Stability-indicating methods for the determination of mosapride citrate in the presence of its degradation products according to ICH guidelines

被引:4
作者
Hegazy, Maha A. [1 ]
Yehia, Ali M. [1 ]
Mostafa, Azza A. [1 ]
机构
[1] Fac Pharm, Dept Pharmaceut Analyt Chem, Cairo, Egypt
关键词
mosapride; mosapride degradation products; spectrophotometry; spectrofluorimetry; PERFORMANCE LIQUID-CHROMATOGRAPHY; PHARMACEUTICAL DOSAGE FORMS; BULK DRUG SAMPLES; SPECTROPHOTOMETRIC METHOD; GASTROPROKINETIC DRUG; PROKINETIC AGENTS; RATIO SPECTRA; HUMAN PLASMA; MIXTURES; HPLC;
D O I
10.1002/dta.246
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present work, different spectrophotometric methods and one spectrofluorimetric method have been developed and validated for the determination of mosapride citrate in the presence of its acid-induced degradation products. The drug was subjected to stress stability study including acid, alkali, oxidative, photolytic, and thermal stress degradation. The developed spectrophotometric methods included the use of first order derivative (1D), derivative of ratio spectra (1DD), mean centring of ratio spectra (MC) and H-point standard additions (HPSAM) spectrophotometric methods. For 1D method, the peaks amplitudes at 282.8 and 319.6 nm were measured, while for 1DD method those at 308 nm and 323 nm were measured. Mean centring of ratio spectra method used the values at 317 nm for calibration, while for HPSAM the absorbance at 273 and 288.6 nm were used. These methods were successfully applied for determination of mosapride in the concentration range of 570 mu g.ml-1. The spectrofluorimetric method was based on measuring the native fluorescence of mosapride in 0.1 M NaOH using ?excitation 276 nm and ?emission 344 nm and 684 nm with linearity ranges of 503000 ng.ml-1 and 509000 ng.ml-1, respectively. All the developed methods were validated according to the International Conference on Harmonization (ICH) guidelines and were applied for bulk powder and dosage form. The results obtained were statistically compared to each other using one-way ANOVA testing. Copyright (c) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:104 / 115
页数:12
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