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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >MULTICRITERIA OPTIMIZATION METHODOLOGY IN DEVELOPMENT OF HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF INDAPAMIDE AND PERINDOPRIL IN BULK DRUG AND ITS COMBINED DOSAGE FORM
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MULTICRITERIA OPTIMIZATION METHODOLOGY IN DEVELOPMENT OF HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF INDAPAMIDE AND PERINDOPRIL IN BULK DRUG AND ITS COMBINED DOSAGE FORM

机译:高效液相色谱法同时估算散装毒品中吲哚酰胺和吲哚普利及其混合剂型的多标准优化方法

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Multicriteria optimization methodology was applied for development of isocratic reversed-phased HPLC method for simultaneous determination of Indapamide and Perindopril. In the first stage of method development, pH value of the water phase, percentage of methanol, te mperature of the column and flow rate of the mobile phase were investigated using fractional factorial design. This work is concerned with application of simple, accurate, precise and highly selective reverse phase high performance liquid chromatographic (RP-HPLC) method for simultaneous estimation of Indapamide and Perindopril in combined dosage form. Chromatographic separation was achieved isocratically at 25°C ± 0.5°C on phase Inertsil ODS C8 [250 mm x 4.6mm] 5.m column with a mobile phase composed of Phosphate buffer with pH 2.5 and methanol in the ratio of 40:60 at flow rate of 0.5 ml/min. Detection is carried out using a UV-PDA detector at 215nm. The retention time of Perindopril at and Indapamide at 5.08 min and 6.91 min respectively. The correlation coefficients for all components are close to 1. The developed method was validated according to ICH guidelines and values of accuracy, precision and other statistical analysis were found to be in good accordance with the prescribed values. Thus the proposed method was successfully applied for simultaneous determination of Indapamide and Perindopril in routine analysis
机译:应用多标准优化方法开发了等度反相HPLC方法,同时测定了吲达帕胺和培哚普利。在方法开发的第一阶段,使用分数阶乘设计研究了水相的pH值,甲醇的百分比,色谱柱的温度和流动相的流速。这项工作涉及简单,准确,精确和高选择性的反相高效液相色谱(RP-HPLC)方法的应用,以同时估算联合剂型中的吲达帕胺和培哚普利。在Inertsil ODS C8相[250 mm x 4.6mm] 5.m色谱柱上,在25°C±0.5°C下等度分离,色谱柱的流动相由pH 2.5的磷酸盐缓冲液和比例为40:60的甲醇组成流速为0.5 ml / min。使用215nm的UV-PDA检测器进行检测。培哚普利和Indapamide的保留时间分别为5.08分钟和6.91分钟。所有成分的相关系数都接近1。根据ICH指南验证了开发的方法,发现准确性,精密度和其他统计分析的值与规定值完全一致。因此,该方法成功地用于常规分析中同时测定吲达帕胺和培哚普利

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