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Characterization of Metabolites from Shigella dysenteriae
1. Characterization of Metabolites Produced by Shegilla
dysenteriae and Determination of Its Anti-Fungal Activity
Fatima Moeen Abbas1
, Rafid Hadi Hameed2
, Imad Hadi Hameed3
1
Department of Biology, College of Science for Women, University of Babylon, Hillah city, Iraq, 2
Ministry of Public
Health, Maysan Health Department, Mesan Governorate, Iraq, 3
Biomedical Science Department, University of
Babylon, College of Nursing, Hillah City, Iraq
ABSTRACT
Shigella species generally invade the epithelial lining of the colon, causing severe inflammation and death of
the cells lining the colon. This inflammation results in the diarrhea and even dysentery that are the hallmarks
of Shigella infection. The aims of our research were analysis of the secondary metabolite products and
evaluation antifungal activity. Forty bioactive compounds were identified in the methanolic extract of Shegilla
dysenteriae. GC-MS analysis of Shegilla dysenteriae revealed the existence of the 1-Deoxy-d-mannitol,
γ-Thionodecalactone, Hexaborane, 1-Propanamine, 3-(methylthio), 1H-Pyrrole, 1-pentyl, 2-Propanone,
1-(N-cyanomethylimino-), 1-Pentanol, 5-methoxy, 2-Methyl-4-methoxy-1-butanol, Benzeneethanamine,
2-Butanamine , (S), L-valine , N-glycyl, N-carbobenzyloxy-l-tyrosyl-l-valine, DL-Isoleucine, and 3-Buten-
2-one, 4-(dimethylamino)-3-[(1-methylethyl). Daucus carota was very highly active (6.953±0.22) mm.
The results of anti-fungal activity produced by Shegilla dysenteriae showed that the volatile compounds
were highly effective to suppress the growth of Aspergillus flavus (6.00±0.22). Based on the significance
of employing bioactive compounds in pharmacy to produce drugs for the treatment of many diseases, the
purification of compounds produced by Shegilla dysenteriae can be useful.
Keywords: Shegilla dysenteriae, GC-MS, Anti-microbial, Secondary metabolites.
INTRODUCTION
Shigella infection is typically by ingestion.
Depending on the health of the host, fewer than 100
bacterial cells can be enough to cause an infection. Some
strains of Shigella produce toxins which contribute to
disease during infection. Shigella species invade the host
through the M-cells interspersed in the gut epithelia of
the small intestine, as they do not interact with the apical
surface of epithelial cells, preferring basolateral side1-
5
. After invasion, Shigella cellsmultiply intracellularly and
spread to neighboring epithelial cells, resulting in
tissue destruction and characteristic pathology of
Corresponding author:
Imad Hadi Hameed.
Biomedical Science Department, University of
Babylon, College of Nursing, Hillah City, Iraq; Phone
number: 009647716150716;
E-mail: imad_dna@yahoo.com
shigellosis. Shigella uses a type-III secretion system,
which acts as a biological syringe to translocate toxic
effector proteins to the target human cell. The effector
proteins can alter the metabolism of the target cell, for
instance leading to the lysis of vacuolar membranes
or reorganization of actin polymerization to facilitate
intracellular motility of Shigella bacteria inside
the host cell 6-9
. The most common symptoms
are diarrhea, fever, nausea, vomiting, stomach cramps,
and flatulence. It is also commonly known to cause
large and painful bowel movements. Virulent Shigella
strains produce disease after invading the intestinal
mucosa; the organism only rarely penetrates beyond the
mucosa. The stool may contain blood, mucus, or pus.
Hence, Shigella cells may cause dysentery. Shigella is
implicated as one of the pathogenic causes of reactive
arthritis worldwide.
DOI Number: 10.5958/0976-5506.2018.00486.2
2. Indian Journal of Public Health Research & Development, May 2018, Vol. 9, No. 5 453
MATERIALS AND METHOD
Detection of secondary metabolites
Shegilla dysenteriae metabolites were separated
from the liquid culture and evaporated to dryness
with a rotary evaporator at 45Cº. The residue was
dissolved in 1 ml methanol, filtered through a 0.2 μm
syringe filter, and stored at 4ºC for 24 h before being
used for gas chromatography mass spectrometry10-22
.
