Review Article
wjpls, 2020, Vol. 6, Issue 12, 216-220
Pandey et al.
ISSN 2454-2229
World and
Journal
of Pharmaceutical
World Journal of Pharmaceutical
Life
Sciences and Life Science
WJPLS
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PHYTOCHEMICAL AND PHARMACOLOGICAL INVESTIGATION OF CORDIA
MACLEODII HOOK
Sandeep Pandey*, Sushma Kushwaha, Susma Singh, Subha Chaurasia, Khusboo Mishra
Center for Botany, School of Environmental Biology, APS University, Rewa, India- 486003.
Corresponding Author: Sandeep Pandey
Center for Botany, School of Environmental Biology, APS University, Rewa, India- 486003.
Article Received on 14/10/2020
Article Revised on 04/11/2020
Article Accepted on 25/11/2020
ABSTRACT
Cordia macleodii Hook. an important medicinal plant of family Boraginaceae categorized as endangered taxa has
immense economical and ethno medicinal uses. Several bioactive compounds like alkaloids, tannins, saponins,
phenolics, phytosterols has been isolated from tree bark, stem, leaves, flower, crude and solvent extracts. In
general the plant is anti-microbial, hepato-protective, antioxidant, anti-venom, wound-healer, antihypertensive in
nature with great significance in pharmaceutical industries. This systematic review focuses on screening main
chemical constituents of all the valuable parts and their pharmacological activities so as to be successfully
employed in pharma industries for preparing new drug formulations.
KEYWORDS: Cordia macleodii, chemical composition, pharmaceutical activities.
INTRODUCTION
Plants containing bioactive compounds have been
beneficial for human health since time immoral.
According to an estimate nearly 50 to 80,000 plant
species either native or pharmaceutical derivatives are
used in human healthcare system globally.[1] Drug
discovery from plant products include its chemical
composition, analysis and pharmacological investigation.
The development of new scientific technologies like
GC–MS, IR, NMR, HPLC, HPTLC has helped in
identifying and elucidating natural products and new
drug discovery.[2] Moreover, in recent years tissue
culture techniques has revolutionized the development of
commercially important species and their secondary
metabolites like alkaloids, flavonoids and phytosterols
with pharmacological applications.[3] The continuous
growing economic importance of plant-based
pharmaceuticals is increasing rapidly and shown positive
impact on human healthcare system.[4] In recent years,
various studies have been done on chemical constituents
and pharmacological properties of medicinal plants.[5-10]
Cordia macleodii (Griff) Hook. F. & Thomas., a medium
sized tree belonging to family Boraginaceae is an
important medicinal tree (Figure 1). The tree mainly
occurs in moist and deciduous forests in Central India,
Deccan, Southern and Western region with common
names ‘Dadhiman’, ‘Dahipalas’ or ‘Dahiman’. It
contains various bioactive compounds with significant
pharmaceutical uses. According to available literature
HPTLC, GC/MS, FTIR, UV-Vis scientific techniques
has been applied to isolate many secondary metabolites
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like alkaloids, tannins, glycosides, flavonoids from the
leaves, bark, stem and flowers of the plant. These
bioactive compounds have immense potentiality against
various diseases and thus an important candidate in drug
industries for developing new medicines.
Figure 1. Cordia macleodii.
PHYTOCHEMICAL CONSTITUENTS
The phytochemical composition of any plant is key
factor in determining its pharmaceutical potentiality.
Earlier the author has conducted vast studies on
phytochemical composition of various important
medicinal plants.[11-15] The screening of literatures based
on phytochemical constituents of C. macleodii comes out
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with significant outcomes suggesting that plant parts are
enriched with several bioactive compounds. The
systematic research study reveals that tree bark followed
by leaves and stem are the important parts with essential
secondary metabolites of pharmaceutical importance.
presence of Phenolics and ethanolic leaf extract yielded
Gallic acid (3, 4-dihydroxy-5-methoxybenzoic acid) [20].
