Preparation of monodispersed and cytotoxic silver nanoparticles using Launaea taraxacifolia leaf extract

  • Enobong R. EssienEmail author
  • Violette N. Atasie
  • Esther U. Udobang
  • Goddey Umanu
Open Access
Original Research


The current work investigated the green and low-cost preparation of silver nanoparticles (AgNPs) using the aqueous extract from Launaea taraxacifolia leaf and studied its antimicrobial effects. The leaf extract was analysed in a gas chromatogram–mass spectrometer to assess the phytochemicals present. UV–Vis spectrophotometer was used to monitor the formation of AgNPs, the morphological assessment was performed by a scanning electron microscope, energy dispersive X-ray analysis was used to determine the elemental composition, the particle size and shape were studied using transmission electron microscopy, and the vibrational modes of bonds in the AgNPs were assessed by Fourier transformed infrared spectroscopy. The AgNPs produced were spherical and in a size range of 9–15.5 nm, monodispersed with a large surface area. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of the AgNPs against Pseudomonas aeruginosa and Proteus mirabilis were very low. Against P. aeruginosa, the MIC was 0.10 mg/mL and the MBC was 0.15 mg/mL, while the MIC and MBC against P. mirabilis were 0.05 and 0.25 mg/mL, respectively. Therefore, the AgNPs prepared using L. taraxacifolia leaf extract showed high antibacterial activities and could be a candidate antimicrobial agent for biomedical applications.

Graphic Abstract


Launaea taraxacifolia Silver nanoparticles Antimicrobial agent Phytochemicals Monodisperse 


Nanotechnology has great potential in the field of materials science for producing materials of various types at nanoscale level. Nanomaterials have minimum dimension in the nonmetre scale (1–100 nm), which is in the size dimension of microorganisms like viruses or bacteria. In this dimension, nanomaterials can generate therapeutic activities and several other unique properties [1] compared with their corresponding bulk materials. This is because their physicochemical properties, like surface charge, surface area, size, and shape greatly influence their properties. The ‘green approach’ method of synthesizing silver nanoparticles (AgNPs) has become very attractive in chemical synthesis, thanks to the sustained worldwide awareness campaigns and concerns regarding the dangers associated with environmental pollution [2]. At the nanometre scale, silver has applications in various fields, including medicine, biosensors, and analysis. AgNPs have long been credited with strong inhibitory effects against bacteria and fungi found in medical and industrial processes [3, 4]. Thus, AgNPs have been applied in topical ointments to stop burns and open wounds from being infected [5]. Besides, biologically synthesized AgNPs are highly toxic to several multi-drug resistant human pathogens, and in monodisperse morphology, they are more effective in drug delivery, resonance imaging, and medical diagnostics [6].

There are many chemical techniques of synthesizing AgNPs, some involve reducing silver ions chemically in aqueous solutions, which could employ stabilizing agents. Others are decomposing silver ion thermally in organic solvents, chemical reduction and carrying out photoreduction in reverse micelles [7, 8], and using radiation chemical reduction method [9]. However, most of these techniques are complex and involve the use of very expensive equipment [10]. Furthermore, these processes may release harmful gases into the atmosphere and the chemicals used may be hazardous and dangerous to health and pollute the environment as well [10].

The plant extract alternative pathway for synthesizing AgNPs, apart from its eco-friendliness, has the advantages of being facile and cost effective [11, 12]. Additionally, in plant-mediated synthesis, the phytochemicals inherent in the plants, after playing a reducing role, also act as capping agents towards forming the nanoparticles. Based on this, the AgNPs obtained from this technique are safe for human medical use [12, 13].

Launaea taraxacifolia is a leafy vegetable found mainly in the tropical regions and has the common name ‘Dandelion’. It owes its origin to the family Asteraceae (Compositae) and is commonly found in several African countries including Ghana, Senegal, Benin, and Nigeria. L. taraxacifolia has also been shown to play a crucial role in curbing non-communicable diseases in man. There is a report that the milky fluid which exudes from the plant possesses therapeutic effect against conjunctivitis, and at a specific dosage, the leaves have been shown to provide protection against gentamicin-induced kidney damage in rats [14].

Launaea taraxacifolia is probably one plant that is most grossly understudied among leafy vegetables [15], ranking among “the ten most neglected and underutilized plants” [16, 17], yet it is very easily found as weed and roadside grass. It is against this backdrop that the current work is designed to synthesize AgNPs from L. taraxacifolia leaf and study their inhibitory effects against two strains of bacteria. Based on our investigation, there is currently no report in literature on the preparation of silver AgNPs from L. taraxacifolia.