The identification of the components was based on
comparison of their mass spectra with those of NIST
mass spectral library as well as on comparison of
their retention indices either with those of authentic
compounds or with literature values23-35
.
Materials of Plants Collection and Preparation
In our research, all plant samples were dried at room
temperature for fifteen days and when properly dried the
leaves were powdered using clean pestle and mortar, and
the powdered plant was size reduced with a sieve36-39
.
The fine powder was then packed in airtight container
to avoid the effect of humidity and then stored at room
temperature.
Gas chromatography – Mass Spectrum analysis
Interpretation of mass spectrum was conducted
using the database of National Institute of Standards
and Technology (NIST, USA). The database consists of
more than 62,000 patterns of known compounds. The
spectrum of the extract was matched with the spectrum
of the known components stored in the NIST library.
Shegilla dysenteriae GC–MS analysis were carried out
in a GC system (Agilent 7890A series, USA) 40-42
. The
flow rate of the carrier gas, helium (He) was set to beat 1
mL min−1, split ratio was 1:50. The injector temperature
was adjusted at 250◦C, while the detector temperature
was fixed to280◦C.
Determination of antibacterial and antifungal
activity
Five-millimeter diameter wells were cut from the
agar using a sterile cork-borer, and 25 μl of the plant
samples solutions were delivered into the wells. The
plates were incubated for 48 h at room temperature.
Antimicrobial activity was evaluated by measuring
the zone of inhibition against the test microorganisms.
The studied fungi, Microsporum canis, Streptococcus
faecalis, Aspergillus flavus, Aspergillus fumigatus,
Candida albicans, Penicillium expansum, Trichoderma
horzianum, Aspergillus niger and Aspergillus terreus
were isolated and maintained in potato dextrose agar
slants. Spores were grown in a liquid culture of potato
dextrose broth (PDB) and incubated at 25ºC in a shaker
for 16 days at 130 rpm. The extraction was performed
by adding 25 ml methanol to 100 ml liquid culture in
an Erlenmeyer flask after the infiltration of the culture
43-45
. The antifungal activity was evaluated by measuring
the inhibition-zone diameter observed after 48 h of
incubation.
Data analysis
All the measurements were replicated three times
for each assay and the results are presented as mean ±
SD and mean ± SE. IBM SPSS 20 version statistical
software package was used for statistical analysis of
percentage inhibition and disease incidence and disease
severity in each case.
RESULTS AND DISCUSSION
Gas chromatography and mass spectroscopy
analysis of compounds was carried out in
methanolic extract of Shegilla dysenteriae, shown
in Table 1. Peaks were determined to be 1-Deoxy-
d-mannitol, γ-Thionodecalactone, Hexaborane,
1-Propanamine , 3-(methylthio), 1H-Pyrrole , 1-pentyl,
2-Propanone, 1-(N-cyanomethylimino-), 1-Pentanol
, 5-methoxy, 2-Methyl-4-methoxy-1-butanol,
Benzeneethanamine, 2-Butanamine , (S), L-valine ,
N-glycyl, N-carbobenzyloxy-l-tyrosyl-l-valine, DL-
Isoleucine, and 3-Buten-2-one , 4-(dimethylamino)-
3-[(1-methylethyl). The results of anti-fungal activity
produced by Shegilla dysenteriae showed that the
volatile compounds were highly effective to suppress the
growth of Aspergillus flavus (6.00±0.22) mm, Table 2.
