Sensitive determination of a pharmaceutical compound and its metabolites in human plasma by ultra-high performance liquid chromatography-tandem mass spectrometry with on-line solid-phase extraction

被引:16
作者
Heinig, K. [1 ]
Wirz, T. [1 ]
Bucheli, F. [1 ]
Monin, V. [1 ]
Gloge, A. [1 ]
机构
[1] F Hoffmann La Roche Ltd, Pharma Res, Nonclin Safety, DMPK Dev, CH-4070 Basel, Switzerland
关键词
UHPLC; LC-MS/MS; On-line SPE; Human plasma; Microdosing; MICRODOSE CLINICAL-TRIAL; QUANTITATIVE-DETERMINATION; IONIZATION; DRUGS;
D O I
10.1016/j.jpba.2010.10.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper describes the determination of a drug candidate and two metabolites in human plasma by column-switching LC-MS/MS after protein precipitation. Starting from a standard method with a quantitation limit of 0.5 ng/mL, a highly sensitive assay was developed, employing UHPLC separation and detection on an API 5000 mass spectrometer. The injected plasma equivalent was increased from 6 to 204; conventional column trapping for compound enrichment and removal of matrix constituents was combined with high-pressure analytical separation using small particle columns to improve resolution and signal-to-noise ratio. Quantitation limits were thus lowered to between Sand 20 pg/mL, offering the possibility to provide bioanalytical support for microdosing studies in humans. Excellent assay quality and robustness were achieved by both methods. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:742 / 749
页数:8
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