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dc.contributor.authorRioux, James
dc.date.accessioned2012-08-14T12:27:18Z
dc.date.available2012-08-14T12:27:18Z
dc.date.issued2012-08-14
dc.identifier.urihttp://hdl.handle.net/10222/15229
dc.description.abstractMagnetic Resonance Imaging can now detect cells that are labeled with contrast agents such as superparamagnetic iron oxide (SPIO). Quantitative monitoring, which is desirable for evaluating cellular therapies, remains challenging. In this work, an MRI technique called TurboSPI is implemented for quantitative cellular imaging. TurboSPI acquires maps of the relaxation rate R2', which is directly related to SPIO concentration. Quantification of R2' is demonstrated using micron-sized iron oxide particles and SPIO-labeled cells. To explain experimental results that deviated from predicted behavior, an extended analytical description of MRI signal relaxation near SPIO was developed. This model compares well to Monte Carlo simulations and experimental data, and may allow improved quantification. The slow imaging speed of TurboSPI is overcome using a signal processing technique called compressed sensing to reconstruct undersampled data, enabling in vivo animal imaging with TurboSPI. Such images demonstrate detection of iron with improved specificity and good potential for quantification.en_US
dc.language.isoenen_US
dc.subjectMagnetic Resonance Imagingen_US
dc.subjectCellular Imagingen_US
dc.subjectQuantitative Imagingen_US
dc.subjectMR Relaxometryen_US
dc.subjectCompressed Sensingen_US
dc.titleQuantitative Magnetic Resonance Imaging of Cellular Density with TurboSPIen_US
dc.date.defence2012-08-01
dc.contributor.departmentDepartment of Physics & Atmospheric Scienceen_US
dc.contributor.degreeDoctor of Philosophyen_US
dc.contributor.external-examinerDr. Blaine Chroniken_US
dc.contributor.graduate-coordinatorDr. Randall Martinen_US
dc.contributor.thesis-readerDr. Steven Beyeaen_US
dc.contributor.thesis-readerDr. Laurent Kreplaken_US
dc.contributor.thesis-supervisorDr. Chris Bowen, Dr. Kevin Hewitten_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNot Applicableen_US
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