Selenium belongs to a group of trace elements of special interest in biolog
ical samples for clinical diagnosis. Selenium has antioxidizing functions a
nd is essential for providing the organism with triiodothyronine produced f
rom thyroxine.
Among several analytical techniques used to determine the Se concentration
in serum, Inductively Coupled Plasma Mass Spectrometry (ICP-MS) has been us
ed in the past because of its high sensitivity. Interference problems origi
nating from different ions on the major Se isotopes have been described to
be a limiting factor for the direct determination of Se in these matrices.
Standard addition calibration or isotope dilution is often required to over
come carbon-enhanced ionisation effects in biological sample matrices. In m
ost cases, the typical serum sample volume which is available for the analy
sis is limited to 0.5 mi or less, making multiple sample preparation for st
andard addition calibration impractical. Isotope dilution requires enriched
isotopes and substantial sample preparation. Furthermore, the approximate
Se concentration in every sample has to be known to adjust the appropriate
amount of spike to each sample. Matrix matching with methanol has been desc
ribed to overcome ionisation effects but we found limiting factors of this
application when other trace elements are also determined within one sample
run.
This paper describes an effective sample preparation method which allows th
e direct determination of Se in serum without limiting the analytical capab
ilities for the additional determination of Al, Cu, Ni, Co, Cd; Mn and Zn i
n a single sample run by ICP-MS. Optimization procedures are presented and
results of the analysis of reference samples are discussed, with a comparis
on of more than 150 serum data with those obtained by the GFAAS method.