Isolation and characterization of urinary metabolites of nalorphine in dogs and cats
โ Scribed by S. Y. Yeh; L. A. Woods
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- English
- Weight
- 355 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
โฆ Synopsis
Nalorphine-3-glucuronide dihydrate and nalorphine-6-glucuronide were isolated as urinary metabolites of nalorphine in dogs, and nalorphine-3-ethereal sulfate and nalorphine-3-glucuronide dihydrate were isolated in cats. These metabolites were characterized by UV and IR spectra, phenolic test, nalorphine and glucuronic acid determinations, elemental analyses, and enzymatic hydrolysis.
Keyphrases 0 Nalorphine, urinary metabolites-isolation, characterization, in dogs, cats I J TLC-separation 0 Paper chromatography-separation 0 UV spectrophotometry-identification 0 IR spectrophotometry-identification Nalorphine is N-dealkylated to normorphine in vitro by rat liver microsomes (1) and in vivo in rats (2) and cats (3), and it is conjugated in rats (4) and dogs ACKNOWLEDGMENTS AND ADDRESSES
๐ SIMILAR VOLUMES
The pharmacokinetics and renal excretion of a trichothecene mycotoxin, verrucarol, were studied in six mongrel dogs following IV administration (0.4 mg kg-I). The fraction of verrucarol excreted intact in the urine ranged from 0.9% to 2.7% of the administered dose. The fraction of verrucarol metabo
## Abstract ฮ^8,9^โDehydroestrone is the fifth most abundant component in the conjugated equine estrogen preparation Premarinยฎ, representing about 2 to 6% of the total steroids in the tablet. The metabolism of this estrogen has been determined in female beagle dogs after acute peroral administratio
The urine collected from three dogs for 24 hr. after oral administration of but~olol-'~C contained 61.2% of the administered radioactivity. An acidic metabolite, representing 16% of the urinary IrC, was purified by ether extraction and preparative TLC. The methyl ester of the metabolite was prepared