St. Giroussi et al., SIMULTANEOUS DETERMINATION OF TETRATHIOMOLYBDATES AND MOLYBDATES IN SPIKED BLOOD-PLASMA BY DIFFERENTIAL-PULSE VOLTAMMETRY AND THEIR SPECIATION, Fresenius' journal of analytical chemistry, 356(7), 1996, pp. 452-455
A selective, sensitive and reliable voltametric method for the simulta
neous determination of MoS42- and MoO42- has been developed. The reduc
tion of HgMoS4 at - 0.43 V and the reduction of Mo as complex of MoO2-
oxine(2) at - 0.63 V in acetate buffer at pH 4.9 are utilized for the
simultaneous determination by differential pulse cathodic stripping vo
ltametry (DPCSV). Cadmium and lead form complexes with MoS42-, but do
not interfere with the determination. The limit of detection is 0.59 m
u g/l Mo for MoS42- and 1.8 mu g/l for MoO42-. The R.S.D at a concentr
ation level of 20 mu g/l is 4.7% for MoO42- and 3.6% for MoS42-. The m
ethod is applied to spiked blood plasma samples for the determination
of free tetrathiomolybdates and molybdates. Additionally, labile tetra
thiomolybdates and molybdates can be determined in spiked blood plasma
after treatment of the sample with 0.15 mol/l KCN and ultrafiltration
.