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Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/129864
Título

Niosomes based on synthetic cationic lipids for gene delivery: The influence of polar head-groups on the transfection efficiency in HEK-293, ARPE-19 and MSC-D1 cells

AutorOjeda, Edilberto; Puras, Gustavo; Agirre, Mireia; Zárate, Jon; Grijalvo, Santiago; Pons, Ramon; Eritja Casadellà, Ramón; Martínez Navarrete, Gema C.; Soto-Sánchez, Cristina; Fernandez, E.; Pedraz, José Luís
Palabras claveCells
Genes
Molecular biology
genetic transfection
Lipids
Fecha de publicación14-abr-2015
EditorRoyal Society of Chemistry (Great Britain)
CitaciónOrganic and Biomolecular Chemistry
ResumenWe designed niosomes based on three lipids that differed only in the polar-head group to analyze their influence on the transfection efficiency. These lipids were characterized by small-angle X-ray scattering before being incorporated into the niosomes which were characterized in terms of pKa, size, zeta potential, morphology and physical stability. Nioplexes were obtained upon the addition of a plasmid. Different ratios (w/w) were selected to analyze the influence of this parameter on size, charge and the ability to condense, release and protect the DNA. In vitro transfection experiments were performed in HEK-293, ARPE-19 and MSC-D1 cells. Our results show that the chemical composition of the cationic head-group clearly affects the physicochemical parameters of the niosomes and especially the transfection efficiency. Only niosomes based on cationic lipids with a dimethyl amino head group (lipid 3) showed a transfection capacity when compared with their counterparts amino (lipid 1) and tripeptide head-groups (lipid 2). Regarding cell viability, we clearly observed that nioplexes based on the cationic lipid 3 had a more deleterious effect than their counterparts, especially in ARPE-19 cells at 20/1 and 30/1 ratios. Similar studies could be extended to other series of cationic lipids in order to progress in the research on safe and efficient non-viral vectors for gene delivery purposes.
Versión del editorhttp://pubs.rsc.org/en/content/articlelanding/2015/ob/c4ob02087a#!divAbstract
URIhttp://hdl.handle.net/10261/129864
DOI10.1039/c4ob02087a
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