Centella asiatica (CA) is a medicinal plant widely used in the East, with many of its phytoconstituents remaining unexplored. In this study, compounds were extracted and identified from C. asiatica to determine its medicinal properties. Phytochemical screening was conducted on shoot, callus, and cell suspension extracts, revealing the presence of tannins, flavonoids, terpenoids, saponins, and steroids in all three cultures, with no alkaloids detected. IC50 values were determined to evaluate the antioxidant activity of the extracts, with the highest value observed for cell suspension culture (20 µg/mL), followed by shoot culture (19 µg/mL), and then callus extract (10 µg/mL), with ascorbic acid as the standard at an IC50 value of 26.25 µg/mL. Finally, density functional theory was used to analyze the structure–activity relationships of the identified compounds from C. asiatica extract. The results suggest that ultrasonic-assisted extraction yielded the highest recovery and antioxidant activity, with a scavenging activity of 79%. This study provides valuable insights into the phytochemical composition and antioxidant potential of C. asiatica, which may have implications for its use in traditional medicine and future drug development.

Selective laser sintering (SLS) is an additive manufacturing process that has shown promise in the production of medical devices, including hip cups, knee trays, dental crowns, and hearing aids. SLS-based 3D-printed dosage forms have the potential to revolutionise the production of personalised drugs. The ability to manipulate the porosity of printed materials is a particularly exciting aspect of SLS. Porous tablet formulations produced by SLS can disintegrate orally within seconds, which is challenging to achieve with traditional methods. SLS also enables the creation of amorphous solid dispersions in a single step, rather than the multi-step process required with conventional methods. This review provides an overview of 3D printing, describes the operating mechanism and necessary materials for SLS, and highlights recent advances in SLS for biomedical and pharmaceutical applications. Furthermore, an in-depth comparison and contrast of various 3D printing technologies for their effectiveness in tissue engineering applications is also presented in this review.

ZnCo₂O₄ has emerged as a promising electrode material for supercapacitor applications due to its unique properties and potential for high-performance energy storage. As a transition metal oxide, ZnCo₂O₄ offers eco-friendly characteristics and favorable diffusion properties, making it an attractive candidate for sustainable energy storage systems. However, the poor conductivity and low surface area of ZnCo₂O₄ have posed challenges for its optimal utilization in supercapacitors. Various innovative approaches have been explored to overcome these limitations, including the development of ZnCo₂O₄ with different morphologies such as core-shell and porous structures. This review work aims to provide a comprehensive analysis of diverse synthesis methods employed in recent studies, including hydrothermal growth, solvothermal synthesis, wet chemical methods, and miscellaneous synthesis techniques, each offering unique advantages and influencing the properties of the synthesized materials. The synthesis conditions, such as precursor concentrations, temperature, annealing time, and the incorporation of dopants or additional materials, were found to play a crucial role in determining the electrochemical performance of ZnCo₂O₄-based supercapacitor electrodes. Core-shell heterostructures based on ZnCo₂O₄ exhibited versatility and tunability, with the choice of shell material significantly impacting the electrochemical performance. The incorporation of different materials in composite electrodes, as well as doping strategies, proved effective in enhancing specific capacitance, stability, surface area, and charge transfer characteristics. Controlled synthesis of ZnCo₂O₄ with diverse morphologies and porosity was crucial in improving mechanical strength, surface area, and ion diffusion capabilities. The findings provide valuable insights for the design and engineering of high-performance supercapacitor electrodes based on ZnCo₂O₄, and suggest exciting avenues for further exploration, including advanced characterization techniques, novel doping strategies, scale-up of synthesis methods, and integration into practical supercapacitor devices. Continued research and development in this field will contribute to the advancement of energy storage technologies and the realization of efficient and sustainable energy storage systems.

