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Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents

Among different Candida species triggering vaginal candidiasis, Candida albicans is the most predominant yeast. It is commonly treated using azole drugs such as Tioconazole (TIO) and Econazole (ECO). However, their low water solubility may affect their therapeutic efficiency. Therefore, the aim of t...

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Autores principales: Calvo, Natalia L., Sreekumar, Sruthi, Svetaz, Laura A., Lamas, María C., Moerschbacher, Bruno M., Leonardi, Darío
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695956/
https://www.ncbi.nlm.nih.gov/pubmed/31357647
http://dx.doi.org/10.3390/ijms20153686
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author Calvo, Natalia L.
Sreekumar, Sruthi
Svetaz, Laura A.
Lamas, María C.
Moerschbacher, Bruno M.
Leonardi, Darío
author_facet Calvo, Natalia L.
Sreekumar, Sruthi
Svetaz, Laura A.
Lamas, María C.
Moerschbacher, Bruno M.
Leonardi, Darío
author_sort Calvo, Natalia L.
collection PubMed
description Among different Candida species triggering vaginal candidiasis, Candida albicans is the most predominant yeast. It is commonly treated using azole drugs such as Tioconazole (TIO) and Econazole (ECO). However, their low water solubility may affect their therapeutic efficiency. Therefore, the aim of this research was to produce a novel chitosan nanocapsule based delivery system comprising of TIO or ECO and to study their suitability in vaginal application. These systems were characterized by their physicochemical properties, encapsulation efficiency, in vitro release, storage stability, cytotoxicity, and in vitro biological activity. Both nanocapsules loaded with TIO (average hydrodynamic size of 146.8 ± 0.8 nm, zeta potential of +24.7 ± 1.1 mV) or ECO (average hydrodynamic size of 127.1 ± 1.5 nm, zeta potential of +33.0 ± 1.0 mV) showed excellent association efficiency (99% for TIO and 87% for ECO). The analysis of size, polydispersity index, and zeta potential of the systems at 4, 25, and 37 °C (over a period of two months) showed the stability of the systems. Finally, the developed nanosystems presented fungicidal activity against C. albicans at non-toxic concentrations (studied on model human skin cells). The results obtained from this study are the first step in the development of a pharmaceutical dosage form suitable for the treatment of vaginal candidiasis.
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spelling pubmed-66959562019-09-05 Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents Calvo, Natalia L. Sreekumar, Sruthi Svetaz, Laura A. Lamas, María C. Moerschbacher, Bruno M. Leonardi, Darío Int J Mol Sci Article Among different Candida species triggering vaginal candidiasis, Candida albicans is the most predominant yeast. It is commonly treated using azole drugs such as Tioconazole (TIO) and Econazole (ECO). However, their low water solubility may affect their therapeutic efficiency. Therefore, the aim of this research was to produce a novel chitosan nanocapsule based delivery system comprising of TIO or ECO and to study their suitability in vaginal application. These systems were characterized by their physicochemical properties, encapsulation efficiency, in vitro release, storage stability, cytotoxicity, and in vitro biological activity. Both nanocapsules loaded with TIO (average hydrodynamic size of 146.8 ± 0.8 nm, zeta potential of +24.7 ± 1.1 mV) or ECO (average hydrodynamic size of 127.1 ± 1.5 nm, zeta potential of +33.0 ± 1.0 mV) showed excellent association efficiency (99% for TIO and 87% for ECO). The analysis of size, polydispersity index, and zeta potential of the systems at 4, 25, and 37 °C (over a period of two months) showed the stability of the systems. Finally, the developed nanosystems presented fungicidal activity against C. albicans at non-toxic concentrations (studied on model human skin cells). The results obtained from this study are the first step in the development of a pharmaceutical dosage form suitable for the treatment of vaginal candidiasis. MDPI 2019-07-27 /pmc/articles/PMC6695956/ /pubmed/31357647 http://dx.doi.org/10.3390/ijms20153686 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Calvo, Natalia L.
Sreekumar, Sruthi
Svetaz, Laura A.
Lamas, María C.
Moerschbacher, Bruno M.
Leonardi, Darío
Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents
title Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents
title_full Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents
title_fullStr Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents
title_full_unstemmed Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents
title_short Design and Characterization of Chitosan Nanoformulations for the Delivery of Antifungal Agents
title_sort design and characterization of chitosan nanoformulations for the delivery of antifungal agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695956/
https://www.ncbi.nlm.nih.gov/pubmed/31357647
http://dx.doi.org/10.3390/ijms20153686
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