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International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115
111 | P a g e
ANTIMICROBIAL EFFECT OF MEDICINAL
PLANT PEDALIUM MUREX AGAINST
DIFFERENT MICROORGANISMS
Anandanayaki S1 Uma C2*
1
Department of Plant science, 2
Department of Chemistry,
Avvaiyar govntment College for women,
Karaial 609602 U.T of Puducherry. India.
Umasiva74@gmail.com
Abstract: Indian medicinal plants have a traditional
background that they have potential to use as antimicrobial agents.
Pedalium murex showed broad spectrum antimicrobial activity
against three fungal strains Aspergillus niger, Aspergillus flavus,
Candida albicans and five bacterial strains Escherichia coli,
Staphylococus epidermis, Klebseilla pneumonia,Citrobactor
diverses, Enterococus faecalis.The Ethanolic extracts were tested
against selected test bacteria and fungi through disc diffusion assay
where amoxicillin was used as standard. The results showed that
alcoholic extract possess good antimicrobial activity against selected
test bacteria and fungi. The present results therefore offer a
scientific basis for traditional use of the various extract of Pedalium
murex.
Key words: Antimicrobial activity, Pedalium murex, Bacillus
subtilis.
I. INTRODUCTION
It is generally believed that around 25% of the active
compounds used in modern medicines were derived from plants.
At the same time, hardly 5000 of the over 2,50,000 flowering
plants have been looked at scientifically for their medicinal
properties. Presently there is an increasing interest in the use of
plant microbicides because of the necessity of finding safer
microbicides and the need for preventing environmental
degradation.
Pedalium murex is an important medicinal plant that
contains several alkaloids [1]. The leaf decoction is used to
control white discharge due to excessive body heat. Root
decoction is used as an anti bilious agent, while the juice of the
fruit is used as an emmenagogue and to promote lochial
discharge [2]. The decoction of the seeds and glycosides
obtained from it showed mild diuretic activity and the alcoholic
extract of the fruits reduced blood pressure in dog and rat [3]. It
is reported that many Indian medicinal plants show beneficial
effects against renal injury [4]. A good example is a succulent
herb, Pedalium murex Linn, commonly called Gokhru a member
of family Pedaliaceae. It is commonly found in Deccan and in
some parts of Ceylon and Gujarat and in the coastal areas of
southern India [5]. The fruits are rich in flavonoids, saponin
soluble proteins [6]. An infusion extract prepared using cold
water from the leaves, stems and fruits of P.murex is demulcent,
diuretic and also found to be useful in the treatment of disorders
of urinary systems such as gonorrhea, dysuria, incontinence of
urine, etc. [7-8]. The knowledge of the chemical constituents of
plants would further be valuable in discovering the actual value
of folkloric remedies [9]. Research on medicinal plants has been
increased and screened for their antimicrobial activities in
number of studies. The knowledge of the chemical constituents
of plants would further be valuable in discovering the actual
value of folkloric remedies [9]. Research on medicinal plants has
been increased and screened for their antimicrobial activities in
number of studies.
II. METIRIAL AND METHODS
Plant parts of Pedalium murex for the proposed study were
collected from Karaikal district, U.T of Puducherry and care was
taken to select healthy plants and for normal organs. The identity
of the plant specimens was confirmed by the use of local floras
[10-12] and standard references [13-14]. The botanical identify
was also authenticated by Dr. M. Jegadeesan, Associate
Professor, at the Department of Environment and Herbal
Science. Tamil University, Thanjavur, Tamil Nadu. Herbarium
specimens of the taxa (Plate 1 – 4) were deposited Tamil
University Herbarium during study period. Medicinally useful
parts of the plants were studied in both fresh and dried conditions
[15-18].
ANTIMICROBIAL STUDIES
The concentrate of all the extracts and isolated compounds
were tested for antimicrobial activities against human pathogens.
A. Media preparation
a) Bacterial Media (Muller lfindo Media)
36g of molar find media (Hi–Media) was mixed with distilled
water and then sterilized in autoclave at 15 lb pressure for 15
minutes. The sterilized media were poured in to petri dishes. The
solidified plates were pored with 5 mm dia cork pores. The plates
with wells used for antibacterial studies.
b) Fungal Media (PDA)
200g of potato slices were boiled with distilled water. The potato
infusion was used as water solute of media preparation. 29g of
dextrose was mixed with potato infusion. 20g of agar was added
as a solidifying agent. This constituent ware mixed and
autoclaved. The solidified plates were pored with 6mm dial cork
borer.
c) Bacterial Strains
The bacterial and fungal pathogenic strains were obtained from
the Microbial Type Culture Collection (MTCC), Institute of
Microbial Technology, Chandigarh, India. Bacterial strains used
were Escherichia coli, Staphylococcus aureus, Klebsiela
pneumoniae, Acetobactor diversus.
