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Article: Single-cell membrane drug delivery using porous pen nanodeposition

TitleSingle-cell membrane drug delivery using porous pen nanodeposition
Authors
Issue Date2018
Citation
Nanoscale, 2018, v. 10, p. 12704-12712 How to Cite?
AbstractDelivering molecules onto the plasma membrane of single cells is still a challenging task in profiling cell signaling pathways with single cell resolution. We demonstrated that a large quantity of molecules could be targeted and released onto the membrane of individual cells to trigger signaling responses. This is achieved by a porous pen nanodeposition (PPN) method, in which a multilayer porous structure, serving as a reservoir for a large amount of molecules, is formed on an atomic force microscope (AFM) tip using layer-by-layer assembly and post processing. To demonstrate its capability for single cell membrane drug delivery, PPN was employed to induce a calcium flux triggered by the binding of released antibodies to membrane antigens in an autoimmune skin disease model. This calcium signal propagates from the target cell to its neighbors in a matter of seconds, proving the theory of intercellular communication through cell–cell junctions. Collectively, these results demonstrated the effectiveness of PPN in membrane drug delivery for single cells; to the best of our knowledge, this is the first technique that can perform the targeted transport and delivery in single cell resolution, paving the way for probing complex signaling interactions in multicellular settings.
Persistent Identifierhttp://hdl.handle.net/10722/261774
ISSN
2023 Impact Factor: 5.8
2023 SCImago Journal Rankings: 1.416
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYang, Y-
dc.contributor.authorYu, J-
dc.contributor.authorMonemian Esfahani, A-
dc.contributor.authorSeiffert-Sinha, K-
dc.contributor.authorXi, N-
dc.contributor.authorLee, I-
dc.contributor.authorSinha, A-
dc.contributor.authorChen, L-
dc.contributor.authorSun, Z-
dc.contributor.authorYang, R-
dc.contributor.authorDong, L-
dc.date.accessioned2018-09-28T04:47:38Z-
dc.date.available2018-09-28T04:47:38Z-
dc.date.issued2018-
dc.identifier.citationNanoscale, 2018, v. 10, p. 12704-12712-
dc.identifier.issn2040-3364-
dc.identifier.urihttp://hdl.handle.net/10722/261774-
dc.description.abstractDelivering molecules onto the plasma membrane of single cells is still a challenging task in profiling cell signaling pathways with single cell resolution. We demonstrated that a large quantity of molecules could be targeted and released onto the membrane of individual cells to trigger signaling responses. This is achieved by a porous pen nanodeposition (PPN) method, in which a multilayer porous structure, serving as a reservoir for a large amount of molecules, is formed on an atomic force microscope (AFM) tip using layer-by-layer assembly and post processing. To demonstrate its capability for single cell membrane drug delivery, PPN was employed to induce a calcium flux triggered by the binding of released antibodies to membrane antigens in an autoimmune skin disease model. This calcium signal propagates from the target cell to its neighbors in a matter of seconds, proving the theory of intercellular communication through cell–cell junctions. Collectively, these results demonstrated the effectiveness of PPN in membrane drug delivery for single cells; to the best of our knowledge, this is the first technique that can perform the targeted transport and delivery in single cell resolution, paving the way for probing complex signaling interactions in multicellular settings.-
dc.languageeng-
dc.relation.ispartofNanoscale-
dc.titleSingle-cell membrane drug delivery using porous pen nanodeposition-
dc.typeArticle-
dc.identifier.emailXi, N: xining@hku.hk-
dc.identifier.emailSun, Z: sunzy@hku.hk-
dc.identifier.authorityXi, N=rp02044-
dc.identifier.doi10.1039/C8NR02600A-
dc.identifier.scopuseid_2-s2.0-85049845125-
dc.identifier.hkuros292493-
dc.identifier.volume10-
dc.identifier.spage12704-
dc.identifier.epage12712-
dc.identifier.eissn2040-3372-
dc.identifier.isiWOS:000438246000054-
dc.identifier.issnl2040-3364-

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