FATE OF ERYTHRITOL AFTER SINGLE ORAL-ADMINISTRATION TO RATS AND DOGS

Citation
K. Noda et al., FATE OF ERYTHRITOL AFTER SINGLE ORAL-ADMINISTRATION TO RATS AND DOGS, Regulatory toxicology and pharmacology, 24(2), 1996, pp. 206-213
Citations number
10
Categorie Soggetti
Medicine, Legal","Pharmacology & Pharmacy",Toxicology
ISSN journal
02732300
Volume
24
Issue
2
Year of publication
1996
Part
2
Pages
206 - 213
Database
ISI
SICI code
0273-2300(1996)24:2<206:FOEASO>2.0.ZU;2-O
Abstract
The absorption and distribution of radiolabeled erythritol were studie d in Wistar rats and beagle dogs after a single oral administration in doses ranging from 0.125 to 2.0 g erythritol/kg body wt. Erythritol c oncentrations in blood and plasma of rats reached their maxima 1 hr af ter administration and then declined biexponentially, In the blood and plasma of dogs, the highest concentrations occurred after 1/2 hr foll owed by a similar decline. Blood plasma distribution ratios and plasma protein binding ratios increased as blood plasma levels declined. At 120 hr after administration, 95.68 +/- 2.25% of the radioactivity had been excreted in the urine of dogs and 92.70 +/- 0.44% in the urine of rats; 0.33 +/- 0.05% had been excreted in the feces of dogs and 1.19 +/- 0.09% in the feces of rats; 1.17 +/- 0.04% had been excreted in ex pired air from dogs and 4.80 +/- 0.32% in expired air from rats. The r esults demonstrate that erythritol is rapidly absorbed and excreted, p rincipally through the urinary pathway. (C) 1996 Academic Press, Inc.