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Title: Preparation of biological tissue for determination of arsenic and selenium by graphite furnace atomic absorption spectrometry

Journal Article · · Anal. Chem.; (United States)
DOI:https://doi.org/10.1021/ac00141a034· OSTI ID:6426158

A great deal of interest has been generated in the measurement of selenium in biological tissue. Consequently, a method was needed for the digestion of large numbers of tissue samples (mainly eggs and liver of avian species) for arsenic and selenium analysis. Several wet digestion methods are described for the solubilizing of biological tissues and perchloric acid is often used in these procedures. However, this acid can be dangerous and particularly so in the presence of organic material. To avoid the use of perchloric acid, the authors have used an open flask digestion method which involves the careful evaporation of a 20-mL nitric acid/tissue solution down to 3 mL, directly on a hot plate. The authors have overcome many of the shortcomings of this method through a modification of the nitric acid digestion method in which hydrogen peroxide is added during the digestion process to enhance the solubilizing of the biological tissue. Samples solubilized in this manner were then quantified directly for arsenic and/or selenium by using graphite furnace atomic absorption spectrometry (GFAAS) with Zeeman background correction. The authors were able to have the method for selenium independently verified by stable isotope dilution mass spectrometry (SIDMS). The lower limit of detection, based on a 0.5-g subsample (wet weight) and a 25-mL final volume dilution, was 0.10 pp for both arsenic and selenium. The lower limit of detection, based on a 0.25-g subsample (dry weight) and a 50-mL final volume dilution, was 0.40 ppm for the two elements.

Research Organization:
Fish and Wildlife Service, Laurel, MD
OSTI ID:
6426158
Journal Information:
Anal. Chem.; (United States), Vol. 59:14
Country of Publication:
United States
Language:
English