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Effect of concomitant oral administration of ethanol on the pharmacokinetics of nicardipine in rats.

Young-Heun JungDong-Gyu HeoDong-Cheol LeeYe-Min KwonMi-Ji SeolDidi ZhangTae Cheon JeongJong Oh Kim
Published in: Biomedical chromatography : BMC (2022)
Ethanol intake can alter pharmacokinetics by increasing the solubility or enhancing the absorption of concomitant drugs. Here, a selective, sensitive and reproducible high-performance liquid chromatography-tandem mass spectrometry method for the quantitative analysis of nicardipine in rat plasma was developed using simple protein precipitation. The calibration curve was linear over a concentration range of 1-2,000 ng/ml (r 2  > 0.998). Accuracy ranged from 93.4 to 112.2% and precision was within 12.1% from three independent analytical batches. Stable conditions for the quantification of nicardipine in rat plasma were established in various conditions, including sample storage and handling. The matrix effect was negligible, and recovery was consistent at three different levels of quality control sample. The method was applied to assessment for the effect of ethanol on the pharmacokinetics of nicardipine in rats. The oral bioavailability of nicardipine was increased from 5.4 to 9.4% in Sprague-Dawley rats by concomitant oral administration of ethanol whereas the half-life was not altered. The findings indicated that concomitant ethanol intake can increase systemic drug exposure by increasing gastrointestinal absorption, especially poorly soluble drugs. This study provides an insight for further investigation of the alteration of the pharmacological effect of poorly soluble drugs owing to ethanol intake.
Keyphrases
  • liquid chromatography tandem mass spectrometry
  • quality control
  • weight gain
  • emergency department
  • high resolution
  • protein protein
  • liquid chromatography