Current Research in Complementary & Alternative Medicine (ISSN: 2577-2201)

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Evaluation of Selected Nigerian Medicinal Plants for Phenolic Content, Antimicrobial, and Cytotoxic Activities

Samuel Ayoolu Oguntimehin1*, Edith Oriabure Ajaiyeoba1, Omonike Oluyemisi Ogbole1, Hannah Odunola Dada-Adegbola2, Bosede Bolaji Oluremi3, Adekunle Johnson Adeniji4

1 Department of Pharmacognosy, University of Ibadan, Ibadan, Nigeria

2 Department of Medical Microbiology and Parasitology, University College Hospital, Ibadan, Nigeria

3 Department of Pharmaceutical Microbiology, University of Ibadan, Ibadan, Nigeria

4 Department of Virology, University of Ibadan, Ibadan, Nigeria

*Corresponding author: Samuel Ayoolu Oguntimehin, Department of Pharmacognosy, University of Ibadan, Ibadan, Nigeria

Received Date: 27 July 2022

Accepted Date: 15 August 2022

Published Date: 22 August 2022

Citation: Oguntimehin SA, Ajaiyeoba EO, Ogbole OO, Dada-Adegbola HO, Oluremi BB, et al. (2022) Evaluation of Selected Nigerian Medicinal Plants for Phenolic Content, Antimicrobial, and Cytotoxic Activities. Curr Res Cmpl Alt Med 6: 158. DOI:


Increased exposure to pathogens and free radicals contributes to the high incidence and mortality rate of various types of cancers in Nigeria and globally. This study aimed to screen twenty extracts from fifteen selected Nigerian medicinal plants used traditionally for cancer treatment for phenolic content, antimicrobial, and cytotoxic activities. The phenolic content was determined by Folin – Ciocalteu method, and antimicrobial potentials of the extracts was evaluated using spectrophotometric growth inhibition method while MTT assay was used to assess their cytotoxicity to cancer cell lines. Bark and root extracts of T. tetraptera and X. aethiopica demonstrated satisfactory activities in all the biological tests, which could be linked to their high phenolic contents. The findings support the ethnomedicinal uses of most of the tested medicinal plants.

Keywords: MTT assay; Cytotoxicity; Ethnomedicine; Antioxidants; Antimicrobial


Cancer remains one of the leading causes of death worldwide with an estimated 19.3 million new cancer cases and 10 million cancer deaths [1]. Several factors are associated with the development of cancer, but notable is the actions of free radicals and pathogenic microorganisms [2]. Studies have shown that reactive free radicals interact with macromolecules such as DNA in the cell, leading to damage to cell structure and functions [3]. In addition, pathogenic microbes are associated with cancer [4].

Cancer treatment faces challenges of resistance, toxicities to normal cells, and ineffectiveness of some anticancer agents [5]. The use of an agent with antioxidant and antimicrobial activities will be a good strategy in the treatment of cancer. Medicinal plants are a veritable source of anticancer agents [6], they are a rich source of phenolic compounds which are known to attenuate the actions of free radicals [7] and also showed antimicrobial activities [8].

The dependence of not less than 80% of the African populace on medicinal plants for healthcare needs [9] informed the inquiry into plants used traditionally in the treatment of cancer in Southwestern Nigeria. More so, various studies demonstrated the antioxidant [10], antimicrobial [11], and anticancer [12] activity of some Nigerian medicinal plants. Retrieving information on the pharmacological relevance of medicinal plants is often achieved through the conduction of ethnomedicinal surveys [13]. An ethnomedicinal survey was carried out in Ile-Ife, Osun State, Nigeria between June to December 2017. From the survey, twenty extracts from fifteen plant species were selected for this study based on how they are frequently mentioned. This study aims at identifying plant extracts with antioxidant, antimicrobial, and cytotoxic activities towards the identification of the potential source of new anticancer agents.



The MTT [3-(4,5-dimethylthiazol-2-yl)-2,5diphenyltetrazolium bromide] tetrazolium salt (purity ≥ 97%), vincristine sulphate (purity ≥ 95%), nutrient agar, sabouraud dextrose agar, ketoconazole (purity = ≥ 99%), streptomycin (purity = ≥90%), gallic acid (purity ≥ 90%). All chemicals and media are purchased from Sigma-Aldrich (Germany), Folin – ciocalteu was purchased from Loba Chemie (India).

