In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling

Labeling-assisted visualization is a powerful strategy to track circulating tumor cells (CTCs) for mechanism study (e.g., tumor metastasis). Due to the rarity of CTCs in the whole blood, efficient simultaneous enrichment and labeling of CTCs are needed. Hereby, novel in situ electroporation on a pre...

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Main Authors: Tingting Hun, Yi Zhang, Qingmei Xu, Dong Huang, Qi Wang, Zhihong Li, Wei Wang
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Micromachines
Subjects:
Online Access:https://www.mdpi.com/2072-666X/13/5/672
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author Tingting Hun
Yi Zhang
Qingmei Xu
Dong Huang
Qi Wang
Zhihong Li
Wei Wang
author_facet Tingting Hun
Yi Zhang
Qingmei Xu
Dong Huang
Qi Wang
Zhihong Li
Wei Wang
author_sort Tingting Hun
collection DOAJ
description Labeling-assisted visualization is a powerful strategy to track circulating tumor cells (CTCs) for mechanism study (e.g., tumor metastasis). Due to the rarity of CTCs in the whole blood, efficient simultaneous enrichment and labeling of CTCs are needed. Hereby, novel in situ electroporation on a previously-developed micropore-arrayed filter (PERFECT filter) is proposed. Benefiting from the ultra-small-thickness and high-porosity of the filter plus high precision pore diameter, target rare tumor cells were enriched with less damage and uniform size distribution, contributing to enhanced molecular delivery efficiency and cell viability in the downstream electroporation. Various biomolecules (e.g., small molecule dyes, plasmids, and functional proteins) were used to verify this in situ electroporation system. High labeling efficiency (74.08 ± 2.94%) and high viability (81.15 ± 3.04%, verified via live/dead staining) were achieved by optimizing the parameters of electric field strength and pulse number, ensuring the labeled tumor cells can be used for further culture and down-stream analysis. In addition, high specificity (99.03 ± 1.67%) probing of tumor cells was further achieved by introducing fluorescent dye-conjugated antibodies into target cells. The whole procedure, including cell separation and electroporation, can be finished quickly (<10 min). The proposed in situ electroporation on the PERFECT filter system has great potential to track CTCs for tumor metastasis studies.
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spelling doaj.art-59c3fd15638340f999bf035670bae6592023-11-23T12:11:22ZengMDPI AGMicromachines2072-666X2022-04-0113567210.3390/mi13050672In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell LabelingTingting Hun0Yi Zhang1Qingmei Xu2Dong Huang3Qi Wang4Zhihong Li5Wei Wang6School of Integrated Circuits, Peking University, Beijing 100871, ChinaSchool of Integrated Circuits, Peking University, Beijing 100871, ChinaSchool of Integrated Circuits, Peking University, Beijing 100871, ChinaSchool of Integrated Circuits, Peking University, Beijing 100871, ChinaDepartment of Respiratory Medicine, The Second Affiliated Hospital of Dalian Medical University, Dalian 116027, ChinaSchool of Integrated Circuits, Peking University, Beijing 100871, ChinaSchool of Integrated Circuits, Peking University, Beijing 100871, ChinaLabeling-assisted visualization is a powerful strategy to track circulating tumor cells (CTCs) for mechanism study (e.g., tumor metastasis). Due to the rarity of CTCs in the whole blood, efficient simultaneous enrichment and labeling of CTCs are needed. Hereby, novel in situ electroporation on a previously-developed micropore-arrayed filter (PERFECT filter) is proposed. Benefiting from the ultra-small-thickness and high-porosity of the filter plus high precision pore diameter, target rare tumor cells were enriched with less damage and uniform size distribution, contributing to enhanced molecular delivery efficiency and cell viability in the downstream electroporation. Various biomolecules (e.g., small molecule dyes, plasmids, and functional proteins) were used to verify this in situ electroporation system. High labeling efficiency (74.08 ± 2.94%) and high viability (81.15 ± 3.04%, verified via live/dead staining) were achieved by optimizing the parameters of electric field strength and pulse number, ensuring the labeled tumor cells can be used for further culture and down-stream analysis. In addition, high specificity (99.03 ± 1.67%) probing of tumor cells was further achieved by introducing fluorescent dye-conjugated antibodies into target cells. The whole procedure, including cell separation and electroporation, can be finished quickly (<10 min). The proposed in situ electroporation on the PERFECT filter system has great potential to track CTCs for tumor metastasis studies.https://www.mdpi.com/2072-666X/13/5/672in situ electroporationcirculating tumor cellhigh viability
spellingShingle Tingting Hun
Yi Zhang
Qingmei Xu
Dong Huang
Qi Wang
Zhihong Li
Wei Wang
In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling
Micromachines
in situ electroporation
circulating tumor cell
high viability
title In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling
title_full In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling
title_fullStr In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling
title_full_unstemmed In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling
title_short In Situ Electroporation on PERFECT Filter for High-Efficiency and High-Viability Tumor Cell Labeling
title_sort in situ electroporation on perfect filter for high efficiency and high viability tumor cell labeling
topic in situ electroporation
circulating tumor cell
high viability
url https://www.mdpi.com/2072-666X/13/5/672
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