Full text is available at the source.
Abstract
Ionizable lipid nanoparticles (iLNPs) enable precise delivery of nucleic acids but face challenges in clinical translation.
- Batch-to-batch variability and complex lipid-RNA interactions hinder iLNP development.
- Advanced microfluidic technologies provide precise control over iLNP fabrication.
- Different mixing technologies, such as hydrodynamic flow focusing and staggered herringbone mixers, influence particle size, polydispersity index, and encapsulation efficiency.
- Integrating design-of-experiments methodologies and computational fluid dynamics modeling supports predictive formulation design.
- Machine learning-assisted optimization may enhance reproducibility and scalability in iLNP production.
Simplified