Synthesis Of Metal Nanoparticles Research Articles

Phytochemical fabrication of ZnO nanoparticles and their antibacterial and anti-biofilm activity

The synthesis of metal nanoparticles through bio-reduction is environmentally benign and devoid of impurities, which is very important for biological applications. This method aims to improve ZnO nanoparticle's antibacterial and anti-biofilm activity while reducing the amount of hazardous chemicals used in nanoparticle production. The assembly of zinc oxide nanoparticles (ZnO NPs) is presented via bio-reduction of an aqueous zinc nitrate solution using Echinochloacolona (E. colona) plant aqueous leaf extract comprising various phytochemical components such as phenols, flavonoids, proteins, and sugars. The synthesized nano ZnO NPs are characterized by UV–visible spectrophotometer (UV–vis), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (X-RD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and elemental composition by energy-dispersive x-ray spectroscopy (EDX). The formation of biosynthesized ZnO nanoparticles was confirmed by the absorbance at 360–370 nm in the UV–vis spectrum. The average crystal size of the particles was found to be 15.8 nm, as calculated from XRD. SEM and TEM analysis of prepared ZnO NPs confirmed the spherical and hexagonal shaped nanoparticles. ZnO NPs showed antibacterial activity against Escherichia coli and Klebsiella pneumoniae with the largest zone of inhibition (ZOI) of 17 and 18 mm, respectively, from the disc diffusion method. Furthermore, ZnO NPs exhibited significant anti-biofilm activity in a dose-dependent manner against selected bacterial strains, thus suggesting that ZnO NPs can be deployed in the prevention of infectious diseases and also used in food preservation.

Biologically Synthesized Gold Nanoparticles with Enhanced Antioxidant and Catalytic Properties.

Increasing levels of reactive oxygen species generate oxidative stress in the human body that can lead to various medical conditions. The use of nanomaterials exhibiting antioxidant properties may prevent these effects. The biological synthesis of metallic nanoparticles using plant extracts with antioxidant properties can offer benefits due to their active compounds. The used extracts contained reducing and stabilizing agents, which were shown to be transferred onto the gold nanoparticles, functionalizing them. Herin, we report a gold nanoparticle synthesis by eco-friendly biological methods (b-AuNPs) using extracts of sea buckthorn, lavender, walnuts, and grapes, obtained through ultrasound-assisted extraction and pressure-enhanced extraction. The obtained b-AuNPs were characterized by UV-Vis and FTIR spectroscopies and visualized using transmission electron microscopy. The catalytic and scavenging effect of the b-AuNPs towards H2O2 (as reactive oxygen species) was evaluated electrochemically, highlighting the protective behavior of b-AuNPs towards lipid peroxidation. All experiments demonstrated the stability and reproducibility of prepared b-AuNPs with enhanced antioxidant and catalytic properties, opening a new perspective for their use in biomedical applications.

Alocasia Indica Assisted Green Synthesis of Metallic Cu Nanoparticles for Enhanced Antimicrobial Activities

In the past several years, the widespread utility of copper nanoparticles (CuNPs) has spurred global interest in streamlining synthesis methodologies. Notably, this study introduces an environmentally conscious strategy for synthesizing CuNPs using the extract of Alocasia indica. Employing a chemical reduction process, A. indica, abundant in phenolics and flavonoids, acts as a potent reducing agent. The nanoparticles (NPs) synthesized by A. indica have been carefully characterized by Ultraviolet–Visible (UV–Viz) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDX), Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD) analysis and antimicrobial analysis. UV testing, spanning wave length, elucidates light absorption attributed to the newly formed CuNPs by showcasing a surface plasmonic resonance peak at 204 nm. The evolution of the FTIR spectrum of the produced CuNPs confirms the presence of diverse biomolecules. TEM delineates the synthesis of irregularly shaped particles. Elemental composition analysis via EDX identifies the presence of various elements, including C, O, Al, Cl, K and Cu, with detailed insights into their mass percentages, standard deviations, atom percentages and characteristic X-ray energy levels. The successful synthesis of CuNPs is validated by XRD, which reveals characteristic copper peaks at 2[Formula: see text] = [Formula: see text], [Formula: see text] and [Formula: see text]. The synthesized NP showed 98.99% inhibition against Staphylococcus aureus and 99.99% inhibition against Escherichia coli. This research presents an easy, economical and ecologically friendly process for producing CuNPs utilizing A. indica extracts.

