Indirect three-dimensional printing: A method for fabricating polyurethane-urea based cardiac scaffolds

被引:23
作者
Hernandez-Cordova, R. [1 ]
Mathew, D. A. [2 ]
Balint, R. [3 ]
Carrillo-Escalante, H. J. [1 ]
Cervantes-Uc, J. M. [1 ]
Hidalgo-Bastida, L. A. [2 ]
Hernandez-Sanchez, F. [1 ]
机构
[1] Ctr Invest Cient Yucatan AC, Merida, Yucatan, Mexico
[2] Manchester Metropolitan Univ, Sch Healthcare Sci, Manchester, Lancs, England
[3] Univ Manchester, Sch Mat, Manchester, Lancs, England
关键词
indirect 3D printing; rapid prototyping; scaffold fabrication; polyurethane-urea; cardiac tissue engineering; TISSUE ENGINEERING SCAFFOLDS; 3D CULTURE-SYSTEMS; POLYCAPROLACTONE SCAFFOLD; CHAIN EXTENDERS; ELASTOMERS; PUTRESCINE; CYTOCOMPATIBILITY; DEGRADATION; HYPOXIA; BONE;
D O I
10.1002/jbm.a.35721
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Biomaterial scaffolds are a key part of cardiac tissue engineering therapies. The group has recently synthesized a novel polycaprolactone based polyurethane-urea copolymer that showed improved mechanical properties compared with its previously published counterparts. The aim of this study was to explore whether indirect three-dimensional (3D) printing could provide a means to fabricate this novel, biodegradable polymer into a scaffold suitable for cardiac tissue engineering. Indirect 3D printing was carried out through printing water dissolvable poly(vinyl alcohol) porogens in three different sizes based on a wood-stack model, into which a polyurethane-urea solution was pressure injected. The porogens were removed, leading to soft polyurethane-urea scaffolds with regular tubular pores. The scaffolds were characterized for their compressive and tensile mechanical behavior; and their degradation was monitored for 12 months under simulated physiological conditions. Their compatibility with cardiac myocytes and performance in novel cardiac engineering-related techniques, such as aggregate seeding and bi-directional perfusion, was also assessed. The scaffolds were found to have mechanical properties similar to cardiac tissue, and good biocompatibility with cardiac myocytes. Furthermore, the incorporated cells preserved their phenotype with no signs of de-differentiation. The constructs worked well in perfusion experiments, showing enhanced seeding efficiency. (c) 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 1912-1921, 2016.
引用
收藏
页码:1912 / 1921
页数:10
相关论文
共 34 条
[1]   Mechanical stretch regimen enhances the formation of bioengineered autologous cardiac muscle grafts [J].
Akhyari, P ;
Fedak, PWM ;
Weisel, RD ;
Lee, TYJ ;
Verma, S ;
Mickle, DAG ;
Li, RK .
CIRCULATION, 2002, 106 (13) :I137-I142
[2]   Preparation and characterization of collagen-based ADSC-carrier sheets for cardiovascular application [J].
Arana, Miriam ;
Pena, Estefania ;
Abizanda, Gloria ;
Cilla, Myriam ;
Ochoa, Ignacio ;
Jose Gavira, Juan ;
Espinosa, Gaudencio ;
Doblare, Manuel ;
Pelacho, Beatriz ;
Prosper, Felipe .
ACTA BIOMATERIALIA, 2013, 9 (04) :6075-6083
[3]   Effectiveness and cost effectiveness of cardiovascular disease prevention in whole populations: modelling study [J].
Barton, Pelham ;
Andronis, Lazaros ;
Briggs, Andrew ;
McPherson, Klim ;
Capewell, Simon .
BMJ-BRITISH MEDICAL JOURNAL, 2011, 343
[4]   Polymeric scaffolds for cardiac tissue engineering: requirements and fabrication technologies [J].
Boffito, Monica ;
Sartori, Susanna ;
Ciardelli, Gianluca .
POLYMER INTERNATIONAL, 2014, 63 (01) :2-11
[5]   Enabling Microscale and Nanoscale Approaches for Bioengineered Cardiac Tissue [J].
Chan, Vincent ;
Raman, Ritu ;
Cvetkovic, Caroline ;
Bashir, Rashid .
ACS NANO, 2013, 7 (03) :1830-1837
[6]   Characterization and biocompatibility studies of new degradable poly(urea)urethanes prepared with arginine, glycine or aspartic acid as chain extenders [J].
Chan-Chan, L. H. ;
Tkaczyk, C. ;
Vargas-Coronado, R. F. ;
Cervantes-Uc, J. M. ;
Tabrizian, M. ;
Cauich-Rodriguez, J. V. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2013, 24 (07) :1733-1744
[7]   Degradation studies on segmented polyurethanes prepared with HMDI, PCL and different chain extenders [J].
Chan-Chan, L. H. ;
Solis-Correa, R. ;
Vargas-Coronado, R. F. ;
Cervantes-Uc, J. M. ;
Cauich-Rodriguez, J. V. ;
Quintana, P. ;
Bartolo-Perez, P. .
ACTA BIOMATERIALIA, 2010, 6 (06) :2035-2044
[8]   Characterisation of a soft elastomer poly(glycerol sebacate) designed to match the mechanical properties of myocardial tissue [J].
Chen, Qi-Zhi ;
Bismarck, Alexander ;
Hansen, Ulrich ;
Junaid, Sarah ;
Tran, Michael Q. ;
Harding, Sian E. ;
Ali, Nadire N. ;
Boccaccini, Aldo R. .
BIOMATERIALS, 2008, 29 (01) :47-57
[9]   Human cardiosphere-seeded gelatin and collagen scaffolds as cardiogenic engineered bioconstructs [J].
Chimenti, Isotta ;
Rizzitelli, Giuseppe ;
Gaetani, Roberto ;
Angelini, Francesco ;
Ionta, Vittoria ;
Forte, Elvira ;
Frati, Giacomo ;
Schussler, Olivier ;
Barbetta, Andrea ;
Messina, Elisa ;
Dentini, Mariella ;
Giacomello, Alessandro .
BIOMATERIALS, 2011, 32 (35) :9271-9281
[10]   Polyurethane-based scaffolds for myocardial tissue engineering [J].
Chiono, Valeria ;
Mozetic, Pamela ;
Boffito, Monica ;
Sartori, Susanna ;
Gioffredi, Emilia ;
Silvestri, Antonella ;
Rainer, Alberto ;
Giannitelli, Sara Maria ;
Trombetta, Marcella ;
Nurzynska, Daria ;
Di Meglio, Franca ;
Castaldo, Clotilde ;
Miraglia, Rita ;
Montagnani, Stefania ;
Ciardelli, Gianluca .
INTERFACE FOCUS, 2014, 4 (01)