Phytochemistry, Biological, and Toxicity Study on Aqueous and Methanol Extracts of Chromolaena odorata

The medicinal plant Chromolaena odorata is traditionally used by people living in different communities of Nepal and the globe against diabetes, soft tissue wounds, skin infections, diarrhea, malaria, and several other infectious diseases. The present study focuses on the qualitative and quantitative phytochemical analyses and antioxidant, antidiabetic, antibacterial, and toxicity of the plant for assessing its pharmacological potential. The extracts of flowers, leaves, and stems were prepared using methanol and distilled water as the extracting solvents. Total phenolic content (TPC) and total flavonoid content (TFC) were estimated by using the Folin–Ciocalteu phenol reagent method and the aluminum chloride colorimetric method. Antioxidant and antidiabetic activities were assessed using the DPPH assay and α-glucosidase inhibition assay. A brine shrimp assay was performed to study the toxicity, and the antibacterial activity test was performed by the agar well diffusion method. Phytochemical analysis revealed the presence of phenols, flavonoids, quinones, terpenoids, and coumarins as secondary metabolites. The methanol extract of leaves and flowers displayed the highest phenolic and flavonoid content with 182.26 ± 1.99 mg GAE/g, 128.57 ± 7.62 mg QE/g and 172.65 ± 0.48 mg GAE/g, 121.74 ± 7.06 mg QE/g, respectively. The crude extracts showed the highest DPPH free radical scavenging activity with half maximal inhibitory concentration (IC50) of 32.81 ± 5.26 µg/mL and 41.00 ± 1.10 µg/mL, respectively. The methanol extract of the leaves was found to be effective against bacterial strains such as K. pneumoniae (ZOI = 9.67 ± 0.32 mm), B. subtilis (ZOI = 15.00 ± 0 mm), and E. coli (7.3 ± 0.32 mm). The methanol extract of the flowers showed the most α-glucosidase inhibitory activity (IC50 227.63 ± 11.38 µg/mL), followed by the methanol extract of leaves (IC50 249.50 ± 0.97 µg/mL). The aqueous extract of the flowers showed the toxic effect with LC50 107.31 ± 49.04 µg/mL against the brine shrimp nauplii. In conclusion, C. odorata was found to be a rich source of plant secondary metabolites such as phenolics and flavonoids with potential effects against bacterial infection, diabetes, and oxidative stress in humans. The toxicity study showed that the aqueous extract of flowers possesses pharmacological activities. This study supports the traditional use of the plant against infectious diseases and diabetes and provides some scientific validation.


Introduction
Diabetes mellitus is a chronic disease caused due to metabolic disorder and is noticed by the high blood sugar in the human body.It is a global health problem afecting an estimated 536.6 million people worldwide as mentioned by the International Diabetes Federation [1].Type 1 diabetes is caused by immune-associated destruction of pancreatic beta cells, whereas type 2 diabetes results from beta cell dysfunction and insulin resistance [2].It can lead to cardiovascular and microvascular complications such as retinopathy, neuropathy, and nephropathy [3].Studies have reported hyperglycemia-associated production of high levels of reactive oxygen species that ultimately leads to vascular damage [4].Diabetes can be managed by insulin injection, changes in lifestyle, diet, and medication.Te synthetic antidiabetic drugs available in the modern world are causing several side efects besides lowering the blood glucose level in human beings.Hence, the search of plant-based natural antidiabetic drug candidates or drugs is an urgent need in modern research.Te natural compounds isolated from the plants such as apigenin, curcumin, naringenin, and resveratrol exhibit antihyperglycemic activities showing least side efects with high efcacy [5].
Reactive oxygen species (ROS) including superoxide anion radicals, hydrogen peroxide, and hydroxyl radicals are produced in mitochondria during aerobic respiration [6].Tey can cause structural damage to DNA, protein, carbohydrates, lipids, and enzymes that lead to infammation, age-related cancer, and neurodegeneration [7].Various enzymatic and nonenzymatic antioxidants neutralize reactive oxygen species and protect our bodies from oxidative damage.Primary and secondary plant metabolites such as vitamin C, vitamin E, polyphenols, favonoids, and carotenoids play a signifcant role as natural antioxidants [8].Te rise of multidrug-resistant bacteria that are resistant to almost all available antibiotics has resulted in the need to fnd noble antimicrobial compounds [9].Plant secondary metabolites such as polyphenols, alkaloids, terpenoids, coumarins, and essential oils display signifcant antimicrobial activity [10].Tus, medicinal plants may act as sources of compounds with therapeutic potential [10].Te study of toxicity in plants can be carried out by the brine shrimp lethality assay which is a cheap, simple, and efective method to report toxic bioactive compounds.In this way, plant secondary metabolites pose a variety of medicinal properties.Plant-based medicine makes up about 25% of the global market in modern medicinal practices.Hence, there is a need for an extensive study into medicinal plants and the incorporation of traditional knowledge with modern science in a country like Nepal which is rich in medicinal plants.
Chromolaena odorata (L.) King and Robinson (also Eupatorium odoratum) is a weedy shrub that belongs to the Asteraceae family.It is native to Central and South America and found in most of the tropical and subtropical habitats around the world including Asia, Africa, and Australia [11,12].C. odorata is a rapidly growing, scrambling, perennial shrub.Its leaf and fower give of a pungent odor upon being crushed.Despite being an invasive species that can potentially cause harm to local vegetation, C. odorata has some benefcial efects in the area of agriculture and medicine [13].From a previous study, it has been reported that the plant is used in the treatment of wounds, skin infections, malaria, diarrhea, cough, and diabetes [14][15][16].It has also been found that the plant shows anti-infammatory, antipyretic, analgesic, antimicrobial, antioxidant, antihyperglycemic, cytotoxic, and antispasmodic properties [17].Te present study focuses on qualitative phytochemical analysis, estimation of phenolic and favonoid contents, antioxidant, antidiabetic, and antibacterial activities, and toxicity of the methanol and aqueous plant extracts.To the best of our knowledge, this is the frst report on this plant which is growing in the western part of Nepal (Figure 1).

