锌
活性氧
大肠杆菌
细菌
伤口愈合
体内
细菌生长
抗生素
体外
金属
氧气
化学
微生物学
生物化学
生物
免疫学
有机化学
生物技术
遗传学
基因
作者
Di Zhong,Yuhui Zuo,Yanfeng Shi,Pengfei Zhang,Yuanhong Xu,Bing Li
标识
DOI:10.1016/j.cej.2023.141837
摘要
Iron-based metal–organic frameworks (Fe-MOFs) have been regarded as promising antibacterial alternatives towards antibiotics since they can generate strong reactive oxygen species (ROS) for combating bacterial-infected wounds. But its instability under physiological conditions could not only lead to attenuation of the catalytic activity but also result in a large accumulation of iron ions, which would increase the risk of additional wound infection due to the simultaneous role of iron as a nutrient for bacterial growth. Herein, zinc (Zn) doped Fe-MOFs (ZFMs), which was prepared via stabilizing the structure of Fe-MOFs (FMs) upon Zn doping to enhance the carboxyl group on the frameworks. It can maintain long-term stability in the physiological environment while FMs disintegrate rapidly within one minute. ZFMs inactivated drug-resistant Escherichia coli (E. coli) (1 × 106 CFU mL−1) with high efficiency (>98 %) and accelerated the E. coli infected wounds healed by up-regulating VEGFα factor, which was validated in vivo and vitro. In addition, fibroblast cells (L929) remained at 100 % cell viability after incubating with 150 μg mL−1 ZFMs for 48 h and presented negligible effects on the functions of important organs in animal experiments.
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