European Journal of Lipid Science and Technology · 2006 · 142 citations · 25 references
AgricultureFood ScienceNutritional SciencesFood AnalysisFood ChemistryFood ProcessingFood AntioxidantsLipid OxidationLipid PeroxidationLipids In FoodsOilseed ProcessingAntioxidants In LipidsLipid Oxidation MechanismsLipid Oxidation ProductsNatural AntioxidantsOil ProcessingPhenolic CompoundsSeed Antioxidant CompoundsSeed Tocopherols
Abstract Amongst oilseeds, rapeseed and mustard are rich sources of phenolic compounds, which also prominent in the by‐products of their respective oil processing or in commercial rapeseed and mustard press cakes. These cakes are rich sources of sinapic acid derivatives, which could be extracted as free sinapic acid or sinapine, the choline ester of sinapic acid. Sinapic acid is a widely investigated antioxidative compound. However, the main compound in the press cakes is present as sinapine. Investigations on the free‐radical‐scavenging activity of sinapic acid and sinapine indicate that sinapine had a significant but lower activity as compared to sinapic acid. Apart from this, sinapic acid, sinapine and different tocopherols were compared as antioxidants for inhibition of the formation of lipid oxidation products in purified rapeseed oils. The oxidation at 40 °C was monitored by the formation of hydroperoxides and propanal. The experiments indicate that in contrast to tocopherol mixtures addition of sinapic acid causes increasing inhibition of hydroperoxide formation when enhancing the concentration from 50 to 500 μmol/kg oil. Sinapine was not able to inhibit the formation of hydroperoxides, compared to sinapic acid. This indicates that sinapic acid‐rich extracts, as compared to sinapine‐rich fractions, could better inhibit the lipid oxidation in bulk lipid systems.
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Francisco A. M. Silva, Fernanda Borges, Carla Guimarães et al. · Journal of Agricultural and Food Chemistry · 2000 · 374 citations · Full text
Pharmacy, Biochemistry, Pharmacology +15