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Volumn 16, Issue 1, 2014, Pages 172-180

Use of different parameters and equations for calculation of IC 50 values in efflux assays: Potential sources of variability in IC50 determination

Author keywords

Caco 2; Drug interaction; IC50; Inhibition; P glycoprotein

Indexed keywords

DIGOXIN; ITRACONAZOLE; SPIRONOLACTONE; VARDENAFIL;

EID: 84893688044     PISSN: 15507416     EISSN: None     Source Type: Journal    
DOI: 10.1208/s12248-013-9554-7     Document Type: Article
Times cited : (55)

References (57)
  • 1
    • 65549102615 scopus 로고    scopus 로고
    • P-gp inhibition potential in cell-based models: Which "calculation" method is the most accurate
    • Balimane PV, Marino A, Chong S. P-gp inhibition potential in cell-based models: which "calculation" method is the most accurate? AAPS J. 2008;10:577-86.
    • (2008) AAPS J , vol.10 , pp. 577-586
    • Balimane, P.V.1    Marino, A.2    Chong, S.3
  • 3
    • 79955690629 scopus 로고    scopus 로고
    • European Medicine Agency. Accessed 28 October 2013
    • European Medicine Agency. Guideline on the investigation of drug interactions. 2012. http://www.ema.europa.eu/ema/index.jsp?curl=pages/includes/ document/document-detail.jsp? webContentId=WC500129606&mid= WC0b01ac058009a3dc. Accessed 28 October 2013.
    • (2012) Guideline on the Investigation of Drug Interactions
  • 4
    • 83655197410 scopus 로고    scopus 로고
    • Role of transporters in drug interactions
    • Han HK. Role of transporters in drug interactions. Arch Pharmacol Res. 2011;34:1865-77.
    • (2011) Arch Pharmacol Res , vol.34 , pp. 1865-1877
    • Han, H.K.1
  • 5
    • 33646640645 scopus 로고    scopus 로고
    • Current industrial practices of assessing permeability and P-glycoprotein interaction
    • article 1
    • Balimane PV, Han YH, Chong S. Current industrial practices of assessing permeability and P-glycoprotein interaction. AAPS J. 2006; 8(1):article 1.
    • (2006) AAPS J , vol.8 , Issue.1
    • Balimane, P.V.1    Han, Y.H.2    Chong, S.3
  • 6
    • 33644868785 scopus 로고    scopus 로고
    • Development, validation and utility of an in vitro technique for assessment of potential clinical drug-drug interactions involving P-glycoprotein
    • Keogh JP, Kunta JR. Development, validation and utility of an in vitro technique for assessment of potential clinical drug-drug interactions involving P-glycoprotein. Eur J Pharm Sci. 2006;27:543-54.
    • (2006) Eur J Pharm Sci , vol.27 , pp. 543-554
    • Keogh, J.P.1    Kunta, J.R.2
  • 7
    • 0032907322 scopus 로고    scopus 로고
    • Interrelationships between substrates and inhibitors of human CYP3A and P-glycoprotein
    • Kim RB, Wandel C, Leake B, Cvetkovic M, Fromm MF, Dempsey PJ, et al. Interrelationships between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharm Res. 1999;16:408-14.
    • (1999) Pharm Res , vol.16 , pp. 408-414
    • Kim, R.B.1    Wandel, C.2    Leake, B.3    Cvetkovic, M.4    Fromm, M.F.5    Dempsey, P.J.6
  • 9
    • 27644521247 scopus 로고    scopus 로고
    • Comparison of P-glycoprotein-mediated drugdigoxin interactions in Caco-2 with human and rodent intestine: Relevance to in vivo prediction
    • Collett A, Tanianis-Hughes J, Carlson GL, Harwood MD, Warhurst G. Comparison of P-glycoprotein-mediated drugdigoxin interactions in Caco-2 with human and rodent intestine: relevance to in vivo prediction. Eur J Pharm Sci. 2005;26:386-93.
    • (2005) Eur J Pharm Sci , vol.26 , pp. 386-393
    • Collett, A.1    Tanianis-Hughes, J.2    Carlson, G.L.3    Harwood, M.D.4    Warhurst, G.5
  • 10
    • 39749114622 scopus 로고    scopus 로고
    • Variability in Caco-2 and MDCK cell-based intestinal permeability assays
    • Volpe DA. Variability in Caco-2 and MDCK cell-based intestinal permeability assays. J Pharm Sci. 2008;97:712-25.
