posted on 2016-09-27, 00:00authored byAbdolreza Yazdani, Holly Bilton, Alyssa Vito, Afaf R. Genady, Stephanie
M. Rathmann, Zainab Ahmad, Nancy Janzen, Shannon Czorny, Brian M. Zeglis, Lynn C. Francesconi, John F. Valliant
A high yield synthesis
of a novel, small molecule, bisphosphonate-modified trans-cyclooctene (TCO-BP, 2) that binds to
regions of active bone metabolism and captures functionalized tetrazines
in vivo, via the bioorthogonal inverse electron demand Diels–Alder
(IEDDA) cycloaddition, was developed. A 99mTc-labeled derivative
of 2 demonstrated selective localization to shoulder
and knee joints in a biodistribution study in normal mice. Compound 2 reacted rapidly with a 177Lu-labeled tetrazine
in vitro, and pretargeting experiments in mice, using 2 and the 177Lu-labeled tetrazine, yielded high activity
concentrations in shoulder and knee joints, with minimal uptake in
other tissues. Pretargeting experiments with 2 and a
novel 99mTc-labeled tetrazine also produced high activity
concentrations in the knees and shoulders. Critically, both radiolabeled
tetrazines showed negligible uptake in the skeleton and joints when
administered in the absence of 2. Compound 2 can be utilized to target functionalized tetrazines to bone and
represents a convenient reagent to test novel tetrazines for use with
in vivo bioorthogonal pretargeting strategies.