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UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.

Dracocephalum moldavica L. is a significant component in the Iranian food basket. This study aimed to investigate the bioactive compounds and biological activities of different extracts obtained from D. moldavica aerial parts. From the aerial parts, a crude methanolic (MeOH) extract and its four sub...

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Autores principales: Fattahi, Azin, Shakeri, Abolfazl, Tayarani‐Najaran, Zahra, Kharbach, Mourad, Segers, Karen, Heyden, Yvan Vander, Taghizadeh, Seyedeh Faezeh, Rahmani, Hanieh, Asili, Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358350/
https://www.ncbi.nlm.nih.gov/pubmed/34401078
http://dx.doi.org/10.1002/fsn3.2396
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author Fattahi, Azin
Shakeri, Abolfazl
Tayarani‐Najaran, Zahra
Kharbach, Mourad
Segers, Karen
Heyden, Yvan Vander
Taghizadeh, Seyedeh Faezeh
Rahmani, Hanieh
Asili, Javad
author_facet Fattahi, Azin
Shakeri, Abolfazl
Tayarani‐Najaran, Zahra
Kharbach, Mourad
Segers, Karen
Heyden, Yvan Vander
Taghizadeh, Seyedeh Faezeh
Rahmani, Hanieh
Asili, Javad
author_sort Fattahi, Azin
collection PubMed
description Dracocephalum moldavica L. is a significant component in the Iranian food basket. This study aimed to investigate the bioactive compounds and biological activities of different extracts obtained from D. moldavica aerial parts. From the aerial parts, a crude methanolic (MeOH) extract and its four sub‐fractions, that is, petroleum ether (Pet), ethyl acetate (EtOAc), n‐butanol (n‐BuOH), and aqueous (water) extracts were obtained. The total phenolic and flavonoid contents as well as the antioxidant and cytotoxic activities of the extracts were determined. Moreover, the phytochemical profiles of the essential oil (EO) and of those extracts with the highest antioxidant activity measured by GC/MS and UPLC–PDA‐ESI–QTOF–MS/MS. Results showed that the highest concentrations of phenols and flavonoids as well as the most potent antioxidant potential according to the DPPH method were determined in the EtOAc and MeOH extracts with IC(50) values of 22.0 and 34.4 µg.ml(‐1), respectively. Quantitative analysis of these extracts was subsequently performed by UPLC–PDA‐ESI–QTOF–MS/MS. Both extracts contained mainly rosmarinic acid, caffeic acid, and 2‐hydroxycinnamic acid, which may be responsible for their high antioxidant activity. Moreover, none of the extracts showed cytotoxic effects against MCF7, SW48, and a normal cell line of mouse embryonic fibroblast cells (NIH/3T3) in the tested concentrations (up to 400 μg.ml(‐1)). Additionally, GC‐MS analysis showed that oxygenated monoterpenes (55.4%) were the main constituents of the EO of D. moldavica.
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spelling pubmed-83583502021-08-15 UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L. Fattahi, Azin Shakeri, Abolfazl Tayarani‐Najaran, Zahra Kharbach, Mourad Segers, Karen Heyden, Yvan Vander Taghizadeh, Seyedeh Faezeh Rahmani, Hanieh Asili, Javad Food Sci Nutr Original Research Dracocephalum moldavica L. is a significant component in the Iranian food basket. This study aimed to investigate the bioactive compounds and biological activities of different extracts obtained from D. moldavica aerial parts. From the aerial parts, a crude methanolic (MeOH) extract and its four sub‐fractions, that is, petroleum ether (Pet), ethyl acetate (EtOAc), n‐butanol (n‐BuOH), and aqueous (water) extracts were obtained. The total phenolic and flavonoid contents as well as the antioxidant and cytotoxic activities of the extracts were determined. Moreover, the phytochemical profiles of the essential oil (EO) and of those extracts with the highest antioxidant activity measured by GC/MS and UPLC–PDA‐ESI–QTOF–MS/MS. Results showed that the highest concentrations of phenols and flavonoids as well as the most potent antioxidant potential according to the DPPH method were determined in the EtOAc and MeOH extracts with IC(50) values of 22.0 and 34.4 µg.ml(‐1), respectively. Quantitative analysis of these extracts was subsequently performed by UPLC–PDA‐ESI–QTOF–MS/MS. Both extracts contained mainly rosmarinic acid, caffeic acid, and 2‐hydroxycinnamic acid, which may be responsible for their high antioxidant activity. Moreover, none of the extracts showed cytotoxic effects against MCF7, SW48, and a normal cell line of mouse embryonic fibroblast cells (NIH/3T3) in the tested concentrations (up to 400 μg.ml(‐1)). Additionally, GC‐MS analysis showed that oxygenated monoterpenes (55.4%) were the main constituents of the EO of D. moldavica. John Wiley and Sons Inc. 2021-06-14 /pmc/articles/PMC8358350/ /pubmed/34401078 http://dx.doi.org/10.1002/fsn3.2396 Text en © 2021 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Fattahi, Azin
Shakeri, Abolfazl
Tayarani‐Najaran, Zahra
Kharbach, Mourad
Segers, Karen
Heyden, Yvan Vander
Taghizadeh, Seyedeh Faezeh
Rahmani, Hanieh
Asili, Javad
UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.
title UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.
title_full UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.
title_fullStr UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.
title_full_unstemmed UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.
title_short UPLC–PDA‐ESI–QTOF–MS/MS and GC‐MS analysis of Iranian Dracocephalum moldavica L.
title_sort uplc–pda‐esi–qtof–ms/ms and gc‐ms analysis of iranian dracocephalum moldavica l.
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358350/
https://www.ncbi.nlm.nih.gov/pubmed/34401078
http://dx.doi.org/10.1002/fsn3.2396
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