Show simple item record

dc.contributor.advisorTunnell, James W.en
dc.creatorPark, Jaesooken
dc.date.accessioned2010-11-09T16:36:15Zen
dc.date.accessioned2010-11-09T16:36:35Zen
dc.date.available2010-11-09T16:36:15Zen
dc.date.available2010-11-09T16:36:35Zen
dc.date.created2010-08en
dc.date.issued2010-11-09en
dc.date.submittedAugust 2010en
dc.identifier.urihttp://hdl.handle.net/2152/ETD-UT-2010-08-1885en
dc.descriptiontexten
dc.description.abstractGold nanoparticles (GNP) have been widely used as optical imaging and photothermal therapy agents due to their biocompatibility, simplicity of conjugation chemistry, optical tunability and efficient light conversion to heat. A number of in vitro and in vivo studies have demonstrated that they can be used as effective thermal therapy and imaging contrast agents to treat and diagnose cancer. As clinical applications of GNPs for cancer imaging and therapy have gained interest, efforts for understanding their accumulation kinetics has become more important. Given the recent demonstration of intrinsic two-photon induced photoluminescence (TPIP) of gold nanoshells (GNSs) and gold nanorods (GNRs), TPIP imaging is an efficient tool for investigating the microscopic distribution of the GNPs at intra-organ level. The following work explores these GNPs’ physical and optical properties for effective use of GNPs in TPIP imaging and examines the feasibility of using intrinsic TPIP imaging to investigate GNP’s biodistribution in bulk tumors and thin tissue slices processed for standard histology. Our results showed that GNPs yield a strong TPIP signal, and we found that the direct luminescence-based contrast imaging of GNPs can image both GNPs and nuclei, cytoplasm or vasculature simultaneously. Also, we present the effect of GNP morphology on their distribution within organs. Collected images showed that GNPs had a heterogeneous distribution with higher accumulation at the tumor periphery. However, GNRs had deeper penetration into tumor than GNRs due to their shape and size. In addition, GNPs were observed in unique patterns close to vasculature. Finally, we introduce single- and multiple-dose administrations of GNPs as a way of increasing GNP accumulation in tumor. Our results show that multiple dosing can increase GNP accumulation in tumor 1.6 to 2 times more than single dosing. Histological analysis also demonstrated that there were no signs of acute toxicity in tumor, liver and spleen excised from the mice receiving 1 injection, 5 injections of GNPs and trehalose injection.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.subjectTPIP imagingen
dc.subjectTwo-photon induced photoluminescenceen
dc.subjectGold nanoshellen
dc.subjectGold nanoroden
dc.subjectTwo-photon excitationen
dc.subjectExcitation processen
dc.subjectTumorsen
dc.subjectGNPen
dc.subjectGold nanoparticlesen
dc.titleInvestigation of gold nanoparticle accumulation kinetics for effective cancer targetingen
dc.date.updated2010-11-09T16:36:35Zen
dc.contributor.committeeMemberDunn, Andrew K.en
dc.contributor.committeeMemberSokolov, Konstantinen
dc.contributor.committeeMemberRoy, Krishnenduen
dc.contributor.committeeMemberKrishnan, Sunilen
dc.description.departmentBiomedical Engineeringen
dc.type.genrethesisen
thesis.degree.departmentBiomedical Engineeringen
thesis.degree.disciplineBiomedical Engineeringen
thesis.degree.grantorUniversity of Texas at Austinen
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record