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Intracellular Drug Concentrations and Transporters: Measurement, Modeling, and Implications for the Liver
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2013 (English)In: Clinical Pharmacology and Therapeutics, ISSN 0009-9236, E-ISSN 1532-6519, Vol. 94, no 1, 126-141 p.Article, review/survey (Refereed) Published
Abstract [en]

Intracellular concentrations of drugs and metabolites are often important determinants of efficacy, toxicity, and drug interactions. Hepatic drug distribution can be affected by many factors, including physicochemical properties, uptake/efflux transporters, protein binding, organelle sequestration, and metabolism.This white paper highlights determinants of hepatocyte drug/metabolite concentrations and provides an update on model systems, methods, and modeling/simulation approaches used to quantitatively assess hepatocellular concentrations of molecules. The critical scientific gaps and future research directions in this field are discussed.

Place, publisher, year, edition, pages
2013. Vol. 94, no 1, 126-141 p.
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Medical and Health Sciences
URN: urn:nbn:se:uu:diva-206394DOI: 10.1038/clpt.2013.78ISI: 000321028500018OAI: oai:DiVA.org:uu-206394DiVA: diva2:644536

On behalf of the International Transporter Consortium.

Available from: 2013-08-30 Created: 2013-08-30 Last updated: 2013-08-30Bibliographically approved

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Matsson, Pär
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