Advances in Pharmaceutics

Advances in Pharmaceutics / 2015 / Article

Research Article | Open Access

Volume 2015 |Article ID 485469 | 14 pages |

Preliminary Investigation of Bioactive Compounds and Bioautographic Studies of Whole Plant Extract of Euphorbia pulcherrima on Escherichia coli, Staphylococcus aureus, Salmonella typhi, and Pseudomonas aeruginosa

Academic Editor: Barbara R. Conway
Received14 Aug 2014
Revised09 Dec 2014
Accepted14 Dec 2014
Published21 Jan 2015


The aim of this study is to carry out preliminary investigation of bioactive compounds and bioautographic studies of whole plant extract of Euphorbia pulcherrima on Escherichia coli, Staphylococcus aureus, Salmonella typhi, and Pseudomonas aeruginosa. Tukey HSD test of hierarchy for the effect of different solvents crude extract on bacterial isolates indicates the methanol extract as the most bioactive. The Tukey HSD analysis also showed that the bioactivities of the crude extracts of the various parts of Euphorbia pulcherrima were part dependent and the whole plant was the most bioactive. The ethyl acetate fraction of the methanol extract of the whole plant of Euphorbia pulcherrima has been shown in this work to contain phytochemicals which have shown remarkable activities against Escherichia coli, Staphylococcus aureus, Salmonella typhi, and Pseudomonas aeruginosa. The bioactivities against the test organisms were due to the combined effects of the compounds separated on TLC plates. Families of terpenoids, flavonoids, alkaloids, saponin, and steroids that were detected in the extracts were identified by GC-MS. The various classes of phytochemicals in the E. pulcherrima plant provided the antimicrobial potency of the plant.

1. Introduction

The search for solutions to the global problems of antibiotic resistance in pathogenic microorganisms has often been driven on the isolation and characterization of new antimicrobial compounds from a variety of sources including medicinal plants [1]. Investigations into toxicity of medicinal plants have been reported by [24]. However, there is still an increasing interest in the use of medicinal herbs for meeting the goal of primary health care delivery worldwide [5, 6].

The plant family Euphorbiaceae contains skin irritating and tumor promoting diterpenoids [7].

However, some species are used in folk medicine to treat skin diseases, gonorrhea, migraine, intestinal parasites, and warts [8]. The broad range and diversity of biological activities in the Euphorbia genus may be due to the presence of various components in the plants with different modes of action [9, 10].

The active principles of many drugs found in plants are secondary metabolites [11, 12]. However, there is scanty literature on the bioactive secondary metabolites possessed by Euphorbia pulcherrima that may be responsible for its curative effect.

This present study focused on identification of bioactive compounds in whole plant extract of Euphorbia pulcherrima and bioautographic studies of the whole plant extract with Escherichia coli, Staphylococcus aureus, S. typhi, and Ps. aeruginosa as test organisms. Bioautography is a microbial detection method hyphenated with planar chromatography techniques. It is based mainly on antimicrobial or antifungal properties of analyzed substances. The selection of E. pulcherrima for investigation premised on its use and efficacy in the African ethnopharmacopoeia to treat gastroenteritis related ailments [13], despite its acclaimed toxicity. The medicinal properties of the plant are also contraindicated in the local treatment of respiratory tract infection, malaria, eczema, asthma, and wound healing properties.

2. Materials and Method

2.1. Collection and Authentication of Samples of Euphorbia pulcherrima Plant

The samples of E. pulcherrima were collected from the bushes along Gwarzo road, Kano State, Nigeria, at different sites between November and December 2013. The plants were authenticated at the Herbarium of the Department of Biological Sciences, Bayero University, Kano.

2.2. Preparation of Plant Samples

The E. pulcherrima whole plant samples were washed with distilled water and dried at room temperature in the biological garden at the Department of Applied Science, Kaduna Polytechnic. Dried E. pulcherrima samples were crushed and pulverized using sterilized mortar and pestle. The plant powder was exhaustively and successively extracted with methanol, ethanol, and water in Soxhlet extractor. 500 g of plant was used for the extraction from which the crude extract was obtained. 100 mg/mL, 50 mg/mL, and 25 mg/mL of the crude extract were used to carry out the antimicrobial activity evaluation against the test organisms. The methanol extract was used to carry out further analyses as it indicated the highest activity against the test organisms. Preliminary antimicrobial activity studies confirmed the methanol extract as the most bioactive against Escherichia coli, Staphylococcus aureus, S. typhi, and Ps. aeruginosa as test organisms.

