Potential of LC Coupled to Fluorescence Detection in Food Metabolomics: Determination of Phenolic Compounds in Virgin Olive Oil
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Monasterio, Romina P; Olmo García, Lucía; Bajoub, Aadil; Fernández Gutiérrez, Alberto; Carrasco Pancorbo, AlegríaEditorial
MDPI
Materia
Fluorescence detection Olive oil Phenolic compounds
Date
2016-09-24Referencia bibliográfica
Monasterio, R.P.; Olmo-García, L.; Bajoub, A.; Fernández-Gutiérrez, A.; Carrasco-Pancorbo, A. Potential of LC Coupled to Fluorescence Detection in Food Metabolomics: Determination of Phenolic Compounds in Virgin Olive Oil. Int. J. Mol. Sci. 2016, 17, 1627. https://doi.org/10.3390/ijms17101627
Sponsorship
Spanish Government (Ministry of Education, Culture and Sport) by means of a FPU fellowship (FPU13/06438); Ministry of Economy and Competitiveness with project CTQ2014-53442-P; FONCyT (PICT 2013-0547); CONICET; Fellowship from Fundación Carolina, SpainAbstract
A powerful chromatographic method coupled to a fluorescence detector was developed
to determine the phenolic compounds present in virgin olive oil (VOO), with the aim to propose
an appropriate alternative to liquid chromatography-mass spectrometry. An excitation wavelength
of 285 nm was selected and four different emission wavelengths (316, 328, 350 and 450 nm) were
simultaneously recorded, working therefore on “multi-emission” detection mode. With the use of
commercially available standards and other standards obtained by semipreparative high performance
liquid chromatography, it was possible to identify simple phenols, lignans, several complex phenols,
and other phenolic compounds present in the matrix under study. A total of 26 phenolic compounds
belonging to different chemical families were identified (23 of them were susceptible of being
quantified). The proposed methodology provided detection and quantification limits within the
ranges of 0.004–7.143 µg·mL-1 and 0.013–23.810 µg·mL-1, respectively. As far as the repeatability is
concerned, the relative standard deviation values were below 0.43% for retention time, and 9.05% for
peak area. The developed methodology was applied for the determination of phenolic compounds in
ten VOOs, both monovarietals and blends. Secoiridoids were the most abundant fraction in all the
samples, followed by simple phenolic alcohols, lignans, flavonoids, and phenolic acids (being the
abundance order of the latter chemical classes logically depending on the variety and origin of
the VOOs).