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Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage

Liposomes are versatile and well-proven as a means to deliver nucleic acids into cells. Most of the formulation procedures used are labour intensive and result in unstable end products. We have previously reported on the development of a simple, yet efficient, hydration-of-freeze-dried-matrix (HFDM)...

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Detalles Bibliográficos
Autores principales: Clarke, Daniel, Idris, Adi, McMillan, Nigel A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368384/
https://www.ncbi.nlm.nih.gov/pubmed/30735545
http://dx.doi.org/10.1371/journal.pone.0211954
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author Clarke, Daniel
Idris, Adi
McMillan, Nigel A. J.
author_facet Clarke, Daniel
Idris, Adi
McMillan, Nigel A. J.
author_sort Clarke, Daniel
collection PubMed
description Liposomes are versatile and well-proven as a means to deliver nucleic acids into cells. Most of the formulation procedures used are labour intensive and result in unstable end products. We have previously reported on the development of a simple, yet efficient, hydration-of-freeze-dried-matrix (HFDM) method to entrap siRNA within lipid particles. Here we show that the particles are stable up to 12 months after storage at room temperature (RT), 4°C or -20°C. While RT storage results in changes in particle size and polydispersity, gene silencing of all particles was similar to freshly prepared particles following storage for 3, 6, 9 or 12 months at all temperatures. This is the first report of such long-term stability in siRNA-loaded liposomes.
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spelling pubmed-63683842019-02-22 Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage Clarke, Daniel Idris, Adi McMillan, Nigel A. J. PLoS One Research Article Liposomes are versatile and well-proven as a means to deliver nucleic acids into cells. Most of the formulation procedures used are labour intensive and result in unstable end products. We have previously reported on the development of a simple, yet efficient, hydration-of-freeze-dried-matrix (HFDM) method to entrap siRNA within lipid particles. Here we show that the particles are stable up to 12 months after storage at room temperature (RT), 4°C or -20°C. While RT storage results in changes in particle size and polydispersity, gene silencing of all particles was similar to freshly prepared particles following storage for 3, 6, 9 or 12 months at all temperatures. This is the first report of such long-term stability in siRNA-loaded liposomes. Public Library of Science 2019-02-08 /pmc/articles/PMC6368384/ /pubmed/30735545 http://dx.doi.org/10.1371/journal.pone.0211954 Text en © 2019 Clarke et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Clarke, Daniel
Idris, Adi
McMillan, Nigel A. J.
Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage
title Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage
title_full Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage
title_fullStr Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage
title_full_unstemmed Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage
title_short Development of novel lipidic particles for siRNA delivery that are highly effective after 12 months storage
title_sort development of novel lipidic particles for sirna delivery that are highly effective after 12 months storage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368384/
https://www.ncbi.nlm.nih.gov/pubmed/30735545
http://dx.doi.org/10.1371/journal.pone.0211954
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