Oral quinine pharmacokinetics and dietary salt intake

Eur J Clin Pharmacol. 2001 May;57(2):111-3. doi: 10.1007/s002280100283.

Abstract

Objectives: The objective was to determine whether or not dietary salt intake affects the relative bioavailability of oral quinine. Salt intake has been shown to alter quinidine bioavailability.

Methods: The pharmacokinetic properties of oral quinine sulphate (600 mg salt) were investigated in seven healthy Caucasian volunteers, in a randomised, crossover study, on low- and high-salt diets. Plasma quinine concentrations were measured by high-performance liquid chromatography (HPLC) and the 24-h urinary sodium excretion was assayed.

Results: Although the 24-h urine sodium excretion was significantly higher when the volunteers were on a high-salt diet, there were no significant differences in quinine AUC0-infinity, tmax, and Cmax after the two diets. The median (range) quinine elimination half-life was significantly shorter after a high-salt diet [8.5 (4.3-10.2) h] than after a low-salt diet [10.0 (7.6-14.8) h] (P = 0.04).

Conclusion: Dietary salt does not affect the relative oral bioavailability of quinine sulphate.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Antimalarials / administration & dosage
  • Antimalarials / pharmacokinetics*
  • Area Under Curve
  • Biological Availability
  • Cross-Over Studies
  • Half-Life
  • Humans
  • Male
  • Metabolic Clearance Rate
  • Middle Aged
  • Quinine / administration & dosage
  • Quinine / pharmacokinetics*
  • Sodium Chloride, Dietary / administration & dosage
  • Sodium Chloride, Dietary / pharmacology*

Substances

  • Antimalarials
  • Sodium Chloride, Dietary
  • Quinine