Crosslinker Architectures Impact Viscoelasticity in Dynamic Covalent Hydrogels
Abstract
Dynamic covalent crosslinked (DCC) hydrogels represent a significant advance in biomaterials for regenerative medicine and mechanobiology. These gels typically offer viscoelasticity and self-healing properties that more closely mimic in vivo tissue mechanics than traditional, predominantly elastic, covalent crosslinked hydrogels. Despite their promise, the effects of varying crosslinker architecture - side chain versus telechelic crosslinks - on the viscoelastic properties of DCC hydrogels have not been thoroughly investigated. This study introduces hydrazone-based alginate hydrogels and examines how side-chain and telechelic crosslinker architectures impact hydrogel viscoelasticity and stiffness. In hydrogels with side-chain crosslinking (SCX), higher polymer concentrations enhance stiffness and decelerates stress relaxation, while an off-stoichiometric hydrazine-to-aldehyde ratio leads to reduced stiffness and shorter relaxation time. In hydrogels with telechelic crosslinking, maximal stiffness and slowest stress relaxation occurs at intermediate crosslinker concentrations for both linear and star crosslinkers, with higher crosslinker valency further increasing stiffness and relaxation time. Our result suggested different ranges of stiffness and stress relaxation are accessible with the different crosslinker architectures, with SCX hydrogels leading to slower stress relaxation relative to the other architectures, and hydrogels with star crosslinking (SX) providing increased stiffness and slower stress relaxation relative to hydrogels with linear crosslinking (LX). The mechanical properties of SX hydrogels are more robust to changes induced by competing chemical reactions compared to LX hydrogels. Our research underscores the pivotal role of crosslinker architecture in defining hydrogel stiffness and viscoelasticity, providing crucial insights for the design of DCC hydrogels with tailored mechanical properties for specific biomedical applications.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 35
- FWCI
- 2.92
- Field percentile
- top 7%
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Tuning viscoelasticity of dynamic covalent hydrogels for human tissue modeling
Narelli de Paiva Narciso, Fotis Christakopoulos, … Sarah C. Heilshorn·Advanced Functional MaterialsPeer-reviewed·Aug 14, 2026
- Mechanical cues of an interpenetrating polysaccharide matrix regulate self-assembly of collagen fibers
Fatemeh Tavakoli Joorabi, Nicholas J. Derr, … Kyle H. Vining·Science AdvancesPeer-reviewed·Sep 2, 2026
- Correlating Structure and Rheology in Ionically Crosslinked Alginate Biopolymer Hydrogels - A Case for Why "Less" can be "More"
Vinay Kopnar, Peter S. Sherin, … Anders Aufderhorst-Roberts·bioRxiv·Jul 26, 2026
- Lipid Network Crosslinked Hydrogels: Controlling MaterialDynamics Across Multiple Length Scales Through Lipid Movement
Neil J. Baugh, Michelle S. Huang, … Sarah C. Heilshorn·bioRxiv·Jun 25, 2026
- Linking Polysaccharide Structure, Gelation Kinetics, and Function in Dynamic Acylhydrazone Hydrogels
Fereshteh Kazemi-Aghdam, Zuzana Varchulova, … Abolfazl Heydari·bioRxiv·Sep 28, 2026
- Crosslinker Structure Modulates Bulk Mechanical Properties and Dictates hMSC Behavior on Hyaluronic Acid Hydrogels
L. D. Morton, D. A. Castilla Casadiego, … A. Rosales·bioRxiv·Aug 3, 2022