Oxidative Transformation of Fluoroquinolone Antibacterial Agents and Structurally Related Amines by Manganese Oxide

摘要

Various members of the popularfluoroquinolone antibacterial agents (FQs) have been frequently detected in municipal wastewater and surface water bodies in recent years.This study was conducted to gain a better understanding of the fate of FQs in the sediment-water environment.Seven FQs were examined for adsorptive and oxidative interactions with delta-Mn0_2 under environmental conditions and exhibited reactivity in the order of ciprofloxacin ~ enrofloxacin approx norfloxacin ~ ofloxacin > lomefloxacin > pipemidic acid flumequine.Four amines that are structurally related to the aniline and piperazine functional groups of FQs showed reactivity to oxidation by delta-Mn0_2 in the order of 1-phenylpiperazine > aniline > N-phenyl-morpholine > 4-phenylpiperidine.Comparison among the above compounds clearly indicates that the piperazine moiety of FQs is the predominant adsorptive and oxidative site to Mn0_2.Product analyses showed that oxidation fay MnO_2 results in dealkylation and hydroxylation at the piperazine moiety of FQs,with the quinolone ring essentially intact The reaction kinetics,reactivity comparison,and product characterization point to a surface reaction mechanism that likely begins with formation of a surface complex between FQ and the surface-bound Mn~(IV),followed by oxidation at the aromatic N_1 atom of FQ's piperazine moiety to generate an anilinyl radical intermediate.The radical intermediates subsequently undergo N-dealkylation,C-hydroxylation,and possibly coupling to yield a range of products.Even though the quinolone ring appears to be stable with respect to Mn02,it affects the overall reactivity and potentially product distribution of FQs via substituent effects.Results of this study strongly suggest that manganese oxides commonly present in soils will likely play an important role in the abiotic degradation of fluoroquinolone antibacterial agents in the environment.