Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, University of Alexandria, Alexandria 21521, Egypt.
Drug Test Anal. 2013 Apr;5(4):234-41. doi: 10.1002/dta.297. Epub 2012 Jan 31.
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 8-16 μg ml(-1) . 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.
格拉司琼是一种选择性 5-HT3 受体拮抗剂,用于预防和治疗化疗引起的恶心和呕吐。该药物有片剂和含苯甲醇作为防腐剂的注射剂型。格拉司琼的主要降解途径是水解。本工作描述了一种简单、快速和可靠的一阶导数分光光度法,用于测定存在水解产物以及赋形剂和苯甲醇的格拉司琼。该方法基于格拉司琼在 290nm 处的一阶导数响应的测量,其中水解产物、共同配制的赋形剂和苯甲醇的干扰完全消除。该方法在专属性、线性、选择性、准确性、精密度、稳健性、检测限和定量限方面进行了验证。回归分析表明,在 8-16μgml(-1)范围内,一阶导数响应与格拉司琼浓度之间具有良好的相关性。统计分析证明了与参考稳定性指示高效液相色谱法相比,该方法的准确性。该方法成功地应用于不同批次片剂和安瓿中格拉司琼的测定。本研究中的测定结果强烈鼓励我们应用验证的方法对含有格拉司琼的片剂和注射制剂进行质量控制和常规分析。