Asian Pac J Trop Biomed 2016; 6(12): 1037–1043 1037

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Asian Pacific Journal of Tropical Biomedicine

journal homepage: www.elsevier.com/locate/apjtb

Original article http://dx.doi.org/10.1016/j.apjtb.2016.10.004

Phytochemical and antioxidant properties of different solvent extracts of Kirkia wilmsii

tubers

Kayini Chigayo1, Paul Eanas Lesedi Mojapelo1, Simon Mnyakeni-Moleele1*, Jane Masiiwa Misihairabgwi2*
1
Department of Chemistry, School of Mathematical and Natural Sciences, University of Venda, Private Bag x5050,
Thohoyandou, 0950, South Africa
2
Department of Biochemistry, School of Medicine, University of Namibia, Private Bag 13301, Windhoek, Namibia

A R TI C L E I N F O ABSTRACT

Article history: Objective: To determine suitable phytochemical extraction solvents, screen for phyto-
Received 2 Mar 2016 chemicals, determine the total phenol and flavonoid contents and the antioxidant activities of
Accepted 15 Aug 2016 different solvent extracts of Kirkia wilmsii (K. wilmsii), an ethnomedicine in South Africa.
Available online 17 Oct 2016 Methods: Extractions were performed from dried tubers of the K. wilmsii plant, using several
solvents and varying extraction times. Extract yields were determined and suitable extraction
solvents were selected. Total phenol and flavonoid contents of the extracts were determined
Keywords:
spectrophotometrically using gallic acid and quercetin as standards. The free radical scav-
Kirkia wilmsii
enging activity of the extracts was investigated using 1,1-diphenyl-2-picrylhydrazyl radical.
Phytochemical
Results: Phytochemical screening confirmed the presence of phenolics, flavonoids, terpe-
Total phenol
noids, tannins, cardenolide deoxy sugars and reducing sugars. Of the 12 solvent extracts used,
Flavonoid
six gave yields higher than 5%, while the other six gave yields less than 1%. The highest
Antioxidant
extract yield of 52.9% was obtained using 80% methanol while the lowest yield of 7.3% was
obtained using ethanol at 60 min. The 80% methanol, methanol/chloroform/water (12:5:3)
and 60% methanol extracts were significantly higher than those of ethanol, methanol and
water (P < 0.05). Total phenolic content recorded extracts ranged from (45.32 ± 0.50) to
(122.84 ± 0.31) mg gallic acid equivalent per gram. A maximum total flavonoid content of
(917.02 ± 0.10) mg quercetin equivalent per gram and a minimum of (206.26 ± 0.10) mg
quercetin equivalent per gram were recorded for methanol and water, respectively. The
flavonoid content for methanol was significantly higher than all the other extracts (P < 0.05).
The scavenging profiles of K. wilmsii extracts were significantly lower (P < 0.05) than that of
ascorbic acid and IC50 values ranged from 129.94 mg/mL for methanol to 225.04 mg/mL for
water. An IC50 value of 56.52 mg/mL was obtained with ascorbic acid.
Conclusions: Ethanol, methanol, methanol/chloroform/water, 80% methanol, 60%
methanol and water can be used as suitable phytochemical extraction solvents for
K. wilmsii tubers. Total phenolic content and total flavonoid content analysis proved the
presence of high levels of phenolic compounds as well as flavonoids. The presence of
phenols and flavonoid could be responsible for the radical scavenging activities observed.

*Corresponding authors: Simon Mnyakeni-Moleele, Department of Chemistry, 1. Introduction

School of Mathematical and Natural Sciences, University of Venda, Private Bag
x5050, Thohoyandou, 0950, South Africa.
Tel: +27 159628190 Secondary metabolites are produced by plants mainly as
Fax: +27 159624749 products of primary metabolism and as part of the defence
E-mail: mnyakeni.moleele@univen.ac.za mechanisms of plants. Phytochemicals such as, alkaloids, tan-
Jane Masiiwa Misihairabgwi, Department of Biochemistry, School of Medicine,
University of Namibia, Private Bag 13301, Windhoek, Namibia. nins and flavonoids are examples of secondary metabolites
Tel: +264 612065039 produced by plants, from which the plants are thought to get
Fax: +264 886526605 their healing properties [1]. Phenolic compounds have been
E-mail: jmisihairabgwi@unam.na
Foundation Project: Supported by BIOPAD (Project Code SMNS/12/MBY/05)
associated with antioxidant activity due to their free radical
and the Department of Research & Innovation (IS63), University of Venda who both scavenging activities [2,3].
provided funding for this research. Common names of Kirkia wilmsii (K. wilmsii) are wild
Peer review under responsibility of Hainan Medical University. The journal
implements double-blind peer review practiced by specially invited international
pepper or Mountain Seringa (English) and Legaba or Modumela
editorial board members. (Northern Sotho) [4]. The K. wilmsii belongs to the Sapindales

