Available via license: CC BY-NC 4.0
Content may be subject to copyright.
1
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
Potential ofmoringa (Moringa oleifera) leaf powder
for functional food ingredients: Areview
L N A1, T E2*, W B S2, A K3
1Department ofFood Science – doctoral program, Faculty ofAgricultural Technology,
Universitas Brawijaya, Malang, Indonesia
2Department ofFood Science and Technology, Faculty ofAgricultural Technology,
Universitas Brawijaya, Malang, Indonesia
3Kuliyyah ofPharmacy, International Islamic University ofMalaysia, Kuantan, Malaysia
*Corresponding author: teties@ub.ac.id
Citation: Ariani L.N., Estiasih T., Sunarharum W.B., Khatib A. (2023): Potential ofmoringa (Moringa oleifera) leaf powder for
functional food ingredients: Areview. Czech Journal ofFood Science.
Abstract: One of the efforts toproduce functional foods is using ingredients containing health-beneficial bioactive
compounds. Another way toproduce functional foods isfermentation generating bioactive compounds orfortification
with the bioactive compound extract. Aningredient historically believed tohave benefits onhealth ismoringa (Moringa
oleifera) leaf powder. Moringa leaf powder isavaluable source offunctional ingredients, including protein, vitamins,
minerals, and phytonutrients such ascarotenoids, tocopherols, polyphenols, flavonoids, alkaloids, and tannins. How-
ever, moringa isaplant that isdistributed invarious tropical countries inthe world. Its quality depends ongeographical
differences, cultivars, environmental conditions, seasons, genotypes, and varieties. is article reviews the bioactive
compounds ofmoringa leaf powder and the characteristics ofmoringa leaf powder extract. eeffect ofmoringa leaf
powder fortification onfood product characteristics isalso discussed. Moringa leaf powder possesses many pharma-
cological properties, such as anticancer, anti-inflammatory, hepatoprotective, cardioprotective, and antioxidant ones.
ebioactivity ofleaf extract isextracting solvent dependent. erefore, fortification results innutritional improvement
and increasing health benefits offood products. However, the adverse effect isfound insensory. us properties, thus
the moringa leaf powder fortification level usually isless than 10%. Changes inthe functional properties offoods due
tomoringa leaf powder fortification have been studied toalimited extent. Alow level offortification might not affect
the properties offood products. erefore, moringa leaf powder ispotentially used as afunctional food ingredient.
Some studies reported the toxicological effects ofmoringa leaf powder and the use ofthis ingredient, should bebelow
the harmful doses.
Keywords: bioactive compounds; fortification; leaf extract; phytochemicals
Supported bythe Universitas Brawijaya, Project No.975.9/UN10.C10/PN/2021.
© eauthors. is work islicensed under aCreative Commons Attribution-NonCommercial 4.0 International (CC BY-NC4.0).
Moringa oleifera isa miracle tree because of its nu-
merous uses and adaptability; it contains nutrients,
aswell assecondary metabolites that have health ben-
efits (Biswas et al. 2020; Zainab etal. 2020). In many
developing countries, moringa isused asaningredient
in traditional medicine (Magaji et al. 2020). Moringa
isatropical plant that isrich inbioactive compounds.
Moringa has pharmacological activities such as anti-
cancer, antidiabetic (Chigurupati et al. 2021), anti-in-
flammatory (Cuellar-Nunez etal.2021), and antioxidant
2
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
(Mahmoud etal.2022). epharmacological properties
ofmoringa are adequately related tothe presence ofits
bioactive compounds (Ma etal.2020). Moringa leaves
are effective asanantidiabetic (Chigurupati etal.2021).
Invitro and invivo studies confirmed various biological
activities such as antioxidant (Mahmoud et al. 2022),
anti-inflammatory (Cuellar-Nunez et al. 2021), anti-
diabetic (Mahmoud et al. 2022), anticancer (Kumar
et al. 2023), cardioprotective (Aju et al. 2020), hypo-
cholesterolemic (Chen et al. 2020), hepatoprotective
(Asgari-Kafrani etal.2020; Fotio etal.2020), antihyper-
tensive (Acuram2019), and antibacterial (van den Berg
and Kuipers2022).
M.oleifera leaves were also found tocontain substan-
tial amounts oftotal phenol, protein, calcium, potas-
sium, magnesium, iron, manganese and copper (Owon
etal. 2021). M.oleifera leaves are also a good source
ofphytonutrients such ascarotenoids, tocopherols and
ascorbic acid (Mahato etal.2021). ese nutrients are
known toscavenge free radicals when combined with
abalanced diet and may have immunosuppressive ef-
fects. Inaddition toleaves, flowers and fruits, M.oleif-
era and significant amounts ofcarotenoids (Oyeyinka
and Oyeyinka2018).
Moringa leaf metabolite profiles are determined
bygenotype, cultivation method (Managa etal.2021),
agroclimatic (Rébufa etal. 2021), geographic, variety,
environmental conditions, and season (Maetal.2020).
e moringa leaf metabolite profile is influenced
by cultivation method, harvest time and genotype
(Managa etal.2021). Moringa trees have high genetic
diversity between genotypes (Ravi etal. 2022). ere
are three types ofmoringa based onthe stem's colour,
namely white, green, and red. Cholesterol reduction
ofhypercholesterolaemic rats fed red and white mor-
inga leaf powder was different (Asrifah etal.2017).
e food industry tends todevelop high-fibre prod-
ucts tofulfil the demand for dietary fibre consumption,
one ofwhich isafortification with moringa leaf pow-
der. is powder isrich infibre and has the potential
todecrease postprandial glucose and insulin respons-
es, maintain or reduce cholesterol and lipid levels,
improve gastrointestinal function, immunomodulato-
ryand antitumour effects, and prevent type2diabetes
and cardiovascular diseases (Ortiz etal.2020).
Fortifying bread dough with M.oleifera leaf powder
has been reported to increase bread nutrition (Abu
et al. 2013; Ogunsina et al. 2014; Azeez et al. 2022).
Substitution ofmoringa leaf powder for flour inbread
isprobable toproduce healthy functional bread topre-
vent hypercholesterolaemia. Forexample, the protein
and crude fibre content ofwheat flour enriched with
5% moringa leaf powder was confirmed to increase
by about 54 and 56%, respectively (Abu et al. 2013).
Another study on bread enriched with moringa leaf
powder reported anincrease inprotein and crude fibre
content byaround 17and 88% (Azeez etal.2022). is
fortification increases micro and macro nutrients (Bo-
larinwa etal.2019).
is article aims toreview the bioactive compounds
ofmoringa leaf powder, their extraction, moringa leaf
powder characteristics, and its potential asafunction-
al food ingredient.
Moringa oleifera. M.oleifera, also known asamira-
cle tree, isatree belonging tothe family Moringaceae
inthe order Brassicales. e family Moringaceae has
13 species which are the most widely cultivated and
studied (Singh etal.2020). M.oleifera isnative tothe
sub-Himalayan tract ofNorthern India, where itwas
first described asamedicinal plant. Later, itwas distrib-
uted toAfrica and Ethiopia. Today, because the tree can
grow inavariety ofconditions, itisalso found inplaces
asfar away as Latin America and the Pacific Islands,
among other countries (Avilés-Gaxiola et al. 2021).
