Abstract
The hydroxyl radical scavenging capacity and efficacy of a novel organosiliceous anionic hydride compound, silica hydride, were quantified by a recently developed method. The method measures a direct relationship between the hydroxyl radical scavenging capability of the antioxidant compound and the linear decrease in signal from a fluorescent 2-hydroxyterephthalate product created by reacting an Fe2+-EDTA complex in the presence of a potential radical scavenger. A fluorescence signal half-inhibition, IC50, value of 1.4 ± 0.1 μM was obtained for silica hydride compounds. The validity of the analysis was verified by electron spin resonance spectroscopy, spectrophotometric analysis of NAD+/NADH ratios, mitochondrial membrane potential measurements, and assays of both cytochrome c(Fe3+) to cytochrome c (Fe2+) and epinephrine to adenochrome reductions.
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