*Corresponding Author:
S. Nayaka
Department of Studies in Botany, Karnatak University, Dharwad-580 003, India
E-mail: sreenivasankud@gmail.com
Date of Received 04 November 2019
Date of Revision 23 December 2019
Date of Acceptance 23 January 2020
Indian J Pharm Sci 2020;82(2):260-269

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The present study was focused on the green synthesis of silver nanoparticles using the aqueous extract of Putranjiva roxburghii seed and investigation of antibacterial activity of the nanoparticles. Further, the synthesized silver nanoparticles were tested on human breast cancer cell line the potential tumour suppressing property for antitumour activity. The seed extract was investigated for the presence of secondary metabolites and the formation of silver nanoparticles was indicated by a colour change from pale yellow to brown. The synthesis of the silver nanoparticles was ascertained with UV/Vis spectroscopy, atomic force microscopy, X-ray powder diffraction, energy dispersive X-ray analysis, Fourier Transform infrared spectroscopy and transmission electron microscopy. Antibacterial and anticancer activity of the synthesized silver nanoparticles was tested using agar well diffusion and 96 well plate mean transit time cell proliferation assay methods, respectively. The results showed that silver nanoparticles were spherical, 13-69 nm in size with a maximum absorption peak at 371 nm. These silver nanoparticles showed considerable antibacterial effects on Staphylococcus aureus, Streptococcus pneumoniae and Enterococcus faecalis except on Escherichia coli. The cytotoxic effect of the silver nanoparticles was tested on human breast cancer cell line. The decrease in % viability of the human breast cancer cell line cells was observed at 12.5 to 200 µg/µl concentration with an IC50 of 72.32 µg/ml. It is an easy, inexpensive and eco-friendly approach for the biosynthesis of silver nanoparticles from Putranjiva roxburghii seed extract and the nanoparticles exhibited antibacterial activity and a potential to be used against human breast cancer.


Silver nanoparticles, Putranjiva roxburghii, green synthesis, phytochemical test, antibacterial, anticancer activityy

Nanotechnology is emerging as an area of intense scientific research, due to a wide variety of potential applications in the modern material world [1]. Nanoparticles (NPs) possess a very small size and very high surface to volume ratio[2]. Green nanotechnology is emerging into an important tool for the synthesis of nanoparticles. Biological synthesis of NPs is very well known as green chemistry, and it is growing in to a simple but effective alternative to chemical procedures to obtain NPs and also it is non-toxic, easy and environmental friendly[3-6]. The synthesis of metal NPs can be done by employing many methods such as physical, chemical, photochemical and biological synthesis. The use of microbes and plants for the reduction of metal ions is found to be much faster and stable at different physical conditions[7]. Among the metal NPs, gold and silver NPs have been used more often for various applications[8]. Silver nanoparticles (AgNPs) have some unique properties like surfaceenhanced Raman scattering, high electrical and thermal conductivity, surface plasmon resonance and chemical stability[9]. Plants contain different kinds of metabolites such as alkaloids, terpenoids, polyphenols, phenolic acids, sugars and proteins to play an important role in the bio-reduction of ionic silver (Ag+) to elemental silver (Ag0), and these act as capping and stabilising agents[10]. AgNPs can be obtained through green synthesis using plant extracts and microbial cell biomass or cells[11]. Due to the ease of large-scale synthesis and maintenance-free, plants or plant extracts are more preferred for NP synthesis than microbes[12,13]. The pre-established plant secondary metabolites play an important role in the reduction and stabilization of Ag+ [10]. For the synthesis of AgNPs, various parts of plants or their extracts have been extensively used and phytosynthesis is considered as an easier and more rapid method among the biological processes[14].

Putranjiva roxburghii (P. roxburghii) has been described as an important plant in the traditional Ayurvedic and Unani systems. Various parts of P. roxburghii are used for the treatment of different diseases[15,16]. The leaves are used to treat inflammatory and eye diseases, while the seeds are used orally in the form of a powder for the treatment of burning sensation, thirst, dysuria, elephantiasis, ophthalmic diseases, constipation, semen disorders, infertility, diseases of female genital organs and also as an aphrodisiac[17,18]. There are reports of green synthesis of AgNPs using various parts of P. roxburghii and their antimicrobial activity [19] but the synthesis of AgNPs from seed extract and their biological activity was not reported even though there were reports about the medicinal uses of P. roxburghii seeds[16,17]. The present study is focused on the green synthesis of AgNPs using the aqueous extract of P. roxburghii seeds and investigation of the antibacterial and anticancer activity possessed by these AgNPs.

