Gold-silver Bimetallic Nanoparticles Research Articles

Chitosan film of thiolated TPGS-modified Au-Ag nanoparticles for combating multidrug-resistant bacteria

The widely used vitamin-E based amphiphilic material, tocopheryl polyethylene glycol succinate (TPGS) was further improvised to redox-sensitive thiolated TPGS (TPGS-SH), which has been achieved by attaching 4-aminothiophenol. Further, TPGS and TPGS-SH-coated bimetallic gold-silver nanoparticles (TPGS-Au-Ag-NP and TPGS-SH-Au-Ag-NP) were formulated to explore their antibacterial and wound healing abilities. The prepared NP were monodisperse with a mean hydrodynamic diameter of 69.5±3.23 nm, 59.65±3.23 nm, PDI of 0.3±0.05, 0.2±0.03 and a zeta potential of +29.2±2.71 mV and +35.28±1.53 mV, respectively. The TPGS and TPGS-SH modified Au-Ag-NP were tested for their antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA) and E. coli; minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) results showed that TPGS Au-Ag-NP, TPGS-SH-Au-Ag-NP displayed significantly stronger antibacterial activity than their coating material alone. The anti-efflux pump activity of the most potent antibacterial agent TPGS-SH-Au-Ag-NP was evaluated against MRSA. Toxicity assessment of TPGS-SH-Au-Ag-NP in human dermal fibroblasts showed 88% viability up to 125 µg/mL. The TPGS-SH-Au-Ag-NP, after incorporation in chitosan film (TPGS-SH-Au-Ag-NP-CS), exhibited sustained release and prolonged in vivo residence characteristics, which were evaluated by IVIS. Results also revealed that treatment with TPGS-SH-Au-Ag-NP showed a significant 87% wound healing rate after 12 days of application in the rat model. Hence, we concluded that TPGS-SH-Au-Ag-NP was safe and effective against test bacteria MRSA and capable of efficient wound healing when incorporated in chitosan film.

Synergistic mesoporous bimetallic gold-silver nanoparticles: Synthesis, structure, and superior electrocatalytic activity

Mesoporous bimetallic nanoparticles have gained immense interest due to their unique properties and applications in various fields. In this study, we report a novel and straightforward one-pot chemical reduction method for the synthesis of mesoporous AuAg nanoparticles, featuring a substantial mesopore size (>10 nm) and a well-defined structure. The synthetic route involves employing L-cysteine as a ligand to form thiolate-metal(I) complexes and co-reduction of metal precursors around sacrificial templates of polymeric micelles. The resulting nanoparticles exhibit remarkable uniformity in size and possess a well-ordered mesoporous structure. Structural analyses confirm the formation of an alloy system containing Au and Ag without any distinct phases. By adjusting the initial precursor composition, precise control over the Au:Ag ratios in the final products is achievable. The electrocatalytic activity of mesoporous AuAg nanoparticles in the electrooxidation of small molecules surpasses that of mesoporous Au nanoparticles, owing to the synergistic effect arising from both the alterations in the electronic structure and the benefits offered by the porous architecture. This synthetic approach provides a promising avenue for developing efficient and cost-effective mesoporous Au-based nanoparticles for a diverse range of applications.

Sericin mediated gold/silver bimetallic nanoparticles and exploration of its multi-therapeutic efficiency and photocatalytic degradation potential

