Label-Free and Continuous-Flow Ferrohydrodynamic Separation of HeLa Cells and Blood Cells in Biocompatible Ferrofluids
In this study, a label‐free, low‐cost, and fast ferrohydrodynamic cell separation scheme is demonstrated using HeLa cells (an epithelial cell line) and red blood cells. The separation is based on cell size difference, and conducted in a custom‐made biocompatible ferrofluid that retains the viability...
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Published in | Advanced functional materials Vol. 26; no. 22; pp. 3990 - 3998 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Blackwell Publishing Ltd
14.06.2016
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Subjects | |
Online Access | Get full text |
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Summary: | In this study, a label‐free, low‐cost, and fast ferrohydrodynamic cell separation scheme is demonstrated using HeLa cells (an epithelial cell line) and red blood cells. The separation is based on cell size difference, and conducted in a custom‐made biocompatible ferrofluid that retains the viability of cells during and after the assay for downstream analysis. The scheme offers moderate‐throughput (≈106 cells h−1 for a single channel device) and extremely high recovery rate (>99%) without the use of any label. It is envisioned that this separation scheme will have clinical applications in settings where rapid cell enrichment and removal of contaminating blood will improve efficiency of screening and diagnosis such as cervical cancer screening based on mixed populations in exfoliated samples.
A label‐free, low‐cost, and fast method in biocompatible ferrofluids is developed to ferrohydrodynamically separate HeLa cells and red blood cells based on their size difference. It offers moderate‐throughput (≈106 cells h−1 for a single channel device) and extremely high recovery rate (>99 %) for the enrichment of HeLa cells from blood. |
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Bibliography: | istex:8185AE82DFF5D579B0A9748ADABA22512EEE1EEC ark:/67375/WNG-M9D9P58C-J ArticleID:ADFM201503838 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.201503838 |