Search Results (2,517)

Due to the rapid development of the textile industry and increased consumption of various textiles composed of both synthetic and natural fibers, large amounts of textile waste are produced, leading to environmental and economic problems on a global scale. Turning textile waste into carbon materials that can be used in a broad range of applications has become a viable solution to address this challenge in terms of sustainability and value generation. Natural and synthetic textile fibers have distinctive molecular structures with relatively high carbon content and variable chemical functionality; therefore, they have been identified as highly promising precursors for fabricating carbon materials with various electrochemical and environmental applications. At the same time, the properties of carbonized and activated textile fibers are strongly dependent on the molecular transformations taking place during thermal treatment and functionalization of textile fibers. This review will provide a comprehensive overview of the molecular evolution of natural and synthetic textile fibers during carbonization and activation processes in terms of dehydration, depolymerization, aromatization, heteroatom preservation, and graphitization mechanisms. The effect of precursor chemical composition, pyrolysis conditions, activation process, and heteroatom incorporation on the structure of carbonized and activated textile fibers and their physical and electrochemical properties will be analyzed. Particular emphasis is placed on electrochemical applications, including capacitive deionization, supercapacitors, electrocatalysis, and emerging smart electrochemical textile systems, highlighting how molecular transformation, pore engineering, and surface chemistry govern charge storage, ion adsorption, and catalytic behavior. In addition, major characterization techniques such as Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area analysis will be reviewed and discussed in relation to understanding the interdependence between molecular structure and material properties. Finally, recent issues related to feedstock heterogeneity, scalability, energy efficiency, and sustainability of processing are highlighted, and future perspectives on multifunctional carbon structures and circular utilization of textile waste are discussed. Full article

The nanoscale structural heterogeneity of carbons plays a crucial role in regulating the surface activity, catalytic performance, and wettability of substances. Herein, we quantitatively investigate the nanostructural evolution of a coal-derived carbon during high-temperature treatment, using high-resolution transmission electron microscopy (HRTEM). To elucidate the intrinsic nanoscale structural heterogeneity of carbonaceous materials during thermal treatment, a particle-edge preferential graphitization is hypothesized in this study. Based on quantitative HRTEM analysis of coal-derived carbon heat-treated up to 3000 °C, this study demonstrates that particle boundaries act as intrinsic geometric templates and stress concentrators, governing the carbon nanostructural evolution. The length enhancement of the aromatic structural transformation occurs at 300 °C, 1000 °C, and 2550 °C, respectively, with substantially decreased small-size lattice fringes and substantially increased medium- and large-size lattice fringes. The average curvature displays a non-monotonic decrease and a transient increase during the second carbonization and pregraphitization processes, driven by the formation of concentric and twisted nanostructures. During graphitization, lattice fringe curvature becomes geometrically constrained by particle edges, resulting in an unexpected positive correlation with fringe length. Lattice fringes at particle edges develop highly ordered, boundary-parallel orientations, whereas interior regions experience delayed ordering with randomly oriented graphitic domains. Edge-preferential graphitization explains the non-uniform evolution of carbon structures, providing a crucial theoretical basis for the comprehensive utilization of complex amorphous carbon precursors, including coal and biomass-derived fuels. Full article

Metal oxide nanoparticles have been the subject of intense research interest because of their remarkable physicochemical properties, such as their high surface area, particle size tunability, outstanding chemical stability, optical activity, catalytic efficiency, and antimicrobial behavior. These properties make them very useful in environmental, biomedical, energy, sensing, agricultural and industrial applications. The chosen synthesis method is important in controlling the morphology, crystallinity, surface charge, band gap and overall performance of metal oxide nanoparticles. They have been prepared using various physical, chemical and biological means, such as sol–gel, co-precipitation, hydro/solvothermal, microwave-assisted, sonochemical, combustion and green synthesis. Of these, green synthesis is gaining more interest as it employs plant extracts, microorganisms, and other biological materials as reducing agents, stabilizing and capping agents that make the process more eco-friendly and cost-effective. Recent advancements in the synthesis and application of metal oxide nanoparticles are discussed. There is an emphasis on the major synthesis routes, the main factors that influence the formation of nanoparticles, the characterization techniques used, and the structure–property relationships uncovered. A special focus is given to the influence of synthesis parameters, such as the type of precursor and the pH, temperature, reaction time, solvents and capping agents, on the properties of nanoparticles. In addition, the uses of metal oxide nanoparticles in photocatalysis, wastewater treatment, antimicrobial activity, drug delivery, biosensing, energy storage, gas sensing, and agriculture are also included. Finally, present challenges, toxicity issues, the problems of large-scale production, and future research directions are discussed to support the practical and sustainable uses of metal oxide nanoparticles. Full article

