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Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency

Novel biodegradable and biocompatible formulations of “old” but “gold” drugs such as nystatin (Nys) and amphotericin B (AmB) were made using a biopolymer as a matrix. Medium chain length polyhydroxyalkanoates (mcl-PHA) were used to formulate both polyenes (Nys and AmB) in the form of films (~50 µm)....

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Autores principales: Pekmezovic, Marina, Kalagasidis Krusic, Melina, Malagurski, Ivana, Milovanovic, Jelena, Stępień, Karolina, Guzik, Maciej, Charifou, Romina, Babu, Ramesh, O’Connor, Kevin, Nikodinovic-Runic, Jasmina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234488/
https://www.ncbi.nlm.nih.gov/pubmed/34207011
http://dx.doi.org/10.3390/antibiotics10060737
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author Pekmezovic, Marina
Kalagasidis Krusic, Melina
Malagurski, Ivana
Milovanovic, Jelena
Stępień, Karolina
Guzik, Maciej
Charifou, Romina
Babu, Ramesh
O’Connor, Kevin
Nikodinovic-Runic, Jasmina
author_facet Pekmezovic, Marina
Kalagasidis Krusic, Melina
Malagurski, Ivana
Milovanovic, Jelena
Stępień, Karolina
Guzik, Maciej
Charifou, Romina
Babu, Ramesh
O’Connor, Kevin
Nikodinovic-Runic, Jasmina
author_sort Pekmezovic, Marina
collection PubMed
description Novel biodegradable and biocompatible formulations of “old” but “gold” drugs such as nystatin (Nys) and amphotericin B (AmB) were made using a biopolymer as a matrix. Medium chain length polyhydroxyalkanoates (mcl-PHA) were used to formulate both polyenes (Nys and AmB) in the form of films (~50 µm). Thermal properties and stability of the materials were not significantly altered by the incorporation of polyenes in mcl-PHA, but polyene containing materials were more hydrophobic. These formulations were tested in vitro against a panel of pathogenic fungi and for antibiofilm properties. The films containing 0.1 to 2 weight % polyenes showed good activity and sustained polyene release for up to 4 days. A PHA monomer, namely 3-hydroxydecanoic acid (C10-OH), was added to the films to achieve an enhanced synergistic effect with polyenes against fungal growth. Mcl-PHA based polyene formulations showed excellent growth inhibitory activity against both Candida yeasts (C. albicans ATCC 1023, C. albicans SC5314 (ATCC MYA-2876), C. parapsilosis ATCC 22019) and filamentous fungi (Aspergillus fumigatus ATCC 13073; Trichophyton mentagrophytes ATCC 9533, Microsporum gypseum ATCC 24102). All antifungal PHA film preparations prevented the formation of a C. albicans biofilm, while they were not efficient in eradication of mature biofilms, rendering them suitable for the transdermal application or as coatings of implants.
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spelling pubmed-82344882021-06-27 Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency Pekmezovic, Marina Kalagasidis Krusic, Melina Malagurski, Ivana Milovanovic, Jelena Stępień, Karolina Guzik, Maciej Charifou, Romina Babu, Ramesh O’Connor, Kevin Nikodinovic-Runic, Jasmina Antibiotics (Basel) Article Novel biodegradable and biocompatible formulations of “old” but “gold” drugs such as nystatin (Nys) and amphotericin B (AmB) were made using a biopolymer as a matrix. Medium chain length polyhydroxyalkanoates (mcl-PHA) were used to formulate both polyenes (Nys and AmB) in the form of films (~50 µm). Thermal properties and stability of the materials were not significantly altered by the incorporation of polyenes in mcl-PHA, but polyene containing materials were more hydrophobic. These formulations were tested in vitro against a panel of pathogenic fungi and for antibiofilm properties. The films containing 0.1 to 2 weight % polyenes showed good activity and sustained polyene release for up to 4 days. A PHA monomer, namely 3-hydroxydecanoic acid (C10-OH), was added to the films to achieve an enhanced synergistic effect with polyenes against fungal growth. Mcl-PHA based polyene formulations showed excellent growth inhibitory activity against both Candida yeasts (C. albicans ATCC 1023, C. albicans SC5314 (ATCC MYA-2876), C. parapsilosis ATCC 22019) and filamentous fungi (Aspergillus fumigatus ATCC 13073; Trichophyton mentagrophytes ATCC 9533, Microsporum gypseum ATCC 24102). All antifungal PHA film preparations prevented the formation of a C. albicans biofilm, while they were not efficient in eradication of mature biofilms, rendering them suitable for the transdermal application or as coatings of implants. MDPI 2021-06-18 /pmc/articles/PMC8234488/ /pubmed/34207011 http://dx.doi.org/10.3390/antibiotics10060737 Text en © 2021 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
Pekmezovic, Marina
Kalagasidis Krusic, Melina
Malagurski, Ivana
Milovanovic, Jelena
Stępień, Karolina
Guzik, Maciej
Charifou, Romina
Babu, Ramesh
O’Connor, Kevin
Nikodinovic-Runic, Jasmina
Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency
title Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency
title_full Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency
title_fullStr Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency
title_full_unstemmed Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency
title_short Polyhydroxyalkanoate/Antifungal Polyene Formulations with Monomeric Hydroxyalkanoic Acids for Improved Antifungal Efficiency
title_sort polyhydroxyalkanoate/antifungal polyene formulations with monomeric hydroxyalkanoic acids for improved antifungal efficiency
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234488/
https://www.ncbi.nlm.nih.gov/pubmed/34207011
http://dx.doi.org/10.3390/antibiotics10060737
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