Djokić Divna, Janković Drilia, Nikolić Nadezda
Laboratory for Radioisotopes, The Institute of Nuclear Sciences Vinca, M. Petrovica Alasa 12-14, Belgrade, Serbia.
Cancer Biother Radiopharm. 2009 Feb;24(1):129-36. doi: 10.1089/cbr.2008.0499.
The aim of this study was to find out if (90)Y could form a stabile complex with meso-2,3-dimercaptosuccinic acid (DMSA) and if (90)Y-DMSA may have potential for tumor therapy in the palliative treatment of bone metastases.
The preparing of (90)Y-DMSA was carried out by varying experimental parameters, such as ligand concentration, pH, time, and temperature of the reaction, in order to maximize the labeling yield. Analysis of the complexes enclosed the radiochemical quality control (instant thin-layer chromatography, paper chromatography, and high-performance liquid chromatography), determination of pharmacokinetical parameters as well as biodistribution study in healthy male Wistar rats. In vitro stability of the complexes was tested too.
(90)Y-DMSA could be prepared in high yields (>95%) under optimized conditions of reaction. Stability studies in saline and human serum in vitro showed no significant release of activity from the ligand over 24 hours and 10 days, respectively. The preliminary biodistribution results in rat at 2 hours indicated that (90)Y-DMSA, at both pH levels, was significantly retained into bone. The uptake in the kidneys was lower for (90)Y-DMSA at pH 8.0 then at pH 3.0. The retention in other organs was negligible.
(90)Y complexes could be made with ease with DMSA. (90)Y-DMSA was obtained in good yield and was found to be very stable. A promising biodistribution result of this complex pointed at potential in the palliative treatment of bone metastases.
本研究的目的是探究钇-90(90Y)能否与内消旋-2,3-二巯基丁二酸(DMSA)形成稳定的络合物,以及90Y-DMSA在骨转移瘤姑息治疗中是否具有肿瘤治疗潜力。
通过改变实验参数,如配体浓度、pH值、反应时间和温度等,制备90Y-DMSA,以最大化标记产率。对络合物的分析包括放射化学质量控制(即时薄层色谱法、纸色谱法和高效液相色谱法)、药代动力学参数测定以及在健康雄性Wistar大鼠体内的生物分布研究。同时也测试了络合物的体外稳定性。
在优化的反应条件下,可高产率(>95%)制备90Y-DMSA。体外在生理盐水和人血清中的稳定性研究表明,在24小时和10天内,配体均无明显的活性释放。大鼠在2小时时的初步生物分布结果表明,在两种pH水平下,90Y-DMSA均显著滞留于骨中。pH 8.0时90Y-DMSA在肾脏中的摄取低于pH 3.0时。在其他器官中的滞留可忽略不计。
90Y可轻松与DMSA形成络合物。90Y-DMSA产率良好且非常稳定。该络合物有前景的生物分布结果表明其在骨转移瘤姑息治疗中具有潜力。