| Literature DB >> 21508937 |
K Eechoute1, R M Franke, W J Loos, L A Scherkenbach, I Boere, J Verweij, H Gurney, R B Kim, R G Tirona, R H J Mathijssen, A Sparreboom.
Abstract
The bioavailability of orally administered imatinib is >90%, although the drug is monocationic under the acidic conditions in the duodenum. In vitro, we found that imatinib is transported by the intestinal uptake carrier organic anion transporting polypeptide (OATP1A2) and that this process is sensitive to pH, rosuvastatin, and genetic variants. However, in a study in patients with cancer, imatinib absorption was not associated with OATP1A2 variants and was unaffected by rosuvastatin. These findings highlight the importance of verifying in a clinical setting the drug-transporter interactions observed in in vitro tests.Entities:
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Year: 2011 PMID: 21508937 PMCID: PMC3476732 DOI: 10.1038/clpt.2011.42
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875