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Recommendations for Improving Identification and Quantification in Non-Targeted GC-MS-Based Metabolomic Profiling of Human Plasma

机译:在基于血浆的基于GC-MS的非靶向代谢组学分析中提高鉴定和定量的建议

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摘要

The field of metabolomics as applied to human disease and health is rapidly expanding. In recent efforts of metabolomics research, greater emphasis has been placed on quality control and method validation. In this study, we report an experience with quality control and a practical application of method validation. Specifically, we sought to identify and modify steps in gas chromatography-mass spectrometry (GC-MS)-based, non-targeted metabolomic profiling of human plasma that could influence metabolite identification and quantification. Our experimental design included two studies: (1) a limiting-dilution study, which investigated the effects of dilution on analyte identification and quantification; and (2) a concentration-specific study, which compared the optimal plasma extract volume established in the first study with the volume used in the current institutional protocol. We confirmed that contaminants, concentration, repeatability and intermediate precision are major factors influencing metabolite identification and quantification. In addition, we established methods for improved metabolite identification and quantification, which were summarized to provide recommendations for experimental design of GC-MS-based non-targeted profiling of human plasma.
机译:应用于人类疾病和健康的代谢组学领域正在迅速扩展。在代谢组学研究的最新努力中,人们更加重视质量控制和方法验证。在这项研究中,我们报告了在质量控制和方法验证的实际应用方面的经验。具体而言,我们试图确定和修改基于气相色谱-质谱(GC-MS)的人血浆非目标代谢组学谱分析中可能影响代谢物鉴定和定量的步骤。我们的实验设计包括两项研究:(1)有限稀释研究,研究稀释对分析物鉴定和定量的影响; (2)一项针对浓度的研究,该研究将第一项研究中确定的最佳血浆提取物体积与当前机构协议中使用的体积进行了比较。我们确认污染物,浓度,重复性和中间精度是影响代谢物鉴定和定量的主要因素。此外,我们建立了改善代谢物鉴定和定量的方法,总结了这些方法,可为基于GC-MS的人血浆非靶向分析的实验设计提供建议。

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