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针对色氨酸、酪氨酸和支链氨基酸途径的人血浆和尿液代谢谱分析

Metabolic Profiling of Human Plasma and Urine, Targeting Tryptophan, Tyrosine and Branched Chain Amino Acid Pathways.

作者信息

Anesi Andrea, Rubert Josep, Oluwagbemigun Kolade, Orozco-Ruiz Ximena, Nöthlings Ute, Breteler Monique M B, Mattivi Fulvio

机构信息

Department of Food Quality and Nutrition, Research and Innovation Centre, Fondazione Edmund Mach (FEM), Via E. Mach 1, 38010 San Michele all' Adige, Italy.

CIBIO, Department of Cellular, Computational and Integrative Biology, Via Sommarive 9, 38123 Povo, Italy.

出版信息

Metabolites. 2019 Nov 1;9(11):261. doi: 10.3390/metabo9110261.

Abstract

Tryptophan and tyrosine metabolism has a major effect on human health, and disorders have been associated with the development of several pathologies. Recently, gut microbial metabolism was found to be important for maintaining correct physiology. Here, we describe the development and validation of a UHPLC-ESI-MS/MS method for targeted quantification of 39 metabolites related to tryptophan and tyrosine metabolism, branched chain amino acids and gut-derived metabolites in human plasma and urine. Extraction from plasma was optimised using 96-well plates, shown to be effective in removing phospholipids. Urine was filtered and diluted ten-fold. Metabolites were separated with reverse phase chromatography and detected using triple quadrupole MS. Linear ranges (from ppb to ppm) and correlation coefficients ( > 0.990) were established for both matrices independently and the method was shown to be linear for all tested metabolites. At medium spiked concentration, recovery was over 80% in both matrices, while analytical precision was excellent (CV < 15%). Matrix effects were minimal and retention time stability was excellent. The applicability of the methods was tested on biological samples, and metabolite concentrations were found to be in agreement with available data. The method allows the analysis of up to 96 samples per day and was demonstrated to be stable for up to three weeks from acquisition.

摘要

色氨酸和酪氨酸代谢对人类健康有重大影响,相关紊乱与多种疾病的发生有关。最近,人们发现肠道微生物代谢对于维持正常生理功能很重要。在此,我们描述了一种超高效液相色谱-电喷雾串联质谱(UHPLC-ESI-MS/MS)方法的开发与验证,该方法用于靶向定量人血浆和尿液中与色氨酸和酪氨酸代谢、支链氨基酸及肠道衍生代谢物相关的39种代谢物。使用96孔板对血浆提取进行了优化,结果表明其能有效去除磷脂。尿液经过过滤并稀释10倍。代谢物通过反相色谱进行分离,并用三重四极杆质谱进行检测。分别为两种基质建立了线性范围(从ppb到ppm)和相关系数(>0.990),且该方法对所有测试代谢物均呈线性。在中等加标浓度下,两种基质中的回收率均超过80%,同时分析精密度良好(CV<15%)。基质效应最小,保留时间稳定性良好。该方法在生物样品上进行了适用性测试,发现代谢物浓度与现有数据一致。该方法每天可分析多达96个样品,且从采集起长达三周内都证明是稳定的。

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