抗菌剂
抗生素耐药性
遗传增强
适体
细菌
广谱
抗生素
DNA损伤
微生物学
DNA
基因
材料科学
计算生物学
生物
化学
组合化学
遗传学
作者
Shan Huang,Yuexin Song,Xiaojun Chen,Qianhao Min,Jianrong Zhang,Jun‐Jie Zhu
标识
DOI:10.1002/adfm.202300145
摘要
Abstract Nanoparticle‐based approaches addressed the barriers to antibiotic resistance faced by traditional antimicrobial agents. However, nanotherapies against multibacterial infections still suffered from the lack of broad‐spectrum targeting ability and the mono‐inhibition pathway. In this study, a multimodality therapeutic nanoplatform (denoted as Asza) is introduced, which combines specific recognition, synergistic oxidative damage, and gene therapy, to effectively inhibit the emergence of bacterial resistance, achieving broad‐spectrum sterilization activity against two Gram‐positive ( B. subt , S. epider ) and two Gram‐negative bacteria ( E. coli , E. aero ). In addition to the oxidative damage generated from gold nanoclusters, DNA aptamer, and CRISPR‐Cas modules are combined in the Asza to recognize multiple bacteria and cleave the ftsz gene with high specificity, allowing precision treatment of multibacterial infections without damaging surrounding healthy cells. Furthermore, multimodal antimicrobial strategies can reduce the risk of the generation of bacterial resistance to single‐modality therapy and significantly boost the efficiency of antibacterial therapy. This study offers a promising approach to advance the applications of nanomaterials in clinical antimicrobial therapy.
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