Issue 21, 2024

Facile synthesis of a CeMnOx catalytic gel with bacterial microenvironment-responsive antibacterial properties

Abstract

A nanocatalytic antimicrobial gel responsive to the bacterial infection microenvironment (IME) possessing highly specific antimicrobial properties provides an opportunity to address the bacterial drug resistance. However, the pH conditions and low substrate concentration in the IME limit the catalytic antimicrobial efficiency of these agents, resulting in unsatisfactory performance. The reported transition metal peroxide alleviates endogenous substrate insufficiency due to H2O2 self-supplying properties, but still suffers from difficulties of simple synthesis, long-stem storage and lower intrinsic catalytic efficiency responsive to the IME. In this paper, we report for the first time the use of cerium–manganese bimetallic peroxide nanoparticles (CeMnOx) as a nanocatalyst with high pH responsiveness, H2O2 self-supplying properties, multiple ROS-generating activity and synergistic effect-enhanced cascade catalytic reactions for efficient antimicrobial therapy. CeMnOx achieved more than 95% kill rate at 50 μg mL−1 for E. coli and 100 μg mL−1 for S. aureus, which was superior to those of previously reported works. To further improve the availability, nanoparticle-carrying hydrogels with excellent antimicrobial properties were prepared through in situ gelation, thus adapting to a wider range of antimicrobial application scenarios. Therefore, the in situ molded nanocatalytic antimicrobial gels provide a promising paradigm for efficient treatment of bacterial infections.

Graphical abstract: Facile synthesis of a CeMnOx catalytic gel with bacterial microenvironment-responsive antibacterial properties

Supplementary files

Article information

Article type
Paper
Submitted
27 Mar 2024
Accepted
29 Apr 2024
First published
29 Apr 2024

New J. Chem., 2024,48, 9685-9693

Facile synthesis of a CeMnOx catalytic gel with bacterial microenvironment-responsive antibacterial properties

Z. Wei, Z. Niu, H. Xu, Z. Li, P. Wang, C. Li, G. Wen and X. Li, New J. Chem., 2024, 48, 9685 DOI: 10.1039/D4NJ01440E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements