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1.
Green chemistry of nanomaterials from synthesis to diverse biomedical applications is a discussion of town in the current scientific scenario. In this work, Ocimum basilicum leaves extract was utilized as the reducing agent in the synthesis of ZnO nanoparticles. Green synthesized ZnO NPs mediated via Ocimum basilicum extract were decorated on the reduced graphene oxide (RGO) sheet by the simple one-step method. The prepared green synthesized RGO-ZnO nanocomposites (NCs) were characterized via the X-ray diffractometer. The average crystallite size of ZnO was 25 nm which confirmed the wurtzite hexagonal structure of ZnO. The scanning Electron Microscopy technique confirmed the spherical morphology of particle size of 31 nm. Further, Fourier Transform Infrared Spectroscopy confirms the Zn-O bond stretching in the RGO-ZnO NCs. Antioxidant activity of the green synthesized Ocimum basilicum ZnO NPs and RGO-ZnO NCs were performed by DPPH scavenging activities and found the dose-dependent. RGO-ZnO effectively inhibited the α-amylase and α-glucosidase for in vitro antidiabetic activities. Moreover, RGO-ZnO NCs showed the antibacterial potential with increasing concentration against the gram-positive (Cocci) and gram-negative (E. coli) bacterial strains. In Photocatalytic activity, the ZnO NPs and RGO-ZnO NCs were utilized as the catalyst and degraded the Rh-B dye 91.4% and 96.7% under UV–visible light. Overall, RGO-ZnO NCs showed better results in antibacterial, antidiabetic activity as well as photocatalytic activity against the pure ZnO NPs. Hence, RGO-ZnO nanocomposites have demonstrated the opportunity to be an entrancing material for photocatalysis and biological studies.  相似文献   

2.
The objective of this study is to synthesize ZnO and Mg doped ZnO (Zn1−xMgxO) nanoparticles via the sol-gel method, and characterize their structures and to investigate their biological properties such as antibacterial activity and hemolytic potential.Nanoparticles (NPs) were synthesized by the sol-gel method using zinc acetate dihydrate (Zn(CH3COO)2.2H2O) and magnesium acetate tetrahydrate (Mg(CH3COO)2.4H2O) as precursors. Methanol and monoethanolamine were used as solvent and sol stabilizer, respectively. Structural and morphological characterizations of Zn1−xMgxO nanoparticles were studied by using XRD and SEM-EDX, respectively. Photocatalytic activities of ZnO and selected Mg-doped ZnO (Zn1−xMgxO) nanoparticles were investigated by degradation of methylene blue (MeB). Results indicated that Mg doping (both 10% and 30%) to the ZnO nanoparticles enhanced the photocatalytic activity and a little amount of Zn0.90 Mg0.10 O photocatalyst (1.0 mg/mL) degraded MeB with 99% efficiency after 24 h of irradiation under ambient visible light. Antibacterial activity of nanoparticles versus Escherichia coli ( E. coli ) was determined by the standard plate count method. Hemolytic activities of the NPs were studied by hemolysis tests using human erythrocytes. XRD data proved that the average particle size of nanoparticles was around 30 nm. Moreover, the XRD results indicatedthat the patterns of Mg doped ZnO nanoparticles related to ZnO hexagonal wurtzite structure had no secondary phase for x ≤ 0.2 concentration. For 0 ≤ x ≤ 0.02, NPs showed a concentration dependent antibacterial activity against E. coli . While Zn0.90Mg0.10 O totally inhibited the growth of E. coli , upper and lower dopant concentrations did not show antibacterial activity.  相似文献   

