Pharmacokinetic evaluation of noreximide in rats
โ Scribed by Heinrich P. Koch; Gertrude Pischek; Margarete Holzbecher; Wolfgang A. Ritschel
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 296 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0142-2782
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
The pharmacokinetics of noreximide in the rat after i.v., p.o., and i.p. administration was studied. The biologic halfโlife of approximately 8 h was found almost the same for all three routes. Upon p.o. administration the fraction of drug absorbed is 85 per cent, and the peak concentration in the blood is reached within approximately 4.5 h. Additional pharmacoโkinetic parameters are listed.
๐ SIMILAR VOLUMES
The dispositions of free and liposomal entrapped ampicillin were compared in male and female rats after IV administration. Serial blood samples were collected for 2 h in the free drug study and 12 h for the liposomal formulation. Pharmacokinetic parameters obtained with free drug were not signiยฎcant
## Abstract The pharmacokinetics of a series of novel cyclic, nonโpeptide inhibitors of HIV protease were studied in rats or dogs after intravenous and oral administration. Six symmetrically substituted cyclic urea compounds (XK234, XM311, XM320, XM321, XM323, and XM412), which effectively inhibite
Stereoselectivity of the pharmacokinetics of the nonsteroidal antiinflammatory drug flobufen, 4-(2ะ,4ะ-difluorobiphenyl-4-yl)-2-methyl-4-oxobutanoic acid, was studied in male Wistar rats after intravenous administration. Pharmacokinetic parameters and chiral inversion of flobufen enantiomers were st