АНТИБАКТЕРИАЛЬНОЕ ДЕЙСТВИЕ НАНОЧАСТИЦ СЕРЕБРА

Background. Metal nanoparticles can have unique properties that differ from those of the solid metal from which they are obtained. This is what determines the increased interest in them on the part of researchers from all over the world. Objective of the study: quantitative assessment of the antibacterial effect of silver and zinc oxide nanoparticles on polyantibiotic-resistant strains of gram-positive and gram-negative microorganisms. Material and methods. The synthesis of silver and zinc oxide nanoparticles was performed by laser ablation in a liquid. The physical properties and sizes of these nanoparticles were studied on the basis of spectral characteristics and atomic force microscopy. The study of the antibacterial resistance of the studied microorganisms was carried out, as well as a quantitative assessment of the antibacterial effect of the obtained nanoparticles based on the determination of the minimum inhibitory and minimum bactericidal concentrations. Results. All microorganisms used in the study were clinical pathogenic strains with polyantibacterial resistance. In this case, the minimum inhibitory concentrations of silver nanoparticles ranged from 7.81 to 31.25 μg/ml, and the minimum bactericidal concentrations - from 31.25 to 62.50 μg/ml, while for zinc oxide nanoparticles the values of the minimum inhibitory concentrations were within the range from 125 to 500 μg/ml, and the values of the minimum bactericidal - from 250 to 1000 μg/ml. Conclusions. The laser ablation method allows the synthesis of chemically pure nanoparticles of silver, zinc oxide, and, if necessary, other metals. Silver and zinc oxide nanoparticles are effective antimicrobial agents against polyantibiotic-resistant pathogenic microbial flora. The obtained values of the minimum bactericidal and minimum inhibitory concentrations must be taken into account in the subsequent clinical implementation of medical devices based on the use of metal nanoparticles.

Background: Drug resistance of microorganisms to antimicrobial agents is on the rise. Therefore, an alternative route to overcome drug resistance of various microorganisms is needed. Objectives: This study was conducted to assess antibacterial activity of silver nanoparticles (AgNps) produced by Satureja hortensis extract against Bacillus cereus isolated from soil of Sistan plain (Zabol, Southeastern Iran). Materials and Methods: Bacillus cereus was isolated from collected soil samples by serial dilution and agar plating method. The minimum inhibitory concentrations (MIC) of silver nanoparticles produced by Satureja hortensis extract were evaluated by microdilution method. Results: AgNPs display Gaussian dispensation with a mean diameter of 17.58 nm with some deviations. The highest MIC value was 25 ppm against one Bacillus cereus and the least MIC value was against two Bacillus cereus strains (12.5 ppm). Conclusions: The silver nanoparticles produced by Satureja hortensis extract owed antibacterial activity against Bacillus cereus. Furthermore, antimicrobial activity was based on the concentration of silver NPs to produce the most significant effect against Bacillus cereus.

Antioxidant and antibacterial activity of silver nanoparticles synthesized by Cestrum nocturnum

Date palm silver nanoparticles are a green synthesis method used as antibacterial agents. Today, there is a considerable interest in it because it is safe, nontoxic, low costly and ecofriendly. Biofilm bacteria existing in marketed local milk is at highly risk on population health and may be life-threatening as most biofilm-forming bacteria are multidrug resistance. The goal of current study is to eradicate biofilm-forming bacteria by alternative treatment green synthesis silver nanoparticles. The biofilm formation by bacterial isolates was detected by Congo red method. The silver nanoparticles were prepared from date palm(khestawy) fruit extract. The formed nanoparticles were characterized with UV-Vis and AFM. The antibacterial activity of synthetic silver nanoparticles was evaluated by agar well diffusion method. Gram-negative bacteria isolates were E. coli in 3 isolates and Klebsiella pneumoniae in 5 isolates and all are biofilm producer. The size of synthetic green silver nanoparticles is 18 nm and the generation of silver nanoparticles was confirmed by change of date extract color from yellow to brown with an absorption maximum at 410 nm. Highly antibacterial activity of silver nanoparticles was recorded in comparison to plant extract and silver nitrate against gram-negative biofilm-forming bacteria. From this study, the antibacterial activity of date palm silver nanoparticles was more efficient to eradicate gram negative biofilm[1]forming bacteria isolated from marketed local milk

