2015
DOI: 10.1016/j.foodchem.2014.05.153
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Potential of LC–MS phenolic profiling combined with multivariate analysis as an approach for the determination of the geographical origin of north Moroccan virgin olive oils

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Cited by 55 publications
(47 citation statements)
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“…The mobile phases used were water with acetic acid (0.5%) (Phase A) and acetonitrile (Phase B), and the solvent gradient changed according to the following conditions [7]: 0 to 10 min, 5%–30% B; 10 to 12 min, 30%–33% B; 12 to 17 min, 33%–38% B; 17 to 20 min, 38%–50% B; 20 to 23 min, 50%–95% B. Finally, the B content was decreased to the initial conditions (5%) in 2 min and the column re-equilibrated for 2.5 min.…”
Section: Methodsmentioning
confidence: 99%
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“…The mobile phases used were water with acetic acid (0.5%) (Phase A) and acetonitrile (Phase B), and the solvent gradient changed according to the following conditions [7]: 0 to 10 min, 5%–30% B; 10 to 12 min, 30%–33% B; 12 to 17 min, 33%–38% B; 17 to 20 min, 38%–50% B; 20 to 23 min, 50%–95% B. Finally, the B content was decreased to the initial conditions (5%) in 2 min and the column re-equilibrated for 2.5 min.…”
Section: Methodsmentioning
confidence: 99%
“…Some other important parameters in that detector were 2.31 Hz for signal acquisition rate (0.2 min of peak width which corresponds to a response time of 4 s), 10 units for photomultiplier (PMT) gain, 5% of Zero offset and 100 Lu of attenuation in analog output. Besides, previously optimized conditions for phenolic compounds detection were employed in DAD (240, 280, and 330 nm) (data has not been considered in the manuscript to contain the size of the contribution) and the MS detector [7]. The most relevant ionization source and transferring MS parameters resulted to be: nebulizer pressure, drying gas flow and drying temperature, which were set at 30 psi, 9 L·min −1 and 300 °C, respectively; and voltages in the end plate offset and in the capillary, which were −500 V and +3200 V, apiece.…”
Section: Methodsmentioning
confidence: 99%
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“…This method defines the RI as a function of fruit colour in both skin and pulp (Uceda & Frías, 1975). Oil extraction was performed at laboratory scale by an Oliomio laboratory mill (Oliomio, Italy), following a previously described procedure (Bajoub, Carrasco-Pancorbo, Ajal, Ouazzani, & Fernández-Gutiérrez, 2014). Afterwards, olive oil samples were filtered and stored in dark glass bottles (250 ml), excluding any head space volume, in order to ensure the proper conservation of the olive oil against oxidation, and kept in the freezer at −18 ºC until the analysis.…”
Section: Olive Sampling and Oil Extractionmentioning
confidence: 99%
“…Very few works can be cited to illustrate this point (Bajoub, Carrasco-Pancorbo, Ajal, Ouazzani, & Fernández-Gutiérrez, 2014;Haddi et al, 2013Haddi et al, , 2011Houlali et al, 2014), but they open up great expectations for testing the suitability of some olive oil compounds to be used as geographical markers of Moroccan VOOs.…”
Section: Introductionmentioning
confidence: 99%