Cytotoxic activity of bimetallic Ag@Se green synthesized nanoparticles using Jerusalem Thorn (Parkinsonia aculeata).

Introduction: The process of green synthesis of metal nanoparticles is considered to be eco-friendly and cost-effective. Methods: In this study, bimetallic Ag@Se-P and Ag@Se-S nanoparticles were synthesized successfully using Parkinsonia aculeata aerial parts and seed extracts. The phytochemical contents in P. aculeata aerial parts and seed aqueous extract serve as reducing and stabilizing capping agents without the need for any chemical stabilization additive in the synthesis of bimetallic nanoparticles. Result and Discussion: The obtained results from UV-vis spectrophotometry, scanning electron microscopy (SEM), X-ray powder diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Fourier-transform infrared spectroscopy (FT-IR) confirmed the successful synthesis of bimetallic nanoparticles with cluster irregular spherical morphology, crystalline nature, and average particle sizes of 17.65 and 24.36 nm for Ag@Se-S and Ag@Se-P, respectively. The cytotoxicity assessment of greenly synthesized nanomaterials using seed and plant extracts showed cell inhibition >50 µg/mL. Ag@Se-S and Ag@Se-P seed and plant extracts significantly reduced LPS-induced inflammation, which was assessed by NO and cytokines IL-1ß, IL-6, and TNF-α. The mRNA and protein expression levels of phosphoinositide 3 kinase (PI3K) and nuclear factor kappa B (NFkB) were significantly overexpressed in LPS-induced RAW 264.7 cell lines. Ag@Se-S and Ag@Se-P downregulated the expression of PI3K and NFkB in LPS-induced cell models.

Photocatalytic removal of imidacloprid containing frequently applied insecticide in agriculture industry using Co3O4 modified MoO3 composites.

Water pollution caused by the frequent utilization of pesticides in the agriculture industry is one of the major environmental concerns that require proper attention. In this context, the photocatalytic removal of pesticides from contaminated water in the presence of metallic oxide photocatalysts is quite in approach. In the present study, Orthorhombic MoO3 has been modified with varying amount of cobalt oxide through wet impregnation for the removal of imidacloprid and imidacloprid-containing commercially available insecticide. The solid-state absorption response and band gap evaluation of synthesized composites revealed a significant extension of absorption cross-section and absorption edge in the visible region of the light spectrum than pristine MoO3. The indirect band gap energy varied from ∼2.88 eV (MoO3) to ∼2.15 eV (10% Co3O4-MoO3). The role of Co3O4 in minimizing the photo-excitons' recombination in MoO3 was studied using photoluminescence spectroscopy. The orthorhombic shape of MoO3 was confirmed through X-ray diffraction analysis and scanning electron microscopy. Moreover, the presence of distinct absorption edges and diffraction peaks corresponding to Co3O4 and MoO3 in absorption spectra and XRD patterns, respectively verified the composite nature of 10% Co3O4-MoO3. The photocatalytic study under natural sunlight irradiation showed higher photocatalytic removal (∼98%) of imidacloprid with relatively higher rate by 10% Co3O4-MoO3 composite among all contestants. Furthermore, the photocatalytic removal (∼93%) of commercially applied insecticide, i.e., Greeda was also explored.

Catalytic Reduction of p-Nitrophenol on MnO2/Zeolite -13X Prepared with Lawsonia inermis Extract as a Stabilizing and Capping Agent.