Plant Collection, Identifcation, and Extract Preparation.
Te fowers, leaves, and stems of C. odorata were harvested from the Kaski district of Nepal in September 2021.Te herbarium of the plant was submitted to the Central Department of Botany, Tribhuvan University, Kathmandu, Nepal, for identifcation of the plant.Te identifcation number was TUCH21052.Te harvested plant materials were cleaned, shade-dried, and ground.300 g of each plant powder was kept in the conical fasks in which 500 mL of methanol was added in one conical fask, whereas the same amount of distilled water was added to another conical fask as the extracting solvent.Te fasks were kept for percolation with continuous shaking.After 24 hours, the contents of the conical fask with distilled water were fltered using a clean muslin cloth.Te residue was resuspended in the same conical fask with some additional distilled water.Te fltrate was again fltered using Whatman flter paper 1 and concentrated in a rotatory evaporator at 40 °C.Te same process was repeated three times for the complete extraction of the water-soluble metabolites.A similar process was carried out for methanol solvent at intervals of 72, 48, and 24 hours.Te crude aqueous and methanol extracts were stored at 4 °C to proceed with the biological study and chemical analysis (Table 1).

Phytochemical Analysis.
Te qualitative preliminary phytochemical analysis of the plant extract was performed by adopting standard protocols [19,20].

2.2.1.
Alkaloids.Te plant extract (5 mL) was concentrated to yield a residue.Tus, the obtained residue was dissolved in 1.5 mL of 2% (v/v) HCl. 3 drops of Meyer's reagent were added.Te appearance of a white precipitate indicates the presence of alkaloids.

Phenols.
Te plant extract was mixed with 2 mL of 2% FeCl 3 solution.Te formation of blue-green or black coloration indicates the presence of phenols.

Flavonoids.
Te plant extract was mixed with a few pieces of magnesium ribbon, and then, conc.HCl was added in a dropwise manner.Te formation of a pink scarlet color after a few minutes indicates the presence of favonoids.

2.2.4.
Tannins. 2 mL of 5% FeCl 3 was added to 2 mL of plant extract.Te formation of a yellow or brown precipitate indicates the presence of tannins.
2.2.5.Reducing Sugars.0.5 g of plant extract was added to 2.5 mL of Benedict's solution taken in a test tube and then warmed in a hot waterbath for about 5 minutes.Te formation of green/red or yellow coloration indicates the presence of reducing sugar.
2.2.6.Saponins.Te plant extract was mixed with 5 mL of distilled water and then shaken vigorously.Te formation of stable foam indicates the presence of saponins.

