Edwards David, Lewis Joanne, Battle Mark, Lear Rochelle, Farrar Gill, Barnett D Jon, Godden Vanessa, Oliveira Alexandra, Coombes Catherine, Ahlström Håkan
Research and Development, GE Healthcare Bio-Sciences, The Grove Centre, White Lion Road, Little Chalfont, HP7 9LL, UK.
Eur J Nucl Med Mol Imaging. 2006 Nov;33(11):1258-65. doi: 10.1007/s00259-006-0091-9. Epub 2006 Jun 28.
(99m)Tc-NC100668 is a new radiotracer being developed to aid the diagnosis of thromboembolism. The structure of NC100668 is similar to a region of human alpha(2)-antiplasmin, which is a substrate for factor XIIIa (FXIIIa). The purpose of this study was to confirm the uptake of (99m)Tc-NC100668 into forming plasma clot and to establish the biodistribution of (99m)Tc-NC100668 in Wistar rats.
The in vitro plasma clot uptake of (99m)Tc-NC100668 and other compounds with known affinities to FXIIIa was measured using a plasma clot assay. The biodistribution and blood clot uptake of radioactivity of (99m)Tc-NC100668 in normal Wistar rats and those bearing experimentally induced deep vein thrombi were investigated.
The in vitro uptake of (99m)Tc-NC100668 was greater than that for [(14)C]dansyl cadaverine, a known substrate of FXIIIa in the plasma clot assay. The biodistribution of (99m)Tc-NC100668 in male and female Wistar rats up to 24 h p.i. showed that radioactivity was rapidly excreted, predominantly into the urine, with very little background tissue retention. In vivo the uptake and retention of (99m)Tc-NC100668 into the blood clot was greater than could be accounted for by non-specific accumulation of the radiotracer within the blood clot.
(99m)Tc-NC100668 was retained by plasma clots in vitro and blood clots in vivo. No significant tissue retention which could interfere with the ability to image thrombi in vivo was observed. This evidence suggests that (99m)Tc-NC100668 might be useful in the detection of thromboembolism.
(99m)Tc-NC100668是一种正在研发的新型放射性示踪剂,用于辅助诊断血栓栓塞。NC100668的结构与人类α(2)-抗纤溶酶的一个区域相似,而α(2)-抗纤溶酶是因子XIIIa(FXIIIa)的底物。本研究的目的是确认(99m)Tc-NC100668在形成的血浆凝块中的摄取情况,并确定(99m)Tc-NC100668在Wistar大鼠体内的生物分布。
使用血浆凝块分析法测量(99m)Tc-NC100668和其他对FXIIIa具有已知亲和力的化合物在体外血浆凝块中的摄取情况。研究了(99m)Tc-NC100668在正常Wistar大鼠和实验性诱导深部静脉血栓形成的大鼠体内的生物分布及放射性在血凝块中的摄取情况。
在血浆凝块分析中,(99m)Tc-NC100668的体外摄取量大于已知的FXIIIa底物[(14)C]丹磺酰尸胺。注射后24小时内,(99m)Tc-NC100668在雄性和雌性Wistar大鼠体内的生物分布表明,放射性迅速排出,主要通过尿液排出,背景组织滞留极少。在体内,(99m)Tc-NC100668在血凝块中的摄取和滞留量大于放射性示踪剂在血凝块中非特异性积累所能解释的量。
(99m)Tc-NC100668在体外被血浆凝块保留,在体内被血凝块保留。未观察到会干扰体内血栓成像能力的明显组织滞留。这一证据表明(99m)Tc-NC100668可能对血栓栓塞的检测有用。