In Africa, M.oleifera has also been used to combat
child malnutrition (Avilés-Gaxiola etal.2021).
Amoringa isaplant that proliferates, has along life,
flowers throughout the year, and can endure extreme
heat conditions. is plant is native to tropical and
subtropical regions ofSouth Asia. is plant iscom-
monly used for food and medicine in several parts
ofthe world, mainly Asia and Africa. Most parts ofthe
moringa tree have been exploited and used for food,
including seeds, fruit, and leaves.
Some ofthe other benefits ofthe moringa plant in-
clude the bark ofthe moringa tree as amedicine for
colon inflammation and its leaves asananti-anaemic
agent (White 2015). Moringa leaves and stems can
beused asalowering agent for high blood pressure and
totreat diabetes (Hassan etal.2021). Inseveral devel-
oping countries, M.oleifera has been used to prevent
protein energy malnutrition, especially among children
ataninitial age and pregnant females (Alain etal.2016;
Mune etal.2016).
e moringa tree is declared a miracle tree or tree
oflife because ithas beneficial effects onhealth, nutri-
tion, water sanitation, and the environment. Moringa
ischaracterised bydiversity, isavalued tree innumerous
places inthe tropics and isused innumerous tradition-
alme dicines. Moringa isaversatile traditional medicinal
plant due tothe content ofvarious bioactive compounds
(Duranti etal.2021). Moringa isasource ofvarious nu-
3
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
trients such asprotein, vitamins, minerals, and phyto-
nutrients such ascarotenoids, polyphenols, flavonoids,
alkaloids, and tannins. is plant isused incertain areas
experiencing nutritional problems asanutritional sup-
plement for infants and children (Mahato etal. 2022).
enutritional and bioactive content ofmoringa leaves
isinfluenced byagroclimatic conditions, plant age, and
harvest time (Rébufa et al. 2021). e moringa plant
genotype also affects the bioactive content ofmoringa
leaves (Managa etal.2021). ephysical characteristics
ofmoringa leaves are shown inTable1. Figure1 shows
the genotype ofMObased onthe colour ofits stem.
Moringa oleifera leaf phytochemicals. Phytochem-
icals are secondary metabolites present inplants, which
accumulate in high concentrations but play a small
role inplant growth and development. Humans have
used phytochemicals as medicine to cure and protect
against various diseases. About 80% ofthe population
in developing countries use phytochemicals as tradi-
tional medicines for health. Based on their chemical
structure, vegetable phytochemicals are divided into
five classes, namely polyphenols, carotenoids, alka-
loids, terpenoids, and compounds containing sulphur
(Ma et al. 2020). e majority of these phytochemi-
cals are also present inthe moringa tree. e diverse
biological activities and disease prevention potential
ofmoringa are largely believed tobedue tothe pres-
ence ofthese phytochemicals (Maetal.2020).
Moringa isrich inpolyphenols, including flavonoids,
tannins and phenolic acids (Owon etal. 2021). Of the
various parts of the moringa plant, the leaves contain
the highest number of polyphenols. Moringa phenol
content isstrongly influenced bygeography and envi-
ronmental conditions ofgrowth. Quercetin and kaemp-
ferol glycosides (glucoside, rutinoside and malonyl
glucoside) are the most common flavonoids invarious
parts of the moringa tree except the roots and seeds.
Other flavonols are e.g. myricetin, rutin, and epicat-
echin. Geographical variations in the concentration
offlavonoids have also been observed among the differ-
ent varieties. Phenolic acids are present invarious parts
ofmoringa including gallic acid, caffeic acid, chlorogen-
Figure 1. Moringa leaves with different stem colour: (A) red, (B) green, (C) white
Table 1. Physical characteristics ofMoringa oleifera leaves based oncolour
Characteristics Stem colour
white green red
Leaf shape imperfect fins imperfect fins imperfect fins
Size small oval small oval small oval
Stem colour white green red
Leaf blade colour green green red
Leaf base rounded rounded rounded
Leaf tip blunt blunt blunt
(A) (B) (C)
4
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
ic acid, coumaric acid and ellagic acid. Moringa leaves
also contain asignificant number oftannins which are
complex polyphenols that can bind to proteins. Tan-
nin concentrations vary indifferent parts of the mor-
inga tree, with the highest concentrations inthe leaves
(Maetal.2020).
By using UPLC-Q-TOF-MS(ultra-high performance
liquid chromatography with quadrupole time-of-flight
mass spectrometr y), phenolic acid derivatives were iden-
tified, which included glucomoringin, 3-caffeoyl quinic
acid, 3-p-coumaroylquinic acid, 4-caffeoyl quinic acid,
acetyl 4-(a-L-rhamnopyranosyloxy) benzyl glucosino-
late, apigenin C-diglycoside, 4-p-coumaroylquinic acid,
4-feruloylquinic acid, quercetin-3-O-rutinoside, apigen-
in-C-hexose, quercetin-7-hexose, quercetin-3-hexose,
quercetin-3-acetyl-hexose, kaempferol-3-O-rutinoside,
luteolin-7-O-glucoside, kaempferol-3-hexose, cyanidin
hexose isorhamnetin-hexose, kaempferol acetyl hex-
ose (Teclegeorgish etal.2021), rutin, kaempferol acetyl
glycoside, quercetin-3-glucoside, quercetin-3-acetyl-
glucoside and kaempferol 3-glucoside were identified
by LC-ESI-MS (liquid chromatography electrospray
ionization tandem mass spectrometry) as reported
by Hamed et al. (2019). e results of the identifica-
tion of phytochemical compounds from the ethanol
extract of moringa leaves with GC MS (gas chroma-
tography–mass spectrometry) showed the presence
of 9, 12, 15-octadecatrienoic acid (39.66%), hexadec-
enoic acid (16.71%), palmitic acid, ethyl ester (14.70%),
and phytol (9.81%) asthe largest component (Adeyemi
etal. 2021). eir phenolic compounds inM. oleifera
leaves and their health benefits are shown inTable2.
