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 language | English |
|---|---|
| Pages (from-to) | 367 |
| Number of pages | 1 |
| Journal | Yaoxue Xuebao |
| Volume | 36 |
| Issue number | 5 |
| State | Published - May 2001 |
Keywords
- Chiral separation
- Coupled HPLC
- Enantiomer
- Nicardipine
- Seteroselectivity