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141| P a g e International Standard Serial Number (ISSN): 2319-8141
Full Text Available On www.ijupbs.com
International Journal of Universal Pharmacy and Bio Sciences 6(3): May-June 2017
INTERNATIONAL JOURNAL OF UNIVERSAL
PHARMACY AND BIO SCIENCES IMPACT FACTOR 2.96***
ICV 6.16***
Pharmaceutical Sciences REVIEW ARTICLE …………!!!
A REVIEW ON PLANTS HAVING ANTI-MALARIAL ACTIVITY
Arzoo* and Parina Kumari
Assistant professor of Pharmacology, Shri ram college of pharmacy, Ramba, Karnal,
India.
KEYWORDS:
Malaria, Anti- Malarial
activity, Medicinal
Plants, WHO, Drugs
resistance.
For Correspondence:
Arzoo *
Address:
Assistant professor of
Pharmacology, Shri ram
college of pharmacy,
Ramba, Karnal, India.
ABSTRACT
Malaria has long been recognized as a crucial as well life- threatening
parasitic disease of humans caused by parasites transmitted to human by
bite of female anopheles mosquitoes. There are about 3-500 million
clinical cases of per year and 1.5-2.7 million deaths annually worldwide
just because of malaria. The parasite passes through several stages of
development such as the sporozoites, merozoites, trophozoites and
gametocytes. The symptoms of malaria typically develop within 10 days
to four weeks following the infection. The complications due to malaria
mimic many diseases, so physical examination and blood examination
should be done carefully to confirm the diagnosis. Nations agencies
WHO, UNICEF and UNDP, together with the World Bank, on 30
October 1998, launched the roll back malaria (RBM) initiative, as a bold
new effort to mobilize global partnerships including governments,
donors, non-governmental organizations (NGOS) and communities, to
effectively tackle the increasing global problem of malaria. Now days,
besides the use of medicine for treating malaria, personal protection is
more preferable such as insecticide-treated mosquito nets, mosquito
coils, body repellents and insecticide spraying. In the era of 21st
century
the drug resistance have become a problem. Therefore, the use of
traditional medicines is still on the rise. There are a number of
unidentified plants in the world that can be used as a source of remedy
for malaria. In this review we try to summarize the already documented
plants having anti-malarial activity.
142 | P a g e International Standard Serial Number (ISSN): 2319-8141
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1. INTRODUCTION
Malaria has long been recognized as a crucial parasitic disease of humans a major public health
problem. It is life- threatening blood disease caused by parasites transmitted to human by bite of
female anopheles mosquitoes. Malaria is usually found in tropical and subtropical climates where
the parasites that cause it live. There are about 3-500 million clinical cases of per year and 1.5-2.7
million deaths annually worldwide just because of malaria. Malaria parasite has a complex as well
multistage life cycle [1], [2]. The parasite passes through several stages of development such as the
sporozoites (sporos = seeds; the infectious form injected by the mosquito), merozoites (meros =
piece; the stage invading the erythrocytes), trophozoites (trophes = nourishment; the form
multiplying in erythrocytes), and gametocytes (sexual stages). During these different stages the
parasites have their own unique shapes, structures and protein complements, which keep changing
during different stages. The symptoms of malaria typically develop within 10 days to four weeks
following the infection. Malaria is transmitted by blood, an organ transplant, a transfusion or use of
shared needles or syringes. An early diagnosis of malaria in young children and in pregnant women
is necessary because they may rapidly become very ill and may die within a few days. An infected
mother can also pass the disease to her baby at birth. This is known as congenital malaria [1], [2],
[3].
The complications due to malaria mimic many diseases, so physical examination and blood
examination should be done carefully to confirm the diagnosis. Pregnancy reduces the immune
status of individuals as well as is more difficult to treat, because the parasites tend to hide in the
placenta, making diagnosis and treatment difficult. Therefore, the patient must be monitored closely
to recognize, prevent and treat complications.
