Nitroxides as Building Blocks for Nanoantioxidants

[Image: see text] Nitroxides are an important class of radical trapping antioxidants whose promising biological activities are connected to their ability to scavenge peroxyl (ROO(•)) radicals. We have measured the rate constants of the reaction with ROO(•) (k(inh)) for a series of 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) derivatives as 5.1 × 10(6), 1.1 × 10(6), 5.4 × 10(5), 3.7 × 10(5), 1.1 × 10(5), 1.9 × 10(5), and 5.6 × 10(4) M(–1) s(–1) for −H, −OH, −NH(2), −COOH, −NHCOCH(3), −CONH(CH(2))(3)CH(3), and =O substituents in the 4 position, with a good Marcus relationship between log (k(inh)) and E° for the R(2)NO(•)/R(2)NO(+) couple. Newly synthesized Pluronic-silica nanoparticles (PluS) having nitroxide moieties covalently bound to the silica surface (PluS–NO) through a TEMPO–CONH–R link and coumarin dyes embedded in the silica core, has k(inh) = 1.5 × 10(5) M(–1) s(–1). Each PluS-bound nitroxide displays an inhibition duration nearly double that of a structurally related "free" nitroxide. As each PluS–NO particle bears an average of 30 nitroxide units, this yields an overall ≈60-fold larger inhibition of the PluS–NO nanoantioxidant compared to the molecular analogue. The implications of these results for the development of novel nanoantioxidants based on nitroxide derivatives are discussed, such as the choice of the best linkage group and the importance of the regeneration cycle in determining the duration of inhibition.