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4'-脱氧阿霉素和阿霉素在荷实体瘤小鼠器官中的荧光测定及药代动力学研究。

Fluorescence assays and pharmacokinetic studies of 4'-deoxydoxorubicin and doxorubicin in organs of mice bearing solid tumors.

作者信息

Formelli F, Pollini C, Casazza A M, di Marco A, Mariani A

出版信息

Cancer Chemother Pharmacol. 1981;5(3):139-44. doi: 10.1007/BF00258470.

Abstract

The pharmacokinetic of 4'-deoxydoxorubicin, a new analog of doxorubicin, was compared with that of its parent compound in mice treated with equal and equiactive doses. The levels of total fluorescence due to the initial drugs and to metabolites were determined in tissue extracts by fluorometry. 4'-Deoxydoxorubicin reached the same tissue levels as doxorubicin in all the organs tested except in spleen and lung, where a higher peak was found in the animals treated with the new analog. The rate of elimination of 4'-deoxydoxorubicin from the organs tested was higher than that of doxorubicin.

摘要

在以同等剂量和等效活性剂量治疗的小鼠中,对阿霉素的一种新类似物4'-脱氧阿霉素的药代动力学与其母体化合物的药代动力学进行了比较。通过荧光法测定组织提取物中初始药物及其代谢产物产生的总荧光水平。在所有测试器官中,4'-脱氧阿霉素达到的组织水平与阿霉素相同,但在脾脏和肺中除外,在接受新类似物治疗的动物中,脾脏和肺中发现了更高的峰值。4'-脱氧阿霉素从测试器官中的消除速率高于阿霉素。

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