Bifunctional HPPH-N2S2-99mTc conjugates as tumor imaging agents: synthesis and biodistribution studies

Author:

Ma Bing1,Li Guolin1,Kanter Peter2,Lamonica Dominick1,Grossman Zachary3,Pandey Ravindra K.14

Affiliation:

1. Department of Nuclear Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263, USA

2. Department of Drug and Treatment Development, Roswell Park Cancer Institute, Buffalo, NY 14263, USA

3. Department of Radiology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA

4. PDT center, Roswell Park Cancer Institute, Buffalo, NY 14263, USA

Abstract

Pyropheophorbide-a and the corresponding 3-(1'-hexyloxyethyl)-3-devinyl derivative ( HPPH ), the tumor-avid photosensitizers were conjugated with mono- or di-bisaminoethanethiols ( N 2 S 2 ligand). The in vivo biodistribution study of the related 99m Tc complexes was performed in F-344 rats bearing Ward colon tumors at 4 h and 24 h post injection. These data show that the complexes are stable and among four tracers, HPPH di-99 m Tc N 2 S 2 conjugate reaches the highest tumor uptake (%ID/g). The larger tumors reach higher concentrations of the tracer. However, the short 6 h half life of 99 m Tc is incompatible with the 24 h imaging time, suggesting that the use of a longer-lived isotope such as 111 In could still provide a useful scanning agent, or that further structure-activity screening could yield an HPPH analog with more appropriate pharmacokinetics for tumor imaging with 99 m Tc .

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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