4.7 Article

Effect of hydrophobic tails of plier-like cationic lipids on nucleic acid delivery and intracellular trafficking

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 573, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2019.118798

Keywords

Plier-like cationic lipid; Asymmetry hydrophobic tail; Cationic niosomes; Gemini cationic lipids; DNA and siRNA delivery; Internalization pathway

Funding

  1. Thailand Research Fund through the Golden Jubilee Ph.D Program [PHD/0047/2559]
  2. Thailand Research Fund through Research Team Promotion Grant [RTA6180003]
  3. Research and Creative Fund, Faculty of Pharmacy, Silpakorn University
  4. Faculty of Pharmaceutical Sciences, Burapha University

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In the optimization of transfection efficacy, one of the crucial barriers to effective gene delivery is in fact the intracellular trafficking of nucleic acids, besides the first and the last steps of gene transfer, i.e., delivery to the cell and transcription. Modifications of cationic lipid structure have been reported to have a significant effect on gene delivery. Therefore, the plier-like cationic lipids (PCLs) have been synthesized and the effect of the different types of hydrophobic tails (chain length and unsaturated hydrocarbon) on physicochemical properties, cellular uptake, trafficking process, transfection, and silencing efficiency has been investigated. In this study, the plier-like cationic niosomes (PCNs) containing PCL (A, B, and C) were evaluated their performance to deliver pDNA and siRNA to HeLa cells. Among the PCNs, PCN-B with saturated asymmetric hydrocarbon tails (C18 and C12) provided the highest efficiency for pDNA and siRNA delivery. Furthermore, the results revealed that the structure of the cationic lipids affected the internalization pathway and the intracellular trafficking. PCL-B and PCL-C with asymmetric tails preferred clathrin- and caveolae-mediated endocytosis as the predominant internalization pathways and were also involved in the polymerization process for transfection. However, PCL-A with symmetry hydrocarbon tails (C12) was predominantly taken up via macropinocytosis. All PCNs were able to escape from endosomal-lysosomal systems through facilitation of acidification. Results obtained from the cytotoxicity test revealed that the PCNs were safe in vitro. Therefore, PCNs provide a great prospect as an alternative effective gene delivery system.

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