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Biopharmaceutics & Drug Disposition|October 1, 1995
Comparison of plasma and saliva concentrations of the active monohydroxy metabolite of oxcarbazepine in patients at steady stateJ M Cardot, P Degen, G Flesch, et al.Biopharmaceutics & Drug Disposition|October 1, 1995
Factors influencing the protein binding of azosemide using an equilibrium dialysis techniqueS H Lee, M G LeeBiopharmaceutics & Drug Disposition|November 25, 2016
Selective reduction in the expression of UGTs and SULTs, a novel mechanism by which piperine enhances the bioavailability of curcumin in ratXiaohui Zeng, Dake Cai, Qiaohuang Zeng, et al.Biopharmaceutics & Drug Disposition|March 1, 1989
Primaquine disposition in the isolated perfused rat liver: effect of mefloquine induced bile flow reductionM D Coleman, L Fleckenstein, M H HeifferBiopharmaceutics & Drug Disposition|October 21, 2016
P-gp activity and inhibition in the different regions of human intestine ex vivoMing Li, Inge A M de Graaf, Marina H de Jager, et al.Biopharmaceutics & Drug Disposition|December 23, 2016
The absorption kinetics of ketoconazole plays a major role in explaining the reported variability in the level of interaction with midazolam: Interplay between formulation and inhibition of gut wall and liver metabolismBo Liu, H Kim Crewe, Mahmut Ozdemir, et al.Biopharmaceutics & Drug Disposition|April 23, 2014
Hepatic microsomal UDP-glucuronosyltransferase (UGT) activities in the microminipigEriko Higashi, Akihiro Ando, Shunsuke Iwano, et al.Biopharmaceutics & Drug Disposition|March 4, 2017
Impact of acute fat mobilisation on the pharmacokinetics of the highly fat distributed compound TAK-357, investigated by physiologically based pharmacokinetic (PBPK) modeling and simulationAkihiko Goto, Yoshihiko Tagawa, Yuu Moriya, et al.Biopharmaceutics & Drug Disposition|February 17, 2017
Pharmacokinetic interactions in mice between irinotecan and MBL-II-141, an ABCG2 inhibitorEmilie Hénin, Mylène Honorat, Jérôme Guitton, et al.Biopharmaceutics & Drug Disposition|February 17, 2017
Optimization of intestinal microsomal preparation in the rat: A systematic approach to assess the influence of various methodologies on metabolic activity and scaling factorsOliver J D Hatley, Christopher R Jones, Aleksandra Galetin, et al.Pageof 214