Shegilla dysenteriae produce many important secondary
metabolites with high biological activities. In agar well
diffusion method the selected medicinal plants Ricinus
communis, Datura stramonium, Linum usitatissimum,
Diplotaxis cespitosa, Cassia angustifolia, Celosia
argentea, Apium graveolens, Brassica rapa, Cichorium
endivia, Anethum graveolens, Plantago major, Linum
usitatissimum, A. esculentus, Malva sylvestris, Cordia
myxa, Malva parviflora, Mentha pulegium, Daucus
carota, Vitex agnus-castus, Sambucus nigra, C.
morifolium, Equisetum arvense, Portulaca oleracea,
Malva neglecta, L. angustifolia, Althaea Officinalis, and
3. 454 Indian Journal of Public Health Research & Development, May 2018, Vol. 9, No. 5
Melissa officinalis were effective against Staphylococcus aureus, Table 3. Aspergillus flavus was very highly active
(6.00±0.22) mm against Pseudomonas aeruginosa.
Table 1. Major chemical compounds identified in methanolic extract of Shegilla dysenteriae.
Molecular WeightRT (min)Phytochemical compound
Serial
No.
164.0684743.110Alpha-l-rhamnopyranose1.
166.0841243.1611-Deoxy-d-mannitol2.
186.10783614.949γ-Thionodecalactone3.
76.1340833.482Hexaborane4.
105.061223.8481-Propanamine , 3-(methylthio)-5.
137.1204493.9451H-Pyrrole , 1-pentyl-6.
110.04801274.0882-Propanone, 1-(N-cyanomethylimino-)7.
102.11569834.2371,5-Pentanediamine8.
118.09937954.4321-Pentanol , 5-methoxy-9.
118.09937954.5922-Methyl-4-methoxy-1-butanol10.
248.177634.7462H-Pyran , tetrahydro-2-(2,5-undecadiynyloxy)-11.
121.08914954.941Benzeneethanamine12.
111.10479935.1478-Azabicyclo[5.1.0]octane13.
195.1259295.233Benzenemethanol , 2-(2-aminopropoxy)-3-methyl-14.
97.08914955.5022,5-Dimethyl-1-pyrroline15.
148.0654936.057Cycloheptanol , 2-chloro-,trans-16.
281.0025756.331Phenylhydrazine , 4-nitro-N2-(chloro)(2-thienyl)meth)17.
73.08914956.6922-Butanamine , (S)-18.
174.1004426.955L-valine , N-glycyl-19.
117.05784947.1615H-1-Pyrindine20.
132.0898787.487Ornithine21.
117.07897858.277DL-Valine22.
136.0524299.0492,7-Dioxa-tricyclo[4.4.0.0(3,8)]deca-4,9-diene23.
221.1051939.198Benzenemethanol , α-(2-nitrocyclopentyl)24.
414.1790879.747N-carbobenzyloxy-l-tyrosyl-l-valine25.
338.11149.890N-Carbobenzyloxy-glycylglutamine 26.
594.3682259.988Di-[1,3,2]-oxazino[6,5-f:5’,6’-H]quinoxaline27.
131.09462811.046DL-Isoleucine28.
168.0283412.168Uric acid29.
154.07422712.826Pyrrolo[1,2-a]pyrazine-1,4-dione , hexahydro-30.
154.07422713.592Pyrrolo[1,2-a]pyrazine-1,4-dione , hexahydro-3-(2-me31.
154.17215114.308: 2-Undecene , (Z)32.
230.19942915.046Dihexylamine , N-nitro-33.
170.08037615.704Uracil , 1,3-dimethyl-6-hydrazino-34.
170.14191315.7323-Buten-2-one , 4-(dimethylamino)-3-[(1-methylethyl)35.
184.1463316.362Oxacyclododecan-2-one36.
170.02623216.5568H-[1,2,5]Thiadiazolo[3,4-e][1,4]diazepin-8-one , 437.
226.16812816.7742,5-Piperazinedione , 3,6-bis(2-methylpropyl)-38.
185.14157919.709Methyl 2-diethylamino-3-methyl-but-2-enoate39.
388.1746720.173
L-Prolinamide , 5-oxo-L-prolyl-L-phenylalanyl-4-hydro
40.
4. Indian Journal of Public Health Research & Development, May 2018, Vol. 9, No. 5 455
Table 2. Antifungal activity of Shegilla dysenteriae metabolite products.
