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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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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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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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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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Song KH, Fasano A, Eddington ND 
Effect of the six-mer synthetic peptide (AT1002) fragment of zonula occludens toxin on the intestinal absorption of cyclosporin A. [JOURNAL ARTICLE]
Int J Pharm 2007 Sep 15.
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Sandström R, Karlsson A, Lennernäs H 
The absence of stereoselective P-glycoprotein-mediated transport of R/S-verapamil across the rat jejunum. [Journal Article]
J Pharm Pharmacol 1998 Jul; 50(7):729-35.
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Varma MV, Panchagnula R 
pH-dependent functional activity of P-glycoprotein in limiting intestinal absorption of protic drugs: kinetic analysis of quinidine efflux in situ. [Journal Article]
J Pharm Sci 2005 Dec; 94(12):2632-43.
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Zakeri-Milani P, Valizadeh H, Tajerzadeh H, et al. 
Predicting human intestinal permeability using single-pass intestinal perfusion in rat. [Journal Article]
J Pharm Pharm Sci 2007; 10(3):368-79.
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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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