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Medicinal plants with antioxidant activity – A review

Authors:

Abstract

The production of free radicals occurs continuously in all cells as part of normal cellular function. However, excessive production of free radicals can play a role in many diseases. Antioxidants prevent tissue damage caused by free radicals by inhibition of their production, scavenging them, or by promoting their decomposition. This review highlighted the natural sources of antioxidants to be used as beneficial supplements in prevention of many diseases.
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1980
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Medicinal plants with antioxidant activity – A review
Mahdi M. Thuwaini
Department of Pathology, College of Medical and Healthy Techniques, Southern Technical University, Basrah,
Iraq.
Received: 10.11.2023 Revised: 18.11.2023 Accepted: 26.11.2023 Published: 30.11.2023
________
INTRODUCTION:
The body is constantly producing free radicals due to the
regular use of oxygen. Oxidation is a chemical reaction
that transfers electrons from one molecule to an
oxidizing agent. Oxidation reactions are known to
produce free radicals. These free radicals are responsible
for the cell damage in the body and contribute to various
kinds of health problems, such as heart disease, diabetes,
macular degeneration, and cancer. Antioxidants are a
class of chemical substances naturally found in our food
that can prevent or reduce the oxidative stress of the
physiological system. Plants are the major source of
natural antioxidants. Many previous reviews revealed
that medicinal plants are efficient sources of antioxidant
and free radical scavenging activities [1-3].
Table 1. Medicinal plants with antioxidant effects.
Journal of Pharmaceutical Advanced Research
(An International Multidisciplinary Peer Review Open Access monthly Journal)
Available online at: www.jparonline.com
ABSTRACT:
The production of free radicals occurs continuously in all cells as part of normal cellular function.
However, excessive production of free radicals can play a role in many diseases. Antioxidants prevent
tissue damage caused by free radicals by inhibition of their production, scavenging them, or by
promoting their decomposition. This review highlighted the natural sources of antioxidants to be
used as beneficial supplements in prevention of many diseases.
Corresponding author:
Dr. Mahdi M. Thuwaini
Professor
College of Medical and Healthy Techniques,
Southern Technical University, Basrah, Iraq.
Tel: +91- 9641397949
E. Mail ID: mahdimurshd@stu.edu.iq
Keywords: Medicinal plants, Antioxidant,
Free radicals, Therapeutic.
.
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1981
Table 1. Medicinal plants with antioxidant effects.
Ref. Methods Active extracts or compounds Medicinal plant
7-9
Lipid peroxidation inhibition assay and
DPPH assay
Hydroalcoholic extract Achillea santolina
10-13
Lipid peroxidation inhibition assay, ABTS
and DPPH assays
Leaf extract Adiantum capillus-
veneris
14-16 ABTS and DPPH assays Flavonoids, crude extract Adonis aestivalis
17-18 ABTS and DPPH assays Different extracts and fractions Agrimonia eupatoria
19-20 ABTS and DPPH assays Ethyl acetate (EtOAc) fraction Ailanthus altissima
21-22 FRAP and DPPH assays Aqueous extract Alhagi maurorum
23
In vivo improve superoxide dismutase,
catalase, glutathionperoxidase, and reduced
glutathione
aqueous extract Allium cepa
24-25
DPPH, and inhibition of lipid peroxidation
assays
Allium sativum
26-28
ABTS and DPPH assays and inhibition of
lipid peroxidation assays
Extracts and essential oil Alpinia galangal
29-30
Inhibition of lipid peroxidation assay Scopoletin (7-hydroxy-6-methoxy
coumarin)
Althaea officinalis
31-32 Inhibition of lipid peroxidation assay Methanolic extract Ammanniabaccifera
33-34 DPPH assay Butanolic extract Ammi visnaga
35-36
DPPH assay butamol extract of Anchusa italicaand
two of the triterpenes’ compounds
Anchusa italica
37-39
ABTS and Inhibition of lipid peroxidation
assays
Chamazulene, aqueous extracts Anthemis nobilis
40-41 DPPH assay Absolute methanol extract Antirrhinum majus
42-43 NO, DPPH, ABTS, LPO, and HPO methods leaf extract Apium graveolens
44-46 DPPH assay Peanut peptide Arachis hypogaea
47-49
The antioxidant activities were measured in
a hexane/2-propanol solution of methyl
linoleate in the presence of a radical initiator
caffeoylquinic acid derivatives from the
root
Arctium lappa
50-53
ABTS and DPPH assays and inhibition of
lipid peroxidation assays
Aqueous, Ethyl acetate extracts and
essential oils
Artemisia campestris
54-55
Inhibition of lipid peroxidation and DPPH
assay
Juice, anthocyanins A1 and A2 Asparagus officinalis
56-57
In vivo antioxidant enzymes Rhamnocitrin 4'-β-D-galactopyranoside
(RGP) obtained from leaves
Astragalus hamosus
58-60
DPPHassay, inhibition of lipid peroxidation Phenolic-rich fractions of oats and 3
avenanthramides compounds
Avena sativa
61-63
.