2221-1691/Copyright © 2016 Hainan Medical University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://
creativecommons.org/licenses/by-nc-nd/4.0/).
1038 Kayini Chigayo et al./Asian Pac J Trop Biomed 2016; 6(12): 1037–1043

family [5]. This family (Kirkiaceae) includes a wide range of 2.2. Sample preparation and extraction
small to medium sized trees, mainly found in eastern tropical
Africa, Madagascar and South Africa. This tree is one of the Only the tuber of K. wilmsii tree was used in the study. The
plants that have underground storage organs (such as tubers are covered with a bark which was removed from the
rhizomes, tubers, corms, bulbs and caudex) [6]. tubers as the indigenous people remove the bark from the tubers
The K. wilmsii tuber is used by the Bapedi people in Leb- before eating them. The peeled tubers were washed with
owakgomo district located in the Limpopo Province, South Africa deionised water (Milli-Q Millipore, 0.054 mS/cm) to remove soil
for the treatment of various ailments. The local people believe that and dirt. The tuber was cut into small pieces using an ordinary
chewing it regularly helps to maintain general good health. kitchen knife and dried at ambient temperature (± 30  C in
Studies on the leaves have shown that the leaves of the tree have Thohoyandou) in the laboratory for 5 days. After drying, the
antiplasmodial properties [7]. Studies conducted on leaf extracts plant was ground to a fine powder using a Retsch Muhle
have shown antimicrobial activity against Staphylococcus aureus grinding mill.
(S. aureus), Enterococcus faecal, Escherichia coli (E. coli), The extraction process was performed by adding 25 mL
Pseudomonas aeruginosa, Sporothrix schenckii, Microsporum of each extraction solvent to the weighed portions (2 g) of dried
canis, Cryptococcus neoformans and Candida albicans [8]. The powder in stoppered volumetric flasks and extraction performed
leaves further showed biological activity against the animal by sonicating in an Integral Systems ultrasonic bath for the pre-
fungal pathogen Aspergillus fumigatus. scribed extraction times below. Extraction was performed with the
Extracts of the dried and powdered bark of the K. wilmsii required solvent for the required length of time. The extraction
were found to contain secondary metabolites, lignans, iso- times were 15, 30 and 60 min [15]. The solvents used were ethanol,
coumarins and flavonoids [9]. Ethnobotanical surveys have methanol, methanol/chloroform/water (MCW), 80% methanol,
recorded that K. wilmsii tubers are traditionally used in the 60% methanol, water, dichloromethane, chloroform, acetone,
treatment of diabetes mellitus [4] and hypertension [10]. hexane, diethyl ether, ethyl acetate [16].
Antimicrobial activity against Shigella dysenteriae, Aeromonas For the extracts with the yields higher than 5%, i.e. ethanol,
hydrophila, Salmonella thyphii, Proteus mirabilis, E. coli and methanol, MCW, 80% methanol, 60% methanol and water,
S. aureus was recorded [11]. further extractions were performed in triplicate.
The presence of an excess of oxygen in the human body has In all cases the filtrate was evaporated to dryness using the
some negative effects as it can trigger radical chain reactions in the Vacutex Flexi-dry mp freeze drier. The freeze dried extracts were
presence of reactive species. This can cause health problems, such kept in a deep freezer at −20  C for storage.
as aging and cell destruction [12]. Antioxidants have been found to
be the solution to this problem as they interrupt these chain 2.3. Phytochemical screening tests
reactions to form radicals that can easily be removed from the
human body, thereby generally improving health, assisting cell Phytochemical screening tests were performed according to
rejuvenation, cancer prevention and cardiovascular diseases standardised recent methods as described in literature [1,2,17–20].
prevention [13]. Thus it is important to investigate the antioxidant Various solvent extracts of K. wilmsii were used to screen for
potential of K. wilmsii. phenolics and flavonoids [1,20], steroids and terpenoids [18,20],
A considerable number of publications have been reported on saponins [20], cardiac glycosides [20], cardenolide deoxy sugars
the phytochemistry of leaves and the bark of K. wilmsii [5,7–9,14]. [20], tannins [2], phlobatannins [2], anthraquinone glycosides
Limited studies on the tuber have been directed at the evaluation [17] and reducing sugars [19].
of its traditional medicinal applications [4,10]. No reports are
available on the phytochemical analysis and antioxidant 2.4. Total phenolic content
activities of the tubers of K. wilmsii. The study was therefore
aimed at determining suitable solvents for extraction of A modified method for the determination of total phenolic
phytochemicals, phytochemical screening and quantitative content was carried out using modification of the method
analysis of total phenols, flavonoids and antioxidant activity of cited by Sahu and Saxena [21]. Gallic acid standard solutions
K. wilmsii tubers. Our results provide a basis for future studies were prepared in methanol to give the following final
on isolation, identification and characterization of active concentrations; 20.00, 40.00, 60.00, 80.00, and 100.00 mg/
compounds with potential applications in drug development. mL. Each plant extract was dissolved in methanol to give a
final concentration of 1.0 mg/mL and 0.5 mL of each sample
2. Materials and methods and standards were introduced into different test tubes and
mixed with 2.5 mL of a 10-fold dilute Folin-Ciocalteu re-
2.1. Plant materials agent and 2 mL of 7.5% sodium carbonate were added. The
test tubes were covered with parafilm and allowed to stand for
The tubers of K. wilmsii were collected from the Lebowakgomo 30 min at room temperature before the absorbance was read at
Region in Polokwane District between November 2015 and July 760 nm. The results of the total phenolics were expressed as
2016, which is situated in the Limpopo Province of South Africa. mg of gallic acid equivalents (GAE) per gram of sample and
The plant name was identified by the Department of Botany at the calculated by the formula [22]:
University of Venda and the name was further confirmed by the
National Herbarium (Voucher number MPT00112) in Pretoria, TPC = (C × V)/M
South Africa. The plant name has been checked with www.
theplantlist.org and has been reported as an accepted name (re- where, TPC is total phenolic content (mg/g plant extract in
cord 29400130), website accessed 28 November 2015. GAE), C is concentration of gallic acid established from the
 Kayini Chigayo et al./Asian Pac J Trop Biomed 2016; 6(12): 1037–1043 1039

