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Mechanistic insights into nanotoxicity determined by synchrotron radiation-based Fourier-transform infrared imaging and multivariate analysis

机译:通过基于同步加速器辐射的傅立叶变换红外成像和多元分析确定的纳米毒性机理

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Our ability to identify the mechanisms by which carbon-based nanomaterials (CBNs) exert toxicity in cells is constrained by the lack of standardized methodologies to assay endpoint effects. Herein we describe a method of mechanistically identifying the effects of various CBN types in both prokaryotic and eukaryotic cells using multi-beam synchrotron radiation-based Fourier-transform infrared imaging (SR-FT1RI) at diffraction-limited resolution. This technique overcomes many of the inherent difficulties of assaying nanotoxicity and demonstrates exceptional sensitivity in identifying the effects of CBNs in cells at environmentally-relevant concentrations. We identify key mechanisms of nanotoxicity as the alteration of Amide and lipid biomolecules, but propose more specific bioactivity of CBNs occurs as a result of specific interactions between CBN structural conformation and cellular characteristics.
机译:我们缺乏确定终点效应的标准化方法,因此无法确定碳基纳米材料(CBN)在细胞中发挥毒性作用的机制。本文中,我们描述了一种基于衍射限制分辨率的基于多光束同步加速器辐射的傅立叶变换红外成像(SR-FT1RI)机械识别各种CBN类型在原核和真核细胞中作用的方法。这项技术克服了许多测定纳米毒性的内在困难,并证明了在鉴定与环境相关浓度的细胞中CBNs效应时的出色灵敏度。我们确定纳米毒性的关键机制为酰胺和脂质生物分子的改变,但由于CBN结构构象与细胞特征之间的特异性相互作用,CBNs的生物活性更强。

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