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

被引:24
|
作者
Liu, Shaoqiong [1 ]
Fukushima, Kazuki [2 ]
Venkataraman, Shrinivas [1 ]
Hedrick, James L. [3 ]
Yang, Yi Yan [1 ]
机构
[1] Inst Bioengn & Nanotechnol, 31 Biopolis Way, Singapore 138669, Singapore
[2] Yamagata Univ, Dept Polymer Sci & Engn, Yonezawa, Yamagata, Japan
[3] IBM Almaden Res Ctr, San Jose, CA 95120 USA
关键词
Cationic small molecules; Supramolecular assembly; Nanofibers; Antibiotic delivery; Wound infection; BETA-LACTAM ANTIBIOTICS; CANCER STEM-CELLS; DRUG-DELIVERY; PIPERACILLIN-TAZOBACTAM; TOBRAMYCIN LIPOSOMES; POLYMERIC MICELLES; NANOPARTICLES; RESISTANCE; KERATITIS; THERAPY;
D O I
10.1016/j.nano.2017.09.007
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:165 / 172
页数:8
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