The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.
Surface-bound reactive oxygen species generating nanozymes for selective antibacterial action
Open accessAbstract
Acting by producing reactive oxygen species (ROS) in situ, nanozymes are promising as antimicrobials. ROS’ intrinsic inability to distinguish bacteria from mammalian cells, however, deprives nanozymes of the selectivity necessary for an ideal antimicrobial. Here we report that nanozymes that generate surface-bound ROS selectively kill bacteria over mammalian cells. This result is robust across three distinct nanozymes that universally generate surface-bound ROS, with an oxidase-like silver-palladium bimetallic alloy nanocage, AgPd 0.38, being the lead model. The selectivity is attributable to both the surface-bound nature of ROS these nanozymes generate and an unexpected antidote role of endocytosis. Though surface-bound, the ROS on AgPd 0.38 efficiently eliminated antibiotic-resistant bacteria and effectively delayed the onset of bacterial resistance emergence. When used as coating additives, AgPd 0.38 enabled an inert substrate to inhibit biofilm formation and suppress infection-related immune responses in mouse models. This work opens an avenue toward biocompatible nanozymes and may have implication in our fight against antimicrobial resistance.
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Defect engineering in nanozymes
Wu, Y., Xu, W., Jiao, L., Tang, Y., Chen, Y., Gu, W., & Zhu, C. (2022) · Materials Today · doi:10.1016/j.mattod.2021.10.032 · Cited by 269
Nanozybiotics: advancing antimicrobial strategies through biomimetic mechanisms
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Metadata
- Authors
- Gao, F., Shao, T., Yu, Y., Xiong, Y., & Yang, L.
- Venue
- Nature Communications
- Published
- 2021-02-02
- Volume
- 12
- Issue
- 1
- Pages
- 745-745
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W3128883496
- Cited by
- 465
- References
- 65
- FWCI
- 21.84
- Type
- journal article
- Language
- en
- Open access
- gold
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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