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一种用99mTc标记纤维蛋白原的化学方法。

A chemical method for the labeling of fibrinogen with 99mTc.

作者信息

Jeghers O, Abramovici J, Jonckheer M, Ermans A M

出版信息

Eur J Nucl Med. 1978 Apr 1;3(2):95-100. doi: 10.1007/BF00251631.

Abstract

A new method allowing the labelling of fibrinogen with 99mTcO4- is described. The 99mTcO4- is reduced by stannous chloride in an alkaline medium. After 1 h incubation with fibrinogen, the pH was brought down to 7.1. The study of (1) the pH of the solution, (2) the quantity of the reducer, and (3) the time of incubation allowed us to specify optimal conditions for labeling. The labeling yield varied from 91.68% plus or minus 6.05% to 95.18% plus or minus 2.13% according to the method of control used: the precipitation of fibrinogen by (NH4)2SO4 25% or thin-layer chromatography with methylethylketone as solvent. Clottable radioactivity averaged 72% plus or minus 4.43%. Column chromatography separated the tracer into two radioactive peaks. The first peak corresponded to the fibrinogen and carried 73.36% plus or minus 5.8% of the total radioactivity. The total recovered radioactivity amounted to 89.86% plus or minus 8.07%. Spectroscopic clottability was 88.23% plus or minus 2.42%. The in vivo stability of the labeling and the molecule was followed for 24 h after intravenous injection. If the radioactivity measured in the 5 min sample was considered to equal 100%, the 24 h sample averaged 32.71% plus or minus 3.25%, of which 85.68% plus or minus 2.92% was recovered in the clot. In conclusion, this method enabled us to obtain a stable tracer that we used for routine investigations in man.

摘要

描述了一种用99mTcO4-标记纤维蛋白原的新方法。在碱性介质中,氯化亚锡将99mTcO4-还原。与纤维蛋白原孵育1小时后,将pH值降至7.1。通过研究(1)溶液的pH值、(2)还原剂的量和(3)孵育时间,我们确定了标记的最佳条件。根据所用的对照方法,标记产率在91.68%±6.05%至95.18%±2.13%之间变化:用25%的(NH4)2SO4沉淀纤维蛋白原或用甲基乙基酮作为溶剂进行薄层色谱分析。可凝放射性平均为72%±4.43%。柱色谱将示踪剂分离为两个放射性峰。第一个峰对应于纤维蛋白原,占总放射性的73.36%±5.8%。总回收放射性为89.86%±8.07%。光谱可凝性为88.23%±2.42%。静脉注射后,对标记物和分子的体内稳定性进行了24小时的跟踪。如果将5分钟样品中测得的放射性视为100%,则24小时样品平均为32.71%±3.25%,其中85.68%±2.92%在凝块中回收。总之,该方法使我们能够获得一种稳定的示踪剂,用于人体的常规研究。

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