Preclinical molecular imaging is used in studying animal models of human disease, evaluating new therapeutic drugs, and in carrying out research in basic biology. Optical imaging techniques, such as bioluminescence and multispectral fluorescence imaging, currently are widely used for preclinical functional imaging despite their depth dependent limitations on quantitation, resolution and sensitivity. Nuclear imaging techniques, SPECT and PET, are more closely translational. Dedicated preclinical SPECT and PET systems provide quite good imaging capability, but can be expensive, difficult (for non-experts), and slow to use. Optical systems are widely available, relatively affordable, easy to operate, and quick (for setup, imaging, and data analysis; i.e. high-throughput). For some imaging tasks a dedicated SPECT system would be essential, but for many studies a high-throughput acquisition of projection images would be sufficient and gains from cost reduction and speed could be significant. High resolution planar images of gamma-ray emitting radiotracers can be obtained by retrofitting a small animal optical imaging system (such as an IVIS Spectrum (Perkin-Elmer)) with a pinhole collimator and a large area CsI:Tl scintillator with a novel morphology. Recent progress at Radiation Monitoring Devices (RMD) has led to thick, transparent, crystalline microcolumnar structure (CMS) scintillator detectors of CsI(Tl) that simultaneously provide high gamma-ray absorption efficiency, high intrinsic spatial resolution, and bright light emission. The ability to use an existing commercial preclinical optical imaging system to rapidly acquire planar gamma ray images with good spatial resolution of one or possibly multiple animals would be a new and useful tool for high throughput screening of molecular imaging probes. Adding a nuclear imaging capability to the many existing preclinical optical imaging systems is an appealing opportunity for greatly expanded access to that modality of molecular imaging. The goal of this proposal is to build and characterize an insert which can be placed in an existing optical imaging system, where the insert uses a collimator and scintillator to enable gamma rays to be imaged by the existing sensitive CCD camera. The collimators used will be from a commercial SPECT imaging system. In this project we will: (1) develop protocols for production of large (15 cm diameter) thick (up to 4 mm) CMS CsI(Tl) films with improved light transmission; (2) simulate collimator and detector configurations using the GATE software package; (3) produce three large CMS detectors for use in an optical system insert; (4) fabricate an insert with flexible geometry for a variety of collimator and scintillator configurations, and perform phantom imaging studies to characterize the system; and (5) conduct two proof-of-concept animal imaging studies to demonstrate the potential for dynamic imaging and for high resolution imaging of a smaller field of view.

Public Health Relevance

Single photon emission computed tomography (SPECT) is a method of molecular imaging with gamma-emitting radionuclides; it is used in clinical practice, and also preclinically to study biological processes for both basic science and models of disease. While preclinical commercial SPECT scanners can yield tomographic images of small animals with excellent spatial resolution and good quantitative accuracy, the systems are expensive and complicated to operate for nonexperts. On the other hand, preclinical optical molecular imaging using visible wavelength photons is now in common research use, and commercial optical scanners are comparatively affordable and easy to use. We are developing an insert with a collimator and a crystalline microcolumnar structure (CMS) scintillation detector, to be placed above the animal in an optical imaging system. The insert enables the system's sensitive CCD camera to image gamma rays by their interactions in the scintillator, and thereby obtain a projection image of the distribution of gamma-emitting radiotracer in the animal. There is great potential for increased access by researchers to nuclear imaging; even for researchers with access to modern preclinical SPECT systems, this capability would be useful for high-throughput screening applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21EB018601-02
Application #
8934102
Study Section
Biomedical Imaging Technology Study Section (BMIT)
Program Officer
Sastre, Antonio
Project Start
2014-09-25
Project End
2017-07-31
Budget Start
2015-08-01
Budget End
2017-07-31
Support Year
2
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of California Davis
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618