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A Validated RP-HPLC Method for Estimation of Related Compounds in Hydroxy Naproxen

机译:一种验证的RP-HPLC方法,用于估计羟基萘芬相关化合物

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A simple, linear gradient liquid chromatographic method (RP-HPLC) is proposed for the simultaneous estimation of related compounds in hydroxy naproxen samples. Chromatographic separation was achieved on Zorbax SB C8 (150 x 4.6) mm, 3.5 urn particle size RRLC short column and eluent A used as 0.1% v/v trifluoroacetic acid in water and eluent B used as acetonitrile using Agilent RRLC (UHPLC) system. The mobile phase flow rate was 1.0 mL/min and the eluted compounds were monitored at 235 nm for related substance method and assay method. The excellent resolution was obtained between hydroxy naproxen and its related compounds, which were eluted within 25 min. The performance of the method was validated with respect to ICH guidelines for specificity, limit of detection, limit of quantification, linearity, accuracy, precision and robustness. The correlation coefficient(r) was > 0.995 for both the methods from linearity data and percentage of recovery is 98.0 to 102.0 for assay method and 80.0 to 120.0% for related substance method. Sensitivity of the method was found be less than 0.5 μg/mL. Peak homogeneity data for naproxen in the chromatograms from the selectivity solution obtained by use of the photodiode array detector demonstrated the specificity of the method for analysis of hydroxy naproxen in presence of the related compounds.
机译:提出了一种简单的线性梯度液相色谱法(RP-HPLC),用于同时估计相关化合物在羟基萘普生样品中。在Zorbax Sb C8(150×4.6)mm,3.5瓮粒径RRLC短柱上和洗脱液A在水和洗脱液B中使用的洗脱液A在水和洗脱液B中使用的色谱分离,用作使用Agilent RRLC(UHPLC)系统的0.1%V / V三氟乙酸。流动相流速为1.0ml / min,并在235nm上监测洗脱的化合物,以用于相关物质方法和测定方法。在羟基萘芬及其相关化合物之间获得了优异的分辨率,在25分钟内洗脱。关于特异性,检测极限,定量限制,线性,准确性,精度,精度和鲁棒性的ICH指南,验证了该方法的性能。对于来自线性数据的方法和回收率的方法的相关系数(R)> 0.995为测定方法的98.0至102.0,相关物质方法的80.0至120.0%。发现该方法的敏感性小于0.5μg/ ml。通过使用光电二极管阵列检测器获得的选择性溶液中萘克森的峰均匀性数据证明了在存在相关化合物存在下分析羟基萘芬的方法的特异性。

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