Moringa oleifera leaf extract. Hassan et al. (2021)
described that phenolic compounds from moringa
leaves could beextracted using acombination ofwa-
ter and organic solvents (methanol, ethanol, ethyl
Table 2. Phenolic compounds inMoringa oleifera leaves and their health benefits
Constituents Postulated function Model used Disease protection Reference
Polyphenols
increases antioxidant enzymes and
inhibit the expression ofinflammatory
mediators oftumour necrosis factor-
alpha (TNF-α) and interleukin-6 (IL-6)
Wistar rats diabetes/ nephrotoxic Omodanisi
etal.2017
increases antioxidant enzymes and
decreases nitric oxide levels rats liver disorders El-Hadary and
Ramadan2019
decreases oxidative stress damage and
brain infarct volume Wistar rats cerebral ischemia Kirisattayakul
etal.2013
represses pancreatic α-amylase,
α-glucosidase, and cholesterol esterase in vitro diabetes disease Adisakwattana and
Chanathong2011
Polyphenols:
catechin, epicat-
echin, ferulic acid,
ellagic acid,
and myricetin
increases antioxidant enzymes, sup-
presses ROS (reactive oxygen species)
formation and scavenges free radicals
rats kidney protection Mansour etal.2014
Polyphenols:
gallic acid, caffeic
acid, and quercetin
scavenges free radicals, promotes
antioxidant activity and reduces the
expression ofliver disease markers
Wistar rats non-alcoholic fatty liver
disease
Asgari-Kafrani
etal.2020
Phenolic acid:
chlorogenic acid
reduces the expression ofdifferentia-
tion-68 and sterol regulatory element
binding protein-1c
guinea pigs non-alcoholic fatty liver
disease
Vergara-Jimenez
etal.2017
Flavonoids
prevents the increased level ofinter-
leukin 17(IL-17) via the NFκB (nuclear
factor kappa-light-chain-enhancer)
pathway, supports adecrease ofthe
level ofsoluble vascular endothelial
growth factor receptor1 (sFlt-1),
and angiogenesis
Wistar rats antihypertensive Batmomolin
etal.2020
5
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
Table 2. Tobecontinued
Constituents Postulated function Model used Disease protection Reference
Flavonoids
scavenges free radicals
inhibits the GABAergic system rats Alzheimer's disease Ganguly etal.2010
inhibits the GABAergic system mice epilepsy and anxiety Ingale and
Gandhi2016
influences noradrenergic-serotonergic
agents through the
neurotransmission pathway
mice depressant Aggarwal
etal.2020
decreases oxidative stress
and improves cholinergic function
bysuppressing acetylcholinesterase
(AChE) activity
rats dementia Sutalangka
etal.2013
alter the brain's monoamine level
and electrical activity rats Alzheimer's disease Ganguly and
Guha2008
suppress the activity ofthe crucial
enzymes associated with hypertension,
including angiotensin-1
converting enzyme (ACE), acetylcho-
linesterase (AChE), arginase,
and phosphodiesterase-5 (PDE5)
rats antihypertensive Adefegha
etal.2019
Flavonoids:
quercetin
stimulates endogenous antioxidant
enzymes and scavenges free radicals Wistar rats cerebellar disorders Omotoso
etal.2018
Quercetin
prevents fat accumulation and
increases lipolysis bystimulating the
AMPK (5' adenosine monophosphate-
activated protein kinase)
signalling pathway
in vitro and
mice antiobesity Xie etal.2018
modulates the expression ofgene
glycogen synthase and stimulates
insulin release
rats antidiabetes Abd Eldaim
etal.2017
Flavonoids:
isoquercetin
reduces the blood glucose level
by inhibiting α-amylase
and α-glucosidase activities
Wistar rats antidiabetes Jimoh2018
Kaempferol
regulates activities ofmajor enzymes
causing obesity, including HMG-CoA
(3-hydroxy-3-methylglutaryl coen-
zyme A), FAS (fatty acid synthase),
and increasing the mRNA expression
ofPPARα, MC4R,
enhancing fatty acid β-oxidation
and reducing fat accumulation
rats antiobesity Ezzat etal.2020
Flavonoids:
kaempferol,
apigenin quercetin
decreases pro-inflammatory cytokines
such asTNF-α, IL-1β, and IL-6,
and increases anti-inflammatory
(IL-10) and antioxidant enzymes,
such asSOD (superoxide dismutase),
CAT (catalase), and GSH-Px
(glutathione sulfhydril peroxidase)
mice kidney protection Karthivashan
etal.2016
6
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
acetate, and acetone). eir profile of the bioactive
compounds ofmoringa leaf extract isshown inTable3.
e health benefits of moringa leaves have been
widely studied and have anextended history astradi-
tional medicine inmany countries (Biswas etal.2020).
Moringa has a wide range of pharmacological activi-
ties, antimicrobial, hypotensive, hypoglycaemic, im-
munomodulatory and anti-inflammatory. Moringa
leaves have the potential as a source of natural anti-
oxidants such as flavonoids, quercetin, β-sitosterol
and zeatin. Moringa roots and leaves have antispas-
modic activity. Hot water infusion of leaves, seeds,
flowers, roots, and bark exhibits anti-inflammatory
activity. Various parts ofthe tree, such asleaves, roots,
seeds, pods, fruits, and flowers are used totreat com-
mon illnesses such as skin infections, anaemia, asth-
ma, coughs, diarrhoea, swelling, headaches, hysteria,
cholera, respiratory disorders, scurvy, diabetes, sick-
ness, throat and chest tightness (Padayachee and Bai-
jnath2020). emoringa tree trunk methanol extract
showed the ability torepair glycerol-induced rat kid-
ney damage (Apedapo etal.2020). eethanol extract
ofmoringa leaves shows the ability to inhibit neuro-
toxins from venom sothat itacts asanantivenom and
prevents bleeding (Adeyemi etal.2021). Moringa leaf
bioactive compounds improve physical and metabolic
functioning related tomuscles, they act asantitumor
and cytotoxic (García-Beltrán etal.2020), antiasthma,
anticancer, anti-inflammatory, hepatoprotective, and
cardioprotective agents (Hassan etal.2021). ebioac-
tive compounds ofmoringa leaves, and their potential
as antioxidants, anticancer, antiasthma, antidiabetic,
Table 3. Bioactive compounds inMoringa oleifera leaf extract
Extract Bioactive compounds Reference
Infusion
alkaloids, terpenoids, saponins, plobatin, and cardiac glycosides, but
noflavonoids, steroids, and anthraquinones were detected Akpor etal.2021
phytosterol, steroids, and flavonoids Barodia etal.2022
Ethanol 14 types ofphenolic compounds were identified inethanol extract
ofmoringa leaves Chigurupati etal.2021
Methanol
phenolic compounds decrease atherogenic index, cholesterol,
LDL(low density lipoprotein), triglyceride, and VLDL (very low
density lipoprotein) blood serum levels and increase LDLinhyper-
lipidaemic rats
Jain and Patel2010
polyphenol compounds and flavonoids Duranti etal.2021
Ether
gallic tannins, catechol tannins, saponins, alkaloids and anthraqui-
nones were detected inlow concentrations, steroids and triterpenoids
were detected inhigh concentrations, coumarins were not detected
Kasolo etal.2010
Ethanol
i)gallic tannins and saponins were detected inlow concentrations
ii)steroids, triterpenoids, flavonoids and anthraquinones were
detected inmoderate concentrations
iii)catechol, coumarin and alkaloid were not detected
Kasolo etal.2010
Water
i)gallic tannins, catechol tannins, steroids and triterpenoids, fla-
vonoids, saponins and alkaloids were detected inmoderate con-
centrations
ii)anthraquinone was detected inhigh concentration, coumarin was
not detected
Kasolo etal.2010
Ethanol and water
i)contains phenolic compounds, flavonoids, saponins, condensed
tannins, and cyanogenic glycosides
ii)phenol from moringa leaves can beextracted using acombina-
tion ofwater and organic solvents (methanol, ethanol, ethyl acetate,
and acetone)
García-Beltrán etal.2020
the same phenolic and flavonoid compounds but different concen-
trations Kerdsomboon etal.2021
7
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
anti-inflammatory, hepatoprotective, and cardiopro-
tective agents are shown inTable4.
