High-throughput cell focusing and separation via acoustofluidic tweezers.

Lab Chip

Department of Mechanical Engineering and Material Science, Duke University, Durham, NC 27707, USA.

Published: September 2018

Separation of particles and cells is an important function in many biological and biomedical protocols. Although a variety of microfluidic-based techniques have been developed so far, there is clearly still a demand for a precise, fast, and biocompatible method for separation of microparticles and cells. By combining acoustics and hydrodynamics, we have developed a method which we integrated into three-dimensional acoustofluidic tweezers (3D-AFT) to rapidly and efficiently separate microparticles and cells into multiple high-purity fractions. Compared with other acoustophoresis methods, this 3D-AFT method significantly increases the throughput by an order of magnitude, is label-free and gently handles the sorted cells. We demonstrate not only the separation of 10, 12, and 15 micron particles at a throughput up to 500 μl min-1 using this 3D-AFT method, but also the separation of erythrocytes, leukocytes, and cancer cells. This 3D-AFT method is able to meet various separation demands thus offering a viable alternative with potential for clinical applications.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203445PMC
http://dx.doi.org/10.1039/c8lc00434jDOI Listing

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High-throughput cell focusing and separation via acoustofluidic tweezers.

Lab Chip

September 2018

Department of Mechanical Engineering and Material Science, Duke University, Durham, NC 27707, USA.

Separation of particles and cells is an important function in many biological and biomedical protocols. Although a variety of microfluidic-based techniques have been developed so far, there is clearly still a demand for a precise, fast, and biocompatible method for separation of microparticles and cells. By combining acoustics and hydrodynamics, we have developed a method which we integrated into three-dimensional acoustofluidic tweezers (3D-AFT) to rapidly and efficiently separate microparticles and cells into multiple high-purity fractions.

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