Journal of controlled release : official journal of the Controlled Release SocietyMay 20, 2025

Measuring the charge of single particles to analyze lipid nanoparticles and how they carry mRNA

mRNA Technology Weekly Brief ↗PubMed ↗DOI ↗

Updated Feb 27, 2026

Abstract

A similarly prepared mRNA-packaged lipid nanoparticle sample has a peak mass at 70 MDa, which is 31 MDa higher than that of the empty lipid nanoparticles.

Charge detection mass spectrometry (CDMS) can effectively weigh thousands of individual lipid nanoparticles.
Diameter distributions of empty lipid nanoparticles from CDMS and cryo-TEM measurements show excellent agreement, indicating stability in high vacuum.
Four freeze-thaw cycles lead to a significant reduction in the mass of mRNA-packaged lipid nanoparticles to approximately 26.5 MDa.
After the first freeze-thaw cycle, degraded lipid nanoparticles constitute about 28% of the mRNA-packaged sample.
Two models for the lipid core mass distribution suggest that the average mRNA packaging ranges from 43 to 107 copies, with a rough estimate of 62 copies from cryo-TEM images.

Simplified

Lipid nanoparticles (LNPs) are effective delivery systems for RNA therapeutics, yet their intrinsic heterogeneity in size and composition make them challenging to characterize. Charge detection mass spectrometry (CDMS) was used to rapidly weigh thousands of individual LNPs. Diameter distributions of empty LNPs from CDMS and cryo-TEM measurements are in excellent agreement demonstrating that these particles are sufficiently stable in the high vacuum environment of the mass spectrometer for accurate mass analysis. A similarly prepared mRNA-packaged LNP sample has a peak mass at ∼70 MDa, 31 MDa higher than that of the empty LNP sample. Four freeze-thaw (FT) cycles of the mRNA-LNPs results in a peak mass at ∼26.5 MDa, indicating significantly degraded LNPs. The degraded LNPs are about 28 % of the population of the mRNA-LNP sample after the first FT cycle. A non-linear least squares fitting routine was developed to convolve the mass distribution of the LNP core with a function that describes the packaging distribution to fit the mRNA-LNP data. Two models of the lipid core mass distribution were used to obtain the distribution of mRNA in the packaged LNPs. These two models provide a lower and upper limit to the average mRNA packaging of 43 and 107 mRNA copies, consistent with a rough estimate of an average of 62 mRNA copies obtained from cryo-TEM images. These results demonstrate the potential for label-free, rapid characterization of mass, diameter, packaging, and stability of LNPs with CDMS.

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Measuring the charge of single particles to analyze lipid nanoparticles and how they carry mRNA

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