The current investigation aimed at bimetallic gold-silver nanoparticles (Au/Ag NPs), here called BM-GS NPs, synthesis using sericin protein as the reducing agent in an easy, cost-effective, and sustainable way. The obtained BM-GS NPs were characterized by UV–Visible spectroscopy, Transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDS), atomic force microscopy (AFM), Dynamic light scattering (DLS) and Zeta potential, X-ray Powder Diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and Thermogravimetric analysis followed by evaluation of its multitherapeutic and photocatalytic degradation potentials. The TEM analysis revealed its spherical nature and the EDS result displayed the presence of both Ag and Au elements, confirming the synthesis of BM-GS NPs. The XRD pattern verified the crystalline nature of the nanoparticles (NPs). The DLS analysis showed an average size of 86.08 d nm and the zeta potential showed a highly negative value (−26.3 mV) which specifies that the generated bimetallic NPs are stable. The BM-GS NPs exhibited positive wound healing potential (with 63.38% of wound closure rate at 25 μg/ml, as compared to 54.42% by the untreated control) with very negligible toxicity effect on the cell viability of the normal keratinocyte cells. It also demonstrated promising antioxidant properties with 65.00%, 69.23%, and 63.03% activity at 100 μg/ml concentration for ABTS (2, 2-azinobis) (3-ethylbenzothiazoline-6-sulfonic acid)), DPPH (1, 1 diphenyl-2-picrylhydrazyl) and SOD (superoxide dismutase enzyme) assays respectively, antidiabetic potential (with a significantly high α-glucosidase inhibition potential of 99.69% at 10μg/ml concentration and 62.11% of α-amylase enzyme inhibition at 100 μg/ml concentration) and moderate tyrosinase inhibitory potential (with 17.09% at 100 μg/ml concentration). Besides, it displayed reasonable antibacterial potential with the diameter of zone of inhibition ranging between 10.89 and 12.39 mm. Further, its antibacterial mode of action reveals that its effects could be due to being very smaller, the NPs could have penetrated inside the cellular membrane thereby causing rupture and damage to the interior materials leading to cellular lysis. The photocatalytic evaluation showed that synthesized BM-GS NPs have the efficiency of degrading methylene blue dye by 34.70% within 3 h of treatment. The above findings revealed the multi-therapeutic efficacy of the sericin globular protein-mediated BM-GS NPs and its potential future applications in the cosmetics and food sector and environmental contamination management industries.

Design of novel bioadhesive chitosan film loaded with bimetallic gold-silver nanoparticles for antibiofilm and wound healing activity

Microbial infections and antibiotic resistance are among the leading causes of morbidity and mortality worldwide. The bimetallic chitosan (CS)-capped gold-silver nanoparticles (CS-AuAg-NPs) were prepared by the seeded growth synthesis technique. The nanoparticles were optimized for particle size (PS), zeta potential (ZP) and antibacterial activity by Box–Behnken design at three levels and three factors. The developed CS-AuAg-NPs were polydispersed with mean hydrodynamic PS in the range of 55 – 289 nm and ZP ranges from +8.53 mV to +38.6 mV. The optimized CS-AuAg-NPs found to have a minimum inhibitory concentration and minimal bactericidal concentration of 1.625 ± 0.68 and 3.25 ± 0.74 µg ml−1 towards multidrug resistant (MDR) Staphylococcus aureus ATCC 25923 (MDR AT) and 3.25 ± 0.93 and 3.25 ± 0.86 µg ml−1 towards MDR S. aureus clinical isolate MDR1695 (MDR CI) strain, respectively. The CS-AuAg-NPs were much more effective against MDR AT and MDR CI compared to clindamycin standard. The live/dead assay of clinical isolates strain demonstrated significant reduction of bacterial cells ∼67.52 folds compared to control group in 12 h. The hemolysis study suggested that CS-AuAg-NPs were non-hemolytic and safer for application in the wound. Furthermore, CS-AuAg-NPs were distributed in the CS film, which showed 87% wound recovery after 7 d in mice model. Hence, we concluded that CS-AuAg-NPs was safer and more effective against MDR bacteria and capable of skin regeneration in the infected wound.

