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Grant: Discovery Grants Program - Individual

University of Western Ontario

$15,000.00

Development of SPECT for in vivo 3D cell tracking

FY 2007-08

Summary
Medical imaging is undergoing a revolution fueled by both advances in imaging technology and advances in imaging probes. New probes, arising from discoveries in molecular biology, allow imaging of very specific molecular events - provided that imaging technology can be adapted to their detection. Central to realizing the potential of the medical imaging revolution are three challenges: (1) Imaging molecular pathways: Imaging of multiple probes simultaneously to follow related molecular processes; (2) Providing context: Combining the imaging of probes with the imaging of anatomy to localize the molecular events relative to underlying anatomical structure; and (3) Ensuring accessibility: Making the imaging technology cost-effective and widely deployable. An imaging technology with the potential to meet these challenges is Single Photon Emission Computed Tomography (SPECT). SPECT is inherently multi-spectral, allowing for the simultaneous imaging of multiple radioactively labeled probes. The rich functional information provided by SPECT can be placed into the context of underlying anatomy through hybrid SPECT/CT, which is readily available and increasingly popular. Finally, SPECT is already deployed widely throughout Canada. The inevitable evolution of SPECT to solid-state detector technology promises to multiply its multi-spectral capabilities. Our development of reconstruction algorithms designed for imaging large objects with smaller cost-effective detectors will help make this evolution more economically feasible. We propose to optimize SPECT for in vivo cell tracking - an emerging niche with applications in cardiac, neural, and pancreatic regenerative therapy; oncology; and developmental biology. Our theoretical work includes state-of-the-art computer simulations and reconstruction techniques; while our experimental efforts focus on phantoms and large animals (canines). The focus of our application is monitoring myocardial stem cell therapy in a canine model of heart disease because of availability in our research institute, and because it represents the majority of challenges to be solved in molecular imaging and cell tracking.
Program
Discovery Grants Program - Individual
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
327598-2007
Name nom
Stodilka, Robert
Department département
Medical Biophysics
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2007
Award amount
15000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
29
Committee name en
General Physics
Committee name fr
Physique générale
Area of application code
518
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Medical equipment and apparatus
Area of application fr
Appareils et instruments médicaux
Research subject code
1900
Research subject group en
Biomedical engineering
Research subject group fr
Génie biomédical
Research subject en
Biomedical engineering
Research subject fr
Génie biomédical
Partie
1
Nb partie
3
Application title
Development of SPECT for in vivo 3D cell tracking
Keyword
NA
Application summary
Medical imaging is undergoing a revolution fueled by both advances in imaging technology and advances in imaging probes. New probes, arising from discoveries in molecular biology, allow imaging of very specific molecular events - provided that imaging technology can be adapted to their detection. Central to realizing the potential of the medical imaging revolution are three challenges: (1) Imaging molecular pathways: Imaging of multiple probes simultaneously to follow related molecular processes; (2) Providing context: Combining the imaging of probes with the imaging of anatomy to localize the molecular events relative to underlying anatomical structure; and (3) Ensuring accessibility: Making the imaging technology cost-effective and widely deployable. An imaging technology with the potential to meet these challenges is Single Photon Emission Computed Tomography (SPECT). SPECT is inherently multi-spectral, allowing for the simultaneous imaging of multiple radioactively labeled probes. The rich functional information provided by SPECT can be placed into the context of underlying anatomy through hybrid SPECT/CT, which is readily available and increasingly popular. Finally, SPECT is already deployed widely throughout Canada. The inevitable evolution of SPECT to solid-state detector technology promises to multiply its multi-spectral capabilities. Our development of reconstruction algorithms designed for imaging large objects with smaller cost-effective detectors will help make this evolution more economically feasible. We propose to optimize SPECT for in vivo cell tracking - an emerging niche with applications in cardiac, neural, and pancreatic regenerative therapy; oncology; and developmental biology. Our theoretical work includes state-of-the-art computer simulations and reconstruction techniques; while our experimental efforts focus on phantoms and large animals (canines). The focus of our application is monitoring myocardial stem cell therapy in a canine model of heart disease because of availability in our research institute, and because it represents the majority of challenges to be solved in molecular imaging and cell tracking.