In healthy volunteers, taking flucloxacillin with food does not compromise effective plasma concentrations in most circumstances

Autor: Jared Green, Philip G. Drennan, Sharon J. Gardiner, Stephen T. Chambers, Evan J. Begg, Richard J. Everts, Mei Zhang, Heather Isenman, Ronald Begg
Rok vydání: 2018
Předmět:
Male
Bacterial Diseases
0301 basic medicine
Staphylococcus
lcsh:Medicine
Pathology and Laboratory Medicine
0302 clinical medicine
Healthy volunteers
Medicine and Health Sciences
polycyclic compounds
Staphylococcus Aureus
030212 general & internal medicine
lcsh:Science
Cross-Over Studies
Multidisciplinary
Pharmaceutics
Stomach
Adjustment of Dosage at Steady State
Healthy Volunteers
Anti-Bacterial Agents
Bacterial Pathogens
Infectious Diseases
Medical Microbiology
Plasma concentration
Female
Drug Monitoring
Pathogens
Anatomy
Research Article
medicine.drug
Adult
030106 microbiology
Cmax
Microbial Sensitivity Tests
Bioequivalence
Drug Absorption
Microbiology
Floxacillin
Young Adult
03 medical and health sciences
Dose Prediction Methods
Animal science
Pharmacokinetics
Streptococcal Infections
medicine
Humans
Microbial Pathogens
Pharmacology
Bacteria
business.industry
lcsh:R
Organisms
Biology and Life Sciences
Crossover study
Gastrointestinal Tract
Pharmacodynamics
lcsh:Q
Flucloxacillin
business
Digestive System
Zdroj: PLoS ONE
PLoS ONE, Vol 13, Iss 7, p e0199370 (2018)
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0199370
Popis: It is usually recommended that flucloxacillin is given on an empty stomach. The aim of this study was to compare total and free flucloxacillin concentrations after oral flucloxacillin, given with and without food, based on contemporary pharmacokinetic and pharmacodynamic targets. Flucloxacillin 1000 mg orally was given to 12 volunteers, after a standardised breakfast and while fasting, on two separate occasions. Flucloxacillin concentrations over 12 hours were measured by liquid chromatography-tandem mass spectrometry. Pharmacokinetic parameters, and pharmacodynamic endpoints related to target concentration achievement, were compared in the fed and fasting states. For free flucloxacillin, the fed/fasting area under the concentration-time curve from zero to infinity (AUC0-∞) ratio was 0.80 (p
Databáze: OpenAIRE