Malaria’s cost to human and social well-being is enormous. Several costly medications are
available to prevent malaria in different areas where the disease is common. Malaria is treated with
anti-malarial medications such as chloroquine, doxycycline, amodiaquine, lumefantrine,
mefloquine or sulfadoxine/pyrimethamine ( Table-1). Now drug resistance posses a growing
problem in 21st-century against all classes of anti-malarial drugs apart from artemisinins such as
chloroquine resistant (reported in north Africa, the middle east, rural areas of Mexico, central
America, north and west of the panama canal), pyrimethamine/sulfadoxine resistance ( reported in
south east Asia, the Indian subcontinent, the Amazon basin, many countries in Africa south of the
Sahara and Oceania), mefloquine resistance (reported in south east Asia especially in Thailand,
parts of Africa and south America, the middle east, and Oceania), quinine resistance (reported in
south east Asia, parts of Africa, Brazil and Oceania), halofantrine resistance (reported in Thailand).
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But, the cost of artemisinins limits their use in the developing world. Therefore, prevention of
malaria may be more cost-effective than its treatment [4].
WHO has prioritized four main strategies for malaria control worldwide, which were endorsed by
the global malaria conference for health ministers, held in Amsterdam in 1992 i) provision of early
diagnosis and prompt treatment, ii) planning and implementation of selective and sustainable
prevention measures including vector control, iii) early detection, containment and prevention of
epidemics iv) strengthening of local capacities in basic and applied research, for regular assessment
of the malaria situation within countries. The United Nations agencies WHO, UNICEF and UNDP,
together with the World Bank, on 30 October 1998, launched the roll back malaria (RBM)
initiative, as a bold new effort to mobilize global partnerships including governments, donors, non-
governmental organizations (NGOS) and communities, to effectively tackle the increasing global
problem of malaria. RBM aims at reducing overall mortality due to malaria by 50% by the year
2010. The RBM movement has now been accepted by many heads of state in Africa with the
assistance of the international community who have expressed strong commitment to intensify
malaria prevention and control [5], [6].
Now days, besides the use of medicine for treating malaria, personal protection is more preferable.
In malaria prevention and control, use of insecticide-treated mosquito nets, mosquito coils, body
repellents and insecticide spraying has become a leading strategy. Another way of treating malaria
is use of traditional medicine without any side-effects. There are many traditional anti-malarial
drugs have been used to treat malaria for thousands of years. These anti-malarial plants contain
active constituents which are responsible for their medicinal properties such as artemisinin and
quinine derivatives. In order to develop a cost –effective treatment for the malaria, the development
and identification of safe and effective anti-malarial medicinal plants should be done. In this
review, we try our best to summarize the natural plant having anti-malarial activity.
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Table- 1: Target for anti-malarial chemotherapy [7]
Target
location
Pathway /
mechanism
Target molecules Existing
compounds
Newer compounds
Cytosol Folate metabolism
Glycolysis
Protein synthesis
Glutathione
metabolism
Signal transduction
Unknown
Dihydrofolate reductase
Dihydropteroate synthase
Thymidylate synthase
Lactate dehydrogenase
Peptide deformylase
Heat-shock protein 90
Glutathione reductase
Protein kinases
Ca2+-ATPase
Pyrimethamie,
Proguanil, dapsone,
Sulphadoxine
Artemisinins
Chlorproguanil
5-fluoroorotate
Gossypol derivatives
Actinonin
Geldanamycin
Enzyme inhibitors
Oxindole
derivatives
Parasite
membrane
Phospholipid
Synthesis
Membrane
Transport
Choline transporter
Unique channels
Hexose transporter
Quinolines
G25
Dinucleoside dimers
Hexose derivatives
Food
Vacuole
Haempolymerizatin
Haemoglobin
hydrolysis
Free-radical
Haemozoin,
Plasmepsins,
Falcipains
Unknown
Chloroquine
Artemisinins
New quinolines
Protease inhibitors,
Protease inhibitors
New peroxides
Mitochondria Electron transport Cytochrome c
Oxidoreductase
Atovaquone
Apicoplast Protein synthesis
DNA synthesis
Transcription
Type II fatty acid
BIOSYNTHESIS
Isoprenoid
synthesis
Protein
farnesylation
Apicoplast Ribosome
DNA Gyrase
RNA Polymerase
FabH
FabI/PfENR
DOXP reductoisomerase
Farnesyl transferase
Tetracyclines,
clindamycin
Quinolones
Rifampin
Thiolactomycin
Triclosan
Fosmidomysin
Peptidomimetics
Extracellular Erythrocyte
Invasion
Subtilisin serine
Proteases
Protease inhibitors
145 | P a g e International Standard Serial Number (ISSN): 2319-8141
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SYMPTOMS [1], [8]
Generally, the symptoms of malaria develop within 10 days to four weeks following the infection.