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115
112 | P a g e
d) Fungal strains
Fungal strains were Aspergillus niger (MTCC – 1344)
aspergillus floavus (MTCC – 1973) and Candida albicans.
e) Anti Bacterial Activity of the Plant Extract:
The aqueous extract of dried leaves plant parts was used through
our study. The aqueous extract 10% 20% and 40% were tested
against different bacterial pathogens such as Escherichia coli,
Sstaphylococcus aureus, klebsielia pneumonia, Acetobactor
diversus and Escherichia faccalic for their antimicrobial activity.
It was demonstrated by well diffusion assay.
f) Antifungal Activity of the plant Extract:
The aqueous extract of 10 % 20 % and 40% were tested against
different fungal pathogens such as Aspergillus flavus, Aspergillus
niger and Candida albicans for their antifungal activity. It was
demonstrated by well diffusion assay.
g) Well Diffusion Method:
Antibacterial and antifungal activity of plant extract was test
using well diffusion method (Banel et al, 1996). The prepared
culture plates were inoculated with different strains of bacteria
and fungi using streak plate method. Wells were made on the
agar surface with 5mm cork borer. The extracts were pound into
the well using sterile syringe. The plates were incubated at
37+2ºC for 48 hrs for fungal activity and for 24 hrs for bacterial
activity. The plates were observed for the lone formation around
the wells.
The zone of inhibition was calculated by measuring the diameter
of the inhibition zone around the well (in mm) including the well
diameter. The readings were taken in three different fixed
directions in all three replicates and the average values were
tabulated.
III. RESULTS
A. Anti-microbial activities of Pedalium murex extracts
The extracts of the plant were screened for anti-fungal
activities against Aspergillus niger, Aspergillus flavus and
Candida albicans in three different concentrations (10%, 20%
and 40%) of petroleum ether, benzene, chloroform, alcohol and
water extracts by disc method. In extracts of PM, Aspergillus
niger displayed the inhibition zones in 10% and 20% of
concentrations of petroleum ether, 20 % and 40% of benzene and
all the concentrations of alcohol extracts. Candida albucans
formed the inhibition zone only against chloroform extracts of
PM (Table 1).
Extracts of Pedalium murex (PM) were also tested for
antimicrobial activities against Escherichia coli, Staphylococcus
epidermidis, Klebsiella pneumoniae, Citrobactor diversus and
Enterococcus faecalis. Three different concentrations, namely
10%, 20% and 40% of petroleum ether, benzene, chloroform,
alcohol and water extracts of both plants were used to screen
anti-microbial activity by well and disc method (Table 2) (Plate
1-2).
Benzene, chloroform and alcohol extracts of PM were
showed inhibition zone against the Escherichia coli but
Staphylococcus epidermidis formed the inhibition zone only in
benzene and chloroform extracts. Benzene, chloroform and
petroleum ether (20% and 40 %) extracts of PM showed the zone
of inhibition against Klebsiella pneumoniae and Enterococcus
faecalis whereas Citrobactor diversus did not expressed the anti-
bacterial activity against PM extracts.
Pedalium murex is a valuable plant source of medicinally
useful compounds that has been traditionally used for several
applications. The bioactive compound of plant are that exhibited
good antimicrobial properties. However a detailed study is
required to find out the specific bioactive compounds responsible
for antimicrobial property through various advanced techniques.
Table 1.Antifungal activity of pedalium murex
S.No Organism Zone inhibition of different extracts (mm)
Pet.ether Bezene Chloroform Ethyl alcohol Water
10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30%
1. Aspergillus
niger
0.4 0.1 - - 0.3 0.4 - - - 0.4 0.1 0.7 - - -
2. Aspergillus
flavus
- - - - - - - - - - - - - - -
3. Candida
albicans
- - - - - - 0.1 0.7 0.6 - - - - - -
Table 2.Antibactirial activity of pedalium murex
S.
