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Oxygen-Vacancy-Rich Monolayer BiO 2- X Nanosheets for Bacterial Sepsis Management via Dual Physically Antibacterial and Chemically Anti-inflammatory Functions

Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection. Effective treatment of bacterial sepsis remains challenging due to the rapid progression of infection and the systemic inflammatory response. In this study, monolayer BiO nanosheets (BiO NS...

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Bibliographic Details
Published in:Advanced healthcare materials 2024-07, Vol.13 (18), p.e2304002
Main Authors: Liu, Fang, Zhang, Kun, Lu, Bin, Wang, Xiaochun, Dong, Qingrong, Xue, Tingyu, Tan, Yan, Wang, Xing, Du, Jiangfeng
Format: Article
Language:English
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Summary:Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection. Effective treatment of bacterial sepsis remains challenging due to the rapid progression of infection and the systemic inflammatory response. In this study, monolayer BiO nanosheets (BiO NSs) with oxygen-rich vacancies through sonication-assisted liquid-phase exfoliation are successfully synthesized. Herein, the BiO NSs exhibit a novel nanozyme-enabled intervention strategy for the management of bacterial sepsis, based on its pH dependent dual antibacterial and anti-inflammatory functions. BiO NSs exhibit effective antibacterial by utilizing oxidase (OXD)-like activity. Additionally, BiO NSs can scavenge multiple reactive oxygen species (ROS) and mitigate systemic hyperinflammation by mimicking superoxide dismutase (SOD) and catalase (CAT). These dual capabilities of BiO NSs allow them to address bacterial infection, proinflammatory cytokines secretion and ROS burst collaboratively, effectively reversing the progression of bacterial sepsis. In vivo experiments have demonstrated that BiO NSs significantly reduce bacterial burden, attenuate systemic hyperinflammation, and rapidly rescued organ damage. Importantly, no obvious adverse effects are observed at the administered dose of BiO NSs. This study presents a novel defect engineering strategy for the rational design of high-performance nanozymes and development of new nanomedicines for managing bacterial sepsis.
ISSN:2192-2640
2192-2659
DOI:10.1002/adhm.202304002