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首页> 外文期刊>Investigative radiology >Preclinical profile of the monodisperse iodinated macromolecular blood pool agent P743.
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Preclinical profile of the monodisperse iodinated macromolecular blood pool agent P743.

机译:单分散碘化大分子血池试剂P743的临床前概况。

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RATIONALE AND OBJECTIVES: To summarize the chemical synthesis, physicochemical characterization, pharmacokinetic behavior, and biological evaluation of P743, a new macromolecular iodinated contrast medium. METHODS: The synthesis and molecular modeling of the iodinated macromolecule P743 are described. The pharmacokinetic profile was established in rabbits and rats. Acute toxicity in mice, renal tolerance in normal rabbits, and renal tolerance in uninephrectomized, dehydrated rats undergoing selective intrarenal injection was evaluated. In vitro permeability effects on isolated mastocytes and on the coagulation pathways were carried out. Computed tomography vascular imaging was performed after intravenous injection of P743 (300 mg I/kg) in rabbits and compared with the nonspecific nonionic agent iobitridol. RESULTS: P743 is a monodisperse, macromolecular iodinated contrast medium. In both rabbits and rats, P743 showed a pharmacokinetic profile consistent with that of a rapid-clearance blood-pool agent. Its diffusion through the endothelium was found to be low in vitro, thus confirming early confinement of this macromolecule, unlike nonspecific contrast media. In both species, P743 was excreted by glomerular filtration. Acute toxicity disclosed no mortality at the highest volume that could be injected into mice, leading to a median lethal dose greater than 8.9 g I/kg. Renal tolerance was found to be good in both euvolemic rabbits and uninephrectomized, dehydrated rats. No histamine or leukotriene B4 release was found on RBL-2H3 isolated mastocytes. P743 did not interfere with the coagulation pathways. Imaging experiments confirmed that P743 remains in the vascular compartment for a longer time than does iobitridol, thus allowing vascular enhancement that is twice as high as that of iobitridol in the recirculation phase. CONCLUSIONS: The pharmacokinetic and imaging profiles of P743, a new, monodisperse, macromolecular blood-pool iodinated contrast medium, were consistent with those of a rapid-clearance blood-pool agent. Its initial safety profile is satisfactory. Further experimental imaging studies are required to define the clinical interest in such molecules.
机译:理由和目的:总结一种新型的大分子碘化造影剂P743的化学合成,理化特性,药代动力学行为和生物学评估。方法:描述了碘化大分子P743的合成和分子模型。在兔子和大鼠中建立了药代动力学特征。评估了小鼠的急性毒性,正常兔子的肾耐受性和接受选择性肾内注射的未切除直肠的脱水大鼠的肾耐受性。对离体肥大细胞和凝血途径进行了体外通透性影响。在兔静脉注射P743(300 mg I / kg)后,进行了计算机断层扫描血管成像,并将其与非特异性非离子药物碘比妥醇进行了比较。结果:P743是一种单分散的大分子碘化造影剂。在兔子和大鼠中,P743的药代动力学特征均与速释血池药物一致。发现其在体外的通过内皮的扩散低,从而证实了该大分子的早期限制,这与非特异性造影剂不同。在两个物种中,P743通过肾小球滤过排泄。急性毒性显示,在可注射到小鼠的最大体积下没有死亡,导致中位致死剂量大于8.9 g I / kg。发现在正常血兔和未切除直肠的脱水大鼠中肾耐受性均良好。在分离的RBL-2H3肥大细胞中未发现组胺或白三烯B4释放。 P743不干扰凝血途径。成像实验证实,P743在血管腔室中的停留时间比碘比地多更长,因此在循环阶段的血管增强作用是碘比地多的两倍。结论:一种新的,单分散的,大分子血池碘化造影剂P743的药代动力学和成像特征与快速清除血池剂的相符。其初始安全性令人满意。需要进一步的实验成像研究来确定对此类分子的临床兴趣。

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