UV-Visible and FTIR spectra of Choloformic extract of
leaf confirms the presence of β-carotene, showing
potentiality as a dye sensitized solar cell.[26]
Chemical composition of stem bark
Physico-chemical studies of bark reveal that it contains
total ash, acid insoluble ash, hexane soluble extractive,
alcohol soluble extractive, water soluble extractive,
sugar, starch and tannins. The hexane and chloroform
bark extract mainly contain triterpenoids, acetone,
methanol and aqueous bark extract contains reducing
sugar and aqueous bark extract also contain saponins,
tannins, glycosides, alkaloids.[16, 17] Beside this acetone,
ethyl alcohol, petroleum ether and water extract also
contains carbohydrate, flavanoid, and resin.[17] Moreover,
the physico-chemical analysis of powdered stem bark
using HPTLC reveals foreign matters, loss on drying,
alcohol soluble extractive, water soluble extractive, total
ash and acid in soluble ash in 2.18, 8.40, 7.01, 24.93,
17.07, 5.86 % respectively.[17]
PHARMACOLOGICAL ACTIVITIES
The pharmacological activities of Cordia macleodii has
been studied since many years. The scientific
information suggests that the plant generally possesses
antimicrobial, antioxidant, anti-inflammatory, analgesic,
hepatoprotective, antivenom activities.[27] The plant parts
mainly stem, bark and leave in form of extracts, powder,
and decoction either internal or external applicability,
shows wider pharmacological activities.
The unsaponifiable fraction of petrol-ether bark extract
using GC/MS analysis and IR and UV characterization
yielded three compounds Stigmasterol, Camphesterol
and
Cholest-5-EN
-3OL
(3
Beta)-Carbonyl
chlorinated[18,19] in addition with p-hydroxyphenylacetic
acid and β-sitosterol.[19] The UV spectrum studies of bark
fraction shows presence of flavonoids whereas and
ethanolic[19, 20] and methanolic bark extract shows
presence of Quercetin.[21] Beside this two other
flavonoids apigenin and kaempferol were isolated from
methanolic bark extract.[21] The granular activated
charcoal prepared from the bark at pH 11.5, 330 minute
contact time, 6 mg/l initial metal concentration, 1.4 gm
adsorbent dose, and 650c temperature, has potentiality in
adsorbing toxic element manganese from wastewater.[22]
Chemical composition of stem
The UV-Vis spectrophotometry of silver nitrate colloidal
solution of stem extracts with maximum absorption
spectrum at 424 and 437.4 nm confirms presence of
silver nanoparticles.[23]
Chemical composition of Leaf
Physicochemical studies suggest that the drug moisture
minimizes on drying of leaves, inorganic materials in
total ash content, acid insoluble ash, along with
extractive values that are water and alcohol soluble.[24]
The qualitative analysis of powered, methanolic,
petroleum ether and water extract of leaf shows presence
of glycosides, alkaloids, flavonoids, tannin, fats and
fixed oils, terpenoids, steroids, phenolics compound and
resin.[17,24,25] Physico-chemical analysis of powdered leaf
applying HPTLC technique shows foreign matters, loss
on drying, alcohol soluble extractive, water soluble
extractive, total ash and acid in soluble ash in the range
2.93, 5.22, 4.17, 12.56, 13.68 and 3.12%, respectively.[17]
UV spectrum analysis of pure fraction of leaf shows
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Anti-microbial activities
Plant leaf powder shows moderate effect on gram
positive bacteria Streptococcus and Staphylococcus
aureus.[24] The mixture of plant leave and its ghrita base
in different concentration shows antibacterial activity
against gram negative- P. aeruginosa and E. coli, and
gram positive- S. pyogenes and S. aureus bacteria.[28]
Water and n-hexane extract of leaf exhibited effective
action against gram-positive bacteria Bacillus subtilis
and fungi Aspergilus niger after 12 hrs.[29] Dhal et al.[23]
observed that silver nanoparticles synthesized from plant
stem extract showed high degree of antibacterial activity
against S. aureus, Citrobacter sp. and Klebsiella sp. with
15.1 mm, 14.0 mm and 11.9mm zone of inhibition,
respectively.
The ethanolic bark extract at 100 mg/ml shows
significant antibacterial activity against Comamonas
testosteroni and Pseudomonas plecoglossicida with 7
and 9mm zone of inhibition. Petroleum ether bark extract
of the plant shows significant inhibition of two grampositive bacteria
Streptococcus pyogenes
and
Staphylococcus aureus, and two gram-negative bacteria
Pseudomonas aeruginosa and Escherichia coli.[30] The
chloroform leaf extract exhibit significant anti-fungal
activity against Aspergillus niger, Candida albicans and
Aspergillus clavatus compared to standard drugs.
Moreover, chloroform leaf extract and ethyl acetate leaf
extract shows better anti-malarial activity against
Plasmoduim falciparum.[31]
Anti-oxidant activities
Qureshi et al.[32] reported leaf ethanolic extract at 800
lg/ml dose exhibit maximum inhibition of DPPH and
nitric oxide radicals 81.20 and 72.70%, respectively.
