Abstract

On-chip blood plasma separators using microfluidic channels are typically developed as disposable devices for short-term use only because blood cells tend to clog the microchannels, limiting their application in real-time and continuous systems. In this study, we propose an anti-clogging method. We applied dielectrophoresis to prevent microchannel clogging in a plasma separator that can be used over long periods for real-time and continuous monitoring. Prior to applying the anti-clogging method, the blood plasma separator stopped working after 4 h. In contrast, by manipulating the separator with the new anti-clogging method at a voltage of 20 V, it continued working in a long-term experiment for 12 h without performance deterioration or an increase in cell loss. Two critical performance parameters of the manipulated separator, the purity efficiency and the plasma yield, were 97.23 ± 5.43% and 38.95 ± 9.34%, respectively, at 20 V after 15 min. Interestingly, the two performance parameters did not decrease during the long-term experiment. Hence, the blood plasma separator with the anti-clogging method is an interesting device for use in real-time and continuous blood plasma separation systems because of its consistent performance and improved lifespan.

Highlights

  • When the cells start to attach to the branch channel wall, they reduce the channel diameter and increase the diameter difference between the main and the branch channel

  • To estimate the anti-clogging method, cell loss ηL was defined as where Ci, Co, and Cp is the original concentration of the blood cells at the inlet, the processed concentration at the blood outlet, and the concentration at the plasma product outlet, respectively

  • Unwanted clogging by blood cell adhesion to the microchannel walls has been blocking any progress in this field

Read more

Summary

Introduction

The fluid flow is accelerated where the microchannel splits into more than two narrow branch channels because of the difference in channel dimensions. Blood cells, for example red blood cells (RBCs), white blood cells (WBCs), and platelets (PLTs), approach the microchannel wall because of the change in fluid flow. The cell attachment to the channel wall surface is dramatically accelerated and by cell-to-surface attachment and by cell-to-cell attachment (aggregation), causing microchannel clogging. The adhesion of a single cell to the microchannel wall initiates aggregation and clogging

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call