4.3 Article

Highly efficient isolation and release of circulating tumor cells based on size-dependent filtration and degradable ZnO nanorods substrate in a wedge-shaped microfluidic chip

期刊

BIOMEDICAL MICRODEVICES
卷 19, 期 4, 页码 -

出版社

SPRINGER
DOI: 10.1007/s10544-017-0235-7

关键词

Circulating tumor cells; Cell isolation and release; ZnO nanorods; Microfluidic chip

资金

  1. National Natural Science Foundation of China [81372358, 81527801, 51303140, 81602489]
  2. Natural Science Foundation of Hubei Province, China [2014CFA029]
  3. Colleges of Hubei Province Outstanding Youth Science and Technology Innovation Team [T201305]
  4. Wuhan Municipal Science and Technology Bureau [2015060101010056]
  5. Technology Research and Development Fund in Shenzhen [JCYJ20150403091443300, JCYJ20150403091443271]
  6. Natural Science Foundation of Guangdong [2016A030310242, 2016A030313381]

向作者/读者索取更多资源

Circulating tumor cells (CTCs) have been regarded as the major cause of metastasis, holding significant insights for tumor diagnosis and treatment. Although many efforts have been made to develop methods for CTC isolation and release in microfluidic system, it remains significant challenges to realize highly efficient isolation and gentle release of CTCs for further cellular and bio-molecular analyses. In this study, we demonstrate a novel method for CTC isolation and release using a simple wedge-shaped microfluidic chip embedding degradable znic oxide nanorods (ZnNRs) substrate. By integrating size-dependent filtration with degradable nanostructured substrate, the capture efficiencies over 87.5% were achieved for SKBR3, PC3, HepG2 and A549 cancer cells spiked in healthy blood sample with the flow rate of 100 mu L min(-1). By dissolving ZnNRs substrate with an extremely low concentration of phosphoric acid (12.5 mM), up to 85.6% of the captured SKBR3 cells were released after reverse injection with flow rate of 100 mu L min(-1) for 15 min, which exhibited around 73.6% cell viability within 1 h after release to around 93.9% after re-cultured for 3 days. It is conceivable that our microfluidic device has great potentials in carrying on cell-based biomedical studies and guiding individualized treatment in the future.

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