Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/98184
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Title: Amphiphilic nano-swords for direct penetration and eradication of pathogenic bacterial biofilms
Authors: Zhou, C
Zhou, Y
Zheng, Y
Yu, Y
Yang, K
Chen, Z
Chen, X
Wen, K
Chen, Y
Bai, S
Song, J
Wu, T
Lei, E
Wan, M
Cai, Q
Ma, L
Wong, WL 
Bai, Y
Zhang, C
Feng, X
Issue Date: 26-Apr-2023
Source: ACS applied materials and interfaces, 26 Apr. 2023, v. 15, no. 16, p. 20458–20473
Abstract: Bacterial biofilms are major causes of persistent and recurrent infections and implant failures. Biofilms are formable by most clinically important pathogens worldwide, such as Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli, causing recalcitrance to standard antibiotic therapy or anti-biofilm strategies due to amphiphilic impermeable extracellular polymeric substances (EPS) and the presence of resistant and persistent bacteria within the biofilm matrix. Herein, we report our design of an oligoamidine-based amphiphilic “nano-sword” with high structural compacity and rigidity. Its rigid, amphiphilic structure ensures effective penetration into EPS, and the membrane-DNA dual-targeting mechanism exerts strong bactericidal effect on the dormant bacterial persisters within biofilms. The potency of this oligoamidine is shown in two distinct modes of application: it may be used as a coating agent for polycaprolactone to fully inhibit surface biofilm growth in an implant-site mimicking micro-environment; meanwhile, it cures model mice of biofilm infections in various ex vivo and in vivo studies.
Keywords: Anti-bacterial biofilm
Amphiphilic oligomers
Extracellular polymeric substance
Persister cells
Publisher: American Chemical Society
Journal: ACS applied materials and interfaces 
ISSN: 1944-8244
EISSN: 1944-8252
DOI: 10.1021/acsami.3c03091
Rights: © 2023 American Chemical Society
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials & Interfaces, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://dx.doi.org/10.1021/acsami.3c03091.
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