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A glass microfluidic chip for continuous blood cell sorting by a magnetic gradient without labeling
Bai-Yan Qu1, Zhi-Yong Wu, Fang Fang
1Research Center for Analytical Sciences, Northeastern University, 110004, Shenyang, China.
Analytical and Bioanalytical Chemistry
|September 23, 2008
Summary
This study developed a microfluidic chip using magnetic properties for efficient red blood cell (RBC) separation. The novel chip achieved high RBC recovery rates, offering a promising tool for blood analysis.
Area of Science:
- Biomedical Engineering
- Microfluidics
- Cell Separation
Background:
- Efficient separation of red blood cells (RBCs) from whole blood is crucial for various diagnostic and research applications.
- Existing methods often face challenges with efficiency, throughput, or cell viability.
Purpose of the Study:
- To develop and demonstrate a microfluidic chip for highly efficient RBC separation based on their intrinsic magnetic properties.
- To optimize the chip design and operating parameters for maximum RBC recovery.
Main Methods:
- Fabrication of a glass microfluidic chip using photolithography and thermal bonding.
- Integration of a nickel wire within the separation channel to generate a magnetic gradient.
- Application of an external permanent magnet (0.3 T) to induce magnetic forces on RBCs.
- Optimization of flow rates (0.12-0.92 microL/min) and use of bovine serum albumin to mitigate cell sedimentation.
Main Results:
- Continuous separation of RBCs from diluted whole blood samples.
- Achieved up to 93.7% RBC recovery in the middle outlet at a flow rate of 0.23 microL/min.
- Demonstrated successful visual tracking of the separation process using quantum dot labeling.
Conclusions:
- The developed microfluidic chip provides a highly efficient method for RBC separation using native magnetic properties.
- The technology shows potential for applications in blood analysis, diagnostics, and cell research.
- Further investigation into cell distribution phenomena around the magnetic field source is warranted.