The present work investigates the antibacterial activity of silver nanoparticles (Ag-NPs) synthesized by biological method using Sargassum wightii. The fresh live seaweed was collected from the Mandapam coast of Tamilnadu, India. Solvent extract was prepared using acetone, petroleum ether and methanol. Aqueous extract of the seaweed was also used for the synthesis of silver Ag-NPs. Seaweed extract is used as a reducing agent of 2mM silver nitrate solution for the synthesis of Ag-NPs. Periodical monitoring of reaction mixture was done using UV-vis spectroscopy at 300-750 nm. The scanning electron microscopy (SEM) of the sample confirms the presence of Ag-NPs. The antibacterial activity of solvent extract was done by Minimal inhibitory concentration (MIC) assay. The methanol extract of the seaweed at a concentration of 250µg/ml exhibited potent antimicrobial activity against the test microorganism. The zone of inhibition ranging from 8-14 mm was observed with different extracts. The antibacterial activity of the synthesized Ag-NPs against the organism was also done by MIC test. The MIC of Ag-NPs was found to be 130µg/ml for all pathogenic microorganisms selected for the study. The zone of inhibition against Bacillus cereus, Bacillus anhtracis, Staphylococcus aureus and Vibrio alginoyticus were found to be 10, 8, 10 and 9 mm, respectively. The synthesized Ag-NPs exhibited significant antimicrobial activity against the selected microorganisms than the solvent extract of seaweed.DOI: http://dx.doi.org/10.3329/icpj.v3i10.20337 International Current Pharmaceutical Journal, September 2014, 3(10): 322-325

In this work, the antibacterial activity of silver nanoparticles (AgNPs) synthesized using Areca catechu extracts against three species of antibiotic-susceptible and three species of resistant bacteria was investigated. The effects of this plant were more promising when compared with other medicinal plants tested. The hydrothermal extract of Areca catechu was mixed with silver nitrate to synthesize AgNPs. The synthesized particle characteristics were analyzed by UV–Vis spectrophotometry, scanning electron microscopy (SEM), dynamic light scattering (DLS), and Fourier-transform infrared spectroscopy (FT-IR). Minimum inhibitory concentration and minimum bactericidal concentration tests were conducted to confirm antibacterial activity and the results showed that AgNPs synthesized using Areca catechu extracts effectively inhibited the growth of bacterial species. Moreover, the SEM images of the bacterial species treated with AgNPs synthesized with Areca catechu extracts showed that clusters of AgNPs were attached to the surface of the bacterial cell wall, which could induce destruction of the cell membranes. The results suggest that AgNPs synthesized with Areca catechu extracts have the potential to treat antibiotic-resistant bacteria known as the major cause of nosocomial infections.

ObjectiveThe present work represents the green synthesis of silver nanoparticles using Withania coagulans extract and its antibacterial property. The synergy, additive, bacteriostatic and bactericidal effect of silver nanoparticles was determined against Enterococcus faecalis, Staphylococcus aureus, Escherichia coli, Proteus vulgaris, Salmonella typhi, and Vibrio cholerae. Methods The green silver nanoparticles were characterized by X-ray diffractometry, Transmission Electron Microscopy, Scanning Electron Microscopy and Fourier Transform Infra Red spectroscopy. The Agar dilution, Minimum Inhibitory Concentration and Bacterial Growth Inhibition methods were used for the determination of the antibacterial activity of silver nanoparticles. The Fractional Inhibitory Concentration Index method was performed to check the synergistic activity of conjugated silver nanoparticles. ResultsThe Withania coagulans extract were reduced the silver nitrate into silver nanoparticles which was confirmed by color changes and spectral analysis. The silver nanoparticles were crystalline, elemental and spherical. The antibacterial activity was reported in silver nanoparticles which confirmed by zone of inhibition and pores on the surface of bacteria. The conjugated silver nanoparticles with Levofloxacin have synergy and additive behavior against the tested bacteria. Furthermore, bacteriostatic and bactericidal nature of silver nanoparticles was reported in lower (50 µg/ml) respectively. Conclusion The phenolic compounds of W. coagulans was responsible for the formation of silver nanoparticles. The bacteriostatic and bacteriocidal activity of silver nanoparticles depends upon its concentration. The conjugation of silver nanoparticles with antibiotics may be beneficial due to its synergy and additive effect against the bacteria.

