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Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment
Pycnogenol (PYC) is a concentrate of phenolic compounds derived from French maritime pine; its biological activity as antioxidant, anti-inflammatory and antibacterial suggests its use in the treatment of open wounds. A bioadhesive film, loaded with PYC, was prepared by casting, starting with a combi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002000/ https://www.ncbi.nlm.nih.gov/pubmed/33802607 http://dx.doi.org/10.3390/pharmaceutics13030324 |
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author | Pagano, Cinzia Puglia, Debora Luzi, Francesca Michele, Alessandro Di Scuota, Stefania Primavilla, Sara Ceccarini, Maria Rachele Beccari, Tommaso Iborra, César Antonio Viseras Ramella, Daniele Ricci, Maurizio Perioli, Luana |
author_facet | Pagano, Cinzia Puglia, Debora Luzi, Francesca Michele, Alessandro Di Scuota, Stefania Primavilla, Sara Ceccarini, Maria Rachele Beccari, Tommaso Iborra, César Antonio Viseras Ramella, Daniele Ricci, Maurizio Perioli, Luana |
author_sort | Pagano, Cinzia |
collection | PubMed |
description | Pycnogenol (PYC) is a concentrate of phenolic compounds derived from French maritime pine; its biological activity as antioxidant, anti-inflammatory and antibacterial suggests its use in the treatment of open wounds. A bioadhesive film, loaded with PYC, was prepared by casting, starting with a combination of two biopolymer acqueous solutions: xanthan gum (1% wt/wt) and sodium alginate (1.5% wt/wt), in a 2.5/7.5 (wt/wt) ratio. In both solutions, glycerol (10% wt/wt) was added as plasticizing agent. The film resulted in an adhesive capable to absorb a simulated wound fluid (~ 65% wt/wt within 1 h), therefore suitable for exuding wounds. The mechanical characterization showed that the film is deformable (elastic modulus E = 3.070 ± 0.044 MPa), suggesting adaptability to any type of surface and resistance to mechanical solicitations. PYC is released within 24 h by a sustained mechanism, achieving a maximum concentration of ~0.2 mg/mL, that is safe for keratinocytes, as shown by cytotoxicity studies. A concentration of 0.015 mg/mL is reached in the first 5 min after application, at which point PYC stimulates keratinocyte growth. These preliminary results suggest the use of PYC in formulations designed for topical use. |
format | Online Article Text |
id | pubmed-8002000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80020002021-03-28 Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment Pagano, Cinzia Puglia, Debora Luzi, Francesca Michele, Alessandro Di Scuota, Stefania Primavilla, Sara Ceccarini, Maria Rachele Beccari, Tommaso Iborra, César Antonio Viseras Ramella, Daniele Ricci, Maurizio Perioli, Luana Pharmaceutics Article Pycnogenol (PYC) is a concentrate of phenolic compounds derived from French maritime pine; its biological activity as antioxidant, anti-inflammatory and antibacterial suggests its use in the treatment of open wounds. A bioadhesive film, loaded with PYC, was prepared by casting, starting with a combination of two biopolymer acqueous solutions: xanthan gum (1% wt/wt) and sodium alginate (1.5% wt/wt), in a 2.5/7.5 (wt/wt) ratio. In both solutions, glycerol (10% wt/wt) was added as plasticizing agent. The film resulted in an adhesive capable to absorb a simulated wound fluid (~ 65% wt/wt within 1 h), therefore suitable for exuding wounds. The mechanical characterization showed that the film is deformable (elastic modulus E = 3.070 ± 0.044 MPa), suggesting adaptability to any type of surface and resistance to mechanical solicitations. PYC is released within 24 h by a sustained mechanism, achieving a maximum concentration of ~0.2 mg/mL, that is safe for keratinocytes, as shown by cytotoxicity studies. A concentration of 0.015 mg/mL is reached in the first 5 min after application, at which point PYC stimulates keratinocyte growth. These preliminary results suggest the use of PYC in formulations designed for topical use. MDPI 2021-03-03 /pmc/articles/PMC8002000/ /pubmed/33802607 http://dx.doi.org/10.3390/pharmaceutics13030324 Text en © 2021 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 (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Pagano, Cinzia Puglia, Debora Luzi, Francesca Michele, Alessandro Di Scuota, Stefania Primavilla, Sara Ceccarini, Maria Rachele Beccari, Tommaso Iborra, César Antonio Viseras Ramella, Daniele Ricci, Maurizio Perioli, Luana Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment |
title | Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment |
title_full | Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment |
title_fullStr | Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment |
title_full_unstemmed | Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment |
title_short | Development and Characterization of Xanthan Gum and Alginate Based Bioadhesive Film for Pycnogenol Topical Use in Wound Treatment |
title_sort | development and characterization of xanthan gum and alginate based bioadhesive film for pycnogenol topical use in wound treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002000/ https://www.ncbi.nlm.nih.gov/pubmed/33802607 http://dx.doi.org/10.3390/pharmaceutics13030324 |
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