Cefixime is an orally administered cephalosporin with physicochemical
properties able to account for a possibly significant biliary excretio
n. In addition, over 50 % of total clearance of the drug has been show
n to operate through extra renal pathways in healthy volunteers. The a
im of the study was to quantify and to delineate the kinetics of cefix
ime biliary elimination in ten patients provided with external drainag
e. Following a single 200 mg oral dose of cefixime, biliary clearance
of the drug appears to vary from 0.85 to 27.3 ml/min. Contribution of
the latter to the apparent total clearance is relatively low since ran
ging from 0.8 to 18.6 % (mean 5 %). Additionaly, biliary clearance kin
etics of the drug proves non linear and well described according to a
sigmoidal model. On account of these results, and given the dianionic
charge of the molecule as well as the absence of any metabolite report
ed so far, an intrahepatic binding and accumulating process, mediated
by ligandin, seems to underlie the hepatobiliary excretion of cefixime
, as previously reported for other anionic betalactam antibiotics.