The L. taraxacifolia leaves used for this research work were obtained from the premises of Bells University of Technology, Ota, Ogun State, southwest Nigeria and identified at the Herbarium section of Botany Department, University of Lagos, Nigeria. AgNO3 was purchased from Sigma-Aldrich.

Preparation of L. taraxacifolia leaf aqueous extract

The L. taraxacifolia leaves were first washed with tap water and further rinsed with distilled water to remove dust and particulate impurities. Thereafter, they were allowed to dry at ambient condition and at 70 °C in an oven before milling into a fine powder, and then stored in an airtight container for further use. Then, the powder (4.0 g) was added to distilled water (100 mL), sealed and heated to 65 °C for 15 min in a thermostatic water bath. After allowing to cool to room temperature, the mixture was filtered to obtain the L. taraxacifolia aqueous leaves extract. The obtained extract was stored at a temperature range 5–10 °C in a refrigerator for subsequent experiments.

Synthesis of AgNPs

The synthesis was performed by modifying a previous method by Krishnamoorthy and Jayalakshmi [18]. Briefly, 1 mL of the L. taraxacifolia aqueous leaf extract was added to 9 mL of 10 mM solution of AgNO3. The reaction was performed in a dark room at room temperature and left overnight to minimize photoactivation of the AgNO3. After the desired reaction period, the solution containing the AgNPs was centrifuged at 15,000 rpm for 15 min to separate them from the reaction solution. The particles formed were washed in deionized water to remove any residual organic compounds still present in the AgNPs. This washing procedure was repeated thrice to increase the purity of the AgNPs, and, thereafter, the wet particles were dried at 60 °C in an oven. Finally, the particles were stirred in absolute ethanol to reduce aggregation and then dried at 60 °C for 30 min in an oven to expel the solvent.

Characterization techniques

A gas chromatograph–mass spectrometer (GC–MS) (Shimadzu, QP2010SE) performing at a 1:1 injection ratio was used to determine the phytochemicals present in the ethanolic solution of the L. taraxacifolia leaf extract. The phytochemicals were identified using a software having a database incorporated into the GC–MS machine.

UV–Vis spectral details were recorded in a UV–visible absorption spectrophotometer (Uniscope SM 7504) in the wavelength between 300 nm and 700 nm to monitor the formation of AgNPs in the reaction medium between L. Taraxacifolia leaf extract and AgNO3. The UV–visible spectrum of the L. Taraxacifolia leaf extract was also obtained at a similar wavelength range.

A morphological evaluation to determine the microstructure, particle distribution and elemental composition of the AgNPs was performed in a scanning electron microscope (SEM) having an energy dispersive X-ray analysis (EDX) unit (SEM: JEOL JSM 7660F). The sample was analysed using an accelerating voltage of 15 kV.

The particle size and structure of the AgNPs were assessed by transmission electron microscopy (TEM) (TEM: JEM-ARM200F-G) operating at 200 kV accelerating voltage. The average particle size and distribution were determined from the TEM micrograph using a software—ImageJ.

The type of bonds present in the L. taraxacifolia aqueous leaf extract and AgNPs was assessed using Fourier transform infrared (FTIR) spectroscopy (FTIR: Nicolet iS10) in the wavenumber range of 350–4000 cm−1.

Antimicrobial analysis

Broth dilution method as described by Krishnan et al., 2015 [19] was employed in the preparation of the AgNPs samples to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). The Luria–Bertani (LB) broth used for the experimental analysis was prepared based on the manufacturer’s instructions using deionized water as the broth diluent.

