| Literature DB >> 34286581 |
Andrew J Sinegra, Michael Evangelopoulos, Jungsoo Park, Ziyin Huang, Chad A Mirkin.
Abstract
Lipid nanoparticle SNAs (LNP-SNAs) have been synthesized for the delivery of DNA and RNA to targets in the cytoplasm of cells. Both the composition of the LNP core and surface-presented DNA sequences contribute to LNP-SNA activity. G-rich sequences enhance the activity of LNP-SNAs compared to T-rich sequences. In the LNP core, increased cholesterol content leads to greater activity. Optimized LNP-SNA candidates reduce the siRNA concentration required to silence mRNA by 2 orders of magnitude compared to liposome-based SNAs. In addition, the LNP-SNA architectures alter biodistribution and efficacy profiles in mice. For example, mRNA within LNP-SNAs injected intravenously is primarily expressed in the spleen, while mRNA encapsulated by LNPs (no DNA on the surface) was expressed primarily in the liver with a relatively small amount in the spleen. These data show that the activity and biodistribution of LNP-SNA architectures are different from those of conventional liposomal SNAs and therefore potentially can be used to target tissues.Entities:
Keywords: RNA; Spherical nucleic acids; drug delivery; lipid nanoparticles
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Year: 2021 PMID: 34286581 PMCID: PMC8385759 DOI: 10.1021/acs.nanolett.1c01973
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 12.262