Characterization of mRNA Lipid Nanoparticles by Electron Density Mapping Reconstruction: X-ray Scattering with Density from Solution Scattering (DENSS) Algorithm

• Published in: Pharmaceutical research 2024-03, Vol.41 (3), p.501-512
• Main Authors: Dao, Huy M., AboulFotouh, Khaled, Hussain, Aasim Faheem, Marras, Alexander E., Johnston, Keith P., Cui, Zhengrong, Williams, Robert O.
• Format: Article
• Language: English
• Subjects: Algorithms; Biochemistry; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Biomedicine; Diffraction; Electrons; Ethylenediaminetetraacetic acid; Freeze-thawing; Light scattering; Lipids; Mapping; Medical Law; Messenger RNA; Morphology; mRNA; Nanoparticles; Original Research Article; Pharmacology/Toxicology; Pharmacy; Transmission electron microscopy; X-ray scattering; X-rays
• ISSN: 0724-8741; 1573-904X
• DOI: 10.1007/s11095-024-03671-9

Purpose This study aimed to test the feasibility of using Small Angle X-ray Scattering (SAXS) coupled with Density from Solution Scattering (DENSS) algorithm to characterize the internal architecture of messenger RNA-containing lipid nanoparticles (mRNA-LNPs). Methods The DENSS algorithm was employed to construct a three-dimensional model of average individual mRNA-LNP. The reconstructed models were cross validated with cryogenic transmission electron microscopy (cryo-TEM), and dynamic light scattering (DLS) to assess size, morphology, and internal structure. Results Cryo-TEM and DLS complemented SAXS, revealed a core–shell mRNA-LNP structure with electron-rich mRNA-rich region at the core, surrounded by lipids. The reconstructed model, utilizing the DENSS algorithm, effectively distinguishes mRNA and lipids via electron density mapping. Notably, DENSS accurately models the morphology of the mRNA-LNPs as an ellipsoidal shape with a "bleb" architecture or a two-compartment structure with contrasting electron densities, corresponding to mRNA-filled and empty lipid compartments, respectively. Finally, subtle changes in the LNP structure after three freeze–thaw cycles were detected by SAXS, demonstrating an increase in radius of gyration (Rg) associated with mRNA leakage. Conclusion Analyzing SAXS profiles based on DENSS algorithm to yield a reconstructed electron density based three-dimensional model can be a useful physicochemical characterization method in the toolbox to study mRNA-LNPs and facilitate their development.