4.8 Article

Hydrogen-bonding topological remodeling modulated ultra-fine bacterial cellulose nanofibril-reinforced hydrogels for sustainable bioelectronics

Journal

BIOSENSORS & BIOELECTRONICS
Volume 231, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2023.115288

Keywords

Nanofibrils; Bacterial cellulose; Electrophysiological interface; Bioelectronics; Skin dressing; Electronic skin

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By using gelatin and glycerol to mediate the rearrangement of the hydrogen-bonding topological structure of bacterial cellulose (BC), an ultra-fine nanofibril-reinforced composite hydrogel with high transparency, stretchability, and toughness has been developed. The hydrogel also possesses tissue adhesiveness and long-lasting water-retaining capacity, making it suitable for bio-electronic skin applications and optical identification of bacterial infections. This work provides a green, low-cost, and sustainable strategy for designing skin-like bioelectronics by regulating the hierarchical structure of natural materials.
Bacterial cellulose (BC) with its inherent nanofibrils framework is an attractive building block for the fabrication of sustainable bioelectronics, but there still lacks an effective and green strategy to regulate the hydrogenbonding topological structure of BC to improve its optical transparency and mechanical stretchability. Herein, we report an ultra-fine nanofibril-reinforced composite hydrogel by utilizing gelatin and glycerol as hydrogenbonding donor/acceptor to mediate the rearrangement of the hydrogen-bonding topological structure of BC. Attributing to the hydrogen-bonding structural transition, the ultra-fine nanofibrils were extracted from the original BC nanofibrils, which reduced the light scattering and endowed the hydrogel with high transparency. Meanwhile, the extracted nanofibrils were connected with gelatin and glycerol to establish an effective energy dissipation network, leading to an increase in stretchability and toughness of hydrogels. The hydrogel also displayed tissue-adhesiveness and long-lasting water-retaining capacity, which acted as bio-electronic skin to stably acquire the electrophysiological signals and external stimuli even after the hydrogel was exposing to air condition for 30 days. Moreover, the transparent hydrogel could also serve as a smart skin dressing for optical identification of bacterial infection and on-demand antibacterial therapy after combined with phenol red and indocyanine green. This work offers a strategy to regulate the hierarchical structure of natural materials for designing skin-like bioelectronics toward green, low cost, and sustainability.

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