Drug transporters expressed on the hepatocyte membrane play an important role in hepatic drug disposition. In the last two decades, systematic research has resulted in a better understanding of the diversity, expression and substrate specificities of drug transporters in the liver. Here we review recent studies on the role of transporters in drug-drug interactions and disease states such as cirrhosis. We conclude the review by considering techniques and model systems used to study hepatic transporters, including the latest technological developments such as multiphoton microscopy
Correct dosing in pharmacotherapeutics is based on the idea that too much of a drug will cause toxic...
Carrier-mediated transport of drugs occurs in various tissues in the body and may largely affect the...
Detailed knowledge regarding the influence of hepatic transport proteins on drug disposition has adv...
Cells need to strictly control their internal milieu, a function which is performed by the plasma me...
For drugs with hepatobiliary transport across hepatocytes, the interplay between uptake and efflux t...
For drugs with hepatobiliary transport across hepatocytes, the interplay between uptake and efflux t...
The liver is the primary organ for the metabolic degradation of xenobiotics. Transmembrane transport...
Hepatic drug uptake and intrinsic clearance are key determinants of hepatic drug disposition in norm...
Together with drug metabolising enzymes, transmembrane transporters are important determinants of dr...
A better understanding of the role of hepatic transporters in drug elimination is of crucial importa...
Over the last two decades drug tranporter proteins have been the focus of increased study to determi...
This review brings you up-to-date with the hepatocyte research on: 1) in vitro-in vivo correlations ...
This review brings you up-to-date with the hepatocyte research on: 1) in vitro-in vivo correlations ...
ABSTRACT Pharmacodynamical studies showed that most drugs elicit their effects by acting on 3 kinds...
The role of hepatobiliary transporters in drug-induced liver injury remains poorly understood. Vario...
Correct dosing in pharmacotherapeutics is based on the idea that too much of a drug will cause toxic...
Carrier-mediated transport of drugs occurs in various tissues in the body and may largely affect the...
Detailed knowledge regarding the influence of hepatic transport proteins on drug disposition has adv...
Cells need to strictly control their internal milieu, a function which is performed by the plasma me...
For drugs with hepatobiliary transport across hepatocytes, the interplay between uptake and efflux t...
For drugs with hepatobiliary transport across hepatocytes, the interplay between uptake and efflux t...
The liver is the primary organ for the metabolic degradation of xenobiotics. Transmembrane transport...
Hepatic drug uptake and intrinsic clearance are key determinants of hepatic drug disposition in norm...
Together with drug metabolising enzymes, transmembrane transporters are important determinants of dr...
A better understanding of the role of hepatic transporters in drug elimination is of crucial importa...
Over the last two decades drug tranporter proteins have been the focus of increased study to determi...
This review brings you up-to-date with the hepatocyte research on: 1) in vitro-in vivo correlations ...
This review brings you up-to-date with the hepatocyte research on: 1) in vitro-in vivo correlations ...
ABSTRACT Pharmacodynamical studies showed that most drugs elicit their effects by acting on 3 kinds...
The role of hepatobiliary transporters in drug-induced liver injury remains poorly understood. Vario...
Correct dosing in pharmacotherapeutics is based on the idea that too much of a drug will cause toxic...
Carrier-mediated transport of drugs occurs in various tissues in the body and may largely affect the...
Detailed knowledge regarding the influence of hepatic transport proteins on drug disposition has adv...