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Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics

Elasticity and bio-adhesiveness of circulating tumor cells (CTCs) are important biomarkers of cancer. CTCs are rare in blood, thus their capture and atomic force microscopy (AFM)-based biomechanical characterization require use of multifunctional microfluidic device. Here, we describe procedures for...

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Detalles Bibliográficos
Autores principales: Deliorman, Muhammedin, Glia, Ayoub, Qasaimeh, Mohammad A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157559/
https://www.ncbi.nlm.nih.gov/pubmed/35664257
http://dx.doi.org/10.1016/j.xpro.2022.101433
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author Deliorman, Muhammedin
Glia, Ayoub
Qasaimeh, Mohammad A.
author_facet Deliorman, Muhammedin
Glia, Ayoub
Qasaimeh, Mohammad A.
author_sort Deliorman, Muhammedin
collection PubMed
description Elasticity and bio-adhesiveness of circulating tumor cells (CTCs) are important biomarkers of cancer. CTCs are rare in blood, thus their capture and atomic force microscopy (AFM)-based biomechanical characterization require use of multifunctional microfluidic device. Here, we describe procedures for fabrication of such device, AFM-Chip, and give details on its use in affinity-based CTC capture, and integration with AFM via reversable physical assembly. In the AFM-Chip, CTC capture is efficient, and transition to AFM characterization is seamless with minimal cell loss. For complete details on the use and execution of this protocol, please refer to Deliorman et al. (2020).
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spelling pubmed-91575592022-06-02 Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics Deliorman, Muhammedin Glia, Ayoub Qasaimeh, Mohammad A. STAR Protoc Protocol Elasticity and bio-adhesiveness of circulating tumor cells (CTCs) are important biomarkers of cancer. CTCs are rare in blood, thus their capture and atomic force microscopy (AFM)-based biomechanical characterization require use of multifunctional microfluidic device. Here, we describe procedures for fabrication of such device, AFM-Chip, and give details on its use in affinity-based CTC capture, and integration with AFM via reversable physical assembly. In the AFM-Chip, CTC capture is efficient, and transition to AFM characterization is seamless with minimal cell loss. For complete details on the use and execution of this protocol, please refer to Deliorman et al. (2020). Elsevier 2022-05-27 /pmc/articles/PMC9157559/ /pubmed/35664257 http://dx.doi.org/10.1016/j.xpro.2022.101433 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Deliorman, Muhammedin
Glia, Ayoub
Qasaimeh, Mohammad A.
Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics
title Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics
title_full Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics
title_fullStr Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics
title_full_unstemmed Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics
title_short Characterizing circulating tumor cells using affinity-based microfluidic capture and AFM-based biomechanics
title_sort characterizing circulating tumor cells using affinity-based microfluidic capture and afm-based biomechanics
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157559/
https://www.ncbi.nlm.nih.gov/pubmed/35664257
http://dx.doi.org/10.1016/j.xpro.2022.101433
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