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  2. Process Robustness in Lipid Nanoparticle Production: A Comparison of Microfluidic and Turbulent Jet Mixing

Process Robustness in Lipid Nanoparticle Production: A Comparison of Microfluidic and Turbulent Jet Mixing

  • Mol Pharm. 2023 Jul 18. doi: 10.1021/acs.molpharmaceut.3c00390.
Matthew N O'Brien Laramy 1 Antonio P Costa 2 Yareli Maciel Cebrero 1 Johnson Joseph 2 Apoorva Sarode 1 Nanzhi Zang 1 Lee Joon Kim 3 Kate Hofmann 1 Shirley Wang 1 Alexandre Goyon 1 Stefan G Koenig 1 Michal Hammel 3 Greg L Hura 3 4
Affiliations

Affiliations

  • 1 Genentech, Inc., Genentech Research and Early Development, Synthetic Molecule Pharmaceutical Sciences, 1 DNA Way, South San Francisco, California 94060, United States.
  • 2 DIANT Pharma, Inc., 130 Utopia Road, Manchester, Connecticut 06042, United States.
  • 3 Lawrence Berkeley National Laboratory, Molecular Biophysics and Integrated Bioimaging Division, Berkeley, California 94720, United States.
  • 4 University of California Santa Cruz, Department of Chemistry and Biochemistry, Santa Cruz, California 95064, United States.
Abstract

The recent clinical and commercial success of lipid nanoparticles (LNPs) for nucleic acid delivery has incentivized the development of new technologies to manufacture LNPs. As new technologies emerge, researchers must determine which technologies to assess and how to perform comparative evaluations. In this article, we use a quality-by-design approach to systematically investigate how the mixer technology used to form LNPs influences LNPstructure. Specifically, a coaxial turbulent jet mixer and a staggered herringbone microfluidic mixer were systematically compared via matched formulation and process conditions. A full-factorial design-of-experiments study with three factors and three levels was executed for each mixer to compare process robustness in the production of antisense oligonucleotide (ASO) LNPs. ASO-LNPs generated with the coaxial turbulent jet mixer were consistently smaller, had a narrower particle size distribution, and had a higher ASO encapsulation as compared to the microfluidic mixer, but had a greater variation in internal structure with less ordered cores. A subset of the study was replicated for mRNA-LNPs with comparable trends in particle size and encapsulation, but more frequent bleb features for LNPs produced by the coaxial turbulent jet mixer. The study design used here provides a road map for how researchers may compare different mixer technologies (or process changes more broadly) and how such studies can inform process robustness and manufacturing control strategies.

Keywords

antisense oligonucleotide; lipid nanoparticle; messenger RNA; microfluidic mixer; nucleic acid; turbulent jet mixer.

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