You are on page 1of 3

EXTRACTION OF PHYTOCHEMICAL COMPONENTS FROM THE

FRUIT OF MOMORDICA CHARANTIA AND EVALUATION OF ITS


ANTIMICROBIAL ACTIVITY
1
ABHINAY THAKRE, 2VAIBHAV DEORE, 3SAYALI GAIKWAD, 4SAYALI KAWADE
1
M.Tech, 2,3,4B.Tech

Abstract- Momordica charantia, commonly used in Indian sub-continent known for its medicinal properties. It belongs to
the family of cucurbitaceae and widely used against many diseases since ancient times. The aim of this study was to extract
the phytochemical compounds of bitter melon and to evaluate its antimicrobial activity. Extraction of polyphenolic
compounds was carried out using phytochemical screening which shows presence of different compounds such as
flavonoids, saponins, carbohydrates, tannins, and terpenoids. The highest amount estimated from the ultra-sonication
extraction was found to be 12.83mg for water extract. The antimicrobial Momordica charantia fruit extracted in different
solvents such as methanol, ethanol, distilled water, chloroform, n-hexane, heptane, against various bacterial species like
Staphylococcus aureus, Klebsiella Pneumoniae, Bacillus subtilis, Escherichia coli, were tested using well diffusion method.
The maximum antimicrobial activities were observed for methanol and n-heptane extracts. M.charantia plant extract along
with methanol and n-heptane can be used as an effective antimicrobial agent.

Index terms- Antimicrobial activity, Momordica Charantia, Phytochemical Compounds

I. INTRODUCTION II. MATERIALS AND METHODS

Momordica charantia originated on the Indian Collection of Vegetable


subcontinent which is also called as bitter melon, Fruits of Momordica charantia were obtained from
balsam pear or karela. It is a tropical vegetable, a local parts of pune region, India. The fruits were
common food in Indian, cuisine and extensively used brought to the laboratory rinsed with water, were cut
as medicinal remedy for many diseases, specifically into small circular shapes, then dried and crushed to
for diabetes. It belongs to the family of cucurbitaceae. small pieces using pastel and mortar and further finely
All parts of the plant including the fruit taste bitter. powered in an electric grinder. 4 g of powder was
The immature fruits are eaten as vegetable and are mixed with 40 ml of different solvents and different
good source of vitamin c, vitamin A, phosphorous and extracts were prepared. (Aqueous extract, ethanol
iron. Fruits and seeds of bitter gourd possess extract, methanol extract, n-hexane extract, n-heptane
medicinal property such as anti-HIV, anti-ulcer, anti- extract and chloroform extract)
inflammatory, anti-leukemic, anti-microbial, anti-
tumor, and last but not the least the important anti Two methods were used for obtaining plant extract
diabetic property. Although the different parts of the were
plants of bitter gourd are used as food and drug, but 1) Maceration
the fruit is most important part of the plant. 2) ultra-sonication
1) Maceration: In maceration the prepared powder of
The present report gives an account of the M. charantia fruit was kept in contact with solvent at
antimicrobial effect of Momordica charantia. It has 300C and 120 rpm for 36 hrs. in a stoppered container
been seen that it has strong antimicrobial activity until the soluble matter is dissolved. After the
against wide range of gram positive and gram extraction, extract with solvent is collected and
negative bacterias. As the Momordica charantia fruit evaporated using rotary evaporator.
contains many important phytochemicals, the
emphasis of the present study has given to the use of 2) Ultra-sonication: ultrasound has a potential benefit
it as a remedy for inhibition of various pathogenic in the extraction and isolation of novel potentially
bacterias. In present study phytochemical components bioactive compounds. The irradiation of liquid sample
of Momordica charantia were extracted using two with ultrasonic waves results in agitation. The
methods Maceration and Ultra-sonication with solvents were mixed with powder and kept for
various solvents viz. chloroform, methanol, N-hexane, extraction, the caps of the bottles were slightly loose.
N-heptane, ethanol and water. The yield of extraction In this method due to high frequency ultrasound the
was used to check antimicrobial activity of various solvents gets heated and extraction takes place. After
extracts on pathogenic strength as E.coli ,S.aureus, the extraction the obtained extract was stored in petri
Bacillus subtilis, K.neumoniae, were examined. dishes overnight until it gets solidified. The obtained

