Hsieh Yunsheng, Duncan Christine J G, Liu Ming
Drug Metabolism and Pharmacokinetics Department, Schering-Plough Research Institute, Kenilworth, NJ 07033, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Jul 1;854(1-2):8-12. doi: 10.1016/j.jchromb.2007.03.034. Epub 2007 Apr 5.
A novel mixed-mode high performance liquid chromatographic system (HPLC) interfaced with an atmospheric pressure chemical ionization (APCI) source and a tandem mass spectrometer (MS/MS) was developed for the determination of cytarabine (ara-C) in mouse plasma to support pharmacodynamic studies. The mixed-mode reversed-phase ion-exchange chromatography column was adapted for sufficient retention and separation of a small and polar analyte. The impact of the mobile phase composition on both chromatographic separation and the ionization efficiency of the test compound in the positive mode was investigated. The potential of ionization suppression from endogenous biological matrices on the mixed-mode LC-APCI/MS/MS method was evaluated using the post-column infusion technique. Furthermore, the feasibility of using the mixed-mode HPLC-MS/MS method for the determination of the plasma concentrations of cytarabine in mice was demonstrated by comparing those obtained by the ion-pairing HPLC-MS/MS method.
为支持药效学研究,开发了一种新型的混合模式高效液相色谱系统(HPLC),该系统与大气压化学电离(APCI)源和串联质谱仪(MS/MS)联用,用于测定小鼠血浆中的阿糖胞苷(ara-C)。混合模式反相离子交换色谱柱适用于对小分子极性分析物进行充分保留和分离。研究了流动相组成对色谱分离以及正模式下被测化合物电离效率的影响。采用柱后注入技术评估了内源性生物基质对混合模式LC-APCI/MS/MS方法的电离抑制潜力。此外,通过比较离子对HPLC-MS/MS方法获得的结果,证明了使用混合模式HPLC-MS/MS方法测定小鼠血浆中阿糖胞苷浓度的可行性。