A stock solution containing 10 mg/mL of the AgNPs was used for the determination of the MICs. It was prepared by sonicating the AgNPs in deionized water at 40 °C in an ultrasonic cleaner (CLEAN–120HD) for 5 h to achieve a homogeneous, cloudy solution. The antibacterial potencies of the AgNPs against clinically isolated Gram-negative Pseudomonas aeruginosa and Proteus mirabilis were determined by inoculating varying amounts of the AgNPs (prepared from the stock solution, Table 1) with suspensions of the test microorganisms. Bacterial suspensions of the test strains were prepared using a 0.5 McFarland turbidity standard. 50 μL of the prepared suspension was inoculated into each of the serially diluted tubes containing the AgNPs at concentrations of 4–0.01 mg/mL (Table 1). Negative and positive control tubes were also prepared to check the sterility of the procedure and the bacterial activity, respectively. The negative control tube contained only sterile broth, while the positive control tube contained the broth and bacterial inoculum, but no antimicrobial agent. After 24 h of incubation at 37 °C, the MIC values were obtained by checking for visual turbidity in the tubes. The lowest concentrations of the AgNPs that visually inhibited the growth of the test microorganisms were taken as the MICs.
Table 1

Working concentrations of the AgNPs for MIC determination using Pseudomonas aeruginosa and Proteus mirabilis as test microorganisms

Pseudomonas aeruginosa

Proteus mirabilis

Dilution code

AgNPs concentration (mg/mL)

Dilution code

AgNPs concentration (mg/mL)









































To determine the minimum bactericidal concentration (MBC), 50 μL aliquots from all the tubes which showed no visible bacterial growth were seeded in LB agar plates devoid of the antimicrobial agent (AgNPs). The plates were labelled according to the dilution tubes from where their inoculums were obtained and then incubated for 24 h at 37 °C. Thereafter, the agar plates were observed for the presence or absence of bacterial growth. The plate representing the lowest concentration of the AgNPs which did not exhibit any bacterial growth or colony was taken as the MBC. MBC is defined as the lowest concentration of antimicrobial agent that kills 99.9% of the initial test bacterial population [19].

Results and discussion

UV–Vis spectrophotometry

During the biosynthesis reaction, colour change occurred as the solution changed colour from buff to brown as a result surface plasmon resonance (SPR) phenomenon caused by the formation of the AgNPs [20]. The solution was analysed immediately after the colour change was observed, which indicated a reduction of the silver ion (Ag+) to pure silver (Ag0). The UV–Vis absorption spectrum of the AgNPs solution showed a strong and sharp absorption band centred at 440 nm (Fig. 1a) which corresponds to the dipole resonance of Ag nanospheres and agrees with previous findings [21, 22, 23]. The absence of additional absorption bands at higher wavelengths indicates spherical shape uniformity of the nanoparticles [24]. The UV–Vis spectrum recorded and the visual observation made indicated that a bio-reduction reaction occurred giving rise to the formation of AgNPs. This is in contrast to the UV–Vis spectrum of the AgNO3 (Fig. 1b) solution, which appeared as a band without an absorption peak.
Fig. 1

UV-Vis spectra of a the colloidal solution containing AgNPs showing absorption at 440 nm and b aqueous extract of L. taraxacifolia leaf showing no absorption peaks

Phytochemicals present in the L. taraxacifolia leaf extract and probable mechanism of AgNPs formation

The retention times and peak heights of the major metabolites identified in the L. taraxacifolia leaf extract by GC–MS are shown in the chromatogram in Fig. 2 and Table 2. The result indicated that most of the biomolecules are alcohols, amides and carbohydrates. Reports indicate that plant leaf extracts containing carbohydrate and proteins with amino functional groups serve as reductants to reduce silver ions (Ag+) to silver nanoparticles (Ag0) [25, 26]. Amides, in particular, have been shown to act as reducing and capping agents to obtain AgNPs [27, 28].
Fig. 2

Chromatogram showing peaks with different intensities of the phytochemicals present in the L. taraxacifolia leaf extract (shown in Table 2)

Table 2

Major phytochemicals identified in the L. taraxacifolia leaf extract using GC–MS

Peak no.

Retention time

Peak height

















Methyl N-hydroxybenzenecarboximidoate








2,2′-Dihydroxydipropyl ether








(E)-2-isopropyl-5-methylphenyl 2-methylbut-2-enoate




























Ethyl 14-methyl-hexadecanoate





Microstructure and elemental composition of the AgNPs

The morphological features of the AgNPs are presented in Fig. 3. As observed, the microstructure shows homogeneous spherical particles that are mostly devoid of agglomeration, and consequently, presents excellent distribution and large surface area. Particle topography, including size and distribution are known to be important for nanoparticles to exhibit antimicrobial and optical properties [28, 29, 30]. The shape of the AgNPs as observed in the SEM micrograph was spherical and uniform, thus supporting the UV–Vis result.
Fig. 3

