Antibiotic Contamination Research Articles

Bioconversion of sulfamethazine-contaminated chicken manure by black soldier fly larvae: Effects on antibiotic resistance genes and microbial communities.

Sulfamethazine (SM2), a widely detected antibiotic in livestock manure, poses environmental and health risks due to its persistence and the proliferation of antibiotic resistance genes (ARGs). In this study, we investigated the degradation of SM2 and the elimination of sulfonamide ARGs (sul1 and sul2) in chicken manure contaminated with varying concentration of SM2 by black soldier fly larvae (BSFL). Quantitative PCR and 16S rRNA gene sequencing were employed to monitor changes in sulfa ARGs and microbial community composition within both the larvae gut and chicken manure. During the 12-day test period, BSFL exhibited strong tolerance to SM2, significantly reducing SM2 concentrations by 80.54%-92.22% across different treatment groups. Concurrently, the abundance of sul1 and sul2 decreased by 79.27% and 79.92% in chicken manure, respectively. Additionally, microbial genera such as Firmicutes (47.18-65%) and Bacillus (9.32-10.25%), which were enriched in both the BSFL gut and chicken manure, were identified as potential contributors to SM2 degradation. These findings provide a promising biotechnological strategy for mitigating antibiotic contamination in livestock manure.

Cold Plasma for Enhanced Water Purification

Abstract Access to clean water remains a critical global challenge, with traditional water treatment methods often failing to eliminate complex pollutants such as pharmaceuticals, dyes, and antibiotics. Cold atmospheric plasma technology offers a promising solution by generating reactive oxygen and nitrogen species at room temperature, effectively degrading these contaminants and inactivating pathogens. Recent advancements in cold plasma have shown significant potential in water treatment applications. Cold plasma has demonstrated efficacy in disrupting bacterial biofilms, reducing antibiotic contaminants, and degrading complex organic pollutants, making it an innovative and eco-friendly alternative to conventional methods. This review examines the principles of plasma technology, evaluates its performance in water sanitation, and addresses the challenges of scalability and economic feasibility. By integrating cold plasma into existing water treatment systems and developing standardized protocols, this technology can significantly contribute to sustainable water management and public health, supporting the Sustainable Development Goals (SDGs).

Antibiotic contaminants and their impact in Gingee River, Puducherry: insights from SPE-UPLC-MS/MS and zebrafish study.

The accumulation of antibiotic residues in ecosystems is intricately tied to the proliferation of bacterial resistance to antibiotics, with far-reaching consequences for the health and welfare of both humans and animal well-being. The analytical approach integrates solid phase extraction (SPE) with ultra performance liquid chromatography-mass spectrometry (UPLC-MS/MS) for quantification of multiclass antibiotic residues. Upon applying the aforementioned method to analyse water samples collected from the Gingee River, revealed the existence of five distinct antibiotics. This is the first study reporting antibiotic concentration in the Gingee River, Puducherry. The concentrations of nalidixic acid, sulfamethoxazole, and tetracycline were determined to be 8.5, 6.9, and 4.8μg/L, respectively. Metronidazole and trimethoprim were detected at concentrations below the quantifiable limit. The microbial study of water samples also indicated that Shigella sp. and Acinetobacter sp. were the most predominant bacterial species present. Our preliminary observation underscores the importance of comprehending the intricate relationship between the presence of antibiotics in water and the concurrent proliferation of antibiotic-resistant bacteria within bacterial populations in the Gingee River. Further, we evaluated the developmental toxicity of environmentally relevant concentrations of antibiotics in zebrafish. The zebrafish model confirms that these antibiotics are sublethally hazardous to human health at environmentally relevant concentrations. This integrated approach allows unique views on the environmental impact of antibiotic residues, their role in the evolution of antibiotic resistance, and their impact on human health.