BackgroundAntibiotic resistance is a global issue that threatens public health. The excessive use of antibiotics contributes to this problem as the genes of antibiotic resistance can be transferred between the bacteria in humans, animals and aquatic organisms. Metallic nanoparticles could serve as future substitutes for some conventional antibiotics because of their antimicrobial activity. The aim of this study was to evaluate the antimicrobial effects of silver and zinc oxide nanoparticles against major fish pathogens and assess their safety in vitro. Silver nanoparticles were synthesized by chemical reduction and characterized with UV–Vis spectroscopy, transmission electron microscopy and zeta sizer. The concentrations of silver and zinc oxide nanoparticles were measured using inductively coupled plasma-mass spectrometry. Subsequently, silver and zinc oxide nanoparticles were tested for their antimicrobial activity against Aeromonas hydrophila, Aeromonas salmonicida subsp. salmonicida, Edwardsiella ictaluri, Edwardsiella tarda, Francisella noatunensis subsp. orientalis, Yersinia ruckeri and Aphanomyces invadans and the minimum inhibitory concentrations were determined. MTT assay was performed on eel kidney cell line (EK-1) to determine the cell viability after incubation with nanoparticles. The interaction between silver nanoparticles and A. salmonicida was investigated by transmission electron microscopy.ResultsThe tested nanoparticles exhibited marked antimicrobial activity. Silver nanoparticles inhibited the growth of both A. salmonicida and A. invadans at a concentration of 17 µg/mL. Zinc oxide nanoparticles inhibited the growth of A. salmonicida, Y. ruckeri and A. invadans at concentrations of 15.75, 31.5 and 3.15 µg/mL respectively. Silver nanoparticles showed higher cell viability when compared to zinc oxide nanoparticles in the MTT assay. Transmission electron microscopy showed the attachment of silver nanoparticles to the bacterial membrane and disruption of its integrity.ConclusionsThis is the first study on inhibitory effects of silver and zinc oxide nanoparticles towards A. salmonicida and A. invadans. Moreover, zinc oxide nanoparticles inhibited the growth of Y. ruckeri. In low concentrations, silver nanoparticles were less cytotoxic than zinc oxide nanoparticles and represent an alternative antimicrobial compound against A. hydrophila, A. salmonicida and A. invadans.

In the present study, antibacterial activity of silver nanoparticles synthesized from stem of Tinospora cordifolia were analysed against multidrug-resistant strains of Pseudomonas aeruginosa isolated from burn patients. As Pseudomonas aeruginosa is a scourge of hospital burn units and its emergence as multidrug-resistant strains is a major problem in the control of nosocomial infections. Therefore, we tried to establish a combination of medicinal values of Tinospora cordifolia and nanotechnology possibly with the field of medicine for the development of antibacterial agents against these MDR strains.The synthesized silver nanoparticles were characterized by UV-visible spectroscopy, Energy Dispersive Spectroscopy and Fourier Transform Infrared Spectroscopy. Transmission Electron Microscopy and X-Ray Diffraction have revealed the size of silver nanoparticles 9 ± 36 nm and 12.49 nm respectively. Further antibacterial activity of silver nanoparticles prepared from Tinospora cordifolia against multidrug resistant strains was determined by agar well diffusion assay and Minimum Inhibitory Concentration (MIC) was estimated by qualitative experimentation by resazurin based micro broth dilution method. All experiments were done in triplicate. The silver nanoparticles of stem of Tinospora cordifolia showed the zone of inhibition ranges from 10 ± 0.58 to 21 ± 0.25mm. The MIC of AgNPs from stem extract was found to be 6.25 to 200 μg/ml against Pseudomonas aeruginosa strains. Silver nanoparticles from Tinospora cordifolia possess very good antibacterial activity which makes them a potent source of antibacterial agent.

Antimicrobial activity of silver nanoparticles is gaining importance due its broad spectrum of targets in cell compared to conventional antimicrobial agents. In this context, a UV photo-reduction method was used for the synthesis and the nanoparticles were characterized by UV–Visible spectroscopy, transmission electron microscopy, atomic force microscopy and thermogravimetric analysis techniques. The antibacterial activity of the synthesized silver nanoparticles was evaluated both in liquid and solid growth media employing various susceptibility assays on Pseudomonas aeruginosa, a ubiquitous bacterium. The dose dependent growth suppression by nanoparticles was studied with well diffusion method. By broth dilution method, the minimum inhibitory concentration (MIC) was found to be 2 μg/ml. It was observed that the bactericidal effect depends both on nanoparticle concentration and number of bacteria present. In our study, we could demonstrate the complete antibiofilm activity of silver nanoparticles at a concentration as low as 1 μg/ml. Our observations substantiated the association of reactive oxygen species and cell membrane damage in the antibacterial mechanism of silver nanoparticles. Our findings suggested that these nanoparticles can be exploited towards the development of potential antibacterial coatings for various biomedical and environmental applications.

