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Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior
In the present study, gels based on xanthan gum and poloxamer 407 have been developed and characterized in order to convey natural antioxidant molecules included in niosomes. Specifically, the studies were conducted to evaluate how the vesicular systems affect the release of the active ingredient an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9956392/ https://www.ncbi.nlm.nih.gov/pubmed/36826277 http://dx.doi.org/10.3390/gels9020107 |
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author | Sguizzato, Maddalena Pepe, Alessia Baldisserotto, Anna Barbari, Riccardo Montesi, Leda Drechsler, Markus Mariani, Paolo Cortesi, Rita |
author_facet | Sguizzato, Maddalena Pepe, Alessia Baldisserotto, Anna Barbari, Riccardo Montesi, Leda Drechsler, Markus Mariani, Paolo Cortesi, Rita |
author_sort | Sguizzato, Maddalena |
collection | PubMed |
description | In the present study, gels based on xanthan gum and poloxamer 407 have been developed and characterized in order to convey natural antioxidant molecules included in niosomes. Specifically, the studies were conducted to evaluate how the vesicular systems affect the release of the active ingredient and which formulation is most suitable for cutaneous application. Niosomes, composed of Span 20 or Tween 20, were produced through the direct hydration method, and therefore, borate buffer or a micellar solution of poloxamer 188 was used as the aqueous phase. The niosomes were firstly characterized in terms of morphology, dimensional and encapsulation stability. Afterwards, gels based on poloxamer 407 or xanthan gum were compared in terms of spreadability and adhesiveness. It was found to have greater spreadability for gels based on poloxamer 407 and 100% adhesiveness for those based on xanthan gum. The in vitro diffusion of drugs studied using Franz cells associated with membranes of mixed cellulose esters showed that the use of a poloxamer micellar hydration phase determined a lower release as well as the use of Span 20. The thickened niosomes ensured controlled diffusion of the antioxidant molecules. Lastly, the in vivo irritation test confirmed the safeness of niosomal gels after cutaneous application. |
format | Online Article Text |
id | pubmed-9956392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99563922023-02-25 Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior Sguizzato, Maddalena Pepe, Alessia Baldisserotto, Anna Barbari, Riccardo Montesi, Leda Drechsler, Markus Mariani, Paolo Cortesi, Rita Gels Article In the present study, gels based on xanthan gum and poloxamer 407 have been developed and characterized in order to convey natural antioxidant molecules included in niosomes. Specifically, the studies were conducted to evaluate how the vesicular systems affect the release of the active ingredient and which formulation is most suitable for cutaneous application. Niosomes, composed of Span 20 or Tween 20, were produced through the direct hydration method, and therefore, borate buffer or a micellar solution of poloxamer 188 was used as the aqueous phase. The niosomes were firstly characterized in terms of morphology, dimensional and encapsulation stability. Afterwards, gels based on poloxamer 407 or xanthan gum were compared in terms of spreadability and adhesiveness. It was found to have greater spreadability for gels based on poloxamer 407 and 100% adhesiveness for those based on xanthan gum. The in vitro diffusion of drugs studied using Franz cells associated with membranes of mixed cellulose esters showed that the use of a poloxamer micellar hydration phase determined a lower release as well as the use of Span 20. The thickened niosomes ensured controlled diffusion of the antioxidant molecules. Lastly, the in vivo irritation test confirmed the safeness of niosomal gels after cutaneous application. MDPI 2023-01-26 /pmc/articles/PMC9956392/ /pubmed/36826277 http://dx.doi.org/10.3390/gels9020107 Text en © 2023 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 Sguizzato, Maddalena Pepe, Alessia Baldisserotto, Anna Barbari, Riccardo Montesi, Leda Drechsler, Markus Mariani, Paolo Cortesi, Rita Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior |
title | Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior |
title_full | Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior |
title_fullStr | Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior |
title_full_unstemmed | Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior |
title_short | Niosomes for Topical Application of Antioxidant Molecules: Design and In Vitro Behavior |
title_sort | niosomes for topical application of antioxidant molecules: design and in vitro behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9956392/ https://www.ncbi.nlm.nih.gov/pubmed/36826277 http://dx.doi.org/10.3390/gels9020107 |
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