Preliminary Phytochemical Screening and Macroscopic Analysis of
Ficus dalhousiae Miq
Syed SafiullahGhori1,3*,
Mohib Khan2 and Mohammed Shamim Qureshi3
1Department of Pharmacology, Himalayan
University, Naharlagun, Itanagar,
Arunachal Pradesh
2Department of Pharmacognosy and
Phytochemistry, Oriental College of Pharmacy, Sector 2,
Plot 3, 4, 5 Sanpada
(E), Navi Mumbai
3Anwarul Uloom
College of Pharmacy, New Mallepally, Hyderabad
500001, Telangana, India
*Corresponding Author E-mail: safiullahghori@gmail.com
ABSTRACT:
The present study was designed to carry out
preliminary phytochemical screening of different
parts (aerial roots, leaves, and stem bark) of Ficus dalhousiae Miq
(Moraceae).The
aqueous extracts of the plant revealed the presence of phytoconstituents
like alkaloids, carbohydrates, flavanoids, and terpenoids in
the, stem bark and leaves .Sterols, tannins and phenols were present in aerial
roots. The macroscopic study of the plant was also conducted which provided
information for identification and characterization of this plant from the
allied species.
KEYWORDS: Ficus dalhousiae,
Moraceae, Phytochemical screening.
INTRODUCTION:
The use of herbal
medicine has become an integral part of human life. Plants contain phytochemicals which have medicinal properties. Phytochemicals are
nonnutritive plant chemicals which have disease preventive properties[1]Some
important phytochemicals extracted from medicinal
plants include alkaloids, flavanoids, phenolic compounds which show biological activity[2]Tannins
have antimicrobial properties, flavanoids have
antibacterial, antifungal properties, terpenes and
steroids also have antimicrobial property against various pathogens[3]. Ficus genus which
belongs to the family Moraceae, represents a vital
group of plants which have immense medicinal value. Ficus dalhousiae Miq is one the species of this family which is
widely used in traditional medicine. Ficus dalhousiae is an
umbrageous tree 9–12 Meters having young branches at first softly pubescent and
afterwards glabrous. It is mainly found in Kerala and Tamil Nadu states
(Coimbatore, Dundigal, Namkkal,
Niligiri, Salem, Theni, Tirunaveli and Vellore districts) The leaves and bark of Ficus dalhousiae Miq are recommended for liver complaints. Fruit is used as cardiotonic.[4]. In the present study preliminary phytochemical screening and macroscopic analysis of
different parts of the plant is conducted to differentiate it from the other
species.
Description:
Ficus dalhousiae is an umbrageous tree 9-12 m having young
branches at first softly pubescent and afterwards glabrous. Leaves are 10-23 cm
in length, subcoriaceous petiolate elliptic
or broadly ovate acute entire, base is cordate, 3-7
nerved, minutely dotted and puberulous or glabrous
above, beneath softly minutely pubescent; nerves 10-12 pairs, rather prominent
beneath, with midrib minutely pubescent; petiole 2.5-6.3 cm., pubescent;
stipules are 1.3-2.5cm., ovate-lanceolate, much acuminate,
puberulous or glabrous.[5] Receptacles are in pairs,
shortly peduncled axillary obovoid with three broad triangular sometimes bifid basal
bracts are densely hairy when ripe i.e about 13mm.
diameter, peduncles are about 8mm in diameter, densely hairy. Male flowers are very few, only near apex of
receptacle, sessile, globose; sepals are three,
concave, rounded; stamen is one; connective wide, filament is thick adnate. Gall flowers on thick pedicels; perianth
is gamophyllous; Ovary is obovoid,
smooth; style is short. Female flowers are sessile; achene
ovate; style is long, lateral, stigma is cylindrical.
Taxanomical classification:
Domain : Eukaryota
Kingdom : Plantae
Subkingdom :
Viridaeplantae
Phylum : Tracheophyta
Subphylum :
Euphyllophytina
Infraphylum :
Radiatopses
Class : Mangoliopsida
Subclass : Dilleniidae
Super order :
Urticanae
Order : Urticales
Family : Moraceae
Genus : Ficus
Specific epithet : dalhousiae Miq
MATERIAL AND
METHODS:
Collection and identification of plant
material:
Fresh aerial
roots, stem bark and leaves of the plant were collected from Tirupati The specimen S. No. 112, Voucher No. 0949 was
deposited in the herbarium, Department of Botany, Osmania University, Hyderabad, Telangana.
The plant was identified by a taxonomist of the same department.
Processing of plant material:
Each part of the
plant was washed under running water to make it free from dust and foreign
particles. The plant parts were powdered and kept in airtight container before
analysis.
Preparation of aqueous extracts:
5gm powder of
each part was soaked in 30ml of distilled water, heated at 50-60şC for 10
minutes and filtered using (Whatman filter paper No.1).The filtrate was
centrifuged at 3000 rpm for 20 minutes and analysed
by phytochemical tests[6].
Phytochemical analysis:
Phytochemical
analysis was carried according to the method of Siddiqui[6]and
Edeoga[7] The phytochemicals
analysed were alkaloids, amino acids ,carbohydrates, cardiac
glycosides, flavanoids phenolic
compounds, proteins, saponins, sterols, tannins, terpenoids.
Screening methods:
Test for alkaloids:
200gm of powdered
plant was dissolved in 10 ml CH3OH and then filtered.1ml HCl (1%aqueous) was added to 2ml filtrate and warmed in a
water bath. while stirring 6 drops of Dragendroff’s
reagent was added to 1ml of the filtrate .Reddish brown precipitate indicates
the presence of alkaloids.