In some people, these symptoms may not develop for several months because malarial parasites can
enter the body but will be dormant for long periods of time. Common symptoms of malaria include:
Shaking chills that can range from moderate to severe
High fever
Anorexia
Hepatomegaly: the liver may be slightly tender
Anemia
Jaundice: destruction of erythrocytes cause jaundice in malaria
Profuse sweating
Dehydration
Headache
Nausea
Vomiting
Diarrhoea
Anaemia
Muscle pain
Convulsions
Coma
Bloody stools
Yellow skin
Blood in urine
Life-threatening complications associated with malaria
An accumulation of fluid in the lungs that causes breathing problems, or pulmonary oedema
Organ failure of the kidneys, liver, or spleen
Swelling of the blood vessels of the brain, or cerebral malaria
Anaemia due to the destruction of red blood cells
Low blood sugar
HISTORY OF MALARIA
Malaria is the oldest and cumulatively the most virulent of the human infectious diseases, hastened
into very earliest human history. In 2700 BCE, NeiChing (Chinese Canon of Medicine) discussed
malaria symptoms and the relationship between fevers and enlarged spleens. Ebers Papyrus
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mentions fevers, rigors, splenomegaly, and oil from Balantines tree as mosquito repellent in1550
BCE. Hippocrates in Egypt was the first to make connection between nearness of stagnant bodies of
water and occurrence of fevers in local population. And he described malarial symptoms also, such
as paroxysmal fever, shaking chills, sweating. Malaria was once known as ague, a term of Italian
origin (from the Latin acuta meaning sharp, as in an acute fever). Although malaria primarily
associated with tropical climates, but we can see that malaria was historically also present in non-
tropical climates, from Britain to the south-eastern United States. It is hypothecated that Alexander
the Great may have died of malaria in Babylonia.
The British Empire amplified into tropical regions of Africa, India and the Caribbean and has the
risk of exposure to malaria. As malaria was one of the most common, debilitating and so deadly
that West Africa earned the nickname “the white man’s grave”. The malarial fevers often resulted
in increased susceptibility to other diseases. Therefore, significantly to decrease the death rate of
populations, it was necessary to solve the puzzle of malaria. Spanish conquistadors and Jesuit
missionaries in South America entered the Amazonian jungles in search of indigenous peoples to
convert to Christian. Thus far, Cinchona spp., as well as Artemisia annua, was discovered for
Plasmodium treatment. In the 15th
century, the Spaniards Juan Fragoso and Nicolas Monardes,
wrote the first known record about cinchona as a malaria remedy. South American Indians had used
cinchona brews for fevers and other conditions, which called as “quinas”. In 1633 Calancha of
Lima (an Augustinian monk), wrote that a powder of quina, a Native American word meaning bark
“given as a beverage, cures the fevers and tertian”. By 1643, Jesuits import and distribute the
cinchona bark to the Europe. Therefore, in European medical literature this remedy earned the
name “Jesuit’s bark” in the British apothecaries.
In 17th
century, according to PC Garnham, an earthquake caused destruction in Loxain which make
many cinchona trees collapsed and fell into small lake or pond. Then water became very bitter as to
be almost undrinkable. Yet an Indian so thirsty with a violent fever quenched his thirst with this
cinchona bark contaminated water and was better in a day or two. Alternatively, Indians working in
mountain mines drank cinchona tea to stop shivering. In the late 17th century, the famed physician
Francesco Torti began using high doses of the powdered bark at the first signs of malarial fevers.
