| Literature DB >> 28831798 |
Theresia Arbring Sjöström1, Amanda Jonsson1, Erik Gabrielsson1, Loïg Kergoat1, Klas Tybrandt1, Magnus Berggren1, Daniel T Simon1.
Abstract
On-demand local release of biomolecules enables fine-tuned stimulation for the next generation of neuromodulation therapies. Such chemical stimulation is achievable using iontronic devices based on microfabricated, highly selective ion exchange membranes (IEMs). Current limitations in processability and performance of thin film IEMs hamper future developments of this technology. Here we address this limitation by developing a cationic IEM with excellent processability and ionic selectivity: poly(4-styrenesulfonic acid-co-maleic acid) (PSS-co-MA) cross-linked with polyethylene glycol (PEG). This enables new design opportunities and provides enhanced compatibility with in vitro cell studies. PSSA-co-MA/PEG is shown to out-perform the cation selectivity of the previously used iontronic material.Entities:
Keywords: ion exchange membranes; iontronics; microfabrication; neurotransmitter release; organic bioelectronics
Year: 2017 PMID: 28831798 DOI: 10.1021/acsami.7b05949
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229