Amlacher R, Baumgart J, Mackowiak A, Sühnel J, Horn U, Bubner M, Hoffmann H
Central Institutes of Microbiology and Experimental Therapy, Jena.
Pharmazie. 1991 Jan;46(1):44-6.
In this study, the influence of different stages and transplantation routes of the experimentally widely used solid tumor melanoma B16 on the pharmacokinetics of the antineoplastic agent mitoguazone was investigated in B6D2F1 mice. It could be shown that changes of the pharmacokinetic parameters as well as the distribution pattern of this drug were clearly influenced and dependent on the tumor stage but not by the tumor inoculation route. Advanced melanoma (d16) led to a sharp decrease in the terminal elimination half-life as well as to decreased spleen levels and increased initial liver concentrations of the drug. With respect to the results obtained in leukemia P388-bearing mice it can be concluded that the tumor stage as well as the tumor model are to be considered as important factors in which way and to which extent a tumor may alter the pharmacokinetics of antineoplastic agents.
在本研究中,在B6D2F1小鼠中研究了实验中广泛使用的实体瘤黑色素瘤B16的不同阶段和移植途径对抗肿瘤药物米托胍腙药代动力学的影响。结果表明,该药物的药代动力学参数变化以及分布模式明显受到影响,且取决于肿瘤阶段,而非肿瘤接种途径。晚期黑色素瘤(第16天)导致药物的终末消除半衰期急剧缩短,脾脏药物水平降低,肝脏初始药物浓度升高。关于在携带白血病P388的小鼠中获得的结果,可以得出结论,肿瘤阶段以及肿瘤模型应被视为肿瘤可能以何种方式以及在何种程度上改变抗肿瘤药物药代动力学的重要因素。