3.9 Article

A microfluidic chip carrier including temperature control and perfusion system for long-term cell imaging

期刊

HARDWAREX
卷 10, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.ohx.2021.e00245

关键词

Microphysiological system; Long-term cell monitoring; Functional assay on-chip; Portable microfluidics

资金

  1. European Union [812954]
  2. European Research Council (ERC) [757444]
  3. Knut and Alice Wallenberg Foundation [WAF 2016.0112]
  4. European Research Council (ERC) [757444] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

The presented carrier is a cost-effective option for maintaining physiological conditions of microfluidic chips while minimizing device manipulation. By integrating a perfusion system and a film resistive heater, the carrier can sustain the environmental conditions and temperature of the microfluidic chips.
Microfluidic devices are widely used for biomedical applications but there is still a lack of affordable, reliable and user-friendly systems for transferring microfluidic chips from an incubator to a microscope while maintaining physiological conditions when performing microscopy. The presented carrier represents a cost-effective option for sustaining environmental conditions of microfluidic chips in combination with minimizing the device manipulation required for reagent injection, media exchange or sample collection. The carrier, which has the outer dimension of a standard well plate size, contains an integrated perfusion system that can recirculate the media using piezo pumps, operated in either continuous or intermittent modes (50-1000 mu l/min). Furthermore, a film resistive heater made from 37 mu m-thick copper wires, including temperature feedback control, was used to maintain the microfluidic chip temperature at 37 degrees C when outside the incubator. The heater characterisation showed a uniform temperature distribution along the chip channel for perfusion flow rates up to 10 mu l/min. To demonstrate the feasibility of our platform for long term cell culture monitoring, mouse brain endothelial cells (bEnd.3) were repeatedly monitored for a period of 10 days, demonstrating a system with both the versatility and the potential for long imaging in microphysiological system cell cultures. (C) 2021 The Authors. Published by Elsevier Ltd.

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