This eventually encouraged fellow physicians also to follow his protocol.
The German chemist Sertürner’s in 1805, isolated the morphine from opium poppy (Papaver
somniferum Papaveraceae). In 1820, Pelletier and Caventou (French chemist-pharmacists) isolated
quinine out of the 30 + alkaloids in cinchona. Charles Louis Alphonse Laveran (the military
surgeon) in 1880, observed the pigment in cyst-like bodies within red blood cells. And this made
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him realize that these bodies were the parasite of the 4 species of malaria parasites that infect
humans Plasmodium falciparum, P. vivax, P. ovale, P. malariae and P. falciparum.
During World War II the United States military experimented with a mixture of cinchona alkaloids
named totaquine (containing 7 – 12% anhydrous quinine, and 70 – 80% of total anhydrous
crystallizable cinchona alkaloids). The military found that totaquine was as effective as quinine in
terminating acute attacks of malaria, but had a slightly higher rate of nausea and blurred vision.
However, they also found two alkaloids cinchonine and cinchonidine were less toxic than quinine.
A more recent study has done with a mixture of these three of the chinchona alkaloids, quinine,
quinidine, and cinchonine, showing a synergic effect against a culture of P. Falciparum. Today,
Studies with plants traditionally used for malaria treatment from various parts of the world as the
multi-drug resistance has become a leading obstacle to curing malaria and protecting against
infection.
MALARIA MOSQUITO LIFE [1]
In the world there are many different kinds of mosquitoes exist, but only female Anopheles
mosquitoes is responsible for passage of malaria parasites. The Anopheles mosquito can be
recognized by its upturning tail. The Anopheles mosquito needs blood to produce eggs. These eggs
are very small (2-5mm wide) and can be seen as small black spots on the surface of water. The
malaria mosquito chooses slow-flowing water to lay her eggs. After two or three days the eggs are
laid on the water, mosquito larva as come out of each egg. The larva feeds on microscopic
organisms and plants in the water. Then larva grows until it becomes a pupa. The pupa remains in
the water, but does not feed. A mosquito egg, larva or pupa does not have malaria parasites inside
it. After a few days the adult mosquito comes out of the pupa and flies away. After feeding, the
mosquito usually rests on a nearby surface before it flies away. Then it laid eggs and the cycle starts
all over again. It takes 7-14 days for a mosquito to grow from an egg to an adult mosquito. If adult
mosquitoes have bitten someone who has malaria, then they may have malaria parasites in their
bodies. The average lifespan of the mosquito is roughly the same as the time taken for the parasite
to go through its growth and development. The survival of the parasite depends upon the weather.
Once the average temperature drops below a certain point, the mosquito tends to die before it can
transmit malaria.
RECOGNIZATION OF MALARIA [1],[2]
It is difficult to judge a sickness is caused by malaria or some other disease, because the features
may be similar. For the enquiry ask the patient, whether there has been any fever at any time during
the past 2-3 days. Patients who have had fever during the last 2-3 days may have malaria. In this
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case, ask and then look for danger signs such as changes in behaviour (convulsions (fits);
unconsciousness; sleepiness; confusion; inability to walk, sit, speak or recognize relatives),
repeated vomiting; inability to retain oral medication; inability to eat or to drink, passage of small
quantities of urine or no urine, or passage of dark urine, severe diarrhoea, unexplained heavy
bleeding from nose, gums, or other sites, high fever (above 39 degrees centigrade), severe
dehydration (loose skin and sunken eyes), anaemia (look at the patient’s facial colour and hands –
the palms of a patient with anaemia do not have the redness of a healthy person’s palms),
yellowness of the eyes.
