Pharmacokinetics of N-2-chloroethylaziridine, a volatile cytotoxic metabolite of cyclophosphamide, in the rat
β Scribed by Hong Lu; Kenneth K. Chan
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 282 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0344-5704
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π SIMILAR VOLUMES
## Abstract The main objective of this study was to determine the pharmacokinetics of the enantiomers of desbutylhalofantrine (DHF), a metabolite of halofantrine (HF), in the rat. Rats received either intravenous (2 mg/kg) or oral (7 mg/kg) (Β±)βDHF HCl, or (Β±)βHF HCl intravenously (3 mg/kg). Enanti
Alcophosphamide was identified in urine obtained from Sprague-Dawley rats treated with a 1 : l mixture of cyclophosphamide and f3-(2H4)cyclophosphamide using chemical ionization mass spectrometry and the ion cluster technique. This compound was also quantified in rat plasma using gas chromatographic