p-nitrophenol (pNP) is a highly toxic organic compound and is considered carcinogenic and mutagenic. It is a very stable compound with high resistance to chemical or biological degradation. As a result, the elimination of this pollutant has been very challenging for many researchers. Catalytic reduction is one of the most promising techniques, if a suitable catalyst is developed. Thus, this work aims to prepare an eco-friendly catalyst via a simple and low-cost route and apply it for the conversion of the toxic p-nitrophenol (pNP) into a non-toxic p-aminophenol (pAP) that is widely used in industry. Manganese oxide was prepared in an environmentally friendly manner with the aid of Lawsonia inermis (henna) extract as a stabilizing and capping agent and loaded on the surface of 13X molecular sieve zeolite. The UV-Vis spectrum, EDS, and XRD patterns confirmed the formation of the pure MnO2 loaded on the zeolite crystalline network. The TGA analysis showed that the samples prepared by loading MnO2 on zeolite (Mn2Z, Mn3Z, and Mn4Z) lost more mass than pure MnO2 (Mn) or zeolite (Z), which is mainly moisture adsorbed on the surface. This indicates a better dispersion of MnO2 on the surface of zeolite compared to pure MnO2, and thus a higher number of active adsorption sites. SEM images and EDS confirmed the dispersion of the MnO2 on the surface of the zeolite. Results showed a very fast reduction rate, following the order Mn2Z > Mn3Z > Mn4Z > Mn > Z. With sample Mn2Z, 96% reduction of pNP was achieved in 9 min and 100% in 30 min. For Mn3Z, Mn4Z, and Mn, 98% reduction was achieved in 20 min and 100% in 30 min. Zeolite was the slowest, with only a 40% reduction in 30 min. Increasing the amount of zeolite in the synthesis mixture resulted in lower reduction efficiency. The kinetic study indicated that the reduction of p-nitrophenol on the surface of the prepared nanocomposite follows the pseudo-first-order model. The results show that the proposed nanocomposite is very effective and very promising to be commercially applied in water treatment, due to its low cost, simple synthesis procedure, and reusability.

Facile Green Synthesis of Ni(OH)2@Mn3O4 Cactus-Type Nanocomposite: Characterization and Cytotoxicity Properties.

In the present work, the facile eco-friendly synthesis and evaluation of the anti-tumor activity of Ni(OH)2@Mn3O4 nanocomposite were carried out. The synthesis of Ni(OH)2@Mn3O4 nanocomposite from chia-seed extract was mediated by sonication. The obtained materials were characterized by different spectroscopic techniques such as transmission electron microscopy (TEM), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible (UV-Vis), and Fourier transform infrared (FT-IR) spectroscopies. The results of XRD, SEM, EDS, TEM, FT-IR, and UV-Vis analysis indicate the successful manufacturing of a crystalline, cactus-type Ni(OH)2@Mn3O4 nanocomposite of 10.10 nm average particle size. XPS analysis confirms that the synthesized materials consist mainly of Ni2+, Mn2+, and Mn3+. The antitumor activity of the nanocomposite was tested against a breast cancer (MCF-7) cell line. The results showed Ni(OH)2@Mn3O4 nanocomposite possesses insignificant cytotoxicity. The cell-death percentage was 34% at a 100 ppm concentration of Ni(OH)2@Mn3O4 nanocomposite. The obtained results imply that the synthesized nanocomposite could be suitable and safe for drug delivery and water treatment.

Sonochemical-Assisted Biogenic Synthesis of Theophrasite ß-Ni(OH)2 Nanocluster Using Chia Seeds Extract: Characterization and Anticancer Activity.

Theophrasite ß-Ni(OH)2 nanocluster were fabricated via the sonochemical-assisted biogenic method using chia seeds extract as a reducing and stabilizing agent. The optical and morphological feature of the synthesized nanocluster was characterized using UV-Vis, FTIR, FE-SEM-EDS, HR-TEM, DLS, XPS, and XRD analysis. According to FE-SEM and HR-TEM images of the synthesized materials, ß-Ni(OH)2 nanocluster illustrates the hexagonal particle shape with an average size of 5.8 nm, while the EDS results confirm the high purity of the synthesized nanocluster. Moreover, the XRD pattern of the synthesized materials shows typical peaks that match the reference pattern of the Theophrasite form of ß-Ni(OH)2 with a hexagonal crystal system. The XPS analysis illustrates that the prepared samples exhibit both Ni2+ and Ni3+ with the predominance of Ni2+ species. Additionally the in-vitro cytotoxic activity of ß-Ni(OH)2 nanocluster is tested against the MCF7 cell lines (breast cancer cells). The MTT assay results proved that the synthesized ß-Ni(OH)2 nanocluster has potent cytotoxic activity against breast cancer cell lines (IC50: 62.7 µg/mL).

