Qiu X-J, Zheng S-L, Wang Y-F, Wang R, Ye L
Department of Pharmacology, Medical College of Henan University of Science and Technology, Luoyang, China.
The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Drug Res (Stuttg). 2014 Jun;64(6):330-4. doi: 10.1055/s-0034-1368702. Epub 2014 Feb 18.
In this study, a simple, rapid and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method is described for determination of domperidone in human plasma samples using oxcarbazepine as the internal standard (IS). Sample preparation was accomplished through protein precipitation with methanol, and chromatographic separation was performed on an Acquity BEH C18 column (2.1 mm×50 mm, 1.7 μm) with gradient profile at a flow 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 transition of m/z 426.3→175.2 was used to quantify for domperidone. The linearity of this method was found to be within the concentration range of 0.25-100.0 ng/mL for domperidone in human plasma. Only 1.5 min was needed for an analytical run. The method herein described was superior to previous methods and was successfully applied to the pharmacokinetic study of domperidone in healthy Chinese volunteers after oral administration.
在本研究中,描述了一种简单、快速且灵敏的超高效液相色谱串联质谱法(UPLC-MS/MS),以奥卡西平作为内标(IS)测定人血浆样品中的多潘立酮。样品制备通过用甲醇进行蛋白沉淀完成,色谱分离在Acquity BEH C18柱(2.1 mm×50 mm,1.7 μm)上进行,采用梯度洗脱,流速为0.45 mL/min。质谱分析使用配备电喷雾电离(ESI)源的QTrap5500质谱仪在正离子模式下进行。m/z 426.3→175.2的多反应监测(MRM)转换用于定量多潘立酮。该方法在人血浆中多潘立酮的浓度范围为0.25 - 100.0 ng/mL内呈线性。一次分析运行仅需1.5分钟。本文所述方法优于先前方法,并成功应用于健康中国志愿者口服多潘立酮后的药代动力学研究。