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

Author:

Shepherd Sarah J.1,Han Xuexiang1,Mukalel Alvin J.1,El-Mayta Rakan1ORCID,Thatte Ajay S.1,Wu Jingyu2,Padilla Marshall S.1,Alameh Mohamad-Gabriel3,Srikumar Neha4,Lee Daeyeon2,Weissman Drew3,Issadore David125,Mitchell Michael J.16789ORCID

Affiliation:

1. Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104

2. Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104

3. Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104

4. Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104

5. Department of Electrical and Systems Engineering, University of Pennsylvania, Philadelphia, PA 19104

6. Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104

7. Cardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104

8. Institute for Regenerative Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104

9. Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104

Abstract

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.

Funder

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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