Anti-CD38 monoclonal antibodies have substantially improved outcomes in multiple myeloma (MM). Although daratumumab and isatuximab target the same antigen, accumulating evidence indicates that they differ in epitope recognition, biological activity, and immunomodulatory properties, suggesting these agents may not be therapeutically interchangeable. This review summarizes the molecular and immunological mechanisms underlying their distinct antitumor effects and their implications for treatment selection. Isatuximab binds near the catalytic site of CD38, resulting in potent enzymatic inhibition, enhanced antibody internalization, FOXM1 suppression, and reactive oxygen species-mediated cytotoxicity, which may preferentially target MM cells harboring 1q21 amplification. In contrast, daratumumab exerts prominent Fc-dependent immune effects, including trogocytosis-mediated downregulation of CD38 and VLA-4, suppression of cell adhesion-mediated drug resistance, and modulation of the immune microenvironment, potentially enhancing subsequent T-cell-redirecting therapies. We further discuss the relevance of these mechanistic differences to measurable residual disease, extramedullary disease, and sequencing with BCMA- and GPRC5D-directed immunotherapies. Finally, we propose a biology-guided treatment-selection model integrating genomic alterations, tumor biology, and immune remodeling to support precision medicine for patients with MM. Full article

This study analyzes a low-cost potassium feldspar mineral from Chihuahua, Mexico, for removing cationic dyes (methylene blue and rhodamine 6G) from water. The raw mineral, characterized by Rietveld refinement as a polymineralic composite of sanidine (49 vol%), muscovite (27 vol%), calcite (16 vol%), and anorthoclase (7 vol%), demonstrated significant dual functionality. In darkness, it acted as an effective adsorbent, achieving 98% and 76% removal of MB and R6G, respectively, after 120 min, with adsorption behavior fitting the Langmuir isotherm. Under solar irradiation, the mineral facilitated photocatalytic degradation, evidenced by a faster intensity decrease and a shift in the absorption bands, and the near-complete decolorization of the dyes. The degradation kinetics were significantly accelerated in a synergistic advanced oxidation process (AOP) with added hydrogen peroxide (H₂O₂), achieving 98% degradation for MB and 93% degradation for R6G within 15 min, compared with 97% for MB and 65% for R6G under sunlight irradiation alone. Kinetic analysis revealed that the process consistently followed a pseudo-second-order model, indicating a surface-controlled mechanism dependent on dye concentration and the availability of active sites. Additional fitting with the Elovich and Avrami models suggested heterogeneous surface behavior and multistep degradation pathways, implying that the overall process involved concurrent adsorption, surface-mediated catalytic reactions, and oxidative degradation driven by photogenerated reactive species. Additionally, the scavenger tests revealed that the dominant reactive species depended on the presence of ${\mathrm{H}}_2{\mathrm{O}}_2$: ${\mathrm{O}}_2^{•-}$ radicals prevailed in the peroxide-free system, whereas $•\mathrm{OH}$ radicals dominated under ${\mathrm{H}}_2{\mathrm{O}}_2$- assisted conditions. Photoluminescence spectroscopy analysis provided mechanistic insights, tracking the evolution of dye monomers, dimers, and aggregates, confirming structural degradation of the dyes and revealing the formation of specific fluorescent intermediates. Together, these findings highlight the mineral’s potential as an abundant, eco-friendly material for solar-driven wastewater treatment. Full article

