Introducing Degradable Cationic Nanogels Carrying TLR9 Stimulating Oligonucleotides.
Autor: | Fuchs A; Chair of Macromolecular Chemistry, Institute of Functional Materials and Biofabrication, Faculty of Chemistry and Pharmacy, Julius -Maximilians-Universität-Würzburg, Röntgenring 11, 97070, Würzburg, Germany., Czysch C; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Maxeiner K; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Winterwerber P; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Schmitt S; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Stickdorn J; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Zhong Z; Department of Pharmaceutics, Ghent University, Ghent, 9000, Belgium., Medina-Montano C; Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 55131, Mainz, Germany., Räder HJ; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Bros M; Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 55131, Mainz, Germany., De Geest BG; Department of Pharmaceutics, Ghent University, Ghent, 9000, Belgium., Koynov K; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany., Grabbe S; Department of Dermatology, University Medical Center Mainz, Langenbeckstraße 1, 55131, Mainz, Germany., Nuhn L; Chair of Macromolecular Chemistry, Institute of Functional Materials and Biofabrication, Faculty of Chemistry and Pharmacy, Julius -Maximilians-Universität-Würzburg, Röntgenring 11, 97070, Würzburg, Germany. |
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Jazyk: | angličtina |
Zdroj: | Small (Weinheim an der Bergstrasse, Germany) [Small] 2024 Dec 01, pp. e2406082. Date of Electronic Publication: 2024 Dec 01. |
DOI: | 10.1002/smll.202406082 |
Abstrakt: | Cationic, core-crosslinked nanogel particles are prepared from synthetic biodegradable materials. These fully hydrophilic nanogels offer superior customizability compared to common lipid nanoparticles, thereby circumventing intrinsic immune stimulatory properties. Electrostatic loading allows for complexation of nucleic acids including the immune stimulatory Toll-like receptor 9 (TLR9) agonistCpG-ODN (cytidine-phosphate-guanosine oligodeoxynucleotide). Only when complexed inside nanogels, one can control CpG-ODN's biodistribution, prevent systemic toxicity, and increase bioavailability at target locations. Nanogels are prepared from cyclic aliphatic carbonate monomers with reactive pentafluorophenyl (PFP) esters. First, block copolymers are acquired via cationic ring opening polymerization (CROP) onto polyethylene glycol (PEG). Upon self-assembly in ethanol, the micelles' core is cationically core-crosslinked, and the resulting fully hydrophilic particles exhibit sizes of ≈20 nm, also upon loading with CpG-ODN. In vitro, they promote intracellular delivery devoid of carrier-related toxicities, while retaining the immune stimulatory properties of the TLR agonist cargo. In vivo, the nanogels reduce systemic liver immune responses and remain near the injection site. Additionally, delivery into cDC1 (conventional dentritic cells type 1) antigen-presenting cells, which are highly relevant for antitumoral T-cell immune responses, is confirmed. Altogether, cationic, core-crosslinked polycarbonate nanogels show promise for nucleic acid delivery, showcasing controlled immunostimulatory cargo delivery and an enhanced hydrolytic biodegradability profile, highly valuable for cancer immunotherapy. (© 2024 The Author(s). Small published by Wiley‐VCH GmbH.) |
Databáze: | MEDLINE |
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