Formation Of NPs Research Articles

Antibacterial Activity of V2O5 Nanoparticles

The chemical synthesis of vanadium pentoxide nanoparticles (V2O5 NPs) is presented in this article. The formation of V2O5 NPs is confirmed by the 508 cm-1 band visible in the Fourier-transform infrared spectrum. According to the scanning electron microscopy analysis, the 40–50 nm-sized V2O5 NPs resemble sponges. The size of V2O5 NPs is in between 33.72 and 52.78 nm, as shown by XRD. The antibacterial capabilities of V2O5 NPs were evaluated against Staphylococcus aureus and Bacillus cereus. Moderate antibacterial activity is exhibited by the synthesized V2O5 NPs.

Green synthesis of silver nanoparticle by Hyoscyamus muticus L. extract and study of its effect on tomato infected with Meloidogyne javanica

In this study, the aqueous leaf extract of Hyoscyamus muticus L Plant leaf was prepared using three methods: maceration (MAC), microwave-assisted extraction (MAE), and ultrasonic-assisted extraction (UAE). Then, the extracts were used to synthesize silver nanoparticles (Ag NPs) in an environmentally friendly approach. The characterization of the synthesized Ag NPs was carried out by various techniques. The XRD results confirmed the successful synthesis of nano-sized Ag crystals with spherical structure. The SEM images showed the formation of Ag NPs, which were smaller than 75 nm. The UV-Vis studies showed an obvious absorption peak for Ag NPs between 400-500 nm, with a clear peak around 450 nm for all samples. The elemental analysis using the EDS technique confirmed the presence of silver in the synthesized Ag NPs. Furthermore, the effect of different concentrations of Ag NPs was investigated on hatching and second-stage juvenile (J2s) mortality of Meloidogyne javanica, under controlled conditions. The results showed that increasing concentrations of Ag NPs led to higher percentages of inhibition of egg hatching and J2s mortality. Additionally, the Ag NPs synthesized by ultrasonic-assisted extraction with lower lethal concentration were found to be more toxic to M. javanica than the extract prepared by soaking. According to the results, Ag NPs showed a stronger inhibitory effect on M. javanica egg hatching and J2s mortality compared to the total extracts and chemically synthesized Ag NPs. Also, the lowest LC50 was observed for the Ag NPs synthesized using the plant extract as: UAE > MAE (180 w) > MAE (90 w) > MAC methods. The highest inhibition of egg hatch occurred at 0.5 % v/v of Ag NPs after 72 hours and remained consistent after 120 hours.

Encapsulation of Antarctic krill peptide by polysaccharide-based nanoparticles: Preparation, characterization, evaluation of stability and hypoglycemic activity

The aim of this study was to construct a chitosan quaternary ammonium salt (HTCC)/sodium alginate (SA) nanoparticle delivery system for the encapsulation of Antarctic krill peptide (AKP), with the goal of enhancing its stability and post-digestive hypoglycemic activity. Additionally, the effect of the content and encapsulation sequence of HTCC/SA on the structure and properties of AKP-loaded nanoparticles (AKP-loaded NPs) was investigated. As the content of the outermost wall material (HTCC) increased, the particle size of nanoparticles initially increased and then decreased. Concurrently, the zeta potential showed a trend of increase, ranging from -38.77 to 46.07 mV. When SA was used as the outermost wall material, the nanoparticles exhibited a smaller particle size (240.1 nm) and better dispersibility. Electrostatic interaction and hydrogen bonding were the major forces involved in the formation of AKP-loaded NPs. X-ray diffraction revealed that AKP was successfully encapsulated in an amorphous state. Scanning electron microscopy showed that AKP-loaded NPs had an elliptical or blocky appearance. Moreover, AKP-loaded NPs demonstrated good storage and temperature stability, while nanoparticles with HTCC in the outermost layer (HTCC:SA=2:1) showed good pH and ionic stability. During simulated digestion, AKP-loaded NPs inhibited the release of AKP in gastric fluid. Consequently, the hypoglycemic activity of digested AKP-loaded NPs was remarkably higher than unencapsulated AKP. Notably, the nanoparticles with HTCC in the outermost layer provided superior hypoglycemic activity. In summary, the polysaccharide-based delivery system exhibited great potential to improve the stability and post-digestive hypoglycemic activity of AKP, broadening its applications in the food and pharmaceutical industries.

Green synthesis of silver nanoparticles on polyamide fabrics using Scrophularia striata Boiss extract: Characterization, dyeing, and antibacterial properties

The green synthesis of silver nanoparticles (Ag NPs) on textiles using natural extracts is emerging as an innovative, eco-friendly approach for enhancing both antibacterial properties and dyeing performance. This study introduces a novel in-situ method for synthesizing Ag NPs directly on polyamide (PA) fabrics, utilizing Scrophularia striata Boiss extract (SBE) as a natural dye and reducing agent. UV–visible spectroscopy and dynamic light scattering (DLS) were used to characterize the synthesis process and determine the average particle size of Ag NPs. The data showed particle sizes of 62.5 nm and 56.1 nm when using flower and stem extracts, respectively. Surface morphology findings from scanning electron microscopy (SEM) and corresponding diffraction peaks in X-ray diffraction (XRD) confirmed the in situ formation of Ag NPs on the surface of PA fabric. Fabrics dyed with SBE and Ag NPs exhibited higher color strength (K/S values of 4.1 and 5.6 for flower and stem, respectively), showing 64 % and 100 % increases compared to samples without silver. Additionally, PA fabrics exhibited 100 % inhibition against E. coli and S. aureus bacteria. After 10 washing cycles, antibacterial activity was maintained at 88 % and 85 % for the stem extract and 83 % and 79 % for the flower extract. This research highlights the novel integration of natural dye and nanoparticle synthesis, providing a sustainable route for multifunctional textile development.

Capping agent-free aqueous gold nanoparticles generated by an environmentally friendly plasma-liquid method

This study investigates a simple approach for synthesizing gold nanoparticles (Au NPs) using atmospheric pressure plasma without the need for reducing agents, additives, or capping agents. The size, morphology, optical properties, and aggregation stability of the synthesized Au NPs were characterized using scanning electron microscopy, UV-vis spectroscopy, and zeta potential analysis. The UV-vis absorption spectra of the gold nanoparticles, obtained at various Au3+ concentrations and treatment durations with anode plasma discharge, were analyzed. The UV-vis spectra revealed a surface plasmon resonance absorption band between 530–600 nm, indicative of Au NP formation. Results demonstrated that the size of Au NPs can be tuned within the range of 30–75 nm by adjusting the gold salt precursor concentration from 0.3 to 2.5 mmol/L. It was found that plasma treatment for 3–10 minutes, at different Au3+ concentrations, resulted in the formation of Au NPs with varying sizes and morphologies. The study showed that particles with different shapes – spherical, hexagonal, and triangular – were formed depending on the initial concentration of Au3+. The plasma-chemically synthesized nanoparticles at an Au3+ concentration of 0.06 mmol/L were predominantly spherical and exhibited the highest stability (lasting 12–24 hours), with a zeta potential of –20 to –22 mV, compared to samples with Au3+ concentrations ranging from 0.3 to 2.5 mmol/L.

Biofabrication of highly effective and easily regenerated CuO nanoparticles as adsorbents for Congo red and malachite green removal

An effective and easily regenerated adsorbent is the one for which scientists are making an effort to explore. In this study, copper oxide nanoparticles (CuO NPs) were synthesized in a green manner from a leaf extract of Moringa stenopetala and used for dye adsorption. XRD, FTIR, and SEM were employed for the characterization of CuO NPs. The crystallite size of the CuO NPs was calculated via Debye–Scherrer equation from the XRD data and was found to be 8.33 nm. The Cu–O bonding bending vibration at 1116 cm− 1 and stretching vibration at 1649 cm− 1 observed from the FTIR data strongly confirmed the formation of CuO NPs. SEM morphology analysis confirmed the formation of nanoparticles with a plate-like morphology and a spherically random orientation. The zero-point charge of CuO NPs was investigated and reported to be at pH 7. The adsorption of dyes on the greenly produced CuO NPs was studied by optimizing different adsorption parameters. The removal efficiencies of the green CuO NPs adsorbent were 99.54% at the optimum conditions (pH, 4; dye concentration, 30 mg/L; amount of adsorbent, 0.25 g; and contact time, 80 min) and 98.33% at the optimum conditions (pH, 11; dye concentration, 20 mg/L; amount of adsorbent, 0.4 g; and contact time, 80 min) for congo red and malachite green, respectively. The adsorption efficiency of the biosynthesized CuO NPs for the mixture of the two dyes was 92.3%. The green synthesized adsorbent was regenerated and able to work effectively for four cycles for the two dyes. The results of the kinetics-type investigation indicate that the adsorption of both dyes by the CuO NPs adsorbent best fits a pseudo-second-order model. The isotherm model-type investigation resulted in the fitting of the Langmuir adsorption isotherm for both the congo red and malachite green dyes.

