Gas chromatographic–mass spectrometric analysis of dichlorobenzene isomers in human blood with headspace solid-phase microextraction

Abstract\n\t\t\t\t\n\t\t\t\t\tHeadspace solid-phase microextraction (HS-SPME) was utilized for the determination of three dichlorobenzene isomers (DCBs) in human blood. In the headspace at 30°C, DCBs were absorbed for 15 min by a 100-μm polydimethylsiloxane (PDMS) fiber. They were then analyzed by capillary column gas chromatography–mass spectrometry (GC–MS). By setting the initial column oven temperature at 20°C, the three isomers were resolved at the baseline level. \n\t\t\t\t\t\tp-Xylene-d\n\t\t\t\t\t\t10 was used as the internal standard (I.S.). For quantitation, the molecular ion at \n\t\t\t\t\t\tm/\n\t\t\t\t\t\tz 146 for each isomer and the molecular ion at \n\t\t\t\t\t\tm/\n\t\t\t\t\t\tz 116 for I.S. were selected. For day-to-day precision, relative standard deviations in the range 3.2–10.7% were found at blood concentrations of 1.0 and 10 μg/ml. Each compound was detectable at a level of at least 0.02 μg per 1 g of whole blood (by full mass scanning). HS-SPME–GC–MS, when performed at relatively low temperatures, was found to be feasible in toxicological laboratories. Using this method, the plasma levels of one patient who had drunk a pesticide-like material were measured.