2.3. Chromatographic Studies

The crude methanol extract of whole plant of E. pulcherrima (L) was fractionated using ethyl acetate. The whole plant ethyl acetate fraction was subjected to thin layer chromatography (TLC) using normal TLC precoated silica gel G micro slides. Various solvent systems consisting of hexane and ethyl acetate in the ratios 9 : 1, 4 : 1, 7 : 3, 3 : 2, and 1 : 1 were used at different concentrations to determine the solvent system that provided maximum separation of compounds when the slides were sprayed with p-anisaldehyde and visualized under UV light. Hexane : ethyl acetate in ratio 7 : 3 was used to separate the components of the extract and the Rf values were thus calculated. The developed chromatograms were subjected to antimicrobial activity test by the Agar overlay bioautography method (Onawumi, 2000) and observed the zones of inhibition on the TLC plates. The ethyl acetate fraction was used in its crude form.

2.3.1. Column Chromatography

The ethyl acetate extract used for the column chromatography was in crude form. The weight of the extract used was 4 g. This was eluted with 200 mL of 100% n-hexane first and then with varying ratios of hexane : ethyl acetate used. 20 mL of eluents was collected at intervals and similar compounds were pooled together after TLC.

A glass column of length 30 cm and width 3 cm parked with silica gel was used for the partitioning of the ethyl acetate fraction. The ethyl acetate fraction was first eluted with 200 mL of 100% n-hexane and two different sets of fractions were collected and labeled as A and B. The fraction obtained by eluting the column with 9 : 1 n-hexane : ethyl acetate was labeled as C. n-Hexane : ethyl acetate in the ratio 4 : 1 eluted fractions D, E, F, and G. 7 : 3 n-hexane : ethyl acetate mixture eluted the fraction labeled H. The fractions were further used to confirm the bioactivity of the ethyl acetate fraction.

2.4. FT-IR and GC-MS Analysis

The A, B, C, D, E, F, G, and H fractions obtained from the column chromatography were concentrated on rotary evaporator and analysed using GC-MS-QP2010 Plus Shimadzu and FT-IR model 8400S scanned in accordance with ATSM1252-98 to determine the probable compounds responsible for the bioactivity of the fractions.

2.5. Characterization and Authentication of Test Organisms

The test organisms were typed cultures of E. coli ATCC 25922, Ps. aeruginosa ATCC 27853, S. aureus ATCC 25923, and the clinical isolates of S. typhi obtained from the Pharmaceutical Microbiology Laboratory, Department of Pharmaceutical Sciences, Ahmadu Bello University, Zaria. The standard strains of bacteria were grown on nutrient agar and tested for purity while the clinical isolates of S. typhi were characterized as described by Cheesebrough [14] by observing their cultural characteristics when subcultured on SS agar, MacConkey agar, and nutrient agar and the Gram staining reaction for bacteria. Biochemical tests for motility, citrate, and methyl red as positive confirmatory tests were performed for S. typhi.

2.6. Preparation and Standardization of Inocula

McFarland’s standard method was adopted from Cheesebrough [14] to standardize the organisms to 1.0 × 108 cfu/mL using Genesys 20 spectrophotometer for the bacterial test organisms at 625 nm optical density.

2.7. Antimicrobial Susceptibility Test

The agar well diffusion method of the National Committee on Clinical Laboratory Standard [16] was adopted to test for the antimicrobial activity of the extracts on the test organisms. Sterile media plates of nutrient agar were prepared for the bacteria. These plates were then separately flooded with diluted standardized overnight cultures and then drained off to remove excess. Wells of 6 mm diameter were made in triplicate in each plate with a central well for the control using 6 mm sterile cork borer. The wells were filled with 0.1 mL of diluted concentrations of extracts with the aid of sterile pipettes per well. 100, 50, and 25 mg/mL of extract were used and 1 mg/mL of the standard antibiotics (ciprofloxacin 500 mg and flucamed 50 mg) was used as positive controls. Sterile distilled water was used as negative control on a separate plate. Diameters of zones inhibition were measured after incubating the plates at 37°C for 24 hrs (bacteria). The plates were replicated in triplicate and the diameter of zones of inhibition was recorded.

