NSECT - Research Imaging Institute
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Transcript NSECT - Research Imaging Institute
Neutron Stimulated Emission
Computed Tomography (NSECT)
Drosoula Giantsoudi
Spring 2007
Presentation for Diagnostic Imaging II class
Outline
Introduction – What is NSECT
The physics behind
Methods of NSECT
Potential applications
Neutron radiation dose
Directions of present and future
research
What is NSECT?
Spectroscopic measurement of element
concentrations in the body using a neutron beam
γ emission computed tomography (ECT), γ rays
from stable isotopes stimulated by neutron
collisions
Image the naturally existing distribution of stable
isotopes along the path of the neutron beam
Not clinically applied yet
The physics behind NSECT
Fast neutron interactions:
– Elastic scattering
– Inelastic scattering
Energy given to the nucleus leaving
it in an excited state.
Characteristic gamma emission from
the γ-decay of the nucleus
Gamma energies for all elements:
100keV-6600keV except H and
He(25MeV)
Method description
Three required components:
Neutron source
2.8 MeV deuteron beam gas cell 6MeV
neutron beam
Imaging target – sample
– Energy emitted characteristic of the specific
element
Gamma spectrometer
– High purity germanium (HPGe) detector
Acquisition setup
Acquisition setup
Collimated neutron beam (2x2cm2, 1x1cm2 or
narrower)
Low – dose beam is scanned over the body
Cylindrical HPGe detectors - fine energy resolution
– Energy spectrum acquisition for each position of the beam
– Reconstruction of nuclei distribution into a tomographic
image – seperate for each element
– Image intensity corresponding to the concentration of that
element
Experimental Setup
http://dailabs.duhs.duke.edu
Disadvantages
Spatial resolution determined by the
collimated beam
Neutron beam collimation in a small size
not a trivial task
Limitations: narrow beams result in
decreased neutron flux
Longer acquisition time - patient motion
Another approach
Broad neutron beam geometry
– No translation of the target
or the beam necessary
Collimated Ge detector –
rotational collimators
Compton Coincidence Detector
(CCD) 2D projection
Spatial resolution determined by the detector
Decreased detection efficiency of the CCD due to
multiple coincidence requirement
Considerations-Challenges
Background suppression
– ‘sample-in-sample-out’ subtraction
– pulsed neutron beam, acquisition in the time window that
the photons are produced - TOF measurements
Normalization
– monitoring of the deuteron flux: collecting the charge
deposited onto the gas target cell
– neutron monitoring: thin plastic scintillator
– neutron monitor to beam current ratio
List-mode data acquisition, allowing for post setting
of parameters (detector bias, TOF windows)
Identification of specific elements
Spectra from basic elements: C, Ca, Fe, Cu,
water phantom (for O)
Analysis identifying the peaks (NNDC
databases)
γ-ray flux~(# target nuclei)×(neutron flux)×
(differential cross section)
Neutron and γ attenuation have small effect
for biomedical targets
http://www.sns.gov/workshops/ian2006/TU2/IAN2006oct_Kapadia.pdf
http://www.sns.gov/workshops/ian2006/TU2/IAN2006oct_Kapadia.pdf
Reconstructed Images
http://dailabs.duhs.duke.edu
Potential medical applications
Cancer diagnosis:
– difference in trace element concentrations in
tissues when malignancy begins to occur
– In vivo non destructive spectrometry=non invasive
biopsy long before anatomical changes
Non-invasive measurement of iron
– Important for thalassanemia, heamochromatosis
mutations, chronic blood transfusions
– No delay or morbidity associated with repeated
biopsy
Potential medical applications
Small animal spectroscopic imaging.
Molecular biology research
Study of metallo-protein transport
Follow the transport of stable
isotopesnew tool for pharmaceutical
development
Neutron radiation dose
Monte Carlo simulations – GEANT4 for 2.5 MeV neutron beam:
Two necessary factors:
– Fraction of # of incident neutrons that deposit energy in the subject (0.6)
– Average fraction of each neutron’s energy deposited (1.4MeV)
For a gamma peak of 30 counts, 10×106 incident neutrons (liver in
the abdomen)
1cm2 beam area, 10cm path through the liver, density 1.1g cm-3
Eabs= (Eav per neutron)×(#of incident neutrons)×(fraction of
neutrons interacting)=1.4MeV×107×0.6=8.4×106 MeV=1.34×10-6J
Effective Dose = Eabs ×QF ×WF=(1.34×10-6 J/0.011 kg)×10×0.5 =
0.0061 mSv < 0.02 mSv for a chest x-ray
Directions of present and
future research
High flux neutron source
– shorter scan time
– smaller collimation of the neutron beam
More efficient, multiple or collimated detectors
– better signal to noise ratio
– better spatial resolution
Extended dose simulations
Thank you!
References:
– Carey Floyd, C Howell, A Kapadia et al, Introduction
to neutron stimulated emission computed tomography,
Phys. Med. Biol. 51 (2006) 3375–3390
– http://www.sns.gov/workshops/ian2006/TU2/IAN2006
oct_Kapadia.pdf
– http://deckard.mc.duke.edu/research8.html
– http://www.aapm.org/meetings/04AM/VirtualPressRoo
m/NeutronImaging.pdf