Fluoroquinolones are a valuable synthetic antibacterial class widely used in the treatment of infectious diseases both in humans and animals. Until recently, it has been thought that bacterial resistance to fluoroquinolones develops very slowly. Nowadays, there are multiple studies that reveal the alarming occurrence of bacterial resistance and there is a high risk of becoming therapeutically useless. The emergence of this phenomenon comes from injudicious usage in therapy, the presence of residues and their metabolites in food of animal origin and also in sewage, compost and domestic waste, which end up in soil and water sources. In the present paper, we reviewed important issues regarding fluoroquinolones impact on the environment in connection with the development of bacterial resistance: (1) the presence of fluoroquinolones as pollutants in soil, surface waters, and food. Fluoroquinolones are persistent with high specificity to interact with soil compared to other antibiotics. Pollution of water sources raises concerns regarding the effects of small concentrations (ng L⁻¹) on human health and also of the environment. The non-therapeutic use in animal farms conducts to food pollution; the cultivated plants could concentrate the fluoroquinolones (over 100 μg L⁻¹); (2) the increase of bacterial resistance to fluoroquinolones occurring with specific mutations in the target enzymes as well by the plasmid-mediated resistance and active efflux of the cell; (3) international regulations of the fluoroquinolone residues in food that are far to encompass all compounds; (4) fluoroquinolones residues analysis with standardized methods should provide limits of detection lower than maximum residue limit values; and (5) trends and perspectives: (a) a wider process of harmonization of regulations; (b) the fluoroquinolones restriction, necessary for low levels of bacterial resistance; (c) the soil and waste water purification methods; (d) the practice of soil planting scheme as an alternative; and (e) an environmental label in order to facilitate the selection of drugs.

A sensitive liquid–chromatography–electrospray tandem mass spectrometry multiclass method for determination of 45 veterinary compounds belonging to 9 different antibiotic groups, including aminoglicosides (4), β-lactams (13), diaminopyrimidines (1), fluoroquinolones (10), lincosamides (1), macrolides (5), pleuromutilins (1), sulfonamides (6) and tetracyclines (4), in water from breeding animal watering supply system has been developed. Isolation of the analytes was carried out by solid phase extraction with heptafluorobutyric acid as an ion-pair agent on the Strata-X reversed phase cartridges. All analytes were determined simultaneously in one single run on a C18 column with gradient elution and short analysis time (13min). Method was validated, average relative recoveries were in the range of 84.3–109.3% with satisfactory precision are repeatability for all compounds are in the range of 4.7–12.2%, within-laboratory reproducibility are in the range of 4.4–13.5% for. The limit of quantitation (LOQ) of the method was in the range of 0.02–10μgL−1, depending of analyte. The applicability of the method was tested by determining antimicrobial compounds in real water samples collected from water supply systems in breeding animal farms. The average antibiotics concentration in real water samples were, respectively, in the range of 0.14–1670μgL−1.

Antimicrobial resistances (AMR) present an emerging concern in human and animal health policy, as well as in water policy as a consequence of the pollution of water resources by antibiotic substances stemming from manure and sewage treatment plants. In 2017, the European Commission passed an AMR Action Plan and urged member states to develop national action plans to coordinate action across human, animal and environmental health. Building on the literature on policy integration we conduct comparative case studies in order to explore how European countries address the AMR challenge and if policies respond to the cross-sectoral character of AMR. We find that policy integration varies across countries provide explanations for why this is the case and come to three main conclusions: Firstly, and confirming previous research, a pronounced executive capacity, the presence of green parties in parliament, and a consensus democracy are each necessary but not sufficient conditions in configurations leading to policy integration. Secondly, executive capacity only results in policy integration if there is no important agricultural sector articulating its interests. Thirdly, even if there is an important agricultural and/or livestock sector, green parties in parliament or consensus democracies can balance these interests towards a successful policy integration.

The residues of antibiotics in the environment pose a potential health hazard, so highly sensitive detection of antibiotics has always appealed to analytical chemists. With the widespread use of new low-dimensional materials, graphene-modified electrochemical sensors have emerged as an excellent candidate for highly sensitive detection of antibiotics. Graphene, its derivatives and its composites have been used in this field of exploration in the last decade. In this review, we have not only described the field using traditional summaries, but also used bibliometrics to quantify the development of the field. The literature between 2011 and 2021 was included in the analysis. Also, the sensing performance and detection targets of different sensors were compared. We were able to trace not only the flow of research themes, but also the future areas of development. Graphene is a material that has a high potential to be used on a large scale in the preparation of electrochemical sensors. How to design a sensor with selectivity and low cost is the key to bring this material from the laboratory to practical applications.

