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Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application

Quercus Suber Bark from Quercus suber L. is a natural, renewable and biodegradable biomaterial with multifunctional proprieties. In this study, we used it as solid particles to stabilize a Pickering emulsion. The main goal was to produce an optimized topical formulation using biocompatible organic p...

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Autores principales: Carriço, Catarina, Pinto, Pedro, Graça, Angélica, Gonçalves, Lídia Maria, Ribeiro, Helena Margarida, Marto, Joana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471441/
https://www.ncbi.nlm.nih.gov/pubmed/30893873
http://dx.doi.org/10.3390/pharmaceutics11030131
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author Carriço, Catarina
Pinto, Pedro
Graça, Angélica
Gonçalves, Lídia Maria
Ribeiro, Helena Margarida
Marto, Joana
author_facet Carriço, Catarina
Pinto, Pedro
Graça, Angélica
Gonçalves, Lídia Maria
Ribeiro, Helena Margarida
Marto, Joana
author_sort Carriço, Catarina
collection PubMed
description Quercus Suber Bark from Quercus suber L. is a natural, renewable and biodegradable biomaterial with multifunctional proprieties. In this study, we used it as solid particles to stabilize a Pickering emulsion. The main goal was to produce an optimized topical formulation using biocompatible organic particles as stabilizers of the emulsion instead of the common surfactants, whilst benefiting from Quercus suber L. proprieties. In this work, a Quality by Design (QbD) approach was successfully applied to the production of this emulsion. A screening design was conducted, identifying the critical variables of the formula and process, affecting the critical quality attributes of the emulsion (droplet size distribution). The optimization of the production was made through the establishment of the design space. The stability was also investigated during 30 days, demonstrating that Quercus Suber Bark-stabilized emulsions are stable since the droplet size distribution lowers. In vitro studies were performed to assess antioxidant and antiaging efficacy, which revealed that the formulation had indeed antioxidant proprieties. A physicochemical characterization demonstrated that the formulation presents a shear-thinning fluid, ideal for topical administration. The in vivo compatibility study confirmed that the final formulation is not skin irritant, being safe for human use. A sensorial analysis was also performed, using a simple sensory questionnaire, revealing very positive results. Thus, the use of Quercus Suber Bark particles as a multifunctional solid ingredient contributed to achieve a stable, effective and innovative Pickering emulsion with a meaningful synergistic protection against oxidative stress.
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spelling pubmed-64714412019-04-27 Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application Carriço, Catarina Pinto, Pedro Graça, Angélica Gonçalves, Lídia Maria Ribeiro, Helena Margarida Marto, Joana Pharmaceutics Article Quercus Suber Bark from Quercus suber L. is a natural, renewable and biodegradable biomaterial with multifunctional proprieties. In this study, we used it as solid particles to stabilize a Pickering emulsion. The main goal was to produce an optimized topical formulation using biocompatible organic particles as stabilizers of the emulsion instead of the common surfactants, whilst benefiting from Quercus suber L. proprieties. In this work, a Quality by Design (QbD) approach was successfully applied to the production of this emulsion. A screening design was conducted, identifying the critical variables of the formula and process, affecting the critical quality attributes of the emulsion (droplet size distribution). The optimization of the production was made through the establishment of the design space. The stability was also investigated during 30 days, demonstrating that Quercus Suber Bark-stabilized emulsions are stable since the droplet size distribution lowers. In vitro studies were performed to assess antioxidant and antiaging efficacy, which revealed that the formulation had indeed antioxidant proprieties. A physicochemical characterization demonstrated that the formulation presents a shear-thinning fluid, ideal for topical administration. The in vivo compatibility study confirmed that the final formulation is not skin irritant, being safe for human use. A sensorial analysis was also performed, using a simple sensory questionnaire, revealing very positive results. Thus, the use of Quercus Suber Bark particles as a multifunctional solid ingredient contributed to achieve a stable, effective and innovative Pickering emulsion with a meaningful synergistic protection against oxidative stress. MDPI 2019-03-19 /pmc/articles/PMC6471441/ /pubmed/30893873 http://dx.doi.org/10.3390/pharmaceutics11030131 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
Carriço, Catarina
Pinto, Pedro
Graça, Angélica
Gonçalves, Lídia Maria
Ribeiro, Helena Margarida
Marto, Joana
Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application
title Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application
title_full Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application
title_fullStr Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application
title_full_unstemmed Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application
title_short Design and Characterization of a New Quercus Suber-Based Pickering Emulsion for Topical Application
title_sort design and characterization of a new quercus suber-based pickering emulsion for topical application
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471441/
https://www.ncbi.nlm.nih.gov/pubmed/30893873
http://dx.doi.org/10.3390/pharmaceutics11030131
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