Zeng Ming-Ze, Wei Dan, Ding Jie, Tian Yuan, Wu Xiao-Yang, Chen Zhi-Hong, Wu Cheng-Heng, Sun Jing, Yin Hua-Bing, Fan Hong-Song
National Engineering Research Center for Biomaterials, College of Biomedical Engineering, Sichuan University, Chengdu 610064, Sichuan, China.
National Engineering Research Center for Biomaterials, College of Biomedical Engineering, Sichuan University, Chengdu 610064, Sichuan, China; Institute of Regulatory Science for Medical Devices, Sichuan University, Chengdu 610065, Sichuan, China.
Carbohydr Polym. 2023 Feb 15;302:120403. doi: 10.1016/j.carbpol.2022.120403. Epub 2022 Nov 26.
Conductive hydrogel (CH) as flexible electrophysiology interface has become the new trend of bioelectronics, but still challenging in synergizing the biocompatibility, mechanics and comprehensive electrical performance. Hyaluronic acid (HA), featured with abundant active sites for personalized-modification and well-known biocompatibility, is one of the alterative candidates. The obstacle lies in the unstable conductivity from the ionic conduction, and the electronic conduction by embedding conductive nanoparticles (NPs) is likely to result in inhomogeneous CH with poor stretchability and discontinuous conductive network. Herein, inspired by catechol chemistry, dopamine (DA)-modified HA was homogeneously composited with DA-modified poly (3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, named PP), to produce particle-free conductive hydrogel (HA-DA-PP). The DA-introduced multiple bondings in HA network and PP molecules brought aqueous conductive PP into HA hydrogel to form a homogeneous crosslinking network, imparted the flexible stretchability. By accurately regulation, HA-DA-PP achieved high stretchability with large tensile deformation (over 470 %) in the category of natural polymer-based hydrogels. Moreover, the interaction between DA and PP (conformational transition and charge transfer) could effectively enhance the hydrogel's conductivity. Consequently, HA-DA-PP hydrogel showed high sensibility to human movement, epidermal and in vivo electrophysiological signals monitoring. Overall, DA-mediated multiple bonding is a powerful strategy for constructing CH with high performance for bioelectronics.
导电水凝胶(CH)作为柔性电生理接口已成为生物电子学的新趋势,但在协同生物相容性、力学性能和综合电学性能方面仍具有挑战性。透明质酸(HA)具有丰富的可用于个性化修饰的活性位点且具有众所周知的生物相容性,是替代候选材料之一。障碍在于离子传导导致的导电性不稳定,而通过嵌入导电纳米颗粒(NPs)进行电子传导可能会导致CH不均匀,拉伸性差且导电网络不连续。在此,受儿茶酚化学启发,将多巴胺(DA)修饰的HA与DA修饰的聚(3,4 - 乙撑二氧噻吩):聚(苯乙烯磺酸盐)(PEDOT:PSS,简称PP)均匀复合,制备出无颗粒导电水凝胶(HA - DA - PP)。DA在HA网络和PP分子中引入的多重键合将水性导电PP引入HA水凝胶中形成均匀的交联网络,赋予其柔性拉伸性。通过精确调控,HA - DA - PP在天然聚合物基水凝胶类别中实现了高达470%以上的大拉伸变形的高拉伸性。此外,DA与PP之间的相互作用(构象转变和电荷转移)可有效提高水凝胶的导电性。因此,HA - DA - PP水凝胶对人体运动、表皮和体内电生理信号监测表现出高灵敏度。总体而言,DA介导的多重键合是构建用于生物电子学的高性能CH的有力策略。