Lipid nanoparticles are an extension of earlier RNA transfection methods such as cationic liposomes.[8] Such systems are needed to protect the delicate mRNA molecules and shuttle them into cells without the immune system destroying them first. The nanoparticles enter the cells by triggering receptor-mediated endocytosis.
Ionisable lipids like SM-102 hold a relatively (/ close to) neutral charge at physiological pH but are positively charged within the nanoparticle (the amine group is protonated to form an ammonium cation). This allows them to bind to the negatively charged backbone of mRNA. The rest of the nanoparticle is formed from PEGylated lipids, which help stabilize the particle, and phospholipids and cholesterol molecules that contribute to the particle’s structure.[8]
SM-102 is also used for non-invasive bioluminescence imaging when SM-102 containing luciferase-encoding mRNA is used for in-vivo luciferase expression in animal models.[9][10][11]
Synthesis
The preparation of SM-102 was first described in a patent application to lipid nanoparticles by Moderna in 2017.[12]: 139–142 The final step is an alkylation reaction in which a secondary amine is combined with a lipid bromo ester.
^WO application 2017049245, Benenato K.E.; Kumarasinghe E.S. & Cornebise M., "Compounds and compositions for intracellular delivery of therapeutic agents", published 2017-03-23, assigned to ModernaTX, Inc.
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