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Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment

Psoriasis is a chronic autoimmune systemic disease with an approximate incidence of 2% worldwide; it is commonly characterized by squamous lesions on the skin that present the typical pain, stinging, and bleeding associated with an inflammatory response. In this work, poly(methyl vinyl ether-alt-mal...

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Autores principales: Martínez-Ortega, Leticia, Mira, Amalia, Fernandez-Carvajal, Asia, Mateo, C. Reyes, Mallavia, Ricardo, Falco, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359116/
https://www.ncbi.nlm.nih.gov/pubmed/30621136
http://dx.doi.org/10.3390/pharmaceutics11010014
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author Martínez-Ortega, Leticia
Mira, Amalia
Fernandez-Carvajal, Asia
Mateo, C. Reyes
Mallavia, Ricardo
Falco, Alberto
author_facet Martínez-Ortega, Leticia
Mira, Amalia
Fernandez-Carvajal, Asia
Mateo, C. Reyes
Mallavia, Ricardo
Falco, Alberto
author_sort Martínez-Ortega, Leticia
collection PubMed
description Psoriasis is a chronic autoimmune systemic disease with an approximate incidence of 2% worldwide; it is commonly characterized by squamous lesions on the skin that present the typical pain, stinging, and bleeding associated with an inflammatory response. In this work, poly(methyl vinyl ether-alt-maleic ethyl monoester) (PMVEMA-ES) nanofibers have been designed as a delivery vehicle for three therapeutic agents with palliative properties for the symptoms of this disease (salicylic acid, methyl salicylate, and capsaicin). For such a task, the production of these nanofibers by means of the electrospinning technique has been optimized. Their morphology and size have been characterized by optical microscopy and scanning electron microscopy (SEM). By selecting the optimal conditions to achieve the smallest and most uniform nanofibers, approximate diameters of up to 800–900 nm were obtained. It was also determined that the therapeutic agents that were used were encapsulated with high efficiency. The analysis of their stability over time by GC-MS showed no significant losses of the encapsulated compounds 15 days after their preparation, except in the case of methyl salicylate. Likewise, it was demonstrated that the therapeutic compounds that were encapsulated conserved, and even improved, their capacity to activate the transient receptor potential cation channel 1 (TRPV1) channel, which has been associated with the formation of psoriatic lesions.
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spelling pubmed-63591162019-02-14 Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment Martínez-Ortega, Leticia Mira, Amalia Fernandez-Carvajal, Asia Mateo, C. Reyes Mallavia, Ricardo Falco, Alberto Pharmaceutics Article Psoriasis is a chronic autoimmune systemic disease with an approximate incidence of 2% worldwide; it is commonly characterized by squamous lesions on the skin that present the typical pain, stinging, and bleeding associated with an inflammatory response. In this work, poly(methyl vinyl ether-alt-maleic ethyl monoester) (PMVEMA-ES) nanofibers have been designed as a delivery vehicle for three therapeutic agents with palliative properties for the symptoms of this disease (salicylic acid, methyl salicylate, and capsaicin). For such a task, the production of these nanofibers by means of the electrospinning technique has been optimized. Their morphology and size have been characterized by optical microscopy and scanning electron microscopy (SEM). By selecting the optimal conditions to achieve the smallest and most uniform nanofibers, approximate diameters of up to 800–900 nm were obtained. It was also determined that the therapeutic agents that were used were encapsulated with high efficiency. The analysis of their stability over time by GC-MS showed no significant losses of the encapsulated compounds 15 days after their preparation, except in the case of methyl salicylate. Likewise, it was demonstrated that the therapeutic compounds that were encapsulated conserved, and even improved, their capacity to activate the transient receptor potential cation channel 1 (TRPV1) channel, which has been associated with the formation of psoriatic lesions. MDPI 2019-01-04 /pmc/articles/PMC6359116/ /pubmed/30621136 http://dx.doi.org/10.3390/pharmaceutics11010014 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
Martínez-Ortega, Leticia
Mira, Amalia
Fernandez-Carvajal, Asia
Mateo, C. Reyes
Mallavia, Ricardo
Falco, Alberto
Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment
title Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment
title_full Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment
title_fullStr Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment
title_full_unstemmed Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment
title_short Development of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatment
title_sort development of a new delivery system based on drug-loadable electrospun nanofibers for psoriasis treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359116/
https://www.ncbi.nlm.nih.gov/pubmed/30621136
http://dx.doi.org/10.3390/pharmaceutics11010014
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