Karube Y, Ito S, Katsuno K, Takata J
Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.
Ann Nucl Med. 1996 Feb;10(1):63-9. doi: 10.1007/BF03165055.
Fibrinogen was labeled with Tc-99m by two methods and in vitro stability and the in vivo behavior in mice were studied. The Tc-99m labeling was performed by mixing an unreduced fibrinogen (UnFib) or a reduced fibrinogen (ReFib) with Tc-99m pertechnetate in the presence of stannous chloride. In both of them, chelation with Tc-99m resulted in a single radiochemical product. For the in vitro stability studies, Tc-99m labeled fibrinogen (Tc-99m UnFib) was prepared with UnFib, and transchelation with cysteine solution was easy to produce compared to Tc-99m labeled fibrinogen (Tc-99m ReFib) prepared with ReFib. The radioactivity bound to clottable protein for Tc-99m UnFib and Tc-99m ReFib was about 70% and about 69%, respectively. The in vivo behavior of these labeled fibrinogens was studied, and their efficiencies for imaging an abscess and Ehrlich tumor in mice were determined with a gamma camera. Technetium-99m UnFib underwent a rapid partial exchange of the Tc-99m with compounds of the blood buffer system in vivo, resulting in early biologically active and would be incorporated into the abscess and tumor. The uptake in the abscess increased slightly over time with Tc-99m ReFib, but the abscess to blood and abscess to muscle ratios were 0.09 and 2.6 at 5 hr, respectively. Clearly delineated images of abscess were obtained beginning at about 5 hr after injection. The tumor to blood and tumor to muscle ratios were 0.05 and 1.4 at 5 hr, respectively. The Ehrlich tumor image in mice was slightly visible at 10 hr. The short half-life of Tc-99m was inappropriate for fibrinogen with a low pharmacokinetic value, because it was necessary for imaging of the abscess and tumor to take a long time.
采用两种方法用Tc-99m标记纤维蛋白原,并研究了其体外稳定性及在小鼠体内的行为。通过在氯化亚锡存在的情况下,将未还原的纤维蛋白原(UnFib)或还原的纤维蛋白原(ReFib)与高锝酸盐Tc-99m混合来进行Tc-99m标记。在这两种情况下,与Tc-99m的螯合都产生了单一的放射化学产物。对于体外稳定性研究,用UnFib制备了Tc-99m标记的纤维蛋白原(Tc-99m UnFib),与用ReFib制备的Tc-99m标记的纤维蛋白原(Tc-99m ReFib)相比,其与半胱氨酸溶液的转螯合更容易发生。Tc-99m UnFib和Tc-99m ReFib与可凝蛋白结合的放射性分别约为70%和约69%。研究了这些标记纤维蛋白原的体内行为,并用γ相机测定了它们对小鼠脓肿和艾氏瘤成像的效率。Tc-99m UnFib在体内与血液缓冲系统的化合物发生了Tc-99m的快速部分交换,产生了早期生物活性物质,并会被脓肿和肿瘤摄取。随着时间的推移,Tc-99m ReFib在脓肿中的摄取略有增加,但在5小时时,脓肿与血液的比值和脓肿与肌肉的比值分别为0.09和2.6。在注射后约5小时开始获得清晰的脓肿图像。在5小时时,肿瘤与血液的比值和肿瘤与肌肉的比值分别为0.05和1.4。小鼠的艾氏瘤图像在10小时时略有可见。Tc-99m的半衰期较短,不适用于药代动力学值较低的纤维蛋白原,因为脓肿和肿瘤成像需要较长时间。