Rosebrough S F, Hashmi M
Department of Radiology, University of Rochester Medical Center, New York, USA.
J Pharmacol Exp Ther. 1996 Feb;276(2):770-5.
Diagnostic and therapeutic procedures utilizing the high affinity streptavidin (SA)/biotin system are being investigated for in vivo use. We are developing a rapid two-step imaging technique for the diagnosis of deep venous thrombosis and pulmonary embolism. The optimal SA-bound targeting moiety would circulate adequately for sufficient lesion accumulation, but nonbound reagent would clear in a reasonably short time before the injection of radiolabeled biotin. The objective of this study was to cross-link SA and galactose-modified SA to GC4 antifibrin monoclonal antibody and to study the pharmacokinetics and biodistribution of the radiolabeled GC4-SA conjugates after injection into rabbits. A cross-linking method was developed for the synthesis of the GC4-SA conjugates via the addition reaction of sulfhydryl containing SA derivatives with maleimide-GC4. In vivo, radiolabeled trigalactose modified SA-GC4 exhibited a much faster blood clearance compared to mono-galactose modified GC4-SA or GC4-SA containing no galactose.
正在研究利用高亲和力链霉亲和素(SA)/生物素系统的诊断和治疗程序用于体内应用。我们正在开发一种快速两步成像技术用于诊断深静脉血栓形成和肺栓塞。最佳的SA结合靶向部分应能充分循环以实现足够的病变积累,但未结合的试剂应在注射放射性标记的生物素之前在合理的短时间内清除。本研究的目的是将SA和半乳糖修饰的SA与GC4抗纤维蛋白单克隆抗体交联,并研究放射性标记的GC4-SA缀合物注入兔子后的药代动力学和生物分布。开发了一种交联方法,通过含巯基的SA衍生物与马来酰亚胺-GC4的加成反应合成GC4-SA缀合物。在体内,与单半乳糖修饰的GC4-SA或不含半乳糖的GC4-SA相比,放射性标记的三半乳糖修饰的SA-GC4表现出快得多的血液清除率。