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用于血栓成像的铟-111标记重组组织型纤溶酶原激活剂的特性研究

Characterization of indium-111 labeled recombinant tissue plasminogen activator for the imaging of thrombi.

作者信息

Hnatowich D J, Virzi F, Doherty P W, Wilson J, Rosa J, Ansell J E

机构信息

Department of Nuclear Medicine, University of Massachusetts Medical Center, Worcester 01605.

出版信息

Eur J Nucl Med. 1987;13(9):467-73. doi: 10.1007/BF00281862.

Abstract

The in vitro functional properties of recombinant tissue plasminogen activator (rt-PA), its biodistribution in mice, and its pharmacokinetics and clot localization properties in dogs have been investigated after labeling rt-PA with 111In. The rt-PA was coupled with the bicyclic anhydride of DTPA using standard methodology. Amidolytic and fibrinolytic assays showed retention of protein activity when rt-PA was conjugated with an average of one DTPA group or less per molecule. Size exclusion HPLC showed each preparation to be radiochemically pure with 111In bound exclusively to the attached DTPA groups. Biodistribution in mice showed major accumulation of activity in the liver and kidneys. After administration of 0.5-1.0 mg of the labeled protein to dogs, blood activity decreased with a half time of approximately 5 min in agreement with previous reports of rapid blood clearance. Largely because of decreased blood levels, clot: blood ratios of labeled protein increased rapidly, in one study reaching 6.3 after 31 min, and satisfactory images of fibrin thrombi were obtained. The rt-PA may be labeled with 111In without destroying the ability of the protein to localize in clot and images of forming clot can be obtained with this agent within 1 h after administration.

摘要

用111铟标记重组组织型纤溶酶原激活剂(rt-PA)后,对其体外功能特性、在小鼠体内的生物分布以及在犬体内的药代动力学和凝块定位特性进行了研究。采用标准方法将rt-PA与二乙三胺五乙酸(DTPA)的双环酸酐偶联。酰胺水解和纤维蛋白溶解试验表明,当rt-PA与每个分子平均一个或更少的DTPA基团缀合时,蛋白质活性得以保留。尺寸排阻高效液相色谱显示每种制剂放射化学纯,111铟仅与连接的DTPA基团结合。小鼠体内的生物分布显示,活性主要在肝脏和肾脏中积累。给犬注射0.5-1.0mg标记蛋白后,血液活性下降,半衰期约为5分钟,这与先前关于血液快速清除的报道一致。很大程度上由于血液水平降低,标记蛋白的凝块:血液比率迅速增加,在一项研究中,31分钟后达到6.3,并获得了纤维蛋白血栓的满意图像。rt-PA可用111铟标记,而不会破坏蛋白质定位于凝块的能力,并且在给药后1小时内可用该试剂获得正在形成的凝块的图像。

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