Total Phenolic Content (TPC).
Te total phenolic content of plant extracts was measured by using the Folin-Ciocalteu phenol (FCR) reagent method with slight modifcations [21].
A set of gallic acid solutions with concentrations 10, 20, 30, 40, 50, 60, 70, 80, 90, and 100 µg/mL in methanol and 5 mg/ mL plant extract solution in 50% DMSO were prepared.20 µL each of gallic acid and diferent plant extract solutions were flled in diferent bores of a 96-well plate in triplicates.100 µL of FCR (1 : 10 v/v diluted with distilled water) and 80 µL of Na 2 CO 3 (1 M) were added to each bore.Te reaction mixture was placed in the dark for 25 minutes, and then, absorbance was measured at 760 nm by using a microplate reader (SYNERGYILX, BioTek Instruments.Inc., USA).A standard calibration curve was constructed using the absorbance against the diferent concentrations of gallic acid.TPC of plant extracts was calculated using the standard calibration curve and expressed in terms of milligrams of gallic acid equivalent per gram dry weight of plant extract (mg GAE/g).

Total Flavonoid Content (TFC).
Te total favonoid content of the plant extract was measured by using the aluminum chloride colorimetric method with slight changes   [22].A set of quercetin solutions of concentrations 15.4, 30.8, 46.2, 61.6, 77, 92.4, 107.8, 123.2, 138.6, and 154 µg/mL were prepared in methanol.130 µL quercetin solution, 60 µL of ethanol, 5 µL of AlCl 3 , and 5 µL of CH 3 COOK were flled in the bores of the 96-well plates in triplicates.Similarly, 20 µL of plant extract (5 mg/mL in 50% DMSO), 110 µL of distilled water, 60 µL of ethanol, 5 µL of AlCl 3 , and 5 µL of CH 3 COOK were added in triplicates to the remaining bores.Te reaction mixture was allowed to stand for 30 minutes in the dark, and then, absorbance was measured at 415 nm using a microplate reader.A standard calibration curve was constructed using absorbances of quercetin solutions.TFC of plant extracts was calculated by using the calibration curve constructed, and the values were expressed as milligrams of quercetin equivalent per gram dry weight of plant extract (mg QE/g).
2.5.Antioxidant Assay.2, 2-Diphenyl-1-picrylhydrazyl (DPPH) assay was used to evaluate the free radical scavenging activity of plant extracts [23].Plant extract solutions of 500, 250, 125, 62.5, 31.25, and 15.625 µg/mL were prepared by serial dilution of stock solution (5 mg/mL in 50% DMSO).100 µL of DPPH solution (0.1 mM in ethanol) and 100 µL of plant extract solution were flled in the bores of a microplate in triplicates.Te reaction mixture was placed in the dark for 30 minutes, and then, absorbance was measured at 517 nm.50% DMSO was used as control, and quercetin was used as standard.Te percentage of free radical scavenging was calculated by using the following equation: Half maximal inhibitory concentration (IC 50 ) was calculated from the plot of percentage scavenging against concentrations of plant extract using GraphPad Prism 9 software.

Antidiabetic Assay.
Te antidiabetic activity of plant extracts was estimated by using an α-glucosidase enzyme inhibition assay [24].Plant extract solutions of 1000, 500, 250, and 125 µg/mL concentrations were prepared by diluting stock solution (5 mg/mL in 30% DMSO).20 µL of α-glucosidase enzyme (0.5 unit/mL) was premixed with 20 µL of plant extract solution.Ten, 120 µL of potassium phosphate bufer (pH 6.8) was added to the mixture followed by the addition of 40 µL of pNPG (4-nitrophenyl-α-d-glucopyranoside) as the substrate.Te reaction mixture was incubated at 37 °C for 15 minutes, and absorbance was measured at 405 nm.Te absorbance of the control was recorded from a reaction mixture in which the enzyme was substituted by the same volume of bufer solution.Te percentage of enzyme inhibition was calculated by using the following equation: Te IC 50 values for plant extracts were calculated by using GraphPad Prism 9 software.

