Poly(vinyl pyrrolidone) derivatives as PEG alternatives for stealth, non-toxic and less immunogenic siRNA-containing lipoplex delivery

• Published in: Journal of controlled release Vol. 361; pp. 87 - 101
• Main Authors: Berger, Manon, Toussaint, François, Djemaa, Sanaa Ben, Laloy, Julie, Pendeville, Hélène, Evrard, Brigitte, Jerôme, Christine, Lechanteur, Anna, Mottet, Denis, Debuigne, Antoine, Piel, Géraldine
• Format: Journal Article Web Resource
• Language: English
• Published: Netherlands Elsevier B.V 01-09-2023; Elsevier BV
• Subjects: Human health sciences; Immune reaction; Lipoplexes; PEG derivatives; Pharmacie, pharmacologie & toxicologie; Pharmacy, pharmacology & toxicology; Poly(vinyl pyrrolidone); Protein corona; Sciences de la santé humaine; Stealth properties; Poly(vinyl pyrrolidone); Stealth properties; Protein corona; Immune reaction; Lipoplexes; PEG derivatives
• ISSN: 0168-3659; 1873-4995; 1873-4995
• DOI: 10.1016/j.jconrel.2023.07.031

The recent approval of Onpattro® and COVID-19 vaccines has highlighted the value of lipid nanoparticles (LNPs) for the delivery of genetic material. If it is known that PEGylation is crucial to confer stealth properties to LNPs, it is also known that PEGylation is responsible for the decrease of the cellular uptake and endosomal escape and for the production of anti-PEG antibodies inducing accelerated blood clearance (ABC) and hypersensitivity reactions. Today, the development of PEG alternatives is crucial. Poly(N-vinyl pyrrolidone) (PNVP) has shown promising results for liposome decoration but has never been tested for the delivery of nucleic acids. Our aim is to develop a series of amphiphilic PNVP compounds to replace lipids-PEG for the post-insertion of lipoplexes dedicated to siRNA delivery. PNVP compounds with different degrees of polymerization and hydrophobic segments, such as octadecyl, dioctadecyl and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine (DSPE), were generated. Based on the physicochemical properties and the efficiency to reduce protein corona formation, we showed that the DSPE segment is essential for the integration into the lipoplexes. Lipoplexes post-grafted with 15% DSPE-PNVP30 resulted in gene silencing efficiency close to that of lipoplexes grafted with 15% DSPE-PEG. Finally, an in vivo study in mice confirmed the stealth properties of DSPE-PNVP30 lipoplexes as well as a lower immune response ABC effect compared to DSPE-PEG lipoplexes. Furthermore, we showed a lower immune response after the second injection with DSPE-PNVP30 lipoplexes compared to DSPE-PEG lipoplexes. All these observations suggest that DSPE-PNVP30 appears to be a promising alternative to PEG, with no toxicity, good stealth properties and lower immunological response.
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