Wu Qi, Ghosal Krishanu, Kana'an Nadine, Roy Shounak, Rashed Nagham, Majumder Ranabir, Mandal Mahitosh, Gao Liang, Farah Shady
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.
School of Medical Science and Technology, Indian Institute of Technology Kharagpur, West Bengal, 721302, India.
Bioact Mater. 2024 Oct 15;44:116-130. doi: 10.1016/j.bioactmat.2024.10.003. eCollection 2025 Feb.
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. 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, 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.
细菌伤口感染在医疗保健领域正成为日益严峻的挑战,会带来诸如全身感染、器官衰竭和败血症等严重风险,据预测到2050年每年将有超过1000万人死亡。具有类似细胞外基质特性的抗菌水凝胶正成为治疗感染性伤口的有前景的解决方案。然而,这些水凝胶大多的抗菌性能很大程度上归因于外在试剂,其作用机制仍知之甚少。在此,我们首次引入改性咪唑烷基脲(IU)作为开发类似组织的抗菌水凝胶的聚合物主链。所设计的水凝胶具有类似组织的机械特性、出色的抗冻性能和快速的自愈能力。采用分子动力学(MD)模拟和密度泛函理论(DFT)计算来深入了解氢键和金属 - 配体配位的程度,以微调水凝胶的性能。研究表明水凝胶对小鼠成纤维细胞以及人类皮肤、肺和红细胞具有良好的生物相容性,并具有潜在的伤口愈合能力。此外,水凝胶表现出良好的3D打印性和显著的抗菌活性,这归因于浓度依赖性的活性氧生成、氧化应激诱导以及随后对细菌膜的破坏。最重要的是,生物膜研究证实所开发的水凝胶在预防生物膜形成方面是有效的。因此,这些模拟组织的水凝胶为加速伤口愈合同时控制细菌感染提供了一个有前景且有效的平台,为伤口护理的未来带来了希望。