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Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced Sirna Delivery and Silencing Publisher Pubmed



Shaabani E1, 2 ; Sharifiaghdam M1, 2 ; De Keersmaecker H2, 3 ; De Rycke R4, 5, 6 ; De Smedt S2, 3 ; Faridimajidi R1 ; Braeckmans K2, 3 ; Fraire JC2
Authors
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Authors Affiliations
  1. 1. Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Laboratory of General Biochemistry and Physical Pharmacy, Faculty of Pharmacy, Ghent University, Ghent, B-9000, Belgium
  3. 3. Center for Advanced Light Microscopy, Ghent University, Ghent, 9000, Belgium
  4. 4. Department of Biomedical Molecular Biology, Ghent University, Ghent, 9052, Belgium
  5. 5. VIB Center for Inflammation Research, Ghent, 9052, Belgium
  6. 6. Ghent University Expertise Centre for Transmission Electron Microscopy and VIB BioImaging Core, Ghent, 9052, Belgium

Source: International Journal of Molecular Sciences Published:2021


Abstract

Delivery of small interfering RNA (siRNA) provides one of the most powerful strategies for downregulation of therapeutic targets. Despite the widely explored capabilities of this strategy, intracellular delivery is hindered by a lack of carriers that have high stability, low toxicity and high transfection efficiency. Here we propose a layer by layer (LBL) self-assembly method to fabricate chitosan-coated gold nanoparticles (CS-AuNPs) as a more stable and efficient siRNA delivery system. Direct reduction of HAuCl4 in the presence of chitosan led to the formation of positively charged CS-AuNPs, which were subsequently modified with a layer of siRNA cargo molecules and a final chitosan layer to protect the siRNA and to have a net positive charge for good interaction with cells. Cytotoxicity, uptake, and downregulation of enhanced Green Fluorescent Protein (eGFP) in H1299-eGFP lung epithelial cells indicated that LBL-CS-AuNPs provided excellent protection of siRNA against enzymatic degradation, ensured good uptake in cells by endocytosis, facilitated endosomal escape of siRNA, and improved the overall silencing effect in comparison with commercial transfection reagents Lipofectamine and jetPEI®. Therefore, this work shows that LBL assembled CS-AuNPs are promising nanocarriers for enhanced intracellular siRNA delivery and silencing. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.