Moringa oleifera leaf powder as a food ingredi-
ent. M.oleifera has great potential touse in biscuits,
cakes, brownies, meats, juices and sandwiches. ese
uses are interesting, asthe product's nutritional value
and health function increase. Still, the concentration
should not behigh because ofthe harmful effect onthe
organoleptic properties (Milla et al. 2021). Cattan
et al. (2022) described that moringa leaf powder has
aprotein content of27.4%, oil of5.6%, and dietary fi-
bre of23.7% somoringa leaf powder has the potential
tobeused as a food ingredient. Moringa leaf protein
extract has good emulsification and solubility ability.
Giuberti et al. (2021) reviewed various studies show-
ing that moringa leaves have the potential tobeadd-
ed to numerous products and cause improvements
in protein, lipid/fat, minerals, fibre, and antioxidant
activity. e effect of adding moringa leaf powder
on the anticholesterol activity of the bread has been
reported (Aly etal.2022). Food products that are said
to have been fortified are biscuits that can prevent
anaemiainpregnant women with anindicator ofanin-
crease inhaemoglobin due toiron and zinc intake with
biscuits containing moringa leaf powder (Páramo-Cal-
derón etal.2019; Manggul etal.2021), tortillas, soit
has a higher antioxidant activity (Páramo-Calderón
etal.2019). Adding moringa flour totortillas increases
the total phenolic content, oleic acid, palmitic acid,
protein, lipids significantly, and snacks with better nu-
tritional quality are produced (Zungu etal.2020).
e study by Bolarinwa et al. (2019) showed that
bread fortification with moringa leaf powder in-
creased protein (8.55–13.46%), ash (0.63–1.76%), fat
(7.31–15.75%) and fibre (0.08–0.62%) with adecrease
in water and carbohydrate content of 22.90–20.01%
and mineral content (P, K, Ca, Fe) increased through
46.73–57.68% compared tothe bread without Morin-
ga leaf powder fortification. Sensory analysis revealed
that adding 5% moringa leaf powder did not show
any differences from the unfortified bread. Moringa
isafortificant for amala, ogi, bread, biscuits, yoghurt,
cheese, and soups (Oyeyinka and Oyeyinka 2018).
e fortification of bread with moringa dried leaves
increased protein, ash, fat, and fibre but moisture con-
tent decreased (Aly et al. 2022). Bread fortification
with moringa leaf powder showed the same physical
properties of volume and skin colour as the control
ata5% fortification level. Colour isanimportant sen-
sory attribute. e moringa leaf protein concentrate
isapotential ingredient for bakeryproducts and isone
of the ways to remove the adverse effect of chloro-
phyll onfortified foods. Lower sensory properties due
tomoringa leaf powder fortification are related todif-
ferent breadcrumbs and crust colour and lower volume
than unfortified bread (Oyeyinka and Oyeyinka2018).
efortified bread revealed improvement inthe blood
lipid profile and, aswell asliver and kidney functions.
Table 4. Moringa oleifera leaf bioactive compounds and their potential
Bioactive compounds Application Reference
Moringa leaf phenolic
compounds potential asanantioxidant and antidiabetic agent Chigurupati etal.2021
Phenolic compounds antiasthma, anticancer, anti-inflammatory,
hepatoprotective and cardioprotective effects Hassan etal.2021
Moringa leaf phenolic
compounds
moringa leaf bioactive compounds improve physical
and metabolic performance related tomuscle, antitumor
and cytotoxic effects
García-Beltrán etal.2020
Moringa leaf ethanol
extract
the ability toinhibit neurotoxin from venom
so that itacts asanantivenom, besides also playing arole
in preventing bleeding
Adeyemi etal.2021
Moringa leaf water extract
protects mice from hepatotoxicity because itacts asananti-
oxidant and anti-inflammatory agent totreat liver disease Fotio etal.2020
potential asanimmunostimulant, cytotoxic, antitumor,
antibacterial and antioxidant effects García-Beltran etal.2020
potential torepair damaged brain tissue García-Beltran etal.2020
antioxidant and anti-inflammatory potential
to treat liver disease Fotio etal.2020
8
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
euse ofmoringa leaf powder inbakery products and
its effect onproduct quality are shown inTable5.
Oyeyinka and Oyeyinka (2018) studied the sweet po-
tato flour-based amala fortification with moringa leaf
powder atnumerous concentrations of2.5, 5, 7.5, and
10%. e addition of 10% moringa leaf powder was
found to increase the protein content by about 48%.
Similarly, fortified amala's calcium, magnesium, potas-
sium, sodium, and iron content increased after fortifica-
tion. However, the sensory perception ofamala colour
enriched with10% moringa leaf powder decreased.
Moringa leaves are high in fibre and low in fat.
Itis very important touse in the formulation oflow-
calorie food products. ecombination ofmoringa leaf
powder will increase the nutritional value and the con-
tribution ofmacro and micronutrients, including pro-
tein, fibre, vitamins, and minerals (Milla et al.2021).
Inaddition, besides having nutritional purposes, forti-
fication with moringa leaf powder also provides other
benefits such asincreased digestibility, dough stability,
antioxidant capacity, and preservation (Oyeyinka and
Oyeyinka 2018). erefore, itcan besaid that morin-
ga leaf powder can beused as a functional ingredient
inbakery products.
e safety profile ofMoringa oleifera leaf extract
and powder. Toxicity studies onM.oleifera are scarce
(Asare etal.2012). einternational regulation ofhu-
man health-related products requires that the toxicity
of nutraceutical products should be tested to ensure
their safety. ekey toensuring safety istoxicity testing
onboth invitro and invivo models (Robinson etal.2008).
