Ohmomo Y, Yokoyama A, Kawai K, Arano Y, Horiuchi K, Tanaka C, Saji H, Torizuka K
Eur J Nucl Med. 1985;10(5-6):269-75. doi: 10.1007/BF00254473.
In our search for a platelet-specific labeling agent, metaraminol (MA), a low-toxic pharmaceutical for the treatment of hypotension and cardiogenic shock, attracted our attention. Its active incorporation and accumulation by platelets have been recognized. At first, the preparation of 125I radioiodinated metaraminol (125I-MA) was carried out using the chloramine-T method. Then, upon the harvest of platelets as platelet-rich plasma (PRP), their labeling with this new radiopharmaceutical was easily performed by incubation for 10 min at 37 degrees C. The cell-labeling efficiency was dependent on cell density, reaching 63.0% +/- 3.1% at 2.4 X 10(9) cells/ml. The specific incorporation of 125I-MA by an active transport system similar to that of 5-hydroxytryptamine (5-HT) as well as by passive diffusion was demonstrated. In in vitro studies, the unaltered state of 125I-MA-labeled platelets with their cellular functions fully retained was estimated. In vivo studies carried out in rabbits with induced thrombi in the femoral artery showed a rather rapid disappearance of the radioactivity from circulating blood, reaching a high thrombus-to-blood activity ratio of 19.8 +/- 4.3 within 30 min of the administration of 125I-MA-labeled autologous platelets. Thus, with the potential availability of 123I, 123I-MA-labeled platelets appear to be a promising agent for thrombus imaging using single-emission computed tomography (CT) studies.
在寻找血小板特异性标记剂的过程中,间羟胺(MA),一种用于治疗低血压和心源性休克的低毒药物,引起了我们的注意。它能被血小板主动摄取和积累这一点已得到认可。起初,采用氯胺-T法制备了125I放射性碘化间羟胺(125I-MA)。然后,当采集富含血小板血浆(PRP)形式的血小板时,通过在37℃孵育10分钟,很容易用这种新的放射性药物对其进行标记。细胞标记效率取决于细胞密度,在细胞密度为2.4×10⁹个细胞/毫升时达到63.0%±3.1%。结果表明,125I-MA通过类似于5-羟色胺(5-HT)的主动转运系统以及被动扩散进行特异性摄取。在体外研究中,评估了125I-MA标记的血小板其细胞功能完全保留的未改变状态。在兔股动脉诱导形成血栓的体内研究中,显示给药125I-MA标记的自体血小板后30分钟内,循环血液中的放射性迅速消失,血栓与血液的放射性活度比高达19.8±4.3。因此,鉴于123I的潜在可用性,123I-MA标记的血小板似乎是一种有前景的用于单光子发射计算机断层扫描(CT)研究的血栓成像剂。