Abstract

This work presents a capillary electrophoresis methodology for the enantiodetermination of cathinones in urine employing a liquid-liquid extraction sample pretreatment. The cathinones were enantioseparated by adding a mixture of 8mM 2-hydroxypropyl β-cyclodextrin and 5mM β-cyclodextrin to the background electrolyte, which consists of 70mM of monosodium phosphate aqueous solution at pH 2.5. Field-amplified sample injection was used as preconcentration strategy to improve the sensitivity. We studied various parameters that affect this stacking strategy, in particular, the sample solvent and its pH, the presence or absence of a low conductivity solvent plug introduced before the sample injection, the nature and volume of this plug, and the voltage and time of the electrokinetic injection of the sample. The optimum conditions were achieved by injecting a plug of isopropanol:H2 O 50/50 at 50mbar for 5s prior to the electrokinetic injection of the sample prepared in an aqueous solution of HCl 10-6 M. The sensitivity enhancement factors were from 562 to 601 in terms of peak area and from 444 to 472 in terms of peak height. The method was validated by analyzing spiked urine samples, obtaining a linear range of 25 to 1000ng/mL and limits of detection ranging from 15 to 45ng/mL.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call