Mano N, Oda Y, Takakuwa S, Chiku S, Nakata H, Asakawa N
Tsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
J Pharm Sci. 1996 Sep;85(9):903-7. doi: 10.1021/js960172n.
A high-performance liquid chromatographic method using the column-switching technique was developed for the simultaneous determination of E3810 and its metabolites (M1-M4). An avidin column was used for in-line pretreatment to exclude plasma proteins, allowing direct injection of a large volume of plasma. A flavoprotein-conjugated chiral stationary phase in a gradient elution mode then gave baseline separation of E3810 and the four metabolites. The enantiomers of E3810 and M3 were also separated. The method is simple, rapid, accurate, and precise. Since no extraction procedure is employed, which might involve different recoveries of different metabolites, no internal standard is necessary. The method was applied to analyze E3810 and its metabolites in plasma after intravenous injection of the drug in beagle dogs.
建立了一种采用柱切换技术的高效液相色谱法,用于同时测定E3810及其代谢物(M1 - M4)。使用抗生物素蛋白柱进行在线预处理以排除血浆蛋白,从而允许直接进样大量血浆。然后,在梯度洗脱模式下使用黄素蛋白偶联手性固定相,实现了E3810及其四种代谢物的基线分离。E3810和M3的对映体也得以分离。该方法简便、快速、准确且精密。由于未采用可能涉及不同代谢物回收率不同的提取程序,因此无需内标。该方法应用于分析比格犬静脉注射该药物后血浆中的E3810及其代谢物。