Formulation and characterization of a novel anti-human endometrial cancer supplement by gold nanoparticles green-synthesized using Spinacia oleracea L. Leaf aqueous extract

Gold nanoparticles as one of the productions of the chemistry field have a special place in the cure of many diseases. Many experiences in medicinal researches have indicated that the plants enhance the anticancer effects of gold nanoparticles. According to the above contents, we investigated the capacities of Spinacia oleracea L. leaf aqueous extract green-mediated gold nanoparticles (AuNPs) as a modern chemotherapeutic material in treating endometrial cancer. The physicochemical characterization tests including UV–Visible Spectroscopy (UV–Vis), Field Emission Scanning Electron Microscopy (FE‐SEM), Fourier Transformed Infrared Spectroscopy (FT‐IR), and Transmission Electron Microscopy (TEM) were used for investigating the physicochemical properties of AuNPs. To survey the antioxidant potentials of AuNPs, one of the common antioxidant techniques i.e., DPPH was used. Determination of anti-endometrial cancer effects of AuNPs was carried out by the MTT assay and against Ishikawa, KLE, HEC-1-A, and HEC-1-B cell lines. The physicochemical characterization analyses revealed that the AuNPs had been formulated as the best possible. The results of the DPPH test confirmed excellent antioxidant properties of AuNPs in comparison to the butylated hydroxytoluene. The AuNPs IC50 was 194 µg/mL in the antioxidant test. The results of the MTT assay confirmed removing Ishikawa, KLE, HEC-1-A, and HEC-1-B cell lines after treating with low concentrations of AuNPs. The IC50 of the AuNPs was 341, 335, 316, and 325 µg/mL against Ishikawa, KLE, HEC-1-A, and HEC-1-B cell lines, respectively. The best finding of anti-endometrial cancer potentials was determined in the HEC-1-A cell line. According to the above results, significant anti-endometrial cancer effects of Au nanoparticles green-mediated by S. oleracea leaf extract are confirmed. It is offered that the studies of the clinical trial are performed for approving the above findings in humans.     

Application of organometallic chemistry in the formulation of a modern therapeutic drug by Ag nanoparticles green-mediated by Allium to treat the breast cancer

In the recent study, we decided to survey the capacities of metallic nanoparticles formulated by Allium monanthum (AgNPs) as a novel chemotherapeutic drug in the treatment of several types of breast cancers. Characterization of AgNPs was done by UV–Visible Spectroscopy (UV–Vis), Fourier Transformed Infrared Spectroscopy (FT‐IR), Transmission Electron Microscopy (TEM), and Field Emission Scanning Electron Microscopy (FE‐SEM). For investigating the antioxidant properties of AgNO₃, Allium monanthum, and AgNPs, the DPPH test was used in the presence of butylated hydroxytoluene as the positive control. To survey the cytotoxicity and anti-breast cancer effects of AgNO₃, Allium monanthum, and AgNPs, MTT assay was used on the breast adenocarcinoma (MCF7), breast carcinoma (Hs 578Bst), infiltrating ductal cell carcinoma (Hs 319.T), infiltrating lobular carcinoma of breast (UACC-3133), inflammatory carcinoma of the breast (UACC-732), and metastatic carcinoma (MDA-MB-453) cell lines. DPPH test revealed similar antioxidant potentials for Allium monanthum, AgNPs, and butylated hydroxytoluene. Silver nanoparticles had very low cell viability and anti-breast cancer properties dose-dependently against MCF7, Hs 578Bst, Hs 319.T, UACC-3133, UACC-732, and MDA-MB-453 cell lines without any cytotoxicity on the normal cell line. The best result of anti-breast cancer properties of AgNPs against the above cell lines was seen in the case of the UACC-3133 cell line. According to the above findings, the silver nanoparticles containing Allium monanthum aqueous extract can be administrated in humans for the treatment of several types of breast cancer especially breast adenocarcinoma, breast carcinoma, infiltrating ductal cell carcinoma, infiltrating lobular carcinoma of breast, inflammatory carcinoma of the breast, and metastatic carcinoma.     

