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Título
Non-separative determination of isomeric polycyclic aromatic hydrocarbons by electrospray Ag(I) cationization mass spectrometry and multivariate calibration
Autor(es)
Palabras clave
Flow injection analysis
Mass spectrometry
Ag (I) cationization
Polycyclic aromatic hydrocarbons
PLS models
Experimental design
Clasificación UNESCO
23 Química
Fecha de publicación
2022
Editor
Elsevier
Citación
María Casas-Ferreira, A., Del Nogal Sánchez, M., Rodríguez-Gonzalo, E., & Pérez Pavón, J. L. (2022). Non-separative determination of isomeric polycyclic aromatic hydrocarbons by electrospray Ag(I) cationization mass spectrometry and multivariate calibration. Microchemical Journal, 183, 108072. https://doi.org/10.1016/j.microc.2022.108072
Resumen
[EN] A new approach for the determination of isomeric polycyclic aromatic hydrocarbons using a stand-alone mass
spectrometry method is proposed. The aim of the work is to study quantitative possibilities of multivariate
calibration and electrospray Ag(I) cationization mass spectrometry for the non-separative determination of
polycyclic aromatic hydrocarbons isomers. The method is based on flow injection analysis, electrospray ionization and tandem mass spectrometry (FIA-ESI-MS/MS). No chromatographic column was included into the
instrumental configuration and the analysis time was 1.7 min. Seven polycyclic aromatic hydrocarbons were
selected as test compounds and the ionization was achieved by forming complexes with Ag (I). Individual
quantification of all the isomers was carried out by using PLS multivariate calibration and experimental design
for calibration modeling. The PLS models were used to predict the concentration of the analytes in a set of
external validation samples and satisfactory results were obtained. RMSE, expressed as a relative value, were
found to be between 23 and 34 %. Results obtained with multivariate analysis were compared with those corresponding to univariate calibration to show its high potential.
URI
ISSN
0026-265X
DOI
10.1016/j.microc.2022.108072
Versión del editor
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Patrocinador
Publicación en abierto financiada por la Universidad de Salamanca como participante en el Acuerdo Transformativo CRUE-CSIC con Elsevier, 2021-2024