Fungi
Antibiotics / Shegilla dysenteriae metabolite products
Shegilla dysenteriae
metabolite products
Amphotericin B Fluconazol
Miconazole
nitrate
Microsporum canis 2.80±0.18 ª 2.11±0.11 3.06±0.17 2.97±0.17
Streptococcus faecalis 3.01±0.19 3.03±0.16 2.88±0.15 1.81±0.10
Aspergillus flavus 6.00±0.22 2.75±0.12 3.97±0.19 3.06±0.18
Aspergillus fumigatus 5.91±0.21 2.38±0.11 2.76±0.16 2.04±0.16
Candida albicans 5.53±0.19 3.55±0.19 2.85.±0.13 1.85±0.10
Penicillium expansum 4.00±0.17 3.10±0.18 3.02±0.18 1.99±0.10
Trichoderma horzianum 3.87±0.19 1.09±0.09 3.84±0.19 2.98±0.17
Aspergillus niger 5.00±0.19 2.00±0.10 2.95±0.17 2.03±0.15
Aspergillus terreus 4.83±0.18 2.83±0.11 3.07±0.19 3.00±0.18
ª The values ( average of triplicate) are diameter of zone of inhibition at 100 mg/mL crude extract and 30 μg/mL
of (Amphotericin B; Fluconazol and Miconazole nitrate).
Table 3. Zone of inhibition (mm) of test different bioactive compounds and standard antibiotics of
medicinal plants to Shegilla dysenteriae.
Plant
Inhibition
(mm)
Plant
Inhibition
(mm)
Ricinus communis 2.951±0.17 Cordia myxa 2.881±0.16
Datura stramonium 3.617±0.19 Malva parviflora 3.704±0.19
Linum usitatissimum 4.991±0.20 Mentha pulegium 6.100±0.21
Diplotaxis cespitosa 5.984±0.21 Daucus carota 6.953±0.22
Cassia angustifolia 5.977±0.21 Vitex agnus-castus 5.800±0.20
Celosia argentea 3.271±0.18 Sambucus nigra 2.952±0.16
Apium graveolens 4.880±0.20 C. morifolium 5.996±0.20
Brassica rapa 6.274±0.22 Equisetum arvense 5.851±0.21
Cichorium endivia 5.628±0.21 Portulaca oleracea 6.000±0.22
Anethum graveolens 5.749±0.20 Malva neglecta 5.572±0.19
Plantago major 4.951±0.19 L. angustifolia 2.871±0.16
Linum usitatissimum 4.000±0.18 Althaea Officinalis 6.002±0.20
A. esculentus 5.981±0.21 Melissa officinalis 6.704±0.22
Malva sylvestris 6.400±0.22 Control 0.00
CONCLUSION
Forty bioactive chemical constituents have been
identified from methanolic extract of the Pseudomonas
aeruginosa by gas chromatogram mass spectrometry
(GC-MS). In vitro antifungal and antibacterial evaluation
of secondary metabolite products of Pseudomonas
aeruginosa forms a primary platform for further
phytochemical and pharmacological investigation for the
development of new potential antimicrobial compounds.
Financial Disclosure: There is no financial
disclosure.
Conflict of Interest: None to declare.
Ethical Clearance: All experimental protocols
5. 456 Indian Journal of Public Health Research & Development, May 2018, Vol. 9, No. 5
were approved under the Department of Biology, College
of Science, Hillah city, Iraq and all experiments were
carried out in accordance with approved guidelines.
REFERENCES
1. Edwards BH. Salmonella and Shigella species. Clin
Lab Med. 1999; 19(3):469-87
2. Hill J. Arthritis associated with enteric
infection. Best Practice & Research Clinical
Rheumatology. 2003;17(2): 219–39.
