First derivative spectrophotometric determination of granisetron hydrochloride in presence of its hydrolytic products and preservative and application to pharmaceutical preparations

被引:11
|
作者
Hewala, Ismail I. [1 ]
Bedair, Mona M. [2 ]
Shousha, Sherif M. [3 ]
机构
[1] Univ Alexandria, Dept Pharmaceut Analyt Chem, Fac Pharm, Alexandria 21521, Egypt
[2] Pharos Univ, Fac Pharm & Drug Mfg, Dept Pharmaceut Chem, Alexandria, Egypt
[3] Univ Montreal, Fac Pharm, Montreal, PQ H3C 3J7, Canada
关键词
granisetron; hydrolytic degradation; first derivative; spectrophotometry; pharmaceutical preparations; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; HUMAN PLASMA; FLUORESCENCE DETECTION; HPLC METHOD; 7-HYDROXY METABOLITE; VALIDATION; ASSAY; RAT;
D O I
10.1002/dta.297
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Granisetron is a selective 5-HT3 receptor antagonist used in prevention and treatment of chemotherapy-induced nausea and vomiting. The drug is available in tablet dosage form and parenteral dosage form containing benzyl alcohol as a preservative. The main route of degradation of granisetron is through hydrolysis. The present work describes the development of a simple, rapid, and reliable first derivative spectrophotometric method for the determination of granisetron in presence of its hydrolytic products as well as the formulations adjuvant and benzyl alcohol. The method is based on the measurement of the first derivative response of granisetron at 290 nm where the interference of the hydrolytic products, the co-formulated adjuvant and benzyl alcohol is completely eliminated. The proposed method was validated with respect to specificity, linearity, selectivity, accuracy, precision, robustness, detection, and quantification limits. Regression analysis showed good correlation between the first derivative response and the concentration of granisetron over a range of 816 g ml1. Statistical analysis proved the accuracy of the proposed method compared with a reference stability indicating high performance liquid chromatography method. The described method was successfully applied to the determination of granisetron in different batches of tablets and ampoules. The assay results obtained in this study strongly encourage us to apply the validated method for the quality control and routine analysis of tablets and parenteral preparations containing granisetron. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:234 / 241
页数:8
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