Synthesis and evaluation of new iodine-125 radiopharmaceuticals as potential tracers for malignant melanoma

J Nucl Med. 1991 Aug;32(8):1573-80.

Abstract

The synthesis, labeling, and biodistribution of four 125I radiopharmaceuticals designed to localize in melanoma were tested. Uptake in tumors was demonstrated by autoradiography of whole-body sections and quantitated by measurement of radioactivity of selected tissues and tumors using melanoma-bearing mice. N-(2-diethylaminoethyl)-4-iodobenzamide was selected for its highest melanoma uptake: 60 min after IV injection of 6.5% and 4% ID/g, respectively for murine B16 and human melanotic melanoma. Tumor uptake showed the highest values of all analyzed tissues from 6 to 24 hr after injection. High uptake in melanotic tumor tissue with relatively low uptake in blood, muscle, brain, lung, and liver tissue resulted in high tumor/nontumor ratios (at 24 hr for B16, tumor/blood = 37, tumor/brain = 147, tumor/muscle = 95). This agent was compared with iodoamphetamine. Scintigraphic images of the tumor confirmed that external detection of melanoma is possible with this new radiopharmaceutical.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amphetamines
  • Animals
  • Benzamides* / chemical synthesis
  • Iodine Radioisotopes*
  • Iofetamine
  • Male
  • Melanoma, Experimental / diagnostic imaging*
  • Mice
  • Mice, Inbred Strains
  • Radionuclide Imaging
  • Tissue Distribution

Substances

  • Amphetamines
  • Benzamides
  • Iodine Radioisotopes
  • N-(2-(diethylamino)ethyl)-4-iodobenzamide
  • Iofetamine