| Literature DB >> 28011336 |
Benjamin M Geilich1, Ilia Gelfat2, Srinivas Sridhar3, Anne L van de Ven3, Thomas J Webster4.
Abstract
The rising prevalence and severity of antibiotic-resistant biofilm infections poses an alarming threat to public health worldwide. Here, biocompatible multi-compartment nanocarriers were synthesized to contain both hydrophobic superparamagnetic iron oxide nanoparticles (SPIONs) and the hydrophilic antibiotic methicillin for the treatment of medical device-associated infections. SPION co-encapsulation was found to confer unique properties, enhancing both nanocarrier relaxivity and magneticity compared to individual SPIONs. These iron oxide-encapsulating polymersomes (IOPs) penetrated 20 μm thick Staphylococcus epidermidis biofilms with high efficiency following the application of an external magnetic field. Three-dimensional laser scanning confocal microscopy revealed differential bacteria death as a function of drug and SPION loading. Complete eradication of all bacteria throughout the biofilm thickness was achieved using an optimized IOP formulation containing 40 μg/mL SPION and 20 μg/mL of methicillin. Importantly, this formulation was selectively toxic towards methicillin-resistant biofilm cells but not towards mammalian cells. These novel iron oxide-encapsulating polymersomes demonstrate that it is possible to overcome antibiotic-resistant biofilms by controlling the positioning of nanocarriers containing two or more therapeutics.Entities:
Keywords: Antibiotic-resistance; Biofilm; Nanomedicine; Polymersome; SPION; Staphylococcus epidermidis
Mesh:
Substances:
Year: 2016 PMID: 28011336 DOI: 10.1016/j.biomaterials.2016.12.011
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479