Obtaining and sustaining an erection are common problems for the male spinal cord injury patient. Intracavernous injection of vasoactive substances offers a new treatment option but it must be approached with caution in this population. In this work, the use of an alpha-adrenergic blocking agent, mo
Kinetics of cocaine in humans after intravenous and intranasal administration
β Scribed by J. I. Javaid; Mahmoud N. Musa; Marian Fischman; C. R. Schuster; John M. Davis
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 416 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0142-2782
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
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
## Abstract The aim of this study was to investigate the pharmacokinetic behavior of huperzine A (Hup A) in plasma and cerebrospinal fluid (CSF) after intranasal administration (0.5βmg/kg) in male SpragueβDawley rats. A pharmacokinetic study of intravenous Hup A (0.5βmg/kg) was also performed. The