Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/11067
Title: Comprehensive analysis by liquid chromatography Q‐Orbitrap mass spectrometry : fast screening of peptides and organic molecules.
Authors: Sardela, Vinícius Figueiredo
Martucci, Maria Elvira Poleti
Araujo, Amanda Lessa Dutra de
Leal, E. C.
Oliveira, D. S.
Carneiro, G. R. A.
Deventer, K.
Eenoo, P. Van
Pereira, Henrique Marcelo Gualberto
Aquino Neto, Francisco Radler de
Keywords: Anti‐doping control
High‐resolution mass spectrometry
Olympic Games
Q‐Exactive
Issue Date: 2018
Citation: SARDELA, V. F. et al. Comprehensive analysis by liquid chromatography Q‐Orbitrap mass spectrometry : fast screening of peptides and organic molecules. Journal of Mass Spectrometry, v. 53, n. 6, p. 476-503, jun. 2018. Disponível em: <https://onlinelibrary.wiley.com/doi/full/10.1002/jms.4077>. Acesso em: 25 fev. 2019.
Abstract: The number of substances nominally listed in the prohibited list of the World Anti‐ Doping Agency increases each year. Moreover, many of these substances do not have a single analytical target and must be monitored through different metabolites, artifacts, degradation products, or biomarkers. A new analytical method was developed and validated for the simultaneous analysis of peptides and organic molecules using a single sample preparation and LC‐Q‐HRMS detection. The simultaneous analysis of 450 target molecules was performed after cleanup on a mixed‐mode solid‐phase extraction cartridge, combined with untreated urine. The cleanup solvent and reconstitution solvent were the most important parameters for achieving a comprehensive sample preparation approach. A fast chromatographic run based on a multistep gradient was optimized under different flows; the detection of all substances without isomeric coelution was achieved in 11 minutes, and the chromatographic resolution was considered a critical parameter, even in high‐resolution mass spectrometry detection. The mass spectrometer was set to operate by switching between positive and negative ionization mode for FULL‐MS, all‐ion fragmentation, and FULL‐MS/MS2 . The suitable parameters for the curved linear trap (c‐trap) conditions were determined and found to be the most important factors for the development of the method. Only FULL‐MS/ MS2 enables the detection of steroids and peptides at concentrations lower than the minimum required performance levels set by World Anti‐Doping Agency (1 ng mL−1 ). The combination of the maximum injection time of the ions into the c‐trap, multiplexing experiments, and loop count under optimized conditions enabled the method to be applied to over 10 000 samples in only 2 months during the 2016 Rio Summer Olympic and Paralympic Games. The procedure details all aspects, from sample preparation to mass spectrometry detection. FULL‐MS data acquisition is performed in positive and negative ion mode simultaneously and can be applied to untargeted approaches.
URI: http://www.repositorio.ufop.br/handle/123456789/11067
metadata.dc.identifier.uri2: https://onlinelibrary.wiley.com/doi/full/10.1002/jms.4077
metadata.dc.identifier.doi: https://doi.org/10.1002/jms.4077
ISSN: 1096-9888
Appears in Collections:DEFAR - Artigos publicados em periódicos

Files in This Item:
File Description SizeFormat 
ARTIGO_ComprehensiveAnalysisLiquid.pdf1,73 MBAdobe PDFView/Open    Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.