Nakamura M, Fukui M, Morisada S, Inaba M, Tsukagoshi S, Sakurai Y
Gan To Kagaku Ryoho. 1985 Oct;12(10):2030-6.
We investigated the antitumor effect of orally administered SM-108. The drug showed strong antitumor activities against Ehrlich carcinoma, sarcoma 180, P388 leukemia, L1210 leukemia, colon 26 adenocarcinoma, colon 38 adenocarcinoma, and Lewis lung carcinoma. The antitumor activity of SM-108 against Ehrlich carcinoma was so remarkable, in fact, that all mice in a group survived for a long time. The antitumor effect of SM-108 depends on its administration schedule. Treatment involving a schedule of one dose every 6 h for 24 h at intervals of 3 days brought about a much stronger effect than daily single treatment. The maintenance of a high serum level of SM-108 for 24 h by the former treatment is responsible for the strong therapeutic effects, because the action of SM-108 is time-dependent. The antitumor activities of SM-108 administered orally are excellent enough to be comparable with those obtained by intraperitoneal administration as previously reported.
我们研究了口服SM - 108的抗肿瘤作用。该药物对艾氏癌、肉瘤180、P388白血病、L1210白血病、结肠26腺癌、结肠38腺癌和Lewis肺癌显示出强大的抗肿瘤活性。实际上,SM - 108对艾氏癌的抗肿瘤活性非常显著,以至于一组中的所有小鼠都存活了很长时间。SM - 108的抗肿瘤作用取决于其给药方案。每6小时给药一次,持续24小时,间隔3天的治疗方案比每日单次治疗产生的效果要强得多。前一种治疗方案使SM - 108血清高水平维持24小时,这是产生强大治疗效果的原因,因为SM - 108的作用具有时间依赖性。口服给药的SM - 108的抗肿瘤活性非常出色,足以与先前报道的腹腔注射所获得的活性相媲美。