Gray Evan P, Browning Cynthia L, Vaslet Charles A, Gion Kyle D, Green Allen, Liu Muchun, Kane Agnes B, Hurt Robert H
The Department of Civil Environmental and Construction Engineering, Texas Tech University, Lubbock, TX, 79409, USA.
Department of Pathology and Laboratory Medicine, Brown University, Providence, RI 02912, USA.
Small. 2020 May;16(21):e2000303. doi: 10.1002/smll.202000303. Epub 2020 Mar 19.
Many layered crystal phases can be exfoliated or assembled into ultrathin 2D nanosheets with novel properties not achievable by particulate or fibrous nanoforms. Among these 2D materials are manganese dioxide (MnO ) nanosheets, which have applications in batteries, catalysts, and biomedical probes. A novel feature of MnO is its sensitivity to chemical reduction leading to dissolution and Mn release. Biodissolution is critical for nanosafety assessment of 2D materials, but the timing and location of MnO biodissolution in environmental or occupational exposure scenarios are poorly understood. This work investigates the chemical and colloidal dynamics of MnO nanosheets in biological media for environmental and human health risk assessment. MnO nanosheets are insoluble in most aqueous phases, but react with strong and weak reducing agents in biological fluid environments. In vitro, reductive dissolution can be slow enough in cell culture media for MnO internalization by cells in the form of intact nanosheets, which localize in vacuoles, react to deplete intracellular glutathione, and induce cytotoxicity that is likely mediated by intracellular Mn release. The results are used to classify MnO nanosheets within a new hazard screening framework for 2D materials, and the implications of MnO transformations for nanotoxicity testing and nanosafety assessment are discussed.
许多层状晶体相可以被剥离或组装成超薄二维纳米片,这些纳米片具有颗粒状或纤维状纳米形式无法实现的新特性。在这些二维材料中,二氧化锰(MnO)纳米片在电池、催化剂和生物医学探针方面有应用。MnO的一个新特性是其对化学还原的敏感性,会导致溶解和锰释放。生物溶解对于二维材料的纳米安全性评估至关重要,但在环境或职业暴露场景中,MnO生物溶解的时间和位置却知之甚少。这项工作研究了生物介质中MnO纳米片的化学和胶体动力学,以进行环境和人类健康风险评估。MnO纳米片在大多数水相中不溶,但在生物流体环境中会与强还原剂和弱还原剂发生反应。在体外,在细胞培养基中还原溶解可能足够缓慢,使得细胞能够以完整纳米片的形式内化MnO,这些纳米片定位于液泡中,消耗细胞内的谷胱甘肽,并诱导可能由细胞内锰释放介导的细胞毒性。这些结果被用于在二维材料的新危害筛选框架内对MnO纳米片进行分类,并讨论了MnO转化对纳米毒性测试和纳米安全性评估的影响。