Plant material

Following the methods of Olorunniola et al. [14], an ethnobotanical survey was previously conducted in Ile-Ife, Osun state Nigeria. The plant parts of frequently mentioned plants were used for this study (Table 1). Plants were collected on the campus of the University of Ibadan, Nigeria, and authenticated at the herbarium of the Forest Research Institute of Nigeria, where voucher specimens were also deposited. The plant materials were dried at room temperature and pulverized into powder.



Local name

Identification number

Part used

Ethnomedicinal use


Asystasia gangetica

(L.) T.Anderson

Akpuarachi (I)

FHI 109634


Antihelmintic, asthma, astringent, diaphoretic, stomachic



Xylopia aethiopica (Dunal) A.Rich.

Kimba (H), Uda (I),

Eruu, girinja (Y),

Ethiopian pepper (E)

FHI 108978



Amenorrhea, biliousness, bronchitis, cough, dysentery, fibroid, malaria, rheumatism [16]


Anchomanes difformis (Blume) Engl.

Igo langbodo,


Ogirisako (Y), Oje (I), Chakara (H)

FHI 109638

Leaves Root

Asthma, diabetes, gastrointestinal disturbances, inflammation, microbial infections, pain, ulcerations [17]

Culcasia scandens P.Beauv.

Oji azu ari nkwu (I),

FHI 110050


Cancer, stomachache [18]


Aspilia africana (Pers.) C.D.Adams

Jamajina (H), Oranjila

(I), Yunyun, Ako yunyun (Y)

FHI 107511


abortifacients, dysentery, hemorrhoid, hemostatic, nervous disorders, skin diseases, stomach disorders,

tuberculosis, ulcers [18]


Crotalaria retusa L.

Koropo, Alatunse,

Saworo (Y), Rattle pea (E)

FHI 109052


cold, fever, flatulence, hemoptysis fever, leprosy, lung disease, skin infections [19]


Tetrapleura tetraptera (Schum et Thonn) Taub.

Dawo (H), Uyayak (IB), Aridan/Aidan (Y)

FHI 110141



febrile convulsions, infantile flatulence, inflammation, rheumatic aches, stomach gripes [20]

Pterocarpus osun


Madubiya (H), Osun (Y)

FHI 108415

Leaves Bark

antipyretic, anti-sickling, asthma, blood supplement, candidiasis, eczema, skin infections[18]


Triclisia subcordata Oliv.

Alugbonron (Y)

FHI 109638


Breast cancer [18]


Treculia africana

Decne. ex Trécul

Barafuta (H), Ukwa (I), Afon (Y)

FHI 106992


anemia, cough, guinea worm infections, hemorrhoid, malaria, ulcer, venereal disease [18]


Olax subscorpioidea Oliv.

Gwano kurmi (H), Aziza (I), Ifon (Y)

FHI 109983


abscess, antisickling, breast cancer, diabetes, hemorrhoid,

jaundice, mental disorders, scalp infection in children,

yellow fever [18]


Petiveria alliacea L.

Guinea Hen weed

(E), Awogbaarun,

Arunyanyan (Y)

FHI 106992

Leaves Roots

Anticancer, guinea worm infections [18]


Morinda lucida Benth.

Oruwo (Y),

Morinda, Indian mulberry (E)

FHI 110086


anticancer, candidiasis, diabetes, female infertility, malaria, vaginitis [18]


Capsicum frutescens L.

Ata wewe (Y), Chilli pepper (E)

FHI 108325


anticancer, antisickling, breast cancer, diabetes, dysentery, fever, stimulant, measles [18]

Nicotiana tabacum L.

Ewe taba (Y), Taba (H), Anwere (I)

FH 107924


candidiasis, cancer, diabetes, epistasis, gonorrhea, hemorrhoid, typhoid fever [18]

E – English; H – Hausa; I – Igbo; IB – Ibibio; Y – Yoruba

Table 1: List of study plants, ethnomedicinal uses, and identification numbers.


