Tuning the ATP-triggered pro-oxidant activity of iron oxide-based nanozyme towards an efficient antibacterial strategy.
Tuning the ATP-triggered pro-oxidant activity of iron oxide-based nanozyme towards an efficient antibacterial strategy.
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DOI:
10.1016/j.jcis.2020.01.099
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发表时间:
2020-01
影响因子:
9.9
通讯作者:
N. V. S. Vallabani;A. Vinu;Sanjay Singh;Ajay S. Karakoti;Ajay S. Karakoti
中科院分区:
文献类型:
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作者:
N. V. S. Vallabani;A. Vinu;Sanjay Singh;Ajay S. Karakoti;Ajay S. Karakoti
An alarming increase in bacterial resistance towards various types of antibiotics makes it imperative to design alternate or combinational therapies to treat stubborn bacterial infections. In this perspective, emerging tools like nanozymes, nanomaterials with biological enzyme like characteristics, are being utilised to control infections caused by bacterial pathogens. Among several nanozymes used for antibacterial applications, Fe3O4nanoparticles (NP) received great attention due to their effective peroxidase like activity. The pH dependent peroxidase activity of Fe3O4NP results in generation ofradical dotOH radical via the unique Fenton chemistry of iron. However, their pH dependent activity is restricted to acidic environment and dramatic loss in antibacterial activity is observed at near neutral pH. Here we describe a novel strategy to overcome the pH lacunae of citrate coated Fe3O4NP by utilizing adenosine triphosphate disodium salt (ATP) as a synergistic agent to accelerate theradical dotOH radical production and restore its antibacterial activity over a wide range of pH. This synergistic combination (30 µg/mL Fe3O4NP and 2.5 mM ATP) shows a high bactericidal activity against both gram positive (B. subtilis) and gram negative (E. coli) bacterial strains, in presence of H2O2, at neutral pH. The synergistic effect (Fe3O4NP + ATP) is determined from the viability assessment and membrane damage studies and is further confirmed by comparing the concentration of generatedradical dotOH radicals. Over all, this study illustrates ATP assisted andradical dotOH-mediated bactericidal activity of Fe3O4nanozyme at near neutral pH.