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

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle
  • Drug Evaluation, Preclinical
  • Flow Cytometry
  • Half-Life
  • Kinetics
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nitrogen Mustard Compounds / metabolism*
  • Nitrogen Mustard Compounds / therapeutic use
  • Regression Analysis

Substances

  • Nitrogen Mustard Compounds
  • mitozolomide