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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/ma11040580</dc:identifier><dc:language>eng</dc:language><dc:creator>Batool, F.</dc:creator><dc:creator>Morand, D.-N.</dc:creator><dc:creator>Thomas, L.</dc:creator><dc:creator>Bugueno, I.M.</dc:creator><dc:creator>Aragon, J.</dc:creator><dc:creator>Irusta, S.</dc:creator><dc:creator>Keller, L.</dc:creator><dc:creator>Benkirane-Jessel, N.</dc:creator><dc:creator>Tenenbaum, H.</dc:creator><dc:creator>Huck, O.</dc:creator><dc:title>Synthesis of a novel electrospun polycaprolactone scaffold functionalized with ibuprofen for periodontal regeneration: An in vitro and in vivo study</dc:title><dc:identifier>ART-2018-105903</dc:identifier><dc:description>Ibuprofen (IBU) has been shown to improve periodontal treatment outcomes. The aimof this study was to develop a new anti-inflammatory scaffold by functionalizing an electrospun nanofibrous poly-e-caprolactone membrane with IBU (IBU-PCL) and to evaluate its impact on periodontal inflammation, wound healing and regeneration in vitro and in vivo. IBU-PCL was synthesized through electrospinning. The effects of IBU-PCL on the proliferation and migration of epithelial cells (EC) and fibroblasts (FB) exposed to Porphyromonas gingivlais lipopolysaccharide (Pg-LPS) were evaluated through the AlamarBlue test and scratch assay, respectively. Anti-inflammatory and remodeling properties were investigated through Real time qPCR. Finally, the in vivo efficacy of the IBU-PCL membrane was assessed in an experimental periodontitis mouse model through histomorphometric analysis. The results showed that the anti-inflammatory effects of IBU on gingival cells were effectively amplified using the functionalizedmembrane. IBU-PCL reduced the proliferation and migration of cells challenged by Pg-LPS, as well as the expression of fibronectin-1, collagen-IV, integrin a3ß1 and laminin-5. In vivo, the membranes significantly improved the clinical attachment and IBU-PCL also reduced inflammation-induced bone destruction. These data showed that the IBU-PCL membrane could efficiently and differentially control inflammatory and migratory gingival cell responses and potentially promote periodontal regeneration.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/70281</dc:source><dc:doi>10.3390/ma11040580</dc:doi><dc:identifier>http://zaguan.unizar.es/record/70281</dc:identifier><dc:identifier>oai:zaguan.unizar.es:70281</dc:identifier><dc:identifier.citation>Materials 11, 4 (2018), 580 [18 pp]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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