Synthesis and electrochemical characteristics of metal nanoparticles decorated composite anode made of domestic alloy, used in lithium ion batteries

In this work, appropriate material selection and process design enable the succesful production of high energy density electrode active material in the form of XAZ (where X, A and Z stand for electrochemically active, electrochemically inactive and carbon materials, respectively). Herein, the precipitates rich in iron and chromium are extracted selectively from a local ferrochromium alloy utilizing hydrometallurgy procedures. The precipitates are then exposed to separate calcination to get iron-rich and chromium-rich oxides seperately. In the end, a composite (XAZ) is fabricated under the mild synthesis conditions by combining these oxides with activated carbon and aluminum powder in a planetary ball mill. The composite's morphological, structural, and chemical properties are all optimized. The galvanostatic test results clearly demonstrate that the powder made of XAZ composite with embedded metal nanoparticles delivers 798 mAh g-1 after 100th cycle under a current load of 50 mA g-1 and high capacity (600 mAh g−1) over 300 cycles with an exceptional rate performance. It is anticipated that this research will create novel opportunities for producing high-value electrode active materials from accessible, low-cost raw ingredients.

(Invited) Nanosecond Electrical Discharges in Liquids: Applications in the Synthesis of Nanoparticles, Including Nanoalloys

In recent decades, the field of nanotechnology has witnessed rapid growth, fueled by the exceptional physical, chemical, mechanical, and electrical properties of nanoscale materials. Nanomaterials have found applications across various domains, including catalysis, drug delivery, microelectronics, and more. Notably, plasma-based methods have emerged as promising avenues for nanomaterial synthesis, offering versatile approaches through both bottom-up and top-down techniques.One particularly innovative area of research is the plasma-liquid system, which has demonstrated remarkable efficiency in nanomaterial synthesis. This system involves the generation of plasma in a gas phase in contact with a liquid or directly within the liquid, sometimes aided by the introduction of bubbles. This communication has two goals: 1) present an overview of the physics of different discharge mechanisms, with a particular focus on the intriguing phenomena occurring at the interfaces, and 2) show different cases where nanomaterials of interest are produced. For instance, we will show that in-liquid spark discharges prouce nanoparticles through electrode erosion, and notably, the properties of these materials are highly sensitive to both the nature of the electrode and the composition of the liquid. In the second part, we introduce an innovative plasma-liquid system where a discharge can be produced at or close the interface of two immiscible liquids. In specific cases where the system is composed of a conductive solution (e.g. salty water) and a hydrocarbon liquid, spark discharges can be generated between a pin in liquid hydrocarbon and the surface of the conductive solution. This unique configuration facilitates therefore an interaction between a high-density plasma (generated in liquid) and a solution containing metal ions. At this stage, many reactions may occur and lead to the reduction of ions to produce nanomaterials. We found that the particles collected from hydrocarbon liquid are different from those collected from the solution, in terms of composition and size distribution. This finding suggests the triggering of different chemical reactions in each liquid, involving thus species with short- as well as long-lifetime species. Consequently, we adopted this approach to synthesize metal nanoparticles as well as binary and ternary nanoalloys, expanding the scope of possibilities in nanomaterial synthesis.

