Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Determination of multiple drugs of abuse in human urine using dispersive liquid–liquid microextraction and capillary electrophoresis with PDA detection

Bibliographic Data

ID13119751
AuthorsLiang Meng (0000-0002-0470-7818, Guangdong Police College, corresponding author), Shuhai Ye (Institute of Forensic Science), Yilin Wu (0000-0002-4994-3822, Guangdong Police College), Linda You (Guangdong Police College)
Year2021
Volume7
Issue2
Pages265-271
Publication date2021-12-09
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueForensic Sciences Research (JOURNAL)
Journal identifiersISSN: 2471-1411 • E-ISSN: 2096-1790
PublisherTaylor & Francis (PUBLISHER • GB)
DOI10.1080/20961790.2021.1986771
PMID35784428
OpenAlexW4200016329
LanguageEN
References cited32

A new method was developed for pre-concentration and determination of multiple drugs of abuse in human urine using dispersive liquid-liquid microextraction (DLLME) and capillary electrophoresis (CE) with photodiode array detection. The method was based on the formation of tiny droplets of an organic extractant in the prepared sample solution using water-immiscible organic solvent (chloroform) dissolved in water-miscible organic dispersive solvent (isopropyl alcohol). The organic phase, which extracted eight drugs of abuse from the prepared urine solution, was separated by centrifugation. The sedimented phase was transferred into a small volume CE auto-sampler vial with 10 μL of 1% HCl methanol solution and evaporated to dryness. The residue was reconstituted in lidocaine hydrochloride (internal standard) aqueous solution and introduced by electrokinetic injection into CE. Under the optimum conditions, acceptable linear relationship was observed in the range of 3.0-500 ng/mL with the correlation coefficient ( r ) of 0.9982-0.9994 for spiked urine samples. The limit of detection (LOD) (S/N = 3) was estimated to be 1.0 ng/mL. A recovery of 75.7%-90.6% was obtained for spiked samples. The mean relative error (MRE) was within ±7.0% and the relative standard deviation (RSD) was less than 6.9%. The proposed DLLME-CE procedure offers an alternative analytical approach for the sensitive detection of drugs of abuse in real urine samples.Key pointsThe dispersive liquid-liquid microextraction (DLLME) was involved for the determination of drugs in urine with capillary electrophoresis with photodiode array detection (CE-PDA).Good linearity, sensitivity, recovery and precision were achieved.The proposed method was eco-friendly with microliter scale solvent consumption

Analytical Chemistry (journal · Capillary electrophoresis · Chromatography · Detection limit · Solvent · Urine · Analytical chemistry methods development · Chemistry · Forensic Toxicology and Drug Analysis · Microfluidic and Capillary Electrophoresis Applications

  • Determination of amphetamines, ketamine and their metabolites in hair with high-speed grinding and solid-phase microextraction followed by LC-MS

    Open Access•Liang Meng, Yong Dai et al.•Forensic Sciences Research•2021

Citation velocityhistorical
Highly citedNo

Tools

Open DOIOpen Access
Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae