Abstract

A liquid chromatography–inductively coupled plasma mass spectrometric (LC–ICP-MS) method for lead and mercury speciation analysis was described. Sample containing ionic lead and mercury compounds was subjected to liquid chromatographic separation before injection into the direct injection high efficiency nebulizer (DIHEN, 170-AA). The species studied include inorganic lead (Pb(II)), trimethyl lead (trimethyl-Pb), triethyl lead (triethyl-Pb), inorganic mercury (Hg(II)), methyl mercury (methyl-Hg) and ethyl mercury (ethyl-Hg), which were well separated by reversed-phase liquid chromatography with a C18 column as the stationary phase and a pH 2.8 solution of 0.2% (v/v) 2-mercaptoethanol, 1 mg L −1 ETDA, 174.2 mg L −1 sodium 1-pentanesulfonate and 12% (v/v) methanol as the mobile phase. The lead and mercury species in biological tissues were quantitatively extracted, into 10 g L −1 EDTA and 0.2% (v/v) 2-mercaptoethanol solution taken in a closed centrifuge tube and kept on water bath, using microwaves at 65 °C for 2 min. The spike recovery of individual lead and mercury species determined by spiking the samples with suitable concentration of lead and mercury mixture standard were between 93% and 99%. The detection limits of the species studied were in the range 0.1–0.3 μg Pb L −1 and 0.2–0.3 μg Hg L −1. The procedure has been applied for the speciation analysis of two reference samples namely NRCC DOLT-3 Dogfish Liver and DORM-2 Dogfish Muscle and a swordfish sample obtained locally. The sum of the concentrations of individual species has been compared with the certified values for total lead and mercury to verify the accuracy of the method. The precision between sample replicates was better than 10% with LC–DIHEN-ICP-MS method.

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