Thiol‐ene/acrylate substrates for softening intracortical electrodes. Issue 1 (13th May 2013)

• Record Type: Journal Article
• Authors: Ware, Taylor; Simon, Dustin; Liu, Clive; Musa, Tabassum; Vasudevan, Srikanth; Sloan, Andrew; Keefer, Edward W.; Rennaker, Robert L.; Voit, Walter
• Is Part Of: Journal of biomedical materials research. Volume 102:Issue 1(2014:Jan.)
• Page Start: 1
• Page End: 11
• Publication Date: 2013-05-13
• Subjects: Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/jbmb.32946
• Languages: English
• ISSNs: 1552-4973

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <p>Neural interfaces have traditionally been fabricated on rigid and planar substrates, including silicon and engineering thermoplastics. However, the neural tissue with which these devices interact is both 3D and highly compliant. The mechanical mismatch at the biotic–abiotic interface is expected to contribute to the tissue response that limits chronic signal recording and stimulation. In this work, novel ternary thiol‐ene/acrylate polymer networks are used to create softening substrates for neural recording electrodes. Thermomechanical properties of the substrates are studied through differential scanning calorimetry and dynamic mechanical analysis both before and after exposure physiological conditions. This substrate system softens from more than 1 GPa to 18 MPa on exposure to physiological conditions: reaching body temperature and taking up less than 3% fluid. The impedance of 177 µm<sup>2</sup> gold electrodes electroplated with platinum black fabricated on these substrates is measured to be 206 kΩ at 1 kHz. Specifically, intracortical electrodes are fabricated, implanted, and used to record driven neural activity. This work describes the first substrate system that can use the full capabilities of photolithography, respond to physiological conditions by softening markedly after insertion, and record driven neural activity for 4 weeks. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 102B: 1–11, 2014.</p> </abstract>