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解析 CeO 纳米颗粒在亚铁离子和硫离子存在下对大肠杆菌的影响:物理化学转化诱导的毒性和解毒机制。

Deciphering the effects of CeO nanoparticles on Escherichia coli in the presence of ferrous and sulfide ions: Physicochemical transformation-induced toxicity and detoxification mechanisms.

机构信息

Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes, Ministry of Education, Hohai University, Nanjing 210098, People's Republic of China; College of Environment, Hohai University, 1 Xikang Road, Nanjing 210098, People's Republic of China.

College of Agricultural Engineering, Hohai University, Nanjing 210098, People's Republic of China.

出版信息

J Hazard Mater. 2021 Jul 5;413:125300. doi: 10.1016/j.jhazmat.2021.125300. Epub 2021 Feb 6.

DOI:10.1016/j.jhazmat.2021.125300
PMID:33578093
Abstract

The physicochemical transformations as well as the redox reaction-induced toxicity changes of ceria nanoparticles (CeO NPs) in reducing conditions is extremely lacking. Herein, the behaviors, chemical modifications and toxicity of CeO NPs in the presence of reduction-active ions (namely Fe and S) were investigated, with a particular emphasis on the cytotoxicity mechanism associated with their physicochemical transformations. The presence of Fe and S differently altered the surface properties and toxicity of CeO NPs. Redox reactions with Fe led to form small aggregates, boosted the reduction of CeO and enhanced dissolved Ce concentration. Moreover, CeO NPs possessed a high affinity for Escherichia coli (E. coli) and induced the generation of •OH abiotically after reaction with Fe, provoking serious disruption of cell membranes and causing high toxicity to E. coli. In contrast, the amending of S protected E. coli from direct contact with CeO NPs by creating new CeS precipitated on the surface, accelerating the aggregation of NPs and reducing the concentration of dissolved Ce. This study suggested that the chemical interactions between the reactive surfaces of CeO and reduction-active ions highly determined the stability and cytotoxicity of CeO NPs, which provides fundamental insights into the environmental risks of CeO NPs.

摘要

在还原条件下,氧化铈纳米颗粒(CeO NPs)的物理化学转化以及氧化还原反应诱导的毒性变化极其缺乏。在此,研究了还原活性离子(即 Fe 和 S)存在下 CeO NPs 的行为、化学修饰和毒性,特别强调了与其物理化学转化相关的细胞毒性机制。Fe 和 S 的存在以不同的方式改变了 CeO NPs 的表面性质和毒性。与 Fe 的氧化还原反应导致形成小的聚集物,促进 CeO 的还原并增加溶解的 Ce 浓度。此外,CeO NPs 对大肠杆菌(E. coli)具有高亲和力,并在与 Fe 反应后产生•OH,严重破坏细胞膜并对 E. coli 造成高毒性。相比之下,S 的添加通过在表面上形成新的 CeS 沉淀来保护大肠杆菌免受 CeO NPs 的直接接触,加速 NPs 的聚集并降低溶解的 Ce 浓度。本研究表明,CeO 与还原活性离子的反应表面之间的化学相互作用高度决定了 CeO NPs 的稳定性和细胞毒性,为 CeO NPs 的环境风险提供了基本的认识。

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