Fosinopril: Pharmacokinetics and pharmacodynamics in Chinese subjects

This study examined the pharmacokinetics and pharmacodynamics of fosinopril (IV oral) in Chinese subjects to determine whether they were different from a group of somewhat heavier and older Western control subjects previously published using the same methods. It was an open-label, randomized, balance d, two-way crossover study comparing oral and IV pharmacokinetics in 12 hea lthy Chinese subjects in a clinic in Taiwan. Each subject received 10 mg of oral fosinopril or 7.5 mg of IV fosinoprilat in a randomized sequence with sampling for fosinoprilat concentrations over 48 hours. Standard pharmacok inetics, including AUC, C-max, T-max, T-1/2, V-ss, bioavailability, total c learance, and renal and nonrenal clearance, were determined as well as phar macodynamic effects on angiotensin-converting enzyme (ACE) activity. Follow ing oral administration of 10 mg fosinopril, AUC(0-T) and AUC(inf) were 155 6 +/- 586 ng . hr/mL and 1636 +/- 620 ng . hr/mL; respectively; T-1/2 was 1 7.4 +/- 11.4 hr, C-max was 183.4 +/- 59.4 ng/mL; and median T-max was 4.0 h r, with > 99% protein binding. Following IV administration of 7.5 mg fosino prilat, AUC(0-T) and AUC(inf) were 7727 +/- 2638 ng . hr/mL and 7727 +/- 26 38 ng . hr/mL, respectively; T-1/2 was 13.0 +/- 5.2 hr; and median T-max wa s 4.0 hr, with 99.5% +/- 0.22% protein binding and a V-ss of 5850 +/- 2780 mL. Bioavailability was 22.3% +/- 7.9%. Percent urinary excretion was 7.6% +/- 2.6% after oral dosing and 42.6% +/- 6.1% after IV dosing. After IV, do sing total clearance was 1088 +/- 439 mL/hr, renal clearance was 472 +/- 21 3 mL/hr, and nonrenal clearance was 617 +/- 246 mL/hr. ACE inhibition was e ssentially complete through 12 hours and markedly reduced through 24 hours. Compared to a somewhat heavier and older previously reported control group , pharmacokinetic values were similar except for a slightly lower AUC and t otal clearance in Chinese and a statistically significantly lower nonrenal clearance. Pharmacodynamic effects on ACE activity were essentially identic al. There is no reason to expect significant differences in fosinopril dosi ng or effect in a Chinese population compared to a Western population. (C) 1999 the American College of Clinical Pharmacology.