(Invited) Plasmonic and Electrochemical Approaches to the Synthesis of Tailored Catalyst Materials

The development of novel photo- and electrocatalytic processes requires the design of catalyst materials that are specifically optimized to take advantage of these driving forces. This talk will describe approaches developed in our lab for (1) using visible light stimulus to control the structure of plasmonically responsive and hybrid materials and (2) using electrodeposition to grow shape-controlled nanostructures on electrode surfaces. In the first case, the reduction of more catalytically active metals onto plasmonically active metals requires fine control over competing reductive and oxidative chemical processes. Differentially modulating the rates of these reactions using only chemical and thermal parameters can be prohibitively challenging. However, excitation of the plasmon resonance of the growing nanoparticles using visible light can yield hybrid structures that are not accessible via standard colloidal approaches. In the second case, while particles synthesized in colloidal solution can be processed and cast onto electrodes, this adds an additional fabrication step—increasing time and cost—and faces challenges in controlling particle dispersion on the surface. Meanwhile, direct chemical reduction-based synthesis of well-defined nanoparticles on electrodes has proven difficult. We have developed an integrated electrochemical approach that enables directed synthesis of shaped nanoparticles on electrode surfaces. Our approach links metal nanoparticle synthesis with real-time monitoring of chemical changes in the reaction solution using a combination of colloidal particle synthesis, electrochemical particle synthesis, and electrochemical measurements. This provides a pathway for the directed adaptation of the extensive library of existing shaped colloidal nanoparticle syntheses to growth on a surface—something that remains a non-trivial challenge.

Implications of White Light-Emitting Diode-Based Photoirradiation on Green Synthesis of Silver Nanoparticles by Methanol- and Aqueous-Based Extracts of Bergenia ciliata Leaves.

Bergenia ciliata (BC) is a perennial herb that is frequently used as a traditional medicine. Its leaves and rhizomes are reported to have significant antioxidant, metal-reducing, and chelating properties. Although the rhizomes have the potential to synthesize silver nanoparticles (AgNPs), the leaves are yet to be studied for the green synthesis of metal nanoparticles. Likewise, photoirradiation also plays a significant role in the green synthesis of metal nanoparticles. In the current study, we intended to demonstrate the implications of photoirradiation by white light-emitting diode (LED) on the aqueous and methanol extracts (AE and ME, respectively) of BC leaf-mediated green synthesis of AgNPs. In this regard, the AgNP synthesis of the two extracts was performed in the dark and under 250-lumen (lm) and 825 lm LED bulbs. The physicochemical characterization of the synthesized nanoparticles was also performed, wherein percent nanoparticles yield, morphology of the nanoparticles, shape, size, percent elemental composition, crystallinity, and nanoparticle stability were studied. The nanoparticle-synthesizing potential of the two extracts contradicted significantly in the presence and absence of light, while the AE produced a significantly high number of nanoparticles in the dark (17.26%), and increasing light intensities only attenuated the nanoparticle synthesis, whereas ME synthesized comparatively negligible silver nanoparticles in the dark (1.23%). However, increasing light intensities significantly enhanced the number of nanoparticles synthesized in 825 lms (7.41%). The GCMS analysis further gave a comparative insight into the phytochemical composition of both extracts, wherein catechol and pyrogallol were identified as major reducing agents for nanoparticle synthesis. The influence of light intensities on the physiochemical characterization of AgNPs was predominant. While the size of both the AE- and ME-mediated AgNPs increased considerably (20-50 nm diameter) with increasing light intensities, the percent of silver atoms decreased significantly with increasing light intensities in both the AE- and ME-mediated AgNPs with ranges of 13-18% and 14-24%, respectively. The nanoparticle stability studies suggested that both the AE- and ME-mediated AgNPs were stable for up to 15 days when stored at 4 °C. The stability of both nanoparticles was attributed to the presence of a wide range of phytochemicals. In conclusion, the AE of BC leaves was reported to have significantly higher AgNP-synthesizing potential as compared to the ME. However, AE-mediated AgNP synthesis is attenuated by photoirradiation, whereas ME-mediated AgNP synthesis is enhanced by photoirradiation. The photoirradiation by white LED light increases the size of the AgNPs, while the percent silver composition declines, irrespective of the extract type. Both extracts, however, have nanoparticle stabilizing potential, thereby producing stable nanoparticles.