Versatile silicate-modified hydrochar based on Scutellaria baicalensis-residue for efficiently removing heavy metal-antibiotic co-contamination and relevant bio-contaminants from wastewater

In this study, we utilized typical Chinese medicine herbal residues (CMHRs)－Scutellaria baicalensis (Scutellaria baicalensis Georgi) residue (SR), as the raw material and employed Na2SiO3 and Fe2(SO4)3 as modifying agents to fabricate a novel and multifunctional hydrochar (FeSi-SRHC), which was designed for comprehensive removal of typical contaminants such as Cu2+, Zn2+, tetracycline (TC), and ciprofloxacin (CIP), along with relevant bio-contaminants (resistant bacteria (RBs) and resistance genes (RGs)) present in wastewater. Based on the analysis of adsorption kinetics and Freundlich isotherm, it was found that FeSi-SRHC exhibited physical monolayer adsorption for Cu2+/Zn2+ while mainly chemical multilayer adsorption for TC/CIP in single-contamination system. Furthermore, Langmuir isotherm demonstrated excellent adsorption capacity of FeSi-SRHC towards Cu2+/Zn2+/TC/CIP with maximum capacities of 255.75, 265.26, 425.53, and 404.86 mg/g, respectively. In the co-contamination system, the presence of Cu2+, Zn2+, TC, and CIP exhibited varying degrees of inhibitory or promotive effects on the mutual adsorption by FeSi-SRHC. This divergence stemmed from differences in complexation intensities and concentration ratios among diverse co-existing contaminants. Based on XPS and Density Functional Theory (DFT) analyses, the adsorption process for Cu2+, Zn2+, TC, and CIP by FeSi-SRHC primarily involves pore fill, complexation reactions, ion exchange, hydrogen bonding, π-π stacking interactions, and electrostatic interactions. Bio-contaminant removal experiments revealed that the release of baicalin and wogonoside from FeSi-SRHC disrupts the structure of RBs cells and compromises the integrity of resistance plasmids. The practical application experiment showed that FeSi-SRHC displayed favorable performance for removing heavy metals, antibiotics, and bio-contaminants in actual wastewater. This study presented a “Treating waste with waste” strategy, which provided a method with low carbon, eco-friendly, and inexpensive for CMHRs resources and turning waste into treasure while proposing a idea to address the challenges associated with treating heavy metal, antibiotic, and bio-contaminant contamination in wastewater.

Polyacrylonitrile nanofibrous mat modified with cysteamine and ionic liquid as a recyclable and efficient adsorbent for selective removal of sulfonamides and Cu(II) from aqueous solution: Roles of multi-function adsorption

The combined contamination of heavy metals and antibiotics is a prevalent occurrence, yet the distinct chemical characteristics of these substances pose a significant obstacle to their simultaneous elimination. In this work, novel polyacrylonitrile nanofibrous mat (NFsM) modified with cysteamine and ionic liquid (IL@Cys@PAN NFsM) was developed using a cascade thiol-ene click reaction. The IL@Cys@PAN NFsM exhibits a rich array of functional groups and demonstrates strong binding affinity, fast mass transfer, and exceptional selectivity for sulfonamides (SAs) and Cu(II). The maximum adsorption capacities for SAs and Cu(II) in single-component systems were 122.3 and 97.4 mg/g respectively, according to the Langmuir isotherm model. The time dependent adsorption capacities followed a pseudo-second-order kinetic model, demonstrating a chemisorption-dominant process for each analyte. In binary pollutant systems, the co-occurrence of SAs and Cu(II) in water produced a competitive effect; however, the decrease in adsorption capacity was minimal. Through experimental analysis, FTIR characterization and density functional theory (DFT) studies, reasonable interactions of hydrogen-bond, electrostatic interactions, π-π stacking for SAs, and chelation effect for Cu(II) were proposed. Additionally, the reusability and recyclability of IL@Cys@PAN NFsM enhance its practicality for real-world applications. This paper presents the first systematic study on the simultaneous adsorption of heavy metals and antibiotics using NFsM, offering a novel perspective on the design of custom adsorbents capable of efficiently removing multiple contaminants with diverse characteristics while balancing eco-friendliness, excellent adsorption performance, and impressive recyclability for wastewater remediation.

