Spectrophotometric assay of artesunate using benzaldehydes with electron withdrawing substituents

G. E. Aghayere, H. A. Okeri
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Abstract

Different analytical methods have been reported for the assay of artesunate. However, these methods require the use of sophisticated and expensive equipment and reagents which are not readily available in many developing countries like Nigeria. This study is aimed at developing a method that is accurate, simple and cost effective using readily available reagents for the assay of artesunate in pure form and in pharmaceutical formulations. The developed spectrophotometric assay method is based on the fact that reactive methylene centre of the acid decomposed product of artesunate readily donates a proton that reacts with benzaldehyde to form a chromogen. This study involves the use of two benzaldehydes with electron withdrawing substituents, 3-bromobenzaldehyde and 4-chlorobenzaldehyde. Both gave immediate yellow coloured products and the wavelength of maximum absorption for the product obtained using 3-bromobenzaldehyde was 452 nm, while it was 456 nm for the product obtained with 4-chlorobenzaldehyde. However, the dissolution of 3-bromobenzaldehyde was incomplete in the acidic medium. The result obtained with 4-chlorobenzaldehyde revealed that Beer’s law was obeyed at the range of 20-100 μg/ml artesunate concentration with a linear coefficient of 0.9996 and the molar absorptivity was 2.1261×10 3 mol -1 cm -1 . The limits of detection and quantification were 1.3832 μg/ml and 4.6109 μg/ml, respectively. The method required water as diluent. The result obtained from recovery studies by standard addition method confirmed that there was no interference from pharmaceutical excipients. The developed method was used to assay five brands of artesunate tablets successfully. The results compared favourably well with those obtained using the method described in the International Pharmacopoeia. Keywords: Artesunate, Benzaldehydes, spectrophotometry, recovery studies
用带吸电子取代基的苯甲醛分光光度法测定青蒿琥酯
不同的分析方法已报道的测定青蒿琥酯。然而,这些方法需要使用复杂和昂贵的设备和试剂,而这些设备和试剂在尼日利亚等许多发展中国家并不容易获得。本研究旨在开发一种准确、简单和成本有效的方法,使用现成的试剂来测定纯形式和药物制剂中的青蒿琥酯。所开发的分光光度测定方法是基于青蒿琥酯酸分解产物的活性亚甲基中心容易提供一个质子与苯甲醛反应形成显色剂的事实。本研究涉及使用两种具有吸电子取代基的苯甲醛,3-溴苯甲醛和4-氯苯甲醛。用3-溴苯甲醛制得的产物的最大吸收波长为452nm,用4-氯苯甲醛制得的产物的最大吸收波长为456nm。而3-溴苯甲醛在酸性介质中溶解不完全。以4-氯苯甲醛为溶剂,在青蒿琥酯浓度20 ~ 100 μg/ml范围内符合比尔定律,线性系数为0.9996,摩尔吸光度为2.1261×10 3 mol -1 cm -1。检测限为1.3832 μg/ml,定量限为4.6109 μg/ml。这种方法需要水作为稀释剂。标准加样法回收率研究结果证实,该方法不受药用辅料的干扰。该方法成功地测定了5个牌号的青蒿琥酯片的含量。结果与用国际药典中所描述的方法得到的结果比较良好。关键词:青蒿琥酯,苯甲醛,分光光度法,回收率研究
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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