Laboratory of Organic Electronics, Department of Science and Technology, Linköping University , 601 74 Norrköping, Sweden.
ACS Appl Mater Interfaces. 2017 Sep 13;9(36):30247-30252. doi: 10.1021/acsami.7b05949. Epub 2017 Aug 28.
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.
按需局部释放生物分子可实现下一代神经调节治疗的精细刺激。这种化学刺激可以使用基于微加工的、高度选择性的离子交换膜 (IEM) 的离子电子器件来实现。目前,薄膜 IEM 在加工和性能方面的局限性阻碍了这项技术的未来发展。在这里,我们通过开发一种具有优异加工性能和离子选择性的阳离子 IEM 来解决这一限制:聚(4-苯乙烯磺酸-co-马来酸) (PSS-co-MA) 与聚乙二醇 (PEG) 交联。这为新的设计机会提供了可能性,并提高了与体外细胞研究的兼容性。结果表明,PSSA-co-MA/PEG 的阳离子选择性优于之前使用的离子电子材料。