Formulation of gold nanoparticles with hibiscus and curcumin extracts induced anti-cancer activity

Gold nanoparticles (AuNPs) have shown a potential for biological applications due to their biocompatibility and high efficiency in drug delivery. Most of the times, the chemical routs are being used to synthesize the AuNPs products. In this paper, eco-friendly non-chemical rout was used to prepare AuNPs by utilizing hibiscus and curcumin extracts as reducing and stabilizing agents, and subsequently their anticancer activities were investigated. The synthesized AuNPs were characterized by using ultraviolet–visible spectroscopy (UV–Vis spectroscopy), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). UV–Vis spectroscopy analysis confirmed the characteristics absorption peak of gold, and FTIR findings were highlighted the characteristics boding. SEM and TEM analyses showed that the particles were predominantly spherical in shape. The particles were well dispersed when they were prepared under Hibiscus extracts with average size ～ 13 nm. An interesting morphology was observed when AuNPs were prepared with curcumin, where particles displayed an interconnected morphology (average size ～ 18 nm). The anticancer cell activity of AuNPs was studied against human colorectal carcinoma cells (HCT-116) and breast cancer cells (Michigan Cancer Foundation-7 (MCF-7)). The results of anticancer study showed that the treatment of cancer cells with AuNPs decreased the number of cells significantly as compared to control cells. The AuNPs -Hibiscus specimen showed a better inhibiting property than AuNPs -Curcumin, which is attributed to their uniform dispersion and small size.     

Green formulation,chemical characterization,and antioxidant,cytotoxicity, and anti-human cervical cancer effects of vanadium nanoparticles: A pre-clinical study

In this study, V₂O₅ nanoparticles were synthesized in an aqueous medium using Calendula officinalis extract as stabilizing and reducing agents. The synthesized nanoparticles (VNPs@C.officinalis) were characterized using different techniques including UV–Vis. and FT-IR Spectroscopy, X‐ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive X-ray Spectrometry (EDS). According to the XRD analysis, 28.83 nm was measured for VNPs@C.officinalis crystal size. SEM images exhibited a uniform spherical morphology in size of 38.14 nm for the biosynthesized nanoparticles. To survey the cytotoxicity and anti-human cervical cancer effects of C. officinalis aqueous extract and vanadium nanoparticles, MTT assay was used on C-33 A [c-33a], SiHa, Ca Ski, DoTc2 4510, HT-3, and LM-MEL-41 cell lines. The IC50 of the vanadium nanoparticles were237, 259, 226, 409, 335, and 192 µg/mL against C-33 A [c-33a], SiHa, Ca Ski, DoTc2 4510, HT-3, and LM-MEL-41 cell lines, respectively. To survey the antioxidant properties of Calendula officinalis aqueous extract and vanadium nanoparticles, the DPPH test was used. The vanadium nanoparticles inhibited half of the DPPH molecules in a concentration of 125 µg/mL. As mentioned, the vanadium nanoparticles had significant antioxidant and anti-human cervical cancer effects.     

Nephroprotective properties of chitosan/sodium lignosulfonate/Au nanoparticles in streptozotocin-induced nephropathy in mice: Introducing a novel therapeutic drug for the treatment of nephropathy

In this study, we report the green synthesis of nontoxic, stable, and small size gold nanoparticle by using chitosan/sodium lignosulfonate hydrogel with capping/reducing ability for the synthesis of CS/NaLS/Au NPs. The prepared bio-nanocomposite were characterized by advanced physicochemical techniques like Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Energy Dispersive X-ray spectroscopy (EDX) and X-ray Diffraction (XRD) study. It has been established that CS/NaLS/Au NPs have a spherical shape with a mean diameter from 20 to 30 nm. Diabetes was induced by administration of 60 mg/kg of streptozotocin (STZ) intraperitoneally in 100 mature male mice and they were randomly divided into 5 groups. The negative control group received normal saline and treatment groups received glibenclamide with dose 0.5 mg/kg and 10 and 40 μg/kg of CS/NaLS/Au NPs through gavage for 50 days. In addition, one group considered as positive control (in treated-diabetic). On the last day, serum levels of samples blood glucose, urea and creatinine were measured. After tissue processing, 5 μm sections of the kidneys were prepared and they were stained by periodic acid Schiff (PAS) and used for stereological analysis. In the antioxidant test, the IC50 of CS/NaLS/Au NPs and BHT against DPPH free radicals were 117 and 86 µg/mL, respectively. In the cellular and molecular part of the recent study, the treated cells with CS/NaLS/Au NPs were assessed by MTT assay for 48 h about the cytotoxicity properties on normal (HUVEC) cell line. The increased levels of blood glucose and urea were decreased (p < 0.05) significantly in CS/NaLS/Au NPs-treated groups as compared to the untreated diabetic. The kidney weight, kidney volume (Volume of cortex, medulla, glomerulus, proximal and distal tubules, collecting ducts, loop of Henle, interstitial tissues, and vessels) and kidney structures length (length of proximal and distal tubules, collecting ducts, loop of Henle, and vessels) decreased significantly (p < 0.05) after treatment with high dose of CS/NaLS/Au NPs (p < 0.05). According to the obtained results, CS/NaLS/Au NPs can regulates the levels of blood glucose and urea and inhibits from kidney damages in STZ-induced diabetic mice. This study suggested CS/NaLS/Au NPs as an antidiabetic and nephroprotective drug in the developing countries.     

