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直接进样高分辨质谱法测定干血斑中的代谢物。

Quantification of metabolites in dried blood spots by direct infusion high resolution mass spectrometry.

机构信息

Department of Genetics and Center for Molecular Medicine, UMC Utrecht, Utrecht, The Netherlands.

出版信息

Anal Chim Acta. 2017 Aug 1;979:45-50. doi: 10.1016/j.aca.2017.04.038. Epub 2017 Apr 26.

DOI:10.1016/j.aca.2017.04.038
PMID:28599708
Abstract

Diagnosis and treatment of inborn errors of metabolism (IEM) require the analysis of a variety of metabolites. These compounds are usually quantified by targeted platforms. High resolution mass spectrometry (HRMS) has the potential to detect hundreds to thousands of metabolites simultaneously. A chip-based nanoelectrospray source (chip-based nanoESI) enables the direct infusion of biological samples. Major advantages of this system include high sample throughput, no sample carryover, and low sample consumption. The combination, chip-based nanoESI-HRMS enables untargeted metabolomics of biological samples but its potential for quantification of metabolites has not been reported. We investigated whether chip-based nanoESI-HRMS is suitable for quantification of metabolites in dried blood spots (DBS). After addition of internal standards, metabolites were extracted with methanol. Aliquots of each extract were analysed by chip-based nanoESI-HRMS operating in both positive and negative mode with an m/z window of 70-600 and a resolution of 140,000. Total run time was 4.5 min per sample and a full report could be generated within 40 min. Concentrations of all 21 investigated diagnostic metabolites in DBS as quantified by chip-based nanoESI-HRMS correlated well with those obtained by targeted liquid chromatography-tandem mass spectrometry. We conclude that chip-based nanoESI-HRMS is suitable for quantification.

摘要

诊断和治疗先天性代谢错误(IEM)需要分析各种代谢物。这些化合物通常通过靶向平台进行定量。高分辨率质谱(HRMS)具有同时检测数百到数千种代谢物的潜力。基于芯片的纳喷雾源(基于芯片的纳 ESI)可实现生物样本的直接注入。该系统的主要优点包括高样品通量、无样品残留和低样品消耗。该系统与基于芯片的纳 ESI-HRMS 相结合,可实现生物样本的非靶向代谢组学分析,但尚未报道其对代谢物定量的潜力。我们研究了基于芯片的纳 ESI-HRMS 是否适合定量干血斑(DBS)中的代谢物。加入内标后,用甲醇提取代谢物。每份提取物的等分试样分别通过正、负离子模式下的基于芯片的纳 ESI-HRMS 进行分析,m/z 窗口为 70-600,分辨率为 140,000。每个样本的总运行时间为 4.5 分钟,在 40 分钟内可以生成完整报告。通过基于芯片的纳 ESI-HRMS 定量的 DBS 中 21 种研究诊断代谢物的浓度与靶向液相色谱-串联质谱法获得的浓度密切相关。我们得出结论,基于芯片的纳 ESI-HRMS 适合定量。

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