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Radiolabelling of DOTA-TATE with ~177Lu. Preliminary Studies with a View to Somatostatin Receptor Radionuclide Therapy

机译:用〜177室的Dota-tate放射性标记。初步研究以索抑素受体放射性核素治疗的视图

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This study describes the radiolabelling method of DOTA-TATE with ~177Lu as well as the in vitro experiments for quantification of the biological properties. The radiolabelling was performed taking into account the usual biological and radioactively therapeutic doses. Radiochemical purities higher than 95% were obtained for the following parameters: ~177Lu to DOTA-TATE molar ratio: 3.8; pH: 4.5 in acetate buffer; incubation time: 30min; temperature: 80°C; HABA (3hydroxi-4aminobenzoic acid) as stabilizer. The competition binding assay of natLu-DOTA-TATE/~125I-Tyr3-Octreotide and the saturation binding assay of ~177Lu-DOTA-TATE using rat brain cortex membrane as somatostatin receptor model were done. The obtained results, analyzed using Prism 2 software, allow determination of IC_(50) (4.74 nM) and K_d (142.8 pM). These pharmacological parameters values illustrate the excellent capacity of ~177Lu-DOTA-TATE to bind to somatostatin receptors as well as the formed bounds stability.
机译:该研究描述了与〜177LU的达塔酸的放射性标记方法以及用于定量生物学性质的体外实验。考虑到通常的生物和放射性治疗剂量进行放射性标记。下列参数获得高于95%的放射化学纯度:〜177LU至DOTA-Tate摩尔比:3.8; pH:4.5乙酸盐缓冲液;孵化时间:30min;温度:80°C; Haba(3Hydroxi-4氨基苯甲酸)作为稳定剂。使用大鼠脑皮层膜作为生长抑素受体模型,NaTlu-dota-tate /〜125i-Tyr3-奥曲霉和〜177lu-dota-tate的饱和结合测定的竞争结合测定和〜177lu-dota-tate的饱和结合测定。使用棱镜2软件分析所得结果,允许确定IC_(50)(4.74nm)和K_D(142.8 PM)。这些药理学参数值说明〜177lu-dota-tate的优异容量,以结合生长抑素受体以及形成的界面稳定性。

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