    • (2008) J Pharm Sci , vol.97 , pp. 712-725
    • Volpe, D.A.1
  • 11
    • 27544483787 scopus 로고    scopus 로고
    • Functional assessment of multiple P-glycoprotein (P-gp) probe substrates: Influence of cell line and modulator concentration on P-gp activity
    • Taub ME, Podila L, Ely D, Almeida I. Functional assessment of multiple P-glycoprotein (P-gp) probe substrates: influence of cell line and modulator concentration on P-gp activity. Drug Metab Dispos. 2005;33:1679-87.
    • (2005) Drug Metab Dispos , vol.33 , pp. 1679-1687
    • Taub, M.E.1    Podila, L.2    Ely, D.3    Almeida, I.4
  • 12
    • 84879085257 scopus 로고    scopus 로고
    • Variability in P-glycoprotein inhibitory potency (IC50) using various in vitro experimental systems: Implications for universal digoxin DDI risk assessment decision criteria
    • Bentz J, O'Connor MP, Bednarczyk D, Coleman J, Lee C, Palm J, et al. Variability in P-glycoprotein inhibitory potency (IC50) using various in vitro experimental systems: implications for universal digoxin DDI risk assessment decision criteria. Drug Metab Dispos. 2013;41:1347-66.
    • (2013) Drug Metab Dispos , vol.41 , pp. 1347-1366
    • Bentz, J.1    O'Connor, M.P.2    Bednarczyk, D.3    Coleman, J.4    Lee, C.5    Palm, J.6
  • 13
    • 79960150931 scopus 로고    scopus 로고
    • Establishment of in vitro P-glycoprotein inhibition assay and its exclusion criteria to assess the risk of drug-drug interaction at the drug discovery stage
    • Sugimoto H, Matsumoto S, Tachibana M, Niwa S, Hirabayashi H, Amano N, et al. Establishment of in vitro P-glycoprotein inhibition assay and its exclusion criteria to assess the risk of drug-drug interaction at the drug discovery stage. J Pharm Sci. 2011;100:4013-23.
    • (2011) J Pharm Sci , vol.100 , pp. 4013-4023
    • Sugimoto, H.1    Matsumoto, S.2    Tachibana, M.3    Niwa, S.4    Hirabayashi, H.5    Amano, N.6
  • 14
    • 56749164877 scopus 로고    scopus 로고
    • Effects of dietary flavonoids on the transport of cimetidine via P-glycoprotein and cationic transporters in Caco-2 and LLC-PK1 cell models
    • Taur JS, Rodriguez-Proteau R. Effects of dietary flavonoids on the transport of cimetidine via P-glycoprotein and cationic transporters in Caco-2 and LLC-PK1 cell models. Xenobiotica. 2008;38:1536-50.
    • (2008) Xenobiotica , vol.38 , pp. 1536-1550
    • Taur, J.S.1    Rodriguez-Proteau, R.2
  • 16
    • 68249162213 scopus 로고    scopus 로고
    • Predicting drug-drug interactions: An FDA perspective
    • Zhang L, Zhang Y, Zhao P, Huang SM. Predicting drug-drug interactions: an FDA perspective. AAPS J. 2009;11:300-6.
    • (2009) AAPS J , vol.11 , pp. 300-306
    • Zhang, L.1    Zhang, Y.2    Zhao, P.3    Huang, S.M.4
  • 17
    • 58549088199 scopus 로고    scopus 로고
    • Drug-drug interactions mediated through Pglycoprotein: Clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug
    • Fenner KS, Troutman MD, Kempshall S, Cook JA, Ware JA, Smith DA, et al. Drug-drug interactions mediated through Pglycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug. Clin Pharmacol Ther. 2009;85:173-81.
    • (2009) Clin Pharmacol Ther , vol.85 , pp. 173-181
    • Fenner, K.S.1    Troutman, M.D.2    Kempshall, S.3    Cook, J.A.4    Ware, J.A.5    Smith, D.A.6
  • 18
    • 33645805657 scopus 로고    scopus 로고
    • In vitro P-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: A recommendation for probe substrates
    • Rautio J, Humphreys JE, Webster LO, Balakrishnan A, Keogh JP, Kunta JR, et al. In vitro P-glycoprotein inhibition assays for assessment of clinical drug interaction potential of new drug candidates: a recommendation for probe substrates. Drug Metab Dispos. 2006;34:786-92.
