Wenzel M, Asindraza P
Strahlenther Onkol. 1986 Jan;162(1):51-6.
The organ distribution of 103Ru labelled ruthenocenyl derivatives of tyramine, histamine, benzylamine, phenylethylamine and homoveratrylamine were measured in rats. The derivatives of tyramine, histamine and benzylamine showed a high affinity for the adrenal and ovar. Adrenal/muscle ratios up to 2000:1 were gained but only if the dose was administered i.v. and was below 0.1 mumol/kg. The ruthenocenyl derivatives of tyramine labelled with 103Ru in the ruthenocene moiety or with 14C in the tyramine moiety showed a parallel distribution pattern but completely different from the distribution of 103RuCl3. This indicates that the tyramine derivatives are not destroyed in the body yielding Ru-ions. The advantages of the ruthenocenyl derivatives in comparison with the known amphetamine derivatives labelled with radioactive iodine are discussed.
在大鼠体内测定了103Ru标记的酪胺、组胺、苄胺、苯乙胺和高香草基胺的钌茂基衍生物的器官分布。酪胺、组胺和苄胺的衍生物对肾上腺和卵巢具有高亲和力。只有静脉注射剂量低于0.1 μmol/kg时,肾上腺/肌肉比率才能达到2000:1。在钌茂部分用103Ru标记或在酪胺部分用14C标记的酪胺钌茂基衍生物显示出平行的分布模式,但与103RuCl3的分布完全不同。这表明酪胺衍生物在体内不会被破坏而产生Ru离子。讨论了钌茂基衍生物与已知的放射性碘标记的苯丙胺衍生物相比的优势。