L. Dunemann et al., Simultaneous determination of Hg(II) and alkylated Hg, Pb, and Sn species in human body fluids using SPME-GC/MS-MS, FRESEN J AN, 363(5-6), 1999, pp. 466-468
A GC/MS-MS method for the determination of Hg(II) and alkylated Hg, Pb, and
So species in human urine is described. Separation and identification of t
he metal species are performed by capillary gas chromatography coupled with
an ion-trap mass spectrometer with electron impact ionization in the tande
m-MS mode. For sample preparation a very promising technique was applied th
at is based on a derivatization with sodium tetraethylborate followed by he
adspace solid phase microextraction (SPME). Operation of the used ion trap
in the tandem-MS mode yields in improved detection limits because of a sign
al-to-noise ratio that is at least one order of magnitude better than in th
e MS mode. The detection limits in real matrices like urine are between 7 a
nd 22 ng/L for all species investigated. Urinary levels of inorganic Hg in
non-occupationally exposed persons with and without dental amalgam were fou
nd to be between 0.1 and 1.4 mu g/L. A reference material ("ClinRep, Level
I") was used for quality assurance. Compared to the coupling of GC with ICP
-MS ("inorganic" MS), the advantage of the proposed method using an "organi
c" MS is that (i) the species can be directly identified via their precurso
r and daughter ions and (ii) analysis can be performed with a commercially
available hyphenated technique at moderate costs and needs no lab-made inte
rfacing. Moreover, it offers a real multi-element/multi-species capability
with low detection limits and a minimum of sample preparation.