calibration curve (mg/mL), V is volume of the extract (mL), M is Table 1

mass of the extract of the plant (g). Phytochemical screening test results.

2.5. Total flavonoid content Test Extract

Water Methanol Acetone Ether Ethyl Chloroform
Total flavonoid content was estimated using standard methods acetate
with minor modifications [21,23] using quercetin as a standard. The Phenolics + + + − + −
standard solutions with the following final concentrations were Flavonoids + + + − + −
(Alkaline test)
prepared; 50, 100, 150, 200 and 250 mg/mL. One milliliter of
Flavonoids + + + − + −
each standard solution and extract solutions was taken into (Lead acetate)
10 mL volumetric flask, containing 4 mL of deionised water. Terpenoids − − − − − +
Then 0.3 mL of 10% AlCl3 was added to the mixture. At the 6th Saponins − − − − − −
min, 2 mL of NaOH (1 mol/L) was added and volume made up Cardiac − − − − − −
glycosides
to 10 mL with distilled water. The absorbance was read at Cardenolide − + + − − −
510 nm using Beckman Coulter DU 650i UV–vis deoxy sugar
spectrophotometer. The results of the total flavonoids were Tannins + + + − − −
expressed as quercetin equivalents (QE). Phlobatannins − − − − − −
Anthraquinone − − − − − −
glycosides
2.6. Antioxidant activity Reducing sugars + + + − − −

1,1-Diphenyl-2-picrylhydrazyl (DPPH) radical scavenging

60
activity of the different plant extracts were compared by
adapting the procedure reported by Iqbal et al. and Sahu et al.
[17,24]. Each extract was dissolved in an appropriate volume of 50
methanol to give final concentrations ranging from 10.00 to
250.00 mg/mL. Standard ascorbic acid solutions were also 40
prepared in methanol to give the same concentration range.
% Yield

