Water-responsive supercontractile polymer films for bioelectronic interfaces

• Published in: Nature (London) Vol. 624; no. 7991; pp. 295 - 302
• Main Authors: Yi, Junqi, Zou, Guijin, Huang, Jianping, Ren, Xueyang, Tian, Qiong, Yu, Qianhengyuan, Wang, Ping, Yuan, Yuehui, Tang, Wenjie, Wang, Changxian, Liang, Linlin, Cao, Zhengshuai, Li, Yuanheng, Yu, Mei, Jiang, Ying, Zhang, Feilong, Yang, Xue, Li, Wenlong, Wang, Xiaoshi, Luo, Yifei, Loh, Xian Jun, Li, Guanglin, Hu, Benhui, Liu, Zhiyuan, Gao, Huajian, Chen, Xiaodong
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 14.12.2023; Nature Publishing Group
• Subjects: 14; 639/166/985; 639/301/1005/1009; 639/638/298/54/989; Bioelectricity; Biomedical materials; Body temperature; Cardiac muscle; Cold; Cyclodextrin; Cyclodextrins; Electrodes; Electronic equipment; Electronics; Humanities and Social Sciences; Humidity; Hydrogels; Hydrogen bonds; In vivo methods and tests; Inclusion complexes; Interfaces; Mechanical properties; Motion Pictures; multidisciplinary; Muscles; Nerves; Polyethylene glycol; Polyethylene Glycols; Polyethylene oxide; Polymer films; Polymers; Polymers - chemistry; Science; Science (multidisciplinary); Silk; Stimuli; Thin films; Tissues; Water - chemistry
• ISSN: 0028-0836; 1476-4687
• DOI: 10.1038/s41586-023-06732-y

Connecting different electronic devices is usually straightforward because they have paired, standardized interfaces, in which the shapes and sizes match each other perfectly. Tissue–electronics interfaces, however, cannot be standardized, because tissues are soft 1 – 3 and have arbitrary shapes and sizes 4 – 6 . Shape-adaptive wrapping and covering around irregularly sized and shaped objects have been achieved using heat-shrink films because they can contract largely and rapidly when heated 7 . However, these materials are unsuitable for biological applications because they are usually much harder than tissues and contract at temperatures higher than 90 °C (refs.  8 , 9 ). Therefore, it is challenging to prepare stimuli-responsive films with large and rapid contractions for which the stimuli and mechanical properties are compatible with vulnerable tissues and electronic integration processes. Here, inspired by spider silk 10 – 12 , we designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials. Water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex contract by more than 50% of their original length within seconds after wetting and become soft and stretchable hydrogel thin films that can be used in bioelectronic interfaces.