Dopamine
is one of the most important neurotransmitters released
by neurons in the central nervous system, and a variety of neurological
illnesses and mental disorders are associated with impairments in
the secretion and functionality of dopamine. Dopamine, depending on
the type of receptors, can act as a stimulant or an inhibitor. In
this study, dendrimer-conjugated dopamine was utilized as a chelating
agent for Technetium-99m to investigate the organ distribution of
this compound in vivo using the single-photon emission
computed tomography (SPECT) technique. For this purpose, dendrimers
were synthesized using polyethylene glycol diacid and citric acid
precursors, and dopamine was conjugated to the dendrimer using EDC/NHS
cross-linker. The results showed no sign of toxicity of the dopamine-functionalized
dendrimers on HEK-293 cell lines. The optimization of labeling conditions
was conducted using the experimental design method (i.e., conjugate
value, pH, and the amount of reducing agent), and then labeling efficiency
was evaluated by thin-layer chromatography (TLC). Finally, the study
of organ distribution in normal mice using SPECT imaging and comparing
it with gene expression in different organs revealed that dopamine
D1 receptors exhibited the highest accumulation in the liver and that
the drug retained its specificity.