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Colistin-Functionalized Nanoparticles for the Rapid Capture of Acinetobacter baumannii

dc.creatorMiller, Sinead Emily
dc.date.accessioned2020-08-23T15:48:44Z
dc.date.available2015-11-23
dc.date.issued2015-11-23
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-11202015-152348
dc.identifier.urihttp://hdl.handle.net/1803/14665
dc.description.abstractGold nanoparticles (AuNPs) were functionalized for rapid binding of Acinetobacter baumannii (A. baumannii), a Gram-negative bacterium. AuNPs were functionalized with colistin (Col), a polycationic antibiotic, using a two-step self-assembly process, in which heterobifunctional polyethylene glycol (PEG) was used as a linker. Colistin was successfully conjugated to the AuNPs (Col-PEG-AuNP), as validated by dynamic light scattering (DLS) and proton nuclear magnetic resonance (H1 NMR). Images taken using a scanning transmission electron microscope (STEM), in combination with x-ray energy dispersive spectroscopy (EDS), confirmed binding of Col-PEG-AuNPs to the cell wall of A. baumannii. Results generated from a rapid binding assay indicated that the reaction rate of Col-PEG-AuNP complexation with A. baumannii reached half-maximum saturation in approximately 7 minutes. Quantitative measurement of the kinetics of Col-PEG-AuNP binding to A. baumannii is essential to inform the design of colistin-functionalized magnetic nanoparticles for magnetic separation of nanoparticle-bound A. baumannii.
dc.format.mimetypeapplication/pdf
dc.subjectLipopolysaccharide
dc.subjectGram-negative
dc.subjectMulti-Drug Resistance
dc.subjectGold
dc.titleColistin-Functionalized Nanoparticles for the Rapid Capture of Acinetobacter baumannii
dc.typethesis
dc.contributor.committeeMemberFrederick R. Haselton
dc.type.materialtext
thesis.degree.nameMS
thesis.degree.levelthesis
thesis.degree.disciplineBiomedical Engineering
thesis.degree.grantorVanderbilt University
local.embargo.terms2015-11-23
local.embargo.lift2015-11-23
dc.contributor.committeeChairTodd D. Giorgio


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