Materials and Methods

P. roxburghii seeds were collected from a commercial Ayurvedic store near Dharwad, Karnataka and authenticated by comparing with the sample existing in the herbarium at the depository of plants and animals museum, Karnatak University, Dharwad and literature of traditional medicinal plants. AgNO3 and nutrient agar were procured from Himedia Laboratory. Staphylococcus aureus (MTCC 6908), Escherichia coli (MTCC 40), Streptococcus pneumoniae (MTCC 9238) and Enterococcus faecalis (MTCC 6845) were procured from NCL Pune.

Preparation of seed extract:.

P. roxburghii seeds were used to synthesise AgNPs. The seeds were washed several times with distilled water to remove dust particles and other debris. Then the dried seeds were crushed into a fine powder using a mortar and pestle. Ten grams of the seed powder was suspended in 100 ml of distilled water, heated for 1 h at 80°. The mixture was allowed to cool, filtered through Whatman No.1 filter paper and then centrifuged at 5000 rpm for 5 min. The filtrate was collected in a conical flask and was stored in a refrigerator at 4° for further use[19]. Standard methods was used for the phytochemical analysis of P. roxburghii seed aqueous extract[20,21].

Preparation of AgNPs from the seed extract:

For the synthesis of AgNPs, 0.1 mM AgNO3 solution was prepared, 86% of AgNO3 solution was mixed with 14% seed extract and the pH was adjusted to 8.5. The colour change from yellow to reddish-brown was observed, which indicated reduction of Ag+ to Ag0 NPs. Finally, the synthesized nanoparticles were air-dried and collected in Eppendorf tubes to carry out further analysis[19].

UV/Vis spectroscopy:

The spectrophotometric analysis of the synthesized AgNPs was carried out to measure the absorption maximum of AgNPs on a UV/Vis double-beam spectrophotometer (Metash UV-9000A). The synthesized AgNPs were scanned at different wavelengths periodically from 200 to 700 nm at room temperature. The absorption spectrum of the AgNPs was plotted with wavelength on X-axis and absorbance on Y-axis[14].

Atomic force microscopy (AFM):

The purified AgNP suspension was freeze-dried to obtain a powder and a thin film of sample was prepared to perform AFM which reveals the morphological details. The AgNPs were scanned with AFM (Nano Surf Flex AFM) to determine the distribution and surface morphology of the synthesized AgNPs[22].

X-ray diffraction (XRD):

XRD measurement of the AgNPs was carried out using a solution drop coated on a glass substrate on an X-ray diffractometer, operated at a voltage of 3 keV. The phase formation was analysed by XRD analyser (Rigaku Miniflex 600) in the 2θ range from 30 to 80° at the scanning rate of 4º/min. The intensities measured with XRD can provide quantitative, accurate information on the atomic arrangements at interfaces[14].

Energy-dispersive X-ray (EDX) spectroscopy:

EDX was employed to determine the presence of various elements and to measure their relative proportions. Initial EDX analysis usually involved the generation of an X-ray spectrum from the entire scan area to detect the different elements in a sample[14].

Transmission electron microscopy (TEM):

TEM is helpful for the direct imaging of the atomic structure of the sample, the exact structure and diameter of the sample particle can be determined by the high- resolution images. The dried AgNPs were characterized by TEM (Hitachi, Model: S-3400N)[11].

Fourier transform infrared (FTIR) spectroscopy

The functional group analysis was characterized by FTIR (Nicolet 6700) and a spectrum was recorded in the region of 4000 to 400 cm-1. The sample gave peaks at different wavenumbers, according to the peak values the possible functional groups are interpreted to know the structure of the synthesized NPs[19].

Antibacterial activity of AgNPs:

The antibacterial activity of AgNPs was determined against Gram-positive bacteria such as Streptococcus pneumoniae, Staphylococcus aureus, Enterococcus faecalis and a Gram-negative bacterium Escherichia coli using the agar well diffusion method[10] on Mueller- Hinton agar medium (pH 7.4). The test organisms were spread on separate Mueller-Hinton agar medium plates and wells of 6 mm diameter were made on 4 mm thick media. AgNO3 solution was filled in a well as a control, AgNPs suspension at concentrations of 25, 50, 75 and 100µg/ml were filled in separate wells. These plates were incubated overnight at 37º for 24 h[4]. After the incubation period, the antibacterial activities were determined by measuring inhibition zone diameter.

