Neutralization of ionic interactions by dextran-based single-chain nanoparticles improves tobramycin diffusion into a mature biofilm

被引:21
作者
Blanco-Cabra, Nuria [1 ,2 ]
Movellan, Julie [3 ]
Marradi, Marco [3 ,4 ]
Gracia, Raquel [3 ]
Salvador, Cristian [3 ]
Dupin, Damien [3 ]
Loinaz, Iraida [3 ]
Torrents, Eduard [1 ,2 ]
机构
[1] Barcelona Inst Sci & Technol BIST, Inst Bioengn Catalonia IBEC, Bacterial Infect Antimicrobial Therapies Grp, Barcelona, Spain
[2] Univ Barcelona, Microbiol Sect, Biol Fac, Dept Genet Microbiol & Stat, Barcelona, Spain
[3] CIDETEC, Basque Res & Technol Alliance BRTA, Parque Cientif & Tecnol Gipuzkoa, Donostia San Sebastian, Spain
[4] Univ Florence, Dept Chem Ugo Schiff, Sesto Fiorentino, FI, Italy
关键词
CYSTIC-FIBROSIS SPUTUM; PSEUDOMONAS-AERUGINOSA; EXTRACELLULAR DNA; INFECTIONS; DELIVERY; TRANSPORT;
D O I
10.1038/s41522-022-00317-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The extracellular matrix protects biofilm cells by reducing diffusion of antimicrobials. Tobramycin is an antibiotic used extensively to treat P. aeruginosa biofilms, but it is sequestered in the biofilm periphery by the extracellular negative charge matrix and loses its efficacy significantly. Dispersal of the biofilm extracellular matrix with enzymes such as DNase I is another promising therapy that enhances antibiotic diffusion into the biofilm. Here, we combine the charge neutralization of tobramycin provided by dextran-based single-chain polymer nanoparticles (SCPNs) together with DNase I to break the biofilm matrix. Our study demonstrates that the SCPNs improve the activity of tobramycin and DNase I by neutralizing the ionic interactions that keep this antibiotic in the biofilm periphery. Moreover, the detailed effects and interactions of nanoformulations with extracellular matrix components were revealed through time-lapse imaging of the P. aeruginosa biofilms by laser scanning confocal microscopy with specific labeling of the different biofilm components.
引用
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页数:12
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