3. Suzuki T, Sasakawa C. Molecular basis of the
intracellular spreading of Shigella. Infection and
Immunity. 69 (10): 5959–66
4. KamalSA,HamzaLF,IbraheamIA.Characterization
of Antifungal Metabolites Produced by Aeromonas
hydrophila andAnalysis of its Chemical Compounds
Using GC-MS. Research Journal of Pharmacy and
Technology. 2017; 10 (11): 3845-3851.
5. Mohammed GJ, Kadhim MJ, Hameed IH. Proteus
species: Characterization and herbal antibacterial: A
review. International Journal of Pharmacognosy and
Phytochemical Research. 2016; 8(11): 1844-1854.
6. ShireenSK,HameedIH,HamzaLF.Acoruscalamus:
Parts used, insecticidal, anti-fungal, antitumour and
anti-inflammatory activity: A review. International
Journal of Pharmaceutical Quality Assurance. 2017;
8(3): 153-157.
7. Huda JA, Hameed IH, Hamza LF. Anethum
graveolens: Physicochemical properties, medicinal
uses, antimicrobial effects, antioxidant effect,
anti-inflammatory and analgesic effects: A review.
International Journal of Pharmaceutical Quality
Assurance. 2017; 8(3): 88-91.
8. Altaee N, Kadhim MJ, Hameed IH. Detection of
volatile compounds produced by pseudomonas
aeruginosa isolated from UTI patients by gas
chromatography-mass spectrometry. International
Journal of Toxicological and Pharmacological
Research. 2016; 8(6): 462-470.
9. Hussein HM, Hameed IH, Ubaid JM.Analysis of the
secondary metabolite products of Ammi majus and
evaluation anti-insect activity. International journal
of pharmacognosy and phytochemical research.
2016; 8(8): 1192-1189.
10. Hussein HM, Ubaid JM, Hameed IH. Inscticidal
activity of methanolic seeds extract of Ricinus
communis on adult of callosobruchus maculatus
(coleopteran:brauchidae) and analysis of its
phytochemical composition. International journal of
pharmacognosy and phytochemical research. 2016;
8(8): 1385-1397.
11. Ubaid JM, Hussein HM, Hameed IH. Determination
ofbioactivechemicalcompositionofCallosobruchus
maculutus and investigation of its anti-fungal
activity. International journal of pharmcognosy and
phytochemical research. 2016; 8(8): 1293-1299.
12. Ibraheam IA, Hussein HM, Hameed IH. Cyclamen
persicum: Methanolic Extract Using Gas
Chromatography-Mass Spectrometry (GC-MS)
Technique. International Journal of Pharmaceutical
Quality Assurance. 2017; 8(4); 200-213.
13. Ibraheam IA, Hadi MY, Hameed IH. Analysis of
Bioactive Compounds of Methanolic Leaves extract
of Mentha pulegium Using Gas Chromatography-
Mass Spectrometry (GC-MS) Technique.
International Journal of Pharmaceutical Quality
Assurance. 2017; 8(4); 174-182.
14. Hadi MY, Hameed IH, Ibraheam IA. Ceratonia
siliqua: Characterization, Pharmaceutical Products
and Analysis of Bioactive Compounds: A Review.
Research Journal of Pharmacy and Technology.
2017; 10(10): 3585-3589.
15. Hadi MY, Hameed IH, Ibraheam IA. Mentha
pulegium: Medicinal uses, Anti-Hepatic,
Antibacterial, Antioxidant effect and Analysis of
Bioactive Natural Compounds: A Review. Research
Journal of Pharmacy and Technology. 2017; 10(10):
3580-3584.
16. Kadhim MJ, Sosa AA, Hameed IH. Evaluation of
anti-bacterialactivityandbioactivechemicalanalysis
of Ocimum basilicum using Fourier transform
infrared (FT-IR) and gas chromatography-mass
spectrometry (GC-MS) techniques. International
Journal of Pharmacognosy and Phytochemical
Research. 2016; 8(6): 127-146.
17. Mohammed GJ, Kadhim MJ, Hussein HM.
Characterization of bioactive chemical compounds
from Aspergillus terreus and evaluation of
antibacterial and antifungal activity. International
Journal of Pharmacognosy and Phytochemical
Research. 2016; 8(6): 889-905.
