首页> 外文期刊>Nuclear Medicine and Biology >186Re-1,4,8,11-tetraaza cyclotetradecyl-1,4,8,11-tetramethylene phosphonic acid: a novel agent for possible use in metastatic bone-pain palliation.
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186Re-1,4,8,11-tetraaza cyclotetradecyl-1,4,8,11-tetramethylene phosphonic acid: a novel agent for possible use in metastatic bone-pain palliation.

机译:186Re-1,4,8,11-四氮杂环十四烷基-1,4,8,11-四亚甲基膦酸:一种可能用于转移性骨痛减轻的新型药物。

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In connection with our work on the development of 186Re-tetra-phosphonates with optimum properties for use in bone pain palliation, a novel cyclic tetraphosphonate derivative, has been synthesized, complexed with 186Re and evaluated with promising results. The ligand, which consists of a cyclic array of tetra-aminomethylphosphonate groups, was synthesized using orthophosphorus acid, 1,4,8,11-tetraazacyclotetradecane and formaldehyde. The labeling conditions with 186Re have been standardized under varying reaction conditions to give maximum yield. In a reaction volume of 1 mL, maximum complexation yield of 98% was observed at pH 2 using 0.1 mg Re (37-370 MBq) for a ligand concentration at 9 x 10(-2) M/L, under heating at 100 degrees C for 30 min with 2 mg of stannous chloride. The complex was found to be stable for 6 days with RC purity remaining approximately 97%. The complex was characterized by paper chromatography in saline and acetone, wherein the R(f) exhibited were 0.9 and 0, respectively. Biodistribution studies of the complex were performed in male Wistar rats. Activity in femur which was observed to be 1.8%/g (equivalent to about 23% of the injected activity in skeleton) at 3 h post injection remained almost constant up to 48 h. Minimum activity was observed in blood and other soft tissues. The complex showed major renal clearance. Scintigraphic images in rabbits after injecting 70-100 MBq of 186Re-CTMP and using a dual head gamma camera were observed to be superior to 186Re-HEDP, prepared by a procedure standardized by us. Insignificant activity was observed in other vital organs. The results suggest the suitability of the complex for further evaluation in higher animals for bone pain palliation.
机译:结合我们开发的具有最佳特性的186Re-四膦酸酯用于缓解骨痛的研究工作,已合成了一种新型环状四膦酸酯衍生物,与186Re络合,并获得了可喜的结果。使用正磷酸,1,4,8,11-四氮杂环十四烷和甲醛合成了由四氨基甲基膦酸酯基团的环状阵列组成的配体。 186Re的标记条件已在各种反应条件下标准化,以提供最大的收率。在1 mL的反应体积中,在100°C的加热温度下,对于配体浓度为9 x 10(-2)M / L的配体浓度为0.1 mg Re(37-370 MBq),在pH 2下观察到最大络合产率为98%用2毫克氯化亚锡在C中加热30分钟。发现该络合物稳定6天,RC纯度保持约97%。通过在盐水和丙酮中​​的纸色谱法对该配合物进行表征,其中显示的R(f)分别为0.9和0。在雄性Wistar大鼠中进行了复合物的生物分布研究。注射后3小时观察到的股骨活性为1.8%/ g(相当于骨架中注射活性的约23%),直至48小时几乎保持恒定。在血液和其他软组织中观察到最小的活性。该复合物显示出主要的肾脏清除率。观察到在注射70-100 MBq的186Re-CTMP并使用双头伽玛照相机后,兔子的闪烁图像优于通过我们标准化的程序制备的186Re-HEDP。在其他重要器官中观察到微不足道的活动。结果表明该复合物适合在高等动物中进一步评估其骨痛减轻情况。

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