MSc (Chemistry) | Department of Chemistry | Antibiotics and perfluoroalkyl substances (PFAS) are groups of anthropogenic substances that are found in industries and consumer products, i.e., antibiotics are used in healthcare facilities, pharmaceutical companies, and agriculture, whereas PFAS are used in industries and households. These compounds find their way into the environment through emission, landfill disposal, agricultural run-offs, irrigations, leaching and wastewater spillage. Their residues are widely detected in almost every environmental compartment. Their detection in drinking water and food is one of the global concerns. Their effect in living organisms have been widely documented ranging from allergic reaction to carcinogenic effect, and in serious situations they can lead to death. In this project, the background review on the behaviour of antibiotics and PFAS in different environments are discussed in chapter two. This has been done by looking into their physico-chemical properties, distribution pathways, accumulation and toxicity in various environmental compartments through available literature. After understanding their behaviour in the environment two review papers, namely Paper I and Paper II, were written. Paper I was a book chapter which focused on the application of miniaturised liquid phase extraction techniques used for extraction of antibiotics in environmental water samples. In this book chapter, the use of liquid-liquid extraction techniques was discussed and the evolution of liquid-liquid extraction technique into miniaturised extraction technique was reviewed. Paper II was a critical review which focuses on the application of dispersive liquid-liquid micro-extraction of PFAS in different environmental samples. In this paper, the principles of dispersive liquid-liquid micro-extraction was explained. Later, its application for pre-concentration of PFAS was reviewed and the future trends were discussed. In chapter four, three lab-based papers, namely Paper III, Paper IV and Paper V, were written. In Paper III, for the first time a dispersive liquid-liquid microextraction technique was developed and applied for extraction of multi-class antibiotics in macadamia nuts prior to UHPLC-qToF-MS analysis. In paper IV, a novel deep eutectic solvent was synthesised and characterised using FTIR spectroscopy. For the first time the synthesised deep eutectic solvent was applied for extraction of multiclass antibiotics in green beans prior to UHPLC-qToF-MS analysis. In Paper V, for the first a dispersive liquid-liquid micro-extraction technique was developed and applied for extraction of PFAS in food contact materials prior to UHPLC-qToF-MS analysis. Owing to their ease of operation, efficiency and sensitivity, these techniques can also be applied for preconcentration of antibiotics and PFAS in different food, environmental and biological samples. | NRF

Seaweeds are rich in bioactive compounds which have well-documented antioxidant properties. They also have antimicrobial activities against food pathogenic microorganisms. This study uses an extract of the brown seaweed, Saccharina (Laminaria) japonica, produced by subcritical water hydrolysis (SWH) for investigating its potential to inhibit bacteria. De-oiled S. japonica was obtained by supercritical carbon dioxide extraction. The reaction temperatures for hydrolysis of raw and de-oiled S. japonica were maintained from 200 to 280 °C. The experiment was done with condition 1.3–6.0 MPa for the reaction pressure and 1:10 (w/v) for the ratio of material to water. The antibacterial activities of raw and de-oiled S. japonica produced by SWH were determined by using the agar diffusion method. Antibacterial activity was tested against two Gram-negative (Escherichia coli and Salmonella typhimurium) and two Gram-positive bacteria (Staphylococcus aureus and Bacillus cereus). The antibacterial activities of hydrolysate water with catalyst at 240 °C showed better bacterial inhibition than the others. Strong antibacterial activity was found using de-oiled material with acetic acid added, with a zone of inhibition of S. typhimurium (14.33 ± 0.06 mm) and E. coli (13.00 ± 0.09 mm). On the other hand, the weakest antibacterial inhibition was found for S. aureus (12.83 ± 0.10 mm) and B. cereus (12.50 ± 0.09 mm).

Greywater is increasingly treated and reused for agricultural irrigation in off-grid communities in the Middle East and other water scarce regions of the world. However, there is a dearth of data regarding levels of antibiotics and herbicides in off-grid greywater treatment systems. To address this knowledge gap, we evaluated levels of these contaminants in two types of greywater treatment systems on four farms in the West Bank, Palestinian Territories. Samples of household greywater (influent, n = 23), treated greywater effluent intended for agricultural irrigation (n = 23) and pumped groundwater held in irrigation water ponds (n = 12) were collected from October 2017 to June 2018. Samples were analyzed using high performance liquid chromatography tandem mass spectrometry (LC-MS/MS) for the following antibiotics and herbicides: alachlor, ampicillin, atrazine, azithromycin, ciprofloxacin, erythromycin, linezolid, oxacillin, oxolinic acid, penicillin G, pipemidic acid, sulfamethoxazole, triclocarban, tetracycline, triflualin, and vancomycin. All tested antibiotics and herbicides were detected in greywater influent samples at concentrations ranging from 1.3 to 1592.9 ng/L and 3.1–22.4 ng/L, respectively. When comparing influent to effluent concentrations, removal was observed for azithromycin, alachlor, linezolid, oxacillin, penicillin G, pipemidic acid, sulfamethoxazole, triclocarban, and vancomycin. Removal was not observed for atrazine, ciprofloxacin, erythromycin, oxolinic acid, tetracycline, and trifluralin. Pond water also contained the majority of tested contaminants, but at generally lower concentrations. To our knowledge, this is the first description of an extensive array of antibiotics and herbicides detected in household greywater from off-grid treatment systems.

Water contamination by pathogenic bacteria is a global public health problem. Contamination of surface water utilized to irrigate food products, or for human consumption, causes outbreaks of foodborne and waterborne disease. Of these, those caused by diarrheagenic Escherichia coli (DEC) strains present substantial morbidity and mortality. The aim of this study was, therefore, to investigate the microbiological quality of surface water and the presence of DEC strains in different water bodies. A total of 472 water samples were collected from irrigation canal, dam, river, and dike water bodies from January through December 2015 in Sinaloa, a State located in Northwestern Mexico. Our studies demonstrated that 47.0% (222/472) of samples contained thermotolerant coliforms above permissive levels whereas E. coli strains were isolated from 43.6% (206/472). Among these E. coli isolates, DEC strains were identified in 14% (29/206) of samples including in irrigation canal (26/29) and river water (3/29) collected from the northern (83%) and central area (17%). Isolated DEC strains were classified as enteroaggregative E. coli (EAEC) 34.4% (10/29), enteropathogenic E. coli (EPEC) 31.0% (9/29), diffuse adherent E. coli (DAEC) 27.5% (8/29), and enterotoxigenic E. coli (ETEC) 6.8% (2/29). Moreover, 90% of isolated DEC strains exhibited resistance to at least one commonly prescribed antibiotic in Mexico whereas 17% were multi-drug resistant. In conclusion, the presence of DEC strains in surface water represents a potential source for human infection, and thus routine monitoring of DEC in surface water and other indirect affected areas should be considered at northwestern Mexico.

A molybdenum disulfide(MoS2)-based core-shell magnetic nanocomposite (Fe₃O₄@MoS₂) was synthesized by the stepwise hydrothermal method. Two-dimension ultrathin MoS₂ sheets with a thickness of approximately 20 nm were grown in situ on the surface of Fe₃O₄ (∼200 nm). They were employed as an adsorbent for the magnetic solid-phase extraction (MSPE) of sulfonamide antibiotics (SAs) from water samples. High-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) was used for SA quantitation. Extraction parameters, including the pH effect, amount of Fe₃O₄@MoS₂, extraction time, temperature, and desorption conditions, were systematically investigated. The electrostatic interaction between the positively charged SAs and negatively charged MoS₂ nanoparticles in the optimal extraction conditions enhanced the adsorption of SAs on the sorbent surface. Under chosen conditions, the proposed strategy achieved wide linear range of 1.0–1000 ng·L⁻¹ SAs, low limits of detection (LOD, 0.20–1.15 ng·L⁻¹, S/N = 3:1), good trueness (recoveries between 85.50–111.5%), satisfactory repeatability and reproducibility (relative standard deviation, <10%, n = 5), and excellent recoveries between 80.20% and 108.6% for SAs determination in spiked waste water samples. The proposed strategy was validated and successfully applied for the analysis of water, milk, pork meat and fish meat. The nanocomposites, which have the combined advantages of magnetic separation and high adsorption affinity toward SAs, are a promising sorbent for antibiotics extraction from real samples.