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Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS
BACKGROUND: Ginsenosides are the characteristic and principal components which manifest a variety of the biological and pharmacological activities of the roots and rhizomes of Panax ginseng (GRR). This study was carried out to qualitatively and quantitatively determine the ginsenosides in the cultiv...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052439/ https://www.ncbi.nlm.nih.gov/pubmed/27746691 http://dx.doi.org/10.1016/j.jgr.2015.12.001 |
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author | Wang, Hong-Ping Zhang, You-Bo Yang, Xiu-Wei Zhao, Da-Qing Wang, Ying-Ping |
author_facet | Wang, Hong-Ping Zhang, You-Bo Yang, Xiu-Wei Zhao, Da-Qing Wang, Ying-Ping |
author_sort | Wang, Hong-Ping |
collection | PubMed |
description | BACKGROUND: Ginsenosides are the characteristic and principal components which manifest a variety of the biological and pharmacological activities of the roots and rhizomes of Panax ginseng (GRR). This study was carried out to qualitatively and quantitatively determine the ginsenosides in the cultivated and forest GRR. METHODS: A rapid and sensitive ultra-high-performance liquid chromatography coupled with diode-array detector and quadrupole/time of flight tandem mass spectrometry (UPLC-DAD-QTOF-MS/MS) was applied to the qualitative analysis of ginsenosides and a 4000 QTRAP triple quadrupole tandem mass spectrometer (HPLC-ESI-MS) was applied to quantitative analysis of 19 ginsenosides. RESULTS: In the qualitative analysis, all ingredients were separated in 10 min. A total of 131 ginsenosides were detected in cultivated and forest GRR. The method for the quantitative determination was validated for linearity, precision, and limits of detection and quantification. 19 representative ginsenosides were quantitated. The total content of all 19 ginsenosides in the forest GRR were much higher than those in the cultivated GRR, and were increased with the growing ages. CONCLUSION: This newly developed analysis method could be applied to the quality assessment of GRR as well as the distinction between cultivated and forest GRR. |
format | Online Article Text |
id | pubmed-5052439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50524392016-10-14 Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS Wang, Hong-Ping Zhang, You-Bo Yang, Xiu-Wei Zhao, Da-Qing Wang, Ying-Ping J Ginseng Res Research Article BACKGROUND: Ginsenosides are the characteristic and principal components which manifest a variety of the biological and pharmacological activities of the roots and rhizomes of Panax ginseng (GRR). This study was carried out to qualitatively and quantitatively determine the ginsenosides in the cultivated and forest GRR. METHODS: A rapid and sensitive ultra-high-performance liquid chromatography coupled with diode-array detector and quadrupole/time of flight tandem mass spectrometry (UPLC-DAD-QTOF-MS/MS) was applied to the qualitative analysis of ginsenosides and a 4000 QTRAP triple quadrupole tandem mass spectrometer (HPLC-ESI-MS) was applied to quantitative analysis of 19 ginsenosides. RESULTS: In the qualitative analysis, all ingredients were separated in 10 min. A total of 131 ginsenosides were detected in cultivated and forest GRR. The method for the quantitative determination was validated for linearity, precision, and limits of detection and quantification. 19 representative ginsenosides were quantitated. The total content of all 19 ginsenosides in the forest GRR were much higher than those in the cultivated GRR, and were increased with the growing ages. CONCLUSION: This newly developed analysis method could be applied to the quality assessment of GRR as well as the distinction between cultivated and forest GRR. Elsevier 2016-10 2015-12-17 /pmc/articles/PMC5052439/ /pubmed/27746691 http://dx.doi.org/10.1016/j.jgr.2015.12.001 Text en Copyright © 2016, The Korean Society of Ginseng, Published by Elsevier. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Wang, Hong-Ping Zhang, You-Bo Yang, Xiu-Wei Zhao, Da-Qing Wang, Ying-Ping Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS |
title | Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS |
title_full | Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS |
title_fullStr | Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS |
title_full_unstemmed | Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS |
title_short | Rapid characterization of ginsenosides in the roots and rhizomes of Panax ginseng by UPLC-DAD-QTOF-MS/MS and simultaneous determination of 19 ginsenosides by HPLC-ESI-MS |
title_sort | rapid characterization of ginsenosides in the roots and rhizomes of panax ginseng by uplc-dad-qtof-ms/ms and simultaneous determination of 19 ginsenosides by hplc-esi-ms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052439/ https://www.ncbi.nlm.nih.gov/pubmed/27746691 http://dx.doi.org/10.1016/j.jgr.2015.12.001 |
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