Literature DB >> 22684249

SSA-MOA: a novel CTC isolation platform using selective size amplification (SSA) and a multi-obstacle architecture (MOA) filter.

Minseok S Kim1, Tae Seok Sim, Yeon Jeong Kim, Sun Soo Kim, Hyoyoung Jeong, Jong-Myeon Park, Hui-Sung Moon, Seung Il Kim, Ogan Gurel, Soo Suk Lee, Jeong-Gun Lee, Jae Chan Park.   

Abstract

Circulating tumor cells (CTCs) have gained increasing attention as physicians and scientists learn more about the role these extraordinarily rare cells play in metastatic cancer. In developing CTC technology, the critical criteria are high recovery rates and high purity. Current isolation methods suffer from an inherent trade-off between these two goals. Moreover, ensuring minimal cell stress and robust reproducibility is also important for the clinical application of CTCs. In this paper, we introduce a novel CTC isolation technology using selective size amplification (SSA) for target cells and a multi-obstacle architecture (MOA) filter to overcome this trade-off, improving both recovery rate and purity. We also demonstrate SSA-MOA's advantages in minimizing cell deformation during filter transit, resulting in more stable and robust CTC isolation. In this technique, polymer microbeads conjugated with anti-epithelial cell adhesion molecules (anti-EpCAM) were used to selectively size-amplify MCF-7 breast cancer cells, definitively differentiating from the white blood cells (WBCs) by avoiding the size overlap that compromises other size selection methods. 3 μm was determined to be the optimal microbead diameter, not only for size discrimination but also in maximizing CTC surface coverage. A multi-obstacle architecture filter was fabricated using silicon-on-glass (SOG) technology-a first such application of this fabrication technique-to create a precise microfilter structure with a high aspect ratio. The filter was designed to minimize cell deformation as simulation results predicted that cells captured via this MOA filter would experience 22% less moving force than with a single-obstacle architecture. This was verified by experiments, as we observed reliable cell capture and reduced cell deformation, with a 92% average recovery rate and 351 peripheral blood leukocytes (PBL) per millilitre (average). We expect the SSA-MOA platform to optimize CTC recovery rates, purity, and stability, increasing the sensitivity and reliability of such tests, thereby potentially expanding the utilization of CTC technologies in the clinic.

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Year:  2012        PMID: 22684249     DOI: 10.1039/c2lc40065k

Source DB:  PubMed          Journal:  Lab Chip        ISSN: 1473-0189            Impact factor:   6.799


  29 in total

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6.  Circulating tumor cell detection: A direct comparison between negative and unbiased enrichment in lung cancer.

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Review 7.  Recent advances in microfluidic methods in cancer liquid biopsy.

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Journal:  Biomicrofluidics       Date:  2019-07-23       Impact factor: 2.800

Review 8.  Comprehensive characterization of circulating and bone marrow-derived multiple myeloma cells at minimal residual disease.

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Journal:  Semin Hematol       Date:  2018-03-01       Impact factor: 3.851

Review 9.  Circulating tumor cell isolation, culture, and downstream molecular analysis.

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Journal:  Biotechnol Adv       Date:  2018-03-17       Impact factor: 14.227

Review 10.  Microfluidic blood cell sorting: now and beyond.

Authors:  Zeta Tak For Yu; Koh Meng Aw Yong; Jianping Fu
Journal:  Small       Date:  2014-02-10       Impact factor: 13.281

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