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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/polym13193399</dc:identifier><dc:language>eng</dc:language><dc:creator>Ren, Jiongyu</dc:creator><dc:creator>Kohli, Nupur</dc:creator><dc:creator>Sharma, Vaibhav</dc:creator><dc:creator>Shakouri, Taleen</dc:creator><dc:creator>Keskin-Erdogan, Zalike</dc:creator><dc:creator>Saifzadeh, Siamak</dc:creator><dc:creator>Brierly, Gary I.</dc:creator><dc:creator>Knowles, Jonathan C.</dc:creator><dc:creator>Woodruff, Maria A.</dc:creator><dc:creator>García-Gareta, Elena</dc:creator><dc:title>Poly-e-Caprolactone/Fibrin-Alginate scaffold: a new Pro-Angiogenic composite biomaterial for the treatment of bone defects</dc:title><dc:identifier>ART-2021-131314</dc:identifier><dc:description>We hypothesized that a composite of 3D porous melt-electrowritten poly-ɛ-caprolactone (PCL) coated throughout with a porous and slowly biodegradable fibrin/alginate (FA) matrix would accelerate bone repair due to its angiogenic potential. Scanning electron microscopy showed that the open pore structure of the FA matrix was maintained in the PCL/FA composites. Fourier transform infrared spectroscopy and differential scanning calorimetry showed complete coverage of the PCL fibres by FA, and the PCL/FA crystallinity was decreased compared with PCL. In vitro cell work with osteoprogenitor cells showed that they preferentially bound to the FA component and proliferated on all scaffolds over 28 days. A chorioallantoic membrane assay showed more blood vessel infiltration into FA and PCL/FA compared with PCL, and a significantly higher number of bifurcation points for PCL/FA compared with both FA and PCL. Implantation into a rat cranial defect model followed by microcomputed tomography, histology, and immunohistochemistry after 4- and 12-weeks post operation showed fast early bone formation at week 4, with significantly higher bone formation for FA and PCL/FA compared with PCL. However, this phenomenon was not extrapolated to week 12. Therefore, for long-term bone regeneration, tuning of FA degradation to ensure syncing with new bone formation is likely necessary.</dc:description><dc:date>2021</dc:date><dc:source>http://zaguan.unizar.es/record/121330</dc:source><dc:doi>10.3390/polym13193399</dc:doi><dc:identifier>http://zaguan.unizar.es/record/121330</dc:identifier><dc:identifier>oai:zaguan.unizar.es:121330</dc:identifier><dc:identifier.citation>Polymers 13, 19 (2021), 3399 [22 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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