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Contemporary technological and industrial advancements have led to increased reliance on chemicals for product innovation, leading to heightened contamination of water sources by traditional pollutants (organic dyes, heavy metals) and disease-causing microorganisms. Wastewater treatment processes now reveal “emerging pollutants”, including pharmaceuticals, endocrine disruptors, and agricultural chemicals. While some are benign, certain emerging pollutants can harm diverse organisms. Researchers seek cost-effective water purification methods that completely degrade pollutants without generating harmful by-products. Semiconductor-based photocatalytic degradation, particularly using titanium dioxide (TiO2), is popular for addressing water pollution. This study focuses on recent applications of TiO2 nanostructures in photocatalysis for eliminating various water pollutants. Structural modifications, like doping and nanocomposite formation, enhance photocatalyst performance. The study emphasizes photocatalytic elimination mechanisms and comprehensively discusses factors impacting both the mechanism and performance of nano-TiO2-based photocatalysts. Characteristics of TiO2, such as crystal structure and energy band-gap, along with its photocatalytic activity mechanism, are presented. The review covers the advantages and limitations of different TiO2 nanostructure production approaches and addresses potential toxicity to human health and the environment. In summary, this review provides a holistic perspective on applying nano-TiO2 materials to mitigate water pollution.

In recent times, there has been considerable interest among researchers in magnesium oxide (MgO) nanoparticles, due to their excellent biocompatibility, stability, and diverse biomedical uses, such as antimicrobial, antioxidant, anticancer, and antidiabetic properties, as well as tissue engineering, bioimaging, and drug delivery applications. Consequently, the escalating utilization of magnesium oxide nanoparticles in medical contexts necessitates the in-depth exploration of these nanoparticles. Notably, existing literature lacks a comprehensive review of magnesium oxide nanoparticles’ synthesis methods, detailed biomedical applications with mechanisms, and toxicity assessments. Thus, this review aims to bridge this gap by furnishing a comprehensive insight into various synthetic approaches for the development of MgO nanoparticles. Additionally, it elucidates their noteworthy biomedical applications as well as their potential mechanisms of action, alongside summarizing their toxicity profiles. This article also highlights challenges and future prospects for further exploring MgO nanoparticles in the biomedical field. Existing literature indicates that synthesized magnesium oxide nanoparticles demonstrate substantial biocompatibility and display significant antibacterial, antifungal, anticancer, and antioxidant properties. Consequently, this review intends to enhance readers’ comprehension regarding recent advancements in synthesizing MgO nanoparticles through diverse approaches and their promising applications in biomedicine.

The Enhanced Permeability and Retention (EPR) effect is a key mechanism for passive tumor targeting, which involves the selective accumulation of therapeutic nanoparticles in tumors due to their unique vascular characteristics. While previous reviews have explored this phenomenon, the present review offers a comprehensive, multidisciplinary approach, highlighting recent advancements in strategies to enhance the EPR effect, as well as novel insights into the role of tumor microenvironment heterogeneity and the multifaceted approaches to overcome EPR-related challenges. This review provides a detailed analysis of the latest developments in nanocarriers’ design, including size, shape, and surface modifications, as well as cutting-edge multi-stage drug delivery systems. Furthermore, the integration of physical, pharmacological, and combinatory therapies to optimize the EPR effect is also discussed, aiming to improve the clinical translation of nanomedicines. Unlike other reviews, this work emphasizes the dynamic interaction between the tumor microenvironment and the vascular network, which remains underexplored in the current literature. In addition, specific clinical trials’ outcomes are highlighted and future directions to address existing limitations are proposed, offering a clearer roadmap regarding clinical applications in cancer therapy.

The increasing global requirement for clean and safe drinking water has necessitated the development of efficient methods for the elimination of organic contaminants, especially dyes, from wastewater. This study reports the synthesis of magnesium oxide (MgO) nanoparticles via a simple precipitation approach and their thorough characterization using various techniques, including XRD, FT-IR, XPS, TGA, DLS, and FESEM. Synthesized MgO nanoparticles’ photocatalytic effectiveness was evaluated towards rhodamine B and rhodamine 6G degradation under both UV and visible light irradiation. The results indicated that the MgO nanoparticles possess a face-centered cubic structure with enhanced crystallinity and purity, as well as an average crystallite size of approximately 3.20 nm. The nanoparticles demonstrated a significant BET surface area (52 m2/g) and a bandgap value equal to 5.27 eV. Photocatalytic experiments indicated complete degradation of rhodamine B dye under UV light within 180 min and 83.23% degradation under visible light. For rhodamine 6G, the degradation efficiency was 92.62% under UV light and 38.71% under visible light, thus verifying the MgO catalyst’s selectivity towards degradation of rhodamine B dye. Also, reusability of MgO was investigated for five experimental photocatalytic trials with very promising results, mainly against rhodamine B. Scavenging experiments confirmed that •OH radicals were the major reactive oxygen species involved in the photodegradation procedure, unraveling the molecular mechanism of the photocatalytic efficiency of MgO.

