二硫化钼
氮化硼
纳米材料
细胞毒性
流出
化学
钼
硼
无机化学
核化学
材料科学
冶金
纳米技术
生物化学
有机化学
体外
作者
Su Liu,Zhuoyan Shen,Bing Wu,Yue Yu,Hui Hou,Xuxiang Zhang,Hongqiang Ren
标识
DOI:10.1021/acs.est.7b02463
摘要
Sheetlike molybdenum disulfide (MoS2) and boron nitride (BN) nanomaterials have attracted attention in the past few years due to their unique material properties. However, information on adverse effects and their underlying mechanisms for sheetlike MoS2 and BN nanomaterials is rare. In this study, cytotoxicities of sheetlike MoS2 and BN nanomaterials on human hepatoma HepG2 cells were systematically investigated at different toxic end points. Results showed that MoS2 and BN nanomaterials decreased cell viability at 30 μg/mL and induced adverse effects on intracellular ROS generation (≥2 μg/mL), mitochondrial depolarization (≥4 μg/mL), and membrane integrity (≥8 μg/mL for MoS2 and ≥2 μg/mL for BN). Furthermore, this study first found that low exposure concentrations (0.2–2 μg/mL) of MoS2 and BN nanomaterials could increase plasma membrane fluidity and inhibit transmembrane ATP binding cassette (ABC) efflux transporter activity, which make both nanomaterials act as a chemosensitizer (increasing arsenic toxicity). Damage to plasma membrane and release of soluble Mo or B species might be two reasons that both nanomaterials inhibit efflux pump activities. This study provides a systematic understanding of the cytotoxicity of sheetlike MoS2 and BN nanomaterials at different exposure levels, which is important for their safe use.
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