What Kinds of Substrates Show P-Glycoprotein-Dependent Intestinal Absorption? Comparison of Verapamil with Vinblastine-Reference-Cited by-同舟云学术

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What Kinds of Substrates Show P-Glycoprotein-Dependent Intestinal Absorption? Comparison of Verapamil with Vinblastine

Published:2006 Issue:3 Volume:21 Page:238-244
ISSN:1347-4367
Container-title:Drug Metabolism and Pharmacokinetics
language:en
Short-container-title:Drug Metabolism and Pharmacokinetics

Author:

Ogihara Takuo,Kamiya Masatsugu,Ozawa Makoto,Fujita Takuya,Yamamoto Akira,Yamashita Shinji,Ohnishi Shuhei,Isomura Yasuo

Publisher

Japanese Society for the Study of Xenobiotics

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology

Reference21 articles.

1. Importance of P-glycoprotein at blood-tissue barriers;Fromm;Trends Pharmacol. Sci.,2004

2. Toxic digoxin-drug interactions: the major role of renal P-glycoprotein;Koren;Vet. Hum. Toxicol.,1998

3. Molecular and pharmacokinetic properties of 222 commercially available oral drugs in humans;Sakaeda;Biol. Pharm. Bull.,2001

4. Limited influence of P-glycoprotein on small-intestinal absorption of cilostazol, a high absorptive permeability drug;Toyobuku;J. Pharm. Sci.,2003

5. A comprehensive account on the role of efflux transporters in the gastrointestinal absorption of 13 commonly used substrate drugs in humans;Chiou;Int. J. Clin. Pharmacol. Ther.,2001

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