Chakraborty S, Das T, Unni P R, Sarma H D, Samuel G, Banerjee S, Venkatesh M, Ramamoorthy N, Pillai M R A
Radiopharmaceuticals Division, Bhabha Atomic Research Centre, Mumbai, India.
Nucl Med Commun. 2002 Jan;23(1):67-74. doi: 10.1097/00006231-200201000-00011.
Polyphosphonate ligands labelled with radioisotopes decaying by moderate energy beta emission have shown utility as palliative agents for painful bone metastasis. 177Lu (T(1/2)=6.71 d, Ebetamax=497 keV) has radionuclidic properties suitable for use in palliative therapy of bone metastasis. 177Lu was produced at a high specific activity and excellent radionuclidic purity by thermal neutron bombardment of a target prepared from natural Lu. Three polyaminomethylene phosphonate ligands, abbreviated as EDTMP, DTPMP and TTHMP, were synthesized and radiolabelled with 177Lu. Complexation parameters were optimized to achieve maximum yields (97-99.5%). All the complexes were found to retain their stability at room temperature even 14 days after preparation. Biodistribution studies of the complexes were carried out in Wistar rats. All the complexes showed significant bone uptake (6-6.5%/g in tibia at 3 h post-injection (p.i.)) with rapid clearance from blood and minimum uptake in soft tissues. These studies reveal that 177Lu complexes with the synthesized ligands have a potential use in palliative treatment of painful bone metastasis.
通过中等能量β发射衰变的放射性同位素标记的多膦酸盐配体已显示出作为疼痛性骨转移姑息治疗剂的效用。177Lu(T(1/2)=6.71天,Ebetamax=497keV)具有适用于骨转移姑息治疗的放射性核素特性。通过对由天然Lu制备的靶进行热中子轰击,以高比活度和优异的放射性核素纯度制备了177Lu。合成了三种多氨基亚甲基膦酸盐配体,简称为EDTMP、DTPMP和TTHMP,并用177Lu进行放射性标记。优化络合参数以实现最大产率(97-99.5%)。发现所有络合物在室温下即使在制备后14天仍保持其稳定性。在Wistar大鼠中进行了络合物的生物分布研究。所有络合物均显示出显著的骨摄取(注射后3小时(p.i.)胫骨中为6-6.5%/克),血液清除迅速,软组织摄取最少。这些研究表明,177Lu与合成配体形成的络合物在疼痛性骨转移的姑息治疗中具有潜在用途。