Abstract
When formulating mRNA into lipid nanoparticles (LNP), various copy numbers of mRNA are encapsulated, leading to a distribution of mRNA loading levels within LNPs. It is unclear if the mRNA loading level affects the functional delivery of the message. Here we show that depending on the mRNA loading level, LNPs exhibit distinct mass densities and can be fractionated via ultracentrifugation. Upon fractionation, we investigated if mRNA loading levels influence LNP sizing, lipid composition and morphology. We further conducted in vitro and in vivo functional delivery of mRNA and found that the LNP fraction with highest mRNA loading levels were the least transfection competent.
Supplementary materials
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Supporting information
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In the document: mathematical process of Equation1, FigS1~3
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