3.
《印度化学会志》2023,100(2):100920
In the present work, silver-doped ZnO (Ag–ZnO NPs) with different concentrations of silver ions (0.3, 0.5, 1.0 and 1.5 mol %) were synthesized by using a simple co-precipitation method. The Ag–ZnO NPs were primarily characterized by XRD, FT-IR, SEM, EDS, TEM, UV–Vis. DRS, PL and BET surface area. The XRD analysis of Ag–ZnO NPs shows a wurtzite structure and optimized Ag–ZnO NPs (1.0 mol %) exhibit a lower crystallite size of 15.96 nm than that of bare ZnO (19.07 nm). Optical study shows a decrease in band gap from 3.13 to 2.97 eV as the concentration of Ag ions increases from 0.3 to 1.5 mol%. TEM images reveal the spherical shape particle with sizes ranging between 10 and 15 nm. From the multipoint BET plot, the surface area of Ag–ZnO NPs found 38.06 m2/gwhich is higher than the ZnO NPs (34.48 m2/g). The photocatalytic study demonstrated that the Ag–ZnO NPs (1.0 mol %) has an excellent photodegradation efficiency of Methyl Orange (96.74%)with a 26% increment as compared to bare ZnO (70.47%). Furthermore, the bactericidal activity of Ag–ZnO NPs (1.0 mol %) was investigated against four different bacterial strains. The results explored that the Gram-negative bacteria (E. coli and P. vulgaris) are more sensitive than Gram-positive (S. aureus and B. cereus) to Ag–ZnO NPs. Overall, the anticipated material is economical and reusable for photodegradation and antibacterial activity.  相似文献   

4.
Nowadays, the industrial wastewater pollutants including toxic dyes and pathogenic microbes have caused serious environmental contaminations and human health problems. In the present study, eco-friendly and facile green synthesis of Ag modified ZnO nanoparticles (ZnO-Ag NPs) using Crataegus monogyna (C. monogyna) extract (ZnO-Ag@CME NPs) is reported. The morphology and structure of the as-biosynthesized product were characterized by field emission scanning electron microscopy (FESEM), X-Ray diffraction (XRD), differential reflectance spectroscopy (DRS), dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), and energy-dispersive X-ray spectroscopy (EDS) techniques. TEM and FESEM images confirmed the oval and spherical-like structure of the products with a size of 55–70 nm. The EDS analysis confirmed the presence of Zn, Ag, and O elements in the biosynthesized product. The photocatalytic results showed ZnO-Ag@CME NPs were degraded (89.8% and 75.3%) and (94.2% and 84.7%) of methyl orange (MO) and basic violet 10 (BV10), under UV and sunlight irradiations, respectively. The Ag modified ZnO nanoparticles exhibited enhanced catalytic activity towards organic pollutants, and showed better performance than the pure ZnO nanoparticles under UV and sunlight irradiations. This performance was probably due to the presence of silver nanoparticles as a plasmonic material. Antibacterial activity was performed against different bacteria. ZnO-Ag@CME NPs showed high antibacterial activity against K. pneumoniae, S. typhimurium, P. vulgaris, S. mitis, and S. faecalis with MIC values of 50, 12.5, 12.5, 12.5, and 12.45 µg/mL, respectively. All in all, the present investigation suggests a promising method to achieve high-efficiency antibacterial and catalytic performance.  相似文献   

5.
In the present work, the properties of ZnO nanoparticles obtained using an eco-friendly synthesis (biomediated methods in microwave irradiation) were studied. Saponaria officinalis extracts were used as both reducing and capping agents in the green nanochemistry synthesis of ZnO. Inorganic zinc oxide nanopowders were successfully prepared by a modified hydrothermal method and plant extract-mediated method. The influence of microwave irradiation was studied in both cases. The size, composition, crystallinity and morphology of inorganic nanoparticles (NPs) were investigated using dynamic light scattering (DLS), powder X-ray diffraction (XRD), SEM-EDX microscopy. Tunings of the nanochemistry reaction conditions (Zn precursor, structuring agent), ZnO NPs with various shapes were obtained, from quasi-spherical to flower-like. The optical properties and photocatalytic activity (degradation of methylene blue as model compound) were also investigated. ZnO nanopowders’ antibacterial activity was tested against Gram-positive and Gram-negative bacterial strains to evidence the influence of the vegetal extract-mediated synthesis on the biological activity.  相似文献   