18. Mohammed GJ, Omran AM, Hussein HM.
Antibacterial and Phytochemical Analysis of Piper
6. Indian Journal of Public Health Research & Development, May 2018, Vol. 9, No. 5 457
nigrum using Gas Chromatography-Mass Spectrum
and Fourier-Transform Infrared Spectroscopy.
International Journal of Pharmacognosy and
Phytochemical Research. 2016; 8(6): 977-996.
19. Shareef HK, Muhammed HJ, Hussein HM,
Hameed IH. Antibacterial effect of ginger (Zingiber
officinale) roscoe and bioactive chemical analysis
using gas chromatography mass spectrum. Oriental
Journal of Chemistry. 2016; 32(2): 20-40.
20. Mohammed GJ, Al-Jassani MJ, Hameed IH. Anti-
bacterial,AntifungalActivity and Chemical analysis
of Punica grantanum (Pomegranate peel) using GC-
MS and FTIR spectroscopy. International Journal
of Pharmacognosy and Phytochemical Research.
2016; 8(3): 480-494.
21. Dhahir BM, Hameed IH, Jaber AR. Prospective
and Retrospective Study of Fractures According
to Trauma Mechanism and Type of Bone Fracture.
Research Journal of Pharmacy and Technology.
2017; 10(10):1827-1835.
22. Hapeep MA, Hameed IH, Jasim AA. Risk Factors,
Cause and Site of Firearm Injuries: A Prospective
and Retrospective Study. Research Journal of
Pharmacy and Technology. 2017; 10(10): 3420-
3425.
23. Jasim AA, Hameed IH, Hapeep MA. Traumatic
Events in an Urban and Rural Population of
Children, Adolescents and Adults in Babylon
Governorate - Iraq. Research Journal of Pharmacy
and Technology. 2017; 10(10): 3429-3434.
24. Altameme HJ, Hameed IH, Abu-Serag NA.
Analysis of bioactive phytochemical compounds
of two medicinal plants, Equisetum arvense and
Alchemila valgaris seed using gas chromatography-
mass spectrometry and fourier-transform infrared
spectroscopy. Malays. Appl. Biol. 2015; 44(4):
47–58.
25. Hussein HM, Hameed IH, Ibraheem OA.
AntimicrobialActivityandspectralchemicalanalysis
of methanolic leaves extract of Adiantum Capillus-
Veneris using GC-MS and FT-IR spectroscopy.
International Journal of Pharmacognosy and
Phytochemical Research. 2016; 8(3): 369-385.
26. Hussein HJ, Hadi MY, Hameed IH. Study of
chemical composition of Foeniculum vulgare using
Fourier transform infrared spectrophotometer and
gas chromatography - mass spectrometry. Journal of
Pharmacognosy and Phytotherapy. 2016; 8(3): 60-
89.
27. Kadhim MJ, Mohammed GJ, Hameed IH. In vitro
antibacterial, antifungal and phytochemical analysis
of methanolic fruit extract of Cassia fistula. Oriental
Journal of Chemistry. 2016; 32(2): 10-30.
28. Altameme HJ, Hameed IH, Idan SA, Hadi MY.
Biochemical analysis of Origanum vulgare seeds by
fourier-transform infrared (FT-IR) spectroscopy and
gas chromatography-mass spectrometry (GC-MS).
Journal of Pharmacognosy and Phytotherapy. 2015;
7(9): 221-237.
29. Jaddoa HH, Hameed IH, Mohammed GJ. Analysis
of volatile metabolites released by Staphylococcus
aureus using gas chromatography-Mass
spectrometry and determination of its antifungal
activity. Oriental Journal of Chemistry. 2016; 32(4):
8-24.
30. Hameed IH, SalmanHD, Mohammed GJ. Evaluation
of antifungal and antibacterial activity and
analysis of bioactive phytochemical compounds of
Cinnamomum zeylanicum (Cinnamon bark) using
gas chromatography-mass spectrometry. Oriental
Journal of Chemistry. 2016; 32(4): 16-25.
