首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of ABT-888, a poly (ADP-ribose) polymerase inhibitor, and its metabolite in human plasma by liquid chromatography/tandem mass spectrometry
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Simultaneous determination of ABT-888, a poly (ADP-ribose) polymerase inhibitor, and its metabolite in human plasma by liquid chromatography/tandem mass spectrometry

机译:液相色谱/串联质谱法同时测定人血浆中的聚(ADP-核糖)聚合酶抑制剂ABT-888及其代谢物

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摘要

A reversed-phase liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) method was developed and validated for Simultaneous determination of ABT-888 and its major metabolite (M8) in human plasma. Sample preparation involved a liquid-liquid extraction by the addition of 0.25 ml of plasma with 10 mu l of 1M NaOH and 1.0 ml ethyl acetate containing 50 ng/ml of the internal standard zileuton. The analytes were separated on a Waters XBridge C-18 Column using a gradient mobile phase consisting of methanol/water containing 0.45% formic acid at the flow rate of 0.2 ml/min. The analytes were monitored by tandem mass spectrometry with electrospray positive ionization. Linear calibration curves were generated over the ABT-888 and M8 concentration ranges of 1-2000 ng/ml in human plasma. The lower limits of quantitation (LLOQ) were 1 ng/ml for both ABT-888 and M8 in human plasma. The accuracy and within-and between-day precisions were within the generally accepted criteria for bioanalytical method (<15%). This method was successfully employed to characterize the plasma concentration-time profile of ABT-888 after its oral administration in cancer patients.
机译:建立了反相液相色谱-串联质谱(LC-MS / MS)方法,并验证了该方法可同时测定人血浆中的ABT-888及其主要代谢物(M8)。样品制备涉及通过向0.25 ml血浆中加入10μl1M NaOH和1.0 ml含50 ng / ml内标齐留通的乙酸乙酯进行液-液萃取。在Waters XBridge C-18色谱柱上使用流速为0.2 ml / min的包含0.45%甲酸的甲醇/水组成的梯度流动相分离分析物。通过串联质谱联用电喷雾正电离监测分析物。在人血浆中1-2000 ng / ml的ABT-888和M8浓度范围内生成线性校准曲线。人血浆中ABT-888和M8的定量下限(LLOQ)均为1 ng / ml。准确性以及日间和日间精度均在生物分析方法公认的标准之内(<15%)。该方法已成功用于表征ABT-888在癌症患者中口服后的血浆浓度-时间曲线。

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