Rose bengal–encapsulated chitosan nanoparticles for the photodynamic treatment of Trichophyton species

Author:

Bekmukhametova Alina1ORCID,Antony Anu2,Halliday Catriona3,Chen Sharon34,Ho Chun‐Hoong15,Uddin Mir Muhammad Nasir16,Longo Leonardo7,Pedrinazzi Christian8,George Laurel9,Wuhrer Richard9,Myers Simon2,Mawad Damia1011,Houang Jessica1,Lauto Antonio112ORCID

Affiliation:

1. School of Science Western Sydney University Penrith New South Wales Australia

2. School of Medicine Western Sydney University Penrith New South Wales Australia

3. Centre for Infectious Diseases and Microbiology Laboratory Services, ICPMR, Westmead Hospital Westmead New South Wales Australia

4. Sydney Medical School University of Sydney Westmead New South Wales Australia

5. School of Biomedical Sciences The University of Queensland Brisbane Queensland Australia

6. Department of Pharmacy, Faculty of Biological Science University of Chittagong Chittagong Bangladesh

7. School of Medicine University of Siena Siena Italy

8. School of Medicine University of Pavia Pavia Italy

9. Advanced Materials Characterisation Facility (AMCF) Western Sydney University Penrith New South Wales Australia

10. School of Materials Science and Engineering University of New South Wales Kensington New South Wales Australia

11. Australian Centre for NanoMedicine, UNSW Australia Sydney New South Wales Australia

12. Biomedical Engineering & Neuroscience Research Group, The MARCS Institute Western Sydney University Penrith New South Wales Australia

Abstract

AbstractRose bengal (RB) solutions coupled with a green laser have proven to be efficient in clearing resilient nail infections caused by Trichophyton rubrum in a human pilot study and in extensive in vitro experiments. Nonetheless, the RB solution can become diluted or dispersed over the tissue and prevented from penetrating the nail plate to reach the subungual area where fungal infection proliferates. Nanoparticles carrying RB can mitigate the problem of dilution and are reported to effectively penetrate through the nail. For this reason, we have synthesized RB‐encapsulated chitosan nanoparticles with a peak distribution size of ~200 nm and high reactive oxygen species (ROS) production. The RB‐encapsulated chitosan nanoparticles aPDT were shown to kill more than 99% of T. rubrum, T. mentagrophytes, and T. interdigitale spores, which are the common clinically relevant pathogens in onychomycosis. These nanoparticles are not cytotoxic against human fibroblasts, which promotes their safe application in clinical translation.

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,General Medicine,Biochemistry

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