Determination of three antidepressants in urine using simultaneous derivatization and temperature‐assisted dispersive liquid–liquid microextraction followed by gas chromatography–flame ionization detection. (16th December 2014)

• Record Type: Journal Article
• Authors: Alizadeh Nabil, Ali Akbar; Nouri, Nina; Farajzadeh, Mir Ali
• Is Part Of: Biomedical chromatography. Volume 29:Number 7(2015:Jul.)
• Page Start: 1094
• Page End: 1102
• Publication Date: 2014-12-16
• Subjects: Chromatographic analysis -- Periodicals; Biology -- Periodicals; Medicine -- Periodicals; Biology -- Periodicals; Chromatography -- methods -- Periodicals; Medicine -- Periodicals; 543.089
• DOI: 10.1002/bmc.3396
• Languages: English
• ISSNs: 0269-3879

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <p>This paper presents a fast and simple method for the extraction, preconcentration and determination of fluvoxamine, nortriptyline and maprotiline in urine using simultaneous derivatization and temperature‐assisted dispersive liquid–liquid microextraction (TA‐DLLME) followed by gas chromatography–flame ionization detection (GC‐FID). An appropriate mixture of dimethylformamide (disperser solvent), 1, 1, 2, 2‐tetrachloroethane (extraction solvent) and acetic anhydride (derivatization agent) was rapidly injected into the heated sample. Then the solution was cooled to room temperature and cloudy solution formed was centrifuged. Finally a portion of the sedimented phase was injected into the GC‐FID. The effect of several factors affecting the performance of the method, including the selection of suitable extraction and disperser solvents and their volumes, volume of derivatization agent, temperature, salt addition, pH and centrifugation time and speed were investigated and optimized. Figures of merit of the proposed method, such as linearity (<italic>r</italic><sup>2</sup> > 0.993), enrichment factors (820–1070), limits of detection (2–4 ng mL<sup>−1</sup>) and quantification (8–12 ng mL<sup>−1</sup>), and relative standard deviations (3–6%) for both intraday and interday precisions (concentration = 50 ng mL<sup>−1</sup>) were satisfactory for determination of the selected antidepressants. Finally the method was successfully applied to determine the target pharmaceuticals in urine. Copyright © 2014 John Wiley & Sons, Ltd.</p> </abstract>