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Method development and validation of Guanfacine in rat plasma by liquid chromatography–tandem mass spectrometry: Application to a pharmacokinetic study

机译:液相色谱-串联质谱法在大鼠血浆中胍法辛的方法开发和验证:在药代动力学研究中的应用

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摘要

A selective, sensitive and high-throughput liquid chromatography–tandem mass spectrometry (LC–ESI-MS/MS) method has been developed and validated for the quantitation of Guanfacine in rat plasma. Sample clean-up involved liquid–liquid extraction (LLE) and 100 μL of rat plasma was used. YMC BASIC column (50 mm×2.0 mm, 3.5 µm) was used. Mobile phase used was 10 mM ammonium formate (pH 4.0):acetonitrile (70:30, v/v) at a flow rate of 0.3 mL/min. The parent→product ion transitions for the drug (m/z 246.0→159.0) and IS (m/z 252.0→161.1) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and positive ion mode. The method was validated over the concentration range of 50.00–10,000.00 pg/mL for Guanfacine. The method was successfully applied into a pharmacokinetic study in rat plasma.
机译:一种选择性,灵敏,高通量的液相色谱-串联质谱(LC-ESI-MS / MS)方法已经开发出来,并已用于大鼠血浆中胍法辛的定量验证。样品净化涉及液液萃取(LLE),并使用100μL大鼠血浆。使用YMC BASIC色谱柱(50mm×2.0mm,3.5μm)。使用的流动相为10 mM甲酸铵(pH 4.0):乙腈(70:30,v / v),流速为0.3 mL / min。在三重四极杆质谱仪上以多反应监测(MRM)和正离子模式运行,监测药物的母体→产物离子跃迁(m / z 246.0→159.0)和IS(m / z 252.0→161.1)。该方法在胍法辛的50.00–10,000.00 pg / mL浓度范围内得到验证。该方法已成功地应用于大鼠血浆的药代动力学研究。

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