A Mechanistic Insight into Superoxide Elimination by Mesalazine through Proton-Coupled Electron Transfer

Abstract

This research clarifies a mechanistic insight into the elimination of the superoxide radical anion (O₂\(^\bullet\)^-) by 5-amino-2-hydroxybenzoic acid (mesalazine, 5-ASA). The elimination of O₂\(^\bullet\)^- by 5-ASA, 4-amino-2-hydroxybenzoic acid (4-ASA), and related compounds used for ulcerative colitis treatment was investigated using cyclic voltammetry and electron spin resonance (ESR) analyses aided by density functional theory (DFT) calculations. Quasi-reversible O₂/O₂\(^\bullet\)^- redox was found to be modified by the compounds, suggesting that an acid-base reaction in which a hydroperoxyl radical (HO₂^{\(^\bullet\)}) is formed from O₂\(^\bullet\)^- occurs. However, the deprotonated 5-ASA anion can eliminate O₂\(^\bullet\)- through proton-coupled electron transfer (PCET), forming a radical product. This electron transfer (ET) was confirmed by ESR analysis. The 4-aminophenol moiety in 5-ASA plays an important role in the PCET, involving two proton transfers and one ET based on TT-conjugation. The electrochemical and DFT results indicated that O₂\(^\bullet\)^- elimination by 5-ASA proceeds efficiently through the PCET mechanism after deprotonation of the 1-carboxyl group. Thus, 5-ASA may act as an anti-inflammatory agent in the alkali intestine through PCET-based O₂\(^\bullet\)^- elimination.