Clinical pharmacology of moxalactam in patients with malignant disease

Antimicrob Agents Chemother. 1981 Apr;19(4):639-44. doi: 10.1128/AAC.19.4.639.

Abstract

Pharmacological studies of moxalactam were conducted with 37 cancer patients. Intramuscular administration of 500 mg of moxalactam to 10 patients produced a mean peak serum concentration of 12.4 micrograms/ml. The serum terminal-phase half-life was 3.9 h. Intravenous administration of 500 mg of moxalactam over 5 min to the same 10 patients produced a mean serum concentration of 42.0 micrograms/ml at 15 min, which decreased to 3.3 micrograms/ml at 6 h. A dose of 1 g of moxalactam was given in an identical manner to the same 10 patients. The mean serum concentration was 69.7 micrograms/ml at 15 min and 7.4 micrograms/ml at 6 h. The mean proportions of a drug recovered in the urine by 12 h after administration were 59% after the intramuscular dose and 61 and 55% after the single intravenous doses. Multiple-dose intravenous studies were also conducted. The serum terminal-phase half-life varied from 2.0 to 3.2 h. Continuous infusion studies were performed by up to 9 days by using a loading dose of 1 g over 0.5 h, followed by 2 g every 6 h. Serum concentrations were maintained at about 30.0 micrograms/ml during the study period.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Biological Assay
  • Cephalosporins / metabolism*
  • Cephamycins / metabolism*
  • Escherichia coli / drug effects
  • Humans
  • Injections, Intravenous
  • Kinetics
  • Middle Aged
  • Moxalactam
  • Neoplasms / metabolism*
  • Time Factors

Substances

  • Cephalosporins
  • Cephamycins
  • Moxalactam