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Local siRNA delivery by non-viral vectors

Since the discovery of the RNA interference (RNAi) phenomenon, RNAi-based therapies now present a huge potential for the treatment of many diseases, including inflammatory and infectious diseases and cancers. While numerous reports have described the development of small interfering RNA (siRNA) deli...

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Detalles Bibliográficos
Autores principales: Beilvert, F., Mével, M., Chatin, Benoît, Pitard, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128187/
http://dx.doi.org/10.1016/S1773-2247(12)50002-X
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author Beilvert, F.
Mével, M.
Chatin, Benoît
Pitard, B.
author_facet Beilvert, F.
Mével, M.
Chatin, Benoît
Pitard, B.
author_sort Beilvert, F.
collection PubMed
description Since the discovery of the RNA interference (RNAi) phenomenon, RNAi-based therapies now present a huge potential for the treatment of many diseases, including inflammatory and infectious diseases and cancers. While numerous reports have described the development of small interfering RNA (siRNA) delivery systems for in-vivo applications, only a small number of siRNA-based therapies are currently under clinical development. This is essentially due to the lack of efficient and safe siRNA delivery systems for intravenous administration. However, the delivery of siRNA after local injection could represent an attractive route of administration to limit the issues of toxicity associated with systemic injection. We will describe here the different synthetic vectors which have been developed for the local delivery of siRNA in various organs.
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spelling pubmed-71281872020-04-08 Local siRNA delivery by non-viral vectors Beilvert, F. Mével, M. Chatin, Benoît Pitard, B. J Drug Deliv Sci Technol Article Since the discovery of the RNA interference (RNAi) phenomenon, RNAi-based therapies now present a huge potential for the treatment of many diseases, including inflammatory and infectious diseases and cancers. While numerous reports have described the development of small interfering RNA (siRNA) delivery systems for in-vivo applications, only a small number of siRNA-based therapies are currently under clinical development. This is essentially due to the lack of efficient and safe siRNA delivery systems for intravenous administration. However, the delivery of siRNA after local injection could represent an attractive route of administration to limit the issues of toxicity associated with systemic injection. We will describe here the different synthetic vectors which have been developed for the local delivery of siRNA in various organs. Elsevier B.V. 2012 2014-12-17 /pmc/articles/PMC7128187/ http://dx.doi.org/10.1016/S1773-2247(12)50002-X Text en Copyright © 2012 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Beilvert, F.
Mével, M.
Chatin, Benoît
Pitard, B.
Local siRNA delivery by non-viral vectors
title Local siRNA delivery by non-viral vectors
title_full Local siRNA delivery by non-viral vectors
title_fullStr Local siRNA delivery by non-viral vectors
title_full_unstemmed Local siRNA delivery by non-viral vectors
title_short Local siRNA delivery by non-viral vectors
title_sort local sirna delivery by non-viral vectors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128187/
http://dx.doi.org/10.1016/S1773-2247(12)50002-X
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