L
Leon D. Li
Researcher at Massachusetts Institute of Technology
Publications - 8
Citations - 889
Leon D. Li is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Whole blood & Mucin. The author has an hindex of 8, co-authored 8 publications receiving 803 citations.
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Journal ArticleDOI
Pinched flow coupled shear-modulated inertial microfluidics for high-throughput rare blood cell separation.
Ali Asgar S. Bhagat,Han Wei Hou,Han Wei Hou,Leon D. Li,Chwee Teck Lim,Jongyoon Han,Jongyoon Han +6 more
TL;DR: A high-throughput size-based separation method for processing diluted blood using inertial microfluidics is introduced, demonstrating the isolation of cancer cells spiked in blood by exploiting the difference in size between CTCs and hematologic cells.
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Amplified Electrokinetic Response by Concentration Polarization near Nanofluidic Channel
TL;DR: The first direct measurements of detailed flow and electric potential profiles within and near the depletion region are reported, measuring and confirming that the electric field inside an ion depletion region is amplified more than 30-fold compared to outside of the depletion zone.
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Spatial Configuration and Composition of Charge Modulates Transport into a Mucin Hydrogel Barrier
TL;DR: It is shown that certain configurations of positive and negative charges result in enhanced uptake into a mucin barrier, a remarkable effect that is not observed with either charge alone, and suggest that spatial charge distribution is a critical parameter to modulate transport through mucin-based barriers.
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A microfluidics approach towards high-throughput pathogen removal from blood using margination.
Han Wei Hou,Han Wei Hou,Hiong Yap Gan,Hiong Yap Gan,Ali Asgar S. Bhagat,Leon D. Li,Chwee Teck Lim,Chwee Teck Lim,Jongyoon Han,Jongyoon Han +9 more
TL;DR: A simple microfluidic approach for intrinsic, non-specific removal of both microbes and inflammatory cellular components from whole blood, inspired by the invivo phenomenon of leukocyte margination is reported, which offers significant advantages including high throughput and label-free separation.
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Massively parallel concentration device for multiplexed immunoassays
TL;DR: Using multiplexed, successive-concentration enhanced detection in the device, it is shown that the dynamic range and reliability of the immunoassay can be significantly increased.