Marine microbial exopolysaccharide route synthesis of Ag and Pd metal nanoparticles: A possible anticancer, and antioxidant applications

The present research aimed develop an innovative and efficient method for fabricating silver and palladium nanoparticles (NPs)by using exopolysaccharide (EPS) from the seaweed-associated endo-symbiotic bacteria Exiguobacterium profundum (OP919469). Through, the application is a combined precipitation approach, EPS acts as a reducing and stabilising agent for the production of NPs. The major functional groups of NPs such as C–H, N–H, C–C, and C–O stretching’s were detected. The structural morphology of NPs showed a mixture of needle, spherical, and triangle-shaped with size between 10 and 50 nm. The purity of EPS was confirmed by high-performance liquid chromatography which revealed 99.81% purity. The NPs revealed strong anti-cancer and antioxidant properties. In addition, the NPs have been shown to dose-dependent toxicity with reduced hatching, survival rate, and abnormalities in zebrafish. The biochemical assay revealed that the EPS loaded NPsdid not induce oxidative stress up to 120 hpf in contrast to hydrogen peroxide which had a significant effect (P < 0.0001) on glutathione-S-transferase, catalase (P < 0.0017), and superoxide dismutase (P < 0.0001). Overall, our finding indicates that the molecular and functional characteristics of EPS and EPS loaded NPs represent future potential applications in the drug delivery and healthcare sectors.

Bacterial synthesis of metal nanoparticles as antimicrobials.

Nanoscience, a pivotal field spanning multiple industries, including healthcare, focuses on nanomaterials characterized by their dimensions. These materials are synthesized through conventional chemical and physical methods, often involving costly and energy-intensive processes. Alternatively, biogenic synthesis using bacteria, fungi, or plant extracts offers a potentially sustainable and non-toxic approach for producing metal-based nanoparticles (NP). This eco-friendly synthesis approach not only reduces environmental impact but also enhances features of NP production due to the unique biochemistry of the biological systems. Recent advancements have shown that along with chemically synthesized NPs, biogenic NPs possess significant antimicrobial properties. The inherent biochemistry of bacteria enables the efficient conversion of metal salts into NPs through reduction processes, which are further stabilized by biomolecular capping layers that improve biocompatibility and functional properties. This mini review explores the use of bacteria to produce NPs with antimicrobial activities. Microbial technologies to produce NP antimicrobials have considerable potential to help address the antimicrobial resistance crisis, thus addressing critical health issues aligned with the United Nations Sustainability Goal #3 of good health and well-being.

Biosynthesis and characterization of gold nanoparticles from citrullus colocynthis (L.) schrad pulp ethanolic extract: Their cytotoxic, genotoxic, apoptotic, and antioxidant activities

The age-old discipline of plant therapy has gained renewed importance through the utilization of plants for the synthesis of metal nanoparticles. However, toxicity testing and characterization of the recently synthesized nanomaterials are essential to evaluating their appropriate application. Citrullus colocynthis is a medicinal plant with several health benefits. Herein, we used its ethanolic pulp extract (PE) to manufacture gold nanoparticles (PE-AuNPs). Various approaches were employed to assess the MTT50 and NR50 values of PE and PE-AuNPs at different concentrations in the human hepatocarcinoma cell line (HepG2). The study aimed to assess the genotoxic effects and in vivo toxicity of PE and PE-AuNPs at MTT50 dosages. The quasi-spherical, cubic/triangular prisms, and nail-looking particles exhibited no antioxidant properties. They had an absorbance peak between 540 and 560 nm, diameters of less than 20 nm, hydrodynamic diameters of 177.9 nm, and a negative surface charge (−10.3 mV). The significant role of plant phytochemicals in the formation of metal nanoparticles is confirmed by the diminished antioxidant capacity of extract residues following PE-AuNP synthesis. PE-AuNPs exhibited in vivo and cytotoxic effects at relatively lower concentrations compared to PE. In contrast to PE, PE-AuNPs exhibited lower genotoxic at MTT50 dosages. Despite having MTT50 values of approximately 1.95 ± 0.06 and 0.89 ± 0.03 mg/ml, PE and PE-AuNPs can still be considered biocompatible. Nonetheless, our results suggest that the characteristics of recently produced nanoparticles can differ from those of the matching plant. Further investigation can provide a better understanding of the possible therapeutic and pharmacological impacts of PE-AuNPs.

