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Abstract
The viscosity of biofluids such as blood and saliva can reflect an individual’s health conditions, and viscosity measurements are therefore considered in health monitoring and disease diagnosis. However, conventional viscometers can only handle a larger liquid volume beyond the quantity that can be extracted from a person. Though very effective, micro-sensors based on electrokinetic, ultrasonic, or other principles often have strict requirements for the supporting equipment and complicated procedures and signal processing. Sample contamination is always an important issue. In this paper, we report a microfluidic viscometer requiring a small volume of biosamples (<50 µL) and straightforward operation procedures. It is fabricated with low-cost and biocompatible polymeric materials as one-time-use devices, such that contamination is no longer the concern. It contains a suspending micromembrane located along a microchannel. Under a steady driving pressure, the membrane displacement is a function of viscosity of the liquid sample being tested. We derived a simple analytical relation and perform a simulation for converting the membrane displacement to the sample viscosity. We conducted experiments with liquids (water and mineral oil) with defined properties to verify such a relation. We further applied the micro-viscometer to measure bovine blood samples with different hematocrit levels. It can be concluded that the microfluidic viscometer has a high compatibility with a broad range of biomedical applications.
| Original language | English |
|---|---|
| Article number | 934 |
| Journal | Micromachines |
| Volume | 11 |
| Issue number | 10 |
| Online published | 14 Oct 2020 |
| DOIs | |
| Publication status | Published - Oct 2020 |
Research Keywords
- Microfluidic
- Sensor
- Viscosity
Publisher's Copyright Statement
- This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
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- 1 Finished
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GRF: Automation of a Viscoelasticity Microcytometer for High-Throughput Biomechanical Phenotyping of Floating Cancer Cells
LAM, H. W. R. (Principal Investigator / Project Coordinator)
1/09/20 → 28/02/25
Project: Research