The encapsulation of bioactive compounds using proteins as wall materials has emerged as an effective strategy to enhance their stability, bioavailability, and controlled release. Proteins offer unique functional properties, including amphiphilic behavior, gel-forming ability, and interactions with bioactives, making them ideal candidates for encapsulation. Animal-derived proteins, such as whey and casein, exhibit superior performance in stabilizing lipophilic compounds, whereas plant proteins, including soy and pea protein, demonstrate greater affinity for hydrophilic bioactives. Advances in protein modification and the formation of protein–polysaccharide complexes have further improved encapsulation efficiency, particularly for heat- and pH-sensitive compounds. This review explores the physicochemical characteristics of proteins used in encapsulation, the interactions between proteins and bioactives, and the main encapsulation techniques, including spray drying, complex coacervation, nanoemulsions, and electrospinning. Furthermore, the potential applications of encapsulated bioactives in functional foods, pharmaceuticals, and nutraceuticals are discussed, highlighting the role of emerging technologies in optimizing delivery systems. Understanding the synergy between proteins, bioactives, and encapsulation methods is essential for developing more stable, bioavailable, and sustainable functional products.

Free-standing copper oxide (Cu2O)-copper hydroxide (Cu(OH)2) nanocomposites with enhanced catalytic and antibacterial functionalities were synthesized on copper mesh using a green method based on spinach leaf extract and glycerol. EDX, SEM, and TEM analyses confirmed the chemical composition and morphology. The resulting Cu2O-Cu(OH)2@Cu mesh exhibited notable hydrophobicity, achieving a contact angle of 137.5° ± 0.6, and demonstrated the ability to separate thick oils, such as HD-40 engine oil, from water with a 90% separation efficiency. Concurrently, its photocatalytic performance was evaluated by the degradation of methylene blue (MB) under a weak light intensity of 5 mW/cm2, achieving 85.5% degradation within 30 min. Although its application as a functional membrane in water treatment may raise safety concerns, the mesh showed significant antibacterial activity against both Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria under both dark and light conditions. Using the disk diffusion method, strong bacterial inhibition was observed after 24 h of exposure in the dark. Upon visible light irradiation, bactericidal efficiency was further enhanced—by 17% for S. aureus and 2% for E. coli. These findings highlight the potential of the Cu2O-Cu(OH)2@Cu microfibers as a multifunctional membrane for industrial wastewater treatment, capable of simultaneously removing oil, degrading organic dyes, and inactivating pathogenic bacteria through photo-assisted processes.

In this work, we present the development and validation of an automated system for the Successive Ionic Layer Adsorption and Reaction (SILAR) method, aimed at depositing Cu2ZnSnS4 (CZTS) thin films. The system is based on a Raspberry Pi Pico microcontroller programmed in Micro-Python (Thonny 4.0.2), allowing precise control over immersion sequences, timing intervals, and substrate positioning along two degrees of freedom. Automation enhances reproducibility, safety, and reduces human error compared with manual operation. CZTS films were deposited on borosilicate glass and optically and structurally characterized. A gradual darkening of the films with increasing deposition cycles indicates controlled material accumulation. X-ray diffraction (XRD) and Raman spectroscopy confirmed the presence of CZTS phases, although with a partially amorphous structure. The estimated optical bandgap of ~1.34 eV is consistent with photovoltaic applications. These results validate the functionality of the automated SILAR platform for repeatable and scalable thin-film fabrication, offering a low-cost alternative for producing semiconductor absorber layers in solar energy technologies.

Microfluidic devices are tiny tools used to manipulate small volumes of liquids in various fields. However, these devices frequently require additional equipment to control fluid flow, increasing the cost and complexity of the systems and limiting their potential for widespread use in low-resource biomedical applications. Here, we present a cost-effective and simple fabrication method for PMMA microfluidic chips using laser cutting technology, along with a low-cost and open-source peristaltic pump constructed with common hardware. The pump, programmed with an Arduino microcontroller, offers precise flow control in microfluidic devices for small volume applications. The developed application for controlling the peristaltic pump is user-friendly and open source. The microfluidic chip and pump system was tested using Jurkat cells. The cells were cultured for 24 h in conventional cell culture and a microfluidic chip. The LDH assay indicated higher cell viability in the microfluidic chip (111.99 ± 7.79%) compared to conventional culture (100 ± 15.80%). Apoptosis assay indicated 76.1% live cells, 18.7% early apoptosis in microfluidic culture and 99.2% live cells, with 0.5% early apoptosis in conventional culture. The findings from the LDH and apoptosis analyses demonstrated an increase in both cell proliferation and cellular stress in the microfluidic system. Despite the increased stress, the majority of cells maintained membrane integrity and continued to proliferate. In conclusion, the chip fabrication method and the pump offer advantages, including design flexibility and precise flow rate control. This study promises solutions that can be tailored to specific needs for biomedical applications.

