Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sguizzato, Maddalena, Pepe, Alessia, Baldisserotto, Anna, Barbari, Riccardo, Montesi, Leda, Drechsler, Markus, Mariani, Paolo, Cortesi, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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
_version_ 1784894580042235904
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
work_keys_str_mv AT sguizzatomaddalena niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT pepealessia niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT baldisserottoanna niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT barbaririccardo niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT montesileda niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT drechslermarkus niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT marianipaolo niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior
AT cortesirita niosomesfortopicalapplicationofantioxidantmoleculesdesignandinvitrobehavior