The development and validation of a Thin Layer Chromatography densitometry method for the analysis of diclofenac sodium tablets

Eliangiringa Kaale , Bugusu C. Nyamweru , Vicky Manyanga , Mhina Chambuso , Thomas Layloff
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引用次数: 24

Abstract

Aims

Diclofenac sodium is a Nonsteroidal Anti-Inflammatory Drug (NSAID) with anti-inflammatory, antipyretic, and analgesic action as a result of the blockade of prostaglandin synthesis by inhibition of the cyclooxygenase enzyme. Analysis of the active pharmaceutical ingredient as well as finished pharmaceutical product is of vital importance to help ensure that good quality products are manufactured and supplied to the patient end users. The aim of the study was to develop a simple and rapid method to enable timely release of products.

Methods

The method was developed using a mobile phase prepared with environment-friendly analytical grade solvents: toluene, acetone and glacial acetic acid (10:15:0.2 v/v/v). Diclofenac sodium reference material and samples were chromatographed using pre-coated TLC silica gel 60 F254 glass plates with a saturation time of 25 minutes and a densitometer detection wavelength of 284 nm in the reflectance absorbance mode. Detection and part of analysis was done using densitometer TLC Scanner 3 operated with Wincats (version 1.4.3) planar chromatograph software.

Results

A Thin Layer Chromatography (TLC) method for the qualitative and quantitative analysis of diclofenac sodium tablets was developed and validated according to ICH and USP guidelines. The Rf of diclofenac sodium was at 0.60 and the method was repeatable, robust with good selectivity and specificity. Regression functions were established over the range of 250–600 ng/spot with r2 of 0.993 and 0.999 for the linear and polynomial regressions respectively. The accuracy at nominal concentration was found to be 100.2%, and the results of the assay of three brands for diclofenac sodium tablets were found to meet the USP 95–105% assay limits thus demonstrating the usefulness of the method for the assay of these products.

The developed assay method for diclofenac sodium in tablets is simple, accurate, and inexpensive, with good precision and should be especially useful in resource constrained countries.

双氯芬酸钠片薄层色谱密度分析法的建立与验证
目的双氯芬酸钠是一种非甾体抗炎药(NSAID),具有抗炎、解热和镇痛作用,这是由于双氯芬酸钠通过抑制环加氧酶来阻断前列腺素的合成。活性药物成分和成品药物的分析对于帮助确保生产出高质量的产品并供应给患者最终用户至关重要。本研究的目的是开发一种简单快速的方法,使产品能够及时释放。方法采用环境友好型分析级溶剂:甲苯、丙酮和冰醋酸(10:15:20 .2 v/v/v)制备流动相。双氯芬酸钠标准品和样品采用预涂TLC硅胶60 F254玻璃板进行色谱,饱和时间为25分钟,反射吸光度模式下,密度计检测波长为284 nm。使用密度计TLC Scanner 3进行检测和部分分析,并使用Wincats (version 1.4.3)平面色谱仪软件。结果建立了双氯芬酸钠片的薄层色谱(TLC)定性和定量分析方法,并按照ICH和USP标准进行了验证。双氯芬酸钠的Rf值为0.60,方法重复性好,具有良好的选择性和特异性。在250 ~ 600 ng/spot范围内建立回归函数,线性和多项式回归的r2分别为0.993和0.999。在标称浓度下的准确度为100.2%,三个品牌双氯芬酸钠片的测定结果符合USP 95-105%的测定限,从而证明了该方法对这些产品的测定的有效性。所开发的片剂双氯芬酸钠测定方法简便、准确、廉价,精密度好,在资源有限的国家应特别有用。
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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