Designed Synthesis of Nanostructured Magnetic Hydroxyapatite Based Drug Nanocarrier for Anti-Cancer Drug Delivery toward the Treatment of Human Epidermoid Carcinoma

Superparamagnetic Fe3O4 nanoparticles on hydroxyapatite nanorod based nanostructures (Fe3O4/HAp) were synthesized using hydrothermal techniques at 180 °C for 12 h and were used as drug delivery nanocarriers for cancer cell therapeutic applications. The synthesized Fe3O4/HAp nanocomposites were characterized by X-ray diffraction analysis (XRD), Field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET)-analysis, and vibrating sample magnetometry (VSM). The morphologies of the Fe3O4/HAp nanocomposites show 15 nm Fe3O4 nanoparticles dispersed in the form of rods. The BET result shows that the synthesized samples have a high specific surface area of 80 m2 g−1 with mesoporous structures. Magnetic measurements revealed that the sample has high saturation magnetization of 18 emu/g with low coercivity. The Fe3O4/HAp nanocomposites had a large specific surface area (SSA), high mesoporous volume, and good magnetic property, which made it a suitable nanocarrier for targeted drug delivery systems. The chemotherapeutic agent, andrographolide, was used to investigate the drug delivery behavior of the Fe3O4/HAp nanocomposites. The human epidermoid skin cancer cells (A431) were used as the model targeting cell lines by treating with andrographolide loaded Fe3O4/HAp nanosystems and were further evaluated for their antiproliferative activities and the induction of apoptosis. Also, the present nanocomposite shows better biocompatibility, therefore it can be used as suitable drug vehicle for cancer therapy applications

Method to Model Input Voltage Ripple in Multi-Domain Fully Integrated Voltage Regulators

The on-chip power domains of the latest generation of high performance server microprocessors are generated using integrated switched mode dc-dc converters also known as Fully Integrated Voltage regulators (FIVR). The multi-domain FIVRs in the chip share a common input power supply and the input voltage ripple can be quite high when all of them switch together. The modeling of the input voltage ripple in multi-domain FIVRs using circuit simulation tools such as SPICE is a tedious task. This paper proposes a simple method to accurately model the steady state input voltage ripple using the Harmonic Domain (HD) method

Pd-Decorated 2D MXene (2D Ti₃C₂Ti_x) as a High-Performance Electrocatalyst for Reduction of Carbon Dioxide into Fuels toward Climate Change Mitigation

Palladium nanoparticles (Pd NPs) have attracted considerable attention recently for their excellent catalytic properties in various catalysis reactions. However, Pd NPs have some drawbacks, including their high cost, susceptibility to deactivation, and the possibility of poisoning by intermediate products. Herein, Pd nanoparticles with an average diameter of 6.5 nm were successfully incorporated on electronically transparent 2D MXene (Ti3C2Tix) nanosheets (Pd-MXene) by microwave irradiation. Considering the synergetic effects of ultra-fine Pd NPs, together with the intrinsic properties of 2D MXene, the obtained Pd-MXene showed a specific surface area of 97.5 m2g−1 and multiple pore channels that enabled excellent electrocatalytic activity for the reduction of CO2. Further, the 2D Pd-MXene hybrid nanocatalyst enables selective electroreduction of CO2 into selective production of CH3OH in ambient conditions by multiple electron transfer. A detailed explanation of the CO2RR mechanism is presented, and the faradic efficiency (FE) of CH3OH is tuned by varying the cell potential. Recyclability studies were conducted to demonstrate the practical application of CO2 reduction into selective production of CH3OH. In this study, metal and MXene interfaces were created to achieve a highly selective electroreduction of CO2 into fuels and other value-added chemical products

Ni_(1−x)Pd_x Alloyed Nanostructures for Electrocatalytic Conversion of Furfural into Fuels

A continuous electrocatalytic reactor offers a promising method for producing fuels and value-added chemicals via electrocatalytic hydrogenation of biomass-derived compounds. However, such processes require a better understanding of the impact of different types of active electrodes and reaction conditions on electrocatalytic biomass conversion and product selectivity. In this work, Ni1−xPdx (x = 0.25, 0.20, and 0.15) alloyed nanostructures were synthesized as heterogeneous catalysts for the electrocatalytic conversion of furfural. Various analytical tools, including XRD, SEM, EDS, and TEM, were used to characterize the Ni1−xPdx catalysts. The alloyed catalysts, with varying Ni to Pd ratios, showed a superior electrocatalytic activity of over 65% for furfural conversion after 4.5 h of reaction. In addition, various experimental parameters on the furfural conversion reactions, including electrolyte pH, furfural (FF) concentration, reaction time, and applied potential, were investigated to tune the hydrogenated products. The results indicated that the production of 2-methylfuran as a primary product (S = 29.78% after 1 h), using Ni0.85Pd0.15 electrocatalyst, was attributed to the incorporation of palladium and thus the promotion of water-assisted proton transfer processes. Results obtained from this study provide evidence that alloying a common catalyst, such as Ni with small amounts of Pd metal, can significantly enhance its electrocatalytic activity and selectivity