Hemocompatible polyurethane/gelatin-heparin nanofibrous scaffolds formed by a bi-layer electrospinning technique as potential artificial blood vessels

被引:26
作者
Wang H. [1 ]
Feng Y. [1 ,2 ,3 ,4 ]
Behl M. [2 ,3 ,4 ]
Lendlein A. [2 ,3 ,4 ]
Zhao H. [1 ]
Xiao R. [1 ]
Lu J. [1 ]
Zhang L. [1 ]
Guo J. [1 ,2 ,3 ,4 ]
机构
[1] School of Chemical Engineering and Technology, Tianjin University
[2] Joint Laboratory for Biomaterials and Regenerative Medicine, Tianjin University-Helmholtz-Zentrum Geesthacht
[3] 14513 Teltow
[4] Helmholtz-Zentrum Geesthacht, Center for Biomaterial Development and Berlin Brandenburg Center for Regenerative Therapies (BCRT), Institute of Polymer Research, 14513 Teltow
关键词
artificial blood vessels; electrospinning; gelatin; hemocompatibility; nanofiber; polyurethane; scaffold;
D O I
10.1007/s11705-011-1202-0
中图分类号
学科分类号
摘要
In this paper, a scaffold, which mimics the morphology and mechanical properties of a native blood vessel is reported. The scaffold was prepared by sequential bi-layer electrospinning on a rotating mandrel-type collector. The tubular scaffolds (inner diameter 4 mm, length 3 cm) are composed of a polyurethane (PU) fibrous outer-layer and a gelatin-heparin fibrous inner-layer. They were fabricated by electrospinning technology, which enables control of the composition, structure, and mechanical properties of the scaffolds. The microstructure, fiber morphology and mechanical properties of the scaffolds were examined by means of scanning electron microscopy (SEM) and tensile tests. The PU/gelatinheparin tubular scaffolds have a porous structure. The scaffolds achieved a breaking strength (3. 7±0. 13 MPa) and an elongation at break (110±8%) that are appropriate for artificial blood vessels. When the scaffolds were immersed in water for 1 h, the breaking strength decreased slightly to 2. 2±0. 3 MPa, but the elongation at break increased to 145±21%. In platelet adhesion tests the gelatin-heparin fibrous scaffolds showed a significant suppression of platelet adhesion. Heparin was released from the scaffolds at a fairly uniform rate during the period of 2nd day to 9th day. The scaffolds are expected to mimic the complex matrix structure of native arteries, and to have good biocompatibility as an artificial blood vessel owing to the heparin release. © 2011 Higher Education Press and Springer-Verlag Berlin Heidelberg.
引用
收藏
页码:392 / 400
页数:8
相关论文
共 29 条
[1]  
Barron V., Lyons E., Stenson-Cox C., McHugh P.E., Pandit A., Bioreactors for cardiovascular cell and tissue growth: a review, Annals of Biomedical Engineering, 31, 9, pp. 1017-1030, (2003)
[2]  
Hoenig M.R., Campbell G.R., Rolfe B.E., Campbell J.H., Tissueengineered blood vessels: alternative to autologous grafts?, Arteriosclerosis, Thrombosis, and Vascular Biology, 25, 6, pp. 1128-1134, (2005)
[3]  
Tiwari A., Salacinski H.J., Punshon G., Hamilton G., Seifalian A.M., Development of a hybrid cardiovascular graft using a tissue engineering approach, The FASEB Journal, 16, 8, pp. 791-796, (2002)
[4]  
Jeong S.I., Kim S.Y., Cho S.K., Chong M.S., Kim K.S., Kim H., Lee S.B., Lee Y.M., Tissue-engineered vascular grafts composed of marine collagen and PLGA fibers using pulsatile perfusion bioreactors, Biomaterials, 28, 6, pp. 1115-1122, (2007)
[5]  
Buttafoco L., Engbers-Buijtenhuijs P., Poot A.A., Dijkstra P.J., Vermes I., Feijen J., Physical characterization of vascular grafts cultured in a bioreactor, Biomaterials, 27, 11, pp. 2380-2389, (2006)
[6]  
Couet F., Rajan N., Mantovani D., Macromolecular biomaterials for scaffold-based vascular tissue engineering, Macromolecular Bioscience, 7, 5, pp. 701-718, (2007)
[7]  
Jung F., Wischke C., Lendlein A., Degradable, multifunctional cardiovascular implants: challenges and hurdles, MRS Bulletin, 35, 8, pp. 607-613, (2010)
[8]  
Baguneid M.S., Seifalian A.M., Salacinski H.J., Murray D., Hamilton G., Walker M.G., Tissue engineering of blood vessels, The British Journal of Surgery, 93, 3, pp. 282-290, (2006)
[9]  
Ko J.H., Yin H., An J., Chung D.J., Kim J.H., Lee S.B., Pyun D.G., Characterization of cross-linked gelatin nanofibers through electrospinning, Macromolecular Research, 18, 2, pp. 137-143, (2010)
[10]  
Feng Y.K., Meng F.R., Xiao R.F., Zhao H.Y., Guo J.T., Electrospinning of polycarbonate urethane biomaterials, Frontiers of Chemical Science and Engineering, 5, 1, pp. 11-18, (2011)