fuji IX CGIC中不会影响它们的生物相容性,因此将其添加到这些材料中可以提供良好的生物学特性,特别是考虑到其对玻璃离子水门汀其他性能的有益影响。