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Updated: Feb 23, 2026

Author Spotlight: Asymmetric Field Flow Fractionation for Bioreactor Integration
Published on: February 2, 2024
Non-equilibrium Inertial Separation Array for High-throughput, Large-volume Blood Fractionation
Baris R Mutlu1, Kyle C Smith2, Jon F Edd1,3
1BioMEMS Resource Center, Center for Engineering in Medicine and Surgical Services, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, 02114, USA.
A new non-equilibrium inertial separation array (NISA) enables rapid, label-free blood fractionation. This microfluidic device processes large blood volumes efficiently for transfusion, cell therapy, and diagnostics.
Area of Science:
- Biomedical Engineering
- Microfluidics
- Cell Separation Technology
Background:
- Microfluidic blood processing is crucial for diagnostics and therapeutics.
- Clinical translation requires scalable, high-throughput, and robust blood processing methods.
- Current methods face challenges in processing large volumes quickly and reliably.
Purpose of the Study:
- To introduce a scaled, label-free cell separation mechanism for efficient blood processing.
- To demonstrate a microfluidic device capable of processing large blood volumes rapidly.
- To provide a robust solution for clinical applications requiring precise cell fractionation.
Main Methods:
- Development of a non-equilibrium inertial separation array (NISA) using passive islands.
- Utilizing inertial lift forces for gentle, label-free cell manipulation.
- Siphoning a fraction of flow to separate cells based on size-dependent deterministic paths.
Main Results:
- Successfully fractionated 400 mL of whole blood in under 3 hours.
- Achieved an ultrapure buffy coat with 96.6% white blood cell yield.
- Demonstrated minimal red blood cell carryover (0.0059%) at a processing rate of 3 mL/min.
Conclusions:
- The NISA device offers a feasible and efficient alternative for blood fractionation.
- This technology can support blood transfusion, cellular therapy, and diagnostics.
- Improved sensitivity for rare cell isolation is possible by increasing processed blood volumes.
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