Surfactant-driven modifications to AlFeO3 for degradation of emerging antibiotic contaminants

We show that residues of unused antibiotics Sulfamethoxazole (SMZ) and tetracycline (TC) in wastewater can be treated by photocatalytic degradation. Here, a magnetic photocatalyst known as aluminum ferrite (AlFeO3) is employed to assess the degradation of SMZ and TC under visible light conditions. The structural and functional properties of co-precipitated AlFeO3 with four different surfactants are examined. The little-known relevance of surfactant usage in AlFeO3 synthesis, its characteristics, and its impact on emergent particle morphology for SMZ and TC degradation is reported. The results indicate that the catalyst can completely (100 %) degrade SMZ and TC in ∼60 mins. We propose a distinct degradation pathway for the same. Significantly, AlFeO3 can decompose TC and SMZ to yield rather small compounds (m/z ∼ 60), thereby showing potential for practical use. Also, the use of different surfactants indicates that surface potential plays a significant role in photocatalytic degradation. Despite the large size and low surface area, AlFeO3 performed well due to the surface potential of the catalyst. Findings suggest that using bulk catalysts with adjusted surface potentials offers sufficient performance, thereby bypassing the need for nano-sizing and concern about nano-toxicity. Further, the magnetic property of AlFeO3 facilitates the recovery and reuse of the catalyst post-degradation.

Impacts of micro/nano plastics on the ecotoxicological effects of antibiotics in agricultural soil: A comprehensive study based on meta-analysis and machine learning prediction

Micro/nano plastics (M/NPs) and antibiotics, as widely coexisting pollutants in environment, pose serious threats to soil ecosystem. The purpose of this study was to systematically evaluate the ecological effects of the co-exposure of M/NPs and antibiotics on soil organisms through the meta-analysis and machine learning prediction. Totally, 1002 data set from 38 articles were studied. The co-exposure of M/NPs significantly promoted the abundance (62.68 %) and migration level (55.22 %) of antibiotic contamination in soil, and caused serious biotoxicity to plants (−12.31 %), animals (−12.03 %), and microorganisms (35.07 %). Using 10 variables, such as risk response categories, basic physicochemical properties, exposure objects, and exposure time of M/NPs, as data sources, Random Forests (RF) and eXtreme Gradient Boosting (XGBoost) models were developed to predict the impacts of M/NPs on the ecotoxicological effects of antibiotics in agricultural soil. The effective R2 values (0.58 and 0.60, respectively) indicated that both models can be used to predict the future ecological risk of M/NPs and antibiotics coexistence in soil. Particle size (13.54 %), concentration (5.02 %), and type (11.18 %) of M/NPs were the key characteristic parameters that affected the prediction results. The findings of this study indicate that the co-exposure of M/NPs and antibiotics in soil not only exacerbates antibiotic contamination levels but also causes severe toxic effects to soil organism. Furthermore, this study provides an effective approach for ecological risk assessment of the coexistence of M/NPs and antibiotics in environment.

Adsorption of amoxicillin by chitosan and alginate biopolymers composite beads.

Due to its widespread use and incomplete breakdown in the human body, amoxicillin has been detected in receiving water bodies. This raises significant concerns, like the promotion of antibiotic resistance, toxicity towards aquatic life, disruption of the natural balance of microbial communities within these water bodies, and the struggle of effectively removal by the traditional wastewater treatment plants. Consequently, exploring new processes to complement the existing methods is crucial. Adsorption, a promising highly efficient, selective, and versatile technique, can effectively remove contaminants, making it useful in various industries such as water treatment, pharmaceuticals, and environmental remediation. Several adsorbents are documented in the literature for drug adsorption; however, their fabrication often involves more complex steps and substances compared to chitosan and alginate, which are natural polymers that are biocompatible, non-toxic, and biodegradable. Their tunable properties and ease of modification enhance their efficacy in environmental remediation. Therefore, the novelty of this article is to understand the interaction of amoxicillin with chitosan and alginate adsorbents easily synthetized using the dripping technique. This approach allows us to explore basic principles that can be applied to more complex systems in future studies. The optimal pH for both beads was found to be 4, with adsorption capacities of 74.2 ± 0.3mgg-1 for alginate and 80.4 ± 0.2mgg-1 for chitosan, using 1g of adsorbent. Kinetics studies indicated that external diffusion governs adsorption for alginate, while internal diffusion governs adsorption for chitosan. This approach underscores the potential of chitosan and alginate beads as effective adsorbents for mitigating antibiotic contamination in water systems, offering a sustainable complement to traditional treatment methods.

