3 resultados para Jacquinet, Ag.-Magd.

em Archivo Digital para la Docencia y la Investigación - Repositorio Institucional de la Universidad del País Vasco


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Laburpena: Ikerlan hau itsasoaren kutsaduran zentratzen da, itsasoak arriskutsuak eta kaltegarriak diren substantziak jasotzen dituelako, bai ibaietako ekarpenarengatik, baita zuzeneko karguetatik. Organismo behale gisa ostrak erabiliko dira, izaki iragazleak izanik elikagaien irenstearen ondorioz medio urtsutik kutsatzaileak metatzen dituztelako eta gainera, ingurugiroan dauden mailen gainetik kontzentratzen dituztelako. Ostretan zilarra (Ag) eta kobrea (Cu) bezalako metalen eragina aztertuko da, horretarako, metalen aurreko esposizio biomarkatzaileak erabiliko dira. Besteak beste, autometalografia erabiliko da metalen mailak eta banaketa ostren ehunetan neurtzeko eta metalotioneinen mailak ere neurtuko dira. Ostrek metalekiko izan duten esposizio denborak 0, 6, 7, 13 eta 14 egunetakoak izan dira, bai itsasoko eta bai estuarioko uretan mantenduz. Emaitzak ikusita behatu da estuarioko laginek, normalean, metal kontzentrazio baxuagoak aurkezten dituztela, eta zenbait kasutan kontrolek metalen pean jarritako laginak baino metal kontzentrazio handiagoak erakutsi dituzte aste bat igaro eta gero. Bigarren astean, metal mailen jaitsiera bat behatu da. Beste alde batetik, metalotioneinetan neurtutako indukzio mailak oso baxuak izan dira. Metalen distribuzioa ehun desberdinetan aldez aurretik beste molusku batzuetan deskribatutakoen oso antzekoa izan da ostretan.

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The fields of organic electronics and spintronics have the potential to revolutionize the electronics industry. Finding the right materials that can retain their electrical and spin properties when combined is a technological and fundamental challenge. We carry out the study of three archetypal organic molecules in intimate contact with the BiAg2 surface alloy. We show that the BiAg2 alloy is an especially suited substrate due to its inertness as support for molecular films, exhibiting an almost complete absence of substrate-molecular interactions. This is inferred from the persistence of a completely unaltered giant spin-orbit split surface state of the BiAg2 substrate, and from the absence of significant metallic screening of charged molecular levels in the organic layer. Spin-orbit split states in BiAg2 turn out to be far more robust to organic overlayers than previously thought.

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Silver nanoparticles (Ag NPs) are increasingly used in many products and are expected to end up in the aquatic environment. Mussels have been proposed as marine model species to evaluate NP toxicity in vitro. The objective of this work was to assess the mechanisms of toxicity of Ag NPs on mussel hemocytes and gill cells, in comparison to ionic and bulk Ag. Firstly, cytotoxicity of commercial and maltose stabilized Ag NPs was screened in parallel with the ionic and bulk forms at a wide range of concentrations in isolated mussel cells using cell viability assays. Toxicity of maltose alone was also tested. LC50 values were calculated and the most toxic Ag NPs tested were selected for a second step where sublethal concentrations of each Ag form were tested using a wide array of mechanistic tests in both cell types. Maltose-stabilized Ag NPs showed size-dependent cytotoxicity, smaller (20 nm) NPs being more toxic than larger (40 and 100 nm) NPs. Maltose alone provoked minor effects on cell viability. Ionic Ag was the most cytotoxic Ag form tested whereas bulk Ag showed similar cytotoxicity to the commercial Ag NPs. Main mechanisms of action of Ag NPs involved oxidative stress and genotoxicity in the two cell types, activation of lysosomal AcP activity, disruption of actin cytoskeleton and stimulation of phagocytosis in hemocytes and increase of MXR transport activity and inhibition of Na-K-ATPase in gill cells. Similar effects were observed after exposure to ionic and bulk Ag in the two cell types, although generally effects were more marked for the ionic form. In conclusion, results suggest that most observed responses were due at least in part to dissolved Ag.