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dc.contributor.authorGuan, B.
dc.contributor.authorMagenau, A.
dc.contributor.authorCiampi, Simone
dc.contributor.authorGaus, K.
dc.contributor.authorReece, P.
dc.contributor.authorGooding, J.
dc.date.accessioned2017-01-30T12:40:35Z
dc.date.available2017-01-30T12:40:35Z
dc.date.created2016-07-24T19:30:45Z
dc.date.issued2014
dc.identifier.citationGuan, B. and Magenau, A. and Ciampi, S. and Gaus, K. and Reece, P. and Gooding, J. 2014. Antibody modified porous silicon microparticles for the selective capture of cells. Bioconjugate Chemistry. 25 (7): pp. 1282-1289.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/24036
dc.identifier.doi10.1021/bc500144u
dc.description.abstract

Herein, the ability of porous silicon (PSi) particles for selectively binding to specific cells is investigated. PSi microparticles with a high reflectance band in the reflectivity profile are fabricated, and subsequently passivated and modified with antibodies via the Cu(I)-catalyzed alkyne-azide cycloaddition reaction and succimidyl activation. To demonstrate the ability of the antibody-modified PSi particles to selectively bind to one cell type over others, HeLa cells were transfected with surface epitopes fused to fluorescent proteins. The antibody-functionalized PSi particles showed good selectivity for the corresponding surface protein on HeLa cells, with no significant cross-reactivity. The results are important for the application of PSi particles in cell sensing and drug delivery.

dc.titleAntibody modified porous silicon microparticles for the selective capture of cells
dc.typeJournal Article
dcterms.source.volume25
dcterms.source.number7
dcterms.source.startPage1282
dcterms.source.endPage1289
dcterms.source.issn1043-1802
dcterms.source.titleBioconjugate Chemistry
curtin.departmentNanochemistry Research Institute
curtin.accessStatusFulltext not available


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