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Identification of critical points in colloidal delivery systems for intravenous administration and intracellular delivery of nucleic acids as therapeutic agents

dc.contributor.advisorVideira, Mafaldapor
dc.contributor.advisorGaspar, Rogériopor
dc.contributor.authorMouro, Andreia Alexandra Dias
dc.date.accessioned2014-05-12T15:31:13Z
dc.date.available2014-05-12T15:31:13Z
dc.date.issued2012
dc.descriptionTese de mestrado, Farmacotecnia Avançada (Tecnologia Farmacêutica), Universidade de Lisboa, Faculdade de Farmácia, 2012por
dc.description.abstractThe RNA-mediated gene-silencing technology, carried out by small interfering RNAs (siRNAs), has attracted a great deal of attention as novel promising therapeutic strategy in oncology. One of the common themes emerging from the studies on cell-specific delivery of siRNA is the need for optimizing the intracellular trafficking of the siRNA to elicit a silencing response. Polymer nanoparticles have become recognized as an efficiency strategy for oligonucleotide delivery to a specific cell population. Among these carriers, PLGA-co-PEG nanoparticles have attracted much attention since they are assumed to meet the criteria required for successful siRNA delivery: they are sufficiently small for efficient tissue penetration and cellular uptake and offer physical protection against RNase activity as well as a favorable colloidal stability. In this study the ability of a polymeric micelle based system for the targeting and delivery of a siRNA to breast cancer cells was proved using as model the siRNA against the Green Fluorescence Protein (GFP). The efficiencies observed during in vitro studies with a MDA-MB-436/GFP cell line confirmed the potential of this new delivery system but it needs further investigation.por
dc.identifier.urihttp://hdl.handle.net/10451/11011
dc.language.isoengpor
dc.peerreviewedyespor
dc.subjectPolymeric micellespor
dc.subjectsiRNApor
dc.subjectPLGA-co-PEGpor
dc.subjectGreen Fluorescence Protein (GFP)por
dc.subjectTeses de mestrado - 2012por
dc.titleIdentification of critical points in colloidal delivery systems for intravenous administration and intracellular delivery of nucleic acids as therapeutic agentspor
dc.typemaster thesis
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typemasterThesispor

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