Permeation studies in vitro and in vivo of potential radiopharmaceuticals with affinity to neuro receptors

PURPOSE:

To check the influence of structural characteristics on their permeation through the blood-Brain barrier (BBB), a set of radioactive [^99mTc]chelates bearing amine groups was synthesized and tested in vitro as well as in vivo.

METHODS:

Compounds with different log P and pK_a values were obtained by complex forming reactions of [^99mTc]pertechnetate with varying substituents. Transport was studied in rats and mice, as well as in an ECV304 cell culture model.

RESULTS:

In vitro higher permeation was found for compounds with electron attracting substituents in beta-position to the amine group (pK_a values 7.4 to 8.3) than for those with more basic amine groups (pK_a values > 8.9) even for similar logD_{ph 7.4}. In vivo brain uptake between 0.8 and 4.8% of the injected dose (ID) per organ was found for the former, whereas < 0.4% ID were present for the latter.

CONCLUSIONS:

Three structurally diverse classes of [^99mTc]chelates showed distinct patterns with regard to brain uptake in vivo and BBB permeability in vitro which could not be predicted by their lipophilicity alone. The close correlation between the data from rats and mice and those obtained with cell cultures render the ECV304 cells an attractive model for the screening of new compounds.