~(211)At通过DTPA酸酐标记IgG

    • 摘要: 研究了211At通过二乙撑三胺五乙酸(DTPA)酸酐标记人免疫球蛋白G(IgG)的方法。合成DTPA酸酐后与人IgG反应,制得DTPA-IgG。Na211At溶液与分离纯化后的DTPA-IgG在室温下反应30min,经SephadexG50柱分离纯化,得211At-DTPA-IgG的0.1mol/LPBS淋洗液。整个标记过程可在1.5h完成,全程标记率在60%以上。测定了211At-DTPA-IgG在体外的稳定性,并通过比较标记物与Na211At注射液在NIH小鼠体内的分布和代谢,评价了211At-DTPA-IgG在体内的稳定性。

       

      Abstract: LABELING IgG WITH 211At VIA DTPA ANHYDRIDELiu Ning Jin Jiannan Mo Shangwu Chen Hengliu Yu Yanping(Institute of Nuclear Science and Technology,Sichuan University,Chengdu 610064)ABSTRACTA method for labeling human IgG with 211At via DTPA anhydride is described.DTPAIgG is prepared and 211At is conjugated to human IgG by adding Na 211At to DTPAIgG and reaction for 30min at room temperature.The astatinated IgG is isolated by a Sephadex G50 column and identified by size exclusion HPLC.The labeling procedure is executed in 1.5h and at least 60% of the added 211At are found in the product.The stability of 211At DTPAIgG in vitro and vivo is evaluated.Keywords 211At Labeling method DTPA IgG Stability Biodistribution

       

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