Improved sensitivity of the nano ultra-high performance liquid chromatography-tandem mass spectrometric analysis of low-concentrated neuropeptides by reducing aspecific adsorption and optimizing the injection solvent

被引:36
作者
Maes, Katrien [1 ]
Van Liefferinge, Joeri [1 ]
Viaene, Johan [2 ]
Van Schoors, Jolien [1 ]
Van Wanseele, Yannick [1 ]
Bechade, Guillaume [3 ]
Chambers, Erin E. [4 ]
Morren, Hugo [1 ]
Michotte, Yvette [1 ]
Heyden, Yvan Vander [2 ]
Claereboudt, Jan [3 ]
Smolders, Ilse [1 ]
Van Eeckhauta, Ann [1 ]
机构
[1] Vrije Univ Brussel, Ctr Neurosci C4N, Dept Pharmaceut Chem & Drug Anal, B-1090 Brussels, Belgium
[2] Vrije Univ Brussel, Dept Analyt Chem & Pharmaceut Technol, B-1090 Brussels, Belgium
[3] Waters Corp, B-1731 Zellik, Belgium
[4] Waters Corp, Milford, MA 01757 USA
关键词
Neuropeptides; Nano ultra-high performance liquid chromatography-tandem mass spectrometry; Sensitivity; Aspecific adsorption; Design of experiments; Statistical analysis; IN-VIVO; SOLID-SURFACE; NEUROMEDIN S; LC-MS/MS; PEPTIDES; QUANTIFICATION; SOLUBILITY; PHYSIOLOGY; SULFOXIDE; RECEPTORS;
D O I
10.1016/j.chroma.2014.07.086
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Obtaining maximal sensitivity of nano UHPLC-MS/MS methods is primordial to quantify picomolar concentrations of neuropeptides in microdialysis samples. Since aspecific adsorption of peptides to Eppendorf tubes, pipette tips and UHPLC vials is detrimental for method sensitivity, a strategy is presented to reduce adsorption of these peptides during standard preparation. Within this respect, all procedural steps from dissolution of the lyophilized powder until the injection of the sample onto the system are investigated. Two peptides of the neuromedin family, i.e. neuromedin B and neuromedin N, and a neuromedin N-related neuropeptide, neurotensin, are evaluated. The first part of this study outlines a number of parameters which are known to affect peptide solubility. The main focus of the second part involves the optimization of the sample composition in the UHPLC vial by using design of experiments. Contradictory findings are observed concerning the influence of acetonitrile, salts and matrix components. They are found important for injection of the peptides into the system, but crucially need to be excluded from the dilution solvent. Furthermore, the type of surface material, temperature and the pipetting protocol considerably affect the adsorption phenomenon. Statistical analysis on the results of the central composite design reveals that the highest peptide responses are obtained with the injection solvent consisting of 13.1% V/V ACN and 4.4% V/V FA. This aspect of the optimization strategy can be identified as the main contributor to the gain in method sensitivity. Since the reduction of peptide adsorption and the optimization of the injection solvent resulted in a clear and quantifiable signal of the three peptides, optimization of both issues should be considered in the early stage of method development, in particular when the analysis of low-concentration peptide solutions is envisaged. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:217 / 228
页数:12
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