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dc.contributor.advisorDarrell J. Irvine.en_US
dc.contributor.authorYang, Yu-Sang Sabrinaen_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Materials Science and Engineering.en_US
dc.date.accessioned2013-09-24T19:40:17Z
dc.date.available2013-09-24T19:40:17Z
dc.date.copyright2013en_US
dc.date.issued2013en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/81061
dc.descriptionThesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2013.en_US
dc.descriptionCataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (p. 70-72).en_US
dc.description.abstractStriped gold nanoparticles (NPs), inorganic particles protected by an amphiphilic mixed organic ligand shell, are the most recent and potent evolution of gold nanoparticle intracellular delivery vectors. Here we propose the combination of striped gold nanoparticles with lipid vesicles of diameter < 200 nm in order to concentrate their delivery and couple their delivery to the delivery of pharmaceuticals. Mechanisms of penetration of striped gold nanoparticles into live cell membranes via non-endocytic pathways was poorly understood, therefore this work focuses on the interaction of striped NPs with synthetic lipid membranes as models for cellular membranes, and interactions with bacterial membranes have been investigated to provide a more stringent test of their interaction capacity. Cellular uptake of striped gold nanoparticles has been observed to be homogeneous when delivered via interbilayer crosslinked multilamellar lipid vesicles, which resulted in enhancement of striped gold nanoparticle induced radiosensitization causing membrane rupture and genomic damage.en_US
dc.description.statementofresponsibilityby Yu-Sang Yang.en_US
dc.format.extent72 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectMaterials Science and Engineering.en_US
dc.titleInteraction of amphiphilic gold nanoparticles with lipid membranes and their application to cancer radiotherapyen_US
dc.typeThesisen_US
dc.description.degreeS.M.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.oclc857792301en_US


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