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dc.contributor.authorZhong, Ruibo
dc.contributor.authorTalebian, Sepehr
dc.contributor.authorMendes, Bárbara B
dc.contributor.authorWallace, Gordon
dc.contributor.authorLanger, Robert
dc.contributor.authorConde, João
dc.contributor.authorShi, Jinjun
dc.date.accessioned2025-10-16T15:53:40Z
dc.date.available2025-10-16T15:53:40Z
dc.date.issued2023-03-20
dc.identifier.urihttps://hdl.handle.net/1721.1/163187
dc.description.abstractRNA-based therapeutics have shown tremendous promise in disease intervention at the genetic level, and some have been approved for clinical use, including the recent COVID-19 messenger RNA vaccines. The clinical success of RNA therapy is largely dependent on the use of chemical modification, ligand conjugation or non-viral nanoparticles to improve RNA stability and facilitate intracellular delivery. Unlike molecular-level or nanoscale approaches, macroscopic hydrogels are soft, water-swollen three-dimensional structures that possess remarkable features such as biodegradability, tunable physiochemical properties and injectability, and recently they have attracted enormous attention for use in RNA therapy. Specifically, hydrogels can be engineered to exert precise spatiotemporal control over the release of RNA therapeutics, potentially minimizing systemic toxicity and enhancing in vivo efficacy. This Review provides a comprehensive overview of hydrogel loading of RNAs and hydrogel design for controlled release, highlights their biomedical applications and offers our perspectives on the opportunities and challenges in this exciting field of RNA delivery.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/s41563-023-01472-wen_US
dc.rightsCreative Commons Attribution-Noncommercial-ShareAlikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePubMed Centralen_US
dc.titleHydrogels for RNA deliveryen_US
dc.typeArticleen_US
dc.identifier.citationZhong, R., Talebian, S., Mendes, B.B. et al. Hydrogels for RNA delivery. Nat. Mater. 22, 818–831 (2023).en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.relation.journalNature Materialsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2025-10-16T15:44:43Z
dspace.orderedauthorsZhong, R; Talebian, S; Mendes, BB; Wallace, G; Langer, R; Conde, J; Shi, Jen_US
dspace.date.submission2025-10-16T15:44:44Z
mit.journal.volume22en_US
mit.journal.issue7en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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