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UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves

This study aimed to determine the total phenolic content, DPPH scavenging, α-glucosidase, and nitric oxide (NO) inhibition of Gynura procumbens and Cleome gynandra extracts obtained with five different ethanolic concentrations. The findings showed that the 100% ethanolic extract of G. procumbens had...

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Autores principales: Chandradevan, Machap, Simoh, Sanimah, Mediani, Ahmed, Ismail, Nor Hadiani, Ismail, Intan Safinar, Abas, Faridah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007755/
https://www.ncbi.nlm.nih.gov/pubmed/32047522
http://dx.doi.org/10.1155/2020/3238561
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author Chandradevan, Machap
Simoh, Sanimah
Mediani, Ahmed
Ismail, Nor Hadiani
Ismail, Intan Safinar
Abas, Faridah
author_facet Chandradevan, Machap
Simoh, Sanimah
Mediani, Ahmed
Ismail, Nor Hadiani
Ismail, Intan Safinar
Abas, Faridah
author_sort Chandradevan, Machap
collection PubMed
description This study aimed to determine the total phenolic content, DPPH scavenging, α-glucosidase, and nitric oxide (NO) inhibition of Gynura procumbens and Cleome gynandra extracts obtained with five different ethanolic concentrations. The findings showed that the 100% ethanolic extract of G. procumbens had the highest phenolic content and the lowest IC(50) values for DPPH scavenging and NO inhibition activity compared to the properties of the other extracts. For C. gynandra, the 20% and 100% ethanolic extracts had comparably high total phenolic contents, and the latter possessed the lowest IC(50) value in the NO inhibition assay. In addition, the 20% ethanolic extract of C. gynandra had the lowest IC(50) value in the DPPH scavenging assay. However, none of the extracts from either herb had the ability to inhibit α-glucosidase enzyme. Pearson correlation analysis indicated a strong relationship between the phenolic content and DPPH scavenging activity in both herb extracts. A moderately strong relationship was also observed between the phenolic content and NO inhibition in G. procumbens extracts and not in C. gynandra extracts. The UHPLC-ESI-Orbitrap-MS revealed major phenolics from the groups of hydroxycinnamic acids, hydroxybenzoic acids, and flavonoid derivatives from both herbs, which could be the key contributors to their bioactivities. Among the identified metabolites, 24 metabolites were tentatively assigned for the first time from both species of studied herbs. These two herbs could be recommended as prospective natural products with valuable medicinal properties.
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spelling pubmed-70077552020-02-11 UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves Chandradevan, Machap Simoh, Sanimah Mediani, Ahmed Ismail, Nor Hadiani Ismail, Intan Safinar Abas, Faridah Evid Based Complement Alternat Med Research Article This study aimed to determine the total phenolic content, DPPH scavenging, α-glucosidase, and nitric oxide (NO) inhibition of Gynura procumbens and Cleome gynandra extracts obtained with five different ethanolic concentrations. The findings showed that the 100% ethanolic extract of G. procumbens had the highest phenolic content and the lowest IC(50) values for DPPH scavenging and NO inhibition activity compared to the properties of the other extracts. For C. gynandra, the 20% and 100% ethanolic extracts had comparably high total phenolic contents, and the latter possessed the lowest IC(50) value in the NO inhibition assay. In addition, the 20% ethanolic extract of C. gynandra had the lowest IC(50) value in the DPPH scavenging assay. However, none of the extracts from either herb had the ability to inhibit α-glucosidase enzyme. Pearson correlation analysis indicated a strong relationship between the phenolic content and DPPH scavenging activity in both herb extracts. A moderately strong relationship was also observed between the phenolic content and NO inhibition in G. procumbens extracts and not in C. gynandra extracts. The UHPLC-ESI-Orbitrap-MS revealed major phenolics from the groups of hydroxycinnamic acids, hydroxybenzoic acids, and flavonoid derivatives from both herbs, which could be the key contributors to their bioactivities. Among the identified metabolites, 24 metabolites were tentatively assigned for the first time from both species of studied herbs. These two herbs could be recommended as prospective natural products with valuable medicinal properties. Hindawi 2020-01-27 /pmc/articles/PMC7007755/ /pubmed/32047522 http://dx.doi.org/10.1155/2020/3238561 Text en Copyright © 2020 Machap Chandradevan et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chandradevan, Machap
Simoh, Sanimah
Mediani, Ahmed
Ismail, Nor Hadiani
Ismail, Intan Safinar
Abas, Faridah
UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves
title UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves
title_full UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves
title_fullStr UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves
title_full_unstemmed UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves
title_short UHPLC-ESI-Orbitrap-MS Analysis of Biologically Active Extracts from Gynura procumbens (Lour.) Merr. and Cleome gynandra L. Leaves
title_sort uhplc-esi-orbitrap-ms analysis of biologically active extracts from gynura procumbens (lour.) merr. and cleome gynandra l. leaves
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007755/
https://www.ncbi.nlm.nih.gov/pubmed/32047522
http://dx.doi.org/10.1155/2020/3238561
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