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PMID: 3199227 Published · ppublish English Journal Article

Quantitative X-ray microanalysis of biological specimens.

Journal of electron microscopy technique ·Vol. 9 ·No. 1 ·1988-05-00 ·Pages 19-43

Roomans GM

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.

MeSH Terms
Animals Electron Probe Microanalysis/standards Freeze Drying Frozen Sections Humans
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Roomans G M
Department of Ultrastructure Research, Wenner-Gren Institute, University of Stockholm, Sweden.
Article Info
Journal
Journal of electron microscopy technique
Abbr.
J Electron Microsc Tech
ISSN
0741-0581
Published
1988-05-00
Pages
19-43
Language
English
Region
United States
NLM ID
8502171
Subset
IM
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