Biogenic synthesis of metal nanoparticles: promoting green nanotechnology and sustainable development goals

Biogenic synthesis of metal nanoparticles: promoting green nanotechnology and sustainable development goals

Tuning the Selectivity of Catalytic Nitrile Hydrogenation with Phase-Controlled Co Nanoparticles Prepared by Hydrosilane-Assisted Method.

Cobalt (Co) is a promising candidate to replace noble metals in the hydrogenation process, which is widely employed in the chemical industry. Although the catalytic performance for this reaction has been considered to be significantly dependent on the Co crystal phase, no satisfactory systematic studies have been conducted, because it is difficult to synthesize metal nanoparticles that have different crystalline structures with similar sizes. Here we report a new method for the synthesis of cobalt nanoparticles using hydrosilane as a reducing agent (hydrosilane-assisted method). This new method uses 1,3-butanediol and propylene glycol to successfully prepare fcc and hcp cobalt nanoparticles, respectively. These two types of Co nanoparticles have similar sizes and surface areas. The hcp Co nanoparticles exhibit higher catalytic performance than fcc nanoparticles for the hydrogenation of benzonitrile under mild conditions. The present hcp Co catalyst is also effective for highly selective benzyl amine production from benzonitrile without ammonia addition, whereas many catalytic systems require ammonia addition for selective benzyl amine production. Mechanistic studies revealed that the fast formation of the primary amine and the prevention of condensation and secondary amine hydrogenation promote selective benzonitrile hydrogenation for benzylamine over hcp Co nanoparticles.

Development of AgNPs-PVP/TPU based flexible strain sensors for structural health monitoring of composite structures

Real-time in-stu structural health monitoring (SHM) of composite structure developed through highly sensitive and flexible smart sensors based on colloidal solution of Silver Nano Particles (AgNPs). Synthesis of AgNPs through chemical reduction method by citrate and then in Haxen phase transferred by using surfactant Cetyltrimethylammonium bromide (CTAB). Colloidal solution of AgNPs-Haxen and Polyvinylpyrrolidone (PVP) - Haxen has been followed by mixed, calcined and deposited that thick paste on flexible Thermoplastic Polyurethane (TPU) film. These sensors become more sensitive than metallic foil made sensors and farther this sensor pasted on polymer composite for monotonic loading like tensile loading. The data extracted from sensors was monitored effectively by data acquisitioning technique using Keithley KUSB-3100. This research based on chemical synthesis of metallic nanoparticles like silver, its functionalization, protection of these nanoparticles from environment by capping agents and by creating inert atmosphere respectively. Then these functionalized capped nanoparticles are embedded on the surface of thermoplastic Urethane (TPU) film to make piezo resistive semi conductive strips which serve as flexible strain gauge/smart sensor. One other technique is also being used to make sensor is that colloidal solution of metallic Nanoparticles sprays over TPU substrate using Connective Self Assembly (CSA) method. The sensor then properly attached to Glass fabric reinforced polymer (GFRP) composite and calibrated using data acquisitioning (DAQ) under different mode of testing.