Each plant material (200 g) was macerated in 80% methanol for 78 h at room temperature. Extracts were filtered through filter paper (Whatman No. 1) and concentrated to dryness in vacuo.

Total phenolic content (TPC) assay

The total phenolic content of the extracts was determined using Folin – Ciocalteu (FC) reagent following the method of Karakas et al. [21] with slight modification. The extracts were made into 100 µg/mL, while 10% FC (v/v) in methanol was freshly prepared. The FC reagent (25 µL) was added to 50 µL of the extracts in 96 – well plates and allowed to stand for 3 min. For the blank, methanol was used in place of the extracts. A solution of 7.5% Na2CO3 (125 µL) was added to each well and afterward incubated in the dark for 2 h at 25 ± 2oC. The absorbance was recorded with a Thermo Fisher Scientific microplate reader at 758 nm. The experiment was carried out in triplicates. The total phenolic content was expressed as Gallic acid equivalents (GAE) [22].

In vitro antimicrobial assay

Test organisms

Reference bacterial and fungi strains were obtained from the Department of Medical Microbiology and Parasitology, University

College Hospital, Ibadan Nigeria. The bacterial strains used include Escherichia coli ATCC 25923, Pseudomonas aeruginosa ATCC 10145, and Salmonella typhi ATCC 24683 while the fungi strain used was Candida albicans ATCC 24433. Nutrient broth and sabouraud dextrose broth were used for the maintenance of the bacterial and fungal strains respectively at 4oC.

Preparation of inoculums

A small piece of a colony from a day-old culture of each test organism was adjusted to a cell density of 1x108 CFU/mL in sterile distilled water using McFarland Standard No. 0.5.

Spectrophotometric growth inhibition method

% Inhibition = ∆Absorbance of control - ∆Absorbance of test sample x 100

The method of Ahmad et al. [23] was adopted with some modifications. Extracts and standard drugs (streptomycin and ketoconazole) were made into concentrations of 1000, 500, 250, 125, 62.50, 31.25, and 15.63 µg/mL in freshly prepared nutrient or sabouraud dextrose broth. An aliquot of 75 µL of each test concentration was gently mixed with 75 µL of the inoculum in 96 –well plates. Sterile distilled water was used as the control. The absorbance at 540 nm was taken before and after 24 h of incubation at 37 oC. Differences in optical densities were taken as microbial growth indexes. The experiment was carried out in triplicates. The concentration at which there is 50% microbial inhibition (IC50) was determined using Graph pad prism (5.0) while the percentage of microbial inhibition was calculated by using the equation: ∆Absorbance of control

Cytotoxicity assay

Cell culture

Culture of human larynx epithelioma (Hep 2), Human Rhabdomyosarcoma (RD), and cervical adenocarcinoma (HeLa) cell lines were obtained from the Department of Virology, University College Hospital (UCH), University of Ibadan, Nigeria. The cells were maintained in Eagle’s Minimum Essential Medium (MEM) supplemented with 10% fetal bovine serum (FBS) (v/v), 100 units/mL of penicillin, 100 µg/mL of streptomycin, 0.07% NaHCO3 (w/v), 2 mM L-glutamine and 1% non-essential amino acids.

MTT assay

The MTT [3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyl tetrazolium bromide] viability assay was carried out following a mildly modified method by Ogbole et al. [24]. Each cell line was seeded into a 96-well plate and incubated at 37°C for 24 h. Extracts and positive control (vincristine sulphate) were freshly made into concentrations of 1000, 100, 10, 1, 0.1 and 0.01 ug/mL with 5% (v/v) DMSO in maintenance medium. At the expiration of 24 h, medium in wells with confluent monolayer cells were carefully replaced with 200 uL of various concentrations of the extracts and were further incubated at 37 °C for 72 h. Cytopathic effects of the extracts at various concentrations after 72 h was evaluated and scored using AmScope 40X-600X microscope. Medium in wells was carefully replaced with 25 uL of 2% (w/v) MTT dye in PBS and incubated at 37 °C for 2 h. DMSO (125 uL) was added to each well and left on a shaker for 30min to ease the solubility and evenness of the color formed. Absorbance at 492 nm was recorded with a Thermo Fisher Scientific microplate reader. The experiment was performed in triplicate while the CC50 was determined using graph pad prism 5.0. Percentage cytotoxicity of the extracts at various concentrations was calculated using the formula;