Two milliliter of each solution was transferred to a test tube

30
and mixed with 4 mL of 0.3 mmol/L DPPH. A control
solution was prepared by adding methanol (2 mL) to
0.3 mmol/L DPPH (4 mL). The experiment was run in 20
triplicate. The solutions were mixed well and left in the dark
for 30 min. After 30 min the solutions were analyzed on a 10
UV–vis spectrophotometer at 517 nm. The percentage of
antioxidant potential was calculated using the formula:
0
A B C
D E F G H I J K L
Ac − As Solvents used for extraction
% Inhibition = × 100
Ac 15 min 30 min 60 min
Figure 1. Effect of varying extraction time and extraction solvent on
where, Ac is absorbance of the control solution, As is absorbance extract yield of K. wilmsii.
of the sample or standard. A: Methanol; B: Ethanol; C: Dichloromethane; D: Chloroform; E: Acetone;
F: MCW; G: 80% Methanol; H: 60% Methanol; I: Water; J: Hexane; K:
Diethyl ether; L: Ethyl acetate.
2.7. Statistical analysis

Means of triplicate analysis were calculated and data was different from 48.2% to 46.9% extract yields for MCW and 60%
expressed as mean ± SD. Post hoc ANOVA statistical analysis methanol, respectively (P > 0.05). The results for ethanol (7.3%),
was performed using SPSS 22 software for comparison between water (20.9%) and methanol (36.6%) were significantly lower than
two or more treatments. A difference was considered to be the above mentioned results. An increase in the extraction time
statistically significant when P < 0.05. also showed a significant increase in the % yield obtained
(P < 0.05). We conclude that 80% methanol is the best solvent to
use for extraction as the extracts are more soluble in polar solvents
3. Results and 80% methanol has more polar organic properties.

3.1. Phytochemical screening 3.3. Total phenolic content

The phytochemical screening tests of the tuber revealed the The total phenolic contents of K. wilmsii extracts ranged from
presence of phenolics, flavonoids, terpenoids, tannins, carde- 45.32 to 122.84 mg GAE/g from water and methanol extracts,
nolide deoxy sugars and reducing sugars (Table 1). respectively (Table 2). Pure methanol produced extracts with the
highest levels of total phenolics. The content is significantly
3.2. Solvent extraction higher than the phenolic contents of all the other solvents used
(P < 0.05). No significant differences were recorded in the total
The highest extract yield (52.9%) was obtained from extraction phenolic contents of ethanol, 80% methanol, MCW, 60%
with 80% methanol (Figure 1). This result was not significantly methanol and water (P > 0.05).
1040 Kayini Chigayo et al./Asian Pac J Trop Biomed 2016; 6(12): 1037–1043

3.4. Total flavonoid content Table 3

IC50 values for the extracts as well as ascorbic acid.
The total flavonoid contents of K. wilmsii were recorded
Extract IC50 (mg/g)
ranging from 206.26 mg QE/g to 917.02 mg QE/g from the
Ethanol 204.78 ± 1.51a
water extract and the methanol extract, respectively. The meth-
Methanol 129.94 ± 0.20b
anol extract exhibited a total flavonoid content that is signifi- MCW 172.44 ± 0.62c
cantly higher than the rest of the extractants (P < 0.05). The 80% Methanol 194.62 ± 1.00d
flavonoid contents of the rest of the solvents are also signifi- 60% Methanol 167.27 ± 0.57c
cantly different (P < 0.05) from each other except for ethanol, Water 225.04 ± 0.72e
Ascorbic acid 56.52 ± 0.07f
60% methanol and water extracts whose flavonoid contents are
not significantly different (Table 2). All extracts with different superscripts are statistically different
The total flavonoid content for the methanol extract was very (P < 0.05).
high (917 mg/g) and the other extracts exhibited results ranging
from 200 to 450 mg/g.
4. Discussion
Table 2
Total phenolic content and total flavonoid content of the different extracts 4.1. Phytochemical screening
of K. wilmsii.
Compounds such as cardenolides, flavonoids, resins, sapo-
Extract Total phenolic Total flavonoid
content GAE (mg/g) content QE (mg/g) nins and tannins have been shown to have healing properties
against most disease causing organisms [20,25]. These properties
Ethanol 58.98 ± 0.45a 256.95 ± 0.45c
Methanol 122.84 ± 0.31b 917.02 ± 0.10d include antioxidant activity, anti-allergic, anti-inflammatory and
MCW 69.34 ± 0.91a 437.64 ± 0.17e many others. In our earlier research, water extracts of K. wilmsii
80% Methanol 57.16 ± 0.47a 351.37 ± 0.06f tuber were found to be active against Shigella dysenteriae,
60% Methanol 62.05 ± 0.30a 262.49 ± 0.25c Aeromonas hydrophila, Salmonella thyphii, Proteus mirabilis,
Water 45.32 ± 0.50a 206.26 ± 0.10c
E. coli and S. aureus [11].
Results with different superscripts are significantly different from each The methanol, water and acetone extracts yielded positive
other (P < 0.05). results for many groups of compounds in the phytochemical
screening tests. These results are consistent with other reported
3.5. DPPH free radical scavenging activity results, where methanol extracts tested positive for the highest
number of different classes of phytochemicals in Bauhinia
The scavenging profiles of the extracts and ascorbic acid are variegata L. bark [26] as well as in tests on the extracts from
shown in Figure 2, from which it can be observed that all the Anamirta cocculus seeds [27]. Further, the root and bark of
extracts possess radical scavenging potential. Methanol proved Eurycoma longifolia also showed that the methanol, ethyl
to be the most active of the extracts while the water extract was acetate and chloroform extracts were good sources of different
the least. classes of compounds [20]. However, the methanol and ethanol
extracts of Strychnos minor Dennst leaves gave poor results
120.00 [2]. Further the extracts gave different results with methanol,
ethyl acetate and chloroform extracts testing positive for
100.00
phenolics, flavonoids, terpenoids, alkaloids, proteins and
cardiac glycosides in the study done on root and stem extracts
80.00
of wild Eurycoma longifolia Jack by Zakia et al. [20]. Our
ethyl acetate and chloroform extracts tested negative for most
% Inhibition

