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Advances in oligonucleotide drug delivery

Oligonucleotides can be used to modulate gene expression via a range of processes including RNAi, target degradation by RNase H-mediated cleavage, splicing modulation, non-coding RNA inhibition, gene activation and programmed gene editing. As such, these molecules have potential therapeutic applicat...

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Detalles Bibliográficos
Autores principales: Roberts, Thomas C., Langer, Robert, Wood, Matthew J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419031/
https://www.ncbi.nlm.nih.gov/pubmed/32782413
http://dx.doi.org/10.1038/s41573-020-0075-7
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author Roberts, Thomas C.
Langer, Robert
Wood, Matthew J. A.
author_facet Roberts, Thomas C.
Langer, Robert
Wood, Matthew J. A.
author_sort Roberts, Thomas C.
collection PubMed
description Oligonucleotides can be used to modulate gene expression via a range of processes including RNAi, target degradation by RNase H-mediated cleavage, splicing modulation, non-coding RNA inhibition, gene activation and programmed gene editing. As such, these molecules have potential therapeutic applications for myriad indications, with several oligonucleotide drugs recently gaining approval. However, despite recent technological advances, achieving efficient oligonucleotide delivery, particularly to extrahepatic tissues, remains a major translational limitation. Here, we provide an overview of oligonucleotide-based drug platforms, focusing on key approaches — including chemical modification, bioconjugation and the use of nanocarriers — which aim to address the delivery challenge.
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spelling pubmed-74190312020-08-12 Advances in oligonucleotide drug delivery Roberts, Thomas C. Langer, Robert Wood, Matthew J. A. Nat Rev Drug Discov Review Article Oligonucleotides can be used to modulate gene expression via a range of processes including RNAi, target degradation by RNase H-mediated cleavage, splicing modulation, non-coding RNA inhibition, gene activation and programmed gene editing. As such, these molecules have potential therapeutic applications for myriad indications, with several oligonucleotide drugs recently gaining approval. However, despite recent technological advances, achieving efficient oligonucleotide delivery, particularly to extrahepatic tissues, remains a major translational limitation. Here, we provide an overview of oligonucleotide-based drug platforms, focusing on key approaches — including chemical modification, bioconjugation and the use of nanocarriers — which aim to address the delivery challenge. Nature Publishing Group UK 2020-08-11 2020 /pmc/articles/PMC7419031/ /pubmed/32782413 http://dx.doi.org/10.1038/s41573-020-0075-7 Text en © Springer Nature Limited 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Roberts, Thomas C.
Langer, Robert
Wood, Matthew J. A.
Advances in oligonucleotide drug delivery
title Advances in oligonucleotide drug delivery
title_full Advances in oligonucleotide drug delivery
title_fullStr Advances in oligonucleotide drug delivery
title_full_unstemmed Advances in oligonucleotide drug delivery
title_short Advances in oligonucleotide drug delivery
title_sort advances in oligonucleotide drug delivery
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419031/
https://www.ncbi.nlm.nih.gov/pubmed/32782413
http://dx.doi.org/10.1038/s41573-020-0075-7
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