% Cytotoxicity (CC) = (A - B) x 100


Where: A = the optical density of untreated cells

B = the optical density of cells treated with plant extracts/ control drug

Statistical analysis

Graphpad Prism, version 5.0 was used for the statistical analysis of data. The data obtained were expressed as Mean ± SD (Standard deviation) values of three independent assessments. The IC50 and CC50 values of all test samples were determined with a nonlinear regression plot of log (cytotoxic concentration) against normalized percentage cytotoxicity. One-way at P < 0.05 followed by Tukey’s test was used to test for the significant difference between the extracts and the standard drugs.


Among all tested extracts, leaf extracts of N. tabacum and P. osun, bark extract of T. tetraptera, and root extract of X. aethiopica had the highest phenolic contents (Table 2) with gallic acid equivalences of 58.35, 56.35, 67.99, 63.84 mg GAE/g, respectively. However, these four extracts are statistically different (P<0.05) in their phenolic contents.

Plant extract

TPC (mg GAE/g)

A. africana (leaf)

4.66 ± 0.23c,e

A. difformis (leaf)

0.17 ± 0.01d

A. difformis (root)

6.32 ± 0.36b,e

A. gangetica (leaf)

7.31 ± 0.21a,b

C. frutescens (leaf)

11.64 ± 0.48k

C. retusa (Root)

8.81 ± 0.78a

C. scandens (leaf)

8.31 ± 0.46a

M. lucida (leaf)

14.63 ± 0.56g

N. tabacum (leaf)

58.35 ± 0.85h

O. subscopoides (leaf)

7.98 ± 0.43a

P. alliaceae (leaf)

3.33 ± 0.48c

P. alliaceae (root)

1.66 ± 0.12d

P. osun (Bark)

8.31 ± 0.60a

P. osun (leaf)

56.35 ± 0.74l

T. africana (leaf)

8.81 ± 0.34a

T. subcordata (leaf)

5.15 ± 0.82e

T. tetraptera (bark)

67.99 ± 0.67i

T. tetraptera (root)

28.59 ± 0.60f

X. aethiopica (bark)

28.59 ± 0.45f

X. aethiopica (root)

63.84 ± 0.38j

Data obtained were expressed as means ± standard deviation (SD), n = 3, for TPC, samples with different superscripts are significantly different (P<0.05) from one another.

Table 2: Total phenolic content of crude plant extracts

The antimicrobial study showed that the extracts exhibit inhibitory activity against tested bacterial and fungal strains (Table 3). The root and bark extracts of X. aethiopica and leaf extracts of A. difformis, Morinda lucida, and Pterocarpus osun had IC50 of 1.5, 20.0, 3.8, 16.9, and 4.1 against Salmonella typhi. Similarly, A. difformis and bark extract ofX. aethiopica produced comparable activities againstE. coli. All tested extracts were active against Pseudomonas aeruginosa; however, none was comparable (P<0.05) to the activity of Streptomycin with IC50 of 0.9 µg mL-1. Root extracts of X. aethiopica and leaf extract of A. difformis showed a broad spectrum of antibacterial activities. Antifungal studies againstCandida albicans showed that root extracts of C. retusa, T. tetraptera, and Ketoconazole exhibited comparable (P<0.05) antifungal activities.

