JAC Advance Access published online on January 14, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkg082
© 2003 by The British Society for Antimicrobial Chemotherapy
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Original article
1 Institute for Anaesthesiology,
University Medical Centre Sint Radboud, PO Box 9101, 6500 HB Nijmegen
* Corresponding author. E-mail: T.Vree{at}anes.azn.nl.
Received 26 October 2001
; revised 20 June 2002
; accepted 6 November 2002
The aims of this investigation were to calculate the
pharmacokinetic parameters of amoxicillin and clavulanic acid, and
to identify parameters that may affect their observed differences
in absorption. Data were obtained from plasma concentration-time
curves from four different open, randomized, two-treatment, two-period,
two-sequence, crossover Phase I bioequivalence studies, with the
following co-amoxiclav formulations: tablets 250/125, 500/125 and
875/125 mg, or 10 mL of an oral suspension 250/62.5 mg per 5 mL.
Data from 144 subjects and 288 drug administrations were available
for evaluation. After a 125 mg clavulanic acid dose (administered
as potassium clavulanate) for all four different formulations, the
clavulanic acid AUCt data ranged from 1.5 to 8 mg·h/L,
varying by a factor of 5. The absorption of clavulanic acid was
not related to the absorption of amoxicillin, or demographic factors,
and we were unable to identify the reasons for the large variability
in the absorption of clavulanic acid. We conclude that the absorption
of clavulanic acid, after oral administration, is highly variable
and may vary over a five-fold range between patients.
Keywords: amoxicillin-clavulanate, co-amoxiclav, amoxiclav,
pharmacokinetics, variable absorption, AUC,
amoxicillin/clavulanate ratio
Identical pattern of highly variable absorption
of clavulanic acid from four different oral formulations of co-amoxiclav
in healthy subjects
2 DADA Consultancy, Dennenstraat
109, 6543 JR Nijmegen
3 Disphar
International, Winkelskamp 6,
7522 PZ Hengelo (Gld), The Netherlands
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