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Multiple Time-of-Flight/Time-of-Flight Events in a Single Laser Shot for Improved Matrix-Assisted Laser Desorption/Ionization Tandem Mass Spectrometry Quantification

机译:单次激光发射中的多个飞行时间/飞行时间事件,用于改进的基质辅助激光解吸/电离串联质谱定量

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摘要

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 internal technology allows the reference of analyte intensity to that of the 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-2) 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.
机译:过去,定量基质辅助激光解吸/电离飞行时间(MALDI TOF)方法的准确性和精密度较差,这主要是由于基质和分析物在目标表面的分布不均匀,基质干扰和电离抑制所致。串联质谱(MS / MS)可用于消除化学噪声干扰,从而减轻对动态范围的担忧,从而确保化学特异性并改善信噪比。但是,传统的MALDI TOF / TOF模式通常每次激光扫描仅扫描一次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,该方法允许在单个激光照射中执行多个TOF / TOF碎片事件。这种内部技术即使在分析物和内标物的m / z差异很大的情况下,也能使每次激光照射中的分析物强度参考标准物的强度,从而在保持化学特异性和占空比的同时提高了定量。在以雷米普利作为内标物对合并的人血浆中的依那普利进行定量分析时,观察到相对标准偏差(<10%)的改善幅度超过4倍,测定系数(R-2)和准确性(> 85%的质量控制)。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对三种药物(异丙嗪,依那普利和维拉帕米)进行了同时定量分析。

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