Antimicrobial Activity of Amino-Modified Cellulose Nanofibrils Decorated with Silver Nanoparticles.

Silver nanoparticles (Ag NPs) conjugated with amino-functionalized cellulose nanofibrils (NH2-CNFs) were in situ-prepared by reducing silver ions with free amino groups from NH2-CNFs. The spectroscopy and transmission electron microscopy measurements confirmed the presence of non-agglomerated nanometer-in-size Ag NPs within micrometer-large NH2-CNFs of high (20 wt.-%) content. Although the consumption of amino groups during the formation of Ag NPs lowers the ζ-potential and surface charge of prepared inorganic-organic hybrids (from +31.3 to +19.9 mV and from 2.4 to 1.0 mmol/g at pH 7, respectively), their values are sufficiently positive to ensure electrostatic interaction with negatively charged cell walls of pathogens in acidic and slightly (up to pH ~8.5) alkaline solutions. The antimicrobial activity of hybrid microparticles against various pathogens (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans) is comparable with pristine NH2-CNFs. However, a long-timescale use of hybrids ensures the slow and controlled release of Ag+ ions to surrounding media (less than 1.0 wt.-% for one month).

Novel ophthalmic hyaluronic acid-hydrogel with curcumin nanoparticles for enhanced healing of ulcerative keratitis in rabbit model

Corneal ulcers, whether melting or indolent, are common in humans and companion animals. Treatment involves local administration of antibiotic eye drops and corneal healing drugs. Compared to traditional treatments for ulcerative keratitis, herbal medicines offer unique advantages, such as potent anti-inflammatory effects and inhibition of proinflammatory cytokines. Curcumin, extracted from the Curcuma Longa plant, possesses extensive pharmacological properties, such as anti-inflammatory, anti-cancer, and antioxidant properties, and is used in various medicines. In this study, we developed a novel ophthalmic drop hydrogel using a formulation of Curcumin NPs encapsulated with β-cyclodextrin and hyaluronic acid, to accelerate corneal healing and improve the quality of healed structures. The formation of Curcumin NPs into Hyaluronic acid-based hydrogels was characterized by zeta, FTIR, and scanning electron microscope (SEM) analyses. A total of 25 healthy male New Zealand Albino rabbits were experimentally induced with ulcerative keratitis and treated individually with topical medication. Rabbits were divided into five groups. Fluorescein dye staining, corneal clarity score, Schirmer tear test, proinflammatory cytokine measurement, and pathologic factors assessments were used to evaluate the optimised Curcumin NPs with β-cyclodextrin in Hyaluronic acid hydrogel. Our results demonstrated that the optimized Curcumin NPs with β-cyclodextrin in hyaluronic acid hydrogel significantly reduced the frequency of medication administration compared to conventional therapies, enhancing the quality of healed structures and effectively treating ulcerative keratitis. All findings in this study provide new insight into designing and fabricating novel ophthalmic medicine for ulcerative keratitis for topical usage.

