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Chiu YY, Higaki K, Neudeck BL, et al. 
Human jejunal permeability of cyclosporin A: influence of surfactants on P-glycoprotein efflux in Caco-2 cells. [Journal Article]
Pharm Res 2003 May; 20(5):749-56.
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Zakeri-Milani P, Valizadeh H, Islambulchilar Z, et al. 
Investigation of the intestinal permeability of ciclosporin using the in situ technique in rats and the relevance of P-glycoprotein. [Journal Article]
Arzneimittelforschung 2008; 58(4):188-92.
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Sharma P, Varma MV, Chawla HP, et al. 
In situ and in vivo efficacy of peroral absorption enhancers in rats and correlation to in vitro mechanistic studies. [Journal Article]
Farmaco 2005 Nov-Dec; 60(11-12):874-83.
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Lee YJ, Chung SJ, Shim CK 
Limited role of P-glycoprotein in the intestinal absorption of cyclosporin A. [Journal Article]
Biol Pharm Bull 2005 Apr; 28(4):760-3.
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Tamura S, Ohike A, Ibuki R, et al. 
Tacrolimus is a class II low-solubility high-permeability drug: the effect of P-glycoprotein efflux on regional permeability of tacrolimus in rats. [Journal Article]
J Pharm Sci 2002 Mar; 91(3):719-29.
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Hilgendorf C, Spahn-Langguth H, Regårdh CG, et al. 
Caco-2 versus Caco-2/HT29-MTX co-cultured cell lines: permeabilities via diffusion, inside- and outside-directed carrier-mediated transport. [Journal Article]
J Pharm Sci 2000 Jan; 89(1):63-75.
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Bogman K, Zysset Y, Degen L, et al. 
P-glycoprotein and surfactants: effect on intestinal talinolol absorption. [Clinical Trial, Journal Article, Randomized Controlled Trial]
Clin Pharmacol Ther 2005 Jan; 77(1):24-32.
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Takamatsu N, Kim ON, Welage LS, et al. 
Human jejunal permeability of two polar drugs: cimetidine and ranitidine. [Comparative Study , Journal Article, Research Support, Non-U.S. Gov't , Research Support, U.S. Gov't, P.H.S. ]
Pharm Res 2001 Jun; 18(6):742-4.
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Svensson US, Sandström R, Carlborg O, et al. 
High in situ rat intestinal permeability of artemisinin unaffected by multiple dosing and with no evidence of P-glycoprotein involvement. [Journal Article]
Drug Metab Dispos 1999 Feb; 27(2):227-32.
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