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A Simple and Efficient Method to Determine Rivaroxaban in Rat Plasma Using Liquid-Liquid Extraction and LC-MRM

机译:液相萃取和LC-MRM法测定大鼠血浆中利伐沙班的简单高效方法

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Rivaroxaban (RRN) is the first available active direct factor Xa inhibitor (anticoagulant) with oral administration. Due to its success in market, there have been efforts to develop various RRN formulations, and the development of good analytical methods for its in vivo evaluation is an essential prerequisite. Thus, here, a simple and efficient method to determine RRN in rat plasma using liquid-liquid extraction (LLE) and liquid chromatography and multiple reaction monitoring (LC-MRM) was presented. The use of ethyl acetate as the LLE solvent results appropriate extraction and purification of RRN and it also helps the significant reduction of rat plasma volume required for RRN quantitation. The developed method showed good analytical performance including specificity, linearity ( $r^2{geq}0.999$ within 0.5 - 500 ng/mL), sensitivity (the lower limit of quantitation at 0.5 ng/mL), accuracy (89.3 - 107.0%), precision ( ${geq}12.7%$ ), and recovery (89.2 - 105.7%). Additionally, RRN in sample extracts showed good stability. Finally, the applicability of the validated method to the PK evaluation of RRN was confirmed after its oral administration to normal rats. The present method is the first analytical method employing LLE for the simple and efficient extraction and purification of RRN in rat plasma. Therefore, the present method can contribute to the development of new RRN formulations as well as to the monitoring of RRN in special clinical situations through its efficient determination in various samples with or without minor modification.
机译:利伐沙班(RRN)是第一种口服的活性直接因子Xa抑制剂(抗凝剂)。由于其在市场上的成功,人们一直在努力开发各种RRN配方,开发用于其体内评估的良好分析方法是必不可少的前提。因此,在这里,提出了一种简单有效的方法,使用液-液萃取(LLE)和液相色谱法以及多反应监测(LC-MRM)测定大鼠血浆中的RRN。乙酸乙酯作为LLE溶剂的使用可适当地提取和纯化RRN,并且还有助于显着减少RRN定量所需的大鼠血浆体积。所开发的方法显示出良好的分析性能,包括特异性,线性($ r ^ 2 { geq} 0.999 $在0.5-500 ng / mL之内),灵敏度(定量下限为0.5 ng / mL),准确性(89.3-107.0) %),精度($ { geq} 12.7%$)和恢复(89.2-105.7%)。此外,样品提取物中的RRN表现出良好的稳定性。最后,证实了该方法对正常大鼠口服后RNR的PK评估的适用性。本方法是使用LLE进行大鼠血浆中RRN的简单有效提取和纯化的第一种分析方法。因此,本方法可以通过在各种样品中进行有效的测定而无需进行较小的修改就有助于开发新的RRN制剂以及在特殊临床情况下监测RRN。

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