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Time- and distance-resolved robotic imaging of fluid flow in vertical microfluidic strips: a new technique for quantitative, multiparameter measurement of global haemostasis

Time- and distance-resolved robotic imaging of fluid flow in vertical microfluidic strips: a new technique for quantitative, multiparameter measurement of global haemostasis
Time- and distance-resolved robotic imaging of fluid flow in vertical microfluidic strips: a new technique for quantitative, multiparameter measurement of global haemostasis
Measuring the complex processes of blood coagulation, haemostasis and thrombosis that are central to cardiovascular health and disease typically requires a choice between high-resolution low-throughput laboratory assays, or simpler less quantitative tests. We propose combining mass-produced microfluidic devices with open-source robotic instrumentation to enable rapid development of affordable and portable, yet high-throughput and performance haematological testing. A time- and distance-resolved fluid flow analysis by Raspberry Pi imaging integrated with controlled sample addition and illumination, enabled simultaneous tracking of capillary rise in 120 individual capillaries (∼160, 200 or 270 μm internal diameter), in 12 parallel disposable devices. We found time-resolved tracking of capillary rise in each individual microcapillary provides quantitative information about fluid properties and most importantly enables quantitation of dynamic changes in these properties following stimulation. Fluid properties were derived from flow kinetics using a pressure balance model validated with glycerol–water mixtures and blood components. Time-resolved imaging revealed fluid properties that were harder to determine from a single endpoint image or equilibrium analysis alone. Surprisingly, instantaneous superficial fluid velocity during capillary rise was found to be largely independent of capillary diameter at initial time points. We tested if blood function could be measured dynamically by stimulating blood with thrombin to trigger activation of global haemostasis. Thrombin stimulation slowed vertical fluid velocity consistent with a dynamic increase in viscosity. The dynamics were concentration-dependent, with highest doses reducing flow velocity faster (within 10 s) than lower doses (10–30 s). This open-source imaging instrumentation expands the capability of affordable microfluidic devices for haematological testing, towards high-throughput multi-parameter blood analysis needed to understand and improve cardiovascular health.

2635-0998
1623-1637
Sarıyer, Rüya Meltem
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Gill, Kirandeep
730b1b27-d75d-43c6-b38a-0b90daa5adba
Needs, Sarah H.
24425556-99e3-4c46-995b-2381776a0a38
Hodge, Daniel
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Reis, Nuno M.
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Jones, Chris I.
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Edwards, Alexander D.
bc3d9b93-a533-4144-937b-c673d0a28879
Sarıyer, Rüya Meltem
12396c8e-9415-4be0-958b-bb419f3aef24
Gill, Kirandeep
730b1b27-d75d-43c6-b38a-0b90daa5adba
Needs, Sarah H.
24425556-99e3-4c46-995b-2381776a0a38
Hodge, Daniel
a8b05703-e8c8-441f-84af-aed1f05b55b0
Reis, Nuno M.
898670e7-a794-4302-81ce-03a4d86cc17a
Jones, Chris I.
8ccc6ae4-311c-4e90-b4e6-ee4536fa49bc
Edwards, Alexander D.
bc3d9b93-a533-4144-937b-c673d0a28879

Sarıyer, Rüya Meltem, Gill, Kirandeep, Needs, Sarah H., Hodge, Daniel, Reis, Nuno M., Jones, Chris I. and Edwards, Alexander D. (2023) Time- and distance-resolved robotic imaging of fluid flow in vertical microfluidic strips: a new technique for quantitative, multiparameter measurement of global haemostasis. Sensors & Diagnostics, 2, 1623-1637. (doi:10.1039/D3SD00162H).

Record type: Article

Abstract

Measuring the complex processes of blood coagulation, haemostasis and thrombosis that are central to cardiovascular health and disease typically requires a choice between high-resolution low-throughput laboratory assays, or simpler less quantitative tests. We propose combining mass-produced microfluidic devices with open-source robotic instrumentation to enable rapid development of affordable and portable, yet high-throughput and performance haematological testing. A time- and distance-resolved fluid flow analysis by Raspberry Pi imaging integrated with controlled sample addition and illumination, enabled simultaneous tracking of capillary rise in 120 individual capillaries (∼160, 200 or 270 μm internal diameter), in 12 parallel disposable devices. We found time-resolved tracking of capillary rise in each individual microcapillary provides quantitative information about fluid properties and most importantly enables quantitation of dynamic changes in these properties following stimulation. Fluid properties were derived from flow kinetics using a pressure balance model validated with glycerol–water mixtures and blood components. Time-resolved imaging revealed fluid properties that were harder to determine from a single endpoint image or equilibrium analysis alone. Surprisingly, instantaneous superficial fluid velocity during capillary rise was found to be largely independent of capillary diameter at initial time points. We tested if blood function could be measured dynamically by stimulating blood with thrombin to trigger activation of global haemostasis. Thrombin stimulation slowed vertical fluid velocity consistent with a dynamic increase in viscosity. The dynamics were concentration-dependent, with highest doses reducing flow velocity faster (within 10 s) than lower doses (10–30 s). This open-source imaging instrumentation expands the capability of affordable microfluidic devices for haematological testing, towards high-throughput multi-parameter blood analysis needed to understand and improve cardiovascular health.

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Accepted/In Press date: 26 September 2023
Published date: 17 October 2023

Identifiers

Local EPrints ID: 494769
URI: http://eprints.soton.ac.uk/id/eprint/494769
ISSN: 2635-0998
PURE UUID: 6f494532-63e4-44ac-982f-239e7b639bb2
ORCID for Alexander D. Edwards: ORCID iD orcid.org/0000-0003-2369-989X

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Date deposited: 15 Oct 2024 16:44
Last modified: 16 Oct 2024 02:12

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Contributors

Author: Rüya Meltem Sarıyer
Author: Kirandeep Gill
Author: Sarah H. Needs
Author: Daniel Hodge
Author: Nuno M. Reis
Author: Chris I. Jones
Author: Alexander D. Edwards ORCID iD

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