Ashraf Hengameh, Moradimajd Nima, Mozayeni Mohammad Ali, Dianat Omid, Mahjour Faranak, Yadegari Zahra
Department of Endodontic, Iranian Center of Endodontic Research, Tehran, Iran.
Dent Res J (Isfahan). 2012 Sep;9(5):549-53. doi: 10.4103/1735-3327.104872.
Endodontic sealers usually come in contact with adjacent tissues and their biocompatibility is key in a successful treatment. The purpose of this study was to assess the cytotoxicity of three resin-based sealers, namely AH Plus, EndoREZ, and Epiphany in set and fresh states on an L929 cell line.
In this in vitro experimental study, the materials were mixed according to the manufacturers' instructions, and were divided into two groups, fresh and set. The elutes of materials were prepared separately and were incubated with L929 fibroblasts for 1 hour, 24 hours, and 72 hours. Pulp Canal Sealer and Dulbecco's Modified Eagle Medium (DMEM) served as positive and negative controls respectively. Cell viability was evaluated by MTT assay ([3-4,5-dimethyl thiazol-2-yl]-2,5-diphenyltetrazolium bromide succinate), after 1 hour, 24 hours, and 72 hours. The data were analyzed by analysis of variance (ANOVA), and Tukey multiple comparison test.
After 1 hour, fresh Epiphany and fresh AH Plus were significantly more cytotoxic than their set samples. No significant difference was perceived between cytotoxicity of fresh state of sealers and positive control, or between set state and negative control. After 24 hours, both fresh and set samples of all materials were significantly more cytotoxic than the negative control group, and were less cytotoxic than the positive control group. After 72 hours, the fresh and set samples of all materials were as cytotoxic as the positive control group. At each time point, no significant difference was perceived among different materials in terms of cell viability.
The observed differences among the cytotoxicity of AH Plus, EndoREZ, and Epiphany did not reach a significant level at comparable time points after exposure.
根管封闭剂通常会与相邻组织接触,其生物相容性是成功治疗的关键。本研究的目的是评估三种树脂基封闭剂,即AH Plus、EndoREZ和Epiphany在凝固状态和新鲜状态下对L929细胞系的细胞毒性。
在这项体外实验研究中,材料按照制造商的说明进行混合,并分为两组,即新鲜组和凝固组。分别制备材料的洗脱液,并与L929成纤维细胞孵育1小时、24小时和72小时。牙髓根管封闭剂和杜氏改良 Eagle 培养基(DMEM)分别作为阳性和阴性对照。在1小时、24小时和72小时后,通过MTT法([3-4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴化物琥珀酸盐)评估细胞活力。数据通过方差分析(ANOVA)和Tukey多重比较检验进行分析。
1小时后,新鲜的Epiphany和新鲜的AH Plus的细胞毒性明显高于其凝固后的样本。封闭剂新鲜状态的细胞毒性与阳性对照之间,或凝固状态与阴性对照之间均未观察到显著差异。24小时后,所有材料的新鲜和凝固样本的细胞毒性均显著高于阴性对照组,且低于阳性对照组。72小时后,所有材料的新鲜和凝固样本的细胞毒性与阳性对照组相同。在每个时间点,不同材料之间在细胞活力方面未观察到显著差异。
在暴露后的可比时间点,AH Plus、EndoREZ和Epiphany的细胞毒性之间观察到的差异未达到显著水平。