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Novel 99mTc-labelled complexes with thymidine isocyanide: radiosynthesis and evaluation as potential tumor imaging tracers

机译:新型99mTc标记的与胸苷异氰化物的复合物:放射合成和评估作为潜在的肿瘤成像示踪剂

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摘要

A novel thymidine isocyanide (CN-TdR) functionalized at the N3 position of thymidine was synthesized and then radiolabelled with 99mTc(i) and [99mTc(i)(CO)3]+ cores to produce [99mTc(CN-TdR)6]+ and [99mTc(CO)3(CN-TdR)3]+, respectively. Both of them were prepared with high radiochemical purity and were stable over 6 h in saline at ambient temperature and in serum at 37 °C. The partition coefficient results demonstrated that they were hydrophilic. The cell internalization studies showed that their uptake might be mediated by nucleoside transporters. Biodistribution of these complexes in mice bearing the S180 tumor showed that they accumulated in the tumor with high uptake and cleared rapidly from blood and muscles, producing high tumor/blood and tumor/muscle ratios. Between them, [99mTc(CN-TdR)6]+ exhibited advantages concerning a higher tumor uptake, tumor/blood ratio and tumor/muscle ratio at 60 min post-injection. Single photon emission computed tomography imaging studies showed that there was a clear accumulation in tumor sites, suggesting that [99mTc(CN-TdR)6]+ could be a promising candidate for tumor imaging.
机译:合成了在胸苷的N3位官能化的新型胸苷异氰化物(CN-TdR),然后用 99m Tc(i)和[ 99m Tc(i)(CO)进行放射性标记)3] + 内核产生[ 99m Tc(CN-TdR)6] + 和[ 99m Tc (CO)3(CN-TdR)3] + 。两者均以高放射化学纯度制备,并在环境温度的盐水中和37°C的血清中稳定超过6小时。分配系数结果表明它们是亲水的。细胞内在化研究表明,其摄取可能是由核苷转运蛋白介导的。这些复合物在患有S180肿瘤的小鼠中的生物分布表明,它们在肿瘤中具有高吸收性,并迅速从血液和肌肉中清除,从而产生高的肿瘤/血液和肿瘤/肌肉比率。在它们之间,[ 99m Tc(CN-TdR)6] + 表现出以下优势:在术后60分钟时,肿瘤的摄取更高,肿瘤/血液比率和肿瘤/肌肉比率更高注射。单光子发射计算机断层摄影成像研究表明,肿瘤部位明显积聚,表明[ 99m Tc(CN-TdR)6] + 可能是有希望的候选者用于肿瘤成像。

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