6.
To increase the profitability and sustainability of agricultural waste, a facile green approach was established to synthesize zinc oxide nanoparticles (ZnO NPs) using saffron leaf extract as a reducing and stabilizing agent. Structural characteristics of NPs were investigated by X-ray diffraction (XRD), Fourier-transform infrared (FTIR), field emission scanning electron microscopy (FESEM), and UV–Visible (UV–Vis) spectroscopy. Characterization results revealed that ZnO NPs is highly crystalline with a hexagonal wurtzite structure and spherical particles with diameter less than 50 nm, as confirmed by XRD and FESEM techniques. UV–Vis absorption spectra depicted an absorption peak at 370 nm, which confirms the formation of ZnO NPs. FTIR spectral analysis confirmed the presence of functional groups and metal oxygen groups. The biological activities of ZnO NPs were also investigated. The antibacterial effect of ZnO NPs was investigated against selected food pathogens (Salmonella Typhimurium, Listeria monocytogenes, and Enterococcus faecalis). The study results prove that the green synthesized ZnO NPs show enhanced antibacterial activity against S. Typhimurium when compared with other strains. A dose-dependent free radical scavenging activity was observed for ZnO NPs in both 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) and fluorescence recovery after photobleaching (FRAP) assays. The ZnO NPs were evaluated for their photocatalytic activity during the degradation of methylene blue (MB) dye in aqueous solutions. The maximum removal of MB achieved was 64% with an initial ZnO NP concentration of 12 mg/mL under UV light. The present study revealed that the agricultural waste (saffron leaf) provides a simple and eco-friendly option to sustainably synthesize ZnO NPs for use as a photocatalyst. In addition, this is the first report on saffron leaf-mediated synthesis of ZnO NPs.  相似文献   

7.
Silver nanoparticles (Ag NPs) were successfully synthesized using AgNO3 via an eco-friendly and simple green route using Abelmoschus esculentus (L.) pulp extract at room temperature. The phytochemicals present in A. esculentus (L.) pulp extract were used both as a reducing and a stabilizing agent for the synthesis of Ag NPs. The stabilization of Ag NPs with phytochemicals was justified using Fourier-transform infrared spectroscopy. The size of the as-synthesized Ag NPs was examined using dynamic light scattering and confirmed by transmission electron microscopy. The crystalline nature of Ag NPs had been identified using X-ray diffraction. The present study demonstrated the efficacy of Ag NPs against Jurkat cells in vitro. Our study also showed that the IC50 dose of Ag NPs leads to the increase in intracellular reactive oxygen species and significantly diminished mitochondrial membrane potential, indicating the effective involvement of apoptosis in cell death. The synthesized Ag NPs also exhibited good antimicrobial activity against different gram class bacteria.  相似文献   

8.
The green biosynthesis of nanoparticles by plant extracts is an attractive and promising technique for medicinal applications. In the current study, we chose one of the daisy plants, Aaronsohnia factorovskyi (which grows in the Najd region, Saudi Arabia), to investigate its anti-microbial efficacy, in combination with silver nanoparticles. The biosynthesized nanoparticles were evaluated for antibacterial activity against Staphylococcus aureus, Bacillus subtilis (Gram-positive), Pseudomonas aeruginosa, and Escherichia coli, (Gram-negative) using the disc diffusion method, while the antifungal activity was assessed against Fusarium oxysporum, Fusarium solani, Helminthosporium rostratum, and Alternaria alternata. The potential phytoconstituents of the plant extracts were identified by Fourier-transform infrared spectroscopy (FT-IR) techniques, the Field emission scanning electron microscopy (FE-SEM), Chromatography/Mass Spectrometry (GC-MS) techniques, and Zeta potential analysis. The current study revealed the ability of the tested plant extract to convert silver ions to silver nanoparticles with an average diameter of 104–140 nm. Biogenic Aaronsohnia factorovskyi-silver nanoparticles (AF-AgNPs) showed significant antibacterial activity against Staphylococcus aureus with inhibition zone diameter to 19.00 ± 2.94 mm, and antifungal activity against Fusarium solani, which reduced the growth of fungal yarn to 1.5 mm. The innovation of the present study is that the green synthesis of NPs, which is simple, cost-effective, provides stable nano-materials, and can be an alternative for the large-scale synthesis of silver nanoparticles.  相似文献   

