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1.
Environ Monit Assess ; 190(12): 723, 2018 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-30430263

RESUMO

Human pharmaceutical residues are a serious environmental concern. They have been reported to have eco, geno, and human toxic effects, and thus their importance as micropollutants cannot be ignored. These have been studied extensively in Europe and North America. However, African countries are still lagging behind in research on these micropollutants. In this study, the wastewaters of the University Teaching Hospital of Yaoundé (UTHY) were screened for the presence of active pharmaceutical ingredients and their metabolites. The screening was carried out using two methods: high-performance liquid chromatography coupled to a triple quadrupole analyzer (LC/QQQ) and high-performance coupled to a mass spectrometer with a time of flight analyzer (LC/Q-TOF). A total of 19 active pharmaceutical ingredients and metabolites were identified and quantified. The compounds identified include paracetamol (211.93 µg/L), ibuprofen (141 µg/L), tramadol (76 µg/L), O-demethyltramadol (141 µg/L), erythromycinanhydrate (7 µg/L), ciprofloxacin (24 µg/L), clarinthromycine (0.088 µg/L), azitromycine (0.39 µg/L), sulfamethoxazole 0.16 µg/L), trimetoprime (0.27 µg/L), caffeine (5.8 µg/L), carnamaeepine (0.94 µg/L), atenolol (0.43 µg/L), propranolol (0.3 µg/L), cimetidine (34 µg/L), hydroxy omeprazole (5 µg/L), diphenhydramine (0.38 µg/L), metformine (154 µg/L), and sucralose (13.07 µg/L).


Assuntos
Cromatografia Líquida de Alta Pressão/métodos , Monitoramento Ambiental/métodos , Águas Residuárias/análise , Poluentes Químicos da Água/análise , Camarões , Hospitais , Humanos , Espectrometria de Massas/métodos , Preparações Farmacêuticas/metabolismo , Águas Residuárias/química
2.
Environ Sci Pollut Res Int ; 18(8): 1253-63, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21380533

RESUMO

INTRODUCTION: To use biomarkers in monitoring programmes, potential confounding factors must be considered. In the clam Scrobicularia plana, the influence of size and salinity on biomarkers at different levels of biological organisation has been examined. MATERIAL AND METHODS: Biochemical (glutathione-S-transferase, lactate dehydrogenase, acetylcholinesterase, digestive enzymes, metallothionein), physiological (energy reserves) and behavioural (burrowing) responses were compared (a) in specimens of different sizes from the Loire estuary; (b) in specimens from the Belon estuary at two sites with salinities of 30.1 or 11.5. RESULTS: Amongst the biomarkers able to reveal pollution effects, several are influenced by the size of the clams (Ag, Cu, Ni and glycogen concentrations, GST and AChE activities, condition indices). Salinity differences induced variations of the same order of magnitude (GST, AChE) or even higher (lactate dehydrogenase, digestive enzymes in the crystalline style) than contamination-induced variations. In burrowing tests, the number of burrowed specimens was similar at both salinities after an experiment time <3 h. CONCLUSIONS: Size is a factor necessarily but easily controlled. Because the weight may be different in clams of identical size, correction factors may be used to minimise the influence of weight changes on biomarkers. A correction factor taking into account salinity levels can also be used. The protein concentrations in the clams did not differ with salinity, a very favourable outcome since all enzyme activities are classically expressed by reference to total protein concentrations. For burrowing tests, the number of burrowed specimens at a particular time is an endpoint that is preferable to measures of burrowing speed.


Assuntos
Bivalves/metabolismo , Monitoramento Ambiental , Poluição da Água/análise , Acetilcolinesterase/metabolismo , Animais , Comportamento Animal , Biomarcadores/metabolismo , Bivalves/anatomia & histologia , Bivalves/enzimologia , Tamanho Corporal , Metabolismo Energético , França , Sedimentos Geológicos/química , Glutationa Transferase/metabolismo , L-Lactato Desidrogenase/metabolismo , Metalotioneína/metabolismo , Salinidade , Água do Mar/química , Cloreto de Sódio/análise
3.
Chemosphere ; 84(1): 166-74, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21354594

RESUMO

Engineered nano-sized Cu oxide particles are extensively used in diverse applications. Because aquatic environments are the ultimate "sink" for all contaminants, it is expected that nanoparticles (NP) will follow the same fate. In this study, two marine invertebrates Scrobicularia plana and Hediste diversicolor were chosen as ecotoxicological models. The aim was to evaluate behavioural (burrowing kinetics, feeding rate) and biochemical (biomarkers) responses of S. plana and H. diversicolor exposed in the laboratory to Cu (10 µg L(-1)) added in natural seawater either in the form of engineered nanoparticles (NPs) of CuO or as dissolved Cu in 2% HNO(3). Exposure was characterized by considering (i) the physico-chemical fate of NP (ii) the fraction of labile Cu in experimental media and (iii) Cu bioaccumulation. Results showed high aggregation of CuO NPs in seawater and no additional bioavailable Cu concentrations. Behavioural impairments were observed in S. plana exposed to CuO NPs or soluble Cu whereas in H. diversicolor, only the exposure to soluble Cu led to a burrowing decrease. No obvious neurotoxicity effects were revealed since in both species, no changes in cholinesterasic activity occurred in response to both forms of Cu exposure. Biomarkers of oxidative-stress catalase and glutathione-S-transferase were enhanced in both species whereas superoxide dismutase was increased only in S. plana exposed to CuO NPs. Metallothionein-like protein was increased in bivalves exposed to both forms of Cu. Since, no detectable release of soluble Cu from CuO NPs occurred during the time of experiment, ecotoxicity effects seem to be related to CuO NPs themselves.


Assuntos
Bivalves/efeitos dos fármacos , Cobre/toxicidade , Nanopartículas Metálicas/toxicidade , Poliquetos/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Animais , Comportamento Animal/efeitos dos fármacos , Biomarcadores/metabolismo , Bivalves/fisiologia , Catalase/metabolismo , Glutationa Transferase/metabolismo , Metalotioneína/metabolismo , Poliquetos/fisiologia , Superóxido Dismutase/metabolismo
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