Volume 27, Issue 4 pp. 732-738
Full Paper

Monitoring of Methyldopa by Fast Fourier Transform Continuous Cyclic Voltammetry at Gold Microelectrode

Parviz NOROUZI

Parviz NOROUZI

Center of Excellence in Electrochemistry, Department of Chemistry, University of Tehran, Tehran, Iran

Endocrinology & Metabolism Research Center, Tehran University of Medical Science, Tehran, Iran

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Mohammad Reza GANJALI

Mohammad Reza GANJALI

Center of Excellence in Electrochemistry, Department of Chemistry, University of Tehran, Tehran, Iran

Endocrinology & Metabolism Research Center, Tehran University of Medical Science, Tehran, Iran

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Sayed Jamaleddin SHAHTAHERI

Sayed Jamaleddin SHAHTAHERI

Environmental Research Center, School of Public Health, University of Tehran, Tehran, Iran

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Rasoul DINARVAND

Rasoul DINARVAND

Medicinal Nanotechnology Research Center, University of Tehran, Tehran, Iran

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Ali HAMZEHPOOR

Ali HAMZEHPOOR

Center of Excellence in Electrochemistry, Department of Chemistry, University of Tehran, Tehran, Iran

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First published: 06 May 2009
Citations: 5

Abstract

A continuous cyclic voltammetric study of methyldopa at gold micro electrode was carried out. The drug in phosphate buffer (pH 2.0) is adsorpted at 400 mV, giving rise to change in the current of well-defined oxidation peak of gold in the flow injection system. The proposed detection method has some of advantages, the greatest one of which are as follows: first, it is no more necessary to remove oxygen from the analyte solution and second, this is a very fast and appropriate technique for determination of the drug compound in a wide variety of chromatographic analysis methods. Signal-to-noise ratio has significantly increased by application of discrete Fast Fourier transform (FFT) method, background subtraction and two-dimensional integration of the electrode response over a selected potential range and time window. Also in this work some parameters such as sweep rate, eluent pH, and accumulation time and potential were optimized. The linear concentration range was of 1.0×10−7−1.0×10−11 mol·L−1 (r=0.9975) with a limit of detection and quantitation 0.004 nmol·L−1 and 0.03 nmol·L−1, respectively. The method has the requisite accuracy, sensitivity, precision and selectivity to assay methyldopa in tablets. The influences of pH of eluent, accumulation potential, sweep rate, and accumulation time on the determination of the methyldopa were considered.

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