Proceedings of IRF International Conference, 30th March-2014, Pune, India, ISBN: 978-93-82702-69-6
31
Extraction of Phytochemical Components from the Fruit of Momordica Charantia and Evaluation of Its Antimicrobial Activity

extract was mixed with DMSO and stored for further III. RESULTS AND DISCUSSION:
use.
B) Screening of phytochemical components. In the present study M. charantia fruit extract was
Phytochemical components were analyzed studied for its antimicrobial activity and screening of
qualitatively. its phytochemical compounds. The results revealed
the presence of different bioactive compounds present
C) Antibacterial activity assay in M. charantia. Also qualitatively analysis of
Screening of antibacterial activity assay was carried different phytochemical compounds using different
out using well diffusion method. A loop full of extracts were carried out as the results are shown in
different Bacterial Strains were inoculated in 30 ml of table 1
nutrient broths in a conical flask and incubated for 72
hrs. to get active strain by using agar well diffusion IV. ANTIMICROBIAL ACTIVITY:
method. Nutrient agar was poured into petri dishes.
After solidification 0.50 ml of test strains were Different strains such as E.coli, S.aureus, Bacillus
inoculated in the media separately. subtilis, K. Pneumonia were used to analyse the
antimicrobial activity of M. charantia. Further
The experiment was performed under strict aseptic antimicrobial activity was also checked at different
conditions. After the medium in petri dishes solidified concentration (40µl,80µl,120µl).
wells were made using a sterile borer. The extract
compound was introduced into the well and plates The maximum antimicrobial activity was observed for
were incubated at 370C for 24 hrs. All samples were methanol extract against K.pneumoniae. The results
tested in triplicates. Antimicrobial activity was for antimicrobial activity are shown in table 2 and
determined by measuring the diameter of zone of table 3.
inhibition. For control ampicillin was used as a
standard antibiotic for all test strains.
Table 1.
Results of qualitative analysis of phytochemical components

Table 2.
Antimicrobial activity analysis of different solvent extract zone of inhibition (mean diameter in mm)

Proceedings of IRF International Conference, 30th March-2014, Pune, India, ISBN: 978-93-82702-69-6
32
Extraction of Phytochemical Components from the Fruit of Momordica Charantia and Evaluation of Its Antimicrobial Activity
Table 3
Antimicrobial activity analysis of different solvent extract zone of inhibition for different concentration (mean diameter in mm)

REFERENCES

[1] Sultana R.S.,Bari Miah M.A. (2003) In vitro Propagation of [4] Assubaie NF , EI-Garawany MM (2004) Evaluation of
Karella (Momordica charantea Linn.) from nodal segment Some Importance Chemical Constituents Of Momordica
and shoot tip. Journal of Biological Sciences, 3: 1134-1139. charantia Cultivated in Hofuf, Saudi Arabia. Journal of
Biological Sciences 4:628-630.
[2] Paul A.,Mitter K., Sen Raychaudhuri S. (2009) effect of
polyamines in vitro Somatic Embrogenesis in Momocardica [5] Praep Kshant Tiwari, Bimlesh Kumar, mandeep Kaur,
charantia L. Plant Cell Tissue and Organ Culture, 97: 303- Gurpeet Kaur, Harllen Kaur, 2011.journal of Internationale
311. pharmaceutica sciencia Vol.1: 098-106

[3] Taylor L. (2000) Technical Data Report for Bitter Melon [6] Ejoba Raphael, 2012. Global Advanced Research Journal
(Momordica charantia). Herbal Secrets of the Rainforest 2nd of Environmental Science and Toxicology Vol. 1(2): 014-
ed, Sage Press Inc. 017.



Proceedings of IRF International Conference, 30th March-2014, Pune, India, ISBN: 978-93-82702-69-6
33

You might also like