Unbound MEDLINE

Identical pattern of highly variable absorption of clavulanic acid from four different oral formulations of co-amoxiclav in healthy subjects. The Journal of antimicrobial chemotherapy. [J Antimicrob Chemother] Journal article

 
TitleIdentical pattern of highly variable absorption of clavulanic acid from four different oral formulations of co-amoxiclav in healthy subjects.
Author(s)Vree TB, Dammers E, Exler PS 
InstitutionInstitute for Anaesthesiology, University Medical Centre Sint Radboud, PO Box 9101, 6500 HB Nijmegen. T.Vree@anes.azn.nl
SourceJ Antimicrob Chemother 2003 Feb; 51(2):373-8.
MeSHAdult
Amoxicillin
Amoxicillin-Potassium Clavulanate Combination
Anti-Bacterial Agents
Area Under Curve
Chemistry, Pharmaceutical
Chromatography, Liquid
Clavulanic Acid
Comparative Study
Cross-Over Studies
Drug Therapy, Combination
Half-Life
Humans
Male
Spectrum Analysis, Mass
AbstractThe 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 AUC(t) 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.
Languageeng
Pub Type(s)Clinical Trial
Journal Article
Randomized Controlled Trial
PubMed ID12562705
  
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