Abstract

Probe electrospray ionization (PESI) is an ambient ionization mass spectrometry technique (AIMS) that is primarily used in qualitative studies, though researchers have recently combined it with sample preparation for the quantitative analysis of various analytes in biological matrices. This study presents a method that integrates solid-phase microextraction with PESI for direct coupling to a triple quadrupole mass spectrometer, and examines its ability to quantitate drugs of abuse. Intra- and inter-probe reproducibility experiments were conducted to assess the stability and reproducibility of the extraction-phase-coated PESI probes (coating length: 2 mm; coating thickness: 6.5 μm). This research is the first documented instance wherein highly sensitive determinations were successfully attained using these microextraction and micro-desorption techniques in conjunction with small volumes of sample and extraction phase. A mixture consisting of IPA/H2O (1/1 v/v) + 0.1% FA was determined to be the optimal desorption solvent for SPME-PESI-MS/MS, as it facilitated high analyte enrichment in a picolitre of the solvent, which acted at the same time as efficient electrospray media. Furthermore, a method of quantifying drugs of abuse in 30 μL of plasma without matrix modification was also developed. This method had an intra-day accuracy within the 80–120% range for all eight drugs of abuse at concentrations of 3, 30, and 90 pg μL−1; the exception to this result was lorazepam at 30 pg μL−1, which had an intra-day accuracy of 122%. The lower limit of quantification (LLOQ) for fentanyl and nordiazepam was pg μL−1; the LLOQ for buprenorphine, codeine, diazepam, lorazepam, and propranolol was 5 pg μL−1; and the LLOQ of oxazepam was 10 pg μL−1.

Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.