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International Journal of Trend in Scientific Research and Development (IJTSRD)
Volume 4 Issue 3, April 2020 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470
@ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 292
Phytochemical Screening and Review of the
Pharmacological Importance of Erythrina Senegalensis
*Bioltif, Yilni Edward; Sase, Terver John; Nehemiah, Tonkum Obadiah
Department of Chemistry, Plateau State University, Bokkos, Nigeria
ABSTRACT
The plant Erythrina senegalensis have been observed by the natives to have
medicinal values. The present study was carried out to investigate the
phytochemicals of the root and pharmacological importance of the plant. The
crushed root was subjected to sequential extraction (maceration) by
increasing polarity index ofsolvents (hexane, ethyl acetateand methanol).The
methanol extract gave the highest percentage yield (4.28%) followed by
Ethylacetate (3.62%) and Hexane (2.48%) was the least in the yield in
extraction. All the three solvent extracts were then used for phytochemicals
screening test. The phytochemical screening has shown the presence of
Flavonoids, alkaloids, anthraquinones, phenols, quinones, steroids, saponins,
tannins, terpenoids, Xanthoproteins.Allthephytochemiscals werefoundtobe
present in atleast one of theextractwithFlavonoids, Quinone,Anthraquinones
and Xanthoproprotein present in all the three extracts. This result of the
phytochemical screening of the root shows why the plant Erythrina
senegalensis has such pharmacological importance.
KEYWORDS: Erythrina senegalensis; extraction; pharmacological;
phytochemicals
How to cite this paper: Bioltif, Yilni
Edward | Sase, Terver John | Nehemiah,
Tonkum Obadiah "Phytochemical
Screening and Review of the
Pharmacological Importance of Erythrina
Senegalensis"
Published in
International Journal
of Trend in Scientific
Research and
Development(ijtsrd),
ISSN: 2456-6470,
Volume-4 | Issue-3,
April 2020, pp.292-296, URL:
www.ijtsrd.com/papers/ijtsrd30350.pdf
Copyright © 2020 by author(s) and
International Journal ofTrendinScientific
Research and Development Journal. This
is an Open Access article distributed
under the terms of
the Creative
Commons Attribution
License (CC BY 4.0)
(http://creativecommons.org/licenses/by
/4.0)
INTRODUCTION
Plant material has remained central to traditional medical
practices and has remained useful sources of new drugs [1].
For a long period of time, plants have been a valuable source
of natural products for maintaining human health especially
in the last decade, with more intensive studies for natural
therapies [2]. Medicinal plant would be the best source to
obtain a variety of drugs while 80% of the developing
countries rely directly on crude concoctions, infusions,
decoctions of plants in traditional medicine for their health
remedies [3]. Phytochemical and pharmacological studies
are very important since a single plant may contain up to
thousands of compounds, the possibility of making new
discovery become evident [4]. The understanding of plants
and investigation to better understand their properties,
safety and efficiency in therefore important.
Phytochemicals are chemicals produced by means of
secondary reactions resulting from primary carbohydrates,
amino acids and lipids [5]. Such chemicals are known to
participate in plant defense mechanisms against herbivores
and pathogens [6]. The most common classes of these
chemicals are saponins, tannins, anthraqinones, flavonoids,
and alkaloids which are widely distributed amongst various
plant families in abundant quantities. It is these chemicals
which attract so much attention from scientists due to their
ability to inhibit the growth of microbes pathogenic to man
and to aid in drug discovery [7, 8].
Plants have served as models for drugs development for
three basic reasons; 25% percent of all prescription drugs
contain active compounds from higher plants, secondly
because secondary plant metabolites are useful in studying
biological systems and disease processes, and lastlybecause
biologically active compounds sometimes have poor
pharmacological activity in humans, and in this case these
compounds are used as template for synthetic modification
and or manufacturing [9].
A. Erythrina senegalensis
Figure 1: Erythrina senegalensis Plant
IJTSRD30350
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 293
1. Taxonomy
Kingdom Plantae
Phylum Tracheophyta
Class Equisetopda
Subclass Magnoliidae
Superclass Rosanae
Order Fabales
Family Leguminosae
Genus Erythrina
Scientific Name— Erythrina senegalensis D.C
Vernacular Names: English- coral tree, Hausa –Mijirya, Tiv –
shor, Yoruba –ologun
2. Geographical Location and Distribution
The plant is commonly found in savannah areas of West
Africa and is native to Senegal, Gambia, Guinea, Guinea-
Bissau, Sierra Leone, Liberia, Mali,Burkina Faso,IvoryCoast,
Niger, Ghana, Togo, Benin, Nigeria and Cameroon. There are
about 108 species of Erythrina distributed allovertheworld
today. Such species exist in different forms as trees, shrubs,
and herbs in Africa, America and Australia [10].
