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1.
Environ Sci Pollut Res Int ; 28(47): 67822-67832, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34268682

RESUMO

Antibiotics have become a concern in the aquatic environments owing to the potential development of bacterial resistances. Thus, this study evaluated the removal of cephalexin (CEP) and erythromycin (ERY) from a local wastewater treatment plant (WWTP) effluent, mediated by microalgae-bacteria consortium. Likewise, the removal of correlated antibiotics resistance genes blaTEM and ermB was also assessed. The incubation results showed that the added concentrations of selected antibiotics did not restrain the consortium growth. Moreover, CEP and ERY were almost completely removed after the cultivation period, reaching total removals of 96.54% and 92.38%, respectively. The symbiotic interaction between microalgae and bacteria plays a role in the kinetics removal of CEP and ERY. The abundance of blaTEM and ermB was reduced by 0.56 and 1.75 logs, respectively. Lastly, our results suggest that technology based on natural microalgae-bacteria consortium could be a potential alternative to improve the quality of WWTP effluents.


Assuntos
Microalgas , Purificação da Água , Antibacterianos , Bactérias/genética , Cefalexina , Eritromicina , Águas Residuárias/análise
2.
Water Res ; 189: 116545, 2021 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-33160237

RESUMO

A widely used herbicide, metribuzin, was evaluated for degradation, mineralization and disinfection by-products (DBPs) formation during aqueous chlorination. In addition, to assess the toxicity effects of chlorination on metribuzin solution the following tests were performed: acute toxicity using Artemia salina nauplii; cell viability using MTT assay; estrogenicity using a re-engineered Bioluminescent Yeast Estrogen Screen (BLYES) and a constitutively bioluminescent strain (BLYR); mutagenicity and developmental toxicity using Q(SAR) methodology. Metribuzin at 10 mg·L-1 was degraded by chlorination, achieving 93% of removal at 30 min of reaction. TOC analysis showed that the herbicide does not suffer complete mineralization, even after 24 h of contact with free chlorine. Seventeen DBPs were detected and their structural formulae were elucidated by high resolution mass spectrometry. Toxicity effects for chlorinated solutions increased when compared to the unreacted metribuzin solution. DBPs were more toxic to Artemia salina nauplii, increasing around 20% on nauplii mortality. It was also observed high estrogenicity to human receptors in BLYES assays and mutagenic and developmental toxicant effects to animals and humans in Q(SAR) methodology, suggesting that DBPs are potentially more toxic than the precursor metribuzin. Metribuzin solutions at 10 mg·L-1 showed equivalent 17-ß-estradiol values ranged from 0.061 to 6.71 µg·L-1 after to be chlorinated at different reaction times.


Assuntos
Desinfetantes , Herbicidas , Poluentes Químicos da Água , Purificação da Água , Animais , Cloro/análise , Desinfecção , Halogenação , Herbicidas/toxicidade , Humanos , Triazinas , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/toxicidade
3.
Environ Sci Pollut Res Int ; 26(31): 31609-31622, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31482525

RESUMO

During this research, chemometric approaches were applied for optimization of the low-temperature partitioning extraction (LTPE) for the simultaneous analysis of the pesticides: acephate, difenoconazole, fenamidone, fluazifop, fluazinam, methamidophos, and thiamethoxam from surface water samples and determination by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry. It was used the 23 full factorial and the Doehlert experimental designs. The extraction technique was optimized by evaluating the effects of the three variables: sample pH, ionic strength (addition of Na2HPO4), and organic solvent volume. Considering the interest to find an optimal condition for all analytes simultaneously, the best extraction parameters found were as follows: pH = 5.33, concentration of Na2HPO4 = 0.0088 mol L-1 and organic phase volume = 4.5 mL. The optimized methodology showed LOD and LOQ levels from 0.33 to 8.13 ng L-1 and from 1.09 to 26.84 ng L-1, respectively. The recovery values ranged from 38.37 and 99.83% and the RSD values varied from 2.33 to 18.92%. The method was applied to surface water analysis sampled in areas with intensive agricultural practices in Ouro Branco City, Minas Gerais, Brazil. The difenoconazole was detected in concentrations between 12.53 and 94.76 ng L-1.


Assuntos
Cromatografia Líquida de Alta Pressão/métodos , Praguicidas/análise , Espectrometria de Massas em Tandem/métodos , Água/análise , Agricultura , Brasil , Compostos Organotiofosforados , Praguicidas/química , Fosforamidas , Projetos de Pesquisa , Temperatura
4.
Environ Sci Pollut Res Int ; 25(20): 19962-19974, 2018 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-29744776

RESUMO

A simple, inexpensive, versatile, and environment-friendly extraction method, using low-temperature partitioning extraction (LTPE), was validated to quantify pharmaceutical-active compounds (PhACs) in surface water samples by high-performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS). The PhACs analyzed were acetaminophen, bezafibrate, diclofenac, diltiazem, fluconazole, linezolid, miconazole, ondansetron hydrochloride, and trimethoprim. The detection and quantification limits ranged from 0.15 to 12.30 ng L-1 and 0.43 to 40.60 ng L-1, respectively. Recovery rates ranged from 46 to 135%, and relative standard deviation (RSD%) varied between 0.49 and 6.13%. This method was applied to monitor water contamination by PhACs in the Paraopeba River Basin (PRB), Minas Gerais state, Brazil. All PhACs, except linezolid which was not detected, were found in PRB water samples in concentrations that ranged from 2.6 ng L-1 to 2.62 µg L-1.


Assuntos
Preparações Farmacêuticas/análise , Poluentes Químicos da Água/análise , Brasil , Cromatografia Líquida de Alta Pressão , Monitoramento Ambiental , Água Doce/análise , Espectrometria de Massas por Ionização por Electrospray , Espectrometria de Massas em Tandem
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