Peptide-Reinforced Photocrosslinkable PEG-based Hydrogels
Date
2026-01-05
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Publisher
RSC Applied Polymers
Abstract
Hydrogels are polymer networks that swell in aqueous solvents. These materials have applications in many fields, including drug delivery, tissue engineering, and soft robotics. For example, polyethylene glycol (PEG) diacrylate is often used as a light-curable crosslinker for the synthesis of PEG-based hydrogels, e.g., in bioinks for 3D printing. However, a common limitation of PEG hydrogels is their typically poor mechanical properties, particularly when in a swollen state. The mechanical strength of natural polymeric materials, such as spider silk and collagen, arises from the formation of hierarchical secondary protein structures that unfold under mechanical load. Here, we present a bio-inspired approach to reinforcing PEG-based hydrogels that mimic these hierarchical structures by incorporating poly(β-benzyl-L-aspartate) (PBLA) blocks between cross-linking end groups and PEG chain segments. We used this peptide-containing crosslinker in combination with a small hydrophilic comonomer, 2-hydroxyethyl acrylate, to synthesise PHEA-linked by-(PBLA-b-PEG-b-PBLA) conetworks with tailored compositions, yielding improved and tailorable mechanical properties. This approach affords hydrogels with increased strength and toughness while retaining the networks’ swelling ability. This research presents a promising avenue for developing robust photocrosslinkable hydrogels with broad practical applications.
Description
Open Access Article. Published on 05 January 2026. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence https://creativecommons.org/licenses/by/3.0/
This article was originally published in RCS Applied Polymers. The version of record is available at: https://doi.org/10.1039/D5LP00335K
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Citation
Russell, S. M., Thomas, J. A., Jang, D., Grysan, P., Sprandl, L., Biesalski, M., Korley, L., & Bruns, N. (2026). Peptide-Reinforced Photocrosslinkable PEG-based Hydrogels. RSC Applied Polymers. https://doi.org/10.1039/D5LP00335K
