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首页> 外文期刊>Journal of separation science. >Quantitation of ribavirin in human plasma and red blood cells using LC-MS/MS
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Quantitation of ribavirin in human plasma and red blood cells using LC-MS/MS

机译:使用LC-MS / MS定量测定人血浆和红细胞中的利巴韦林

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LC-MS/MS has been applied for the rapid determination of the nucleoside analogue ribavirin in human plasma and red blood cells. The incorporation of ribavirin to the erythrocytes has been assayed after in vitro incubation of the cells at different concentrations of the antiviral drug. After protein precipitation, samples were injected into a C_8 column, achieving a complete separation of ribavirin from the endogenous isobaric compound uridine. Calibration ranges varied from 10 to 10 000 ng/mL in plasma and from 0.2 to 200 ng/cell pellet in red blood cells. Precision and accuracy values were always below 10 and 13%, respectively, in all assayed matrices. Ribavirin was demonstrated to remain unchanged after short and long time storage. No matrix effects could be assessed for the analyzed matrices. The developed method has been fully validated. Monitoring of ribavirin concentration in red blood cells in addition to the classic plasma monitoring of the drug could help to explain its efficacy and safety profiles in patients.
机译:LC-MS / MS已用于快速测定人血浆和红细胞中核苷类似物利巴韦林。在不同浓度的抗病毒药物进行体外温育后,已经测定了病毒唑结合到红细胞中的情况。蛋白质沉淀后,将样品注入C_8色谱柱中,从而实现了病毒唑从内源性同量异位化合物尿苷中的完全分离。血浆的校准范围从10到10000 ng / mL,红细胞的校准范围从0.2到200 ng /细胞沉淀。在所有测定的基质中,精密度和准确度值始终始终分别低于10%和13%。利巴韦林经短期和长期保存后保持不变。对于分析的矩阵,无法评估任何矩阵效应。所开发的方法已得到充分验证。除了经典的血浆药物监测以外,监测红细胞中利巴韦林的浓度还有助于解释其对患者的疗效和安全性。

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