Anticancer activity of AgNPs:

Cell viability was measured using MTT assay, which would give effect of AgNPs on cell proliferation and cytotoxicity. Briefly, the MTT assay is based on the reduction of yellow coloured water-soluble tetrazolium dye to formazan crystals. The human breast cancer (MCF-7) cell line was procured from NCCS, Pune. The cells were sub cultured and maintained until they reach 70 % confluence in T25 flasks at 37º in a 5% CO2 incubator. Medium control (medium without cells), negative control (medium with cells but without test compound) and positive control (medium with cells and 15 µM of camptothecin) were used. During the assay, the MCF-7 cells were plated onto 96 well (Thermoscientific Nunc, Cat. No. 167008) flat-bottom plates at a cell density of 20 000 cells/well and the cells were allowed to grow for 24 h. These cells were then treated with 12.5, 25, 50, 100 and 200 µg/ml concentrations of AgNPs suspension for 24 h followed by the addition of MTT reagent to get a final concentration of 0.5 mg/ ml. The plates were incubated for 24 h at 37º in a 5 % CO2 atmosphere. After incubation, the spent media was removed and the plates were wrapped with aluminium foil to avoid exposure to light and again incubated for 3h. Then the product of MTT reduction (formazan) was dissolved in 100 µl of DMSO with gentle shaking and the absorbance was read on an ELISA reader at 570 nm and 630 nm was used as reference wavelength[23].

Results and Discussion

Preliminary screening for secondary metabolites of the P. roxburghii seed extract indicated the presence of alkaloids, flavonoids, amino acids, proteins, saponins, fats and oils, while cardiac glycosides, phenols, phlobatannins, tannins, and quinones were absent (Table 1). These phytochemicals in the seed extract could be extracted by polar solvents water, methanol and ethanol, while the remaining phytochemicals listed above could not be extracted due to their non- polar nature. Previously similar phytochemical analysis results were reported from aqueous and methanol extracts of various parts of P. roxburghii plant[20,21]. The AgNPs were successfully synthesized using the aqueous extract of P. roxburghii seeds as the reducing source. Fig. 1a and b show the P. roxburghii seeds and the finely ground seed powder, respectively. The AgNO3 solution (0.1 mM) was colourless and the colour of the seed extract before and after the addition of AgNO3 was changed from pale yellow to brown as shown in fig. 1c and d. This colour change was due to the interaction of AgNO3 with plant extract leading to the reduction of silver nitrate to elemental silver (Ag+ to Ag0)[24]. The UV/Vis spectrum of AgNPs synthesized in the range of 200 to 700 nm is shown in fig. 2 and the AgNPs gave the maximum absorption peak at 371 nm. The appearance of the peak was the characteristic of surface plasmon resonance (SPR) of AgNPs and the free electrons gave rise to the SPR absorption band, which occurred due to the collective oscillation of AgNP in resonance with the light wave[25]. Some other reports also stated that the UV/Vis absorption peaks for biogenic AgNPs were obtained at 378 nm and 384 nm[24,26].


Fig. 1: Synthesis of AgNPs from P. roxburghii seed extract
a) P. roxburghii seeds with seed coat b) seed powder c) aqueous seed extract d) colour change after adding 0.1 mM AgNO3 solution


Fig. 2: UV/Vis absorbance spectra of synthesized AgNPs from P. roxburghii seed extract

                          Test for                          Results
cardiac glycosides
amino acid and proteins
fats and oils

Table 1: Phytochemical Analysis of p. Roxburghii Seed Aqueous Extract

The AFM data revealed that the AgNPs were mono- dispersed and spherical in shape. The size of the nanoparticles ranged from 13.64 to 69.04 nm in 2 and 3-dimensional structures with a height of 18.9 nm. The distance from each other was 38.43 nm and was shown in fig. 3a-c. Almost similar result about the morphology and size of AgNPs around 30-50 nm was reported[22].


Fig. 3: AFM image of synthesized AgNPs from P. roxburghii seed extract
a) Two dimensional structure b) three dimensional structure and c) particle size distribution

The synthesised AgNPs from P. roxburghii were characterized using powder XRD to confirm the particles as Ag and to know the structural information. Fig. 4 revealed the XRD pattern of the synthesized AgNPs and the characteristic diffraction peaks were found at 38.12º, 46.39º, 64.60º and 76.79º with the XRD planes at 111, 200, 220 and 311, respectively. These values corresponded with the previously reported values for AgNPs prepared from plant extracts and also the AgNPs appeared to be face centred cubic (FCC) crystals in nature[5,12].


