Delivery of oligonucleotide‐based therapeutics: challenges and opportunities

Detalhes bibliográficos
Autor(a) principal: Hammond, Suzan M.
Data de Publicação: 2021
Outros Autores: Aartsma‐Rus, Annemieke, Alves, Sandra, Borgos, Sven E, Buijsen, Ronald A.M., Collin, Rob W.J., Covello, Giuseppina, Denti, Michela A., Desviat, Lourdes R., Echevarría, Lucía, Foged, Camilla, Gaina, Gisela, Garanto, Alejandro, Goyenvalle, Aurelie T., Guzowska, Magdalena, Holodnuka, Irina, Jones, David R., Krause, Sabine, Lehto, Taavi, Montolio, Marisol, Van Roon‐Mom, Willeke, Arechavala‐Gomeza, Virginia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10400.18/7983
Resumo: Nucleic acid-based therapeutics that regulate gene expression have been developed towards clinical use at a steady pace for several decades, but in recent years the field has been accelerating. To date, there are 11 marketed products based on antisense oligonucleotides, aptamers and small interfering RNAs, and many others are in the pipeline for both academia and industry. A major technology trigger for this development has been progress in oligonucleotide chemistry to improve the drug properties and reduce cost of goods, but the main hurdle for the application to a wider range of disorders is delivery to target tissues. The adoption of delivery technologies, such as conjugates or nanoparticles, has been a game changer for many therapeutic indications, but many others are still awaiting their eureka moment. Here, we cover the variety of methods developed to deliver nucleic acid-based therapeutics across biological barriers and the model systems used to test them. We discuss important safety considerations and regulatory requirements for synthetic oligonucleotide chemistries and the hurdles for translating laboratory breakthroughs to the clinic. Recent advances in the delivery of nucleic acid-based therapeutics and in the development of model systems, as well as safety considerations and regulatory requirements for synthetic oligonucleotide chemistries are discussed in this review on oligonucleotide-based therapeutics.
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spelling Delivery of oligonucleotide‐based therapeutics: challenges and opportunitiesRNA TherapeuticsDeliveryOligonucleotidesAntisense OligonucleotidesPreclinical ModelsSafetyDoenças GenéticasGenetica HumanaNucleic acid-based therapeutics that regulate gene expression have been developed towards clinical use at a steady pace for several decades, but in recent years the field has been accelerating. To date, there are 11 marketed products based on antisense oligonucleotides, aptamers and small interfering RNAs, and many others are in the pipeline for both academia and industry. A major technology trigger for this development has been progress in oligonucleotide chemistry to improve the drug properties and reduce cost of goods, but the main hurdle for the application to a wider range of disorders is delivery to target tissues. The adoption of delivery technologies, such as conjugates or nanoparticles, has been a game changer for many therapeutic indications, but many others are still awaiting their eureka moment. Here, we cover the variety of methods developed to deliver nucleic acid-based therapeutics across biological barriers and the model systems used to test them. We discuss important safety considerations and regulatory requirements for synthetic oligonucleotide chemistries and the hurdles for translating laboratory breakthroughs to the clinic. Recent advances in the delivery of nucleic acid-based therapeutics and in the development of model systems, as well as safety considerations and regulatory requirements for synthetic oligonucleotide chemistries are discussed in this review on oligonucleotide-based therapeutics.EMBO Press/ Wiley Open AccessRepositório Científico do Instituto Nacional de SaúdeHammond, Suzan M.Aartsma‐Rus, AnnemiekeAlves, SandraBorgos, Sven EBuijsen, Ronald A.M.Collin, Rob W.J.Covello, GiuseppinaDenti, Michela A.Desviat, Lourdes R.Echevarría, LucíaFoged, CamillaGaina, GiselaGaranto, AlejandroGoyenvalle, Aurelie T.Guzowska, MagdalenaHolodnuka, IrinaJones, David R.Krause, SabineLehto, TaaviMontolio, MarisolVan Roon‐Mom, WillekeArechavala‐Gomeza, Virginia2022-03-10T16:32:16Z2021-04-062021-04-06T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/7983eng1757-468410.15252/emmm.202013243info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-26T14:18:42Zoai:repositorio.insa.pt:10400.18/7983Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T21:33:05.246232Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
title Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
spellingShingle Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
Hammond, Suzan M.
