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Paracetamol, a contaminant of emerging concern, has been detected in different bodies of water, where it can impact ecological and human health. To quantify this paracetamol, electroanalytical methods have gained support. Thus, the present study developed a simple, inexpensive, and environmentally friendly method for paracetamol quantification using a carbon fiber microelectrode based on commercial carbon fiber. To improve the carbon fiber microelectrode's paracetamol sensitivity and selectivity, it was subjected to an activation process via electrochemical oxidation in an acid medium (H2SO4 or HNO3), using 20 consecutive cycles of cyclic voltammetry. The treated (activated) carbon fiber microelectrode was characterized using scanning electron microscopy and electrochemical techniques, including chronoamperometry and electrochemical impedance spectroscopy. The H2SO4-activated carbon fiber microelectrode exhibited enhanced figures of merit, with a linear dynamic range of paracetamol detection from 0.5 to 11 µmol L-1 and a limit of detection of 0.21 µmol L-1 under optimized conditions. The method was optimized by quantifying paracetamol in commercial pharmaceutical tablets, spiked running tap water, and river water (Pita River, Quito, Ecuador, latitude -0.364955°, longitude -78.404538°); the respective recovery values were 102.89, 103.93, and 112.40%. The results demonstrated an acceptable level of accuracy and the promising applicability of this carbon fiber microelectrode as a sensor to detect paracetamol.
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Acetaminofen , Carvão Vegetal , Humanos , Microeletrodos , Fibra de Carbono , ÁguaRESUMO
A green magnetic composite mCS/GO was synthesized using water hyacinth extract, as a reducing agent, and proanthocyanidin, as a crosslinking agent, for the adsorption of naphthalene from effluents. The green composite was evaluated using different characterization techniques to determine its thermal (TG/DTG), structural (BET, XPS and FTIR), crystallographic (XRD), and textural (SEM) properties in natura and post-adsorption. The results obtained through a central composite design (CCD) experiment indicated that the initial concentration of NAP and the adsorbent dosage are significant for the adsorption capacity. The adsorption assays indicated that physisorption, through π-π and hydrophobic interactions, were the main mechanism involved in the NAP adsorption. However, the adjustment to the PSO and Freundlich models, obtained through kinetic and equilibrium studies, indicated that chemisorption also influences the adsorptive process. The thermodynamic study indicated physisorption as the mechanism responsible for the NAP adsorption. Also, the adsorbent has high affinity for the adsorbate and the process is spontaneous and endothermic. The maximum adsorption capacity (qmax) of the green mCS/GO was 334.37 mg g-1 at 20 °C. Furthermore, the green mCS/GO was effectively regenerated with methanol and reused for five consecutive cycles, the percentage of NAP recovery went from approximately 91 to 75% after the fifth cycle. The green composite was also applied in the adsorption of NAP from river water samples, aiming to evaluate the feasibility of the method in real applications. The adsorption efficiency was approximately 70%. From what we know, this it is the first time that a green adsorbent was recycled after the polycyclic aromatic hydrocarbon (PAHs) adsorption process.
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Quitosana , Grafite , Hidrocarbonetos Policíclicos Aromáticos , Poluentes Químicos da Água , Adsorção , Quitosana/química , Águas Residuárias , Naftalenos , Grafite/química , Fenômenos Magnéticos , CinéticaRESUMO
Salmonella enterica is a leading cause of human gastrointestinal disease worldwide. Given that Salmonella is persistent in aquatic environments, this study examined the prevalence, levels and genotypic diversity of Salmonella isolates recovered from major rivers in an important agricultural region in northwestern Mexico. During a 13-month period, a total of 143 river water samples were collected and subjected to size-exclusion ultrafiltration, followed by enrichment, and selective media for Salmonella isolation and quantitation. The recovered Salmonella isolates were examined by next-generation sequencing for genome characterization. Salmonella prevalence in river water was lower in the winter months (0.65 MPN/100 mL) and significantly higher in the summer months (13.98 MPN/100 mL), and a Poisson regression model indicated a negative effect of pH and salinity and a positive effect of river water temperature (p = 0.00) on Salmonella levels. Molecular subtyping revealed Oranienburg, Anatum and Saintpaul were the most predominant Salmonella serovars. Single nucleotide polymorphism (SNP)-based phylogeny revealed that the detected 27 distinct serovars from river water clustered in two major clades. Multiple nonsynonymous SNPs were detected in stiA, sivH, and ratA, genes required for Salmonella fitness and survival, and these findings identified relevant markers to potentially develop improved methods for characterizing this pathogen.
