Issue 19, 2022

Co-exchanged montmorillonite: a potential antibacterial agent with good antibacterial activity and cytocompatibility

Abstract

As a biocompatible material with rich resources and economic benefits, montmorillonite (MMT) has been widely used in the antibacterial field as a drug carrier and toxin adsorbent. In addition, the distinctive structure of MMT provides a possibility to tune its property in a wide range through ion-exchange. In this study, Co-montmorillonite (CoMMT) was prepared by the ion-exchanging method in a Co(NO3)2 solution and its antibacterial activity and cytocompatibility were investigated. The results showed that Co was introduced into MMT successfully and led to an increase in the interlayer spacing of MMT. Also, CoMMT showed a morphology of irregular aggregates consisting of stacked and intertwined lamellae with a uniform cobalt distribution. Besides, CoMMT had better dispersity and higher specific surface area than unmodified MMT. The antibacterial test results showed that CoMMT had good antibacterial activity against S. aureus and E. coli when the CoMMT concentration was higher than 0.2 mg mL−1 and 0.4 mg mL−1, respectively. The possible antibacterial mechanism of CoMMT was speculated and verified by a combination of SEM and EDS results. In addition, CoMMT showed no obvious cytotoxicity to MC3TC-E1 at the observed antibacterial concentration. These findings demonstrated that CoMMT with good biocompatibility and antibacterial activity could be used as a novel antibacterial agent for tissue engineering.

Graphical abstract: Co-exchanged montmorillonite: a potential antibacterial agent with good antibacterial activity and cytocompatibility

Article information

Article type
Paper
Submitted
06 Jan 2022
Accepted
05 Apr 2022
First published
05 Apr 2022

J. Mater. Chem. B, 2022,10, 3705-3715

Co-exchanged montmorillonite: a potential antibacterial agent with good antibacterial activity and cytocompatibility

S. Yang, Y. Ji, F. Deng, X. Sun and C. Ning, J. Mater. Chem. B, 2022, 10, 3705 DOI: 10.1039/D2TB00032F

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