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Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole

The mucosal membrane of the oral cavity, due to its unique structure and availability, constitutes an appropriate site for the delivery of drugs, both with local and systemic effects. Mucoadhesive buccal films are drug dosage forms that due to their convenience of application, flexibility and size,...

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Autores principales: Szekalska, Marta, Czajkowska-Kośnik, Anna, Maciejewski, Bartosz, Misztalewska-Turkowicz, Iwona, Wilczewska, Agnieszka Zofia, Bernatoniene, Jurga, Winnicka, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610174/
https://www.ncbi.nlm.nih.gov/pubmed/37896175
http://dx.doi.org/10.3390/pharmaceutics15102415
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author Szekalska, Marta
Czajkowska-Kośnik, Anna
Maciejewski, Bartosz
Misztalewska-Turkowicz, Iwona
Wilczewska, Agnieszka Zofia
Bernatoniene, Jurga
Winnicka, Katarzyna
author_facet Szekalska, Marta
Czajkowska-Kośnik, Anna
Maciejewski, Bartosz
Misztalewska-Turkowicz, Iwona
Wilczewska, Agnieszka Zofia
Bernatoniene, Jurga
Winnicka, Katarzyna
author_sort Szekalska, Marta
collection PubMed
description The mucosal membrane of the oral cavity, due to its unique structure and availability, constitutes an appropriate site for the delivery of drugs, both with local and systemic effects. Mucoadhesive buccal films are drug dosage forms that due to their convenience of application, flexibility and size, are characterized by patients’ compliance. Sodium alginate and pectin are natural polymers from the polysaccharides group, with mucoadhesive properties, that are widely applied to obtain buccal films. However, their hydrophilic nature and poor water resistance limit their application in sustained drug release formulations. Hence, the aim of this investigation was to design alginate/pectin buccal films by a one-step crosslinking technique—with the application of calcium carbonate. This technique was applied to prepare crosslinked alginate and alginate/pectin mucoadhesive films with a model antifungal drug—posaconazole. The obtained formulations were evaluated for the impact of crosslinking and pectin’s presence on their pharmaceutical, mucoadhesive, mechanical and physicochemical properties. Additionally, the antifungal activity of the prepared films against Candida spp. was evaluated. It was shown that pectin’s presence in the formulations improved flexibility, mucoadhesion and antifungal activity. The crosslinking process reduced mucoadhesiveness and antifungal activity but significantly enhanced the mechanical properties and stability and enabled prolonged drug release.
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spelling pubmed-106101742023-10-28 Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole Szekalska, Marta Czajkowska-Kośnik, Anna Maciejewski, Bartosz Misztalewska-Turkowicz, Iwona Wilczewska, Agnieszka Zofia Bernatoniene, Jurga Winnicka, Katarzyna Pharmaceutics Article The mucosal membrane of the oral cavity, due to its unique structure and availability, constitutes an appropriate site for the delivery of drugs, both with local and systemic effects. Mucoadhesive buccal films are drug dosage forms that due to their convenience of application, flexibility and size, are characterized by patients’ compliance. Sodium alginate and pectin are natural polymers from the polysaccharides group, with mucoadhesive properties, that are widely applied to obtain buccal films. However, their hydrophilic nature and poor water resistance limit their application in sustained drug release formulations. Hence, the aim of this investigation was to design alginate/pectin buccal films by a one-step crosslinking technique—with the application of calcium carbonate. This technique was applied to prepare crosslinked alginate and alginate/pectin mucoadhesive films with a model antifungal drug—posaconazole. The obtained formulations were evaluated for the impact of crosslinking and pectin’s presence on their pharmaceutical, mucoadhesive, mechanical and physicochemical properties. Additionally, the antifungal activity of the prepared films against Candida spp. was evaluated. It was shown that pectin’s presence in the formulations improved flexibility, mucoadhesion and antifungal activity. The crosslinking process reduced mucoadhesiveness and antifungal activity but significantly enhanced the mechanical properties and stability and enabled prolonged drug release. MDPI 2023-10-03 /pmc/articles/PMC10610174/ /pubmed/37896175 http://dx.doi.org/10.3390/pharmaceutics15102415 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
Szekalska, Marta
Czajkowska-Kośnik, Anna
Maciejewski, Bartosz
Misztalewska-Turkowicz, Iwona
Wilczewska, Agnieszka Zofia
Bernatoniene, Jurga
Winnicka, Katarzyna
Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole
title Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole
title_full Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole
title_fullStr Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole
title_full_unstemmed Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole
title_short Mucoadhesive Alginate/Pectin Films Crosslinked by Calcium Carbonate as Carriers of a Model Antifungal Drug—Posaconazole
title_sort mucoadhesive alginate/pectin films crosslinked by calcium carbonate as carriers of a model antifungal drug—posaconazole
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610174/
https://www.ncbi.nlm.nih.gov/pubmed/37896175
http://dx.doi.org/10.3390/pharmaceutics15102415
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