(111)Indium Labelling of Recombinant Activated Coagulation Factor VII: In Vitro and Preliminary In Vivo Studies in Healthy Rats.

International journal of molecular imaging Pub Date : 2012-01-01 Epub Date: 2012-02-12 DOI:10.1155/2012/464810
Amarnadh Nalla, Inge Buch, Maibritt Sigvardt, Rasmus Poul Bodholdt, Andreas Kjaer, Birger Hesse
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引用次数: 2

Abstract

The aim of this study is to investigate whether (111)Indium-labelled recombinant FVIIa (rFVIIa) could be a potential radiopharmaceutical for localization of bleeding sources. DTPA-conjugated rFVIIa was radiolabelled with (111)In chloride. In vitro binding efficiency of (111)In-DTPA-rFVIIa to F1A2-Mab-sepharose was 99% in buffer, while it was 88-82% in serum. The binding efficiency of (111)In-DTPA-rFVIIa to TF (1-209)-sepharose was 48% in buffer whereas 39%-36% in serum, respectively. In vivo experiment was conducted in healthy rats, and gamma camera images were taken immediately after iv. administration of 1.6-1.8 MBq (111)In-DTPA-rFVIIa up to 120-130 min. Five min after administration of (111)In-DTPA-rFVIIa, percentage of (111)In activity was 6.0% in the cardiac region and 24.5% in the liver region. After 2 hours activity was decreased to 3.3% in heart while it had increased to 42.0% in the liver. The (111)In-DTPA-rFVIIa might be a potential radiopharmaceutical for visualisation of tissues with significant TF expression such as acute bleeding lesions in the gastrointestinal tract.

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(111)重组活化凝血因子VII的铟标记:体外和健康大鼠体内初步研究。
本研究的目的是探讨(111)铟标记重组FVIIa (rFVIIa)是否可能成为定位出血源的潜在放射性药物。dtpa偶联的rFVIIa用氯化(111)In进行放射性标记。(111)In- dtpa - rfviia与F1A2-Mab-sepharose的体外结合效率在缓冲液中为99%,在血清中为88-82%。(111) in - dtpa - rfviia与TF (1-209)-sepharose的结合效率在缓冲液中为48%,在血清中为39% ~ 36%。在健康大鼠体内进行实验,注射1.6-1.8 MBq (111)In- dtpa - rfviia后立即拍摄伽马相机图像,持续120-130分钟。注射(111)In- dtpa - rfviia后5分钟,心脏区(111)In- dtpa - rfviia活性百分比为6.0%,肝脏区(111)In活性百分比为24.5%。2小时后,心脏的活跃性降至3.3%,而肝脏的活跃性上升至42.0%。(111) in - dtpa - rfviia可能是一种潜在的放射性药物,用于可视化具有显著TF表达的组织,如胃肠道急性出血病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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