In the present era, the treatment of skin-infected wounds and their associated inflammation constitutes a significant challenge. These infections have the potential to impede the healing process and become a life-threatening pathology, particularly due to the rise of bacterial resistance. Hydrogels could successfully address this issue due to their unique capabilities and versatility. Among them, natural polymer-based hydrogels are especially advantageous as they resemble the extracellular matrix (ECM) and mechanical properties of natural tissues. In this study, we propose a dual-action hydrogel composed of methacrylated gelatin as a matrix and a salicylate (Sal) anion-exchanged polymerizable ionic liquid (PIL) to achieve anti-inflammatory and antibacterial activities. This material facilitated cell attachment and colonization with mouse endothelial fibroblasts. A flow cytometry assay was conducted to evaluate the anti-inflammatory effect, and demonstrated the differentiation of mouse macrophages to an M2 (reparative) phenotype. Therefore, the levels of TNF-α, interleukin-6 (IL-6), and interleukin (IL-10) were quantified to further evaluate this effect, demonstrating an inhibition on the pro-inflammatory ones. The inherent antibacterial capacity of the PIL was demonstrated against Staphylococcus aureus and Escherichia coli, thereby corroborating its potential as a wound dressing. To the best of our knowledge, this is the first reported hydrogel incorporating an anion-exchanged polymerizable ionic liquid that is capable of promoting macrophage differentiation into a reparative phenotype, of reducing pro-inflammatory cytokines, and of simultaneously retaining antibacterial activity. These features open the gate to the potential application of this hydrogel as a wound dressing. STATEMENT OF SIGNIFICANCE: Bacterial wound infections may lead to severe problems due to their associate tissue inflammation and the emergence of bacterial resistance. In this sense, local therapies such as hydrogels have gathered much attention as alternative therapies for these pathologies. In this work, we have developed a natural polymer-based hydrogel copolymerized with a polymerizable ionic liquid containing salicylate as an anion. The hydrogel was shown to be biocompatible, and promoted macrophage differentiation to a reparative phenotype, while reducing the levels of pro-inflammatory cytokines. Finally, the high antibacterial capability against both gram-positive and gram-negative bacteria makes it a promising candidate for use in wound dressings.
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http://dx.doi.org/10.1016/j.actbio.2025.03.015 | DOI Listing |
Acta Biomater
March 2025
Department of Chemistry in Pharmaceutical Sciences, School of Pharmacy, Institute Hospital 12 de Octubre (imas12), Universidad Complutense de Madrid (UCM), 28040, Spain; Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid 28029, Spain. Electronic address:
In the present era, the treatment of skin-infected wounds and their associated inflammation constitutes a significant challenge. These infections have the potential to impede the healing process and become a life-threatening pathology, particularly due to the rise of bacterial resistance. Hydrogels could successfully address this issue due to their unique capabilities and versatility.
View Article and Find Full Text PDFACS Appl Mater Interfaces
March 2025
School of Chemistry and Materials Science, Ludong University, Yantai 264025, China.
Endowing flexible sensors with self-powering capabilities is of significant importance. However, the thermoelectric conversion gels reported so far suffer from the limitations of insufficient flexibility, signal distortion under repetitive deformation, and insufficient comprehensive performance, which seriously hinder their wide application. In this work, we designed and prepared eutectogels by an ionic liquid and a polymerizable deep eutectic solvent (PDES), which exhibit good mechanical properties, adhesion, and excellent thermoelectric conversion and thermoelectric response performance.
View Article and Find Full Text PDFSmall
March 2025
National Engineering Research Center for Colloidal Materials, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
The inherent acid diffusion during post-exposure baking poses significant challenges in balancing resolution, line-edge roughness, and sensitivity (RLS), thereby constraining the performance of chemically amplified photoresists (CARs) in advanced lithography. This study introduces a novel series of alkene-functionalized imino/imido benzenesulfonate photoacid generators (PAGs), characterized by their solubility, thermal stability, and polymerization attributes. These derivatives can copolymerize with acrylates and methacrylates to form PAG-bound copolymers, integrating non-ionic PAG units and acid-cleavable bulky alicyclic substituents, facilitating their use as "single-component" resists devoid of additives.
View Article and Find Full Text PDFAdv Mater
March 2025
Key Laboratory of Functional Polymer Materials of Ministry of Education, College of Chemistry, Nankai University, Tianjin, 300071, China.
Eutectogels are emerging as the next-generation stretchable electronics due to their superior ionic conductivity, non-volatility, and cost-effectiveness. Nevertheless, most eutectogels suffer from weak mechanical strength and toughness and pronounced hygroscopicity. Herein, a strategy is proposed to fabricate phase-separated eutectogels with dual ionic channels (PSDIC-gel), which exhibit exceptional integrative properties, especially water resistance.
View Article and Find Full Text PDFSmall Methods
January 2025
State Key Laboratory of Material Processing and Die & Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.
Next-generation ionic skin (i-skin) should be self-healing and self-powered, promoting its development toward lightweight, miniaturization, compact, and portable designs. Previously reported self-powered i-skin mostly either lack the ability to self-repair damaged parts or only have self-healing capabilities some components, falling short of achieving complete device self-healability. In this work, a self-bonding strategy is presented to obtain an all-polymerizable deep eutectic solvent (PDES) magnetoelectric i-skin (MIS) that simultaneously achieves self-powering and full-device autonomous self-healability.
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