3. Habitat and Ecology
E. senegalensis is a tree which occurs in dry open savannah
woodlands, burned savannah, plateau with fine gravel,
degraded regrowths, coastal savannah (in Ghana), bank of
streams and roadsides by grassland.
4. Morphological Description
Overview: A tree growing up to 7m tall, rarely to 15m, with
deeply fissured, corky bark. The branches and bark are
armed slightly hooked spines up to 10mm long.
Leaves: The leaves are composed of three leaflets, each
measuring 5-15×4-10cm and having a thorny stalk
Flowers: The flowers appear in large groups atthe endofthe
branches, when the tree is leafless (in the first half of the dry
season). The flowers are bright red and 4-5cm long.
Fruits: The fruit is a bent, twisted and slightly hairy pod, 7-
15×1cm. it is constricted between the seeds, which are
bright red.
B. Uses and Application of The Plant
Erythrina senegalensis is used by traditional healers to treat
many ailments, infections, and used as diuretic for horses.
The bark of Erythrina senegalensis is use by traditional
healers in Northern Nigeria to treat jaundice and other
ailments. The bark infusion with spices and honey is widely
used for the treatment of gonorrhoea and as musclerelaxant
[10]. In Ghana, the bark is recommended as emmenagogue
and in French Guinea it is given to women after child birth.
In Senegal the bark is considered as remedy for dysentery
and colitis. The fruits of Erythrinasenegalensisareused injos
locally for treatment of malaria fever. Therootsarepounded
and use as sponge by the Dagombas. The bark and leaves
decoction are sometimes given as drinks, baths or as tonic
for children with rickets and also to weak old men [11].
Some phytochemicals such as alkaloids, flavonoids, tannins,
saponins, phenols, steroid, quinone, xanthoprotein and
terpenoid have been identified in the Erythrina sengalensis
root [12]. The root extract of the plant has been reported in
Nigeria studies to have antimalarial, analgesic, anti-
inflammatory and antibacterial action. The root bark is used
by traditional herbalist to cure wide range of illnesses [13].
C. Pharmacological Activities ofErythrinasenegalensis
The pharmacological studies of this plant are demonstrated
and include antibacterial, antifungal, and antiplasmodial
activities, it also induces analgesic and antipyretic action.
Erythrina senegalensis is used by traditional healers to treat
many ailments, infections, and used as diuretic for horses
[12]. In Gambia and Senegal, the sap from thecrushedleaves
is applied to wounds for two or three days to promote
healing. The pounded bark and leaves are also used in
Nigeria as a tooth ache remedy and inIvoryCoast forgeneral
disease treatment [14]. In Mali, ethanol extract of the plant
was found to contain active bacteriocides against
staphylococcus aureus,Enteracoccusfaccalis,Bacillussubtilis
and Streptococcus pyogenes and thus have found application
in the treatment of bronchial infect, cough and throat
inflammation, malaria, jaundice, sterility, onchocerchiasis,
body pain and wound infection [15].
MATERIALS AND METHODS
D. Plant Material
Erythrina senegalensis root extract was collected from
federal college of forestry Jos, Plateau State. The plant taken
was identified and authenticated at the Department of
herbarium federal college of forestry Jos. The sample was
then chopped into small sizes and dried at room
temperature for four (4) weeks.Thedrysamplewas crushed
into small sizes using mortar and pestle.
E. Preparation of Plant Extract
The dried sample (50g/200ml) was extracted successively
extracted with n-hexane, ethyl acetate and methanol using
cold extraction method (maceration). The solvent is left in
contact with the plant for 72 hours (3 days) in each case.The
extract is decanted and allowed to stand, after which it is
filtered through a Whatman No. 42 filter paper. The extract
was concentrated using a rotary evaporator.Theextract was
transferred into a pre-weighed beakerand placedonawater
bath at 40oC until a plastic form of the extract is obtained.All
the crude extracts were then weighed to determine the
percentages yield of extraction. The percentage yield of
extraction was calculated by using the following equation:
100%
F. Preliminary Phytochemical Screening
The phytochemical test for various phytochemicals present
in the extract was carried out using standard methods as
described below [16].
Test for Alkaloid
0.2g of the molten extract was mixed with little amount of
HCl and then wagners reagent. Formation of a white
precipitate indicates the presence of alkaloid.
Test for Flavonoid
0.2g of the molten extract was mixed with 1ml of 2%
ammonium chloride and the exposed to light. Yellow
precipitate indicates the presence of Flavonoid.
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 294
Test for Anthraquinone
A few drops magnesium acetate was added to 0.2g of the
molten extract. Pink colour formationindicatesthepresence
of anthraquinone.
Test for Quinone
0.2g of the molten extract was treated with few drops of
conc. H2SO4 or aqueous NaOH solution.Red colourformation
indicates the presence of quinone.
Test for Phenols
0.2g of molten extract was mixed with ferric chloride
solution. A green or dirty green precipitate indicates the
presence of phenol.
