Studies on in-vivo process of the enantiomers of nicardipine in rabbit by coupled chiral and achiral HPLC

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Abstract

AIM To study the differences of the pharmacokinetics and tissue distribution of two enantiomers of nicardipine in the rabbit. METHODS Biological samples were diluted by 1 mol·L-1 NaOH solution and extracted with n-hexane-ethyl acetate (1:1). The concentrations of S-nicardipine and R-nicardipine in samples were determined by coupled achiral C18 column (150 mm x 4.6 mm, 5 μm) and chiral OJ column (250 mm x 4.6 mm, 10 μm) chromatography. RESULTS The racemic nicardipine and the enantiomers in sample were separated well by the coupled system. The linear range was 55-550 ng·mL-1 for both enantiomers. The within-day and between-days RSD (n = 5) were 5.25% and 8.97%, and the relative recoveries were 99.99% and 97.10% for R- and S-enantiomer, respectively. The mean Tmax, Cmax and AUC values were (2.49 ± 0.03) h, (134 ± 2) ng·mL-1 and (1082 ± 32) ng·mL-1·h for S-nicardipine and (1.24 ± 0.05) h, (109 ± 2) ng·mL-1 and (778 ± 22) ng·mL-1·h for R-nicardipine. The concentration of S-nicardipine were generally higher than that of R-nicardipine in main target tissues and cells. CONCLUSION There were significant differences between the two enantiomers of nicardipine in rabbit in pharmacokinetics and tissue distribution.

Original languageEnglish
Pages (from-to)367
Number of pages1
JournalYaoxue Xuebao
Volume36
Issue number5
StatePublished - May 2001

Keywords

  • Chiral separation
  • Coupled HPLC
  • Enantiomer
  • Nicardipine
  • Seteroselectivity

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