Photocatalysts workable under direct sunlight are the safe and cost-effective option for water purification. The nanocomposites of strontium oxide and zinc oxide (SZ NCs) were synthesized using coprecipitation method. The respective precursors of SZ NCs were subjected to alkaline hydrolysis and subsequently thermally treated to yield SZ NCs. The SZ NCs with different ZnO composition was synthesized by varying the concentration of ZnO precursor from 0.2 to 1 M. The structural properties of SZ NCs evaluated using X-Ray diffraction (XRD), Thermogravimetric analysis (TGA), and Differential thermal analysis DTA). The optical properties of SZ NCs studied using ultraviolet–visible (UV–Vis) spectroscopic study. The trend observed in the intensity of XRD peaks indicated the occurrence of Zn doping in the crystalline lattice of SrO and the formation of SrO–ZnO composite. Upon incorporation of 1 M of ZnO precursor, the grain size of the SrO was decreased from 49.3 to 27.6 nm. The weight loss in the thermal analysis indicates the removal of carbonates from the sample upon heating and shows the formation of an oxide structure. UV–Vis spectra confirmed that the presence of SrO enhanced the sunlight absorption of SZ NCs. The increase in the composition of ZnO precursors increased the bandgap of SrO (2.09 eV) to the level of ZnO (3.14 eV). SZ NCs exhibited heterostructure morphology, where the nanosized domains with varying shapes (layered and rod-like) were observed. Under direct sunlight conditions, SZ NCs prepared using 1 M/0.6 M of SrO/ZnO precursors exhibited 15–20 % higher photocatalytic efficiency than neat SrO and ZnO. In precise, 1 mg of this SZ NC was degraded 98 % of malachite green dye dissolved in water (10 ppm) under direct sunlight. Additionally, the thermal stability results showed that 18 % decomposition was obtained due to the degradation impurities in SrO/ZnO catalysts and the XRD results revealed that no structural change is obtained in SrO/ZnO photocatalysts after stability test. The SZ NCs can be effectively used as safe and economic sunlight photocatalysts for water purification in remote areas without the electricity.

Sodium-ion batteries (SIBs) are among the most cost-effective and environmentally benign electrical energy storage devices required to match the needs of commercialized stationary and automotive applications. Because of its excellent chemical characteristics, infinite abundance, and low cost, the SIB is an excellent technology for grid energy storage compared with others. When used as anodes, titanium compounds based on the Ti⁴⁺/Ti³⁺ redox couple have a potential of typically 0.5–1.0 V, which is far from the potential of dangerous sodium plating (0.0–0.1 V). This ensures the operational safety of large-scale SIBs. Low lattice strain, usually associated with Ti-based materials, is also helpful for the longevity of the cycling of SIBs. Numerous Ti-based anode materials are being developed for use in SIBs. In particular, due to adequate electrode–electrolyte interaction and rapid charge transportation, hierarchical porous (HP) Ti-based anode materials were reported as having high specific capacity, current density, and cycling stability. HPTi-based anode materials for SIBs have the potential to be used in automobiles and portable, flexible, and wearable electronic devices. This review addresses recent developments in HPTiO₂-based SIBs and their preparation, properties, performance, and challenges.

Sodium-ion batteries (SIBs) have emerged as a promising alternative to lithium-ion batteries (LIBs) in sectors requiring extensive energy storage. The abundant availability of sodium at a low cost addresses concerns associated with lithium, such as environmental contamination and limited availability. However, SIBs exhibit lower energy density and cyclic stability compared to LIBs. One of the key challenges in improving the performance of SIBs lies in the electrochemical properties of the cathode materials. Among the various cathodes utilized in SIBs, sodium vanadium phosphates (NVPs) and sodium vanadium fluorophosphates (NVPFs) are particularly advantageous. These vanadium-based cathodes offer high theoretical capacity and are cost-effective. Commercialization of SIBs with NVPF cathodes has already begun. However, the poor conductivity of these cathode materials leads to a short cycle life and inferior rate performance. Various synthesis methods have been explored to enhance the conductivity, including heteroatom doping (N, S, and Co), surface modification, the fabrication of porous nanostructures, and composite formation with conductive carbon materials. In particular, cathodes with interconnected hierarchical micro- and nano-porous morphologies have shown promise. This review focuses on the diverse synthesis methods reported for preparing hierarchically porous cathodes. With increased attention, particular emphasis has been placed on carbon composites of NVPs and NVPFs. Additionally, the synthesis of vanadium pentoxide-based cathodes is also discussed.