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碘甘葡胺(一种用于静脉尿路造影的新型造影剂)的药代动力学及临床研究

Pharmacokinetics and clinical studies of ioglicinate, a new contrast medium for intravenous urography.

作者信息

Nagel R, Leistenschneider W, Speck U, Clauss W

出版信息

Int J Clin Pharmacol Biopharm. 1978 Feb;16(2):49-53.

PMID:631971
Abstract

The new amino acid-bound contrast medium ioglicinate was first of all studied in respect of its pharmacokinetics in comparison to iothalamate and amidotrizoate in groups of 4 patients. The distribution volume was very similar for all 3 substances. Ioglicinate was found to have the shortest half-life. The elimination of the contrast media studied was mainly via the kidneys. The plasma protein binding of ioglicinate was again lower than that of amidotrizoate and iothalamate. These good experimental results were confirmed for ioglicinate in respect of the tolerance and opacification in a subsequently conducted clinical double-blind study in groups of 50 patients in comparison with iothalamate.

摘要

新型氨基酸结合型造影剂碘甘葡胺首先在4名患者组成的小组中,与碘肽酸盐和泛影酸盐对比,对其药代动力学进行了研究。这三种物质的分布容积非常相似。发现碘甘葡胺的半衰期最短。所研究的造影剂主要通过肾脏排泄。碘甘葡胺与血浆蛋白的结合率再次低于泛影酸盐和碘肽酸盐。随后在50名患者组成的小组中进行的临床双盲研究,将碘甘葡胺与碘肽酸盐对比,在耐受性和造影清晰度方面,这些良好的实验结果得到了证实。

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