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A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells
BACKGROUND: Due to the high transfer ability of cancer cell, cancer has been regarded as a world-wide high mortality disease. Quantitative analysis of circulating tumor cells (CTCs) can provide some valuable clinical information that is particularly critical for cancer diagnosis and treatment. Along...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131777/ https://www.ncbi.nlm.nih.gov/pubmed/30205821 http://dx.doi.org/10.1186/s12951-018-0390-x |
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author | Wu, Xuan Xiao, Tingyu Luo, Zhang He, Rongxiang Cao, Yiping Guo, Zhenzhong Zhang, Weiying Chen, Yong |
author_facet | Wu, Xuan Xiao, Tingyu Luo, Zhang He, Rongxiang Cao, Yiping Guo, Zhenzhong Zhang, Weiying Chen, Yong |
author_sort | Wu, Xuan |
collection | PubMed |
description | BACKGROUND: Due to the high transfer ability of cancer cell, cancer has been regarded as a world-wide high mortality disease. Quantitative analysis of circulating tumor cells (CTCs) can provide some valuable clinical information that is particularly critical for cancer diagnosis and treatment. Along with the rapid development of micro-/nano-fabrication technique, the three-dimensional (3D) bionic interface-based analysis method has become a hot research topic in the area of nanotechnology and life science. Micro-/nano-structure-based devices have been identified as being one of the easiest and most effective techniques for CTCs capture applications. METHODS: We demonstrated an electrospun nanofibers-deposited nickel (Ni) micropillars-based cytosensor for electrochemical detection of CTCs. Breast cancer cell line with rich EpCAM expression (MCF7) were selected as model CTCs. The ultra-long poly (lactic-co-glycolic acid) (PLGA) nanofibers were firstly-crosswise stacked onto the surface of Ni micropillars by electrospinning to construct a 3D bionic interface for capturing EpCAM-expressing CTCs, following immuno-recognition with quantum dots functionalized anti-EpCAM antibody (QDs-Ab) and forming immunocomplexes on the micro-/nano-chip. RESULTS: The Ni micropillars in the longitudinal direction not only play a certain electrical conductivity in the electrochemical detection, but also its special structure improves the efficiency of cell capture. The cross-aligned nanofibers could simulate the extracellular matrix to provide a good microenvironment which is better for cell adhesion and physiological functions. Bioprobe containing quantum dots will release Cd(2+) in the process of acid dissolution, resulting in a change in current. Beneath favourable conditions, the suggested 3D cytosensor demonstrated high sensitivity with a broad range of 10(1)–10(5) cells mL(−1) and a detection limit of 8 cells mL(−1). CONCLUSIONS: We constructed a novel 3D electrochemical cytosensor based on Ni micropillars, PLGA electrospun nanofibers and quantum dots bioprobe, which could be used to highly sensitive and selective analysis of CTCs. More significantly, the 3D cytosensor can efficiently identify CTCs from whole blood, which suggested the potential applications of our technique for the clinical diagnosis and therapeutic monitoring of cancers. |
format | Online Article Text |
id | pubmed-6131777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61317772018-09-13 A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells Wu, Xuan Xiao, Tingyu Luo, Zhang He, Rongxiang Cao, Yiping Guo, Zhenzhong Zhang, Weiying Chen, Yong J Nanobiotechnology Research BACKGROUND: Due to the high transfer ability of cancer cell, cancer has been regarded as a world-wide high mortality disease. Quantitative analysis of circulating tumor cells (CTCs) can provide some valuable clinical information that is particularly critical for cancer diagnosis and treatment. Along with the rapid development of micro-/nano-fabrication technique, the three-dimensional (3D) bionic interface-based analysis method has become a hot research topic in the area of nanotechnology and life science. Micro-/nano-structure-based devices have been identified as being one of the easiest and most effective techniques for CTCs capture applications. METHODS: We demonstrated an electrospun nanofibers-deposited nickel (Ni) micropillars-based cytosensor for electrochemical detection of CTCs. Breast cancer cell line with rich EpCAM expression (MCF7) were selected as model CTCs. The ultra-long poly (lactic-co-glycolic acid) (PLGA) nanofibers were firstly-crosswise stacked onto the surface of Ni micropillars by electrospinning to construct a 3D bionic interface for capturing EpCAM-expressing CTCs, following immuno-recognition with quantum dots functionalized anti-EpCAM antibody (QDs-Ab) and forming immunocomplexes on the micro-/nano-chip. RESULTS: The Ni micropillars in the longitudinal direction not only play a certain electrical conductivity in the electrochemical detection, but also its special structure improves the efficiency of cell capture. The cross-aligned nanofibers could simulate the extracellular matrix to provide a good microenvironment which is better for cell adhesion and physiological functions. Bioprobe containing quantum dots will release Cd(2+) in the process of acid dissolution, resulting in a change in current. Beneath favourable conditions, the suggested 3D cytosensor demonstrated high sensitivity with a broad range of 10(1)–10(5) cells mL(−1) and a detection limit of 8 cells mL(−1). CONCLUSIONS: We constructed a novel 3D electrochemical cytosensor based on Ni micropillars, PLGA electrospun nanofibers and quantum dots bioprobe, which could be used to highly sensitive and selective analysis of CTCs. More significantly, the 3D cytosensor can efficiently identify CTCs from whole blood, which suggested the potential applications of our technique for the clinical diagnosis and therapeutic monitoring of cancers. BioMed Central 2018-09-11 /pmc/articles/PMC6131777/ /pubmed/30205821 http://dx.doi.org/10.1186/s12951-018-0390-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wu, Xuan Xiao, Tingyu Luo, Zhang He, Rongxiang Cao, Yiping Guo, Zhenzhong Zhang, Weiying Chen, Yong A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells |
title | A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells |
title_full | A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells |
title_fullStr | A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells |
title_full_unstemmed | A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells |
title_short | A micro-/nano-chip and quantum dots-based 3D cytosensor for quantitative analysis of circulating tumor cells |
title_sort | micro-/nano-chip and quantum dots-based 3d cytosensor for quantitative analysis of circulating tumor cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131777/ https://www.ncbi.nlm.nih.gov/pubmed/30205821 http://dx.doi.org/10.1186/s12951-018-0390-x |
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