自愈水凝胶
荧光
抗菌活性
聚合物
共轭体系
纳米技术
材料科学
控制释放
聚电解质
化学
自愈
组合化学
生物物理学
细菌
有机化学
高分子化学
物理
病理
生物
医学
量子力学
替代医学
遗传学
作者
Y. Wang,Jian‐Liang Zhao,Zhenzhen Dong,C. Wang,Hanting Meng,Yan Li,Hongwei Jin,C. Wang
标识
DOI:10.1016/j.mtchem.2021.100537
摘要
Although antibacterial hydrogels are emerging as promising biomaterials for effective inhibition of bacterial infections, monitoring their dynamic release behaviors in a visual manner remains greatly challenging. Herein, non-conjugated luminescent polymers (NCLPs) with aggregation-induced emission (AIE) characteristics are used for the first time to develop a visualization strategy to monitor the release process of the drug-loaded hydrogel. The novel antimicrobial peptide polymers with intrinsic AIE effect, namely nanoengineered peptide-grafted hyperbranched polymers (NPGHPs), are encapsulated in an anionic polyelectrolyte to construct the AIE-active fluorescent polymeric hydrogel (NPGHPs/SA gel). Interestingly, the rigid environment mediated by hydrogen bonding and electrostatic interaction contributes to promoting the unconventional luminescence of fluorescent clusters. Moreover, the successive drug release process of NPGHPs/SA gel can be tracked in real time by using fluorescence microscopy. The hydrogel also has potent antibacterial activities against Gram-negative bacteria (E. coli, P. aeruginosa) and Gram-positive bacteria (S. aureus, B. subtilis). Overall, this work not only provides an advanced biomedical material with broad-spectrum antibacterial ability but also opens a facile avenue up for the investigation of drug release from gel systems.
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