Antibacterial and Angiogenic Poly(ionic liquid) Hydrogels

Gels. 2022 Jul 28;8(8):476. doi: 10.3390/gels8080476.

Abstract

Wounds, particularly under low-hydration conditions, require more time to repair successfully. Therefore, there is an urgent need to develop wound dressings that can accelerate wound healing. Hydrogels, which can maintain a moist environment around the wound and allow gas to pass through the material, act as antibacterial hydrogels as dressings and have great application value in the treatment of wounds. In addition, wound dressings (hydrogels) containing antibacterial capacity have lasting antibacterial effects and reduce damage to cells. In this work, we firstly synthesized two antibacterial agents: imidazolium poly(ionic liquids) containing sulfhydryl (Imidazole-SH) and ε-Poly(lysine) containing SH (EPL-SH). Then, lysine as a cross-linking agent, by "thiol-ene" click reaction, was mixed with Deferoxamine (DFO) to prepare the antibacterial hydrogels. The in vitro assays showed that the hydrogels could effectively kill Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). In addition, it also could reduce the inflammatory response produced by Lipopolysaccharide (LPS). More importantly, according to the transwell and angiogenesis assays, DFO-incorporated hydrogels promoted the migration and vascular repair of human umbilical vein endothelial cells (HUVECs). All the results revealed that the hydrogels provided new strategies for wound dressings.

Keywords: anti-inflammatory; antibacterial hydrogels; deferoxamine; imidazolium poly(ionic liquids); vascular repair.

Grants and funding

This research was funded by the Open Project of State Key Laboratory of Supramolecular Structure and Materials (sklssm2022037), Scientific Research Project of Hunan Provincial Education Department of China (No. 19C0990), Joint Construction Project of Medical Science and Technology Research Plan of Henan Province of China (LHGJ20191000) and Fundamental Research Funds for the Central Universities: Southwest University (5330500110).