Removal of phenol from aqueous solutions by magnetic oxide graphene nanoparticles modified with ionic liquids using the Taguchi optimization approach.

A magnetic graphene oxide nanocomposite modified by the ionic liquid 1-amino-3-methylimidazole chloride (LI-MGO) was prepared by the chemical coprecipitation method as a phenol adsorbent for the treatment of contaminated aqueous environments. The structure of the prepared nanocomposite was investigated using Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The prepared nanoparticles exhibited a BET (Brunauer-Emmett-Teller) specific surface area of 110.44 m2 g-1 and total pore volume of 0.2839 cm3 g-1. The results revealed that the adsorption process had the highest phenol removal percentage (95.3%) under optimum conditions (pH = 3, nanocomposite concentration = 0.04 g/l at room temperature). Kinetic studies showed a significant fit to the pseudo-second-order kinetic model (R2 > 0.9997) giving an equilibrium rate constant (K2) of 0.000119 gmg-1 min-1 for phenol loaded. The experimental adsorption data were better fitted with the Langmuir isotherm model than with the Freundlich isotherm model. To further investigate the phenol removal optimization process of the modified magnetic nanoparticles, and to determine the effect of each parameter on the adsorption process, the Taguchi optimization approach was used. The adsorption of these synthesized nanocomposites is among the low-cost, high-efficiency processes that can be used for the reduction/elimination of environmental pollutants, especially in aqueous environments.

Formulation and Physicochemical Characterization of Lycopene-Loaded Solid Lipid Nanoparticles.

PURPOSE: Lycopene belongs to the carotenoids that shows good pharmacological properties including antioxidant, anti-inflammatory and anticancer. However, as a result of very low aqueous solubility, it has a limited systemic absorption, following oral administration. METHODS: Here, we prepared a stable lycopene-loaded solid lipid nanoparticles using Precirol® ATO5, Compritol 888 ATO and myristic acid by hot homogenization method with some modification. The size and morphological characteristics of nanoparticles were evaluated using Scanning Electron Microscopy (SEM). Moreover, zeta potential and dispersity index (DI) were measured using zeta sizer. In addition, encapsulation efficiency (EE%), drug loading (DL) and cumulative drug release were quantified. RESULTS: The results showed that the size and DI of particles was generally smaller in the case of SLNs prepared with precirol when compared to SLNs prepared with compritol. Scanning electron microscopy (SEM) and particle size analyses showed spherical SLNs (125 ± 3.89 nm), monodispersed distribution, and zeta potential of -10.06 ± 0.08 mV. High EE (98.4 ± 0.5 %) and DL (44.8 ± 0.46 mg/g) were achieved in the case of nanoparticles prepared by precirol. The stability study of the lycopene-SLNs in aqueous medium (4 °C) was showed that after 2 months there is no significant differences seen in size and DI compared with the fresh formulation. CONCLUSION: Conclusively, in this investigation we prepared a stable lycopene-SLNs with good physicochemical characteristic which candidate it for the future in vivo trials in nutraceutical industries.