Influence of swift heavy ion irradiation on bimetallic gold-silver nanoparticles in dielectric matrices and their optical properties

Nanosized gold-silver (AuAg) alloy nanoparticles (NPs) of sizes, 2 nm -25 nm embedded in fused quartz are synthesized using sequential implantation and post annealing at 900℃ for 1 h in Argon environment. The post annealed film is irradiated using swift heavy ions (SHI), 120 MeV Ag ions to investigate the effect of electronic energy deposition, (Se×ϕ), on size, shape and composition of the alloy NPs. Transmission electron microscopy (TEM) analysis of the as- implanted AuAg film reveals the formation of small sized, 1.8 nm-3.5 nm, bimetallic AuAg NPs. Rutherford backscattering spectroscopy (RBS) spectra along with its fitted graph convey the annealing induced out diffusion, mixing and formation of larger sized, 2 nm -25 nm, alloy NPs through Ostwald ripening. SHI irradiation results in deformation in shape from spherical to ellipsoidal alloy NPs with major axis align along the beam direction and the average aspect ratio is about 1.20. RBS analysis results convey the formation of Ag enriched alloy NPs after irradiation. The smaller nanoparticles are found dissolved while larger ones grow and elongate along the ion beam direction. SPR properties are modified by SHI induced processes of melting, sputtering and re-precipitation in the ion tracks.The un-irradiated film exhibits a single intense SPR peak at 536 nm, while the irradiated film gives rise two SPR peaks: Ist, a blue shifted SPR peak from 536 nm to 515 nm with significantly reduced intensity and much wider FWHM; and, IInd, a small SPR peak around 460 nm. SHI induced modifications on the NPs are understood in terms of thermal spike model. The detailed analysis shows that SHI can be used as a tool to tailor size, shape and composition of the bimetallic AuAg alloy NPs and their SPR properties.

Rapid Biotransformation of Luminescent Bimetallic Nanoparticles in Hepatic Sinusoids.

Liver sequestration, mainly resulting from the phagocytosis of mononuclear phagocyte system (MPS) cells, is a long-standing barrier in nanoparticle delivery, which severely decreases the disease-targeting ability, leads to nanotoxicity, and inhibits clinical translation. To avoid long-term liver sequestration, we elaborately designed luminescent gold-silver bimetallic nanoparticles that could be rapidly transformed by the hepatic sinusoidal microenvironment rich in glutathione and oxygen, significantly different from monometallic gold nanoparticles that were rapidly sequestrated by Kupffer cells due to the much slower biotransformation. We found that the rapid sinusoidal biotransformation induced by the synergistic reactions of glutathione and oxygen with the reactive silver atoms could help bimetallic nanoparticles to avoid MPS phagocytosis, promote fast release from the liver, prolong blood circulation, enhance renal clearance, and increase disease targeting. With the fast biotransformation in sinusoids, liver sequestration could be turned into a beneficial storage mechanism for nanomedicines to maximize targeting.

Single gold nanowire-based nanosensor for adenosine triphosphate sensing by using in-situ surface-enhanced Raman scattering technique

Development of new hot spots for surface enhanced Raman scattering (SERS) technique is of great significance recently. Herein, we developed a single Au nanowire (NW)-based nanosensor for adenosine triphosphate (ATP) sensing by using in-situ SERS technique. Single Au NWs, fabricated by laser-assisted pulling method and hydrofluoric acid (HF) etching process, were linked with single-stranded HS-terminated DNA. After that, gold-silver bimetallic nanoparticles (Au/Ag NPs), attached with thiol-containing Raman dyes and ATP aptamer, were immobilized on DNA-modified single AuNW due to the designed affinity between ATP aptamer and single-stranded DNA. This single AuNW-based device exhibited strong SERS signals. In the presence of adenosine triphosphate (ATP), due to the strong specific affinity between the aptamer and the target, the Au/Ag NPs will be separated from the AuNW, resulting in the obvious decrease of the Raman signals, which can be used for ATP sensing with high sensitivity, selectivity and stability. This nanosensor can be used as an ideal platform for real applications, especially at some confined-space samples, such as trace detection, single cell and in vivo analysis.