Green synthesis of Ag/Fe3O4 nanoparticles using Mentha extract: Preparation,characterization and investigation of its anti-human lung cancer application

In this study, silver nanoparticles (Ag NPs) were decorated on the surface of magnetic nanoparticles in an eco-friendly pathway applying Mentha extract as reducing/stabilizing agent. The morphological and physicochemical features of the prepared Ag/Fe₃O₄nanocomposite were determined using several advanced techniques. Hence, our protocol is green and advantageous in terms of- i) biochemical modified biocompatible nanocomposite; ii) nanomaterial providing high surface area and larger number reactive sites; iii) very simplistic synthetic procedure; vi) very low load of metal in the composite and v) high yield in short time. In the medicinal part, the anticancer properties of Ag/Fe₃O₄ nanocomposite against lung cancer cell lines were determined. The free radical for the antioxidant effects was DPPH. The IC₅₀ of Ag/Fe₃O₄ nanocomposite was 200 µg/ml in the antioxidant test. The IC₅₀ of the Ag/Fe₃O₄ nanocomposite were 183, 176, 169, and 125 µg/mL against lung cancer (NCI-H661, NCI-H1975, NCI-H1573, and NCI-H1563) cell lines, respectively. In addition, the current study offer that Ag/Fe₃O₄ nanocomposite could be a new potential adjuvant chemopreventive and chemotherapeutic agent against cytotoxic cells.     

Green fluorescent protein for in situ synthesis of highly uniform Au nanoparticles and monitoring protein denaturation

Purified recombinant green fluorescent protein (GFP) expressed in E. coli was used for single-step synthesis of gold nanoparticles (Au NPs) with extraordinary size specificity in aqueous medium. The fluorescence of GFP offered a probe for concomitant changes in the protein during the course of synthesis, in addition to the monitoring of the time-dependent formation of Au NPs by the surface plasmon resonance. Reaction of AuCl⁻₄ with the protein produced spherical Au NPs having diameters ranging from 5–70 nm. Remarkably, addition of 1.0×10⁻⁵ M AgNO₃ in the medium produced uniform spherical Au NPs with particle diameter of 2.2±0.5 nm. Fluorescence spectroscopic measurements suggest that during synthesis of Au NPs in absence of AgNO₃, partial denaturation of the protein occurred resulting in the lowering of fluorescence intensity. On the other hand, when the NPs were synthesized in the presence of AgNO₃ complete denaturation of the protein with complete loss of fluorescence could be observed, which was further confirmed by native and sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis (PAGE). However, use of AgNO₃ only resulted neither in the formation of NPs nor had any significant effect on the fluorescence of GFP.     

