Canada Spends Logo

Explorez notre analyse du budget 2026

Grant: Engage Grants Program

University of Ontario Institute of Technology

$23,500.00

Radiation Dose Estimates to Populations in Urban and Rural Settings from Accidental or Malicious Release of Radionuclides for Development of Automated Cytogenetic Dosimetry

EF 2016-17

Résumé
In a large scale release of radionuclides from a nuclear accident or malicious event, there may be masscasualties requiring rapid triage and treatment to prevent or mitigate illness from the radiation exposure. The""Gold Standard"" for determining the magnitude of radiation exposure post-event is a cytogenetic techniquescalled chromosome aberration analysis (CAA). The most useful CAA technique is chromosome dicentricanalysis. One of the issues for using dicentric analysis in a mass casualty event is that it is extremely timeconsuming, as typically it is personnel intensive to look at metaphase spreads for aberrations. To speed up theprocess, automated software is desirable to examine the spreads and determine the number of aberrations.Since aberration count is proportional to dose, it is then possible to estimate dose in exposure persons.CytoGnomics has developed a state-of-the art image analyzer for estimating dicentrics, called ADCI.However, to demonstrate the efficacy of this software for mass casualty events, the image analysis softwareneeds to be benchmarked. To this end, a simulated biodosimetry analysis on a population, incorporatinggeographic information system (GIS)-calibrated population dose estimates into these analyses will beperformed. Patient datasets will be sampled from radiation calibrated metaphase cell images fromCytoGnomix. HPAC software will be used to model physical dosimetry exposures in an actual radiologicaldispersal scenario. HPAC estimates of physical doses will be used to calibrate the cytogenetic biodosimetrydata. Key issues to be addressed from this analysis are: 1) To interpolate biological radiation exposures forindividuals who were not tested using dose estimates from those who were tested, 2) To determine the densityof individuals affected, 3) To determine the minimum number of individuals that need to be sampled from thetotal population exposed, 4) To determine the variance on dose estimates based on population locationclustering and sampling of clusters. We will further determine 5) the compute time required to complete theseanalyses. The overall goal of this project will be to provide a fully-operational prototype system.
Programme
Engage Grants Program
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
507587-2016
Name nom
Waller, Edward
Department département
Energy Systems & Nuclear Science, Faculty of
Organization id
19222
Institution établissement
University of Ontario Institute of Technology
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2016
Competition year année de concours
2016
Award amount
23500
Program id
EGP
Program name en
Engage Grants Program
Program name fr
Programme de subventions d'engagement partenariat
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
1553
Committee name en
Ontario Internal Decision Committee
Committee name fr
Comité de décision interne pour l'Ontario
Area of application code
405
Area of application group en
Environment
Area of application group fr
Environnement
Area of application en
Modelling and mathematical simulation of natural processes
Area of application fr
Modélisation et simulation mathématique des processus naturels
Research subject code
2402
Research subject group en
Nuclear engineering
Research subject group fr
Génie nucléaire
Research subject en
Radioactive materials
Research subject fr
Matériaux radioactifs
Partie
1
Nb partie
1
Application title
Radiation Dose Estimates to Populations in Urban and Rural Settings from Accidental or Malicious Release of Radionuclides for Development of Automated Cytogenetic Dosimetry
Keyword
NSERC
Application summary
In a large scale release of radionuclides from a nuclear accident or malicious event, there may be masscasualties requiring rapid triage and treatment to prevent or mitigate illness from the radiation exposure. The""Gold Standard"" for determining the magnitude of radiation exposure post-event is a cytogenetic techniquescalled chromosome aberration analysis (CAA). The most useful CAA technique is chromosome dicentricanalysis. One of the issues for using dicentric analysis in a mass casualty event is that it is extremely timeconsuming, as typically it is personnel intensive to look at metaphase spreads for aberrations. To speed up theprocess, automated software is desirable to examine the spreads and determine the number of aberrations.Since aberration count is proportional to dose, it is then possible to estimate dose in exposure persons.CytoGnomics has developed a state-of-the art image analyzer for estimating dicentrics, called ADCI.However, to demonstrate the efficacy of this software for mass casualty events, the image analysis softwareneeds to be benchmarked. To this end, a simulated biodosimetry analysis on a population, incorporatinggeographic information system (GIS)-calibrated population dose estimates into these analyses will beperformed. Patient datasets will be sampled from radiation calibrated metaphase cell images fromCytoGnomix. HPAC software will be used to model physical dosimetry exposures in an actual radiologicaldispersal scenario. HPAC estimates of physical doses will be used to calibrate the cytogenetic biodosimetrydata. Key issues to be addressed from this analysis are: 1) To interpolate biological radiation exposures forindividuals who were not tested using dose estimates from those who were tested, 2) To determine the densityof individuals affected, 3) To determine the minimum number of individuals that need to be sampled from thetotal population exposed, 4) To determine the variance on dose estimates based on population locationclustering and sampling of clusters. We will further determine 5) the compute time required to complete theseanalyses. The overall goal of this project will be to provide a fully-operational prototype system.