A combination of isocratic and gradient elution modes in HPLC with the aid of time-overlapping process for rapid determination of methyldopa in human urine

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Date

2015

Journal Title

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Volume Title

Type

Article

Publisher

Taylor and Francis Inc.

Series Info

Journal of Liquid Chromatography and Related Technologies
38

Abstract

A new rapid time-overlapping high-performance liquid chromatography method using coupled-column double-injection technique with fluorescence detection has been developed and validated to determine methyldopa (MTD) in human urine. The method was based on injecting a new sample onto the second column before finalizing the cleanup and the re-equilibration of the first column for the former sample. A combination of isocratic and gradient elution was employed according to a pre-set program. At the beginning, isocratic step of acetate buffer solution (0.1 M, pH 2.4) was set until 7 min. Subsequently, a gradient elution step using acetate buffer (0.1 M, pH 2.4) as mobile phase A and acetonitrile as mobile phase B was employed. After the end of each gradient step, the column was re-equilibrated with 4 mL of the starting isocratic elution system before the next analysis. The overall cycle time was 7 min per each sample. The calibration curve was linear over the concentration range of 0.1-40 ?g/mL MTD. The overall mean recoveries were in the range of 98.29-101.39%. The applicability of the method was successfully evaluated by monitoring the incremental urinary excretion of MTD in human urine over 12 hr after a single oral administration of 250 mg. � 2015 Taylor & Francis Group, LLC.

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Scopus

Keywords

October University for Modern Sciences and Arts, جامعة أكتوبر للعلوم الحديثة والآداب, University of Modern Sciences and Arts, MSA University, coupled-column, double injection, fluorescence detection, HPLC, methyldopa, mixed elution modes, Coupled-column, Elution modes, Fluorescence detection, HPLC, Methyldopa, acetic acid, acetonitrile, buffer, methyldopa, Article, calibration, elution, fluorescence, high performance liquid chromatography, human, pH, quality control, time, urinalysis, urinary excretion, validation study

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