RNA Therapeutics
Delivery
Oligonucleotides
Antisense Oligonucleotides
Preclinical Models
Safety
Doenças Genéticas
Genetica Humana
title_short Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
title_full Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
title_fullStr Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
title_full_unstemmed Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
title_sort Delivery of oligonucleotide‐based therapeutics: challenges and opportunities
author Hammond, Suzan M.
author_facet Hammond, Suzan M.
Aartsma‐Rus, Annemieke
Alves, Sandra
Borgos, Sven E
Buijsen, Ronald A.M.
Collin, Rob W.J.
Covello, Giuseppina
Denti, Michela A.
Desviat, Lourdes R.
Echevarría, Lucía
Foged, Camilla
Gaina, Gisela
Garanto, Alejandro
Goyenvalle, Aurelie T.
Guzowska, Magdalena
Holodnuka, Irina
Jones, David R.
Krause, Sabine
Lehto, Taavi
Montolio, Marisol
Van Roon‐Mom, Willeke
Arechavala‐Gomeza, Virginia
author_role author
author2 Aartsma‐Rus, Annemieke
Alves, Sandra
Borgos, Sven E
Buijsen, Ronald A.M.
Collin, Rob W.J.
Covello, Giuseppina
Denti, Michela A.
Desviat, Lourdes R.
Echevarría, Lucía
Foged, Camilla
Gaina, Gisela
Garanto, Alejandro
Goyenvalle, Aurelie T.
Guzowska, Magdalena
Holodnuka, Irina
Jones, David R.
Krause, Sabine
Lehto, Taavi
Montolio, Marisol
Van Roon‐Mom, Willeke
Arechavala‐Gomeza, Virginia
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Nacional de Saúde
dc.contributor.author.fl_str_mv Hammond, Suzan M.
Aartsma‐Rus, Annemieke
Alves, Sandra
Borgos, Sven E
Buijsen, Ronald A.M.
Collin, Rob W.J.
Covello, Giuseppina
Denti, Michela A.
Desviat, Lourdes R.
Echevarría, Lucía
Foged, Camilla
Gaina, Gisela
Garanto, Alejandro
Goyenvalle, Aurelie T.
Guzowska, Magdalena
Holodnuka, Irina
Jones, David R.
Krause, Sabine
Lehto, Taavi
Montolio, Marisol
Van Roon‐Mom, Willeke
Arechavala‐Gomeza, Virginia
dc.subject.por.fl_str_mv RNA Therapeutics
Delivery
Oligonucleotides
Antisense Oligonucleotides
Preclinical Models
Safety
Doenças Genéticas
Genetica Humana
topic RNA Therapeutics
Delivery
Oligonucleotides
Antisense Oligonucleotides
Preclinical Models
Safety
Doenças Genéticas
Genetica Humana
description Nucleic acid-based therapeutics that regulate gene expression have been developed towards clinical use at a steady pace for several decades, but in recent years the field has been accelerating. To date, there are 11 marketed products based on antisense oligonucleotides, aptamers and small interfering RNAs, and many others are in the pipeline for both academia and industry. A major technology trigger for this development has been progress in oligonucleotide chemistry to improve the drug properties and reduce cost of goods, but the main hurdle for the application to a wider range of disorders is delivery to target tissues. The adoption of delivery technologies, such as conjugates or nanoparticles, has been a game changer for many therapeutic indications, but many others are still awaiting their eureka moment. Here, we cover the variety of methods developed to deliver nucleic acid-based therapeutics across biological barriers and the model systems used to test them. We discuss important safety considerations and regulatory requirements for synthetic oligonucleotide chemistries and the hurdles for translating laboratory breakthroughs to the clinic. Recent advances in the delivery of nucleic acid-based therapeutics and in the development of model systems, as well as safety considerations and regulatory requirements for synthetic oligonucleotide chemistries are discussed in this review on oligonucleotide-based therapeutics.
publishDate 2021
dc.date.none.fl_str_mv 2021-04-06
2021-04-06T00:00:00Z
2022-03-10T16:32:16Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.18/7983
url http://hdl.handle.net/10400.18/7983
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 1757-4684
10.15252/emmm.202013243
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv EMBO Press/ Wiley Open Access
publisher.none.fl_str_mv EMBO Press/ Wiley Open Access
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