Bioengineered Nickel Oxide Nanofabrication for Energy Storage Systems, Degradation of Refractory Water Toxicity, and Antibacterial Study

AbstractNickel oxide (NiO) nanoparticles were synthesized using a green method involving Pterolobium hexapetalum flower extract as the reducing agent. Synthesized nickel oxide nanoparticles (NiO NPs) were thoroughly characterized using X‐ray diffraction, UV–vis spectroscopy, Fourier‐transform infrared spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Brunauer–Emmett–Teller (BET) surface area analysis. The XRD analysis confirmed the pure formation of NiO NPs. TEM and SEM images revealed the size, shape, and surface morphology of the nanoparticles. BET analysis indicated a high surface area, making these nanoparticles suitable for various applications. The NiO NPs were further investigated for their potential in supercapacitor applications, demonstrating excellent electrochemical performance. NiO@rGO electrode with graphene proportion showed a maximum specific capacity of 1266 Fg−1 at 1 Ag−1. Moreover, following the 3000‐cycle assessment, the specific retention of 98.2% confirmed that the electrode had high cyclic stability. Additionally, their effectiveness in dye degradation was evaluated, showing promising results in removing organic dyes from wastewater. The antibacterial activity of the NiO nanoparticles was also assessed, indicating significant inhibition against various bacterial strains. These multifaceted studies suggest that NiO NPs synthesized from plant extract hold great promise for applications in energy storage, environmental remediation, and antimicrobial treatments.

Preparation of curcumin-loaded chitosan/lecithin nanoparticles with increased anti-oxidant activity and in vivo bioavailability

As a natural polyphenol, curcumin (Cur) has exhibited a range of bioactive properties, including anti-inflammatory, anti-oxidant, and anti-infection properties. However, the chemical instability and low water solubility of Cur hinder its wide application. Herein, Cur-loaded chitosan/lecithin nanoparticles (CCL NPs) were prepared by the electrostatic self-assembly method. The prepared CCL NPs showed a small particle size (122.86 ± 1.53 nm) with homogeneous distribution (PDI = 0.17 ± 0.01). The high EE (79.34 ± 2.93 %) and LC (9.33 ± 0.34 %) indicated that most of Cur was encapsulated in CCL NPs. Meanwhile, the Cur was released from CCL NPs in a quick and sustained way after being exposed to simulated gastrointestinal fluids. The CCL NPs displayed superior anti-oxidant activity than that of free Cur. Moreover, the in vivo pharmacokinetic studies showed that the CCL NPs could lead to a ~ 2.64-fold increase in oral bioavailability compared with that of free Cur. All these findings indicated that the formation of CCL NPs would be a promising platform to deliver Cur in the food industry.

Hepatoprotective Activity of Gingko biloba‐Mediated TiO2 NPs Against Acetaminophen‐Induced Albino Rats‐ In Vitro Studies

AbstractNumerous effects of “titanium dioxide nanoparticles (TiO2 NPs)” have been described and significantly utilized in complementary drugs for many decades. This study is conducted to analyze the therapeutic efficiency of TiO2 NPs against the acetaminophen‐(AMP) induced toxicity. TiO2 NPs were initially prepared using Ginkgo biloba leaf extract as reducing and stabilizing agent. The prepared TiO2 NPs were studied using various spectroscopic and microscopic techniques. AFM, TEM, XRD, and DLS studies have confirmed the formation of TiO2 NPs with size between 20 to 60 nm with negative surface charge of about −12 mV. Later, hepatoprotective studies were performed by administering AMP to albino mice only once at a dosage of 2 g/kg p.o. Post 24 h of AMP intoxication, the animals were treated orally with three different doses of TiO2 NPs (150, 100, and 50 mg/kg) or silymarin at an amount of 50 mg/kg p.o., administered only once. Post 24 h of last treatment, all the animals were surrendered to death. The group of mice administered with AMP displayed a substantial raise in the serum alkaline phosphatase (560 ± 31.90), lactate dehydrogenase (167 ± 10.17), aspartate amino transferase (251 ± 14.82), alanine amino transferase (326 + 18.96), bilirubin (2.2 ± 1.066), cholesterol (96.7 ± 6.2), and albumin (6.0 ± 1.27) in serum, which signified the liver damage. A considerably depleted level of glutathione (5.4 + 1.24) was detected in the mice intoxicated with AMP. The activities of catalase (33.2 ± 2.66) and superoxide dismutase (36 ± 2.93) declined after exposure to acetaminophen, resulting in oxidative stress in liver. The performance of adenosine triphosphatase (901 ± 50.7) and glucose‐6‐phosphatase (3.9 + 1.15) were considerably inhibited after administrating with AMP. On treating with TiO2 NPs, all the variables reversed significantly towards regular levels and were noticed to be nontoxic. The groups treated with TiO2 NPs exhibited less activity of ALT, AST, LDH, and SALP in serum, indicating the protective effect of TiO2 NPs to prevent liver damage. Exposure with TiO2 NPs inverted the cholesterol, albumin, and bilirubin levels towards normal, which is similar to silymarin treatment. TiO2 NPs exhibited a substantial change in tissue and blood biochemical parameters with that of control groups. These results indicate that TiO2 NPs possesses hepatoprotective properties that mitigate the hepatotoxicity induced by acetaminophen in rats. Hence, TiO2 NPs can be further utilized in the preparation of medicine against hepatic and renal diseases, post further clinical and preclinical studies.

