Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-23T04:14:09.776Z Has data issue: false hasContentIssue false

(Bio)degradable Urethane-Elastomers for Electrospun Vascular Grafts

Published online by Cambridge University Press:  31 January 2011

Stefan Baudis
Affiliation:
[email protected], Vienna University of Technology, Institute of Applied Synthetic Chemistry - Division Macromolecular Chemistry, Vienna, Austria
Maria Schwarz
Affiliation:
[email protected], Vienna University of Technology, Institute of Applied Synthetic Chemistry - Division Macromolecular Chemistry, Vienna, Austria
Christian Grasl
Affiliation:
[email protected], Medical University of Vienna, Center for Biomedical Engineering and Physics, Vienna, Austria
Helga Bergmeister
Affiliation:
[email protected], Medical University of Vienna, Division of Biomedical Research, Vienna, Austria
Guenter Weigel
Affiliation:
[email protected], Ludwig-Boltzmann Cluster for Cardiovascular Research, Vienna, Austria
Heinrich Schima
Affiliation:
[email protected], Medical University of Vienna, Center for Biomedical Engineering and Physics, Vienna, Austria
Robert Liska
Affiliation:
[email protected], Vienna University of Technology, Institute of Applied Synthetic Chemistry - Division Macromolecular Chemistry, Vienna, Austria
Get access

Abstract

Electrospinning is a very powerful method to create cellular scaffolds for regenerative medicine – especially for artificial vascular grafts. Commercially available thermoplastic polyurethane elastomers (TPUs), like Pellethane™ are FDA approved and have already shown excellent biomechanical properties as electrospun vascular grafts. In order to induce the growth of a neo artery and hence increase the long-term patency of the graft, the use of biodegradable TPUs is beneficial. Therefore we aim for the development of degradable TPUs. In preliminary studies the mechanical properties of segmented TPUs were examined. The tendencies of the properties of the compression-molded bulk materials were also found for the electrospun materials. It could also be shown that the substitution of the aromatic 4,4′-methylene diphenyl diisocyanate building blocks in Pellethane™ with the aliphatic hexamethylene diisocyanate – to avoid toxic aromatic amines as degradation products - only causes minor loss of strength. To obtain degradable TPUs, our concept is to incorporate cleavable ester bonds into the polymer chain. For this purpose, lactic- and terephthalic ester-based cleavable chain extenders were used. The expected degradation products showed no cytotoxicity in-vitro. Degradation tests of polymer samples in phosphate buffered saline at elevated temperatures confirmed the degradability of the new polymers.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Shalaby, S. W. and Burg, K. J. L., “Absorbable and Biodegradable Polymers,” in Advances in Polymeric Biomaterials Boca Raton; London; New York; Washington, D.C.: CRC press, 2004, pp. 175.Google Scholar
2 Gogolewski, S., Galletti, G., and Ussia, G., Colloid and Polymer Science 265, 774 (1987).Google Scholar
3 Carampin, P., Conconi, M. T., Lora, S., Menti, A. M., Baiguera, S., Bellini, S., Grandi, C., and Parnigotto, P. P., Journal of Biomedical Materials Research Part A 80A, 661 (2007).Google Scholar
4 Sell, S. A. and Bowlin, G. L., Journal of Materials Chemistry 18, 260 (2008).Google Scholar
5 Grasl, C., Bergmeister, H., Stoiber, M., Schima, H., and Weigel, G., Journal of Biomedical Materials Research Part A 91A, N/A (2009).Google Scholar
6 Gorna, K. and Gogolewski, S., Polymer Degradation and Stability 75, 113 (2001).Google Scholar
7 Assumption, H. J. and Mathias, L. J., Polymer 44, 5131 (2003).Google Scholar
8 Baudis, S., Heller, C., Liska, R., Stampfl, J., Bergmeister, H., and Weigel, G., Journal of Polymer Science, Part A: Polymer Chemistry 47, 2664 (2009).Google Scholar