Author
Listed:
- Yunjiang Jiang
(Texas Tech University Health Sciences Center
Shenzhen Bay Lab)
- Wan Zheng
(Texas Tech University Health Sciences Center)
- Keith Tran
(Texas Tech University Health Sciences Center)
- Elizabeth Kamilar
(Texas Tech University Health Sciences Center)
- Jitender Bariwal
(Texas Tech University Health Sciences Center)
- Hairong Ma
(Texas Tech University Health Sciences Center)
- Hongjun Liang
(Texas Tech University Health Sciences Center)
Abstract
To dissect the antibiotic role of nanostructures from chemical moieties belligerent to both bacterial and mammalian cells, here we show the antimicrobial activity and cytotoxicity of nanoparticle-pinched polymer brushes (NPPBs) consisting of chemically inert silica nanospheres of systematically varied diameters covalently grafted with hydrophilic polymer brushes that are non-toxic and non-bactericidal. Assembly of the hydrophilic polymers into nanostructured NPPBs doesn’t alter their amicability with mammalian cells, but it incurs a transformation of their antimicrobial potential against bacteria, including clinical multidrug-resistant strains, that depends critically on the nanoparticle sizes. The acquired antimicrobial potency intensifies with small nanoparticles but subsides quickly with large ones. We identify a threshold size (dsilica ~ 50 nm) only beneath which NPPBs remodel bacteria-mimicking membrane into 2D columnar phase, the epitome of membrane pore formation. This study illuminates nanoengineering as a viable approach to develop nanoantibiotics that kill bacteria upon contact yet remain nontoxic when engulfed by mammalian cells.
Suggested Citation
Yunjiang Jiang & Wan Zheng & Keith Tran & Elizabeth Kamilar & Jitender Bariwal & Hairong Ma & Hongjun Liang, 2022.
"Hydrophilic nanoparticles that kill bacteria while sparing mammalian cells reveal the antibiotic role of nanostructures,"
Nature Communications, Nature, vol. 13(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-021-27193-9
DOI: 10.1038/s41467-021-27193-9
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