Cytotoxicity of silver nanoparticles was influenced by dispersion media in HepG2 cells

Yuying Xue, Yanmei Huang, F. Gong, Ting Zhang, M. Tang
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Abstract

The present investigations were carried out to evaluate the cellular toxic effects of silver nanoparticles (AgNPs) suspended in different solvents using human hepatocellular carcinoma cell line (HepG2). MTT assay was used to examine the proliferation activities of cells. The effects of AgNPs on cell cycle and apoptosis were analyzed using flow cytometry. The ionization of AgNPs in different dispersion media (deionized water, PBS, saline and cell culture medium) was found to be different, with the concentrations of silver ion in deionized water were the highest in all suspensions. AgNPs could inhibit the viability of HepG2 cells. AgNPs (40, 80, 160 μg/mL) could cause cell cycle arrest in G2/M phase and significantly increase the apoptosis rate in HepG2 cells after exposure for 24 or 48 h, especially suspended in deionized water. The results showed that AgNPs possessed cytotoxic effects to HepG2 cells with a time/dose-dependent manner. The cytotoxicity was also affected by the dispersion media of AgNPs.
银纳米颗粒对HepG2细胞毒性的影响
本研究以人肝癌细胞株(HepG2)为实验对象,研究了悬浮在不同溶剂中的银纳米颗粒(AgNPs)对细胞的毒性作用。MTT法检测细胞的增殖活性。流式细胞术分析AgNPs对细胞周期和凋亡的影响。AgNPs在不同分散介质(去离子水、PBS、生理盐水和细胞培养基)中的电离情况不同,去离子水中银离子浓度最高。AgNPs可抑制HepG2细胞的活力。AgNPs(40、80、160 μg/mL)暴露于HepG2细胞24、48 h后可使细胞周期阻滞在G2/M期,并显著提高细胞凋亡率,其中去离子水悬浮效果更明显。结果表明,AgNPs对HepG2细胞具有时间/剂量依赖性的细胞毒作用。细胞毒性也受AgNPs分散介质的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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