Stability indicating spectrophotometric methods for determination of bumadizone in the presence of its alkaline degradation product

Hala E. Zaazaa , Nouruddin W. Ali , Maimana A. Magdy , Mohamed Abdelkawy
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引用次数: 4

Abstract

Objectives

Simple, selective and precise stability indicating spectrophotometric methods were adopted and validated for the quantitative determination of Bumadizone calcium semihydrate (BUM) in presence of its alkaline degradation product (DEG I).

Methods

Method A is based on the application of first derivative (1D) spectrophotometry, then measuring the amplitude of BUM at 245.4 nm. Method B depends on measuring the peak amplitude of the first derivative of the ratio spectra (1DD) at 242.6, 260 and 274 nm over a concentration range of 6–20 μg mL−1. Method C is isoabsorptive point spectrophotometry where total concentration of BUM and DEG I was calculated at their isoabsorptive point at 242.2 nm (Aiso) while DEG I concentration alone can be determined at λmax 320 nm, and then BUM concentration can be determined by subtraction. In Method D ratio subtraction spectrophotometry is applied.

Results

The four methods were found to be specific for determination BUM in presence of different concentrations of DEG I and were successfully applied for the determination of BUM in Octomotol® tablets.

Conclusion

Statistical comparison between the results obtained by applying the proposed methods and that obtained by the manufacturer one for the determination of the drug was done, and it was found that there is no significant difference between them.

Abstract Image

稳定性指示分光光度法测定碱降解产物中人类酮的含量
目的采用一阶导数(1D)分光光度法,在245.4 nm处测定半水合布玛地酮钙(BUM)的振幅,建立了一阶导数(1D)分光光度法测定其碱性降解产物(DEG)的方法。方法B依赖于在6-20 μg mL−1的浓度范围内,在242.6、260和274 nm处测量比值光谱(1DD)一阶导数的峰值幅度。方法C为等吸收点分光光度法,在242.2 nm处计算BUM和DEG I的等吸收点总浓度(Aiso),在λmax 320 nm处单独测定DEG I浓度,然后通过相减法测定BUM浓度。方法D采用比减法分光光度法。结果4种方法均能在不同浓度的DEG I存在下特异测定BUM,并可成功应用于八tomotool®片剂中BUM的测定。结论将所建方法与生产厂家方法测定的结果进行了统计比较,两者无显著性差异。
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