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The COVID-19 pandemic has been monitored by applying different strategies, including SARS-CoV-2 detection with clinical testing or through wastewater-based epidemiology (WBE). We used the latter approach to follow SARS-CoV-2 dispersion in Tapachula city, located in Mexico's tropical southern border region. Tapachula is a dynamic entry point for people seeking asylum in Mexico or traveling to the USA. Clinical testing facilities for SARS-CoV-2 monitoring are limited in the city. A total of eighty water samples were collected from urban and suburban rivers and sewage and a wastewater treatment plant over 4 months in Tapachula. We concentrated viral particles with a PEG-8000-based method, performed RNA extraction, and detected SARS-CoV-2 particles through RT-PCR. We considered the pepper mild mottle virus as a fecal water pollution biomarker and analytical control. SARS-CoV-2 viral loads (N1 and N2 markers) were quantified and correlated with official regional statistics of COVID-19 bed occupancy and confirmed cases (r > 91%). Our results concluded that WBE proved a valuable tool for tracing and tracking the COVID-19 pandemic in tropical countries with similar water temperatures (21-29 °C). Monitoring SARS-CoV-2 through urban and suburban river water sampling would be helpful in places lacking a wastewater treatment plant or water bodies with sewage discharges.
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COVID-19 , SARS-CoV-2 , COVID-19/epidemiologia , Humanos , México/epidemiologia , Pandemias , RNA Viral/genética , Rios , SARS-CoV-2/genética , Esgotos , Águas Residuárias , ÁguaRESUMO
In January 25, 2019, the B1 dam of Córrego do Feijão mine located in Brumadinho municipality (Minas Gerais, Brazil) collapsed and injected nearly 2.8 Mm3 of iron (Fe)- and manganese (Mn)-rich tailings in the Paraopeba River. This study assessed the contribution of tailings to the contamination of sediments and water by those metals. The dataset was built through daily to weekly samplings executed in the two years following the event, at 27 sites located along the Paraopeba plus 9 sites located at the confluence of main tributaries. The results evidenced a distinct contribution in the sectors "Anomalous" (8.6-63.3 km downstream from the dam) and "Natural" (115.8-341.6 km). The "Anomalous" sector presented large Fe/Al (12.2 ± 6.4) and Mn/Al (0.33 ± 0.19) ratios in sediments, thus being rich in tailings, while the "Natural" sector presented small ratios (2.4 ± 1.0; 0.06 ± 0.03) comparable to the natural sediments. A 500-700 m3/s stream flow discharge in the Paraopeba caused pronounced drops to the Fe/Al and Mn/Al ratios in the "Anomalous" sector, attributed to the mixture of contaminated sediments from the main water course with uncontaminated sediments injected by the tributaries during the event. Non-linear regressions showed Fe/Al and Mn/Al declines in the "Anomalous" sector, related with tailings mobilization downstream. The concentrations of Fe and Al in the sediments correlated positively with the corresponding concentrations in the Paraopeba water, conditioned by raising discharge rates and variations in the water pH. The contribution of tailings to the Fe correlation was demonstrated. No direct relation was established between the Mn concentrations in water and stream discharge, because manganese is associated with fine particles in the tailings that are mobilized to the water column even under low flows. The preliminary results of Seasonal Autoregressive Integrated Moving Average models predicted the return of Paraopeba to a pre-collapse condition in 7-11 years.
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Poluentes Químicos da Água , Água , Brasil , Monitoramento Ambiental , Sedimentos Geológicos , Rios , Poluentes Químicos da Água/análiseRESUMO
In this work, a novel and effective hydrochar was prepared by hydrothermal treatment of Prunus serrulata bark to remove the pesticide atrazine in river waters. The hydrothermal treatment has generated hydrochar with a rough surface and small cavities, favoring the atrazine adsorption. The adsorption equilibrium time was not influenced by different atrazine concentrations used, being reached after 240 min. The Elovich adsorption kinetic model presented the best adjustment to the kinetic data. The Langmuir model presented the greatest compliance to the isotherm data and indicated a higher affinity between atrazine and hydrochar, reaching a maximum adsorption capacity of 63.35 mg g-1. Thermodynamic parameters showed that the adsorption process was highly spontaneous, endothermic, and favorable, with a predominance of physical attraction forces. In treating three real river samples containing atrazine, the adsorbent showed high removal efficiency, being above 70 %. The hydrochar from Prunus serrulata bark waste proved highly viable to remove atrazine from river waters due to its high efficiency and low precursor material cost.
