Zell M, Husser C, Hopfgartner G
Department of Drug Metabolism & Pharmacokinetics, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Rapid Commun Mass Spectrom. 1997;11(10):1107-14. doi: 10.1002/(SICI)1097-0231(19970630)11:10<1107::AID-RCM959>3.0.CO;2-0.
A coupled liquid chromatography/tandem mass spectrometry assay was developed for simultaneous determination of Ro 48-6791 and its secondary amine metabolite in human plasma samples with a quantification limit for both compounds of 1 pg/mL using a 1 mL plasma aliquot. The method exploits the enhanced mass sensitivity of a microbore (300 microns i.d.) reversed-phase capillary column coupled to an ion spray probe combined with tandem mass spectrometry. A straightforward column-switching system was utilized to focus the analytes onto a microbore trapping column following solid-phase extraction of a 50 microL plasma sample extract from liquid/liquid extraction. Backflushing of the retained analytes from the trapping column onto the microbore capillary column provided the requisite high peak concentration for high sensitivity. The inter-assay precision and accuracy for Ro 48-6791 and its metabolite, at 10 pg/mL, were found to be 3.4%, and 105%, and 9.1%, and 99.9%, respectively. The calibration curves were linear over the range 1 to 1000 pg/mL. The method proved to be sufficiently rugged for analysis of samples.
开发了一种液相色谱/串联质谱联用测定法,用于同时测定人血浆样品中的Ro 48-6791及其仲胺代谢物,使用1 mL血浆等分试样时,两种化合物的定量限均为1 pg/mL。该方法利用了内径为300微米的微径反相毛细管柱与离子喷雾探针联用串联质谱所具有的增强的质量灵敏度。采用了一种简单的柱切换系统,在对50微升血浆样品提取物进行液/液萃取后的固相萃取过程中,将分析物聚焦到微径捕集柱上。将保留在捕集柱上的分析物反冲至微径毛细管柱上,可提供高灵敏度所需的高峰浓度。发现Ro 48-6791及其代谢物在10 pg/mL时的批间精密度和准确度分别为3.4%、105%以及9.1%、99.9%。校准曲线在1至1000 pg/mL范围内呈线性。该方法经证明对样品分析具有足够的耐用性。