Dual-Site Biomacromolecule Doped Poly(3, 4-ethylenedioxythiophene) for Bosting Both Anticoagulant and Electrochemical Performances
Poly(3, 4-ethylenedioxythiophene) as a new generation of intelligent conductive polymers, is attracting much attention in the field of tissue engineering. However, its water dispersibility, conductivity, and biocompatibility are incompatible, which limits its further development. In this work, bioco...
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Veröffentlicht in: | Advanced healthcare materials 2024-05, p.e2401134-e2401134 |
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Sprache: | eng |
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Zusammenfassung: | Poly(3, 4-ethylenedioxythiophene) as a new generation of intelligent conductive polymers, is attracting much attention in the field of tissue engineering. However, its water dispersibility, conductivity, and biocompatibility are incompatible, which limits its further development. In this work, biocompatible electrode material of poly(3, 4-ethylenedioxythiophene) doped by sodium sulfonated alginate which contains two functional groups of sulfonic acid and carboxylic acid per repeat unit of the macromolecule. The as dual-site doping strategy simultaneously boosts anticoagulant and electrochemical performances, for examples, good hydrophilicity (water contact angle of 59.40°), well dispersibility (dispersion solution unstratified in 30 days), high conductivity (4.45 S·m
), and enhanced anticoagulant property (extended APTT value of 59.0 s), forming an adjustable poly(3, 4-ethylenedioxythiophene): biomacromolecule interface; this fills the technical gap of implantable bioelectronics in terms of coagulation and thrombosis risk. At the same time, the assembled all-in-one supercapacitor with anticoagulant properties is prepared by poly(3, 4-ethylenedioxythiophene): sodium sulfonated alginate as electrode material and sodium alginate hydrogel as electrolyte layer. The dual-site doping strategy provides a new opinion for design and optimization of functional conductive polymers and its applications in implantable energy storage fields. This article is protected by copyright. All rights reserved. |
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ISSN: | 2192-2640 2192-2659 |
DOI: | 10.1002/adhm.202401134 |