Over the last ten years, there has been a growing interest in metal–organic frameworks (MOFs), which are a unique category of porous materials that combine organic and inorganic components. MOFs have garnered significant attention due to their highly favorable characteristics, such as environmentally friendly nature, enhanced surface area and pore volume, hierarchical arrangements, and adjustable properties, as well as their versatile applications in fields such as chemical engineering, materials science, and the environmental and biomedical sectors. This article centers on examining the advancements in using MOFs for environmental remediation purposes. Additionally, it discusses the latest developments in employing MOFs as potential tools for disease diagnosis and drug delivery across various ailments, including cancer, diabetes, neurological disorders, and ocular diseases. Firstly, a concise overview of MOF evolution and the synthetic techniques employed for creating MOFs are provided, presenting their advantages and limitations. Subsequently, the challenges, potential avenues, and perspectives for future advancements in the utilization of MOFs in the respective application domains are addressed. Lastly, a comprehensive comparison of the materials presently employed in these applications is conducted.

Semiconductor photocatalysts, particularly ZnO nanoparticles, were synthesized via the precipitation method using four different precursors (zinc acetate/zinc nitrate/zinc sulfate/zinc chloride) and compared, according to their optical, structural, photocatalytic, and anticancer properties. The materials were characterized via X-ray Diffraction method (XRD), micro-Raman, Fourier Transform Infrared Spectroscopy (FT-IR), Brunauer–Emmett–Teller (BET), Dynamic Light Scattering (DLS), and Field Emission Scanning Electron Microscope (FESEM) analysis. Photocatalysis was conducted under UV and visible light irradiation, using Rhodamine B as the organic pollutant. It was observed that the highest photocatalysis efficiency was obtained by the nanoparticles synthesized from the zinc acetate used as precursor material. A cell-dependent anticancer efficiency of the tested ZnO nanoparticles was also observed, that was also attributed to the different precursors and the synthesis method, revealing that the nanoparticles that were synthesized from zinc acetate were more bioactive among the four tested precursors. Overall, the data revealed that both the enhanced photocatalytic and biological activity of ZnO nanoparticles derived from zinc acetate precursor could be attributed to the reduced crystalline size, increased surface area, as well as the observed hexagonal crystalline morphology.

Organic pollutants found in industrial effluents contribute to significant environmental risks. Degradation of these pollutants, particularly through photocatalysis, is a promising strategy ensuring water purification and supporting wastewater treatment. Thus, photodegradation of rhodamine B and phenol under visible-light irradiation using TiO2/SiO2 composite nanoparticles was within the main scopes of this study. The nanocomposite was synthesized through a wet impregnation method using TiO2 and SiO2 nanopowders previously prepared via a facile sol–gel approach and was fully characterized. The obtained results indicated a pure anatase phase, coupled with increased crystallinity (85.22%) and a relative smaller crystallite size (1.82 nm) in relation to pure TiO2 and SiO2 and an enhanced specific surface area (50 m2/g) and a reduced energy band gap (3.18 eV). Photodegradation of rhodamine B upon visible-light irradiation was studied, showing that the TiO2/SiO2 composite reached total (100%) degradation within 210 min compared to pure TiO2 and SiO2 analogues, which achieved a ≈45% and ≈43% degradation rate, respectively. Similarly, the composite catalyst presented enhanced photocatalytic performance under the same irradiation conditions towards the degradation of phenol, leading to 43.19% degradation within 210 min and verifying the composite catalyst’s selectivity towards degradation of rhodamine B dye as well as its enhanced photocatalytic efficiency towards both organic compounds compared to pure TiO2 and SiO2. Additionally, based on the acquired experimental results, ●O2−, h+ and e− were found to be the major reactive oxygen species involved in rhodamine B’s photocatalytic degradation, while ●OH radicals were pivotal in the photodegradation of phenol under visible irradiation. Finally, after the TiO2/SiO2 composite catalyst was reused five times, it indicated negligible photodegradation efficiency decrease towards both organic compounds.

