Wang K, Davis P P, Crews T, Gabriel L, Edom R W
Department of Drug Metabolism and Pharmacokinetics, Hoffmann-La Roche, Incorporated, Nutley, New Jersey 07110, USA.
Anal Biochem. 1996 Dec 1;243(1):28-40. doi: 10.1006/abio.1996.0478.
A practical analytical method has been developed for the determination of an analog of vitamin D3 (Ro 24-2090) in plasma samples. The method employs liquid-liquid extraction, precolumn derivatization, HPLC separation using an automated column-switching system, and particle-beam negative ionization MS determination. An electron-capture derivatization reagent, 4-pentafluorobenzyl-1,2,4-triazoline-3,5-dione, is utilized to attain high sensitivity through a unique ionization mechanism. The method achieved a lower limit of quantitation of 25 pg (63 fmol) of Ro 24-2090 in plasma aliquots ranging from 0.125 to 1.0 ml. Method validation data were obtained for the quantitation of Ro 24-2090 in plasma from humans and seven animal species. Intraassay precision [mean percent relative standard deviation (%RSD)] ranged from 1.49 to 7.12% among the various species. Interassay precision (mean %RSD) ranged from 4.28 to 17.5%. Mean overall recovery ranged from 71 to 89%. The method has been successfully used to analyze plasma samples from several pharmacokinetic studies. The potential use of this method for determination of vitamin D2, vitamin D3, 1 alpha, 25-dihydroxyvitamin D3, and other drugs containing a diene structural moiety is discussed.
已开发出一种实用的分析方法,用于测定血浆样品中维生素D3类似物(Ro 24-2090)。该方法采用液-液萃取、柱前衍生化、使用自动柱切换系统的高效液相色谱分离以及粒子束负离子化质谱测定。利用电子捕获衍生化试剂4-五氟苄基-1,2,4-三唑啉-3,5-二酮,通过独特的电离机制实现高灵敏度。该方法在0.125至1.0 ml的血浆等分试样中,Ro 24-2090的定量下限达到25 pg(63 fmol)。获得了用于定量人及七种动物物种血浆中Ro 24-2090的方法验证数据。各物种内的批内精密度[平均相对标准偏差百分比(%RSD)]在1.49%至7.12%之间。批间精密度(平均%RSD)在4.28%至17.5%之间。平均总回收率在71%至89%之间。该方法已成功用于多项药代动力学研究的血浆样品分析。还讨论了该方法用于测定维生素D2、维生素D3、1α,25-二羟基维生素D3以及其他含有二烯结构部分的药物的潜在用途。