首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous quantification of venlafaxine and O-desmethylvenlafaxine in human plasma by ultra performance liquid chromatography–tandem mass spectrometry and its application in a pharmacokinetic study
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Simultaneous quantification of venlafaxine and O-desmethylvenlafaxine in human plasma by ultra performance liquid chromatography–tandem mass spectrometry and its application in a pharmacokinetic study

机译:超高效液相色谱-串联质谱法同时定量测定人血浆中的文拉法辛和O-去甲基文拉法辛及其在药代动力学研究中的应用

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摘要

A rapid, selective and sensitive ultra performance liquid chromatography–tandem mass spectrometry (UPLC-MS/MS) method was developed to simultaneously determine venlafaxine (VEN) and O-desmethylvenlafaxine (ODV) in human plasma. Sample pretreatment involved a one-step extraction with diethyl ether of 0.5mL plasma. The separation was carried out on an ACQUITY UPLC~(TM) BEH C_(18) column with 10 mmol/L ammonium acetate and methanol as the mobile phase at a flow rate of 0.30 mL/min. The detection was performed on a triple–quadrupole tandem mass spectrometer by multiple reaction monitoring(MRM)modevia electrospray ionization (ESI) source. The linear calibration curves forVENand ODV were both obtained in the concentration range of 0.200–200 ng/mL (r~2 ≥0.99) with the lower limit of quantification (LLOQ) of 0.200 ng/mL. The intra- and inter-day precision (relative standard deviation, R.S.D.) values were less than 13% and the accuracy (relative error, R.E.) was within ±5.3% and ±3.6% for VEN and ODV. The method herein described was superior to previous methods in sensitivity and sample throughput and successfully applied to clinical pharmacokinetic study of venlafaxine sustained-release capsule in healthy male volunteers after oral administration.
机译:建立了一种快速,选择性和灵敏的超高效液相色谱-串联质谱(UPLC-MS / MS)方法,可同时测定人血浆中的文拉法辛(VEN)和O-去甲基文拉法辛(ODV)。样品预处理涉及用0.5mL血浆的乙醚一步萃取。分离在ACQUITY UPLC TM BEH C_(18)柱上进行,其中以10mmol / L乙酸铵和甲醇作为流动相,以0.30mL / min的流速进行分离。通过电喷雾电离(ESI)源进行多反应监测(MRM)模式,在三重四极串联质谱仪上进行检测。 VEN和ODV的线性校准曲线均在0.200–200 ng / mL的浓度范围内(r〜2≥0.99)获得,定量下限(LLOQ)为0.200 ng / mL。日内和日间精度(相对标准偏差,R.S.D。)值均小于13%,而VEN和ODV的精度(相对误差,R.E。)均在±5.3%和±3.6%之内。本文描述的方法在灵敏度和样品通量方面均优于先前的方法,并成功地用于健康男性志愿者口服后文拉法辛缓释胶囊的临床药代动力学研究。

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