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An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells
Recently there has been a more focus on the development of an efficient technique for detection of circulating tumor cells (CTCs), due to their significance in prognosis and therapy of metastatic cancer. However, it remains a challenge because of the low count of CTCs in the blood. Herein, a rapid a...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309797/ https://www.ncbi.nlm.nih.gov/pubmed/28198402 http://dx.doi.org/10.1038/srep42612 |
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author | Jiang, Jianing Zhao, Hui Shu, Weiliang Tian, Jing Huang, Yuqing Song, Yongxin Wang, Ruoyu Li, Encheng Slamon, Dennis Hou, Dongmei Du, Xiaohui Zhang, Lichuan Chen, Yan Wang, Qi |
author_facet | Jiang, Jianing Zhao, Hui Shu, Weiliang Tian, Jing Huang, Yuqing Song, Yongxin Wang, Ruoyu Li, Encheng Slamon, Dennis Hou, Dongmei Du, Xiaohui Zhang, Lichuan Chen, Yan Wang, Qi |
author_sort | Jiang, Jianing |
collection | PubMed |
description | Recently there has been a more focus on the development of an efficient technique for detection of circulating tumor cells (CTCs), due to their significance in prognosis and therapy of metastatic cancer. However, it remains a challenge because of the low count of CTCs in the blood. Herein, a rapid and high-sensitivity approach for CTCs detection using an integrated microfluidic system, consisting of a deterministic lateral displacement (DLD) isolating structure, an automatic purifying device with CD45-labeled immunomagnetic beads and a capturing platform coated with rat-tail collagen was reported. We observed high capture rate of 90%, purity of about 50% and viability of more than 90% at the high throughput of 1 mL/min by capturing green fluorescent protein (GFP)-positive cells from blood. Further capturing of CTCs from metastatic cancers patients revealed a positive capture rate of 83.3%. Furthermore, our device was compared with CellSearch system via parallel analysis of 30 cancer patients, to find no significant difference between the capture efficiency of both methods. However, our device displayed advantage in terms of time, sample volume and cost for analysis. Thus, our integrated device with sterile environment and convenient use will be a promising platform for CTCs detection with potential clinical application. |
format | Online Article Text |
id | pubmed-5309797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53097972017-02-22 An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells Jiang, Jianing Zhao, Hui Shu, Weiliang Tian, Jing Huang, Yuqing Song, Yongxin Wang, Ruoyu Li, Encheng Slamon, Dennis Hou, Dongmei Du, Xiaohui Zhang, Lichuan Chen, Yan Wang, Qi Sci Rep Article Recently there has been a more focus on the development of an efficient technique for detection of circulating tumor cells (CTCs), due to their significance in prognosis and therapy of metastatic cancer. However, it remains a challenge because of the low count of CTCs in the blood. Herein, a rapid and high-sensitivity approach for CTCs detection using an integrated microfluidic system, consisting of a deterministic lateral displacement (DLD) isolating structure, an automatic purifying device with CD45-labeled immunomagnetic beads and a capturing platform coated with rat-tail collagen was reported. We observed high capture rate of 90%, purity of about 50% and viability of more than 90% at the high throughput of 1 mL/min by capturing green fluorescent protein (GFP)-positive cells from blood. Further capturing of CTCs from metastatic cancers patients revealed a positive capture rate of 83.3%. Furthermore, our device was compared with CellSearch system via parallel analysis of 30 cancer patients, to find no significant difference between the capture efficiency of both methods. However, our device displayed advantage in terms of time, sample volume and cost for analysis. Thus, our integrated device with sterile environment and convenient use will be a promising platform for CTCs detection with potential clinical application. Nature Publishing Group 2017-02-15 /pmc/articles/PMC5309797/ /pubmed/28198402 http://dx.doi.org/10.1038/srep42612 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jiang, Jianing Zhao, Hui Shu, Weiliang Tian, Jing Huang, Yuqing Song, Yongxin Wang, Ruoyu Li, Encheng Slamon, Dennis Hou, Dongmei Du, Xiaohui Zhang, Lichuan Chen, Yan Wang, Qi An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
title | An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
title_full | An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
title_fullStr | An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
title_full_unstemmed | An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
title_short | An integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
title_sort | integrated microfluidic device for rapid and high-sensitivity analysis of circulating tumor cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309797/ https://www.ncbi.nlm.nih.gov/pubmed/28198402 http://dx.doi.org/10.1038/srep42612 |
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