Abstract

Air compliance has been used effectively to stabilize fluidic instability resulting from a syringe pump. It has also been employed to measure blood viscosity under constant shearing flows. However, due to a longer time delay, it is difficult to quantify the aggregation of red blood cells (RBCs) or blood viscoelasticity. To quantify the mechanical properties of blood samples (blood viscosity, RBC aggregation, and viscoelasticity) effectively, it is necessary to quantify contributions of air compliance to dynamic blood flows in microfluidic channels. In this study, the effect of air compliance on measurement of blood mechanical properties was experimentally quantified with respect to the air cavity in two driving syringes. Under periodic on–off blood flows, three mechanical properties of blood samples were sequentially obtained by quantifying microscopic image intensity (<I>) and interface (α) in a co-flowing channel. Based on a differential equation derived with a fluid circuit model, the time constant was obtained by analyzing the temporal variations of β = 1/(1–α). According to experimental results, the time constant significantly decreased by securing the air cavity in a reference fluid syringe (~0.1 mL). However, the time constant increased substantially by securing the air cavity in a blood sample syringe (~0.1 mL). Given that the air cavity in the blood sample syringe significantly contributed to delaying transient behaviors of blood flows, it hindered the quantification of RBC aggregation and blood viscoelasticity. In addition, it was impossible to obtain the viscosity and time constant when the blood flow rate was not available. Thus, to measure the three aforementioned mechanical properties of blood samples effectively, the air cavity in the blood sample syringe must be minimized (Vair, R = 0). Concerning the air cavity in the reference fluid syringe, it must be sufficiently secured about Vair, R = 0.1 mL for regulating fluidic instability because it does not affect dynamic blood flows.

Highlights

  • A blood sample is composed of cells (i.e., red blood cells (RBCs), white blood cells, and platelets) and plasma

  • We inferred that the air cavity increased or decreased the time constant depending on whether it existed in the reference fluid syringe or the blood sample syringe

  • Based on a differential equation derived with a fluid circuit model, the time constant was obtained by analyzing temporal variations of β = 1/(1–α)

Read more

Summary

Introduction

A blood sample is composed of cells (i.e., red blood cells (RBCs), white blood cells, and platelets) and plasma. In contrast with bulky viscometers [5,6], a microfluidic-based device can provide numerous advantages including fast response, small volume consumption, and disposability. Such devices are widely employed for quantifying mechanical properties of blood samples (viscosity [7,8,9,10], RBC aggregation [11,12,13,14], RBC deformability [3,15], and hematocrit (Hct) [16,17,18]). A microfluidic device has been employed to separate RBCs or tumor cells from whole blood sample [19,20,21]

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