DPPHassay, inhibition of lipid peroxidation
and invivo antioxidant enzymes
Aqueous andalcoholic extract Bacopa monniera
64-66
DPPH assay and inhibition of lipid
peroxidation
Aerial parts extracts, diterpenoid and
flavonoid
Ballota nigra
67-68 DPPH assay crude extracts and fractions Bauhinia variegate
69-71 DPPH assay The the aerial parts Bellis perennis
72-75
DPPH, ABTS and in vivo inhibition of lipid
peroxidation
Seeds and fruit extracts Benincasa hispida
76-77 DPPH assay Crude extracts of the herb and flowers Bidens tripartitus
78-79 DPPH assay Crude extract Brassica nigra
80-81
Inhibition of lipid peroxidation and DPPH
assay
Root extract and the carbohydrate
derivatives of the roots
Brassica rapa
82-83 DPPH assay leaf extracts Bryophyllumcalycinum
84-86
Inhibition of lipid peroxidation and DPPH
assay
Seeds extracts Caesalpinia crista
87-88
DPPH and inhibition of lipid peroxidation Crude extracts of the leaves and
flavanone glycosides
Calamintha graveolens
89-91
DPPH, ABTS and in vivo inhibition of lipid
peroxidation and effect on antioxidant
enzymes
Crude extracts Calendula officinalis
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1982
92-94
DPPH and inhibition of lipid peroxidation Crude extracts, latex, flavonoids and
phenols
Calotropaprocera
95-96 DPPH assay The aerial parts methanolic extract Canna indica
97-99 DPPH, ABTS, FRAP assays Aerial part and root extracts Capparis spinosa
100-103
DPPH, ABTS, FRAP assays and α -
carotene-linoleic acid system
Crude extracts and flavonoids Capsicum species
104-107
DPPH, FRAP assays and inhibition of lipid
peroxidation
Seeds extracts, serotonin and flavonoids
derivatives
Carthamus tinctorius
108-111
DPPHassayand inhibition oflipid
peroxidation,
Seeds extracts and essential oils Carum Carvi
112-114
DPPHassay, nitric oxide scavenging activity,
β- carotene-linoleic acid model system,
hydroxyl radical scavenging activity,
reducing power, metal chelating activity and
superoxide radical scavenging activity
The methanolic extracts of leaves,
stems and seeds
Cassia occidentalis
115-116 DPPH and FRAP assays Crude extracts Casuarina equisetifolia
117-119 DPPH, ABTS and FRAP assays Ethanol extract Celosia cristata
120-121
Chemiluminescence‟s method – system
luminol/H
2
O
Crude extract Centaurea cyanus
122-124 DPPH assay Ethanolic leaf extract Chenopodium album
125-126 DPPH assay Methanol leaf extract Chrozophora tinctoria
127-134
DPPH and hydrogen peroxide radical, and in
vivo effect on superoxide dismutase,
catalase, GSH, increased MDA levels.
Crude seeds and roots extracts and
lectin
Cicer arietinum
135-138
(DPPH) and hydrogen peroxide radical, and
in vivo effect on superoxide dismutase,
catalase, GSH, increased MDA levels.
