Jump to main content
Jump to site search

Issue 23, 2011
Previous Article Next Article

Synthesis and evaluation of analogues of HYNIC as bifunctional chelators for technetium

Author affiliations

Abstract

6-Hydrazinonicotinic acid (HYNIC, 1) is a well-established bifunctional technetium-binding ligand often used to synthesise bioconjugates for radiolabelling with Tc-99m. It is capable of efficient capture of technetium at extremely low concentrations, but the structure of the labelled complexes is heterogeneous and incompletely understood. In particular, it is of interest to determine whether, at the no-carrier-added level, it acts in a chelating or non-chelating mode. Here we report two new isomers of HYNIC: 2-hydrazinonicotinic acid (2-HYNIC, 2), which (like 1) is capable of chelation through the mutually orthohydrazine and pyridine nitrogens and 4-hydrazinonicotinic acid (4-HYNIC, 3), which is not (due to the para-relationship of the hydrazine and pyridine nitrogens). LCMS shows that the coordination chemistry of 2 with technetium closely parallels that of conventional 1, and no advantages of one over the other in terms of potential labelling efficiency or isomerism were discernable. Both 1 and 2 formed complexes with the loss of 5 protons from the ligand set, whether the co-ligand was tricine or EDDA. Ligand 3, however, failed to complex technetium except at very high ligand concentration: the marked contrast with 1 and 2 suggests that chelation, rather than nonchelating coordination, is a key feature of technetium coordination by HYNIC. Two further new HYNIC analogues, 2-chloro-6-hydrazinonicotinic acid (2-chloro-HYNIC, 4a) and 2,6-dihydrazinonicotinic acid (diHYNIC, 5) were also synthesised. The coordination chemistry of 4a with technetium was broadly parallel to that of 1 and 2 although it was a less efficient chelator, while 5 also behaved as an efficient chelator of technetium, but its coordination chemistry remains poorly defined and requires further investigation before it can sensibly be adopted for 99mTc-labelling. The new analogues 4a and 5 present an opportunity to develop trifunctional HYNIC analogues for more complex bioconjugate synthesis.

Graphical abstract: Synthesis and evaluation of analogues of HYNIC as bifunctional chelators for technetium

Back to tab navigation

Supplementary files

Article information


Submitted
18 Nov 2010
Accepted
04 Jan 2011
First published
25 Feb 2011

Dalton Trans., 2011,40, 6260-6267
Article type
Paper

Synthesis and evaluation of analogues of HYNIC as bifunctional chelators for technetium

L. K. Meszaros, A. Dose, S. C. G. Biagini and P. J. Blower, Dalton Trans., 2011, 40, 6260
DOI: 10.1039/C0DT01608J

Social activity

Search articles by author

Spotlight

Advertisements