60.00
groups of compounds. The ether extract proved negative for
40.00 all the tests conducted.
We therefore conclude that water, methanol and acetone or
20.00 their combinations would give good extraction yields that can be
used for the phytochemical screening of K. wilmsii.
0.00
0.00 50.00 100.00 150.00 200.00 250.00 300.00
Concentration (μg/mL)
4.2. Solvent extraction
-20.00
Ascorbic Ethanol Methanol MCW
Since biologically active compounds occur naturally in very
80% Methanol 60% Methanol Water small concentrations, the choice of an extraction method and the
Figure 2. Percentage inhibition of the various extracts on DPPH. corresponding suitable solvent is an important step in the drug
discovery process.
The IC50 values of all our extracts are significantly different Solvents with a wide range of polarity were used for the
from each other (P < 0.05) except for MCW and 60% methanol extraction. The results suggest that polar solvents gave better
which are not significantly different (Table 3). Therefore, the extraction yields [28], which is true in our study.
IC50 value for the methanol extract is significantly lower than all Therefore, the K. wilmsii tuber secondary metabolites can be
the other values. The best activity was recorded by the methanol extracted with polar protic solvents with high yields ranging from
extract with an IC50 value of 129.94 mg/mL while the water 7.3% to 52.9%. Non polar solvents, such as, hexane, ether pro-
extract gave the lowest IC50 around 225.04 mg/mL. duced very small amounts of extracts, less than 1%. This
 Kayini Chigayo et al./Asian Pac J Trop Biomed 2016; 6(12): 1037–1043 1041

