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

Abstract Sterile, apyrogenic [ 123 I]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 μg, as measured by a UV spectrophotometer at 254 and 308 nm. Animal biodistribution studies revealed that the [ 123 I]IBZM prepared by this method which contained 5.9 μg of BZM, compared to the standard preparation method containing 0 μg 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 D 2 receptor binding capacity in the rat brain of [ 123 I]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.