IC50 (µg/mL)


Salmonella typhi

Pseudomonas aeroginosa

Escherichia coli

Candida albicans

A. africana (leaf)

183.2 ± 7.5***

4.58 ± 0.47***

2.52 ± 0.17***

29.17 ± 0.74***

A. difformis (leaf)

3.8 ± 0.3

4.56 ± 0.21***

0.70 ± 0.05

28.01 ± 1.84***

A. difformis (root)

337.5 ± 6.5***

4.58 ± 0.67***

4.41± 0.72***

14.19 ± 2.57**

A. gangetica (leaf)

280.9 ± 7.4***

4.06 ± 0.89***

1.99 ±.0.04***

28.94 ± 3.22***

C. frutescens (leaf)

146.0 ± 2.3***

3.97 ± 0.38***

3.03 ± 0.048***

24.21 ± 0.52***

C. retusa (Root)

296.7 ± 20.4***

4.73 ± 0.37***

3.14 ± 0.47***

4.52 ± 0.32

C. scandens (leaf)

318.0 ± 25.7***

4.22 ± 0.36***

4.13 ± 0.19***

24.19 ± 4.29***

M. lucida (leaf)

16.9 ± 2.9

3.32 ± 0.44***

3.18 ± 0.15***

46.82 ± 0.37***

N. tabacum (leaf)

324.8 ± 5.1***

4.18 ± 0.30***

2.39 ± 0.08***

41.20 ± 0.53***

O. subscopoides (leaf)

427.7 ± 17.3***

3.26 ± 0.24***

1.95 ± 0.05***

29.36 ± 0.38***

P. alliaceae (leaf)

242.1 ± 23.9***

4.42 ± 0.24***

2.75 ± 0.10***

22.69 ± 1.56***

P. alliaceae (root)

307.2 ± 15.5***

4.12 ± 0.23***

3.24 ± 0.51***

79.71 ± 4.21***

P. osun (Bark)

310.4 ± 18.7***


15.89 ± 0.31***

17.05 ± 1.98***

P. osun (leaf)

4.1 ± 0.6

7.44 ± 0.23***

2.74 ± 0.14***

15.21 ± 1.85***

T. africana (leaf)

401.8 ± 20.3***

4.78 ± 0.31***

3.00 ± 0.17***

35.89 ± 2.56***

T. subcordata (leaf)

177.5 ± 2.1***

3.58 ± 0.39***

2.28 ± 0.39***

53.78 ± 3.26***

T. tetraptera (bark)

238.9 ± 35.8***


2.40 ± 0.15***

13.83 ± 3.47**

T. tetraptera (root)

153.7 ± 18.8***


3.02 ± 0.56***

10.62 ± 2.56

X. aethiopica (bark)

20.0 ± 2.6

3.59 ± 0.05***

0.75 ± 0.09

20.29 ± 3.06***

X. aethiopica (root)

1.5 ± 0.7

4.90 ± 0.05***

1.52 ± 0.51**

30.78 ± 4.07***


0.1 ± 0.00

0.98 ± 0.12

0.24 ± 0.04






3.95 ± 0.36

Data obtained were expressed as means ± standard deviation (SD), ND = Not determined, n = 3, level of significant difference from positive control/ standard drug (P<0.05) is represented by *,**,*** while samples without asterisks are not significantly different from the standard drug.

Table 3: Antibacterial and antifungal activities of crude plant extracts.

Extracts were also evaluated for their cytotoxicity on Hep 2, RD, and HeLa cell lines. MTT (3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyl tetrazolium bromide) assay was used to monitor viable cells after treatment with extracts. Most extracts were active against Hep 2, with extracts of A. africana, T. tetraptera, and N. tabacum being the most cytotoxic with IC50 of 1.3, 1.7, and 2.9 µg/mL respectively which were comparable (P<0.05) to the standard drug (Table 4). On RD cell line, the cytotoxicity of the standard drug was comparable to that of C. scandens, C. frutescens, and root extract of X. aethiopica with IC50 of 0.9, 1.6, and 1.6 µg/mL, respectively. Only the bark extract of X. aethiopica demonstrated comparable (P<0.05) cytotoxic activity against the HeLa cell line when compared with the standard drug. Extracts of C. frutescens, A. africana, X. aethiopica, T. tetraptera, and C. retusa showed a broad spectrum of cytotoxic activities against the tested cell lines.

