Chen Guodong, Daaro Ibrahim, Pramanik Birendra N, Piwinski John J
Schering-Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA.
J Mass Spectrom. 2009 Feb;44(2):203-13. doi: 10.1002/jms.1498.
In vitro drug metabolism study is an integral part of drug discovery process. In this report, we have described the application of LTQ-Orbitrap hybrid mass spectrometer in conjunction with online hydrogen (H)/deuterium (D) exchange high resolution (HR)-LC/MS for structural characterization of in vitro rat liver microsomal metabolites of antihistamine desloratadine. Five metabolites M1--M5 have been identified, including three hydroxylated metabolites M1--M3, one N-oxide M4 and one uncommon aromatized N-oxide M5. Accurate mass data have been obtained in both full scan and MSn mode support assignments of metabolite structures with reported mass errors less than 3 ppm. Online H/D exchange HR-LC/MS experiments provide additional evidence in differentiating hydroxylated metabolites from N-oxides. This study demonstrates the effectiveness of this approach in structural characterization of drug metabolites.
体外药物代谢研究是药物研发过程中不可或缺的一部分。在本报告中,我们描述了LTQ-轨道阱混合质谱仪与在线氢(H)/氘(D)交换高分辨率(HR)-液相色谱/质谱联用技术在抗组胺药地氯雷他定体外大鼠肝微粒体代谢产物结构表征中的应用。已鉴定出五种代谢产物M1 - M5,包括三种羟基化代谢产物M1 - M3、一种N-氧化物M4和一种不常见的芳构化N-氧化物M5。在全扫描和MSn模式下均获得了精确质量数据,支持代谢产物结构的归属,所报告的质量误差小于3 ppm。在线H/D交换HR-液相色谱/质谱实验为区分羟基化代谢产物和N-氧化物提供了额外证据。本研究证明了该方法在药物代谢产物结构表征中的有效性。