Adaptive hydrogels with spatiotemporal stiffening using pH-modulating enzymes
Natascha Gray, Zoe Gr\"amiger, Andr\'e R. Studart, Rafael Libanori

TL;DR
This paper demonstrates a synthetic enzymatic hydrogel system where chemical waves induce mechanical stiffening, revealing the mechanistic principles of chemomechanical transduction and enabling adaptive material design.
Contribution
It introduces a glucose oxidase-embedded hydrogel with slower kinetics that decouples chemical and mechanical waves, providing insights into energy-dependent chemomechanical coupling.
Findings
Chemical waves propagate at 15-44 μm/min
Mechanical wavefronts lag behind chemical waves at 12 μm/min
System achieves up to 2.1-fold increase in stiffness
Abstract
Biological systems achieve adaptive mechanical responses through reaction-diffusion processes that couple chemical wave propagation to structural transitions. Although synthetic hydrogels with enzymatic reactions offer a platform for replicating such autonomous behavior, the mechanistic principles governing chemomechanical transduction remain poorly understood. Here, we present a glucose oxidase-embedded polyacrylamide-alginate hydrogel with slower transduction kinetics that enable independent resolution of chemical waves and mechanical adaptation. Enzymatic pH waves propagate at 15-44 um/min, triggering calcium-mediated alginate crosslinking through pH-responsive calcium-EDTA dissociation. Independent tracking of chemical and mechanical waves reveals that mechanical wavefronts (12 um/min) lag behind chemical propagation, establishing transduction as the rate-limiting step in this…
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