AI Article Synopsis

  • Lipid nanoparticles (LNPs) are effective delivery systems for RNA vaccines, especially formulations with ionizable cationic lipids that change with pH levels.
  • Understanding the dynamic processes of LNP formation is essential for improving their performance, but gaps exist in knowledge about how these processes affect drug delivery.
  • This study uses advanced microscopy and energy transfer techniques to analyze LNP fusion dynamics based on various formulation factors, revealing a strong link between these dynamics and the formulation choices made.

Article Abstract

Lipid nanoparticles (LNPs) have proven to be promising delivery vehicles for RNA-based vaccines and therapeutics, particularly in LNP formulations containing ionizable cationic lipids that undergo protonation/deprotonation in response to buffer pH changes. These nanoparticles are typically formulated using a rapid mixing technique at low pH, followed by a return to physiological pH that triggers LNP-LNP fusion. A detailed understanding of these dynamic processes is crucial to optimize the overall performance and efficiency of LNPs. However, knowledge gaps persist regarding how particle formation mechanisms impact drug loading and delivery functions. In this work, we employ single-molecule Convex Lens-induced Confinement (CLiC) microscopy in combination with Förster resonance energy transfer (FRET) measurements to study LNP fusion dynamics in relation to various formulation parameters, including lipid concentration, buffer conditions, drug loading ratio, PEG-lipid concentrations, and ionizable lipid selection. Our results reveal a strong correlation between the measured fusion dynamics and the formulation parameters used; these findings are consistent with DLS and Cryo-TEM-based assays. These measurements offer a cost-effective method for characterizing and screening potential drug candidates and can provide additional insights into their design, with opportunities for optimization.

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http://dx.doi.org/10.1021/acsnano.3c12981DOI Listing

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