    • (2006) Drug Metab Dispos , vol.34 , pp. 786-792
    • Rautio, J.1    Humphreys, J.E.2    Webster, L.O.3    Balakrishnan, A.4    Keogh, J.P.5    Kunta, J.R.6
  • 21
    • 3042520870 scopus 로고    scopus 로고
    • Digoxin in the management of cardiovascular disorders
    • Gheorghiade M, Adams KF, Colucci WS. Digoxin in the management of cardiovascular disorders. Circulation. 2004;109:2959-64.
    • (2004) Circulation , vol.109 , pp. 2959-2964
    • Gheorghiade, M.1    Adams, K.F.2    Colucci, W.S.3
  • 24
    • 0026522904 scopus 로고
    • Digoxininteractions in man: Spironolactone reduces renal but not biliary digoxin clearance
    • Hedman A, Angelin B, Arvidsson A, Dahlqvist R. Digoxininteractions in man: spironolactone reduces renal but not biliary digoxin clearance. Eur J Clin Pharmacol. 1992;42:481-5.
    • (1992) Eur J Clin Pharmacol , vol.42 , pp. 481-485
    • Hedman, A.1    Angelin, B.2    Arvidsson, A.3    Dahlqvist, R.4
  • 28
    • 0033372992 scopus 로고    scopus 로고
    • Cellular pharmacokinetic aspects of reversal effect of itraconazole on P-glycoprotein-mediated resistance of anticancer drugs
    • Takara K, Tanigawara Y, Komada F, Nishiguchi K, Sakaeda T, Okumura K. Cellular pharmacokinetic aspects of reversal effect of itraconazole on P-glycoprotein-mediated resistance of anticancer drugs. Biol Pharm Bull. 1999;22:1355-9.
    • (1999) Biol Pharm Bull , vol.22 , pp. 1355-1359
    • Takara, K.1    Tanigawara, Y.2    Komada, F.3    Nishiguchi, K.4    Sakaeda, T.5    Okumura, K.6
  • 29
    • 33845365814 scopus 로고    scopus 로고
    • Factors influencing the magnitude and clinical significance of drug interactions between azole antifungals and select immunosuppressants
    • Saad AH, De Pestel DD, Carver PL. Factors influencing the magnitude and clinical significance of drug interactions between azole antifungals and select immunosuppressants. Pharmacotherapy. 2006;26:1730-44.
    • (2006) Pharmacotherapy , vol.26 , pp. 1730-1744
    • Saad, A.H.1    De Pestel, D.D.2    Carver, P.L.3
  • 30
    • 77955448192 scopus 로고    scopus 로고
    • Management of drug and food interactions with azole antifungal agents in transplant recipients
    • Dodds-Ashley E. Management of drug and food interactions with azole antifungal agents in transplant recipients. Pharmacotherapy. 2010;30:842-54.
    • (2010) Pharmacotherapy , vol.30 , pp. 842-854
    • Dodds-Ashley, E.1
  • 31
  • 33
    • 79955726360 scopus 로고    scopus 로고
    • The phosphodiesterase-5 inhibitor vardenafil is a potent inhibitor of ABCB1/P-glycoprotein transporter
    • Ding PR, Tiwari AK, Ohnuma S, Lee JW, An X, Dai CL, et al. The phosphodiesterase-5 inhibitor vardenafil is a potent inhibitor of ABCB1/P-glycoprotein transporter. PLoS One. 2011;6:e19329.
    • (2011) PLoS One , vol.6
    • Ding, P.R.1    Tiwari, A.K.2    Ohnuma, S.3    Lee, J.W.4    An, X.5    Dai, C.L.6
  • 34
    • 79957924845 scopus 로고    scopus 로고
    • Roles of sildenafil in enhancing drug sensitivity in cancer
    • Shi Z, Tiwari AK, Patel AS, Fu LW, Chen ZS. Roles of sildenafil in enhancing drug sensitivity in cancer. Cancer Res. 2011;71:3735-8.