Asare etal.(2012) evaluated the possible acute toxic-
ity ofanaqueous extract ofmoringa leaf powder. at
study showed that levels≥20mg·mL–1 of M.oleifera
aqueous extract were cytotoxic. eLD50(LD–lethal
dose) of M.oleifera water extract was previously de-
termined to be ≥ 3 000 mg·kg–1 b.wt. (body weight).
e study of Monera et al. (2008) indicated that the
lower concentration (6mg·mL–1) of aqueous leaf ex-
tract was cytotoxic to HepG2 (human hepatocellular
carcinoma cells). Another study byPavathy and Um-
amaheshwari (2007) showed much lower cytotoxic-
ity ataconcentration of0.6mg·mL–1of aqueous leaf
extract. edifferences intoxicity levels might beaf-
Table 5. Moringa leaf powder effects onbakery products
Food products Fortification level (%) Result Reference
Cookies
2.5, 5, 7.5
wheat flour bread fortified with moringa leaf powder
showed anincrease innutritional values
(protein, fibre, and minerals)
Olson and
Fahey2011
10, 20, 30, 50 bread with 10% and cake with 20% ofmoringa leaf
powder had higher protein, iron and calcium
Timilsena
etal.2017
5, 10 the best formula was fortification with moringa leaf
powder level of10% Martín etal.2013
0, 10, 20, 30, 50 the best formula was fortification with moringa leaf
powder level of10% Nwakalor2014
Brownies (cake) 0, 5, 10 improved physicochemical characteristics and increased ash
content, and lowered lipid content compared tothe control
Castro-López
etal.2017
Bread 5, 10, 15, 20
Fortification ofbread increased the nutrition ofprotein,
ash and minerals but the carbohydrate content decreased.
Acceptability decreased byincreasing fortification. ebest
acceptability was 5% and 10% fortification level.
Shah etal.2015
Rice crackers 1, 2, 5
fortification with 1% and 2% resulted inhigher carotene,
vitamin C and calcium compared tothe control;
the sensory score was comparable with the power
even atthe end ofthe storage test
Manaois and
Hashmi2013
Bread 1, 2, 3, 4, 5
nutritional composition ofprotein, ash, fibre, minerals,
and carotene was enhanced; acceptability decreased
when the fortification level increased; fortification affected
bread's physical and sensory attributes
Abu etal.2013
9
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
fected by the method of extraction and purification,
toxicity assays, types ofcells used, and different char-
acteristics ofthe leaves due tothe geographical loca-
tions and soil constituents (Asare etal.2012). emost
important finding ofthe study ofAsare etal.(2012) was
that M.oleifera leaves were genotoxic ata high dose
(3000 mg·kg–1 b.wt.), and the intake issafe at levels
of≤1000mg·kg–1b.wt.
Sagrera etal.(2021) presented acase ofararely de-
scribed adverse action ofmoringa that was cutaneous
toxicity inapatient who consumed moringa powder.
Abiopsy showed necrotic keratinocytes with inflam-
matory infiltrate. eharmful effect ofmoringa pow-
der might be caused by its components, interaction
with drugs, or contaminants. e exact mechanism
ofthis cutaneous toxicity was still unknown because
most studies reveal anti-inflammatory properties.
e acute toxicity assay study of de Barros
et al. (2022) used mice and oral administration
in a single dose in 2 000 and 5 000 mg·kg–1 of infu-
sionorpowder, and for 28days, the assay with oral ad-
ministration ofinfusion orpowder atthe doses of250,
500 and 1000mg·kg–1. at study showed that altera-
tions inbehaviour were observed inthe first 2hafter
5000mg·kg–1dose administration inboth treatments.
No toxicity was observed in the infusion treatment
during 28-day administration. However, 500 and
1000mg·kg–1powder dose promoted kidney and liver
damage. Ata dose of2 000mg·kg–1, no genotoxicity
and mutagenicity were observed (deBarros etal.2022).
Previously, the study ofAwodele etal.(2012) showed
that the aqueous moringa leaf extract had the estima-
tion ofLD50tobe1585 mg·kg–1. eextract did not
exhibit asignificant difference from the control inbio-
chemical and haematological parameters, and sperm
quality aswell.
So far, there have been no studies that reported
the mutagenicity and carcinogenicity ofmoringa leaf
powder since this ingredient is claimed scientifically
asanticancer inmany studies (Chigurupati etal.2021;
Hassan etal.2021; Kumar etal.2023). ebeneficial
effect ofmoringa leaf powder and its use asaningredi-
ent for functional foods should consider the toxicologi-
cal effects, and the uses should bebelow the reported
harmful doses.
CONCLUSION
Moringa leaf powder is a valuable source of func-
tional ingredients for the food industry and contains
a large amount of protein, vitamins, minerals, and
phytonutrients that are efficacious for health. enu-
tritional and bioactive content of moringa leaves
isinfluenced by agro-climate, plant age, harvest time
and genotype. Moringa leaf powder contributes sig-
nificantly tothe intake ofsome essential nutrients and
health-promoting human phytochemicals. Itpossesses
many pharmacological properties such as anticancer,
anti-inflammatory, hepatoprotective, cardioprotective
and antioxidant ones. euse ofmoringa leaf powder
asafunctional food ingredient iswidely popular and
enhances the improvements innutritional quality as-
pects, its health-promoting phytochemicals inhumans
could beused asauseful additive infood products.
Acknowledgement. eauthors would like tothank
Universitas Brawijaya for funding the Moringa oleifera
leaf powder research about the M.oleifera leaf powder
for functional food ingredients through Hibah Peneli-
tian Unggulan2022.
REFERENCES
Abd Eldaim M.A., Shaban Abd Elrasoul A., Abd ElazizS.A.
(2017): Anaqueous extract from Moringa oleifera leaves
ameliorates hepatotoxicity inalloxan-induced diabetic rats .
Biochemistry and Cell Biology, 95:524–530.
Abu O., J., Gernah D.I., Sengev A.I., Abu J.O., GernahD.I.
(2013): Effect ofMoringa oleifera leaf powder supplementa-
tion onsome quality characteristics ofwheat bread. Food
and Nutrition Sciences, 4:270–275.
Acuram L.K., Christine L., Hernandez C. (2019): Antihyper-
tensive effect ofMoringa oleifera L am. Cogent Biology, 5:1.
Adefegha S.A., Oboh G., Iyoha A.E., OyagbemiA.A. (2019):
Comparative effects ofhorseradish (Moringa oleifera)
leaves and seeds onblood pressure and crucial enzymes rel-
evant tohypertension inrat. PharmaNutrition, 9:100152.
Adedapo A.A., Etim U., Falayi O.O., Ogunpolu B.S., Omo-
bowaleT.O., Oyagbemi A.A., OguntibejuO.O. (2020):
Methanol stem extract ofMoringa oleifera mitigates
glycerol-induced acute kidney damage in rats through
modulation ofKIM-1 and NF-kB signaling pathways.
Scientific African, 9:e00493.
Adeyemi S., Larayetan R., Onoja A.D., AjayiA., YahayaA.,
OgunmolaO.O., AdeyiA.O., ChijiokeO. (2021): Antihem-
orrhagic activity ofethanol extract ofMoringa oleifera leaf
onenvenomed albino rats. Scientific African, 12:e00742.
Aggarwal V., Tuli H.S., Tania M., SrivastavaS., RitzerE.E ., Pan-
deyA., AggarwalD., Barwal T.S., JainA., KaurG., SakK.,
VarolM., Bishayee A. (2020): Molecular mechanisms ofac-
tion ofepigallocatechin gallate incancer: Recent trends and
advancement. Seminars inCancer Biology, 80:256–275.
10
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
Aju B.Y., Rajalakshmi R., Mini S. (2020): Protective role
ofMoringa oleifera leaf extract oncardiac antioxidant
status and lipid peroxidation instreptozotocin induced
diabetic rats. Heliyon, 6:e02935.
