Elsevier

Analytica Chimica Acta

Volume 140, Issue 1, 1 August 1982, Pages 221-227
Analytica Chimica Acta

Determination of selenium in small volumes of blood plasma and serum by electrothermal atomic absorption spectrometry

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Abstract

A graphite-furnace atomic absorption spectrometric method is described for the determination of selenium in blood plasma and serum. Samples are diluted (1 + 9) with a solution containing nickel and nitric acid and measured by a standard additions method. Repeatability for a serum sample containing 87 μg Se l-1 was 4.4%. The mean recovery of selenium(IV) from a human protein solution was 97.5%. The method was further tested in an interlaboratory comparison study. The standard additions procedure requires a sample volume of 200 μl and a total time of about 7.5 min. A secondary calibration graph can be used, however, resulting in increased throughput up to 13 samples per hour, and a decrease in the sample volume needed to 100 μl.

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    Citation Excerpt :

    Moreover, selenium can be present in serum in several chemical forms, and so the use of inorganic selenium as standard for spiking may lead to errors if the analytical method used does not guarantee complete atomisation of all these selenium species. However, inorganic standard selenium is mainly used for spiking [3,13–15,17,19,21,23,31,52,61,66,68] and selenomethionine is seldom added [13,19]. Interlaboratory exercises provide external evaluation of the performance and the quality of the data obtained [32,33,37,39,52,72,89].

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