4.6 Article

Synergistic or antagonistic antioxidant combinations - a case study exploring flavonoid-nitroxide hybrids

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 21, Issue 8, Pages 1780-1792

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ob02101c

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Neurodegenerative diseases impose a significant burden on global populations. Oxidative stress, caused by an imbalance in pro-oxidant/antioxidant levels, plays a role in these diseases. Manipulating reactive oxygen species (ROS) levels may be a promising treatment option, but effective treatments have not been achieved yet. By combining free radical nitroxide antioxidants with natural antioxidants called flavonoids, a potential multitargeted antioxidant was formed.
Neurodegenerative diseases impose a considerable medical and public health burden on populations throughout the world. Oxidative stress, an imbalance in pro-oxidant/antioxidant homeostasis that leads to the generation of reactive oxygen species (ROS), has been implicated in the progression of a number of neurodegenerative diseases. The manipulation of ROS levels may represent a promising treatment option to slow down neurodegeneration, although adequate potency of treatments has not yet been achieved. Using a hybrid pharmacology approach, free radical nitroxide antioxidants were hybridised with a class of natural antioxidants, flavonoids, to form a potential multitargeted antioxidant. Modification of the Baker-Venkataraman reaction achieved the flavonoid-nitroxide hybrids (6-9) in modest yields. Antioxidant evaluation of the hybrids by cyclic voltammetry showed both redox functionalities were still active, with little influence on oxidation potential. Assessment of the peroxyl radical scavenging ability through an ORAC assay showed reduced antioxidant activity of the hybrids compared to their individual components. It was hypothesized that the presence of the phenol in the hybrids creates a more acidic medium which does not favour regeneration of the nitroxide from the corresponding oxammonium cation, disturbing the typical catalytic cycle of peroxyl radical scavenging by nitroxides. This work highlights the potential intricacies involved with drug hybridization as a strategy for new therapeutic development.

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