A quantitative assessment of the antibacterial effect of silver nanoparticles on polyantibiotic-resistant grampositive and gram-negative microorganisms was carried out. Silver nanoparticles were synthesized by the environmentally friendly metal-steam synthesis method. The size and electronic state of nanoparticles were investigated by transmission electron and X-ray photoelectron spectroscopy. The antibacterial properties of nanomaterials were assessed on two clinical pathogenic strains of gram-positive and four strains of gram-negative microorganisms. The typing and assessment of bacterial resistance to antibiotics were carried out on a microbiological analyzer. The antibacterial effect of nanoparticles was quantitatively assessed using the dilution method and the determination of the minimum inhibitory and minimum bactericidal concentrations.It was found that the studied silver nanoparticles have sizes in the range from 5 to 24 nm with an average diameter of 10.8 nm. It was shown that all clinical strains of microorganisms used in the study are characterized by multiple antibacterial resistance; the percentage of their antibiotic resistance ranges from 12.5 to 93.3 %. It was found that for the studied microorganism, the values of the minimum inhibitory concentration (MIC) are in the range from 7.81 to 31.25 μg/ml, and the minimum bactericidal concentration (MBC) is in the range from 31.25 to 62.50 μg/ml. The obtained MIC and MBC data can be used to create promising antimicrobial drugs and medical next generation devices.

Multidrug-resistant bacteria continue to pose the greatest threat to public health. Metallic nanoparticles are one of the more promising strategies for combating antibiotic resistance. This research aims to determine the effect of gold and silver nanoparticles and gold-silver alloy nanoparticles as antibacterial agents. On the other hand, biogenic synthesized gold and silver nanoparticles using Ziziphus spina-christi leaf extract and preparation of gold-silver alloy nanoparticles for treatment of multidrug-resistant bacteria were studied. The formation of nanoparticles was characterized using ultraviolet-visible spectrophotometer, fourier transforms infrared spectroscopy, X-ray diffraction and transmission electron microscopy. Antibacterial activity of the biosynthesized gold nanoparticles, silver nanoparticles and gold-silver alloy nanoparticles was studied against Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Acinetobacter baumannii and Enterococcus faecalis. In the present study, the minimum inhibitory concentration ranged from 61.33 to 64 μg/ml and the minimum bactericidal concentration of the silver nanoparticles ranged from 85.33 to 93.33 μg/ml against multidrug-resistant strains. Synthesized gold nanoparticles had no inhibition zone, indicating that silver nanoparticles have no negative effect on multidrug-resistant bacteria. Minimum inhibitory concentration of gold nanoparticles was in high concentration against multidrug-resistant strain was not bactericidal. The highest minimum inhibitory concentration of gold nanoparticles was 114 μg/ml. Finally, the minimum inhibitory concentration ranged from 53.33 to 62 μg/ml and the minimum bactericidal concentration of the gold-silver alloy nanoparticles ranged from 77.33 to 93.33 μg/ml against multidrug-resistant strains. These results indicate that gold-silver alloy nanoparticles showed higher antimicrobial ability when compared to silver nanoparticles and gold nanoparticles alone. Finally, the synthesized nanoparticles could be used as an alternative antimicrobial agent against multidrug-resistant bacteria, according to our findings.

