基于ICH Q2 (R1)方向同时测定片剂苯磺酸氨氯地平和替米沙坦含量的高效液相色谱方法的建立与验证

T. Deshmukh, S. Deo, F. Inam, T. Lambat
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引用次数: 6

摘要

摘要建立了一种简便、特异、准确、精密度高、稳健性好的正相高效薄层色谱(HPTLC)方法,用于同时测定两种降压药苯磺酸氨氯地平(AMB)和替米沙坦(TEL)的药物剂型。以三氯甲烷:甲醇:甲酸(8:2.5:0.5 v/v/v)为固定相,以硅胶60F254预包覆的铝板为固定相进行色谱分离。在251 nm处对分离区进行密度测定。根据ICH指南,从线性、准确度、精密度、检测和定量限、稳健性和特异性等方面验证了所建议的HPTLC方法的分析性能。两种药物对AMB和TEL的Rf值分别为0.57±0.02和0.77±0.02,具有满意的消解效果。在100 ~ 600 μg/ml浓度范围内,研究了AMB和TEL的线性关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and validation of novel HPTLC method for the simultaneous estimation of Amlodipine Besylate and Telmisartan in tablet dosage form using ICH Q2 (R1) directions
AbstractA new simple, specific, accurate, precise and robust normal phase high performance thin layer chromatography (HPTLC) method were developed and validated for simultaneous estimation of two antihypertensive drugs Amlodipine Besylate (AMB) and Telmisartan (TEL) in pharmaceutical dosage form. Chromatographic separation of the drugs was performed over aluminium plates precoated with silica gel 60F254 as the stationary phase and solvent system comprised of chloroform: methanol: formic acid (8:2.5:0.5 v/v/v). Densitometric evaluation of the separated zones was performed at 251 nm. Analytical performance of the suggested HPTLC method was validated according to the ICH guidelines with respect to the linearity, accuracy, precision, detection and quantitation limits, robustness and specificity. The two drugs were satisfactory resolve with Rf values 0.57 ± 0.02 and 0.77 ± 0.02 for AMB and TEL, respectively. The linearity was studied in the concentration range 100–600 μg/ml for both AMB and TEL with a correlat...
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