给药后兔体内生物分布及密度变化的时间过程。与碘己醇的比较研究。

Acta radiologica. Supplementum Pub Date : 1996-01-01
P Rouleau, D Alison, P Bertrand, S Benderbous, P Havard, C Chambon
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引用次数: 0

摘要

目的:研究一种新型非离子低渗透压造影剂——碘比妥(Xenetix 350)与碘己醇(Omnipaque)在麻醉家兔体内静脉注射后的CT检查和生物分布。材料与方法:比较了碘腈醇350和碘己醇在家兔体内的密度及药理学和生物分布。注射造影剂前后分别行脑、肝、腹主动脉及肾脏CT检查。结果:在水介质中,碘腈醇对x射线的吸收与碘己醇完全相同。在注射碘己醇和碘比尼多300 mg /kg剂量后15分钟内,两种造影剂均导致主动脉增强,并随时间降低。肝脏的衰减也增加,随时间减少。脑内未见明显强化,但肾肾盂腔在注射后10分钟可见强化。在研究条件下,两种造影剂之间无显著差异。结论:从其作为细胞外液示踪剂的行为可以预期,碘比醇和其在家兔体内的血管、肝脏和肾脏药代动力学相关的信号发生了显著变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time course of biodistribution and changes in density following administration of iobitridol in rabbits. A comparative study vs iohexol.

Purpose: A new nonionic low-osmolality contrast medium, iobitridol (Xenetix 350) was compared with iohexol (Omnipaque) after i.v. injection in anesthetized rabbits to assess efficacy in CT examinations and biodistribution.

Material and methods: The densities in test tubes and the pharmacogenetics and biodistribution of iobitridol 350 and iohexol were compared in rabbits. CT of the brain, liver, the abdominal aorta and the kidneys was performed before and after injection of the contrast media.

Results: In aqueous medium, iobitridol absorbed roentgen rays in a manner exactly identical to that of iohexol. Within 15 min following injection of iohexol and iobitridol at a dose of 300 mg I/kg, both contrast agents resulted in aortic enhancement which decreased with time. An increased attenuation of the liver also occurred, decreasing with time. There was no significant enhancement in the brain but enhancement was found in the renal pelvocalyceal cavities 10 min postinjection. No significant difference was found between the 2 contrast agents under the study conditions.

Conclusion: As could be expected from its behavior as a tracer of extracellular fluid, iobitridol resulted in significant changes in the signal, corresponding to its vascular, hepatic and renal pharmacokinetics in rabbits.

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