Crude extracts and fractions, Cichorium intybus
139-144
DPPH assay Crude seeds extracts and flavonoids,
isosaponarin, isovitexin and isoorientin
3’-O-methyl ether, isolated from the
fruits
Citrullus colocynthis
145-153
DPPHassay and inhibition of lipid
peroxidation
The leaf extracts and leaf essential oil
of Citrus aurantifolia, Citrus medica,
Citrus limonumand Citrus sinensis
Citrus species
154-156
DPPH Assay, reducing power assay and
total antioxidant activity
Methanolic extract of the aerial parts,
and compound -hydroxy-6,7,4′-
trimethoxy flavones
Clerodendrominerme
157-161
DPPH Assay Different solvent extractsof different
parts
Clitoriaternatea
162-163 DPPH, ABST and FRAP assays Methanol and ethanol extracts Colchicum candidum
164-170 DPPH, ABST and FRAP assays Crude extracts of the aerial parts Convolvulus arvens
171-172 DPPH Assay The crude methanolic extract Convolvulus scammonia
173-175 DPPH assay Crude extracts Cordia myxa
176-183
DPPH assay, lipoxygenase inhibition,
phospholipid peroxidation inhibition, iron
chelating activity, hydroxyl radical
scavenging activity, superoxide dismutation,
glutathione reduction and antilipid
peroxidation
Seed powder, essential oil and crude
extracts
Coriandrum sativum
184-186
DPPH assay Racemiside, scopoletin, 7,8-dimethoxy-
6-hydroxycoumarin, 3,3',4'-tri-O-
methylellagic acid, and
cereotagloperoxide isolated from the
ethyl acetate-soluble fraction
Cotoneaster racimiflora
187-189
DPPH assay n-Butanol, methanolic and ethyl acetate
extracts
Cressa cretica
190-198
DPPH, ABTS assay and in vivo antioxidant
enzymes
petals, stigmas, entire flowersand
crocin
Crocus sativus
199-200
DPPH assay and in vivo antioxidant
enzymes
Crude extracts Crotalaria juncea
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1983
201-210
DPPH assay and in vivo antioxidant
enzymes
Crude extracts and β-pinene, p-cymene,
γ-terpinene, cuminaldehyde and cumin
oils
Cuminum cyminum
211-217
DPPH, ABTS assay and in vivo antioxidant
enzymes
The chloroform and methanol leaf
extracts and essential oils
Cupressus sempervirens
218-225
DPPH assay, β-carotene–linoleic acid
bleaching method, and lipid peroxidation
inhibition assay
Crude leaves, fruits, pulps, peels and
seeds, phenolic extracts and essential
oils
Cydonia oblonga
226-230
DPPH, superoxide anion radical scavenging,
nitric oxide scavenging assay, ferrous
chelating ability, hydroxyl radical
scavenging assay, hydrogen peroxide
scavenging activity and ABTS assay
Ethyl acetate, hexane, ethyl acetate, and
methanol leaves extracts
Cynodondactylon
231-233
DPPH, superoxide anion radicals, hydroxyl
radicals, nitric oxide radical, hydrogen
peroxide, in addition to property of metal
chelating and reducing power.
Extracts by different extraction solvents Cyperus rotundus
234-235
DPPH method Crude extract Dactylocteniumaegyptia
cum
236-238
lipid peroxidation inhibitory (LPO), DPPH
method
ethanol extract of the bark; aqueous and
methanol extracts of the stem bark
Dalbergia sisso
239-241
DPPH method, hydroxyl radical scavenging
activity, reducing power assay, and β –
carotene bleaching activity
different solvent extracts from the
leaves
Datura fastuosa
242 DPPH method Crude extracts Datura stramonium
243-245 TBARS and DPPH methods Dry matter Daucus carota
246-248
DPPH, nitric oxide, hydrogen peroxide,
hydroxyl radical scavenging activities and
DNA damage protection.
methanolic extract
Desmostachyabipinnata
249-250
DPPH assay volatile oil Dianthus caryophyllus
251-253 DPPH and the total antioxidant capacity alcoholic extractof Digitalis purpurea Digitalis species
254-255
DPPH assay Ethanolic and Methanolic
extractsextract
Dodonaeaviscosa
256-257 DPPH assay methanol extracts, Dolichos lablab
258-260 DPPH assay Seeds and aerial parts extracts Echinochloa crus-galli
261-262
DPPH, Fe
2+
- chelating ability, total phenolic
contents and total flavonoid contents
methods.
