Title : Physiologically based pharmacokinetic (PBPK) modeling for prediction of celecoxib pharmacokinetics according to CYP2C9 genetic polymorphism.

Pub. Date : 2021 Jul

PMID : 34304363






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1 Physiologically based pharmacokinetic (PBPK) modeling for prediction of celecoxib pharmacokinetics according to CYP2C9 genetic polymorphism. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens
2 Many studies reported that CYP2C9 genetic polymorphism has significant effects on the pharmacokinetics of celecoxib and the occurrence of adverse drug reactions. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens
3 The aim of this study was to develop a physiologically based pharmacokinetic (PBPK) model of celecoxib according to CYP2C9 genetic polymorphism for personalized pharmacotherapy. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens
4 Based on the conducted pharmacokinetic study and a previous pharmacokinetic study involving subjects with CYP2C9*1/*13 and CYP2C9*3/*3 genotype, PBPK model for celecoxib was developed. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens
5 Based on the conducted pharmacokinetic study and a previous pharmacokinetic study involving subjects with CYP2C9*1/*13 and CYP2C9*3/*3 genotype, PBPK model for celecoxib was developed. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens
6 As a result, the developed PBPK model of celecoxib successfully described the pharmacokinetics of each CYP2C9 genotype group and its predicted values were within the acceptance criterion. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens
7 This study demonstrates the possibility of determining the appropriate dosage of celecoxib for each individual through the PBPK modeling with CYP2C9 genomic information. Celecoxib cytochrome P450 family 2 subfamily C member 9 Homo sapiens