Role of N-Acetylcysteine and Coenzyme Q10 in the Amelioration of Myocardial Energy Expenditure and Oxidative Stress, Induced by Carbon Tetrachloride Intoxication in Rats

This study is designed to evaluate the potential impact of N-acetyl cysteine (NAC) and coenzyme Q10 (CoQ10) each alone or in combination against carbon tetrachloride (CCl 4 )-induced cardiac damage in rats. Animals were treated with CCl 4 in single intraperitoneal dose of 1 mL/Kg body weight; CCl 4 -intoxicated animals were pretreated with 20 mg/kg/d NAC or pretreated with 200 mg/kg/d CoQ10 or NAC and CoQ10 with the same previously mentioned doses. Carbon tetrachloride–intoxicated rats showed a significant elevation in nitric oxide and lipid peroxides and downregulation in reduced glutathione level and calcium adenosine triphosphatase. Cardiac glycolytic enzymes levels such as lactate dehydrogenase, phosphofructokinase, and hexokinase were declined coupled with a reduction in glucose content after CCl 4 treatment. Moreover, myocardial hydroxyproline level was significantly increased after CCl 4 -treatment indicating accumulation of interstitial collagen. N-acetyl cysteine and/or CoQ10 effectively alleviated the disturbances in myocardial oxidative stress and antioxidant markers. These antioxidants effectively upregulated the reduction in cardiac energetic biomarkers due to CCl 4 treatment. N-acetyl cysteine and/or CoQ10 significantly decreased hydroxyproline level compared to that of CCl 4 -treated rats. The current data showed that the aforementioned antioxidants have a remarkable cardioprotective effect, suggesting that they may be useful as prophylactic agents against the detrimental effects of cardiotoxins

Biosynthesis, Physicochemical and Magnetic Properties of Inverse Spinel Nickel Ferrite System

Nanosized Ni ferrite has been prepared by an ecofriendly green synthesis approach based on the self-combustion method. In this route, the egg white as a green fuel was employed with two different amounts (3 and 10 mL). The XRD results display the formation of a stoichiometric NiFe2O4-type inverse spinel structure with a lattice parameter located at 0.8284 nm and 0.8322 nm. Additionally, the nickel ferrites’ typical crystallite size, as synthesized, ranged between 4 and 18 nm. Indicating the development of ferrite material, FTIR analysis shows two distinctive vibrational modes around 600 cm−1 and 400 cm−1. TEM measurements show the formation of nanosized particles with semispherical-type structure and some agglomerations. As the egg white concentration rises, the surface area, total pore volume, and mean pore radius of the material, as prepared, all decrease, and according to the surface area parameters discovered using BET analysis. Based on VSM analysis, the values of saturation magnetization are 6.6589 emu/g and 37.727 emu/g, whereas the coercivity are 159.15 G and 113.74 G. The as-synthesized Ni ferrites fit into the pseudo-single domain predicated by the squareness values (0.1526 and 0.1824). It is mentioned that increasing the egg white content would promote the magnetization of NiFe2O4

Biosynthesis, Physicochemical and Magnetic Properties of Inverse Spinel Nickel Ferrite System

Nanosized Ni ferrite has been prepared by an ecofriendly green synthesis approach based on the self-combustion method. In this route, the egg white as a green fuel was employed with two different amounts (3 and 10 mL). The XRD results display the formation of a stoichiometric NiFe2O4-type inverse spinel structure with a lattice parameter located at 0.8284 nm and 0.8322 nm. Additionally, the nickel ferrites’ typical crystallite size, as synthesized, ranged between 4 and 18 nm. Indicating the development of ferrite material, FTIR analysis shows two distinctive vibrational modes around 600 cm−1 and 400 cm−1. TEM measurements show the formation of nanosized particles with semispherical-type structure and some agglomerations. As the egg white concentration rises, the surface area, total pore volume, and mean pore radius of the material, as prepared, all decrease, and according to the surface area parameters discovered using BET analysis. Based on VSM analysis, the values of saturation magnetization are 6.6589 emu/g and 37.727 emu/g, whereas the coercivity are 159.15 G and 113.74 G. The as-synthesized Ni ferrites fit into the pseudo-single domain predicated by the squareness values (0.1526 and 0.1824). It is mentioned that increasing the egg white content would promote the magnetization of NiFe2O4