Phytofabrication of gold and bimetallic gold-silver nanoparticles using water extract of wheatgrass (Triticum aestivum), their characterization and comparative assessment of antibacterial potential

In the present study, gold (AuNPs) and gold-silver bimetallic nanoparticles (Au-Ag BMNPs) were fabricated by using water extract of leaves of Triticum aestivum - a crop plant, and their bactericidal potency was checked against selected pathogenic bacterial strains. The phytofabricated AuNPs and BMNPs were analyzed for their physical attributes using UV–Visible and Fourier transformed infrared spectroscopy, Dynamic light scattering, High-resolution transmission electron microscopy, Energy-dispersive X-ray spectroscopy. HRTEM analysis revealed that both kinds of NPs were highly crystalline in nature and of spherical and oval-shaped. AuNPs size was found in the range of 5-40 nm, whereas BMNPs showed their size in the range of 5-30 nm. HRTEM results were corroborated by DLS results which revealed the average hydrodynamic diameter of AuNPs and BMNPs in the range of 29.08 and 26.56 nm, respectively. UV-visible spectroscopy showed high-intensity single spectral peaks at 540 and 480 nm for AuNPs and BMNPs, respectively. FTIR analysis demonstrated that protein, flavanones, hydroxyl, carboxylate groups, and reducing sugars were responsible for reducing and capping of both NPs. Bactericidal efficiency of synthesized NPs was evaluated using agar-well diffusion and XTT-colorimetric assays against K. pneumoniae, S. typhimurium, E. aerogenes, E. coli, M. luteus, S. aureus, S. mutans and S. epidermidis. K. pneumonia and S. typhimurium were found to be the most sensitive bacteria towards BMNPs-mediated (MIC: 400 µg/ml) and AuNPs-mediated toxicity (MIC: 800 µg/ml). It was observed that BMNPs generally possessed more powerful bactericidal effect against all bacterial strains in comparison to AuNPs. MIC and MBC values were observed in the concentration range of 400 µg/ml-1.5 mg /ml for different bacterial strains. Furthermore, it was demonstrated that phytosynthesized AuNPs have their own bactericidal effect, but at higher concentrations (>100 µg/ml), and bactericidal effect of BMNPs was due to the synergistic effect of both Ag and Au ions, which was also observed to be concentration-dependent.

Influence of elemental composition on structural, thermal and hydration behavior of gold-silver bimetallic nanoparticles.

In this study, molecular dynamics simulations (MDs) have been employed to explore the influence of elemental composition on the structural, thermal, and hydration behavior of the core-shell gold-silver bimetallic nanoparticles with three different concentrations Au135Ag114, Au87Ag162, and Au55Ag194. The pure gold and silver metal nanoparticles have also been studied for the sake of comparison. The calculated cohesive and formation energy values reveal the enhancement in the stability of gold-silver bimetallic nanoparticles with the increase in the concentration of gold. The specific heat capacity value of the bimetallic gold-silver nanoparticles has been found to increase linearly with the concentration of silver. This suggests that the specific heat capacity value of the gold-silver bimetallic nanoparticles may be improved by raising their silver concentration. The enhancement of specific heat capacity value with respect to the concentration of silver may be attributed to the enhanced phonon density. There is no significant difference in the computed hydration shell and water residence time of the gold-silver bimetallic nanoparticles with respect to their mixing ratio. The obtained stable structure, tunable specific heat capacity values, and the predicted hydration properties of the gold-silver bimetallic nanoparticles may be harnessed for their technological and biological applications.

One Pot Synthesis of PEGylated Bimetallic Gold-Silver Nanoparticles for Imaging and Radiosensitization of Oral Cancers.