Ethanolic extracts Echium italicum
263-264 DPPH assay Methanolic extractof Ephedraalata Ephedra species
265-268 ABTS and DPPH assays Aqueous and ethanol extract Equisetum arvense
269-272
DPPH and against nitrative and oxidative
damage induced by ONOO
Methanolic, hexane, chloroform, ethyl
acetate, butanol and 70% ethanolic
extract
Erigeron canadensis
273-276
DPPH assay Methanolic, extract, tannin, gallic acid,
(+)-catechin and vitamin C
Erodium cicutarium
277-279
DPPH assay Aqueous and ethanolic extracts from
different parts (leaves, stems, roots, and
the whole plant)
Eryngium creticum
280-284
DPPH The essential oil and the subfractions of
methanol extract from leaves of
Eucalyptus largiflorens. The leaves
extract and essential oil of Eucalyptus
camaldulensis
Eucalyptus Species
grown in iraq
285-287
DPPH assay
The hydro-alcoholic extractandcaffeoyl
derivatives
Eupatorium cannabinum
288-290
DPPH assay different parts (leaves, stems, flowers
and roots) extracts of Euphorbia hirta
Euphorbia hirta
291-294 DPPH assay Extracts of the leaves and stems Euphorbia tinctoria
295-298 DPPH assay Seed components, epicatechin, (+)-Fagopyrum esculentum
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1984
catechin 7-O-β-D-glucopyranoside, (−)-
epicatechin 3-O-p-hydroxybenzoate,
and (−)-epicatechin 3-O-(3,4-di-O-
methyl) gallate
299-303
DPPH assay Leaves extracts, Cyanidin-3-
rhamnoglucosideand crude hot-water
soluble polysaccharide
Ficus carica
304-305 DPPH assay Crude extracts Ficus carica
306-307 inhibition of lipid peroxidation assay aqueous and ethanolic bark extracts Ficus religiosa
308-312
DPPH, FRAPassays and total antioxidant
capacity
Crude seeds extracts and 3-
caffeoylquinic acid, 4-caffeoylquinic
acid,
1.5-Odicaffeoylquinicacid, rosmarinic
acid, eriodictyol-7-Orutinoside,
quercetin-3-O-galactoside, kaempferol-
3-Orutinoside, kaempferol-3-
Oglucoside,
hydroxylcinnamic acid derivatives,
flavonoid glycosides and
flavonoid aglycones
Foeniculum vulgare
313-315
DPPH assays and inhibition of lipid
peroxidation
Ethanolic extractof bark, as well as
esculetin,
esculin, fraxetin and fraxin
Fraxinus ornus
316-319
Ferric reducing antioxidant power assay,
cupric reducing antioxidant capacity assay,
DPPH radical scavenging, ß-caroten-linoleic
acid assay, metal chelating capacity and
inhibition of the organic compounds and the
conjugated diene hydroperoxides arising
from linoleic acid oxidation
Methanolic extract of aerial parts Fumaria officinalis
320-321
In vivo, evaluation of SOD, glutathione
Peroxidase and glutathione reductase
Crude extract Fumaria parviflora
322-326
DPPH assay, H2O2 scavenging assay and
metal ion chelating ability
Methanol, ethyl acetate and ethanol
crude aerial parts extracts
Galium aparine
327-331
DPPH and nitric
oxide radical scavenging, reducing power
and H2O2 scavenging
Aerial parts extracts Galium verum
332-334
DPPH, FRAP assays and percentage
inhibition of linoleic acid oxidation capacity
Crude extracts of different parts Geum urbanum
335-339
DPPH assay Roots extracts and Chalcone derivative,
a novel group of neolignan lipid esters,
and seven
known phenolic compounds
(formononetin, glabridin,
hemileiocarpin,
hispaglabridin B, isoliquiritigenin, 4‘-
O-methylglabridin, and
paratocarpin B)
Glycyrrhiza glabra
340-341 DPPH assay Methanol extracts Gnaphalium luteoalbum
342-346
Free radical scavenging
activity, reducing power assay, DNA
damage prevention
Hydroalcoholic, aqueous and ethanolic
leaves extracts andgossypol
Gossypium Species
347-350
β-carotene bleaching test, the
reducing power test and H2O2 induced cell
damage
Aerial parts extracts and essential oils Haplophyllum species
351-355
DPPH assay Ethyl acetate, methanol and
dichloromethane stem extracts,
methanol extract of leaves,methanolic
extract of the whole plant and α-
hederin, hederasaponin-C, and
hederacolchisides-E and F.