Antibacterial Assay.
Antibacterial assay of plant extract was performed by using the agar well difusion method [25].Common human pathogens Klebsiella pneumoniae (ATCC700603), Staphylococcus aureus (ATCC25923), Bacillus subtilis (ATCC35021), and Escherichia coli (ATCC25922) were tested against plant extracts.Overnight incubated broth cultures of test organisms were prepared in nutrient broth media.Te concentration of test organisms was maintained at 0.5 McFarland standard (10 6− 8 CFU/mL).About 100 µL of inoculum was taken and spread on MHA agar plates.Ten, wells of 7 mm diameter were bored on MHA plates with the help of a sterile cork-borer.20 µL of plant extract (25 mg/mL in DMSO) was added to the wells in triplicates.Te plates were incubated at 37 °C for 24 hours.After this, the zone of inhibition (ZOI) was measured using a ruler.100% DMSO was used as control, and ampicillin (1 mg/mL) was used as standard.

Brine Shrimp Toxicity.
A brine shrimp toxicity assay was performed to estimate the lethality of plant extracts.Te assay was performed according to standard protocols as described by Meyer et al. [26].Plant extract solutions of 1000, 100, and 10 µg/mL concentrations in methanol were prepared by the serial dilution of stock solution (10 mg/mL). 2 mL of each concentration was taken in three test tubes for triplicates, and the solvent was evaporated to dryness using a water bath.Equal volume of methanol was also taken in a test tube as a control and evaporated to dryness.Te leftover residue was dissolved by adding 5 mL of artifcial seawater.10 healthy brine shrimp larvae (nauplii) were added to each test tube and left for 24 hours, after which the number of surviving nauplii was counted.Tus, the obtained data were used to construct a percentage mortality versus concentration curve.Te curve was then used to calculate the concentration of the plant extract lethal to half of the test organisms (LC 50 ).

Phytochemical Analysis.
Many important groups of phytochemicals were detected in the extracts of C. odorata.Polyphenols, favonoids, quinones, coumarins, reducing sugar, and terpenoids were observed in all extracts of C. odorata (Table 2).CLM, CFM, CSM, and CSA displayed 10 out of 12 phytochemicals screened.CFA and CLA each showed the presence of 9 phytochemicals.Alkaloids were only present in CFM and CLM.Te absence of glycosides in CLA, sterols in CFA, and tannins in CSA was observed.Saponins were found only in aqueous extracts.

Total Phenolic and Flavonoid Content.
Methanol and aqueous extracts of C. odorata contained signifcant amounts of phenolics and favonoids (Table 3).CLM displayed the highest TPC and TFC values with 182.26 ± 1.92 mg GAE/g and 128.57± 7.62 mg QE/g, respectively.It was followed by that of CFM with TPC and TFC of 172.65 ± 0.48 mg GAE/g and 128.57± 7.62 mg QE/g, respectively.Te lowest value of TPC was found in CSM (113.6 ± 3.51 mg GAE/g) and that of TFC in CSA (13.14 ± 1.98 mg QE/g).Te decreasing order of TPC was CLM > CFM > CFA > CSA > CLA > CSM, whereas the decreasing order of TFC was found to be CLM > CFM > CFA > CLA > CSM > CSA.

Antioxidant Activity.
Plant extracts displayed concentration-dependent increments in radical scavenging activities as shown in Figure 2. Methanol extracts showed comparatively higher radical scavenging and lower IC 50 values than their respective aqueous extracts.Leaf and fower extracts were higher in antioxidant activity than stem extracts.Te decreasing order of observed antioxidant activities for diferent plant extracts is CLM > CFM > CFA > CLA > CSM > CSA (Table 3).Tis order correlates with the decreasing order of TPC and TFC observed in the study.Extracts having higher concentrations of phenolic and favonoids showed lower IC 50 values and thus higher antioxidant activity which is in agreement with the previous reports [27].Phenolic compounds are known to scavenge free radicals by donating hydrogen atoms from their hydroxyl groups.Among all extracts, CLM was found to contain the highest antioxidant activity as it displayed the lowest IC 50 value of 32.81 ± 5.26 µg/mL followed by CFM with 41.00 ± 1.10 µg/mL.However, both values were slightly higher than the value of quercetin (3.74 ± 0.15 µg/mL) used as standard.Nevertheless, fower and leaf extracts of C. odorata displayed signifcant radical scavenging activity.CSA displayed the least antioxidant activity with its highest IC 50 value of 152.93 ± 4.71 µg/mL.Te correlation between antioxidant activity and the TPC and TFC content and antidiabetic activity in the plant extracts is shown in Figure 3.

