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Bacteria-Activated Theranostic Nanoprobes against Methicillin-Resistant Staphylococcus aureus Infection
Abstract
Despite numerous advanced imaging and sterilization techniques available nowadays, the sensitive in vivo diagnosis and complete elimination of drug-resistant bacterial infections remain big challenges. Here we report a strategy to design activatable theranostic nanoprobes against methicillin-resistant Staphylococcus aureus (MRSA) infections. This probe is based on silica nanoparticles coated with vancomycin-modified polyelectrolyte-cypate complexes (SiO 2 -Cy-Van), which is activated by an interesting phenomenon of bacteria-responsive dissociation of the polyelectrolyte from silica nanoparticles. Due to the aggregation of hydrophobic cypate fluorophores on silica nanoparticles to induce ground-state quenching, the SiO 2 -Cy-Van nanoprobes are nonfluorescent in aqueous environments. We demonstrate that MRSA can effectively pull out the vancomycin-modified polyelectrolyte-cypate complexes from silica nanoparticles and draw them onto their own surface, changing the state of cypate from off (aggregation) to on (disaggregation) and leading to in vitro MRSA-activated near-infrared fluorescence (NIRF) and photothermal elimination involving bacterial cell wall and membrane disruption. In vivo experiments show that this de novo -designed nanoprobe can selectively enable rapid (4 h postinjection) NIRF imaging with high sensitivity (10 5 colony-forming units) and efficient photothermal therapy (PTT) of MRSA infections in mice. Remarkably, the SiO 2 -Cy-Van nanoprobes can also afford a long-term tracking (16 days) of the development of MRSA infections, allowing real-time estimation of bacterial load in infected tissues and further providing a possible way to monitor the efficacy of antimicrobial treatment. The strategy of bacteria-activated polyelectrolyte dissociation from nanoparticles proposed in this work could also be used as a general method for the design and fabrication of bacteria-responsive functional nanomaterials that offer possibilities to combat drug-resistant bacterial infections.
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Koch, G., Yepes, A., Förstner, K. U., Wermser, C., Stengel, S. T., Modamio, J., Ohlsen, K., Foster, K. R., & Lopez, D. (2014) · Cell · doi:10.1016/j.cell.2014.06.046 · Cited by 211
Cited by
Huang, Y., Guo, X., Wu, Y., Chen, X., Feng, L., Xie, N., & Shen, G. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01745-z · Cited by 490
Gao, G., Jiang, Y.-W., Jia, H.-R., & Wu, F.-G. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2018.09.045 · Cited by 485
Yu, Y., Li, P., Zhu, C., Ning, N., Zhang, S., & Vancso, G. J. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201904402 · Cited by 363
Nanomaterials for Nanotheranostics: Tuning Their Properties According to Disease Needs
Wong, X. Y., Sena-Torralba, A., Álvarez-Diduk, R., Muthoosamy, K., & Merkoçi, A. (2020) · ACS Nano · doi:10.1021/acsnano.9b08133 · Cited by 363
Li, J., Tan, L., Liu, X., Cui, Z., Yang, X., Yeung, K. W. K., Chu, P. K., & Wu, S. (2017) · ACS Nano · doi:10.1021/acsnano.7b05620 · Cited by 300
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Metadata
- Authors
- Zhao, Z., Yan, R., Yi, X., Li, J., Rao, J., Guo, Z., Yang, Y., Li, W., Li, Y.-Q., & Chen, C.
- Venue
- ACS Nano
- Publisher
- American Chemical Society (ACS)
- Published
- 2017-03-30
- Volume
- 11
- Issue
- 5
- Pages
- 4428-4438
- ISSN
- 1936-0851 (ISSN-L)
- 1936-086X
- OpenAlex
- W2599117579
- Cited by
- 182
- References
- 1
- FWCI
- 9.78
- Type
- journal article
- Language
- en
- Open access
- closed
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- Zhao, Z., Yan, R., Yi, X., Li, J., Rao, J., Guo, Z., Yang, Y., Li, W., Li, Y.-Q., & Chen, C. (2017). Bacteria-Activated Theranostic Nanoprobes against Methicillin-Resistant Staphylococcus aureus Infection. ACS Nano. https://doi.org/10.1021/acsnano.7b00041
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