Abstract
The synthesis of 7-bromo-5-[123I]-iodokynurenic acid is described. The tracer was prepared using a nucleophilic non-isotopic exchange reaction from the corresponding bromo derivative. Optimisation of the reaction parameters and HPLC purification were performed and the radiotracer was obtained in a chemical and radiochemical purity >95% and a specific activity of 235 Ci/μmol.
References
R. Schwarcz, B. Meldrum, Lancet, 2 (1986) 140.
R. Gill, A. Foster, G. Woodruff, Neuroscience, 25 (1988) 847.
T. Greenamyre, J. Young, Neurobiol. Aging, 10 (1989) 593.
M. Kessler, T. Terramani, G. Lynch, M. Baudry, J. Neurochem., 52 (1989) 1319.
J. E. Huettner, Biochem. Pharmacol., 41 (1991) 9.
J. W. Johnson, P. Ascher, Nature, 325 (1987) 529.
J. A. Kemp, A. C. Foster, P. D. Leeson, T. Priestley, R. Tridget, L. L. Iversen, G. N. Woodruff, Proc. Natl. Acad. Sci., 85 (1988) 6547.
P. D. Leeson, R. Baker, R. W. Carling, N. R. Curtis, K. W. Moore, B. J. Williams, A. C. Foster, A. E. Donald, J. A. Kemp, G. R. Marshall, J. Med. Chem., 34 (1991) 1243.
J. Mertens, W. Vanryckegem, M. Gysemans, J. Eersels, E. Finda-Panek, L. Carlsen, Eur. J. Nucl. Med., 13 (1987) 380.
F. Dumont, G. Slegers, Bull. Soc. Chim. Belg., 104 (1995) 505.
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Dumont, F., Slegers, G. Radiolabelling optimisation of 7-bromo-5-[123I]-iodo-4-oxo-1,4-dihidroquinoline-2-carboxylic acid: a potential tracer for NMDA SPECT studies. J Radioanal Nucl Chem 218, 239–241 (1997). https://doi.org/10.1007/BF02039342
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DOI: https://doi.org/10.1007/BF02039342