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Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines

Lipid nanoparticles (LNPs) are a potent delivery technology that have made it possible for the recent clinical breakthroughs in mRNA therapeutics and vaccines. A key challenge to the broader implementation of mRNA therapeutics and vaccines is the development of technology to produce precisely define...

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Autores principales: Shepherd, Sarah J., Han, Xuexiang, Mukalel, Alvin J., El-Mayta, Rakan, Thatte, Ajay S., Wu, Jingyu, Padilla, Marshall S., Alameh, Mohamad-Gabriel, Srikumar, Neha, Lee, Daeyeon, Weissman, Drew, Issadore, David, Mitchell, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438381/
https://www.ncbi.nlm.nih.gov/pubmed/37556502
http://dx.doi.org/10.1073/pnas.2303567120
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author Shepherd, Sarah J.
Han, Xuexiang
Mukalel, Alvin J.
El-Mayta, Rakan
Thatte, Ajay S.
Wu, Jingyu
Padilla, Marshall S.
Alameh, Mohamad-Gabriel
Srikumar, Neha
Lee, Daeyeon
Weissman, Drew
Issadore, David
Mitchell, Michael J.
author_facet Shepherd, Sarah J.
Han, Xuexiang
Mukalel, Alvin J.
El-Mayta, Rakan
Thatte, Ajay S.
Wu, Jingyu
Padilla, Marshall S.
Alameh, Mohamad-Gabriel
Srikumar, Neha
Lee, Daeyeon
Weissman, Drew
Issadore, David
Mitchell, Michael J.
author_sort Shepherd, Sarah J.
collection PubMed
description Lipid nanoparticles (LNPs) are a potent delivery technology that have made it possible for the recent clinical breakthroughs in mRNA therapeutics and vaccines. A key challenge to the broader implementation of mRNA therapeutics and vaccines is the development of technology to produce precisely defined LNP formulations, with throughput that can scale from discovery to commercial manufacturing and meet the stringent manufacturing standards of the pharmaceutical industry. To address these challenges, we have developed a microfluidic chip that incorporates 1×, 10×, or 256× LNP-generating units that achieve scalable production rates of up to 17 L/h of precisely defined LNPs. Using these chips, we demonstrate that LNP physical properties and potency in vivo are unchanged as throughput is scaled. Our chips are fabricated out of silicon and glass substrates, which have excellent solvent compatibility, compatibility with pharmaceutical manufacturing, and can be fully reset and reused. SARS-CoV-2 mRNA-LNP vaccines formulated by our chips triggered potent antibody responses in a preclinical study. These results demonstrate the feasibility of directly translating microfluidic-generated LNPs to the scale necessary for commercial production.
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spelling pubmed-104383812023-08-19 Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines Shepherd, Sarah J. Han, Xuexiang Mukalel, Alvin J. El-Mayta, Rakan Thatte, Ajay S. Wu, Jingyu Padilla, Marshall S. Alameh, Mohamad-Gabriel Srikumar, Neha Lee, Daeyeon Weissman, Drew Issadore, David Mitchell, Michael J. Proc Natl Acad Sci U S A Physical Sciences Lipid nanoparticles (LNPs) are a potent delivery technology that have made it possible for the recent clinical breakthroughs in mRNA therapeutics and vaccines. A key challenge to the broader implementation of mRNA therapeutics and vaccines is the development of technology to produce precisely defined LNP formulations, with throughput that can scale from discovery to commercial manufacturing and meet the stringent manufacturing standards of the pharmaceutical industry. To address these challenges, we have developed a microfluidic chip that incorporates 1×, 10×, or 256× LNP-generating units that achieve scalable production rates of up to 17 L/h of precisely defined LNPs. Using these chips, we demonstrate that LNP physical properties and potency in vivo are unchanged as throughput is scaled. Our chips are fabricated out of silicon and glass substrates, which have excellent solvent compatibility, compatibility with pharmaceutical manufacturing, and can be fully reset and reused. SARS-CoV-2 mRNA-LNP vaccines formulated by our chips triggered potent antibody responses in a preclinical study. These results demonstrate the feasibility of directly translating microfluidic-generated LNPs to the scale necessary for commercial production. National Academy of Sciences 2023-08-09 2023-08-15 /pmc/articles/PMC10438381/ /pubmed/37556502 http://dx.doi.org/10.1073/pnas.2303567120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Physical Sciences
Shepherd, Sarah J.
Han, Xuexiang
Mukalel, Alvin J.
El-Mayta, Rakan
Thatte, Ajay S.
Wu, Jingyu
Padilla, Marshall S.
Alameh, Mohamad-Gabriel
Srikumar, Neha
Lee, Daeyeon
Weissman, Drew
Issadore, David
Mitchell, Michael J.
Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines
title Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines
title_full Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines
title_fullStr Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines
title_full_unstemmed Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines
title_short Throughput-scalable manufacturing of SARS-CoV-2 mRNA lipid nanoparticle vaccines
title_sort throughput-scalable manufacturing of sars-cov-2 mrna lipid nanoparticle vaccines
topic Physical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438381/
https://www.ncbi.nlm.nih.gov/pubmed/37556502
http://dx.doi.org/10.1073/pnas.2303567120
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