EventsThe 1st International Online Conference on Xenobiotics
Published
This submission belongs to the session S3. Emerging Chemicals: Environment Risks and Health Effects of the event The 1st International Online Conference on Xenobiotics
Published date
17 Jun, 2026
Academic Editor
author-avatarLin-Chi Wang
Citation
Dimitra Florou, Thaleia Vlachou, Amvrosios Orfanidis, Vasilios Sakkas, Vassiliki Boumba, FPSE–LC–MS/MS as a Reliable Tool for Quantifying Drugs of Abuse in Oral Fluid, in Proceedings of The 1st International Online Conference on Xenobiotics, 22 June–23 June 2026, MDPI: Basel, Switzerland
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FPSE–LC–MS/MS as a Reliable Tool for Quantifying Drugs of Abuse in Oral Fluid

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1. Department of Forensic Medicine and Toxicology, Faculty of Medicine, School of Health Sciences, University of Ioannina, University Campus, Ioannina 45500, Greece., Greece
2. Department of Forensic Medicine and Toxicology, Faculty of Medicine, School of Health Sciences, University of Ioannina, University Campus, 5110 Ioannina, Greece., Greece
3. Department of Analytical Chemistry, Faculty of Chemistry, University of Ioannina, 5110 Ioannina, Greece.
4. Department of Analytical Chemistry, Faculty of Chemistry, University of Ioannina, 5110 Ioannina, Greece., Greece
Abstract

The widespread use of drugs of abuse (DOA) constitutes a significant public health and social concern, highlighting the need for sensitive and reliable analytical methods particularly for alternative biological matrices. Oral fluid (OF) has emerged as a valuable matrix for the detection of recent drug intake and is extensively employed in forensic and toxicological investigations. Fabric phase sorptive extraction (FPSE) is a recently introduced sample preparation technique, characterized by simplicity, cost-effectiveness, rapidness, low solvent consumption and high analytical performance. A fully developed and validated FPSE-based method for oral fluid analysis will be presented, employing liquid chromatography–tandem mass spectrometry (LC–MS/MS) for the quantitative determination of ten commonly encountered DOA and metabolites including morphine, codeine, 6-monoacetylmorphine (6-MAM), methadone, amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine (MDA), cocaine, benzoylecgonine (BE), and ecgonine methyl ester (EME). The method demonstrated excellent linearity for all analytes (R² = 0.990–0.999), with absolute recoveries ranging from 10 to 93%, coefficients of variation between 2 and 17%. Limits of detection (LOD) and quantification (LOQ) ranged from 0.01 to 2 ng/mL and 0.03 to 6 ng/mL, respectively. Autosampler stability (24h) and short-term (one week) freeze stability exceeded 95 % and 90 % for all analytes. No significant matrix effects, interferences from the analytes or carryover were observed. Overall, the presented FPSE-LC–MS/MS method provides a sensitive, selective, and environmentally friendly analytical approach for the determination of DOA in oral fluid.

Keywords
forensic toxicology
oral fluid
drugs of abuse
FPSE
LC-MS/MS
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