New Capillary Electrophoretic Method for On-line Screenings of Drug Metabolism Mediated by Cytochrome P450 Enzymes

Investor logo
Investor logo

Warning

This publication doesn't include Faculty of Sports Studies. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

ŘEMÍNEK Roman ZEISBERGEROVÁ Marta LANGMAJEROVÁ Monika GLATZ Zdeněk

Year of publication 2013
Type Article in Periodical
Magazine / Source Electrophoresis
MU Faculty or unit

Faculty of Science

Citation
Doi http://dx.doi.org/10.1002/elps.201300124
Field Biochemistry
Keywords CE; Cytochrome P450; Drug Metabolism;
Description A new method for the determination of kinetic and inhibition parameters of cytochromes P450 reactions by means of on-line capillary electrophoresis was developed. It is based on transverse diffusion of laminar flow profiles methodology introduced by Krylov et al. which injection procedure was modified. The solutions of an enzyme and its substrates are injected by hydrodynamic pressure as a series of repeated consecutive plugs. Proposed injection of 3 plugs of enzyme surrounded with plugs of substrates represents a certain trade-off to obtain the reaction mixture with the satisfying homogeneity by the short injection procedure as possible. Mathematical modelling confirmed the assumption of a consistent distribution of reactants in the final reaction mixture. Kinetic and inhibition studies of cytochrome P450 2C9’s reaction with diclofenac as a probe substrate and sulfaphenazole as a probe inhibitor were conducted in order to prove the practical applicability of the proposed method for on-line screenings of drug metabolism mediated by cytochrome P450 enzymes. As a result, an apparent Michaelis constant of 2.66 +- 0.18 uM, apparent maximum reaction velocity of 7.91 +- 0.22 nmol min-1 nmol-1, Hill coefficient of 1.59 +- 0.16, half maximal inhibitory concentration of 0.94 +- 0.04 uM and apparent inhibition constant of 0.39 +- 0.07 uM were determined. All these values are in agreement with literature data obtained using different techniques. In addition, less than 30 nL of cytochrome P450 2C9 solution was consumed per analysis in the kinetic and inhibition studies using this method.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info