Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection
Apigenin is a naturally occurring plant flavone that exhibits strong antioxidant, anti-inflammatory, and antitumor properties. A MEKC-UV based method was developed for the determination of total apigenin in selected herbs. Application of pseudostationary phase in the form of SDS micelles resulted in...
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doaj-e2c0cbade2534814ab067e6a58f8eaaf2020-11-25T01:50:34ZengHindawi LimitedJournal of Analytical Methods in Chemistry2090-88652090-88732016-01-01201610.1155/2016/38278323827832Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV DetectionRafał Głowacki0Paulina Furmaniak1Paweł Kubalczyk2Kamila Borowczyk3Department of Environmental Chemistry, Faculty of Chemistry, University of Łódź, 163 Pomorska Street, 90-236 Łódź, PolandDepartment of Environmental Chemistry, Faculty of Chemistry, University of Łódź, 163 Pomorska Street, 90-236 Łódź, PolandDepartment of Environmental Chemistry, Faculty of Chemistry, University of Łódź, 163 Pomorska Street, 90-236 Łódź, PolandDepartment of Environmental Chemistry, Faculty of Chemistry, University of Łódź, 163 Pomorska Street, 90-236 Łódź, PolandApigenin is a naturally occurring plant flavone that exhibits strong antioxidant, anti-inflammatory, and antitumor properties. A MEKC-UV based method was developed for the determination of total apigenin in selected herbs. Application of pseudostationary phase in the form of SDS micelles resulted in great repeatability of retention times and peak areas. A buffer solution consisting of 30 mmol/L sodium borate (pH 10.2), 10% acetonitrile, and 10 mmol/L sodium dodecyl sulfate was found to be the most suitable BGE for the separation. The method was validated and calibrated for total apigenin in the range of 1.0–100 μmol/L (R2=0.9994). The limits of detection and quantification were 0.48 μmol/L and 0.92 μmol/L, respectively. This precise and robust method was successfully applied to the analysis of plant samples for total apigenin content.http://dx.doi.org/10.1155/2016/3827832 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rafał Głowacki Paulina Furmaniak Paweł Kubalczyk Kamila Borowczyk |
spellingShingle |
Rafał Głowacki Paulina Furmaniak Paweł Kubalczyk Kamila Borowczyk Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection Journal of Analytical Methods in Chemistry |
author_facet |
Rafał Głowacki Paulina Furmaniak Paweł Kubalczyk Kamila Borowczyk |
author_sort |
Rafał Głowacki |
title |
Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection |
title_short |
Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection |
title_full |
Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection |
title_fullStr |
Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection |
title_full_unstemmed |
Determination of Total Apigenin in Herbs by Micellar Electrokinetic Chromatography with UV Detection |
title_sort |
determination of total apigenin in herbs by micellar electrokinetic chromatography with uv detection |
publisher |
Hindawi Limited |
series |
Journal of Analytical Methods in Chemistry |
issn |
2090-8865 2090-8873 |
publishDate |
2016-01-01 |
description |
Apigenin is a naturally occurring plant flavone that exhibits strong antioxidant, anti-inflammatory, and antitumor properties. A MEKC-UV based method was developed for the determination of total apigenin in selected herbs. Application of pseudostationary phase in the form of SDS micelles resulted in great repeatability of retention times and peak areas. A buffer solution consisting of 30 mmol/L sodium borate (pH 10.2), 10% acetonitrile, and 10 mmol/L sodium dodecyl sulfate was found to be the most suitable BGE for the separation. The method was validated and calibrated for total apigenin in the range of 1.0–100 μmol/L (R2=0.9994). The limits of detection and quantification were 0.48 μmol/L and 0.92 μmol/L, respectively. This precise and robust method was successfully applied to the analysis of plant samples for total apigenin content. |
url |
http://dx.doi.org/10.1155/2016/3827832 |
work_keys_str_mv |
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