Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/100773
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorSarret i Pons, Maria-
dc.contributor.advisorMitjans Arnal, Montserrat-
dc.contributor.authorBilbao Asensio, Marc-
dc.date.accessioned2016-07-22T11:02:50Z-
dc.date.available2016-07-22T11:02:50Z-
dc.date.issued2016-06-
dc.identifier.urihttp://hdl.handle.net/2445/100773-
dc.descriptionTreballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2016, Tutores: Maria Sarret Pons i Montserrat Mitjans Arnalca
dc.description.abstractNanotechnology has been advancing relentlessly and the use of nanoparticles has increased rapidly as they have been applied in numerous industrial and medical sectors. For instance, Silver nanoparticles can be found in aerosols, Zinc and Titanium oxides are important components of sunscreen and applications of different nanoparticles have proved to be relevant in biomedicine as multifunctional drug carriers or in novel cancer therapies. Nevertheless, potential dangers from nanoparticle exposure cannot be ignored. Nanoparticles may damage organisms. In vitro, studies have found certain nanoparticles to be able to break DNA helices, denaturalise vital proteins, disrupt gene expression or alter plasma coagulation. In vivo, they can induce inflammation and stimulate or suppress the immune system. Due to the ease of exposure to nanoparticles, the study and understanding of their potential toxicity is fundamental. The area of this research goes by the name of Nanotoxicology. Herein, different sized particles of ZnO, characterized by different methods, were used to study their interaction with plasma proteins, both human and rat. Plasma proteome alteration, as a result of the presence of ZnO in different conditions, has been evaluated in order to gain knowledge of potential toxicity from these nanoparticles and its consequences. Experimental results reported plasma coagulation delays, especially when studying the intrinsic coagulation pathway. Rat and human plasma were not equally affected by the ZnO particle’s presence; SDS-PAGE gels revealed significant differences among proteins adsorbed on the particles depending on the organism studied. The formation of a proteic coating on ZnO particles, the protein corona, was confirmed through observations on TEM and consequent stabilization of particle dispersion was reported by DLS-
dc.format.extent59 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoengca
dc.rightscc-by-nc-nd (c) Bilbao, 2016-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/-
dc.sourceTreballs Finals de Grau (TFG) - Química-
dc.subject.classificationÒxid de zinccat
dc.subject.classificationNanopartículescat
dc.subject.classificationNanotoxicologiacat
dc.subject.classificationTreballs de fi de graucat
dc.subject.otherZinc oxideeng
dc.subject.otherNanoparticleseng
dc.subject.otherNanotoxicologyeng
dc.subject.otherBachelor's theses-
dc.titleIn vitro safety assessment of nanomaterials: Protein corona studies on ZnO particleseng
dc.title.alternativeEstudi de la seguretat de nanomaterials in vitro: Estudis de la corona proteica en partícules de ZnOca
dc.typeinfo:eu-repo/semantics/bachelorThesisca
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca
Appears in Collections:Treballs Finals de Grau (TFG) - Química

Files in This Item:
File Description SizeFormat 
FG_QU Bilbao Asensio Marc.pdf1.62 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons