Journal of Pharmacy Practice · 2005 · 16 citations · 84 references
MedicinePharmacokineticsPharmacologyBioavailabilityClinical PharmacologyPharmacodynamicsAntibiotic ResistanceAntimicrobial PharmacodynamicsDose OptimizationDrug DispositionPharmacokinetics Of AntimicrobialsRespiratory PharmacologyAntibiotic Regimen OptimizationFluoroquinolone AntibioticsMultidrug-resistant OrganismsPharmacodynamics Of AntibioticsPharmacokinetics Of Antimicrobial AgentsRespiratory Bacterial Infections TreatmentSerum Half-lifeTissue Bioavailability
In this review, the authors describe the pharmacokinetic (PK) and pharmacodynamic (PD) characteristics of the new quinolones (levofloxacin, gatifloxacin, moxifloxacin, gemifloxacin, and garenoxacin) and discuss their implications on adequate therapy of patients with respiratory infections. The newer quinolones display excellent bioavailability and have longer serum half-lives than ciprofloxacin. In addition, they have the ability to concentrate in respiratory tract tissues and fluids at levels that exceed serum-drug concentrations. Also, the newer quinolones exhibit broad-spectrum activity against both susceptible and resistant organisms. Those favorable PK/PD properties make the new quinolones an attractive therapeutic alternative to traditional agents for common respiratory infections. Understanding the PK/PD of quinolone antibiotics can facilitate selection of optimal regimens to hasten response, prevent treatment failures, and minimize the development of resistance.
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Pharmacodynamics of Levofloxacin
Sandra L. Preston · JAMA · 1998 · 587 citations · Full text
Jennifer Thomas, Alan Forrest, Sujata M. Bhavnani et al. · Antimicrobial Agents and Chemotherapy · 1998 · 514 citations · Full text
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