Biosynthesis of Silver and Gold Nanoparticles Using Geum urbanum L. Rhizome Extracts and Their Biological Efficiency

AbstractThe present study evaluates the biosynthesis of AgNPs and AuNPs using aqueous and ethanolic Geum urbanum L. rhizome extracts. The biosynthesized metal nanoparticles (MNPs) were characterized using UV-Vis spectroscopy, FTIR, DLS, SEM, EDX, and TEM. The UV-Vis spectra confirmed the synthesis of AgNPs and AuNPs through peaks corresponding to the surface plasmon effect of metallic Ag (400–430 nm) and Au (530–570 nm). FTIR analysis indicated that alcohols, phenols, proteins, and carbohydrates from G. urbanum rhizome extracts composition are involved in MNPs synthesis. In DLS analysis, AgNPs (34.26–41.14 nm) showed smaller hydrodynamic diameters than AuNPs (46.26–70.29 nm). At the same time, all values for zeta potential were negative, between − 21 and − 13 mV, suggesting good stabilities for all the colloidal MNPs systems in dispersion. TEM analysis showed that the biosynthesized AgNPs had a spherical morphology, while AuNPs were quasi-spherical, polygonal, and triangular. According to TEM data, AgNPs synthesized using aqueous and ethanolic G. urbanum rhizome extracts were characterized by mean diameters of 9.82 ± 3.68 and 14.29 ± 3.46 nm, while AuNPs by 15.88 ± 6.28 and 24.89 ± 10.75 nm, respectively. EDX analysis confirmed the presence of metallic Ag and Au in the MNPs composition by detecting strong signals at 3 (AgNPs) and 2.2 keW (AuNPs). In disc diffusion assay, MNPs showed good antimicrobial activity against Gram-positive (S. aureus MSSA, S. aureus MRSA, S. epidermidis) and Gram-negative (E. coli, P. aeruginosa, K. pneumoniae) bacteria and yeasts (C. albicans). AgNPs and AuNPs were also characterized by a significant antioxidant potential, evaluated through in vitro assays (lipoxygenase inhibition, DPPH radical scavenging activity, metal ion chelating activity, and hydroxyl radical scavenging assays). An overall better activity was obtained for the ethanolic G. urbanum rhizome extract and its derived AgNPs (EC50 = 34.2 ± 1.86 mg/mL in lipoxygenase inhibition assay). Therefore, the G. urbanum rhizome extracts proved to be excellent sources for biologically active AgNPs and AuNPs.

An acoustofluidic picoinjector

Droplet microfluidics has emerged as a valuable technology for a multitude of chemical and biomedical applications, offering the capability to create independent microenvironments for high-throughput assays. Central to numerous droplet microfluidic applications is the picoinjection of materials into individual droplets, yet existing picoinjection methods often exhibit high power requirements, lack biocompatibility, and/or suffer from limited controllability. Here, we present an acoustofluidic picoinjector that generates acoustic pressure at the droplet interface to enable on-demand, energy-efficient, and biocompatible injection at high precision. We validate our platform by performing acid-base titrations by iteratively injecting picoliter volume reagents into droplets to induce pH transitions detectable by color change in solution. Additionally, we demonstrate the versatility of the acoustofluidic picoinjector in the synthesis of metallic nanoparticles, yielding highly monodisperse and reproducible particle morphologies compared to conventional bulk-phase techniques. By facilitating controlled delivery of reagents or biological samples with unparalleled accuracy, acoustofluidic picoinjection broadens the utility of droplet microfluidics for a myriad of applications in chemical and biological research.

Synthesis of Metallic and Metal Oxide Nanoparticles Using Homopolymers as Solid Templates: Luminescent Properties of the Eu+3 Nanoparticle Products