Desert truffles are an obligate hypogenous ectomycorrhizal fungi in association with host plant roots Helianthemum sp. and are of socioeconomically important and naturally grown in the Middle East, North Africa, Southern Europe, Mediterranean countries including Arab Gulf countries. Truffles are edible and a rich source of protein and various chemical compounds and traditionally have been used as folk medicine in the Arabian countries. The last decade has witnessed an increase research interest focused on the biosynthesis of metal nanoparticles using fungi as natural sources and as a good tool in nanobiotechnology. Nevertheless, recently metal nanoparticles have been widely applied in multidisciplinary fields including medical and pharmaceutical applications. Among nanometals, silver nanoparticles are of great significance to be used in pharmaceutical aspect as antimicrobial agent. According to our knowledge little information so far is available regarding biosynthesis of silver nanoparticles by the truffles and to search for new antimicrobial alternatives, therefore, the objective of this study was to explore the desert truffle (Tirmania nivea) for its potentiality to biosynthesize silver nanoparticles (AgNPs) and to examine their efficacy against five strains of human pathogenic bacteria namely; Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Salmonella typhi and Staphylococcus aureus. Fruiting bodies (Ascocarps) of the truffle T. nivea were collected from the sandy desert of Iraq and brought to the laboratory, washed thoroughly with distilled water and dried at room temperature. Twenty gram of dried fruit bodies of truffle were grounded and dissolved in boiled water and filtered using Whatman filter paper No 1. For synthesis process of silver nanoparticles, 100 mL of truffle extract filtrate was treated with 1 mM of AgNO3 solution and kept for 24 hr at dark condition and synthesis of silver nanoparticles (AgNPs) was checked by visual observation of color changes from pale yellow to dark brown and was further confirmed by UV – Vis spectrum. Fungal filtrate without AgNO3 was maintained as control. The potentiality of silver nanoparticles was examined for their antibacterial efficiency using agar well diffusion method against the selected strains of pathogenic bacteria. Wells (5 mm diam) were made in Muller-Hinton agar (MHA) plates streaked with swabs of each bacterial strain. The wells were loaded with two concentrations (50 and 100 μl) of synthesized silver nanoparticles solutions, incubated at 37 °C for 24 hr and examined for the appearance of inhibition zones around the wells and their diameters were measured. Minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) assay was carried out using the micro dilution method with serial dilutions (100, 50, 25, 12, 6.5, 3.13, 1.56, 0.78, 0.39, 0.2, 0.1, 0.05, 0.025 μg/L) of the truffle extract filtrate against two strains of bacteria E. coli (ATCC 25922) and S. aureus (NCTC 6571). Disc diffusion method was used to assay the synergistic effect of synthesized AgNPs with commonly used antibiotic Gentamycin. Cytotoxicity of the truffle extract was examined against human blood. Characterization of the biosynthesized silver nanoparticles from truffle extract was carried out by using UV-Vis spectrophotometer analysis, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). The results showed that the biosynthesized silver nanoparticles exhibited a high growth inhibition activity at 50 μl/ml concentration (12–25.5 mm inhibition zones dim) and at 100 μl/ml (14.5–28 mm inhibition zones diam) against the tested pathogenic bacterial strains. Among the tested bacteria, highest growth inhibition was noticed against P. aeruginosa (25.5 and 228 mm diam) at the two concentrations of AgNPs, respectively. However, a remarkable increase of bacterial growth inhibition zones (23–37 mm diam) was observed for a combination of silver nanoparticles and Gentamycin compared with Gentamycin alone (20–30 mm diam). MIC values were very low (0.312 and 0.0097 μg/ml) against the two tested bacterial strains E. coli and S. aureus, respectively. The truffle extract did not show any toxicity against human blood. UV-Vis spectrophotometer analysis revealed a peak at 420 nm indicating the biosynthesis of silver nanoparticles, FTIR analysis verified the detection of protein capping of biosynthesized AgNPs while SEM images showed that the synthesized silver nanoparticles are dispersed or aggregated and mostly spherical shape and their size ranging between 3–41 nm. It can be concluded that the biosynthesized silver nanoparticles by the desert truffle T. nivea are a promising for future medical and pharmaceutical applications as antibacterial agent and a further investigation to examine their efficacy in vivo is recommended.

