Assessment of fibrinolytic status in whole blood using a dielectric coagulometry microsensor

Biosens Bioelectron. 2022 Aug 15:210:114299. doi: 10.1016/j.bios.2022.114299. Epub 2022 Apr 26.

Abstract

Rapid assessment of the fibrinolytic status in whole blood at the point-of-care/point-of-injury (POC/POI) is clinically important to guide timely management of uncontrolled bleeding in patients suffering from hyperfibrinolysis after a traumatic injury. In this work, we present a three-dimensional, parallel-plate, capacitive sensor - termed ClotChip - that measures the temporal variation in the real part of blood dielectric permittivity at 1 MHz as the sample undergoes coagulation within a microfluidic channel with <10 μL of total volume. The ClotChip sensor features two distinct readout parameters, namely, lysis time (LT) and maximum lysis rate (MLR) that are shown to be sensitive to the fibrinolytic status in whole blood. Specifically, LT identifies the time that it takes from the onset of coagulation for the fibrin clot to mostly dissolve in the blood sample during fibrinolysis, whereas MLR captures the rate of fibrin clot lysis. Our findings are validated through correlative measurements with a rotational thromboelastometry (ROTEM) assay of clot viscoelasticity, qualitative/quantitative assessments of clot stability, and scanning electron microscope imaging of clot ultrastructural changes, all in a tissue plasminogen activator (tPA)-induced fibrinolytic environment. Moreover, we demonstrate the ClotChip sensor ability to detect the hemostatic rescue that occurs when the tPA-induced upregulated fibrinolysis is inhibited by addition of tranexamic acid (TXA) - a potent antifibrinolytic drug. This work demonstrates the potential of ClotChip as a diagnostic platform for rapid POC/POI assessment of fibrinolysis-related hemostatic abnormalities in whole blood to guide therapy.

Keywords: Dielectric coagulometry; Dielectric spectroscopy; Fibrinolysis monitoring; Microfluidics; Point-of-care diagnostics; Whole blood coagulation.

MeSH terms

  • Antifibrinolytic Agents* / pharmacology
  • Biosensing Techniques*
  • Fibrin
  • Fibrinolysis
  • Humans
  • Thrombosis*
  • Tissue Plasminogen Activator / pharmacology

Substances

  • Antifibrinolytic Agents
  • Fibrin
  • Tissue Plasminogen Activator