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Development of a microfluidic-based optical sensing device for label-free detection of circulating tumor cells (CTCs) through their lactic acid metabolism
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Development of a microfluidic-based optical sensing device for label-free detection of circulating tumor cells (CTCs) through their lactic acid metabolism

Tzu-Keng Chiu, Kin-Fong Lei, Chia-Hsun Hsieh, Hung-Bo Hsiao, Hung-Ming Wang 和 Min-Hsien Wu
Sensors (Basel, Switzerland), 卷.15(3), 頁碼.6789-6806
19/03/2015
PMID: 25808775
Web of Science ID: WOS:000354160900109

摘要

Biosensing Techniques Cell Line, Tumor Cell Separation Cell Survival Humans Lactic Acid - metabolism Leukocytes - metabolism Leukocytes - pathology Microfluidic Analytical Techniques Neoplasms - diagnosis Neoplasms - metabolism Neoplastic Cells, Circulating - metabolism Neoplastic Cells, Circulating - pathology Optical Devices
This study reports a microfluidic-based optical sensing device for label-free detection of circulating tumor cells (CTCs), a rare cell species in blood circulation. Based on the metabolic features of cancer cells, live CTCs can be quantified indirectly through their lactic acid production. Compared with the conventional schemes for CTC detection, this label-free approach could prevent the biological bias due to the heterogeneity of the surface antigens on cancer cells. In this study, a microfluidic device was proposed to generate uniform water-in-oil cell-encapsulating micro-droplets, followed by the fluorescence-based optical detection of lactic acid produced within the micro-droplets. To test its feasibility to quantify cancer cells, experiments were carried out. Results showed that the detection signals were proportional to the number of cancer cells within the micro-droplets, whereas such signals were insensitive to the existence and number of leukocytes within. To further demonstrate its feasibility for cancer cell detection, the cancer cells with known cell number in a cell suspension was detected based on the method. Results revealed that there was no significant difference between the detected number and the real number of cancer cells. As a whole, the proposed method opens up a new route to detect live CTCs in a label-free manner.

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https://doi.org/10.3390/s150306789檢視
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