Quantitative analysis of phenylalanine, tyrosine, tryptophan and kynurenine in rat model for tauopathies by ultra-high performance liquid chromatography with fluorescence and mass spectrometry detection

被引:27
作者
Galba, Jaroslav [1 ,3 ]
Michalicova, Alena [1 ,2 ]
Parrak, Vojtech [1 ,2 ]
Novak, Michal [1 ,2 ]
Kovac, Andrej [1 ,2 ]
机构
[1] Slovak Acad Sci, Inst Neuroimmunol, Bratislava 84510, Slovakia
[2] AXON Neurosci SE, Bratislava 81102, Slovakia
[3] Comenius Univ, Fac Pharm, Dept Pharmaceut Anal & Nucl Pharm, Bratislava 83232, Slovakia
关键词
Tauopathy; UPLC/FLD/MS; QDa; Immune system; Plasma; Rat model; Tau protein; BLOOD-BRAIN-BARRIER; ALZHEIMERS-DISEASE; IMMUNE ACTIVATION; METABOLISM;
D O I
10.1016/j.jpba.2015.08.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We developed and validated a simple and sensitive ultra-high performance liquid chromatography (UHPLC) method for the analysis of phenylalanine (Phe), tyrosine (Tyr), tryptophan (Trp) and kynurenine (Kyn) in rat plasma. Analytes were separated on Acquity UPLC HSS T3 column (2.1 mm x 50 mm, 1.8 mu m particle size) using a 4 min ammonium acetate (pH 5) gradient and detected by fluorescence and positive ESI mass spectrometry. Sample preparation involved dilution of plasma, deproteinization by trichloroacetic acid and centrifugation. The procedure was validated in compliance with the FDA guideline. The limits of quantification (LOQ) were 0.3 mu M for Kyn and from 1.5 to 3 mu M for Phe, Tyr, Trp. The method showed excellent linearity with regression coefficients higher than 0.99. The accuracy was within the range of 86-108%. The inter-day precision (n = 5 days), expressed as % RSD, was in the range 1-13%. The benefit of using UHPLC is a short analysis period and thus, a very good sample throughput. Using this method, we analyzed plasma samples and detected significant changes of Kyn and Phe in transgenic rat model for tauopathies. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:85 / 90
页数:6
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