Ma D, McDevitt M R, Finn R D, Scheinberg D A
Department of Pharmacology and Molecular Therapeutics, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Appl Radiat Isot. 2001 Oct;55(4):463-70. doi: 10.1016/s0969-8043(01)00048-3.
Alpha emitting radionuclides are of considerable interest for targeted radioimmunotherapy. Generator supplied 213Bi emitting 8.5 MeV alpha particles with a 45.6 min half-life has been conjugated to a monoclonal antibody (HuM195-CHX-A-DTPA) for targeted therapy of leukemia in a clinical trial. The clinical dose preparation of pharmaceutical formulation by a pair of skilled radiochemists took 25 min, which corresponds, to an overall decay loss of 30% of the initial 213Bi activity eluted from the generator. In order to allow more widespread and practical clinical use of targeted 213Bi alpha particle therapy, we developed a new procedure that is simpler, more rapid and adaptable to a hospital pharmacy. The new 10 min process includes a tandem elution and labeling, and an anion exchange column purification method that can be reproducibly used.
发射α粒子的放射性核素在靶向放射免疫治疗中备受关注。在一项临床试验中,由发生器提供的半衰期为45.6分钟、发射8.5兆电子伏特α粒子的213Bi已与单克隆抗体(HuM195-CHX-A-DTPA)偶联,用于白血病的靶向治疗。由一对熟练的放射化学家制备药物制剂的临床剂量需要25分钟,这相当于从发生器洗脱的初始213Bi活性总体衰变损失30%。为了使靶向213Biα粒子治疗更广泛、更实际地应用于临床,我们开发了一种新方法,该方法更简单、更快速,且适用于医院药房。新的10分钟流程包括串联洗脱和标记,以及可重复使用的阴离子交换柱纯化方法。