Akpor O.B., Ndakotsu J., Evbuomwan I.O., OlaoluT.D.,
OsemwegieO.O. (2021): Bacterial growth inhibition and
antioxidant potentials ofleaves infusions of (Moringa
oleifera), locust beans (Parkia biglobosa) and bitter leaves
(Vernonia amygladina). Scientific African, 14:e01001.
Alain M., Mune M., Bernard C., Bassogog B., Nyobe C.,
RenéS., Minka R., Mune MuneM.A., Bakwo Bassog-
ogC.B., NyobeE.C., MinkaS.R. (2016): Physicochemical
and functional properties ofMoringa oleifera seed and leaf
flour. Cogent Food&Agriculture, 2:1220352.
Aly A.A., Zaky E.A., Khatab N.R., HameedA.M., KadasahS.
(2022): eBiological and chemical ameliorative effects
ofbread substituted with dried moringa leaves. Arabian
Journal ofChemistry, 15:103875.
Asare G.A., Gyan B., Bugyei K., Adjei S Mahama R., AddoP.,
Otu-NyarkoL., WireduE.K., Nyarko A. (2012): Toxicity
potentials ofthe nutraceutical Moringa oleifera atsupra-
supplementation levels. Journal of Ethnopharmacology,
139:265–272.
Asgari-Kafrani A., Fazilati M., Nazem H. (2020): Hepato-
protective and antioxidant activity ofaerial parts ofMor-
inga oleifera inprevention ofnon-alcoholic fatty liver
disease inWistar rats. South African Journal ofBotany,
129:82–90.
Asrifah I., Estiasih T., Sujuti H. (2017): Potential hypocholes-
terolemic activity offlour from leaves ofMoringa (Moringa
oleiferaL.). Malaysian Journal ofNutrition, 23:449–460.
Avilés-Gaxiola S., León-Félix J., Jiménez-NevárezY.B., Angu-
lo-EscalanteM.A., Ramos-PayánR., Colado-VelázquezJ.,
HerediaJ.B. (2021): Antioxidant and antiinflammatory
properties ofnovel peptides from Moringa oleifera Lam.
leaves. South African Journal ofBotany, 141:466–473.
Awodele O., Oreagbaa I.A., OdomaS., DaSilvaJ.A.T., Os-
unkaluV.O. (2012): Toxicological evaluation ofthe aqueous
leaf extract ofMoringa oleifera Lam. (Moringaceae). Journal
ofEthnopharmacology, 139:330–336.
Azeez S.O., Chinma C.E., Bassey S.O., EzeU.R ., MakindeA.F.,
SakariyahA.A., OkubanjoS.S., DanbabaN., AdeboO.A.
(2022): Impact ofgermination alone or in combination
with solid-state fermentation onthe physicochemical,
antioxidant, invitro digestibility, functional and thermal
properties of brown finger millet flours. Lebensmittel-
Wissenschaft+Technologie, 154:112734.
Barodia K., Cheruku S.P., Kanwal A., MenonA., RajeevanR.,
RukadeA., Kumar Shenoy R.U., PrabhuC., Sharma V.,
Divya K.P., SumalathaS., Nayak Y., KumarN. (2022):
Effect ofMoringa oleifera leaves extract onexercise and
dexamethasone-induced functional impairment inskeletal
muscles. Journal ofAyurveda and Integrative Medicine,
13:100503.
Batmomolin A., Ahsan A., Wayan I., WiyasaA., SantosoS.
(2020): Ethanolic extract ofMoringa oleifera leaves improve
inflammation, angiogenesis, and blood pressure in rat
model ofpreeclampsia. Journal ofApplied Pharmaceutical
Science, 10:52–057.
Biswas D., Nandy S., Mukherjee A., Pandey D.K., Dey A.
(2020): Moringa oleifera Lam. and derived phytochemicals
aspromising antiviral agents: A review. South African
Journal ofBotany, 129:272–282.
Bolarinwa I.F., Aruna T.E., Raji A.O. (2019): Nutritive value
and acceptability ofbread fortified with moringa seed
powder. Journal ofthe Saudi Society ofAgricultural Sci-
ences, 18:195–200.
Castro-López C., Ventura-SobrevillaJ.M., G onzález-Hernán-
dezM.D., Rojas R., Ascacio-ValdésJ.A., Aguilar C.N.,
Martínez-ÁvilaG.C.G. (2017): Impact of extraction
techniques onantioxidant capacities and phytochemical
composition ofpolyphenol-rich extracts. Food Chemistry,
237:1139–1148.
Cattan Y., Patil D., Vaknin Y., Rytwo G., LakemondC., Benja-
minO. (2022): Characterization ofMoringa oleifera leaves
and seed protein extract functionality inemulsion model
system. Innovative Food Science & Emerging Technolo-
gies, 75:102903.
Chen G.L., Yong-Bing Xu Y.B., Wu J.L., LiN., GuoM.G.
(2020): Hypoglycemic and hypolipidemic effects ofMor-
inga oleifera leaves and their functional chemical constitu-
ents. Food Chemistry, 333:127478.
Chigurupati S., Al-Murikhy A., Almahmoud S.A., Al-
moshariY., Saber AhmedA., VijayabalanS., DasS., Raj
PalanimuthuV. (2021): Molecular docking ofphenolic
compounds and screening ofantioxidant and antidiabetic
potential ofMoringa oleifera ethanolic leaves extract from
Qassim region, Saudi Arabia. Saudi Journal ofBiological
Sciences, 29:854–859.
Cuellar-Nunez M.L., de Mejia E.G., PinaG.L. (2021): Moringa
oleifera leaves alleviated inflammation through down-
regulation ofIL-2, IL-6, and TNF-α inacolitis-associated
colorectal cancer model. Food Research International,
144:110318.
De Barros M.C., Silva A.G.B., Souza T.G.D.S., ChagasC.A.,
MachadoJ.C.B., FerreiraM.R.A ., SoaresL.A .L., XavierV.L.,
De AraújoL.C.C., BorbaE.F.O., DaSilvaT.G., AlvesR.R.V.,
CoelhoL.C.B.B., DeOliveiraA.M., Napoleão T.H.,
PaivaP.M.G. (2022): Evaluation of acute toxicity, 28-day
repeated dose toxicity, and genotoxicity ofMoringa oleifera
leaves infusion and powder. Journal ofEthnopharmacology,
296:115504.
11
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
Duranti G., Maldini M., Crognale D., SabatiniS., CoranaF.,
HornerK., CeciR. (2021): Moringa oleifera leaves extract in-
fluences oxidative metabolism inC2C12 myotubes through
SIRT1-PPARα pathway. Phytomedicine Plus, 1:100014.
El-Hadary A.E., RamadanM.F. (2019): Phenolic profiles,
antihyperglycemic, antihyperlipidemic, and antioxidant
properties ofpomegranate (Punica granatum) peel extract.
