Akademik Veri Yönetim Sistemi
TALANTA, cilt.72, sa.3, ss.1172-1177, 2007 (SCI-Expanded)
A sensitive and specific high-performance liquid chromatography (HPLC) method has been developed and validated for the quantification of mexiletine (MEX) in human plasma and urine. It uses solid-phase extraction (SPE) followed by an automated reversed-phase HPLC with a pre-column derivatization with 4-chloro-7-nitrobenzofurazan (NBD-Cl) and UV-vis Absorbance detection. The process was set as: the UV-vis Absorbance wavelength was set at 458 nm. Chromatographic separation was performed on a Phenomenex-C-18 Column (Aqua, 150 mm x 4.6 mm i.d. with 5 Lm particle size) with the mobile phase consisting of acetonitrile and water (80:20, v/v), and the flow rate was set at 1.0 mL min(-1). Calibration of the overall analytical procedure gave a linear signal (r > 0.9998) over a MEX concentration range of 0.2-2.0 mu g mL(-1) in human plasma and urine. The detection limit in plasma and urine was 0.1 mu g mL(-1). Intra- and inter-day precision of the assay at three concentrations within this range were 0.31-2.50%. The high specificity and sensitivity have been achieved by this fast method (total run-time <6 min). The method has been successfully validated in human plasma and urine and it has been shown to be precise, accurate and reliable. (C) 2007 Elsevier B.V. All rights reserved.