9.
A facile biosynthesis route was followed to prepare zinc oxide nanoparticles (ZnO NPs) using Euphorbia milii (E. milii) leaf constituents. The SEM images exhibited presence of spherical ZnO NPs and the corresponding TEM images disclosed monodisperse nature of the ZnO NPs with diameter ranges between 12 and 20 nm. The Brunauer–Emmett–Teller (BET) analysis revealed that the ZnO NPs have specific surface area of 20.46 m2/g with pore diameter of 2 nm–10 nm and pore volume of 0.908 cm3/g. The EDAX spectrum exemplified the existence of Zn and O elements and non-appearance of impurities that confirmed pristine nature of the ZnO NPs. The XRD pattern indicated crystalline peaks corresponding to hexagonal wurtzite structured ZnO with an average crystallite size of 16.11 nm. The FTIR spectrum displayed strong absorption bands at 512 and 534 cm?1 related to ZnO. The photocatalytic action of ZnO NPs exhibited noteworthy degradation of methylene blue dye under natural sunlight illumination. The maximum degradation efficiency achieved was 98.17% at an illumination period of 50 min. The reusability study proved considerable photostability of the ZnO NPs during photocatalytic experiments. These findings suggest that the E. milii leaf constituents can be utilized as suitable biological source to synthesis ZnO NPs for photocatalytic applications.  相似文献   

10.
In the present investigation novel Polyimide/functionalized ZnO (PI/ZnO) bionanocomposites containing amino acid (Methionine) and benzimidazole pendent groups with different amounts of modified ZnO nanoparticles (ZnO NPs) were successfully prepared through ultrasonic irradiation technique. Due to the high surface energy and tendency for agglomeration, the surface ZnO NPs was modified by a coupling agent as 3- methacryloxypropyl-trimethoxysilane (MPS) to form MPS-ZnO nanoparticles. The ultrasonic irradiation effectively changes the rheology and the glass transition temperature and the crystallinity of the composite polymer. PI/ZnO nanocomposites were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscope (TEM). TEM analysis showed that the modified ZnO nanoparticles were homogeneously dispersed in polymer matrix. The TGA results of PI/ZnO nanocomposites showed that the thermal stability is obviously improved the presence of MPS-ZnO NPs in comparison with the pure PI and that this increase is higher when the NP content increases. The permeabilities of pure H2, CH4, O2, and N2 gases through prepared membranes were determined at room temperature (25 °C) and 20 bar feed pressure. The membranes having 20% ZnO showed higher values of H2 permeability, and H2/CH4 and H2/N2 ideal selectivities (the ratio of pair gas permeabilities) compared with other membranes. The antibacterial activity of bionanocomposite films was tested against gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa). Further, it was observed that antibacterial activity of the resulting hybrid biofilms showed somewhat higher for gram-positive bacteria compared to gram-negative bacteria.  相似文献   

11.
This research aimed to enhance the antibacterial activity of silver nanoparticles (AgNPs) synthesized from silver nitrate (AgNO3) using aloe vera extract. It was performed by means of incorporating AgNPs on an activated carbon nanoparticle (ACNPs) under ultrasonic agitation (40 kHz, 2 × 50 watt) for 30 min in an aqueous colloidal medium. The successful AgNPs synthesis was clarified with both Ultraviolet-Visible (UV-Vis) and Fourier Transform Infrared (FTIR) spectrophotometers. The successful AgNPs–ACNPs incorporation and its particle size analysis was performed using Transmission Electron Microscope (TEM). The brown color suspension generation and UV-Vis’s spectra maximum wavelength at around 480 nm confirmed the existence of AgNPs. The particle sizes of the produced AgNPs were about 5 to 10 nm in the majority number, which collectively surrounded the aloe vera extract secondary metabolites formed core-shell like nanostructure of 8.20 ± 2.05 nm in average size, while ACNPs themselves were about 20.10 ± 1.52 nm in average size formed particles cluster, and 48.00 ± 8.37 nm in average size as stacking of other particles. The antibacterial activity of the synthesized AgNPs and AgNPs-immobilized ACNPs was 57.58% and 63.64%, respectively (for E. coli); 61.25%, and 93.49%, respectively (for S. aureus). In addition, when the AgNPs-immobilized ACNPs material was coated on the cotton and polyester fabrics, the antibacterial activity of the materials changed, becoming 19.23% (cotton; E. coli), 31.73% (polyester; E. coli), 13.36% (cotton; S. aureus), 21.15% (polyester; S. aureus).  相似文献   

