Antinociceptive Interaction and Pharmacokinetics of the Combination Treatments of Methyleugenol Plus Diclofenac or Ketorolac

Molecules. 2020 Nov 3;25(21):5106. doi: 10.3390/molecules25215106.

Abstract

Although nonsteroidal anti-inflammatory drugs (NSAIDs) are one of the main types of drugs used to treat pain, they have several adverse effects, and such effects can be reduced by combining two analgesic drugs. The aim of this study was to evaluate the nociceptive activity of methyleugenol combined with either diclofenac or ketorolac, and determine certain parameters of pharmacokinetics. For the isobolographic analysis, the experimental effective dose 30 (ED30) was calculated for the drugs applied individually. With these effective doses, the peak plasma concentration (Cmax) was found and the other parameters of pharmacokinetics were established. Methyleugenol plus diclofenac and methyleugenol plus ketorolac decreased licking behavior in a dose-dependent manner in phase II, with an efficacy of 32.9 ± 9.3 and 39.8 ± 9.6%, respectively. According to the isobolographic analysis, the experimental and theoretical ED30 values were similar for methyleugenol plus diclofenac, suggesting an additive effect, but significantly different for methyleugenol plus ketorolac (3.6 ± 0.5 vs. 7.7 ± 0.6 mg/kg, respectively), indicating a probable synergistic interaction. Regarding pharmacokinetics, the only parameter showing a significant difference was Cmax for the methyleugenol plus diclofenac combination. Even with this difference, the combinations studied may be advantageous for treating inflammatory pain, especially for the combination methyleugenol plus ketorolac.

Keywords: diclofenac; isobolographic analysis; ketorolac; methyleugenol; synergism.

MeSH terms

  • Analgesics* / pharmacokinetics
  • Analgesics* / pharmacology
  • Animals
  • Diclofenac* / agonists
  • Diclofenac* / pharmacokinetics
  • Diclofenac* / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Eugenol / agonists
  • Eugenol / analogs & derivatives*
  • Eugenol / pharmacokinetics
  • Eugenol / pharmacology
  • Ketorolac* / agonists
  • Ketorolac* / pharmacokinetics
  • Ketorolac* / pharmacology
  • Male
  • Mice
  • Mice, Inbred ICR

Substances

  • Analgesics
  • Diclofenac
  • methyleugenol
  • Eugenol
  • Ketorolac