Cargando…

Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines

Lipid nanoparticles (LNPs) are currently the most advanced non-viral clinically approved messenger ribonucleic acid (mRNA) delivery systems. The ability of a mRNA vaccine to have a therapeutic effect is related to the capacity of LNPs to deliver the nucleic acid intact into cells. The role of LNPs i...

Descripción completa

Detalles Bibliográficos
Autores principales: Malburet, Camille, Leclercq, Laurent, Cotte, Jean-François, Thiebaud, Jérôme, Bazin, Emilie, Garinot, Marie, Cottet, Hervé
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628342/
https://www.ncbi.nlm.nih.gov/pubmed/36316446
http://dx.doi.org/10.1038/s41434-022-00370-1
_version_ 1784823174357057536
author Malburet, Camille
Leclercq, Laurent
Cotte, Jean-François
Thiebaud, Jérôme
Bazin, Emilie
Garinot, Marie
Cottet, Hervé
author_facet Malburet, Camille
Leclercq, Laurent
Cotte, Jean-François
Thiebaud, Jérôme
Bazin, Emilie
Garinot, Marie
Cottet, Hervé
author_sort Malburet, Camille
collection PubMed
description Lipid nanoparticles (LNPs) are currently the most advanced non-viral clinically approved messenger ribonucleic acid (mRNA) delivery systems. The ability of a mRNA vaccine to have a therapeutic effect is related to the capacity of LNPs to deliver the nucleic acid intact into cells. The role of LNPs is to protect mRNA, especially from degradation by ribonucleases (RNases) and to allow it to access the cytoplasm of cells where it can be translated into the protein of interest. LNPs enter cells by endocytosis and their size is a critical parameter impacting their cellular internalization. In this work, we studied different formulation process parameters impacting LNPs size. Taylor dispersion analysis (TDA) was used to determine the LNPs size and size distribution and the results were compared with those obtained by Dynamic Light Scattering (DLS). TDA was also used to study both the degradation of mRNA in the presence of RNases and the percentage of mRNA encapsulation within LNPs. [Image: see text]
format Online
Article
Text
id pubmed-9628342
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-96283422022-11-02 Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines Malburet, Camille Leclercq, Laurent Cotte, Jean-François Thiebaud, Jérôme Bazin, Emilie Garinot, Marie Cottet, Hervé Gene Ther Article Lipid nanoparticles (LNPs) are currently the most advanced non-viral clinically approved messenger ribonucleic acid (mRNA) delivery systems. The ability of a mRNA vaccine to have a therapeutic effect is related to the capacity of LNPs to deliver the nucleic acid intact into cells. The role of LNPs is to protect mRNA, especially from degradation by ribonucleases (RNases) and to allow it to access the cytoplasm of cells where it can be translated into the protein of interest. LNPs enter cells by endocytosis and their size is a critical parameter impacting their cellular internalization. In this work, we studied different formulation process parameters impacting LNPs size. Taylor dispersion analysis (TDA) was used to determine the LNPs size and size distribution and the results were compared with those obtained by Dynamic Light Scattering (DLS). TDA was also used to study both the degradation of mRNA in the presence of RNases and the percentage of mRNA encapsulation within LNPs. [Image: see text] Nature Publishing Group UK 2022-11-01 2023 /pmc/articles/PMC9628342/ /pubmed/36316446 http://dx.doi.org/10.1038/s41434-022-00370-1 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. 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 Article
Malburet, Camille
Leclercq, Laurent
Cotte, Jean-François
Thiebaud, Jérôme
Bazin, Emilie
Garinot, Marie
Cottet, Hervé
Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines
title Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines
title_full Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines
title_fullStr Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines
title_full_unstemmed Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines
title_short Taylor Dispersion Analysis to support lipid-nanoparticle formulations for mRNA vaccines
title_sort taylor dispersion analysis to support lipid-nanoparticle formulations for mrna vaccines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628342/
https://www.ncbi.nlm.nih.gov/pubmed/36316446
http://dx.doi.org/10.1038/s41434-022-00370-1
work_keys_str_mv AT malburetcamille taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines
AT leclercqlaurent taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines
AT cottejeanfrancois taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines
AT thiebaudjerome taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines
AT bazinemilie taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines
AT garinotmarie taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines
AT cottetherve taylordispersionanalysistosupportlipidnanoparticleformulationsformrnavaccines