Modulating hesperetin bioavailability at the level of its intestinal metabolism and ABC transporter mediated efflux studied in Caco-2 monolayers

W. Brand; P.A.I. van der Wel; G. Williamson; P.J. van Bladeren; I. Rietjens

doi:10.1016/j.toxlet.2007.05.276

Modulating hesperetin bioavailability at the level of its intestinal metabolism and ABC transporter mediated efflux studied in Caco-2 monolayers

W. Brand, P.A.I. van der Wel, G. Williamson, P.J. van Bladeren, I. Rietjens

Research output: Contribution to journal › Abstract › Academic

Abstract

In: Abstracts of the 44th congress of the European societies of toxicolgy, EUROTOX 2007

Original language	English
Pages (from-to)	S101
Journal	Toxicology Letters
Volume	172
Issue number	Suppl. 1
DOIs	https://doi.org/10.1016/j.toxlet.2007.05.276
Publication status	Published - 2007

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10.1016/j.toxlet.2007.05.276

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title = "Modulating hesperetin bioavailability at the level of its intestinal metabolism and ABC transporter mediated efflux studied in Caco-2 monolayers",

abstract = "In: Abstracts of the 44th congress of the European societies of toxicolgy, EUROTOX 2007",

author = "W. Brand and {van der Wel}, P.A.I. and G. Williamson and {van Bladeren}, P.J. and I. Rietjens",

year = "2007",

doi = "10.1016/j.toxlet.2007.05.276",

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volume = "172",

pages = "S101",

journal = "Toxicology Letters",

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T1 - Modulating hesperetin bioavailability at the level of its intestinal metabolism and ABC transporter mediated efflux studied in Caco-2 monolayers

AU - Brand, W.

AU - van der Wel, P.A.I.

AU - Williamson, G.

AU - van Bladeren, P.J.

AU - Rietjens, I.

PY - 2007

Y1 - 2007

N2 - In: Abstracts of the 44th congress of the European societies of toxicolgy, EUROTOX 2007

AB - In: Abstracts of the 44th congress of the European societies of toxicolgy, EUROTOX 2007

U2 - 10.1016/j.toxlet.2007.05.276

DO - 10.1016/j.toxlet.2007.05.276

M3 - Abstract

SN - 0378-4274

VL - 172

SP - S101

JO - Toxicology Letters

JF - Toxicology Letters

IS - Suppl. 1

ER -

Modulating hesperetin bioavailability at the level of its intestinal metabolism and ABC transporter mediated efflux studied in Caco-2 monolayers

Abstract

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