Search Results (79)

Emerging and re-emerging viruses continue to pose major threats to public health. Their ability to adapt, cross species barriers, and spread rapidly can trigger severe outbreaks or even pandemics. Strengthening preparedness with comprehensive and efficient strategies is therefore essential. Here, we explore the key components of viral outbreak preparedness, including surveillance systems, diagnostic capacity, prevention and control measures, non-pharmaceutical interventions, antiviral therapeutics, and research and development. We emphasize the increasing importance of genomic surveillance, wastewater-based surveillance, real-time data sharing, and the One Health approach to better anticipate zoonotic spillovers. Current challenges and future directions are also discussed. Effective preparedness requires transparent risk communication and equitable access to diagnostics, vaccines, and therapeutics. The COVID-19 pandemic highlighted both the promise of next-generation vaccine platforms and the necessity of maintaining diagnostic capacity, as early testing delays hindered containment efforts. Countries adopted various non-pharmaceutical interventions: risk communication and social distancing proved to be the most effective, while combined workplace infection-prevention measures outperformed single strategies. These experiences highlight the importance of early detection, rapid response, and multisectoral collaboration in mitigating the impact of viral outbreaks. By applying best practices and lessons learned from recent events, global health systems can strengthen resilience and improve readiness for future viral threats. Full article

Pharmaceutical residues are increasingly emerging in global drinking water sources, posing serious ecological and public health challenges by altering the physicochemical balance of aquatic systems. Among available purification approaches, adsorption remains one of the most promising techniques due to its simplicity, cost-effectiveness, and efficiency. In this work, a ternary nanocomposite of Cu- and ZnO-decorated carboxylated graphene oxide (Cu/ZnO@CGO) was synthesized and utilized for highly efficient and ultrafast removal of the antidiabetic drug metformin from aqueous environments. The adsorption mechanism arises from a synergistic combination of surface complexation on Cu nanoparticles, cation–π and π–π electron donor–acceptor interactions with the CGO aromatic structure, and hydrogen bonding through the amino groups of metformin and the oxygen-rich functional moieties of ZnO and CGO. The nanocomposite was thoroughly characterized using FTIR, XPS, XRD, SEM, HRTEM, and TGA analyses, confirming its well-defined hybrid structure. Unlike conventional single-phase or binary systems, the Cu/ZnO@CGO nanocomposite demonstrated remarkable cooperative effects that enhanced its performance through the integration of metal–ligand coordination, π–π stacking, cation–π forces, and hydrogen bonding. These interactions contributed to an outstanding adsorption capacity of 232.56 mg·g⁻¹ and an exceptionally fast equilibrium time of only 25 min. Moreover, the material maintained excellent reusability, with merely a 4.1% decline in efficiency after five regeneration cycles, and achieved almost complete removal of metformin (99.7 ± 3.4%) from several real water samples, namely river, tap, and bottled water. The unique structural design of Cu/ZnO@CGO prevents CGO aggregation and facilitates efficient contaminant capture even at trace concentrations, establishing it as a highly competitive and sustainable adsorbent for pharmaceutical wastewater treatment. Overall, this study highlights a novel and rationally engineered nanocomposite whose synergistic surface chemistry bridges adsorption and detoxification, providing valuable insight into the next generation of multifunctional graphene-based materials for environmental remediation. Full article

The widespread use of anticancer drugs (ACDs) in human therapies determines the occurrence of these potent cytotoxic chemicals into aquatic ecosystems. Nowadays, ACDs are ubiquitous contaminants in wastewater effluents and freshwater compartments, raising urgent questions about their environmental impact. Designed to disrupt cellular proliferation, these compounds are inherently bioactive and can exert toxic effects on non-target organisms even at trace concentrations. Conventional fate and toxicity tests provide important initial data but are limited in ecological realism, often focusing on single-specie and single-endpoint under controlled conditions and overlooking complex interactions, trophic dynamics, and long-term chronic exposures. Knowledge of all these aspects is needed for proper monitoring, assessment, and regulation of ACDs. Simulated ecosystem experiments, such as mesocosms, provide intermediate-scale, semi-controlled platforms for investigating real-world exposure scenarios, assessing ACD fate, and identifying both direct and indirect ecological effects. They offer distinct advantages for evaluating the chronic toxicity of persistent pollutants by enabling realistic long-term contamination simulations and supporting the simultaneous collection of comprehensive hazard and exposure endpoints. This perspective underscores the growing concern surrounding the contamination of ACDs, examines the limitations of traditional assessment approaches, and advocates for mesocosm-based studies as a critical bridge between laboratory research and ecosystem-level understanding. By integrating mesocosm experiments into environmental fate and risk evaluation, we can better predict the behavior and ecological consequences of anticancer pharmaceuticals, guiding strategies to mitigate their impact on aquatic life. Full article

