Mouse tissue distribution and persistence of the food-born fusariotoxins Enniatin B and Beauvericin
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Development of a LC–MS/MS method for Enn B and Bea quantification in mice tissue.

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Nine days i.p. treatment of Enn B or Bea showed no systemic toxicity in mice.

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Contribution of hepatic/intestinal metabolism for Enn B but not Bea was suggested.

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Both substances showed distinct tissue accumulation with Bea being more potent.

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Tumor accumulation of Enn B and Bea emphasizes their anticancer potential

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