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Bio-metals imaging and speciation in cells using proton and synchrotron radiation X-ray microspectroscopy

机译:使用质子和同步辐射X射线显微光谱法对细胞中的生物金属成像和物种形成

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摘要

The direct detection of biologically relevant metals in single cells and of their speciation is a challenging task that requires sophisticated analytical developments. The aim of this article is to present the recent achievements in the field of cellular chemical element imaging, and direct speciation analysis, using proton and synchrotron radiation X-ray micro- and nano-analysis. The recent improvements in focusing optics for MeV-accelerated particles and keV X-rays allow application to chemical element analysis in subcellular compartments. The imaging and quantification of trace elements in single cells can be obtained using particle-induced X-ray emission (PIXE). The combination of PIXE with backscattering spectrometry and scanning transmission ion microscopy provides a high accuracy in elemental quantification of cellular organelles. On the other hand, synchrotron radiation X-ray fluorescence provides chemical element imaging with less than 100 nm spatial resolution. Moreover, synchrotron radiation offers the unique capability of spatially resolved chemical speciation using micro-X-ray absorption spectroscopy. The potential of these methods in biomedical investigations will be illustrated with examples of application in the fields of cellular toxicology, and pharmacology, bio-metals and metal-based nano-particles.
机译:直接检测单细胞中的生物相关金属及其形态是一项艰巨的任务,需要复杂的分析开发。本文的目的是介绍使用质子和同步加速器辐射X射线显微和纳米分析在细胞化学元素成像和直接形态分析领域中的最新成就。 MeV加速粒子和keV X射线聚焦光学器件的最新改进允许应用于亚细胞区室的化学元素分析。单个细胞中微量元素的成像和定量可以使用粒子诱导的X射线发射(PIXE)获得。 PIXE与背向散射光谱法和扫描透射离子显微镜相结合,可为细胞器的元素定量提供高精度。另一方面,同步加速器辐射X射线荧光可以提供小于100 nm空间分辨率的化学元素成像。此外,同步加速器辐射提供了使用微X射线吸收光谱法进行空间分辨的化学形态形成的独特功能。这些方法在生物医学研究中的潜力将通过在细胞毒理学,药理学,生物金属和金属基纳米粒子领域的应用实例加以说明。

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