123I的制备及其标记新型小分子融合肽的初步研究

    Preparation of 123I and a New 123I Labeled Fusion Peptide

    • 摘要: 本工作利用天然锑靶,通过121Sb(α,2n)123I核反应,在控制锑靶厚度为62.2~64.3mg/cm2和α粒子能量为26.5 MeV的情况下,可以得到11.1 TBq/(A•h)以上且核纯度高达98.6%的123I。利用制备的123I进行了小分子融合肽拟似物VHCDR1-VHFR2-VLCDR3123I标记,并对标记物的体外稳定性及在正常小鼠体内的分布进行了初步研究。结果表明,123I标记VHCDR1-VHFR2-VLCDR3的标记率可达90%以上,123I标记物在体内不易脱碘且具有较高的体外稳定性。

       

      Abstract: 123I with radioactivity of 11.1 TBq/(A•h) and nuclear purity of more than 98.6% was prepared in the CS-30 cyclotron of Sichuan University via 121Sb(α,2n)123I nuclear reaction by α-energy of 26.5 MeV and using Sb target of 62.2-64.3 mg/cm2. Furthermore, VHCDR1-VHFR2-VLCDR3, a new fusion peptide was labeled with 123I, and in vitro and in vivo of the labeled peptide was evaluated. The results show that the labeling yield of 123I VHCDR1-VHFR2-VLCDR3 is more than 90%. The deiodination of 123I labeled VHCDR1-VHFR2-VLCDR3 in vivo is minimal, and 123I VHCDR1-VHFR2-VLCDR3 has a high stability in vitro.

       

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