Test for amino acids:
5-7 drops of Ninhydrin reagent was added to 2ml of filtrate and heated
on a water bath for 5 miutes. Purple colour indicates the presence of amino acids.
Test for carbohydrates:
5-8 drops of
Fehling’s (A and B) solution was added to 1ml of filtrate and the resultant
mixture was boiled for 2 minutes. Brick red precipitate indicated the presence
of carbohydrates.
Test for cardiac glycosides:
To 1ml of glacial
acetic acid, 3 drops of FeCl3 and 3 drops of concentrated H2SO4was
added. Green or blue precipitate indicated the presence of cardiac glycosides.
Test for flavanoids:
To 200gm of
powdered plant material 10ml of ethanol was added, stirred and filtered. To 2ml
of filtrate few pieces of magnesium ribbons were added along with few drops of
concentrated HCl. Red colour
indicated the presence of flavanoids.
Test for proteins:
5-7 drops of 5% NaOH and 5-7 drops of 1% Cu(SO4) was added in 2
ml of filtrate. Violet colour indicated the presence
of proteins
Test for saponins:
About 1ml of the
filtrate was stirred with distilled water. Persistence of froth indicated the
presence of saponins.
Test for steroids:
To 200mg of
powdered plant material 10ml of CHCl3was added and filtered, then
2ml of glacial acetic anhydride and few drops of concentrated H2SO4
was added in 2ml filtrate. Green ring indicated the presence of steroids.
Test for tannins:
200gm of powdered
plant was dissolved in 10 ml water, stirred and filtered.2ml of ferric chloride
was added to the filtrate. Blue –black precipitate was observed for tannins and
phenols.
Test for terpenoids:
To 2ml of powder
solution, 2ml of acetic anhydride and few drops of concentrated H2SO4
was added. Blue green ring indicated the presence of terpenoids.
Macroscopic Characters:
Physical characteristic
features of different plant parts like colour odour, taste etc were determined.
Table No-1 Phytochemical screening report
|
Contents |
Aerial
Roots |
Leaves |
Stem
Bark |
|
Alkaloids |
++ |
+ |
+ |
|
Amino acids |
- |
- |
- |
|
Cardiac glycosides |
- |
- |
- |
|
Carbohydrates |
++ |
++ |
++ |
|
Flavanoids |
+ |
++ |
++ |
|
Phenols |
+ |
++ |
+ |
|
Saponins |
+ |
+ |
++ |
|
Sterols |
++ |
++ |
|
|
Tannins |
++ |
++ |
+ |
|
Terpenoids |
+ |
++ |
+ |
+ Present; ++More
Quantity; -Absent
Table No-2 Aerial Roots
|
S .No |
Features |
Observations |
|
1 |
Colour |
Dark brown |
|
2 |
Odour |
Odourless |
|
3 |
Taste |
Bland |
|
4 |
Shape |
Cylindrical |
|
5 |
Texture |
Smooth |
RESULTS AND DISCUSSION:
Results of phytochemical
screening:
The results of phytochemical screening of
aerial roots ,leaf and stem bark aqueous extracts showed the presence of
alkaloids, carbohydrates, flavanoids phenolic compounds,
saponins, tannins, and terpenoids
in the root and leaf fractions as shown
in table no 1.In the stem bark carbohydrates,
flavanoids
phenolic compounds, saponins,
tannins, and terpenoids were detected.
Fig no.1 Aerial roots of Ficus dalhousiae Miq.
Table No-3 Leaves:
|
S .No |
Features |
Observations |
|
1 |
Colour |
Light green |
|
2 |
Odour |
Aromatic |
|
3 |
Taste |
Bitter |
|
4 |
Shape |
ovate |
|
5 |
Size |
20 cm |
|
6 |
Margin |
Serrulate |
|
7 |
Surface |
Glabrous |
|
8 |
Apex |
obtuse |
|
9 |
Venation |
Reticulate |
|
10 |
Texture |
Smooth |
Fig no.2 Leaves of Ficus dalhousiae Miq.
Table No-4 Stem bark
|
S .No |
Features |
Observations |
|
1 |
Colour |
Brown |
|
2 |
Odour |
Odourless |
|
3 |
Taste |
Tasteless |
|
4 |
Shape |
Cylindrical |
|
5 |
Texture |
Glabrous |
Fig no.3 Stem bark of Ficus dalhousiae Miq
The pharmacological
activities of medicinal plants are due
to the presence of secondary metabolites such as flavanoids
,sterols, alkaloids, phenols, glycosides,
saponins
etc.[8] As the plant contains tannin, flavanoids
and phenolic compounds, there is possibility of
antioxidant property in the plant. The medicinal properties of plants have been
explored all over the world due to their antioxidant activity, economic
viability and side effects[9]. The phytochemicals
play a vital role in preventing renal diseases, cholesterol and carcinomas[10].
The phytochemical screening reports can suggest
possible pharmacological activity of the plant in relation of the chemical
constituents in the plant to the known group of constituents[11]. The results
of macroscopic characters of root, is depicted in table no-2 and fig no.1,
leaves in table no 3 and fig no.2,stem
bark in table no.4 and fig no.3.
CONCLUSION:
In conclusion it
can be said that the plant parts like root and leaves have got chemical
constituents in a larger amount than in the stem bark. The results of
macroscopic analysis can be considered as characteristic features of the plant
and can provide help in separating this plant from the other species.
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Received
on 11.09.2014 Modified on 30.09.2014
Accepted
on 04.10.2014 ©A&V Publications All right reserved
Res. J. Pharmacognosy & Phytochem.
7(1): Jan.-Mar. 2015; Page 09-12
DOI: 10.5958/0975-4385.2015.00003.5