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Atrazina , Herbicidas , Prunus , Poluentes Químicos da Água , Adsorção , Concentração de Íons de Hidrogênio , Cinética , Casca de Planta/química , Rios , Poluentes Químicos da Água/análiseRESUMO
The dissemination of antibiotic-resistant bacteria (ARB) from water used for crop irrigation to vegetables is poorly studied. During a year, five farmer markets in a city in Central Chile were visited, and 478 vegetable samples (parsleys, corianders, celeries, lettuces, chards, and beets) were collected. Simultaneously, 32 water samples were collected from two rivers which are used to irrigate the vegetables produced in the area. Resistant Enterobacterales were isolated and identified. Colistin resistance gene mcr-1 and extended spectrum ß-lactamases (ESBL) were molecularly detected. The association of environmental factors was evaluated, with the outcomes being the presence of Enterobacterales resistant to four antibiotic families and the presence of multidrug resistance (MDR) phenotypes. Parsley, coriander, and celery showed the highest prevalence of resistant Enterobacterales (41.9% for ciprofloxacin and 18.5% for ceftazidime). A total of 155 isolates were obtained, including Escherichia coli (n=109), Citrobacter sp. (n=20), Enterobacter cloacae complex (n=8), Klebsiella pneumoniae (n=8), and Klebsiella aerogenes (n=1). Resistance to ampicillin (63.2%) and ciprofloxacin (74.2%) was most frequently found; 34.5% of the isolates showed resistance to third-generation cephalosporins, and the MDR phenotype represented 51.6% of the isolates. In two E. coli isolates (1.29%), the gene mcr-1 was found and ESBL genes were found in 23/62 isolates (37%), with bla CTX-M being the most frequently found in 20 isolates (32%). Resistant Enterobacterales isolated during the rainy season were less likely to be MDR as compared to the dry season. Understanding environmental associations represent the first step toward an improved understanding of the public health impact of ARB in vegetables and water.
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Lead (Pb) is a potentially toxic element with significant environmental interest. Simple and sensitive analytical methods are necessary to allow determination of this element at trace levels using sample preparation procedures related to green chemistry. For this, calcium alginate beads (CA-beads), a low-cost and environmentally friendly biopolymer, have been proposed for extraction and preconcentration of Pb2+ in river water samples and determination by flame atomic absorption spectrometry (FAAS). CA-beads were prepared and applied to extract and preconcentrate Pb2+ in river water samples, providing an enrichment factor (EF) of 50, enhancement factor (E) of 54, a detection limit of 2 µg L-1, and a relative standard deviation < 5%. The extraction of Pb2+ in CA-beads achieved good selectivity, with recoveries from 94.8 to 100.2% in real samples, demonstrating the good accuracy of the proposed method. The results were also compared to those obtained by ICP-MS. The reuse of CA-beads was evaluated for six cycles, and under these conditions, the extraction and preconcentration efficiency of Pb2+ were not significantly affected. The developed methodology was applied to determine Pb2+ in water samples from rivers that are part of the hydrographic areas of Tibagi and Pitangui Rivers, in which the Pb2+ concentration was less than 2 µg L-1, a concentration lower than that established by Brazilian legislation for class I and II rivers.