12.
Nanoworld is an attractive sphere with the potential to explore novel nanomaterials with valuable applications in medicinal science. Herein, we report an efficient and ecofriendly approach for the synthesis of Nickel oxide nanoparticles (NiO NPs) via a solution combustion method using Areca catechu leaf extract. As-prepared NiO NPs were characterized using various analytical tools such as powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-Visible spectroscopy (UV-Vis). XRD analysis illustrates that synthesized NiO NPs are hexagonal structured crystallites with an average size of 5.46 nm and a hexagonal-shaped morphology with slight agglomeration. The morphology, size, and shape of the obtained material was further confirmed using SEM and TEM analysis. In addition, as-prepared NiO NPs have shown potential antidiabetic and anticancer properties. Our results suggest that the inhibition of α-amylase enzyme with IC 50 value 268.13 µg/mL may be one of the feasible ways through which the NiO NPs exert their hypoglycemic effect. Furthermore, cytotoxic activity performed using NiO NPs exhibited against human lung cancer cell line (A549) proved that the prepared NiO NPs have significant anticancer activity with 93.349 μg/mL at 50% inhibition concentration. The biological assay results revealed that NiO NPs exhibited significant cytotoxicity against human lung cancer cell line (A549) in a dose-dependent manner from 0–100 μg/mL, showing considerable cell viability. Further, the systematic approach deliberates the NiO NPs as a function of phenolic extracts of A. catechu with vast potential for many biological and biomedical applications.  相似文献   

13.
《印度化学会志》2023,100(2):100879
The technique of pulsed laser ablation in liquid media was successfully used to prepare zinc oxide ZnO nanoparticles NPs to enhance glass ionomer GI restorative. The synthesized ZnO NPs were confirmed using UV–Visible spectroscopy, XRD, and TEM. The absorption spectra revealed that the absorbance intensity of the prepared ZnO NPs increased as the number of laser pulses increased, with an absorbance peak at 230 nm due to quantum confinement. The crystalline nature of NPs with hexagonal structure is revealed by XRD analysis. The TEM images demonstrated the nanorod shape with a length of about 3.33 nm and there were spherical nanoparticles ranging from 5 nm to 30 nm. ZnO NPs with and without GI were tested for antibacterial activity against Streptococcus mutans bacteria, which shows slight improvement after adding ZnO NPs to glass ionomer as a result of containing effective ingredients in its composition. The agar well diffusion method results revealed that ZnO with GI had a higher antibacterial activity compared with pure ZnO NPs. Finally, the compressive strength test illustrated significant enhancement of up to 50% associated with the ZnO NP's concentration increase.  相似文献   

14.
Silver and copper nanoparticles were produced by an ecologically safe metal vapor synthesis (MVS) method using acetone as an organic dispersion medium. Transmission electron microscopy (TEM) showed that the specimens are spherical and polydisperse, and their average size is 2.5 nm for silver nanoparticles (Ag NPs) and 2.6 nm for copper nanoparticles (Cu NPs). X-ray photoelectron spectroscopy analyses showed that the state of silver in the nanoparticles is close to that of silver in the Ag0 state, whereas copper black contains two oxidized states of the metal—Cu+ and Cu2+. Biological in vitro studies demonstrated that the nanoparticles have antibacterial activity against Gram-positive and Gram-negative bacterial species. Cu NPs exhibited more prominent antibacterial effects and induced significant growth inhibition of Bacillus cereus and Escherichia coli. Both types of nanoparticles showed anticancer properties in vitro. Cu NPs induced intense cytotoxicity in cancer and normal fibroblasts in vitro cultures, but their inhibitory effect against noncancerous cells was milder compared with cancer cell lines. Ag NPs demonstrated selective cytotoxicity against human lung and cervical adenocarcinoma cell lines. Further in vitro studies indicated that the mechanism of Ag NPs and Cu NPs anticancer effects involves induction of apoptosis. The present study describes a green synthesis approach for production of biologically active silver and copper nanoparticles and highlights their potential for medical application.  相似文献   