Acacia nilotica Pods' Extract Assisted-Hydrothermal Synthesis and Characterization of ZnO-CuO Nanocomposites.

This work represents a novel combination between Acacia nilotica pods' extract and the hydrothermal method to prepare nanoparticles of pure zinc oxide and pure copper oxide and nanocomposites of both oxides in different ratios. Five samples were prepared with different ratios of zinc oxide and copper oxide; 100% ZnO (ZC0), 75% ZnO: 25% CuO (ZC25), 50% ZnO: 50% CuO (ZC50), 25% ZnO: 75% CuO (ZC75), and 100% CuO (ZC100). Several techniques have been applied to characterize the prepared powders as FTIR, XRD, SEM, and TEM. The XRD results confirm the formation of the hexagonal wurtzite phase of zinc oxide and the monoclinic tenorite phase of copper oxide. The microscopy results show the formation of a heterostructure of nanocomposites with an average particle size of 13-27 nm.

Phyto-Assisted Assembly of Metal Nanoparticles in Chitosan Matrix Using S. argel Leaf Extract and Its Application for Catalytic Oxidation of Benzyl Alcohol.

The design and synthesis of eco-friendly solid-supported metal nanoparticles with remarkable stability and catalytic performance have gained much attention for both industrial and environmental applications. This study provides a novel, low-cost, simple, and eco-friendly approach for decorating cross-linked chitosan with gold nanoparticles (AuNPs), greenly prepared with Solenostemma argel (S. argel) leaf extract under mild conditions. Glutaraldehyde-modified chitosan beads were used to coordinate with Au(III) ions and act as stabilizing agents, and S. argel leaf extract was used as a cost-effective phyto-reducing agent to reduce gold ions to elemental Au nanoparticles. The successful cross-linking of chitosan with glutaraldehyde, the coordination of Au(III) ions into the chitosan matrix, and the phytochemical reduction of Au(III) to Au nanoparticles were investigated via FT-IR spectroscopy. The obtained Au nanoparticles have a uniform spherical shape and size <10 nm, as confirmed by both X-ray diffraction (XRD) (~8.8 nm) and TEM (6.0 ± 3 nm). The uniformity of the AuNPs' size was confirmed by Scanning Electron Microscopy (SEM) and Transition Electron Microscopy (TEM). The powder X-ray diffraction technique showed crystalline AuNPs with a face-centered cubic structure. The elemental analysis and the Energy Dispersive Spectroscopy (EDS) analysis both confirmed the successful integration of Au nanoparticles with the chitosan network. The catalytic activity of this highly stable nanocomposite was systematically investigated via the selective oxidation of benzyl alcohol to benzaldehyde. Results showed a remarkable conversion (97%) and excellent selectivity (99%) in the formation of benzaldehyde over other side products.

Green Synthesis of an Activated Carbon-Supported Ag and ZnO Nanocomposite for Photocatalytic Degradation and Its Antibacterial Activities.

In this study Ag nanoparticles (AgNPs), ZnO nanoparticles (ZnONPs), and Ag/ZnO nanocomposites were greenly synthesized and loaded on activated carbon via three different routes: simple impregnation, successive precipitation, and co-precipitation. Neem leaf extract was used as a reducing and stabilizing agent. The morphological and structural properties of the synthesized nanocomposites have been examined using different analytical techniques such as XRD, SEM, FTIR, and UV. The antibacterial and catalytic activity of the synthesized nanocomposites were examined and compared. The results showed that AgNPs loaded on activated carbon (Ag/AC) has the best catalytic activity compared to the other nanocomposites, which is attributed to the good dispersal of AgNPs on the surface of activated carbon. Furthermore, AgNPs showed the best antibacterial effect on eight out of 16 tested pathogens. Results also showed that the order of precipitation is an important factor, as both antibacterial activities and photodegradation activities were higher for ZnO/Ag/AC than Ag/ZnO/AC. Furthermore, the co-precipitation method was shown to be better than the successive precipitation method for 4-nitrophenol photodegradation and 14 out of the 16 antibacterial tests performed.