N
o
Organism Zone inhibition of different extracts (mm)
Pet.ether Bezene Chloroform Ethyl alcohol Water
10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30%
1 Escherichia coli - - - 0.6 0.7 0.9 1.2 1.6 2.5 1.5 1.9 1.2 - - -
2 Staphylococcus
epidermis
- - - 0.7 1.0 1.8 0.4 1.2 1.2 - - - - - -
3 Klebsiella
Pneumoniae
- 1.3 0.4 0.6 1.5 1.3 0.6 1.6 0.7 - - - - - -
4 Citrobactor
diverses
- - - - - - - - - - - - - - -
5 Enterococus
faecalis
0.7 - 0.3 0.4 0.7 1.6 1.2 1.9 0.6 - - - - - -
 Standard: Amoxycyllin
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115
113 | P a g e
Plate – 1
A B
C D
E F
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115
114 | P a g e
Plate –2
Plate 1: Anti-microbial activity of Pedalium murex extract
A. Inhibition zone formed by Escherichia coli against
benzene extract
B. Inhibition zone formed by Escherichia coli against
chloroform extract
C. Inhibition zone formed by Escherichia coli against
alcohol extract
D. Inhibition zone formed by Staphylococcus epidermidis
against benzene extract
E. Inhibition zone formed by Staphylococcus epidermidis
against chloroform extract
F. Inhibition zone formed by Klebsiella pneumoniae
against petroleum ether extract
Plate 2: Anti-microbial activity of Pedalium murex
A. Inhibition zone formed by Klebsiella pneumoniae
against benzene extract of Pedalium murex
B. Inhibition zone formed by Klebsiella pneumoniae
against chloroform extract of Pedalium murex
C. Inhibition zone formed by Enterococcus faecalis against
petroleum ether extract of Pedalium murex
D. Inhibition zone formed by Enterococcus faecalis against
benzene extract of Pedalium murex
E. Inhibition zone formed by Enterococcus faecalis against
chloroform extract of Pedalium murex
A B
E
DC
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115
115 | P a g e
REFERENCES
[1] Subramanian SS, Nair AGR (1972). Flavonoids of the Leaves of
Pedalium-Murex-D. Phytochemistry (Oxford).11:464-465
[2] Satyavathi, G., V. Ashoke, K.Gupta and T. Neeraj. (1987).
Medicinal plants of india, Vol.II, Indian Council of Medicinal
Research, New Delhi, p: 392.
[3] Harvey, S.K.(1996). A preliminary experimental study of the
diuretic activity of some indigenous drugs, IJMR 54;8: 774-778.
[4] Ali,B.H and M.S.Al Moundhru,. (2006).Food
Chem.Toxicol,44:1173-1183.
[5] Nadkarani K.M. (1982). Indian Material Medica 3rd
Edn.
Volume 2, Popular prakashan, Bombay.ISBN 81218600889.
[6] Mukherjee (2002). Quality control of herbal Drugs: An
approach of evalution of Botanicals, Business Horizens
Pharmceuticals publishers, New Delhi.
[7] Chopra R.N., S.L. Nayar and I.C.Chopra.(1999). Glossary of
Indian Medicinal Plants. National Institute of Science
Communication (CSIR), New Delhi.
[8] Shukla, Y.N and S.P.S. Khanuja. (2004). J. Med. Aromatic
Plant.Sci. 26:64-69.
[9] Farnsworth, N.R. (1996). Biological and Phytochemical
screening of plants. J.Pharm Sci, 55:225-276.
[10] Hooker, J.D. (1985). Flora of British India, L.Reeve and Co.
Ltd., London, 4:131-132.
[11] Henry, A.N., Kumari,. G.R. and Chitra, V.Flora of Tamilnadu,
IndiaSeries I: Analysis. Botanical Survey of India, Southern
circle, Coimbatore.1987; II: 190-92.
[12] Matthew KM.The Flora of Tamil Nadu Carnatic (Vols, 1-3),
Diocesan Press, Madras, Tamil Nadu, India.1983.
[13] Anonymous. The Wealth of India, CSIR, New Delhi.1992; III:
414-415.
[14] Chatterjee, A. and Pakrashi, S.C. The Treatise on Indian
Medicinal Plants,Publication and Information Directorate, New
Delhi.1994;I: 70 - 75.
[15] Trease, G.E. and Evans, W.C. 1983. Pharmacognosy. (12th
edn.), University Press, Cambridge, UK.
[16] Kokate CK. Practical Pharmacognosy, 4th ed.,
VallabhPrakashan, New Delhi, India.1994; pp. 112-120.
[17] Kokate, C.K., Khandelwal, K.R., Pawar, A.P. and Gohale, S.B.
Practical Pharmacognosy. NiraliPrakashan, Pune.1995; 3rd
edn., 137-139.
[18] Wallis, T.E. Text book of Pharmacognosy. C.B.S. Publishers
and Distributors, Shahdara, Delhi (India).1985; 566-570.

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Antimicrobial Activity of Medicinal Plant Pedalium Murex

  • 1. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115 111 | P a g e ANTIMICROBIAL EFFECT OF MEDICINAL PLANT PEDALIUM MUREX AGAINST DIFFERENT MICROORGANISMS Anandanayaki S1 Uma C2* 1 Department of Plant science, 2 Department of Chemistry, Avvaiyar govntment College for women, Karaial 609602 U.T of Puducherry. India. Umasiva74@gmail.com Abstract: Indian medicinal plants have a traditional background that they have potential to use as antimicrobial agents. Pedalium murex showed broad spectrum antimicrobial activity against three fungal strains Aspergillus niger, Aspergillus flavus, Candida albicans and five bacterial strains Escherichia coli, Staphylococus epidermis, Klebseilla pneumonia,Citrobactor diverses, Enterococus faecalis.The Ethanolic extracts were tested against selected test bacteria and fungi through disc diffusion assay where amoxicillin was used as standard. The results showed that alcoholic extract possess good antimicrobial activity against selected test bacteria and fungi. The present results therefore offer a scientific basis for traditional use of the various extract of Pedalium murex. Key words: Antimicrobial activity, Pedalium murex, Bacillus subtilis. I. INTRODUCTION It is generally believed that around 25% of the active compounds used in modern medicines were derived from plants. At the same time, hardly 5000 of the over 2,50,000 flowering plants have been looked at scientifically for their medicinal properties. Presently there is an increasing interest in the use of plant microbicides because of the necessity of finding safer microbicides and the need for preventing environmental degradation. Pedalium murex is an important medicinal plant that contains several alkaloids [1]. The leaf decoction is used to control white discharge due to excessive body heat. Root decoction is used as an anti bilious agent, while the juice of the fruit is used as an emmenagogue and to promote lochial discharge [2]. The decoction of the seeds and glycosides obtained from it showed mild diuretic activity and the alcoholic extract of the fruits reduced blood pressure in dog and rat [3]. It is reported that many Indian medicinal plants show beneficial effects against renal injury [4]. A good example is a succulent herb, Pedalium murex Linn, commonly called Gokhru a member of family Pedaliaceae. It is commonly found in Deccan and in some parts of Ceylon and Gujarat and in the coastal areas of southern India [5]. The fruits are rich in flavonoids, saponin soluble proteins [6]. An infusion extract prepared using cold water from the leaves, stems and fruits of P.murex is demulcent, diuretic and also found to be useful in the treatment of disorders of urinary systems such as gonorrhea, dysuria, incontinence of urine, etc. [7-8]. The knowledge of the chemical constituents of plants would further be valuable in discovering the actual value of folkloric remedies [9]. Research on medicinal plants has been increased and screened for their antimicrobial activities in number of studies. The knowledge of the chemical constituents of plants would further be valuable in discovering the actual value of folkloric remedies [9]. Research on medicinal plants has been increased and screened for their antimicrobial activities in number of studies. II. METIRIAL AND METHODS Plant parts of Pedalium murex for the proposed study were collected from Karaikal district, U.T of Puducherry and care was taken to select healthy plants and for normal organs. The identity of the plant specimens was confirmed by the use of local floras [10-12] and standard references [13-14]. The botanical identify was also authenticated by Dr. M. Jegadeesan, Associate Professor, at the Department of Environment and Herbal Science. Tamil University, Thanjavur, Tamil Nadu. Herbarium specimens of the taxa (Plate 1 – 4) were deposited Tamil University Herbarium during study period. Medicinally useful parts of the plants were studied in both fresh and dried conditions [15-18]. ANTIMICROBIAL STUDIES The concentrate of all the extracts and isolated compounds were tested for antimicrobial activities against human pathogens. A. Media preparation a) Bacterial Media (Muller lfindo Media) 36g of molar find media (Hi–Media) was mixed with distilled water and then sterilized in autoclave at 15 lb pressure for 15 minutes. The sterilized media were poured in to petri dishes. The solidified plates were pored with 5 mm dia cork pores. The plates with wells used for antibacterial studies. b) Fungal Media (PDA) 200g of potato slices were boiled with distilled water. The potato infusion was used as water solute of media preparation. 29g of dextrose was mixed with potato infusion. 20g of agar was added as a solidifying agent. This constituent ware mixed and autoclaved. The solidified plates were pored with 6mm dial cork borer. c) Bacterial Strains The bacterial and fungal pathogenic strains were obtained from the Microbial Type Culture Collection (MTCC), Institute of Microbial Technology, Chandigarh, India. Bacterial strains used were Escherichia coli, Staphylococcus aureus, Klebsiela pneumoniae, Acetobactor diversus.
  • 2. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115 112 | P a g e d) Fungal strains Fungal strains were Aspergillus niger (MTCC – 1344) aspergillus floavus (MTCC – 1973) and Candida albicans. e) Anti Bacterial Activity of the Plant Extract: The aqueous extract of dried leaves plant parts was used through our study. The aqueous extract 10% 20% and 40% were tested against different bacterial pathogens such as Escherichia coli, Sstaphylococcus aureus, klebsielia pneumonia, Acetobactor diversus and Escherichia faccalic for their antimicrobial activity. It was demonstrated by well diffusion assay. f) Antifungal Activity of the plant Extract: The aqueous extract of 10 % 20 % and 40% were tested against different fungal pathogens such as Aspergillus flavus, Aspergillus niger and Candida albicans for their antifungal activity. It was demonstrated by well diffusion assay. g) Well Diffusion Method: Antibacterial and antifungal activity of plant extract was test using well diffusion method (Banel et al, 1996). The prepared culture plates were inoculated with different strains of bacteria and fungi using streak plate method. Wells were made on the agar surface with 5mm cork borer. The extracts were pound into the well using sterile syringe. The plates were incubated at 37+2ºC for 48 hrs for fungal activity and for 24 hrs for bacterial activity. The plates were observed for the lone formation around the wells. The zone of inhibition was calculated by measuring the diameter of the inhibition zone around the well (in mm) including the well diameter. The readings were taken in three different fixed directions in all three replicates and the average values were tabulated. III. RESULTS A. Anti-microbial activities of Pedalium murex extracts The extracts of the plant were screened for anti-fungal activities against Aspergillus niger, Aspergillus flavus and Candida albicans in three different concentrations (10%, 20% and 40%) of petroleum ether, benzene, chloroform, alcohol and water extracts by disc method. In extracts of PM, Aspergillus niger displayed the inhibition zones in 10% and 20% of concentrations of petroleum ether, 20 % and 40% of benzene and all the concentrations of alcohol extracts. Candida albucans formed the inhibition zone only against chloroform extracts of PM (Table 1). Extracts of Pedalium murex (PM) were also tested for antimicrobial activities against Escherichia coli, Staphylococcus epidermidis, Klebsiella pneumoniae, Citrobactor diversus and Enterococcus faecalis. Three different concentrations, namely 10%, 20% and 40% of petroleum ether, benzene, chloroform, alcohol and water extracts of both plants were used to screen anti-microbial activity by well and disc method (Table 2) (Plate 1-2). Benzene, chloroform and alcohol extracts of PM were showed inhibition zone against the Escherichia coli but Staphylococcus epidermidis formed the inhibition zone only in benzene and chloroform extracts. Benzene, chloroform and petroleum ether (20% and 40 %) extracts of PM showed the zone of inhibition against Klebsiella pneumoniae and Enterococcus faecalis whereas Citrobactor diversus did not expressed the anti- bacterial activity against PM extracts. Pedalium murex is a valuable plant source of medicinally useful compounds that has been traditionally used for several applications. The bioactive compound of plant are that exhibited good antimicrobial properties. However a detailed study is required to find out the specific bioactive compounds responsible for antimicrobial property through various advanced techniques. Table 1.Antifungal activity of pedalium murex S.No Organism Zone inhibition of different extracts (mm) Pet.ether Bezene Chloroform Ethyl alcohol Water 10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30% 1. Aspergillus niger 0.4 0.1 - - 0.3 0.4 - - - 0.4 0.1 0.7 - - - 2. Aspergillus flavus - - - - - - - - - - - - - - - 3. Candida albicans - - - - - - 0.1 0.7 0.6 - - - - - - Table 2.Antibactirial activity of pedalium murex S. N o Organism Zone inhibition of different extracts (mm) Pet.ether Bezene Chloroform Ethyl alcohol Water 10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30% 10% 20% 30% 1 Escherichia coli - - - 0.6 0.7 0.9 1.2 1.6 2.5 1.5 1.9 1.2 - - - 2 Staphylococcus epidermis - - - 0.7 1.0 1.8 0.4 1.2 1.2 - - - - - - 3 Klebsiella Pneumoniae - 1.3 0.4 0.6 1.5 1.3 0.6 1.6 0.7 - - - - - - 4 Citrobactor diverses - - - - - - - - - - - - - - - 5 Enterococus faecalis 0.7 - 0.3 0.4 0.7 1.6 1.2 1.9 0.6 - - - - - -  Standard: Amoxycyllin
  • 3. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115 113 | P a g e Plate – 1 A B C D E F
  • 4. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115 114 | P a g e Plate –2 Plate 1: Anti-microbial activity of Pedalium murex extract A. Inhibition zone formed by Escherichia coli against benzene extract B. Inhibition zone formed by Escherichia coli against chloroform extract C. Inhibition zone formed by Escherichia coli against alcohol extract D. Inhibition zone formed by Staphylococcus epidermidis against benzene extract E. Inhibition zone formed by Staphylococcus epidermidis against chloroform extract F. Inhibition zone formed by Klebsiella pneumoniae against petroleum ether extract Plate 2: Anti-microbial activity of Pedalium murex A. Inhibition zone formed by Klebsiella pneumoniae against benzene extract of Pedalium murex B. Inhibition zone formed by Klebsiella pneumoniae against chloroform extract of Pedalium murex C. Inhibition zone formed by Enterococcus faecalis against petroleum ether extract of Pedalium murex D. Inhibition zone formed by Enterococcus faecalis against benzene extract of Pedalium murex E. Inhibition zone formed by Enterococcus faecalis against chloroform extract of Pedalium murex A B E DC
  • 5. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 6 (Nov-Dec 2014), PP. 111-115 115 | P a g e REFERENCES [1] Subramanian SS, Nair AGR (1972). Flavonoids of the Leaves of Pedalium-Murex-D. Phytochemistry (Oxford).11:464-465 [2] Satyavathi, G., V. Ashoke, K.Gupta and T. Neeraj. (1987). Medicinal plants of india, Vol.II, Indian Council of Medicinal Research, New Delhi, p: 392. [3] Harvey, S.K.(1996). A preliminary experimental study of the diuretic activity of some indigenous drugs, IJMR 54;8: 774-778. [4] Ali,B.H and M.S.Al Moundhru,. (2006).Food Chem.Toxicol,44:1173-1183. [5] Nadkarani K.M. (1982). Indian Material Medica 3rd Edn. Volume 2, Popular prakashan, Bombay.ISBN 81218600889. [6] Mukherjee (2002). Quality control of herbal Drugs: An approach of evalution of Botanicals, Business Horizens Pharmceuticals publishers, New Delhi. [7] Chopra R.N., S.L. Nayar and I.C.Chopra.(1999). Glossary of Indian Medicinal Plants. National Institute of Science Communication (CSIR), New Delhi. [8] Shukla, Y.N and S.P.S. Khanuja. (2004). J. Med. Aromatic Plant.Sci. 26:64-69. [9] Farnsworth, N.R. (1996). Biological and Phytochemical screening of plants. J.Pharm Sci, 55:225-276. [10] Hooker, J.D. (1985). Flora of British India, L.Reeve and Co. Ltd., London, 4:131-132. [11] Henry, A.N., Kumari,. G.R. and Chitra, V.Flora of Tamilnadu, IndiaSeries I: Analysis. Botanical Survey of India, Southern circle, Coimbatore.1987; II: 190-92. [12] Matthew KM.The Flora of Tamil Nadu Carnatic (Vols, 1-3), Diocesan Press, Madras, Tamil Nadu, India.1983. [13] Anonymous. The Wealth of India, CSIR, New Delhi.1992; III: 414-415. [14] Chatterjee, A. and Pakrashi, S.C. The Treatise on Indian Medicinal Plants,Publication and Information Directorate, New Delhi.1994;I: 70 - 75. [15] Trease, G.E. and Evans, W.C. 1983. Pharmacognosy. (12th edn.), University Press, Cambridge, UK. [16] Kokate CK. Practical Pharmacognosy, 4th ed., VallabhPrakashan, New Delhi, India.1994; pp. 112-120. [17] Kokate, C.K., Khandelwal, K.R., Pawar, A.P. and Gohale, S.B. Practical Pharmacognosy. NiraliPrakashan, Pune.1995; 3rd edn., 137-139. [18] Wallis, T.E. Text book of Pharmacognosy. C.B.S. Publishers and Distributors, Shahdara, Delhi (India).1985; 566-570.