LIFE CYCLE OF MALARIA [1]
The malaria parasite life cycle involves two hosts: human and female Anapheles mosquitoes. There
are four main species of malaria parasites Plasmodium falciparum, Plasmodium vivax, ovale and
malariae. Plasmodium falciparum causes the severest type of malaria, and the other three species
cause less severe symptoms. Malaria is transmitted through the bite of an infected, female
Anopheles mosquito through blood transfusion. Whenever a mosquito bites a person, it sucks up
blood. If the person has malaria then some of the parasites transmitted into the mosquito. After 10-
14 days, malaria parasites are found in mosquitoes’ salivary glands. Then, the parasites multiply
and develop in the mosquito and after they are mature and ready to passed on to someone else.
Now, when the mosquito bites a healthy person, then the malaria parasites enter the body of the
healthy person. The parasites are transported in the victim's liver by bloodstream. In the liver
malaria parasite multiply and then re-enter the bloodstream. The malaria parasites destroyed the red
blood cells as well as infecting new cells. The victim will become ill with malaria and symptoms
appearing from about a week to several months after infection.
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When malaria infected female anopheles mosquito bites a human host, it inoculates sporozoites into
the human blood stream of malaria’s next victim. The sporozoites are rapidly taken up by the liver
cells and mature into schizonts (the multinucleate stage of the cell during asexual reproduction)
which rupture and release merozoites. This stage is known as exo-erythrocytic schizogony cycle.
The released merozoites rapidly invade the red blood cells replicate asexually and destroying each
red blood cell they infect, leading to the clinical symptoms of malaria. Within 48 to 72 hours, the
parasites inside the red blood cells multiply, causing the infected cells to burst open. The ring stage
trophozoites mature into schizonts, which rupture releasing merozoites. This stage is known as
erythrocytes. Some of the ring stage trophozoites become mature trophozoites, which further
differentiate into sexual stages (gametocytes). The gametocytes, male (microgametocytes) and
female (macrogametocytes), are ingested by an Anopheles mosquito during a blood meal. It is these
gametocytes that cause the cycle of transmission to continue back to the mosquito. The parasites’
multiplication in the mosquito is known as the sporogonic cycle. In this cycle the microgametes
penetrate the macrogametes generating diploid zygotes in the mosquito's stomach. The diploid
zygotes in turn become motile and elongated ookinetes. These ookinetes migrate to the midgut of
the insect, pass through the gut wall and form the oocysts. The oocysts grow, rupture, and release
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sporozoites, which make their way to the mosquito's salivary glands. Inoculation of the sporozoites
into a new human host perpetuates the malaria life cycle.
PLANTS HAVING ANT-MALARIAL ACTIVITY
The following plants are documented for their anti-malarial activity.
Table- 2: Medicinal plants having anti-malarial activity [9-40]
Sr. No. Botanical name Common name Part used
1. Acacia albida Apple Ring Acacia Bark
2. Acacia nilotica Babul Root, Bark, Seed
3. Acacia sieberiana Paperbark Thorn Root
4. Acanthospermum hispidum Starbur Roots, Leaf
5. Adansonia digitata Monkey Bread Bark
6. Albizia amara Bitter Albizia Fruit
7. Albizia zygia Lakpokpo Bark