2.8. Bioautographic Studies

The agar overlay method was adopted for the bioautographic studies. The agar media were applied directly onto the developed TLC plate of the whole plant ethyl acetate fraction, TLC chromatogram. 19 mL of molten nutrient agar was seeded with 1 mL of standardized overnight culture of the susceptible organism. This was poured over the developed chromatogram TLC plate kept in a Petri dish. This was allowed to solidify and prediffuse for 2 hrs before incubation at 37°C for 24 hrs for the bacterial isolates. The plates were sprayed with aqueous solution of methyl thiazolyl tetrazolium (MTT) chloride for the detection of dehydrogenase activity. Zones of inhibition were observed as clear spots against purple background.

3. Results

The percentage yield for the E. pulcherrima methanol extract was 5.14% with dark green appearance and gummy texture. Ethanol extract was 4.55% with dark green appearance and gummy texture. The aqueous extract was 4.16% and appeared as a dark solid extract. The ethyl acetate fraction of the methanol extract was consistently giving higher antimicrobial activity against the test organisms in comparison to other fractions and so it was used for the study.

3.1. Chromatography Studies

The thin layer chromatograms of the ethyl acetate fraction revealed the presence of eight compounds with different Rf values as shown in Table 1.


Rf values0.160.420.540.650.710.780.830.89

The partitioning of the ethyl acetate fraction on silica gel column using 100% n-hexane, 9 : 1 hexane : ethyl acetate, 4 : 1 hexane : ethyl acetate, and 7 : 3 hexane : ethyl acetate also revealed sixty-eight fractions of different colours that were grouped into eight using the similarity in their Rf values (Table 2).

Serial numberSolvent systemFractions elutedColourGroup

1n-Hexane1, 2, 3BlackA
2n-Hexane4, 5, 6, 7, 8, 9, 10Light greenB
3Hexane : ethyl acetate (9 : 1)11, 12, 13, 14, 15, 16, 17, 18, 19, 20WhiteC
4Hexane : ethyl acetate (4 : 1)21, 22, 23, 24YellowD
5Hexane : ethyl acetate (4 : 1)25, 26, 27, 28, 29, 30, 31, 32, 33Dark brownE
6Hexane : ethyl acetate (4 : 1)34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48Dark greenF
7Hexane : ethyl acetate (4 : 1)49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62GreenG
8Hexane : ethyl acetate (7 : 3)63, 64, 65, 66, 67, 68BrownH

The results of the GC-MS analysis of fractions A, B, C, D, E, F, G, and H revealed different phytochemicals (terpenoids, flavonoids, alkaloids, saponin, and steroids) as shown in Tables 411. The chromatograms of the extracts are in Figures 18. The presence of the compounds was further confirmed by functional groups such as

These functional groups were revealed by the FT-IR analysis of the ethyl acetate fraction (see Table 3).

Serial numberPeaks in ethyl acetate extractMotionFunctional group

C–H bending out of planeAromatics

C–N stretching
C–O–C stretch


41373.36CH3 bendAlkanes

51456CH3 bendAlkanes

N–H stretchingNitrogenous compounds

73379.4O–H stretchAlcohol/phenol

81041.6C–O stretchPhenol

91724C=O stretchingAliphatic aldehydes

102856.67Carboxylic acid O–H stretchAcid

112924.18C–H stretchingAliphatic hydrocarbons

Peak numberNameStructure

43-Fluorophenyl 2-fluoro-6-(trifluoromethyl)benzoate

144-Bromophenyl heptyl phthalate 

19O-(3-(tert-Butyl)cyclohexa-2,4-dien-1-yl) (6-methoxypyridin-2-yl)(methyl)carbamothioate 

34Bis(4-methylheptan-3-yl) phthalate 

Peak numberNameStructure

8Menthyl acetate

102,4,4-Trimethylpentyl 2-ethylbutanoate 


19Heptan-3-yl isobutyl phthalate  



25Butyl heptan-3-yl phthalate 





44Bis(2-ethylhexyl) phthalate  




12Diisobutyl phthalate 


17Dibutyl phthalate 


34Lup-20(29)-en-3-ol, acetate 





8Heptan-4-yl isobutyl phthalate 

13Dibutyl phthalate 



24(8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl nonadecanoate 





7Diisobutyl phthalate


29Bis(2-ethylhexyl) phthalate

34 (E)-1,2-Bis(5-methylbenzo[d]oxazol-2-yl)ethene


12-Phenylacetic acid 




9Triethyl 2-hydroxypropane-1,2,3-tricarboxylate 

32(E)-17-(5-Ethyl-6-methylhept-3-en-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate 


