Polymers with high conductivity and cross-linking ability are ideal materials for the preparation of conductive hydrogels for application in wearable electronic devices. However, the fabrication of conductive polymer-incorporated hydrogels with good synergistic properties remains a great challenge due to the hydrophobicity and opacity of conjugated π conductive polymers. In this study, a multifunctional hybrid hydrogel was prepared by incorporating hemicellulose-decorated polypyrrole (H/PPY), polyvinyl alcohol (PVA), and tannic acid (TA) into a polyacrylamide (PAM) network. The addition of excess ammonium persulfate (APS) in the process of gelation not only initiated the polymerization of PAM but also resulted in the change of the hydrogel from opaque to transparent by continuously breaking and reducing the size of the PPY particles. The hybrid hydrogel exhibited high transparency and conductivity, good adhesion ability and mechanical performance, and high resistance strain sensitivity and could accurately monitor the strain signals of the index finger and elbow flexion and pulse beat during rest and exercise, which has promising potential for use in wearable or implantable smart sensor devices, electronic skins, and artificial intelligence applications.
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http://dx.doi.org/10.1016/j.ijbiomac.2022.10.262 | DOI Listing |
Int J Biol Macromol
January 2025
Istanbul Technical University, Faculty of Science and Letters, Department of Chemistry, Soft Materials Research Laboratory, 34469, Maslak, Istanbul, Turkey. Electronic address:
Controllable macromolecular architecture formation via polysaccharide integrated ternary copolymerization was explored in the design of amino-functionalized n-alkyl methacrylate ester-based biohybrids. Ternary poly(dimethylaminoethyl methacrylate-co-glycidyl methacrylate-co-hydroxypropyl methacrylate)/sodium-alginate, PDGH/ALG, hybrids were designed using anionic polysaccharide through in-situ radical polymerization. An insight into the effect of ALG on physicochemical structure of ternary hybrids, particularly the interactions between polymeric chains, was created.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Department of Chemistry, Himachal Pradesh University, Shimla 171005, India. Electronic address:
Introduction: The rapid progress in polymer science has designed innovative materials for biomedical applications. In the case of drug design, for each new therapeutic agent, a drug delivery system (DDS) is required to improve its pharmacokinetic and pharmacodynamic parameters. Therefore, significant research has been carried out to develop drug delivery (DD) carriers for these new therapeutic agents.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Health Sciences and Technology, ETH Zürich, 8092 Zürich, Switzerland.
Enzyme immobilization is an efficient and cost-effective approach to recovering, stabilizing, and enhancing enzyme catalytic properties. It is a challenge, however, for coimmobilized multiple enzymes to perform consecutive reactions without being inactivated under similar conditions. Here, we present a facile enzyme immobilization platform using β-lactoglobulin amyloid fibril hydrogels.
View Article and Find Full Text PDFBiomaterials
January 2025
Department of Pharmacy, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, 450008, China. Electronic address:
Chronic consequences of diabetes that are most commonly encountered are diabetic foot ulcers (DFUs), driven by microbiota-immune system dyshomeostasis, eventually leading to delayed wound healing. Available therapies, such as systemic or topical administration of anti-inflammatory or antimicrobial agents, are limited due to antibiotic resistance and immune dysfunction. Herein, a hybrid hydrogel dressing is developed as the artificial bioadhesive barrier at wound sites to maintain microbial and immunological homeostasis locally and have potent anti-inflammatory effects.
View Article and Find Full Text PDFGels
January 2025
Institute for Polymers and Composites, University of Minho, 5800-048 Guimarães, Portugal.
A set of carrageenans produced in the potassium form and with chemical structures varying from pure iota-carrageenans to nearly pure kappa-carrageenans is submitted to ultrasonication to reduce their molecular masses Mw while maintaining a constant chemical structure and a polydispersity index around 2. The kinetics of ultrasound-induced chain scission are found to be slower for polysaccharides richer in kappa-carrageenan disaccharide units. From the elasticity of samples directly gelled in a rheometer at 1 /% in 0.
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