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 (
✦ LIBER ✦
Reduction and Lumping of Physiologically Based Pharmacokinetic Models: Prediction of the Disposition of Fentanyl and Pethidine in Humans by Successively Simplified Models
✍ Scribed by Sven Björkman
- Book ID
- 111558415
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 247 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1573-8744
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