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PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation
In this work, a one-shot process for the simultaneous foaming of polycaprolactone (PCL) and impregnation of mesoglycan (MSG) into the porous structure was successfully attempted. Supercritical carbon dioxide plays the role of the foaming agent with respect to PCL and of the solvent with respect to M...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956126/ https://www.ncbi.nlm.nih.gov/pubmed/31779148 http://dx.doi.org/10.3390/pharmaceutics11120631 |
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author | Franco, Paola Belvedere, Raffaella Pessolano, Emanuela Liparoti, Sara Pantani, Roberto Petrella, Antonello De Marco, Iolanda |
author_facet | Franco, Paola Belvedere, Raffaella Pessolano, Emanuela Liparoti, Sara Pantani, Roberto Petrella, Antonello De Marco, Iolanda |
author_sort | Franco, Paola |
collection | PubMed |
description | In this work, a one-shot process for the simultaneous foaming of polycaprolactone (PCL) and impregnation of mesoglycan (MSG) into the porous structure was successfully attempted. Supercritical carbon dioxide plays the role of the foaming agent with respect to PCL and of the solvent with respect to MSG. The main objective is to produce an innovative topical device for application on skin lesions, promoting prolonged pro-resolving effects. The obtained device offers a protective barrier to ensure a favorable and sterilized environment for the wound healing process. The impregnation kinetics revealed that a pressure of 17 MPa, a temperature of 35 °C, and a time of impregnation of 24 h assured a proper foaming of PCL in addition to the impregnation of the maximum amount of MSG; i.e., 0.22 mg(MSG)/mg(PCL). After a preliminary study conducted on PCL granules used as brought, the MSG impregnation was performed at the optimized process conditions also on a PCL film, produced by compression molding, with the final goal of producing medical patches. Comparing the dissolution profiles in phosphate buffered saline solution (PBS) of pure MSG and MSG impregnated on foamed PCL, it was demonstrated that the release of MSG was significantly prolonged up to 70 times. Next, we performed functional assays of in vitro wound healing, cell invasion, and angiogenesis to evaluate the biological effects of the PCL-derived MSG. Interestingly, we found the ability of this composite system to promote the activation of human keratinocytes, fibroblasts, and endothelial cells, as the main actors of tissue regeneration, confirming what we previously showed for the MSG alone. |
format | Online Article Text |
id | pubmed-6956126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69561262020-01-23 PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation Franco, Paola Belvedere, Raffaella Pessolano, Emanuela Liparoti, Sara Pantani, Roberto Petrella, Antonello De Marco, Iolanda Pharmaceutics Article In this work, a one-shot process for the simultaneous foaming of polycaprolactone (PCL) and impregnation of mesoglycan (MSG) into the porous structure was successfully attempted. Supercritical carbon dioxide plays the role of the foaming agent with respect to PCL and of the solvent with respect to MSG. The main objective is to produce an innovative topical device for application on skin lesions, promoting prolonged pro-resolving effects. The obtained device offers a protective barrier to ensure a favorable and sterilized environment for the wound healing process. The impregnation kinetics revealed that a pressure of 17 MPa, a temperature of 35 °C, and a time of impregnation of 24 h assured a proper foaming of PCL in addition to the impregnation of the maximum amount of MSG; i.e., 0.22 mg(MSG)/mg(PCL). After a preliminary study conducted on PCL granules used as brought, the MSG impregnation was performed at the optimized process conditions also on a PCL film, produced by compression molding, with the final goal of producing medical patches. Comparing the dissolution profiles in phosphate buffered saline solution (PBS) of pure MSG and MSG impregnated on foamed PCL, it was demonstrated that the release of MSG was significantly prolonged up to 70 times. Next, we performed functional assays of in vitro wound healing, cell invasion, and angiogenesis to evaluate the biological effects of the PCL-derived MSG. Interestingly, we found the ability of this composite system to promote the activation of human keratinocytes, fibroblasts, and endothelial cells, as the main actors of tissue regeneration, confirming what we previously showed for the MSG alone. MDPI 2019-11-26 /pmc/articles/PMC6956126/ /pubmed/31779148 http://dx.doi.org/10.3390/pharmaceutics11120631 Text en © 2019 by the authors. 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/). |
spellingShingle | Article Franco, Paola Belvedere, Raffaella Pessolano, Emanuela Liparoti, Sara Pantani, Roberto Petrella, Antonello De Marco, Iolanda PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation |
title | PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation |
title_full | PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation |
title_fullStr | PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation |
title_full_unstemmed | PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation |
title_short | PCL/Mesoglycan Devices Obtained by Supercritical Foaming and Impregnation |
title_sort | pcl/mesoglycan devices obtained by supercritical foaming and impregnation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956126/ https://www.ncbi.nlm.nih.gov/pubmed/31779148 http://dx.doi.org/10.3390/pharmaceutics11120631 |
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