Labeling of ethambutol with 99mTc using a new reduction procedure. Pharmacokinetic study in the mouse and rat

Int J Rad Appl Instrum A. 1990;41(5):493-6. doi: 10.1016/0883-2889(90)90010-e.

Abstract

Certain 99mTc-labeled derivatives of ethylene diamine substituted in NN', when labeled with 99mTc, have been proposed for studying renal excretion, and others for brain imaging. Ethambutol, a well known antituberculosis drug, possesses a structure very similar to these derivatives. We prepared a complex of [99mTc]ethambutol using hypophosphorus acid as the reducing agent. The complex was then analyzed by paper and cellulose F chromatography and by FAB mass spectrometry. A pharmacokinetic study in the mouse and rat indicated that the complex is eliminated by the kidney faster than DTPA, slower than [131I]hippuran and without significant renal retention. The [99mTc]ethambutol complex is easy to prepare and shows good stability in water at physiological pH, making it potentially useful in renal excretion studies.

MeSH terms

  • Animals
  • Ethambutol* / pharmacokinetics*
  • Isotope Labeling / methods
  • Kidney / diagnostic imaging
  • Kidney / metabolism
  • Mice
  • Organotechnetium Compounds* / pharmacokinetics*
  • Radionuclide Imaging
  • Rats
  • Tissue Distribution

Substances

  • Organotechnetium Compounds
  • technetium Tc 99m ethambutol
  • Ethambutol