Starting from poly(4-vinylpyridine) ((P4VP)n), poly(2-vinylpyridine) ((P2VP)n), and [N=P(O2CH2CF3)]m-b-P2VP20 block copolymers, a series of metal-containing homopolymers, (P4VP)n⊕MXm, (P2VP)n⊕MXm, and [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm MXm = PtCl2, ZnCl2, and Eu(NO3)3, have been successfully prepared by using a direct and simple solution methodology. Solid-state pyrolysis of the prepared metal-containing polymeric precursors led to the formation of a variety of different metallic and metal oxide nanoparticles (Pt, ZnO, Eu2O3, and EuPO4) depending on the composition and nature of the polymeric template precursor. Thus, whereas Eu2O3 nanostructures were obtained from europium-containing homopolymers ((P4VP)n⊕MXm and (P2VP)n⊕MXm), EuPO4 nanostructures were achieved using phosphorus-containing block copolymer precursors, [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm with MXm = Eu(NO3)3. Importantly, and although both Eu2O3 and EuPO4 nanostructures exhibited a strong luminescence emission, these were strongly influenced by the nature and composition of the macromolecular metal-containing polymer template. Thus, for P2VP europium-containing homopolymers ((P4VP)n⊕MXm and (P2VP)n⊕MXm), the highest emission intensity corresponded to the lowest-molecular-weight homopolymer template, [P4VP(Eu(NO3)3]6000, whereas the opposite behavior was observed when block copolymer precursors, [N=P(O2CH2CF3)]m-b-P2VP20]⊕MXm MXm= Eu(NO3)3, were used (highest emission intensity corresponded to [N=P(O2CH2CF3)]100-b-[P2VP(Eu(NO3)3)x]20). The intensity ratio of the emission transitions: 5D0 → 7F2/5D0 → 7F1, suggested a different symmetry around the Eu3+ ions depending on the nature of the polymeric precursor, which also influenced the sizes of the prepared Pt°, ZnO, Eu2O3, and EuPO4 nanostructures.

Antimicrobial Activity of Green Synthesized Silver and Copper Oxide Nanoparticles against the Foodborne Pathogen Campylobacter jejuni.

Campylobacter jejuni is a major cause of global foodborne illnesses. To develop alternative antimicrobial strategies against C. jejuni, this study designed and optimized the green synthesis of metallic nanoparticles (NPs) with intracellular components of the medicinal fungus Ganoderma sessile to provide the needed reducing and stabilizing agents. NPs were characterized by transmission electron microscopy and dynamic light scattering, and the quasi-spherical NPs had sizes of 2.9 ± 0.9 nm for the copper oxide NPs and 14.7 ± 0.6 nm for the silver NPs. Surface charge assessment revealed zeta potentials of -21.0 ± 6.5 mV and -24.4 ± 7.9 mV for the copper oxide and silver NPs, respectively. The growth inhibition of C. jejuni by the NPs occurred through attachment to the outer cell membrane and subsequent intracellular internalization and resulted in minimum inhibitory concentrations of the silver NPs at 6 µg/mL and copper oxide NPs at 10 µg/mL. On the other hand, a differential ROS production caused by silver and copper NPs was observed. In summary, this research presents the first demonstration of using green synthesis with the medicinal fungus G. sessile to produce metallic NPs that effectively inhibit C. jejuni growth, providing a sustainable and effective approach to the traditional use of antimicrobials.

Harnessing Coordination‐Assisted Surface Functionalization for Ligand‐Induced Growth of Ultrafine Metal Nanoparticles on MXene

AbstractThe synthesis of ultrafine metal nanoparticles and their integration onto 2D nanomaterials have attracted significant interest due to their outstanding chemical and electrochemical activity. Among 2D materials, MXenes have emerged as promising candidates for hybridization owing to their abundant surface nucleation sites and high electrical conductivity. However, achieving uniform growth of ultrafine metal nanoparticles on MXene surfaces remains a challenge due to non‐uniform metal nucleation and growth behaviors. In this study, a novel coordination‐assisted surface functionalization method is presented to graft organic ligands onto MXene, promoting the uniform growth of ultrafine metal nanoparticles. By leveraging the mutual attraction between metal ions, organic ligands, and MXene surface functional groups, MXene surfaces are efficiently functionalized through palladium coordination complexes. Subsequent ligand‐induced growth facilitated the uniform nucleation of ultrafine metal nanoparticles, resulting in densely anchored nanoparticles of 1–3 nm in size on MXene. Comprehensive characterizations reveal the effectiveness of the method, demonstrating exceptional properties of the MXene‐metal nanoparticle hybrid, particularly in hydrogen sensing applications. This study highlights the potential of coordination‐assisted surface functionalization for the controlled synthesis of MXene‐based nanomaterials with tailored properties for diverse applications.