8. Alchornea laxiflora Murunda-malofha Leaf, Root
9. Alchorneacordifolia Christmas Bush Leaf
10. Allium cepa Onions Bulb
11. Allium sativum Garlic Bulb
12. Aloe vera Aloe, Kumari Leaf
13. Anacardium occidentale Cashew Leaf, Stem
14. Ananas comosus Pineapple Bark
15. Annona muricata Soursop Fruit, Leaf
16. Annona senegalensis Custard-Apple Leaf
17. Anogeissus leiocarpus African Birch Leaf, Bark, Stem
18. Arachis hypogeal Peanut Seed
19. Aradirachta indica Sunsugree Leaf
20. Artemisia maeiverae Pasture Sage Whole Plant
21. Asparagus racemosus Shatavri Leaf
22. Asparagus remota Satavar Leaf
23. Azadirachta indica Neem Leaf, Stem, Bark, Root,
Fruit
24. Balanites aegyptiaca Desert Date Bark
25. Bauhinia strychnifolia White orchid tree Leaf
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26. Boswellia dalzielii Boswellia Bark
27. Bothriocline longipes Ekyoganyanja Leaf
28. Brassica Nigra Black mustard Seeds
29. Caesalpinia bonducella Grey nicker Root
30. Cajanus cajan Pigeon Pea Leaf
31. Capsicum frutescens Chili Pepper Fruit
32. Carica papaya Papaya Leaf, Fruit
33. Carissa edulis Akamba Root
34. Carpobrotus edulis Ice- plant Root
35. Cassia occidentalis Senna Leaf
36. Cassia sieberiana Nansaalesunsugree Leaf
37. Chenopodium ambrosio¨ıdes Goosefoot Leaf
38. Chenopodium opulifolium Seaport Goosefoot Leaf
39. Chrysanthellum americanum Wild Daisy Whole Plant
40. Cissampelos pareira Velvet Leaf Bark
41. Citrus aurantifolia Lime Leaf, Fruit
42. Citrus limonum Lemon Fruits, Leaf
43. Citrus sinensis Sweet Orange Leaf
44. Cleome viscosa Dog mustard Whole plant
45. Clerodendrum myricoides Bagflower Leaf
46. Clerodendrum rotundifolium Glorybower Leaf, Root
47. Clutia abbysinica Groot-bliksembos Root
48. Cochlospermumtinctorium Gbalenbili Roots
49. Coffea canephora Robusta Coffee Leaf
50. Combretum molle Mubondo Leaf
51. Combretumghasalense Bushwillows Leaf
52. Conyza sp. Horseweed Leaf, Bark
53. Conyza sumatrensis Fleabane Leaf
54. Corchorus olitorius Nalta Jute Seed
55. Cymbopogon citrates Lemon Grass Leaf
56. Dalbergia nitidula Pea Leaf, Root, Bark
57. Diospyros mesiliformis Ebony Tree Stem, Bark
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58. Erlangea cordifolia (oliv.)
S.moore
Roquette Leaf, Root
59. Erythrina schliebenii Sassywood Bark
60. Erythrophleum suaveolens Ordeal Tree Leaf, Root
61. Eucalyptus globu Eucalyptus Leaf, Bark
62. Ficus platyphylla Gutta Percha Leaf, Barks
63. Ficus polita Wild Rubber Tree Leaf, Barks
64. Ficus thonningii Blume Strangler fig Leaf
65. Flueggea virosa Bushweed Root
66. Fuerstia africana Birirwo Whole plant
67. Gnidia kraussiana Yellow-Heads Leaf
68. Gossypium arboreum Tree Cotton Leaf
69. Guiera senegalensis Moshi Medicine Leaf
70. Gynostemma pentaphyllums Miracle grass Leaf
71. Haemastotaphis barteri Tursujee Ripe Fruits, Leaf
72. Harrisonia abyssinica Msamburini Leaf
73. Hibiscus cannabinus Kenaf Leaf
74. Hibiscus sabdariffa Roselle Flowers
75. Himatanthus articulatus Vahl Stem, bark
76. Holarrhena pubescens Kurchi Roots
77. Hoslundiaopposita Nyegimaalee Leaf
78. Hyptis spicigera Marubio Whole Plant
79. Jatropha curcas Barbados Nut Leaf,Seed
80. Kalancho¨e densiflora Flaming Katy Leaf
81. Kalanchoe pinnata lam Kataka-Taka Leaf
82. Khaya senegalensis Koke Leaf, Fruit, Root, Stem,
Bark
83. Lanea acida Atina Bateri Stem, Bark
84. Lannea discolour Bakhout Bark And Root
85. Lanneaacida Bembé Leaf
86. Lantana camara Yellow Sage Leaf
87. Lantana trifolia Shrub Verbena Leaf, Root
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88. Leonotis nepetifolia Lion's Ear, Bara
