Delgado-Povedano M M, Calderón-Santiago M, Priego-Capote F, Luque de Castro M D
Department of Analytical Chemistry, Annex Marie Curie Building, Campus of Rabanales, University of Córdoba, Córdoba, Spain; ceiA3 Agroalimentary Excellence Campus, University of Córdoba, Córdoba, Spain; Maimónides Institute of Biomedical Research (IMIBIC), Reina Sofía University Hospital, Córdoba, Spain.
Department of Analytical Chemistry, Annex Marie Curie Building, Campus of Rabanales, University of Córdoba, Córdoba, Spain; ceiA3 Agroalimentary Excellence Campus, University of Córdoba, Córdoba, Spain; Maimónides Institute of Biomedical Research (IMIBIC), Reina Sofía University Hospital, Córdoba, Spain.
Anal Chim Acta. 2016 Jan 28;905:115-25. doi: 10.1016/j.aca.2015.11.048. Epub 2015 Dec 17.
Sweat has recently gained popularity as clinical sample in metabolomics analysis as it is a non-invasive biofluid the composition of which could be modified by certain pathologies, as is the case with cystic fibrosis that increases chloride levels in sweat. However, the whole composition of sweat is still unknown and there is a lack of analytical strategies for sweat analysis. The aim of the present study was to develop and validate a method for metabolomic analysis of human sweat by gas chromatography-time of flight/mass spectrometry (GC-TOF/MS) in high resolution mode. Thus, different sample preparation strategies were compared to check their effect on the profile of sweat metabolites. Sixty-six compounds were tentatively identified by the obtained MS information. Amino acids, dicarboxylic acids and other interesting metabolites such as myo-inositol and urocanic acid were identified. Among the tested protocols, methyoxiamination plus silylation after deproteinization was the most suited option to obtain a representative snapshot of sweat metabolome. The intra-day repeatability of the method ranged from 0.60 to 16.99% and the inter-day repeatability from 2.75 to 31.25%. As most of the identified metabolites are involved in key biochemical pathways, this study opens new possibilities to the use of sweat as a source of metabolite biomarkers of specific disorders.
汗液作为代谢组学分析中的临床样本最近受到了关注,因为它是一种非侵入性生物流体,其成分可因某些病理状况而改变,如囊性纤维化会使汗液中的氯化物水平升高。然而,汗液的整体成分仍然未知,且缺乏用于汗液分析的分析策略。本研究的目的是开发并验证一种通过高分辨率模式的气相色谱 - 飞行时间/质谱(GC - TOF/MS)对人汗液进行代谢组学分析的方法。因此,比较了不同的样品制备策略,以检查它们对汗液代谢物谱的影响。通过获得的质谱信息初步鉴定出66种化合物。鉴定出了氨基酸、二羧酸以及其他有趣的代谢物,如肌醇和尿刊酸。在所测试的方案中,脱蛋白后进行甲氧基胺化加硅烷化是获得汗液代谢组代表性快照的最合适选择。该方法的日内重复性范围为0.60%至16.99%,日间重复性范围为2.75%至31.25%。由于大多数鉴定出的代谢物参与关键生化途径,本研究为将汗液用作特定疾病代谢物生物标志物的来源开辟了新的可能性。