College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Rapid Commun Mass Spectrom. 2010 Jan;24(1):75-84. doi: 10.1002/rcm.4365.
Recent advances in liquid chromatography/tandem mass spectrometry (LC/MS/MS) technology have provided an opportunity for the development of more specific approaches to achieve the 'screen' and 'confirmation' goals in a single analytical step. For this purpose, this study adapts the electrospray ionization ion trap LC/MS/MS instrumentation (LC/ESI-MS/MS) for the screening and confirmation of over 800 drugs and toxic compounds in biological specimens. Liquid-liquid and solid-phase extraction protocols were coupled to LC/ESI-MS/MS using a 1.8-microm particle size analytical column operated at 50 degrees C. Gradient elution of the analytes was conducted using a solvent system composed of methanol and water containing 0.1% formic acid. Positive-ion ESI-MS/MS spectra and retention times for each of the 800 drugs and toxic compounds were first established using 1-10 microg/mL standard solutions. This spectra and retention time information was then transferred to the library and searched by the identification algorithm for the confirmation of compounds found in test specimens - based on retention time matches and scores of fit, reverse fit, and purity resulting from the searching process. The established method was found highly effective when applied to the analyses of postmortem specimens (blood, urine, and hair) and external proficiency test samples provided by the College of American Pathology (CAP). The development of this approach has significantly improved the efficiency of our routine laboratory operation that was based on a two-step (immunoassay and GC/MS) approach in the past.
近年来,液相色谱/串联质谱(LC/MS/MS)技术的进步为开发更具特异性的方法提供了机会,以实现单一分析步骤中的“筛选”和“确证”目标。为此,本研究采用电喷雾离子阱 LC/MS/MS 仪器(LC/ESI-MS/MS),对生物标本中的 800 多种药物和有毒化合物进行筛选和确证。采用液相-液相和固相萃取方案,将其与 LC/ESI-MS/MS 联用,使用 1.8 微米粒径的分析柱,在 50°C 下操作。采用甲醇和水组成的溶剂系统,含有 0.1%甲酸,对分析物进行梯度洗脱。使用 1-10μg/mL 标准溶液,首先为 800 种药物和有毒化合物中的每一种建立正离子 ESI-MS/MS 图谱和保留时间。然后,将这些图谱和保留时间信息转移到库中,并通过鉴定算法进行搜索,以确认在测试标本中发现的化合物-基于保留时间匹配和拟合、反向拟合以及搜索过程产生的纯度的分数。该方法在对法医标本(血液、尿液和头发)和美国病理学院(CAP)提供的外部能力验证样本进行分析时,效果非常显著。该方法的建立极大地提高了我们常规实验室操作的效率,过去我们的实验室操作是基于两步法(免疫测定和 GC/MS)进行的。