PUBLICATION

A Rapid Capillary-Pressure Driven Micro-Channel to Demonstrate Newtonian Fluid Behavior of Zebrafish Blood at High Shear Rates

Authors
Lee, J., Chou, T.C., Kang, D., Kang, H., Chen, J., Baek, K.I., Wang, W., Ding, Y., Carlo, D.D., Tai, Y.C., Hsiai, T.K.
ID
ZDB-PUB-170518-4
Date
2017
Source
Scientific Reports   7: 1980 (Journal)
Registered Authors
Keywords
Animal physiology, Biomedical engineering
MeSH Terms
  • Animals
  • Biomechanical Phenomena
  • Blood Viscosity
  • Hemodynamics*
  • Hemorheology*
  • Microfluidics/methods
  • Reproducibility of Results
  • Stress, Mechanical
  • Zebrafish/physiology*
PubMed
28512313 Full text @ Sci. Rep.
Abstract
Blood viscosity provides the rheological basis to elucidate shear stress underlying developmental cardiac mechanics and physiology. Zebrafish is a high throughput model for developmental biology, forward-genetics, and drug discovery. The micro-scale posed an experimental challenge to measure blood viscosity. To address this challenge, a microfluidic viscometer driven by surface tension was developed to reduce the sample volume required (3μL) for rapid (<2 min) and continuous viscosity measurement. By fitting the power-law fluid model to the travel distance of blood through the micro-channel as a function of time and channel configuration, the experimentally acquired blood viscosity was compared with a vacuum-driven capillary viscometer at high shear rates (>500 s-1), at which the power law exponent (n) of zebrafish blood was nearly 1 behaving as a Newtonian fluid. The measured values of whole blood from the micro-channel (4.17cP) and the vacuum method (4.22cP) at 500 s-1 were closely correlated at 27 °C. A calibration curve was established for viscosity as a function of hematocrits to predict a rise and fall in viscosity during embryonic development. Thus, our rapid capillary pressure-driven micro-channel revealed the Newtonian fluid behavior of zebrafish blood at high shear rates and the dynamic viscosity during development.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping