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The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery

The earliest example of in vivo expression of exogenous mRNA is by direct intramuscular injection in mice without the aid of a delivery vehicle. The current state of the art for therapeutic nucleic acid delivery is lipid nanoparticles (LNP), which are composed of cholesterol, a helper lipid, a PEGyl...

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Autores principales: Kularatne, Ruvanthi N., Crist, Rachael M., Stern, Stephan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322927/
https://www.ncbi.nlm.nih.gov/pubmed/35890195
http://dx.doi.org/10.3390/ph15070897
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author Kularatne, Ruvanthi N.
Crist, Rachael M.
Stern, Stephan T.
author_facet Kularatne, Ruvanthi N.
Crist, Rachael M.
Stern, Stephan T.
author_sort Kularatne, Ruvanthi N.
collection PubMed
description The earliest example of in vivo expression of exogenous mRNA is by direct intramuscular injection in mice without the aid of a delivery vehicle. The current state of the art for therapeutic nucleic acid delivery is lipid nanoparticles (LNP), which are composed of cholesterol, a helper lipid, a PEGylated lipid and an ionizable amine-containing lipid. The liver is the primary organ of LNP accumulation following intravenous administration and is also observed to varying degrees following intramuscular and subcutaneous routes. Delivery of nucleic acid to hepatocytes by LNP has therapeutic potential, but there are many disease indications that would benefit from non-hepatic LNP tissue and cell population targeting, such as cancer, and neurological, cardiovascular and infectious diseases. This review will concentrate on the current efforts to develop the next generation of tissue-targeted LNP constructs for therapeutic nucleic acids.
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spelling pubmed-93229272022-07-27 The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery Kularatne, Ruvanthi N. Crist, Rachael M. Stern, Stephan T. Pharmaceuticals (Basel) Review The earliest example of in vivo expression of exogenous mRNA is by direct intramuscular injection in mice without the aid of a delivery vehicle. The current state of the art for therapeutic nucleic acid delivery is lipid nanoparticles (LNP), which are composed of cholesterol, a helper lipid, a PEGylated lipid and an ionizable amine-containing lipid. The liver is the primary organ of LNP accumulation following intravenous administration and is also observed to varying degrees following intramuscular and subcutaneous routes. Delivery of nucleic acid to hepatocytes by LNP has therapeutic potential, but there are many disease indications that would benefit from non-hepatic LNP tissue and cell population targeting, such as cancer, and neurological, cardiovascular and infectious diseases. This review will concentrate on the current efforts to develop the next generation of tissue-targeted LNP constructs for therapeutic nucleic acids. MDPI 2022-07-20 /pmc/articles/PMC9322927/ /pubmed/35890195 http://dx.doi.org/10.3390/ph15070897 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kularatne, Ruvanthi N.
Crist, Rachael M.
Stern, Stephan T.
The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery
title The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery
title_full The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery
title_fullStr The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery
title_full_unstemmed The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery
title_short The Future of Tissue-Targeted Lipid Nanoparticle-Mediated Nucleic Acid Delivery
title_sort future of tissue-targeted lipid nanoparticle-mediated nucleic acid delivery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322927/
https://www.ncbi.nlm.nih.gov/pubmed/35890195
http://dx.doi.org/10.3390/ph15070897
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