Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging
The development of hybrid PET/MRI imaging systems needs to be paralleled with the development of a hybrid intrinsic PET/MRI probes. The aim of this work was to develop and validate a novel radio-superparamagnetic nanoparticle (r-SPNP) for hybrid PET/MRI imaging. This was achieved with the synthesis...
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ndltd-vcu.edu-oai-scholarscompass.vcu.edu-etd-42522017-03-17T08:27:14Z Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging Hoffman, David The development of hybrid PET/MRI imaging systems needs to be paralleled with the development of a hybrid intrinsic PET/MRI probes. The aim of this work was to develop and validate a novel radio-superparamagnetic nanoparticle (r-SPNP) for hybrid PET/MRI imaging. This was achieved with the synthesis of superparamagnetic iron oxide nanoparticles (SPIONs) that intrinsically incorporated 59Fe and manganese iron oxide nanoparticles (MIONs) that intrinsically incorporated 52Mn. Both [59Fe]-SPIONs and [52Mn]-MIONs were produced through thermal decomposition synthesis. The physiochemical characteristics of the r-SPNPs were assessed with TEM, DLS, and zeta-potential measurements, as well as in imaging phantom studies. The [59Fe]-SPIONs were evaluated in vivo with biodistribution and MR imaging studies. The biodistrubution studies of [59Fe]-SPIONs showed uptake in the liver. This corresponded with major MR signal contrast measured in the liver. 52Mn was produced on natural chromium through the 52Cr(p,n)52Mn reaction. The manganese radionuclides were separated from the target material through a liquid-liquid extraction. The αVβ3 integrin binding of [52Mn]-MION-cRGDs was evaluated with αVβ3 integrin solid phase assays, and the expression of αVβ3 integrin in U87MG xenograft tumors was characterized with fluorescence flow cytometry. [52Mn]-MION-cRGDs were used for in vivo PET and MR imaging of U87MG xenograft tumor bearing mice. PET data showed increased [52Mn]-MION-cRGD uptake compared with untargeted [52Mn]-MIONs. ROI analysis of PET and MRI data showed that MR contrasted corresponded with PET signal. Future work will utilize [52Mn]-MION-cRGDs in other tumor models and with hybrid PET/MRI imaging systems. 2013-12-03T08:00:00Z text application/pdf http://scholarscompass.vcu.edu/etd/3253 http://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=4252&context=etd © The Author Theses and Dissertations VCU Scholars Compass PET MRI Nanoparticle Medical Imaging Molecular Imaging Health and Medical Physics Medicine and Health Sciences Public Health |
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PET MRI Nanoparticle Medical Imaging Molecular Imaging Health and Medical Physics Medicine and Health Sciences Public Health Hoffman, David Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging |
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The development of hybrid PET/MRI imaging systems needs to be paralleled with the development of a hybrid intrinsic PET/MRI probes. The aim of this work was to develop and validate a novel radio-superparamagnetic nanoparticle (r-SPNP) for hybrid PET/MRI imaging. This was achieved with the synthesis of superparamagnetic iron oxide nanoparticles (SPIONs) that intrinsically incorporated 59Fe and manganese iron oxide nanoparticles (MIONs) that intrinsically incorporated 52Mn. Both [59Fe]-SPIONs and [52Mn]-MIONs were produced through thermal decomposition synthesis. The physiochemical characteristics of the r-SPNPs were assessed with TEM, DLS, and zeta-potential measurements, as well as in imaging phantom studies. The [59Fe]-SPIONs were evaluated in vivo with biodistribution and MR imaging studies. The biodistrubution studies of [59Fe]-SPIONs showed uptake in the liver. This corresponded with major MR signal contrast measured in the liver. 52Mn was produced on natural chromium through the 52Cr(p,n)52Mn reaction. The manganese radionuclides were separated from the target material through a liquid-liquid extraction. The αVβ3 integrin binding of [52Mn]-MION-cRGDs was evaluated with αVβ3 integrin solid phase assays, and the expression of αVβ3 integrin in U87MG xenograft tumors was characterized with fluorescence flow cytometry. [52Mn]-MION-cRGDs were used for in vivo PET and MR imaging of U87MG xenograft tumor bearing mice. PET data showed increased [52Mn]-MION-cRGD uptake compared with untargeted [52Mn]-MIONs. ROI analysis of PET and MRI data showed that MR contrasted corresponded with PET signal. Future work will utilize [52Mn]-MION-cRGDs in other tumor models and with hybrid PET/MRI imaging systems. |
author |
Hoffman, David |
author_facet |
Hoffman, David |
author_sort |
Hoffman, David |
title |
Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging |
title_short |
Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging |
title_full |
Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging |
title_fullStr |
Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging |
title_full_unstemmed |
Hybrid PET/MRI Nanoparticle Development and Multi-Modal Imaging |
title_sort |
hybrid pet/mri nanoparticle development and multi-modal imaging |
publisher |
VCU Scholars Compass |
publishDate |
2013 |
url |
http://scholarscompass.vcu.edu/etd/3253 http://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=4252&context=etd |
work_keys_str_mv |
AT hoffmandavid hybridpetmrinanoparticledevelopmentandmultimodalimaging |
_version_ |
1718427981036126208 |