12,4-Di-tert-butylphenyl 5-hydroxypentanoate

















3.2. Bioautography Studies

The results of the bioautography tests of ethyl acetate extract against E. coli (EC), Ps. aeruginosa (Ps), S. typhi (ST), and S. aureus (SA) are shown in Figure 9. It revealed that all the eight compounds separated by TLC had good activities against all the test organisms. Figure 9 compares the original TLC plates displaying the separated components with the developed TLC plate of the whole plant ethyl acetate fraction carrying 19 mL of molten nutrient agar which was seeded with 1 mL of standardized overnight culture of the susceptible organism in Petri dishes.

4. Discussion

The chromatogram of the Euphorbia pulcherrima extracts A, B, C, D, E, F, G, and H obtained from the GC-MS confirmed the numerous compounds extracted by the ethyl acetate solution. However not all of the compounds represented by the peaks may be of relevance in the light of antimicrobial activity. The useful antimicrobial phytochemicals include terpenoids, flavonoids, alkaloids, saponin, and steroids. These categories of phytochemicals have been detected in the extracts and their names are presented in Tables 411. The antimicrobial activities of the plant may be attributable to the presence of the identified phytochemicals in the extracts. Terpenes or terpenoids are active against bacteria [1726]. Flavonoids which are hydroxylated phenolic substances but occur as C6-C3 units linked to an aromatic ring were present in all extracts. Since they are known to be synthesized by plants in response to microbial infection [27], it should not be surprising that they have been found to be effective antimicrobial substances against microorganisms. Their activity is probably due to their ability to complex with extracellular and soluble proteins and to complex with bacterial cell walls similar to quinones. More lipophilic flavonoids may also disrupt microbial membranes [28]. The Euphorbia pulcherrima fractions A, B, C, D, E, F, G, and H have been found to be largely similar in composition but fraction H obtained from hexane : ethyl acetate (7 : 3) appears to contain more alkaloids and terpenoids than other fractions. Generally the mixtures of hexane and ethyl acetate were more effective than only hexane in the extraction of the phytochemicals from the Euphorbia pulcherrima.

All the compounds A, B, C, D, E, F, G, and H showed good activity against the test organisms with zones of inhibitions ranging between 18 and 35 mm at the highest concentration level (100 mg/mL).

The bioautography results confirmed the presence of different antimicrobial compounds in the ethyl acetate fraction. All the compounds A, B, C, D, E, F, G, and H showed good activity against the test organisms with zones of inhibitions evident from the clearing of the spots from the TLC plates (Figure 9). The bioactivity against the test organisms was observed to be attributable to the combined effects of the compounds separated on the TLC plate. This is because all the spots on the TLC plates were cleared consequently upon activity against the test organisms. It is indicative of the synergistic effects of the components of the extract against the test organisms. This finding corroborates the works of Esimone et al. [29]. The identified compounds might have found their way into the cells of the test organisms and ensured the production of efflux pump inhibitors (resistance modifying agents) which may have facilitated the penetration of more phytochemicals into the microbial cells especially of the multidrug resistant organisms. Researches have shown that plant medicinal compounds have resistance modifying activities in vitro [1]. Similarly, Tegos et al. [30] reported that two MDR inhibitors (IN271 and MC207110) from Berberine plant were found to have increased the effectiveness of 13 plants antimicrobial compounds against both Gram-positive and Gram-negative bacteria including those known to express efflux pumps.

5. Conclusion

The ethyl acetate fraction of the methanol extract of the whole plant of Euphorbia pulcherrima contains phytochemicals which have shown remarkable activities against Escherichia coli, Staphylococcus aureus, S. typhi, and Ps. aeruginosa. The bioactivities against the test organisms were due to the combined effects of the compounds separated on the TLC plates. Preparative TLC of the various hexane : ethyl acetate fractions are therefore suggested. This should lead to the isolation of the individual bioactive agent and investigation of their independent bioactivity.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


The authors are grateful to Benedict O. Odjobo, Analytical Unit, Federal Institute of Industrial Research, Oshodi, for the GC-MS analysis and the National Research Institute for Chemical Technology, Zaria, for the FT-IR.


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Copyright © 2015 H. B. Sharif et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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