Comparative efflux of saquinavir, ritonavir and lopinavir from primary human cells

B. Diker, Omar Janneh, R.P.G. van Heeswijk, K.F.T. Copeland

    Research output: Contribution to journalArticle

    4 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)241-245
    JournalDrug Metabolism Letters
    Volume4
    Issue number4
    Publication statusPublished - 2010

    Bibliographical note

    The full text of this item is not available from the repository.
    The journal homepage can be found at: http://www.benthamscience.com/dml/index.htm

    Keywords

    • Protease inhibitor
    • HIV-1
    • release
    • peripheral blood
    • saquinavir
    • ritonavir
    • lopinavir
    • Therapeutic drug monitoring
    • plasma drug concentrations
    • Peripheral blood mononuclear cells
    • cell-associated drug concentrations
    • Highly active antiretroviral therapy (HAART)
    • non-nucleoside
    • lymphocytes
    • Multi-drug resistance
    • breast cancer resistance protein (BCRP)
    • lipophilicity
    • anti-coagulated
    • Octanol-Saline Partition Coefficient
    • efflux proteins
    • drug-containing bathing media

    Cite this

    Diker, B., Janneh, O., van Heeswijk, R. P. G., & Copeland, K. F. T. (2010). Comparative efflux of saquinavir, ritonavir and lopinavir from primary human cells. Drug Metabolism Letters, 4(4), 241-245.