BackgroundRadiotherapy is an important treatment modality for many types of head and neck squamous cell carcinomas. Nanomaterials comprised of high atomic number (Z) elements are novel radiosensitizers enhance radiation injury by production of free radicals and subsequent DNA damage. Gold nanoparticles are upcoming as promising radiosensitizers due to their high (Z) biocompatibility, and ease for surface engineering. Bimetallic nanoparticles have shown enhanced anticancer activity compared to monometallic nanoparticles.Materials and MethodsPEG-coated Au–Ag alloy nanoparticles (BNPs) were synthesized using facile one pot synthesis techniques. Size of ~50±5nm measured by dynamic light scattering. Morphology, structural composition and elemental mapping were analyzed by electron microscopy and SAXS (small-angle X-ray scattering). The radiosensitization effects on KB oral cancer cells were evaluated by irradiation with 6MV X-rays on linear accelerator. Nuclear damage was imaged using confocal microscopy staining cells with Hoechst stain. Computed tomography (CT) contrast enhancement of BNPs was compared to that of the clinically used agent, Omnipaque.ResultsBNPs were synthesized using PEG 600 as reducing and stabilizing agent. The surface charge of well dispersed colloidal BNPs solution was −5mV. Electron microscopy reveals spherical morphology. HAADF-STEM and elemental mapping studies showed that the constituent metals were Au and Ag intermixed nanoalloy. Hydrodynamic diameter was ~50±5nm due to PEG layer and water molecules absorption. SAXS measurement confirmed BNPs size around 35nm. Raman shift of around 20 cm−1 was observed when BNPs were coated with PEG. 1H NMR showed extended involvement of −OH in synthesis. BNPs efficiently enter cytoplasm of KB cells and demonstrated potent in vitro radiosensitization with enhancement ratio ~1.5–1.7. Imaging Hoechst-stained nuclei demonstrated apoptosis in a dose-dependent manner. BNPs exhibit better CT contrast enhancement ability compared to Omnipaque.ConclusionThis bimetallic intermix nanoparticles could serve a dual function as radiosensitizer and CT contrast agent against oral cancers, and by extension possibly other cancers as well.

One-pot green synthesis of Au-Ag bimetallic nanoparticles from Lawsonia inermis seed extract and its catalytic reduction of environmental polluted methyl orange and 4-nitrophenol

BackgroundBimetallic nanoparticles (BNPs) are used in attractive applications in the medicinal, green catalyst, optics, electrochemical and so on. Apart from the catalytic activity, the chemical synthesized BNPs is less energy and environmentally highly toxic. Hence, Au-Ag BNPs prepared by the green synthesis method is suggested to be eco-friendly and have a potential catalytic reduction/degradation activity against environmentally polluted organic dyes. Materials and methodIn this present work, Ultrasound-Assisted green synthesis of Gold-Silver Bimetallic Nanoparticles (Au-Ag BNPs) was synthesized from Lawsonia inermis seed extract aqueous fraction. The effects of the extract volume, metal ions concentration, pH, and temperature were investigated to determine the optimum conditions of the synthesis of Au-Ag BNPs. Results and discussionUV-vis absorbance of the surface Plasmon resonance centre at 537 nm was confirmed the product of Au-Ag BNPs. FT-IR spectroscopy to determine the phytochemicals groups of the plant extract and Au-Ag BNPs. High-resolution transmission electron microscopy image of Au-Ag BNPs shows polygonal, spherical and irregular shaped with particle sizes 15-35 nm. Under UV-vis the light source, the obtained BNPs had a strong photocatalytic reduction/degradation activity against 4-nitrophenol and methyl orange dye in the presence of NaBH4.

Single-Particle Hyperspectral Imaging Reveals Kinetics of Silver Ion Leaching from Alloy Nanoparticles

Gold-silver alloy nanoparticles are have attracted attention for multiple applications, including heterogeneous catalysis, optical sensing, and antimicrobial properties. The inert element gold can act as a stabilizer for silver to prevent particle corrosion to slow down silver ion leaching and increase the durability of plasmonic alloy nanoparticles in sensing or catalytic applications. On the other hand, intentional release of antimicrobial silver ions has been used to fight infections caused by bacteria. Understanding silver ion leaching from gold-silver alloy nanoparticles is a therefore prerequisite to designing alloy nanoparticles with either unintended or intended corrosion. However, little is known about the mechanism and kinetics of silver ion leaching from bimetallic gold-silver nanoparticles and how it is correlated with particle size and silver content, especially not on a single-particle level. To characterize the kinetics of silver ion release from gold-silver alloy nanoparticles, we employed a combination of electron microscopy and single-particle hyperspectral imaging with an acquisition speed fast enough to capture silver ion leaching for a statistically relevant number of individual nanoparticles. Our studies confirmed a reduction in corrosion rate due to the alloying with as little as 10-20 mole% gold. Single-particle leaching profiles revealed two leaching stages, with a large heterogeneity in rate constants. We modelled the initial leaching stage with a shrinking-particle model with a rate constant that exponentially depends on the silver mole fraction. The second, slower leaching stage is controlled by diffusion of silver atoms through a passivating gold rich lattice, and a change in electrochemical potential of the nanoparticle. Individual nanoparticles with similar sizes and compositions exhibited completely different dealloying yields. Most nanoparticles released silver completely, but 25% of them appeared to arrest corrosion. Calculations of average size together with SEM revealed that nanoparticles became slightly porous. Our findings suggest that alloy nanoparticles, produced by scalable laser ablation in liquid, together with kinetic studies of silver ion leaching, provide an approach to selectively design the durability or anti-microbial bioactivity of alloy nanoparticles. Figure 1

Gum Arabic polymer-stabilized and Gamma rays-assisted synthesis of bimetallic silver-gold nanoparticles: Powerful antimicrobial and antibiofilm activities against pathogenic microbes isolated from diabetic foot patients

In this research, irradiation by gamma rays was employed as an eco-friendly route for the construction of bimetallic silver-gold nanoparticles (Ag-Au NPs), while Gum Arabic polymer was used as a capping agent. Ag-Au NPs were characterized through UV–Vis., XRD, EDX, HR-TEM, FTIR, SEM/mapping and EDX analysis. Antibiofilm and antimicrobial activities were examined against some bacteria and Candida sp. isolates from diabetic foot patients. Our results revealed that the synthesis of Ag-Au NPs depended on the concentrations of tetra-chloroauric acid and silver nitrate. HR-TEM analysis confirmed the spherical nature and an average diameter of 18.58 nm. FTIR results assured many functional groups in Gum Arabic which assisted in increasing the susceptibility of incorporation with Ag-Au NPs. Our results showed that, Ag-Au NPs exhibited the highest antimicrobial performance against B. subtilis (14.30 mm ZOI) followed by E. coli (12.50 mm ZOI) and C. tropicalis (11.90 mm ZOI). In addition, Ag-Au NPs were able to inhibit the biofilm formation by 99.64%, 94.15%, and 90.79% against B. subtilis, E. coli, and C. tropicalis, respectively. Consequently, based on the promising properties, they showed superior antimicrobial potential at low concentration and continued-phase durability, they can be extensively-used in many pharmaceutical and biomedical applications.

Gold-Silver Bimetallic Nanoparticles Reduced with Herbal Leaf Extracts Induce ROS-Mediated Death in Both Promastigote and Amastigote Stages of Leishmania donovani.

Resistance to antileishmanial drugs such as sodium stibogluconate (SSG), amphotericin B (Amp-B), and miltefosine is on the rise, and alternate strategies for effective treatment have gained importance in recent years. Although nanoparticle (NP)-based composite drugs that have emerged recently have been found to be effective, the associated toxicity limits their usage. Bimetallic NPs produced through reduction with medicinal plant extracts are proposed to overcome the toxicity of the NPs. In the present study, three types of gold–silver bimetallic nanoparticles (Au–Ag BNPs) were synthesized through a single-step reduction process using fenugreek, coriander, and soybean leaf extracts. All of the three types of BNPs exhibited high antileishmanial effects against promastigotes with half-inhibitory concentration (IC50) values in the range of 0.03–0.035 μg/mL. The IC50 values of the BNPs are much lower compared to those of miltefosine (IC50 = 10 μg/mL). The synthesized BNPs induced the reactive oxygen species (ROS)-mediated apoptosis-like death in the promastigotes and could potentiate the antileishmanial activity of macrophages. The intracellular amastigotes were reduced by 31–46% in macrophages. The biogenic BNPs synthesized in this study and their potent antileishmanial activity provide further impetus to the ongoing quest for novel drugs to effectively manage leishmaniasis.

On demand release of ionic silver from gold-silver alloy nanoparticles: fundamental antibacterial mechanisms study

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.

An in situ SAXS investigation of the formation of silver nanoparticles and bimetallic silver-gold nanoparticles in controlled wet-chemical reduction synthesis.

