International Journal of Indigenous Medicinal Plants, ISSN: 2051-4263, Vol.47, Issue.2 1652
© RECENT SCIENCE PUBLICATIONS ARCHIVES | September 2014|$25.00 | 27703710|
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GC/MS Profiling, in Vitro Antioxidant and
Cytotoxic Activities of Bidens Pilosa
Amal A. Mohamed
Plant Biochemistry Dept., National Research Centre (NRC), Dokki-Cairo, Egypt.
Email: amin_amal@yahoo.com
Sami I. Ali
Plant Biochemistry Dept., National Research Centre (NRC), Dokki-Cairo, Egypt.
Email: samiali.nrc@gmail.com
Salwa M. El-Hallouty
Pharmacognosy Dept. National Research Centre (NRC), Dokki-Cairo, Egypt.
Email: hallouty68@yahoo.com
Farouk K. El-Baz
Plant Biochemistry Dept., National Research Centre (NRC), Dokki-Cairo, Egypt.
Email: fa_elbaz@hotmail.com
Amarendra N. Misra
Centre for Life Sciences, Central University of Jharkhand, Ratu-Lohardaga Road, Ranchi, India.
Email: misraan@yahoo.co.uk
ABSTRACT
Bidens pilosa is traditionally used as food and medicinal
plant. Methanolic extracts from shoots and roots of
Egyptian B. pilosa were analyzed for their phenolic,
flavonoid contents, in vitro antioxidant activity and
cytotoxicity. The shoots extract exhibited 52.67±0.39 mg
total phenolic/g DW, and 12.33±1.1 mg total flavonoid /g
DW, compared to 15.56±0.21mg/g DW, and 2.85±0.01
mg/g DW, respectively for that in roots extract. The shoots
extract showed better ability to scavenge 2, 2-diphenyl-1-
picrylhydrazyl (DPPH) radicals (IC
50
value 44.57±0.84
μg/ml) than the roots extract (IC
50
value 133.42±1.10
μg/ml). The shoots extract showed higher ferrous ion
chelation ability compared to roots, as measured by
inhibition of ferrozine-Fe
+2
complex. Cytotoxic activities
of methanolic extracts were assayed using 4 human cancer
cell lines (MCF-7, A-549, HEPG-2 and HCT-116). The
shoots extract showed selective inhibition (% of control)
of 63.8±0.02 and 40.5±0.03 against MCF-7 and A-549 cell
lines at concentration 100μg/ml plant extract with IC
50
values 80.4μg/ml and 105.5μg/ml, respectively. GC-MS
analysis depicts heterocyclic compounds; these
compounds could be responsible for antioxidant activity
and cytotoxic effects. Further studies are in progress to
investigate the individual compounds isolated from B.
pilosa to understand the traditional uses, and develop the
pharmaceutical applications of each of these isolated
compounds.
Keywords - Bidens pilosa, cancer cells, DPPH,
flavonoid, GC-MS, phenolic.
1. INTRODUCTION
Plants are one of the most important sources of
biologically active natural products, often used by the
pharmaceutical industry as medicines [1]. Phenols,
including phenolic acids, flavonoids, tannins, lignans and
others, are prevalent in medicinal plants. Plant phenolics
act as free radical scavengers, reducing agents, quenchers
of reactive oxygen species (ROS), and antioxidants against
membrane lipid peroxidation [2]. Antioxidants play an
important role in human health and prevention of several
diseases [3].
Bidens pilosa is a perennial herb widely distributed across
temperate and tropical regions [4]. It is a rich source of
food and medicine for animals and humans [5]. The
medicinal use of B. pilosa, either as a plant part or whole
plant, is reported in Africa, Asia, and Oceania [6]. All
parts of B. pilosa plant such as, the aerial parts (leaves,
flowers, seeds, and stems), and the roots, were used as
ingredients in folk medicines [7]. The fresh or dried parts
of shoot and root are used as antihyperglycemic [8], anti-
ulcerogenic [9], antitumor [10], and antioxidant [11]
agents. Phytochemical analysis of B. pilosa extracts
revealed a broad profile of chemical constituents useful in
food and medicine. The main compounds isolated from the
plant are flavonoids, terpenoids, phenyl propanoids,
aromatic compounds, porphyrins and other substances [12].
However, the bioactive potential of B. pilosa extracts is
not yet fully established and is the focus for future
investigations. Therefore, the present work aims to
determine the total phenolic, flavonoid contents, and
chemical profiling by GC-MS in the methanolic extracts
of B. pilosa shoots and roots, and assay their antioxidant
activities and bioactive potential in cancer cells.
2. MATERIALS AND METHODS
2.1. Chemicals and Reagents
Folin-Ciocalteu reagent, 2, 2-diphenyl-1-picrylhydrazyl
(DPPH), sodium carbonate and aluminum chloride were
purchased from Sigma Chemical Co., Ltd (St. Louis, MO,
USA). Ferrozine or 3-(2-pyridyl)-5, 6-bis (4-
phenylsulfonic acid)-1, 2, 4-triazine monosodium salt and
3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium