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International Journal of Pharmaceutical  Biological Archives 2019; 10(2):78-82
ISSN 2581 – 4303
RESEARCH ARTICLE
Fourier-transform Infrared Analysis and In Vitro Antibacterial Activity of
Ormocarpum cochinchinense (Elumbotti)
Sivakumar Thirumal1,2
*, Gajalakshmi Duraikannu3
1
Department of Botany, Annamalai University, Annamalai Nagar, Tamil Nadu, India, 2
Department of Botany,
Thiru A. Govindasamy Govt. Arts College, Tindivanam, Tamil Nadu, India, 3
Department of Chemistry,
University College of Engineering Kakuppam, Villupuram (A Constituent College of Anna University-Chennai)
Tamil Nadu, India
Received: 02 January 2019; Revised: 01 March 2019; Accepted: 4 April 2019
ABSTRACT
The present research is to assess the Fourier transform infrared (FT-IR) analysis and antibacterial activities
of Ormocarpum cochinchinense leaf extract using different solvents dimethyl sulfoxide (DMSO), ethyl
acetate, ethanol (EtOH), methanol (MeOH), and chloroform. To investigation of FT-IR analysis and
antibacterial activities become used agar well diffusion method. FT-IR vibrational bands confirmed that
the fractions of O. cochinchinense had lots of biologically active compounds which include H–Bonded
Phenols, alkanes, carboxylic acid, carboxylic acid, flavonoids, polyphenols, catechins, aromatics, and
aliphatic amines. Antibacterial activity showed that the strongest activities had been produced by MeOH
solvent reaction with all the human pathogens. This research may be concluded that MeOH solvent
extract of O. cochinchinense might be a capability for the treatment of antibacterial activities.
Keywords:Antimicrobial activity, Fourier-transform infrared, methanol, Ormocarpum cochinchinense,
solvents
INTRODUCTION
Plant medicine had been used for historic time to
fashionable for human diseases.[1]
Medicinal plants
are geared up from a variety of plant substances
as leaves, stems, roots, barks, inflorescence,
etc.[2]
Amedicinal plant contains biologic energetic
principles with unique therapeutic effects. Herbal
vegetations are herbal resources of phytochemical
constituents that may be used in opposition to
many human diseases in present day.[3]
Novel
healing sellers were advanced through the use
of pharmacological houses of plants and may be
used as leads.[4]
The therapeutic values of this
herbal lie in bioactive compounds that produce
genuine physiological moves in the human body.
Those phytochemical parts in the medicinal
plant include alkaloids, steroids, flavonoids,
terpenoids, saponins, acidic glycosides, tannins,
fats and oil compounds, and coumarins.[5]
The
separation is now seeking to India due to its
*Corresponding Author:
Sivakumar Thirumal,
E-mail: drtsivanano@gmail.com
wealthy biodiversity of medicinal plant life and
an abundance of traditional therapeutic systems[6].
In India, many herbal flowers are generally used
by all sections of people either immediately as
folk remedies or indirectly in prescription drugs
arrangements of a cutting-edge medical drug.
There is a required that the medicinal flowers
be evaluated for phytochemistry if you want
to determine the potentials of these indigenous
resources of drugs. Consequently, in cutting-edge
study, one medicinal plant changed into decided
on for phytochemical analysis. Ormocarpum
cochinchinense (OC) is a small herb observed in
Tamil Nadu, typically referred to as “Elumbotti”
belongs to Leguminosae family.
This herb was confirmed as a medicinal drug
using people from in advance days to until now.
Maximum drugs in practice were formulated
by plant-based metabolites.[7]
The traditional
expertise about medicinal herbs and their effect
in opposition to sicknesses became recognized
by historic Indians.[8]
However, clinical evidence
turned into unknown because it has been kept
secreted using village vaidyas.[9]
However, there is
no clinical evidence justifying the traditional use
Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti
IJPBA/Apr-Jun-2019/Vol 10/Issue 2 79
of O. cochinchinense leaves inside the treatment
of “bone healing.” The existing research turned
into made to look at the biochemically energetic
herbal products, observed antimicrobial activity
inside the extraordinary solvent extracts prepared
from the leaves of OC. The prepared solvent leaf
extract of O. cochinchinense qualitative, in vitro
antioxidant activities, GC-MS analysis.[10-12]
In the
present work, I reported that Fourier-transform
infrared (FTIR) analysis and antimicrobial activity
of OC.
MATERIALS AND METHODS
Plant materials
The leaves of OC leaves collected from local place
of Villupuram District, Tamil Nadu, India, during
October–January, 2015.
Preparation of plant extract
In green leaves had been dried powdered the
usage of with a mechanical grinder and stored in
a jib lack cover. Leaf powder (1.5 kg) turned into
refluxed with unique solvents, dimethyl sulfoxide
(DMSO), ethyl acetate (EtoAc), ethanol (EtOH),
methanol (MeOH), and chloroform (CHCl3
) for
7 days. The filtrate changed into concentrated to
dryness in a warm air oven at 32o
C to render five
solvent extract for research.
Chemicals
All chemical had been purchased from SD fine
chemical company Mumbai, and all chemical
substances had been an analytical agent.
Antibacterial activity
Bacterial strains of Klebsiella aerogenes (MTCC
98), Escherichia coli (MTCC 443), Bacillus
subtilis (MTCC 2295), and Staphylococcus
aureus (MTCC 3160) were used and maintained
in nutrient agar (HiMedia, Mumbai) slants at
4°C. Muller-Hinton agar (HiMedia, Mumbai)
plates had been prepared, sterilized, solidified,
and swabbed uniformly. In vitro antibacterial
activity assay of aqueous solvents DMSO, EtoAc,
EtOH, MeOH, and CHCl3
was determined by
way of agar well diffusion methods. The various
concentrations of aqueous solvents 10, 20, 30, 40,
and 50 μl have loaded into the wells of all plates.
All bacterial strains are (K. aerogenes, E. coli,
B. substilis, and S. aureus), obtained from Rajah
Muthiah Medical College, Annamalai University,
Annamalai Nagar. Area of inhibition changed into
measured(mm) after incubating the plates at 37°C
for 24 h triplicates have been maintained.
FT-IR evaluation of aqueous leaf extract
In order to identify the biomolecules present in the
leaf extract of O. cochichinense, FT-IR spectra of
the aqueous leaf extract had been analyzed with
the aid of FT-IR spectroscopy (FT-IR Shimadzu
8400 s, Japan). The FT-IR analysis changed into
complete with KBR pellets at the Department
of Chemistry, Annamalai University, Annamalai
Nagar, Tamil Nadu, India. The FT-IR turned into
recorded inside the range of 4000–500 cm/g. The
various modes of vibrations had been recognized
and assigned to determine the phytochemicals are
a presence in the leaf extract.
Statistical analysis
Experimentshavebeenperformedintriplicatesand
the results have been expressed as mean±standard
deviation. The statistical analysis was made with
origin software (Origin Pro evaluation, 2018).
RESULTS AND DISCUSSION
FT-IR analysis
The FT-IR spectrum of clean and dried leaf
extracts of O. cochinchinense are shown in
Figure 
1 resolved peaks at 3938, 3911, 3874,
3763, 3381, 2922, 2854, 2335, 2034, 2007, 1965,
and 466 cm/g unresolved height at 1645, 1425,
1381, 1321, 1244,1153, 1024, 829, 665, 615, and
1730 the peaks received have been due to amide i,
ii, and iii, H–Bonded Phenols, alkanes, carboxylic
acid, alkanes, aromatic rings, aliphatic amines,
and saturated methyl agencies discovered in the
O. cochinchinense leaf extracts.
The FT-IR spectra of the leaf extracts are shown
in Tables 1 and 2 as the dependence of radiation
absorption on wave number. The FT-IR spectrum
indicates three absorption bands between 2854 and
3938 cm−1
that correspond to the c–h stretching
Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti
IJPBA/Apr-Jun-2019/Vol 10/Issue 2 80
500
750
1000
1250
1500
1750
2000
2500
3000
3500
4000
1/cm
30
45
60
75
90
%T
3938.64
3911.64
3874.99
3763.12
3381.21
2922.16
2854.65
2335.80
2034.90
2007.90
1965.46
1730.15
1645.28
1425.40
1381.03
1321.24
1244.09
1153.43
1024.20
829.39
665.44
615.29
466.77
Figure 1: Fourier-transform infrared analysis of Ormocarpum cochinchinense leaf extracts
Table 1: Infrared vibrational bands, intensity, area of Ormocarpum cochinchinense leaf extract
S.no Peak Intensity Correlated intensity Base (H) Base (L) Area Correlated area
1 466.77 73.126 1.265 478.35 405.05 8.649 0.23
2 615.29 65.352 1.767 646.15 480.28 28.015 1.761
3 665.44 65.311 1.593 813.96 648.08 25.547 1.043
4 829.39 76.988 1.021 866.04 815.89 5.353 0.131
5 1024.2 45.485 20.529 1139.93 867.97 62.396 15.587
6 1153.43 55.044 2.379 1195.87 1141.86 12.455 0.439
7 1244.09 58.34 4.476 1290.38 1197.79 20.021 1.34
8 1321.24 58.404 1.665 1340.53 1292.31 10.899 0.291
9 1381.03 55.649 1.159 1394.53 1342.46 12.689 0.253
10 1425.4 55.146 3.912 1489.05 1396.46 22.313 2.203
11 1645.28 39.488 21.549 1716.65 1490.97 68.439 22.071
12 1730.15 58.457 1.332 1948.1 1718.58 30.139 0.189
13 1965.46 80.083 0.009 1973.18 1950.03 2.232 0.001
14 2007.9 79.989 0.017 2013.68 1975.11 3.73 0.002
15 2034.9 79.958 0.187 2328.08 2015.61 28.898 0.674
16 2335.8 82.473 0.074 2355.08 2330.01 2.089 0.008
17 2854.65 60.367 2.124 2870.08 2357.01 60.356 0.221
18 2922.16 50.588 11.902 3001.24 2872.01 30.811 4.564
19 3381.21 37.921 35.113 3745.76 3003.17 218.647 113.714
20 3763.12 82.113 0.022 3765.05 3747.69 1.479 0.002
21 3874.99 84.507 0.123 3894.28 3867.28 1.963 0.01
22 3911.64 84.59 0.147 3932.86 3896.21 2.651 0.015
23 3938.64 84.717 0.027 4000.36 3934.78 4.69 0.014
Table 2: Infrared vibrational bands of Ormocarpum cochinchinense leaf extract
Wave number (cm−1) Vibration band/group Chemical group
3938–3381 O–H stretch H–bonded phenols
2922–2007 C–H stretch (asym.), O–H stretch, C–H stretch (sym.) Alkanes, carboxylic acid, alkanes
1965–1730 Asymmetric –CH2–, symmetric –CH3 and –CH2– stretching vibrations Carboxylic acid
1645–1425 C=O stretch (carbonyls) Flavonoids, polyphenols, catechins
1381–1244 C–C stretch (in ring) Aromatics
1153–1024 C–N stretch Aliphatic amines
829–466 C–H strech Alkanes
Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti
IJPBA/Apr-Jun-2019/Vol 10/Issue 2 81
vibration in aliphatic and H-Bonded phenols. The
aromatic systems are showed using the skeleton
vibration bands among 1381 and 1645 cm−1
.[13,14]
The variety of those bands and their intensities
relies on substitution in fragrant compounds.
Among 1024 and 1200 cm−1
, you could have a
look at a stretching absorption band of CAO for
phenols. The “shoulder” peak at 1105 cm−1[15]
is
from carbohydrate, whereas the bands at 1024 cm−1
and 829 cm−1
are from the vibrational frequency
of the CH2
OH groups of carbohydrates.[16]
The
vibration band of OH is located between 1381
and 1024 cm−1
. An absorption band of low depth
is visible at 1645 cm−1
, which can be related to
the stretching vibration of the carbonyl group.
The evaluation of the leaf extract FT-IR spectra
confirms the presence of aromatic and/or aliphatic
compounds that have hydroxyl and likely carbonyl
groups. The following additional absorption band
at1645cm−1
correspondstothestretchingvibration
of the carbonyl group while the absorption bands
at 1425 cm−1
, 1381, and 1244 cm−1
may be related
to the presence of chlorophyll.[17]
The location of
that band depends at the presence and location
of different functional groups. The presence of
the wideband between 3300 and 3900 cm−1
and
the bands inside the variety of 1024–1381 cm−1
can suggest that carbonyl group is derived from
carboxyl groups or it can be found in phenyl
compounds.
Antibacterial activity
Organic solvent leaf extracts exhibited more
consistent antibacterial activity than aqueous leaf
extract. Antibacterial activity is extended with
the increase inside the attention of the extract
MeOH DMSO, EtoAc, EtOH, and CHCl3
. The
maximum zone of inhibition of (24±0.25 
mm)
turned into exhibited by way of MeOH leaf extract
of O. cochinchinense. The DMSO, EtoAc, EtOH,
and CHCl3
ethanolic and aqueous leaf extract
confirmed that the maximum area of inhibition in
the various concentrations is shown in Figure 2.
This activity can be due to the potential of the
secondary metabolites to shape a complex with
extracellular proteins and with the cell wall of
microorganism.[17]
The inhibitory effect of MeOH
leaf extract, on the increase of bacteria, might
be due to better solubility of these capability
secondary metabolites, which shows the presence
of a wide spectrum of antibiotic compounds.[18]
The organic solvent of the plant extract had greater
antibacterial ability than the aqueous extract. This
observation can be correlated with the polarity of
thesolventusedforextraction,essentialbioactivity,
and capability to diffuse in media utilized in
assay.[19,20]
Therefore, in many elements of the
plant for herbal safety against microbial infection
are packed with phytochemical substances. The
phytochemical analysis of the leaves extracts
h-bonded phenols, alkanes, carboxylic acid,
Figure 2: Antibacterial activity of Ormocarpum cochinchinense leaf extracts against different human pathogens
Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti
IJPBA/Apr-Jun-2019/Vol 10/Issue 2 82
alkanes, fragrant earrings, aliphatic amines, and
saturated methylation organizations. Therefore,
phytochemical products can be responsible for the
bacterial activity of O. cochinchinense.
CONCLUSION
Various solvent extractions of O. cochinchinense
leave contain significant phytochemical and
antibacterial activity. Therefore, the current study
leads the mixture from this research and creates a
powerful design for bone treatment.
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8.	 Bisht C, Badoni A. Distribution and indigenous
uses of some medicinal plants in district Uttarkashi,
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10.	 Sivakumar T, Gajalakshmi D. In vitro antioxidant and
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Assessment of Asymptomatic Urinary Tract Infection and Susceptibility of Antimicrobials Agents and Resistant Patterns among Suspected Females Patients of Two Major Hospitals of Western Nepal

  • 1. © 2019, IJPBA. All Rights Reserved 78 Available Online at www.ijpba.info International Journal of Pharmaceutical Biological Archives 2019; 10(2):78-82 ISSN 2581 – 4303 RESEARCH ARTICLE Fourier-transform Infrared Analysis and In Vitro Antibacterial Activity of Ormocarpum cochinchinense (Elumbotti) Sivakumar Thirumal1,2 *, Gajalakshmi Duraikannu3 1 Department of Botany, Annamalai University, Annamalai Nagar, Tamil Nadu, India, 2 Department of Botany, Thiru A. Govindasamy Govt. Arts College, Tindivanam, Tamil Nadu, India, 3 Department of Chemistry, University College of Engineering Kakuppam, Villupuram (A Constituent College of Anna University-Chennai) Tamil Nadu, India Received: 02 January 2019; Revised: 01 March 2019; Accepted: 4 April 2019 ABSTRACT The present research is to assess the Fourier transform infrared (FT-IR) analysis and antibacterial activities of Ormocarpum cochinchinense leaf extract using different solvents dimethyl sulfoxide (DMSO), ethyl acetate, ethanol (EtOH), methanol (MeOH), and chloroform. To investigation of FT-IR analysis and antibacterial activities become used agar well diffusion method. FT-IR vibrational bands confirmed that the fractions of O. cochinchinense had lots of biologically active compounds which include H–Bonded Phenols, alkanes, carboxylic acid, carboxylic acid, flavonoids, polyphenols, catechins, aromatics, and aliphatic amines. Antibacterial activity showed that the strongest activities had been produced by MeOH solvent reaction with all the human pathogens. This research may be concluded that MeOH solvent extract of O. cochinchinense might be a capability for the treatment of antibacterial activities. Keywords:Antimicrobial activity, Fourier-transform infrared, methanol, Ormocarpum cochinchinense, solvents INTRODUCTION Plant medicine had been used for historic time to fashionable for human diseases.[1] Medicinal plants are geared up from a variety of plant substances as leaves, stems, roots, barks, inflorescence, etc.[2] Amedicinal plant contains biologic energetic principles with unique therapeutic effects. Herbal vegetations are herbal resources of phytochemical constituents that may be used in opposition to many human diseases in present day.[3] Novel healing sellers were advanced through the use of pharmacological houses of plants and may be used as leads.[4] The therapeutic values of this herbal lie in bioactive compounds that produce genuine physiological moves in the human body. Those phytochemical parts in the medicinal plant include alkaloids, steroids, flavonoids, terpenoids, saponins, acidic glycosides, tannins, fats and oil compounds, and coumarins.[5] The separation is now seeking to India due to its *Corresponding Author: Sivakumar Thirumal, E-mail: drtsivanano@gmail.com wealthy biodiversity of medicinal plant life and an abundance of traditional therapeutic systems[6]. In India, many herbal flowers are generally used by all sections of people either immediately as folk remedies or indirectly in prescription drugs arrangements of a cutting-edge medical drug. There is a required that the medicinal flowers be evaluated for phytochemistry if you want to determine the potentials of these indigenous resources of drugs. Consequently, in cutting-edge study, one medicinal plant changed into decided on for phytochemical analysis. Ormocarpum cochinchinense (OC) is a small herb observed in Tamil Nadu, typically referred to as “Elumbotti” belongs to Leguminosae family. This herb was confirmed as a medicinal drug using people from in advance days to until now. Maximum drugs in practice were formulated by plant-based metabolites.[7] The traditional expertise about medicinal herbs and their effect in opposition to sicknesses became recognized by historic Indians.[8] However, clinical evidence turned into unknown because it has been kept secreted using village vaidyas.[9] However, there is no clinical evidence justifying the traditional use
  • 2. Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti IJPBA/Apr-Jun-2019/Vol 10/Issue 2 79 of O. cochinchinense leaves inside the treatment of “bone healing.” The existing research turned into made to look at the biochemically energetic herbal products, observed antimicrobial activity inside the extraordinary solvent extracts prepared from the leaves of OC. The prepared solvent leaf extract of O. cochinchinense qualitative, in vitro antioxidant activities, GC-MS analysis.[10-12] In the present work, I reported that Fourier-transform infrared (FTIR) analysis and antimicrobial activity of OC. MATERIALS AND METHODS Plant materials The leaves of OC leaves collected from local place of Villupuram District, Tamil Nadu, India, during October–January, 2015. Preparation of plant extract In green leaves had been dried powdered the usage of with a mechanical grinder and stored in a jib lack cover. Leaf powder (1.5 kg) turned into refluxed with unique solvents, dimethyl sulfoxide (DMSO), ethyl acetate (EtoAc), ethanol (EtOH), methanol (MeOH), and chloroform (CHCl3 ) for 7 days. The filtrate changed into concentrated to dryness in a warm air oven at 32o C to render five solvent extract for research. Chemicals All chemical had been purchased from SD fine chemical company Mumbai, and all chemical substances had been an analytical agent. Antibacterial activity Bacterial strains of Klebsiella aerogenes (MTCC 98), Escherichia coli (MTCC 443), Bacillus subtilis (MTCC 2295), and Staphylococcus aureus (MTCC 3160) were used and maintained in nutrient agar (HiMedia, Mumbai) slants at 4°C. Muller-Hinton agar (HiMedia, Mumbai) plates had been prepared, sterilized, solidified, and swabbed uniformly. In vitro antibacterial activity assay of aqueous solvents DMSO, EtoAc, EtOH, MeOH, and CHCl3 was determined by way of agar well diffusion methods. The various concentrations of aqueous solvents 10, 20, 30, 40, and 50 μl have loaded into the wells of all plates. All bacterial strains are (K. aerogenes, E. coli, B. substilis, and S. aureus), obtained from Rajah Muthiah Medical College, Annamalai University, Annamalai Nagar. Area of inhibition changed into measured(mm) after incubating the plates at 37°C for 24 h triplicates have been maintained. FT-IR evaluation of aqueous leaf extract In order to identify the biomolecules present in the leaf extract of O. cochichinense, FT-IR spectra of the aqueous leaf extract had been analyzed with the aid of FT-IR spectroscopy (FT-IR Shimadzu 8400 s, Japan). The FT-IR analysis changed into complete with KBR pellets at the Department of Chemistry, Annamalai University, Annamalai Nagar, Tamil Nadu, India. The FT-IR turned into recorded inside the range of 4000–500 cm/g. The various modes of vibrations had been recognized and assigned to determine the phytochemicals are a presence in the leaf extract. Statistical analysis Experimentshavebeenperformedintriplicatesand the results have been expressed as mean±standard deviation. The statistical analysis was made with origin software (Origin Pro evaluation, 2018). RESULTS AND DISCUSSION FT-IR analysis The FT-IR spectrum of clean and dried leaf extracts of O. cochinchinense are shown in Figure  1 resolved peaks at 3938, 3911, 3874, 3763, 3381, 2922, 2854, 2335, 2034, 2007, 1965, and 466 cm/g unresolved height at 1645, 1425, 1381, 1321, 1244,1153, 1024, 829, 665, 615, and 1730 the peaks received have been due to amide i, ii, and iii, H–Bonded Phenols, alkanes, carboxylic acid, alkanes, aromatic rings, aliphatic amines, and saturated methyl agencies discovered in the O. cochinchinense leaf extracts. The FT-IR spectra of the leaf extracts are shown in Tables 1 and 2 as the dependence of radiation absorption on wave number. The FT-IR spectrum indicates three absorption bands between 2854 and 3938 cm−1 that correspond to the c–h stretching
  • 3. Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti IJPBA/Apr-Jun-2019/Vol 10/Issue 2 80 500 750 1000 1250 1500 1750 2000 2500 3000 3500 4000 1/cm 30 45 60 75 90 %T 3938.64 3911.64 3874.99 3763.12 3381.21 2922.16 2854.65 2335.80 2034.90 2007.90 1965.46 1730.15 1645.28 1425.40 1381.03 1321.24 1244.09 1153.43 1024.20 829.39 665.44 615.29 466.77 Figure 1: Fourier-transform infrared analysis of Ormocarpum cochinchinense leaf extracts Table 1: Infrared vibrational bands, intensity, area of Ormocarpum cochinchinense leaf extract S.no Peak Intensity Correlated intensity Base (H) Base (L) Area Correlated area 1 466.77 73.126 1.265 478.35 405.05 8.649 0.23 2 615.29 65.352 1.767 646.15 480.28 28.015 1.761 3 665.44 65.311 1.593 813.96 648.08 25.547 1.043 4 829.39 76.988 1.021 866.04 815.89 5.353 0.131 5 1024.2 45.485 20.529 1139.93 867.97 62.396 15.587 6 1153.43 55.044 2.379 1195.87 1141.86 12.455 0.439 7 1244.09 58.34 4.476 1290.38 1197.79 20.021 1.34 8 1321.24 58.404 1.665 1340.53 1292.31 10.899 0.291 9 1381.03 55.649 1.159 1394.53 1342.46 12.689 0.253 10 1425.4 55.146 3.912 1489.05 1396.46 22.313 2.203 11 1645.28 39.488 21.549 1716.65 1490.97 68.439 22.071 12 1730.15 58.457 1.332 1948.1 1718.58 30.139 0.189 13 1965.46 80.083 0.009 1973.18 1950.03 2.232 0.001 14 2007.9 79.989 0.017 2013.68 1975.11 3.73 0.002 15 2034.9 79.958 0.187 2328.08 2015.61 28.898 0.674 16 2335.8 82.473 0.074 2355.08 2330.01 2.089 0.008 17 2854.65 60.367 2.124 2870.08 2357.01 60.356 0.221 18 2922.16 50.588 11.902 3001.24 2872.01 30.811 4.564 19 3381.21 37.921 35.113 3745.76 3003.17 218.647 113.714 20 3763.12 82.113 0.022 3765.05 3747.69 1.479 0.002 21 3874.99 84.507 0.123 3894.28 3867.28 1.963 0.01 22 3911.64 84.59 0.147 3932.86 3896.21 2.651 0.015 23 3938.64 84.717 0.027 4000.36 3934.78 4.69 0.014 Table 2: Infrared vibrational bands of Ormocarpum cochinchinense leaf extract Wave number (cm−1) Vibration band/group Chemical group 3938–3381 O–H stretch H–bonded phenols 2922–2007 C–H stretch (asym.), O–H stretch, C–H stretch (sym.) Alkanes, carboxylic acid, alkanes 1965–1730 Asymmetric –CH2–, symmetric –CH3 and –CH2– stretching vibrations Carboxylic acid 1645–1425 C=O stretch (carbonyls) Flavonoids, polyphenols, catechins 1381–1244 C–C stretch (in ring) Aromatics 1153–1024 C–N stretch Aliphatic amines 829–466 C–H strech Alkanes
  • 4. Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti IJPBA/Apr-Jun-2019/Vol 10/Issue 2 81 vibration in aliphatic and H-Bonded phenols. The aromatic systems are showed using the skeleton vibration bands among 1381 and 1645 cm−1 .[13,14] The variety of those bands and their intensities relies on substitution in fragrant compounds. Among 1024 and 1200 cm−1 , you could have a look at a stretching absorption band of CAO for phenols. The “shoulder” peak at 1105 cm−1[15] is from carbohydrate, whereas the bands at 1024 cm−1 and 829 cm−1 are from the vibrational frequency of the CH2 OH groups of carbohydrates.[16] The vibration band of OH is located between 1381 and 1024 cm−1 . An absorption band of low depth is visible at 1645 cm−1 , which can be related to the stretching vibration of the carbonyl group. The evaluation of the leaf extract FT-IR spectra confirms the presence of aromatic and/or aliphatic compounds that have hydroxyl and likely carbonyl groups. The following additional absorption band at1645cm−1 correspondstothestretchingvibration of the carbonyl group while the absorption bands at 1425 cm−1 , 1381, and 1244 cm−1 may be related to the presence of chlorophyll.[17] The location of that band depends at the presence and location of different functional groups. The presence of the wideband between 3300 and 3900 cm−1 and the bands inside the variety of 1024–1381 cm−1 can suggest that carbonyl group is derived from carboxyl groups or it can be found in phenyl compounds. Antibacterial activity Organic solvent leaf extracts exhibited more consistent antibacterial activity than aqueous leaf extract. Antibacterial activity is extended with the increase inside the attention of the extract MeOH DMSO, EtoAc, EtOH, and CHCl3 . The maximum zone of inhibition of (24±0.25  mm) turned into exhibited by way of MeOH leaf extract of O. cochinchinense. The DMSO, EtoAc, EtOH, and CHCl3 ethanolic and aqueous leaf extract confirmed that the maximum area of inhibition in the various concentrations is shown in Figure 2. This activity can be due to the potential of the secondary metabolites to shape a complex with extracellular proteins and with the cell wall of microorganism.[17] The inhibitory effect of MeOH leaf extract, on the increase of bacteria, might be due to better solubility of these capability secondary metabolites, which shows the presence of a wide spectrum of antibiotic compounds.[18] The organic solvent of the plant extract had greater antibacterial ability than the aqueous extract. This observation can be correlated with the polarity of thesolventusedforextraction,essentialbioactivity, and capability to diffuse in media utilized in assay.[19,20] Therefore, in many elements of the plant for herbal safety against microbial infection are packed with phytochemical substances. The phytochemical analysis of the leaves extracts h-bonded phenols, alkanes, carboxylic acid, Figure 2: Antibacterial activity of Ormocarpum cochinchinense leaf extracts against different human pathogens
  • 5. Thirumal and Duraikannu: Invitro antibacterial activity of elumbotti IJPBA/Apr-Jun-2019/Vol 10/Issue 2 82 alkanes, fragrant earrings, aliphatic amines, and saturated methylation organizations. Therefore, phytochemical products can be responsible for the bacterial activity of O. cochinchinense. CONCLUSION Various solvent extractions of O. cochinchinense leave contain significant phytochemical and antibacterial activity. Therefore, the current study leads the mixture from this research and creates a powerful design for bone treatment. REFERENCES 1. Arokiyaraj S, Radha R, Martin S, Perinbam K. Phytochemical analysis and antidiabetic activity of Cadaba fruticosa R.Br. Indian J Sci Technol 2008;1:1-4. 2. Gordon DM. Geographical structure and host specificity in bacteria and the implications for tracing the source of coliform contamination. Microbiology 2001;147:1079-85. 3. Kubmarawa D, Ajoku GA, Okorie DA, Enwerem NM. Preliminary phytochemical and antimicrobial screening of 50 medicinal plants from Nigeria. Afr J Biotechnol 2007;6:1690-6. 4. Fawad SA, Rehman MU, Khalid N, Khan SA. Antimicrobial activity of Eucalyptus tereticornis and comparison with daily life antibiotics. Int J Pharmacol Sci Rev Res 2012:12;21-9. 5. Krishnaiah D, Devi T, Bon A, Sarbtly R. Studies on phytochemical constituents of six Malaysian medicinal plants. J Med Plant Res 2009;3:67-72. 6. Salahuddin A, Rahman MS, Jasim UC, Anwar MN. Antimicrobialactivitiesofseedextractsandtruealkaloids of Aegle marmelos. Greener J Sci 1998;22:77-81. 7. Samy RP, Pushparaj PN, Gopalakrishnakone P. A compilation of bioactive compounds from ayurveda. Bioinformation 2008;3:100-10. 8. Bisht C, Badoni A. Distribution and indigenous uses of some medicinal plants in district Uttarkashi, Uttarakhand. Indian J Res 2009;1:38-40. 9. Vedavathy S. Sustainability of traditional herbal medicinepracticedinAnthrapradesh,India.Proceedings of the Workshop Sharing Local and National Experience in South Asia, 21-23 January. Pokhara, Nepal; 2001. p. 220-5. 10. Sivakumar T, Gajalakshmi D. In vitro antioxidant and chemical constituents from the leaves of Ormocarpum cochinchinense elumbotti. Am J Plant Physiol 2013;8:51-60. 11. Sivakumar T, Gajalakshmi D. Gas chromatography- mass spectroscopy analysis of Ormocarpum cochinchinense leaf extract-traditional bone healing plants. Int J Pharm Res Biosci 2014;3:352-9. 12. Sivakumar T, Gajalakshmi D. Phytochemical screening and GC-MS analysis of root extract from Asparagus racemosus L. 2014. Int J Pharm Sci Res 2014;5:1000-5. 13. Lu X, Wang J, Al-Qadiri HM, Ross CF, Powers JR, Tang J, et al. Determination of total phenolic content and antioxidant capacity of onion (Allium cepa) and shallot (Allium oschaninii) using infrared spectroscopy. Food Chem 2011;129:637-44. 14. Schulz H, Baranska M. Identification and quantification of valuable plant substances by IR and Raman spectroscopy. Vib Spectrosc 2007;43:13-25. 15. Andrus PG. Cancer monitoring by FTIR spectroscopy. Technol Cancer Res Treat 2006;5:157-67. 16. Mordechai S, Mordechai J, Ramesh J, Levi C, Huleihel M, Erukhimovitch V. Application of FTIR microspectroscopy for the follow-up of childhood leukaemia chemotherapy. Proceedings of SPIE Subsurface and Surface Sensing Technologies and Applications III. Vol. 44. San Diego, USA: Society of Photo Optical; 2001. p. 243-50. 17. Kuete V, Nguemeving JR, Beng VP, Azebaze AG, Etoa  FX, Meyer M. Antimicrobial activity of the methanolic extracts and compounds from Vismia laurentii de wild (Guttiferae). J  Ethnopharmacol 2007;109:372-9. 18. Ikigai H, Nakae T, Hara Y, Shimamura T. Bactericidal catechins damage the lipid bilayer. Biochim Biophys Acta 1993;1147:132-6. 19. Jigna PA, Darshana JA, Sumitra CH. Efficacy of aqueous and methanol extracts of some medicinal plants for potential antibacterial activity. Turk J Biol 2005;29:203-10. 20. Sivakumar T, Gajalakshmi D, Subramanian VK, Palanisamy K. Tuber extract mediated biosynthesis of silver nanoparticles and its antioxidant, antibacterial activity. J Biol Sci 2015;15:68-7.