Issue 51, 2023

Dual anticancer and antibacterial activity of fluorescent naphthoimidazolium salts

Abstract

Cancer has emerged as a significant global health challenge, ranking as the second leading cause of death worldwide. Moreover, cancer patients frequently experience compromised immune systems, rendering them susceptible to bacterial infections. Combining anticancer and antibacterial properties in a single drug could lead to improved overall treatment outcomes and patient well-being. In this context, the present study focused on a series of hydrophilic naphthoimidazolium salts with donor groups (NI-R), aiming to create dual-functional agents with antibacterial and anticancer activities. Among these compounds, NI-TPA demonstrated notable antibacterial activity, particularly against drug-resistant bacteria, with MIC value of 7.8 μg mL−1. Furthermore, NI-TPA exhibited the most potent cytotoxicity against four different cancer cell lines, with an IC50 range of 0.67–2.01 μg mL−1. The observed high cytotoxicity of NI-TPA agreed with molecular docking and dynamic simulation studies targeting c-Met kinase protein. Additionally, NI-TPA stood out as the most promising candidate for two-photo excitation, fluorescence bioimaging, and localization in lysosomes. The study findings open new avenues for the design and development of imidazolium salts that could be employed in phototheranostic applications for cancer treatment and bacterial infections.

Graphical abstract: Dual anticancer and antibacterial activity of fluorescent naphthoimidazolium salts

Supplementary files

Article information

Article type
Paper
Submitted
26 Sep 2023
Accepted
05 Dec 2023
First published
14 Dec 2023
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2023,13, 36430-36438

Dual anticancer and antibacterial activity of fluorescent naphthoimidazolium salts

D. N. Tran, T. T. H. Hoang, S. Nandanwar, V. T. T. X. Ho, V. T. Pham, H. D. Vu, X. H. Nguyen, H. T. Nguyen, T. V. Nguyen, T. K. V. Nguyen, D. L. Tran, M. Park, S. Lee and T. C. Pham, RSC Adv., 2023, 13, 36430 DOI: 10.1039/D3RA06555C

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