Abstract
The possibility of tightly controlling the cellular microenvironment within microfluidic devices represents an important step toward precision analysis of cellular phenotypes in vitro. Microfluidic platforms that allow both long-term mammalian cell culture and dynamic modulation of the culture environment can support quantitative studies of cells’ responses to drugs. Here, we report the design and testing of a novel microfluidic device of simple production (single Polydimethylsiloxane layer), which integrates a micromixer with vacuum-assisted cell loading for long-term mammalian cell culture and dynamic mixing of four different culture media. Finite element modeling was used to predict flow rates and device dimensions to achieve diffusion-based fluid mixing. The device showed efficient mixing and dynamic exchange of media in the cell-trapping chambers, and viability of mammalian cells cultured for long-term in the device. This work represents the first attempt to integrate single-layer microfluidic mixing devices with vacuum-assisted cell-loading systems for mammalian cell culture and dynamic stimulation.
| Original language | English |
|---|---|
| Article number | 427 |
| Journal | Biosensors |
| Volume | 15 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Jul 2025 |
Bibliographical note
Publisher Copyright:© 2025 by the authors.
Keywords
- PDMS
- mammalian cells
- microfluidics
- micromixers
- single layer
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