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Chumbo , Poluentes Químicos da Água , Alginatos , Monitoramento Ambiental , Estudos de Viabilidade , Concentração de Íons de Hidrogênio , Rios , Espectrofotometria Atômica , Água , Poluentes Químicos da Água/análiseRESUMO
This study evaluated the impact of a 50% reduction of filter media depth in Household Slow Sand Filters (HSSFs) on continuous flow to remove physicochemical and microbiological parameters from river water. Furthermore, simple pre-treatment and disinfection processes were evaluated as additional treatments. Two filter models with different filtration layer depths were evaluated: a traditional one with 50 cm media depth (T-HSSF) and a compact one (C-HSSF) with 25 cm. HSSFs were fed with pre-treated river water (24-h water sedimentation followed by synthetic fabric filtration) for 436 days at a constant filtration rate of 0.90 m3 m-2 day-1 with a daily production of 48 L day-1. Sodium hypochlorite (2.0 mg L-1 of NaOCl 2.5% for 30 min) was used to disinfect the filtered water. Water samples were analysed weekly for parameters such as turbidity, organic matter, colour and E. coli, among others. Removal of protozoan cysts and oocysts by the HSSFs were also evaluated. After pretreatment, turbidity from the HSSF river water was reduced to 13.2 ± 14.6 NTU, allowing the filters to operate. Statistical analysis indicated no significant difference (p > 0.05) between T-HSSF and C-HSSF efficiencies in all evaluated parameters throughout operation time. Hence, media depth reduction did not hinder continuous HSSF performance for almost all the evaluated parameters. However, it may have affected Giardia cysts retaining, which passed through the thinner media on one evaluation day. Disinfection was effective in reducing remaining bacteria from filtered water; however, it was ineffective to inactivate protozoa. The reduction in the filtration layer did not affect the overall filtered water quality or quantity showing that a compact HSSF model may be a viable option for decentralized water treatment.
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Areia , Purificação da Água , Escherichia coli , Características da Família , Filtração , Dióxido de SilícioRESUMO
In this work, nanoporous gold (NPG) was prepared according to three different approaches, such as (i) anodization-electrochemical reduction (A-ECR, NPGA), (ii) dynamic hydrogen bubble template (DHBT, NPGB), and (iii) the combination of both methods (NPGA+B). Field-emission scanning electron microscopy (FE-SEM) and cyclic voltammetry (CV) were used to investigate the structural morphology and the electrochemical behavior of the fabricated materials. The NPGA+B electrode showed a large amount of surface defects and/or edges, greater electrochemical surface area (2.5 cm2), and increased roughness factor (35.4). Such outstanding features of the NPGA+B platform were demonstrated by the sensitive detection of methyl parathion (MP) in river water samples. CV results indicated nearly 25-fold, 6-fold, and 2.5-fold higher sensitivity for NPGA+B compared to that of bare Au, NPGA, and NPGB, respectively. Differential pulse voltammetry (DPV) results show a linear behavior in the MP concentration range of 5-50 ng mL-1 with a limit of detection (LOD) of 0.6 ng mL-1 and limit of quantification (LOQ) of 2.0 ng mL-1. Besides, the NPGA+B sensor also revealed excellent selectivity towards MP detection in the presence of other interfering molecules or ions, reproducibility, and repeatability.
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This study provided a monitoring of phenolic compounds occurrence in a river and in its treated water by a conventional water treatment plant (WTP) throughout a year-period, in Minas Gerais - Brazil. Furthermore, the environmental risk (hazard quotient - HQ), the human health risk (margin of exposure - MOE), and the cancer risk were calculated for the compounds. The results indicated that sixteen out of the seventeen investigated phenolic compounds were detected at some point during the sampling campaign. The most frequent compounds in the raw surface water were 2,3,4-trichlorophenol (234TCP), 2,4-dimethylphenol (24DMP), and 4-nitrophenol (4NP), whereas in treated water were 4NP and bisphenol A (BPA). In addition, the highest total concentration values were corelated to the months in which there was less precipitation, demonstrating that the presence of this micropollutants may be subject to seasonality. From the treated water results, it was not possible to state the efficiency of the conventional WTP in eliminating the phenols, since in some samples the phenolic compounds were totally removed and in others their increase or formation occurred. Regarding to the risk assessments, most of the evaluated compounds were considered highly toxic to some trophic level and posed a significant human health risk. Additionally, the risk reduction of phenolics using conventional WTP was low. The sixteen phenols contamination in surface and drinking waters appears to be subject to seasonality. Besides that, an alarming risk for environment and human health was identified.
