Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783462707766231040 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6812780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT leeseungjoon microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT simtaeseok microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT shinhyunyoung microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT leejungmin microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT kimminyoung microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT sunoojoseph microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT leejeonggun microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT yeakyungmoo microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT kimyoungzoon microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT vannoortdanny microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT parksookyung microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT kimwoonhae microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT parkkyunwoo microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads AT kimminseoks microslitonachipasimplifiedfiltertocapturecirculatingtumorcellsenlargedwithmicrobeads |