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Research Article

Stability-Indicating Spectrophotometric and Densitometric Methods for Determination of Aceclofenac

, &
Pages 571-582 | Published online: 30 May 2002
 

ABSTRACT

Three methods were developed for the determination of aceclofenac in the presence of its degradation product, diclofenac. In the first method, third-derivative spectrophotometry (D3) is used. The D3 absorbance is measured at 283 nm where its hydrolytic degradation product diclofenac does not interfere. The suggested method shows a linear relationship in the range of 4–24 µg mL−1 with mean percentage accuracy of 100.05±0.88. This method determines the intact drug in the presence of up to 70% degradation product with mean percentage recovery of 100.42±0.94. The second method depends on ratio-spectra first-derivative (RSD1) spectrophotometry at 252 nm for aceclofenac and at 248 nm for determination of degradation product over concentration ranges of 4–32 µg mL−1 for both aceclofenac and diclofenac with mean percentage accuracy of 99.81±0.84 and 100.19±0.72 for pure drugs and 100.17±0.94 and 99.73±0.74 for laboratory-prepared mixtures, respectively. The third method depends on the quantitative evaluation of thin-layer chromatography of aceclofenac using chloroform:methanol: ammonia (48:11.5:0.5 v/v/v) as a mobile phase. Chromatograms were scanned at 274 and 283 nm for aceclofenac and diclofenac, respectively. The method determined aceclofenac and diclofenac in concentration ranges of 2–10 and 1–9 µg spot−1 with mean percentage accuracy of 100.20±1.03 and 100.14±0.98 for pure drugs and 99.77±0.74 and 100.07±0.78 for laboratory-prepared mixtures, respectively. This method retains its accuracy in the presence of up to 80% degradation product for the studied drug.

The suggested procedures were checked using laboratory-prepared mixtures and were successfully applied for the analysis of their pharmaceutical preparation. The validity of the proposed methods was further assessed by applying a standard addition technique. The obtained results agreed statistically with those obtained by the reported method.

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