Immunocapturing rare cells from blood: A simple and robust microsystem approach
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
36821992
DOI
10.1016/j.bios.2023.115155
PII: S0956-5663(23)00097-0
Knihovny.cz E-zdroje
- Klíčová slova
- Cell immunocapture, Circulating endothelial cells, Circulating tumor cells, Microsystems, Rare cell population,
- MeSH
- biosenzitivní techniky * MeSH
- lidé MeSH
- mikrofluidní analytické techniky * metody MeSH
- nádorové buněčné linie MeSH
- nádorové cirkulující buňky * metabolismus MeSH
- protilátky MeSH
- separace buněk metody MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- protilátky MeSH
Cell immunocapture microsystems are a fast-emerging field with several potential medical diagnostic applications. Isolation and quantification of circulating rare cells (CRCs) show great importance in the early stages of disease diagnostics and prognostics. Here, we present a simple and robust stop-flow microsystem (fabricated by a combination of glass microblasting and 3D printing) based on a planar antibody-coated surface that is effective in the immunocapture of the model as well as naturally occurring rare cells. A chip with a planar immunocapture channel working in the so-called stop-flow dynamic regime was designed to enable monitoring the efficiency of the cell capture by fluorescence microscopy. Up to 90% immunocapture efficiency of MCF-7 cells spiked into whole blood on CD326 antibody-coated planar surfaces was achieved. We discuss the role of the planar surface modifications, the influence of the set stop-flow dynamic conditions, and medium complexity on the efficiency of cell immunocapture. The presented results could be further employed in the design of microsystems for cell-size-independent isolation and identification of rare cells from blood.
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