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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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 |
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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 |
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