CC50 (µg/mL)


Hep 2



A. africana (leaf)

1.3 ± 0.3

8.3 ± 0.2*

12.9 ± 0.6***

A. difformis (leaf)

284.2 ± 6.3***

62.0 ± 0.6***


A. difformis (root)

65.3 ± 4.3***

5.1 ± 0.3

89.7 ± 1.6***

A. gangetica (leaf)

31.6 ± 1.6***

8.7 ± 0.2*


C. frutescens (leaf)

5.1 ± 0.4

1.6 ± 0.0

5.1 ± 0.4***

C. retusa (Root)

8.0 ± 1.2

8.6 ± 0.2*

14.7 ± 0.4***

C. scandens (leaf)

14.4 ± 0.9***

0.9 ± 0.0

92.4 ± 0.6***

M. lucida (leaf)

100.5 ± 9.0***

14.7 ± 0.7***

85.4 ± 0.3***

N. tabacum (leaf)

2.9 ± 0.4

54.0 ± 0.3***


O. subscopoides (leaf)

5.3 ± 0.7

62.0 ± 0.9***


P. alliaceae (leaf)

5.3 ± 1.0

237.0 ± 2.3***

9.0 ± 0.7***

P. alliaceae (root)

8.5 ± 0.2

31.6 ± 4.3***

253.7 ± 0.7***

P. osun (Bark)

5.4 ± 0.1

14.3 ± 1.5***

144.1 ± 1.1***

P. osun (leaf)

18.5 ± 2.5***

35.2 ± 6.2***

161.4 ± 0.6***

T. africana (leaf)

100.5 ± 3.7***

5.2 ± 0.6


T. subcordata (leaf)

54.0 ± 0.9***

62.0 ± 6.3***

58.1 ± 0.5***

T. tetraptera (bark)

1.7 ± 0.2

14.9 ± 1.1***

14.0 ± 1.3***

T. tetraptera (root)

3.4 ± 0.5

14.1 ± 0.6***

12.9 ± 0.9***

X. aethiopica (bark)

31.6 ± 0.7***

3.3 ± 0.9

0.2 ± 0.0

X. aethiopica (root)

8.6 ± 0.2

1.6 ± 0.2

10.0 ± 0.6***

Vincristine sulfate

0.01 ± 0.0

0.6 ± 0.0

0.6 ± 0.0

Data obtained were expressed as means ± standard deviation (SD), ND = Not determined, n = 3, level of significant difference from vincristine sulfate (P<0.05) is represented by *,**,*** while samples without asterisks are not significantly different from vincristine sulfate.

Table 4: Cytotoxic activities of crude plant extracts


In developing nations, medicinal plants are very important in health care delivery [9]. The prevalence and rising mortality rate of cancers, and related diseases necessitated sourcing treatment alternatives from medicinal plants [12]. Bioactive compounds in extracts of medicinal plants are responsible for the diverse pharmacological activities demonstrated by these plants [25]. Identifying potential medicinal plants for cancer treatment is often achieved through information retrieved from traditional health practitioners (TMPs) [13]. This present study seeks to scientifically justify the ethnomedicinal use of fifteen (15) medicinal plant species used in the treatment of cancer and microbial infections.

Free radicals are proven contributors to the development and progression of most diseases via their damaging effects on macromolecules including proteins, DNA, and RNA [26]. Antioxidants, on the other hand, inhibit the actions of free radicals and therefore could potentially prevent the onset and progression of these diseases [27]. Previous reports showed that Nigerian medicinal plants have antioxidant activities [22,27].

Phenols are known to contribute to the antioxidant activities of medicinal plants [20]. Extract of T. tetraptera was shown to have high phenolic content and was demonstrated to have antioxidant, anti-inflammatory, antimicrobial, hypoglycemic, and antilipidemic activities. Other extracts including bark and root extracts of X. aethiopica and root extract of T. tetraptera also showed high total phenolic contents.

In addition, evidences linking free radicals and chronic microbial infections with cancer have been reported. Salmonella typhi for example has been linked to the development of cancer of the gall bladder [28] while Helicobacter pylori have been linked to gastric cancer [4]. Phenolic compounds in extracts of medicinal plants contribute to their antimicrobial activities due to their damaging effect on the cell membrane and disruption of metabolism and synthesis of nucleic acids [29].

