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dc.contributor.authorGalliková, D.
dc.contributor.authorLiskayová, G.
dc.contributor.authorBúcsi, A.
dc.contributor.authorHubcík, L.
dc.contributor.authorMartinez, Jorge
dc.contributor.authorUhríková, D.
dc.date.accessioned2018-08-08T04:41:39Z
dc.date.available2018-08-08T04:41:39Z
dc.date.created2018-08-08T03:50:59Z
dc.date.issued2018
dc.identifier.citationGalliková, D. and Liskayová, G. and Búcsi, A. and Hubcík, L. and Martinez, J. and Uhríková, D. 2018. DOPE–oleic acid–Ca2+ as DNA condensing agent. European Pharmaceutical Journal. 65 (1): pp. 1-9.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/69628
dc.identifier.doi10.2478/afpuc-2018-0001
dc.description.abstract

Phospholipid-based non-viral carriers composed of neutral phospholipid dioleoylphosphatidylethanolamine (DOPE) and the binary mixture DOPE-oleic acid (OA) are examined as potential DNA delivery vectors. The process of DNA condensation in the presence of Ca2+ions has been monitored through changes in emmision intensity of fluorescent probe ethidium bromide. The decline in fluorescence intensity with increasing Ca2+concentration at two different time intervals was correlated with the binding capacity of complexes and possible release of DNA from the complex. The microstructure of DOPE-OA mixtures at different OA/DOPE molar ratios and that of DOPE-OA-DNA-Ca2+complexes were determined using synchrotron small angle X-ray diffraction (SAXD). We identified inverted hexagonal phase HIIas the dominant structure. OA affects the lattice parameter of HIIformed by DOPE. With the increasing OA/DOPE molar ratio, the lattice parameter decreases, which results in significantly lower fraction of DNA bound to the OA-enriched complexes.

dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.titleDOPE–oleic acid–Ca2+ as DNA condensing agent
dc.typeJournal Article
dcterms.source.issn2453-6725
dcterms.source.titleEuropean Pharmaceutical Journal
curtin.departmentSchool of Pharmacy and Biomedical Sciences
curtin.accessStatusOpen access


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