Green Synthesis of Metallic Nanoparticles from Quercus Bark Extracts: Characterization and Functional Properties.

Quercus species are utilized for their durable wood, providing sustenance for wildlife, conserving biodiversity, and contributing ecological, medicinal, and esthetic benefits to ecosystems and landscapes. In this study, we aimed to use the bark of three Quercus species (Q. dalechampi, Q. fraineto, and Q. petraea) for the synthesis of silver and gold nanoparticles (AgNPs and AuNPs). The aqueous extracts from the bark of Quercus sp. acted both as reducing and stabilizing agent, facilitating the rapid synthesis of AuNPs (AuQD, AuQF, and AuQP) and AgNPs (AgQD, AgQF, and AgQP). The obtained nanoparticles were characterized using UV-vis spectroscopy, TEM, DLS, and FTIR. Characterizations revealed that the nanoparticles exhibited a variety of shapes, such as polygonal, triangular, and spherical forms, with sizes ranging between 14 and 24 nm for AuNPs and 45-70 nm for AgNPs. The total phenolic content was assessed through spectroscopic methods, while several individual phenolic compounds were identified and quantified using UPLC-PDA. Furthermore, we assessed the antioxidant, antibacterial, and antifungal capacities of AuNPs, AgNPs, and raw extracts. The highest antioxidant activity was observed for raw extracts, followed by AgNPs and AuNPs, while the most potent antibacterial and antifungal activity was observed in AgQP. Moreover, cytotoxicity was examined in a human keratinocyte cell line (HaCaT). The results indicated no cytotoxic effects for AuNPs, while AgNPs and the raw extracts exhibited cytotoxic effects after 48 h of incubation. This research underscores the multifaceted utility of Quercus bark extracts in the green synthesis of metallic nanoparticles and their subsequent bioactivity assessment, suggesting promising perspectives for their application in various fields while urging cautious consideration of their cytotoxic implications.

Green synthesis of silver nanoparticles using Senna alexandrina leaf extracts and their antibacterial, larvicidal, nanotoxicity and photocatalytic activity

Biological synthesis of metal nanoparticles has been discovered in recent years, and they have been effectively manufactured and studied from diverse plant extracts. Recent research has shown that nanoparticles have extremely promising antibacterial, larvicidal and anticancer effects. The current study aimed to synthesize Senna alexandrina leaf extract-mediated silver nanoparticles (SA-AgNPs) as are reducing and capping agent. The produced SA-AgNPs were characterized by using UV–visible spectroscopy, Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), and Field emission scanning electron microscopy with energy dispersive spectroscopy (FESEM-EDS). The result showed synthesized SA-AgNPs were confirmed by UV–visible spectroscopy with 440 nm absorption. FT-IR analysis shows the presence of phosphine, primary amines, carboxylic acids, ether, and alkyl halides biomolecules in both plant extract and SA-AgNPs. XRD findings revealed the crystalline structures of produced SA-AgNPs. The spherical shape of SA-AgNPs with an average size of 20–35 nm was confirmed using FESEM. The SA-AgNPs show better antibacterial activity against E. coli (18.0 ± 0.25 mm), S. aureus (17.2 ± 0.36 mm), P. aeruginosa (16.8 ± 0.12 mm), and leaf extract of S. alexandrina showed minimal antibacterial activity. The SA-AgNPs show 100 % mortality for both Cx. quinquefasciatus and Ae. aegypti after 48 hrs. The brine shrimp lethal assay of the SA-AgNPs shows 100 % at 30 µg after 24 hrs of brine shrimp which indicated the presence of cytotoxicity this suggests that produced SA-AgNPs are slightly toxic. The photocatalytic activity was also tested using reactive orange 16 (RO16) and phenol red (PR) with the percentage of degradation being about 93.95 % and 92.91 % respectively. These results suggest that biosynthesized SA-AgNPs have promising properties that can be used as an effective biomedical and environmental protectant.