Author:
Ashbaugh Alyssa G.,Jiang Xuesong,Zheng Jesse,Tsai Andrew S.,Kim Woo-Shin,Thompson John M.,Miller Robert J.,Shahbazian Jonathan H.,Wang Yu,Dillen Carly A.,Ordonez Alvaro A.,Chang Yong S.,Jain Sanjay K.,Jones Lynne C.,Sterling Robert S.,Mao Hai-Quan,Miller Lloyd S.
Abstract
Bacterial biofilm formation is a major complication of implantable medical devices that results in therapeutically challenging chronic infections, especially in cases involving antibiotic-resistant bacteria. As an approach to prevent these infections, an electrospun composite coating comprised of poly(lactic-coglycolic acid) (PLGA) nanofibers embedded in a poly(ε-caprolactone) (PCL) film was developed to locally codeliver combinatorial antibiotics from the implant surface. The release of each antibiotic could be adjusted by loading each drug into the different polymers or by varying PLGA:PCL polymer ratios. In a mouse model of biofilm-associated orthopedic-implant infection, three different combinations of antibiotic-loaded coatings were highly effective in preventing infection of the bone/joint tissue and implant biofilm formation and were biocompatible with enhanced osseointegration. This nanofiber composite-coating technology could be used to tailor the delivery of combinatorial antimicrobial agents from various metallic implantable devices or prostheses to effectively decrease biofilm-associated infections in patients.
Funder
Nexus Award, Johns Hopkins Institute for Clinical and Translational Research (ICTR) funded in part by the National Center for Advancing Translational Sciences (NCTS) of the U.S. NIH
Publisher
Proceedings of the National Academy of Sciences
Cited by
90 articles.
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