Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/4935
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dc.contributor.authorVhangani, Lusani Norah-
dc.contributor.authorVan Wyk, Jessy-
dc.date.accessioned2016-08-17T11:42:49Z-
dc.date.available2016-08-17T11:42:49Z-
dc.date.issued2013-
dc.identifier.urihttp://dx.doi.org/10.1016/j.foodchem.2012.09.030-
dc.identifier.urihttp://hdl.handle.net/11189/4935-
dc.description.abstractMaillard reaction products (MRPs) were prepared from aqueous ribose-lysine (RL) and fructose-lysine (FL) model systems at pH 9, heated at 60, 80 and 120 °C for 15, 60 and 120 min. Browning intensity (BI) and pH reduction were monitored throughout the reaction. 1,1-Diphenyl-2-picryl-hydrazyl (DPPH-RS), peroxyl (PRS), and hydroxyl radical scavenging (HRS) and reducing power (RP) measured their antioxidant activity. The pH of FL and RL system decreased (p < 0.05) as reaction temperatures and times increased. This reduction coincided with the increase (p < 0.05) in BI for all MRPs. With the exception of HRS activity, the antioxidant activity of FL increased (p < 0.05) with increased reaction temperature, while that of RL systems decreased (p < 0.05). Concerning sugar reactivity, RL systems exhibited higher (p < 0.05) reduction in pH, BI, DPPH-RS, PRS and RP than FL model systems, with no considerable differences (p > 0.05) in HRS activity.en_US
dc.description.sponsorshipCape Peninsula University of Technology (Food Technology Department). This study was supported by the university and the National Research Fund of South Africaen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/en
dc.subjectMaillard reaction productsen_US
dc.subjectBrowningen_US
dc.subjectRadical scavengingen_US
dc.subjectAntioxidanten_US
dc.titleAntioxidant activity of Maillard reaction products (MRPs) derived from fructose–lysine and ribose–lysine model systemsen_US
dc.type.patentArticleen_US
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
Prof. Jessy Van Wyk
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