Numéro |
J. Phys. IV France
Volume 104, March 2003
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Page(s) | 321 - 324 | |
DOI | https://doi.org/10.1051/jp4:200300090 |
J. Phys. IV France 104 (2003) 321
DOI: 10.1051/jp4:200300090
Imaging and quantification of trace metals in thin biological specimens using microprobe techniques: Synchrotron induced X-ray fluorescence microprobe and nuclear microprobe
T. Pinheiro1, L.C. Alves1, A. Barreiros2, F. Araujo1, S. Bohic3 and A. Simionovici31 ITN-Instituto Tecnologico e Nuclear, E.N. 10, 2685-953 Sacavém, Portugal
2 INETI, Instituto National de Engenharia e Tecnologia Industrial, Az. Lameiros, 1649-038 Lisboa, Portugal
3 ESRF, European Synchrotron Radiation Facility, BP. 220, 38043 Grenoble cedex, France
Abstract
The combination of Synchrotron X-Ray Fluorescence microprobe (SXRF) with other micro-analytical
techniques based on accelerated particle beams. such as Rutherford Backscattering Spectrometry (RBS), and
Particle Induced X-ray Emission (PIXE) enable to quantify SXRF results of thin biological specimens. The same
specimens were analysed by both techniques. The average thickness calculated by RBS of discrete tissue regions in
equivalent sample sections was used to normalise SXRF data. Analysing the same sample region with PIXE
technique, simultaneously to RBS, can validate the methodology once it will enable to compare concentrations
obtained for elements that are detected by both SXRF and PIXE. Major departures were found for the quantification
of Ca and Ti. For Cr and Fe a good agreement was found between both micro-analytical techniques. Differences
below 20% were obtained for the majority of the elements and samples analysed. The procedure can be applied to
produce quantitative elemental maps and it will be advantageous to quantify toxic elements present at low
concentrations in tissues, such as Cr, Ni and Pb, which can only be efficiently assessed by SXRF.
© EDP Sciences 2003