Pesticide and veterinary drug residues, heavy metals and other hazardous contaminants in agricultural products and food systems pose severe threats to food safety and agro-ecological security. Conventional detection techniques are plagued by complicated operations, long testing cycles and insufficient sensitivity, which fail to meet the practical requirements for rapid, accurate on-site detection and in situ remediation. This paper systematically introduces the fundamental physicochemical properties of typical carbon-based nanomaterials, including graphene, carbon nanotubes, carbon quantum dots and biomass-derived carbon. It comprehensively reviews the latest research advances of these materials in the detection of heavy metal ions, pesticide residues, mycotoxins and illegal additives, as well as in the non-destructive monitoring of food quality. Meanwhile, relevant applications of carbon-based nanomaterials in the adsorption, enrichment and catalytic remediation of heavy metals and organic pollutants in farmland soil and water environments are summarized. The intrinsic mechanisms underlying their performance in high-precision detection and environmental remediation are elaborated from the perspectives of optical sensing response and adsorption–separation effects. Furthermore, the current technical limitations and bottlenecks restricting the practical application of carbon-based nanomaterials are discussed. Combined with the industrial demands for rapid screening of agro-food safety risks and in situ treatment of farmland environments, the future development prospects of carbon-based nanomaterials in agriculture and food safety fields are outlined. This work aims to provide theoretical references for the development and industrialization of high-performance carbon-based sensing and remediation materials, and to facilitate the risk prevention and control of agro-food safety as well as the green and sustainable development of agricultural ecosystems. Full article

4-(2-Nitrobenzoyl)isoxazoles are readily available from 3,5-disubstituted 4-iodoisoxazoles through iodine–lithium exchange and trapping with 2-nitrobenzaldeyde, followed by Jones oxidation of the obtained secondary alcohols. Reductive ring transformation by means of treatment with iron in acetic acid gives 2-substituted 3-acyl-4-quinolones. The mechanism of the cyclization reaction was elucidated by using appropriately substituted isoxazole building blocks and 2D NMR investigation of the products. In contrast, catalytic hydrogenation leaves the isoxazole ring untouched, whereas reduction with NaBH₄/NiCl₂ gives 2-substituted 3-acylquinolines in an unprecedented reductive ring transformation. Full article

Breast cancer remains one of the most prevalent malignancies affecting women worldwide and continues to be a leading cause of cancer-related morbidity and mortality. Patients may present with either localized or advanced disease, with clinical outcomes increasingly influenced by molecular subtype and genetic profile. This review highlights the key genetic factors involved in breast cancer, current diagnostic and therapeutic strategies, and promising emerging approaches that may shape future clinical management. Breast cancer diagnosis typically involves clinical breast examination, imaging techniques such as mammography and ultrasound, and confirmatory biopsies. Genetic mutations in specific genes are strongly linked to the development, progression, and metastasis of the disease. Treatment options for localized breast cancer continue to include surgery (lumpectomy or mastectomy) and radiotherapy, combined with systemic therapies tailored to tumor biology, such as endocrine therapy, human epidermal growth factor receptor 2 (HER2)-targeted therapy, and cyclin-dependent kinase (CDK)4/6 inhibitors. For advanced or metastatic breast cancer, recent therapeutic advances include the use of immunotherapy (e.g., immune checkpoint inhibitors), Poly (ADP-ribose) polymerase (PARP) inhibitors for Breast Cancer gene (BRCA)-mutated cancers, antibody–drug conjugates, and novel targeted agents, which have significantly improved patient outcomes in selected populations. Recent findings in breast cancer genetics have highlighted the critical role of germline and somatic mutations, particularly in genes such as BRCA1, BRCA2, phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA), and TP53, in driving tumor initiation, progression, and therapeutic response. Molecular profiling and next-generation sequencing technologies have enabled more precise tumor classification and facilitated the development of personalized treatment strategies. Despite these advances, treatment resistance and disease recurrence remain major challenges, particularly in aggressive subtypes such as triple-negative breast cancer. Consequently, ongoing research is exploring alternative and complementary approaches, including nanotechnology-based drug delivery systems, gene editing techniques such as clustered regularly interspaced short palindromic repeats-Cas9 (CRISPR-associated protein 9) (CRISPR-Cas9), cancer vaccines, and the integration of traditional and plant-derived compounds. These strategies aim to enhance therapeutic efficacy, reduce systemic toxicity, and overcome resistance mechanisms. Full article

