Many in vitro data on physicochemical properties and specific absorption, distribution, metabolism, and elimination (ADME) processes are already available at early stages of drug discovery. These data about new drug candidates could be integrated/ connected in physiologically based pharmacokinetic (
Effect of parameter variability on physiologically-based pharmacokinetic model predicted drug concentrations
✍ Scribed by Peter Varkonyi; James V. Bruckner; James M. Gallo
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 446 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0022-3549
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