Clays have been used widely as sorbents of potentially toxic elements, especially Pb. However, their adsorption efficiency has been studied mostly under static experimental conditions, which are labour-intensive. In this study, dynamic adsorption experiments were established using micro-columns to assess the adsorption behaviour of natural Fe-Mg-rich clays for Pb ions by varying the inlet solution pH, Pb concentration and flow rate. The clays, consisting of varying amounts of palygorskite and Fe-smectite, were diluted with quartz (Qz) sand to enhance their permeability. Greater adsorption capacity was observed for the mixed palygorskite/Fe-smectite-rich clay beds (45.2±0.01 mg g-1) followed by the Fe-smectite-rich (35.7±0.07 mg g-1) and palygorskite-rich (20.0±0.03 mg g-1) clay beds. The results indicated that the greater adsorption efficiency of palygorskite/Fe-smectite-rich clays could be attributed to synergistic effects due to the coexistence of palygorskite and Fe-smectite clay phases, which have distinct physicochemical characteristics. Moreover, the results obtained showed good agreement with the static experiments, implying that the use of micro-columns could describe adsorption adequately over shorter experimental times.

Zinc oxide (ZnO) possesses exceptional potential to be utilized in water and wastewater treatment applications, either as a photocatalyst or in membrane incorporation. In the present study, ZnO nanoparticles were synthesized using the precipitation method. The Taguchi approach with the L32b orthogonal array was utilized in order to optimize the experimental conditions for the synthesis of the nanoparticles and to ensure that relatively smaller-sized particles were obtained. The design was characterized by ten factors, where nine of them possessed four levels, while one had two levels. This study’s design factors were the type of Zn precursor, the concentration of the Zn precursor, the type of precipitating agent, the precipitation agent’s concentration, the type of utilized solvent, the pH value of the solvent, the temperature used during the synthetic procedure, the calcination temperature, the time of stirring during synthesis, as well as the stirring speed. The influences of those factors on the selected response parameters (the average crystallite size, degree of crystallinity, energy band gap (Eg), and photodegradation constant (k)) were then evaluated. XRD analysis and the calculated Eg values indicated that the hexagonal wurtzite structure was the only crystalline phase present in the produced samples. The photocatalytic efficiency of all ZnO nanoparticles was examined in the degradation of rhodamine B under UV light irradiation. The optimal conditions were achieved using zinc acetate dihydrate as the Zn precursor at a concentration equal to 0.3 M, sodium hydroxide as the precipitating agent (1.5 M), methanol as the solvent (the pH value of the solvent was equal to 13), a temperature during the synthetic procedure of 70 °C, 600 °C as calcination temperature, a 90 min stirring time, and 700 rpm as the stirring speed. The optimized ZnO sample was synthesized based on the aforementioned conditions and thoroughly characterized. The acquired results confirmed the prediction of the Taguchi approach, and the most enhanced k-value was observed.

In recent years, remarkable progress in nanomedicine has been achieved, leading to the development of several nanocarriers which aim to enhance the therapeutic efficacy in cancer treatment. Owing to their high versatility and highly tunable physicochemical properties, alumina (Al2O3) and silica (SiO2) substrates represent promising and innovative nanoplatforms that are widely used in biomedical applications, such as drug-delivery, diagnosis, and biosensing in cancer. In particular, such platforms possess multiple advantageous properties, including mechanical stability, high loading capacity, tunable porosity, excellent biocompatibility, and in vitro and in vivo low toxicity. In this review article, we discuss their emerging role as biosensing platforms and drug delivery systems in oncology. As such, we describe how these substrates enable the incorporation of antibodies against various cancer biomarkers [e.g., cancer antigen 15-3 (CA15-3), serum amyloid A1 (SAA1), epithelial cell adhesion molecule (EpCAM), or human epidermal growth factor receptor 2 (HER2)] for the detection of multiple malignancies. Furthermore, we highlight the development of highly promising alumina- and silica-based platforms for drug delivery (e.g., chemotherapeutics, photosensitizers, or gene delivery agents) in cancer. Ultimately, by providing a comprehensive overview alongside a critical analysis, we demonstrate that such nanostructures represent promising platforms for potential clinical translation in cancer medicine, helping to mitigate the limitations of conventional cancer therapies.