DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA

A new, simple, specific, and rapid ultra high performance liquid chromatography method was developed and validated for the determination of aripiprazole and its active metabolite dehydroaripiprazole in rat plasma. The analysis was performed on a Zorbax Eclipse Plus C18 (50 mm × 2.1 mm, 1.8 &#956...

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Autores principales: YENICELI UĞUR,DUYGU, YILMAZ,IŞIL T, ŞENER,EROL
Lenguaje:English
Publicado: Sociedad Chilena de Química 2015
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072015000300016
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spelling oai:scielo:S0717-970720150003000162015-12-04DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMAYENICELI UĞUR,DUYGUYILMAZ,IŞIL TŞENER,EROL Aripiprazole dehydroaripiprazole UHPLC rat plasma validation protein precipitation A new, simple, specific, and rapid ultra high performance liquid chromatography method was developed and validated for the determination of aripiprazole and its active metabolite dehydroaripiprazole in rat plasma. The analysis was performed on a Zorbax Eclipse Plus C18 (50 mm × 2.1 mm, 1.8 μm particles) column using gradient elution with a mobile phase consisting of acetonitrile and acetate buffer (30 mM, pH 5). Plasma samples were analyzed after a simple, one-step protein precipitation with acetonitrile. The method was validated and the specificity, linearity, limit of detection, limit of quantitation, precision, accuracy, recoveries, matrix effect, stability and robustness were determined. The analytes and internal standard were separated in 3.5 min and the total analysis time including the clean-up step was 8 min. Limit of detection was 0.012 μg mL-1 and 0.009 μg mL-1 for aripiprazole and dehydroaripiprazole, respectively. Limit of quantitation was 0.039 μg mL-1 and 0.029 μg mL-1 for aripiprazole and dehydroaripiprazole, respectively. The intra- and inter-day assay variability was less than 2% for the analytes. The proposed method is rapid, reproducible and accurate to quantify both aripiprazole and dehydroaripiprazole. It involves a simple plasma deproteination technique using one step protein precipitation with acetonitrile. This validated method was successfully used to quantify plasma concentrations of the analytes in rat plasma.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.60 n.3 20152015-09-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072015000300016en10.4067/S0717-97072015000300016
institution Scielo Chile
collection Scielo Chile
language English
topic Aripiprazole
dehydroaripiprazole
UHPLC
rat plasma
validation
protein precipitation
spellingShingle Aripiprazole
dehydroaripiprazole
UHPLC
rat plasma
validation
protein precipitation
YENICELI UĞUR,DUYGU
YILMAZ,IŞIL T
ŞENER,EROL
DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA
description A new, simple, specific, and rapid ultra high performance liquid chromatography method was developed and validated for the determination of aripiprazole and its active metabolite dehydroaripiprazole in rat plasma. The analysis was performed on a Zorbax Eclipse Plus C18 (50 mm × 2.1 mm, 1.8 μm particles) column using gradient elution with a mobile phase consisting of acetonitrile and acetate buffer (30 mM, pH 5). Plasma samples were analyzed after a simple, one-step protein precipitation with acetonitrile. The method was validated and the specificity, linearity, limit of detection, limit of quantitation, precision, accuracy, recoveries, matrix effect, stability and robustness were determined. The analytes and internal standard were separated in 3.5 min and the total analysis time including the clean-up step was 8 min. Limit of detection was 0.012 μg mL-1 and 0.009 μg mL-1 for aripiprazole and dehydroaripiprazole, respectively. Limit of quantitation was 0.039 μg mL-1 and 0.029 μg mL-1 for aripiprazole and dehydroaripiprazole, respectively. The intra- and inter-day assay variability was less than 2% for the analytes. The proposed method is rapid, reproducible and accurate to quantify both aripiprazole and dehydroaripiprazole. It involves a simple plasma deproteination technique using one step protein precipitation with acetonitrile. This validated method was successfully used to quantify plasma concentrations of the analytes in rat plasma.
author YENICELI UĞUR,DUYGU
YILMAZ,IŞIL T
ŞENER,EROL
author_facet YENICELI UĞUR,DUYGU
YILMAZ,IŞIL T
ŞENER,EROL
author_sort YENICELI UĞUR,DUYGU
title DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA
title_short DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA
title_full DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA
title_fullStr DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA
title_full_unstemmed DEVELOPMENT OF A SIMPLE AND SPECIFIC UHPLC ASSAY FOR THE DETERMINATION OF ARIPIPRAZOLE AND DEHYDROARDPDPRAZOLE IN RAT PLASMA
title_sort development of a simple and specific uhplc assay for the determination of aripiprazole and dehydroardpdprazole in rat plasma
publisher Sociedad Chilena de Química
publishDate 2015
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072015000300016
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AT yilmazi350ilt developmentofasimpleandspecificuhplcassayforthedeterminationofaripiprazoleanddehydroardpdprazoleinratplasma
AT 350enererol developmentofasimpleandspecificuhplcassayforthedeterminationofaripiprazoleanddehydroardpdprazoleinratplasma
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