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dc.contributor.authorŞenel, B.
dc.contributor.authorBüyükköroğlu, G.
dc.contributor.authorYazan, Yasemin
dc.date.accessioned2019-10-19T14:44:06Z
dc.date.available2019-10-19T14:44:06Z
dc.date.issued2015
dc.identifier.issn0031-7144
dc.identifier.urihttps://dx.doi.org/10.1691/ph.2015.5026
dc.identifier.urihttps://hdl.handle.net/11421/13393
dc.descriptionWOS: 000369614300002en_US
dc.descriptionPubMed ID: 26790185en_US
dc.description.abstractDue to the recent advances in molecular biology, there are promising gene therapy studies for prevention and treatment of cancer, genetic and infectious diseases. Many technologies in molecular biology and biotechnology were developed, and among those technologies, 'antisense technology' has become prominent in recent years. In this study, non-viral gene delivery systems such as solid lipid and chitosan nanoparticles were developed for improving intercellular delivery of siRNA. Commercially available Bcl-2 siRNA which is specific for Bcl-2 mRNA was used as a genetic material. Particle size, zeta potential, siRNA binding abilities and cytotoxic properties of the systems were evaluated and transfection assay was performed on among the prepared formulations. When the results of those studies were compared with Lipofectamine((R)) 2000, prepared formulations were found to show usable results. A novel method was developed in this study for producing solid lipid nanoparticles (SLNs) with highly efficient siRNA encapsulation. The results of this study showed that the genetic materials can be encapsulated in SLNs and SLNs have the potential to be used as a transfection agents.en_US
dc.description.sponsorshipScience Foundation of Anadolu University [09-0345]en_US
dc.description.sponsorshipThis work was financially supported by the Science Foundation of Anadolu University (Project number: 09-0345).en_US
dc.language.isoengen_US
dc.publisherGovi-Verlag Pharmazeutischer Verlag GMBHen_US
dc.relation.isversionof10.1691/ph.2015.5026en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSolid lipid and chitosan particulate systems for delivery of siRNAen_US
dc.typearticleen_US
dc.relation.journalPharmazieen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Biyoteknoloji Anabilim Dalıen_US
dc.identifier.volume70en_US
dc.identifier.issue11en_US
dc.identifier.startpage698en_US
dc.identifier.endpage705en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorYazan, Yasemin


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