A simple method of preparation for [123I]-(S)-(-)-IBZM

Appl Radiat Isot. 1998 Apr;49(4):369-72. doi: 10.1016/s0969-8043(97)00290-x.

Abstract

Sterile, apyrogenic [123I]IBZM was prepared in a sealed, capped 'V' vial, followed by SEP-PAK C-18 cartridge purification, and then was placed under sealed vial condensation. The quantity of BZM present in the final product ranged from 3.3-5.9 micrograms, as measured by a UV spectrophotometer at 254 and 308 nm. Animal biodistribution studies revealed that the [123I]IBZM prepared by this method which contained 5.9 micrograms of BZM, compared to the standard preparation method containing 0 microgram of BZM, resulted in identical brain uptakes at 15, 30, 60, and 120 min post-injection. The in vitro and in vivo studies demonstrated that a small amount of BZM presence in the final product did not affect the radiochemical purity, nor the D2 receptor binding capacity in the rat brain of [123I]IBZM. The preparation time can be shortened to 1.5 h compared with at least 2-4 h needed for the standard method of preparation. This factor may be important in routine clinical application.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzamides / chemical synthesis*
  • Benzamides / pharmacokinetics
  • Contrast Media / chemical synthesis*
  • Contrast Media / pharmacokinetics
  • Dopamine Antagonists / chemical synthesis*
  • Iodine Radioisotopes / chemistry*
  • Isotope Labeling / methods
  • Male
  • Pyrrolidines / chemical synthesis*
  • Pyrrolidines / pharmacokinetics
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Benzamides
  • Contrast Media
  • Dopamine Antagonists
  • Iodine Radioisotopes
  • Pyrrolidines
  • 3-iodo-2-hydroxy-6-methoxy-N-((1-ethyl-2-pyrrolidinyl)methyl)benzamide