Fig. 4: XRD pattern of synthesized AgNPs from P. roxburghii seed extract

The sample was analysed with EDX at 3 keV to measure the elemental constituents involved in the formation of these AgNPs from P. roxburghii seed extract because generally metallic AgNPs show typical optical absorption peak approximately at 3 keV due to SPR[14,27]. The EDX was employed for the qualitative and quantitative analysis of the possible elements in the synthesized NPs and that showed 31.21±0.82 % of carbon, 37.84±1.93 % of oxygen, 4.82±0.33 % of phosphorous, 2.28±0.30 % of sulphur, 2.77±0.76 % of molybdenum and 21.08±1.00 % of silver and among these elements carbon was from plant and the other elements were from the plant metabolites involved in the capping of the synthesized AgNPs[28]. All these values were presented in fig. 5.


Fig. 5: EDX image of synthesized AgNPs from P. roxburghii seed extract

The synthesized AgNPs were analysed with TEM to confirm the morphology and size and the TEM image shown in fig. 6 depicted that the AgNPs were spherical in shape with a high surface area. The size of these AgNPs was in the range of 13.94 to 52.46 nm with average size of 25.68 nm. The TEM analysis of AgNPs synthesized from various plants and plant extracts showed more variation in size from 5 to 100 nm and the shape was somewhat oblong to spherical[11,12,19].


Fig. 6: TEM images of synthesized AgNPs from P. roxburghii seed extract
a) Image showing the shape of AgNPs and b) image showing average size

The FTIR analysis of P. roxburghii seed aqueous extract and that of AgNPs prepared from aqueous seed extract revealed IR bands at wavenumbers 464 to 3401 cm-1 and 470 to 3393 cm-1, respectively as shown in figs. 7a and b. The FTIR spectrum of seed powder revealed a medium band at 3401 cm-1, which attributed to stretching aliphatic primary amines (N-H), the strong and sharp band at 2923 cm-1 corresponded to C-H stretching alkane and the medium band at 2852 cm-1 represented C-H stretching aldehydes. The two strong sharp bands at 2359 and 2341 cm-1 were due to O=C=O stretching CO2, the bands at 1633, 1538, 1455, and 1384 belonged to C=C stretching alkenes, N-O stretching nitro compound and C-H bending alkane, respectively. The weak bands at 1257, 1032, and 668 represented C-N stretching amines, S=O stretching sulfoxide and C=C bending alkene, respectively. For the synthesized AgNPs, the FTIR band at 3393 cm-1 attributed to the free-OH stretching alcohol/phenols, the sharp band at 2924 cm-1 arose from the stretching modes of alkanes (C-H), whereas the band at 2853 cm-1 corresponded to the aldehyde group (CHO). The medium 3 peaks at 2428, 2360 and 2341 cm-1 belonged to stretching phosphine (P-H), stretching silane (Si-H) and stretching phosphine (P-H) respectively. The remaining bands at 1617, 1384, 1268, 1044, 779, 666 and 617 cm-1 showed the presence of bending amines (N-H), stretching sulphate esters (S=O), wagging alkyl halides (CH2X), stretching amines (C-N), stretching meta di-substituted aromatics (C-H), stretching alkyl halides (C-Br) and bending alkynes (C-H), respectively, which were involved in the formation as well as in the reduction, capping and stabilization of AgNPs of P. roxburghii seed aqueous extract. The presence of the possible bio-reducing agents in the plant extract used and the synthesized AgNPs were confirmed by the FTIR analysis[19,26].


Fig. 6: TEM images of synthesized AgNPs from P. roxburghii seed extract
a) Image showing the shape of AgNPs and b) image showing average size


Fig. 7: FTIR spectra of P. roxburghii seed and the synthesized AgNPs
FTIR spectra of a) P. roxburghii seed powder and b) synthesized AgNPs

Antibacterial activity of AgNPs was studied at 25, 50, 75 and 100 µg/ml concentrations and the concentrations above 100 µg/ml were not studied. The AgNO3 solution was taken as positive control and the plant extract as a negative control. The formation of zones of inhibition at different concentrations of AgNPs is shown in fig. 8. The zones of inhibition was more for 100 µg/ml concentration against all organisms tested and thatE. coli was less-sensitivecomparedtothethreeorganisms to AgNPs prepared from P. roxburghii seed extract. S. aureus was more sensitive than the other bacteria tested and 10, 18, 22 and 23 mm of inhibition zones were obtained with 25, 50, 75 and 100 µg/ml concentrations of AgNPs, respectively. The results of the antibacterial activity were shown in fig. 9. Some other authors also stated that gram-positive bacteria were more sensitive to AgNPs compared to gram-negative bacteria[29,30]. Depending upon the concentration of AgNPs exposed to bacteria and the type of bacteria, different inhibition zones are formed and along with that the structural and molecular compositions of bacterial species[31] and inoculated concentration of bacteria and the size, shape, concentrations of AgNPs contribute to the varying results of inhibition zones[32].


Fig. 8: Antibacterial activity of AgNPs at different concentrations
(■) Control, image 25 μg/ml, image 50 μg/ml, image 75 μg/ml andimage 100 μg/ml


Fig. 9: Antibacterial effects and zones of inhibition produced by synthesized AgNPs
Effects of AgNPs on a) S. aureus b) S. pneumoniae c) E. faecalis and d) E. coli

The human breast cancer cell line (MCF-7) was selected due to the high incidence of breast cancer in India[33] to study the cytotoxic activity of the synthesized AgNPs using MTT assay. When treated with concentrations of AgNPs between 12.5 to 200 μg/ml, about 50 % of MCF-7 cells died. The cell cytotoxicity results from the ELISA reader showed that against MCF-7 cells,P. roxburghii seed extract NPs showed IC50 at 72.32 µg/ ml. The morphological changes of breast carcinoma cell line MCF-7 at different concentration of samples along with the untreated cells were recorded using an inverted phase-contrast tissue culture microscope. The rounding or shrinking of the cells or other morphological changes in the cells to varying degree was visible in the images and it was a clear indication of the cytotoxic effect of synthesized AgNPs. MCF-7 cells treated with different concentrations of AgNPs were shown in fig. 10 and Table 2, respectively and the reduction in % viability of MCF-7 cells with increasing AgNPs concentrations was shown in fig. 11. The synthesized AgNPs exhibited dose-dependent cytotoxic effects on breast cancer cells in vitro[34]. AgNPs synthesised from Embelia ribes showed potential anticancer activity against MCF- cells[35], Bauhinia tomentosa against A-549, Hep-2 and MCF-7 cells[36]. AgNPs synthesized from plant extracts exhibited remarkable antitumour activity against MCF- 7, HT29 and EAC cell lines[37], the AgNPs from Salacia chinensis showed anticancer activity with IC50 values ranging from 4.0 to 14.37 µg/ml against seven selected cancer cell lines[38], also another report suggested that the AgNPs from plant extracts exhibited considerable cytotoxic activity against almost all tested human cancer cell lines[39].


Fig. 10: Cytotoxicity of synthesized AgNPs against MCF-7 cell line
a) MCF-7 control cells b) cells treated with 12.5 μg/ml c) cells treated with 25 μg/ml d) cells treated with 50 μg/ml e) cells treated with 100 μg/ml and f) cells treated with 200 μg/ml of AgNPs


Fig. 11: Reduction in % viability of MCF-7 cells with increasing concentrations of AgNPs

Cell Line Concentrations
Untreated MCF-7 No treatment
camptothecin MCF-7 15 µM
Blank --- Only media without cells
PR-1 MCF-7 12.5, 25, 50,100, 200 µg/ml

Table 2: Concentrations Of Silver Nanoparticles used in Cytotoxicity Assay

The results of the present study showed that the P. roxburghii seed extract is a good reducing agent to prepare AgNPs via green synthesis, ranging 10 to 70 nm in size (average 25.68 nm). It was found to be an ideal method for eco-friendly synthesis of inexpensive AgNPs. The antibacterial activity of the AgNPs was tested on both gram-positive and gram- negative bacteria and the AgNPs showed activity at concentrations ranging from 25-100 µg/µl. Further, the cytotoxic activity of these AgNPs was tested on MCF-7 cell line to find that >12.5 µg/ml of AgNPs reduced cell proliferation and % cell viability giving rise to a possibility that these NPs could be developed as potential anticancer agents.


The authors are grateful to the chairman of the Department of Studies in Botany, Karnatak University, Dharwad for extending laboratory facilities. The authors wish to thank the University Scientific Instrument Centre (USIC), Karnatak University Dharwad for providing instrumentations facilities.

Conflicts of Interest

The authors declare that there is no conflict of interests.