Capturing cancer cells using aptamer-immobilized square capillary channels
Molecular BioSystems, ISSN: 1742-2051, Vol: 7, Issue: 5, Page: 1720-1727
2011
- 28Citations
- 40Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations28
- Citation Indexes27
- 27
- CrossRef25
- Patent Family Citations1
- Patent Families1
- Captures40
- Readers40
- 40
Article Description
We report a simple square capillary-based cell affinity chromatography device that utilizes a coating of aptamers for selective capture of target cancer cells from a flowing suspension. The device consists of a square capillary with an inner diameter of roughly five cell diameters, connected via Teflon tubing to a syringe. Aptamers are immobilized on the inner surface of the capillary through biotin-avidin chemistry, the extent of which can be controlled by adjusting the aptamer concentration. Introduction of different cell types into separate devices, as well as mixtures of target and non-target cells, demonstrated that aptamer-target cells can be captured in significantly higher concentrations compared to non-target cells. Once optimized, 91.1 ± 3.5% capture efficiency of target leukemia cells was reported, as well as 97.2 ± 2.8% and 83.6 ± 5.8% for two different colon cancer cell lines. In addition, cells captured in the device were imaged, and the square capillary exhibited better optical properties than standard cylindrical capillaries, leading to the detection of leukemia cells in blood samples. Compared to current microfluidic cell affinity devices, this capture device requires no complicated design or fabrication steps. By providing a simple means of detecting and imaging cancer cells in the blood, this work has potential to directly assist clinicians in determining disease prognosis and measuring therapeutic response. © The Royal Society of Chemistry 2011.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79954474908&origin=inward; http://dx.doi.org/10.1039/c0mb00311e; http://www.ncbi.nlm.nih.gov/pubmed/21424012; https://xlink.rsc.org/?DOI=c0mb00311e; https://dx.doi.org/10.1039/c0mb00311e; https://pubs.rsc.org/en/content/articlelanding/2011/mb/c0mb00311e
Royal Society of Chemistry (RSC)
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