心肌成像中潜在的67Ga放射性药物:三(1-芳基-3-羟基-2-甲基-4-吡啶醌)镓(III)配合物

Zaihui Zhang , Donald M. Lyster , Gordon A. Webb , Chris Orvig
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引用次数: 10

摘要

一系列高度亲脂性的1-芳基-3-羟基-2-甲基-4-吡啶酮与镓(III)-67的配合物已作为潜在的放射性药物在体外和体内进行了评价。吡啶酮在苯环的对位上有不同的取代基:R = H、CH3、OCH3和NO2。67Ga复合物的生物分布研究已在家兔、小鼠、大鼠和狗身上进行。兔和狗的心脏对这种放射性核素的吸收量很高。小鼠和大鼠体内不同的生物分布模式表明,这些复合物的生物分布存在物种差异。兔子和狗表现出快速的心脏吸收和血液清除。基于现有的热力学数据,在体外用简单的血浆模型模拟体内Ga3+离子的形态形成。
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Potential 67Ga radiopharmaceuticals for myocardial imaging: Tris(1-aryl-3-hydroxy-2-methyl-4-pyridinonato)gallium(III) complexes

A series of highly lipophilic complexes of 1-aryl-3-hydroxy-2-methyl-4-pyridinones with gallium(III)-67 has been evaluated in vitro and in vivo as potential radiopharmaceuticals. The pyridinones have different substituents at the para-position of the phenyl ring: R = H, CH3, OCH3 and NO2. Biodistribution studies of 67Ga complexes have been carried out in rabbits, mice, rats and a dog. High heart uptake of the radionuclide has been shown in rabbits and the dog. The different biodistribution patterns in mice and rats indicate that there is a species difference in the biodistribution of these complexes. Rabbits and the dog show rapid heart uptake and blood clearance. The speciation of the Ga3+ ion in vivo is simulated in vitro with a simple blood plasma model based on the available thermodynamic data.

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