Stability of meropenem and effect of 1 beta-methyl substitution on its stability in the presence of renal dehydropeptidase I

Antimicrob Agents Chemother. 1992 Jul;36(7):1577-9. doi: 10.1128/AAC.36.7.1577.

Abstract

The stability of meropenem in the presence of renal dehydropeptidase I (DHP-I) varied extremely with the animal source of the enzyme. Meropenem, compared with imipenem, was rather easily hydrolyzed by DHP-Is from mice, rabbits, and monkeys, while it showed a higher resistance to guinea pig and beagle dog DHP-Is. In addition, meropenem was four times more resistant than imipenem to human DHP-I. The 1 beta-methyl substituent on carbapenems, i.e., meropenem and 1 beta-methyl imipenem, made them considerably more resistant to mouse and swine DHP-Is than the 1-unsubstituted derivatives are.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Dipeptidases / metabolism*
  • Dogs
  • Drug Stability
  • Guinea Pigs
  • Humans
  • Hydrolysis
  • Imipenem / pharmacokinetics
  • Macaca mulatta
  • Meropenem
  • Mice
  • Rabbits
  • Rats
  • Species Specificity
  • Structure-Activity Relationship
  • Swine
  • Thienamycins / pharmacokinetics*

Substances

  • Thienamycins
  • Imipenem
  • Dipeptidases
  • dipeptidase
  • Meropenem