Plant-mediated synthesis of zinc oxide (ZnO) nanoparticles using Alnus nepalensis D. Don for biological applications

An aqueous bark extract of A. nepalensis D. Don was utilized to prepare zinc oxide (ZnO) nanoparticles through a green method, which is more economical, eco-friendly, and effective for exploring several biological applications and toxicity assessments against brine shrimp nauplii. The prepared ZnO nanoparticles were characterized using several characterizing techniques. The surface morphology and the elemental composition of the prepared ZnO NPs was analyzed by field emission scanning electron microscopy (FE-SEM), and energy dispersive X-ray (EDX) analysis. The colour of the solution was changed from reddish-brown to white indicating the formation of ZnO NPs which shows UV–vis absorption at 361 nm. The various functional groups of the organic compounds present in plant extract act as reducing and stabilizing agents in the formation of nanoparticles. The involvement of these functionalities in the formation of nanoparticles is indicated by the shifts and changes in the IR spectra of both the plant extract and the ZnO nanoparticles. The size of the nanoparticles was determined to be 15.31 nm with XRD analysis while the FE-SEM revealed the average grain size of 67.29 nm with irregular shape. The elemental composition of ZnO NPs shows a greater atomic percentage of zinc compared to other elements (C, N, Ni, O, and Ag), with an intense peak of zinc observed at approximately 1 keV. The trace amount of silver is due to the impurities present in the reagent used in the experiment. The antioxidant property of ZnO nanoparticles was evaluated with an IC₅₀ of 53.02 ± 3.43 μg/mL. The ZnO nanoparticles exhibited significant antibacterial activity against Klebsiella pneumoniae and Escherichia coli, with zones of inhibition (ZOI) of 18 mm and 23 mm, respectively as compared to the positive control neomycin of ZOI 28 mm against K. pneumoniae. The potential antibacterial activity of the ZnO NPS was revealed as the MIC and MBC against K. pneumoniae of 0.39 mg/mL and 0.78 mg/mL, respectively. In addition, the prepared ZnO nanoparticles showed toxicity against brine shrimp nauplii of LC₅₀ 16.59 μg/mL. The results of this study impart that plant-assisted synthesized ZnO nanoparticles possess significant antibacterial properties that reduce oxidative stress in human cells, ultimately contributing to cancer prevention.

Oxalic acid capped tungsten oxide nanozyme mimicking peroxidase activity, its synthesis characterization, and kinetic data validation via spectrophotometric studies