Test for Tannins
0.2g of the molten extract was mixed with few drops ferric
chloride solution. A blue-black, green or blue-green
precipitate indicates the presence of tannin.
Test for Saponins
0.2g of extract was shaken 5ml of distilled water in a test
tube. Frothing which persists on warming indicates the
presence of saponin.
Test for Xanthoproteins
0.2g of extract was mixed with few drops of conc. HNO3 and
then few drops of ammonia. A red precipitate indicates the
presence of xanthoproteins.
Test for Steroids (Salkowski’s test)
0.2g of the extract was mixed with 3ml of chloroform and
2ml of conc. H2SO4. A red colour appearance indicates the
presence of steroid.
Test for Terpenoid
About 0.2g extract was mixed with 2ml Chloroform and 3ml
of concentrated sulphuric acid was added carefully toforma
layer. A reddish brown coloration of the interface formed
indicates the presence of terpenoids
RESULTS
Table1: Weight and Percentage Yield of Extract
Extract Colour of extract Wt. of sample (g) Wt. of extract (g) %Yield (w/w)
Hexane Extract Yellow 500 14.2 2.84
Ethylacetate Extract Orange 500 18.1 3.62
Methanol Extract Orange 500 21.4 4.28
Total Extract 1500 53.7 10.74
Table2. Showing the results for the phytochemical screening of the root extract of Erythrina senegalensis
Phytochemicals Hexane Extract Ethyl acetate Extract Methanol Extract
Alkaloids + - +
Flavonoids + + +
Steriods - - +
Tannins - + +
Phenols + - -
Quinones + + +
Saponins + + -
Terpenoids - - +
Anthraquinones + + +
Xanthoproteins + + +
Present (+) Absent (-)
DISCUSSION
The solvents used in the present study were selected based
on their different polarity ranges. In termofchemistry, polar
substances would dissolve in polar solvents while non-polar
substances will dissolve in non-polar solvents. [17].
The percentage yield of crude methanol extract (4.28%) is
the highest among the three solvent extracts, followed by
ethylacetate extract (3.62%), whereas hexane extract
showed the lowest percentage yield (2.84%). Thus total
percentage yield by E. senegalensis root was found to be
10.74%.
The result of the preliminary phytochemicals screening of
three solvent(N-hexane,ethylacetateand methanol) extracts
of the plant Erythrina senegalensis root is presented in the
Table 2. The result revealed that root bark of Erythrina
senegalensis contain alkaloids, flavonoid, steroid, tannin,
phenol, quinine, saponin, terpenoid, anthraquinone and
xanthoprotein. The N-hexane root extracts of the plant
reveal that the root contain alkaloid, flavonoid, phenol,
quinine, xanthoprotein, saponon, and anthraquinone but
showed a negative test for steroid, tannins and terpenoid.
The ethylacetate root extracts of the plant reveal that its
contain flavonoid, tannins, quinone, xanthoprotein,saponin,
anthraquinone but show negative result for alkaloid,
terpenoid, steroid and phenol. The methanol root extract of
the plant revealed that the root contain alkaloid, flavoniod,
steroid, tannin, quinine, terpenoid, xanthoproteins and
anthraquinone but show negative result forphenol,saponin.
The preliminary phytochemical screening ofthe root extract
of Erythrina senegalensis is similar with other research
findings [18].
The present research brings out information on different
active compounds in plants from root extracts of Erythrina
senegalensis.
Flavonoids shows biological activities like antimicrobial,
anti-inflammatory, analgesic, anti-allergic, antioxidant
properties and anticancer activities [19]. Because of the
presence of flavonoids in the plant, thus makes the plant to
be use as antioxidants and antimicrobial.
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 295
Tannins are known to interact with protein to give the
astringent effects which is important forthetreatment.They
form irreversiblecomplexwithproline-richprotein resulting
in the inhibition of cell protein synthesis. E. senegalensis is
thus useful as antiseptic and this activity is due to presence
of tannins [20, 21].
Phenolic compound in the plant proves that they have anti-
microbial and anti-fungal effect. Also, plants that contain
phenols could be used as anti-inflammatory, immune
enhancers and hormone modulators [22]. Phenolic
compounds are well known potential phytotoxins and exist
as free forms, esters or as glycoside when combined with
sugars. Such compounds contribute to the bitter taste [23].
Plant steroids (cardiac glycosides) are naturally occurring
plant phytoconstituents that have found therapeutic
applications as arrow poisons or cardiacdrugs [24].Steroids
are reported to exhibit strong antiviral and antibacterial
activities; they are used as treatment for congestive heart
failure [18].
Saponins are often referred to as "soap like behaviour" in
water, because of their foamy nature. They have anti-
carcinogenic properties, immune modulation activities and
regulation of cell proliferation as well as healthbenefits such
as inhibition of the growth of cancer cell and cholesterol
lowering activity [25]. Saponins are also important
therapeutically as they are showntohavehypolipidemicand
anticancer and anticancer activity.
