๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Brain pharmacokinetics and tissue distribution of tetrahydropalmatine enantiomers in rats after oral administration of the racemate

โœ Scribed by Zhanying Hong; Guorong Fan; Jian Le; Yifeng Chai; Xueping Yin; Yutian Wu

Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
282 KB
Volume
27
Category
Article
ISSN
0142-2782

No coin nor oath required. For personal study only.

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

Stereospecific pharmacokinetics and toxi
Stereospecific pharmacokinetics and toxicodynamics of ketorolac after oral administration of the racemate and optically pure enantiomers to the rat
โœ F. Jamali; R. Lovlin; B.W. Corrigan; N.M. Davies; G. Aberg ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 114 KB ๐Ÿ‘ 2 views

To determine the stereospecific pharmacokinetics and gastrointestinal permeability (GI) changes (surrogate measures of toxicity) in the rat following oral administration of S, R, and racemic ketorolac (KT),optically pure enantiomers (S and R 2.5 mg/kg), and racemic KT (5 mg/kg) were administered ora

PHARMACOKINETICS OF SUPEROXIDE DISMUTASE
PHARMACOKINETICS OF SUPEROXIDE DISMUTASE IN RATS AFTER ORAL ADMINISTRATION
โœ C. Regnault; M. Soursac; M. Roch-Arveiller; E. Postaire; G. Hazebroucq ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 479 KB ๐Ÿ‘ 2 views

The kinetic behaviour of bovine erythrocyte Cu-Zn SOD was investigated in Sprague Dawley male rats after subcutaneous and oral administrations of doses ranging from 0.5 to 20mgkg-I. Studies have been carried out with SOD and SOD encapsulated into liposomes containing or not containing ceramides. The

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

Circadian variations in the pharmacokine
Circadian variations in the pharmacokinetics, tissue distribution and urinary excretion of nifedipine after a single oral administration to rats
โœ Qing-Ri Cao; Tae-Wan Kim; Jun Shik Choi; Beom-Jin Lee ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 129 KB ๐Ÿ‘ 2 views

## Abstract Circadian variations in the pharmacokinetics, tissue distribution and urinary excretion of nifedipine were examined in fasted rats after administering a single oral dose at three different dosing times (08:00 am, 16:00 pm, 00:00 am). The plasma concentrations, the areas under the plasma