Lipid nanoparticles for nucleic acid delivery beyond the liver

Nadine Saber, Mariona Estape Senti, Raymond Michel Schiffelers*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Lipid nanoparticles (LNPs) are the most clinically advanced drug delivery system for nucleic acid therapeutics, exemplified by the success of the COVID-19 mRNA vaccines. However, their clinical use is currently limited to hepatic diseases and vaccines due to their tendency to accumulate in the liver upon intravenous administration. To fully leverage their potential, it is essential to understand and address their liver tropism, while also developing strategies to enhance delivery to tissues beyond the liver. Ensuring that these therapeutics reach their target cells while avoiding off-target cells is essential for both their efficacy and safety. There are three potential targeting strategies—passive, active, and endogenous—which can be used individually or in combination to target nonhepatic tissues. In this review, we delve into the recent advancements in LNP engineering for delivering nucleic acid beyond the liver.

Original languageEnglish
Pages (from-to)617-627
Number of pages11
JournalHuman gene therapy
Volume35
Issue number17-18
Early online date14 Aug 2024
DOIs
Publication statusPublished - Sept 2024

Keywords

  • drug delivery
  • extrahepatic delivery
  • gene therapy
  • lipid nanoparticle
  • nanomedicine
  • nucleic acid
  • targeted delivery

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