Characterization of the phagocytic ability of white blood cells separated using a single curvature spiral microfluidic device.

Biomed Eng Lett

Department of Mechanical Engineering, BITS-Pilani, K K Birla Goa Campus, Goa, 403726 India.

Published: November 2024

AI Article Synopsis

  • This study introduces a microfluidic device designed to efficiently separate white blood cells (WBCs) from red blood cells (RBCs) for the Nitroblue Tetrazolium (NBT) bioassay, which measures phagocytic activity in cells.
  • The device successfully removes 99.99% of RBCs from WBC samples, improving the RBC to WBC ratio from 848:1 to 2:3, and is effective even at a hematocrit concentration of 1% blood.
  • The microfluidic device is easy to fabricate, cost-effective, and can process a single drop of blood in under 10 minutes, without the need for complex methods like RBC lysis or expensive

Article Abstract

Unlabelled: The present work describes a microfluidic device developed for separating white blood cells (WBCs) for the Nitroblue Tetrazolium (NBT) bioassay, which quantifies the phagocytic ability of cells. The NBT test requires a small number of phagocytic cells but is highly susceptible to the presence of red blood cells (RBCs). Our inertial microfluidic device can deliver a WBC sample by removing 99.99% of RBCs and subsequently reducing the ratio of RBC to WBC from 848:1 to 2:3. The microdevice operates on a relatively higher hematocrit concentration (1% Hct) of blood. Compared to conventional WBC separation methods, the microdevice's passive, label-free nature preserves the cell properties of the original sample. A single-turn spiral microfluidic device with a rectangular cross-section is simple to fabricate, cost-effective, and easy to operate. The reported microfluidic device requires only a single drop of whole blood (⁓20 µl) obtained via the finger prick method for efficient phagocytic analysis. Also, the microdevice reported in this study achieves WBC separation in under 10 min, omitting the need for RBC lysis, density gradient centrifugation, or expensive antibodies.

Supplementary Information: The online version contains supplementary material available at 10.1007/s13534-024-00414-y.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11502713PMC
http://dx.doi.org/10.1007/s13534-024-00414-yDOI Listing

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