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首页> 外文期刊>International Journal of Biomedical Science >Liquid chromatographic determination of alogliptin in bulk and in its pharmaceutical preparation
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Liquid chromatographic determination of alogliptin in bulk and in its pharmaceutical preparation

机译:液相色谱法测定散装及其药物制剂中的阿格列汀

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In this work, a reversed-phase liquid chromatographic (RP-LC) method has been developed for the determination of alogliptin (ALG) based on isocratic elution using a mobile phase consisting of potassium dihydrogen phosphate buffer pH (4.6) - acetonitrile (20:80, v/v) at a flow rate of 1 mL min ~-1 with UV detection at 215 nm. Chromatographic separation was achieved on a Symmetry? cyanide column (150 mm × 4.6 mm, 5 μm). Linearity, accuracy and precision were found to be acceptable over the concentration range of 5-160 μg mL ~-1 for ALG in bulk. The optimized method was validated and proved to be specific, robust and accurate for the quality control of ALG in pharmaceutical preparations.
机译:在这项工作中,已经开发了一种反相液相色谱(RP-LC)方法,用于基于等度洗脱的阿格列汀(ALG)测定,该流动相使用由磷酸二氢钾缓冲液pH(4.6)-乙腈组成的流动相(20: 80,v / v)的流速为1 mL min〜-1,并在215 nm处进行UV检测。色谱分离是通过Symmetry实现的?氰化物柱(150 mm×4.6 mm,5μm)。线性,准确度和精密度在散装ALG的5-160μgmL〜-1的浓度范围内均可接受。经过验证的优化方法对药物制剂中的ALG的质量控制具有特异性,鲁棒性和准确性。

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