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Development and Validation of RP-HPLC Method for Simultaneous Estimation of Atorvastatin Calcium and Fenofibrate in Tablet Dosage Forms

机译:RP-HPLC法同时测定片剂剂量形式中阿托伐他汀钙和非诺贝特的建立与验证

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摘要

A reverse phase high performance liquid chromatographic method was developed for the simultaneous estimation of atorvastatin calcium and fenofibrate in tablet formulation. The separation was achieved by Luna C18 column and methanol:acetate buffer pH 3.7 (82:18 v/v) as mobile phase, at a flow rate of 1.5 ml/min. Detection was carried out at 248 nm. Retention time of atorvastatin calcium and fenofibrate was found to be 3.02+0.1 and 9.05+0.2 min, respectively. The method has been validated for linearity, accuracy and precision. Linearity for atorvastatin calcium and Fenofibrate were in the range of 1-5 μg/ml and 16-80 μg/ml, respectively. The mean recoveries obtained for Atorvastatin calcium and fenofibrate were 101.76% and 100.06%, respectively. Developed method was found to be accurate, precise, selective and rapid for simultaneous estimation of atorvastatin calcium and fenofibrate in tablets.
机译:开发了一种反相高效液相色谱方法,用于同时估算片剂中阿托伐他汀钙和非诺贝特的含量。通过Luna C18色谱柱和甲醇:乙酸盐缓冲液pH 3.7(82:18 v / v)作为流动相,以1.5 ml / min的流速进行分离。检测在248nm进行。阿托伐他汀钙和非诺贝特的保留时间分别为3.02 + 0.1和9.05 + 0.2分钟。该方法已经过线性,准确性和精确性验证。阿托伐他汀钙和非诺贝特的线性分别在1-5μg/ ml和16-80μg/ ml的范围内。阿托伐他汀钙和非诺贝特的平均回收率分别为101.76%和100.06%。发现开发的方法准确,精确,选择性和快速,可同时估算片剂中的阿托伐他汀钙和非诺贝特。

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