一步自蚀刻牙胶对体外人牙周韧带成纤维细胞的细胞毒作用。

Fangfang Sun, Peng Mao, Cong Wang, Chaowen Shi, Rongrong Nie, Ningning Han, Xiaodong Han
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引用次数: 13

摘要

目的探讨四种一步自蚀牙胶粘剂[Adper Easy One (AEO)、iBond (IB)、Clearfil S³Bond (CSB)和G-Bond (GB)]对培养的人牙周韧带成纤维细胞的潜在细胞毒性作用。材料与方法将固化的胶粘剂浸泡在完全的DMEM或去离子水中,在37°C下保持24 h,然后灭菌。用去离子水基提取物进行傅里叶变换红外光谱分析。将dmem提取液稀释成不同浓度进行细胞毒性试验。用CCK-8法、显微镜和流式细胞术检测培养的人牙周韧带成纤维细胞的活力、完整性和凋亡情况。结果4种胶粘剂均可引起细胞活力丧失、细胞形态改变和细胞死亡。GB诱导细胞凋亡和坏死的细胞毒性最大,而IB对培养细胞的细胞毒性作用最弱。结论所有牙粘接剂对细胞活力均有明显的不良影响。因此,在临床使用牙黏剂时,应采取预防措施保护牙周组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytotoxic Effects of One-step Self-etching Dental Adhesives on Human Periodontal Ligament Fibroblasts In Vitro.
PURPOSE To evaluate the potential cytotoxic effects of four one-step self-etching dental adhesives [Adper Easy One (AEO), iBond (IB), Clearfil S³ Bond (CSB), and G-Bond (GB)] on cultured human periodontal ligament fibroblasts. MATERIALS AND METHODS Cured adhesives were immersed in complete DMEM or deionized water and maintained at 37°C for 24 h, followed by sterilization. The deionized water-based extract was used for Fourier transform infrared spectroscopy analysis. The DMEM-based extract was diluted into various concentrations for cytotoxicity tests. The viability, integrity, and apoptosis of cultured human periodontal ligament fibroblasts upon treatment with the extracts were determined using the CCK-8 assay, microscopy, and flow cytometry. RESULTS All of the four adhesives induced cell viability loss, cell morphology alteration, and cell death. GB showed the greatest cytotoxicity by inducing cell apoptosis and necrosis, while IB had the weakest cytotoxic effect on the cultured cells. CONCLUSION All tested dental adhesives have significant adverse effects on cell viability. Therefore, precautions should be taken to protect the periodontal tissues when dental adhesives are applied in the clinic.
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