Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis

A capillary zone electrophoresis (CZE) method has been developed for the analysis of cabergoline in its pharmaceutical preparations. Optimized analysis conditions for cabergoline analysis were performed using 110 mM pH 5.0 phosphate buffer containing 30 % acetonitrile as an electrolyte solution. Sep...

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Autores principales: Dogan, Aysegul, Pehlivan, Ismail, Basci, Nursabah E.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8112
http://www.latamjpharm.org/resumenes/30/1/LAJOP_30_1_1_20.pdf
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id I19-R120-10915-8112
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
Ergolinas
cabergoline; capillary zone electrophoresis; pharmaceutical preparations; tablet; validation
Electroforesis Capilar
spellingShingle Farmacia
Ergolinas
cabergoline; capillary zone electrophoresis; pharmaceutical preparations; tablet; validation
Electroforesis Capilar
Dogan, Aysegul
Pehlivan, Ismail
Basci, Nursabah E.
Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
topic_facet Farmacia
Ergolinas
cabergoline; capillary zone electrophoresis; pharmaceutical preparations; tablet; validation
Electroforesis Capilar
description A capillary zone electrophoresis (CZE) method has been developed for the analysis of cabergoline in its pharmaceutical preparations. Optimized analysis conditions for cabergoline analysis were performed using 110 mM pH 5.0 phosphate buffer containing 30 % acetonitrile as an electrolyte solution. Separation was performed through a fused silica capillary (50 μm i.d., total length 64.5 cm, 50.0 cm effective length) at 30 ºC with an applied voltage of 30 kV and hydrodynamic injection for 4 s. Cabergoline and internal standard verapamil were detected at a wavelength of 220 nm. The calibration was liner from 5.0 to 90.0 μg mL–1 and the limit of detection and quantification were 1.25 and 3.77 μg mL–1 Optimized CE . method was validated on the basis of related ICH guideline and found as an accurate, sensitive, precise and reproducible method for cabergoline determination. Developed method is also successfully applied for the analysis of pharmaceutical preparations containing cabergoline.
format Articulo
Articulo
author Dogan, Aysegul
Pehlivan, Ismail
Basci, Nursabah E.
author_facet Dogan, Aysegul
Pehlivan, Ismail
Basci, Nursabah E.
author_sort Dogan, Aysegul
title Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
title_short Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
title_full Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
title_fullStr Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
title_full_unstemmed Method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
title_sort method development and validation for the determination of cabergoline in tablets by capillary zone electrophoresis
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8112
http://www.latamjpharm.org/resumenes/30/1/LAJOP_30_1_1_20.pdf
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AT pehlivanismail methoddevelopmentandvalidationforthedeterminationofcabergolineintabletsbycapillaryzoneelectrophoresis
AT bascinursabahe methoddevelopmentandvalidationforthedeterminationofcabergolineintabletsbycapillaryzoneelectrophoresis
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