z-logo
Premium
Enantioselective disposition of omeprazole, pantoprazole, and lansoprazole in a same Brazilian subjects group
Author(s) -
Cassiano Neila M.,
Oliveira Regina V.,
Bernasconi Gilberto C.R.,
Cass Quezia B.
Publication year - 2012
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.21995
Subject(s) - lansoprazole , omeprazole , pantoprazole , chemistry , proton pump inhibitor , volunteer , pharmacology , enantiomer , cyp2c19 , stereochemistry , medicine , biochemistry , metabolism , cytochrome p450 , agronomy , biology
This work reports the result of the enantioselective disposition of pantoprazole, omeprazole, and lansoprazole in a same group of Brazilian health subjects. Ten nongenotyped healthy subjects were used for this study. Each subject received a single oral dose of 80 mg of pantoprazole, 40 mg of omeprazole, and 30 mg of lansoprazole, and the plasma concentrations of the enantiomers were measured for 8 h postdose. For pantoprazole and omeprazole, among the 10 volunteers investigated, only one volunteer (Subject # 4) presented higher plasma concentrations of the (+)‐enantiomer than those of (−)‐enantiomer. Nevertheless, the area under the concentration–time curve of the (+)‐lansoprazole was higher than those the (−)‐lansoprazole for all subjects. The comparison of proton pump inhibitors' enantiomers disposition from a single group volunteer demonstrated that pantoprazole and omeprazole can be used to differentiate extensive from poor CYP2C19 metabolizer while lansoprazole cannot do it. Chirality, 2012. © 2012 Wiley Periodicals, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom