生物膜
胞外聚合物
化学
细菌
活性氧
生物物理学
抗菌剂
药代动力学
微生物学
生物化学
生物
药理学
遗传学
作者
Xue Han,Qi Lou,Feng Feng,Guanhua Xu,Song Hong,Li Yao,Shijie Qin,Dazhuan Wu,Xiaoping Ouyang,Zhiguo Zhang,Xiuyu Wang
标识
DOI:10.1002/anie.202202559
摘要
Abstract The heterogeneity in biofilms is a major challenge in biofilm therapies due to different susceptibility of bacteria and extracellular polymeric substances (EPS) to antibacterial agents. Here, we describe a therapeutic strategy that overcame biofilm heterogeneity, where antibacterial agent (NO) and EPS dispersant (reactive oxygen species (ROS)‐inducing Fe 3+ ) were separately loaded in the yolk and shell compartment of a yolk–shell nanoplatform. Compared with traditional combinational chemotherapies which suffer from inconsistent pharmacokinetics profiles, this strategy drew on the pharmacokinetic complementarity of ROS and NO, where ROS with a short diffusion distance and a high redox potential corrupted the EPS, facilitating NO, which has a long diffusion distance and a broad antimicrobial spectrum, to penetrate the biofilm and eliminate the resident bacteria. Additionally, the construction of a three‐dimensional spherical biofilm model is novel and clinically relevant.
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