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Biopharmaceutics & Drug Disposition|July 12, 2019
Biopharmaceutics classification and intestinal absorption of chikusetsusaponin IVaWenzhou Zhang, Hui Liu, Chongfeng LiuBiopharmaceutics & Drug Disposition|June 11, 2011
Physiological modeling and assessments of regional drug bioavailability of danoprevir to determine whether a controlled release formulation is feasibleMicaela B Reddy, Alyson Connor, Barbara J Brennan, et al.Biopharmaceutics & Drug Disposition|July 5, 2011
Are there differences in the catalytic activity per unit enzyme of recombinantly expressed and human liver microsomal cytochrome P450 2C9? A systematic investigation into inter-system extrapolation factorsH K Crewe, Z E Barter, K Rowland Yeo, et al.Biopharmaceutics & Drug Disposition|November 22, 2015
Possible interaction of quinolone antibiotics with peptide transporter 1 in oral absorption of peptide-mimetic drugsHiroshi Arakawa, Hiroki Kamioka, Masahiko Kanagawa, et al.Biopharmaceutics & Drug Disposition|January 11, 2016
Tissue distribution of teneligliptin in rats and comparisons with data reported for other dipeptidyl peptidase-4 inhibitorsYoshinobu Nakamaru, Fumihiko Akahoshi, Hiroaki Iijima, et al.Biopharmaceutics & Drug Disposition|April 10, 2016
Biliary excretion of pravastatin and taurocholate in rats with bile salt export pump (Bsep) impairmentYaofeng Cheng, Chris Freeden, Yueping Zhang, et al.Biopharmaceutics & Drug Disposition|March 1, 1989
Pharmacokinetics and pharmacodynamics of physostigmine in the rat after oral administrationS M SomaniBiopharmaceutics & Drug Disposition|February 11, 2016
Establishing population distribution of drug-metabolizing enzyme activities for the use of salivary caffeine as a dynamic liver function marker in a Singaporean Chinese populationHazel Yiting Chia, Wai-Ping Yau, Han Kiat HoBiopharmaceutics & Drug Disposition|August 22, 2015
Development of a physiologically based pharmacokinetic/pharmacodynamic model to identify mechanisms contributing to entacapone low bioavailabilitySaeed Alqahtani, Amal KaddoumiBiopharmaceutics & Drug Disposition|November 5, 2015
A physiologically based pharmacokinetic model to predict the pharmacokinetics of highly protein-bound drugs and the impact of errors in plasma protein bindingMin Ye, Swati Nagar, Ken KorzekwaPageof 214