Abstract
The rheological properties of red blood cells (RBCs) are crucial for human health. Combining optical tweezers with microfluidics provides a non-contact, sensitive, and high-throughput method for studying RBC rheology. However, the limited trapping capacity of optical tweezers restricts RBC flow within microchannels, reducing individual RBC capture efficiency. To address this, we developed a multichannel microfluidic chip with a pressure relief structure. Integrating this with optical tweezers using time-division multiplexing enabled simultaneous capture of RBCs across multiple microchannels. This method not only enhances sample throughput during optical tweezer measurements but also allows individual capture and analysis of multiple flowing RBCs in the same timeframe. Image recognition analysis of RBCs captured by optical tweezers revealed distinct morphological differences between normal and diseased RBCs, consistent with finite element method simulations of RBC rheological behavior. This approach provides quantitative characterization of RBC rheology and enables effective detection.
Published Version
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