SEM micrograph of the AgNPs showing well-distributed particles

The formation of AgNPs was further supported by the presence of Ag peak at high intensity in the EDX spectrum (Fig. 4). The carbon and oxygen atoms observed in the spectrum are from the plant phytochemicals which participated in the reducing and capping reactions to produce the AgNPs. However, the K, Si, and S appearing in the spectrum at very low intensity could be residual impurities from the aqueous leaf extract which were not completely removed after washing the nanoparticles following their centrifugation.
Fig. 4

EDX spectrum of the AgNPs showing the presence of silver at high concentration

Particle size dimension and distribution

TEM evaluation reveals that the particles were spherical, monodisperse with no agglomerates (Fig. 5). This could be the result of the efficient reduction of the Ag+ to Ag0 followed by growth into isolated nanoparticles. It also reflects, jointly, the capping ability of the biomolecules present and the effect of the ethanol medium to prevent agglomeration, and thus verifies the result obtained by the absorption spectrophotometry. The AgNPs vary in sizes from 9 to 15.5 nm as shown in the histogram presented in Fig. 6, but with an average size of 12 nm. This result is quite remarkable because synthesizing monodisperse nanoparticles with uniform size, shape, and composition is a challenging endeavour [31].
Fig. 5

TEM image of the AgNPs showing monodisperse particles

Fig. 6

Particle size distribution of the AgNPs showing that the particle size was distributed between 9 and 15.5 nm with the average at 12 nm

Bond characteristics of the AgNPs

Figure 7 depicts the FTIR spectra of the AgNPs and the aqueous leaf extract of L. taraxacifolia. The spectrum of the AgNPs (Fig. 7a) reveals the presence of vibrational modes at 3780, 3459, 1636, 1441 and 1143 cm−1. The small peak appearing as a shoulder around 3780 cm−1 is considered to be N–H stretching vibration resulting from the presence NH group in the sample [32]. The broad band centred at 3459 cm−1 is attributed to O–H stretching vibration of water molecules or N–H [32], while the sharp peak near 1636 cm−1 is associated with C=O stretching vibration of an amide [27], which is further confirmed by the C–O deformation mode at 1143 cm−1. The small peak around 1441 cm−1 signifies the presence of C–H bond in CH2 [33]. The result of the FTIR confirms that the phytochemicals present in the leaf extract were involved in the reduction and stabilization reaction for the formation of the AgNPs. Several peaks are observed between 3780 and 530 cm−1 in the FTIR spectrum of the aqueous leaf extract (Fig. 7b). These peaks are vibrations of the bonds of different phytochemicals earlier identified by GC–MS and shown previously in Table 2.
Fig. 7

FTIR spectra of a the AgNPs and b the L. taraxacifolia aqueous leaf extract

Antibacterial activity of the AgNPs

The dilution tubes of the AgNPs solutions which were used to determine the MIC which inhibited the growth of the clinically isolated P. aeruginosa and P. mirabilis are presented in Figs. 8 and 9, respectively. In the antimicrobial test against P. aeruginosa (Fig. 8), the negative control (test tube TX) containing only sterilized LB broth showed no turbidity, and thus verifies the sterility of the experimental procedure; and the positive control (test tube TY) containing sterilized LB broth and the test organism only validates the results of the experiment by showing heavy turbidity as a result of bacterial growth. Turbidity was also visible in tube P16 at 0.05 mg/ml concentration of the AgNPs, while MIC for the AgNPs was recorded at 0.10 mg/mL (P15), the lowest concentration with no visible turbidity.
Fig. 8

Broth dilution tubes for the determination of MIC of AgNPs against clinically isolated Pseudomonas aeruginosa showing MIC at 0.10 mg/ml in P15

Fig. 9

Broth dilution tubes for the determination of MIC of AgNPs against clinically isolated Proteus mirabilis showing MIC at 0.05 mg/mL in N12

For the antibacterial action against P. mirabilis (Fig. 9), turbidity was observed up to the value 0.04 mg/mL of AgNPs concentration (test tube N13), while MIC was recorded at a concentration of 0.05 mg/mL (test tube N12).