The need for parody enzymes has attracted the interest of researchers globally. Nanomaterials have provided promising results as mimic catalysts termed nanozymes (NZMs). This article briefs the peroxidase mimicking behavior of Oxalic acid-capped WO3 nanoparticles (Ox-WO3 NPs), which were hydrothermally synthesized. The peroxidase parodying behavior of the synthesized NZMs was studied for H2O2 as substrate and PPDD-NEDA and TMB as a chromogenic reagent in Phosphate buffer at pH 6.5. The coupled product of PPDD-NEDA showed λmax=480 nm, and the method was linear between 0.2413 and 1.93 mM. The oxidized product of TMB λmax=650 nm was linear in the range of 0.1938–1.9386 mM. Km values corresponding to TMB, and PPDD-NEDA were 0.5308 and 0.3957 mM. Kinetic constants with respect to PPDD-NEDA i.e., Vmax, Kcat, Keff, and Kpow were found to be 0.1913 mM/min, 3.3639 min−1, 8.4999 mM−1 min−1, and 0.4833 min−1. The precision study for intra-day (1.27–2.49 %) and inter-day (1.09–1.52 %) has been calculated. LOD and LOQ of the reaction was found to be 56.34 and 170.73 µM respectively. Characterization of synthesized NPs were carried out with respect to morphology, crystallinity, size, zeta potential and others. The XRD of the sample revealed the crystallite size to be 42.6 nm (Williamson-Hall equation) and 35 nm (Scherrer equation), Crystal structure was identified to be a mixture of monoclinic and orthorhombic as compared with the JCPDS file and the crystallinity of the sample was found to be 79.75 %. The SEM images provided the morphology to be spherical in nature with more aggregation due to lower zeta potential value as recorded by the DLS. The elemental composition by EDS recorded the formation of WO3 NPs. The broad peak of FT-IR spectra between 2900 and 3900 cm−1 confirms the capping of oxalic acid to WO3 NPs.

Unveiling Cu Nanoparticles Formed During Li Deposition in Anode-Free Batteries.

Developing high-energy-density Li metal batteries is essential for sustainable progress, necessitating in-depth studies of complex battery reactions. The presence of metallic Cu impurities detrimentally impacts battery performance, leading to issues such as self-discharging and internal soft short-circuit. Nevertheless, their formation mechanism and structural characteristics have not been revealed clearly. Here the formation of single-crystalline Cu nanoparticles during the Li deposition process in anode-free cells was identified by transmission electron microscopy. Through investigation of the chemical state of Cu before and after Li deposition, the formation of Cu NPs was attributed to the reduction of the oxide layers formed on the surface of Cu current collectors. Additionally, it was observed that Cu nanoparticles can be formed inside of deposited Li metal. This work reveals the formation pathway and microstructural characteristics of Cu nanoparticles appearing during Li deposition, underscoring the importance of nanoscale investigations into the underlying battery reactions.

Synthesis of Palladium Nanomaterials Using Plant Leaf Extract and their Enhanced Photocatalytic Activities against Organic Dyes

Aims and Objectives: This study aimed to carry out the green synthesis of palladium nanoparticles (Pd NPs) using the aqueous leaves extract of Eclipta alba. The appearance of a characteristic surface plasmon resonance peak at 410 nm confirmed the synthesis of Pd NPs. Method: The average particle sizes of 13 nm were observed by using the leaf concentrations of 10 mL with a certain amount of PdCl2 (0.001 M) at 25 ̊ C. The Pd NPs, as synthesized under the optimized conditions (10 mL extract + 60 ̊ C + 0.001 M PdCl2), were spherical in shape, small in size, and uniformly distributed, as depicted by HR-TEM images. Results: FTIR, XRD, DLS, and zeta potential further confirmed the formation of Pd NPs. The Pd NPs synthesized at optimized conditions exhibited strong catalytic activity in dye Eosin yellow, Rose Bengal, Tartrazine, and Ponceau S degradation by discoloration of dyes in 3 hrs. The removal of all dyes by the Pd NPs was optimized by varying specific operating parameters, such as initial dye concentration, solution pH, irradiation time, and temperature. Conclusion: This high activity of Pd NPs may be due to their small size, high dispersion, and surface- capping phytochemicals. result: Bio-fabrication of metallic Pd NPs using different plant extracts compared to other reducing agents is more scalable, rapid, and cost-effective for generating bulk nanoparticles. The phytochemical principles, such as phytoconstituents, reduce the PdCl2 to Pd NPs and are implicated in the capping and stability of the nanoparticles. Hence, the leaves of Eclipta alba have different polyols and are well known. Apart from this, hydroxyl groups in phenolic compounds may participate in the bio-reduction of PdCl2. Such compounds can chelate metal ions to form their quinones form, which is an intermediate palladium complex. Then, stabilization of the intermediate form and reduction of Pd2+ to Pd0 occurred due to free electrons or nascent hydrogen produced during the bio-reduction reaction. Finally, Pd-NPs were prepared due to the collision of neighboring Pd0 atoms. These significant conjugations exist in the keto-enol system within the quinone form of the compound.