We present a study on the formation of silver (Ag) and bimetallic silver–gold (AgAu) nanoparticles monitored by in situ SAXS as well as by ex situ TEM, XRD and UV-vis analysis in a flow reactor at controlled reaction temperature. The formation mechanism of the nanoparticles is derived from the structural parameters obtained from the experimental data. The evolution of the average particle size of pure and alloyed nanoparticles shows that the particle growth occurs initially by a coalescence mechanism. The later growth of pure silver nanoparticles is well described by Ostwald ripening and for the alloyed nanoparticles by a process with a significantly slower growth rate. Additionally, the SAXS data of pure silver nanoparticles revealed two major populations of nanoparticles, the first one with a continuous crystal growth to a saturation plateau, and the second one probably with a continuous emergence of small new crystals. The particle sizes obtained by SAXS agree well with the results from transmission electron microscopy and X-ray diffraction. The present study demonstrates the capability of an in situ investigation of synthesis processes using a laboratory based SAXS instrument. Online monitoring of the synthesis permitted a detailed investigation of the structural evolution of the system.

Bimetallic gold-silver nanoparticles mediate bacterial killing by disrupting the actin cytoskeleton MreB.

The actin cytoskeleton is required for the maintenance of the cell shape and viability of bacteria. It remains unknown to which extent nanoparticles (NPs) can orchestrate the mechanical instability by disrupting the cytoskeletal network in bacterial cells. Our work demonstrates that Au-Ag NPs disrupt the bacterial actin cytoskeleton specifically, fluidize the inner membrane and lead to killing of bacterial cells. In this study, we have tried to emphasize on the key parameters important for NP-cell interactions and found that the shape, specific elemental surface localization and enhanced electrostatic interaction developed due to the acquired partial positive charge by silver atoms in the aggregated NPs are some of the major factors contributing towards better NP interactions and subsequent cell death. In vivo studies in bacterial cells showed that the NPs exerted a mild perturbation of the membrane potential. However, its most striking effect was on the actin cytoskeleton MreB resulting in morphological changes in the bacterial cell shape from rods to predominantly spheres. Exposure to NPs resulted in the delocalization of MreB patches from the membrane but not the tubulin homologue FtsZ. Concomitant with the redistribution of MreB localization, a dramatic increase of membrane fluid regions was observed. Our studies reveal for the first time that Au-Ag NPs can mediate bacterial killing and disrupt the actin cytoskeletal functions in bacteria.

Oligodynamic Boons of Daptomycin and Noble Metal Nanoparticles Packaged in an Anti-MRSA Topical Gel Formulation.