The minimum bactericidal concentration (MBC) was determined by seeding LB agar plates devoid of antimicrobial agent (AgNPs) with aliquots 50 μl from all tubes which showed no visible bacterial growth. After incubation, the MBC was obtained by observing the plates for the presence or absence of bacterial growth (Figs. 10, 11). The plates inoculated with inoculum from the lowest AgNPs concentration tube that showed no growth (no visible colony) is the MBC. The plate inoculated with inoculum from tube P16 (the highest concentration which showed visible turbidity) was used as control to verify that the turbidity was indeed the result of bacterial growth of the test P. aeruginosa (Fig. 10). After overnight incubation, heavy growth, shown by green coloration on the agar plate was observed (Fig. 10), which resulted from the chromogenic nature of the test bacteria. It was observed that in plate P15 (0.10 mg/mL), the bacterial cells had resumed growth, while P14 containing 0.15 mg/mL concentration of AgNPs showed no bacterial growth and was hence recorded as the MBC of the AgNPs against the P. aeruginosa strain.
Fig. 10

Agar plates showing antibacterial potency of AgNPs against Pseudomonas aeruginosa. MBC was recorded at 0.15 mg/mL in P14

Fig. 11

Agar plates showing antibacterial potency of AgNPs against Proteus mirabilis. MBC was detected at 0.25 mg/mL (N8)

Proteus mirabilis agar plates are shown in Fig. 11. MBC for this strain of bacteria was recorded at 0.25 mg/mL (plate N8). There was a resumption of bacterial proliferation in agar plate N12 (0.05 mg/mL concentration), indicating that the bacterial activity was only inhibited at that concentration.

From the MIC and MBC determination results obtained from this study, the synthesized AgNPs showed cytotoxicity at unusually low concentrations, which is in contrast with previous studies on AgNPs synthesized via plant-mediated routes [19, 34, 35] that lay between 5 and 15 mg/mL. However, the data agree with other reports that obtained MIC and MBC from plant-derived AgNPs between 0.05 and 0.1 mg/mL [36, 37].

The high degree of potency could be due to the excellent surface topography containing homogeneous, spherical, monodisperse particles of average size 12 nm. Several in vitro studies [29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40] have provided evidence that particle size and shape uniformity are important in cytotoxicity, because they influence cellular membrane deformability, biodistribution and the kinetics of absorbability [30]. Furthermore, the monodisperse nature of the AgNPs promoted toxicity due to better penetration and destruction of the cell walls of the bacteria [41, 42].


Silver nanoparticles have been synthesized successfully using the phytochemicals in aqueous leaf extract of L. taraxacifolia as the reducing agent. The AgNPs obtained were spherical, monodisperse and in the size range 9–15.5 nm. These properties were attributed to the inherent phytochemicals present in the leaf of the L. taraxacifolia plant which, effectively reduced the Ag+ in the solution to Ag0 and subsequently stabilized the formed AgNPs by preventing oxidation. FTIR analysis further supported the involvement of these metabolites in the capping reaction with the nanoparticles. Antimicrobial investigation on two strains of bacteria, P. aeruginosa and P. mirabilis, revealed high cytotoxicity kinetics for the AgNPs. For P. aeruginosa, MICs were detected at 0.10 and MBC at 0.15 mg/mL, while for P. mirabilis, the MIC and MBC were detected at 0.05 and 0.25 mg/mL, respectively. This indicated high AgNPs penetration across the bacteria cell walls, even at low concentration, attributable to the desirable particle topography.

Interestingly, the synthesis of the monodisperse AgNPs was facile and could be performed without requiring complex equipment and reagents compared to those in previous studies. GC–MS investigation shows that L. taraxacifolia leaf, which is yet to be explored in the ever-evolving field of plant-based synthesis of nanoparticles, contains important metabolites that could be useful as reducing and capping agents for preparing highly cytotoxic AgNPs. Additionally, L. taraxacifolia is regarded as a weed, its consumption as food vegetable is not documented, hence being widely available, could be very useful for large-scale plant-mediated synthesis of AgNPs.

The future perspectives for L. taraxacifolia in this study would be its use for the green and economic synthesis of other metal and metal oxide nanoparticles.



We are grateful to Mr. Ata Samuel Akhihiero, Geology Department of the University of Ibadan, Nigeria for helping in the SEM, EDX, TEM and FTIR analysis of the samples. We also thank the Department of Microbiology, Bells University of Technology, Ota for providing access to their laboratory to conduct the antimicrobial studies.


