SummaryA gas chromatographic method for the analysis of nine organochlorine pesticides in wildlife plasma is described. Reversed-phase solid phase extraction is utilized to extract the organochlorine pesticides from plasma. This is followed by a normal phase solid phase extraction clean-up as the pesticides are recovered by elution with hexane:ethyl ether (1:l) and quantified by gas chromatography/electron capture detection. Method limits of detection range from 7.0-25 pg/L. The mean recovery for all pesticides is 81%.
A fast and sensitive LC-MS method was developed for the simultaneous analysis of 11 cyanotoxins in drinking water. The toxins in this method included eight microcystins, as well as nodularin, anatoxin-a, and cylindrospermopsin. Sample processing involved a small sample volume and a direct dilution procedure that could be performed in minutes rather than hours using traditional SPE procedures. This method also featured a short acquisition time of 12 min with an adequate separation of all analytes. Validation results demonstrated good sensitivity with LODs <100 ng/L and good precision (RSD < 20%) and accuracy. Analyte stability was also thoroughly studied. The matrix effect was minimal, and tap water used for calibrators and controls. No sample carryover was observed after the highest concentration calibrator.
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