References
- Batrakova, E. V., Han, H. Y., Alakhov, V. Y., Miller, D. W., and Kabanov, A. V., Effects of pluronic block copolymers on drug absorption in Caco-2 cell monolayers. Pharm. Res., 15, 850-855 (1998) https://doi.org/10.1023/A:1011964213024
- Borst, P., Evers, R., Kool, M., and Wijnholds, J., The multidrug resistance protein family. Biophys. Acta, 1461, 347-357 (1999) https://doi.org/10.1016/S0005-2736(99)00167-4
- Cornaire, G., Woodley, J. F., Saivin, S., Legendre, J.Y., Decourt, S., Cloarec, A., and Houin, G., Effect of polyoxyl 35 castor oil and Polysorbate 80 on the intestinal absorption of digoxin in vitro. Arzneimittel-forschung., 50, 576-579 (2000)
- Fromm, M. F., Kim, R. B., Stein, C. M., Wilkinson, G. R., and Roden, D. M., Inhibition of P-glycoprotein-mediated drug transport: A unifying mechanism to explain the interaction between digoxin and quinidine. Circulation, 99, 552-557 (1999) https://doi.org/10.1161/01.CIR.99.4.552
- Gottesman, M. M. and Pastan, I., Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu. Rev. Biochem., 62, 385-427 (1993) https://doi.org/10.1146/annurev.bi.62.070193.002125
- Hedman, A., Angelin, B., Arvidsson, A., Dahlqvist, R., and Nilsson, B.. Interactions in the renal and biliary elimination of digoxin: stereoselective difference between quinine and quinidine. Clin. Pharmacol. Ther., 47, 20-26 (1990) https://doi.org/10.1038/clpt.1990.3
- Hinderling, P. H. and Hartmann, D., Pharmacokinetics of digoxin and main metabolites/ derivatives in healthy humans. Ther. Drug Monit., 13, 381-401 (1991) https://doi.org/10.1097/00007691-199109000-00001
- Hugger, E. D., Novak, B. L., Burton, P. S., Audus, K. L., and Borchardt, R. T., A comparison of commonly used polyehtoxylated pharmaceutical excipients on their ability to inhibit P-glycoprotein activity in vitro. J. Pharm. Sci., 91, 1991-2002 (2002) https://doi.org/10.1002/jps.10176
- Iisalo, E., Clinical pharmacokinetics of digoxin. Clin. Pharmacokinet., 2, 1-16 (1977) https://doi.org/10.2165/00003088-197702010-00001
- Knutsen, T., Mickley, L. A., Ried, T., Green, E. D., du Manoir, S., Schrock, E., Macville, M., Ning, Y., Robey, R., Polymeropoulos, M., Torres, R., and Fojo, T., Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL. Genes Chromosomes Cancer, 23, 44-54 (1998) https://doi.org/10.1002/(SICI)1098-2264(199809)23:1<44::AID-GCC7>3.0.CO;2-6
- Litman, T., Druley, T. E., Stein, W. D., and Bates, S. E., From MDR to MXR: new understanding of multidrug resistance systems, their properties and clinical significance. Cell. Mol. Life Sci. 58, 931-959 (2001) https://doi.org/10.1007/PL00000912
- Malingre, M M., Schellens, J. H., Van Tellingen, O., Ouwehand, M., Bardelmeijer, H. A., Rosing, H., Koopman, F. J., Schot, M. E., Ten Bokkel Huinink, W. W., and Beijnen, J. H., The cosolvent Cremophor EL limits absorption of orally administered paclitaxel in cancer patients. Br. J. Cancer, 85, 1472-1477 (2001) https://doi.org/10.1054/bjoc.2001.2118
- Nerurkar, M. M., Ho, N. F., Burton, P. S., Vidmar, T. J., and Borchardt, R. T., Mechanistic roles of neutral surfactants on concurrent polarized and passive membrane transport a model peptide in Caco-2 cells. J. Pharm. Sci., 86, 813-821 (1997) https://doi.org/10.1021/js960483y
- Salphati, L. and Benet, L. Z., Effects of ketoconazole on digoxin absorption and disposition in rat. Pharmacology, 56, 308-313 (1998) https://doi.org/10.1159/000028214
- Salphati, L. and Benet, L. Z., Metabolism of digoxin and digoxigenin digitoxosides in rat liver microsomes: involvement of cytochrome P4503A. Xenobiotica, 29, 171-85 (1999) https://doi.org/10.1080/004982599238722
- Silverman, J. A., Multidrug-resistance transporters. Pharm. Biotechnol., 12, 353-86 (1999)
- Song, S., Suzuki, H., Kawai, R., and Sugiyama, Y., Effect of PSC 833, a P-glycoprotein modulator, on the disposition of vincristine and digoxin in rats. Drug Metab. Disp., 27, 689-694 (1999)
- Stephens, R. H., O'Neill, C. A., Warhurst, A., Carlson, G. L., Rowland, M., and Warhurst, G., Kinetic profiling of P-glycoprotein-mediated drug efflux in rat and human intestinal epithelia. J. Pharmacol. Exp. Ther., 296, 584-591 (2001)
- Tanigawara, Y., Role of P-glycoprotein in drug disposition. Ther. Drug Monit., 22, 137-140 (2000) https://doi.org/10.1097/00007691-200002000-00029
- Troutman, M. D., Luo, G., Gan, L. S., and Thakker, D. R., The role of P-glycoprotein in drug disposition: significance to drug development. In Rodrigues, A. D. (ed.). Drug-drug interactions. Marcel Dekker, New York. pp. 295-357 (2001)
- van Zuylen, L., Verweij, J., and Sparreboom, A., Role of formulation vehicles in taxane pharmacology. Invest. New Drugs, 19,125-141 (2001) https://doi.org/10.1023/A:1010618632738
- Verschraagen, M., Koks, C. H., Schellens, J. H., and Beijnen, J. H., P-glycoprotein system as a determinant of drug interactions: the case of digoxin-verapamil. Pharmacol. Res., 40, 301-306 (1999) https://doi.org/10.1006/phrs.1999.0535
- Yamazaki, M., Neway, W. E., Ohe, T., Chen, I., Rowe, J. F., Hochman, J. H., Chiba, M., and Lin, J. H., In vitro substrate identification studies for p-glycoprotein-mediated transport: species difference and predictability of in vivo results. J. Pharmacol. Exp. Ther., 296, 723-735 (2001)
- Yao, M., Zhang, H., Chong, S., Zhu, M., and Morrison, R. A., A rapid and sensitive LC/MS/MS assay for quantitative determination of digoxin in rat plasma. J. Pharmaceu. Biomed. Anal., 32, 1189-1197 (2003) https://doi.org/10.1016/S0731-7085(03)00050-5