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Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections

Antimicrobial photodynamic therapy (aPDT) is a potent tool to surpass the global rise of antimicrobial resistance; still, the effective topical administration of photosensitizers remains a challenge. Biopolymer-based adhesive films can safely extend the residence time of photosensitizers. However, t...

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Autores principales: Pedro, Sónia N., Valente, Bruno F.A., Vilela, Carla, Oliveira, Helena, Almeida, Adelaide, Freire, Mara G., Silvestre, Armando J.D., Freire, Carmen S.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392606/
https://www.ncbi.nlm.nih.gov/pubmed/37533730
http://dx.doi.org/10.1016/j.mtbio.2023.100733
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author Pedro, Sónia N.
Valente, Bruno F.A.
Vilela, Carla
Oliveira, Helena
Almeida, Adelaide
Freire, Mara G.
Silvestre, Armando J.D.
Freire, Carmen S.R.
author_facet Pedro, Sónia N.
Valente, Bruno F.A.
Vilela, Carla
Oliveira, Helena
Almeida, Adelaide
Freire, Mara G.
Silvestre, Armando J.D.
Freire, Carmen S.R.
author_sort Pedro, Sónia N.
collection PubMed
description Antimicrobial photodynamic therapy (aPDT) is a potent tool to surpass the global rise of antimicrobial resistance; still, the effective topical administration of photosensitizers remains a challenge. Biopolymer-based adhesive films can safely extend the residence time of photosensitizers. However, their wide application is narrowed by their limited water absorption capacity and gel strength. In this study, pullulan-based films with a switchable character (from a solid film to an adhesive hydrogel) were developed. This was accomplished by the incorporation of a betaine-based deep eutectic solvent (DES) containing curcumin (4.4 μg.cm(−2)) into the pullulan films, which tuned the films’ skin moisture absorption ability, and therefore they switch into an adhesive hydrogel capable of delivering the photosensitizer. The obtained transparent films presented higher extensibility (elongation at break up to 338.2%) than the pullulan counterparts (6.08%), when stored at 54% of relative humidity, and the corresponding hydrogels a 4-fold higher adhesiveness than commercial hydrogels. These non-cytotoxic adhesives allowed the inactivation (∼5 log reduction), down to the detection limit of the method, of multiresistant strains of Staphylococcus aureus in ex vivo skin samples. Overall, these materials are promising for aPDT in the treatment of resistant skin infections, while being easily removed from the skin.
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spelling pubmed-103926062023-08-02 Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections Pedro, Sónia N. Valente, Bruno F.A. Vilela, Carla Oliveira, Helena Almeida, Adelaide Freire, Mara G. Silvestre, Armando J.D. Freire, Carmen S.R. Mater Today Bio Full Length Article Antimicrobial photodynamic therapy (aPDT) is a potent tool to surpass the global rise of antimicrobial resistance; still, the effective topical administration of photosensitizers remains a challenge. Biopolymer-based adhesive films can safely extend the residence time of photosensitizers. However, their wide application is narrowed by their limited water absorption capacity and gel strength. In this study, pullulan-based films with a switchable character (from a solid film to an adhesive hydrogel) were developed. This was accomplished by the incorporation of a betaine-based deep eutectic solvent (DES) containing curcumin (4.4 μg.cm(−2)) into the pullulan films, which tuned the films’ skin moisture absorption ability, and therefore they switch into an adhesive hydrogel capable of delivering the photosensitizer. The obtained transparent films presented higher extensibility (elongation at break up to 338.2%) than the pullulan counterparts (6.08%), when stored at 54% of relative humidity, and the corresponding hydrogels a 4-fold higher adhesiveness than commercial hydrogels. These non-cytotoxic adhesives allowed the inactivation (∼5 log reduction), down to the detection limit of the method, of multiresistant strains of Staphylococcus aureus in ex vivo skin samples. Overall, these materials are promising for aPDT in the treatment of resistant skin infections, while being easily removed from the skin. Elsevier 2023-07-14 /pmc/articles/PMC10392606/ /pubmed/37533730 http://dx.doi.org/10.1016/j.mtbio.2023.100733 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Pedro, Sónia N.
Valente, Bruno F.A.
Vilela, Carla
Oliveira, Helena
Almeida, Adelaide
Freire, Mara G.
Silvestre, Armando J.D.
Freire, Carmen S.R.
Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
title Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
title_full Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
title_fullStr Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
title_full_unstemmed Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
title_short Switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
title_sort switchable adhesive films of pullulan loaded with a deep eutectic solvent-curcumin formulation for the photodynamic treatment of drug-resistant skin infections
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392606/
https://www.ncbi.nlm.nih.gov/pubmed/37533730
http://dx.doi.org/10.1016/j.mtbio.2023.100733
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