Alkaloids have wonderful physiological effectonhumanand
used for the development of powerful analgesic drugs [26].
Alkaloids have pharmacological applications as anesthetics
and CNS stimulants, also serve as muscle relaxant [27].
Anthraquinones are also used as laxatives such as in the
drug senna glycoside
The curative properties of medicinal plants are perhaps due
to the presence of various chemicals. Therefore, apart from
giving an insight into valuable chemical constituents,
screening of different parts of medicinal plants would be a
prerequisite for evaluation of the pharmacological activities
of a plant and drug development.
CONCLUSION
The study has shown that the plant extract from the root of
Erythrina senegalensis possessed bioactive constituents like
saponins, tannins, alkaloids, terpenes andcardiacglycosides
which shows that it has high medicinal potential and can be
utilized in treatment of diseases. This confirms its
phamarcological importance and justifies its usage for
various health remedies.
REFERENCES
[1] Anishetty, R., Swapna, S., Aishwarya, B., & Sravanthi, K.
C. (2012). Evaluation of antibacterial activity potential
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[2] Sofowora, A. (1981). Problems and Prospects of
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[3] Sofowora, A. (1993). Recent trends in research into
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[8] Balunas, M. J., & Kinghorn, A. D. (2005). Drug discovery
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[9] Farnsworth, N. R. (1994). Ethnopharmacology and
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[10] Daziel, J. (1955). The Useful Plants of West Tropical
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[11] Games, D. E., Jackson, A. H., Khan, N. A., & Millington, D.
S. (1974). Alkaloids of some African, Asian, Polynesian
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[12] Rawaa, A., Adawai, K., & Mohammed, H. (2016).
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[14] Udem, S. C., Obidoa, O., & Asuzu, I. U. (2010). Acute and
chronic toxicity studies of Erythrina senegalensis DC
stem bark extract in mice. Comparative Clinical
Pathology, 19(3), 275-282.
[15] Togola, A., Austarheim, I., Theïs,A.,Diallo,D.,&Paulsen,
B. S. (2008). Ethnopharmacological uses of Erythrina
senegalensis: a comparison ofthreeareas inMali,and a
link between traditional knowledge and modern
biological science. Journal of ethnobiology and
ethnomedicine, 4(1), 6.
[16] Trease, G.E. and Evans, W.C. 1989. Pharmacognosy.
Thirteenth Edition.
[17] Ali, R. M., Houghton, P. J., Raman, A., & Hoult, J. R. S.
(1998). Antimicrobial and anti-inflammatoryactivities
of extracts and constituents of Oroxylum indicum (L.)
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[18] Saidu, K., Onah, J., Orisadipe, A., Olusola, A., Wambebe,
C., & Gamaniel, K. (2000). Antiplasmodial, analgesic,
and anti-inflammatory activities oftheaqueous extract
International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470
@ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 296
of the stem bark of Erythrina senegalensis. Journal of
ethnopharmacology, 71(1-2), 275-280.
[19] Hodek, P., Trefil, P., & Stiborová,M.(2002).Flavonoids-
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[22] Okwu, D. E., & Omodamiro, O. D. (2006). Effects of
hexane extract and phytochemical content of Xylopia
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[23] Okwu, D. E. (2005). Phytochemicals, vitamins and
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[25] Jimoh, F. O., & Oladiji, A. T. (2005). Preliminary studies
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Phytochemical Screening and Review of the Pharmacological Importance of Erythrina Senegalensis

  • 1. International Journal of Trend in Scientific Research and Development (IJTSRD) Volume 4 Issue 3, April 2020 Available Online: www.ijtsrd.com e-ISSN: 2456 – 6470 @ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 292 Phytochemical Screening and Review of the Pharmacological Importance of Erythrina Senegalensis *Bioltif, Yilni Edward; Sase, Terver John; Nehemiah, Tonkum Obadiah Department of Chemistry, Plateau State University, Bokkos, Nigeria ABSTRACT The plant Erythrina senegalensis have been observed by the natives to have medicinal values. The present study was carried out to investigate the phytochemicals of the root and pharmacological importance of the plant. The crushed root was subjected to sequential extraction (maceration) by increasing polarity index ofsolvents (hexane, ethyl acetateand methanol).The methanol extract gave the highest percentage yield (4.28%) followed by Ethylacetate (3.62%) and Hexane (2.48%) was the least in the yield in extraction. All the three solvent extracts were then used for phytochemicals screening test. The phytochemical screening has shown the presence of Flavonoids, alkaloids, anthraquinones, phenols, quinones, steroids, saponins, tannins, terpenoids, Xanthoproteins.Allthephytochemiscals