15.
Synthesis and biomedical research of bimetallic gold-silver nanoparticles (Au–Ag NPs) have gained much attention due to their unique properties. Antibacterial mechanism of gold-silver nanoparticles is a current topic of interest in nanomedicine engineering. We used three routes in the synthesis of Au–Ag NPs alloy: i) Co-reduction of [HOOC-4-C6H4NN]AuCl4/AgNO3, ii) Seeding of AuNPs-COOH/AgNO3 and iii) immobilization of AgNPs over the parent AuNPs-COOH. Two mild reducing agents, NaBH4 and 9-BBN (9-borabicyclo(3.3.1)nonane), were used. Colloidal alloy nanoparticles structure was confirmed using transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The particles reduced using NaBH4 were larger (~20 nm) than those synthesized using 9-BBN (<10 nm). The synthesized nanoparticles showed high stability under notoriously leaching conditions of chloride-containing electrolytes. Moreover, we studied the Au–Ag NPs antibacterial activity against the growth of Gram-negative Escherichia coli ATCC strain 25922 and Gram-positive Staphylococcus aureus ATCC strain 29213. The antibacterial mechanisms were evaluated by studying the time-dependent generation of reactive oxygen species (ROS). A major destruction of the bacterial cell wall and leakage of cell components were observed by scanning electron microscopy (SEM), which is clearly visible towards E. coli more than S. aureus bacterial strain. The destruction of the bacterial cell wall was further confirmed by detecting the DNA leakage using gel electrophoresis. The synergistic effect of gold enhanced the antibacterial properties, however, with low cytotoxicity to human dermal fibroblast cells. This study deals with the important aspects of time-dependent mechanisms of the antibacterial action of Au–Ag NPs since the leaching out of Ag ion is slow compared to AgNPs. The Au–Ag NPs alloy efficiently tackles microbial activity that can be controlled to minimize cytotoxicity and thus opens their future applications as antibacterial agents.  相似文献   

16.
ABSTRACT

We reported a green and simple method for biosynthesizing zinc oxide nanoparticles (ZnO NPs) using Corymbia citriodora leaf extract as reducing and stabilizing agent. SEM, EDX, XRD, UV–VIS spectroscopy, Raman spectroscopy and TGA have been used for characterizing the biosynthesized ZnO NPs. The results indicating the ZnO NPs synthesized by C. citriodora leaf extract have high purity and the average size is 64?nm. The photocatalytic activity of the ZnO NPs has been investigated by degradation methylene blue under visible light irradiation. Due to the smaller size, the biosynthesized ZnO NPs showed an excellent photocatalytic performance.  相似文献   

17.
ABSTRACT

The synthesized ZnO NPs using durian rind in solution has shown maximum absorption at 355.5?nm with the bandgap of 3.33?eV, spectrophotometrically. SEM and TEM studies revealed that the shape of the synthesized ZnO NPs was spherical with an average size of 280 and 283?nm, respectively. However, DLS analysis of ZnO NPs revealed the average particle size of 456?d.nm. The presence of [100], [002], [101], [102], [110], [103], [200], [112] and [201] planes in XRD corroborate the formation of pure wurtzite structure of ZnO NPs. Synthesized ZnO NPs showed remarkable photocatalytic activity on degradation of methylene blue and sulfanilamide, antioxidant activity, considerable antimicrobial activity against Escherichia coli and Staphylococcus aureus, and considerable cytotoxic activity against brine shrimp. The sulfanilamide degradation was found to be 96.70%, under natural sunlight and in the presence of 0.1% ZnO NPs at pH 10 with a time of 3?h. The dye degradation was found to be 84% under sunlight in the presence of 0.01% ZnO NPs at pH 10 with a time of 40?min. The synthesized ZnO NPs may be explored furthermore in the fields of wastewater treatment, biomedicine, biosensor, and nanotechnology.  相似文献   