    • (2011) Cancer Res , vol.71 , pp. 3735-3738
    • Shi, Z.1    Tiwari, A.K.2    Patel, A.S.3    Fu, L.W.4    Chen, Z.S.5
  • 35
    • 84893688515 scopus 로고    scopus 로고
    • Characterization of efflux transport of PDE5 inhibitors, sildenafil, vardenafil, and udenafil
    • Jian-Wei D, Song I, Shon J, Shin J. Characterization of efflux transport of PDE5 inhibitors, sildenafil, vardenafil, and udenafil. Clin Pharmacol Ther. 2009;85 Suppl 1:S49.
    • (2009) Clin Pharmacol Ther , vol.85 , Issue.SUPPL. 1
    • Jian-Wei, D.1    Song, I.2    Shon, J.3    Shin, J.4
  • 36
    • 84863716828 scopus 로고    scopus 로고
    • Characterization of efflux transport of the PDE5 inhibitors, vardenafil and sildenafil
    • Choi MK, Song IS. Characterization of efflux transport of the PDE5 inhibitors, vardenafil and sildenafil. J Pharm Pharmacol. 2012;64:1074-83.
    • (2012) J Pharm Pharmacol , vol.64 , pp. 1074-1083
    • Choi, M.K.1    Song, I.S.2
  • 37
    • 0001087629 scopus 로고    scopus 로고
    • Vardenafil, a new selective PDE5 inhibitor, produces no interaction with digoxin
    • Rohde G, Bauer R-J, Unger S, Ahr G, Wensing G. Vardenafil, a new selective PDE5 inhibitor, produces no interaction with digoxin. Pharmacotherapy. 2001;21:1254.
    • (2001) Pharmacotherapy , vol.21 , pp. 1254
    • Rohde, G.1    Bauer, R.-J.2    Unger, S.3    Ahr, G.4    Wensing, G.5
  • 38
    • 0036293772 scopus 로고    scopus 로고
    • Are MDCK cells transfected with the human MDR1 gene a good model of the human intestinal mucosa
    • Tang F, Horie K, Borchardt RT. Are MDCK cells transfected with the human MDR1 gene a good model of the human intestinal mucosa? Pharm Res. 2002;19:765-72.
    • (2002) Pharm Res , vol.19 , pp. 765-772
    • Tang, F.1    Horie, K.2    Borchardt, R.T.3
  • 40
    • 34547663275 scopus 로고    scopus 로고
    • Effect of cell differentiation and passage number on the expression of efflux proteins in wild type and vinblastineinduced Caco-2 cell lines
    • Siissalo S, Laitinen L, Koljonen M, Vellonen KS, Kortejärvi H, Urtti A, et al. Effect of cell differentiation and passage number on the expression of efflux proteins in wild type and vinblastineinduced Caco-2 cell lines. Eur J Pharm Biopharm. 2007;67:548-54.
    • (2007) Eur J Pharm Biopharm , vol.67 , pp. 548-554
    • Siissalo, S.1    Laitinen, L.2    Koljonen, M.3    Vellonen, K.S.4    Kortejärvi, H.5    Urtti, A.6
  • 41
    • 70349095606 scopus 로고    scopus 로고
    • Culture period-dependent change of function and expression of ATP-binding cassette transporters in Caco-2 cells
    • Kamiyama E, Sugiyama D, Nakai D, Miura S, Okazaki O. Culture period-dependent change of function and expression of ATP-binding cassette transporters in Caco-2 cells. Drug Metab Dipos. 2009;37:1956-62.
    • (2009) Drug Metab Dipos , vol.37 , pp. 1956-1962
    • Kamiyama, E.1    Sugiyama, D.2    Nakai, D.3    Miura, S.4    Okazaki, O.5
  • 42
    • 84864299679 scopus 로고    scopus 로고
    • Differential selectivity of efflux transporter inhibitors in Caco-2 and MDCK-MDR1 monolayers: A strategy to assess the interaction of a new chemical entity with P-gp, BCRP, and MRP2
    • Mease K, Sane R, Podila L, Taub ME. Differential selectivity of efflux transporter inhibitors in Caco-2 and MDCK-MDR1 monolayers: a strategy to assess the interaction of a new chemical entity with P-gp, BCRP, and MRP2. J Pharm Sci. 2012;101:1888-97.