werefoundtobe present in atleast one of theextractwithFlavonoids, Quinone,Anthraquinones and Xanthoproprotein present in all the three extracts. This result of the phytochemical screening of the root shows why the plant Erythrina senegalensis has such pharmacological importance. KEYWORDS: Erythrina senegalensis; extraction; pharmacological; phytochemicals How to cite this paper: Bioltif, Yilni Edward | Sase, Terver John | Nehemiah, Tonkum Obadiah "Phytochemical Screening and Review of the Pharmacological Importance of Erythrina Senegalensis" Published in International Journal of Trend in Scientific Research and Development(ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-3, April 2020, pp.292-296, URL: www.ijtsrd.com/papers/ijtsrd30350.pdf Copyright © 2020 by author(s) and International Journal ofTrendinScientific Research and Development Journal. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (http://creativecommons.org/licenses/by /4.0) INTRODUCTION Plant material has remained central to traditional medical practices and has remained useful sources of new drugs [1]. For a long period of time, plants have been a valuable source of natural products for maintaining human health especially in the last decade, with more intensive studies for natural therapies [2]. Medicinal plant would be the best source to obtain a variety of drugs while 80% of the developing countries rely directly on crude concoctions, infusions, decoctions of plants in traditional medicine for their health remedies [3]. Phytochemical and pharmacological studies are very important since a single plant may contain up to thousands of compounds, the possibility of making new discovery become evident [4]. The understanding of plants and investigation to better understand their properties, safety and efficiency in therefore important. Phytochemicals are chemicals produced by means of secondary reactions resulting from primary carbohydrates, amino acids and lipids [5]. Such chemicals are known to participate in plant defense mechanisms against herbivores and pathogens [6]. The most common classes of these chemicals are saponins, tannins, anthraqinones, flavonoids, and alkaloids which are widely distributed amongst various plant families in abundant quantities. It is these chemicals which attract so much attention from scientists due to their ability to inhibit the growth of microbes pathogenic to man and to aid in drug discovery [7, 8]. Plants have served as models for drugs development for three basic reasons; 25% percent of all prescription drugs contain active compounds from higher plants, secondly because secondary plant metabolites are useful in studying biological systems and disease processes, and lastlybecause biologically active compounds sometimes have poor pharmacological activity in humans, and in this case these compounds are used as template for synthetic modification and or manufacturing [9]. A. Erythrina senegalensis Figure 1: Erythrina senegalensis Plant IJTSRD30350
  • 2. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 293 1. Taxonomy Kingdom Plantae Phylum Tracheophyta Class Equisetopda Subclass Magnoliidae Superclass Rosanae Order Fabales Family Leguminosae Genus Erythrina Scientific Name— Erythrina senegalensis D.C Vernacular Names: English- coral tree, Hausa –Mijirya, Tiv – shor, Yoruba –ologun 2. Geographical Location and Distribution The plant is commonly found in savannah areas of West Africa and is native to Senegal, Gambia, Guinea, Guinea- Bissau, Sierra Leone, Liberia, Mali,Burkina Faso,IvoryCoast, Niger, Ghana, Togo, Benin, Nigeria and Cameroon. There are about 108 species of Erythrina distributed allovertheworld today. Such species exist in different forms as trees, shrubs, and herbs in Africa, America and Australia [10]. 3. Habitat and Ecology E. senegalensis is a tree which occurs in dry open savannah woodlands, burned savannah, plateau with fine gravel, degraded regrowths, coastal savannah (in Ghana), bank of streams and roadsides by grassland. 4. Morphological Description Overview: A tree growing up to 7m tall, rarely to 15m, with deeply fissured, corky bark. The branches and bark are armed slightly hooked spines up to 10mm long. Leaves: The leaves are composed of three leaflets, each measuring 5-15×4-10cm and having a thorny stalk Flowers: The flowers appear in large groups atthe endofthe branches, when the tree is leafless (in the first half of the dry season). The flowers are bright red and 4-5cm long. Fruits: The fruit is a bent, twisted and slightly hairy pod, 7- 15×1cm. it is constricted between the seeds, which are bright red. B. Uses and Application of The Plant Erythrina senegalensis is used by traditional healers to treat many ailments, infections, and used as diuretic for horses. The bark of Erythrina senegalensis is use by traditional healers in Northern Nigeria to treat jaundice and other ailments. The bark infusion with spices and honey is widely used for the treatment of gonorrhoea and as musclerelaxant [10]. In Ghana, the bark is