Abstract
Degradable shape-memory polymer networks intended for biomedical applications are highlighted. These polymer networks were synthesized from oligo(ε-caprolactone)dimethacrylate (PCL), or oligo[(L-lactide)-ran-glycolide]dimethacrylate (PLG), or from starlike hydroxytelechelic oligo[(rac-lactide)-co-glycolide] and a low molecular weight linker. While the thermal transition related to the switching phase is a melting point in case of the PCL-based materials, the switching transition of oligo[(L-lactide)-ran-glycolide]dimethacrylate networks and copolyesterurethane networks is a glass transition. In this chapter, the influence of the nature of thermal transition on the shape-memory behavior of polymer networks is described. Furthermore, different polymer network architectures are introduced, which enable the tailoring of polymer network properties as well as the shape-memory capability.
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Lendlein, A., Behl, M., Kamlage, S. (2010). The Nature of the Thermal Transition Influences the Shape-Memory Behavior of Polymer Networks. In: Shastri, V., Altankov, G., Lendlein, A. (eds) Advances in Regenerative Medicine: Role of Nanotechnology, and Engineering Principles. NATO Science for Peace and Security Series A: Chemistry and Biology. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-8790-4_8
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DOI: https://doi.org/10.1007/978-90-481-8790-4_8
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