自愈水凝胶
材料科学
纳米技术
胶束
药物输送
生物电子学
可穿戴计算机
疏水效应
离子键合
计算机科学
化学
水溶液
高分子化学
生物传感器
有机化学
离子
嵌入式系统
生物化学
物理化学
作者
Xiaozhuang Zhou,Nan Zhang,Shruthi Kandalai,Huapeng Li,Farzana Hossain,Shiqi Zhang,Jiangjiang Zhu,Junran Zhang,Jiaxi Cui,Qingfei Zheng
标识
DOI:10.1021/acsami.2c21942
摘要
Electro-responsive dynamic hydrogels, which possess robust mechanical properties and precise spatiotemporal resolution, have a wide range of applications in biomedicine and energy science. However, it is still challenging to design and prepare electro-responsive hydrogels (ERHs) which have all of these properties. Here, we report one such class of ERHs with these features, based on the direct current voltage (DCV)-induced rearrangement of sodium dodecyl sulfate (SDS) micelles, where the rearrangement can tune the hydrogel networks that are originally maintained by the SDS micelle-assisted hydrophobic interactions. An enlarged mesh size is demonstrated for these ERHs after DCV treatment. Given the unique structure and properties of these ERHs, hydrophobic cargo (thiostrepton) has been incorporated into the hydrogels and is released upon DCV loading. Additionally, these hydrogels are highly stretchable (>6000%) and tough (507 J/m2), showing robust mechanical properties. Moreover, these hydrogels have a high spatiotemporal resolution. As the cross-links within our ERHs are enabled by the non-covalent (i.e., hydrophobic) interactions, these hydrogels are self-healing and malleable. Considering the robust mechanical properties, precise spatiotemporal resolution, dynamic nature (e.g., injectable and self-healing), and on-demand drug delivery ability, this class of ERHs will be of great interest in the fields of wearable bioelectronics and smart drug delivery systems.
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