𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Effect of perfusion rate and distribution factors on drug elimination kinetics in a perfused organ system

✍ Scribed by Renpei Nagashima; Gerhard Levy


Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
271 KB
Volume
57
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Effect of flow rate on the distribution
✍ Renpei Nagashima; Gerhard Levy πŸ“‚ Article πŸ“… 1968 πŸ› John Wiley and Sons 🌐 English βš– 302 KB πŸ‘ 1 views

sulfoxide. The previous findings showed that the same magnitude of inhibitory activity was obtained regardless of the use of these two solvents (1). Incubation was carried out with N-acetylserotonin and S-adenosyl-~-rnethionine-methyl-~~C according to the previously described procedure (1).

Effect of mode of administration on drug
✍ Milo Gibaldi πŸ“‚ Article πŸ“… 1969 πŸ› John Wiley and Sons 🌐 English βš– 459 KB πŸ‘ 1 views

The pharmacokinetics of drug distribution are evaluated for two types of drug administration, uiz., constant-rate intravenous infusion and instantaneous intravenous injection. Both modes of administration eventually result in a constant tissue compartmentcentral compartment distribution ratio of dru

Effects of shear stress on 3-D human mes
✍ Feng Zhao; Ravindran Chella; Teng Ma πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 264 KB πŸ‘ 2 views

## Abstract Shear stress is an important biomechanical parameter in regulating human mesenchymal stem cell (hMSC) construct development. In this study, the biomechanical characteristics of hMSCs within highly porous 3‐D poly (ethylene terephthalate) (PET) matrices in a perfusion bioreactor system w

A valid equation for the well-stirred pe
✍ Leonid M. Berezhkovskiy πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 165 KB πŸ‘ 1 views

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