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首页> 外文期刊>Bioanalysis >Analysis of losartan and carvedilol in urine and plasma samples using a dispersive liquid-liquid microextraction isocratic HPLC-UV method
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Analysis of losartan and carvedilol in urine and plasma samples using a dispersive liquid-liquid microextraction isocratic HPLC-UV method

机译:使用色散液 - 液微量萃取等分散液 - 液体微萃取等尿液和血浆样品氯沙坦和卡维地洛的分析

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摘要

Background: A simple, precise and sensitive HPLC method has been developed for simultaneous determination of carvedilol and losartan in human plasma and urine samples. The analytes were extracted by a dispersive liquid-liquid microextraction method. A mobile phase of 15 mM sodium dihydrogen phosphate buffer (pH 4.0)/acetonitrile/2-propanol (70/27.5/2.5, v/v/v) was used to separate the drugs using a Waters? ODS column (250 * 4.6 mm) and detected by a UV detector at 222 nm. Results: The developed method is selective for studied drugs possessing a linearity range of 0.1-1.0 and 0.05-0.75 ug/ml, respectively, for losartan and carvedilol with precision <15%. The accuracy is better than 15% and the mean recovery of carvedilol and losartan was 98.9 and 100.2% for plasma and 100.7 and 100.5% for urine samples, respectively. Conclusion: The developed method is applicable for therapeutic drug monitoring and PK analyses.
机译:背景:已经开发了一种简单,精确和敏感的HPLC方法,用于同时测定人血浆和尿液样品中的卡维洛尔和氯沙坦。 通过分散液 - 液微萃取方法提取分析物。 使用15mM磷酸二氢钠缓冲液(pH4.0)/乙腈/ 2-丙醇(70 / 27.5 / 2.5,v / v / v)的流动相用于使用水分离药物? ODS列(250 * 4.6 mm)并由UV探测器在222nm处检测。 结果:开发方法是用于分别具有0.1-1.0和0.05-0.75 ug / ml的线性范围的研究的选择性,用于氯沙坦和Carvedilol,精度<15%。 精度优于15%,血浆的平均恢复分别为98.9和100.7%,尿液样品的100.7和100.5%。 结论:开发方法适用于治疗药物监测和PK分析。

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