Further, ethanolic extract in the same dose was found
effective in inhibiting reducing power and iron chelation
with absorbance mean of 1.53 and 0.433, respectively in
animal models. The ligand cordia-1, an important
phytochemicals of the plant binds with anti-oxidant
enzymes Catalase (CAT), Super oxide dismutase (SOD)
and Glutathione peroxidase (GPx) showing scavenging
action, and have wider impact on anti-oxidant
activities.[33]
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Antihypertensive activities
Dikshit and Jaishwal[34] investigated that dadhimanth
powder obtained from leaves, administered 3-6 gm twice
daily in plain water for one month, reduces hypertension
and also found significant in controlling blood urea.
Wound-healing activities
The plant leaves exhibit low degree of wound healing
capacity. The external application of 100 g dose of plant
leaf powder shows wound healing in wistar rats after 29
days with 88% healing capacity. Moreover, the incision
wound shows nearly 318 g/100g body weight tensile
strength along with neo- vascularization in the dead
space wounds, presenting weak recovery in tested animal
model.[35] However, Sharma et al.[36] observed that
formulation of fresh leaf powder and Cow’s ghrita shows
high percentage of relief from wound healing after third
week of application. The unhealthy granules, discharge
and wound margin were effectively controlled whereas
wound floor, wound size and swelling exhibit promising
reduction. The wound colour, pain and tenderness show
significant changes in the tested patient after 21 days.
Anti-venom activities
Ethanolic bark extract with a dose of 400 and 800 mg/kg
has potentiality in inhibiting Naja venom induced
hemorrhagic lesion, lethality, edema and necrotizing
lesion in male Wistar albino rats.[37]
Hepatoprotective activities
The plants like C. macleodii and others, with effective
chemical constituents show better efficacies against liver
diseases.[38] Qureshi et al.[32] reported the efficacy of leaf
ethanolic extract against CCl4 induced hepatotoxicity in
rats and observed that the dose of 400 mg/kg minimize
the elevation of glutamic pyruvic transaminase
(GPT), glutamic oxaloacetic transaminase (GOT),
alkaline phosphatase (ALP) and Bilirubin up to 23.2 U/I,
25 U/I, 81 U/I and 0.43 mg/dl, along with reducing liver
weight to 6.38 g, respectively. The hepatoprotective
action of stem bark and leaf was also confirmed by other
research works.[39] Shukla et al.[40] reported
hepatoprotective activity of aqueous and ethanolic bark
extract in ethanol and CCl4 induced hepatotoxicity in
male wistar rats. In both the cases, the extract reduces
level of Serum glutamic Pyruvate transaminase (SGPT)
enzyme activity in liver. Further, these extract shows
significant reduction in the level of mitochondrial
enzyme serum Glutamic Oxaloacetic Transaminase
(SGOT) and Alkaline phosphatase (ALP) an enzyme
obtained from hepatic parenchyma, along with
maintaining liver weight.
Chronic diseases
Khan[41] reported that cordia-1((4 5)-1formy 1-4dihydroxy-3oxo 3-4 dihydro-2H-pyran-1-ium) molecular
formula C6H7O5, a bioactive molecule obtained from C.
macleodii has potential in binding and blocking mitogenactivated protein kinases (MAPKs) thus used to develop
drug against chronic diseases like Alzheimer's, Cancer,
Parkinson's, amyotrophic lateral sclerosis, neurological,
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diabetes, cardiovascular, pulmonary and inflammatory
bowel diseases.
CONCLUSION
In conclusion Cordia macleodii although a threatened
species, is an important medicinal plant with highly
significant bioactive compounds. The continuous
exploitation of this species for various economic uses by
human civilization has created a great havoc to this
valuable taxa, thus there is a need to preserve this species
for its sustainable socio-economic uses. The global
scientific communities should take special responsibility
to carry detailed study on its internal composition for
developing new drugs formulation used to combat
various chronic diseases and to prepare medicine to fight
common stresses like hypertension, cardiac and neural
disorders. However, the first and foremost things to be
applied is, proper identification, nomenclature and
increasing species population through tissue culture or
mother nursery techniques and above all the conservation
of mother species throughout the globe.
REFERENCES
1. Ozturk M, Hakeem KR. Plant and Human Health,
Pharmacology and Therapeutic Uses. 3rd ed.
Springer International Publishing. 2019.
2. Koparde AA, Doijad RC, Magdum CS. Natural
Products in Drug Discovery. Open access peerreviewed chapter. 2019.
3. Jain C, Khatana S, Vijayvergia R. Bioactivity of
secondary metabolites of various plants: a review.
Int J Pharm Sci & Res, 2019; 10: 494-504.
