给予抗体酰胺- dtpa -铟-111后大鼠肝脏和血清中的放射性标记产物

C.H. Paik , V.K. Sood , N. Le , L. Cioloca , J.A. Carrasquillo , J.C. Reynolds , R.D. Neumann , R.C. Reba
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引用次数: 14

摘要

以抗人血清白蛋白抗体(Ab)作为模型抗体。采用环DTPA二酐反应将Ab与DTPA偶联,并用111In进行放射性标记。通过亲和层析纯化标记的Ab。该产物的大小排斥高效液相色谱显示,62%的111In与单分子Ab结合,38%的活性与分子量在300,000 - 450,000之间的抗体低聚物结合。标记抗体制剂经大鼠尾静脉注射。分析血清和肝脏匀浆上清中的放射性物质的分子量和免疫反应性。血清样品的大小排除高效液相色谱法表明,在48小时内,单体和二聚体抗体以相似的速度从血清中消失。此外,血清中出现了一种新的放射性物质,估计分子量为35000。循环中的111In物质的免疫反应部分下降缓慢,与代谢物的外观成一定比例。另一方面,肝脏匀浆上清液中的111In物质的免疫反应性迅速下降,48 h后未观察到明显的免疫反应性。标记的抗体在肝脏中分解代谢非常迅速,上清液中的主要活性与小分子量代谢物有关,该代谢物具有与DTPA-111In相同的HPLC保留时间。第二种代谢物估计分子量为35000。转铁蛋白无放射性。
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Radiolabeled products in rat liver and serum after administration of antibody—amide—DTPA—indium-111

Anti-human serum albumin antibody (Ab) was used as a model antibody. Ab was conjugated with DTPA using cyclic DTPA dianhydride reaction and radiolabeled with 111In. The labeled Ab was purified by affinity chromatography. Size exclusion HPLC of this product showed 62% of 111In bound to monomeric Ab and 38% of the activity bound to antibody oligomers with molecular weights ranging from 300,000 to 450,000. The labeled antibody preparation was injected into the tail vein of rats. The radioactive substances in serum and the supernatant from liver homogenates were analyzed for molecular weight and immunoreactivity. Size exclusion HPLC of the serum samples indicated that the monomeric and dimeric Abs disappeared from the serum at a similar rate over a 48 h period. In addition, a new radioactive substance with an estimated molecular weight of 35,000 appeared in the serum. The immunoreactive fraction of the circulating 111In substances decreased slowly, somewhat proportional to the appearance of the metabolite. On the other hand, the immunoreactivity of the 111In substances in the supernatant from the liver homogenate decreased rapidly and no appreciable immunoreactivity was observed after 48 h. The labeled antibody was catabolized very rapidly in the liver and the major activity in the supernatant was associated with a small molecular weight metabolite which had a HPLC retention time identical to that of DTPA-111In. The second metabolite had an estimated molecular weight of 35,000. No radioactivity was associated with transferrin.

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