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Simultaneous determination of free methamphetamine, pethidine, ketamine and tramadol in urine by dispersive liquid–liquid microextraction combined with GC–MS

Bibliographic Data

ID21220171
AuthorsFangmin Xu (0000-0003-0529-7424, Institute of Forensic Science, corresponding author), Lingyun Liu (0000-0002-7431-7399, Institute of Forensic Science)
Year2019
Volume4
Issue2
Pages188-194
Publication date2019-04-03
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueForensic Sciences Research (JOURNAL)
Journal identifiersISSN: 2471-1411 • E-ISSN: 2096-1790
PublisherShanghai Institute of Optics and Fine Mechanics (PUBLISHER • CN)
DOI10.1080/20961790.2017.1377386
PMID31304447
OpenAlexW2758792411
LanguageEN
References cited20

A simple and rapid dispersive liquid-liquid microextraction (DLLME) technique coupled with gas chromatography-ion trap mass spectrometry (GC-MS) was developed for the extraction and analysis of methamphetamine (MA), pethidine (PD), ketamine (KT) and tramadol (TD) from human urine. In this study, different parameters affecting the extraction process such as the type and volume of extraction solvent, type and volume of disperser solvent, extraction time and pH value and salt effect were studied and optimized. Under optimized conditions, the enrichment factor ranged from 185 to 226 and the average recovery ranged from 80.45% to 95.55%. The linear range was 10.0-1000.0 μg/L, the limit of detection and quantitation were in the range 0.43-1.96 μg/L and 1.44-6.53 μg/L, respectively. The relative standard deviations were in the range 1.98%-3.90% ( n = 7). The obtained results show that DLLME combined with GC-MS is a fast and simple method for the determination of MA, PD, KT and TD in human urine

Anesthesia · Chromatography · Detection limit · Disperser · Enrichment factor · Gas chromatography–mass spectrometry · Linear range · Mass spectrometry · Pethidine · Solvent · Urine · Analytical chemistry methods development · Chemistry · Forensic Toxicology and Drug Analysis · Materials Science · Medicine · Pharmacological Effects and Assays

Citation velocityhistorical
Highly citedNo

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