PHYSICAL CHARACTERIZATION OF DNA CONDENSED WITH CATIONIC AGENTS

dc.contributor.advisorBriber, Robert Men_US
dc.contributor.authorSalgado, Eddyen_US
dc.contributor.departmentMaterial Science and Engineeringen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.date.accessioned2017-06-22T05:31:04Z
dc.date.available2017-06-22T05:31:04Z
dc.date.issued2016en_US
dc.description.abstractGene therapy using non viral vectors remains a challenging problem of maximizing efficiency while minimizing risks due to the multiple biological hurdles for a carrier agent to deliver its genetic cargo. The precise connection between the physical properties of the vectors and their transfection behaviors remains to be fully realized. We have used atomic force microscopy as well as dynamic light scattering and zeta potential measurements in order to image and characterize DNA complexes with polyethylenimine (PEI), histidine-lysine (HK) peptide, and triethylenetetramine (TETA)-functionalized gold nanoparticles. The resulting complex structures are analyzed as a function of amine to phosphate (N/P) ratios and as a function of sample preparation protocols. This work aims to not only characterize these specific complexes, but to aid in the general understanding of complex formation and how it relates to transfection observations to promote a more rational design of future gene delivery agents.en_US
dc.identifierhttps://doi.org/10.13016/M29G4S
dc.identifier.urihttp://hdl.handle.net/1903/19265
dc.language.isoenen_US
dc.subject.pqcontrolledMaterials Scienceen_US
dc.subject.pqcontrolledBiomedical engineeringen_US
dc.subject.pqcontrolledBiophysicsen_US
dc.subject.pquncontrolledAFMen_US
dc.subject.pquncontrolledDNA condensationen_US
dc.subject.pquncontrolledGene deliveryen_US
dc.subject.pquncontrolledHKen_US
dc.subject.pquncontrollednanoparticlesen_US
dc.subject.pquncontrolledPEIen_US
dc.titlePHYSICAL CHARACTERIZATION OF DNA CONDENSED WITH CATIONIC AGENTSen_US
dc.typeThesisen_US

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