自愈水凝胶
抗菌活性
化学计量学
摩尔比
齿合度
化学
配位复合体
水溶液中的金属离子
化学工程
放松(心理学)
纳米技术
金属
离子
材料科学
协调数
分子动力学
组织工程
机械强度
组合化学
高分子化学
纳米复合材料
合理设计
配体(生物化学)
作者
Kaixuan Ren,Qing Tao,Xiao Du,Chengfeng Cai,Jingbo Yin
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2026-03-12
卷期号:27 (4): 2524-2535
被引量:2
标识
DOI:10.1021/acs.biomac.5c02161
摘要
The coordination ratio between metal ions and ligands governs the density, strength, and dynamics of coordination bonds in metal-coordinated hydrogels. However, the relationship between coordination stoichiometry and hydrogel properties remains insufficiently understood. In this study, dual-cross-linked poly(histidine methacrylamide) (PHisMA)-Ni 2+ hydrogels were fabricated by varying the HisMA:Ni 2+ molar ratio, enabling precise regulation of network architecture, mechanical performance, and relaxation behavior. Remarkably, by tuning the HisMA:Ni 2+ molar ratio, Ni 2+ ions generated multidentate coordination with HisMA groups, yielding extraordinary mechanical reinforcement, achieving up to 75-fold higher fracture strength, 55-fold higher Young’s modulus, and 492-fold higher toughness. The hydrogels also exhibited strong strain-rate dependence, tunable viscoelasticity, extended relaxation time, excellent energy dissipation, and rapid recovery. Furthermore, the hydrogels displayed potent antibacterial activity against S. aureus . These findings establish the control of metal–ligand coordination ratio as an effective design principle for engineering dual-cross-linked hydrogels with tailored mechanical and antibacterial functionality, holding great promise for biomedical and wearable applications.
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