Cinnamic acid-derived carbon dots by microwave irradiation synergise the ciprofloxacin effect against Staphylococcus aureus and promote its skin permeability

Abstract

Aqueous solubility and biocompatibility have encouraged the development of carbon dots (CDs) for multiple applications. Considering the significance of natural molecules as precursors, cinnamic acid (CA) was used to develop carbon dots (CA-CDs) using an efficient microwave irradiation method which gave a higher quantum yield in comparison with other conventional methods. The positively charged CA-CDs showed a broad spectrum of action against Gram-positive (S. aureus) and Gram-negative (E. coli) bacteria. Unlike ciprofloxacin (CIP), CA-CDs showed potent inhibition of clinically resistant S. aureus (SA-DR) while reducing biofilm production, leading to synergy with CIP. CA-CDs also acted as carriers to enhance the skin-permeability of CIP through their ionic complex (CIP-CA-CDs). The complex retained the antimicrobial properties and showed the ability to gradually release CIP like a reservoir. Considering the poor permeability of CIP as a limitation, this work can encourage the translational application of CIP for topical application. This work provides a novel method of developing CDs for antimicrobial properties and can encourage their use as a complementary therapy or as carriers for further application.

Graphical abstract: Cinnamic acid-derived carbon dots by microwave irradiation synergise the ciprofloxacin effect against Staphylococcus aureus and promote its skin permeability

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Paper
Submitted
19 Mar 2025
Accepted
12 May 2025
First published
14 May 2025
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2025, Advance Article

Cinnamic acid-derived carbon dots by microwave irradiation synergise the ciprofloxacin effect against Staphylococcus aureus and promote its skin permeability

T. K. Vitthal, V. R. Regu, B. Shankar Das, A. Sarangi, M. Gaur, A. Ray, A. K. Pradhan, S. Chattopadhyay and B. B. Subudhi, Mater. Adv., 2025, Advance Article , DOI: 10.1039/D5MA00247H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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