18.
A chalcone series (3a–f) with electron push–pull effect was synthesized via a one-pot Claisen–Schmidt reaction with a simple purification step. The compounds exhibited strong emission, peaking around 512–567 nm with mega-stokes shift (∆λ = 93–139 nm) in polar solvents (DMSO, MeOH, and PBS) and showed good photo-stability. Therefore, 3a–f were applied in cellular imaging. After 3 h of incubation, green fluorescence was clearly brighter in cancer cells (HepG2) compared to normal cells (HEK-293), suggesting preferential accumulation in cancer cells. Moreover, all compounds exhibited higher cytotoxicity within 24 h toward cancer cells (IC50 values ranging from 45 to 100 μM) than normal cells (IC50 value >100 μM). Furthermore, the antimicrobial properties of chalcones 3a–f were investigated. Interestingly, 3a–f exhibited antibacterial activities against Escherichia coli and Staphylococcus aureus, with minimum bactericidal concentrations (MBC) of 0.10–0.60 mg/mL (375–1000 µM), suggesting their potential antibacterial activity against both Gram-negative and Gram-positive bacteria. Thus, this series of chalcone-derived fluorescent dyes with facile synthesis shows great potential for the development of antibiotics and cancer cell staining agents.  相似文献   

19.
Synthesis of nanomaterials is an emerging field due to their fascinating properties for applications in different field and green synthesis offers various advantages versus physical and chemical methods. Herein, green protocol has been adopted for the synthesis of silver nanoparticles (Ag NPs) using seeds extract of strawberry. The Ag NPs were characterized using advanced techniques comprising UV/Vis, XRD, FTIR, SEM, DLS and EDX. The λmax for the Ag NPs was recorded at 405 nm. The functional groups present in the extract and involved in Ag ions reduction were determined using FTIR analysis. The SEM-EDX analysis confirmed the mono-dispersive nature of Ag NPs along with confirmation of elemental composition. The nanoparticles size distribution was recorded in 50-70 nm range. Bio-fabricated Ag NPs were appraised for antioxidant activity (DPPH with % inhibition 56.61 and ABTS with % inhibition 77.81) and antimicrobial activity, i.e., Escherichia coli, Salmonella typhimurium, Shigella sonnei, Halomonas halophile, Staphylococcus aureus and Bacillus subtilis. It is concluded that these synthesized NPs could probably be applied as potent antibacterial and antioxidant materials.  相似文献   

20.
Bio synthesis of nanoparticles using plant parts has gained considerable attention, given the fact that the method is green, environment friendly, cheaper, simple and involves no hazardous substances. The present study involves the green synthesis of copper oxide nanoparticles (CuO NPs) using chitosan and the aqueous leaf extract of Elsholtzia blanda, an aromatic medicinal herb. The synthesized E.blanda-chitosan mediated copper oxide nanoparticles (CPCE) and E. blanda mediated copper oxide nanoparticles (PCE) were subjected to different characterization techniques, Ultraviolet–visible (UV–Vis), Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive X-ray Analysis (EDAX), High Resolution Transmission Electron Microscopy (HRTEM) and Selected Area Electron Diffraction (SAED). The absorbance peaks in UV–Vis spectroscopy at 286 nm and 278 nm for CPCE and PCE respectively indicated the formation of nanoparticles. TEM and SEM employed for studying the surface morphology showed rod-like and spherical morphology bearing average size of 47.71 nm for CPCE and 36.07 nm for PCE. The antibacterial activities of the prepared nanoparticles were tested against Enterococcus faecalis, Staphylococcus aureus, Escherichia coli and Salmonella typhi by agar well diffusion method. The results indicate that CuO NPs possess effective antibacterial potential against all tested bacteria with a maximum zone of inhibition of 18 mm for Enterococcus faecalis. Antioxidant studies revealed the highest DPPH scavenging activity of 89% at 25 μg/mL concentration of the nanoparticles. The percentage of the photo catalytic degradation of Congo red was found to be 95% after 10 h.  相似文献   

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