Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches
The current study was designed to isolate and characterize some bioactive secondary metabolites by using repeated chromatographic and spectroscopic techniques, targeting their anticancer, antimicrobial, and antioxidant properties through in vitro and in silico approaches. Six compounds were isolated...
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oai:doaj.org-article:742be85c42e9427ca7a6c53db38839ea2021-12-02T05:03:22ZIsolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches2405-844010.1016/j.heliyon.2021.e08475https://doaj.org/article/742be85c42e9427ca7a6c53db38839ea2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2405844021025780https://doaj.org/toc/2405-8440The current study was designed to isolate and characterize some bioactive secondary metabolites by using repeated chromatographic and spectroscopic techniques, targeting their anticancer, antimicrobial, and antioxidant properties through in vitro and in silico approaches. Six compounds were isolated and analyzed by thin layer chromatographic technique and the compounds were identified as 5-O-caffeoyl quinic acid (1), syringin (2), luteolin (3), apigenin (4), jhanol (5), and jhanidiol (6) based on spectroscopic methods. The cytotoxic effect of each compound was dose-dependent, and compound 1 showed a higher anti-proliferative effect (IC50 = 181.3 μg/ml) than other compounds (compound 2, 4, 5, and 6). Besides, compound 1 showed the most promising antibacterial activity with a zone of inhibition ranges from 12–15 mm against different strains compared to ciprofloxacin (14–22 mm). In contrast, compound 3 exerted the highest scavenging property against DPPH free radical. Finally, the in vitro bioactivities were also supported by molecular docking studies. The computational study demonstrated that the isolated compounds exerted stronger affinity compared to the standard drugs towards the binding sites of dihydrofolate reductase (DHFR), glutathione reductase, and urase oxidase.Most. Chand Sultana KhatunMd. Abdul MuhitMd. Jamal HossainMuhammad Abdullah Al-MansurS.M. Abdur RahmanElsevierarticleStevia rebaudianaPhenolic constituentsCytotoxicityAntimicrobialAntioxidantMolecular dockingScience (General)Q1-390Social sciences (General)H1-99ENHeliyon, Vol 7, Iss 12, Pp e08475- (2021) |
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Stevia rebaudiana Phenolic constituents Cytotoxicity Antimicrobial Antioxidant Molecular docking Science (General) Q1-390 Social sciences (General) H1-99 |
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Stevia rebaudiana Phenolic constituents Cytotoxicity Antimicrobial Antioxidant Molecular docking Science (General) Q1-390 Social sciences (General) H1-99 Most. Chand Sultana Khatun Md. Abdul Muhit Md. Jamal Hossain Muhammad Abdullah Al-Mansur S.M. Abdur Rahman Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
description |
The current study was designed to isolate and characterize some bioactive secondary metabolites by using repeated chromatographic and spectroscopic techniques, targeting their anticancer, antimicrobial, and antioxidant properties through in vitro and in silico approaches. Six compounds were isolated and analyzed by thin layer chromatographic technique and the compounds were identified as 5-O-caffeoyl quinic acid (1), syringin (2), luteolin (3), apigenin (4), jhanol (5), and jhanidiol (6) based on spectroscopic methods. The cytotoxic effect of each compound was dose-dependent, and compound 1 showed a higher anti-proliferative effect (IC50 = 181.3 μg/ml) than other compounds (compound 2, 4, 5, and 6). Besides, compound 1 showed the most promising antibacterial activity with a zone of inhibition ranges from 12–15 mm against different strains compared to ciprofloxacin (14–22 mm). In contrast, compound 3 exerted the highest scavenging property against DPPH free radical. Finally, the in vitro bioactivities were also supported by molecular docking studies. The computational study demonstrated that the isolated compounds exerted stronger affinity compared to the standard drugs towards the binding sites of dihydrofolate reductase (DHFR), glutathione reductase, and urase oxidase. |
format |
article |
author |
Most. Chand Sultana Khatun Md. Abdul Muhit Md. Jamal Hossain Muhammad Abdullah Al-Mansur S.M. Abdur Rahman |
author_facet |
Most. Chand Sultana Khatun Md. Abdul Muhit Md. Jamal Hossain Muhammad Abdullah Al-Mansur S.M. Abdur Rahman |
author_sort |
Most. Chand Sultana Khatun |
title |
Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
title_short |
Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
title_full |
Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
title_fullStr |
Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
title_full_unstemmed |
Isolation of phytochemical constituents from Stevia rebaudiana (Bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
title_sort |
isolation of phytochemical constituents from stevia rebaudiana (bert.) and evaluation of their anticancer, antimicrobial and antioxidant properties via in vitro and in silico approaches |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/742be85c42e9427ca7a6c53db38839ea |
work_keys_str_mv |
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