Caproate is a valuable medium-chain fatty acid (MCFA) that is found to be extensively used in biofuel production, food preservation, and the pharmaceutical industries. Short-chain fatty acids (SCFAs) from waste streams can be upgraded sustainably through their biological synthesis via anaerobic chain elongation. However, caproate production is frequently limited in real-world systems due to low carbon conversion efficiency and a lack of electron donors. In this study, we developed a two-stage fermentation strategy employing yellow water—a high-strength organic wastewater from liquor manufacturing—as a novel substrate. During primary fermentation, Lactobacillus provided endogenous electron donors by converting the residual carbohydrates in the yellow water into lactic acid. Nano zero-valent iron (NZVI) was introduced to the secondary fermentation to enhance power reduction and electron flow, further promoting caproate biosynthesis. The caproate production increased significantly due to the synergistic action of lactic acid and NZVI, reaching a maximum concentration of 20.41 g·L⁻¹ and a conversion efficiency of 69.50%. This strategy enhances carbon recovery and electron transport kinetics while lowering dependency on expensive external donors like hydrogen or ethanol. Microbial community analysis using 16S rRNA sequencing revealed enrichment of chain-elongating bacteria such as Clostridium kluyveri. These findings demonstrate the feasibility of employing an integrated fermentation–electron management technique to valorize industrial yellow water into compounds with added value. This study offers a scalable and environmentally sound pathway for MCFA production from waste-derived resources. Full article

Currently, continuous population growth and unsustainable industrialization have caused ongoing water pollution, with harmful consequences for human health and the environment. Persistent organic pollutants (dyes, active pharmaceutical compounds, pesticides, etc.) are discharged into water from various industrial, agricultural, and domestic activities. Therefore, wastewater treatment through sustainable technologies is imperative, representing a great and real challenge for worldwide research. Photocatalysis, an innovative and green technology, uses advanced oxidation processes in the presence of a photocatalyst, usually a semiconductor with expanded light absorption ability and high conductivity for photogenerated charge carriers. Molybdenum disulfide (MoS₂) is an n-type semiconductor with different morphologies, variable bandgap energies (Eg = 1.1–2.63 eV), and numerous applications. Although pristine MoS₂ exhibits special structural and optoelectronic properties, its photocatalytic activity can be further improved through various strategies, and constructions with the heterojunctions construction with other semiconductors being frequently pursued. This review extensively studies the recent research (the last 4 years) on MoS₂ and MoS₂-based heterojunction (I-type, II-type, Z-scheme, S-scheme) photocatalysts for degrading organic contaminants under simulated and sunlight irradiation in wastewater treatment. Even if in a relatively short time (a few years) valuable studies have been reported on this topic, there are still numerous challenges facing future research. Full article

This study explores the effectiveness of ultraviolet (UV) irradiation, ozonation (O₃), granular activated carbon (GAC) adsorption, and their combinations (UV/GAC, O₃/GAC) in removing selected pharmaceuticals and common wastewater micropollutants under controlled laboratory-scale conditions. Eight target compounds—candesartan, irbesartan, valsartan, metoprolol, diclofenac, metformin, sucralose, and caffeine—were identified and quantified in real wastewater samples collected from a municipal wastewater treatment plant. Ozonation proved to be the most effective standalone method, achieving complete removal (100%) of five pharmaceuticals and partial removal of sucralose (~60%) and metformin (~17%). The combined O₃/GAC treatment further enhanced overall removal efficiency. In contrast, UV irradiation alone showed limited effectiveness. Importantly, all substances except metformin were fully removed by at least one of the tested methods. These findings underscore the potential of advanced and hybrid treatment technologies—validated here at the laboratory scale—for improving pharmaceutical removal from wastewater and mitigating their environmental impact. Full article

