Amlacher R, Weber H, Preiss R, Hoffmann H
Institute of Microbiology and Experimental Therapie Jena.
Pharmazie. 1992 May;47(5):378-81.
It was the aim of this study to investigate whether leukemia P388 being an important murine transplantation tumor may alter the plasma concentration-time profiles of the alkylating antineoplastic agent bendamustine (1) in mice. In an advanced tumor stage the rapid decline of 1 plasma levels was found to be retarded in tumor-bearing in comparison to tumor-free animals both after i.v. and p.o. drug administration. These changes cannot be explained by the neoplasia-related depression of drug metabolism whereas the 1-containing ascitic fluid may be a possible reason for the prolonged drug levels in plasma. After p.o. administration of 1, the bioavailability of the drug was found to be increased in the leukemia-bearing animals.
本研究的目的是调查作为一种重要的小鼠移植性肿瘤的白血病P388是否会改变烷化剂抗肿瘤药物苯达莫司汀(1)在小鼠体内的血浆浓度-时间曲线。在肿瘤晚期,静脉注射和口服给药后,与无肿瘤动物相比,荷瘤动物体内1的血浆水平快速下降的情况均受到抑制。这些变化不能用肿瘤相关的药物代谢抑制来解释,而含有1的腹水可能是血浆中药物水平延长的一个可能原因。口服1后,发现荷白血病动物体内该药物的生物利用度有所增加。