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Optimising the use of phenolic compounds in foods

Andersen, R. Kragh Lauridsen and L.H. Skibsted, The Royal Veterinary and Agricultural University, Denmark [Pg.315]

Oxidation is initiated by formation of radicals which may be the result of enzyme catalysed reactions like oxygen activation by xanthine oxidase in [Pg.315]

Lipid hydroperoxides are either formed in an autocatalytic process initiated by hydroxyl radicals or they are formed photochemically. Lipid hydroperoxides, known as the primary lipid oxidation products, are tasteless and odourless, but may be cleaved into the so-called secondary lipid oxidation products by heat or by metal ion catalysis. This transformation of hydroperoxides to secondary lipid oxidation products can thus be seen during chill storage of pork (Nielsen et al, 1997). The secondary lipid oxidation products, like hexanal from linoleic acid, are volatile and provide precooked meats, dried milk products and used frying oil with characteristic off-flavours (Shahidi and Pegg, 1994). They may further react with proteins forming fluorescent protein derivatives derived from initially formed Schiff bases (Tappel, 1956). [Pg.316]

The chemical formulae for a variety of plant phenols are given in Fig. 16.2, including examples of simpler phenols, such as cinnamic acid derivative, and of tocopherols, flavonoids, flavonoid glycosides and anthocyanidins. The flavonoids include the following subclasses flavanones (taxifolin), flavones (luteolin), flavonols (quercetin) and flavanols (catechin/epicatechin). The [Pg.317]

Natural antioxidants may be classified according to their nutritive value or according to their solubility. The hydrophobic vitamin E and the hydrophilic vitamin C are thus important both as nutrients and as antioxidants. The nonnutritive antioxidants may similarly be divided into lipid-soluble and water-soluble antioxidants, as shown in Fig. 16.3, which will also form the basis for a discussion of exploitation of combinations of anhoxidants in order to improve protective effects. [Pg.320]


Optimising the use of phenolic compounds in foods 317 16.1.2 Classifying natural antioxidants... [Pg.317]


See other pages where Optimising the use of phenolic compounds in foods is mentioned: [Pg.315]    [Pg.323]    [Pg.325]    [Pg.329]    [Pg.333]    [Pg.341]    [Pg.343]    [Pg.345]    [Pg.315]    [Pg.323]    [Pg.325]    [Pg.329]    [Pg.333]    [Pg.341]    [Pg.343]    [Pg.345]    [Pg.333]   


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