Supramolecular nanofibers self-assembled from cationic small molecules derived from repurposed poly(ethylene teraphthalate) for antibiotic delivery

Low molecular weight cationic compounds were synthesized from re-purposed poly(ethylene teraphthalate) (PET) and used to self-assemble into high aspect ratio supramolecular nanofibers for encapsulation and delivery of anionic antibiotics. The antibiotic piperacillin/tazobactam (PT) was successfully...

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Veröffentlicht in:Nanomedicine 2018-01, Vol.14 (1), p.165-172
Hauptverfasser: Liu, Shaoqiong, Fukushima, Kazuki, Venkataraman, Shrinivas, Hedrick, James L., Yang, Yi Yan
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Sprache:eng
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Zusammenfassung:Low molecular weight cationic compounds were synthesized from re-purposed poly(ethylene teraphthalate) (PET) and used to self-assemble into high aspect ratio supramolecular nanofibers for encapsulation and delivery of anionic antibiotics. The antibiotic piperacillin/tazobactam (PT) was successfully loaded into the nanofibers through ionic interaction between anionic PT and the cationic nanofibers without loss of the nanofiber features. These PT-loaded nanofibers demonstrated high loading efficiency and sustained delivery for PT. The antimicrobial activity of PT-loaded nanofibers remained potent towards both Gram-positive and Gram-negative bacteria. Importantly, in a P. aeruginosa-infected mouse skin wound model, the treatment with the PT-loaded nanofibers was more effective than free PT for wound healing as evidenced by the significantly lower P. aeruginosa counts at the wound sites and histological analysis. This strategy can be applied to deliver a variety of anionic antibiotics for improved treatment efficacy of various infections. Low molecular weight cationic compounds self-assembled into high aspect ratio supramolecular nanofibers for encapsulation and delivery of anionic antibiotics piperacillin/tazobactam (PT). These nanofibers exhibited high loading efficiency and sustained release of PT. PT-loaded nanofibers demonstrated high antibacterial activity both in vitro and in a P. aeruginosa-infected mouse skin wound model. [Display omitted]
ISSN:1549-9634
1549-9642
DOI:10.1016/j.nano.2017.09.007