Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractGenetic and functional characterization of dpp genes encoding a dipeptide transport system in Lactococcus lactis    Next AbstractAnti-Acanthamoeba activity of Tunisian Thymus capitatus essential oil and organic extracts »

Fundam Appl Toxicol


Title:"Effect of Emulphor, an emulsifier, on the pharmacokinetics and hepatotoxicity of oral carbon tetrachloride in the rat"
Author(s):Sanzgiri UY; Bruckner JV;
Address:"College of Pharmacy, University of Georgia, Athens, Georgia 30602-2356, USA"
Journal Title:Fundam Appl Toxicol
Year:1997
Volume:36
Issue:1
Page Number:54 - 61
DOI: 10.1006/faat.1997.2290
ISSN/ISBN:0272-0590 (Print) 0272-0590 (Linking)
Abstract:"Emulphor, a polyethoxylated vegetable oil, is now being used widely to incorporate volatile organic compounds (VOCs) and other lipophilic compounds into aqueous solutions for biochemical, pharmacokinetic, and toxicological studies. Previous work in this laboratory demonstrated that 0.25% Emulphor did not alter the kinetics or hepatotoxicity of low doses of CCl4 compared to when the halocarbon was given to rats orally in water. The present study was undertaken as there was concern that higher concentrations of Emulphor (necessary to maintain lipophilic VOCs in stable aqueous emulsions for extended periods) might alter the VOCs' absorption, disposition, and/or toxicity. Dosages of 10 and 180 mg CCl4/kg bw were given, as an aqueous emulsion using 1, 2.5, 5, or 10% Emulphor, by gavage to fasted male Sprague-Dawley rats. Serial microsamples of blood were collected from an indwelling cannula in unanesthetized, freely moving rats at intervals of 2-60 min for up to 12 hr. The samples' CCl4 content was measured by headspace gas chromatography. Thereby, it was possible to obtain blood CCl4 concentration-versus-time profiles. Animals were euthanized 24 hr postdosing and blood was collected for measurement of serum enzymes as indices of hepatotoxicity. No toxicologically significant differences in pharmacokinetic parameters as a function of Emulphor concentration were found. Similarly the hepatotoxic potency of 10 and 180 mg/kg CCl4, as reflected by elevation in serum enzyme activities, did not vary significantly with the concentration of Emulphor utilized. Hence, it can be concluded that Emulphor, in concentrations as high as 10% (equivalent to 260 mg Emulphor/kg bw) in aqueous emulsions, does not significantly affect the absorption, disposition, or acute hepatotoxicity of CCl4 in male Sprague-Dawley rats"
Keywords:"Administration, Oral Alanine Transaminase/drug effects/metabolism Animals Area Under Curve Carbon Tetrachloride/administration & dosage/*pharmacokinetics *Chemical and Drug Induced Liver Injury Drug Interactions L-Iditol 2-Dehydrogenase/drug effects/metab;"
Notes:"MedlineSanzgiri, U Y Bruckner, J V eng Research Support, U.S. Gov't, Non-P.H.S. 1997/03/01 Fundam Appl Toxicol. 1997 Mar; 36(1):54-61. doi: 10.1006/faat.1997.2290"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024