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Pilot toxicokinetic study and absolute oral bioavailability of the Fusarium mycotoxin enniatin B1 in pigs

Food Chem Toxicol. 2014 Jan:63:161-5. doi: 10.1016/j.fct.2013.11.005. Epub 2013 Nov 13.

Abstract

The aim of present study was to reveal the toxicokinetic properties and absolute oral bioavailability of enniatin B1 in pigs. Five pigs were administered this Fusarium mycotoxin per os and intravenously in a two-way cross-over design. The toxicokinetic profile fitted a two-compartmental model. Enniatin B1 is rapidly absorbed after oral administration (T(1/2a)=0.15 h, Tmax=0.24h) and rapidly distributed and eliminated as well (T(1/2elα)=0.15 h; T(1/2elβ)=1.57 h). The absolute oral bioavailability is high (90.9%), indicating a clear systemic exposure. After intravenous administration, the mycotoxin is distributed and eliminated rapidly (T(1/2elα)=0.15 h; T(1/2elβ)=1.13 h), in accordance with oral administration.

Keywords: Absolute oral bioavailability; Enniatin B1; Mycotoxin; Pig; Toxicokinetics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Administration, Oral
  • Animals
  • Area Under Curve
  • Biological Availability
  • Chromatography, Liquid
  • Depsipeptides / administration & dosage
  • Depsipeptides / pharmacokinetics*
  • Depsipeptides / toxicity*
  • Fusarium / chemistry*
  • Half-Life
  • Pilot Projects
  • Swine
  • Tandem Mass Spectrometry

Substances

  • Depsipeptides
  • enniatins