Articles producció científica> Bioquímica i Biotecnologia

Development and validation of a UHPLC-ESI-MS/MS method for the simultaneous quantification of mammal lysophosphatidylcholines and lysophosphatidylethanolamines in serum

  • Datos identificativos

    Identificador: PC:2741
    Handle: http://hdl.handle.net/20.500.11797/PC2741
  • Autores:

    Suárez-García, S.
    Arola, L.
    Pascual-Serrano, A.
    Arola-Arnal, A.
    Aragonès, G.
    Bladé, C.
    Suárez, M.
  • Otros:

    Autor según el artículo: Suárez-García, S.; Arola, L.; Pascual-Serrano, A.; Arola-Arnal, A.; Aragonès, G.; Bladé, C.; Suárez, M.
    Departamento: Bioquímica i Biotecnologia
    Autor/es de la URV: SUÁREZ GARCÍA, SUSANA; AROLA FERRER, LUIS MARIA; PASCUAL SERRANO, AÏDA; AROLA ARNAL, ANNA; ARAGONÈS BARGALLÓ, GERARD; BLADÉ SEGARRA, MARIA CINTA; SUÁREZ RECIO, MANUEL
    Palabras clave: Biomarkers Cafeteria diet Glycerophospholipid
    Resumen: Recent investigations based on non-targeted metabolomics have proposed lysophospholipids (Lyso-PLs) as biomarkers of different diseases. In particular, lysophosphatidylcholines (Lyso-PCs) and lysophosphatidylethanolamines (Lyso-PEs) have been associated with serious lipid pathologies. Methods to determine the different molecular species in a biological sample and to quantify even less abundant species are required for the evaluation of the Lyso-PL pattern as a novel comprehensive biomarker of dyslipidemia. This study describes the development and validation of an ultra-high-performance liquid chromatography coupled to tandem mass spectrometry assay for the determination of a large number of Lyso-PCs and Lyso-PEs in biological samples. The method was validated in rat serum using two simple methanol-based extractions with low sample volumes (5–50 μL) that covered the wide concentration range of these metabolites. In total, thirty-one Lyso-PLs were separated and quantified with low method limits of detection and quantification, reaching values of 0.2 and 0.8 nM, respectively. The method was subsequently applied in the identification of Lyso-PL-related changes produced by the chronic intake of a cafeteria diet. The results showed alterations in the majority of Lyso-PCs and Lyso-PEs in rat serum. Furthermore, multivariate analysis indicated that the comprehensive evaluation of serum Lyso-PLs could be an excellent indicator of the nutritional phenotype associated with an increased risk of lipid disorders.
    Grupo de investigación: Grup de Recerca en Nutrigenòmica Unitat de Recerca Biomèdica
    Áreas temáticas: Bioquímica i biotecnologia Bioquímica y tecnología Biochemistry and technology
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 1570-0232
    Identificador del autor: ; 0000-0003-2767-1974; ; 0000-0001-6529-1345; 0000-0001-8657-5726; 0000-0003-2838-2402;
    Fecha de alta del registro: 2017-05-17
    Página final: 97
    Volumen de revista: 1055-1056
    Versión del articulo depositado: info:eu-repo/semantics/publishedVersion
    Enlace a la fuente original: http://www.sciencedirect.com/science/article/pii/S1570023217303082
    DOI del artículo: 10.1016/j.jchromb.2017.04.028
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2017
    Página inicial: 86
    Tipo de publicación: Article Artículo Article
  • Palabras clave:

    Marcadors bioquímics
    Lipids
    Biomarkers
    Cafeteria diet
    Glycerophospholipid
    Bioquímica i biotecnologia
    Bioquímica y tecnología
    Biochemistry and technology
    1570-0232
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