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Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads

Microchips are widely used to separate circulating tumor cells (CTCs) from whole blood by virtues of sophisticated manipulation for microparticles. Here, we present a chip with an 8 μm high and 27.9 mm wide slit to capture cancer cells bound to 3 μm beads. Apart from a higher purity and recovery rat...

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Autores principales: Lee, Seung Joon, Sim, Tae Seok, Shin, Hyun Young, Lee, Jungmin, Kim, Min Young, Sunoo, Joseph, Lee, Jeong-Gun, Yea, Kyungmoo, Kim, Young Zoon, van Noort, Danny, Park, Soo Kyung, Kim, Woon-Hae, Park, Kyun Woo, Kim, Minseok S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812780/
https://www.ncbi.nlm.nih.gov/pubmed/31647823
http://dx.doi.org/10.1371/journal.pone.0223193
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author Lee, Seung Joon
Sim, Tae Seok
Shin, Hyun Young
Lee, Jungmin
Kim, Min Young
Sunoo, Joseph
Lee, Jeong-Gun
Yea, Kyungmoo
Kim, Young Zoon
van Noort, Danny
Park, Soo Kyung
Kim, Woon-Hae
Park, Kyun Woo
Kim, Minseok S.
author_facet Lee, Seung Joon
Sim, Tae Seok
Shin, Hyun Young
Lee, Jungmin
Kim, Min Young
Sunoo, Joseph
Lee, Jeong-Gun
Yea, Kyungmoo
Kim, Young Zoon
van Noort, Danny
Park, Soo Kyung
Kim, Woon-Hae
Park, Kyun Woo
Kim, Minseok S.
author_sort Lee, Seung Joon
collection PubMed
description Microchips are widely used to separate circulating tumor cells (CTCs) from whole blood by virtues of sophisticated manipulation for microparticles. Here, we present a chip with an 8 μm high and 27.9 mm wide slit to capture cancer cells bound to 3 μm beads. Apart from a higher purity and recovery rate, the slit design allows for simplified fabrication, easy cell imaging, less clogging, lower chamber pressure and, therefore, higher throughput. The beads were conjugated with anti-epithelial cell adhesion molecules (anti-EpCAM) to selectively bind to breast cancer cells (MCF-7) used to spike the whole blood. The diameter of the cell-bead construct was in average 23.1 μm, making them separable from other cells in the blood. As a result, the cancer cells were separated from 5 mL of whole blood with a purity of 52.0% and a recovery rate of 91.1%, and also we confirmed that the device can be applicable to clinical samples of human breast cancer patients. The simple design with microslit, by eliminating any high-aspect ratio features, is expected to reduce possible defects on the chip and, therefore, more suitable for mass production without false separation outputs.
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spelling pubmed-68127802019-11-03 Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads Lee, Seung Joon Sim, Tae Seok Shin, Hyun Young Lee, Jungmin Kim, Min Young Sunoo, Joseph Lee, Jeong-Gun Yea, Kyungmoo Kim, Young Zoon van Noort, Danny Park, Soo Kyung Kim, Woon-Hae Park, Kyun Woo Kim, Minseok S. PLoS One Research Article Microchips are widely used to separate circulating tumor cells (CTCs) from whole blood by virtues of sophisticated manipulation for microparticles. Here, we present a chip with an 8 μm high and 27.9 mm wide slit to capture cancer cells bound to 3 μm beads. Apart from a higher purity and recovery rate, the slit design allows for simplified fabrication, easy cell imaging, less clogging, lower chamber pressure and, therefore, higher throughput. The beads were conjugated with anti-epithelial cell adhesion molecules (anti-EpCAM) to selectively bind to breast cancer cells (MCF-7) used to spike the whole blood. The diameter of the cell-bead construct was in average 23.1 μm, making them separable from other cells in the blood. As a result, the cancer cells were separated from 5 mL of whole blood with a purity of 52.0% and a recovery rate of 91.1%, and also we confirmed that the device can be applicable to clinical samples of human breast cancer patients. The simple design with microslit, by eliminating any high-aspect ratio features, is expected to reduce possible defects on the chip and, therefore, more suitable for mass production without false separation outputs. Public Library of Science 2019-10-24 /pmc/articles/PMC6812780/ /pubmed/31647823 http://dx.doi.org/10.1371/journal.pone.0223193 Text en © 2019 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lee, Seung Joon
Sim, Tae Seok
Shin, Hyun Young
Lee, Jungmin
Kim, Min Young
Sunoo, Joseph
Lee, Jeong-Gun
Yea, Kyungmoo
Kim, Young Zoon
van Noort, Danny
Park, Soo Kyung
Kim, Woon-Hae
Park, Kyun Woo
Kim, Minseok S.
Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads
title Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads
title_full Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads
title_fullStr Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads
title_full_unstemmed Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads
title_short Microslit on a chip: A simplified filter to capture circulating tumor cells enlarged with microbeads
title_sort microslit on a chip: a simplified filter to capture circulating tumor cells enlarged with microbeads
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812780/
https://www.ncbi.nlm.nih.gov/pubmed/31647823
http://dx.doi.org/10.1371/journal.pone.0223193
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