Pharmaceutical residues, including a wide range of therapeutic drugs, have been increasingly reported in drinking water sources worldwide, raising environmental concerns due to their potential impact on aquatic ecosystems. Among the available treatment approaches, adsorption has emerged as one of the most reliable methods for eliminating these pollutants. In the present study, metformin was effectively removed from water using a nanocomposite adsorbent consisting of copper nanoparticles anchored onto magnetic chitosan (Cu@MCS). The removal of metformin by Cu@MCS was governed by several mechanisms: surface complexation with copper species, electrostatic interactions, hydrophobic associations between the drug’s methyl groups and magnetite, and hydrogen bonding between metformin’s amino groups and oxygenated functional groups of chitosan. The structural and surface properties of the nanocomposite were characterized through FTIR, XPS, XRD, SEM, and HRTEM analyses. Key experimental factors, such as initial drug concentration, contact time, pH, and ionic strength, were systematically optimized to maximize adsorption efficiency. Adsorption data closely followed the Langmuir isotherm model, with a maximum capacity (q_m;) of 52.91 mg·g⁻¹ at 298 K. Regeneration tests demonstrated excellent reusability, showing only a 3.7% decline in performance after six adsorption–desorption cycles. The Cu@MCS material also proved effective in removing metformin from diverse real water samples, including river water, wastewater, bottled water, and tap water. A notable advantage of this nanosorbent is its magnetic separability, which enables straightforward recovery from solution, even at low contaminant levels and with large sample volumes. These results underline the potential of magnetic chitosan-based nanocomposites as fast, efficient, and reusable adsorbents for the removal of pharmaceutical contaminants from aquatic systems. Full article

Wastewater treatment plants (WWTPs) can still be considered point sources of contamination into receiving aquatic ecosystems, especially for many emerging contaminants, which require additional treatments for their removal. In this study, the impact of a WWTP on the water quality of a river located in the metropolitan area of Milan, Northern Italy, was investigated. A wide range of emerging contaminants (i.e., perfluorinated compounds, pharmaceuticals, and synthetic fragrances) and traditional contaminants (i.e., heavy metals, nutrients, and microbiological parameters) were analyzed, both in the river water and in the wastewater at the inlet and outlet of the WWTP, with the aim of evaluating removal efficiency and the risk for the riverine ecosystem. The results showed that wastewater treatment acts differently on the analyzed compounds, effectively removing nutrients, bacteria, few pharmaceuticals, and most heavy metals, but leaving others unchanged such as perfluorinated compounds and synthetic fragrances, that are thus discharged into the receiving river, especially during rain events due to the activation of sewer overflows. The calculation of the Risk Quotient for organic compounds confirmed the negative impact of the WWTP effluent on the chemical quality of the river water, with a consequent potential ecological risk for riverine biota. This study also verified that certain traditional contaminants (i.e., total nitrogen (TN), total phosphorous (TP), thermotolerant coliforms, Escherichia coli), and contamination tracer (i.e., chloride (Cl), boron (B), and MBAS (Methylene Blue Active Substances) could be effectively measured in real time rather than through classical laboratory analysis and could support timely risk assessment. Full article

Metal–organic frameworks (MOFs) are promising materials for environmental remediation, particularly in photocatalysis. In this work, a novel ZMIP nanocomposite was fabricated by integrating MIP-202(Zr) bio-MOF with ZnO nanoparticles. For the first time, ZnO nanoparticles were green-synthesized using water lettuce extract and incorporated into MIP-202(Zr) via a mild hydrothermal route. The resulting hybrid was applied as a visible-light photocatalyst for carbamazepine (CBZ) degradation in real pharmaceutical wastewater. Structural analyses (XRD, FTIR, TEM, EDS) verified the successful incorporation of ZnO into the MIP-202(Zr) framework. The composite exhibited a narrowed bandgap of 2.74 ± 0.1 eV compared to 4.05 ± 0.06 eV for pristine MIP-202 and 3.77 ± 0.04 eV for ZnO, highlighting enhanced visible-light utilization in ZMIP. Operational parameters were optimized using response surface methodology, where CBZ removal reached 99.37% with 84.39% TOC mineralization under the optimal conditions (90 min, pH 6, 15 mg/L CBZ, 1.25 g/L catalyst). The catalyst maintained stable performance over five reuse cycles. Radical quenching and UHPLC-MS analyses identified the dominant reactive oxygen species and generated intermediates, elucidating the degradation mechanism and pathways. Beyond CBZ, the ZMIP photocatalyst effectively degraded other pharmaceuticals, including doxorubicin, tetracycline, paracetamol, and ibuprofen, achieving degradation efficiencies of 82.93%, 76.84%, 72.08%, and 67.71%, respectively. Application on real pharmaceutical wastewater achieved 78.37% TOC removal under the optimum conditions. Furthermore, the supplementation of the photocatalytic system by inorganic oxidants ameliorated the degradation performance, following the order KIO₄ > K₂S₂O₈ > KHSO₅ > H₂O₂. Overall, ZMIP demonstrates excellent activity, reusability, and versatility, underscoring its potential as a sustainable photocatalyst for real wastewater treatment. Full article

