Plasma tryptophan, kynurenine and 3-hydroxykynurenine measurement using automated on-line solid-phase extraction HPLC-tandem mass spectrometry

被引:91
作者
de Jong, Wilhelmina H. A. [1 ]
Smit, Reinier [1 ]
Bakker, Stephan J. L. [2 ]
de Vries, Elisabeth G. E. [3 ]
Kema, Ido P. [1 ]
机构
[1] Univ Groningen, Dept Lab Med, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Dept Nephrol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen, Dept Med Oncol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 07期
关键词
Tryptophan; Kynurenine; Tryptophan-to-kynurenine ratio; IDO; 3-hydroxykynurenine; On-line SPE; Mass spectrometry; XLC-MS/MS; Plasma; PERFORMANCE LIQUID-CHROMATOGRAPHY; URINARY ALBUMIN EXCRETION; INDOLEAMINE 2,3-DIOXYGENASE; FLUORESCENCE DETECTION; SERUM; METABOLITES; ACID; CATABOLISM; SEROTONIN;
D O I
10.1016/j.jchromb.2009.01.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Tryptophan metabolism plays a key role in several (patho)physiological conditions. In order to study the clinical importance of tryptophan and its predominant metabolites (kynurenines), it is important to be able to measure large series of samples with high accuracy and reliability. We aimed to develop a high-throughput on-line solid-phase extraction-liquid chromatographic-tandem mass spectrometric (XLC-MS/MS) method that enables the measurement of tryptophan and its metabolites kynurenine and 3-hydroxykynurenine in plasma. Fifty microliters plasma equivalent was pre-purified by automated on-line solid-phase extraction, using strong cation exchange (PRS. propylsulphonic) cartridges. Chromatographic separation of the analytes and deuterated analogues occurred by C18 reversed phase chromatography. Mass spectrometric detection was performed in the multiple reaction-monitoring mode using a quadrupole tandem mass spectrometer with positive electrospray ionization. Total run-time including sample clean-up was 8 min. Intra- and inter-assay analytical variations were less than 9%. Linearity in the 0.11 -1200 (tryptophan) and 0.050 and 0.023-45 mu mol/L (kynurenine and 3-hydroxylkynurenine, respectively) calibration range was excellent (R > 0.99). Detection limits were 30 nmol/L for tryptophan, I nmol/L for kyriurenine and 5 nmol/L for 3-hydroxykynurenine. Reference intervals for 120 healthy adults were 45.5-83.1 mu mol/L (tryptophan), 1.14-3.02 mu mol/L (kynurenine), <0.13 mu mol/L (3-hydroxylkynurenine) and 19.0-49.8 for tryptophan-to-kynurenine ratio. Blood sampling for tryptophan and tryptophan-tokynurenine ratio should be performed before breakfast, due to biological variation during the day. This Study describes how plasma tryptophan, kynurenine and 3-hydroxykynurenine can be measured accurately and precisely by automated high-throughput XLC-MS/MS. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:603 / 609
页数:7
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