4.8 Article

Tissue-Mimetic Supramolecular Polymer Networks for Bioelectronics

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ADVANCED MATERIALS
卷 35, 期 1, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202207634

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bioelectronics; conducting polymers; host-guest chemistry; hydrogels; supramolecular networks

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This study introduces an electrically conductive supramolecular polymer network that exhibits both electronic and ionic conductivity and maintains tissue-mimetic mechanical properties. By designing an ultrahigh affinity host-guest ternary complex and embedding it as dynamic cross-links, a conducting polymer with high stretchability and rapid self-recovery was synthesized.
Addressing the mechanical mismatch between biological tissue and traditional electronic materials remains a major challenge in bioelectronics. While rigidity of such materials limits biocompatibility, supramolecular polymer networks can harmoniously interface with biological tissues as they are soft, wet, and stretchable. Here, an electrically conductive supramolecular polymer network that simultaneously exhibits both electronic and ionic conductivity while maintaining tissue-mimetic mechanical properties, providing an ideal electronic interface with the human body, is introduced. Rational design of an ultrahigh affinity host-guest ternary complex led to binding affinities (>10(13) M-2) of over an order of magnitude greater than previous reports. Embedding these complexes as dynamic cross-links, coupled with in situ synthesis of a conducting polymer, resulted in electrically conductive supramolecular polymer networks with tissue-mimetic Young's moduli (<5 kPa), high stretchability (>500%), rapid self-recovery and high water content (>84%). Achieving such properties enabled fabrication of intrinsically-stretchable stand-alone bioelectrodes, capable of accurately monitoring electromyography signals, free from any rigid materials.

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