VALIDATION OF A LIQUID-CHROMATOGRAPHY POSTCOLUMN DERIVATIZATION ASSAY FOR THE DETERMINATION OF CISPLATIN IN PLASMA

Method validation results are described for a cisplatin LC post-column derivatization assay. Cisplatin plasma samples were treated with acetonitrile and a citrate buffer solution to enhance cisplatin stability. Processed samples were analysed on a chemically generated anion exchange column using a customized post-column derivatization platform and refrigerated autosampler. The UV response was monitored at 290 nm. The retention time of cisplatin was 9 min. The assay was linear from 0.06 to 30.0 mug ml-1 (r > = 0.998) with inter-run precisions (RSD) of 8.2% (n = 8), 5.9% (n = 8) and 4.0% (n = 8) for low (0.18 mug ml-1), medium (1.5 mug ml-1) and high (24.0 mug ml-1) quality control samples, respectively. The validated assay was used to monitor cisplatin levels in cisplatin drug interaction studies.