The principal aim of the research is to provide a method of reconstruction for tomography (SPECT, PET, TOFPET, X-CT) which represents a substantial improvement in terms of image quality and instrument design flexibility over the presently available techniques. The new proposed method is based on calculating accurately the response matrix of an imaging instrument, optimizing its design by mathematical analytic methods and using the final response matrix as the probability function needed for a maximum likelihood estimator (MLE) reconstruction algorithm. In addition, we propose to study processor architectures for the purpose of designing and building a prototype processor that can open the way to a future cost-effective implementation of the MLE algorithm. The MLE algorithm has been shown to provide substantial improvements in image quality in PET tomography. Unfortunately the long computation times and/or the large amount of storage needed for its implementation make immediate use and even research on the method impractical. By providing a well validated group of programs that calculate the probability functions for an imaging instrument including effects due to incidence angle and position, energy resolution and cross-talk, and by developing an effective method of image analysis, we expect to optimize the MLE imaging problem. The demonstrated favorable computing power-to-cost ratio of microprocessor cluster architectures and array processors can then be exploited to implement the MLE algorithm. The proposed research program could have a substantial impact in all areas of medical research and diagnosis which use tomography by providing higher sensitivity, spatial accuracy, contrast, resolution design flexibility and better utilization of emitted radiation. This is particularly more important now, with the development of new high resolution instruments.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA039501-02
Application #
3178549
Study Section
Diagnostic Radiology Study Section (RNM)
Project Start
1986-05-01
Project End
1988-04-30
Budget Start
1987-05-01
Budget End
1988-04-30
Support Year
2
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Lawrence Berkeley National Laboratory
Department
Type
Organized Research Units
DUNS #
078576738
City
Berkeley
State
CA
Country
United States
Zip Code
94720
Llacer, J; Veklerov, E; Nunez, J (1991) Stopping rules, Bayesian reconstructions and sieves. Prog Clin Biol Res 363:81-93
Kupfer, A; Singer, S J; Dennert, G (1986) On the mechanism of unidirectional killing in mixtures of two cytotoxic T lymphocytes. Unidirectional polarization of cytoplasmic organelles and the membrane-associated cytoskeleton in the effector cell. J Exp Med 163:489-98
Dennert, G; Anderson, C G; Warner, J (1986) Induction of bone marrow allograft rejection and hybrid resistance in nonresponder recipients by antibody: is there evidence for a dual receptor interaction in acute marrow graft rejection? J Immunol 136:3981-6
Criado, M; Lindstrom, J M; Anderson, C G et al. (1985) Cytotoxic granules from killer cells: specificity of granules and insertion of channels of defined size into target membranes. J Immunol 135:4245-51
Dennert, G (1985) Mechanism of cell-mediated cytolysis by natural killer cells. Surv Synth Pathol Res 4:69-83
Dennert, G (1985) Immunostimulation by retinoic acid. Ciba Found Symp 113:117-31
Dennert, G; Anderson, C G; Warner, J (1985) T killer cells play a role in allogeneic bone marrow graft rejection but not in hybrid resistance. J Immunol 135:3729-34
Kupfer, A; Dennert, G; Singer, S J (1985) The reorientation of the Golgi apparatus and the microtubule-organizing center in the cytotoxic effector cell is a prerequisite in the lysis of bound target cells. J Mol Cell Immunol 2:37-49
Schulz, G; Staffileno, L K; Reisfeld, R A et al. (1985) Eradication of established human melanoma tumors in nude mice by antibody-directed effector cells. J Exp Med 161:1315-25