4. Bukar BB, Dayom DW, Uguru MO. The Growing
Economic Importance of Medicinal Plants and The
Need For Developing Countries To Harness From it:
A Mini Review. IOSR Journal of Pharmacy 2016; 6:
42-52.
5. Kumar S, Pandey S. An ethnobotanical study of
local plants and their medicinal importance in Tons
river area, Dehradun, Uttarakhand. Indian J Trop
Biodiv 2015; 23: 227-231.
6. Pandey S, Shukla A, Pandey S, Pandey A. An
overview
of
resurrecting
herb
‘Sanjeevani’(Selaginella
bryopteris)
and
its
pharmacological and ethnomedicinal uses. The
Pharma Innovation Journal 2017; 6: 11-14.
7. Pandey S. Antibacterial and antifungal activities of
Ocimum gratissimum L. Int J Pharm and Pharmaceul
Sci 2017; 9: 26-31.
8. Pandey S, Singh SK, Kumar N, Manjhi R. Antiviral,
antiprotozoal, antimalarial and insecticidal activities
of Ocimum gratissimum L. Asian J Pharmaceu Res
Devp 2017; 5:1-9.
9. Pandey S. Ethnomedicinal potential of Sarcostemma
acidum in different regions in India. Asian J
Pharmaceu Clini Res 2018; 11: 395-400.
10. Pandey S, Sharma A, Panika G, Kumar M.
Morphological studies, traditional and industrial
uses of Bixa Orellana. A review. Curr Sci Int 2019;
8: 70-74.
ISO 9001:2015 Certified Journal
│
218
Pandey et al.
World Journal of Pharmaceutical and Life Science
11. Pandey S, Shukla A, Pandey S, Pandey A.
Morphology, chemical composition and therapeutic
potential of Somlata (Sarcostemma acidum Wight.
& Arn.). Pharma Sci Monitor 2017; 8: 54-60.
12. Pandey
S.
Phytochemical
constituents,
pharmacological and traditional uses of Ocimum
gratissimum L in tropics. Ind Am J P Sci 2017; 4:
4234-4242.
13. Pandey S, Kushwaha GR, Singh A, Singh A.
Chemical composition and medicinal uses of
Anacyclus pyrethrum. Pharma Sci Monitor 2018; 9:
551-560.
14. Pandey S. Morphology, chemical composition and
therapeutic potential of Stevia rebaudiana. Indo Am
J P Sci 2018; 5: 2260-2266.
15. Pandey S, Patel A, Singh B, Gupta RK.
Morphological, anatomical and phytochemical
screening of medicinal herb Boerhaavia diffusa L.
Int J Adv Innov Res 2019; 6: 96-100.
16. Kumar V, Tiwari SS, Shukla AN, Srivastava S,
Rawat AKS. Pharmacognostic and phytochemical
evaluation of Cordia macleodii. Journal of
Medicinal and Aromatic Plant Sciences 2011; 33:
59-63.
17. Kushwaha
J,
Singh
R,
Tripathi
MK.
Pharmacognostic and phytochemical evaluation of
Cordia macleodii (Hook. F & Thomson). EJPMR
2015; 2: 823-831.
18. Nariya PB, Shukla VJ, Nariya MB, Bhatt PV, Pandit
CM, Acharya RN. et al., Isolation and
characterization of phytosterols from Cordia
macleodii (Hook F. and Thomson) bark by
chromatographic and spectroscopic method. Asian
Journal of Pharmaceutical and Clinical Research
2014; 7: 86-88.
19. Nayak P, Kalidass C. Ethnobotany, Phytochemistry,
Pharmacognostic and Pharmacological Aspects of
Cordia macleodii Hook.f. & Thomson - A review.
Journal of Non-timber forest products 2016; 23: 6771.
20. Chaubey ON, Upadhyay R, Tripathi NK, Ranjan A.
Isolations & Characterization of Compounds from
Cordia macleodii Hook Bark & Leaves. IOSR
Journal of Applied Chemistry 2016; 9: 83-85.
21. Nariya PKB, Shukla VJ, Acharya R, Nariya MKB.
Isolation and simultaneous determination of three
biologically active flavonoids from some
indigenous Cordia species
by
thin-layer
chromatography with UV absorption densitometry
method. Journal of Planar Chromatography-Modern
TLC 2017; 30.
22. Wanjari AK. Adsorption of manganese (II) by nitric
acid treated granular activated charcoal prepared
from Cordia Macleodii tree bark. Der Pharma
Chemica 2016; 8: 87-94.
