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Characterization of mRNA Lipid Nanoparticles by Electron Density Mapping Reconstruction: X-ray Scattering with Density from Solution Scattering (DENSS) Algorithm.
Dao, Huy M; AboulFotouh, Khaled; Hussain, Aasim Faheem; Marras, Alexander E; Johnston, Keith P; Cui, Zhengrong; Williams, Robert O.
Afiliación
  • Dao HM; Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX, 78712, USA.
  • AboulFotouh K; Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Hussain AF; Department of Biomedical Engineering, Cockrell School of Engineering, The University of Texas at Austin, Austin, TX, USA.
  • Marras AE; Department of Biomedical Engineering, Cockrell School of Engineering, The University of Texas at Austin, Austin, TX, USA.
  • Johnston KP; Materials Science and Engineering Graduate Program, Texas Materials Institute, The University of Texas at Austin, Austin, TX, USA.
  • Cui Z; Walker Department of Mechanical Engineering, The University of Texas at Austin, Austin, TX, USA.
  • Williams RO; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, USA.
Pharm Res ; 41(3): 501-512, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38326530
ABSTRACT

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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Electrones / Nanopartículas / Liposomas Tipo de estudio: Prognostic_studies Idioma: En Revista: Pharm Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Electrones / Nanopartículas / Liposomas Tipo de estudio: Prognostic_studies Idioma: En Revista: Pharm Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos