Electro-Actuation of a Smart Hydrogel Compatible With 3D Printing.

Mikalef, Georgios; Schofield, Zoe; Moxon, Samuel Robert; Robinson, Thomas Edward; Chu, Hin On; Nugent, Peter Freddie; Baiocco, Daniele; Esteban, Patricia Perez et al. · J Biomed Mater Res A · 2025

basic_science · Level V

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Abstract

Hydrogels that can change shape on the application of an electric field are receiving increasing attention due to their potential to fulfill a range of functions in biomedicine, including the controlled release of therapeutic agents or the creation of replacements for contractile tissues. In this manuscript, a novel electroactive polymer was reported based on the copolymerisation of 2-acrylamido-2-methylpronane sulfonic acid and poly(ethylene glycol) diacrylate (AMPS-co-PEGDA), via free radical polymerization using UV light. It was shown that to enable curing and the production of a material that could repeatably actuate without cracking, 900 mJ/cm<sup>2</sup> (at 365 nm<sup>-1</sup>) of UV exposure was optimal. Further increasing the curing time resulted in the production of a brittle material that cracked following actuation, preventing multiple actuations from occurring. The polymer that was cured for 900 mJ/cm<sup>2</sup> was shown to be non-cytotoxic to dermal fibroblast cells, showing potential in biomedical applications. Furthermore, it was shown that the optimized polymer could be structured using a process of suspended 3D printing, allowing for the manufacture of complex, electro-actuatable geometries. Processing in an agarose supporting bed resulted in a reduction in the Young's modulus of the printed polymer and an associated greater degree of bending. These results demonstrate that the optimized (AMPS-co-PEGDA) polymer is a promising electroactive material with tuneable properties and complex geometries, suitable for advanced biomedical applications.

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