• Media type: E-Article
  • Title: Qualitative Screening of Amphetamine- and Ketamine-Type Abuse Drugs in Urine Employing Dual Mode Extraction Column by Liquid Chromatography–Tandem Mass Spectrometry (LC–MS-MS)
  • Contributor: Wong, George Fai; Lee, Wing-Man; Li, Chi-Keung
  • imprint: Oxford University Press (OUP), 2023
  • Published in: Journal of Analytical Toxicology
  • Language: English
  • DOI: 10.1093/jat/bkac004
  • ISSN: 1945-2403; 0146-4760
  • Keywords: Chemical Health and Safety ; Health, Toxicology and Mutagenesis ; Toxicology ; Environmental Chemistry ; Analytical Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title> <jats:p>This manuscript reported a fast and rapid qualitative screening method for abuse drugs in urine by liquid chromatography–tandem mass spectrometry (LC–MS-MS). The scope of the abuse drugs under investigation included methamphetamine (MA), amphetamine (AMP), methylenedioxymethamphetamine (MDMA), methylenedioxyamphetamine (MDA), paramethoxymethamphetamine (PMMA), ephedrine, pseudoephedrine, ketamine (KET), deschloroketamine (DCK), 2-fluorodeschloroketamine (2 F-DCK) and deschloro-N-ethylketamine (2-oxo-PCE). The method employed a dual mode extraction (DME) column as a novel clean-up method for the urine matrix. To an aliquot of 0.2 mL urine, internal standards (ISTDs) and 0.4 mL of acidified methanol were added. After vortex and centrifugation, the supernatant was passed through a DME column before LC–MS-MS analysis. Chromatographic separation was achieved with a C18 column by gradient elution. The limits of detection (LODs) for MA, AMP, MDMA, MDA and PMMA were 3 ng/mL, whereas those for ephedrine and pseudoephedrine were 10 ng/mL and those for KET, DCK, 2 F-DCK and 2-oxo-PCE were 1 ng/mL. The matrix effects ranged from −12% to 7% (%CV from 4% to 19%). This method is fit for the intended purpose for forensic toxicology, as well as for forensic analysis of drugs facilitating sexual assault and other criminal acts.</jats:p>
  • Access State: Open Access