23. Dhal S, Panda SS, Rout NC, Dhal NK. Biosynthesis
of silver nanoparticles using Cordia macleodii
(Griff.) Hook. F & Thomas and its antibacterial
activity. World J Pharm Sci 2014; 2: 1051-1057.
www.wjpls.org
│
Vol 6, Issue 12, 2020.
│
24. Bhide B, Pillai APG, Shukla VJ, Acharya RN.
Pharmacognostic evaluation of leaf of Cordia
macleodii Hook.: An ethnomedicinally important
plant. AYU 2011; 32: 254-257.
25. Gamit R, Patel AG, Shukla VJ, Nariya MB, Acharya
RN. Phytochemical analysis of successive extracts
of the Cordia macleodii leaves Hook.: A Folklore
medicinal plant. Journal of Ayurvedic and Herbal
Medicine 2018; 4: 14-17.
26. Wanjari AK, Chaudhari UE, Wanjari NW, Barde
MP, Kumre ND. Characterization of chloroform
extract of Cordia macleodii leaf for possible
application in dye sensitized solar cell. IJESRT
2016; 5: 705-708.
27. Oza MJ, Kulkarni YA. Traditional uses,
phytochemistry and pharmacology of the medicinal
species of the genus Cordia (Boraginaceae). Journal
of Pharmacy and Pharmacology 2017; 69: 755–789.
28. Sharma A, Acharya RN, Shukla VJ, Gupta SK. A
comparative antimicrobial study on Cordia
macleodii. hook leaf water extract and its ghrita base
formulation. International Journal of Ayurvedic
Medicine 2013; 4: 9-16.
29. Joshi DK, Patel R, Patel N, Patel D, Pandya C.
Antimicrobial Evaluation of Leaf and Stem Extract
of Cordia macleodii. Open Pharmaceutical Sciences
Journal 2014; 1: 1-3.
30. Chaubey ON, Upadhyay R, Tripathi NK, Ranjan A.
Comparative antimicrobial study of Cordia
macleodii Hook. IOSR Journal of Pharmacy and
Biological Sciences 2015; 10: 1-3.
31. Gamit SB, Sapra P, Vasava MS, Solanki HA, Patel
H, Dhanji R. Antimicrobial and antimalarial
activities of some selected ethno-medicinal plants
used by tribal communities of Tapi District, Gujarat,
India. Int Res J Pharm 2018; 9:151-156.
32. Qureshi NN, Kuchekar BS, Logade NA, Haleem
MA. Antioxidant and hepatoprotective activity of
Cordia macleodii leaves. Saudi pharmaceutical
journal 2009; 17: 299–302.
33. Khan MN, Qureshi J, Kaushar H, Pusham N. Silico
Analyses of Antioxidant-Related Compounds on
Selected Medicinal Plant Cordia macleodii EnzymeBased Targets. AJB2T 2018; Article no. AJB2T
41131, 4: 1-9.
34. Dikshit M, Jaiswal ML. A Study of
Antihypertensive Action of Dadhimanth Hook
(Cordia macleodii.f. and Thomson.). Journal of
Ayurveda 2011; V: 58-65.
35. Bhide B, Ashok BK, Acharya RN, Ravishankar B.
Anti-microbial and wound healing activities
of Cordia macleodii Hook. f & Thoms. Leaves.
Indian J Nat Prod Res 2011; 2:198-203.
36. Sharma A, Acharya RN, Gupta SK, Dudhamal TS,
Mohanto VD. Clinical evaluation of Shikari (Cordia
macleodii) ghrita on vrana ropana (wound healing)
property. Ayurpharm Int J Ayur Alli Sci 2013; 2:
98–104.
37. Soni P, Bodakhe SH. Antivenom potential of
ethanolic extract of Cordia macleodii bark against
ISO 9001:2015 Certified Journal
│
219
Pandey et al.
38.
39.
40.
41.
World Journal of Pharmaceutical and Life Science
Naja venom. Asian Pac J Trop Biomed 2014;
4(Suppl 1): S449-S454.
Verma R. A review on hepatoprotective activity of
medicinal plants. Journal of Medicinal Plants
Studies 2018; 6: 188-190.
Pandey G. Medicinal plants against Liver diseases.
IRJP 2011; 2:115-121.
Shukla P, Patel R, Saraswat R. Evaluation of
hepatoprotective activity on the leaves of Cordia
macleodii. Pramana Research Journal 2019; 9: 337347.
Khan MN. MAPK signaling protein molecular target
of Cordia macleodii phytochemicals for prevention
of chronic diseases. IOSR Journal of Engineering
(IOSRJEN) 2018; 8: 54-60.
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