A consistent account of the assumptions of the well-stirred perfusion limited model leads to the equation for the organ tissue that does not coincide with that often presented in books and papers. The difference in pharmacokinetic profiles calculated by the valid and the commonly used equations coul
✦ LIBER ✦
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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