Antidiabetic Activity.
Te stem extracts of C. odorata did not display signifcant enzyme inhibition during the screening of α-glucosidase inhibition assay and hence were excluded from the determination of IC 50 , but signifcant antidiabetic activity was observed in fower and leaf extracts of the plant.Te increasing order of IC 50 values was found to be CFM > CLM > CLA > CFA (Table 3).Hence, CFM displayed the highest antidiabetic activity with the lowest IC 50 value of 227.63 ± 11.38 µg/mL closely followed by CLM with 249.50 ± 5.97 µg/mL.Te presence of alkaloids, a high concentration of phenolics, and favonoids in addition to tannins and terpenoids may be responsible for such higher α-glucosidase inhibitory activity in CFM and CLM [28] (Figure 4).

Antibacterial Activity.
Te plant extracts displayed signifcant activity against Gram-positive (Bacillus subtilis) and Gram-negative bacteria (Klebsiella pneumoniae and Escherichia coli).CLM displayed the most bioactivity as it displayed a signifcant zone of inhibition against three (K.pneumoniae, B. subtilis, and E. coli) out of four bacterial strains employed in the assay (Table 4, Figure 5).Te highest ZOI (15 ± 0 mm) was displayed against B. subtilis and was found to be more potent than ampicillin (14.5 ± 0.48 mm).CFM, CLA, and CSA were found active against two bacteria.CFA was found to be only active against B. subtilis, and CSM was found to be active only against K. pneumoniae.None of the extracts displayed any signifcant ZOI against S. aureus, whereas K. pneumoniae and B. subtilis were found to be highly susceptible to C. odorata.All the ZOI recorded for plant extracts were found to be less than that recorded for ampicillin except for CLM against B. subtilis.
3.6.Toxicity.Te toxicity is reported in decreasing order of LC 50 for diferent extracts as CSM > CLA > CLM > CFM > CSA > CFA (Table 5).Extracts having LC 50 less than 1000 are considered pharmacologically active.All the extracts except CSM showed a toxic efect against brine shrimp nauplii.CFA showed the highest lethality with an LC 50 of Te Scientifc World Journal 107.31 ± 49.04 µg/mL, followed by CSA with 470.23 ± 87.08 µg/mL.Te aqueous extracts were found to be more toxic than their methanol extract counterparts.Te fndings of this study suggest that the fower of C. odorata is comparatively more toxic than its leaf and stem.Te high toxicity in plant extracts can be used in toxic or side efect-based drug discovery strategies (Figure 6).

