Abstract

Methods are described for the accurate and precise determination of total lead and its isotopic composition in whole blood using inductively coupled plasma source mass spectrometry (ICP-MS). The sample preparation is a simple 1 + 24 dilution of blood (400 µl for total lead; 2000 µl for isotope ratios) using a diluent containing ammonia solution, (NH4)2H2EDTA, NH4H2PO4 and Triton X-100, which allows prolonged pneumatic aerosol generation without blockage of the Meinhard nebuliser.Sensitivities of up to 3 × 106 counts s–1 for 208Pb at a total lead concentration of 5 µmol l–1(1 µg ml–1) enabled total blood lead levels to be measured in 4 min per sample, with a detection limit of 0.072 µmol l–1(15 µg l–1). The agreement between ICP-MS and atomic absorption spectrometry (AAS) for this analysis was excellent: ICP-MS = 0.996 × AAS – 0.0165 µmol l–1; r= 0.994.Isotope ratio measurements required 15 min to achieve the required accuracy and precision both of which were generally better than 0.5% for 206Pb : 207Pb and 208Pb : 206Pb isotopic lead ratios. The ICP-MS data for these ratios in ten quality control blood specimens had a mean bias relative to isotope dilution mass spectrometry of –0.412% for 206Pb : 207Pb ratios and of +0.055% for the 208Pb : 206Pb ratios. This level of accuracy and that of the total blood lead measurements is sufficient to permit application of these ICP-MS methods to environmental studies.

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