Radiotherapy is a cornerstone of breast cancer treatment, but its efficacy is frequently limited by intrinsic and acquired radioresistance as well as dose-limiting toxicity to surrounding normal tissues. Nanoparticle-mediated radiosensitization has emerged as a promising strategy to enhance the therapeutic index of irradiation by combining physical dose amplification with biological, microenvironmental, and immunological modulation. In this systematic review, we evaluated preclinical evidence on nanoparticle-mediated radiosensitization in breast cancer, with emphasis on nanoplatform design, mechanistic patterns, therapeutic efficacy, and translational relevance. A total of 66 studies published between 2015 and 2026 were included. The identified systems encompassed a broad range of materials, including gold-, silver-, platinum-, bismuth-, gadolinium-, polymer-, lipid-, and hybrid-based nanoplatforms, frequently incorporating targeting ligands, catalytic components, biomimetic coatings, or therapeutic payloads. Enhanced radiation responses were most commonly associated with high-atomic-number (high-Z)-mediated energy deposition, increased reactive oxygen species generation, and enhanced DNA damage persistence. Additional mechanisms, including redox modulation, hypoxia targeting, regulated cell death, and immune activation, reflect the evolution of nanoparticle-assisted radiotherapy from predominantly physical radioenhancement toward multifunctional physicobiological strategies. Triple-negative breast cancer models predominated throughout the literature. Across preclinical models, nanoparticle-assisted irradiation consistently improved clonogenic survival, tumor control, and, in selected studies, survival. However, substantial heterogeneity in study design and limited use of rigorous radiobiological endpoints restricted cross-study comparability. The available preclinical evidence indicates that the most promising nanoparticle-mediated radiosensitization strategies integrate physical dose enhancement with biologically active mechanisms targeting oxidative stress, hypoxia, persistent DNA damage, immune signaling, and tumor microenvironmental resistance. Collectively, these findings suggest that the field is evolving from predominantly physical radioenhancement toward multifunctional, mechanism-driven physicobiological strategies. However, clinical translation remains constrained by methodological heterogeneity and limited radiobiological validation, highlighting the need for standardized preclinical evaluation and clinically feasible nanoplatforms tailored to subtype-specific mechanisms of radioresistance. Full article

Diabetes mellitus, particularly type 2 diabetes mellitus (T2DM), represents a major global health challenge, driven by the increasing prevalence of obesity and sedentary lifestyles. T2DM is characterized by insulin resistance and progressive β-cell dysfunction, leading to chronic hyperglycemia and multiple complications. Among the molecular targets investigated for therapeutic intervention, protein tyrosine phosphatase 1B (PTP1B) has emerged as a key negative regulator of insulin signaling. By dephosphorylating the insulin receptor and its downstream substrates, PTP1B attenuates insulin action and contributes to metabolic dysfunction. In addition to its role in glucose homeostasis, PTP1B is implicated in obesity, diabetic complications, neurodegenerative disorders, and cancer, highlighting its relevance as a multifunctional therapeutic target. However, the development of PTP1B inhibitors remains challenging due to the highly conserved and polar nature of its catalytic site, which limits selectivity and cell permeability. Recent research has focused on alternative strategies, including allosteric modulation and multi-site inhibition, to overcome these limitations. This review provides a comprehensive overview of PTP1B inhibitors from both synthetic (2019–2025) and natural sources, with particular emphasis on natural products reported from 2022 onwards, while including selected earlier studies to provide historical context and illustrate representative structural classes and inhibition mechanisms. Although PTP1B remains an attractive therapeutic target, its clinical validation for diabetes treatment has yet to be achieved. Continued advances in medicinal chemistry and allosteric modulation may help overcome the current translational barriers. Full article

