Sensitivity improvements in the determination of mercury in biological tissues by neutron activation analysis |
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Authors: | C R Cornett D L Samudralwar W D Ehmann W R Markesbery |
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Institution: | (1) Department of Chemistry, University of Kentucky, 40506-0055 Lexington, KY, USA;(2) Departments of Pathology and Neurology, University of Kentucky, 40506-0230 Lexington, KY, USA;(3) Sanders-Brown Center on Aging, University of Kentucky, 40506-0230 Lexington, KY, USA |
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Abstract: | The possible association of dental amalgam surface exposure, brain mercury (Hg) levels, and pathological markers of Alzheimer's disease (AD) in the brain is the subject of an on-going study in our laboratory. Two radiochemical neutron activation analysis methods and the use of instrumental neutron activation analysis (INAA) with Compton suppression spectrometry have been evaluated for improving our INAA Hg detection limit (2.8±0.6 ng/g, wet-weight basis) in human tissue. Large numbers of samples dictated the use of a purely instrumental method or rapid, simple radiochemical separations. Human brain tissues and NIST biological standards were analyzed using a precipitation of Hg2Cl2, a solvent extraction utilizing sodium diethyldithiocarbomate, conventional INAA, and INAA with Compton suppression. The radiochemical precipitation of Hg2Cl2 proved to be the most useful method for use in our study because it provided a simultaneous, quantitative determination of silver (Ag) and a Hg detection limit in brain tissue of 1.6±0.1 ng/g (wet-weight basis). |
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