Development of a nano-liquid chromatography on chip tandem mass spectrometry method for high-sensitivity hepcidin quantitation

被引:33
|
作者
Houbart, V. [1 ]
Cobraiville, G. [2 ]
Lecomte, F. [3 ]
Debrus, B. [3 ]
Hubert, Ph. [3 ]
Fillet, M. [1 ,2 ]
机构
[1] Univ Liege, Lab Analyt Pharmaceut Chem, Dept Pharm, CIRM, B-4000 Liege, Belgium
[2] Univ Liege, Clin Chem Lab, GIGA Res, B-4000 Liege, Belgium
[3] Univ Liege, Analyt Chem Lab, Dept Pharm, CIRM, B-4000 Liege, Belgium
关键词
LC-chip; Peptide quantitation; Mass spectrometry; Validation; SFSTP PROPOSAL; IRON-METABOLISM; LC-MS; PEPTIDES; HPLC; VALIDATION; SERUM; HARMONIZATION; STRATEGIES; BIOMARKER;
D O I
10.1016/j.chroma.2011.10.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microfluidic LC systems present undeniable advantages over classical LC in terms of sensitivity. Hepcidin, a peptide marker of clinical disorders linked to iron metabolism, was used as model to demonstrate peptide quantification potentialities of LC-chip coupled to a nanoelectrospray source ion trap mass spectrometer in an aqueous sample. First, stable isotope labelled hepcidin was chosen as internal standard and gradient as well as sample compositions were optimised using design of experiments as development tool. The method was then prevalidated using accuracy profiles in order to select the most appropriate response function and to confirm the ability of the technique to quantify low hepcidin concentration. A reliable and very sensitive quantitation method was finally obtained using this integrated microfluidic technology. Indeed, good results with respect to accuracy, trueness and precision were achieved, as well as a very low limit of quantitation (0.07 ng/ml). Method suitability of nano-LC on chip tandem mass spectrometry for hepcidin quantitation was also demonstrated in complex media such as human plasma. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:9046 / 9054
页数:9
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