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Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method
Solanaceae is one of the highly diverse plant families of which Solanum is the largest genera (1700 species) containing several pharmacological properties like anticancer and antimicrobial. This motivated us to explore the anticancer (against HepG2, HEK-293, and MCF-7 cells) and antimicrobial (again...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051100/ https://www.ncbi.nlm.nih.gov/pubmed/30057644 http://dx.doi.org/10.1155/2018/6040815 |
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author | Alajmi, Mohamed Fahad Alam, Perwez Rehman, Md. Tabish Husain, Fohad Mabood Khan, Azmat Ali Siddiqui, Nasir Ali Hussain, Afzal Kalam, Mohd. Abul Parvez, Mohammad Khalid |
author_facet | Alajmi, Mohamed Fahad Alam, Perwez Rehman, Md. Tabish Husain, Fohad Mabood Khan, Azmat Ali Siddiqui, Nasir Ali Hussain, Afzal Kalam, Mohd. Abul Parvez, Mohammad Khalid |
author_sort | Alajmi, Mohamed Fahad |
collection | PubMed |
description | Solanaceae is one of the highly diverse plant families of which Solanum is the largest genera (1700 species) containing several pharmacological properties like anticancer and antimicrobial. This motivated us to explore the anticancer (against HepG2, HEK-293, and MCF-7 cells) and antimicrobial (against S. aureus, E. coli, P. aeruginosa, and C. albicans) properties of S. schimperianum, S. villosum, S. coagulans, S. glabratum, S. incanum, and S. nigrum along with rutin estimation by UPLC-PDA method. Of the studied Solanum extracts, S. nigrum exhibited significant cytotoxic property against HepG2 (IC(50): 20.4 μg/mL) and MCF-7 (IC(50): 30.1 μg/mL); S. coagulans showed toxicity against HepG2 (IC(50): 28.4 μg/mL) and HEK-293 cells (IC(50): 25.7 μg/mL) compared to 5-Fluorouracil (standard). Compared to these, extracts of S. coagulans and S. glabratum exhibited relatively high antimicrobial potency (MIC: 0.4-1.6 mg/mL). Nonetheless, all Solanum extracts significantly reduced the biofilm against PAO1-strain. Rutin was detected in all extracts with the highest content (53.79 μg/mg) in S. coagulans that supported its strong antimicrobial and anticancer properties. Molecular docking analysis showing strong binding of rutin with human DNA and proteins (DNA Topoisomerase IIα and E. coli DNA gyrase B) supported the anticancer and antimicrobial activities of Solanum species. |
format | Online Article Text |
id | pubmed-6051100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60511002018-07-29 Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method Alajmi, Mohamed Fahad Alam, Perwez Rehman, Md. Tabish Husain, Fohad Mabood Khan, Azmat Ali Siddiqui, Nasir Ali Hussain, Afzal Kalam, Mohd. Abul Parvez, Mohammad Khalid Evid Based Complement Alternat Med Research Article Solanaceae is one of the highly diverse plant families of which Solanum is the largest genera (1700 species) containing several pharmacological properties like anticancer and antimicrobial. This motivated us to explore the anticancer (against HepG2, HEK-293, and MCF-7 cells) and antimicrobial (against S. aureus, E. coli, P. aeruginosa, and C. albicans) properties of S. schimperianum, S. villosum, S. coagulans, S. glabratum, S. incanum, and S. nigrum along with rutin estimation by UPLC-PDA method. Of the studied Solanum extracts, S. nigrum exhibited significant cytotoxic property against HepG2 (IC(50): 20.4 μg/mL) and MCF-7 (IC(50): 30.1 μg/mL); S. coagulans showed toxicity against HepG2 (IC(50): 28.4 μg/mL) and HEK-293 cells (IC(50): 25.7 μg/mL) compared to 5-Fluorouracil (standard). Compared to these, extracts of S. coagulans and S. glabratum exhibited relatively high antimicrobial potency (MIC: 0.4-1.6 mg/mL). Nonetheless, all Solanum extracts significantly reduced the biofilm against PAO1-strain. Rutin was detected in all extracts with the highest content (53.79 μg/mg) in S. coagulans that supported its strong antimicrobial and anticancer properties. Molecular docking analysis showing strong binding of rutin with human DNA and proteins (DNA Topoisomerase IIα and E. coli DNA gyrase B) supported the anticancer and antimicrobial activities of Solanum species. Hindawi 2018-07-03 /pmc/articles/PMC6051100/ /pubmed/30057644 http://dx.doi.org/10.1155/2018/6040815 Text en Copyright © 2018 Mohamed Fahad Alajmi et al. https://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 Alajmi, Mohamed Fahad Alam, Perwez Rehman, Md. Tabish Husain, Fohad Mabood Khan, Azmat Ali Siddiqui, Nasir Ali Hussain, Afzal Kalam, Mohd. Abul Parvez, Mohammad Khalid Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method |
title | Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method |
title_full | Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method |
title_fullStr | Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method |
title_full_unstemmed | Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method |
title_short | Interspecies Anticancer and Antimicrobial Activities of Genus Solanum and Estimation of Rutin by Validated UPLC-PDA Method |
title_sort | interspecies anticancer and antimicrobial activities of genus solanum and estimation of rutin by validated uplc-pda method |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051100/ https://www.ncbi.nlm.nih.gov/pubmed/30057644 http://dx.doi.org/10.1155/2018/6040815 |
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