Evidence map›Paper›PMID 38013763›Full record

ArticleSensors & diagnostics2023

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

Rüya Meltem Sarıyer, Kirandeep Gill, Sarah H Needs, Daniel Hodge, Nuno M Reis, Chris I Jones, Alexander D Edwards

Open access · diamondAbstract read
In one paragraph

Article in Sensors & diagnostics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Rüya Meltem SarıyerReading School of Pharmacy, University of Reading Whiteknights Reading RG6 6UB UK r.sariyer@pgr.reading.ac.uk kkgill@uvic.ca s.h.needs@reading.ac.uk a.d.edwards@reading.ac.uk +44 (0)118 378 4253.ORCID https://orcid.org/0000-0002-2155-653X
Kirandeep GillReading School of Pharmacy, University of Reading Whiteknights Reading RG6 6UB UK r.sariyer@pgr.reading.ac.uk kkgill@uvic.ca s.h.needs@reading.ac.uk a.d.edwards@reading.ac.uk +44 (0)118 378 4253.ORCID https://orcid.org/0000-0002-5606-4738
Sarah H NeedsReading School of Pharmacy, University of Reading Whiteknights Reading RG6 6UB UK r.sariyer@pgr.reading.ac.uk kkgill@uvic.ca s.h.needs@reading.ac.uk a.d.edwards@reading.ac.uk +44 (0)118 378 4253.ORCID https://orcid.org/0000-0003-3407-9637
Daniel HodgeReading School of Biological Sciences, University of Reading Whiteknights Reading UK d.j.hodge@pgr.reading.ac.uk c.i.jones@reading.ac.uk.
Nuno M ReisDepartment of Chemical Engineering and Centre for Biosensors, Bioelectronics and Biodevices (CBio), University of Bath Bath BA2 7AY UK n.m.reis@bath.ac.uk.ORCID https://orcid.org/0000-0002-8706-6998
Chris I JonesReading School of Biological Sciences, University of Reading Whiteknights Reading UK d.j.hodge@pgr.reading.ac.uk c.i.jones@reading.ac.uk.
Alexander D EdwardsReading School of Pharmacy, University of Reading Whiteknights Reading RG6 6UB UK r.sariyer@pgr.reading.ac.uk kkgill@uvic.ca s.h.needs@reading.ac.uk a.d.edwards@reading.ac.uk +44 (0)118 378 4253.ORCID https://orcid.org/0000-0003-2369-989X
University of Reading · GBUniversity of Southampton · GBUniversity of Bath · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Identifiers

PMID38013763
PMCPMC10633108
OpenAlexW4387716043

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.