recommended as emmenagogue and in French Guinea it is given to women after child birth. In Senegal the bark is considered as remedy for dysentery and colitis. The fruits of Erythrinasenegalensisareused injos locally for treatment of malaria fever. Therootsarepounded and use as sponge by the Dagombas. The bark and leaves decoction are sometimes given as drinks, baths or as tonic for children with rickets and also to weak old men [11]. Some phytochemicals such as alkaloids, flavonoids, tannins, saponins, phenols, steroid, quinone, xanthoprotein and terpenoid have been identified in the Erythrina sengalensis root [12]. The root extract of the plant has been reported in Nigeria studies to have antimalarial, analgesic, anti- inflammatory and antibacterial action. The root bark is used by traditional herbalist to cure wide range of illnesses [13]. C. Pharmacological Activities ofErythrinasenegalensis The pharmacological studies of this plant are demonstrated and include antibacterial, antifungal, and antiplasmodial activities, it also induces analgesic and antipyretic action. Erythrina senegalensis is used by traditional healers to treat many ailments, infections, and used as diuretic for horses [12]. In Gambia and Senegal, the sap from thecrushedleaves is applied to wounds for two or three days to promote healing. The pounded bark and leaves are also used in Nigeria as a tooth ache remedy and inIvoryCoast forgeneral disease treatment [14]. In Mali, ethanol extract of the plant was found to contain active bacteriocides against staphylococcus aureus,Enteracoccusfaccalis,Bacillussubtilis and Streptococcus pyogenes and thus have found application in the treatment of bronchial infect, cough and throat inflammation, malaria, jaundice, sterility, onchocerchiasis, body pain and wound infection [15]. MATERIALS AND METHODS D. Plant Material Erythrina senegalensis root extract was collected from federal college of forestry Jos, Plateau State. The plant taken was identified and authenticated at the Department of herbarium federal college of forestry Jos. The sample was then chopped into small sizes and dried at room temperature for four (4) weeks.Thedrysamplewas crushed into small sizes using mortar and pestle. E. Preparation of Plant Extract The dried sample (50g/200ml) was extracted successively extracted with n-hexane, ethyl acetate and methanol using cold extraction method (maceration). The solvent is left in contact with the plant for 72 hours (3 days) in each case.The extract is decanted and allowed to stand, after which it is filtered through a Whatman No. 42 filter paper. The extract was concentrated using a rotary evaporator.Theextract was transferred into a pre-weighed beakerand placedonawater bath at 40oC until a plastic form of the extract is obtained.All the crude extracts were then weighed to determine the percentages yield of extraction. The percentage yield of extraction was calculated by using the following equation: 100% F. Preliminary Phytochemical Screening The phytochemical test for various phytochemicals present in the extract was carried out using standard methods as described below [16]. Test for Alkaloid 0.2g of the molten extract was mixed with little amount of HCl and then wagners reagent. Formation of a white precipitate indicates the presence of alkaloid. Test for Flavonoid 0.2g of the molten extract was mixed with 1ml of 2% ammonium chloride and the exposed to light. Yellow precipitate indicates the presence of Flavonoid.
  • 3. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 294 Test for Anthraquinone A few drops magnesium acetate was added to 0.2g of the molten extract. Pink colour formationindicatesthepresence of anthraquinone. Test for Quinone 0.2g of the molten extract was treated with few drops of conc. H2SO4 or aqueous NaOH solution.Red colourformation indicates the presence of quinone. Test for Phenols 0.2g of molten extract was mixed with ferric chloride solution. A green or dirty green precipitate indicates the presence of phenol. Test for Tannins 0.2g of the molten extract was mixed with few drops ferric chloride solution. A blue-black, green or blue-green precipitate indicates the presence of tannin. Test for Saponins 0.2g of extract was shaken 5ml of distilled water in a test tube. Frothing which persists on warming indicates the presence of saponin. Test for Xanthoproteins 0.2g of extract was mixed with few drops of conc. HNO3 and then few drops of ammonia. A red precipitate indicates the presence of xanthoproteins. Test for Steroids (Salkowski’s test) 0.2g of the extract was mixed with 3ml of chloroform and 2ml of conc. H2SO4. A red colour appearance indicates the presence of steroid. Test for Terpenoid About 0.2g extract was mixed with 2ml Chloroform and 3ml of concentrated sulphuric acid was added carefully toforma layer. A reddish brown coloration of the interface formed indicates the presence of terpenoids RESULTS Table1: Weight and Percentage Yield of Extract Extract Colour of extract Wt. of sample (g) Wt. of extract (g) %Yield (w/w) Hexane Extract Yellow 500 14.2 2.84 Ethylacetate Extract Orange 500 18.1 3.62 Methanol Extract Orange 500 21.4 4.28 Total Extract 1500 53.7 10.74 Table2. Showing the results for the phytochemical screening of the root extract of Erythrina senegalensis Phytochemicals Hexane Extract Ethyl acetate Extract Methanol Extract Alkaloids + - + Flavonoids + + + Steriods - - + Tannins - + + Phenols + - - Quinones + + + Saponins + + - Terpenoids - - + Anthraquinones + + + Xanthoproteins + + + Present (+) Absent (-) DISCUSSION The solvents used in the present study were selected based on their different polarity ranges. In termofchemistry, polar substances would dissolve in polar solvents while non-polar substances will dissolve in non-polar solvents. [17]. The percentage yield of crude methanol extract (4.28%) is the highest among the three solvent extracts, followed by ethylacetate extract (3.62%), whereas hexane extract showed the lowest percentage yield (2.84%). Thus total percentage yield by E. senegalensis root was found to be 10.74%. The result of the preliminary phytochemicals screening of three solvent(N-hexane,ethylacetateand methanol) extracts of the plant Erythrina senegalensis root is presented in the Table 2. The result revealed that root bark of Erythrina senegalensis contain alkaloids, flavonoid, steroid, tannin, phenol, quinine, saponin, terpenoid, anthraquinone and xanthoprotein. The N-hexane root extracts of the plant reveal that the root contain alkaloid, flavonoid, phenol, quinine, xanthoprotein, saponon, and anthraquinone but showed a negative test for steroid, tannins and terpenoid. The ethylacetate root extracts of the plant reveal that its contain flavonoid, tannins, quinone, xanthoprotein,saponin, anthraquinone but show negative result for alkaloid, terpenoid, steroid and phenol. The methanol root extract of the plant revealed that the root contain alkaloid, flavoniod, steroid, tannin, quinine, terpenoid, xanthoproteins and anthraquinone but show negative result forphenol,saponin. The preliminary phytochemical screening ofthe root extract of Erythrina senegalensis is similar with other research findings [18]. The present research brings out information on different active compounds in plants from root extracts of Erythrina senegalensis. Flavonoids shows biological activities like antimicrobial, anti-inflammatory, analgesic, anti-allergic, antioxidant properties and anticancer activities [19]. Because of the presence of flavonoids in the plant, thus makes the plant to be use as antioxidants and antimicrobial.
  • 4. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 295 Tannins are known to interact with protein to give the astringent effects which is important forthetreatment.They form irreversiblecomplexwithproline-richprotein resulting in the inhibition of cell protein synthesis. E. senegalensis is thus useful as antiseptic and this activity is due to presence of tannins [20, 21]. Phenolic compound in the plant proves that they have anti- microbial and anti-fungal effect. Also, plants that contain phenols could be used as anti-inflammatory, immune enhancers and hormone modulators [22]. Phenolic compounds are well known potential phytotoxins and exist as free forms, esters or as glycoside when combined with sugars. Such compounds contribute to the bitter taste [23]. Plant steroids (cardiac glycosides) are naturally occurring plant phytoconstituents that have found therapeutic applications as arrow poisons or cardiacdrugs [24].Steroids are reported to exhibit strong antiviral and antibacterial activities; they are used as treatment for congestive heart failure [18]. Saponins are often referred to as "soap like behaviour" in water, because of their foamy nature. They have anti- carcinogenic properties, immune modulation activities and regulation of cell proliferation as well as healthbenefits such as inhibition of the growth of cancer cell and cholesterol lowering activity [25]. Saponins are also important therapeutically as they are showntohavehypolipidemicand anticancer and anticancer activity. Alkaloids have wonderful physiological effectonhumanand used for the development of powerful analgesic drugs [26]. Alkaloids have pharmacological applications as anesthetics and CNS stimulants, also serve as muscle relaxant [27]. Anthraquinones are also used as laxatives such as in the drug senna glycoside The curative properties of medicinal plants are perhaps due to the presence of various chemicals. Therefore, apart from giving an insight into valuable chemical constituents, screening of different parts of medicinal plants would be a prerequisite for evaluation of the pharmacological activities of a plant and drug development. CONCLUSION The study has shown that the plant extract from the root of Erythrina senegalensis possessed bioactive constituents like saponins, tannins, alkaloids, terpenes andcardiacglycosides which shows that it has high medicinal potential and can be utilized in treatment of diseases. This confirms its