Determination of mercury in biological fluids by potentiometric stripping analysis

A method is described for the determination of mercury by potentiometric stripping analysis. The analyte, Hg(2+), is employed for oxidizing a fixed amount of cadmium, previously reduced and amalgamated at a thin mercury film preplated on a glassy carbon electrode. The cadmium stripping signal correlates well with the amount of Hg(2+) added. Correlation coefficients of 0.9971 and 0.9960 were obtained for the two working ranges: (25 ng-2.5 microg) and (5.0-50) microg Hg(2+), respectively, in spiked water samples. The method was investigated with respect to precision and accuracy by spiking a natural water sample with 25 microg Hg(2+).Nine replicate determinations gave a mean value of 24.8 microg with a standard deviation +/-0.31 microg. The 95% confidence limit of the mean suggested the absence of systematic errors. Using the highest possible sensitivity, detection limits of 2.0 ng (167 ng/l) and 0.5 ng (4.2 ng/100 ml of whole blood) were obtained in water and blood samples, respectively. The applicability of the method was successfully extended to include the more complex matrices after recording a zero blank from authentic samples spiked with Cd(2+) (25 microg).The described PSA procedure is a simple and rapid method compared with the cold-vapor technique, with a 5.2% and 4.9% RSD, respectively.