The aim of this application is to develop novel contrast agents functionally specific to Cerenkov imaging. Cerenkov light emission occurs when beta particles emitted during radioactive decay exceed the speed of light in a dielectric medium. Cerenkov emission is multispectral and continuous across the visible wavelengths. A substantial fraction of the photons released are at wavelengths greater than 600 nm and as a result Cerenkov radiation can be detected using optical imaging techniques routinely used in small animals. This could be used to add functional capabilities to positron emission tomography (PET) imaging but can also act as a stand-alone imaging modality. We propose here Cerenkov specific contrast agents that report on function based on selective bandwidth quenching. The absorption of a selected band of photons by a functional chromophore attenuates the emission within a defined wavelength range and allows the measurement of a specific activity using a radiolabeled probe. To demonstrate this we synthesized prototype 18F-labeled pH-responsive Cerenkov probes based on standard pH indicators. A transition from acidic to basic causes a color change that selectively absorbs a band of photons, reducing detected Cerenkov emission. This selective bandwidth quenching can be achieved intermolecularly or intramolecularly and can be measured in vitro and in vivo. Moreover, ratiometric imaging at different wavelengths can report not only on the function imparted by the dye but also estimate other parameters including the depth of the probe. In this application we will synthesize and test Cerenkov specific contrast agents for detection of pH and redox status in tumors. Although the concept of selective bandwidth quenching is generally applicable, we chose these because they are important measures in tumor biology and because there are known dyes and studies available to validate our methods.
In Aim 1 we will synthetically optimize the pKa, max and lipophilicity of the pH sensitive dyes for in vivo detection of tumor pH and test these compounds in a sophisticated murine breast cancer model where lactate dehydrogenase has been silenced.
In Aim 2, we will increase specificity by optimizing acquisition parameters for ratiometric imaging and sensitivity by designing DOTA-chelated 90Y probes to increase detected signal by 20-30 fold.
In Aim 3, we will extend the overall concept by designing Cerenkov specific contrast agents for the detection of redox status in vitro and in vivo. The modulation of Cerenkov emission using selective bandwidth quenching defines a new imaging platform that can be used for the direct imaging of non-fluorescent chromophores in vivo. There are numerous dyes that functionally alter their absorption in response to chemical or physiological stimuli and many of these absorb at wavelengths appropriate for Cerenkov imaging. The successful development of this platform will allow the creation a wide range for contrast agents for dual Cerenkov-PET imaging to comprehensively describe tumor environment, metabolism and treatment.

Public Health Relevance

The goals of this application are to synthesize and test contrast agents to exploit the unique properties of Cerenkov imaging. The concept is based on the selective quenching of Cerenkov radiation by a functional dye that changes absorption wavelength based on pH or redox status. This defines a new paradigm of molecular imaging, allowing the detection of a wide range of reporter dyes that functionally alter their absorption in response to chemical or physiological stimuli. Cerenkov specific contrast can be used to add functionality to PET imaging or as a stand-alone imaging modality.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB018645-03
Application #
9057539
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Conroy, Richard
Project Start
2014-05-01
Project End
2018-04-30
Budget Start
2016-05-01
Budget End
2017-04-30
Support Year
3
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Kall, Stefanie L; Delikatny, Edward J; Lavie, Arnon (2018) Identification of a Unique Inhibitor-Binding Site on Choline Kinase ?. Biochemistry 57:1316-1325
Kachur, Alexander V; Arroyo, Alejandro D; Bryan, Nikaela W et al. (2017) Synthesis of pH indicators for Cerenkov imaging by electrophilic substitution of bromine by fluorine in an aromatic system. J Fluor Chem 200:146-152
Arlauckas, Sean P; Popov, Anatoliy V; Delikatny, E James (2016) Choline kinase alpha-Putting the ChoK-hold on tumor metabolism. Prog Lipid Res 63:28-40
Chiorazzo, Michael G; Bloch, Noah B; Popov, Anatoliy V et al. (2015) Synthesis and Evaluation of Cytosolic Phospholipase A(2) Activatable Fluorophores for Cancer Imaging. Bioconjug Chem 26:2360-70
Czupryna, Julie; Kachur, Alexander V; Blankemeyer, Eric et al. (2015) Cerenkov-specific contrast agents for detection of pH in vivo. J Nucl Med 56:483-8
Kachur, Alexander V; Arroyo, Alejandro D; Popov, Anatoliy V et al. (2015) Synthesis of F-18 labeled resazurin by direct electrophilic fluorination. J Fluor Chem 178:136-141