The use of in vitro metabolism data to predict human clearance has become more significant in the current prediction of large scale drug clearance for all the drugs. The relevant information (in vitro metabolism data and in vivo human clearance values) of thirty-five drugs that satisfied the entry criteria of probe drugs was collated from the literature. Then the performance of different in vitro systems including Escherichia coli system, yeast system, lymphoblastoid system and baculovirus system is compared after in vitro-in vivo extrapolation. Baculovirus system, which can provide most of the data, has almost equal accuracy as the other systems in predicting clearance. And in most cases, baculovirus system has the smaller CV in scaling fa...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
ABSTRACT Prediction of human pharmacokinetics of new drugs, as well as other disposition attributes,...
The safety and efficacy of drugs depend upon appropriate dosing of drugs made possible by understand...
The use of in vitro metabolism data to predict human clearance has become more significant in the cu...
In the present research, we assessed the utility of the structural information of drugs for predicti...
Objectives. Membrane transporters and metabolism are major determinants of the hepatobiliary elimina...
The utility of in vitro generated kinetic data to provide quantitative prediction of in vivo pharmac...
Total human clearance is a key determinant for the pharmacokinetic behavior of drug candidates. Our ...
The literature was searched for drugs where adequate data were available on in vitro human metabolis...
Introduction: In vitro metabolic profiling is used extensively by the pharmaceutical industry to cha...
We describe a comprehensive retrospective analysis in which the abilities of several methods by whic...
Introduction: Successful quantitative prediction of hepatic drug metabolism often requires integrate...
A systematic kinetic analysis of the metabolism of five benzodiaz-epines (low to high clearance comp...
Clearance, or a measure of the body’s ability to remove drug, is a crucial pharmacokinetic parameter...
In order to improve the benefit–risk ratio of pharmacokinetic (PK) research in the early development...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
ABSTRACT Prediction of human pharmacokinetics of new drugs, as well as other disposition attributes,...
The safety and efficacy of drugs depend upon appropriate dosing of drugs made possible by understand...
The use of in vitro metabolism data to predict human clearance has become more significant in the cu...
In the present research, we assessed the utility of the structural information of drugs for predicti...
Objectives. Membrane transporters and metabolism are major determinants of the hepatobiliary elimina...
The utility of in vitro generated kinetic data to provide quantitative prediction of in vivo pharmac...
Total human clearance is a key determinant for the pharmacokinetic behavior of drug candidates. Our ...
The literature was searched for drugs where adequate data were available on in vitro human metabolis...
Introduction: In vitro metabolic profiling is used extensively by the pharmaceutical industry to cha...
We describe a comprehensive retrospective analysis in which the abilities of several methods by whic...
Introduction: Successful quantitative prediction of hepatic drug metabolism often requires integrate...
A systematic kinetic analysis of the metabolism of five benzodiaz-epines (low to high clearance comp...
Clearance, or a measure of the body’s ability to remove drug, is a crucial pharmacokinetic parameter...
In order to improve the benefit–risk ratio of pharmacokinetic (PK) research in the early development...
A comprehensive analysis on the prediction of human clearance based on intravenous pharmacokinetic d...
ABSTRACT Prediction of human pharmacokinetics of new drugs, as well as other disposition attributes,...
The safety and efficacy of drugs depend upon appropriate dosing of drugs made possible by understand...