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首页> 外文期刊>American Journal of PharmTech Research >Method Development and Validation for Simultaneous Estimation of Esomeprazole and Domperidone by RP-HPLC in pharmaceutical dosage form
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Method Development and Validation for Simultaneous Estimation of Esomeprazole and Domperidone by RP-HPLC in pharmaceutical dosage form

机译:RP-HPLC同时估算药物剂型中埃索美拉唑和多潘立酮的方法开发与验证

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ABSTRACT A reverse phase HPLC method is developed for the determination of Esomeprazole and Domperidone in pharmaceutical dosage forms. Chromatography was carried out on a C18 column [4.6 x 100mm, 5mm, Make: BDS] using a mixture of potassium di hydrogen ortho phosphate buffer and acetonitrile (65:35 v/v) as the mobile phase at a flow rate of 1.3 ml/min. Detection was carried out at 298 nm .The retention time of Domperidone and Esomeprazole was 2.788 min and 3.485 min. The linearity was observed In range of 50-130 µg/ml and 60-140 µg/ml with a correlation coefficient of Domperidone and Esomeprazole were 0.999 and 0.999.the proposed method was validated for its linearity, accuracy, precision and robustness .The proposed method is simple, accurate, precise, and reproducible hence it can be applied for routine quality control analysis of Esomeprazole and Domperidone in pharmaceutical dosage form. Keywords: HPLC, Domperidone and Esomeprazole, Estimation, capsules.
机译:摘要建立了反相HPLC方法,用于测定药物剂型中的埃索美拉唑和多潘立酮。使用正磷酸二氢钾缓冲液和乙腈(65:35 v / v)的混合物作为流动相,在C18色谱柱[4.6 x 100mm,5mm,制造:BDS]上进行色谱分离/分钟。在298 nm处进行检测。多潘立酮和埃索美拉唑的保留时间分别为2.788分钟和3.485分钟。在50-130μg/ ml和60-140μg/ ml的范围内观察到线性,多潘立酮和埃索美拉唑的相关系数分别为0.999和0.999。该方法简单,准确,精确且可重现,因此可用于药物剂型中埃索美拉唑和多潘立酮的常规质量控制分析。关键词:高效液相色谱法,多潘立酮和艾美拉唑,估计,胶囊。

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