Bionanocomposite of Au decorated MnO2 via in situ green synthesis route and antimicrobial activity evaluation

Green synthesis gaining a significant importance for the preparation of nanoparticles (NPs) and NPs-based biocomposites gained much attention in biological applications. In the current study, gold (Au) nanoparticles were prepared via green approach using cinnamon extract. The Au nanocomposite (NC) was prepared with MnO₂ nanofiber mesh structure. The NC was characterized by XRD, SEM, FT-IR, EDX, UV–visible and DLS techniques. The MnO₂ nanofibers diameter was in 10–25 nm range, which was arranged in a mesh form and Au NPs was combined with nanofibers randomly. The MnO₂-Au NC antimicrobial activity was measured against Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus strains. The antimicrobial activity of MnO₂-Au NC was highly promising against tested microorganisms in comparison to control (ciprofloxacin, a standard drug). The antimicrobial activity of MnO₂-Au NC was found in following order; > S. aureus > E. coli > P. aeruginosa with the zones inhibition of 22, 18 and 15 (mn), respectively. The MIC (minimum inhibitory concentration) values were 316, 342 and 231 (µg/mL) for E. coli, P. aeruginosa and S. aureus, respectively. In view of promising antimicrobial activity, the MnO₂-Au NC prepared via green approach could have potential applications in medical field and future study can be engrossed on the biocompatibility evaluation of MnO₂-Au NC using bioassays.     

CE‐MS analysis of heroin and its basic impurities using a charged polymer‐protected gold nanoparticle‐coated capillary

The first application of charged polymer‐protected gold nanoparticles (Au NPs) as semi‐permanent capillary coating in CE‐MS was presented. Poly(diallyldimethylammonium chloride) (PDDA) was the only reducing and stabilizing agent for Au NPs preparation. Stable and repeatable coating with good tolerance to 0.1 M HCl, methanol, and ACN was obtained via a simple rinsing procedure. Au NPs enhanced the coating stability toward flushing by methanol, improved the run‐to‐run and capillary‐to‐capillary repeatabilities, and improved the separation efficiency of heroin and its basic impurities for tracing geographical origins of illicit samples. Baseline resolution of eight heroin‐related alkaloids was achieved on the PDDA‐protected Au NPs‐coated capillary under the optimum conditions: 120 mM ammonium acetate (pH 5.2) with addition of 13% methanol, separation temperature 20°C, applied voltage ?20 kV, and capillary effective length 60.0 cm. CE‐MS analysis with run‐to‐run RSDs (n=5) of migration time in the range of 0.43–0.62% and RSDs (n=5) of peak area in the range of 1.49–4.68% was obtained. The established CE‐MS method would offer sensitive detection and confident identification of heroin and related compounds and provide an alternative to LC‐MS and GC‐MS for illicit drug control.     

A novel validated LC method for quantitation of lopinavir in bulk drug and pharmaceutical formulation in the presence of its potential impurities and degradation products

A simple isocratic liquid chromatographic method was developed for determination of lopinavir from its related impurities and assay for the first time. This method involves the use of a C(8) (Symmetry Shield RP8, 150 x 4.6 mm, 5 microm) column. The method was validated over the range of limit of quantitation (LOQ) to 120% of impurity specification limit and LOQ to 150% of working concentration for assay. The mobile phase consisted of a mixture of 50 mM of potassium phosphate buffer, acetonitrile and methanol in the ratio of 40:50:10. The flow rate was set at 1.0 mL/min with UV detection monitored at 210 nm. The drug was subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. The developed method was validated for linearity, range, precision, accuracy and specificity. This method was successfully applied for content determination of lopinavir in pharmaceutical formulations. The method can be conveniently used in a quality control laboratory for routine analysis for assay and related substances as well for the evaluation of stability samples of bulk drugs and pharmaceutical formulations.     

Formulation design, preparation and physicochemical characterizations of solid lipid nanoparticles containing a hydrophobic drug: effects of process variables

This study aimed to prepare solid lipid nanoparticles (SLNs) of a hydrophobic drug, tretinoin, by emulsification-ultrasonication method. Solubility of tretinoin in the solid lipids was examined. Effects of process variables were investigated on particle size, polydispersity index (PI), zeta potential (ZP), drug encapsulation efficiency (EE), and drug loading (L) of the SLNs. Shape and surface morphology of the SLNs were investigated by cryogenic field emission scanning electron microscopy (cryo-FESEM). Complete encapsulation of drug in the nanoparticles was checked by cross-polarized light microscopy and differential scanning calorimetry (DSC). Crystallinity of the formulation was analyzed by DSC and powder X-ray diffraction (PXRD). In addition, drug release and stability studies were also performed. The results indicated that 10mg tretinoin was soluble in 0.45±0.07 g Precirol? ATO5 and 0.36±0.06 g Compritol? 888ATO, respectively. Process variables exhibited significant influence in producing SLNs. SLNs with <120 nm size, <0.2 PI, >I30I mV ZP, >75% EE, and ～0.8% L can be produced following the appropriate formulation conditions. Cryo-FESEM study showed spherical particles with smooth surface. Cross-polarized light microscopy study revealed that drug crystals in the external aqueous phase were absent when the SLNs were prepared at ≤0.05% drug concentration. DSC and PXRD studies indicated complete drug encapsulation within the nanoparticle matrix as amorphous form. The drug release study demonstrated sustained/prolonged drug release from the SLNs. Furthermore, tretinoin-loaded SLNs were stable for 3 months at 4°C. Hence, the developed SLNs can be used as drug carrier for sustained/prolonged drug release and/or to improve oral absorption/bioavailability.     

芦丁在纳米金修饰玻碳电极上的电化学行为及其测定

采用循环伏安法将纳米金电沉积于玻碳电极表面,制备了纳米金修饰玻碳电极(NG/GCE).在pH3.29的Britton-Robinson(B-R)缓冲溶液中,用循环伏安法研究了芦丁在NG/GCE上的电化学行为.结果表明,NG/GCE对芦丁的氧化还原反应有良好的电催化作用.用方波伏安法测得芦丁的还原峰电流与其浓度在2.0×10-8～2.0×10-6mol/L范围内呈线性关系,检出限为1.0×10-8mol/L(S/N=3).     

A novel immunoassay strategy based on combination of chitosan and a gold nanoparticle label

A novel immunoassay strategy based on combination of chitosan (CHIT) and a gold nanoparticle (GNP) label has been developed. The susceptibility of CHIT to further chemical modifications due to the abundant amino groups is explored in order to covalently immobilize antibody (Ab) onto the (3-aminopropyl) triethoxysilane derivatized glass slide by cross-linking with glutaraldehyde (GA). After incubating in antigen (Ag) solution, the obtained substrate is immersed in GNP labeled antibody solution for signal generation. The two steps were repeated alternatively for three times, forming multilayer of gold nanoparticles via antigen-antibody specific reaction. Ultraviolet-visible (UV-vis) absorption spectrum is recorded to obtain quantitative information about the specific antigen. The presented immunoassay strategy is applied for determination of human serum albumin (HSA) as a model analyte. The immunoassay of HSA is specific. Compared to previous correlative work, the proposed immunosensing strategy shows some advantages, such as improved sensitivity as much more gold nanoparticles can be coupled to the functionalized surface making use of the abundant amino groups of CHIT. Moreover, a significantly extended linear detection range of 8.0-512.0 μg/mL is gained under the optimized experimental conditions. In particular, the presented biosensing method shows low cost and simplicity, and only a conventional UV-vis detector is involved.     

Encapsulation and controlled release of a hydrophobic drug using a novel nanoparticle-forming hyperbranched polyester

An amphiphilic, hyperbranched polymer suitable for use in controlled drug delivery is reported. This polymer was obtained by modification of the hyperbranched aliphatic polyester Boltorn H20 (H20) with succinic anhydride and then glycidyl methacrylate, and formed nanoparticles in aqueous solution. The critical association concentration was 7.4 x 10(-3) g . L(-1), as determined by fluorescence spectroscopy using pyrene as a molecular probe. A static/dynamic laser light scattering (LLS) study revealed that the average particle size was 39.4 nm with a low particle size distribution (PDI=0.04), and that each particle was composed of about 350 amphiphilic molecules. Daidzein, a hydrophobic traditional Chinese medicine, was encapsulated during particle formation and the release properties were determined. The optimal feeding concentration of daidzein to hyperbranched polyester was 4.9 x 10(-5) g . mL(-1) to 5.0 x 10(-3) g . mL(-1) with a loading efficiency of 76.1%. In the presence of the enzyme Lipase PS, the drug loaded nanoparticles degraded in a random one-by-one manner and released the drug over a few days. This system is therefore a novel controlled drug release system based on nanoparticles formed of hyperbranched polyester. Encapsulation of daidzein by hyperbranched polyester particles.     

