Spontaneous Formation of Cationic Vesicles in Aqueous DDAB-Lecithin Mixtures for Efficient Plasmid DNA Complexation and Gene Transfection

ACS Appl Bio Mater. 2021 Aug 16;4(8):6005-6015. doi: 10.1021/acsabm.1c00165. Epub 2021 Jun 9.

Abstract

Cationic liposomes have become an attractive tool to deliver genes and interfering RNA into cells. Herein, we report the application of spontaneously formed cationic vesicles in mixtures of lecithin and cationic amphiphiles for efficient transfection of plasmid DNA and siRNA into cells. The average hydrodynamic diameter of the phospholipid vesicles was modulated by changing the ratio of dihexadecyldimethylammonium bromide (DDAB) to phospholipid in the vesicles. The vesicles were characterized by dynamic light scattering, ζ potential, and small-angle X-ray scattering. Depending on the ratio of DDAB to phospholipid, the average size of the vesicles can be varied in the range of 150-300 nm with a ζ potential of +40 mV. The ability of these cationic vesicles to form lipoplexes upon binding with pDNA is demonstrated by ζ potential, isothermal titration calorimetry, gel retardation, and DNase I digestion assay. The enthalpy of binding between pDNA and cationic liposome was found to be -5.7 (±0.8) kJ/mol. The cellular uptake studies of lipoplexes observed by fluorescence microscopy confirmed good transfection efficiency of DDAB liposomes in MCF-7 and HeLa cells. The fluorescent imaging analysis showed effective gene delivery and expression of green fluorescent protein. In addition, the formulation has demonstrated an ability to deliver small interfering RNA (siBRD4) for efficient gene silencing as seen by a significant decrease in BRD4 protein level in siBRD4-treated cells. Comparison of the transfection efficiency of different formulations suggests that DDAB-rich mixed phospholipid vesicles with size <200 nm are better than large size vesicles for improved endocytosis and gene expression.

Keywords: amphiphiles; cationic liposomes; gene delivery; lipoplexes; surface potential; transfection efficiency.

MeSH terms

  • Cations / chemistry
  • Cell Cycle Proteins / genetics
  • DNA / genetics
  • HeLa Cells
  • Humans
  • Lecithins*
  • Liposomes* / chemistry
  • Nuclear Proteins / genetics
  • Plasmids / genetics
  • Quaternary Ammonium Compounds
  • RNA, Small Interfering / genetics
  • Transcription Factors / genetics
  • Transfection

Substances

  • BRD4 protein, human
  • Cations
  • Cell Cycle Proteins
  • Lecithins
  • Liposomes
  • Nuclear Proteins
  • Quaternary Ammonium Compounds
  • RNA, Small Interfering
  • Transcription Factors
  • didodecyldimethylammonium
  • dihexadecyldimethylammonium
  • DNA