  1. 1.
    Iqbal, J., Abbasi, B.A., Ahmad, R., Mahmood, T., Ali, B., Khalil, A.T., Kanwal, S., Shah, S.A., Alam, M.M., Badshah, H., Munir, A.: Nanomedicines for developing cancer nanotherapeutics: from benchtop to bedside and beyond. Appl. Microbiol. Biotechnol. 102, 9449–19470 (2018)CrossRefGoogle Scholar
  2. 2.
    Thuesombat, P.S., Hannongbua, S., Akasit, S., Chadchawan, S.: Effect of silver nanoparticles on rice (Oryza sativa L. cv. KDML 105) seed germination and seedling growth. Ecotox. Environ. Saf. 104C, 302–309 (2014)CrossRefGoogle Scholar
  3. 3.
    Morones, J.R., Elechiguerra, J.L., Camacho, A., Holt, K., Kouri, J.B., Ramírez, J.T., Yacaman, M.J.: The bactericidal effect of silver nanoparticles. Nanotechnology 16, 2346–2353 (2005)CrossRefGoogle Scholar
  4. 4.
    Lok, C., Ho, C., Chen, R., He, Q., Yu, W., Sun, H., Tam, P.K., Chiu, J.F., Che, C.M.: Silver nanoparticles: partial oxidation and antibacterial activities. J. Biol. Inorg. Chem. 12, 527–534 (2007)CrossRefGoogle Scholar
  5. 5.
    Ip, M., Lui, S.L., Poon, V.K.M., Lung, I., Burd, A.: Antimicrobial activities of silver dressings: an in vitro comparison. J. Med. Microbiol. 55, 59–63 (2006)CrossRefGoogle Scholar
  6. 6.
    Xie, J., Peng, S., Brower, N., Pourmand, N., Wang, S., Sun, S.: One-pot synthesis of monodisperse iron oxide nanoparticles for potential biomedical applications. Pure Appl. Chem. 78, 1003–1014 (2006)CrossRefGoogle Scholar
  7. 7.
    Pileni, M.P.: Fabrication and physical properties of self-organized silver nanocrystals. Pure Appl. Chem. 72, 53–65 (2000)CrossRefGoogle Scholar
  8. 8.
    Sun, Y.P., Atorngitjawat, P., Meziani, M.J.: Preparation of silver nanoparticles via rapid expansion of water in carbon dioxide microemulsion into reductant solution. Langmuir 17, 5707–5710 (2001)CrossRefGoogle Scholar
  9. 9.
    Henglein, A.: Reduction of Ag (CN)-2 on silver and platinum colloidal nanoparticles. Langmuir 17, 2329–2333 (2001)CrossRefGoogle Scholar
  10. 10.
    Hazarika, D., Phukan, A., Saikia, E., Chetia, B.: Phytochemical screening and synthesis of silver nanoparticles using leaf extract of Rhynchotechum ellipticum. Int. J. Pharm. Pharm. Sci. 6, 672–674 (2014)Google Scholar
  11. 11.
    Huang, J., Li, Q., Sun, D., Lu, Y., Su, Y., Yang, X., Wang, H., Wang, Y., Shao, W., He, N.: Biosynthesis of silver and gold nanoparticles by novel sundried Cinnamomum camphora leaf. Nanotechnology 18, 105104–105115 (2007)CrossRefGoogle Scholar
  12. 12.
    Iqbal, J., Abbasi, B.A., Mahmood, T., Hameed, S., Munir, A., Kanwal, S.: Green synthesis and characterizations of Nickel oxide nanoparticles using leaf extract of Rhamnus virgata and their potential biological applications. Appl. Organomet. Chem. 33, e4950 (2019)CrossRefGoogle Scholar
  13. 13.
    Kumar, V., Yadav, S.K.: Plant-mediated synthesis of silver and gold nanoparticles and their applications. J. Chem. Technol. Biotechnol. 84, 151–157 (2009)CrossRefGoogle Scholar
  14. 14.
    Koukoui, O., Agbangnan, P., Boucherie, S., Yovo, M., Nusse, O., Combettes, L., Sohounhloué, D.: Phytochemical study and evaluation of cytotoxicity, antioxidant and hypolipidemic properties of Launaea taraxacifolia leaves extracts on cell lines HepG2 and PLB985. Am. J. Plant Sci. 6, 1768–1779 (2015)CrossRefGoogle Scholar
  15. 15.
    Sakpere, A.M.A., Aremu, O.A.: The growth of Launaea taraxacifolia (Asteraceae) and its response to shading. Res. J. Bot. 3, 90–96 (2008)CrossRefGoogle Scholar
  16. 16.