Discussion
Te presence of phenols, favonoids, alkaloids, tannins, terpenoids, and coumarins and the absence of saponin in CLM are reported for C. odorata.Akinmoladun et al. reported the presence of glycosides in CLM; however, it was reported absent by Mathew et al. [29,30].Similarly, the results reported in the literature agreed in the case of alkaloids, saponins, tannins, terpenoids, favonoids, coumarins, and phenols but did not agree in the case of glycosides and quinones for CLA [30][31][32].Tis may be due to the impacts of altitude, plant growth, environmental stress, harvesting period, and laboratory setup.However, the phytochemical analysis of stem and fower extracts using methanol and the aqueous solvent is the frst report in this study.Diferent phytochemicals are responsible for the bioactivity of plants.Flavonoids, phenols, alkaloids, terpenoids, and coumarins display antioxidant, antidiabetic, anticancer, anti-infammatory, and antimicrobial activities [33].Many drugs such as aspirin, digoxin, paclitaxel, artemisinin, and quinine used in modern chemotherapy are isolated or derived from plant sources [34].Te observed prevalence of important phytochemicals in C. odorata makes this plant a viable candidate as a source of bioactive compounds in the drug discovery and development process.In recent years, the metabolites in the plant samples can also be analyzed using GC-MS and LC-MS/MS in which the bioactive target metabolites are known by analyzing the mass spectra with the help of the computer software.In this method, a signifcant peak is detected and the possible fragments and stable ions are analyzed.Te metabolomics study part is not included in this paper, but the preliminary phytochemical analysis is included to make the study from preliminary to advanced.Te estimation of total phenolics and favonoids showed that the extracts were rich in these metabolites.Te content of phenols and favonoids was found to be comparatively higher in fowers and leaves than in stems.Similarly, methanol extracts displayed higher content than their aqueous counterparts.Such trends were also reported in the previous research [35].Te TPC in CLM is reported as 455.55 ± 4.59 mg GAE/g by Melinda et al. [36].
In the case of CLA, the TPC was found to be lower than 379.0 ± 7.00 and 198.02 ± 3.96 mg GAE/g reported in the literature [35,37].Phenolic contents observed in this study for CLM and CSM were found to be higher than 71.08 ± 0.38 mg GAE/g reported in the literature for the methanol extract of the whole plant [38].Although there were slight variations in TPC and TFC values in the present studies and the previous literature, they almost agreed with each other.Slight variations in TPC and TFC among previous studies and the present study may have arisen due to several factors including temperature, rainfall, soil composition, and ultraviolet radiation [39].Flavonoids and phenolic compounds present in C. odorata prevent oxidative damage to proteins and cultured skin cells and display cytotoxicity against cancer cells and pharmacological activity against pathogens [40].In this study, the radical scavenging activity measured in IC 50 for methanol and aqueous leaf extracts was found to be similar to 0.07 ± 0.003 mg/mL reported for the ethanolic extract of leaves by Omoregie et al. [35].Te antioxidant activity shown by the plant extract is due to the presence of various phytochemicals such as phenols, carotenoids, vitamins, and glucosinolates [41].A signifcant correlation between TPC and TFC with antioxidant activity was observed in the present study.Te antioxidant activity in plant extracts carries signifcant importance as it provides protection from oxidative stress, maintains cellular health, supports the immune system, and prevents various cardiovascular and neurodegenerative diseases, diabetes, and cancer [42].Te correlation was also observed between free radical scavenging and antidiabetic activity shown by the plant extracts.Methanol extracts of fowers and leaves displayed signifcantly higher antidiabetic activity than their   2018) also observed no ZOI against E. coli for CLA [31], whereas ZOI of 11 mm against B. subtilis (at 30 mg/mL) was comparable to ZOI of 10 ± 0.57 mm observed in this study [31].Plant secondary metabolites such as alkaloids, favonoids, and tannins are reported to have antibacterial properties [46].Hence, comparatively higher concentrations of favonoids and the presence of alkaloids in CLM may have contributed to the higher antibacterial activity.Te toxicity study showed that LC 50 value of 830.09 ± 115.57µg/mL for CLA was higher than 392 µg/mL as reported by Asomugha et al. [47].Juliani calculated the LC 50 value from the essential oil of C. odorata to be 52.16µg/mL [48].Te fndings of this study suggest that the leaves, stems, and fowers of plants are pharmacologically active.Toxicity in plants may arise due to individual or synergetic interactions of various metabolites.Certain alkaloids, terpenoids, and polyphenols are reported to pose remarkable cytotoxic activities [49].Tis high cytotoxicity activity of the plant extract may be responsible for its insecticidal cytotoxic and antimicrobial properties.

Conclusions
C. odorata displays a signifcant quantity of favonoids and phenolics showing antioxidant, antidiabetic, antibacterial, and cytotoxic activities.Te results showed a correlation between the concentration of phenolics and favonoids with antioxidant, antidiabetic, and antibacterial activities.Te fower and leaf of the plant displayed higher concentrations of phytochemicals and more antioxidant, antibacterial, and antidiabetic activities than the stem extract.Tus, the leaf extract of this plant could be used against bacterial infection which supports the traditional use of this plant against infectious diseases.Te methanol extracts were found to be richer in phenolic and favonoid content and subsequent antioxidant, antimicrobial, and antidiabetic activities than their aqueous extract counterparts.Although the exact cause of such correlation is not known, similar trends were also observed in the literature.Te plant extracts displayed potential free radical scavenging and α-glucosidase inhibitory activities.Te present study authenticates the importance of C. odorata as a valuable medicinal plant with substantial pharmacological activity.However, it also necessitates further work on the isolation, purifcation, characterization, and standardization of bioactive compounds.Te fndings of this study support the traditional use of C. odorata in the control of diabetes as a viable candidate that should be explored for noble therapeutic agents against diabetes.

FreshFigure 1 :
Figure 1: Photographs of plant samples collected from the study area.

Figure 2 :
Figure 2: Plot of percentage radical scavenging against concentrations (µg/mL) of plant extracts and standard (values are signifcantly diferent from their respective controls at p < 0.0001).

Figure 6 :
Figure 6: Plot of percentage mortality against concentrations (µg/ mL) of the plant extract (values are signifcantly diferent from their respective controls at p < 0.0001).

Table 2 :
Qualitative phytochemical analysis of plant extracts.