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Amorphous Polymer Networks Combining Three Functionalities–Shape-memory, Biodegradability, and Drug Release

Published online by Cambridge University Press:  31 January 2011

Christian Wischke
Affiliation:
[email protected], GKSS Research Center Geesthacht GmbH, Center for Biomaterial Development, Teltow, Germany
Axel Thomas Neffe
Affiliation:
[email protected], GKSS Research Center Geesthacht GmbH, Center for Biomaterial Development, Teltow, Germany
Susi Steuer
Affiliation:
[email protected], Intervet Innovation GmbH, Schwabenheim, Germany
Andreas Lendlein
Affiliation:
[email protected], GKSS Research Center Geesthacht GmbH, Center for Biomaterial Development, Teltow, Germany
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Abstract

Shape-memory polymers are of high scientific and technological interest in the biomedical field, e.g., as matrix for self-anchoring implantable devices. In this study, two different star-shaped copolyester tetroles, semi-crystalline oligo[(-caprolactone)-co-glycolide]tetrol (oCG) and amorphous oligo[(rac-lactide)-co-glycolide]tetrol (oLG), were synthesized and subsequently crosslinked by a low molecular weight diisocyanate resulting in copolyester urethane networks (N-CG, N-LG). Both networks could be loaded with model drugs and a diffusion controlled release of the drugs was observed without any effect on the mass loss as measure of hydrolytic degradation. However, the N-CG network’s capability of shape programming was disturbed as the crystallinity of the precursors got lost in the complex three dimensional architecture after crosslinking. By contrast, amorphous N-LG network showed an excellent shape-memory capability with a switching temperature around 36 °C corresponding to their glass transition temperature. This led to triple-functional materials combining biodegradability, shape-memory, and controlled drug release.

Type
Research Article
Copyright
Copyright © Materials Research Society 2009

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References

1 Behl, M., Lendlein, A., Soft Matter 3 (2007), 5867.10.1039/B610611KGoogle Scholar
2 Gall, K., Yakacki, C.M., Liu, Y., Shandas, R., Willett, N., Anseth, K.S., J. Biomed. Mater. Res. Part A 73A (2005) 339348.10.1002/jbm.a.30296Google Scholar
3 Lendlein, A., Langer, R., Science 296 (2002) 16731676.10.1126/science.1066102Google Scholar
4 Sharp, A.A., Panchawagh, H.V., Ortega, A., Artale, R., Richardson-Burns, S., Finch, D.S., Gall, K., Mahajan, R.L., Restrepo, D., J. Neural Eng. 3 (2006) L23–L30.10.1088/1741-2560/3/4/L02Google Scholar
5 Small, W., Wilson, T.S., Buckley, P.R., Benett, W.J., Loge, J.M., Hartman, J., Maitland, D.J., IEEE Trans Biomed Eng 54 (2007) 16571666.10.1109/TBME.2007.892921Google Scholar
6 Weigel, Th., R, Mohr, A, Lendlein, Smart Mater. Struct. 18 (2009) 025011 (9pp).10.1088/0964-1726/18/2/025011Google Scholar
7 Mohr, R., Kratz, K., Weigel, T., Lucka-Gabor, M., Moneke, M., Lendlein, A., Proc. Natl. Acad. Sci. USA 103 (2006) 35403545.10.1073/pnas.0600079103Google Scholar
8 Lendlein, A., Jiang, H., Jünger, O., Langer, R., Nature 434 (2005) 879882.10.1038/nature03496Google Scholar
9 Neffe, A.T., Hanh, D.B., Steuer, S., Lendlein, A., Polymer networks combining controlled drug release, biodegradation, and shape-memory capability, Adv. Mat. in press, DOI: 10.1002/adma.20080233310.1002/adma.200802333Google Scholar
10 Wischke, C., Neffe, A., Steuer, S., Lendlein, A.. Evaluation of a degradable shape-memory polymer network as matrix for controlled drug release. J. Controlled Release in press, doi:10.1016/j.jconrel.2009.05.027.Google Scholar