Phytosynthesis of titanium dioxide nanoparticles using Cynodon dactylon leaf extract and their antibacterial activity

Due to use of nanoparticles, nanotechnology has become an important area of research penetrating in all the fields of science and technology including medicinal chemistry. Titanium dioxide nanoparticles (TiO2 NPs) play an important role in biotechnology and nanomedicine because of their antimicrobial effect against many pathogens such as bacteria, fungus, viruses and yeast. In this article, we propose an eco-friendly phytosynthesis method of TiO2 NPs using aqueous leaf extract of Cynodon dactylon herbal plant as a reducing agent. The formation of TiO2 NPs by plant bio-molecules involved in the reduction of metal ions to nanoparticles is demonstrated. The synthesized TiO2 NPs are analyzed using X-ray diffraction analysis, Fourier transform infrared spectroscopy, laser Raman spectroscopy and field emission scanning electron microscopy. The antibacterial activity of the TiO2 NPs against gram-positive bacterial pathogens like Bacillus subtilis and Staphylococcus aureus as well as gram-negative bacterial pathogen like Escherchia coli is tested. The obtained results demonstrate potent bactericidal activity of the TiO2 NPs.

Green synthesis, chemical characterization, anti-osteoarthritis properties of Cu nanoparticles

In our latest study, we assessed the effectiveness of a green copper nanoparticle formulation containing curcumin on the chick’s knee joint injury. The NPs were characterized using FE-SEM, TEM, XRD, and EDX techniques. The primary cultured chondrocytes were utilized to check the nanoparticles effectiveness on chondrogenesis in the orthopedic experiments. Subsequently, we assessed the functional restoration post copper nanoparticles transplantation using an osteoarthritis articular model in the knee. Histological, PCR, and western blot analyses were conducted to investigate the underlying mechanisms. The XRD results exhibited the CuO formula for CuNPs and a spherical shape with a size <60 nm was obtained for the NPs from the TEM and FE-SEM images. The presence signals in EDX diagram including signals at 0.22 keV for C Lα, 0.51 keV for O Lα, and 0.93 keV for Cu Lα approve the formation of Cu NPs. The use of nanoparticles effectively inhibited abnormal fibrosis and angiogenesis at the injury site. The nanoparticles presence in the histological test resulted in rised synthesis of cartilage matrix and proliferation of chondrocytes, while also reducing the formation of abnormal vasculature. The study unveiled that the use of nanoparticles accelerated the healing process following an injury after three weeks. Furthermore, we highlighted the beneficial effects of copper nanoparticles in promoting cartilage formation in a laboratory setting. In the immunological domain, the copper nanoparticles demonstrated a decrease in the quantities of IL-1β, TNF-α, p-p65, and MMPs expression. This phenomenon could potentially be attributed to the cellular redox homeostasis modulation associated with the Nrf2 pathway. In conclusion, the results of this research confirmed the positive efficacy of copper nanoparticles containing curcumin in accelerating the osteoarthritis articular cartilage repair.

Green synthesis of undoped and Ag-doped NiO nanoparticles: Evaluation and their synergetic effect on antimicrobial, anticancer, and antioxidant activities

In this investigation, we successfully synthesized nickel oxide nanoparticles (NiO NPs) using a combustion method with Acacia nilotica gum as a biofuel, and systematically altered silver (Ag) concentrations within the NiO matrix. Post-calcination at 400 °C, various characterization techniques confirmed the formation, surface morphology, and crystalline characteristics of NiO NPs. The Ag-doped NiO NPs, particularly the NiAg4 sample, demonstrated remarkable antimicrobial efficacy, with superior activity against both fungal and bacterial pathogens. The NiAg4 sample also exhibited potent cytotoxicity against HT-29 human colon cancer cells, achieving an IC50 value of 1.5 mg/mL. Toxicological assessments revealed that both undoped and Ag-doped NiO NPs maintained biocompatibility with human red blood cells, indicating their potential for biomedical applications. Additionally, the NPs showed strong antioxidant activity and protein kinase inhibition, further supporting their therapeutic potential. These findings suggest that Ag-doped NiO NPs synthesized through a green protocol possess enhanced bioactivities, making them promising candidates for future in vivo studies and diverse biomedical applications.

