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Bioadhesive Surfactant Systems for Methotrexate Skin Delivery

Methotrexate (MTX) is an immunosuppressive drug for systemic use in the treatment of skin diseases, however, MTX presents a number of side effects, such as hepatotoxicity. To overcome this limitation, this study developed skin MTX delivery surfactant systems, such as a microemulsion (ME) and a liqui...

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Autores principales: Cintra, Giovana Aparecida de Souza, Pinto, Larissa Alvarenga, Calixto, Giovana Maria Fioramonti, Soares, Christiane Pienna, Von Zuben, Eliete de Souza, Scarpa, Maria Virgínia, Gremião, Maria Palmira Daflon, Chorilli, Marlus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273544/
https://www.ncbi.nlm.nih.gov/pubmed/26901183
http://dx.doi.org/10.3390/molecules21020231
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author Cintra, Giovana Aparecida de Souza
Pinto, Larissa Alvarenga
Calixto, Giovana Maria Fioramonti
Soares, Christiane Pienna
Von Zuben, Eliete de Souza
Scarpa, Maria Virgínia
Gremião, Maria Palmira Daflon
Chorilli, Marlus
author_facet Cintra, Giovana Aparecida de Souza
Pinto, Larissa Alvarenga
Calixto, Giovana Maria Fioramonti
Soares, Christiane Pienna
Von Zuben, Eliete de Souza
Scarpa, Maria Virgínia
Gremião, Maria Palmira Daflon
Chorilli, Marlus
author_sort Cintra, Giovana Aparecida de Souza
collection PubMed
description Methotrexate (MTX) is an immunosuppressive drug for systemic use in the treatment of skin diseases, however, MTX presents a number of side effects, such as hepatotoxicity. To overcome this limitation, this study developed skin MTX delivery surfactant systems, such as a microemulsion (ME) and a liquid crystalline system (LCS), consisting of a glycol copolymer-based silicone fluid (SFGC) as oil phase, polyether functional siloxane (PFS) as surfactant, and carbomer homopolymer type A (C971) dispersion at 0.5% (wt/wt) as aqueous phase. Polarized light microscopy and small-angle X-ray scattering evidenced the presence of hexagonal and lamellar LCSs, and also a ME. Texture profile and in vitro bioadhesion assays showed that these formulations are suitable for topical application, showing interesting hardness, adhesiveness and compressibility values. Rheology analysis confirmed the Newtonian behaviour of the ME, whereas lamellar and hexagonal LCSs behave as pseudoplastic and dilatant non-Newtonian fluids, respectively. In vitro release profiles indicated that MTX could be released in a controlled manner from all the systems, and the Weibull model showed the highest adjusted coefficient of determination. Finally, the formulations were not cytotoxic to the immortalized human keratinocyte line HaCaT. Therefore, these bioadhesive surfactant systems established with PFS and C971 have great potential as skin delivery systems.
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spelling pubmed-62735442018-12-28 Bioadhesive Surfactant Systems for Methotrexate Skin Delivery Cintra, Giovana Aparecida de Souza Pinto, Larissa Alvarenga Calixto, Giovana Maria Fioramonti Soares, Christiane Pienna Von Zuben, Eliete de Souza Scarpa, Maria Virgínia Gremião, Maria Palmira Daflon Chorilli, Marlus Molecules Article Methotrexate (MTX) is an immunosuppressive drug for systemic use in the treatment of skin diseases, however, MTX presents a number of side effects, such as hepatotoxicity. To overcome this limitation, this study developed skin MTX delivery surfactant systems, such as a microemulsion (ME) and a liquid crystalline system (LCS), consisting of a glycol copolymer-based silicone fluid (SFGC) as oil phase, polyether functional siloxane (PFS) as surfactant, and carbomer homopolymer type A (C971) dispersion at 0.5% (wt/wt) as aqueous phase. Polarized light microscopy and small-angle X-ray scattering evidenced the presence of hexagonal and lamellar LCSs, and also a ME. Texture profile and in vitro bioadhesion assays showed that these formulations are suitable for topical application, showing interesting hardness, adhesiveness and compressibility values. Rheology analysis confirmed the Newtonian behaviour of the ME, whereas lamellar and hexagonal LCSs behave as pseudoplastic and dilatant non-Newtonian fluids, respectively. In vitro release profiles indicated that MTX could be released in a controlled manner from all the systems, and the Weibull model showed the highest adjusted coefficient of determination. Finally, the formulations were not cytotoxic to the immortalized human keratinocyte line HaCaT. Therefore, these bioadhesive surfactant systems established with PFS and C971 have great potential as skin delivery systems. MDPI 2016-02-18 /pmc/articles/PMC6273544/ /pubmed/26901183 http://dx.doi.org/10.3390/molecules21020231 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cintra, Giovana Aparecida de Souza
Pinto, Larissa Alvarenga
Calixto, Giovana Maria Fioramonti
Soares, Christiane Pienna
Von Zuben, Eliete de Souza
Scarpa, Maria Virgínia
Gremião, Maria Palmira Daflon
Chorilli, Marlus
Bioadhesive Surfactant Systems for Methotrexate Skin Delivery
title Bioadhesive Surfactant Systems for Methotrexate Skin Delivery
title_full Bioadhesive Surfactant Systems for Methotrexate Skin Delivery
title_fullStr Bioadhesive Surfactant Systems for Methotrexate Skin Delivery
title_full_unstemmed Bioadhesive Surfactant Systems for Methotrexate Skin Delivery
title_short Bioadhesive Surfactant Systems for Methotrexate Skin Delivery
title_sort bioadhesive surfactant systems for methotrexate skin delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273544/
https://www.ncbi.nlm.nih.gov/pubmed/26901183
http://dx.doi.org/10.3390/molecules21020231
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