Issue 23, 2024, Issue in Progress

Evaluation of multi-target iridium(iii)-based metallodrugs in combating antimicrobial resistance and infections caused by Staphylococcus aureus

Abstract

The rapid emergence and spread of multidrug-resistant bacteria pose a serious challenge to human life and health, necessitating the development of novel antibacterial agents. Herein, to address this challenge, three iridium-based antibacterial agents were prepared and their antimicrobial activity were explored. Importantly, the three complexes all showed robust potency against S. aureus with MIC values in the range of 1.9–7.9 μg mL−1. Notably, the most active complex Ir3 also exhibited relative stability in mammalian fluids and a significant antibacterial effect on clinically isolated drug-resistant bacteria. Mechanism studies further demonstrated that the complex Ir3 can kill S. aureus by disrupting the integrity of the bacterial membrane and inducing ROS production. This multi-target advantage allows Ir3 to not only effectively combat bacterial resistance but also efficiently clear the bacterial biofilm. In addition, when used together, complex Ir3 could enhance the antibacterial potency of some clinical antibiotics against S. aureus. Moreover, both G. mellonella wax worms and mouse infection model demonstrated that Ir3 has low toxicity and robust anti-infective efficacy in vivo. Overall, complex Ir3 can serve as a new antibacterial agent for combating Gram-positive bacterial infections.

Graphical abstract: Evaluation of multi-target iridium(iii)-based metallodrugs in combating antimicrobial resistance and infections caused by Staphylococcus aureus

Supplementary files

Article information

Article type
Paper
Submitted
21 Mar 2024
Accepted
28 Apr 2024
First published
20 May 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 16194-16206

Evaluation of multi-target iridium(III)-based metallodrugs in combating antimicrobial resistance and infections caused by Staphylococcus aureus

S. Lin, Y. Chen, Y. Sun, G. Yu, X. Liao and Q. Yang, RSC Adv., 2024, 14, 16194 DOI: 10.1039/D4RA02152E

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