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Drug Metabolism & Disposition

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Research ArticleArticle

Predictive Utility of In Vitro Rifampin Induction Data Generated in Fresh and Cryopreserved Human Hepatocytes, Fa2N-4, and HepaRG Cells

Ian E. Templeton, J. Brian Houston and Aleksandra Galetin
Drug Metabolism and Disposition October 2011, 39 (10) 1921-1929; DOI: https://doi.org/10.1124/dmd.111.040824
Ian E. Templeton
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J. Brian Houston
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Aleksandra Galetin
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Abstract

Rifampin is a potent inducer of CYP3A4 in vitro and precipitates numerous drug-drug interactions (DDIs) when coadministered with CYP3A4 substrates. In the current study, we have critically assessed reported rifampin in vitro CYP3A4 induction data in Fa2N-4, HepaRG, and cryopreserved or primary human hepatocytes, using either CYP3A4 mRNA or probe substrate metabolism as induction endpoints. An in vivo data base of intravenously administered victim drugs (assuming hepatic induction only) was collated (n = 18) to assess the predictive utility of these in vitro systems and to optimize rifampin in vivo Emax. In addition, the effect of substrate hepatic extraction ratio on prediction accuracy was investigated using prediction boundaries proposed recently (Drug Metab Dispos 39:170–173). Incorporation of hepatic extraction ratio in the prediction model resulted in accurate prediction of 89% of intravenous induction DDIs (n = 18), regardless of the in vitro system or induction endpoint (mRNA or CYP3A4 activity). Effects of in vitro parameters from different cellular systems, and optimized in vivo Emax, on the prediction of 21 oral DDIs were assessed. Use of mRNA data resulted in pronounced overprediction across all systems, with 86 to 100% of DDIs outside the acceptable prediction limits; in contrast, CYP3A4 activity predicted up to 62% of the oral DDIs within limits. Although prediction accuracy of oral DDIs was improved when using intravenous optimized rifampin Emax, >35% of DDIs were incorrectly assigned, suggesting potential differential Emax between intestine and liver. Implications of the findings and recommendations for prediction of rifampin DDIs are discussed.

Footnotes

  • This work was supported by a consortium of pharmaceutical companies (GlaxoSmithKline, Lilly, Novartis, Pfizer, and Servier) within the Centre of Applied Pharmacokinetic Research at the University of Manchester.

  • Article, publication date, and citation information can be found at http://dmd.aspetjournals.org.

    doi:10.1124/dmd.111.040824.

  • ↵Embedded Image The online version of this article (available at http://dmd.aspetjournals.org) contains supplemental material.

  • ABBREVIATIONS:

    Emax
    maximum induced fold change
    EH
    hepatic extraction ratio
    AUCiv/AUCivind
    ratio of the intravenous victim drug AUC in the absence and presence of rifampin
    DDI
    drug-drug interaction.

  • Received May 20, 2011.
  • Accepted July 19, 2011.
  • Copyright © 2011 by The American Society for Pharmacology and Experimental Therapeutics
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Drug Metabolism and Disposition: 39 (10)
Drug Metabolism and Disposition
Vol. 39, Issue 10
1 Oct 2011
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Research ArticleArticle

PREDICTION OF RIFAMPIN INDUCTION DRUG-DRUG INTERACTIONS

Ian E. Templeton, J. Brian Houston and Aleksandra Galetin
Drug Metabolism and Disposition October 1, 2011, 39 (10) 1921-1929; DOI: https://doi.org/10.1124/dmd.111.040824

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Research ArticleArticle

PREDICTION OF RIFAMPIN INDUCTION DRUG-DRUG INTERACTIONS

Ian E. Templeton, J. Brian Houston and Aleksandra Galetin
Drug Metabolism and Disposition October 1, 2011, 39 (10) 1921-1929; DOI: https://doi.org/10.1124/dmd.111.040824
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