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Gruschwitz, Franka V. ; Hausig, Franziska ; Schüler, Philipp ; Kimmig, Julian ; Hoeppener, Stephanie ; Pretzel, David ; Schubert, Ulrich S. ; Catrouillet, Sylvain ; Brendel, Johannes C.:
Shear-Thinning and Rapidly Recovering Hydrogels of Polymeric Nanofibers Formed by Supramolecular Self-Assembly.
In: Chemistry of Materials.
Bd. 34
(2022)
Heft 5
.
- S. 2206-2217.
ISSN 1520-5002
DOI: https://doi.org/10.1021/acs.chemmater.1c03931
Abstract
The self-assembly of amphiphilic polymers into worm-like micelles represents a versatile approach to create hydrogels, where interactions and functionalities are widely customizable by the chemistry of the hydrophilic block. However, processing options for such gels remain a bottleneck as fragmentation is often irreversible due to the limited dynamics of the assemblies. We demonstrate here that shear-thinning hydrogels can reversibly be formed by amphiphilic polymers, which assemble into supramolecular polymer nanofibers due to additional directing hydrogen bonds. The addition of bifunctional cross-linkers resulted in robust gels, which feature a surprisingly strong shear-thinning character but recover fully in the absence of shear stress despite the lack of a dynamic exchange of individual building blocks. In addition to increasing the concentration, the strength of the gel can be tuned by varying the content or the length of the bivalent cross-linker. Low viscosities under shear load and the rapid recovery (<5 s) after relief of the strain facilitates an effortless extrusion through even thin needles and subsequent formation of self-supporting structures in a printing process. The polymer covered fiber structure further bestows the gels with an excellent stability in various conditions and good biocompatibility while minimizing cell adhesion. The mesh sizes of the gel allow even large macromolecules to diffuse, but retardation is nevertheless observed for small molecules due to the dense polymer brush structure. This unique set of properties renders these polymer fiber hydrogels a versatile and easily processable scaffold for future applications, for example as an adaptable cell scaffold or injectable drug depots.
Weitere Angaben
| Publikationsform: | Artikel in einer Zeitschrift |
|---|---|
| Begutachteter Beitrag: | Ja |
| Institutionen der Universität: | Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Chemie > Lehrstuhl Makromolekulare Chemie I Fakultäten Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Chemie Fakultäten > Fakultät für Biologie, Chemie und Geowissenschaften > Fachgruppe Chemie > Lehrstuhl Makromolekulare Chemie I > Lehrstuhl Makromolekulare Chemie I - Univ.-Prof. Dr. Johannes C. Brendel |
| Titel an der UBT entstanden: | Nein |
| Themengebiete aus DDC: | 500 Naturwissenschaften und Mathematik > 540 Chemie |
| Eingestellt am: | 20 Feb 2024 13:06 |
| Letzte Änderung: | 02 Mai 2024 07:39 |
| URI: | https://eref.uni-bayreuth.de/id/eprint/88583 |