Cargando…

Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies

Amphotericin B is an antifungal drug used for the treatment of invasive fungal infections. However, its clinical use is limited due to its serious side effects, such as renal and cardiovascular toxicity. Furthermore, amphotericin B is administered in high doses due to its poor water solubility. Henc...

Descripción completa

Detalles Bibliográficos
Autores principales: Uroro, Evelyn Osehontue, Bright, Richard, Hayles, Andrew, Vasilev, Krasimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823996/
https://www.ncbi.nlm.nih.gov/pubmed/36616065
http://dx.doi.org/10.3390/nano13010155
_version_ 1784866300072296448
author Uroro, Evelyn Osehontue
Bright, Richard
Hayles, Andrew
Vasilev, Krasimir
author_facet Uroro, Evelyn Osehontue
Bright, Richard
Hayles, Andrew
Vasilev, Krasimir
author_sort Uroro, Evelyn Osehontue
collection PubMed
description Amphotericin B is an antifungal drug used for the treatment of invasive fungal infections. However, its clinical use is limited due to its serious side effects, such as renal and cardiovascular toxicity. Furthermore, amphotericin B is administered in high doses due to its poor water solubility. Hence, it is necessary to develop an on-demand release strategy for the delivery of amphotericin B to reduce cytotoxicity. The present report describes a novel encapsulation of amphotericin B into lipase-sensitive polycaprolactone to form a nanocomposite. Nanocomposites were produced by the oil-in-water method and their physicochemical properties such as size, hydrodynamic diameter, drug loading, and zeta potential were determined. The in vitro release of amphotericin B was characterized in the presence and absence of lipase. The antifungal activity of the nanocomposites was verified against lipase-secreting Candida albicans, and cytotoxicity was tested against primary human dermal fibroblasts. In the absence of lipase, the release of amphotericin B from the nanocomposites was minimal. However, in the presence of lipase, an enzyme that is abundant at infection sites, a fungicidal concentration of amphotericin B was released from the nanocomposites. The antifungal activity of the nanocomposites showed an enhanced effect against the lipase-secreting fungus, Candida albicans, in comparison to the free drug at the same concentration. Furthermore, nanoencapsulation significantly reduced amphotericin B-related cytotoxicity compared to the free drug. The synthesized nanocomposites can serve as a potent carrier for the responsive delivery of amphotericin B in antifungal applications.
format Online
Article
Text
id pubmed-9823996
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-98239962023-01-08 Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies Uroro, Evelyn Osehontue Bright, Richard Hayles, Andrew Vasilev, Krasimir Nanomaterials (Basel) Article Amphotericin B is an antifungal drug used for the treatment of invasive fungal infections. However, its clinical use is limited due to its serious side effects, such as renal and cardiovascular toxicity. Furthermore, amphotericin B is administered in high doses due to its poor water solubility. Hence, it is necessary to develop an on-demand release strategy for the delivery of amphotericin B to reduce cytotoxicity. The present report describes a novel encapsulation of amphotericin B into lipase-sensitive polycaprolactone to form a nanocomposite. Nanocomposites were produced by the oil-in-water method and their physicochemical properties such as size, hydrodynamic diameter, drug loading, and zeta potential were determined. The in vitro release of amphotericin B was characterized in the presence and absence of lipase. The antifungal activity of the nanocomposites was verified against lipase-secreting Candida albicans, and cytotoxicity was tested against primary human dermal fibroblasts. In the absence of lipase, the release of amphotericin B from the nanocomposites was minimal. However, in the presence of lipase, an enzyme that is abundant at infection sites, a fungicidal concentration of amphotericin B was released from the nanocomposites. The antifungal activity of the nanocomposites showed an enhanced effect against the lipase-secreting fungus, Candida albicans, in comparison to the free drug at the same concentration. Furthermore, nanoencapsulation significantly reduced amphotericin B-related cytotoxicity compared to the free drug. The synthesized nanocomposites can serve as a potent carrier for the responsive delivery of amphotericin B in antifungal applications. MDPI 2022-12-29 /pmc/articles/PMC9823996/ /pubmed/36616065 http://dx.doi.org/10.3390/nano13010155 Text en © 2022 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
Uroro, Evelyn Osehontue
Bright, Richard
Hayles, Andrew
Vasilev, Krasimir
Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
title Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
title_full Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
title_fullStr Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
title_full_unstemmed Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
title_short Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies
title_sort lipase-responsive amphotericin b loaded pcl nanoparticles for antifungal therapies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823996/
https://www.ncbi.nlm.nih.gov/pubmed/36616065
http://dx.doi.org/10.3390/nano13010155
work_keys_str_mv AT uroroevelynosehontue lipaseresponsiveamphotericinbloadedpclnanoparticlesforantifungaltherapies
AT brightrichard lipaseresponsiveamphotericinbloadedpclnanoparticlesforantifungaltherapies
AT haylesandrew lipaseresponsiveamphotericinbloadedpclnanoparticlesforantifungaltherapies
AT vasilevkrasimir lipaseresponsiveamphotericinbloadedpclnanoparticlesforantifungaltherapies