Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
J Chromatogr A ; 1120(1-2): 94-101, 2006 Jul 07.
Article in English | MEDLINE | ID: mdl-16376901

ABSTRACT

Cytochrome P450 (CYP), which is one of the most important enzymes in human liver, is responsible for a large portion of the first-pass metabolism of drugs. Many studies have focused on the determination of CYP activity by substrate assays. Most of them used liquid chromatography (LC) as analytical technique, while only a few studies used capillary electrophoresis (CE) for the separation and quantitation of reaction components. In this study, the feasibility of using CE in an in vitro metabolism study with CYP was tested. Verapamil was chosen as the substrate for CYP 3A4 isozyme (Supersome). A chiral capillary electrophoretic method was developed and validated for the simultaneous determination of R,S-verapamil (VER) and their major metabolites, R,S-norverapamil (NOR). A method for CYP 3A4 activity assay was proposed with VER as a probe. At the same time, the enantioselective metabolism of VER was studied. Michaelis-Menten constants of R- and S-VER were determined. S-VER was metabolised faster and more extensively than R-VER, with K(m)=167+/-23 microM, V(max)=3,418+/-234 pmol/min/mg for S-VER, and K(m)=168+/-35 microM, V(max)=2,502+/-275 pmol/min/mg for R-VER.


Subject(s)
Cytochrome P-450 Enzyme System/metabolism , Electrophoresis, Capillary/methods , Verapamil/analogs & derivatives , Verapamil/metabolism , Cytochrome P-450 CYP3A , Humans , Isoenzymes/metabolism , Molecular Structure , Reproducibility of Results , Stereoisomerism , Verapamil/chemistry , Verapamil/isolation & purification
SELECTION OF CITATIONS
SEARCH DETAIL
...