Department of Restorative Dentistry, Dental School of São Paulo State University, Araraquara, São Paulo, Brazil.
J Endod. 2012 Jul;38(7):971-6. doi: 10.1016/j.joen.2012.02.018. Epub 2012 Apr 6.
The main purpose of this study was to evaluate the biocompatibility and bioactivity of a new mineral trioxide aggregate (MTA)-based endodontic sealer, MTA Fillapex (MTA-F; Angelus, Londrina, Brazil), in human cell culture.
Human osteoblast-like cells (Saos-2) were exposed for 1, 2, 3, and 7 days to MTA-F, Epiphany SE (EP-SE; SybronEndo, Orange, CA), and zinc oxide-eugenol sealer (ZOE). Unexposed cultures were the control group (CT). The viability of the cells was assessed by MTT assay and the morphology by scanning electron microscopy (SEM). The bioactivity of MTA-F was evaluated by alkaline phosphatase activity (ALP) and the detection of calcium deposits in the culture with alizarin red stain (ARS). Energy-dispersive X-ray spectroscopy (EDS) was used to chemically characterize the hydroxyapatite crystallites (HAP). Saos-2 cells were cultured for 21 days for ARS and SEM/EDS. ARS results were expressed as the number of stained nodules per area. Statistical analysis was performed with analysis of variance and Bonferroni tests (P < .01).
MTA-F exposure for 1, 2, and 3 days resulted in increased cytotoxicity. In contrast, viability increased after 7 days of exposure to MTA-F. Exposure to EP-SE and ZOE was cytotoxic at all time points. At day 7, ALP activity increase was significant in the MTA-F group. MTA-F presented the highest percentage of ARS-stained nodules (MTA-F > CT > EP-SE > ZOE). SEM/EDS analysis showed hydroxyapatite crystals only in the MTA-F and CT groups. In the MTA-F group, crystallite morphology and chemical composition were different from CT.
After setting, the cytotoxicity of MTA-F decreases and the sealer presents suitable bioactivity to stimulate HAP crystal nucleation.
本研究的主要目的是评估一种新型矿化三氧化物聚合体(MTA)基根管封闭剂 MTA Fillapex(MTA-F;Angelus,Londrina,巴西)在人细胞培养中的生物相容性和生物活性。
人成骨样细胞(Saos-2)分别暴露于 MTA-F、Epiphany SE(EP-SE;SybronEndo,Orange,CA)和氧化锌丁香酚封闭剂(ZOE)中 1、2、3 和 7 天,未暴露的培养物为对照组(CT)。通过 MTT 测定法评估细胞活力,通过扫描电子显微镜(SEM)评估细胞形态。通过碱性磷酸酶活性(ALP)和茜素红染色(ARS)检测培养物中的钙沉积来评估 MTA-F 的生物活性。能量色散 X 射线光谱法(EDS)用于化学表征羟基磷灰石晶体(HAP)。Saos-2 细胞培养 21 天进行 ARS 和 SEM/EDS 检测。ARS 结果以每个区域染色结节的数量表示。采用方差分析和 Bonferroni 检验进行统计学分析(P<.01)。
暴露于 MTA-F 1、2 和 3 天会导致细胞毒性增加。相反,暴露于 MTA-F 7 天后细胞活力增加。EP-SE 和 ZOE 暴露在所有时间点均具有细胞毒性。在第 7 天,MTA-F 组的 ALP 活性增加显著。MTA-F 组 ARS 染色结节的百分比最高(MTA-F>CT>EP-SE>ZOE)。SEM/EDS 分析仅在 MTA-F 和 CT 组中显示出羟基磷灰石晶体。在 MTA-F 组中,晶体形态和化学成分与 CT 不同。
凝固后,MTA-F 的细胞毒性降低,该封闭剂具有适宜的生物活性,可刺激 HAP 晶体成核。