Chromatographic Methods for the Analysis of the Antipsychotic Drug Clozapine and Its Major Metabolites: A Review.

Clozapine (CLZ), a second-generation antipsychotic, can effectively reduce schizophrenia, bipolar disorder and major depression symptoms. This review provides an overview of all reported chromatographic methods (62 references) for the quantification of CLZ and its two main metabolites, norclozapine and clozapine N-oxide in pharmaceutical formulations, biological matrices and environmental samples.

Photochemical Synthesis of Noble Metal Nanoparticles: Influence of Metal Salt Concentration on Size and Distribution.

This paper explores the photochemical synthesis of noble metal nanoparticles, specifically gold (Au) and silver (Ag) nanoparticles, using a one-component photoinitiator system. The synthesis process involves visible light irradiation at a wavelength of 419 nm and an intensity of 250 mW/cm2. The radical-generating capabilities of the photoinitiators were evaluated using electron spin resonance (ESR) spectroscopy. The main objective of this study was to investigate how the concentration of metal salts influences the size and distribution of the nanoparticles. Proposed mechanisms for the photochemical formation of nanoparticles through photoinitiated radicals were validated using cyclic voltammetry. The results showed that the concentration of AgNO3 significantly impacted the size of silver nanoparticles, with diameters ranging from 1 to 5 nm at 1 wt% and 3 wt% concentrations, while increasing the concentration to 5 wt% led to an increase in the diameter of silver nanoparticles to 16 nm. When HAuCl4 was used instead of AgNO3, it was found that the average diameters of gold nanoparticles synthesized using both photoinitiators at different concentrations ranged between 1 and 4 nm. The findings suggest that variations in HAuCl4 concentration have minimal impact on the size of gold nanoparticles. The photoproduction of AuNPs was shown to be thermodynamically favorable, with the reduction of HAuCl4 to Au0 having ∆G values of approximately -3.51 and -2.96 eV for photoinitiators A and B, respectively. Furthermore, the photoreduction of Ag+1 to Ag0 was demonstrated to be thermodynamically feasible, with ∆G values of approximately -3.459 and -2.91 eV for photoinitiators A and B, respectively, confirming the effectiveness of the new photoinitiators on the production of nanoparticles. The synthesis of nanoparticles was monitored using UV-vis absorption spectroscopy, and their sizes were determined through particle size analysis of transmission electron microscopy (TEM) images.

Surface Modification of PP and PBT Nonwoven Membranes for Enhanced Efficiency in Photocatalytic MB Dye Removal and Antibacterial Activity.

In this study, we developed highly efficient nonwoven membranes by modifying the surface of polypropylene (PP) and poly(butylene terephthalate) (PBT) through photo-grafting polymerization. The nonwoven membrane surfaces of PP and PBT were grafted with poly(ethylene glycol) diacrylate (PEGDA) in the presence of benzophenone (BP) and metal salt. We immobilized tertiary amine groups as BP synergists on commercial nonwoven membranes to improve PP and PBT surfaces. In situ Ag, Au, and Au/Ag nanoparticle formation enhances the nonwoven membrane surface. SEM, FTIR, and EDX were used to analyze the surface. We evaluated modified nonwoven membranes for photocatalytic activity by degrading methylene blue (MB) under LED and sunlight. Additionally, we also tested modified membranes for antibacterial activity against E. coli. The results indicated that the modified membranes exhibited superior efficiency in removing MB from water. The PBT showed the highest efficiency in dye removal, and bimetallic nanoparticles were more effective than monometallic. Modified membranes exposed to sunlight had higher efficiency than those exposed to LED light, with the PBT/Au/Ag membrane showing the highest dye removal at 97% within 90 min. The modified membranes showed reuse potential, with dye removal efficiency decreasing from 97% in the first cycle to 85% in the fifth cycle.

Copper II Complexes Based on Benzimidazole Ligands as a Novel Photoredox Catalysis for Free Radical Polymerization Embedded Gold and Silver Nanoparticles.

