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人体内的3H- cymarol。排泄途径和血清蛋白结合情况。

3H-Cymarol in man. Excretion pathways and serum protein binding.

作者信息

Gundert-Remy U, Weber E, Rabl W

出版信息

Arzneimittelforschung. 1978;28(7):1174-6.

PMID:582706
Abstract

In 10 patients, 5 having received 3H-cymarol i.v., 5 orally, the radioactivity in plasma, urine and in the feces of some patients also was determined. After oral administration the plasma levels rose rapidly reaching maximum levels 1--2 h after administration. After i.v. injection about 30% of the given radioactivity were excreted in the urine. The remaining radioactivity was found in the feces suggesting a high biliary excretion. Only 10% of the radioactivity excreted in the first 24 h were chloroform-extractable. The radioactivity found in the urine after oral administration of the drug amounted to 17.6%. Between 51.1 and 58.5% of the drug were bound to serum proteins.

摘要

在10名患者中,5名静脉注射3H- cymarol,5名口服,还测定了部分患者血浆、尿液和粪便中的放射性。口服给药后,血浆水平迅速上升,给药后1 - 2小时达到最高水平。静脉注射后,约30%的给药放射性从尿液中排出。其余放射性在粪便中发现,提示胆汁排泄较高。在最初24小时内排出的放射性中,只有10%可被氯仿提取。口服该药物后在尿液中发现的放射性占17.6%。51.1%至58.5%的药物与血清蛋白结合。

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