Pharmacokinetic profile of iobitridol.

Acta radiologica. Supplementum Pub Date : 1996-01-01
A Dencausse, X Violas, H Feldman, P Havard, C Chambon
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引用次数: 0

Abstract

Iobitridol (Xenetix) is a new triiodinated monomer, nonionic, low-osmolality contrast agent. Animal pharmacokinetic studies (rats, rabbits, dogs) and in vitro studies show that it is a marker of extracellular fluid, i.e. it is distributed in the interstitial space, it does not penetrate into cells, it does not cross the healthy blood-brain barrier (BBB), it does not bind to proteins, and it is eliminated by glomerular filtration without secretion or reabsorption. These characteristics determine its use as an urography and angiography contrast agent as well as the precautions necessary to be taken, which are classical for contrast agents of this classification, related to administration in pathophysiologic populations (patients with renal failure, pregnant women or nursing mothers, neonates, etc. )

碘吡醇的药动学特征。
Iobitridol (Xenetix)是一种新型的三碘化单体、非离子型、低渗透压造影剂。动物药代动力学研究(大鼠、兔、狗)和体外研究表明,它是细胞外液的标志物,即它分布在间质空间,不渗透到细胞中,不穿过健康的血脑屏障(BBB),不与蛋白质结合,在没有分泌或重吸收的情况下被肾小球滤过消除。这些特点决定了其作为泌尿造影和血管造影造影剂的用途,以及必要的预防措施,这是该分类造影剂的经典应用,与病理生理人群(肾功能衰竭患者、孕妇或哺乳期妇女、新生儿等)的给药有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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