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Effects of verapamil on etoposide pharmacokinetics after intravenous and oral administration in rats

โœ Scribed by Yong-Ji Piao; Xiuguo Li; Jun-Shik Choi

Publisher
Springer-Verlag
Year
2008
Tongue
English
Weight
624 KB
Volume
33
Category
Article
ISSN
0378-7966

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๐Ÿ“œ SIMILAR VOLUMES

PHARMACOKINETICS OF THE ENANTIOMERS OF V
PHARMACOKINETICS OF THE ENANTIOMERS OF VERAPAMIL AFTER INTRAVENOUS AND ORAL ADMINISTRATION OF RACEMIC VERAPAMIL IN A RAT MODEL
โœ M. MASOOD BHATTI; ROBERT T. FOSTER ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 111 KB ๐Ÿ‘ 2 views

Verapamil is a chiral calcium channel blocking drug which is useful clinically as the racemate in treating hypertension and arrhythmia. The published pharmacokinetic data for verapamil enantiomers in the rat model are limited. Utilizing a stereospeciยฎc highperformance liquid chromatographic (HPLC) a

Pharmacokinetics of ethopropazine in the
Pharmacokinetics of ethopropazine in the rat after oral and intravenous administration
โœ Mojdeh Maboudian-Esfahani; Dion R. Brocks ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 115 KB ๐Ÿ‘ 2 views

The pharmacokinetics of the anticholinergic drug ethopropazine (ET) have been studied in the rat after intravenous (i.v.) and oral administration. After i.v. doses of 5 and 10 mg/kg ET HCl, mean +/- S.D. plasma AUC were 9836 +/- 2129 (n = 4 rats) and 13096 +/- 4186 ng h/mL (n = 5 rats), respectively