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A Method of Targeted Cell Isolation via Glass Surface Functionalization
Published on: September 20, 2016
Antibody modified porous silicon microparticles for the selective capture of cells
Bin Guan1, Astrid Magenau, Simone Ciampi
1School of Chemistry, ‡The Australian Centre for NanoMedicine, §ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, ∥Centre for Vascular Research, and ⊥School of Physics, The University of New South Wales , Sydney, Australia 2052.
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.

