Development of a DNA-liposome complex for gene delivery applications

作者:Rasoulianboroujeni M; Kupgan G; Moghadam F; Tahriri M; Boughdachi A; Khoshkenar P; Ambrose J J; Kiaie N; Vashaee D; Ramsey J D; Tayebi L*
来源:Materials Science & Engineering C-Materials for Biological Applications, 2017, 75: 191-197.
DOI:10.1016/j.msec.2017.02.012

摘要

The association structures formed by cationic liposomes and DNA (Deoxyribonucleic acid)-liposome have been effectively utilized as gene carriers in transfection assays. In this research study, cationic liposomes were prepared using a modified lipid film hydration method consisting of a lyophilization step for gene delivery applications. The obtained results demonstrated that the mean particle size had no significant change while the polydispersity (PDI) increased after lyophilization. The mean particle size slightly reduced after lyophilization (520 +/- 12 nm to 464 +/- 25 nm) while the PDI increased after lyophilization (0.094 +/- 0.017 to 0220 +/- 0.004). In addition. The mean particle size of vesicles increases when DNA is incorporated to the liposomes (673 27 nm). According to the Scanning Electron Microscopy (SEM) and transmission electron microscopy (TEM) images, the spherical shape of liposomes confirmed their successful preservation and reconstitution from the powder. It was found that liposomal formulation has enhanced transfection considerably compared to the naked DNA as negative control. Finally, liposomal formulation in this research had a better function than Lipofectamine 2000 as a commercialized product because the cellular activity (cellular protein) was higher in the prepared lipoplex than Lipofectamine (R) 2000.

  • 出版日期2017-6-1