Effective removal of tetracycline antibiotics from water by in-situ nitrogen-doped porous biochar derived from waste antibiotic fermentation residues

This study explored the utilization of waste oxytetracycline fermentation residue (OFR), abundant in nitrogen and organic matter, to prepare in-situ nitrogen-doped porous biochar (activated OFR derived biochar, AOBC) through a coupled pyrolysis process, and investigated the removal of tetracycline antibiotics (TCs) from water with the prepared AOBCs. The physicochemical characterization results showed the characterizations of abundant nitrogen functional groups, high specific surface area (1960.38 m2/g), and the high microporosity (61.6 %) for AOBCs. At 25 ℃, the maximum adsorption capacity calculated by Langmuir model of AOBC-3–600 for tetracycline hydrochloride (TC), chlortetracycline hydrochloride (CTC), oxytetracycline hydrochloride (OTC), and doxycycline hydrochloride (DOC) reached 473.00, 293.28, 220.61, and 282.72 mg/g, respectively. The superior fit of the pseudo-second-order and Langmuir models indicated that the adsorption mechanism involved both the physical effect (pore filling) and chemical interactions (electrostatic attraction, hydrogen bonding, π-π interaction, and Lewis acid-base interaction). Environmental risk assessments substantiated the absence of residual oxytetracycline and antibiotic resistance genes in the prepared biochar, indicating its application safety. This research provides a sustainable route to simultaneously treat the antibiotic contamination in water and rationally utilize antibiotic fermentation residues.

Improvement of tetracycline removal using amino acid ionic liquid modified magnetic biochar based on theoretical design

In current research, biochar is widely used to remove antibiotic contamination from the environment. However, original biochar produced through direct pyrolysis has significant limitations in removing antibiotics. In this paper, response surface methodology provided the laudable choice for magnetic poplar biochar (MPBC) considering the synergistic effect of multi-factors as well as the restrictions abundance experiments during the preparation of MPBC. Amino acid ionic liquids (AAILs) are a class of ionic liquids in which amino acids act as the anionic component, combining the tunable properties of ionic liquids with the biocompatibility and functionality of amino acids. To ameliorate adsorption capacity of MPBC, tetra-ethylammonium glycinate ([TEA][Gly]) with the best affinity for tetracycline (TC) were screened from 600 AAILs based on theoretical predictions using the conductor-like screening model for real solvents (COSMO-RS) without extensive experimental. Furthermore, AAILs-modified magnetic biochar (MPBC-AAIL) was synthesized chemically for the first time. Adsorption kinetics, isotherms, and thermodynamic analyses revealed that TC adsorption by both MPBC and MPBC-AAIL is a monolayer, spontaneous, and exothermic chemical process. Moreover, MPBC-AAIL exhibited a maximum adsorption capacity of 305.9 mg·g−1. Meanwhile, MPBC-AAIL maintains superior adsorption performance for TC in different impurity solutions as well as in real water samples. The excellent reusability and selective adsorption capacity of the material demonstrate the superiority of the theoretical based design. The characterization reveals that the adsorption mechanisms include pore filling, π-π interactions, surface complexation, hydrogen bonding, and electrostatic interactions. In addition, theoretical calculations showed that ionic liquid modification altered the adsorption sites between TC and MPBC-AAIL, leading to enhanced adsorption. This comprehensive study introduces an innovative modification of biochar, providing a novel approach to designing biochar composites and promoting their application in the remediation of complex environmental pollution.