Facile Biogenic synthesis of Europium doped lanthanum silicate nanoparticles as novel supercapacitor electrodes for efficient energy storage applications

In this work, we demonstrated for the first time, use of Europium doped lanthanum silicate nanoparticles (LS NPs) as electrodes for supercapacitor applications. Europium (Eu3+) doped (5 mol%) LS NPs were synthesized by green solution combustion method using Mexican mint leaf extracts. Various analytical techniques such as High-Resolution Transmission Electron Microscopy (HRTEM), Selected Area Diffraction (SAED), Powder X-ray Diffraction (PXRD), Fourier Transform Infra-Red Spectroscopy (FTIR) and Diffuse Reflectance Spectroscopy (DRS) techniques were used to confirm the morphological and structural characteristics of the synthesized nanoparticles. The HRTEM and SAED patterns confirms the formation of NPs having agglomerated structure with a particle size less than 50 nm. The PXRD patterns reveals crystalline cubic structure for the NPs. Further, the FT-IR spectra reveal the successful doping of Europium in Lanthanum Silicate NPs. The DRS (Diffuse Reflectance Spectroscopy) studies confirm the reduced band gap for Europium (Eu3+) doped (5 mol%) LS NPs. Cyclic voltametric and electrochemical impedance spectroscopy experiments were performed in an alkaline medium to compare the electrochemical activity of Eu3+ doped LS NPs with that of their undoped counterpart. The Eu3+ doped (5 %) LS NPs electrodes attained a specific capacitance of 373.3 Fg-1 at a current density of 0.5 Ag-1 in comparison to pure LS NPs which is about 267 Fg-1. The long-term stability of the Eu3+ doped (5 %) LS NPs electrodes show excellent stability up to 4000 cycles of operation in comparison pure LS NPs electrodes. Doping of Eu3+ had a favourable effect on the conductivity and electrochemical activity of LS NPs. Due to favourable green combustion synthesis, superior electrochemical performance, these Eu3+ doped LS NPs could be potential materials for new generation supercapacitors in energy storage applications.

A highly efficient and stable PtNi bimetallic nanoparticles modified on Mo2C decorated N-doped carbon flowers catalysts for the remediation of environmental pollutants

The unregulated discharge of nitroaromatics (NAs) and organic dye contaminants into aquatic ecosystems is a growing global concern, highlighting the urgent need for the development of effective wastewater treatment technology. In this study, we prepared Mo2C decorated on N- doped carbon flowers supported with PtNi bimetallic (PtxNiy@Mo2C/NCF) nanoparticles using the self-polymerization of dopamine and followed by the chemical reduction methods. These catalysts, with varying Pt:Ni ratios, were designed for the highly efficient catalytic reduction of NAs and rhodamine b (RhB) under the mild reaction conditions. The HR-TEM images confirmed the formation of spherical PtNi bimetallic NPs with an average diameter of 1.68 ± 0.6 nm. The prepared PtxNiy@Mo2C/NCF catalysts exhibited significantly higher catalytic efficiency for 4-nitrophenol (4-NP) reduction compared to their respective monometallic counterparts using NaBH4. Particularly, the Pt0.75Ni0.25@Mo2C/NCF catalyst showed superior catalytic activity with the apparent rate constant (kapp: 0.6703 min−1) and TOF (17.0 × 10−7 mol mg−1 min−1) and high recyclability over eight consecutive recycles. Furthermore, the Pt0.75Ni0.25@Mo2C/NCF catalyst also exhibited high catalytic activity for other NAs and RhB dye reduction with excellent yields. This enhanced catalytic activity of Pt0.75Ni0.25@Mo2C/NCF catalyst could be ascribed to the synergistic effect of the bimetallic systems, leading to more efficient reactions. Additional experiments were conducted on a fixed bed reactor to demonstrate that the Pt0.75Ni0.25@Mo2C/NCF catalyst effectively reduce both 4-NP and RhB dye over 15 successive runs. This work may pave the way for using PtxNiy@Mo2C/NCF catalysts in various wastewater treatment applications.