phamarcological importance and justifies its usage for various health remedies. REFERENCES [1] Anishetty, R., Swapna, S., Aishwarya, B., & Sravanthi, K. C. (2012). Evaluation of antibacterial activity potential of extracts of Ricinus communis, Zingiber officinalis and Punica granatum in a Polyherbal Extract. Research Journal ofPharmacyandTechnology, 5(11),1385-1388. [2] Sofowora, A. (1981). Problems and Prospects of Integrating Traditional and Western Medicine in Nigeria. Nigerian Journal of Pharmacy, 12(1), 277-283. [3] Sofowora, A. (1993). Recent trends in research into African medicinal plants. Journal of ethnopharmacology, 38(2-3), 197-208. [4] Banso, A., & Adeyemo, S. O. (2007). Evaluation of antibacterial properties of tannins isolated from Dichrostachys cinerea. African Journal of Biotechnology, 6(15). [5] Hussain, M. S., Fareed, S., Saba Ansari, M., Rahman, A., Ahmad, I. Z., & Saeed, M. (2012). Current approaches toward production of secondary plant metabolites. Journal of pharmacy & bioallied sciences, 4(1), 10. [6] Edreva, A., Velikova, V., Tsonev, T., Dagnon, S.,Gürel,A., Aktaş, L., & Gesheva, E. (2008).Stress-protectiveroleof secondary metabolites: diversity of functions and mechanisms. Gen Appl Plant Physiol, 34(1-2), 67-78. [7] Pereira, D. M., Valentão, P., Pereira, J. A., & Andrade, P. B. (2009). Phenolics: From chemistry to biology. [8] Balunas, M. J., & Kinghorn, A. D. (2005). Drug discovery from medicinal plants. Life sciences, 78(5), 431-441. [9] Farnsworth, N. R. (1994). Ethnopharmacology and drug development. Ethnobotany and thesearchfor new drugs, 185, 42-51. [10] Daziel, J. (1955). The Useful Plants of West Tropical Africa Published by Crown Agents for Overseas Government and Administration. [11] Games, D. E., Jackson, A. H., Khan, N. A., & Millington, D. S. (1974). Alkaloids of some African, Asian, Polynesian and Australianspecies ofErythrina. Lloydia, 37(4),581. [12] Rawaa, A., Adawai, K., & Mohammed, H. (2016). “Antibacterial activity of Asphodelin intea and Asphodelus microcarpus against methicillin. Resistant Staphylococcus aureus isolates”. International Journal of Pharmacognosy and Phytochemical Research, 8 (12); 1964-1968. [13] Obidah, W., Badung, H. L., Ajuji, J., Peter, H., & Bello, H. (2014). Effects of Erythrina senegalensis aqueous leaf extract in rats. American Journal of Research Communication, 2, 179-185. [14] Udem, S. C., Obidoa, O., & Asuzu, I. U. (2010). Acute and chronic toxicity studies of Erythrina senegalensis DC stem bark extract in mice. Comparative Clinical Pathology, 19(3), 275-282. [15] Togola, A., Austarheim, I., Theïs,A.,Diallo,D.,&Paulsen, B. S. (2008). Ethnopharmacological uses of Erythrina senegalensis: a comparison ofthreeareas inMali,and a link between traditional knowledge and modern biological science. Journal of ethnobiology and ethnomedicine, 4(1), 6. [16] Trease, G.E. and Evans, W.C. 1989. Pharmacognosy. Thirteenth Edition. [17] Ali, R. M., Houghton, P. J., Raman, A., & Hoult, J. R. S. (1998). Antimicrobial and anti-inflammatoryactivities of extracts and constituents of Oroxylum indicum (L.) Vent. Phytomedicine, 5(5), 375-381. [18] Saidu, K., Onah, J., Orisadipe, A., Olusola, A., Wambebe, C., & Gamaniel, K. (2000). Antiplasmodial, analgesic, and anti-inflammatory activities oftheaqueous extract
  • 5. International Journal of Trend in Scientific Research and Development (IJTSRD) @ www.ijtsrd.com eISSN: 2456-6470 @ IJTSRD | Unique Paper ID – IJTSRD30350 | Volume – 4 | Issue – 3 | March-April 2020 Page 296 of the stem bark of Erythrina senegalensis. Journal of ethnopharmacology, 71(1-2), 275-280. [19] Hodek, P., Trefil, P., & Stiborová,M.(2002).Flavonoids- potent and versatile biologically active compounds interacting with cytochromes P450. Chemico-biological interactions, 139(1), 1-21. [20] Adegboye, M. F., Akinpelu, D. A., & Okoh, A. I. (2008). The bioactive and phytochemicalproperties ofGarcinia kola (Heckel) seed extract on some pathogens. African Journal of Biotechnology, 7(21). [21] Shimada, T. (2006). Salivary proteins as a defense against dietary tannins. Journal of chemical ecology, 32(6), 1149-1163. [22] Okwu, D. E., & Omodamiro, O. D. (2006). Effects of hexane extract and phytochemical content of Xylopia aethiopica and Ocimum gratissimum on the uterus of guinea pig. Bio-research. [23] Okwu, D. E. (2005). Phytochemicals, vitamins and mineral contents of two Nigerian medicinal plants. Int. J. Mol. Med. Adv. Sci, 1(4), 375-381. [24] Firn, J. (2010). Ten Commitments,ReshapingtheLucky Country's Environment. [25] Jimoh, F. O., & Oladiji, A. T. (2005). Preliminary studies on Piliostigma thonningii seeds: Proximate analysis, mineral composition and phytochemical screening. African Journal of Biotechnology, 4(12). [26] Kam, P. C. A., & Liew, S. (2002). Traditional Chinese herbal medicine and anaesthesia. Anaesthesia, 57(11), 1083-1089. [27] Madziga, H. A., Sanni, S., & Sandabe, U. K. (2010). Phytochemical and elemental analysis of Acalypha wilkesiana leaf. JournalofAmericanScience, 6(11),510- 514.