粘附
聚合
材料科学
自愈水凝胶
胶粘剂
光热治疗
纳米技术
伤口愈合
组织粘连
变形(气象学)
复合材料
化学工程
图层(电子)
聚合物
高分子化学
外科
工程类
医学
作者
Lan Feng,Wenbin Shi,Qin Chen,Huitong Cheng,Jianxu Bao,Chunji Jiang,Weifeng Zhao,Changsheng Zhao
标识
DOI:10.1002/adhm.202100784
摘要
Abstract Multifunctional hydrogels acting as wound dressing have received extensive attention in soft tissue repair; however, it is still a challenge to develop a non‐antibiotic‐dependent antibacterial hydrogel that has tunable adhesion and deformation to achieve on‐demand removal. Herein, an asymmetric adhesive hydrogel with near‐infrared (NIR)‐triggered tunable adhesion, self‐deformation, and bacterial eradication is designed. The hydrogel is prepared by the crosslinking polymerization of N ‐isopropylacrylamide and acrylic acid, during the sedimentation of conductive PPy‐PDA nanoparticles based on the polymerization of pyrrole (Py) and dopamine (DA). Due to the conversion capacity from NIR light into heat for PPy‐PDA NPs, the formed temperature‐sensitive hydrogel exhibits tissue adhesive as well as NIR‐triggered tunable adhesion and self‐deformation property, which can achieve an on‐demand dressing refreshing. Systematically in vitro / in vivo antibacterial experiments indicate that the hydrogel shows excellent disinfection capability to both Gram‐negative and Gram‐positive bacteria. The in vivo experiments in a full‐layer cutaneous wound model demonstrate that the hydrogel has a good treatment effect to promote wound healing. Overall, the asymmetric hydrogel with tunable adhesion, self‐deformation, conductive, and photothermal antibacterial activity may be a promising candidate to fulfill the functions of adhesion on skin tissue, easy removing on‐demand, and accelerating the wound healing process.
科研通智能强力驱动
Strongly Powered by AbleSci AI