Magnetic Behavior of Virgin and Lithiated NiFe₂O₄ Nanoparticles

A series of virgin and lithia-doped Ni ferrites was synthesized using egg-white-mediated combustion. Characterization of the investigated ferrites was performed using several techniques, specifically, X-ray Powder Diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and High-resolution transmission electron microscopy (HRTEM). XRD-based structural parameters were determined. A closer look at these characteristics reveals that lithia doping enhanced the nickel ferrite lattice constant (a), unit cell volume (V), stress (ε), microstrain (σ), and dislocation density (δ). It also enhanced the separation between magnetic ions (LA and LB), ionic radii (rA, rB), and bond lengths (A-O and B-O) between tetrahedral (A) and octahedral (B) locations. Furthermore, it enhanced the X-ray density (Dx) and crystallite size (d) of random spinel nickel ferrite displaying opposing patterns of behavior. FTIR-based functional groups of random spinel nickel ferrite were determined. HRTEM-based morphological properties of the synthesized ferrite were investigated. These characteristics of NiFe2O4 particles, such as their size, shape, and crystallinity, demonstrate that these manufactured particles are present at the nanoscale and that lithia doping caused shape modification of the particles. Additionally, the prepared ferrite’s surface area and total pore volume marginally increased after being treated with lithia, depending on the visibility of the grain boundaries. Last, but not least, as the dopant content was increased through a variety of methods, the magnetization of virgin nickel ferrite fell with a corresponding increase in coercivity. Uniaxial anisotropy, rather than cubic anisotropy, and antisite and cation excess defects developed in virgin and lithia-doped nickel ferrites because the squareness ratio (Mr/Ms) was less than 0.5. Small squareness values strongly recommend using the assessed ferrites in high-frequency applications

Biosynthesis Effect of Egg White on Formation and Characteristics of NiO/NiCo₂O₄ Nanocomposites

For the successful production of NiO/NiCo2O4 nanocomposites, the environmentally friendly method of egg white supplementation has been used. Several analytical techniques were employed to characterize the morphology, purity, and crystal structure of the as-prepared nanocomposites. These techniques included transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The physical adsorption and magnetic properties of the investigated composite were determined using the Brunauer–Emmett–Teller (BET) method and a vibrating-sample magnetometer (VSM), respectively. The results have shown that the as-prepared composite particles had diameters of about 10–25 nm, with uniform distribution. The XRD analysis showed that the as-synthesized composites consisted entirely of cubic structures of both NiO and spinel NiCo2O4 nanoparticles, with a space group of Fd3m. The FTIR analysis showed characteristic vibration modes related to metal oxides, confirming the formation of composites containing NiO and NiCo2O4 crystallites. The investigated composites’ saturation magnetization (MS) and coercivity (HC) were easily controllable because of the ingredients’ ferromagnetic (NiCo2O4) and antiferromagnetic (NiO) characteristics. The excellent combination of the NiO/NiCo2O4 nanocomposites’ properties is anticipated to make this system suitable for a wide range of applications

Fabrication and Characterization of W-Substituted ZnFe2O4 for Gas Sensing Applications

A sol–gel technique was successfully employed in creating pure and W-substituted zinc ferrite, with nominal compositions of ZnFe2−2xWxO4 (0.0 ≤ x ≤ 0.15). For the purposes of investigating the physical and chemical properties of the generated powders, several analytical techniques were used. In TEM images of all the compositions, mixed-shaped particles (cubic, spherical, and hexagonal) were observed. The crystallite size decreases from 82 nm (x = 0.0) to 32 nm (x = 0.15) with an increase in the W doping contents in the ZnFe2O4 lattice. The microstrain increases with increasing W doping content. Furthermore, the surface area of pure ZnFe2O4, 0.05 W-ZnFe2O4, 0.10 W-ZnFe2O4, and 0.15 W-ZnFe2O4 NPs were calculated as being 121.5, 129.1, 134.4 and 143.2 m2 g−1, respectively, with a mesoporous pore structure for all ferrite samples. The calculated BJH pore size distribution was within the range of 160 to 205 Å. All W-doped ZnFe2O4 samples show H-M loops with paramagnetic characteristics. The magnetization (M) directly increases by increasing the applied field (H) without achieving saturation up to 20 kA/m. For comparison, the magnetization at 20 kA/m gradually decreases with increasing W doping content. Among all the synthesized samples, the 0.15 W-ZnFe2O4 NPs demonstrated the highest sensitivity towards acetone gas at 350 °C