Guma
Leaf
89. Leptadenia hastate Pers Root
90. Lippiaadoensis Koseret Leaf
91. Lophira alata Red ironwood Tree Leaf
92. Maesa lanceolata forssk Omuhanga Leaf, Bark
93. Magifera indica Mango Leaf, Stem, Bark
94. Markhamia tomentosa Balanta Leaf
95. Melia azedarach Chinaberry Leaf
96. Microglossa pyrifolia Kuntze Leaf
97. Mitragynainermis Dondoleeyeelee Leaf, Twig
98. Momordica foetida Karela Leaf
99. Morinda lucida Brimstone Tree Root
100. Moringa oleifera Drumstick Tree Leaf
101. Musa sapientum Banana Leaf
102. Musa sinensis Banana Leaf, Root
103. Nicotiana tabaccum l. Tobacco Leaf
104. Ocimum basilicum Sweet Basil Leaf
105. Ocimum gratissimum Clove Basil Leaf
106. Parkia biglobosa Locust Bean Root
107. Paulina pinnata Naahoonyeko Biri Leaf
108. Pennisetum glaucum Pearl Millet Roots, Seed
109. Pentas lanceolata Egyptian Star cluster Whole plant
110. Persea Americana Avocado Leaf
111. Phyllanthus nummulariifolius Gale of wind Whole plant
112. Piliostigma thonningii Camel's Foot Tree Bark
113. Plectranthus forskahlii wild Coleus Leaf
114. Polyalthia longifolia Fir tree Leaf
115. Prosopis africana Iron Tree Leaf, Stem, Bark
116. Pseudarthria hookeri Bug Catcher Leaf, Root
117. Psidium gujava Guava Bark, Leaf
118. Pterocarpus erinaceus Barwood Root
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119. Ricinus communis Castorbean Fruit
120. Sclerocarya birrea Marula Bark
121. Securida longepedonculata Violet Tree Root
122. Senna dybomotrya Candelabra Tree Leaf
123. Senna occidentalis Coffee Seena Leaf
124. Senna tora Senna Seed
125. Sericocomopsis hildebrandtii
Schinz
Schin Whole plant
126. Sida rhombifolia Cuban Jute Leaf
127. Sidaacuta Bedawsaalong Leaf
128. Sorghum bicolour Jowari Root
129. Strychnosinnocua Yual Potiga Leaf
130. Talinum portulacifolium Flameflower Leaf
131. Tamarindusindica Tamarind Leaf, Stem, Bark
132. Theobroma cacao Cacao tree Leaf
133. Toddalia asiatica lam. Orange Climber Leaf, Root
134. Trichilia heudelotii Jasui Stem, bark
135. Tridax procumbens Coatbuttons Whole plant
136. Trimeria bakeri gilg Omwatanshare Roots
137. Vangueria infausta Wild Medlar Root, Leaf
138. Vernonia amygdalina Bitter Leaf Whole Plant
139. Vernonia lasiopus Onugbu Leaf, Root
140. Voandzei subterranean Bambara-Bean Seed
141. Ximenia americana Sea lemon Whole plant
142. Zanthoxylum chalybeum Mjafari Leaf
143. Zea mays Corn Flower
144. Zingiber officinale roscoe Ginger Root
145. Ziziphus abyssinica Catch Thorn Bark, Leaf
146. Ziziphus mauritiana Chinkee Apple Root
147. Satyrium princeae California Buckwheat Leaf
148. Leucas calostachys Oliv Leaf
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CONCLUSION
In the era of 21st
century the use of traditional medicines is still on the rise because of cost-effective,
safe and natural treatment. Therefore, herbal medicine can be a potential source for the
development of new anti-malarial drugs also. The different species of above mentioned medicinal
plants can be studied further for the anti-malarial activity. The active principle constituents
responsible for the anti-malarial activity present in these plants should be studied in order to spread
the results of this work at the national as well at the international level. There are a number of
unidentified plants in the world that can be used as a source of remedy for malaria. Thus, the
involvement of scientific community and governments is very important for the further
development of these anti-malarial plants which are effective against malaria.
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