4.7 Article

Human mammalian cell sorting using a highly integrated micro-fabricated fluorescence-activated cell sorter (mu FACS)

Journal

LAB ON A CHIP
Volume 10, Issue 12, Pages 1567-1573

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c000136h

Keywords

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Funding

  1. NIH
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [R21RR024453] Funding Source: NIH RePORTER
  3. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG004876] Funding Source: NIH RePORTER

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We demonstrate a high performance microfabricated FACS system with highly integrated microfluidics, optics, acoustics, and electronics. Single cell manipulation at a high speed is made possible by the fast response time (similar to 0.1 ms) of the integrated PZT actuator and the nozzle structure at the sorting junction. A Teflon AF-coated optofluidic waveguide along the microfluidic channel guides the illumination light, enabling multi-spot detection, while a novel space-time coding technology enhances the detection sensitivity of the mu FACS system. The real-time control loop system is implemented using a field-programmable-gate-array (FPGA) for automated and accurate sorting. The mu FACS achieves a high purification enrichment factor: up to similar to 230 fold for both polystyrene microbeads and suspended human mammalian cells (K562) at a high throughput (>1000 cells s(-1)). The sorting mechanism is independent of cell properties such as size, density, and shape, thus the presented system can be applied to sort out any pure sub-populations. This new lab-on-a-chip FACS system, therefore, holds promise to revolutionize microfluidic cytometers to meet cost, size, and performance goals.

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