Pharmaceuticals and personal care products (PPCPs) are recognized as emerging contaminants of concern, even at ultra-trace concentrations. However, the current detection systems are prohibitively expensive and typically rely on labor-intensive, lab-based workflows that lack automation in sample pretreatment. In this study, we developed a robotic and on-flow solid-phase extraction (ROF-SPE) system, fully integrated with online liquid chromatography-tandem mass spectrometry (LC-MS/MS), for the on-site and real-time monitoring of 16 PPCPs in wastewater effluent. The system automates the entire pretreatment workflow—including sample collection, filtration, pH adjustment, solid-phase extraction, and injection—prior to seamless coupling with LC–MS/MS analysis. The optimized pretreatment parameters (pH 7 and 10, 12 mL wash volume, 9 mL elution volume) were selected for analytical efficiency and cost-effectiveness. Compared with conventional offline SPE methods (~370 min), the total analysis time was reduced to 80 min (78.4% reduction), and parallel automation significantly enhanced the throughput. The system was capable of quantifying target analytes at concentrations as low as 0.1 ng/L. Among the 16 PPCPs monitored at a municipal wastewater treatment plant in South Korea, only sulfamethazine and ranitidine were not detected. Compounds such as iopromide, caffeine, and paraxanthine were detected at high concentrations, and seasonal variation patterns were also observed This study demonstrates the feasibility of a fully automated and on-site SPE pretreatment system for ultra-trace environmental analysis and presents a practical solution for the real-time monitoring of contaminants in remote areas. Full article

In recent years, one of the major problems facing humanity has been the contamination of the environment by various organic pollutants, with some of them exhibiting environmental persistence or pseudo-persistence. For this reason, it is necessary today, more than ever, to find new and effective methods for degrading these persistent pollutants. Transition metal selenides (TMSes) have emerged as a versatile and promising class of catalysts for the degradation of organic pollutants through various advanced oxidation processes (AOPs). The widespread use of these materials lies in the desirable characteristics they offer, such as unique electronic structures, narrow band gaps, high electrical conductivity, and multi-valent redox behavior. This review comprehensively examines recent progress in the design, synthesis, and application of these TMSes—including both single- and composite systems, such as TMSes/g-C₃N₄, TMSes/TiO₂, and heterojunctions. The catalytic performance of these systems is being highlighted, regarding the degradation of organic pollutants such as dyes, pharmaceuticals, antibiotics, personal care products, etc. Further analysis of the mechanistic insights, structure–activity relationships, and operational parameter effects are critically discussed. Emerging trends, such as hybrid AOPs combining photocatalysis with PMS or electro-activation, and the challenges of stability, scalability, and real wastewater applicability are explored in depth. Finally, future directions emphasize the integration of multifunctional activation methods for the degradation of organic pollutants. This review aims to provide a comprehensive analysis and pave the way for the utilization of TMSe catalysts in sustainable and efficient wastewater remediation technologies. Full article

Laccases, a class of multicopper oxidases found in diverse biological sources, have emerged as key green biocatalysts with significant potential for eco-friendly pollutant degradation. Their ability to drive electron transfer reactions using oxygen, converting pollutants into less harmful products, positions laccases as promising tools for scalable and sustainable treatment of wastewater, soil, and air pollution. This review explores laccase from a translational perspective, tracing its journey from laboratory discovery to real-world applications. Emphasis is placed on recent advances in production optimization, immobilization strategies, and nanotechnology-enabled enhancements that have improved enzyme stability, reusability, and catalytic efficiency under complex field conditions. Applications are critically discussed for both traditional pollutants such as synthetic dyes, phenolics, and pesticides and emerging contaminants, including endocrine-disrupting chemicals, pharmaceuticals, personal care products, microplastic additives, and PFAS. Special attention is given to hybrid systems integrating laccase with advanced oxidation processes, bioelectrochemical systems, and renewable energy-driven reactors to achieve near-complete pollutant mineralization. Challenges such as cost–benefit limitations, limited substrate range without mediators, and regulatory hurdles are evaluated alongside solutions including protein engineering, mediator-free laccase variants, and continuous-flow bioreactors. By consolidating recent mechanistic insights, this study underscores the translational pathways of laccase, highlighting its potential as a cornerstone of next-generation, scalable, and eco-friendly remediation technologies aligned with circular bioeconomy and low-carbon initiatives. Full article