Innovative RGO-bridged S-scheme CuFe2O4@Ag2S heterojunction for efficient Sun-light-driven photocatalytic disintegration of Ciprofloxacin

Antibiotics contamination in water bodies poses a significant threat to public health and the environment, necessitating advanced methods for their removal from wastewater. In response to this issue, developing a novel magnetic nanocomposite (RGO/CuFe2O4@Ag2S) as an efficient photocatalyst for the degradation of pharmaceuticals like ciprofloxacin (CIP) is of great importance. The synthesized nanocomposite underwent comprehensive characterization to elucidate its crystalline structure, chemical bonding, surface morphology, elemental composition, internal structure, optical properties, surface area, particle size distribution, and magnetic properties. Under optimized conditions (pH = 9, nanocomposite dose = 0.5 g/L, CIP concentration of 20 mg/L, and duration of 200 min), the nanocomposite demonstrated complete degradation of CIP. Moreover, post-treatment analysis revealed significant reductions in total organic carbon (TOC) and chemical oxygen demand (COD) of 70.08 % and 85.08 %, respectively, indicating extensive mineralization of the antibiotic. Mechanistic investigations revealed a unique S-scheme heterojunction in the RGO/CuFe2O4@Ag2S nanocomposite, where RGO acts as an electronic bridge between CuFe2O4 and Ag2S. This innovative architecture facilitates efficient charge separation and transfer, significantly enhancing the photocatalytic activity. Reusability tests demonstrated the robust nature of the photocatalyst, with only a modest 6 % decline in efficiency after six consecutive cycles. To further assess the system's effectiveness in real-world applications, its performance was evaluated in treating pharmaceutical wastewater. The biodegradation efficiency was quantified by measuring the Average Oxidation State (AOS) and Carbon Oxidation State (COS) of the wastewater samples before and after treatment.

Efficiency of CaZn₂(OH)₆·2H₂O and ZnO nanoparticles in photocatalytic degradation of amoxicillin after multiple cycles

The widespread use of antibiotics has increased their presence in wastewater, largely due to inadequate removal by conventional treatment methods. This highlights a critical need for effective degradation strategies to mitigate environmental and public health risks. This study reports the photocatalytic degradation of amoxicillin (AMX) using calcium zinc hydroxide dihydrate [CaZn2(OH)6·2H2O] (CZ) and zinc oxide (ZnO) nanoparticles (NPs) synthesized by different routes. X-ray diffraction results confirmed the formation of CZ NPs with an 81–95% crystalline phase, while ZnO NPs present a single crystalline phase. The photolysis of AMX under UV-A light (365 nm) was strongly pH-dependent, with degradation rates of 34.7, 5.7, and 4.2% observed at pH 3, 5, and 13, respectively. Maximum adsorption occurred at pH 3, with ZnO achieving 63–83.2% AMX removal and 23.5–47.1% in the case of CZ. The highest overall AMX removal was observed at pH 3, where adsorption dominated the photocatalytic process for both CZ and ZnO. At pH 5 and 13, degradation was primarily driven by photocatalysis in CZ materials, particularly CZ-HT and CZ-SG, while adsorption remained predominant in ZnO. Proton nuclear magnetic resonance analysis indicates benzene ring cleavage in AMX photodegraded by CZ materials. Furthermore, the residues of photodegraded AMX by CZ materials lost antimicrobial activity against Gram-positive and Gram-negative bacteria. Additionally, the reuse of NPs over four cycles maintained consistent degradation performance, highlighting their potential for repeated applications. The comparative analysis of CZ and ZnO NPs superior photocatalytic efficiency of CZ in degrading AMX. This efficiency, along with its potential for repeated use, establish CZ as a promising material for environmental applications aimed at reducing antibiotic contamination and the associated risks of resistance development.

Source apportionment and ecological risk assessment of antibiotics in Dafeng River Basin using PMF and Monte-Carlo simulation.

