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白血病P388对丙脒腙在B6D2F1小鼠体内药代动力学的影响。

Influence of leukemia P388 on the pharmacokinetics of mitoguazone in B6D2F1 mice.

作者信息

Amlacher R, Sühnel J, Baumgart J, Mackowiak A, Schulze W, Bubner M, Hoffmann H

机构信息

Central Institute of Microbiology and Experimental Therapy, Academy of Sciences, GDR, Jena.

出版信息

Pharmazie. 1990 May;45(5):364-6.

PMID:2395900
Abstract

The aim of the present study was to investigate the influence of different stages of leukemia P388 on the pharmacokinetics of the antineoplastic agent mitoguazone in mice. It could be shown that, independent of the tumor stage investigated, the total clearance of mitoguazone is slightly reduced reflecting a moderate increase of AUC in the serum of leukemia-bearing animals. Furthermore, in an advanced tumor stage the drug levels in kidneys, liver, spleen and serum were found to be elevated to some extent in comparison to tumor-free controls in contrast to an earlier stage of leukemia. In conclusion, the tumor stage has to be considered as an important factor to which extent a neoplasia may alter the pharmacokinetics of drugs used for anticancer chemotherapy.

摘要

本研究的目的是调查白血病P388不同阶段对小鼠抗肿瘤药物丙脒腙药代动力学的影响。结果表明,无论所研究的肿瘤阶段如何,丙脒腙的总清除率略有降低,这反映了荷瘤动物血清中AUC的适度增加。此外,与白血病早期相比,在肿瘤晚期,肾脏、肝脏、脾脏和血清中的药物水平与无肿瘤对照组相比有一定程度的升高。总之,肿瘤阶段必须被视为肿瘤在多大程度上可能改变用于抗癌化疗药物药代动力学的一个重要因素。

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