| Literature DB >> 24900470 |
Alla Darwish1, Megan Blacker2, Nancy Janzen1, Stephanie M Rathmann1, Shannon Czorny1, Shawn M Hillier3, John L Joyal3, John W Babich3, John F Valliant1.
Abstract
A new prosthetic group referred to as the triazole appending agent (TAAG) was developed as a means to prepare targeted radioiodine-based molecular imaging and therapy agents. Tributyltin-TAAG and the fluorous analogue were synthesized in high yield using simple click chemistry and the products labeled in greater than 95% RCY with (123)I. A TAAG derivative of an inhibitor of prostate-specific membrane antigen was prepared and radiolabeled with (123)I in 85% yield where biodistribution studies in LNCap prostate cancer tumor models showed rapid clearance of the agent from nontarget tissues and tumor accumulation of 20% injected dose g(-1) at 1 h. The results presented demonstrate that the TAAG group promotes minimal nonspecific binding and that labeled conjugates can achieve high tumor uptake and exquisite target-to-nontarget ratios.Entities:
Keywords: SPECT; imaging; iodine; radiochemistry; radiopharmaceuticals
Year: 2012 PMID: 24900470 PMCID: PMC4025841 DOI: 10.1021/ml300003v
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345