College of Pharmacy and Nutrition, University of Saskatchewan, 107 Wiggins Rd, Saskatoon, SK, S7N 5E5, Canada.
Faculty of Pharmacy, Alexandria University, Alexandria, 21521, Egypt.
Mass Spectrom Rev. 2017 Mar;36(2):115-134. doi: 10.1002/mas.21455. Epub 2015 Apr 16.
Urine metabolomics has recently emerged as a prominent field for the discovery of non-invasive biomarkers that can detect subtle metabolic discrepancies in response to a specific disease or therapeutic intervention. Urine, compared to other biofluids, is characterized by its ease of collection, richness in metabolites and its ability to reflect imbalances of all biochemical pathways within the body. Following urine collection for metabolomic analysis, samples must be immediately frozen to quench any biogenic and/or non-biogenic chemical reactions. According to the aim of the experiment; sample preparation can vary from simple procedures such as filtration to more specific extraction protocols such as liquid-liquid extraction. Due to the lack of comprehensive studies on urine metabolome stability, higher storage temperatures (i.e. 4°C) and repetitive freeze-thaw cycles should be avoided. To date, among all analytical techniques, mass spectrometry (MS) provides the best sensitivity, selectivity and identification capabilities to analyze the majority of the metabolite composition in the urine. Combined with the qualitative and quantitative capabilities of MS, and due to the continuous improvements in its related technologies (i.e. ultra high-performance liquid chromatography [UPLC] and hydrophilic interaction liquid chromatography [HILIC]), liquid chromatography (LC)-MS is unequivocally the most utilized and the most informative analytical tool employed in urine metabolomics. Furthermore, differential isotope tagging techniques has provided a solution to ion suppression from urine matrix thus allowing for quantitative analysis. In addition to LC-MS, other MS-based technologies have been utilized in urine metabolomics. These include direct injection (infusion)-MS, capillary electrophoresis-MS and gas chromatography-MS. In this article, the current progresses of different MS-based techniques in exploring the urine metabolome as well as the recent findings in providing potentially diagnostic urinary biomarkers are discussed. © 2015 Wiley Periodicals, Inc. Mass Spec Rev 36:115-134, 2017.
尿液代谢组学最近成为一个突出的领域,用于发现非侵入性生物标志物,以检测对特定疾病或治疗干预的微妙代谢差异。与其他生物体液相比,尿液具有采集方便、代谢物丰富、能够反映体内所有生化途径失衡的特点。进行代谢组学分析后,必须立即将尿液样本冷冻以抑制任何生物和/或非生物化学反应。根据实验目的的不同,样品制备可以从简单的过滤程序到更具体的提取方案,如液液萃取。由于缺乏对尿液代谢组稳定性的全面研究,应避免较高的储存温度(如 4°C)和反复的冻融循环。迄今为止,在所有分析技术中,质谱(MS)提供了最好的灵敏度、选择性和识别能力,可用于分析尿液中大多数代谢物的组成。结合 MS 的定性和定量能力,并且由于其相关技术(即超高效液相色谱[UPLC]和亲水相互作用液相色谱[HILIC])的不断改进,LC-MS 无疑是尿液代谢组学中使用最广泛、信息量最大的分析工具。此外,差异同位素标记技术为尿液基质的离子抑制提供了解决方案,从而允许进行定量分析。除了 LC-MS 外,其他基于 MS 的技术也已用于尿液代谢组学。这些技术包括直接进样(注入)-MS、毛细管电泳-MS 和气相色谱-MS。本文讨论了不同基于 MS 的技术在探索尿液代谢组学方面的最新进展,以及在提供潜在诊断性尿液生物标志物方面的最新发现。©2015Wiley Periodicals, Inc. Mass Spec Rev 36:115-134, 2017.