ŘEMÍNEK, Roman, Marta ZEISBERGEROVÁ, Monika LANGMAJEROVÁ and Zdeněk GLATZ. New Capillary Electrophoretic Method for On-line Screenings of Drug Metabolism Mediated by Cytochrome P450 Enzymes. Electrophoresis. Weinheim: WILEY-VCH Verlag GmbH, 2013, vol. 34, No 18, p. 2705-2711. ISSN 0173-0835. Available from: https://dx.doi.org/10.1002/elps.201300124.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name New Capillary Electrophoretic Method for On-line Screenings of Drug Metabolism Mediated by Cytochrome P450 Enzymes
Name in Czech Nová metoda pro on-line studie metabolismu léčiv pomocí CE
Authors ŘEMÍNEK, Roman (203 Czech Republic, guarantor, belonging to the institution), Marta ZEISBERGEROVÁ (203 Czech Republic, belonging to the institution), Monika LANGMAJEROVÁ (203 Czech Republic) and Zdeněk GLATZ (203 Czech Republic, belonging to the institution).
Edition Electrophoresis, Weinheim, WILEY-VCH Verlag GmbH, 2013, 0173-0835.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.161
RIV identification code RIV/00216224:14310/13:00066068
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1002/elps.201300124
UT WoS 000327590900013
Keywords (in Czech) CE; Cytochrom P450; Metabolismus léčiv;
Keywords in English CE; Cytochrome P450; Drug Metabolism;
Tags AKR, rivok, ZR
Tags International impact, Reviewed
Changed by Changed by: Ing. Zdeňka Rašková, učo 140529. Changed: 25/4/2014 14:59.
Abstract
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.
Abstract (in Czech)
Byla nová metoda pro on-line studie metabolismu léčiv pomocí CE
Links
EE2.3.20.0182, research and development projectName: Vytvoření multidisciplinárního výzkumného a vzdělávacího centra bioanalytických technologií
GAP206/10/0057, research and development projectName: Miniaturizovaný systém pro "on-line" studie metabolismu léčiv založený na kapilární elektroforéze
Investor: Czech Science Foundation, Miniaturized on-line drug metabolism system based on capillary electrophoresis
PrintDisplayed: 12/5/2024 14:38