“…This method, which has not been described in the literature before, is expected to yield an unstable radiolabelled product, since there is no driving force that will facilitate the hydrophilic 99m Tc-DTPA to pass the lipid bilayer and entrap the radiolabel inside the liposome. Moreover, the described quality control method (Koukourakis et al, 1999(Koukourakis et al, , 2000a does not discriminate between free 99m Tc-DTPA and liposome-associated 99m Tc-activity. The chromatographic method applied can distinguish between reduced 99m TcO 2 and unreduced 99m TcO 4 -, however, it is more essential to discriminate between liposome-associated 99m Tc-activity and 99m Tc-DTPA in the preparation.…”