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Updated: May 8, 2026

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Multi-Stream Perfusion Bioreactor Integrated with Outlet Fractionation for Dynamic Cell Culture
Published on: July 20, 2022
Pressure-driven microfluidic perfusion culture device for integrated dose-response assays.
Koji Hattori1, Shinji Sugiura, Toshiyuki Kanamori
11Research Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, Japan.
Journal of Laboratory Automation
|September 10, 2013
Summary
Microfluidic cell-based assays, using pressure-driven perfusion, offer reliable, high-throughput drug discovery. This review details advancements in these integrated microfluidic systems for enhanced assay processes.
Area of Science:
- Biotechnology
- Drug Discovery
- Microfluidics
Background:
- Cell-based assays are crucial in drug discovery.
- Microfluidic systems have advanced cell-based assays for reliability and high throughput.
- Integrating microfluidic systems with macro-scale processes is key for industrial applications.
Purpose of the Study:
- To review recent advancements in microfluidic cell-based assays.
- To focus on pressure-driven perfusion culture devices.
- To discuss key techniques in microfluidic assay development.
Main Methods:
- Review of microfluidic cell-based assay device development.
- Discussion of microfluidic network design, fabrication, and liquid/cell manipulation.
- Analysis of detection schemes for pressure-driven perfusion culture.
Main Results:
- Microfluidic systems enable reliable and high-throughput cell-based assays.
- Pressure-driven perfusion culture devices are ideal for integrated assays.
- Recent progress shows semiautomatic and reliable pressure-driven microfluidic assays.
Conclusions:
- Microfluidic cell-based assays, particularly pressure-driven perfusion systems, are powerful tools for drug discovery.
- Advancements in design, fabrication, and manipulation enhance assay integration and reliability.
- The field is progressing towards more automated and dependable microfluidic assay platforms.