Hedera helix
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Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1985
356-359 Inhibition of peroxidation of lipids, hydroxyl
radical formation and DPPH radical
formation
Methanol and hexane extracts of seeds
Helianthus annuus
360-363
Total antioxidants, ABTS and CUPRAC
methods
Leaves and tubers extracts Helianthus tuberosus
364
Lipid peroxidation (inhibition Aqueous extracts of the leaves Helicophyllum crassipes
(Eminiumspiculatum)
365-367
DPPH assay Leaves, flowers stems, and roots
extracts
HeliotropiumSpecies
368-369
DPPH assay Methanol extracts Herniaria glabra and
Herniariahirsuta
370-371
DPPH free radical scavenging activity in
vitro and their capacity to protect DNA from
oxidative damage in vivo.
Flowers extracts Hibiscus cannabinus
372-379
DPPH free radical scavenging activity and
percentage
inhibition of linoleic acid oxidation capacity
Different leaves and flowers extracts Hibiscus rosa-sinensis
380-391
(DPPH) inhibition, lipid peroxidation
inhibition and in vivo antioxidant status
Different calyx, petal, and leaf extracts Hibiscus sabdariffa
392-399
DPPH antiradical, nitric oxide scavenging
and metal chelating activities
Arial parts and leaves extracts Hyoscyamus species
400-404
DPPH free radical scavenging, ferric
Reducingand ferrous chelating,
aerial parts extracts Hypericum
triquetrifolium
405-410
DPPH assay and ferrous ion chelating Methanolic leaves extract, methanolic
and acetone extract of aerial parts
Inula graveolens (Syn:
Dittrichia graveolens)
411-415
DPPH, NO, superoxide and ABTS radicals
in addition to reducing power
assessment.
Crude aqueous, methanolic and
ethanolic leaves extracts
Jasminum officinale
416-420
DPPH free radical scavenging, β-carotene-
linoleic acid assays andhydrogen peroxide
method.
Methanol and ethanol extracts and
essential oils
Jasminum sambac
421-430
DPPH radical scavenging, reductive power
tests, H2O2 scavenging activity, inhibition
of lipid peroxidation andtotal antioxidant
capacity
Water, chloroform, methanol, ethanol,
ethyl acetate and N-butanol extracts of
the leaves, water, hydroalcoholic,
chloroform and petroleum ether of the
bark and polyphenols
Juglans regia
431 DPPH assay Rhizomes extracts Juncus maritimus
432-436
DPPH, ABTS, hydroxyl radical (ОН•)
scavenging and chelating capacity,
superoxide radical (•O2−) scavenging,
xanthine oxidase inhibitory effects and
hydrogen peroxide scavenging.
