Fast, general-purpose metabolome analysis by mixed-mode liquid chromatography – mass spectrometry

IF 3.3 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Analyst Pub Date : 2025-10-02 DOI:10.1039/d5an00641d
Mario S.P. Correia, Alaa Othman, Nicola Zamboni
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引用次数: 0

Abstract

Comprehensive metabolomics requires robust and efficient analytical techniques capable of addressing the chemical diversity, complexity, and high sample throughput demands characteristic of large-scale studies. We introduce a rapid, mixed-mode liquid chromatography method that uniquely integrates anion exchange and hydrophobic interactions within a single stationary phase. Employing an optimized ternary gradient, our method achieves comprehensive separation of diverse metabolite classes over a wide range of polarities within only 4 minutes per run. The performance was tested with standards for ca. 1000 metabolites. For two-thirds of 94 isomeric sets, we could achieve a separation of 2 or more seconds, which is sufficient for correct identification. We demonstrate robustness over 500 consecutive injections of bacterial extracts and with the analysis of complex matrices like plasma, cecum extracts, and urine. Throughout, retention time drifts were < 1 s. Our mixed-mode LC-MS approach offers a routine throughput of 360 samples/day/instrument and is ideally suited for studies that require rapid and comprehensive metabolic profiling.
快速,通用代谢组分析混合模式液相色谱-质谱
综合代谢组学需要强大而高效的分析技术,能够解决化学多样性、复杂性和大规模研究的高样品通量要求。我们介绍了一种快速的混合模式液相色谱方法,该方法独特地将阴离子交换和疏水相互作用集成在单个固定相中。采用优化的三元梯度,我们的方法在每次运行仅4分钟内就可以在广泛的极性范围内实现各种代谢物类别的全面分离。用约1000种代谢物的标准进行性能测试。对于94个同分异构体的三分之二,我们可以实现2秒或更长时间的分离,这足以正确识别。我们证明了500次连续注射细菌提取物的稳健性,并分析了复杂的基质,如血浆、盲肠提取物和尿液。在整个过程中,滞留时间漂移为1 s。我们的混合模式LC-MS方法提供360个样品/天/仪器的常规吞吐量,非常适合需要快速和全面代谢分析的研究。
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来源期刊
Analyst
Analyst 化学-分析化学
CiteScore
7.80
自引率
4.80%
发文量
636
审稿时长
1.9 months
期刊介绍: "Analyst" journal is the home of premier fundamental discoveries, inventions and applications in the analytical and bioanalytical sciences.
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