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dc.contributor.authorPushie, M.J.
dc.contributor.authorSylvain, N.J.
dc.contributor.authorHou, H.
dc.contributor.authorHackett, Mark
dc.contributor.authorKelly, M.E.
dc.contributor.authorWebb, S.M.
dc.date.accessioned2023-08-15T05:41:49Z
dc.date.available2023-08-15T05:41:49Z
dc.date.issued2022
dc.identifier.citationPushie, M.J. and Sylvain, N.J. and Hou, H. and Hackett, M.J. and Kelly, M.E. and Webb, S.M. 2022. X-ray fluorescence microscopy methods for biological tissues. Metallomics. 14 (6): ARTN mfac032.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/92982
dc.identifier.doi10.1093/mtomcs/mfac032
dc.description.abstract

Synchrotron-based X-ray fluorescence microscopy is a flexible tool for identifying the distribution of trace elements in biological specimens across a broad range of sample sizes. The technique is not particularly limited by sample type and can be performed on ancient fossils, fixed or fresh tissue specimens, and in some cases even live tissue and live cells can be studied. The technique can also be expanded to provide chemical specificity to elemental maps, either at individual points of interest in a map or across a large field of view. While virtually any sample type can be characterized with X-ray fluorescence microscopy, common biological sample preparation methods ( often borrowed from other fields, such as histology ) can lead to unforeseen pitfalls, resulting in altered element distributions and concentrations. A general overview of sample preparation and data-acquisition methods for X-ray fluorescence microscopy is presented, along with outlining the general approach for applying this technique to a new field of investigation for prospective new users. Considerations for improving data acquisition and quality are reviewed as well as the effects of sample prepa- ration, with a particular focus on soft tissues. The effects of common sample pretreatment steps as well as the underlying factors that govern which, and to what extent, specific elements are likely to be altered are reviewed along with common artifacts observed in X-ray fluorescence microscopy data.

dc.languageEnglish
dc.publisherOXFORD UNIV PRESS
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiochemistry & Molecular Biology
dc.subjectX-ray fluorescence microscopy
dc.subjectmapping
dc.subjectimaging
dc.subjectXFI
dc.subjectXFM
dc.subjectbiological samples
dc.subjectchemical speciation
dc.subjectALZHEIMERS-DISEASE
dc.subjectK-EDGE
dc.subjectCOPPER
dc.subjectMOUSE
dc.subjectTRANSMISSION
dc.subjectSCRAPIE
dc.subjectIRON
dc.subjectCU
dc.subjectMICROANALYSIS
dc.subjectMECHANISMS
dc.subjectX-ray fluorescence microscopy
dc.subjectXFI
dc.subjectXFM
dc.subjectbiological samples
dc.subjectchemical speciation
dc.subjectimaging
dc.subjectmapping
dc.subjectMicroscopy, Fluorescence
dc.subjectProspective Studies
dc.subjectSpectrometry, X-Ray Emission
dc.subjectSynchrotrons
dc.subjectTrace Elements
dc.subjectX-Rays
dc.subjectTrace Elements
dc.subjectMicroscopy, Fluorescence
dc.subjectSpectrometry, X-Ray Emission
dc.subjectProspective Studies
dc.subjectSynchrotrons
dc.subjectX-Rays
dc.titleX-ray fluorescence microscopy methods for biological tissues
dc.typeJournal Article
dcterms.source.volume14
dcterms.source.number6
dcterms.source.issn1756-5901
dcterms.source.titleMetallomics
dc.date.updated2023-08-15T05:41:46Z
curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.accessStatusOpen access via publisher
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidHackett, Mark [0000-0002-3296-7270]
curtin.identifier.article-numberARTN mfac032
dcterms.source.eissn1756-591X
curtin.contributor.scopusauthoridHackett, Mark [35240056500] [57999521300]
curtin.repositoryagreementV3


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