Biological Activities of Extracts Obtained From Natural Origin
Biological Activities of Extracts Obtained From Natural Origin
Biological Activities of Extracts Obtained From Natural Origin
ABSTRACT
Background: Medicinal plants have been in use for curing ailments since hundreds of centuries. Extracts, both
crude and purified are used in different forms and preparations to cure diseases. Various microorganisms have
gained antibiotic resistance due to the overuse of drugs and widespread use of antibiotics.
Aim: To determine the antibacterial, antiproliferative and antioxidant activities of Aloe vera medinensis,
Azadirachta indica and Citrus aurantium.
Methods: For this study, different parts of the selected medicinal plants were analyzed on various assays. These
plants were collected from Gujranwala, Punjab and the extracts were prepared using the Cold maceration method
in ethyl acetate and ethanol. The antibacterial activity was assessed against Staphylococcus aureus, Escherichia
coli, Pseudomonas aeruginosa, Klebsiella pneumoniae and Proteus mirabilis by disc diffusion method. The
inhibitory zones were recorded in millimetres. The antiproliferative activity was assessed against HeLa cell lines
using MTT assay. The absorbance was recorded at 570 nm. The antioxidant activity was assessed using Catalase
and Superoxide dismutase assay. The absorbance was recorded at 240 nm for Catalase assay and 560 nm for
Superoxide dismutase assay.
Results: The results indicate that commercially available antibiotics have better zones of inhibition against tested
microorganisms. The antiproliferative activity was significant for the extract of neem leaves in ethanol and citrus
fruit seeds in ethyl acetate. Antioxidant activity was found to be higher through SOD assay as compared to
Catalase assay for most extracts. It can be concluded that the microorganisms were found to be susceptible to
most of the extracts. Only two of the extracts showed antiproliferative activity whereas reasonably good
antioxidant activity is shown by all of the extracts. These plants can be explored for further in depth analysis in
animal models.
Keywords: Antimicrobial, antioxidant, antiproliferative, disc diffusion, MTT assay, Catalase assay
preparation of inoculums for disc diffusion assay.(22) Bacterial observe the effects of plant extracts on surviving potential of
suspension (200µl) was poured and adsorbed over the surface cancerous cells. Viable cell number in each of the wells was
of Muller-Hinton agar. Imipenem 5µg was used as positive proportionally taken to be equal to the intensity of absorbance
control for Staphylococcus aureus, Escherichia coli and of light and the measurement of this absorbance was then
Pseudomonas aeruginosa. Amikacin 5µg was used as a read on an ELISA plate reader at 570 nm.
positive control for Klebsiella and Proteus. The results were Data obtained through MTT assay, SOD and Catalase
noted in the form of zone of inhibition (ZOI) in mm. assays were statistically analyzed by Graph pad prism. Values
For antioxidant activity, SOD and Catalase assay were at P ≤ 0.05 were considered to be statistically significant.
performed to determine the antioxidant activity of medicinal
plant extracts. The absorbance was taken at 560 nm on an RESULTS
ELISA plate reader.
For the detection of antiproliferative activity of plant Table 1: Preparation of extracts in respective solvents
extracts, the samples were dissolved in DMSO at S.No Extract No. Preparation of extract
concentration of 20 mg/ml. The stock solutions were further 1 Extract 1-E1 Ethyl acetate+ Aloe vera leaf cuticl
diluted to concentration of 500µg in DMEM in a stock vial; 2 Extract 2-E2 Ethanol+ Aloe vera leaf cuticle
these were filtrated by syringe filters measuring 0.22µm and 3 Extract 3-E3 Ethyl acetate+ Aloe vera gel
later were stored in sterile aliquots in Falcon tubes at -20ºC 4 Extract 4-E4 Ethanol+ Aloe vera gel
until analyzed. HeLa cell lines which are human cervical cell 5 Extract 5-E5 Ethyl acetate +Neem leaves
lines were taken from cell culture laboratory of CRiMM (Center 6 Extract 6-E6 Ethanol+ Neem leaves
of Research in Molecular Medicine). DMEM-HG medium 7 Extract 7-E7 Ethyl acetate+ Neem stems
(Dulbecco’s Modified Eagle’s-High Glucose medium) that is 8 Extract 8-E8 Ethanol + Neem stems
supplemented with 10% heat inactivated (56ºC) fetal bovine 9 Extract 9-E9 Ethyl acetate +Citrus fruit peel
serum, streptomycin (100mg/ ml) and Penicllin (100 IU/ml) was 10 Extract 10-E10 Ethanol +Citrus fruit peel
used to maintain the cervical cell lines. 11 Extract 11-E11 Ethyl acetate+ Citrus fruit seeds
MTT assay (3-(4,5-Dimethylthiazole-2-Yl)-2,5- 12 Extract 12-E12 Extract 12-E12
Diphenyltetrazolium Bromide assay) test was then applied to
14
Zone of inhibition (mm)
12
10
8
6
4
2
0
8
6
4
2
0
12
Zone of inhibition ( mm)
10
8
6
4
2
0
12
10
Zone of inhibition ( mm)
8
6
4
2
0
12
Zone of inhibition ( mm)
10
8
6
4
2
0
Graph-6. Anti-proliferative activity of plant extracts against HeLa cervical cell line
1 MTT
Absorbance (nm)
0.8
0.6
0.4
0.2
0
1.2
1 ***
***
0.8 *** *** ***
0.6 ***
0.4
0.2
0
Pre-treatment extracts
2.5 *** *** ***
*** *** *** *** *** ***
*** ***
2 ***
Absorbance (nm)
1.5
1
0.5
0
antioxidant properties and this is complemented by reports 7. Bibalani GH, Mosazadeh-Sayadmahaleh F .(2011).
presented by Bandyopadhyay et al.,2002 and Amal Kumar Recognition and consumption uses and medicinal properties
Ghimeray et al., 2009. The work on Citrus aurantium has of sour orange (Citrus aurantium) by rural people in East part
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The results of this study state that the extracts of Aloe vera heart rate effects following a single dose of bitter orange.
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method and if the doses of these extracts are increased within
11. Furukawa F, Nishikawa A, Chihara T, Shimpo K, Beppu H,
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