observation is also supported by results obtained from the chloroform, ethyl acetate, butanol, methanol and water extracts
extraction from Paramignya trimera root where the polar protic of Azadirachta indica with results ranging from 63 mg QE/g
solvents, methanol and water, gave the best extraction yields [29]. to 529.5 mg QE/g [37]. In their work, all the other results are
Extraction with a MCW combined solvent also produced a above 350 mg QE/g except for the butanol extract. Research
significantly high yield (48.2%), consistent with other research has proven that flavonoids are important in the fight against
work using the same solvent [16]. However, we reported a diseases and can also act as antioxidants depending on their
slightly higher extract yield of 48.2% as compared to 45% and structure [17]. Coupled with phenols, flavonoids have been
35% extraction yields for Anthocleista grandiflora and reported to have high antioxidant activity [2]. Therefore, these
Combretum erythrophyllum leaves reported by Eloff [16]. high total phenolic content results could mean the abundance
However, the MCW combination tended to separate into of possible compounds of pharmaceutical importance. Other
different phases as chloroform and water are immiscible. published results are very low, pigeon pea extracts gave
Therefore, addition of water to methanol proved that the flavonoid contents ranging from 0.16 to 1.58 mg QE/g [38],
extraction efficiency can be increased significantly as the and from 20 to 80 mg QE/g content for Curcuma extracts [21],
extraction yields obtained with 80% methanol (52.9% yield) and 79.13–82.18 mg QE/g for Hieracium pilosella [35]. Further
60% methanol (46.9% yield) were much higher than the yield work is necessary to determine the flavonoid types, biological,
obtained from the use of pure methanol (36.6% yield). This anti-inflammatory activity, antimicrobial and anticancer activ-
observation is consistent with other reported results [30,31], as the ities of K. wilmsii.
water tends to increase the polarity of the extractant.
4.5. DPPH free radical scavenging activity
4.3. Total phenolic content
Antioxidant agents with high scavenging activity should
The total phenolic content results obtained in our study are have a low IC50 value [39]. This is supported by the lowest value
higher than the results reported by Dhanani et al. [32], who being exhibited by ascorbic acid, a well-known antioxidant. The
reported a maximum of 30 mg GAE/g for Withania somnifera IC50 results obtained are significantly higher than that of
roots extracted with ethanol, 10% ethanol and water [32]. Some ascorbic acid (56 mg/mL). This is to be expected as crude ex-
other researchers reported total phenolic content values tracts were used before purification. Results for purified extracts
between 100 and 150 mg GAE/g, with the methanol and are expected to be much more closely related to those of
acetone extracts of the leaves, stem and flowers of Thermopsis ascorbic acid.
turcica [33]. These values are generally higher than our results The methanol IC50 (130 mg/mL) result is comparable to that
and only our methanol extract matches these values. Our obtained from 90% ethanol Cyclocarya paliurus extracts
methanol extract compares well with these phenolic contents. (146 mg/mL) [31]. Furthermore, this observation closely relates to
The other solvents produced extracts whose total phenolic results obtained by Alkhawalisy and Hossain [40], where they
contents is similar to those reported in literature, from the ex- reported that they recorded the highest antioxidant activity
tracts of Goniothalamus velutinus (G. velutinus) whose bark with methanol extracts. However, the concentration of the
extract gave 68 GAE mg/g and the leaves 78 GAE mg/g [17]. DDPH concentration used in our study is higher (0.3 mmol/L)
G. velutinus is reported to have antitumor and anticancer as compared to 0.1 mmol/L used by Xie et al. [31].
properties. The water extracts of Hedychium spicatum, Other IC50 results from Pistacia atlantica subsp. mutica ex-
Hedychium coronarium and Hedychium rubrum were found to tracts yielded IC50 values ranging from 0.6 to 1 105.3 mg/mL [1],
be 30, 35 and 67 GAE mg/g [21]. However, our results are with protic polar solvents giving higher activity, which is
much lower than total phenolic contents recorded for the consistent with our work. The major differences observed can
resurrection plant Myrothamnus flabellifolius water, ethanol be attributed to the very low concentration of DPPH used by
and methanol extracts (all 400 mg GAE/g) [34]. Stanojevic Rezaie et al. [3].
et al. [35] also reported much higher total phenolic contents of Our results are also comparable to IC50 values of 155 and
250 mg GAE/g when Hieracium pilosella water, ethanol and 204 mg/mL from the leaves and bark respectively of the extracts
methanol extracts were tested. of G. velutinus [17].
Phenolic contents ranging 90–260 mg GAE/g were recorded An extract is considered to be active against free radicals if
with three species of Curcuma methanol extracts [21]. All these IC50 < 5 mg/mL [41]. All our extracts have IC50 values less than
results are also higher than our reported results except for our 5 mg/mL, therefore all the extracts for the solvents used are a
methanol extract. Curcuma species are used for the treatment possible good source of antioxidants. There is a positive
of asthma tumors and also as antifungal. correlation between the IC50, total phenolic content and total
Total phenolic content is an important factor in the consider- flavonoid content (r = 0.853 for IC50 and total flavonoid
ation of antioxidant activity. Therefore, the higher the value of content and r = 0.899 for IC50 and total phenolic content).
phenolic content, the more beneficial the extract is to human health Furthermore, there is also a very high correlation between
as they can quench reactive free radicals or primary oxidants. total flavonoid content and total phenolic content (r = 0.98).
The phytochemical screening and solvent extraction analysis
4.4. Total flavonoid content give a good guide of the phytochemicals present in the extracts as
well as suitable extraction solvents. And 80% methanol is the best
The methanol extract's flavonoid content matches the very solvent to use for extraction as the extracts are more soluble in polar
high flavonoid contents values obtained with wheat methanol solvents and 80% methanol has more polar organic properties.
extracts ranging from 791.3 to 987.7 mg QE/g [36]. All our other Successive extractions proved that yields can be considerably
results are comparable to the results reported with the hexane, increased by performing short repetitive extractions.
1042 Kayini Chigayo et al./Asian Pac J Trop Biomed 2016; 6(12): 1037–1043

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