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Ultrahigh-Performance Liquid Chromatography Tandem Mass Spectrometry with Electrospray Ionization Quantification of Tryptophan Metabolites and Markers of Gut Health in Serum and Plasma—Application to Clinical and Epidemiology Cohorts

色谱法 化学 分析物 串联质谱法 选择性反应监测 电喷雾电离 犬尿氨酸 固相萃取 蛋白质沉淀 质谱法 液相色谱-质谱法 电喷雾 色氨酸 生物化学 氨基酸
作者
Luke Whiley,Leanne C. Nye,Isobelle Grant,Nick Andreas,Katie E. Chappell,Magali Sarafian,Ravi Misra,Robert S. Plumb,Matthew R. Lewis,Jeremy K. Nicholson,Elaine Holmes,Jonathan R. Swann,Ian D. Wilson
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:91 (8): 5207-5216 被引量:89
标识
DOI:10.1021/acs.analchem.8b05884
摘要

A targeted ultrahigh-performance liquid chromatography tandem mass spectrometry with electrospray ionization (UHPLC-ESI-MS/MS) method has been developed for the quantification of tryptophan and its downstream metabolites from the kynurenine and serotonin pathways. The assay coverage also includes markers of gut health and inflammation, including citrulline and neopterin. The method was designed in 96-well plate format for application in multiday, multiplate clinical and epidemiology population studies. A chromatographic cycle time of 7 min enables the analysis of two 96-well plates in 24 h. To protect chromatographic column lifespan, samples underwent a two-step extraction, using solvent protein precipitation followed by delipidation via solid-phase extraction (SPE). Analytical validation reported accuracy of each analyte <20% for the lowest limit of quantification and <15% for all other quality control (QC) levels. The analytical precision for each analyte was 2.1-12.9%. To test the applicability of the method to multiplate and multiday preparations, a serum pool underwent periodic repeat analysis during a run consisting of 18 plates. The % CV (coefficient of variation) values obtained for each analyte were <15%. Additional biological testing applied the assay to samples collected from healthy control participants and two groups diagnosed with inflammatory bowel disease (IBD) (one group treated with the anti-inflammatory 5-aminosalicylic acid (5-ASA) and one group untreated), with results showing significant differences in the concentrations of picolinic acid, kynurenine, and xanthurenic acid. The short analysis time and 96-well plate format of the assay makes it suitable for high-throughput targeted UHPLC-ESI-MS/MS metabolomic analysis in large-scale clinical and epidemiological population studies.
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