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Title: Positron emission tomography (PET) imaging of neuroblastoma and melanoma with 64Cu-SarAr immunoconjugates
Authors: Voss, SD
Smith, SV
DiBartolo, N
McIntosh, LJ
Cyr, EM
Bonab, AA
Dearling, JLJ
Carter, EA
Fischman, AJ
Treves, ST
Gillies, SD
Sargeson, AM
Huston, JS
Packard, AB
Keywords: Positron computed tomography
Tracer techniques
Copper 64
Issue Date: 30-Oct-2007
Publisher: National Academy of Sciences
Citation: Voss, S. D., Smith, S. V., DiBartolo, N., McLntos, L. J., Cyr, E. M., Bonab, A. A., Dearling, J. L. J., Carter, E. A., Fischman, A. J., Treves, S. T., Gillies, S. D., Sargeson, A. M., Huston, J. S., & Packard, A. B. (2007). Positron emission tomography (PET) imaging of neuroblastoma and melanoma with Cu-64-SarAr immunoconjugates. Proceedings of the National Academy of Sciences of the United States of America, 104(44), 17489-17493. doi:10.1073/pnas.0708436104
Abstract: The advancement of positron emission tomography (PET) depends on the development of new radiotracers that will complement 18F-FDG. Copper-64 (64Cu) is a promising PET radionuclide, particularly for antibody-targeted imaging, but the high in vivo lability of conventional chelates has limited its clinical application. The objective of this work was to evaluate the novel chelating agent SarAr (1-N-(4-aminobenzyl)-3, 6,10,13,16,19-hexaazabicyclo[6.6.6] eicosane-1,8-diamine) for use in developing a new class of tumor-specific 64Cu radiopharmaceuticals for imaging neuroblastoma and melanoma. The anti-GD2 monoclonal antibody (mAb) 14.G2a, and its chimeric derivative, ch14.18, target disialogangliosides that are overexpressed on neuroblastoma and melanoma. Both mAbs were conjugated to SarAr using carbodiimide coupling. Radiolabeling with 64Cu resulted in >95% of the 64Cu being chelated by the immunoconjugate. Specific activities of at least 10 μCi/μg (1 Ci = 37 GBq) were routinely achieved, and no additional purification was required after 64Cu labeling. Solid-phase radioimmunoassays and intact cell-binding assays confirmed retention of bioactivity. Biodistribution studies in athymic nude mice bearing s.c. neuroblastoma (IMR-6, NMB-7) and melanoma (M21) xenografts showed that 15–20% of the injected dose per gram accumulated in the tumor at 24 hours after injection, and only 5–10% of the injected dose accumulated in the liver, a lower value than typically seen with other chelators. Uptake by a GD2-negative tumor xenograft was significantly lower (<5% injected dose per gram). MicroPET imaging confirmed significant uptake of the tracer in GD-2-positive tumors, with minimal uptake in GD-2-negative tumors and nontarget tissues such as liver. The 64Cu-SarAr-mAb system described here is potentially applicable to 64Cu-PET imaging with a broad range of antibody or peptide-based imaging agents. © 2007, National Academy of Sciences
Gov't Doc #: 2883
ISSN: 0027-8424
Appears in Collections:Journal Articles

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