31. Kadhim MJ, Mohammed GJ, Hussein HM. Analysis
of bioactive metabolites from Candida albicans
using (GC-MS) and evaluation of antibacterial
activity. International Journal of Pharmaceutical and
Clinical Research. 2016; 8(7): 655-670.
32. Ubaid JM, Hussein HM, Hameed IH. Analysis of
bioactive compounds of Tribolium castaneum and
evaluation of anti-bacterial activity. International
Journal of Pharmaceutical and Clinical Research.
2016; 8(7): 655-670.
33. Hameed, I.H., Al-Rubaye A.F. and Kadhim, M.J.
Antimicrobial Activity of Medicinal Plants and
Urinary Tract Infections. International Journal of
Pharmaceutical and Clinical Research. 2017; 8(11):
44-54.
34. Kadhim WA, Kadhim, M.J., Hameed, I.H.
Antibacterial Activity of Several Plant Extracts
Against Proteus Species. International Journal of
Pharmaceutical and Clinical Research. 2017; 8(11):
88-94.
35. Ahmed MD, Hameed IH, Abd-Ali MQ. Prospective
and Retrospective Study of the Acute Heart Attack
7. 458 Indian Journal of Public Health Research & Development, May 2018, Vol. 9, No. 5
Cases in Marjan Hospital-Hillah City-Iraq. Research
Journal of Pharmacy and Technology. 2017; 10(10):
3408-3416.
36. Fakhir DF, Hameed IH, Flayyih SS. Burns Injuries:
A Prospective Statistical Study of 112 patients.
Research Journal of Pharmacy and Technology.
2017; 10(10): 3401-3407.
37. MekhlefAK, Hameed IH, Khudhair ME. Prevalence
of Physical Injuries on the Head, Neck and Entire
Body in, Hilla, Iraq. Research Journal of Pharmacy
and Technology. 2017; 10(10): 3276-3282.
38. Hameed IH, Al-Rubaye AF, Kadhim MJ.
Antimicrobial Activity of Medicinal Plants and
Urinary Tract Infections. International Journal of
Pharmaceutical and Clinical Research. 2017; 9(1):
44-50.
39. Al-Rubaye AF, Hameed IH, Kadhim MJ. A Review:
Uses of Gas Chromatography-Mass Spectrometry
(GC-MS) Technique for Analysis of Bioactive
Natural Compounds of Some Plants. International
Journal of Toxicological and Pharmacological
Research. 2017; 9(1); 81-85.
40. Kadhim MJ, Kaizal AF, Hameed IH. Medicinal
Plants Used for Treatment of Rheumatoid Arthritis:
A Review. International Journal of Pharmaceutical
and Clinical Research. 2016; 8(12): 1685-1694.
41. Hussein HM, Hameed IH, Ubaid JM.Analysis of the
secondary metabolite products of Ammi majus and
evaluation anti-insect activity. International journal
of pharmacognosy and phytochemical research.
2016; 8(8): 1192-1189.
42. Ubaid JM, Hussein HM, Hameed IH. Determination
ofbioactivechemicalcompositionofCallosobruchus
maculutus and investigation of its anti-fungal
activity. International journal of pharmcognosy and
phytochemical research. 2016; 8(8): 1293-1299.
43. Mohammed GJ, Hameed IH. Anti-fungal,
Antitumor andAnti-inflammatory activity ofAcorus
calamus. Indian Journal of Public Health Research
and Development. 2018; 9(3): 254-258.
44. Hameed IH, Mohammed GJ, Kamal SA. A review:
Uses and Pharmacological activity of Matricaria
chamomilla. Indian Journal of Public Health
Research and Development. 2018; 9(3): 200-205.
45. Mohammed GJ, Hameed IH, Kamal SA. Anti-
inflammatory Effects and other Uses of Cyclamen
species: A review. Indian Journal of Public Health
Research and Development. 2018; 9(3): 206-211.