J 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

Tags

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
Name: Centrum pokročilých bioanalytických technologií