The major aim of this study was to investigate the CYP3A4 metabolism and polarized transport of ropivacaine and its metabolite 2',6'-pipecoloxylidide (PPX) in tissue specimens from the human small and large intestine. Ropivacaine has been shown to be effective in the treatment of ulcerative colitis in human colon. This study was conducted using a modified Ussing-chamber technique with specimens from jejunum, ileum and colon collected from 11 patients. The local kinetics of ropivacaine and PPX were assessed from their concentration-time profiles in mucosal and serosal compartments. The permeability (P-app) in the absorptive direction for both ropivacaine and PPX increased regionally in the order jejunum <ileum<colon. Ropivacaine was not foun...
The primary objective of the study was to develop an approach utilising conventional pharmaceutical ...
The passage number and origin of two populations of Caco-2 cells influence their enterocyte-like cha...
PURPOSE: To evaluate intestinal transport, uptake and metabolism characteristics of the bis(pivaloyl...
One of the aims of this thesis was to investigate the involvement of efflux proteins, such as the P-...
The main objective of this thesis was to investigate the in vivo relevance of membrane transporters ...
The aims of this thesis were to explore the clinical pharmacology of ropivacaine gel as a potential ...
Drug absorption across viable porcine intestines was investigated using an Ussing chamber system. Th...
Introduction: Both efflux transporters and metabolic enzymes are expressed in the intestinal epithel...
The subject of this thesis was to study two intestinal barriers to oral drug bioavailability, drug e...
Three purposes are presented in this study: (1) to study the in vivo regional dependent intestinal a...
Copyright © 2001 by the American Society for Clinical Pharmacology and Therapeutics.Background and A...
Intestinal P-gp and CYP3A4 work coordinately to reduce the intracellular concentration of drugs, and...
AbstractOral administration is the most commonly used route for drug treatment. Intestinal cytochrom...
Induction of drug enzyme activity in the intestine can strongly determine plasma levels of drugs. It...
BACKGROUND AND AIMS: In humans gut wall metabolism can be quantitatively as important as hepatic dru...
The primary objective of the study was to develop an approach utilising conventional pharmaceutical ...
The passage number and origin of two populations of Caco-2 cells influence their enterocyte-like cha...
PURPOSE: To evaluate intestinal transport, uptake and metabolism characteristics of the bis(pivaloyl...
One of the aims of this thesis was to investigate the involvement of efflux proteins, such as the P-...
The main objective of this thesis was to investigate the in vivo relevance of membrane transporters ...
The aims of this thesis were to explore the clinical pharmacology of ropivacaine gel as a potential ...
Drug absorption across viable porcine intestines was investigated using an Ussing chamber system. Th...
Introduction: Both efflux transporters and metabolic enzymes are expressed in the intestinal epithel...
The subject of this thesis was to study two intestinal barriers to oral drug bioavailability, drug e...
Three purposes are presented in this study: (1) to study the in vivo regional dependent intestinal a...
Copyright © 2001 by the American Society for Clinical Pharmacology and Therapeutics.Background and A...
Intestinal P-gp and CYP3A4 work coordinately to reduce the intracellular concentration of drugs, and...
AbstractOral administration is the most commonly used route for drug treatment. Intestinal cytochrom...
Induction of drug enzyme activity in the intestine can strongly determine plasma levels of drugs. It...
BACKGROUND AND AIMS: In humans gut wall metabolism can be quantitatively as important as hepatic dru...
The primary objective of the study was to develop an approach utilising conventional pharmaceutical ...
The passage number and origin of two populations of Caco-2 cells influence their enterocyte-like cha...
PURPOSE: To evaluate intestinal transport, uptake and metabolism characteristics of the bis(pivaloyl...