Isolation, Detection, and Antigen‐Based Profiling of Circulating Tumor Cells Using a Size‐Dictated Immunocapture Chip

Even though the diagnostic and prognostic value of circulating tumor cells (CTCs) has been demonstrated, their clinical utility and widespread adoption have been limited. Herein, we describe a new device, size‐dictated immunocapture chip (SDI‐Chip), for efficient, sensitive, and spatially resolved c...

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Veröffentlicht in:Angewandte Chemie International Edition 2017-08, Vol.56 (36), p.10681-10685
Hauptverfasser: Ahmed, Metages Gashaw, Abate, Mahlet Fasil, Song, Yanling, Zhu, Zhi, Yan, Feng, Xu, Yao, Wang, Xiaomin, Li, Qingbiao, Yang, Chaoyong
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Sprache:eng
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Zusammenfassung:Even though the diagnostic and prognostic value of circulating tumor cells (CTCs) has been demonstrated, their clinical utility and widespread adoption have been limited. Herein, we describe a new device, size‐dictated immunocapture chip (SDI‐Chip), for efficient, sensitive, and spatially resolved capture and detection of CTCs. SDI‐Chip enables selective, frequent, and extended interaction of CTCs with hydrodynamically optimized immunocoated micropillar surfaces. CTCs with different antigen expression levels can be efficiently captured and spatially resolved around the micropillars. Capture efficiency greater than 92 % with a purity of 82 % was achieved with blood samples. CTCs were detected in non‐metastasis colorectal (CRC) patients, while none was detected from healthy volunteers. We believe that SDI‐Chip will facilitate the transition of tumor diagnosis from anatomical pathology to molecular pathology in localized CRC patients. A size‐dictated immunocapture chip (SDI‐Chip) was designed through the rigorous computational analysis of various parameters. Frequent contact with and prolonged retention time on the immunocoated surface, as well as optimum hydrodynamic forces provided by the device, enables the efficient capture of CTCs from cancer patient samples as well as spatial profiling based on antigen expression levels.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201702675