4.8 Article

Integrated Microdevice for Long-Term Automated Perfusion Culture without Shear Stress and Real-Time Electrochemical Monitoring of Cells

期刊

ANALYTICAL CHEMISTRY
卷 83, 期 24, 页码 9524-9530

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ac202302t

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资金

  1. National Natural Science Foundation of China [20975077, 31070995]
  2. Science Fund for Creative Research Groups [20921062]
  3. National Basic Research Program of China (973 Program) [2007CB714507]
  4. Program for New Century Excellent Talents in University [NCET-10-0611]
  5. Program for Changjiang Scholars and Innovative Research Team in University [IRT1030]

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Electrochemical techniques based on ultramicroelectrodes (UMEs) play a significant role in real-time monitoring of chemical messengers' release from single cells. Conversely, precise monitoring of cells in vitro strongly depends on the adequate construction of cellular physiological microenvironment. In this paper, we developed a multilayer microdevice which integrated high aspect ratio poly(dimethylsiloxane) (PDMS) microfluidic device for long-term automated perfusion culture of cells without shear stress and an independently addressable microelectrodes array (IAMEA) for electrochemical monitoring of the cultured cells in real time. Novel design using high aspect ratio between circular moat and ring-shaped micropillar array surrounding cell culture chamber combined with automated circular-centre and 5 bottom-up perfusion model successfully provided continuous fresh medium and a stable and uniform microenvironment for cells. Two weeks automated culture of human umbilical endothelial cell line (ECV304) and neuronal differentiation of rat pheochromocytoma (PC12) cells have been realized using this device. Furthermore, the quantal release of dopamine from individual PC12 cells during their culture or propagation process was amperometrically monitored in real time. The multifunctional microdevice developed in this paper integrated cellular microenvironment construction and real-time monitoring of cells during their physiological process, and would possibly provide a versatile platform for cell-based biomedical analysis.

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