    Dansi, A., Adjatin, A., Adoukonou-Sagbadja, H., Faladé, V., Yedomonhan, H., Odou, D., Dossou, B.: Traditional leafy vegetables and their use in the Benin Republic. Genet. Resour. Crop Evol. 55, 1239–1256 (2008)CrossRefGoogle Scholar
  17. 17.
    Dansi, A., Vodouhè, R., Azokpota, P., Yedomonhan, H., Assogba, P., Adjatin, A., Loko, L., Dossou-Aminon, I., Akpagana, K.: Diversity of the neglected and underutilized crop species of importance in Benin. Sci. World J. 2012, 932947 (2012)CrossRefGoogle Scholar
  18. 18.
    Krishnamoorthy, P., Jayalakshmi, T.: Preparation, characterization and synthesis of silver nanoparticles by using Phyllanthusniruri for the antimicrobial activity and cytotoxic effects. J. Chem. Pharm. Res. 4, 4783–4794 (2012)Google Scholar
  19. 19.
    Krishnan, R., Arumugam, V., Vasaviah, S.K.: The MIC and MBC of silver nanoparticles against Enterococcus faecalis—a facultative anaerobe. J. Nanomed. Nanotechnol. 6, 1000285 (2015)Google Scholar
  20. 20.
    Veerasamy, R., Xin, T.Z., Gunasagaran, S., Xiang, T.F.W., Yang, E.F.C., Jeyakumar, N., Dhanaraj, S.A.: Biosynthesis of silver nanoparticles using Mangosteen leaf extract and evaluation of their antimicrobial activities. J. Saudi Chem. Soc. 15, 113–120 (2011)CrossRefGoogle Scholar
  21. 21.
    Obaid, A.Y., Al-Thabaiti, S.A., Al-Harbi, L.M., Khan, Z.: Extracellular bio-synthesis of silver nanoparticles. Glob. Adv. Res. J. Microbiol. 3, 119–126 (2015)Google Scholar
  22. 22.
    Ebrahiminezhad, A., Barzegar, Y., Ghasemi, Y., Berenjian, A.: Green synthesis and characterization of silver nanoparticles using Alcea rosea flower extract as a new generation of antimicrobials. Chem. Ind. Chem. Eng. Q. 23, 31–37 (2017)CrossRefGoogle Scholar
  23. 23.
    Dhand, V., Soumya, L., Bharadwaj, S., Chakra, S., Bhatt, D., Sreedhar, B.: Green synthesis of silver nanoparticles using Coffea arabica seed extract and its antibacterial activity. Mater. Sci. Eng. C 58, 36–43 (2016)CrossRefGoogle Scholar
  24. 24.
    Nateghi, M.R., Hajimirzababa, H.: Effect of silver nanoparticles morphologies on antimicrobial properties of cotton fabrics. J. Text. Inst. 108, 806–813 (2014)CrossRefGoogle Scholar
  25. 25.
    Richardson, A., Chan, B.C., Crouch, R.D., Janiec, A., Chan, B.C., Crouch, R.D.: Synthesis of silver nanoparticles: an undergraduate laboratory using green approach. Chem. Educ. 11, 331–333 (2006)Google Scholar
  26. 26.
    Li, S., Qui, L., Shen, Y., Xie, A., Yu, X., Zhang, L., Zhang, Q.: Green synthesis of silver nanoparticles using Capsicum annum L extract. Green Chem. 9, 852–858 (2007)CrossRefGoogle Scholar
  27. 27.
    Mirzaei, A., Janghorban, K., Hashemi, B., Bonyani, M., Leonardi, S.G., Neri, G.: Characterization and optical studies of PVP-capped silver nanoparticles. J. Nanostruct. Chem. 7, 37–46 (2017)CrossRefGoogle Scholar
  28. 28.
    Banerjee, P., Satapathy, M., Mukhopahayay, A., Das, P.: Leaf extract mediated green synthesis of silver nanoparticles from widely available Indian plants: synthesis, characterization, antimicrobial property and toxicity analysis. Bioresour. Bioprocess. 1, 3 (2014)CrossRefGoogle Scholar
  29. 29.
    Sarkar, S., Jana, A.D., Samanta, S.K., Mostafa, G.: Facile synthesis of silver nano particles with highly efficient anti-microbial property. Polyhedron 26, 4419–4426 (2007)CrossRefGoogle Scholar
  30. 30.
    Zawadzka, K., Kądzioła, K., Felczak, A., Wrońska, N., Piwoński, I., Kisielewska, A., Lisowska, K.: Surface area or diameter—which factor really determines the antibacterial activity of silver nanoparticles grown on TiO2 coatings? New J. Chem. 38, 3275–3281 (2014)CrossRefGoogle Scholar
