Lee Hon Kit, Ho Chung Shun, Iu Yan Ping Heidi, Lai Po Shan Judy, Shek Chi Chung, Lo Yun-Chuen, Klinke Helene Bendstrup, Wood Michelle
Department of Clinical Pathology, Tuen Mun Hospital, Tuen Mun, Hong Kong.
Anal Chim Acta. 2009 Sep 1;649(1):80-90. doi: 10.1016/j.aca.2009.06.068. Epub 2009 Jul 28.
Withdrawal of the support for the REMEDi HS drug profiling system has necessitated its replacement within our laboratories with an alternative broad toxicological screening technique. To this end, a novel method, based on ultra-performance liquid chromatography (UPLC) and time-of-flight (TOF) mass spectrometry, was developed for the routine analysis of urine samples. Identification was achieved by comparison of acquired data to libraries containing more than 300 common drugs and metabolites, and was based on a combination of retention time, exact mass and fragmentation patterns. Validation data for the method is presented and comprised an evaluation of the following parameters: precision; transferability of the methodology between the six collaborating laboratories; specificity; extraction recovery and stability of processed samples; matrix effects and sensitivity. This paper presents the benefits of supplementary fragmentation data with particular regard to increasing specificity and confidence of identification and its usefulness with overdosed samples. The utility of the method was assessed by the parallel analysis of 30 authentic urine samples using the REMEDi HS and UPLC-TOF. The latter provided enhanced detection, leading to the identification of twice as many drugs. Furthermore it did not miss any compounds that were identified by REMEDi HS. The UPLC-TOF findings were further verified by a combination of data from three other conventional screening techniques, i.e., GC-MS, HPLC-DAD and UPLC-MS/MS.
REMEDi HS药物分析系统的技术支持不再提供,因此我们实验室需要用另一种广泛的毒理学筛查技术取而代之。为此,我们开发了一种基于超高效液相色谱(UPLC)和飞行时间(TOF)质谱的新方法,用于尿液样本的常规分析。通过将采集的数据与包含300多种常见药物和代谢物的数据库进行比较来实现鉴定,鉴定基于保留时间、精确质量和碎片模式的组合。本文给出了该方法的验证数据,包括对以下参数的评估:精密度;该方法在六个合作实验室之间的可转移性;特异性;提取回收率和处理后样品的稳定性;基质效应和灵敏度。本文介绍了补充碎片数据的好处,特别是在提高鉴定的特异性和可信度方面,以及其在过量用药样本中的实用性。通过使用REMEDi HS和UPLC-TOF对30份真实尿液样本进行平行分析,评估了该方法的实用性。后者提供了更强的检测能力,鉴定出的药物数量是前者的两倍。此外,它没有遗漏任何REMEDi HS鉴定出的化合物。UPLC-TOF的结果通过其他三种传统筛查技术(即气相色谱-质谱联用(GC-MS)、高效液相色谱-二极管阵列检测(HPLC-DAD)和超高效液相色谱-串联质谱(UPLC-MS/MS))的数据组合进一步得到验证。