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Sangeeta Ray Banerjee

Researcher at Johns Hopkins University School of Medicine

Publications -  81
Citations -  4099

Sangeeta Ray Banerjee is an academic researcher from Johns Hopkins University School of Medicine. The author has contributed to research in topics: Biodistribution & Prostate cancer. The author has an hindex of 35, co-authored 76 publications receiving 3583 citations. Previous affiliations of Sangeeta Ray Banerjee include Johns Hopkins University & Syracuse University.

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Synthesis and Evaluation of Technetium-99m- and Rhenium-Labeled Inhibitors of the Prostate-Specific Membrane Antigen (PSMA)

TL;DR: The prostate-specific membrane antigen (PSMA) is increasingly recognized as a viable target for imaging and therapy of cancer and can accommodate the steric requirements of (99m)Tc/Re complexes within PSMA inhibitors, the best results achieved with a linker moiety between the epsilon amine of the urea lysine and the chelator.
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Clinical applications of Gallium-68.

TL;DR: This review will focus on the clinical experience of selected, well-established and recently applied (68)Ga-labeled imaging agents used in nuclear medicine.
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68Ga-labeled inhibitors of prostate-specific membrane antigen (PSMA) for imaging prostate cancer.

TL;DR: Gallium-68 is a generator-produced radionuclide for positron emission tomography (PET) that is being increasingly used for radiolabeling of tumor-targeting peptides, and (68)Ga, a cyclotron-free isotope useful for clinical PET studies, with maintenance of target specificity.
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Bridging the gap between in vitro and in vivo imaging: isostructural Re and 99mTc complexes for correlating fluorescence and radioimaging studies.

TL;DR: A bifunctional ligand that is capable of forming Re and 99mTc complexes as complementary fluorescent and radioactive probes was developed and was incorporated into fMLFG, a peptide that binds to the formyl peptide receptor (FPR).
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New directions in the coordination chemistry of 99mTc: a reflection on technetium core structures and a strategy for new chelate design.

TL;DR: It is concluded that the single amino acid analogue chelates (SAAC), which are readily conjugated to small peptides by solid-phase synthesis methods and which form robust complexes with the {Tc(CO)3}1+ core, offer an effective alternative to the previously described methods.