Journal
FOOD RESEARCH INTERNATIONAL
Volume 54, Issue 1, Pages 587-594Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.foodres.2013.07.043
Keywords
Canolol; Mustard seed oil; Lipid oxidation; Antioxidant; Roasting; Phospholipid browning
Categories
Funding
- Special Research Fund - BOF, Ghent University
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The oxidative stability of the roasted and unroasted crude mustard seed oil samples collected from the Nepalese market was evaluated by monitoring the peroxide value (PV) and conjugated diene (CD) during storage in the dark at 50 degrees C. These samples showed a wide variability in the oxidative stability as measured by PV ranging from 5.22 to 42.11 meq oxygen/kg oil after 69 days of storage. The PV after 40 days of storage (PV40) as an index of oxidative stability of the different samples was not significantly correlated (p > 0.05) both with the total radical scavenger concentration (sum of tocopherol, plastochromanol-8 and canolol) and the total radical scavenging capacity of the oil using the di(phenyl)-(2,4,6-trinitrophenyl)iminoazanium (DPPH) assay. Hence, those antioxidants were not solely responsible for the differences in the oxidative stability among the oil samples. On the other hand, the PV40 showed significant negative correlation with the canolol content (p < 0.01), the phospholipid content (p < 0.001) and the different browning reaction markers such as absorbance at 350 nm (p < 0.001), fluorescence (excitation at 350 nm and emission at 440 nm) (p < 0.001), and the pyrrolized phospholipid content (p < 0.01). Moreover, all the browning reaction markers and phospholipid content were also highly positively correlated (p < 0.001) with each other. The phospholipid and its Maillard type browning reaction products together with canolol formed during seed roasting were primarily responsible for the high oxidative stability of the roasted mustard seed oil samples. (C) 2013 Elsevier Ltd. All rights reserved.
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