海藻酸钠
灭菌(经济)
伤口愈合
纤维素
壳聚糖
化学工程
材料科学
纳米晶
羧甲基纤维素钠
钠
化学
高分子化学
纳米技术
有机化学
医学
外科
业务
工程类
财务
外汇市场
汇率
作者
Baijie Cheng,Ruolin Wang,Sheng Wang,Nan Wang,Xiao–kun Ouyang
标识
DOI:10.1016/j.carbpol.2024.122550
摘要
In the realm of natural polysaccharides, hydrogen bonding is a prevalent feature, yet its role in enhancing photocatalytic antimicrobial properties has been underexplored. In this paper, heterojunctions formed by graphene oxide (GO) and ZIF-8 were locked in sodium alginate/ carboxylated cellulose nanocrystals via hydrogen bonding networks, designated as SCGZ. The SCGZ films exhibit superior photocatalytic performance compared to either ZIF-8 or heterojunctions. This enhancement is primarily due to two key factors: firstly, the hydrogen bonding network significantly enhances the transfer of protons and holes, thereby improving the separation efficiency of photo-generated carriers; secondly, the hydrogen bonding between the layers facilitates a more efficient charge transfer, which expedites the movement of electrons from ZIF-8 to GO upon illumination. In vitro studies demonstrated that the SCGZ films possess remarkable antibacterial capabilities, achieving 99.75 % and 99.61 % inhibition rates against S. aureus and E. coli, respectively. In vivo animal experiments have shown that SCGZ films can significantly accelerate the healing process of damaged tissues, with a healing efficiency of up to 90.5 %. This research provides additional insights into the development of natural polysaccharide-based multi‑hydrogen bonded macromolecules with enhanced photocatalytic properties.
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