Determination of ring-substituted amphetamines through automated online hollow fiber liquid-phase microextraction-liquid chromatography.

Autor: Cabal LFR; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, SP, 13566-590, Brazil., Medina DAV; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, SP, 13566-590, Brazil., Costa JL; Faculty of Pharmaceutical Sciences, University of Campinas, Campinas, SP, 13083-859, Brazil., Lanças FM; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, SP, 13566-590, Brazil., Santos-Neto ÁJ; São Carlos Institute of Chemistry, University of São Paulo, São Carlos, SP, 13566-590, Brazil. alvarojsn@iqsc.usp.br.
Jazyk: angličtina
Zdroj: Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2019 Nov; Vol. 411 (29), pp. 7889-7897. Date of Electronic Publication: 2019 Nov 16.
DOI: 10.1007/s00216-019-02196-0
Abstrakt: The present paper describes an original method for the online preconcentration and analysis of ring-substituted amphetamines in urine samples, used on the integration of robot-assisted hollow fiber liquid-phase microextraction (HF-LPME), high-performance liquid chromatography (HPLC), and fluorescence detection (FLD). A lab-made autosampler, actuating a 100-μL syringe and equipped with a three-way solenoid microvalve, allowed the acceptor phase to flow through and be withdrawn from the lumen fiber, enabling the automated online transference of the enriched acceptor phase for chromatographic analysis, through a six-port switching valve. The developed online HF-LPME-LC/FLD method demonstrated high analytical throughput and confidence, facilitating the efficient extraction and determination of the target analytes, with minimal solvent consumption and sample manipulation, in a straightforward way. Sample cleanup, analyte uptake, and analysis were carried out in 14.5 min. Under optimal conditions, automated online HF-LPME showed excellent linearity, precision, and trueness, obtaining intraday RSDs between 2.9 and 9.2% (n = 6) and interday RSDs between 5.3 and 9.3% (n = 6). Enrichment factors (EFs) ranged between 14.2 and 15.7, extraction recoveries (ERs) ranged between 17.7 and 19.5%, and the limits of detection (S/N = 3) were 2.0, 3.0, and 3.0 μg L -1 for MDA, MDMA, and MDEA, respectively. The method proved to be an effortless, rapid, reliable, and environment-friendly approach for the determination of drug abuse in urine samples. Graphical abstract.
Databáze: MEDLINE
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