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碘比醇在兔体内的生物分布时间进程及给药后密度变化。与碘海醇的对比研究。

Time course of biodistribution and changes in density following administration of iobitridol in rabbits. A comparative study vs iohexol.

作者信息

Rouleau P, Alison D, Bertrand P, Benderbous S, Havard P, Chambon C

机构信息

Department of Adult Radiology, Central Hospital of Tours, France.

出版信息

Acta Radiol Suppl. 1996;400:49-55.

PMID:8619352
Abstract

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.

摘要

目的

将一种新型非离子低渗造影剂碘比醇(Xenetix 350)与碘海醇(欧乃派克)在麻醉兔静脉注射后进行比较,以评估其在CT检查中的效能和生物分布。

材料与方法

比较了兔体内试管中的密度以及碘比醇350和碘海醇的药物遗传学和生物分布。在注射造影剂前后对脑、肝、腹主动脉和肾脏进行CT检查。

结果

在水性介质中,碘比醇吸收X射线的方式与碘海醇完全相同。以300 mg I/kg的剂量注射碘海醇和碘比醇后15分钟内,两种造影剂均导致主动脉强化,且强化程度随时间降低。肝脏的衰减也增加,并随时间降低。脑内无明显强化,但注射后10分钟肾盂肾盏腔内出现强化。在研究条件下,两种造影剂之间未发现显著差异。

结论

正如作为细胞外液示踪剂所预期的那样,碘比醇导致信号发生显著变化,这与它在兔体内的血管、肝脏和肾脏药代动力学一致。

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