TY - JOUR
T1 - Elastomeric electrospun scaffolds of a biodegradable aliphatic copolyester containing PEG-like sequences for dynamic culture of human endothelial cells
AU - Fusaro, Luca
AU - Gualandi, Chiara
AU - Antonioli, Diego
AU - Soccio, Michelina
AU - Liguori, Anna
AU - Laus, Michele
AU - Lotti, Nadia
AU - Boccafoschi, Francesca
AU - Focarete, Maria Letizia
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/12
Y1 - 2020/12
N2 - In the field of artificial prostheses for damaged vessel replacement, polymeric scaffolds showing the right combination of mechanical performance, biocompatibility, and biodegradability are still demanded. In the present work, poly(butylene-co-triethylene trans-1,4-cyclohexanedicarboxylate), a biodegradable random aliphatic copolyester, has been synthesized and electrospun in form of aligned and random fibers properly designed for vascular applications. The obtained materials were analyzed through tensile and dynamic-mechanical tests, the latter performed under conditions simulating the mechanical contraction of vascular tissue. Furthermore, the in vitro biological characterization, in terms of hemocompatibility and cytocompatibility in static and dynamic conditions, was also carried out. The mechanical properties of the investigated scaffolds fit within the range of physiological properties for medium-and small-caliber blood vessels, and the aligned scaffolds displayed a strain-stiffening behavior typical of the blood vessels. Furthermore, all the produced scaffolds showed constant storage and loss moduli in the investigated timeframe (24 h), demonstrating the stability of the scaffolds under the applied conditions of mechanical deformation. The biological characterization highlighted that the mats showed high hemocompatibility and low probability of thrombus formation; finally, the cytocompatibility tests demonstrated that cyclic stretch of electrospun fibers increased endothelial cell activity and proliferation, in particular on aligned scaffolds.
AB - In the field of artificial prostheses for damaged vessel replacement, polymeric scaffolds showing the right combination of mechanical performance, biocompatibility, and biodegradability are still demanded. In the present work, poly(butylene-co-triethylene trans-1,4-cyclohexanedicarboxylate), a biodegradable random aliphatic copolyester, has been synthesized and electrospun in form of aligned and random fibers properly designed for vascular applications. The obtained materials were analyzed through tensile and dynamic-mechanical tests, the latter performed under conditions simulating the mechanical contraction of vascular tissue. Furthermore, the in vitro biological characterization, in terms of hemocompatibility and cytocompatibility in static and dynamic conditions, was also carried out. The mechanical properties of the investigated scaffolds fit within the range of physiological properties for medium-and small-caliber blood vessels, and the aligned scaffolds displayed a strain-stiffening behavior typical of the blood vessels. Furthermore, all the produced scaffolds showed constant storage and loss moduli in the investigated timeframe (24 h), demonstrating the stability of the scaffolds under the applied conditions of mechanical deformation. The biological characterization highlighted that the mats showed high hemocompatibility and low probability of thrombus formation; finally, the cytocompatibility tests demonstrated that cyclic stretch of electrospun fibers increased endothelial cell activity and proliferation, in particular on aligned scaffolds.
KW - Artificial prosthesis
KW - Dynamic cell culture
KW - Elastomeric scaffold
KW - Electrospinning
KW - Endothelial cells
KW - Hemocompatibility assay
KW - Mechanical characterization
KW - Poly(butylene-co-triethylene trans-1,4-cyclohexanedicarboxylate)
KW - Vascular tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=85097124193&partnerID=8YFLogxK
U2 - 10.3390/biom10121620
DO - 10.3390/biom10121620
M3 - Article
SN - 2218-273X
VL - 10
SP - 1
EP - 16
JO - Biomolecules
JF - Biomolecules
IS - 12
M1 - 1620
ER -