Current trends and challenges in sample preparation for global metabolomics using liquid chromatography-mass spectrometry

被引:375
作者
Vuckovic, Dajana [1 ]
机构
[1] Univ Toronto, Donnelly Ctr Cellular & Biomol Res, Toronto, ON M5S 3E1, Canada
关键词
Metabolomics; Untargeted metabolite profiling; Sample preparation; Metabolism quenching; Solvent extraction; Ultrafiltration; In vivo sampling; Dried blood spots; Method development; Liquid chromatography-mass spectrometry (LC-MS); Mammalian cells; Tissue; SOLID-PHASE MICROEXTRACTION; DRIED BLOOD SPOTS; TISSUE-TARGETED METABONOMICS; METABOLITE EXTRACTION; HUMAN PLASMA; BIOLOGICAL SAMPLES; QUANTITATIVE METABOLOMICS; RELATIVE QUANTIFICATION; HPLC-MS; TOF-MS;
D O I
10.1007/s00216-012-6039-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The choice of sample-preparation method is extremely important in metabolomic studies because it affects both the observed metabolite content and biological interpretation of the data. An ideal sample-preparation method for global metabolomics should (i) be as non-selective as possible to ensure adequate depth of metabolite coverage; (ii) be simple and fast to prevent metabolite loss and/or degradation during the preparation procedure and enable high-throughput; (iii) be reproducible; and (iv) incorporate a metabolism-quenching step to represent true metabolome composition at the time of sampling. Despite its importance, sample preparation is often an overlooked aspect of metabolomics, so the focus of this review is to explore the role, challenges, and trends in sample preparation specifically within the context of global metabolomics by liquid chromatography-mass spectrometry (LC-MS). This review will cover the most common methods including solvent precipitation and extraction, solid-phase extraction and ultrafiltration, and discuss how to improve analytical quality and metabolite coverage in metabolomic studies of biofluids, tissues, and mammalian cells. Recent developments in this field will also be critically examined, including in vivo methods, turbulent-flow chromatography, and dried blood spot sampling.
引用
收藏
页码:1523 / 1548
页数:26
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