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Poluentes Químicos da Água , Compostos Benzidrílicos/análise , Brasil , Monitoramento Ambiental , Humanos , Fenóis/análise , Medição de Risco , Rios , Estações do Ano , Poluentes Químicos da Água/análiseRESUMO
Rapid, on-site detection of emerging pollutants is critical for monitoring health threats and the environment, especially if performed through autonomous systems. In this paper, we report on a new design of a complete electrochemical system whose working (WE), auxiliary (AE) and reference (RE) electrodes were obtained on a pen (PEN Sensor) made with graphite:polyurethane (GPUE). Working electrodes were decorated with spherical, ca. 200 nm silver nanoparticles (AgNPs) reduced on graphite using the polyol method. Differential pulse voltammetry (DPV) was used to detect bisphenol-A (BPA) in a linear range from 2.5 to 15 µmol L-1 with detection limit of 0.24 µmol L-1. The PEN Sensor could also detect bisphenol-A in tap and river water samples, with satisfactory reproducibility and repeatability, while common interferents did not affect electrooxidation of bisphenol-A. The high sensitivity and rapid detection are suitable for real-time analysis and in loco monitoring of emerging pollutants. With their robustness and versatility, PEN Sensors such as those fabricated here may be integrated into futuristic smart robotic systems.
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Grafite , Nanopartículas Metálicas , Técnicas Eletroquímicas , Eletrodos , Limite de Detecção , Poliuretanos , Reprodutibilidade dos Testes , Rios , Prata , ÁguaRESUMO
Intestinal pathogenic microorganisms are introduced into the water by means of faecal contamination, thus creating a threat to public health and to the environment. Detecting these contaminants has been difficult due to such an analysis being costly and time-intensive; as an alternative, microbiological indicators have been used for this purpose, although they cannot differentiate between human or animal sources of contamination because these indicators are part of the digestive tracts of both. To identify the sources of faecal pollution, the use of chemical, microbiological and molecular markers has been proposed. Currently available markers present some geographical specificity. The aim of this study was to select microbial and molecular markers that could be used to differentiate the sources of faecal pollution in the Bogotá River and to use them as tools for the evaluation and identification of the origin of discharges and for quality control of the water. In addition to existing microbial source markers, a phage host strain (PZ8) that differentiates porcine contamination was isolated from porcine intestinal content. The strain was identified biochemically and genotypically as Bacteroides. The use of this strain as a microbial source tracking indicator was evaluated in bovine and porcine slaughterhouse wastewaters, raw municipal wastewaters and the Bogotá River. The results obtained indicate that the selected microbial and molecular markers enable the determination of the source of faecal contamination in the Bogotá River by using different algorithms to develop prediction models.
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Bacteroides/isolamento & purificação , Monitoramento Ambiental/métodos , Fezes , Poluentes da Água/isolamento & purificação , Poluição da Água , Matadouros , Animais , Bovinos , Colômbia , Aprendizado de Máquina , Rios/microbiologia , Suínos , Águas Residuárias/microbiologia , Microbiologia da ÁguaRESUMO
Recycling of end-of-life polyamide-based thin film composite (TFC) membranes is gaining interest in academic and industrial contexts. The effects of chlorine exposure on the performance of polyamide membranes result in an increase in membrane permeability, whereas the solute rejection decreases. Therefore, the controlled chemical conversion of old reverse osmosis (RO) membranes has been reported by some previous papers. The objectives of this study were to assess recycling of old nanofiltration (NF) membrane, to assess the performance of the recycled membranes for a river water treatment application, and to conduct preliminary cost evaluations. Recycling technique consisted of exposing the membrane to a sodium hypochlorite solution in order to remove its polyamide layer and conversion to a low-pressure membrane. The work conducted bench scale and long-time pilot tests, and the recycled membranes showed a low fouling tendency. The difference between some results in bench- and pilot scale underscores the importance of evaluating design parameters using pilot scale units. Based on the cost analysis, the total cost of chemical recycling end-of-line NF membranes for a river water treatment is approximately 1.1% of the cost of using a new UF membrane. There is a great potential in using recycled membranes for rivers water treatments.
