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A shear gradient-activated microfluidic device for automated monitoring of whole blood haemostasis and platelet function

Abhishek Jain, Amanda Graveline, Anna Waterhouse, Andyna Vernet, Robert Flaumenhaft and Donald E. Ingber ()
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Abhishek Jain: Wyss Institute for Biologically Inspired Engineering, Harvard University
Amanda Graveline: Wyss Institute for Biologically Inspired Engineering, Harvard University
Anna Waterhouse: Wyss Institute for Biologically Inspired Engineering, Harvard University
Andyna Vernet: Wyss Institute for Biologically Inspired Engineering, Harvard University
Robert Flaumenhaft: Beth Israel Deaconess Medical Center and Harvard Medical School
Donald E. Ingber: Wyss Institute for Biologically Inspired Engineering, Harvard University

Nature Communications, 2016, vol. 7, issue 1, 1-10

Abstract: Abstract Accurate assessment of blood haemostasis is essential for the management of patients who use extracorporeal devices, receive anticoagulation therapy or experience coagulopathies. However, current monitoring devices do not measure effects of haemodynamic forces that contribute significantly to platelet function and thrombus formation. Here we describe a microfluidic device that mimics a network of stenosed arteriolar vessels, permitting evaluation of blood clotting within small sample volumes under pathophysiological flow. By applying a clotting time analysis based on a phenomenological mathematical model of thrombus formation, coagulation and platelet function can be accurately measured in vitro in patient blood samples. When the device is integrated into an extracorporeal circuit in pig endotoxemia or heparin therapy models, it produces real-time readouts of alterations in coagulation ex vivo that are more reliable than standard clotting assays. Thus, this disposable device may be useful for personalized diagnostics and for real-time surveillance of antithrombotic therapy in clinic.

Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10176

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DOI: 10.1038/ncomms10176

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