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首页> 外文期刊>Biomedical Chromatography >Development and validation of a high-throughput and robust LC–MS/MS with electrospray ionization method for simultaneous quantitation of oseltamivir phosphate and its oseltamivir carboxylate metabolite in human plasma for pharmacokinetic studies
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Development and validation of a high-throughput and robust LC–MS/MS with electrospray ionization method for simultaneous quantitation of oseltamivir phosphate and its oseltamivir carboxylate metabolite in human plasma for pharmacokinetic studies

机译:开发和验证具有电喷雾电离方法的高通量且功能强大的LC-MS / MS,用于同时定量人体血浆中的磷酸奥司他韦及其羧酸奥司他韦羧酸酯代谢物,用于药代动力学研究

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AbstractA rapid, sensitive and rugged solid-phase extraction ultraperformance liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed for determination of oseltamivir phosphate (OP) and oseltamivir carboxylate (OC) in human plasma. The procedure for sample preparation includes a simple SPE extraction procedure coupled with a Chromatopack C18 column (50 × 3.0?mm, i.d., 3.0?μm) with isocratic elution at a flow-rate of 0.600?mL /min and acyclovir was used as the internal standard. The analysis was performed on a triple-quadrupole tandem mass spectrometer by multiple reaction monitoring mode via electrospray ionization. Using 500?μL plasma, the methods were validated over the concentration ranges 0.92–745.98 and 5.22–497.49?ng/mL for OP and OC, with a lower limit of quantification of 0.92and 5.22?ng/mL. The intra- and inter-day precision and accuracy of the quality control samples were within 10.1%. The recovery was 68.72, 70.66 and 71.59% for OP, OC and IS, respectively. Total run time was only 1.0?min. The method was highly reproducible with excellent chromatography properties. Copyright ? 2010 John Wiley & Sons, Ltd.
机译:摘要建立了一种快速,灵敏,耐用的固相萃取超高效液相色谱串联质谱(LC-MS / MS)方法,用于测定人血浆中的磷酸奥司他韦(OP)和奥司他韦羧酸盐(OC)。样品制备过程包括一个简单的SPE萃取过程,以及一个Chromatopack C 18 色谱柱(50×3.0?mm,内径,3.0?μm),等度洗脱,流速为0.600?mL / min,并使用阿昔洛韦作为内标。该分析是在三重四极串联质谱仪上通过电喷雾电离通过多反应监测模式进行的。使用500 µL血浆,对OP和OC的浓度范围分别为0.92–745.98和5.22–497.49?ng / mL进行了验证,定量下限为0.92和5.22?ng / mL。质量控制样品的日内和日间精度和准确度在10.1%以内。 OP,OC和IS的回收率分别为68.72%,70.66和71.59%。总运行时间仅为1.0分钟。该方法具有高度的重现性和出色的色谱性能。版权? 2010 John Wiley&Sons,Ltd.

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