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Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors
Circulating tumor cells (CTCs) are single cancer cells or cancer cell clusters that are present in the circulatory system. Assessing CTC levels in patients can aid in the early detection of cancer metastasis and is essential for the purposes of accurate cancer prognosis. However, current in vitro bl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687831/ https://www.ncbi.nlm.nih.gov/pubmed/36354476 http://dx.doi.org/10.3390/bios12110968 |
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author | Zhu, Shaodi Xie, Zhenming Chen, Yuzhi Liu, Shiyue Kwan, Yiu-Wa Zeng, Shuwen Yuan, Wu Ho, Ho-Pui |
author_facet | Zhu, Shaodi Xie, Zhenming Chen, Yuzhi Liu, Shiyue Kwan, Yiu-Wa Zeng, Shuwen Yuan, Wu Ho, Ho-Pui |
author_sort | Zhu, Shaodi |
collection | PubMed |
description | Circulating tumor cells (CTCs) are single cancer cells or cancer cell clusters that are present in the circulatory system. Assessing CTC levels in patients can aid in the early detection of cancer metastasis and is essential for the purposes of accurate cancer prognosis. However, current in vitro blood tests are limited by the insufficient blood samples and low concentration levels of CTCs, which presents a major challenge for practical biosensing devices. In this work, we propose the first surface plasmon resonance (SPR) fiber probe to work intravenously, which offers a real-time detection of CTCs in bloodstreams. By exposing the protein-functionalized fiber probe to circulating blood, a continuous capture of CTCs ensures a constant increase in enrichment and hence greatly enhances enumeration accuracy. The performance of our plasmonic fiber probe was demonstrated to specifically detect Michigan Cancer Foundation-7 (MCF-7) breast cancer cells in flowing whole mouse blood. Further, a detection limit of ~1.4 cells per microliter was achieved by using an epithelial cell adhesion molecule (EpCAM) antibody-based receptor layer and a 15 min enrichment period. This pilot study validates real-time CTC detection directly in the bloodstream by using plasmonic fiber probes, which exhibit promising clinical potential for in vivo diagnostic tests involving low concentration biomarkers in circulating blood. |
format | Online Article Text |
id | pubmed-9687831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96878312022-11-25 Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors Zhu, Shaodi Xie, Zhenming Chen, Yuzhi Liu, Shiyue Kwan, Yiu-Wa Zeng, Shuwen Yuan, Wu Ho, Ho-Pui Biosensors (Basel) Article Circulating tumor cells (CTCs) are single cancer cells or cancer cell clusters that are present in the circulatory system. Assessing CTC levels in patients can aid in the early detection of cancer metastasis and is essential for the purposes of accurate cancer prognosis. However, current in vitro blood tests are limited by the insufficient blood samples and low concentration levels of CTCs, which presents a major challenge for practical biosensing devices. In this work, we propose the first surface plasmon resonance (SPR) fiber probe to work intravenously, which offers a real-time detection of CTCs in bloodstreams. By exposing the protein-functionalized fiber probe to circulating blood, a continuous capture of CTCs ensures a constant increase in enrichment and hence greatly enhances enumeration accuracy. The performance of our plasmonic fiber probe was demonstrated to specifically detect Michigan Cancer Foundation-7 (MCF-7) breast cancer cells in flowing whole mouse blood. Further, a detection limit of ~1.4 cells per microliter was achieved by using an epithelial cell adhesion molecule (EpCAM) antibody-based receptor layer and a 15 min enrichment period. This pilot study validates real-time CTC detection directly in the bloodstream by using plasmonic fiber probes, which exhibit promising clinical potential for in vivo diagnostic tests involving low concentration biomarkers in circulating blood. MDPI 2022-11-03 /pmc/articles/PMC9687831/ /pubmed/36354476 http://dx.doi.org/10.3390/bios12110968 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhu, Shaodi Xie, Zhenming Chen, Yuzhi Liu, Shiyue Kwan, Yiu-Wa Zeng, Shuwen Yuan, Wu Ho, Ho-Pui Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors |
title | Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors |
title_full | Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors |
title_fullStr | Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors |
title_full_unstemmed | Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors |
title_short | Real-Time Detection of Circulating Tumor Cells in Bloodstream Using Plasmonic Fiber Sensors |
title_sort | real-time detection of circulating tumor cells in bloodstream using plasmonic fiber sensors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687831/ https://www.ncbi.nlm.nih.gov/pubmed/36354476 http://dx.doi.org/10.3390/bios12110968 |
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