    • (2012) J Pharm Sci , vol.101 , pp. 1888-1897
    • Mease, K.1    Sane, R.2    Podila, L.3    Taub, M.E.4
  • 43
    • 84856372013 scopus 로고    scopus 로고
    • Validation of quinidine as a probe substrate for the in vitro P-gp inhibition assay in Caco-2 cell monolayer
    • Patil AG, D'Souza R, Dixit N, Damre A. Validation of quinidine as a probe substrate for the in vitro P-gp inhibition assay in Caco-2 cell monolayer. Eur J Drug Metab Pharmacokinet. 2011;36:115-9.
    • (2011) Eur J Drug Metab Pharmacokinet , vol.36 , pp. 115-119
    • Patil, A.G.1    D'Souza, R.2    Dixit, N.3    Damre, A.4
  • 44
    • 38349174530 scopus 로고    scopus 로고
    • Effect of P-glycoprotein expression levels on the concentration-dependent permeability of drugs to the cell membrane
    • Shirasaka Y, Sakane T, Yamashita S. Effect of P-glycoprotein expression levels on the concentration-dependent permeability of drugs to the cell membrane. J Pharm Sci. 2008;97:553-65.
    • (2008) J Pharm Sci , vol.97 , pp. 553-565
    • Shirasaka, Y.1    Sakane, T.2    Yamashita, S.3
  • 45
    • 56149087140 scopus 로고    scopus 로고
    • Comparison of drug transporter gene expression and functionality in Caco-2 cells from 10 different laboratories
    • Hayeshi R, Hilgendorf C, Artursson P, Augustijns P, Brodin B, Dehertogh P, et al. Comparison of drug transporter gene expression and functionality in Caco-2 cells from 10 different laboratories. Eur J Pharm Sci. 2008;35:383-96.
    • (2008) Eur J Pharm Sci , vol.35 , pp. 383-396
    • Hayeshi, R.1    Hilgendorf, C.2    Artursson, P.3    Augustijns, P.4    Brodin, B.5    Dehertogh, P.6
  • 46
    • 79959434557 scopus 로고    scopus 로고
    • Use of transporter knockdown Caco-2 cells to investigate the in vitro efflux of statin drugs
    • Li J, Volpe DA, Wang Y, Zhang W, Bode C, Owen A, et al. Use of transporter knockdown Caco-2 cells to investigate the in vitro efflux of statin drugs. Drug Metab Dispos. 2011;39:1196-202.
    • (2011) Drug Metab Dispos , vol.39 , pp. 1196-1202
    • Li, J.1    Volpe, D.A.2    Wang, Y.3    Zhang, W.4    Bode, C.5    Owen, A.6
  • 47
    • 76749153917 scopus 로고    scopus 로고
    • Investigation of the involvement of P-glycoprotein and multidrug resistance-associated protein 2 in the efflux of ximelagatran and its metabolites by using short hairpin RNA knockdown in Caco-2 cells
    • Darnell M, Karlsson JE, Owen A, Hidalgo IJ, Li J, Zhang W, et al. Investigation of the involvement of P-glycoprotein and multidrug resistance-associated protein 2 in the efflux of ximelagatran and its metabolites by using short hairpin RNA knockdown in Caco-2 cells. Drug Metab Dispos. 2010;38:491-7.
    • (2010) Drug Metab Dispos , vol.38 , pp. 491-497
    • Darnell, M.1    Karlsson, J.E.2    Owen, A.3    Hidalgo, I.J.4    Li, J.5    Zhang, W.6
  • 48
    • 48749121103 scopus 로고    scopus 로고
    • Validation and application of Caco-2 assays for the in vitro evaluation of development candidate drugs as substrates or inhibitors of Pglycoprotein to support regulatory submissions
    • Elsby R, Surry DD, Smith VN, Gray AJ. Validation and application of Caco-2 assays for the in vitro evaluation of development candidate drugs as substrates or inhibitors of Pglycoprotein to support regulatory submissions. Xenobiotica. 2008;38:1140-64.
    • (2008) Xenobiotica , vol.38 , pp. 1140-1164
    • Elsby, R.1    Surry, D.D.2    Smith, V.N.3    Gray, A.J.4
  • 49
    • 77449143886 scopus 로고    scopus 로고
    • Interaction of angiotensin II type 1 receptor blockers with P-gp substrates in Caco-2 cells and hMDR1-expressing membranes
    • Kamiyama E, Nakai D, Mikkaichi T, Okudaira N, Okazaki O. Interaction of angiotensin II type 1 receptor blockers with P-gp substrates in Caco-2 cells and hMDR1-expressing membranes. Life Sci. 2010;86:52-8.