Water, ethanol extracts and essential
oils
Juniperus communis
437-441
DPPH, TEAC, and FRAP Aqueous, ethanolic, methanolic extracts
and essential oils
Juniperus oxycedrus
442-445 DPPH assay Crude leaves extracts Jussiaea repens
446-447
DPPH radical assay, Superoxide anion
radical scavenging activity and Lipid
peroxidation inhibition assay
Aqueous and 50% ethanol fructus
kochiae extracts
Kochia scoparia (Syn:
Bassia scoparia)
448-451 DPPH, ABTS and FRAP assays Flowers and leaves extracts Lagerstroemia indica
452-455 DPPH assay Leaves and barks extracts Lagerstroemia speciosa
456-458
DPPH and FRAP assays Ethyl acetate and methanol leaves
extracts and essential oils
Lallemantiaiberica
459-460 DPPH and FRAP assays Seeds different extracts Lallemantiaroyleana
461-466
DPPH, the total phenolic and flavonoids
contents and total antioxidant activity
Extracts of leaves and
Stem, lantadene A, oleanolic acid and
lantanilic acid
Lantana camara
467-471
DPPH scavenging activity, reducing power,
β-carotene bleaching
inhibition and TBARS formation inhibition
Crude extracts Lathyrus sativus
472-478 DPPH and ABTS assays Leaves methanol, petroleum ether and Lawsoniainermis
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1986
ethyl
Acetate extracts
479-480
H2O2 scavenging activity, Ferrous ion
chelating
activity and Superoxide scavenging activity
lyophilized water and ethanol extracts Lemna minor
481-483
ABTS, FRAP and reduction power Lupanine, a quinolizidine alkaloid
isolated from the tubers
Leonticeleontopetalum
484-489
DPPH, ABTS, superoxide
scavenging activity and metal chelating
property
Methanolic, ethyl acetate and ethanolic
extracts
Lepidium sativum
490-494
DPPH assay and inhibition of lipid
peroxidation
Defatted
methanolic extract of aerial parts,
methanol and ethyl
acetate extract of leaf and stem
Lippianodiflora
495-499
DPPH, ABTS, superoxides radical, reducing
power and phosphomolybdenum assay.
Ethyl acetate and ethanol extracts of
dried leaves, peels and seeds extracts
Luffa acutangula
500-504
ferric thiocyanate test, thiobarbituric acid
test,
ferric reducing antioxidant power and DPPH
free radicals
scavenging test
Chloroform, n-hexane, ethyl acetate,
ethanol and methanol extracts of leaves
Luffa cylindriica
505-507 DPPH and ABTS assays Leaves waterand hydroalcholicextracts Lycopus europaeus
508-513
DPPH, nitric oxide and hydrogen peroxide
scavenging activities
Methanolic and ethanolic extracts of the
aerial parts
Lythrumsalicaria
514-518
DPPH, FRAP and ORAC assays.
Leaves, stems, flowers and roots
extracts
Malva neglecta
519-527
DPPH, FRAPassays, and inhibition of lipid
peroxidation
Aqueous-methanolic extracts of pulp,
peel and seed kernels, many crude
extracts, fractions (ethyl
acetate and n-butanol) and many
separated compounds
Mangifera indica
528-532
DPPH and nitric oxide antioxidant activity
and LPO inhibition
Methanolic extract, essential oils and
flavonoids (acacetin, apigenin, and
acacetin-7-rhamnoside).
Marrubium vulgare
533-537
Various antioxidant assays: DPPH, ABTS,
linoleic acid emulsion, ferric ions reducing
antioxidant power, ferrous ions chelating
capacity, superoxide radical scavenging
activity assays
Crude extracts of different parts and
polyphenolic-polysaccharide conjugates
Matricaria chamomilla
538-542
DPPH and FRAP assays Flowers extracts, raw seeds and
germinated seeds
Medicago sativa
543-546
DPPH assay and lipid peroxidation
inhibition
Hexane, 96 and 50% ethanol extract Melilotus officinalis
547-549
DPPH radical scavenging model and
CUPRAC method
Hydroalcoholic extract and infusions
Melissa officinalis
550-553
The total antioxidant capacity, FRAP and
DPPH tests.
Acetone, ethyl acetate, petroleum ether,
methanol and ethanol extracts of leaves
Mirabilis jalapa
554-556 DPPH assay The aqueous and ethanolic extracts Musa paradisiaca
557-559
DPPH and FRAP assays.
Bulb and 11 compounds [tazettones C-
G, (2S)-3′,4′-dihydroxy-7-
methoxyflavan, (2S)-3′,7-dihydroxy-
4′-methoxy8-methylflavan, (2S)-
liquiritigenin 7-methyl ether, 8-
methylnaringenin, farrerol, and
cyrtominetin], isolated from the bulbs.
Narcissus tazetta
560-563
DPPH, ABTS and Inhibition of lipid
peroxidation assays
Ethanolic extract, phenolic, flavonoid,
and anthocyanin contents
Nasturtium officinale
564-567
DPPH assay; β-Carotene/linoleic acid a
bleaching assay and ferric reducing power
assay.
