Department of Biochemistry, ‡Department of Chemistry, §Departments of Pharmacology and Medicine, and ∥Mass Spectrometry Research Center, Vanderbilt University , Nashville, Tennessee 37232, United States.
Anal Chem. 2016 Oct 4;88(19):9780-9788. doi: 10.1021/acs.analchem.6b02821. Epub 2016 Sep 14.
Quantitative matrix-assisted laser desorption/ionization time-of-flight (MALDI TOF) approaches have historically suffered from poor accuracy and precision mainly due to the nonuniform distribution of matrix and analyte across the target surface, matrix interferences, and ionization suppression. Tandem mass spectrometry (MS/MS) can be used to ensure chemical specificity as well as improve signal-to-noise ratios by eliminating interferences from chemical noise, alleviating some concerns about dynamic range. However, conventional MALDI TOF/TOF modalities typically only scan for a single MS/MS event per laser shot, and multiplex assays require sequential analyses. We describe here new methodology that allows for multiple TOF/TOF fragmentation events to be performed in a single laser shot. This technology allows the reference of analyte intensity to that of the internal standard in each laser shot, even when the analyte and internal standard are quite disparate in m/z, thereby improving quantification while maintaining chemical specificity and duty cycle. In the quantitative analysis of the drug enalapril in pooled human plasma with ramipril as an internal standard, a greater than 4-fold improvement in relative standard deviation (<10%) was observed as well as improved coefficients of determination (R) and accuracy (>85% quality controls). Using this approach we have also performed simultaneous quantitative analysis of three drugs (promethazine, enalapril, and verapamil) using deuterated analogues of these drugs as internal standards.
定量基质辅助激光解吸/电离飞行时间(MALDI-TOF)方法在历史上主要由于基质和分析物在靶表面上的不均匀分布、基质干扰和抑制电离而受到准确性和精密度差的困扰。串联质谱(MS/MS)可用于通过消除化学噪声干扰、缓解动态范围的一些担忧来确保化学特异性和提高信噪比。然而,传统的 MALDI-TOF/TOF 模式通常每次激光射击只能扫描单个 MS/MS 事件,并且多重分析需要顺序分析。我们在这里描述了一种新的方法学,允许在单个激光射击中进行多个 TOF/TOF 碎裂事件。这项技术允许在每个激光射击中参考分析物强度与内标物的强度,即使分析物和内标物在 m/z 上有很大的差异,从而在保持化学特异性和工作周期的同时提高定量分析的准确性。在以雷米普利作为内标物对人血浆中依那普利的定量分析中,观察到相对标准偏差(<10%)提高了 4 倍以上,并且改善了决定系数(R)和准确性(>85%的质控)。使用这种方法,我们还使用这些药物的氘代类似物作为内标物对三种药物(苯海拉明、依那普利和维拉帕米)进行了同时定量分析。