Original Research Article | OPEN ACCESS

Development of colorimetric method for the assay of artesunate using 4-nitrobenzaldehyde

Godfrey E Aghayere , Sunday A Adelusi,

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Benin, PMB 1154, Benin City, 300001, Nigeria;

For correspondence:-  Godfrey Aghayere   Email:  godfrey.aghayere@uniben.edu   Tel:  +2347034482650

Published: 11 December 2019

Citation: Aghayere GE, Adelusi SA, Development of colorimetric method for the assay of artesunate using 4-nitrobenzaldehyde. J Sci Pract Pharm 2019; 6(1):298-302 doi: 10.47227/jsppharm.v6i1.3

© 2019 The author(s).
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). This license requires that reusers give credit to the creator. It allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, for noncommercial purposes only. .

Abstract

Purpose: Artesunate is one of the artemisinin derivatives that is commonly used in combination with some anti-malarials as artemisinin-based combination therapies. High performance liquid chromatographic technique is the required standard assay method for artesunate, but this is not readily available or affordable in most developing countries. This study was carried out to develop a simple, accurate and cost-effective assay method for quantitative determination of artesunate.

Methods: The method is an indirect colorimetric assay, which was developed from the formation of yellow coloured product due to the reaction between acid decomposed product of artesunate with 4-nitrobenzaldehyde.

Results: The wavelength of maximum absorption for the yellow coloured product was 474 nm. The Beer’s law was obeyed at the range of 20-100 µg/ml artesunate concentration with a linear coefficient of 0.9996. The molar absorptivity was 2.3183×103 mol-1 cm-1. The limit of detection and quantification were 0.0753 µg/ml and 0.2283 µg/ml, respectively. The method required water as diluent. The result obtained from recovery study confirmed that there was no interference from pharmaceutical excipients. Five brands of artesunate tablets were assayed using the developed method.

Conclusion: The results compared favourably well with those obtained using the official method described in the international pharmacopoeia. The developed method is useful for the quantitative determination of artesunate in tablets and raw pharmaceutical material.

 

 

 

 

Keywords: Artemisinin, quantitative determination, in-direct colorimetric assay, molar absorptivity

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