The use of radiometal-labeled small molecules conjugated to targeting proteins and peptides as diagnostic agents has been increasing. A major challenge in developing radiometal-based radiopharmaceuticals is ensuring metal chelate stability in vivo to avoid decreased contrast and increased radiation doses to non- target tissues and organs. Our current research has demonstrated the in vivo superiority of cross-bridged ligands (chelators) as carriers for copper radionuclides compared to traditional macrocyclic chelators, resulting in improved target uptake and pharmacokinetics of their chelator-peptide conjugates. To build on this advance, we propose to develop a second generation of cross-bridged chelators for copper-, indium- and gallium-based radiopharmaceuticals for diagnostic imaging and targeted radiotherapy of cancer. We will design pendant-armed cross-bridged cyclam and cyclen chelators that have convenient synthetic routes, enhanced radiometal binding ability, and more rapid complexation kinetics to enable efficient radiolabeling of proteins under mild conditions. We will prepare their metal complexes, assay their kinetic and thermodynamic properties, and verify correlations between these properties and in vivo behavior.
In Aim (I), new cross-bridged chelators will be synthesized.
In Aim (II), their copper, gallium, and indium complexes will be prepared and evaluated using acid inertness, electrochemical (Cu only) and stability constant criteria. Our working hypothesis, based on results from the current grant, is that ligands with a single anionic pendant arm are sufficient to ensure superior biological behavior, freeing the other arm for conjugation to targeting moieties.
In Aim (III), the most promising ligands will be labeled with Cu-64 (Ga-67,68 and ln-111) and evaluated in vitro and in vivo for stability and biological clearance. Bifunctional chelators will be synthesized and conjugated to the somatostatin analog Tyr3-octreotate. Biological evaluation of these in tumor-bearing rats will test Aim (II) predictions to optimize ligand design. Development of a second-generation of cross- bridged tetraamine chelators for metal radionuclides will advance the viability of copper, gallium and indium radiopharmaceuticals for diagnostic imaging and therapy of cancer. These will have a wide array of applications in small-molecule-, peptide- and protein-based imaging and therapy agents. Relevance: Effective detection and therapy of cancer by metal-based radiopharmaceuticals depend critically on the intact delivery of these drugs to target organs.
We aim to develop strong-binding radiometal carriers to ensure safe delivery of copper, gallium, and indium radioisotopes for both diagnosis and treatment of cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA093375-10
Application #
8056538
Study Section
Medical Imaging Study Section (MEDI)
Program Officer
Menkens, Anne E
Project Start
2002-01-01
Project End
2014-03-31
Budget Start
2011-04-01
Budget End
2014-03-31
Support Year
10
Fiscal Year
2011
Total Cost
$342,049
Indirect Cost
Name
University of New Hampshire
Department
Chemistry
Type
Schools of Engineering
DUNS #
111089470
City
Durham
State
NH
Country
United States
Zip Code
03824
Cai, Zhengxin; Li, Barbara T Y; Wong, Edward H et al. (2015) Cu(I)-assisted click chemistry strategy for conjugation of non-protected cross-bridged macrocyclic chelators to tumour-targeting peptides. Dalton Trans 44:3945-8
Hu, Lina Y; Bauer, Nadine; Knight, Leah M et al. (2014) Characterization and evaluation of (64)Cu-labeled A20FMDV2 conjugates for imaging the integrin ?v? 6. Mol Imaging Biol 16:567-77
Zeng, Dexing; Guo, Yunjun; White, Alexander G et al. (2014) Comparison of conjugation strategies of cross-bridged macrocyclic chelators with cetuximab for copper-64 radiolabeling and PET imaging of EGFR in colorectal tumor-bearing mice. Mol Pharm 11:3980-7
Cai, Zhengxin; Ouyang, Qin; Zeng, Dexing et al. (2014) 64Cu-labeled somatostatin analogues conjugated with cross-bridged phosphonate-based chelators via strain-promoted click chemistry for PET imaging: in silico through in vivo studies. J Med Chem 57:6019-29
Cai, Zhengxin; Anderson, Carolyn J (2014) Chelators for copper radionuclides in positron emission tomography radiopharmaceuticals. J Labelled Comp Radiopharm 57:224-30
Banerjee, Sangeeta Ray; Pullambhatla, Mrudula; Foss, Catherine A et al. (2014) ??Cu-labeled inhibitors of prostate-specific membrane antigen for PET imaging of prostate cancer. J Med Chem 57:2657-69
Nedrow, Jessie R; White, Alexander G; Modi, Jalpa et al. (2014) Positron emission tomographic imaging of copper 64- and gallium 68-labeled chelator conjugates of the somatostatin agonist tyr3-octreotate. Mol Imaging 13:
Zeng, Dexing; Ouyang, Qin; Cai, Zhengxin et al. (2014) New cross-bridged cyclam derivative CB-TE1K1P, an improved bifunctional chelator for copper radionuclides. Chem Commun (Camb) 50:43-5
Jiang, Majiong; Ferdani, Riccardo; Shokeen, Monica et al. (2013) Comparison of two cross-bridged macrocyclic chelators for the evaluation of 64Cu-labeled-LLP2A, a peptidomimetic ligand targeting VLA-4-positive tumors. Nucl Med Biol 40:245-51
Ferdani, Riccardo; Stigers, Dannon J; Fiamengo, Ashley L et al. (2012) Synthesis, Cu(II) complexation, 64Cu-labeling and biological evaluation of cross-bridged cyclam chelators with phosphonate pendant arms. Dalton Trans 41:1938-50

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