R)-2-Arylpropionates are often inverted to the pharmacologically active S-enantiomers in vivo, although there is significant interspecies variability in inversion. In order to provide a basis for determining the biochemical consequences of this unique process using rats as a model, it was important
Stereoselective disposition of hydroxychloroquine and its metabolites in rats
β Scribed by Yimin Wei; Gloria A. Nygard; Shari L. Ellertson; Shoukry K.W. Khalil
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 576 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0899-0042
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract Liquidβphase microextraction based on polypropylene hollow fibers and CE were applied for the chiral determination of hydroxychloroquine (HCQ) and its metabolites (desethylchloroquine, DCQ; desethylhydroxychloroquine, DHCQ; bisdesethylchloroquine, BDCQ) in human urine. The analytes were
The pharmacokinetics and metabolic chiral inversion of the S(+)-and R(-)-enantiomers of tiaprofenic acid (S -TIA, R-TIA) were assessed in vivo in rats, and in addition the biochemistry of inversion was investigated in vitro in rat liver homogenates. Drug enantiomer concentrations in plasma were inve