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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Functionalization of polycaprolactone 3D scaffolds with hyaluronic acid glycine-peptide conjugates and endothelial cell adhesion</dc:title><dc:creator>Mohan,	Tamilselvan	(Avtor)
	</dc:creator><dc:creator>Gürer,	Fazilet	(Avtor)
	</dc:creator><dc:creator>Bračič,	Doris	(Avtor)
	</dc:creator><dc:creator>Lackner,	Florian	(Avtor)
	</dc:creator><dc:creator>Nagaraj,	Chandran	(Avtor)
	</dc:creator><dc:creator>Maver,	Uroš	(Avtor)
	</dc:creator><dc:creator>Gradišnik,	Lidija	(Avtor)
	</dc:creator><dc:creator>Finšgar,	Matjaž	(Avtor)
	</dc:creator><dc:creator>Kargl,	Rupert	(Avtor)
	</dc:creator><dc:creator>Stana-Kleinschek,	Karin	(Avtor)
	</dc:creator><dc:subject>3D printing</dc:subject><dc:subject>polycaprolactone</dc:subject><dc:subject>hyaluronic acid</dc:subject><dc:description>This study enhances the bioactivity of polycaprolactone (PCL) scaffolds for tissue engineering by functionalizing them with oxidized hyaluronic acid glycine-peptide conjugates to improve endothelial cell adhesion and growth. Hyaluronic acid was conjugated with a glycine-peptide to create a bioactive interface on PCL (static water contact angle, SCA(H2O): 98°). The scaffolds were fabricated using a melt extrusion 3D printing technique. The HA-glycine peptide conjugates were oxidized and immobilized on aminolyzed PCL via Schiff-base chemistry, introducing hydrophilicity (SCA(H2O): 21°), multiple functional groups, and a negative zeta potential (-12.04 mV at pH 7.4). A quartz crystal microbalance confirmed chemical conjugation and quantified the mass (8.5-10.3 mg m-2) of oxidized HA-glycine on PCL. The functionalized scaffolds showed enhanced swelling, improved mechanical properties (2-fold increase in strength, from 26 to 51 MPa), and maintained integrity during degradation. In-vitro experiments demonstrated improved endothelial cell adhesion, proliferation and viability, suggesting the potential for vascularized tissue constructs.</dc:description><dc:publisher>ACS Publications</dc:publisher><dc:date>2025</dc:date><dc:date>2025-03-19 08:32:27</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>92182</dc:identifier><dc:identifier>UDK: 604</dc:identifier><dc:identifier>COBISS_ID: 228392451</dc:identifier><dc:identifier>DOI: 10.1021/acs.biomac.4c01559</dc:identifier><dc:identifier>ISSN pri članku: 1526-4602</dc:identifier><dc:language>sl</dc:language></metadata>
