Ibuprofen loaded PVA/chitosan membranes: A highly efficient strategy towards an improved skin wound healing
•Drug loaded hydrogel-based dressings are efficiently prepared by scCO2-assisted phase inversion.•β-CD_IBP loaded PVA/CS dressings display suitable properties for wound management.•β-CDs assure a sustained IBP release during the peak of the inflammatory phase.•IBP-loaded β-CDs carriers prevent an ex...
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Published in: | Carbohydrate polymers Vol. 159; pp. 136 - 145 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Elsevier Ltd
01-03-2017
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Subjects: | |
Online Access: | Get full text |
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Summary: | •Drug loaded hydrogel-based dressings are efficiently prepared by scCO2-assisted phase inversion.•β-CD_IBP loaded PVA/CS dressings display suitable properties for wound management.•β-CDs assure a sustained IBP release during the peak of the inflammatory phase.•IBP-loaded β-CDs carriers prevent an exuberant inflammatory phase.•IBP, a simple NSAID, improves the skin wound healing.
During wound healing, an early inflammation can cause an increase of the wound size and the healing process can be considerably belated if a disproportionate inflammatory response occurs. (S)-ibuprofen (IBP), a non-steroidal anti-inflammatory agent, has been used for muscle healing and to treat venous leg ulcers, but its effect in skin wound healing has not been thoroughly studied thus far. Herein, IBP-β-cyclodextrins carriers were designed to customise the release profile of IBP from poly(vinyl alcohol)/chitosan (PVA/CS) dressings in order to promote a faster skin regeneration. The dressings were produced using supercritical carbon dioxide (scCO2)-assisted technique. In vitro IBP release studies showed that β-cyclodextrins allowed a controlled drug release from the hydrogels which is crucial for their application in wound management. Moreover, the in vivo assays revealed that the presence of PVA/CS membranes containing IBP-β-cyclodextrins carriers avoided scab formation and an excessive inflammation, enabling an earlier skin healing. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2016.12.029 |