2014
Nonaqueous capillary electrophoresis of dextromethorphan and its metabolites
PELCOVÁ, Marta; Monika LANGMAJEROVÁ; Eliška CVINGRÁFOVÁ; Jan JUŘICA; Zdeněk GLATZ et. al.Basic information
Original name
Nonaqueous capillary electrophoresis of dextromethorphan and its metabolites
Authors
PELCOVÁ, Marta (203 Czech Republic, belonging to the institution); Monika LANGMAJEROVÁ (203 Czech Republic, belonging to the institution); Eliška CVINGRÁFOVÁ (203 Czech Republic, belonging to the institution); Jan JUŘICA (203 Czech Republic, belonging to the institution) and Zdeněk GLATZ (203 Czech Republic, guarantor, belonging to the institution)
Edition
JOURNAL OF SEPARATION SCIENCE, 2014, 1615-9306
Other information
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: 2.737
RIV identification code
RIV/00216224:14310/14:00074172
Organization unit
Faculty of Science
UT WoS
000342909300021
EID Scopus
2-s2.0-84908076583
Keywords in English
Dextromethorphan; Dextrorphan; Methanol; Nonaqueous media
Changed: 13/3/2018 12:00, doc. PharmDr. Jan Juřica, Ph.D.
Abstract
In the original language
This study deals with the nonaqueous capillary electrophoretic separation of dextromethorphan and its metabolites using a methanolic background electrolyte. The optimization of separation conditions was performed in terms of the resolution of dextromethorphan and dextrorphan and the effect of separation temperature, voltage, and the characteristics of the background electrolyte were studied. Complete separation of all analytes was achieved in 40 mM ammonium acetate dissolved in methanol. Hydrodynamic injection was performed at 3 kPa for 4 s. The separation voltage was 20 kV accompanied by a low electric current. The ultraviolet detection was performed at 214 nm, the temperature of the capillary was 25°C. These conditions enabled the separation of four analytes plus the internal standard within 9 min. Further, the developed method was validated in terms of linearity, sensitivity, and repeatability. Rat liver perfusate samples were subjected to the nonaqueous capillary electrophoretic method to illustrate its applicability.
Links
GBP206/12/G014, research and development project |
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