Cover image of the article: Electro-Oxidation Mechanism and Direct Square-Wave Voltammetric Determination of Lidocaine With a Carbon-Paste Electrode

Image Credit:Jundishapur J Nat Pharm Prod

Electro-Oxidation Mechanism and Direct Square-Wave Voltammetric Determination of Lidocaine With a Carbon-Paste Electrode

Authors

Nadereh Rahbar2,*, Zahra Ramezani2, Ahmad Babapour2
2Department of Medicinal Chemistry, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran
*Corresponding Author: Corresponding author: Nadereh Rahbar, Department of Medicinal Chemistry, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran. Tel: +98-6133738378, n_rahbar2010@ajums.ac.ir. Email: n_rahbar2010@ajums.ac.ir

Jundishapur Journal of Natural Pharmaceutical Products:Vol. 10, issue 1; 19382
Published online:Feb 19, 2015
Article type:Research Article
Received:Apr 11, 2014
Accepted:Oct 10, 2014
How to Cite:Rahbar N, Ramezani Z, Babapour A. Electro-Oxidation Mechanism and Direct Square-Wave Voltammetric Determination of Lidocaine With a Carbon-Paste Electrode. Jundishapur J Nat Pharm Prod. 2015;10(1):19382. doi: https://doi.org/10.17795/jjnpp-19382

Abstract

Background:

Lidocaine hydrochloride (LH) is one of the most extensively used local anesthetics and peripheral analgesics. Availability of a simple and sensitive assay method for this analyte in pharmaceutical preparations as well as development of new voltammetric detectors that can be applied in chromatographic systems for determination of this analyte in biological samples are of great importance.

Objectives:

In this study, a square-wave voltammetric (SWV) determination of LH at a bare carbon-paste electrode (CPE) was reported. Moreover, the oxidation mechanism for LH molecule at this electrode was investigated.

Materials and Methods:

The SW voltammogram of LH solution at CPE showed a well-defined peak between +0.80 and +0.88 V depending on a scan rate in potassium nitrate (KNO3) solution. Different chemical and instrumental parameters influencing the voltammetric response, such as the pH level and scan rate were optimized for LH determination.

Results:

A linear range of 8.0 - 1000.0 ?mol L-1 (r2 = 0.999) was obtained. The limit of detection (LOD) was 0.29 ?mol L-1. The relative standard deviations of 2.1% obtained for 0.8 800 ?mol L-1 solution of LH indicated a reasonable reproducibility of the method.

Conclusions:

The results of this study show that LH in different pharmaceutical preparations could be determined with good reliability. In addition, the results reveal that the equal numbers of electrons and protons are involved in the oxidation of LH and the irreversible oxidation of an analyte was performed via amine groups of LH molecule.

Highlights

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Copyright

© 2015, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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