Sladek N E
J Pharmacol Exp Ther. 1977 Jan;200(1):17-24.
Centrophenoxine, without antitumor activity itself, enhanced the cytotoxic action of melphalan and "activated" cyclophosphamide against mouse P388 lymphoma and rat W256 carcinosarcoma cells growing in static suspension culture. The concentration of alkylating agent required for 99% cell-kill was approximately halved when centrophenoxine was also present during exposure to the antitumor drug. Maximum potentiation by centrophenoxine of the cytotoxic action of melphalan occurred when cells were exposed to the two agents simultaneously; little or no potentiation was observed when cells were exposed to centrophenoxine before or after exposure to the alkylating agent.
脑复新本身无抗肿瘤活性,但能增强美法仑和“活化”环磷酰胺对静态悬浮培养的小鼠P388淋巴瘤细胞和大鼠W256癌肉瘤细胞的细胞毒作用。在接触抗肿瘤药物期间同时存在脑复新时,实现99%细胞杀伤所需的烷化剂浓度大约减半。当细胞同时接触这两种药物时,脑复新对美法仑细胞毒作用的增强效果最大;当细胞在接触烷化剂之前或之后接触脑复新时,观察到很少或没有增强作用。