Champailler A, Gremillet E, Decousus M, Kassir A, Voutay M, Healy J C
Eur J Nucl Med. 1985;10(9-10):437-40. doi: 10.1007/BF00256586.
Plasma transport of 99mTc-p-butyl-IDA was measured by four in vitro methods: trichloroacetic acid precipitation, electrophoresis, HPLC, and Scatchard binding isotherm. The data are in accord with protein transport, the main carrier being albumin with two categories of sites. This work suggests that after IV injection of 99mTc-p-butyl-IDA in humans plasma protein binding is one of the limiting factors for the hepatic deposition of the radiopharmaceutical.
采用四种体外方法测量了99mTc-p-丁基-IDA的血浆转运:三氯乙酸沉淀法、电泳法、高效液相色谱法和Scatchard结合等温线法。数据符合蛋白质转运情况,主要载体是白蛋白,存在两类位点。这项研究表明,在人体静脉注射99mTc-p-丁基-IDA后,血浆蛋白结合是放射性药物肝脏沉积的限制因素之一。