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Membranas Artificiais , Purificação da Água , Filtração , Osmose , ReciclagemRESUMO
Organophosphate esters used as flame retardants and plasticizers are ubiquitous contaminants in surface waters. Many studies indicate that these compounds are neurotoxicants, endocrine disruptors, and may affect reproduction and development of aquatic organisms. Thus, analytical methods that allow accurate quantification of these contaminants at environmentally relevant concentrations are desirable for risk assessment studies. In this study, a method based on solid phase extraction and gas chromatography coupled to mass spectrometry was developed for determination of organophosphate esters in river water extracts. Multivariate optimization was used to determine the best conditions for injection of larger volumes of sample in a Programmable Temperature Vaporization inlet. Furthermore, the matrix effect on the instrumental response was evaluated and compensated by association of extraction-blank-matched calibration and isotopically labeled focus standards. The method quantification limits ranged from 0.009 to 0.11 µg/L, staying below the predicted non-effect concentration for the aquatic compartment for all analytes, which is a requisite for using in risk assessment studies. The method was applied to freshwater samples collected in rivers from the Sao Paulo State, Brazil, and eight out of the ten target organophosphate esters were quantified, being tris(2-chloroisopropyl) phosphate and tris(phenyl) phosphate the most frequently detected compounds.
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The growth of urbanization worldwide has contributed to the deterioration of the ecological status of water bodies. Efforts at improving the ecological status have been made either in isolated form or by means of integrated measures by stakeholders, but in many cases, these measures have not been evaluated to determine their benefit. In this study, we implemented a scenario analysis to restore the ecological water quality in the Cuenca River and its tributaries, which are located in the southern Andes of Ecuador. For this analysis, an integrated ecological model (IEM) was developed. The IEM linked an urban wastewater system (IUWS) model, which gave satisfactory results in its calibration and validation processes, with ecological models. The IUWS is a mechanistic model that incorporated the river water quality model, a wastewater treatment plant (WWTP) with activated sludge technology, and discharges from the sewage system. The ecological status of the waterways was evaluated with the Andean Biotic Index (ABI), which was predicted using generalized linear models (GLMs). The GLMs were calculated with physicochemical results from the IUWS model. Four scenarios that would enhance the current ecological water quality were analyzed. In these scenarios, the inclusion of a new WWTP with carbon, and with carbon and nitrogen removal as well as the addition of retention tanks before the discharges of combined sewer overflows (CSOs) were assessed. The new WWTP with carbon and nitrogen removal would bring about a better restoration of the ecological water quality due to better nitrogen removal. The retention tanks would help to enhance the ecological status of the rivers during rainy seasons. The integrated model implemented in this study was shown to be an essential tool to support decisions in the Cuenca River basin management.
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Spent coffee grounds (SCG) immobilized in agarose gel are proposed as a novel binding agent for application in the Diffusive Gradients in Thin films (DGT) technique for the determination of Cd, Cu, Ni, Pb and Zn in waters. The SCG-agarose gel was characterized by Scanning Electron Microscopy, Energy Dispersive X-ray Spectrometry and Porosimetry by nitrogen adsorption. Elution of analytes from the binding agent was effectively performed with 2â¯molâ¯L-1 HCl. The effects of key DGT parameters (e.g. immersion time, ionic strength and pH) were evaluated with a deployment of DGT devices (DGT-SCG) in synthetic solutions with ionic strengths between 0.005â¯molâ¯L-1 and 0.1â¯molâ¯L-1 and within a pH range of 3.5-8.0. The results were in excellent agreement with the predicted theoretical curve for mass uptake. Consistent results were found for solutions with ionic strengths between 0.005â¯molâ¯L-1 and 0.1â¯molâ¯L-1 and within a pH range of 3.5-8.0. The DGT-SCG performance was also evaluated in two spiked river water samples (Corumbataí and Piracicaba river) with satisfactory uptake values (CDGT-SCG/Csol) between 0.74 and 1.53. The proposed DGT-SCG opens opportunities for using residual biomass as binding phase in the DGT technique, showing low costs in production and complying with "green" technology approaches.
