(376) Design and Screening of Ionizable Lipids for Precision mRNA Delivery to Extrahepatic Organs
Introduction: Lipid nanoparticles (LNPs) have emerged as the leading platform for nucleic acid delivery, but their tendency to accumulate in the liver limits broader therapeutic applications. While apolipoprotein E (ApoE)-mediated uptake drives liver accumulation, expanding LNP biodistribution to extrahepatic tissues could increase the clinical potential of mRNA-based therapies. This study explores how structural modifications in ionizable lipids (ILs) influence protein corona formation and organ-specific targeting, aiming to develop LNPs capable of selective delivery to the lungs and spleen.
Learning Objectives:
Upon completion, participants will be able to describe how lipid structure affects organ targeting.
Upon completion, participants will be able to explain how protein corona drives LNP biodistribution.
Upon completion, participants will be able to find strategies to enhance extrahepatic mRNA delivery.