Kanzawa F, Hoshi A, Kuretani K
Gan. 1976 Aug;67(4):595-9.
In order to clarify the mechanism of potentiation of cyclophosphamide activity by centrophenoxine, blood concentration of total and activated cyclophosphamide was examined. Blood concentration of cyclophosphamide increased by the compound and biological half-life of activated cyclophosphamide was markedly increased to 30 min from 18 min in intraperitoneal administration. At the same time, concentration of active form in ascites fluid was also increased and biological half-life of the active form was increased to 50 min from 18 min. Similar increase in blood level of active form was also shown by p-chlorophenoxyacetic acid and probenecid, but concentrations at early stages after injection was not increased. As a result, potentiation of cyclophosphamide activity by centrophenoxine was found to be due to maintenance of active form in both blood and ascites fluid at higher levels than those in the control.
为阐明氯酯醒增强环磷酰胺活性的机制,检测了总环磷酰胺和活化环磷酰胺的血药浓度。该化合物使环磷酰胺的血药浓度升高,腹腔注射时,活化环磷酰胺的生物半衰期从18分钟显著延长至30分钟。同时,腹水中活性形式的浓度也升高,活性形式的生物半衰期从18分钟延长至50分钟。对氯苯氧乙酸和丙磺舒也显示出活性形式血药水平的类似升高,但注射后早期的浓度未升高。结果发现,氯酯醒增强环磷酰胺活性是由于血液和腹水中活性形式的维持水平高于对照组。