Please use this identifier to cite or link to this item: https://doi.org/10.1002/ange.202006890
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dc.titleLight-Induced Self-Escape of Spherical Nucleic Acid from Endo/Lysosome for Efficient Non-Cationic Gene Delivery
dc.contributor.authorShi, L
dc.contributor.authorWu, W
dc.contributor.authorDuan, Y
dc.contributor.authorXu, L
dc.contributor.authorXu, Y
dc.contributor.authorHou, L
dc.contributor.authorMeng, X
dc.contributor.authorZhu, X
dc.contributor.authorLiu, B
dc.date.accessioned2022-02-08T09:38:33Z
dc.date.available2022-02-08T09:38:33Z
dc.date.issued2020-01-01
dc.identifier.citationShi, L, Wu, W, Duan, Y, Xu, L, Xu, Y, Hou, L, Meng, X, Zhu, X, Liu, B (2020-01-01). Light-Induced Self-Escape of Spherical Nucleic Acid from Endo/Lysosome for Efficient Non-Cationic Gene Delivery. Angewandte Chemie 132 (43) : 19330-19336. ScholarBank@NUS Repository. https://doi.org/10.1002/ange.202006890
dc.identifier.issn0044-8249,1521-3757
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/215041
dc.description.abstract© 2020 Wiley-VCH GmbH Developing non-cationic gene carriers and achieving efficient endo/lysosome escape of functional nucleic acids in cytosol are two major challenges faced by the field of gene delivery. Herein, we demonstrate the concept of self-escape spherical nucleic acid (SNA) to achieve light controlled non-cationic gene delivery with sufficient endo/lysosome escape capacity. In this system, Bcl-2 antisense oligonucleotides (OSAs) were conjugated onto the surface of aggregation-induced emission (AIE) photosensitizer (PS) nanoparticles to form core–shell SNA. Once the SNAs were taken up by tumor cells, and upon light irradiation, the accumulative 1O2 produced by the AIE PSs ruptured the lysosome structure to promote OSA escape. Prominent in vitro and in vivo results revealed that the AIE-based core–shell SNA could downregulate the anti-apoptosis protein (Bcl-2) and induce tumor cell apoptosis without any transfection reagent.
dc.publisherWiley
dc.sourceElements
dc.typeArticle
dc.date.updated2022-02-08T07:14:42Z
dc.contributor.departmentDEPT OF CHEMICAL & BIOMOLECULAR ENGG
dc.contributor.departmentDEPT OF COMPUTER SCIENCE
dc.description.doi10.1002/ange.202006890
dc.description.sourcetitleAngewandte Chemie
dc.description.volume132
dc.description.issue43
dc.description.page19330-19336
dc.published.statePublished
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