In Vivo Pharmacodynamics of a New Oxazolidinone (Linezolid)
| Autor: | William A. Craig, M. L. Van Ogtrop, David R. Andes, J. Peng |
|---|---|
| Rok vydání: | 2002 |
| Předmět: |
Staphylococcus aureus
Time Factors Micrococcaceae Microbial Sensitivity Tests Biology medicine.disease_cause Pneumococcal Infections Microbiology Mice Minimum inhibitory concentration chemistry.chemical_compound Pharmacokinetics Acetamides Drug Resistance Bacterial Streptococcus pneumoniae medicine Animals Experimental Therapeutics Pharmacology (medical) Oxazolidinones Antibacterial agent Pharmacology Mice Inbred ICR Linezolid biology.organism_classification Anti-Bacterial Agents Infectious Diseases chemistry Area Under Curve Pharmacodynamics Female |
| Zdroj: | Antimicrobial Agents and Chemotherapy. 46:3484-3489 |
| ISSN: | 1098-6596 0066-4804 |
| DOI: | 10.1128/aac.46.11.3484-3489.2002 |
| Popis: | Linezolid is a new oxazolidinone with activity against gram-positive cocci. We determined the in vivo activity of linezolid against four strains of Staphylococcus aureus (two methicillin-susceptible S. aureus [MSSA] strains and two methicillin-resistant S. aureus strains) and one penicillin-susceptible Streptococcus pneumoniae (PSSP) strain, two penicillin-intermediate S. pneumoniae strains, and five penicillin-resistant S. pneumoniae strains. The mice had 10 6.3 to 10 7.7 CFU/thigh before therapy and were then treated for 24 h with 5 to 1,280 mg of linezolid/kg divided into 1, 2, 4, 8, or 16 doses. The killing activities after 4 h of therapy ranged from 2.4 to 5.0 log 10 CFU/thigh against S. pneumoniae and 1.35 to 2.2 log 10 CFU/thigh against S. aureus . Increasing doses produced minimal concentration-dependent killing; doses of 20 and 80 mg/kg produced no in vivo postantibiotic effects (PAEs) with PSSP and modest PAEs (3.4 and 3.2 h) with MSSA. Pharmacokinetic studies at doses of 20 and 80 mg/kg by high-pressure liquid chromatography analysis exhibited peak dose values of 0.68 and 0.71 and elimination half-lives of 1.02 and 1.00 h. Linezolid MICs ranged from 0.5 to 1.0 μg/ml for S. pneumoniae and from 1.0 to 4.0 μg/ml for S. aureus . A sigmoid dose-response model was used to estimate the dose required to achieve a net bacteriostatic effect over 24 h. Static doses against S. pneumoniae ranged from 22.2 to 97.1 mg/kg/24 h and from 133 to 167 mg/kg/24 h for S. aureus . The 24-h area under the concentration-time curve (AUC)/MIC ratio was the major parameter determining the efficacy of linezolid against PSSP ( R 2 = 82% for AUC/MIC versus 57% for T>MIC and 59% for the peak level in serum/MIC [peak/MIC]). It was difficult to determine the most relevant pharmacokinetic/pharmacodynamic parameter with S. aureus , although the outcomes correlated slightly better with the 24-h AUC/MIC ratio ( R 2 = 75%) than with the other parameters (T>MIC R 2 = 75% and peak/MIC R 2 = 65%). The 24-h AUC/MIC ratio required for a bacteriostatic effect with linezolid varied from 22 to 97 (mean = 48) for pneumococci and from 39 to 167 (mean = 83) for staphylococci. Based upon a pharmacokinetic goal of a 24-h AUC/MIC of 50 to 100, a dosage regimen of 600 mg given either intravenously or orally twice daily would achieve success against organisms with MICs as high as 2 to 4 μg/ml. |
| Databáze: | OpenAIRE |
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