67ga标记尿激酶的体内动力学和血栓积聚

Yoshiro Ohmomo, Akira Yokoyama, Yuko Yamauchi, Kazuko Horiuchi, Hideo Saji, Chiaki Tanaka, Kanji Torizuka
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引用次数: 4

摘要

用去铁胺(DF)作为双功能螯合剂,用67Ga标记高纯度和低分子量尿激酶(H-UK和L-UK)。H-UK和L-UK的标记效率分别为91.7%和90.4%。67Ga标记的UK (67Ga- df -UK)完全保留了亲本UK的酶活性。对67Ga标记的UK在家兔体内行为的研究表明,其血液清除速度非常快,半衰期为4分钟(67Ga- df -L-UK)至8分钟(67Ga- df - h -UK)。对诱发股静脉血栓的家兔进行的研究显示,注射后2小时,h -UK与血液的67Ga- df -UK活性比分别为2.00-3.08,L-UK活性比分别为0.84-1.65,血栓形成时间为4 - 3天。观察67Ga-DF-H-UK对其血栓积聚的剂量效应。从注射了这种放射性药物的动物身上提取的血浆样品的凝胶层析分析显示,由于与蛋白质抑制剂络合,67Ga-DF-UK的有效性降低。这导致高分子量复合物的形成,这反映在非常快的血液清除率上。讨论了其在血栓积聚中的意义。总之,DF在不改变UK酶性质的情况下用67Ga或68Ga标记UK的有效性得到了证明。使用67Ga-DF-UK作为诊断或治疗放射性药物是有希望的。
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In vivo kinetics and thrombus accumulation of 67ga-labeled urokinase

Highly purified high and low molecular weight urokinase (H-UK and L-UK) were labeled with 67Ga using deferoxamine (DF) as a bifunctional chelating agent. The labeling efficiency was 91.7% for the H-UK, and 90.4% for the L-UK, respectively. The 67Ga labeled UK (67Ga-DF-UK) fully retained the enzymatic activity of the parent UK. Studies on the in vivo behavior of the 67Ga labeled UK in rabbits showed a very rapid blood clearance with half-life of 4 min (67Ga-DF-L-UK) to 8 min (67Ga-DF-H-UK Studies carried out in rabbits with induced thrombi in the femoral vein showed thrombus-to-blood 67Ga-DF-UK activity ratios, 2 h after injection, of 2.00–3.08 for the H-UK, and 0.84–1.65 for the L-UK, respectively, with thrombi aged 4 to 3 days. A dose effect of the 67Ga-DF-H-UK on its thrombus accumulation was observed. Gel chromatographic analysis of plasma samples withdrawn from those animals injected with this radiopharmaceutical revealed a reduction of the 67Ga-DF-UK effectiveness due to complexation with protein inhibitors. This led to formation of high molecular weight complexes which was reflected in the very fast blood clearance. Its implication in thrombus accumulation is discussed. In conclusion, usefulness of DF for labeling UK with 67Ga or 68Ga with no alteration of UK enzymatic properties was demonstrated. The use of 67Ga-DF-UK as a diagnostic or therapeutic radiopharmaceutical is promising.

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