In vivo use of a radioiodinated somatostatin analogue: dynamics, metabolism, and binding to somatostatin receptor-positive tumors in man

J Nucl Med. 1991 Jun;32(6):1184-9.

Abstract

Somatostatin analogues, labeled with gamma-emitting radionuclides, are of potential value in the localization of somatostatin receptor-positive tumors with gamma camera imaging. We investigated the application in man of a radioiodinated analogue of somatostatin, 123I-Tyr-3-octreotide, which has similar biologic characteristics as the native peptide. The radiopharmaceutical is cleared rapidly from the circulation (up to 85% of the dose after 10 min) mainly by the liver. Liver radioactivity is rapidly excreted into the biliary system. Until 3 hr after injection, radioactivity in the circulation is mainly in the form of 123I-Tyr-3-octreotide. Thereafter, plasma samples contain increasing proportions of free iodide. Similarly, during the first hours after injection, radioactivity in the urine exists mainly in the form of the unchanged peptide. Thereafter, a progressive increase in radioiodide excretion is observed, indicating degradation of the radiopharmaceutical in vivo. Fecal excretion of radioactivity amounts to only a few percent of the dose. The calculated median effective dose equivalent is comparable with values for applications of other 123I-radiopharmaceuticals (0.019 mSv/MBq).

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Humans
  • Iodine Radioisotopes
  • Neoplasms / diagnostic imaging*
  • Neoplasms / metabolism
  • Octreotide / analogs & derivatives*
  • Octreotide / metabolism
  • Radionuclide Imaging
  • Receptors, Neurotransmitter / metabolism*
  • Receptors, Somatostatin

Substances

  • Iodine Radioisotopes
  • Receptors, Neurotransmitter
  • Receptors, Somatostatin
  • 3-Tyr-octreotide
  • Octreotide