This study describes a method for the screening of metylenedioxyamphetamine- and piperazine-derived compounds in urine by LC-MS/MS. These substances, characterized by possessing common moieties, are screened using precursor ion and neutral loss scan mode and then quantified in MRM acquisition mode. Based on the product-ion spectra (PIS) of different known molecules, chosen as “model”, characteristic neutral losses and product ions were selected: piperazines were detected in precursor ion scan of m/z 44 and neutral loss of 43 and 86 while amphetamines in precursor ion scan of m/z 133, 135 and 163. The applicability of the screening approach was studied in blank urine spiked with selected analytes and processed by SPE. Linearity, matrix effect, precision, accuracy, LODs and LOQs were evaluated both for the screening and the quantification methods. The ability of the screening method to provide semi-quantitative data was demonstrated. This method appears to be an useful tool for the identification of designer drugs derived from piperazines or metylenedioxyamphetamines and can be potentially applied to other drug classes.[...]

Screening of methylenedioxyamphetamine- and piperazine-derived designer drugs in urine by LC-MS/MS using neutral loss and precursor ion scan.

SERGI, Manuel;DEL CARLO, MICHELE;COMPAGNONE, DARIO;
2013-01-01

Abstract

This study describes a method for the screening of metylenedioxyamphetamine- and piperazine-derived compounds in urine by LC-MS/MS. These substances, characterized by possessing common moieties, are screened using precursor ion and neutral loss scan mode and then quantified in MRM acquisition mode. Based on the product-ion spectra (PIS) of different known molecules, chosen as “model”, characteristic neutral losses and product ions were selected: piperazines were detected in precursor ion scan of m/z 44 and neutral loss of 43 and 86 while amphetamines in precursor ion scan of m/z 133, 135 and 163. The applicability of the screening approach was studied in blank urine spiked with selected analytes and processed by SPE. Linearity, matrix effect, precision, accuracy, LODs and LOQs were evaluated both for the screening and the quantification methods. The ability of the screening method to provide semi-quantitative data was demonstrated. This method appears to be an useful tool for the identification of designer drugs derived from piperazines or metylenedioxyamphetamines and can be potentially applied to other drug classes.[...]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11575/16902
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