Ultrasensitive and label free electrochemical immunosensor for detection of ROR1 as an oncofetal biomarker using gold nanoparticles assisted LDH/rGO nanocomposite.

In the present article, we developed a highly sensitive label-free electrochemical immunosensor based on NiFe-layered double hydroxides (LDH)/reduced graphene oxide (rGO)/gold nanoparticles modified glassy carbon electrode for the determination of receptor tyrosine kinase-like orphan receptor (ROR)-1. In this electrochemical immunoassay platform, NiFe-LDH/rGO was used due to great electron mobility, high specific surface area and flexible structures, while Au nanoparticles were prepared and coated on the modified electrodes to improve the detection sensitivity and ROR1 antibody immobilizing (ROR1Ab). The modification procedure was approved by using cyclic voltammetry and differential pulse voltammetry based on the response of peak current to the step by step modifications. Under optimum conditions, the experimental results showed that the immunosensor revealed a sensitive response to ROR1 in the range of 0.01-1 pg mL-1, and with a lower limit of quantification of 10 attogram/mL (10 ag mL-1). Furthermore, the designed immunosensor was applied for the analysis of ROR1 in several serum samples of chronic lymphocytic leukemia suffering patients with acceptable results, and it also exhibited good selectivity, reproducibility and stability.

Sonophotocatalytic activities of FeCuMg and CrCuMg LDHs: Influencing factors, antibacterial effects, and intermediate determination.

Herein, FeCuMg and CrCuMg layered double hydroxides (LDHs) were synthesized and their sonophotocatalytic activities toward Acid blue 113 (AB113) were compared. Sonolysis alone (only ultrasound) led to the decolorization efficiency of 13.0 %. A similar result was obtained in the case of the utilization of photolysis alone using a 10-W LED lamp (13.5 %). The adsorption process of AB113 onto both compounds was not efficient to significantly remove the target contaminant. The bandgap energy of 2.54 eV and 2.41 eV was calculated for FeCuMg and CrCuMg LDHs, respectively, indicating relatively higher photocatalytic activity of Cr-incorporated LDH than FeCuMg LDH. The sonophotocatalysis of AB113 (50 mg L-1) over CrCuMg LDH (81.1 %) was more efficient than that of FeCuMg LDH (57.3 %) within the reaction time of 60 min. Intermediate byproducts of the sonophotocatalytic decomposition of organic dye over the as-synthesized tri-metal layered sonophotocatalysts were also identified. Furthermore, the antibacterial activity of both LDHs was evaluated by the CFU technique and the MBC and MIC values were determined. The antibacterial assessment confirmed the higher antibacterial activity of CrCuMg LDH than that of FeCuMg LDH against Staphylococcus aureus (S. aureus).

Synergistic enhancement in photocatalytic performance of Ce (IV) and Cr (III) co-substituted magnetite nanoparticles loaded on reduced graphene oxide sheets.

Effective utilization of visible-light by a photocatalyst is of great significance in photocatalytic processes. Herein, magnetite structure was modified by co-incorporation of Ce4+ and Cr3+ cations, and deposition on reduced graphene oxide sheets. The as-prepared Fe2.8Cr0.2O4#rGO and Fe2.5Cr0.2Ce0.3O4#rGO nanocomposites were characterized by XRD, SEM, X-ray Dot mapping, EDX, BET, DRS, XPS, FT-IR and VSM techniques and assessed for their photocatalytic performance under visible light irradiation for treatment of methylene blue. The results confirmed the central role of the incorporated Cr and Ce in improving the photocatalytic performance of magnetite through enhanced light harvesting, and the role of Ce3+/Ce4+ redox pair, and rGO sheets in extending the life span of photo-induced e-/h+. Moreover, the influence of enhancers and scavengers were evaluated and oxidation path and generated byproducts were estimated. The results established the Fe2.5Cr0.2Ce0.3O4#rGO nanocomposite as a visible-light-driven photocatalyst for effective degradation of recalcitrant compounds.

Heterogeneous sonocatalytic degradation of anazolene sodium by synthesized dysprosium doped CdSe nanostructures.

Undoped and Dy-doped CdSe nanoparticles are synthesized and then characterized by the SEM, XRD, FT-IR, XPS and BET methods, which verify successful preparation of the doped catalyst. The sonocatalytic degradation of anazolene sodium as a model azo dye is higher than sonolysis process and the 2% Dy-doped CdSe with band gap of 1.42eV exhibits the greatest sonocatalytic performance. The decolorization efficiency (DE%) of sonocatalysis with 2% Dy-doped CdSe, undoped CdSe and sonolysis after 90min of the process is 91.32%, 56.13% and 39.14%, respectively. In addition, the sonocatalytic degradation of anazolene sodium increases with enhancement of the dopant, catalyst dosage, ultrasonic power, dissolved gasses and decreasing of initial anazolene sodium concentration. Furthermore, with addition of chloroform, sulfate, chloride and ethanol as the radical scavengers, the DE% decreases indicating the controlling mechanism of free radicals for the dye degradation. Besides, the results reveal the appropriate reusability of the catalyst and various degradation by-products are identified using the GC-MS technique. Eventually, the empirical kinetic model is expanded by nonlinear regression analysis for prediction of pseudo first-order constants in various operational conditions.

Preparation of zeolite nanorods by corona discharge plasma for degradation of phenazopyridine by heterogeneous sono-Fenton-like process.

The plasma-modified clinoptilolite (PMC) nanorods were prepared from natural clinoptilolite (NC) utilizing environmentally-friendly corona discharge plasma. The PMC and NC were characterized by XRD, FT-IR, SEM, EDX, XPS and BET, which confirmed the nanocatalyst formation. The catalytic performance of the PMC in the heterogeneous sono-Fenton-like process was greater than the NC for treatment of phenazopyridine (PhP). The desired amounts were obtained for experimental parameters including initial pH (5), PMC dosage (2g/L), K2S2O8 concentration (2mmol/L), ultrasonic power (300W) and PhP concentration (10mg/L). Reactive oxygen species scavengers decreased the removal efficiency of the PhP. The treatment process followed pseudo-first order kinetic and seven degradation intermediates were identified by the GC-MS technique.