DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Byungji | ko |
dc.contributor.author | Park, Ji-Ho | ko |
dc.contributor.author | Sailor, Michael J. | ko |
dc.date.accessioned | 2019-12-20T06:20:51Z | - |
dc.date.available | 2019-12-20T06:20:51Z | - |
dc.date.created | 2019-10-22 | - |
dc.date.created | 2019-10-22 | - |
dc.date.issued | 2019-12 | - |
dc.identifier.citation | ADVANCED MATERIALS, v.31, no.49, pp.1903637 | - |
dc.identifier.issn | 0935-9648 | - |
dc.identifier.uri | http://hdl.handle.net/10203/270016 | - |
dc.description.abstract | With the recent FDA approval of the first siRNA-derived therapeutic, RNA interference (RNAi)-mediated gene therapy is undergoing a transition from research to the clinical space. The primary obstacle to realization of RNAi therapy has been the delivery of oligonucleotide payloads. Therefore, the main aims is to identify and describe key design features needed for nanoscale vehicles to achieve effective delivery of siRNA-mediated gene silencing agents in vivo. The problem is broken into three elements: 1) protection of siRNA from degradation and clearance; 2) selective homing to target cell types; and 3) cytoplasmic release of the siRNA payload by escaping or bypassing endocytic uptake. The in vitro and in vivo gene silencing efficiency values that have been reported in publications over the past decade are quantitatively summarized by material type (lipid, polymer, metal, mesoporous silica, and porous silicon), and the overall trends in research publication and in clinical translation are discussed to reflect on the direction of the RNAi therapeutics field. | - |
dc.language | English | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.title | Rekindling RNAi Therapy: Materials Design Requirements for In Vivo siRNA Delivery | - |
dc.type | Article | - |
dc.identifier.wosid | 000488166800001 | - |
dc.identifier.scopusid | 2-s2.0-85073972779 | - |
dc.type.rims | ART | - |
dc.citation.volume | 31 | - |
dc.citation.issue | 49 | - |
dc.citation.beginningpage | 1903637 | - |
dc.citation.publicationname | ADVANCED MATERIALS | - |
dc.identifier.doi | 10.1002/adma.201903637 | - |
dc.contributor.localauthor | Park, Ji-Ho | - |
dc.contributor.nonIdAuthor | Kim, Byungji | - |
dc.contributor.nonIdAuthor | Sailor, Michael J. | - |
dc.description.isOpenAccess | Y | - |
dc.type.journalArticle | Review | - |
dc.subject.keywordAuthor | drug delivery | - |
dc.subject.keywordAuthor | gene therapy | - |
dc.subject.keywordAuthor | nanoparticles | - |
dc.subject.keywordAuthor | RNA interference | - |
dc.subject.keywordAuthor | siRNA | - |
dc.subject.keywordPlus | MESOPOROUS SILICA NANOPARTICLES | - |
dc.subject.keywordPlus | SMALL INTERFERING RNA | - |
dc.subject.keywordPlus | CELL-PENETRATING PEPTIDES | - |
dc.subject.keywordPlus | IRON-OXIDE NANOPARTICLES | - |
dc.subject.keywordPlus | HUMAN-GENOME-PROJECT | - |
dc.subject.keywordPlus | SENSITIVE FUSOGENIC PEPTIDE | - |
dc.subject.keywordPlus | SOLID LIPID NANOPARTICLES | - |
dc.subject.keywordPlus | CORE-SHELL NANOPARTICLES | - |
dc.subject.keywordPlus | TARGETED DELIVERY | - |
dc.subject.keywordPlus | GOLD NANOPARTICLES | - |
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