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首页> 外文期刊>Journal of Chromatographic Science >UPLC-MS-MS Determination of Dihydrocodeine in Human Plasma and Its Application to a Pharmacokinetic Study
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UPLC-MS-MS Determination of Dihydrocodeine in Human Plasma and Its Application to a Pharmacokinetic Study

机译:UPLC-MS-MS测定人血浆中的双氢可待因及其在药代动力学研究中的应用

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A sensitive and rapid ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS-MS) method was developed to determine dihydrocodeine (DHC) in human plasma using diazepam as the internal standard (IS). Sample preparation was accomplished through a liquid-liquid extraction procedure with ethyl acetate. The analyte and IS were separated on an Acquity UPLC BEH C18 column (2.1 x 50 mm, 1.7 mu m) with the mobile phase of acetonitrile and 1% formic acid in water with gradient elution at a flow rate of 0.4 mL/min. The detection was performed on a triple quadrupole tandem mass spectrometer equipped with positive-ion electrospray ionization by multiple reaction monitoring (MRM) of the transitions at m/z 302.3 -> 199.2 for DHC and m/z 285.1 -> 193.1 for IS. The linearity of this method was found to be within the concentration range of 0.5-100 ng/mL with a lower limit of quantification of 0.5 ng/mL. The overall run time was 4.0 min. The method herein described was superior to previous methods and was successfully applied to the pharmacokinetic study of DHC in healthy Chinese volunteers after oral administration.
机译:建立了灵敏快速的超高效液相色谱串联质谱(UPLC-MS-MS)方法,以地西epa为内标(IS)测定人血浆中的双氢可待因(DHC)。通过使用乙酸乙酯的液-液萃取程序完成样品制备。在Acquity UPLC BEH C18色谱柱(2.1 x 50 mm,1.7μm)上,用乙腈和1%甲酸的流动相在水中进行梯度洗脱,以0.4 mL / min的流速分离分析物和IS。该检测是在配备正离子电喷雾电离的三重四极杆串联质谱仪上进行的,通过多反应监测(MRM)进行DHC的m / z 302.3-> 199.2和IS的m / z 285.1-> 193.1的跃迁。发现该方法的线性在0.5-100 ng / mL的浓度范围内,定量下限为0.5 ng / mL。总体运行时间为4.0分钟。本文描述的方法优于先前的方法,并已成功应用于口服后健康中国志愿者DHC的药代动力学研究。

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