Abstract
Nedocromil sodium (an antiasthma drug) and pentamidine isethionate (an antiprotozoal agent) were determined in urine by cathodic stripping voltammetry after adsorptive accumulation at a hanging mercury drop electrode as examples of the use of solid-phase extraction cartridges with this technique. Prior separation from matrix interferents was necessary and this was carried out using either a C18 solid-phase extraction cartridge or liquid–liquid extraction. For nedocromil, a recovery of 100.5 ± 6.5%(± 2 standard deviations) was obtained from urine spiked with 0.42 µg ml–1 of the drug using a C18 cartridge (five determinations). A 97% recovery of pentamidine isethionate was obtained by solid-phase extraction when the drug was added to urine at a level of 1.48 µg ml–1. At lower levels of pentamidine isethionate, better recovery was obtained using liquid–liquid extraction: recoveries of between 60 and 100% were obtained at levels of 0.04–29.6 µg ml–1. Linear calibration graphs were obtained for the determination of both drugs at concentration levels in the measured solution lower than 1 × 10–7 mol l–1(i.e., less than approximately 0.05 µg ml–1): standard additions method was preferred for quantification. Relative standard deviations of 4.5% for the determination of pentamidine isethionate and of 5.2% for the determination of nedocromil (n= 5) were obtained for urine samples containing 2.96 µg ml–1 of pentamidine isethionate and 0.42 µg ml–1 of nedocromil.
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