Antibiotics, prevalent in aquatic ecosystems, pose a grave threat to human health and the ecological well-being. This paper performed a case study on Dafeng River Basin in southern China. Specifically, techniques including positive matrix factorization (PFM) and Monte-Carlo simulation were employed to comprehensively investigate the spatial variations, possible sources, and ecological risks of antibiotics in four groups: sulfonamides (SAs), macrolides (MLs), quinolones (QNs), and tetracyclines (TCs). The major findings were as follows: first, 43 and 39 antibiotics were detected in the surface water and sediments of the basin, respectively, where the respective total content were ND-490.08ng/L and ND-144.34μg/kg, and the QNs and TCs were the two dominating groups. Second, the highest antibiotic content in surface water (441.43ng/L) was observed in the midstream area, whereas the highest concentration in sediments (68.41μg/kg) was found in the upstream region. Third, the investigation identified five sources of antibiotics discharged to surface water: domestic sewage, agricultural drainage, livestock discharge, sewage treatment plants, and aquaculture; three sources were detected for antibiotics in sediments: aquaculture, sewage treatment plants, and livestock discharge. Fourth, QNs had a significantly higher ecological risk than the other three groups of antibiotics, and livestock discharge (31.4% contribution) and aquaculture (23.4% contribution) were the main sources of risks of antibiotic contamination in Dafeng River Basin. This study is expected to provide some reference for control and risk management of antibiotic pollution in Dafeng River Basin.

The remediation performance and mechanism for tetracycline from groundwater using controlled release materials containing mesoporous MnOx with different morphology

Aiming at the effective remediation of antibiotic contaminants in groundwater, in-situ chemical oxidation (ISCO), using controlled release materials (CRMs) as an oxidant deliverer, has emerged as a promising technique due to their long-term effective pollutant removal performance. This study used different microstructures of mesoporous manganese oxide (MnOx) and sodium persulfate as active components to fabricate CRMs. Following that, a comparative study of tetracycline (TC) degradation and the formation of reactive oxygen species (ROS) by mesoporous MnOx powder and CRMs were conducted. The ROS formed during peroxodisulfate (PDS) activation by powder catalysts and CRMs differed, but MnOx powder catalysts and CRMs both had good reaction stoichiometric efficiency (RSE) for PDS, thus completely mineralizing TC. In PDS activation by mesoporous MnOx powder, oxygen vacancies (OVs) caused by defects in the catalysts contributed to the generation of singlet oxygen (1O2). The 1O2 and free radicals (·SO4− and ·OH) both worked as major ROS participating in TC degradation. Concerning the release of CRMs in static groundwater, the immobilization of catalysts inside CRMs made it difficult to release 1O2 in the solution, thus slowing the degradation of TC by CRMs containing MnOx(1) in static groundwater. In the TC remediation in dynamic groundwater, the water flowing slowly passed through the CRM layer, and TC molecules were trapped. Therefore, 1O2 degraded the trapped TC in the CRM layer in dynamic groundwater. Compared to TC, the toxicity of most intermediates during the TC degradation by CRMs has decreased in static and dynamic groundwater.

Insight into efficient photocatalytic degradation of norfloxacin over a simple, economical biochar-based magnetic photocatalyst under solar illumination: a statistical and experimental approach.

The transformation of residual agricultural solid waste into an efficient value-added carbon product has been an ongoing strategy for solid waste management and a sustainable economy. Meanwhile, the upsurgence of antibiotic contamination in water bodies due to their inadvertent use poses a serious threat to human health and leads to antimicrobial resistance. Hence, to neutralize two evils in one stroke simultaneously, a simple, easy, and cost-effective pea shell-based magnetic photocatalyst (PSMC) has been synthesized and characterized by XRD (X-ray diffraction), VSM (vibrating sample magnetometer), XPS (X-ray photoelectron spectroscopy), TGA (thermogravimetric analysis), and FTIR (Fourier-transform infrared) spectroscopy techniques. Batch experimental studies revealed that PSMC efficiently eliminates norfloxacin (91.3%) within 180min from wastewater and mineralizes it into innocuous products at optimum parameters of norfloxacin concentration of 20mg/L, catalyst dosage of 15mg, and pH 3.5. Additionally, statistical parameters for the photodegradation of NX obtained from ANOVA by applying the Box-Behnken design are in close agreement with batch experiment parameters. PSMC has surplus advantages of facile recovery for recycling up to seven consecutive cycles by an external magnet and efficacy in natural solar light, making it cost-effective and economical. Radical scavenging studies revealed that O2•- and OH• were the potent reactive species in the photocatalytic degradation process.

