Cargando…

Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds

Cutaneous chronic wounds impose a silent pandemic that affects the lives of millions worldwide. The delayed healing process is usually complicated by opportunistic bacteria that infect wounds. Staphylococcus aureus is one of the most prevalent bacteria in infected cutaneous wounds, with the ability...

Descripción completa

Detalles Bibliográficos
Autores principales: Awad, Muhammed, Kopecki, Zlatko, Barnes, Timothy J., Wignall, Anthony, Joyce, Paul, Thomas, Nicky, Prestidge, Clive A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964009/
https://www.ncbi.nlm.nih.gov/pubmed/36839628
http://dx.doi.org/10.3390/pharmaceutics15020305
_version_ 1784896396807110656
author Awad, Muhammed
Kopecki, Zlatko
Barnes, Timothy J.
Wignall, Anthony
Joyce, Paul
Thomas, Nicky
Prestidge, Clive A.
author_facet Awad, Muhammed
Kopecki, Zlatko
Barnes, Timothy J.
Wignall, Anthony
Joyce, Paul
Thomas, Nicky
Prestidge, Clive A.
author_sort Awad, Muhammed
collection PubMed
description Cutaneous chronic wounds impose a silent pandemic that affects the lives of millions worldwide. The delayed healing process is usually complicated by opportunistic bacteria that infect wounds. Staphylococcus aureus is one of the most prevalent bacteria in infected cutaneous wounds, with the ability to form antibiotic-resistant biofilms. Recently, we have demonstrated the potential of gallium protoporphyrin lipid liquid crystalline nanoparticles (GaPP-LCNP) as a photosensitizer against S. aureus biofilms in vitro. Herein, we investigate the potential of GaPP-LCNP using a pre-clinical model of infected cutaneous wounds. GaPP-LCNP showed superior antibacterial activity compared to unformulated GaPP, reducing biofilm bacterial viability by 5.5 log(10) compared to 2.5 log(10) in an ex vivo model, and reducing bacterial viability by 1 log(10) in vivo, while unformulated GaPP failed to reduce bacterial burden. Furthermore, GaPP-LCNP significantly promoted wound healing through reduction in the bacterial burden and improved early collagen deposition. These findings pave the way for future pre-clinical investigation and treatment optimizations to translate GaPP-LCNP towards clinical application.
format Online
Article
Text
id pubmed-9964009
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99640092023-02-26 Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds Awad, Muhammed Kopecki, Zlatko Barnes, Timothy J. Wignall, Anthony Joyce, Paul Thomas, Nicky Prestidge, Clive A. Pharmaceutics Article Cutaneous chronic wounds impose a silent pandemic that affects the lives of millions worldwide. The delayed healing process is usually complicated by opportunistic bacteria that infect wounds. Staphylococcus aureus is one of the most prevalent bacteria in infected cutaneous wounds, with the ability to form antibiotic-resistant biofilms. Recently, we have demonstrated the potential of gallium protoporphyrin lipid liquid crystalline nanoparticles (GaPP-LCNP) as a photosensitizer against S. aureus biofilms in vitro. Herein, we investigate the potential of GaPP-LCNP using a pre-clinical model of infected cutaneous wounds. GaPP-LCNP showed superior antibacterial activity compared to unformulated GaPP, reducing biofilm bacterial viability by 5.5 log(10) compared to 2.5 log(10) in an ex vivo model, and reducing bacterial viability by 1 log(10) in vivo, while unformulated GaPP failed to reduce bacterial burden. Furthermore, GaPP-LCNP significantly promoted wound healing through reduction in the bacterial burden and improved early collagen deposition. These findings pave the way for future pre-clinical investigation and treatment optimizations to translate GaPP-LCNP towards clinical application. MDPI 2023-01-17 /pmc/articles/PMC9964009/ /pubmed/36839628 http://dx.doi.org/10.3390/pharmaceutics15020305 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Awad, Muhammed
Kopecki, Zlatko
Barnes, Timothy J.
Wignall, Anthony
Joyce, Paul
Thomas, Nicky
Prestidge, Clive A.
Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds
title Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds
title_full Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds
title_fullStr Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds
title_full_unstemmed Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds
title_short Lipid Liquid Crystal Nanoparticles: Promising Photosensitizer Carriers for the Treatment of Infected Cutaneous Wounds
title_sort lipid liquid crystal nanoparticles: promising photosensitizer carriers for the treatment of infected cutaneous wounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964009/
https://www.ncbi.nlm.nih.gov/pubmed/36839628
http://dx.doi.org/10.3390/pharmaceutics15020305
work_keys_str_mv AT awadmuhammed lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds
AT kopeckizlatko lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds
AT barnestimothyj lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds
AT wignallanthony lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds
AT joycepaul lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds
AT thomasnicky lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds
AT prestidgeclivea lipidliquidcrystalnanoparticlespromisingphotosensitizercarriersforthetreatmentofinfectedcutaneouswounds