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Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing

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 transf...

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Autores principales: Shaabani, Elnaz, Sharifiaghdam, Maryam, De Keersmaecker, Herlinde, De Rycke, Riet, De Smedt, Stefaan, Faridi-Majidi, Reza, Braeckmans, Kevin, Fraire, Juan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830320/
https://www.ncbi.nlm.nih.gov/pubmed/33467656
http://dx.doi.org/10.3390/ijms22020831
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author Shaabani, Elnaz
Sharifiaghdam, Maryam
De Keersmaecker, Herlinde
De Rycke, Riet
De Smedt, Stefaan
Faridi-Majidi, Reza
Braeckmans, Kevin
Fraire, Juan C.
author_facet Shaabani, Elnaz
Sharifiaghdam, Maryam
De Keersmaecker, Herlinde
De Rycke, Riet
De Smedt, Stefaan
Faridi-Majidi, Reza
Braeckmans, Kevin
Fraire, Juan C.
author_sort Shaabani, Elnaz
collection PubMed
description 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 HAuCl(4) 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.
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spelling pubmed-78303202021-01-26 Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing Shaabani, Elnaz Sharifiaghdam, Maryam De Keersmaecker, Herlinde De Rycke, Riet De Smedt, Stefaan Faridi-Majidi, Reza Braeckmans, Kevin Fraire, Juan C. Int J Mol Sci Article 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 HAuCl(4) 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. MDPI 2021-01-15 /pmc/articles/PMC7830320/ /pubmed/33467656 http://dx.doi.org/10.3390/ijms22020831 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shaabani, Elnaz
Sharifiaghdam, Maryam
De Keersmaecker, Herlinde
De Rycke, Riet
De Smedt, Stefaan
Faridi-Majidi, Reza
Braeckmans, Kevin
Fraire, Juan C.
Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing
title Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing
title_full Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing
title_fullStr Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing
title_full_unstemmed Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing
title_short Layer by Layer Assembled Chitosan-Coated Gold Nanoparticles for Enhanced siRNA Delivery and Silencing
title_sort layer by layer assembled chitosan-coated gold nanoparticles for enhanced sirna delivery and silencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830320/
https://www.ncbi.nlm.nih.gov/pubmed/33467656
http://dx.doi.org/10.3390/ijms22020831
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