Essential oil and different extracts
(water, methanol, water: methanol and
acetone).
Nerium oleander
J Pharm Adv Res, 2023; 6(11): 1980-2016. e – ISSN: 2581-6160 (Online)
Mahdi ©Journal of Pharmaceutical Advanced Research 2018. 1987
568-572
DPPH, ABTS, and reducing power tests. The extracts of the stem, flavonoids and
polysaccharides.
Nicotiana tabacum
573-578
DPPH assay
Flavonoids, polyphenols, essential oil
and crude leaf extracts.
Ociumbasilicum
579-584
DPPH, ABTS, total antioxidant capacity
(TAC), xanthine oxidase (XO) inhibitory
assays.
Ethanolic, hydro-alcoholic and aqueous
extracts of leaves, and phenolic
compounds
Olea europea
585-588 DPPH and ABTS assays. Crude extracts and fractions Ononis spinosa
589-592
DPPH assay.
Butanolic, ethanol, and acetone extracts
from flowers and leaves
Onopordonacanthium
593-595 DPPH method and total antioxidant effect. Polysaccharide and crude extracts Orchis masscula
596-600
DPPH and ABTS assays.
The essential oil and aqueous, ethanolic
and methanolic extracts
Origanum vulgare
601-605
DPPH, nitric oxide radical scavenging
activity and against MPTP induced oxidative
stress.
Flavonoids, crude methanolic and
ethanolic leaves extracts.
Oxalis corniculata
606-612
FRAP and DPPH assays.
The fruit extracts and polyphenol,
flavonoid, anthocyanin contents.
Phoenix dacylifera
613-614 FRAP Fruits, water and
methanol extracts of sweet kernels
Pruns armeniae
615-616
DPPH, FRAP, TEAC, CUPRAC and SNP
(silver nanoparticle assay)
Crude extracts of Ranunculussceleratus Ranuculussceleratus
617-618 DPPH Crude extracts of Ranunculus arvensis Ranunculus arvensis
619-620
On the activity of catalase, glutathione-S-
transferase, and glutathione peroxidase
Methanol extracts of the flowers and
leaves of Reseda lutea
Reseda Species
Plant antioxidants are mainly polyphenols (phenolic
acids, flavonoids, anthocyanins, lignans and stilbenes),
carotenoids (xanthophylls and carotenes) and vitamins
(vitamin E and C) [4-5].
The antioxidant effects of medicinal plants are
determined by many chemical-based assays. Among
these assays, some are based on the ability to scavenge
stable free radicals, such as Trolox equivalence
antioxidant capacity (TEAC), DPPH assay and, Folin–
Ciocalteu regent assay, and some assays are based on the
ability to reduce metal ions, such as ferric ion reducing
antioxidant power (FRAP), and cupric reducing
antioxidant capacity (CUPRAC). Meanwhile, HAT-
based assays detect the ability of an antioxidant to
quench free radicals by hydrogen donation, which is
more relevant to the radical chain-breaking antioxidant
capacity. HAT-based assays include oxygen radical
absorbance capacity (ORAC), total radical trapping
antioxidant parameter (TRAP), and inhibiting the
oxidation of low-density lipoprotein (LDL) [6].
This review highlighted the natural sources of
antioxidants to be used as beneficial supplements in
prevention of many diseases.
CONCLUSION:
Antioxidants from plant sources are biologically active
compounds that have medicinal and therapeutic values as
alternatives to their synthetic analogues, due to their
stability, cheapness, and lack of undesirable effects
associated with their use. This review presented plant
sources of antioxidants to encourage further studies on
their effectiveness when used medicinally, their stability,
their pharmacokinetics, and the possibility of side effects
resulting from them.
ACKNOWLEDGMENT:
We acknowledged the dean of college of medical and
healthy techniques, Southern Technical University,
Basrah-Iraq, for his support.
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Conflict of Interest: None
Source of Funding: Nil
Paper Citation: Thuwaini MM. Medicinal plants
with antioxidant activity A review. J Pharm Adv
Res, 2023; 6(11): 1980-2016.
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