    • (2010) Life Sci , vol.86 , pp. 52-58
    • Kamiyama, E.1    Nakai, D.2    Mikkaichi, T.3    Okudaira, N.4    Okazaki, O.5
  • 50
    • 79251518645 scopus 로고    scopus 로고
    • The utility of in vitro data in making accurate predictions of human P-glycoprotein-mediated drug-drug interactions: A case study for AZD5672
    • Elsby R, Gillen M, Butters C, Imisson G, Sharma P, Smith V, et al. The utility of in vitro data in making accurate predictions of human P-glycoprotein-mediated drug-drug interactions: a case study for AZD5672. Drug Metab Dispos. 2011;39:275-82.
    • (2011) Drug Metab Dispos , vol.39 , pp. 275-282
    • Elsby, R.1    Gillen, M.2    Butters, C.3    Imisson, G.4    Sharma, P.5    Smith, V.6
  • 51
    • 84893682843 scopus 로고    scopus 로고
    • Comparison of digoxin efflux inhibition in Caco-2 and MDR1-LLC-PK1 cell monolayers
    • Perloff ES, Mason AK, Kapadnis S, Khun W, Fox LG, Stresser DM. Comparison of digoxin efflux inhibition in Caco-2 and MDR1-LLC-PK1 cell monolayers. Drug Metab Rev. 2011;43 Suppl 2:193.
    • (2011) Drug Metab Rev , vol.43 , Issue.SUPPL. 2 , pp. 193
    • Perloff, E.S.1    Mason, A.K.2    Kapadnis, S.3    Khun, W.4    Fox, L.G.5    Stresser, D.M.6
  • 52
    • 36249014207 scopus 로고    scopus 로고
    • Role of P-glycoprotein inhibition for drug interactions evidence from in vitro and pharmacoepidemiological studies
    • Eberl S, Renner B, Neubert A, Reisig M, Bachmakov I, König J, et al. Role of P-glycoprotein inhibition for drug interactions evidence from in vitro and pharmacoepidemiological studies. Clin Pharmacokinet. 2007;46:1039-49.
    • (2007) Clin Pharmacokinet , vol.46 , pp. 1039-1049
    • Eberl, S.1    Renner, B.2    Neubert, A.3    Reisig, M.4    Bachmakov, I.5    König, J.6
  • 53
    • 0034121122 scopus 로고    scopus 로고
    • Pharmacological inhibition of P-glycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes
    • Choo EF, Leake B, Wandel C, Imamura H, Wood AJJ, Wilkinson GR, et al. Pharmacological inhibition of P-glycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes. Drug Metab Dispos. 2000;28:655-60.
    • (2000) Drug Metab Dispos , vol.28 , pp. 655-660
    • Choo, E.F.1    Leake, B.2    Wandel, C.3    Imamura, H.4    Wood, A.J.J.5    Wilkinson, G.R.6
  • 55
    • 40849145621 scopus 로고    scopus 로고
    • In vitro-to-in vivo prediction of P-glycoprotein-based drug interactions at the human and rodent blood-brain barrier
    • Hsiao P, Bui T, Ho RJY, Unadkat JD. In vitro-to-in vivo prediction of P-glycoprotein-based drug interactions at the human and rodent blood-brain barrier. Drug Metab Dispos. 2008;36:481-4.
    • (2008) Drug Metab Dispos , vol.36 , pp. 481-484
    • Hsiao, P.1    Bui, T.2    Ho, R.J.Y.3    Unadkat, J.D.4
  • 56
    • 31044448805 scopus 로고    scopus 로고
    • Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: F2 values
    • Weiss J, Haefeli WE. Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: F2 values. Drug Metab Dispos. 2006;34:203-7.
    • (2006) Drug Metab Dispos , vol.34 , pp. 203-207
    • Weiss, J.1    Haefeli, W.E.2
  • 57
    • 84893686524 scopus 로고    scopus 로고
    • app values vs. Efflux ratios
    • app values vs. efflux ratios. Drug Metab Rev. 2009;41 Suppl 3:76.
    • (2009) Drug Metab Rev , vol.41 , Issue.SUPPL. 3 , pp. 76
    • Lin, J.1    Grimm, S.2


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