BioAcyl Corp |
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| Resource type: Journal Article DOI: 10.1016/j.addr.2024.115461 ID no. (ISBN etc.): 0169-409X BibTeX citation key: Bader2024 View all bibliographic details |
Categories: BioAcyl Corp Subcategories: Lipid nanovesicles Keywords: Clinical trials, Drug loading, Extracellular vesicles, Gene delivery, Lipid nanoparticles, Nucleic acid therapeutics Creators: Bader, Brigger, Leroux Collection: Advanced Drug Delivery Reviews |
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| Abstract |
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Extracellular vesicles (EVs) are increasingly investigated for delivering nucleic acid (NA) therapeutics, leveraging their natural role in transporting NA and protein-based cargo in cell-to-cell signaling. Their synthetic counterparts, lipid nanoparticles (LNPs), have been developed over the past decades as NA carriers, culminating in the approval of several marketed formulations such as patisiran/Onpattro® and the mRNA-1273/BNT162 COVID-19 vaccines. The success of LNPs has sparked efforts to develop innovative technologies to target extrahepatic organs, and to deliver novel therapeutic modalities, such as tools for in vivo gene editing. Fueled by the recent advancements in both fields, this review aims to provide a comprehensive overview of the basic characteristics of EV and LNP-based NA delivery systems, from EV biogenesis to structural properties of LNPs. It addresses the primary challenges encountered in utilizing these nanocarriers from a drug formulation and delivery perspective. Additionally, biodistribution profiles, in vitro and in vivo transfection outcomes, as well as their status in clinical trials are compared. Overall, this review provides insights into promising research avenues and potential dead ends for EV and LNP-based NA delivery systems.
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