File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

조윤경

Cho, Yoon-Kyoung
FRUITS Lab.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 11356 -
dc.citation.number 22 -
dc.citation.startPage 11349 -
dc.citation.title ANALYTICAL CHEMISTRY -
dc.citation.volume 86 -
dc.contributor.author Lee, Ada -
dc.contributor.author Park, Juhee -
dc.contributor.author Lim, Minji -
dc.contributor.author Sunkara, Vijaya -
dc.contributor.author Kim, Shine Young -
dc.contributor.author Kim, Gwang Ha -
dc.contributor.author Kim, Mi-Hyun -
dc.contributor.author Cho, Yoon-Kyoung -
dc.date.accessioned 2023-12-22T02:06:56Z -
dc.date.available 2023-12-22T02:06:56Z -
dc.date.created 2014-12-26 -
dc.date.issued 2014-11 -
dc.description.abstract Circulating tumor cells (CTCs) have gained increasing attention owing to their roles in cancer recurrence and progression. Due to the rarity of CTCs in the bloodstream, an enrichment process is essential for effective target cell characterization. However, in a typical pressure-driven micro-fluidic system, the enrichment process generally requires complicated equipment and long processing times. Furthermore, the commonly used immunoaffinity-based positive selection method is limited, as its recovery rate relies on EpCAM expression of target CTCs, which shows heterogeneity among cell types. Here, we propose a centrifugal-force-based size-selective CTC isolation platform that can isolate and enumerate C'TCs from whole blood within 30 s with high purity. The device was validated using the MCF-7 breast cancer cell line spiked in phosphate-buffered saline and whole blood, and an average capture efficiency of 61% was achieved, which is typical for size-based filtration. The capture efficiency for whole blood samples varied from 44% to 84% under various flow conditions and dilution factors. Under the optimized operating conditions, a few hundred white blood cells per 1 mL of whole blood were captured, representing a 20-fold decrease compared to those obtained using a commercialized size-based CTC isolation device. In clinical validation, normalized CTC counts varied from 10 to 60 per 7.5 mL of blood from gastric and lung cancer patients, yielding a detection rate of 50% and 38%, respectively. Overall, our CTC isolation device enables rapid and label-free isolation of CTCs with high purity, which should greatly improve downstream molecular analyses of captured CTCs. -
dc.identifier.bibliographicCitation ANALYTICAL CHEMISTRY, v.86, no.22, pp.11349 - 11356 -
dc.identifier.doi 10.1021/ac5035049 -
dc.identifier.issn 0003-2700 -
dc.identifier.scopusid 2-s2.0-84921360711 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/9682 -
dc.identifier.wosid 000345263300052 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title All-in-One Centrifugal Microfluidic Device for Size-Selective Circulating Tumor Cell Isolation with High Purity -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Analytical -
dc.relation.journalResearchArea Chemistry -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.