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Preparation and Evaluation of [55Co](II)DTPA for Blood Cell Labeling

机译:血细胞标记[55Co](II)DTPA的制备与评价

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Co-55 (T1/2=17.53 h) was produced by 150 μA irradiation of a natural nickel target by 15 MeV protons and wasseparated from the irradiated target material by two ion exchange chromatography steps and was used for the preparationof [55Co]diethylenetriaminepentacetate ([55Co]DTPA). Optimization studies were performed using Co-57 due to its longerhalf-life. Cobalt-57 (T1/2=271.79 d) was produced by irradiation of a natural nickel target with 150 μA current of 22 MeVprotons. The 57Co was separated from the irradiated target material using a no carrier added method with a radiochemicalyield of > 97%. The 55Co was separated from the irradiated target material using a two step method with a radiochemicalyield of > 95%. Both products were controlled for radionuclide and chemical purity. The solutions of [55Co]complex wereprepared (radiochemical yield>80%) starting with 55CoOAc ligand at room temperature after 30 min. RTLC showed theradiochemical purity of more than 99%. Specific activity was obtained about 9.1 TBq/mmol. The tracer showed to be stablein the final product and in the presence of human serum at 37°C up to 15 h. [55Co]DTPA was successively used in theradiolabeling of red blood cells for PET1diagnostic studies.
机译:Co-55(T1 / 2 = 17.53 h)是通过15 MeV质子以150μA天然镍靶进行辐照而产生的,并通过两个离子交换色谱步骤从被辐照的靶材料中分离出来,并用于制备[55Co]二亚乙基三胺五乙酸盐( [55Co] DTPA)。由于Co-57的半衰期较长,因此进行了优化研究。钴57(T1 / 2 = 271.79 d)是通过以22 MeVprotons的150μA电流照射天然镍靶产生的。使用无载体方法将57Co与被辐照的目标材料分离,放射化学产率> 97%。使用两步法将55Co与被辐照的目标材料分离,放射化学产率> 95%。两种产品的放射性核素和化学纯度均得到控制。 30分钟后,在室温下从55CoOAc配体开始制备[55Co]复合物的溶液(放射化学产率> 80%)。 RTLC显示放射化学纯度超过99%。获得约9.1 TBq / mmol的比活。示踪剂在最终产品中和存在人血清的情况下(在37°C下长达15小时)显示稳定。 [55Co] DTPA被连续用于红细胞的放射性标记以进行PET1诊断研究。

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