Several clinical investigations have been published regarding the inte
raction of nifedipine and quinidine. The results of these studies are
contradictory. In vitro studies indicate that the 3-hydroxylation and
N-oxigenation of quinidine appear to involve the P4503A4 family, a for
m of cytochrome that predominantly catalyzes the aromatization of nife
dipine, too. The aim of our study was to investigate the effect of ora
l intake of 200 mg quinidine on the kinetics of 20 mg nifedipine as a
retarded formulation and vice versa. Twelve healthy male volunteers be
tween 18 and 40 years were treated. Each subject was studied on three
occasions each separated by a one week washout period. Drug administra
tion consisted of one oral dose of nifedipine (Adalat(R) retard 20 mg)
, one oral dose of quinidine (Chinidin sulfuricum ''Buchler''(R) 200 m
g) or a combination of both (20 mg nifedipine and 200 mg quinidine) in
a randomised 3 way crossover. Administration of the test drugs in com
bination slightly increased the bioavailability of both - nifedipine [
N] to 18% and quinidine [Q] to 16% - and decreased the clearance of bo
th drugs. The results were not statistically significant. Based on our
data, the combination of nifedipine and quinidine seems to lack a cli
nically relevant interaction.