甲氧胺酸、盐酸双环胺和帕玛溴的高效液相色谱法开发与验证

Ajay Kumar, P. Chawla, P. Porwal, R. Rawal, D. Anghore
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引用次数: 4

摘要

采用分光光度和色谱技术对散粉和制剂中的甲芬那酸(MEF)、盐酸二环胺(DCL)和帕玛溴龙(PABr)进行了验证,具有高度的特异性、选择性和保证性,联合用药方法尚未见报道。目的:建立一种简便、精确、准确的紫外分光光度法和高效液相色谱法同时测定多组分片剂中甲氧胺、盐酸二环明和帕玛溴的方法。采用第一种Vierdot法,MEF、DCL和PABr分别在285、218和278 nm处达到最大吸光度。在2 ~ 24 μg/mL范围内建立校准图。停留时间分别为5.789、2.522和4.284 min。建立并验证了紫外分光光度法和高效液相色谱法测定药物剂型的方法。
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 Mefenamic Acid, Dicyclomine HCl and Pamabrom in Marketed Formulation by HPLC
Method has been validated by using spectrophotometric and chromatographic techniques for Mefenamic acid (MEF), Dicyclomine Hydrochloride (DCL) and Pamabrom (PABr) in bulk powder and in pharmaceutical formulations, with a high degree of specificity, selectivity and assurances, method for the drug combination has been not reported. The objectives were to develop and validate a simple, precise and accurate UV and RPHPLC method for simultaneous estimation of mefenamic acid, dicyclomine hydrochloride and pamabrom from multicomponent tablet dosage form. The first Vierdot’s method was performed and absorption maxima of MEF, DCL and PABr at 285, 218 and 278 nm, respectively. Calibration graphs were established in the range of 2-24 μg/mL. The retention time were found to be 5.789, 2.522 and 4.284 min. respectively. UV and HPLC methods were developed and validated for pharmaceutical dosages forms.
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