Pharmaceutical wastewater contains high levels of organic matter, salts, and toxic compounds that are resistant to conventional treatment methods. Even after secondary treatment, traces of dissolved organics and suspended solids often remain, contributing to environmental concerns such as increased microbial resistance and harm to aquatic life. This study introduces a sustainable “waste-to-treat-waste” approach that utilizes discarded white chicken eggshells as a low-cost biosorbent for removing ciprofloxacin, a common antibiotic. Unlike previous eggshell-based adsorption studies that primarily targeted dyes or heavy metals, this work demonstrates the first comprehensive evaluation of both untreated and chemically/thermally modified eggshells for antibiotic removal from real pharmaceutical wastewater. Batch adsorption experiments under optimized conditions showed removal efficiencies of 85% for raw eggshells, 91% after HCl activation, and 96% after thermal conversion to CaO. Batch adsorption experiments under optimized conditions (pH 7, 25 °C, 625 µm particle size, 3 g/100 mL dose, 90 min contact time) showed maximum adsorption capacities of 23.75 mg/g for untreated ES, 4.08 mg/g after HCl activation, and 1.82 mg/g after thermal conversion to CaO, with removal efficiencies of 85%, 91%, and 96%, respectively. The simplicity of preparation, use of an abundant waste material, and high removal efficiency highlight the potential for scalable cost-effective applications in industrial wastewater treatment systems. Full article

The global increase in municipal and industrial wastewater generation has intensified the need for ecologically resilient and technologically advanced treatment systems. Although traditional biological treatment technologies are effective for organic load reduction, they often fail to remove recalcitrant xenobiotics such as pharmaceuticals, synthetic dyes, endocrine disruptors (EDCs), and microplastics (MPs). Engineered microbial consortia offer a promising and sustainable alternative owing to their metabolic flexibility, ecological resilience, and capacity for syntrophic degradation of complex pollutants. This review critically examines emerging strategies for enhancing microbial bioremediation in wastewater treatment systems (WWTS), focusing on co-digestion, biofilm engineering, targeted bioaugmentation, and incorporation of conductive materials to stimulate direct interspecies electron transfer (DIET). This review highlights how multi-omics platforms, including metagenomics, transcriptomics, and metabolomics, enable high-resolution community profiling and pathway reconstructions. The integration of artificial intelligence (AI) and machine learning (ML) algorithms into bioprocess diagnostics facilitates real-time system optimization, predictive modeling of antibiotic resistance gene (ARG) dynamics, and intelligent bioreactor control. Persistent challenges, such as microbial instability, ARG dissemination, reactor fouling, and the absence of region-specific microbial reference databases, are critically analyzed. This review concludes with a translational pathway for the development of next-generation WWTS that integrate synthetic microbial consortia, AI-mediated biosensors, and modular bioreactors within the One Health and Circular Economy framework. Full article

Cost-effective procedures usually cannot achieve complete removal of priority contaminants present in water at very low concentrations (as pesticides or pharmaceuticals). Advanced oxidation processes (AOPs) represent promising technologies for removing priority contaminants from water at trace concentrations, yet practical implementation remains limited due to technical and economic constraints. This study presents an innovative flow-through photodegradation device designed to overcome current limitations while achieving efficient contaminant removal at industrial scale. The device integrates a UVC 254 nm lamp-equipped flow chamber with automated dosing pumps for hydrogen peroxide and/or solid catalyst suspensions, coupled with a 30 nm porous membrane filtration system for catalyst recirculation. This configuration optimizes light–catalyst–pollutant contact while enabling combined catalytic processes. Performance evaluation using acesulfame (ACE) and iohexol (IHX) as model contaminants demonstrated rapid and effective removal. IHX degradation with UVC and 75 μM H₂O₂ achieved complete removal with t₉₅% = 7.23 ± 1.21 min (pseudo-order 0.25, t₁/₂ = 3.27 ± 0.39 min), while ACE photolysis (with UVC only) required t₉₅% = 14.88 ± 2.02 min (pseudo-order 1.27, t₁/₂ = 2.35 ± 0.84 min). The introduction of t₉₅% as a performance metric provides practical insights for near-complete contaminant removal requirements. Real-world efficacy was confirmed using tertiary wastewater treatment plant effluents containing 14 μg/L IHX, achieving complete removal within 8 min. However, carbamazepine degradation proved slower (t₉₅% > 74 h), highlighting the need for combined catalytic approaches for recalcitrant compounds. Spiking experiments (1000 μg/L) revealed concentration-dependent kinetics and synergistic effects between co-present contaminants. Analysis identified degradation byproducts consistent with previous studies, including tri-deiodinated iohexol (474.17 Da) intermediates. This scalable system, constructed from commercially available components, demonstrates potential for cost-effective industrial implementation. The modular design allows adaptation to various contaminants through adjustable AOP combinations (UV/H₂O₂, photocatalysts, ozone), representing a practical advancement toward addressing the gap between laboratory-scale photocatalytic research and full-scale water treatment applications. Full article