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Ionization and Structural Properties of mRNA Lipid Nanoparticles that Influence Expression in Intramuscular and Intravascular Administration
Published
Author(s)
Manuel Carrasco, Suman Alishetty, Mohamad-Gabriel Alameh, Hooda Said, Lacey Wright, Mikell Paige, Ousamah Soliman, Drew Weissman, Thomas Cleveland, Alexander Grishaev, Michael Buschmann
Abstract
Lipid Nanoparticles (LNPs) are used to deliver siRNA and COVID-19 mRNA vaccines. The main factor known to determine their delivery efficiency is the pKa of the LNP containing an ionizable lipid. Herein, we report a method that can predict the LNP pKa from the structure of the ionizable lipid. We used theoretical, NMR, fluorescent-dye binding, and electrophoretic mobility methods to comprehensively measure protonation of both the ionizable lipid and the formulated LNP. The pKa of the ionizable lipid was 2-3 units higher than the pKa of the LNP primarily due to proton solvation energy differences between the LNP and aqueous medium. We exploited these results to explain a wide range of delivery efficiencies in vitro and in vivo for intramuscular (IM) and intravascular (IV) administration of different ionizable lipids at escalating ionizable lipid-to-mRNA ratios in the LNP. In addition, we determined that the more negatively charged LNPs exhibit higher off-target systemic expression of mRNA in the liver following IM administration, that is undesirable for mRNA-LNP vaccines and can be minimized through appropriate design of the ionizable lipid and LNP.
Carrasco, M.
, Alishetty, S.
, Alameh, M.
, Said, H.
, Wright, L.
, Paige, M.
, Soliman, O.
, Weissman, D.
, Cleveland, T.
, Grishaev, A.
and Buschmann, M.
(2021),
Ionization and Structural Properties of mRNA Lipid Nanoparticles that Influence Expression in Intramuscular and Intravascular Administration, Communications Biology, [online], https://doi.org/10.1038/s42003-021-02441-2, https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=932410
(Accessed October 14, 2025)