One-pot synthesis of monodisperse silver-lignin particles: Enhanced antibacterial agents against antibiotic-resistant bacteria

Lignin-based supports for metal nanoparticles (NPs) have attracted significant attention due to their abundant functional groups that facilitate NPs loading. However, many studies involve a two-step process: fabricating lignin particles and then reducing metal ions to NPs using physical energy consumption or chemical reduction. A one-step in-situ reduction method for NP synthesis on carrier surfaces, eliminating energy consumption, is needed for environmentally friendly and sustainable approach. Herein, we demonstrate that poly-l-lysine (PL) controls the self-assembly kinetics of kraft lignin (KL), and reduces silver ion (Ag+) to silver nanoparticles (AgNPs), forming highly monodisperse, co-self-assembled PL-KL particles (Ag@PL-KLPs) without chemical reducing agents or energy consumption. PL facilitated rapid KL desolvation, promoting intermolecular interactions and silver ion adsorption, followed by an efficient, separate nucleation and growth process yielded Ag@PL-KLPs approximately 270 nm in size with a narrow distribution. Notably, Ag@PL-KLPs exhibited enhanced bacteriostatic and bactericidal properties against antibiotic-resistant bacteria (ARB), including both Gram-negative and Gram-positive strains, at concentrations of 250 μg/mL. Leveraging biomass-derived lignin and this cost-effective, one-step green synthesis approach offers a sustainable method for avoiding antibiotic overuse and environmental contamination.

Global quantification and distribution of antibiotic resistance genes in oceans and seas: Anthropogenic impacts and regional variability

The global spread of antibiotic resistance genes (ARGs) in the marine environment poses a significant threat to public health and natural ecosystems. This study quantified and analysed the distribution and co-occurrence patterns of ARGs in a wide range of oceans and high seas, including the Atlantic, Arctic and Indian Ocean, the Mediterranean Sea and the Persian Gulf. Focusing on beta-lactamases (blaOXA-48, blaCTX-M-1 group, and blaTEM), sulfonamides (sul1) and tetracycline (tetA), our results showed that sul1 was ubiquitous, indicating widespread dissemination. Notably, the Mediterranean Sea exhibited higher levels of multiple ARGs in single samples, suggesting significant anthropogenic impact. Interestingly, the Arctic Ocean, particularly around the Svalbard Islands, also showed the presence of multiple ARGs, highlighting the pervasive occurrence of antibiotic resistance in remote areas. We employed two clustering approaches to explore ARG patterns, primarily focusing on identifying geographic trends and differences in ARG abundance. Additionally, we investigated potential sources of contamination, including proximity to wastewater treatment plants, ports, marine traffic, and currents.These findings clearly demonstrate that antibiotic resistance gene contamination is widespread across diverse marine environments, with significant regional variations. This underscores the urgent need for tailored intervention strategies and global collaboration to mitigate the spread of ARGs and manage their complex dynamics in marine ecosystems.

