Drug partitioning III. Kinetics of drug transfer in an in vitro model for drug absorption
β Scribed by James T. Doluisio; Joseph V. Swintosky
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- English
- Weight
- 493 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-3549
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β¦ Synopsis
The kinetics of drug transfer from a buffered aqueous phase (compartment A) through a lipid phase (compartment B ) to another aqueous buffered phase (compartment C) are reported. These kinetics are obtained from an in vifm model system which in important respects mimics drug transfer during the absorptive process. Several kinetic cases were observed-namely, DA -DB, DA DB,
π SIMILAR VOLUMES
The purpose of this research is to simulate the in vivo performance of drugs with a wide range of solubility and permeability characteristics formulated as oral dosage forms. The absorption-disposition model was developed using a number of physiological parameters as well as in vitro permeability da
## Abstract Inhibiting leukocyte recruitment is now a major focus in the design of novel antiβinflammatory drugs. Following the identification of lead compounds from conventional highβthroughput screens using appropriate receptors or enzymes, it is important to validate the action of the compounds