In this work anti-cancer drug curcumin-loaded superparamagnetic iron oxide (Fe3O4) nanoparticles was modified by chitosan (CS). The magnetic iron oxide nanoparticles were synthesized by using reverse micro-emulsion (water-in-oil) method. The magnetic nanoparticles without loaded drug and drug-loaded magnetic nanoparticles were characterized by XRD, FTIR, TG-DTA, SEM, TEM, and VSM techniques. These nanoparticles have almost spherical shape and their diameter varies from 8 nm to 17 nm. Measurement of VSM at room temperature showed that iron oxide nanoparticles have superparamagnetic properties. In vitro drug loading and release behavior of curcumin drug-loaded CS-Fe3O4 nanoparticles were studied by using UV-spectrophotometer. In addition, the cytotoxicity of the modified nanoparticles has shown anticancer activity against A549 cell with IC50 value of 73.03 μg/ml. Therefore, the modified magnetic nanoparticles can be used as drug delivery carriers on target in the treatment of cancer cells.

We have summarized recent developments in SFN-based hybrid designs. The additional interactions, combination effects, and important changes have been analyzed and assessed for LIB, environmental monitoring, and biomedical applications.

Functional two-dimensional (2D) structured nanomaterials, e.g. graphene oxide (GO) and molybdenum disulfide (MoS2), exhibiting many advantages including large surface areas and excellent electronic/mechanical/catalytic properties, were shown to be strong candidates...

In this work, we clarify the roles of phase composition and copper loading amount on the CAP sensing performance of Cu–MoS2 nanocomposite-based electrochemical nanosensors.

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For the first time, the influences of phase purity and crystallinity on the electrochemical and electrocatalytic properties of CuCo2O4 (CCO) and CuFe2O4 (CFO)-based electrochemical sensors for the detection of chloramphenicol (CAP) are reported. A series of CCO and CFO nanoparticles were prepared by a modified coprecipitation method and then annealed at different temperatures under air (400 °C, 600 °C, 800 °C, and 1000 °C). Surface morphology, the evolution of the crystallite size, and crystalline phase transition, as well as phase purity of CCO and CFO at each annealing temperature, were characterized via different techniques. Their electrochemical properties were analyzed using cyclic voltammetry and differential pulse voltammetry measurements conducted with a PalmSens3 workstation. Results obtained show that the phase purity and crystallinity have decisive effects on their electrocatalytic activity, conductivity, and adsorption efficiency. Under an optimized condition (more namely, annealed 600 °C), both CCO and CFO samples offer high phase purity with low percent of CuO side phase (below 38%), small enough size with a large number of defects and available active sites; particularly, the cubic CFO nanoparticles are present due to its tetragonal phase transition. The modified electrodes with CCO-600 and CFO-600 exhibit a better voltammetric response, a higher synergistic electrocatalytic activity, and a greater electrochemical performance of comparing to other modified electrodes. They respond linearly to chloramphenicol (CAP) in the range from 2.5 to 50 μM. Furthermore, they display am excellent long-term stability, reproducibility, and good selectivity, as well as their capacity of detecting CAP in the real milk sample.

To enhance the performance of lithium-ion batteries, zinc oxide (ZnO) has generated interest as an anode candidate owing to its high theoretical capacity. However, because of its limitations such as its slow chemical reaction kinetics, intense capacity fading on potential cycling, and low rate capability, composite anodes of ZnO and other materials are manufactured. In this study, we introduce binary and ternary composites of ZnO with other metal oxides (MOs) and carbon-based materials. Most ZnO-based composite anodes exhibit a higher specific capacity, rate performance, and cycling stability than a single ZnO anode. The synergistic effects between ZnO and the other MOs or carbon-based materials can explain the superior electrochemical characteristics of these ZnO-based composites. This review also discusses some of their current limitations.

MgAC-Fe 3 O 4 /TiO 2 hybrid nanocomposites were synthesized in different ratios of MgAC-Fe 3 O 4 and TiO 2 precursor. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray fluorescence spectrometry (XRF), electron spin resonance spectrometry (ESR), Brunauer-Emmett-Teller (BET), photoluminescence (PL), and UV photoelectron spectroscopy (UPS) were used to characterize the nanocomposites. The increase of MgAC-Fe 3 O 4 , in the hybrid nanocomposites’ core-shell structure, led to the decrease of anatase TiO 2 peaks, thus reducing the photo-Fenton and photocatalytic activities. According to the obtained data, MgAC-Fe 3 O 4 [0.05 g]/TiO 2 showed the best photo-Fenton and photocatalytic activities, having removed ~93% of MB (photo-Fenton reaction) and ~80% of phenol (photocatalytic reaction) after 20 and 80 mins, respectively. On the pilot scale (30 L), MgAC-Fe 3 O 4 [0.05 g]/TiO 2 was completely removed after 27 and 30 hours by the photo-Fenton and photocatalytic activities, respectively. The synergistic effect gained from the combined photo-Fenton and photocatalytic activities of Fe 3 O 4 and TiO 2 , respectively, was credited for the performances of the MgAC-Fe 3 O 4 /TiO 2 hybrid nanocomposites.