We observed that Extracts used in this study demonstrated antimicrobial activities against S. typhi, P. aeroginosa, E. coli, and C. albicans. Extracts of X. aethiopica root and leaf extract of A. difformis produced a broad spectrum of antibacterial activities. Fruit extract of X. aethiopica and derivative of its major constituent had earlier been demonstrated to have antimicrobial activities [30]. Our findings demonstrated that the root and bark extracts of X. aethiopica equally hold antimicrobial properties. The activities observed in this study may be attributed to the high phenolic content as a result of the phenolic constituents of the test samples.

Varying cytotoxic activities against tested cell lines were reported for our study plants as observed in previous reports [12,24,31]. According to the National Cancer Institute (NCI) on screening of medicinal plants for cytotoxic activities, plant extracts with CC50 < 30 μg/mL are considered active [12]. Based on the NCI standard, nineteen (19) extracts were active against at least one (1) cancer cell line, while ten (10) extracts were active against at least two (2) cancer cell lines. Only six (6) extracts were cytotoxic to all the cancer cell lines used.

We are reporting perhaps the first cytotoxicity studies on the root and bark extract of X. aethiopica. The root extract of X. aethiopica produced the most pronounced cytotoxicity against Hep 2, RD, and HeLa cell lines. Earlier studies showed that fruit extract of X. aethiopica was cytotoxic to cancer cell lines of the prostate (DU-145), breast (JIMT-1), pancreatic (MIA-PaCa 2), and cervix through the induction of apoptosis and arrest of the cell cycle [32]. Ent-15-oxokaur-16-en-19-oic acid, 3,4,5-trihydroxy6,6-dimethylpyrano[2,3-g] flavone, and isotetrandrine are some of the cytotoxic constituents in the fruit extract of X. aethiopica [33].

This study also showed that bark and root extracts of T. tetraptera demonstrated cytotoxicity against all tested cancer cell lines. Fadeyi et al. [12] reported the cytotoxicity of extract of T. tetrapleura against breast (BT-549) cancer cell line. Similarly, in vitro, and in vivo models of Ozaslan et al. [34] also demonstrated the cytotoxicity of fruit extract of T. tetraptera against Ehrlich Ascites tumor cells. Bioactive coumarin, saponins, terpenes, and some phenolics have been isolated from extracts of the plants [20]. The high phenolic content of T. tetraptera extract might contribute to its cytotoxicity, however, further works will aim at identifying the active cytotoxic compounds.

Stem extract of C. retusa was found to be more cytotoxic than leaf, seed, pod, and flower extracts of the plant although in an un-selective manner [35]. We report the cytotoxicity of its root extract to Hep 2, RD, and HeLa cell lines. Similarly, leaf extract of A. africana was found to be cytotoxic against the three cell lines used. Niyonizigiye et al. [36] reported the cytotoxicity of extracts of A. africana obtained using various green methods of extraction against AGS, A549, and HeLa cell lines. Gallic acid, chlorogenic acid, syringic acid, ferulic acid, and quercetin were detected in the most active extract of A. africana.

In this study, C. frutescens elicited a broad spectrum of cytotoxicity against all tested cell lines. Its fruits, commonly used in African cuisine are widely studied for their nutritional and health benefits [37]. Although a report suggests that capsaicin, a constituent of the fruits is a human carcinogen [38], however, the same compound has been reported to demonstrate cytotoxic and cancer prevention potentials [37]. A more recent report demonstrated that capsaicin and piperine from Piper nigrum could reverse the resistance of cancer cells to doxorubicin [39].


In this study, we evaluated the antioxidant, antimicrobial, and cytotoxicity of extracts of medicinal plants used traditionally in the treatment of cancer in Southwestern Nigeria. Results from the study justify the traditional use of these extracts in the treatment of cancer and accompanying conditions. Extracts of T. tetraptera and X. aethiopica was active in all the biological tests which could be linked to their high phenolic contents. Further purification might potentiate their pharmacological effects which will favor their pharmaceutical application in the development of anticancer and antimicrobial therapeutics. Our current endeavor is devoted to identifying the active constituents present in the extracts of these plants.


SAO is grateful to the Postgraduate College, the University of Ibadan for the Teaching and Research Assistant Award with which this study was carried out.


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