Fabrication of efficient interface carrier channels on multidimensional O[sbnd]CQD Decorated CN Heterojunction for tetracycline degradation via peroxymonosulfate activation

Graphite carbon nitride (CN) is recognized as a promising non-metallic semiconductor photocatalyst for its excellent chemical stability and visible light response. However, the high electron-hole recombination rate in CN greatly limits its photocatalytic performance. To circumvent these limitations, it is particularly important to explore an efficient way to promote the migration of carriers in CN. This study innovatively designs a multidimensional heterojunction between organic carbon quantum (OCQD) and CN, which named as OCQD-CN. OCQD acts as an carriers transfer channel, which effectively promotes the separation efficiency of carriers. Meanwhile, the introduction of OCQD further improves light absorption scope as well as light reaction intensity of CN. By adding peroxymonosulfate (PMS) to form an advanced oxidation process, OCQD-CN10 exhibits a prominent tetracycline (TC) degradation capacity up to 89.1 % within 60 min. The photocatalytic degradation performance of OCQD-CN is significantly improved by 2.0 times with the addition of OCQD. The first-order rate constant corresponding of OCQD-CN10 (0.0300 min−1) is also 2.8 times higher than CN (0.0107 min−1). Thereby, this research underscores the potential of OCQD-CN/PMS system in mitigating water pollution and advancing eco-friendly technologies, offering a promising route to address antibiotic contaminants in the environment.

Removal of aqueous oxytetracycline using copper-loaded biochar-activated peroxodisulfate: Synergistic mechanism of adsorption and nonradical 1O2

Antibiotic contamination from livestock and poultry farming wastewater has caused substantial adverse effects on the environment and humans. Therefore, in this study, bifunctional adsorption and synergistic degradation of Cu and N codoped biochar (Cu-N/BC) were utilized to efficiently promote the activation of peroxodisulfate (PDS) for removing oxytetracycline (OTC). Cu-N/BC exhibited a high adsorption affinity toward OTC. The adsorption of OTC (50 mg/L) by 0.4 g/L catalyst could reach 36.2 mg/g in 30 min, and the removal of OTC reached 97.24 % in 90 min after adding 0.5 mM PDS. Preadsorption experiments demonstrated that the OTC enriched on the Cu-N/BC surface facilitated the subsequent degradation reaction，its reaction rate constant increases from 0.026 to 0.037. Low-valent copper (Cu0/Cu+), pyridine N, and oxygen-containing functional groups (CO) were the main active sites of Cu-N/BC, and the main contribution toward OTC degradation was from the nonradical pathway of singlet oxygen. Furthermore, potential degradation pathways were revealed, and the intermediates in the OTC degradation process were identified. Cu-N/BC exhibited stable performance, a wide pH application range, and great potential for practical application. This study offers a new concept for designing a bifunctional carbon-based material to remove antibiotics from wastewater.

Simultaneous determination of some coccidiostat antibiotics in food by liquid chromatography tandem mass spectrometry (LC-MS/MS)

Coccidiostats (anticoccidial antibiotics) are veterinary drugs widely used for the prevention and treatment of coccidiosis, especially in poultry farming. The illegal use of anticoccidial antibiotics, in the wrong dosage and duration, can lead to antibiotic residues in animal products and harm the health of consumers. In this study, a highly sensitive and accurate liquid chromatography-tandem mass spectrometry method was developed for the simultaneous analysis of anticoccidial antibiotics (diclazuril, nicarbazin, robenidin and salinomycin) in food. Samples were extracted using the QuEChERS method with acetonitrile (ACN) as the extraction solvent and cleaned with C18 adsorbent. The cleaned extracts were analyzed on an LC-MS/MS system with a C18 reversed-phase chromatography column (2.1 x 150 mm, 3.5 µm) and corresponding pre-column. The mobile phase used was 0.1% HCOOH in water and methanol (MeOH), the flow rate was 0.5 mL/min. The method had good specificity, the linear range was established in the range of 10-100 ng/mL, the correlation coefficient R2 > 0.998. The method recovery was in the range of 81-109% and the relative standard deviation (RSD%) was in the range of 1.77-10.13% for milk and meat samples. The limit of quantification and limit of detection of the method for four coccidiostat antibiotics were 3.0 µg/kg and 10 µg/kg, respectively. The method was applied to analyze the content of these four antibiotics in 31 food samples (meat and meat products, milk and dairy products) randomly purchased in Hanoi. The results did not detect four coccidiostat antibiotics in all 31 samples, initially showing that the residual contamination of coccidiostat antibiotics is basically safely controlled.