Sasai K, Shibamoto Y, Takahashi M, Abe M, Wang J, Zhou L, Nishimoto S, Kagiya T
Department of Radiology, Faculty of Medicine, Kyoto University.
Jpn J Cancer Res. 1989 Nov;80(11):1113-8. doi: 10.1111/j.1349-7006.1989.tb02267.x.
The radiosensitizing activity, acute toxicity and pharmacokinetics of RP170, a new hypoxic cell radiosensitizer, were compared with those of misonidazole (MISO) and SR2508. RP170 belongs to the group of 2-nitroimidazole nucleosides, which are designed to be selectively excluded from the neural tissue. The reduction potential of RP170 was similar to that of MISO and SR2508. The partition coefficients in octanol/water of RP170, MISO, and SR2508 were 0.094, 0.35, and 0.021, respectively. The radiosensitizing activity of RP170 was similar to that of MISO and SR2508 in vitro and in vivo. There was no significant difference in the radiosensitizing activity of RP170 in vivo between intravenous and intraperitoneal administration. The acute toxicity of RP170 was the same as that of SR2508. Pharmacokinetic evaluation showed that the concentration of RP170 in the brain was as low as that of SR2508. RP170 is expected to have the same radiosensitizing effects as MISO and SR2508, and to be less neurotoxic than MISO.
将新型低氧细胞放射增敏剂RP170的放射增敏活性、急性毒性和药代动力学与甲硝唑(MISO)和SR2508进行了比较。RP170属于2-硝基咪唑核苷类,其设计目的是被选择性地排除在神经组织之外。RP170的还原电位与MISO和SR2508相似。RP170、MISO和SR2508在正辛醇/水中的分配系数分别为0.094、0.35和0.021。RP170在体外和体内的放射增敏活性与MISO和SR2508相似。静脉注射和腹腔注射时,RP170在体内的放射增敏活性没有显著差异。RP170的急性毒性与SR2508相同。药代动力学评估表明,RP170在脑中的浓度与SR2508一样低。预计RP170与MISO和SR2508具有相同的放射增敏作用,且神经毒性比MISO小。