Formulation characterization and in vitro evaluation of acacia gum–calcium alginate beads for oral drug delivery systems

In the present work, new matrix bead formulations based on linear and branched polysaccharides have been developed using an ionic gelation technique, and their potential use as oral drug carriers has been evaluated. Using calcium chloride as a cross‐linking agent and sodium diclofenac (SD), as a model drug, acacia gum–calcium alginate matrix beads were formulated. The response surface methodology based on 3² factorial design was used as a statistical method to evaluate and optimize the effects of the biopolymers‐blend ratio and the concentration of calcium chloride on the particle size (mm), density (g/cm³), drug encapsulation efficiency (%), and the cumulative drug release after 8 hours (R_8h,%). The optimized beads with the highest drug encapsulation efficiency were examined for a drug‐excipients compatibility by powder X‐ray diffraction, differential scanning calorimetry, thermo‐gravimetric analysis, and Fourier transform‐infrared spectroscopy analyses. The swelling and degradation of the matrix beads were found to be influenced by the pH of medium. Higher degrees of swelling were observed in intestinal pH than in stomach pH. Accordingly, the drug release study showed that the amount of SD released from the acacia gum–calcium alginate beads was higher in intestinal pH than in stomach pH. Therefore, the in vitro drug release from the SD‐loaded beads appears to follow the controlled‐release (Hixson‐Crowell) pattern involving a case‐2 transport mechanism operated by swelling and relaxation of the polymeric blend matrix.     

A simple method to fabricate a chitosan-gold nanoparticles film and its application in glucose biosensor

A novel film of chitosan-gold nanoparticles is fabricated by a direct and facile electrochemical deposition method and its application in glucose biosensor is investigated. HAuCl(4) solution is mixed with chitosan and electrochemically reduced to gold nanoparticles, which can be stabilized by chitosan and electrodeposited onto glassy carbon electrode surfaces along with the electrodeposition of chitosan. Then a model enzyme, glucose oxidase (GOD) is immobilized onto the resulting film to construct a glucose biosensor through self-assembly. The resulting modified electrode surfaces are characterized with both AFM and cyclic voltammetry. Effects of chitosan and HAuCl(4) concentration in the mixture together with the deposition time and the applied voltage on the amperometric response of the biosensor are also investigated. The linear range of the glucose biosensor is from 5.0 x 10(-5) approximately 1.30 x 10(-3) M with a Michaelis-Menten constant of 3.5 mM and a detection limit of about 13 microM.     

Detection of antinuclear antibodies by a colloidal gold modified optical fiber: comparison with ELISA

A fiberoptic evanescent-wave sensor has been developed for the measurement of antinuclear antibodies in sera from patients and healthy individuals. The sensor was constructed on the basis of modification of the unclad portion of an optical fiber with self-assembled gold colloids, where the colloidal gold surface was further functionalized with extractable nuclear antigens. Results show that detection of antinuclear antibodies by this sensor agrees quantitatively with the clinically accepted enzyme-linked immunosorbent assay (ELISA) method. This sensing platform has the following advantages: label-free and real-time detection capability, simple to construct and use, highly sensitive, and does not require a secondary antibody. The sensitivity of this platform is at least an order of magnitude higher than that of the ELISA method and thus may lead to a new direction in recognition of immune response. Biomolecular binding of antinuclear antibodies (ANA) with extractable nuclear antigens (ENA)-functionalized gold nanoparticles results in a change of surface plasmon absorption. When light propagates in an optical fiber by multiple total internal reflection, such a change in signal can be significantly enhanced.     

多贝斯在纳米金修饰玻碳电极上的电化学行为与测定

采用循环伏安法将纳米金电沉积于玻碳电极表面,制备了纳米金修饰玻碳电极(NG/GCE).在0.05 mol/L H2SO4溶液中,用循环伏安法研究了多贝斯在NG/GCE上的电化学行为.结果表明,NG/GCE对多贝斯的氧化还原反应有明显的电催化作用.建立了测定多贝斯的新方法,用方波伏安法测得多贝斯的氧化峰电流与其浓度在4....     

The surface modification of spherical ZnO with Ag nanoparticles: A novel agent,biogenic synthesis,catalytic and antibacterial activities

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.