期刊
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 48, 期 3, 页码 648-656出版社
AMER CHEMICAL SOC
DOI: 10.1021/jf9908188
关键词
antioxidant; DPPH; kinetics; oil; radical scavenger; spectrophotometry; thin-layer chromatography
The total free radical scavenger capacity (RSC) of 57 edible oils from different sources was studied: olive (24 brands of oils), sunflower (6), safflower (2), rapeseed (3), soybean (3), linseed (2), corn (3), hazelnut (2), walnut (2), sesame (2), almond (2), mixture of oils for salad (2), dietetic oil (2), and peanut (2). Olive oils mere also studied according to their geographical origins (France, Greece, Italy, Morocco, Spain, and Turkey). RSC was determined spectrophotometrically by measuring the disappearance of the radical 2,2-diphenyl-1-picrylhydrazyl radical (DPPH.) at 515 MI. The disappearance of the radical followed a double-exponential equation in the presence of oils and oil fractions, which suggested the presence of two (fast and slow) groups of antioxidants. RSC was studied for the methanol-soluble phase (methanolic fraction, MF) of the oil, the fraction nonsoluble in methanol (lipidic fraction, LF), and the nonfractionated oil (total oil; TF = MF + LF). Only olive, linseed, rapeseed, safflower, sesame, and walnut oils showed significant RSC in the MF due to the presence of phenolic compounds. No significant differences were found in the RSC of olive oils from different geographical origins. Upon heating at 180 degrees C the apparent constant for the disappearance of RSC (k(T)) and the half-life (t(1/2)) of RSC for MF, LF, and TF were calculated. The second-order rate constants (k(2)) for the antiradical activity of some phenolic compounds present in oils are also reported.
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