Dubey Sunil Kumar, Saha R N, Jangala Hemanth, Pasha S
Department of Pharmacy, Birla Institute of Technology & Science, Pilani, India.
Institute of Genomics and Integrative Biology, Mall Road, Delhi, India.
J Pharm Anal. 2013 Dec;3(6):466-471. doi: 10.1016/j.jpha.2013.05.002. Epub 2013 Jun 3.
A new ultra-performance liquid chromatography-electrospray ionization mass spectrometry (UPLC-MS/ESI) method for simultaneous determination of venlafaxine (VEN) and its metabolite O-desmethylvenlafaxine (ODV) in rat plasma has been developed and validated using Venlafaxine d6 as the internal standard. The compounds and internal standard were extracted from plasma by solid phase extraction. The UPLC separation of the analytes was performed on ACQUITY UPLC BEH Shield RP18 (1.7 µm, 100 mm×2.1 mm) column, using isocratic elution with mobile phase constituted of water (containing 2 mM ammonium acetate): acetonitrile (20:80, v/v) at a flow rate of 0.3 mL/min. All of the analytes were eluted within 1.5 min. The compounds were ionized in the electrospray ionization (ESI) ion source of the mass spectrometer, operating in multiple reaction monitoring (MRM) and positive ion mode. The precursor to product ion transitions monitored for VEN, ODV and Venlafaxine d6 were / 278.3→121.08, 264.2→107.1 and 284.4→121.0, respectively. The developed and validated method was used for the pharmacokinetic study of VEN in rats.
建立了一种使用文拉法辛-d6作为内标同时测定大鼠血浆中盐酸文拉法辛(VEN)及其代谢产物O-去甲基文拉法辛(ODV)的超高效液相色谱-电喷雾电离质谱(UPLC-MS/ESI)新方法,并进行了验证。通过固相萃取从血浆中提取化合物和内标。在ACQUITY UPLC BEH Shield RP18(1.7 µm,100 mm×2.1 mm)色谱柱上对分析物进行UPLC分离,采用等度洗脱,流动相由水(含2 mM醋酸铵):乙腈(20:80,v/v)组成,流速为0.3 mL/min。所有分析物在1.5分钟内洗脱完毕。化合物在质谱仪的电喷雾电离(ESI)离子源中电离,以多反应监测(MRM)和正离子模式运行。监测到的VEN、ODV和文拉法辛-d6的前体离子到产物离子的跃迁分别为/ 278.3→121.08、264.2→107.1和284.4→121.0。所建立并验证的方法用于VEN在大鼠体内的药代动力学研究。