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The determination of methylmercury in biological samples by HPLC coupled to ICP‐MS detection
Authors:Daniel S Vidler  Richard O Jenkins  John F Hall  Chris F Harrington
Institution:1. De Monfort University, School of Allied Health Sciences, Faculty of Health and Life Sciences, Leicester LE1 9BH, UK;2. University of Leicester, Cancer Biomarkers and Prevention Group, Biocentre, University Road, Leicester UK LE1 7RH
Abstract:The use of high‐performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP‐MS) for the determination of methylmercury (MeHg+) in fish tissue and hair samples is described. Analysis of these sample types is required when carrying out biomonitoring studies to determine human dietary exposure to this toxic mercurial compound. The developed method used a mobile phase containing an organic modifier and a sulfydryl compound (1:1 v/v methanol:water containing 0.01% v/v 2‐mercaptoethanol) to limit peak tailing and aid separation. The chromatographic separation was coupled to the ICP‐MS detector via a short piece of PEEK tubing, attached to the nebulizer. A cooled spraychamber and oxygen addition post‐nebulization were required to limit the solvent loading on the plasma and reduce carbon build‐up on the cones, respectively. The sample preparation procedure employed a drying step followed by digestion of the sample using tetramethylammonium hydroxide (TMAH) and heating in an open vessel microwave system. Two fish tissue certified reference materials (CRM), tuna fish CRM 463 and 464 (BCR, Brussels), a tuna fish proficiency test sample, IMEP‐20 (IRMM, Geel, Belgium) and a hair CRM NIES no. 13 (National Institute of Environmental Science, Japan), were used to evaluate the method. The recovery of MeHg+ for these four materials was between 83 and 100%, with precisions better than 6% for three separate extractions of the different materials. The limit of quantitation for MeHg+ using the developed protocol was 0.5 µg Hg g?1. The stability of MeHg+ in the fish sample extracts was also assessed and losses of 14–16% were observed after storage of the extracts in a refrigerator at 5 °C, in high‐density polypropylene tubes, for 6 months. The developed protocol has been used previously with atmospheric pressure ionization mass spectrometry (API‐MS) to provide structural characterization and also with calibration via isotope dilution (IDMS) to provide high accuracy quantitation. Copyright © 2006 John Wiley & Sons, Ltd.
Keywords:biomonitoring  elemental speciation  methylmercury  hair  fish tissue  HPLC‐ICP‐MS
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