Zhao Lei, Lu Yuhan, Lu Xinxin, Guo Bihan, Chang Zhiqiang, Ren Qinjuan, Li Xiang, Wang Bingfang, Lv Ailin, Wei Jing, Nie Jianfang, Lv Yingying, Rotenberg Menahem Y, Zhang Ya, Ji Daizong, Fang Yin
Research Center for Translational Medicine, Medical Innovation Center and State Key Laboratory of Cardiology, Shanghai East Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Shanghai, 200120, China.
Institute of Analytical Chemistry and Instrument for Life Science, The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, 710049, China.
Small Methods. 2025 Aug;9(8):e2401844. doi: 10.1002/smtd.202401844. Epub 2025 Mar 31.
Carbon aerogels with exceptional electrical properties are considered promising materials for bioelectronics in signal detection and electrical stimulation. To address the mechanical incompatibilities of carbon aerogels with bio-interfaces, particularly for dynamic tissues and organs, the incorporation of hydrogels is an effective strategy. However, achieving excellent electrical performance in carbon aerogel-hydrogel hybrids remains a significant challenge. Two key factors contribute to this difficulty: 1) unrestricted hydrogel infiltration during preparation can lead to complete encapsulation of the conductive aerogel, and 2) the high swelling behavior of hydrogels can cause disconnection of the aerogel. Herein, a stretchable, highly conductive bioelectronic interface is achieved by forming an interlocking network between hierarchical porous carbon aerogel (PA) with polyvinyl alcohol (PVA) hydrogel. Partial exposure of the PA due to confined infiltration of PVA into the porous structure maintains the electrical performance, while the non-swellable PVA ensures mechanical stretchability and stability. The hybrid demonstrates excellent conductivity (370 S·m), high charge storage capacity (1.66 mC cm), remarkable stretchability (250%), and long-term stability over three months, enabling effective signal recording and electrical stimulation. For the first time, carbon aerogel-hydrogel hybrids enable cardiac pacing both ex vivo and in vivo in rat heart models. Compared to conventional platinum electrodes, the PA-PVA electrodes require lower pacing voltages, suggesting potential advantages in power efficiency and reduced tissue damage. The electrodes can be integrated with a wireless implantable device for in vivo synchronous electrocardiogram monitoring and cardiac pacing, underscoring their potential for arrhythmia management.
具有卓越电学性能的碳气凝胶被认为是生物电子学中用于信号检测和电刺激的有前途的材料。为了解决碳气凝胶与生物界面的机械不相容性问题,特别是对于动态组织和器官,加入水凝胶是一种有效的策略。然而,在碳气凝胶-水凝胶复合材料中实现优异的电学性能仍然是一个重大挑战。造成这一困难的两个关键因素是:1)制备过程中不受限制的水凝胶渗透会导致导电气凝胶被完全包裹,2)水凝胶的高膨胀行为会导致气凝胶断开连接。在此,通过在分级多孔碳气凝胶(PA)与聚乙烯醇(PVA)水凝胶之间形成互锁网络,实现了一种可拉伸、高导电性的生物电子界面。由于PVA受限渗透到多孔结构中而导致PA部分暴露,从而保持了电学性能,而非膨胀性的PVA确保了机械拉伸性和稳定性。该复合材料表现出优异的导电性(370 S·m)、高电荷存储容量(1.66 mC cm)、显著的拉伸性(250%)以及超过三个月的长期稳定性,能够实现有效的信号记录和电刺激。碳气凝胶-水凝胶复合材料首次在大鼠心脏模型中实现了离体和体内心脏起搏。与传统的铂电极相比,PA-PVA电极所需的起搏电压更低,这表明在功率效率和减少组织损伤方面具有潜在优势。这些电极可以与无线植入式设备集成,用于体内同步心电图监测和心脏起搏,突出了它们在心律失常管理方面的潜力。