聚吡咯
壳聚糖
材料科学
纤维素
细菌纤维素
铵
抗菌活性
化学工程
自愈水凝胶
高分子化学
细菌
有机化学
复合材料
聚合
聚合物
化学
生物
工程类
遗传学
作者
Xinru Wang,Jie Zhang,Jinyu Shan,Dong Yang,Jie Yang,Guangming Tian,Yunzhi Dang,Jianhua Ma
标识
DOI:10.1021/acsami.5c12061
摘要
Smart antibacterial materials are gaining attention for their potential in controlled drug release and efficient treatment. This study constructed a composite hydrogel based on oxidized bacterial cellulose (OBC) and quaternary ammonium chitosan (QAC). This hydrogel was loaded with the natural antibacterial drug berberine (Ber) and utilized the abundant functional groups (such as amino and carboxyl groups) on OBC and QAC to achieve pH responsiveness, achieving on-demand drug release in the alkaline microenvironment of simulated chronic wounds. By further in situ polymerization of polypyrrole (PPy) on the hydrogel surface, the composite hydrogel (OBC/QAC/Ber/PPy) was endowed with excellent photothermal and electrothermal conversion properties. Systematic characterization showed that the OBC/QAC/Ber/PPY hydrogel had a high compressive strength of 135.6 kPa, self-healing ability, excellent biocompatibility, and significant antimicrobial activity. Notably, the introduction of the PPy layer also synergistically enhanced the inherent antibacterial properties of QAC and Ber through thermal effects; under photothermal stimulation, inhibition zones against E. coli and S. aureus reached 8.0 and 6.2 mm, respectively. Mouse wound models showed that the OBC/QAC/Ber/PPy composite hydrogel significantly accelerated wound healing, with a 27.03% improvement in the wound healing rate after 15 days compared to pure BC films. In summary, the OBC/QAC/Ber/PPy composite hydrogel, which integrates pH responsiveness, photoelectric thermal synergistic therapy, and multiple antibacterial mechanisms, provides a promising strategy for developing next-generation smart wound dressings and addressing bacterial resistance challenges.
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