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Updated: Jan 20, 2026

Generation of a Simplified Three-Dimensional Skin-on-a-chip Model in a Micromachined Microfluidic Platform
Published on: May 17, 2021
Micromachining of Polymeric Microfluidic Micro/Nanoelectroporation Device
1Department of Material Science and Engineering, Washington State University, Pullman, WA, USA. lei.li2@wsu.edu.
This study presents a microfluidic nanochannel electroporation device for efficient gene/drug delivery. The integrated system enhances cell processing speed and viability for batch cell applications.
Area of Science:
- Biotechnology
- Nanotechnology
- Cell Biology
Background:
- Micro/nanochannel electroporation offers precise single-cell gene/drug delivery with high viability.
- Traditional methods face challenges in efficiency and operational complexity.
- Integrating microfluidics addresses these limitations for large-scale cell processing.
Purpose of the Study:
- To provide a detailed protocol for fabricating microfluidic nanochannel electroporation devices.
- To enable efficient gene/drug delivery to a batch of cells.
- To combine the benefits of single-cell nanochannel electroporation and microfluidic cell manipulation.
Main Methods:
- Device fabrication integrates soft lithography, DNA combing and imprinting, and micromilling.
- The protocol covers device fabrication, holder construction, cell trapping, and electroporation procedures.
- Microfluidic integration with nanochannel electroporation is key.
Main Results:
- The developed device facilitates gene/drug delivery to a large number of cells efficiently.
- The integrated approach overcomes the low efficiency and complex operation issues of single-cell methods.
- Achieved high cell viability and precise dosage control in batch processing.
Conclusions:
- Microfluidic nanochannel electroporation devices offer a powerful platform for efficient and viable gene/drug delivery to cell batches.
- The detailed protocol enables the fabrication and application of these advanced devices.
- This technology merges single-cell precision with microfluidic throughput.
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