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新型抗癌药米托唑胺(NSC 353451)对Lewis肺癌的体内研究。

In vivo studies with the novel anticancer agent mitozolomide (NSC 353451) on Lewis lung carcinoma.

作者信息

Broggini M, Erba E, Morasca L, Horgan C, D'Incalci M

出版信息

Cancer Chemother Pharmacol. 1986;16(2):125-8. doi: 10.1007/BF00256161.

Abstract

Mitozolomide is one of the most effective drugs against Lewis lung carcinoma in the mouse. Two IP doses of 40 mg/kg (days 6 and 15 after IM transplantation of 3LL) or four doses of 20 mg/kg given at various intervals (starting from day 6) increased survival time by 100%. A single IP dose of 80 mg/kg was toxic, and 10 mg/kg was ineffective even when this dose was given on eight occasions. The pharmacokinetics of mitozolomide was investigated in 3LL-bearing mice by HPLC assay. Peak drug levels were achieved in tumor 15 min after IP treatment, after which they declined according to first-order kinetics, with a half-life of 80-100 min (the same as in plasma). No dose-dependent kinetics was observed. Flow cytometry studies showed an accumulation of 3LL cells in G2M 24 h after drug treatment. This cell cycle perturbation was reversed 96 h after the inactive dose of 10 mg/kg, but not after the effective dose of 40 mg/kg.

摘要

米托唑胺是对小鼠Lewis肺癌最有效的药物之一。两次腹腔注射剂量为40mg/kg(在3LL肌内移植后第6天和第15天)或从第6天开始以不同间隔给予四次剂量为20mg/kg,可使存活时间延长100%。单次腹腔注射剂量为80mg/kg有毒性,而10mg/kg即使给药八次也无效。通过高效液相色谱法测定,在携带3LL的小鼠中研究了米托唑胺的药代动力学。腹腔注射治疗后15分钟肿瘤内达到药物峰值水平,此后它们按照一级动力学下降,半衰期为80 - 100分钟(与血浆中相同)。未观察到剂量依赖性动力学。流式细胞术研究表明,药物治疗后24小时3LL细胞在G2M期积累。在无效剂量10mg/kg给药96小时后这种细胞周期扰动得以逆转,但在有效剂量40mg/kg给药后则未逆转。

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