Measurement of serotonin in platelet depleted plasma by liquid chromatography tandem mass spectrometry

被引:29
作者
Monaghan, Phillip J. [1 ,2 ]
Brown, Heather A. [3 ]
Houghton, Lesley A. [4 ]
Keevil, Brian G. [2 ]
机构
[1] Wirral Univ Teaching Hosp, Dept Clin Biochem, Wirral CH49 5PE, Merseyside, England
[2] S Manchester Univ Hosp Trust, Dept Clin Biochem, Manchester M23 9LT, Lancs, England
[3] Waters MS Technol Ctr, Manchester M22 5PP, Lancs, England
[4] S Manchester Univ Hosp Trust, Neurogastroenterol Unit, Manchester M23 9LT, Lancs, England
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2009年 / 877卷 / 22期
关键词
Serotonin; LC-MS/MS; Protein precipitation; Functional gastrointestinal disorders; IRRITABLE-BOWEL-SYNDROME; WHOLE-BLOOD; 5-HYDROXYTRYPTAMINE; PREDOMINANT; VALIDATION; RELEASE;
D O I
10.1016/j.jchromb.2009.05.045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
5-Hydroxytryptamine (5-HT) in human platelet depleted plasma (PDP) is a biomarker in functional gastrointestinal disorders (FGID), with levels reflecting acute changes in circulating 5-HT concentration. POP 5-HT is currently measured by reversed phase high performance liquid chromatography (HPLC) fluorimetric detection. We have developed a simple and rapid liquid chromatography tandem mass spectrometry (LC-MS/MS) method that is two times more rapid than the current HPLC methodology. Our method employs a simple protein precipitation requiring no further downstream sample preparation. 10 mu L of extract was injected directly onto a SecurityGuard SCX cation exchange column followed by isocratic elution onto an Onyx Monolithic C18 analytical column and methanolic gradient elution. Eluant was connected directly to a Quattro Premier XE tandem mass spectrometer operating in ES+ mode. We detected multiple reaction monitoring transitions m/z 160 > 114.9 and m/z 164.1 > 118.9 for 5-HT and d(4)-5-HT, respectively. 5-HT and d(4)-5-HT co-eluted at 2.79 min and cycle time between injections was 6 min. Mean recovery was 98%, limit of detection 1.5 nmol/L, lower limit of quantification 5 nmol/L, linearity to 1000 nmol/L(r(2) = 0.999), imprecision <10% and bias <13.4%. 5-HT eluted with no ion suppression. No interference was found with L-tryptophan or 5-hydroxyindoleacetic acid (5-HIAA). This assay was compared to a previously published HPLC method. Passing-Bablok regression analysis showed LC-MS/MS=0.91 (HPLC)-0.83, r(2) = 0.97, n = 80. Bland Altman analysis showed general agreement, with a mean bias of 3.3 nmol/L We have developed a simple and robust assay for POP 5-HT that will increase throughput for clinical trials. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2163 / 2167
页数:5
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