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Saponin and Fluorine-Modified Polycation As a Versatile Gene Delivery System Publisher Pubmed



Hasanzadeh A1 ; Vahabi AH1 ; Hooshmand SE1 ; Hosseini ES1 ; Azar BKY2 ; Kiani J2, 3 ; Saeedi S1 ; Shahbazi A4 ; Rudra A5, 6, 7 ; Hamblin MR8 ; Karimi M1, 3, 9, 10
Authors
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Authors Affiliations
  1. 1. Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran
  3. 3. Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran
  5. 5. David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, 02139, MA, United States
  6. 6. Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children’s Hospital, 300 Longwood Avenue, Boston, 02115, MA, United States
  7. 7. Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, 02139, MA, United States
  8. 8. Laser Research Centre, Faculty of Health Science, University of Johannesburg, Doornfontein, 2028, South Africa
  9. 9. Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran
  10. 10. Research Center for Science and Technology in Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: Nanotechnology Published:2022


Abstract

Despite the development of many novel carriers for the delivery of various types of genetic material, the lack of a delivery system with high efficiency and low cytotoxicity is a major bottleneck. Herein, low molecular weight polyethylenimine (PEI1.8k) was functionalized with saponin residues using phenylboronic acid (PBA) as an ATP-responsive cross-linker, and a fluorinated side chain to construct PEI-PBA-SAP-F polycation as a highly efficient delivery vector. This vehicle could transfect small plasmid DNA (∼3 kb) with outstanding efficiency into various cells, including HEK 293T, NIH3T3, A549, PC12, MCF7 and HT-29, as well as robust transfection of a large plasmid (∼9 kb) into HEK 293T cells. The carrier indicated good transfection efficacy even at high concentration of serum and low doses of plasmid. The use of green fluorescent protein (GFP) knock-out analysis demonstrated transfection of different types of CRISPR/Cas9 complexes (Cas9/sgRNA ribonucleoproteins RNP, plasmid encoding Cas9 plus sgRNA targeting GFP, Cas9 expression plasmid plus in vitro-prepared sgRNA). In summary, we report an effective PEI-PBA-SAP-F gene carrier with the appropriate lipophilic/cationic balance for biomedical applications. © 2022 IOP Publishing Ltd.
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