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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-7830320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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