Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract

Citrus maxima Merr is a tropical fruit from rutaceae family. Fruits of the plant had been utilized in folk medicine and showed various pharmacological properties. The present study include phytochemical screening, quantitation and identification of phenolics in fruit ethanolic extract of C. maxima. F...

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Main Authors: Zakia Khanam, Nur Hazerra Mohd Zakaria, Kong, Hui Sam, Chua, Hui Ching, Muhammad Che Isa, Irshad Ul Haq Bhat
Format: Conference or Workshop Item
Language:English
Online Access:http://discol.umk.edu.my/id/eprint/9182/1/Phytochemical%20study%20and%20DNA%20cleavage%20activity%20of%20citrus%20maxima%20ethanolic%20fruit%20extract.pdf
http://discol.umk.edu.my/id/eprint/9182/
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spelling my.umk.eprints.91822022-05-23T11:17:43Z http://discol.umk.edu.my/id/eprint/9182/ Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract Zakia Khanam Nur Hazerra Mohd Zakaria Kong, Hui Sam Chua, Hui Ching Muhammad Che Isa Irshad Ul Haq Bhat Citrus maxima Merr is a tropical fruit from rutaceae family. Fruits of the plant had been utilized in folk medicine and showed various pharmacological properties. The present study include phytochemical screening, quantitation and identification of phenolics in fruit ethanolic extract of C. maxima. Furthermore, C. maxima ethanolic extract was evaluated against pathogenic E.coli palmid DNA by DNA cleavage assay. Phytochemical screening was carried out by colour reaction. The total phenolic (TPC) and total flavonoid content (TFC) were determined by Folin-Ciocalteu and aluminium trichloride colorimetric method, respectively. The identification of C. maxima phenolics present in ethanolic extract was done by HPLC equipped with Diode Array Detector. DNA cleavage activity was performed by gel electrophoresis method at various concentrations of the extract (0.125 pg/ul to 0.600 pg/ul). The preliminary phytochemical analyses, TPC and TFC results indicated C. maxima ethanolic extract is a good source of phenolics. 4-hydroxy-3-methoxy cinnamic acid and quercetin were identified as major phenolic acid and flavonoids in the ethanolic extract respectively. DNA cleavage activity exhibited ability of maximum bacterial DNA cleavage up to the linear form in a concentration dependent manner. Thus, overall results of the study suggests, C. maxima possess neutraceutical potential and may be exploited in future for therapeutic applications and anticancer drug discovey. Conference or Workshop Item NonPeerReviewed pdf en http://discol.umk.edu.my/id/eprint/9182/1/Phytochemical%20study%20and%20DNA%20cleavage%20activity%20of%20citrus%20maxima%20ethanolic%20fruit%20extract.pdf Zakia Khanam and Nur Hazerra Mohd Zakaria and Kong, Hui Sam and Chua, Hui Ching and Muhammad Che Isa and Irshad Ul Haq Bhat Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract. In: Proceedings of 4th USM-PSU-NSTRU-MU International Conference on Arts and Sciences, 2015, Universiti Sains Malaysia. (Submitted)
institution Universiti Malaysia Kelantan
building Perpustakaan Universiti Malaysia Kelantan
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Kelantan
content_source UMK Institutional Repository
url_provider http://umkeprints.umk.edu.my/
language English
description Citrus maxima Merr is a tropical fruit from rutaceae family. Fruits of the plant had been utilized in folk medicine and showed various pharmacological properties. The present study include phytochemical screening, quantitation and identification of phenolics in fruit ethanolic extract of C. maxima. Furthermore, C. maxima ethanolic extract was evaluated against pathogenic E.coli palmid DNA by DNA cleavage assay. Phytochemical screening was carried out by colour reaction. The total phenolic (TPC) and total flavonoid content (TFC) were determined by Folin-Ciocalteu and aluminium trichloride colorimetric method, respectively. The identification of C. maxima phenolics present in ethanolic extract was done by HPLC equipped with Diode Array Detector. DNA cleavage activity was performed by gel electrophoresis method at various concentrations of the extract (0.125 pg/ul to 0.600 pg/ul). The preliminary phytochemical analyses, TPC and TFC results indicated C. maxima ethanolic extract is a good source of phenolics. 4-hydroxy-3-methoxy cinnamic acid and quercetin were identified as major phenolic acid and flavonoids in the ethanolic extract respectively. DNA cleavage activity exhibited ability of maximum bacterial DNA cleavage up to the linear form in a concentration dependent manner. Thus, overall results of the study suggests, C. maxima possess neutraceutical potential and may be exploited in future for therapeutic applications and anticancer drug discovey.
format Conference or Workshop Item
author Zakia Khanam
Nur Hazerra Mohd Zakaria
Kong, Hui Sam
Chua, Hui Ching
Muhammad Che Isa
Irshad Ul Haq Bhat
spellingShingle Zakia Khanam
Nur Hazerra Mohd Zakaria
Kong, Hui Sam
Chua, Hui Ching
Muhammad Che Isa
Irshad Ul Haq Bhat
Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract
author_facet Zakia Khanam
Nur Hazerra Mohd Zakaria
Kong, Hui Sam
Chua, Hui Ching
Muhammad Che Isa
Irshad Ul Haq Bhat
author_sort Zakia Khanam
title Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract
title_short Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract
title_full Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract
title_fullStr Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract
title_full_unstemmed Phytochemical study and DNA cleavage activity of citrus maxima ethanolic fruit extract
title_sort phytochemical study and dna cleavage activity of citrus maxima ethanolic fruit extract
url http://discol.umk.edu.my/id/eprint/9182/1/Phytochemical%20study%20and%20DNA%20cleavage%20activity%20of%20citrus%20maxima%20ethanolic%20fruit%20extract.pdf
http://discol.umk.edu.my/id/eprint/9182/
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