King Richard, Fernandez-Metzler Carmen
Department of Drug Metabolism, Merck and Co., Inc., West Point, PA 19486, USA.
Curr Drug Metab. 2006 Jun;7(5):541-5. doi: 10.2174/138920006777697936.
Advances in mass spectrometry continue to bring new and exciting capabilities to the study of drug metabolism. This review covers the hybrid linear ion trap - triple quadrupole mass spectrometer, the QTrap. While still a recent addition to the arsenal of mass spectrometry techniques available to the metabolism scientist, reports in the literature highlight the advantages of the system for metabolite identification. The system combines the selective scans of the triple quadrupole with the high speed, high sensitivity of the ion trap allowing metabolites to be found and characterized in a single scan. Additionally, the system has MS(3) and time delayed fragmentation scans that aid in structure elucidation. Since the fragmentation occurs in the collision cell of the triple quadrupole, the traditionally rich fragmentation of the collision cell fragmentation is preserved. In addition to helping to make traditional processes more efficient, work has been done that shows the potential of the instrument to change traditional DMPK approaches. Researchers have reported methods that allow for both qualitative analysis of circulating metabolites and quantification of parent drug within the same analysis. The approaches reported show how the instrument can be used to collect more information from every sample and potentially streamline typical drug metabolism assays.
质谱技术的进步不断为药物代谢研究带来新的、令人兴奋的能力。本综述涵盖了混合线性离子阱-三重四极杆质谱仪,即QTrap。虽然它在代谢科学家可用的质谱技术中仍是新成员,但文献报道突出了该系统在代谢物鉴定方面的优势。该系统将三重四极杆的选择性扫描与离子阱的高速、高灵敏度相结合,使得代谢物能够在单次扫描中被发现并表征。此外,该系统具有MS(3)和延时碎裂扫描,有助于结构解析。由于碎裂发生在三重四极杆的碰撞池中,碰撞池碎裂传统上丰富的碎裂得以保留。除了有助于提高传统流程的效率外,已有研究表明该仪器有改变传统药物代谢动力学方法的潜力。研究人员报告了一些方法,这些方法能够在同一分析中对循环代谢物进行定性分析,并对母体药物进行定量。所报道的方法展示了该仪器如何用于从每个样品中收集更多信息,并有可能简化典型的药物代谢分析。