Daptomycin is a popular anti-MRSA antibiotic, especially for surgical wound infections. The side-effects of Daptomycin dosage through intravenous administration have prompted the experimental use of topical Daptomycin. Also, combinatorial drug therapy involving noble metal nanoparticles and conventional antibiotics have proved beneficial in the past. The synergistic oligodynamic effect of Daptomycin with nanoparticles for topical application was attempted for the first time in this work. The present study was focused on topical gel formulation containing Daptomycin combined with mycogenic gold, silver and bimetallic gold and silver nanoparticles and evaluation of their synergistic antibacterial effect against an MRSA strain. An efficient approach for fungal growth was discussed wherein the biomass was cultivated under non-limiting conditions, followed by the addition of gold salt, silver salt and bimetallic (Gold and silver) solution. The metal salt reduction efficacy was evaluated using Cyclic Voltammetry. Formation of nanoparticles was observed by visual color changes and confirmed by UV-visible characteristic peaks. The mycosynthesized metallic and bimetallic nanoparticles were characterized by various advanced analytical methods. Further, Daptomycin was combined with nanoparticles in a topical gel formulation. The properties of the topical gels were evaluated and their antimicrobial activity was investigated against an MRSA strain associated with burn infections though disc diffusion method. Formation of nanoparticles was observed by visual color changes and confirmed by UVvisible characteristic peaks. XRD spectra revealed the crystalline nature of nanoparticles whereas TEM confirmed the presence of spherical nanoparticles. The bio fabricated nanoparticles were characterized using ICP-MS, XRD and TEM. The UV-Visible spectrum of the gold, silver, bimetallic nanoparticles showed a characteristic peak at 550 nm, 450 nm, and 480 nm, respectively. ICP-MS of the residual salt concentration depicted more than 75% bioconversion of metal salt to metal nanoparticles. TEM showed the formation of uniform, spherical monometallic nanoparticles. XRD results were in sync with the dynamic light scattering experiments which determined that the gold, silver, bimetallic nanoparticles ranged between 10-20 nm, 5-30 nm, and 20-40 nm respectively and were crystalline in nature with the face centered cubic symmetry. Topical gels combining Daptomycin and nanoparticles were formulated and characterized. The in-vitro drug release studies indicated controlled release of antibiotic from bimetallic nanoparticles and Daptomycin combination in topical gel formulation. The MIC values reduced for the combinatorial drug and the average synergistic antimicrobial effect was 37% and the increase in efficacy of Daptomycin due to the synergistic effect with bimetallic nanoparticles was 43%. Topical gels were formulated using the biologically synthesized gold, silver and bimetallic gold-silver nanoparticles and modern-day antibiotic Daptomycin to combat burn infections. The topical gel formulations showed enhanced antimicrobial activity against methicillin-resistant Staphylococcus aureus at lower MIC values as compared to individual nanoparticle or antibiotic. The best results were obtained with bimetallic nanoparticles in topical gel formulation as it assisted in controlled drug release up to 94.6% and improved antimicrobial effect i.e. 43%.

Unraveling Structural Information of Turkevich Synthesized Plasmonic Gold-Silver Bimetallic Nanoparticles.

For the synthesis of gold-silver bimetallic nanoparticles, the Turkevich method has been the state-of-the-art method for several decades. It is presumed that this procedure results in a homogeneous alloy, although this has been debatable for many years. In this work, it is shown that neither a full alloy, nor a perfect core-shell particle is formed but rather a core-shell-like particle with altering metal composition along the radial direction. In-depth wet-chemical experiments are performed in combination with advanced transmission electron microscopy, including energy-dispersive X-ray tomography, and finite element method modeling to support the observations. From the electron tomography results, the core-shell structure can be clearly visualized and the spatial distribution of gold and silver atoms can be quantified. Theoretical simulations are performed to demonstrate that even though UV-vis spectra show only one plasmon band, this still originates from core-shell type structures. The simulations also indicate that the core-shell morphology does not so much affect the location of the plasmon band, but mainly results in significant band broadening. Wet-chemistry experiments provide the evidence that the synthesis pathway starts with gold enriched alloy cores, and later on in the synthesis mainly silver is incorporated to end up with a silver enriched alloy shell.

An Immunosensor Based on Au-Ag Bimetallic NPs Patterned on a Thermal Resistant Flexible Polymer Substrate for In-Vitro Protein Detection.

Nanosensors based on flexible polymers have emerged as powerful tools for next generation smart devices in the recent years. Here, we report a facile protocol to fabricate an immunosensor supported by a thermally resistant flexible polymer substrate (polyarylene ether nitrile, PEN). The immunosensor is a localized surface plasmon resonance (LSPR) optical sensor for in-vitro protein detection based on anti-body coated gold-silver bimetallic nanoparticles (Au-Ag NPs) immobilized on a PEN substrate. Plasmonic spectroscopy and morphological characterization show that the Au-Ag NPs essentially exhibit a more uniform size distribution and higher quality factors than those from single-component Au NPs. Furthermore, it should be noted that the robust PEN substrate in this nanosensor acts a flexible substrate to support Au-Ag NPs and immobilize the nanoparticles via quick thermal annealing at 290 °C. Thanks to these merits, a prostate-specific antigen (PSA) concentration as low as 1 ng/mL can be specifically discriminated via the prepared PEN/Au-Au NPs, which confirms that the protocol reported in this work can be readily adapted for the construction of various flexible immunosensors for different applications.