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Quantitation of Floxuridine in K2 EDTA Rat Plasma using HPLC Coupled with Tandem Mass Spectrometry

机译:高效液相色谱-串联质谱法定量测定K2 EDTA大鼠血浆中的氟尿苷

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摘要

A rapid, sensitive and specific method based on high performance liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) detection with electro spray ionization in negative ionization mode has been developed for the determination of floxuridine in K2 EDTA rat plasma. Sample preparation involved liquid-liquid extraction with ethyl acetate. Chromatographic separation was performed on Agilent Eclipse XDB column (C_(18) 150 x 4.6 mm 5 μ), with a mobile phase consisting of methanol and 1 mM ammonium acetate at a flow rate of 0.4 mL/min. The analytes were then detected by monitoring the transitions m/z 245.2-155.1 for floxuridine and m/z 321.5-143.9 for 5-bromouridine(IS) using API-400O LC-MS/MS system (applied biosystems). Calibration curves were linear within the range of 0.050 to 50.00 ng/mL. The lower limit of quantitation (LLOQ) was 0.050 ng/mL. The method has been fully validated in rat plasma. This method can be successfully applied to the pharmacokinetic study sample analysis.
机译:建立了一种基于高效液相色谱-串联质谱(LC-MS / MS)的快速,灵敏和特异性的检测方法,该方法采用负离子化模式进行电喷雾离子化,用于测定K2 EDTA大鼠血浆中的氟尿苷。样品制备涉及用乙酸乙酯进行液-液萃取。在Agilent Eclipse XDB色谱柱(C_(18)150 x 4.6 mm 5μ)上进行色谱分离,流动相由甲醇和1 mM乙酸铵组成,流速为0.4 mL / min。然后,使用API​​-400O LC-MS / MS系统(应用的生物系统)通过监测氟尿苷的m / z 245.2-155.1和5-溴尿苷(IS)的m / z 321.5-143.9的变化来检测分析物。校正曲线在0.050至50.00 ng / mL范围内呈线性。定量下限(LLOQ)为0.050 ng / mL。该方法已在大鼠血浆中得到充分验证。该方法可以成功地应用于药代动力学研究样品分析。

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