Thermo-reversible gelation of self-assembled conducting polymer colloids
Abstract
Abstract Electrically conductive hydrogels based on conducting polymers have found increased use in bioelectronics due to their low moduli that mimic biological tissues, their ability to transport both ionic and electronic charges, and their ease of processing in various form factors via printing or injection. Current approaches towards conductive hydrogels, however, rely on covalent and therefore irreversible crosslinking mechanisms. Here, we report a thermo-responsive conducting polymer (TR-CP) that undergoes a fully reversible non-covalent crosslinking at 35 °C within less than a minute to form conductive hydrogels. The TR-CP is based on a block polyelectrolyte complex, that self-assembles into well-defined colloidal particles in water which undergo an isovolumetric sol-gel transition just below physiological temperature. The hydrogels have tunable mechanical properties in the 20 to 200 Pa range, are stable at various pH and salt conditions, self-healing, injectable, and biocompatible in vitro and in vivo. We demonstrate that the TR-CPs can be used to fabricate sensitive, conformal and reusable electrodes for surface electromyography. This thermo-responsive material provides exciting opportunities for stimuli-responsive and adaptive bioelectronics.
Article Details
Authors (20)
Vidhika S. Damani
Xinran Xie
Rachel E. Daso
Khushboo Suman
Masoud Ghasemi
Department of Chemical Engineering, Pennsylvania State University
Weiran Xie
Department of Materials Science and Engineering
Ruiheng Wu
Yuhang Wu
Calvin L. Chao
Julian E. Alberto
Casey M. Lorch
Ai-Nin Yang
Dan My Nguyen
Tulaja Shrestha
Kayla Otero
Chun-Yuan Lo
Darrin J. Pochan
Department of Materials Science and Engineering
Enrique D. Gomez
Department of Chemical Engineering, Pennsylvania State University
Jonathan Rivnay
Department of Biomedical Engineering, McCormick School of Engineering
Laure V. Kayser