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UPLC-MS/MS determination of phentolamine in human plasma and its application to a pharmacokinetic study

机译:UPLC-MS / MS测定人血浆中的酚妥拉明及其在药代动力学研究中的应用

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摘要

A sensitive and rapid ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed to determine phentolamine in human plasma. Sample preparation was accomplished through a simple liquid-liquid extraction with ethyl acetate. Chromatographic separation was carried out on an Acquity UPLC BEH C18 column using an isocratic mobile phase system composed of acetonitrile and 1% formic acid in water (33:67, v/v) at a flow rate of 0.45 mL/min. Mass spectrometric analysis was performed using a QTrap5500 mass spectrometer coupled with an electro-spray ionization (ESI) source in the positive ion mode. The MRM transitions of m/z 282.1 → 212.0 and m/z 237.1 → 194.2 were used to quantify for phentolamine and carbamazepine (internal standard, IS), respectively. The linearity of this method was found to be within the concentration range of 0.5-100.0 ng/mL with a lower limit of quantification of 0.5 ng/mL. Only 1.0 min was needed for an analytical run. This fully validated method was successfully applied to the pharmacokinetic study after oral administration of 60 mg phentolamine to 20 Chinese healthy male volunteers.
机译:建立了灵敏快速的超高效液相色谱串联质谱法(UPLC-MS / MS),用于测定人血浆中的酚妥拉明。通过用乙酸乙酯进行简单的液-液萃取来完成样品的制备。色谱分离在Acquity UPLC BEH C18色谱柱上进行,使用等度流动相系统,该系统由乙腈和1%甲酸的水溶液(33:67,v / v)组成,流速为0.45 mL / min。使用QTrap5500质谱仪和正离子模式下的电喷雾电离(ESI)源进行质谱分析。 m / z 282.1→212.0和m / z 237.1→194.2的MRM跃迁分别用于量化苯妥拉明和卡马西平(内标,IS)。发现该方法的线性在0.5-100.0 ng / mL的浓度范围内,定量下限为0.5 ng / mL。分析运行仅需1.0分钟。在对20位中国健康男性志愿者口服60 mg酚妥拉明后,这种经过充分验证的方法已成功应用于药代动力学研究。

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