Vera D R, Krohn K A, Stadalnik R C, Scheibe P O
Radiology. 1984 Apr;151(1):191-6. doi: 10.1148/radiology.151.1.6701314.
The biodistribution and kinetics of a receptor-binding hepatic radiopharmaceutical, Tc-99m-galactosyl-neoglycoalbumin (Tc-NGA), were investigated using mammalian and avian models. The radiopharmaceutical exhibited four significant features associated with receptor-mediated binding at the hepatocyte membrane in mammals: (a) high tissue specificity, (b) high molecular specificity, (c) affinity-dependent uptake, and (d) dose-dependent uptake. Diminished hepatic uptake by the avian model illustrated low nonspecific binding. The kinetic sensitivity to ligand-receptor affinity and stoichiometry illustrated the principal feature of receptor-binding radio-pharmaceuticals, namely, quantitative assessment of tissue function based upon the biochemical interaction of a ligand and its specific receptor.
使用哺乳动物和禽类模型研究了一种受体结合型肝脏放射性药物锝-99m-半乳糖基新糖白蛋白(Tc-NGA)的生物分布和动力学。该放射性药物在哺乳动物肝细胞膜上表现出与受体介导结合相关的四个显著特征:(a)高组织特异性,(b)高分子特异性,(c)亲和力依赖性摄取,以及(d)剂量依赖性摄取。禽类模型中肝脏摄取减少表明非特异性结合较低。对配体-受体亲和力和化学计量学的动力学敏感性说明了受体结合型放射性药物的主要特征,即基于配体与其特异性受体的生化相互作用对组织功能进行定量评估。