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Physiological perfusion model for cephalosporin antibiotics I: Model selection based on blood drug concentrations

✍ Scribed by D. S. Greene; R. Quintiliani; C. H. Nightingale


Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
563 KB
Volume
67
Category
Article
ISSN
0022-3549

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✦ Synopsis


Various cephalosporins with different degrees of protein binding were administered to human volunteers. Blood samples were collected as a function of time and were assayed for drug content by a microbiological assay. A pharmacokinetic analysis of the data was performed using a two-compartment model with and without protein binding in the central compartment and a perfusion model. Both the two-compartment model without protein binding and the physiological perfusion model adequately described the blood levels of all three cephalosporins.


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