Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Control of the network topology by selection of an appropriate cross-linking chemistry is introduced as a new strategy to improve the elasticity and toughness of bioresorbable networks. The development of novel photocross-linkable and bioresorbable oligomers is essential for the application of light-based 3D-printing techniques in the context of tissue engineering. Although light-based 3D-printing techniques are characterized by an increased resolution and manufacturing speed as compared to extrusion-based 3D-printing, their application remains limited. Via chemical modification, poly-ε-caprolactone (PCL) is functionalized with photoreactive end groups such as acrylates, alkenes, and alkynes. Based on these precursors, networks with different topologies are designed via chain growth polymerization, step growth polymerization, or a combination thereof. The influence of the network topology and the concomitant cross-linking chemistry on the thermal, mechanical, and biological properties are elucidated together with their applicability in digital light processing (DLP). Photocross-linkable PCL with an elongation at break of 736.3 ± 47% and an ultimate strength of 21.3 ± 0.8 MPa is realized, which is approximately tenfold higher compared to the current state-of-the-art. Finally, extremely elastic DLP-printed dog bones are developed which can fully retrieve their initial length upon stress relieve at an elongation of 1000%.

Original publication




Journal article


Advanced functional materials

Publication Date