The copper II complex's novel benzimidazole Schiff base ligands were manufactured and gauged as a new photoredox catalyst/photoinitiator amalgamated with triethylamine (TEA) and iodonium salt (Iod) for the polymerization of ethylene glycol diacrylate while exposed to visible light by an LED Lamp at 405 nm with an intensity of 543 mW/cm2 at 28 °C. Gold and silver nanoparticles were obtained through the reactivity of the copper II complexes with amine/Iod salt. The size of NPs was around 1-30 nm. Lastly, the high performance of copper II complexes for photopolymerization containing nanoparticles is presented and examined. Ultimately, the photochemical mechanisms were observed using cyclic voltammetry. The preparation of the polymer nanocomposite nanoparticles in situ was photogenerated during the irradiation LED at 405 nm with an intensity of 543 mW/cm2 at 28 °C process. UV-Vis, FTIR, and TEM analyses were utilized for the determination of the generation of AuNPs and AgNPs which resided within the polymer matrix.

An Ionic Supported Liquid Membrane for the Recovery of Bisphenol A from Aqueous Solution.

In this work, a flat supported liquid membrane (FSLM) was applied for the extraction of bisphenol A (BPA) from aqueous solutions, using an ionic liquid as a carrier. The liquid membrane consists of tricaprylmethylammonium chloride (aliquat 336®) diluted in 2-octanol. Furthermore, to obtain the best transport efficiency, the impacts of various experimental parameters were investigated. These parameters included aliquat 336® concentration, the concentration of BPA in the feed phase, the pH of the feed phase, the concentration of NaOH in the receiving phase, the polymeric support nature, the percentage of extractant in the organic phase, and the solvent nature. The optimum conditions of the experiment were 50% (v/v) aliquat 336®/2-octanol as the organic phase, a transport time of 8 h, and 1 × 10-2 mol L-1 NaOH as the receiving phase. The BPA was successfully recovered (the recovery percentage was about 89%). Supported liquid membrane-based aliquat 336®/2-octanol displayed an acceptable stability with re-impregnation after 5 days of operation.

Novel Copper Photoredox Catalysts for Polymerization: An In Situ Synthesis of Metal Nanoparticles.

The copper II complex (HLCuCl) carrying 2,4 dinitrophenylhydrazone (L) is synthesized and evaluated as a new photoredox catalyst/photoinitiator in combination with triethylamine (TEA) and iodonium salt (Iod) for the radical polymerization of ethylene glycol diacrylate during exposure to visible light using a photoreactor at 419 nm. The copper complex reactivity with TEA/Iod salt/gold chloride showed a good production and stability of gold nanoparticles. Finally, the high performance of Cu (II) complex for radical photopolymerization incorporating gold nanoparticles is provided. The photochemical mechanisms for the production of initiating radicals are studied using cyclic voltammetry. Polymer nanocomposites containing gold nanoparticles (Au NPs) in situ photogenerated during the irradiation process were prepared. The formation of Au NPs inside the polymer matrix was through UV-Vis and EDS/SEM analyses.

Microstructural analysis, magnetic properties, magnetocaloric effect, and critical behaviors of Ni0.6Cd0.2Cu0.2Fe2O4 ferrites prepared using the sol-gel method under different sintering temperatures.

This work focuses on the microstructural analysis, magnetic properties, magnetocaloric effect, and critical exponents of Ni0.6Cd0.2Cu0.2Fe2O4 ferrites. These samples, denoted as S1000 and S1200, were prepared using the sol-gel method and sintered separately at 1000 °C and 1200 °C, respectively. XRD patterns confirmed the formation of cubic spinel structures and the Rietveld method was used to estimate the different structural parameters. The higher sintering temperature led to an increased lattice constant (a), crystallite size (D), magnetization (M), Curie temperature (T C), and magnetic entropy change (-ΔS M) for samples that exhibited second-order ferromagnetic-paramagnetic (FM-PM) phase transitions. The magnetic entropy changed at an applied magnetic field (µ 0 H) of 5 T, reaching maximum values of about 1.57-2.12 J kg-1 K-1, corresponding to relative cooling powers (RCPs) of 115 and 125 J kg-1 for S1000 and S1200, respectively. Critical exponents (ß, γ, and δ) for samples around their T C values were studied by analyzing the M(µ 0 H, T) isothermal magnetizations using different techniques and checked by analyzing the -ΔS M vs. µ 0 H curves. The estimated values of ß and γ exponents (using the Kouvel-Fisher method) and δ exponent (from M(T C, µ 0 H) critical isotherms) were ß = 0.443 ± 0.003, γ = 1.032 ± 0.001, and δ = 3.311 ± 0.006 for S1000, and ß = 0.403 ± 0.008, γ = 1.073 ± 0.016, and δ = 3.650 ± 0.005 for S1200. Obviously, these critical exponents were affected by an increased sintering temperature and their values were different to those predicted by standard theoretical models.