PHARMACOKINETICS AND BIOAVAILABILITY OF A CONTROLLED RELEASE AMOXICILLIN FORMULATION

Authors:
  • AAA ARANCIBIA
    A ARANCIBIA
  • GGG GONZALEZ
    G GONZALEZ
  • AIA ICARTE
    A ICARTE
  • MAM ARANCIBIA
    M ARANCIBIA
  • PAP ARANCIBIA
    P ARANCIBIA

  • 1 February 1987
    • journal article
    • research article
    • Vol. 25  (2) , 97-100
    • PMID:3557736
Abstract
The pharmacokinetics and bioavailability of an in vitro controlled release amoxicillin formulation were studied in nine healthy volunteers, in comparison with an intravenous injection and a conventional tablet. The experiment was designed in a crossover fashion. The volunteers received the three formulations on separate occasions. The antibiotic was measured in plasma using a microbiological method. The absolute bioavailability of the two solid dosage forms was estimated comparing non-compartmental parameters. The results indicated that there was no correlation between the in vitro dissolution rate and the pharmacokinetic behavior in the body.

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