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Validation of the Mass-Extraction-Window for Quantitative Methods Using Liquid Chromatography High Resolution Mass Spectrometry

机译:使用液相色谱高分辨率质谱对定量方法的质量提取窗口进行验证

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A paradigm shift is underway in the field of quantitative liquid chromatography-mass spectrometry (LC-MS) analysis thanks to the arrival of recent high-resolution mass spectrometers (HRMS). The capability of HRMS to perform sensitive and reliable quantifications of a large variety of analytes in HR-full scan mode is showing that it is now realistic to perform quantitative and qualitative analysis with the same instrument. Moreover, HR-full scan acquisition offers a global view of sample extracts and allows retrospective investigations as virtually all ionized compounds are detected with a high sensitivity. In time, the versatility of HRMS together with the increasing need for relative quantification of hundreds of endogenous metabolites should promote a shift from triple-quadrupole MS to HRMS. However, a current "pitfall" in quantitative LC-HRMS analysis is the lack of HRMS-specific guidance for validated quantitative analyses. Indeed, false positive and false negative HRMS detections are rare, albeit possible, if inadequate parameters are used. Here, we investigated two key parameters for the validation of LC-HRMS quantitative analyses: the mass accuracy (MA) and the mass-extraction-window (MEW) that is used to construct the extracted-ion-chromatograms. We propose MA-parameters, graphs, and equations to calculate rational MEW width for the validation of quantitative LC-HRMS methods. MA measurements were performed on four different LC-HRMS platforms. Experimentally determined MEW values ranged between 5.6 and 16.5 ppm and depended on the HRMS platform, its working environment, the calibration procedure, and the analyte considered. The proposed procedure provides a fit-for-purpose MEW determination and prevents false detections.
机译:由于最近的高分辨率质谱仪(HRMS)的出现,定量液相色谱-质谱(LC-MS)分析领域正在发生范式转变。 HRMS在HR全扫描模式下对多种分析物进行灵敏和可靠的定量分析的能力表明,现在使用同一仪器进行定量和定性分析是现实的。此外,HR全扫描采集提供了样品提取物的全局视图,并允许进行回顾性研究,因为实际上所有离子化化合物都以高灵敏度被检测到。随着时间的流逝,HRMS的多功能性以及对数百种内源性代谢物的相对定量的日益增长的需求应促使从三重四极杆质谱仪向HRMS的转变。但是,定量LC-HRMS分析中的当前“陷阱”是缺乏经过验证的定量分析的HRMS专用指南。确实,即使使用的参数不足,也很少会出现假阳性和假阴性HRMS检测。在这里,我们调查了用于验证LC-HRMS定量分析的两个关键参数:质量准确度(MA)和用于构建提取离子色谱图的质量提取窗口(MEW)。我们提出MA参数,图形和方程式,以计算合理的MEW宽度,以验证定量LC-HRMS方法的有效性。 MA测量是在四个不同的LC-HRMS平台上进行的。实验确定的MEW值介于5.6和16.5 ppm之间,并且取决于HRMS平台,其工作环境,校准程序和所考虑的分析物。所提出的程序提供了适合目的的MEW确定并防止了错误检测。

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