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生物标本的定量X射线微分析

Quantitative X-ray microanalysis of biological specimens.

作者信息

Roomans G M

机构信息

Department of Ultrastructure Research, Wenner-Gren Institute, University of Stockholm, Sweden.

出版信息

J Electron Microsc Tech. 1988 May;9(1):19-43. doi: 10.1002/jemt.1060090104.

Abstract

Qualitative X-ray microanalysis of biological specimens requires an approach that is somewhat different from that used in the materials sciences. The first step is deconvolution and background subtraction on the obtained spectrum. The further treatment depends on the type of specimen: thin, thick, or semithick. For thin sections, the continuum method of quantitation is most often used, but it should be combined with an accurate correction for extraneous background. However, alternative methods to determine local mass should also be considered. In the analysis of biological bulk specimens, the ZAF-correction method appears to be less useful, primarily because of the uneven surface of biological specimens. The peak-to-local background model may be a more adequate method for thick specimens that are not mounted on a thick substrate. Quantitative X-ray microanalysis of biological specimens generally requires the use of standards that preferably should resemble the specimen in chemical and physical properties. Special problems in biological microanalysis include low count rates, specimen instability and mass loss, extraneous contributions to the spectrum, and preparative artifacts affecting quantitation. A relatively recent development in X-ray microanalysis of biological specimens is the quantitative determination of local water content.

摘要

生物标本的定性X射线微分析需要一种与材料科学中所使用的方法有所不同的方法。第一步是对所获得的光谱进行反卷积和背景扣除。进一步的处理取决于标本的类型:薄的、厚的或半厚的。对于薄片,最常使用连续谱定量方法,但应结合对外部背景的精确校正。然而,也应考虑用于确定局部质量的替代方法。在生物大块标本的分析中,ZAF校正方法似乎不太有用,主要是因为生物标本表面不均匀。对于未安装在厚基板上的厚标本,峰到局部背景模型可能是一种更合适的方法。生物标本的定量X射线微分析通常需要使用标准物质,这些标准物质最好在化学和物理性质上与标本相似。生物微分析中的特殊问题包括计数率低、标本不稳定和质量损失、光谱的外部贡献以及影响定量的制备假象。生物标本X射线微分析中一个相对较新的进展是局部含水量的定量测定。

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