The sustained expansion of printing and dyeing operations has led to the discharge of large volumes of organic wastewater containing dyes. The resulting environmental pollution demands urgent solutions, making the development of efficient and eco-friendly methods for the elimination of dyeing wastewater critically important. The combination of alginate hydrogel membranes with advanced oxidation processes (AOPs) for water purification represents an emerging approach in the current field of water treatment. In this study, a calcium alginate membrane was loaded with a glaze containing highly active cobalt oxide to fabricate a glaze-calcium alginate (Glaze-CaAlg) composite membrane. The membrane achieved stable degradation of Orange G dye under optimal conditions, and a series of tests were conducted under varying conditions using pollutant concentrations close to those found in real water bodies. Under optimal conditions (glaze loading = 2.5 mL, PMS = 0.3 mmol/L, cross-flow filtration mode), the membrane achieved a 93.7% degradation efficiency of Orange G (10 ppm) within 45 min, with hydroxyl radicals (·OH, ~79%) identified as the predominant reactive species. The Glaze-CaAlg membrane also exhibited excellent reusability, maintaining a degradation efficiency of over 80% for Orange G across five consecutive cycles. Furthermore, sodium citrate was employed to react with the Glaze-CaAlg membrane, enabling the recovery and secondary application of the glaze. Membranes re-fabricated from the recovered glaze showed mechanical strength and catalytic efficiency comparable to those of the pristine membrane. The Glaze-CaAlg membrane possesses high catalytic activity and good stability. This work offers a sustainable, cost-effective, and recyclable catalytic membrane that converts a traditional ceramic material into an advanced functional material for wastewater remediation, with great potential for practical application in the treatment of refractory organic pollutants. Full article

The treatment of refractory wastewater pollutants requires advanced materials capable of synergistic enrichment and destruction. Cellulose-based aerogels, combining biomass sustainability with a porous structure, are a promising platform, yet a quantitative synthesis of this field’s evolution is lacking. This study presents the first bibliometric and visual analysis of 463 publications on cellulose-based aerogels for wastewater treatment. The field shows S-shaped growth, evolving from a Nascent phase to Exponential Growth and now entering Maturation. Social network analysis reveals a China-centered but increasingly international collaboration pattern, while institutional productivity remains fragmented into multiple small research teams. The foundation rests on two synergistic pillars: adsorptive sequestration and catalytic degradation, with research evolving from their parallel development to active fusion. Current frontiers focus on sustainable system engineering, emphasizing process integration, material regeneration, and advanced precursors like cellulose nanofiber. This analysis maps the field’s maturation from material exploration toward integrated catalytic system design, providing a foundational reference and clear directives for future research to address integration challenges. In addition to bibliometric mapping, this review critically discusses treatment functions (adsorption, catalytic oxidation, and integrated pathways) and deployment barriers (regeneration, recyclability, and scale-up feasibility), thereby linking knowledge evolution to practical wastewater-treatment translation. While China contributes the largest publication share in the present dataset, the field is supported by increasing participation from multiple countries and regions. Full article

Per- and polyfluoroalkyl substances (PFASs) are persistent environmental contaminants widely recognized as “forever chemicals” due to the exceptional stability of their carbon–fluorine (C-F) bonds. Their widespread occurrence in water, soil, sediments, and biota, coupled with increasing evidence of toxicity, bioaccumulation, and long-range transport, has intensified the search for sustainable remediation strategies. Conventional remediation technologies for PFASs have been widely applied but remain constrained by several technical and environmental limitations, such as incomplete mineralization, high energy requirements, secondary waste generation, and the formation of toxic transformation products. Moreover, many conventional treatment processes were not originally designed to handle the chemical stability and structural diversity of PFASs, resulting in variable removal efficiencies across different compounds. Bio-based strategies for PFAS remediation, particularly those targeting C-F bond cleavage and biological defluorination, are gaining attention due to the unique challenges posed by the chemical stability and environmental persistence of these “forever chemicals”. This review addresses the fragmented nature of PFAS remediation research by integrating biological and physicochemical strategies and critically examining mechanisms of C-F bond cleavage and defluorination. Emerging technologies, including bioelectrochemical systems, photocatalytic and electrochemical defluorination, adsorption-assisted degradation, plasma treatment, hydrothermal processes, and synthetic biology approaches, are evaluated in relation to their degradation efficiencies, defluorination capacities, and applicability in diverse environmental matrices. Particular attention is given to integrated “capture-and-destroy” systems that combine adsorption with catalytic or biological degradation to enhance remediation efficiency and reduce energy demand. PFAS treatment performance varies markedly across scalability, destruction, and cost. Key knowledge gaps and future perspectives are outlined, emphasizing the need for scalable, energy-efficient, and environmentally sustainable remediation technologies capable of achieving complete PFAS mineralization in complex environmental systems. Full article