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BACKGROUND: River water has been implicated as a source of non-typhoidal Salmonella (NTS) serovars in Mexico. OBJECTIVE: To dissect the molecular pathogenesis and defense strategies of seven NTS strains isolated from river water in Mexico. METHODS: The genome of Salmonella serovars Give, Pomona, Kedougou, Stanley, Oranienburg, Sandiego, and Muenchen were sequenced using the whole-genome shotgun methodology in the Illumina Miseq platform. The genoma annotation and evolutionary analyses were conducted in the RAST and FigTree servers, respectively. The MLST was performed using the SRST2 tool and the comparisons between strains were clustered and visualized using the Gview server. Experimental virulence assay was included to evaluate the pathogenic potential of strains. RESULTS: We report seven high-quality draft genomes, ranging from ~ 4.61 to ~ 5.12 Mb, with a median G + C value, coding DNA sequence, and protein values of 52.1%, 4697 bp, and 4,589 bp, respectively. The NTS serovars presented with an open pan-genome, offering novel genetic content. Each NTS serovar had an indistinguishable virulotype with a core genome (352 virulence genes) closely associated with Salmonella pathogenicity; 13 genes were characterized as serotype specific, which could explain differences in pathogenicity. All strains maintained highly conserved genetic content regarding the Salmonella pathogenicity islands (1-5) (86.9-100%), fimbriae (84.6%), and hypermutation (100%) genes. Adherence and invasion capacity were confirmed among NTS strains in Caco-2 cells. CONCLUSION: Our results demonstrated the arsenal of virulence and defense molecular factors harbored on NTS serovars and highlight that environmental NTS strains are waterborne pathogens worthy of attention.
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Genoma Bacteriano , Rios/microbiologia , Salmonella/genética , México , Anotação de Sequência Molecular , Filogenia , Salmonella/classificação , Salmonella/isolamento & purificação , Salmonella/patogenicidade , Virulência/genéticaRESUMO
A carbon paste electrode (CPE) was modified with graphite oxide (GrO) and ß-cyclodextrin (CD) to obtain a sensor for simultaneous voltammetric determination of levodopa (LD), piroxicam (PRX), ofloxacin (OFX) and methocarbamol (MCB). The morphology, structure and electrochemical properties of the functionalized GrO were characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, contact angle measurements and cyclic voltammetry. Under the optimal experimental conditions, the sensor is capable of detecting LD, PRX, OFX and MCB by square wave voltammetry (SWV) at working potentials of +0.40, +0.60, +1.03 and + 1.27 V (versus Ag/AgCl), respectively. Response is linear from 1.0 to 20 µM for LD, from 1.0 to 15 µM for PRX, from 1.0 to 20 µM for OFX, and from 1.0 to 50 µM for MCB. The respective limits of detection are 65, 105, 89 and 400 nM. The method was successfully applied to the simultaneous determination of LD, PRX, OFX and MCB in (spiked) real river water and synthetic urine samples, and the results were in agreement with those obtained using a spectrophotometric method, with recoveries close to 100%. Graphical abstract Schematic presentation of a novel electroanalytical method employing a carbon paste electrode modified with graphite oxide and ß-cyclodextrin for the simultaneous determination of levodopa, piroxicam, ofloxacin and methocarbamol in urine and river water samples by square wave voltammetry.
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Grafite/química , Levodopa/urina , Metocarbamol/urina , Ofloxacino/urina , Piroxicam/urina , beta-Ciclodextrinas/química , Técnicas Eletroquímicas/métodos , Eletrodos , Levodopa/química , Limite de Detecção , Metocarbamol/química , Ofloxacino/química , Óxidos/química , Piroxicam/química , Reprodutibilidade dos Testes , Rios/químicaRESUMO
The envisaged ubiquitous sensing and biosensing for varied applications has motivated materials development toward low cost, biocompatible platforms. In this paper, we demonstrate that carbon nanodiamonds (NDs) can be combined with potato starch (PS) and be deposited on a glassy carbon electrode (GCE) in the form of a homogeneous, rough film, with electroanalytical performance tuned by varying the relative ND-PS concentration. As a proof of concept, the ND/PS film served as matrix to immobilize tyrosinase (Tyr) and the resulting Tyr-ND-PS/GCE biosensor was suitable to detect catechol using differential pulse voltammetry with detection limit of 3.9â¯×â¯10-7â¯molâ¯L-1 in the range between 5.0â¯×â¯10-6 and 7.4â¯×â¯10-4â¯molâ¯L-1. Catechol could also be detected in river and tap water samples. This high sensitivity, competitive with biosensors made with more sophisticated procedures and materials in the literature, is attributed to the large surface area and conductivity imparted by the small NDs (<5â¯nm). In addition, the ND-PS matrix may have its use extended to immobilize other enzymes and biomolecules, thus representing a potential biocompatible platform for ubiquitous biosensing.