Desert truffles are an obligate hypogenous ectomycorrhizal fungi in association with host plant roots Helianthemum sp. and are of socioeconomically important and naturally grown in the Middle East, North Africa, Southern Europe, Mediterranean countries including Arab Gulf countries. Truffles are edible and a rich source of protein and various chemical compounds and traditionally have been used as folk medicine in the Arabian countries. The last decade has witnessed an increase research interest focused on the biosynthesis of metal nanoparticles using fungi as natural sources and as a good tool in nanobiotechnology. Nevertheless, recently metal nanoparticles have been widely applied in multidisciplinary fields including medical and pharmaceutical applications. Among nanometals, silver nanoparticles are of great significance to be used in pharmaceutical aspect as antimicrobial agent. According to our knowledge little information so far is available regarding biosynthesis of silver nanoparticles by the truffles and to search for new antimicrobial alternatives, therefore, the objective of this study was to explore the desert truffle (Tirmania nivea) for its potentiality to biosynthesize silver nanoparticles (AgNPs) and to examine their efficacy against five strains of human pathogenic bacteria namely; Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Salmonella typhi and Staphylococcus aureus. Fruiting bodies (Ascocarps) of the truffle T. nivea were collected from the sandy desert of Iraq and brought to the laboratory, washed thoroughly with distilled water and dried at room temperature. Twenty gram of dried fruit bodies of truffle were grounded and dissolved in boiled water and filtered using Whatman filter paper No 1. For synthesis process of silver nanoparticles, 100 mL of truffle extract filtrate was treated with 1 mM of AgNO3 solution and kept for 24 hr at dark condition and synthesis of silver nanoparticles (AgNPs) was checked by visual observation of color changes from pale yellow to dark brown and was further confirmed by UV – Vis spectrum. Fungal filtrate without AgNO3 was maintained as control. The potentiality of silver nanoparticles was examined for their antibacterial efficiency using agar well diffusion method against the selected strains of pathogenic bacteria. Wells (5 mm diam) were made in Muller-Hinton agar (MHA) plates streaked with swabs of each bacterial strain. The wells were loaded with two concentrations (50 and 100 ul) of synthesized silver nanoparticles solutions. Incubated at 37°C for 24 hr and examined for the appearance of inhibition zones around the wells and their diameters were measured. Minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) assay was carried out using the micro dilution method with serial dilutions (100, 50, 25, 12, 6.5, 3.13, 1.56, 0.78, 0.39, 0.2, 0.1, 0.05, 0.025 μg/L) of the truffle extract filtrate against two strains of bacteria E. coli (ATCC 25922) and S. aureus (NCTC 6571). Disc diffusion method was used to assay the synergistic effect of synthesized AgNPs with commonly used antibiotic Gentamycin. Cytotoxicity of the truffle extract was examined against human blood. Characterization of the biosynthesized silver nanoparticles from truffle extract was carried out by using UV-Vis spectrophotometer analysis, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). The results showed that the biosynthesized silver nanoparticles exhibited a high growth inhibition activity at 50 ul/ml concentration (12–25.5 mm inhibition zones dim) and at 100 ul/ml (14.5–28 mm inhibition zones diam) against the tested pathogenic bacterial strains. Among the tested bacteria, highest growth inhibition was noticed against P. aeruginosa (25.5 and 228 mm diam) at the two concentrations of AgNPs, respectively. However, a remarkable increase of bacterial growth inhibition zones (23–37 mm diam) was observed for a combination of silver nanoparticles and Gentamycin compared with Gentamycin alone (20–30 mm diam). MIC values were very low (0.312 and 0.0097 ug/ml) against the two tested bacterial strains E. coli and S. aureus, respectively. The truffle extract did not show any toxicity against human blood. UV-Vis spectrophotometer analysis revealed a peak at 420 nm indicating the biosynthesis of silver nanoparticles, FTIR analysis verified the detection of protein capping of biosynthesized AgNPs while SEM images showed that the synthesized silver nanoparticles are dispersed or aggregated and mostly spherical shape and their size ranging between 3–41 nm. It can be concluded that the biosynthesized silver nanoparticles by the desert truffle T. nivea are a promising for future medical and pharmaceutical applications as antibacterial agent and a further investigation to examine their efficacy in vivo is recommended.

In this study aim was to perform green synthesis of synthesis silver nanoparticles (LAC-AgNPs, RAE-AgNPs and BAE-AgNPs) by using Desmodesmus sp., intracellular and extracellular synthesis methods and to compare the obtained products with physicochemical characterization techniques. The structural, morphological and optical properties of the synthesized nanoparticles were characterized using UV-Vis spectroscopy, TEM, SEM-EDS, FTIR, DLS and zeta potential. These results clearly show that silver nanoparticles (AgNPs) could be synthesized in different sizes and stabilities with various biological materials obtained from Desmodesmus sp. LAC-AgNPs had size of 10-30 nm, RAE-AgNPs had size of 4-8 nm and BAE-AgNPs had size of 3-6 nm. Also, the antibacterial activity of silver nanoparticles synthesized as intracellular and extracellular showed a strong antibacterial effect against pathogens such as Salmonella sp. and Listeria monocytogenes. Additionally, they have effective antifungal activity against Candida parapsilosis. The broth microdilution method was used for examining antibacterial antifungal effect of synthesis AgNPs. The minimum inhibitory concentration against Salmonella sp., Listeria monocytogenesis and Candida parapsilosis were recorded as 3,125 μl, 1,5625 µl and 0,78125 µl synthesis AgNPs, respectively. As a result, it has thought that different sizes of synthesis AgNPs may have a great potential for biomedical applications.