Background/Objectives: Cryptosporidiosis, caused by Cryptosporidium parvum, is a significant cause of diarrheal disease, particularly affecting young children and immunocompromised individuals. With current treatments offering limited efficacy, there is an urgent need for novel therapeutic targets. Methods: In this study, we report the cloning, expression, and functional characterization of a glutathione transferase (GST) from C. parvum (CpGST). Results: Biocomputing analysis revealed a single gene encoding a cytosolic enzyme with distinct structural features, compared to human cytosolic homologs. Structural modeling indicated a non-canonical thioredoxin fold and a truncated C-terminal domain, suggesting functional divergence. CpGST was expressed in Escherichia coli, and its enzymatic properties were characterized. Although the enzyme displayed a narrow substrate spectrum, it showed a distinct substrate preference, retaining catalytic activity toward the standard GST substrates 1-chloro-2,4-dinitrobenzene (CDNB) and cumene hydroperoxide (CuOOH). Steady-state kinetic analysis revealed limited affinity for both reduced glutathione (GSH) and CDNB. Inhibition analysis identified several polyphenols and synthetic curcumin analogues as potent inhibitors, with IC₅₀ values in the low micromolar range. Kinetic analysis with the most potent inhibitor revealed a mixed-type inhibition mechanism. Conclusions: These findings support the classification of CpGST as a structurally and functionally distinct member of the GST family, likely adapted to the parasite’s physiology and metabolism. The enzyme’s divergence from human GSTs, along with its favorable druggability profile, underscores its potential as a target for anti-cryptosporidial drug development, particularly in strategies aimed at disrupting stress response and detoxification pathways. Full article

This review is devoted to the occurrence, extraction, structural characterization and catalytic applications of vanadyl porphyrins present in heavy crude oils and petroleum residues. Vanadyl porphyrins represent the major vanadium-containing compounds in petroleum systems and play a dual role as both catalyst poisons during refining processes and valuable precursors for functional catalytic materials. Particular attention is devoted to recent advances in extraction technologies, including solvent extraction, ionic liquids, deep eutectic solvents, functionalized adsorbents and chelating agents. Process intensification approaches such as ultrasound- and microwave-assisted extraction, are also discussed as promising strategies for improving extraction efficiency and selectivity. Furthermore, recent developments in petroleum characterization using FTICR-MS, EPR, HYSCORE and LA-ICP-MS techniques are reviewed, providing insights into metalloporphyrin speciation, oxidation states, and distribution within complex petroleum matrices. Beyond their traditional role in catalyst deactivation, vanadyl porphyrins have emerged as attractive precursors for catalytic materials applied in oxidation reactions, photocatalysis, oxidative desulfurization, wastewater treatment and selective organic synthesis. The development of hybrid catalytic systems based on mesoporous silica, graphene oxide, carbon nanotubes, polymer matrices, and metal–organic frameworks has significantly improved catalyst stability, activity and recyclability. Current challenges related to the selective extraction, preservation of metalloporphyrin structure and catalytic performance evaluation are also discussed. Overall, this review provides an integrated perspective on the recovery, characterization and valorization of vanadyl porphyrins for sustainable petroleum upgrading and environmental applications. Full article