Diblock Copolymer Targeted Lipid Nanoparticles: Next-Generation Nucleic Acid Delivery System Produced by Confined Impinging Jet Mixers

  • Bumjun Kim
  • , Sai Nikhil Subraveti
  • , Jason X. Liu
  • , Satya K. Nayagam
  • , Safaa Merghoub
  • , Nicholas J. Caggiano
  • , David F. Amelemah
  • , Ting Jiang
  • , Navid Bizmark
  • , Jonathan M. Conway
  • , Andrew Tsourkas
  • , Robert Krafft Prud'homme

Research output: Contribution to journalArticlepeer-review

Abstract

Despite the recent advances and clinical demonstration of lipid nanoparticles (LNPs) for therapeutic and prophylactic applications, the extrahepatic delivery of nucleic acids remains a significant challenge in the field. This limitation arises from the rapid desorption of lipid-PEG in the bloodstream and clearance to the liver, which hinders extrahepatic delivery. In response, we explore the substitution of lipid-PEG with biodegradable block copolymers (BCPs), specifically poly(ϵ-caprolactone)-block-poly(ethylene glycol) (PCL-b-PEG). BCPs offer strong anchoring for large macromolecules, potentially enhancing cell-specific targeting. To develop and optimize BCP-stabilized LNPs (BCP-LNPs), we employed a Design of Experiment (DOE) approach. Through a systematic exploration, we identified optimal formulations for BCP-LNPs, achieving desirable physicochemical properties and encapsulation efficiency. Notably, BCP-LNPs exhibit surprising trends in transfection efficiency, with certain formulations showing up to a 40-fold increase in transfection in Hela cells, while maintaining minimal cytotoxicity. The lipid compositions that optimized PCL-b-PEG LNP transfection were different from the compositions that optimized PEG-lipid LNP transfection. Furthermore, our study confirms the versatility of BCP-LNPs in encapsulating and delivering both mRNA and pDNA, demonstrating their cargo-agnostic nature. Lastly, we showcased the targeted BCP-LNPs using a Cetuximab-conjugated formulation. These targeted LNPs show significant promise in delivering cargo specific to EGFR-overexpressing cells (A549 cells), with up to 2.4 times higher transfection compared to nontargeted LNPs. This finding underscores the potential of BCP-LNPs in targeted gene therapy, especially in challenging scenarios such as tumor targeting. Overall, our study establishes the viability of BCP-LNPs as a versatile, efficient, and targeted delivery platform for nucleic acids, opening avenues for advanced therapeutic applications.

Original languageEnglish (US)
Pages (from-to)7595-7607
Number of pages13
JournalACS Applied Bio Materials
Volume7
Issue number11
DOIs
StatePublished - Nov 18 2024
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biomaterials
  • General Chemistry
  • Biomedical Engineering
  • Biochemistry, medical

Keywords

  • Block copolymers
  • Design of Experiments
  • Flash NanoPrecipitation
  • Lipid Nanoparticles
  • mRNA
  • plasmid DNA

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