  31. 31.
    Robertson, J.D., Rizzello, L., Avila-Olias, M., Gaitzsch, J., Contini, C., Magoń, M.S.: Purification of nanoparticles by size and shape. Sci. Rep. 6, 27494 (2016)CrossRefGoogle Scholar
  32. 32.
    Prabakaran, M., Subha, K., Thennarasu, V., Merinal, S.: Biosynthesis of silver nanoparticles using Sphaerulina albispiculata and evaluation of antibacterial activity. Eur J. Exp. Biol 2, 297–303 (2012)Google Scholar
  33. 33.
    Tontowi, A.E., Perkasa, D.P., Siswomihardjo, W., Darwis, D.: Effect of polyvinyl alcohol (PVA) blending and gamma irradiation on compressive strength of FHAp/Fgel composite as candidate of scaffold. Int. J. Eng. Technol. 8, 108–116 (2016)Google Scholar
  34. 34.
    Deshi, J.J., Barminas, J.T., Onwuka, J.C., Dass, P.M., Maitera, O.N., Muazu, I.: Antimicrobial efficacy of biosynthesized silver nanoparticles from different solvent extracts of Waltheria americana root. J. Anal. Sci. Technol. 7, 23 (2016)CrossRefGoogle Scholar
  35. 35.
    Sheikholeslami, S., Mousavi, S.E., Ashitiani, H.R.A., Doust, S.R.H., Rezayat, S.M.: Antibacterial activity of silver nanoparticles and their combination with Zataria multiflora essential oil and methanol extract. Jundishapur J. Microbiol. 9, e36070 (2016)CrossRefGoogle Scholar
  36. 36.
    Balashanmugam, P., Kalaichelvan, P.T.: Biosynthesis characterization of silver nanoparticles using Cassia roxburghii DC. aqueous extract and coated on cotton cloth for effective antibacterial activity. Int. J. Nanomed. 10, 87–89 (2015)CrossRefGoogle Scholar
  37. 37.
    Banala, R.R., Nagati, V.B., Karnati, P.R.: Green synthesis and characterization of Carica papaya leaf extract coated silver nanoparticles through X-ray diffraction, electron microscopy and evaluation of bactericidal properties. Saudi J. Biol. Sci. 22, 637–644 (2015)CrossRefGoogle Scholar
  38. 38.
    Carlson, C., Hussain, S.M., Schrand, A.M., Braydich-Stolle, L.K., Hess, K.L., Jones, R.L., Schlager, J.J.: Unique cellular interaction of silver nanoparticles: size-dependent generation of reactive oxygen species. J. Phys. Chem. B 112, 13608–13619 (2008)CrossRefGoogle Scholar
  39. 39.
    Park, J., Lim, D.-H., Lim, H.-J., Kwon, T., Choi, J., Jeong, S., Choi, I.-H., Cheon, J.: Size dependent macrophage responses and toxicological effects of Ag nanoparticles. Chem. Commun. 47, 4382–4384 (2011)CrossRefGoogle Scholar
  40. 40.
    Park, M.V.D.Z., Neigh, A.M., Vermeulen, J.P., de la Fonteyne, L.J.J., Verharen, H.W., Briedé, J.J., van Loveren, H., de Jong, W.H.: The effect of particle size on the cytotoxicity, inflammation, developmental toxicity and genotoxicity of silver nanoparticles. Biomaterials 32, 9810–9817 (2011)CrossRefGoogle Scholar
  41. 41.
    Prabhu, S., Poulose, E.K.: Silver nanoparticles: mechanism of antimicrobial action, synthesis, medical applications, and toxicity effects. Int. Nano Lett. 2, 32 (2012)CrossRefGoogle Scholar
  42. 42.
    Sondi, I., Salopek-Sondi, B.: Silver nanoparticles as antimicrobial agent: a case study on E. coli as a model for Gram-negative bacteria. J. Colloid Interface Sci. 27, 177–182 (2004)CrossRefGoogle Scholar

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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Department of Chemical and Food SciencesBells University of TechnologyOtaNigeria
  2. 2.Department of Biological SciencesBells University of TechnologyOtaNigeria

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