1. Academic Validation
  2. On-demand imidazolidinyl urea-based tissue-like, self-healable, and antibacterial hydrogels for infectious wound care

On-demand imidazolidinyl urea-based tissue-like, self-healable, and antibacterial hydrogels for infectious wound care

  • Bioact Mater. 2024 Oct 15:44:116-130. doi: 10.1016/j.bioactmat.2024.10.003.
Qi Wu 1 Krishanu Ghosal 1 Nadine Kana'an 1 Shounak Roy 1 Nagham Rashed 1 Ranabir Majumder 2 Mahitosh Mandal 2 Liang Gao 3 Shady Farah 1 4
Affiliations

Affiliations

  • 1 The Laboratory for Advanced Functional/Medicinal Polymers & Smart Drug Delivery Technologies, The Wolfson Faculty of Chemical Engineering, Technion-Israel Institute of Technology, Haifa, 3200003, Israel.
  • 2 School of Medical Science and Technology, Indian Institute of Technology Kharagpur, West Bengal, 721302, India.
  • 3 Jinan Key Laboratory of High Performance Industrial Software, Jinan Institute of Supercomputing Technology, Jinan, 250000, China.
  • 4 The Russell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa, 3200003, Israel.
Abstract

Bacterial wound infections are a growing challenge in healthcare, posing severe risks like systemic Infection, organ failure, and sepsis, with projections predicting over 10 million deaths annually by 2050. Antibacterial hydrogels, with adaptable extracellular matrix-like features, are emerging as promising solutions for treating infectious wounds. However, the Antibacterial properties of most of these hydrogels are largely attributed to extrinsic agents, and their mechanisms of action remain poorly understood. Herein we introduce for the first time, modified imidazolidinyl urea (IU) as the polymeric backbone for developing tissue-like Antibacterial hydrogels. As-designed hydrogels behave tissue-like mechanical features, outstanding antifreeze behavior, and rapid self-healing capabilities. Molecular dynamics (MD) simulation and density functional theory (DFT) calculation were employed to well-understand the extent of H-bonding and metal-ligand coordination to finetune hydrogels' properties. In vitro studies suggest good biocompatibility of hydrogels against mouse fibroblasts & human skin, lung, and red blood cells, with potential wound healing capacity. Additionally, the hydrogels exhibit good 3D printability and remarkable Antibacterial activity, attributed to concentration dependent ROS generation, oxidative stress induction, and subsequent disruption of Bacterial membrane. On top of that, in vitro biofilm studies confirmed that developed hydrogels are effective in preventing biofilm formation. Therefore, these tissue-mimetic hydrogels present a promising and effective platform for accelerating wound healing while simultaneously controlling Bacterial infections, offering hope for the future of wound care.

Keywords

Antibacterial hydrogel; Antibiofilm hydrogel; Imidazolidinyl urea; Self-healing; Wound care.

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