Decreased biliary excretion of tributylmethyl ammonium in cholestyramine pretreated rats due to reduced formation of ion-pair complexes with hepatic bile salts
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine
Reference22 articles.
1. Hepatobiliary elimination of cationic drugs: the role of P-glycoproteins and other ATP-dependent transporters
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3. Multiple Alterations of Canalicular Membrane Transport Activities in Rats with CCl4-induced Hepatic Injury
4. Mechanism of the Stationary Canalicular Excretion of Tributylmethyl Ammonium in Rats with a CCl4-Induced Acute Hepatic Injury
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1. Ion Pairing with Bile Salts Modulates Intestinal Permeability and Contributes to Food–Drug Interaction of BCS Class III Compound Trospium Chloride;Molecular Pharmaceutics;2013-07-12
2. Transport of organic cationic drugs: Effect of ion-pair formation with bile salts on the biliary excretion and pharmacokinetics;Pharmacology & Therapeutics;2013-04
3. Using resin to generate a non-invasive intestinal bile-depleted rat model was unsuccessful;European Journal of Pharmaceutical Sciences;2012-09
4. Increased Affinity to Canalicular P-gp via Formation of Lipophilic Ion-Pair Complexes with Endogenous Bile Salts is Associated with Mw Threshold in Hepatobiliary Excretion of Quaternary Ammonium Compounds;Pharmaceutical Research;2010-03-10
5. Current World Literature;Current Opinion in Lipidology;2009-06
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