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Self‐Degrading Multifunctional PEG‐Based Hydrogels : Tailormade Substrates for Cell Culture

Titelangaben

Kowalczuk, Kathrin ; Dasgupta, Anindita ; Páez Larios, Francisco ; Ulrich, Hans F. ; Wegner, Valentin ; Brendel, Johannes C. ; Eggeling, Christian ; Mosig, Alexander S. ; Schacher, Felix H.:
Self‐Degrading Multifunctional PEG‐Based Hydrogels : Tailormade Substrates for Cell Culture.
In: Macromolecular Bioscience. (2024) . - 2300383.
ISSN 1616-5195
DOI: https://doi.org/10.1002/mabi.202300383

Abstract

The use of PEG-based hydrogels as cell culture matrix to mimic the natural extracellular matrix (ECM) has been realized using a range of well-defined, tunable, and dynamic scaffolds, although they require cell adhesion ligands such as RGDS-peptide (Arg-Gly-Asp-Ser) to promote cell adhesion. Herein the synthesis of ionic and degradable hydrogels is demonstrated for cell culture by crosslinking [PEG-SH]4 with the zwitterionic crosslinker N,N-bis(acryloxyethyl)-N-methyl-N-(3-sulfopropyl) ammonium betaine (BMSAB) and the cationic crosslinker N,N-bis(acryloxyethyl)-N,N-dimethyl-1-ammonium iodide (BDMAI). Depending on the amount of ionic crosslinker used in gel formation, the hydrogels show tunable gelation time and stiffness. At the same time, the ionic groups act as catalysts for hydrolytic degradation, thereby allowing to define a stability window. The latter could be tailored in a straightforward manner by introducing the non-degradable crosslinker tri(ethylene glycol) divinyl ether. In addition, both ionic crosslinkers favor cell attachment in comparison to the pristine PEG hydrogels. The degradation is examined by swelling behavior, rheology, and fluorescence correlation spectroscopy indicating degradation kinetics depending on diffusion of incorporated fluorescent molecules.

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
Titel an der UBT entstanden: Nein
Themengebiete aus DDC: 500 Naturwissenschaften und Mathematik > 540 Chemie
Eingestellt am: 20 Feb 2024 09:27
Letzte Änderung: 20 Feb 2024 09:27
URI: https://eref.uni-bayreuth.de/id/eprint/88594