Journal ofFood Biochemistry, 43:e12803.
Ezzat S.M., El Bishbishy M.H., Aborehab N.M., SalamaM.M.,
HasheeshA., Motaal A.A., RashadH., Metwally F.M.
(2020): Upregulation ofMC4R and PPAR-α expression
mediates the antiobesity activity ofMoringa oleifera Lam.
inhigh-fat diet-induced obesity inrats. Journal ofEthnop-
harmacology, 251:112541.
Fotio A.L., Nguepi M.S.D., Tonfack L.B., TemdieR.J.G.,
NguelefackT.B. (2020): Acetaminophen induces liver
injury and depletes glutathione in mice brain: Preven-
tion byMoringa oleifera extract. South African Journal
ofBotany, 129:317–323.
Ganguly R., GuhaD. (2008): Alteration ofbrain monoam-
ines & EEG wave pattern inrat model of Alzheimer's
disease&protection byMoringa oleifera. Indian Journal
ofMedical Research, 128:744–751.
García-Beltrán J.M., Mansour A.T., AlsaqufiA.S., AliH.M.,
EstebanM.Á. (2020): Effects ofaqueous and ethanolic
leaves extracts from drumstick tree (Moringa oleifera)
ongilthead seabream (Sparus aurataL.) leucocytes, and
their cytotoxic, antitumor, bactericidal and antioxidant
activities. Fish and Shellfish Immunology, 106:44–55.
Giuberti G., Rocchetti G., Montesano D., LuciniL. (2021):
epotential ofMoringa oleifera infood formulation:
apromising source offunctional compounds with health-
promoting properties. Current Opinion inFood Science,
42:257–269.
Hamed Y.S., Abdin M., Akhtar H.M.S., ChenD., WanP.,
ChenG., ZhengX. (2019): Extraction, purification bymac-
rospores resin and invitro antioxidant activity offlavo-
noids from Moringa oliefera leaves. South African Journal
ofBotany, 124:270–279.
Hassan M.A., Xu T., Tian Y., Zhong Y., AliF.A.Z., YangX.,
LuB. (2021): Health benefits and phenolic compounds
ofMoringa oleifera leaves: Acomprehensive review. Phy-
tomedicine, 93:153771.
Ingale S.P., Gandhi F.P. (2016): Effect of aqueous extract
ofMoringa oleifera leaves onpharmacological mod-
elsofepilepsy and anxiety inmice. International Journal
ofEpilepsy, 3:12–19.
Jain P.G., Patil S., Haswani N., Girase M., SuranaS. (2010):
Hypolipidemic activity ofMoringa oleifera Lam., Morin-
gaceae, onhigh fat diet induced hyperlipidemia inalbino
rats, Revista Brasileira de Farmacognosia, 20: 969–973.
Jimoh T.O. (2018): Enzymes inhibitor y and radical scavenging
potentials oftwo selected tropical vegetable (Moringa oleif-
era and Telfairia occidentalis) leaves relevant totype2dia-
betes mellitus. Revista Brasileira de Farmacognosia,
28:73–79.
Karthivashan G., Masarudin M.J., Kura A.U., Abas F.,
FakuraziS. (2016): Optimization, formulation, and charac-
terization ofmultiflavonoids-loaded flavanosome bybulk
orsequential technique. International Journal of Nano-
medicine, 11:3417–3434.
Kasolo J.N., Bimenya G.S., Ojok L., OchiengJ., Ogwal-
OkengJ.W. (2010): Phytochemicals and uses ofMoringa
oleifera leaves inUgandan rural communities. Journal
ofMedicinal Plants Research, 4:753–757.
Kerdsomboon K., Chumsawat W., AuesukareeC. (2021): Ef-
fects ofMoringa oleifera leaves extracts and its bioactive
compound gallic acid onreducing toxicities ofheavy metals
and metalloid inSaccharomyces cerevisiae. Chemosphere,
270:128659.
Kirisattayakul W., Wattanathorn J., Tong-UnT., Muchima-
puraS., WannanonP., JittiwatJ. (2013): Cerebroprotective
effect ofMoringa oleifera against focal ischemic stroke
induced bymiddle cerebral artery occlusion. Oxidative
Medicine and Cellular Longevity:951415.
Kumar S., Verma P.K., Shukla A., Singh R.K., PatelA.K.,
YadavL., KumarS., KumarN., Kaushalendra AcharyaA.
(2023): Moringa oleiferaL. leaf extract induces cell cycle
arrest and mitochondrial apoptosis inDalton's Lymphoma:
Anin vitro and invivo study. Journal ofEthnopharmacol-
ogy, 302:115849.
Ma Z.F., Ahmad J., Zhang H., Khan I., MuhammadS. (2020):
Evaluation ofphytochemical and medicinal properties
ofMoringa (Moringa oleifera) asapotential functional
food. South African Journal ofBotany, 129:40–46.
Magaji U.F., Sacan O., Yanardag R. (2020): Alpha amylase,
alpha glucosidase and glycation inhibitory activity ofMor-
inga oleifera extracts. South African Journal of Botany,
128:225–230.
Mahato D.K., Kargwal R., Kamle M., Sharma B., PandhiS.,
MishraS., Gupta A., MahmudM.M.C., Gupta M.K.,
SinghaL.B., Kumar P. (2022b): Ethnopharmacological
properties and Nutraceutical potential ofMoringa oleifera.
Phytomedicine Plus, 2:100168.
Mahmoud K.B., Wasli H., MansourR.B., JemaiN., SelmiS.,
JemmaliA., Ksouri R. (2021): Antidiabetic, antioxi-
dantand chemical functionalities of Ziziphus jujuba
(Mill.) andMoringa oleifera (Lam.) plants using multi-
variate data treatment. South African Journal ofBotany,
144L:219–228.
Managa L.R., Du Toit E.S., Prinsloo G. (2021): Variations
inthe leaves metabolite profile between hydroponic and
12
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
field grown Moringa oleifera Lam. genotypes. Biochemical
Systematics and Ecology, 97:104302.
Manaois R.V., Morales A.V., Abilgos-Ramos R.G. (2013):
Acceptability, shelf life and nutritional quality ofmoringa-
supplemented rice crackers. Philippine Journal ofCrop
Science, 2:1–8.
Manggul M.S., Hidayanty H., Arifuddin S., Ahmad M.,
HadjuV., UsmanA.N. (2021): Biscuits containing Moringa
oleifera leaf powder improve conditions ofanemia inpreg-
nant women. Gaceta Sanitaria, 35:S191–S195.
Mansour A.R., Farmer M.A., Baliki M.N., ApkarianA.V.
(2014): Chronic pain: erole oflearning and brain plastic-
ity. Restorative Neurology and Neuroscience, 32:129–139.
Martín Medina C., Martín G., García A., FernándezT.,
HernándezE., Puls J. (2013): Potential applications
ofMoringa oleifera. Acritical review. Pastos yForrajes,
36:137–149.
Milla P.G., Peñalver R., Nieto G. (2021): Health benefits
ofuses and applications of Moringa oleifera inbakery
products. Plants, 10:318.
Monera T.G., Alan R., Maponga C.C., LeslieZ.B., GuglielmoJ.
(2008): Moringa oleifera leaf extracts inhibit 6-hydroxyla-
tion oftestosterone byCYP3A4. eJournal ofInfection
inDeveloping Countries, 2:379–383.
Mune M.M.A., Bakwo Bassogog C.B., Nyobe E.C., René
MinkaS.R. (2016): Physicochemical and functional proper-
ties ofMoringa oleifera seed and leaf powder. Cogent Food
and Agriculture, 2:1220352.
Nwakalor C.N. (2014): Sensory evaluation ofcookies pro-
duced from different blends ofwheat and Moringa oleifera
leaf powder. International Journal ofNutrition and Food
Sciences, 3:307–310.
Ogunsina B.S., Indira T.N., Bhatnagar A.S., RadhaC., Deb-
nathS., Gopala KrishnaA .G. (2014): Quality characteristics
and stability ofMoringa oleifera seed oil ofIndian origin.
Journal ofFood Science and Technology, 51:503–510.
Olson M.E., Fahey J.W. (2011): Moringa oleifera: Amulti-
purpose tree for the dry tropics. Un Revista Mexicana de
Biodiversidad, 82:1071–1082.
Omodanisi E.I., Aboua Y.G., OguntibejuO.O., Lamuela-
RaventósR.M. (2017): Assessment ofthe antihyperglycae-
mic, anti-inflammatory and antioxidant activities of the
methanol extract ofMoringa oleifera indiabetes-induced
nephrotoxic male Wistar rats. Molecules, 22:439.
Omotoso G.O., Gbadamosi I.T., OlajideO.J., Dada-Hab eebS.O.,
ArogundadeT.T., Yawson E.O. (2018): Moringa oleifera
phytochemicals protect the brain against experimental
nicotine-induced neurobehavioral disturbances and cerebel-
lar degeneration. Pathophysiology, 25:57–62.
Owon M., Osman M., Ibrahim A., SalamaM.A., MatthausB.
(2021): Characterisation ofdifferent parts from Moringa
oleifera regarding protein, lipid composition and extract-
able phenolic compounds. Oilseeds & fats, Crops and
Lipids, 28:45.
Oyeyinka A.T., Oyeyinka S.A. (2018): Moringa oleifera
asafood fortificant: Recent trends and prospects. Journal
ofthe Saudi Society ofAgricultural Sciences, 17:127–136.
Padayachee B., Baijnath, H. (2020): Anupdated comprehen-
sive review ofthe medicinal, phytochemical and pharma-
cological properties of Moringa oleifera. South African
Journal ofBotany, 129:304–316.
Páramo-Calderón D.E., Aparicio-SaguilánA., Aguirre-
Cruz A., Carrillo-AhumadaJ., Hernández-Uribe J.P.,
Acevedo-TelloS., Torruco-UcoJ.G. (2019): Tortilla added
with Moringa oleífera flour: Physicochemical, texture
properties and antioxidant capacity. Lebensmittel-Wis-
senschaft+Technologie, 100:409–415.
Pavathy M.V.S., Umamaheshwari A. (2007): Cytotoxic ef-
fect onMoringa oleifera leaf extracts onhuman multiple
myloma cell lines. Trends inMedical Research, 2:44–50.
Rébufa C., Dupuy N., Bombarda I. (2021): AComDim,
amultivariate tool tohighlighting impact ofagroclimatic
factors onMoringa oleifera Lam. leaves' composition
from their FTIR-ATR profiles. Vibrational Spectroscopy,
116:103297.
Ravi D.R.S., Nair B.R., Siril E.A. (2022): Fingerprinting and
genetic variability in drumstick (Moringa oleifera Lam.)
elite trees using RAPD markers – Anunderutilized and
wild edible future crop. South African Journal ofBotany,
145:370–377.
Robinson S., Delongeas J.L., Donald E., DreherD., FestagM.
(2008): European pharmaceutical company initiative
challenging the regulatory requirement for acute toxicity
studies inpharmaceutical drug development. Regulatory
Toxicology and Pharmacology, 50:345–352.
Sagrera A., Montenegro T., B orrego L. (2021): Cutaneous tox-
icity due toMoringa oleifera ACTAS Dermo-Sifiliográficas,
112:928–965.
Shah M.A., Bosco S.J.D., Mir S.A. (2015): Effect ofMoringa
oleifera leaves extract onthe physicochemical properties
ofmodified atmosphere packaged raw beef. Food Packaging
and Shelf Life, 3:31–38.
Singh A.K., Rana H.K., Tshabalala T., Kumar R., GuptaA.,
NdhlalaA.R., PandeyA.K. (2020): Phytochemical, nutra-
ceutical and pharmacological attributes of a functional
crop Moringa oleifera Lam: Anoverview. South African
Journal ofBotany, 129:209–220.
Sutalangka C., Wattanathorn J., MuchimapuraS., ukham-
MeeW. (2013): Moringa oleifera mitigates memory
impairment and neurodegeneration inanimal model
ofage-related dementia. Oxidative Medicine and Cellular
Longevity, 2013:695936.
13
Review Czech Journal of Food Sciences
https://doi.org/10.17221/221/2022-CJFS
Teclegeorgish Z.W., Aphane Y.M., MokgalakaN.S., Steen-
kampP., TembuV.J. (2021): Nutrients, secondary metabo-
lites and antioxidant activity ofMoringa oleifera leaves
and Moringa-based commercial products. South African
Journal ofBotany, 142:409–420.
Timilsena Y.P., Vongsvivut J., Adhikari R., AdhikariB. (2017):
Physicochemical and thermal characteristics ofAustralian
chia seed oil. Food Chemistry, 228:394–402.
Van den Berg J., Kuipers S. (2022): eantibacterial action
ofMoringa oleifera: Asystematic review. South African
Journal ofBotany, 151:224–233.
Vergara-Jimenez M., Almatrafi M.M., FernandezM.L. (2017):
Bioactive components inMoringa oleifera leaves protect
against chronic disease. Antioxidant, 6:94.
White P. (2015): e concept of diseases and health care
inAfrican traditional religion inGhana. HTS Teologiese
Studies/eological Studies, 71:a2762.
Zainab B., Ayaz Z., Alwahibi M.S., Khan S., Rizwana H.,
SolimanD.W., AlawaadA., Mehmood AbbasiA. (2020):
In-silico elucidation ofMoringa oleifera phytochemicals
against diabetes mellitus. Saudi Journal ofBiological Sci-
ences, 27:2299–2307.
Zungu N., Van Onselen A., Kolanisi U., SiwelaM. (2020):
Assessing the nutritional composition and consumer
acceptability ofMoringa oleifera leaf powder (MOLP)-
based snacks for improving food and nutrition security
ofchildren. South African Journal ofBotany, 129:283–290.
Received: November 20, 2022
Accepted: January 16, 2023
Published online: February 9, 2023