Thermal energy storage offers a viable solution for managing intermediate energy availability challenges. Phase change materials (PCMs) have been extensively studied for their capacity to store thermal energy when available and release it when needed, maintaining a narrow temperature range. However, effective utilization of PCMs requires its proper encapsulation in most applications. In this study, microcapsules containing Rubitherm®(RT) 21 PCM (Tpeak = 21 °C, ΔH = 140 kJ/kg), which is suitable for buildings, were synthesized using a suspension polymerization technique at different operating temperatures (45–75 °C). Two different water-insoluble thermal initiators were evaluated: 2,2-Azobis (2,4-dimethyl valeronitrile) (Azo-65) and benzoyl peroxide (BPO). The prepared microcapsules were characterized using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), particle size distribution (PSD), scanning electron microscope (SEM), and optical microscopy (OM). Additionally, the microcapsules were subjected to multiple melting and freezing cycles to assess their thermal reliability and performance stability. DSC results revealed that the microcapsules using BPO exhibited a latent heat of melting comparable to those produced with Azo-65 at an operating temperature of 75 °C. However, the onset crystallization temperature for the BPO-encapsulated PCMs was approximately 2 °C lower than that of the Azo-65-encapsulated PCMs. The greatest latent heat of melting, 107.76 J/g, was exhibited by microcapsules produced at 45 °C, representing a PCM content of 82 wt. %. On the other hand, microcapsules synthesized at 55 °C and 75 °C showed latent heats of 96.02 J/g and 95.66 J/g, respectively. The degree of supercooling for PCM microcapsules was reduced by decreasing the polymerization temperature, with the lowest supercooling observed for microcapsules synthesized at 45 °C. All microcapsules exhibited a monodisperse and narrow PSD of ~10 µm, indicating uniformity in microcapsule size and demonstrating that temperature variations had no significant impact on the particle size distribution. Future research should focus on low-temperature polymerization with extended polymerization times.

In recent years, various types of sensors have been developed at both millimeter (mm) and micrometer (µm) scales for numerous biomedical applications. Each design has its own advantages and limitations. This study compares the electrical characteristics and sensitivity of millimeter- and micrometer-scale sensors, emphasizing the superior performance of millimeter-scale designs for detecting type-2 diabetes. Elevated glucose levels in type-2 diabetes alter the complex permittivity of red blood cells (RBCs), affecting their rheological and electrical properties, such as viscosity, volume, relative permittivity, dielectric loss, and AC conductivity. These alterations may manifest as a unique bio-impedance signature, offering a diagnostic topology for diabetes. In view of this, various concentrations (ranging from 10% to 100%) of 400 µL of normal and diabetic RBCs suspended in phosphate-buffered saline (PBS) solution are examined to record the changes in bio-impedance signatures across a spectrum of frequencies, ranging from 1 MHz to 10 MHz. In this study, simulations are performed using the finite element method (FEM) with COMSOL Multiphysics® to analyze the electrical behavior of the sensors at both millimeter (mm) and micrometer (µm) scales. These simulations provide valuable insights into the performance parameters of the sensors, aiding in the selection of the most effective design by using this topology.

The catalytic conversion of carbon dioxide (CO2) into carbon monoxide (CO) via the reverse water–gas shift (RWGS) reaction offers a promising pathway toward a sustainable carbon cycle. However, the competing Sabatier reaction presents a significant challenge, underscoring the need for highly efficient catalysts. In this study, we developed a novel catalyst comprising cobalt-oxide-supported nickel-hydroxide nanoparticles (denoted as Co@Ni). This catalyst achieved a remarkable CO production yield of ~5144 μmol g−1 at 573 K, with a CO selectivity of 77%. These values represent 30% and 70% improvements over carbon-supported Ni(OH)2 (Ni-AC) and CoO (Co-AC) nanoparticles, respectively. Comprehensive physical characterizations and electrochemical analyses reveal that the exceptional CO yield of the Co@Ni catalyst stems from the synergistic electronic interactions between adjacent active sites. Specifically, cobalt-oxide domains act as electron donors to Ni sites, facilitating efficient H2 splitting. Additionally, the oxygen vacancies in cobalt oxide enhance CO2 adsorption and promote subsequent dissociation. These findings provide critical insights into the design of highly efficient and selective catalysts for the RWGS reaction, paving the way for advancements in sustainable carbon utilization technologies.

Recently, there have been several scientific breakthroughs in the fields of micro- and nanoscience [...]

Carbon dots (C-Dots) have garnered significant attention in various fields, including biomedical applications, photocatalysis, sensing, and optoelectronics, due to their high luminescence, biocompatibility, and ease of functionalization. However, concerns regarding their potential toxicity persist. Conventional synthesis methods for C-Dots often require long reaction times, high pressures, expensive equipment, extreme temperatures, and toxic reagents. In contrast, microwave irradiation provides a rapid, cost-effective, and scalable alternative for the synthesis of high-quality C-Dots. In this study, we report the single-step, 3-min synthesis of water-stable carbon dots at 100 °C, 120 °C, and 140 °C using microwave irradiation. Particle stability was achieved through polyethyleneimine (PEI) functionalization. The toxicity of the synthesized carbon dots was evaluated in marine crustaceans, revealing that C-Dots with an estimated size below 10 nm did not exhibit toxicity after 24 and 48 h of exposure. These findings demonstrate the potential of microwave-synthesized carbon dots as non-toxic, water-stable nanomaterials for environmental and biomedical applications.

The global rise in diabetes has highlighted the urgent need for continuous, non-invasive health monitoring solutions. Traditional glucose monitoring methods, which are invasive and often inconvenient, have created a demand for alternative technologies that can offer comfort, accuracy, and real-time data. In this study, the development of a textile-based organic electrochemical transistor (OECT) is presented, designed for non-invasive glucose sensing, aiming to integrate this technology seamlessly into everyday clothing. The document details the design, optimization, and testing of a one-component textile-based OECT, featuring a porous PEDOT:PSS structure and a glucose oxidase-modified electrolyte for effective glucose detection in sweat. The research demonstrates the feasibility of using this textile-based OECT for non-invasive glucose monitoring, with enhanced sensitivity and specificity achieved through the integration of glucose oxidase within the electrolyte and the innovative porous PEDOT:PSS design. These findings suggest a significant advancement in wearable health monitoring technologies, providing a promising pathway for the development of smart textiles capable of non-invasively tracking glucose levels. Future work should focus on refining this technology for clinical use, including individual calibration for accurate blood glucose correlation and its integration into commercially available smart textiles.